SE Anan ee han a tt Be ee ee ee ee ee ree nr aT oe aT enh a ere ae: Saag Speeinieeeeae ea eee ee Cre : . 5 = stay = mee a eae cen: Se ee lS ae TL Ee Oe TOTO = en neque a ns 5 a ! ¥e : ae . : oars a Lae ee e~ : Peiaiaseet esos :- See andl . : em ‘i = es naan he S - : . “ — ~—* = 7 3 - . teat i ad = - oo 7 7 elie ; : ae a 7 7 , ar nae a a - al ‘omni ote ee ‘ii F Bees 4 Fil LYE = — a ae es “i iD a Se Leen (a “4 - ; — i 2 ne oats ie m a) Se Et a , eo : " hal : | Pran Chiy We Saieincipr. | vy | 7 vi a x 1” , 7 i Bi r ‘i 7 a oft | i SMITHSONIAN MISCELLANEOUS COLLECTIONS VOL. 88 IS A VALUABLE MEMBER OF SOCIETY WHO, BY HIS OBSERVATIONS, RESEARCHES, ““ EVERY MAN AND EXPERIMENTS, PROCURES KNOWLEDGE FOR MEN -——-SMITHSON (PUBLICATION 3240) CITY OF WASHINGTON PUBLISHED BY THE SMITHSONIAN INSTITUTION 1934 The Lord Baltimore Press BALTIMORE, MD., U. S. A. ADVERTISEMENT The present series, entitled “ Smithsonian Miscellaneous Collec- tions,’ is intended to embrace all the octavo publications of the Institution, except the Annual Report. Its scope is not limited, and the volumes thus far issued relate to nearly every branch of science. Among these various subjects zoology, bibliography, geology, mineralogy, anthropology, and astrophysics have predominated. The Institution also publishes a quarto series entitled ‘* Smith- sonian Contributions to Knowledge.” It consists of memoirs based on extended original investigations, which have resulted in important additions to knowledge. CiGeABBOT. Secretary of the Sinithsonian Institution. (iti) Lopes Veh CONTENTS Fow.e, Frepertck E. Smithsonian Physical Tables. Eighth revised edition. 782 pp., Sept. 22, 1933. (Publ. 3171.) (Whole volume. ) (vy) le ny ' 7 yee SMITHSONIAN MISCELLANEOUS COLLECTIONS VOLUME 88 (WHOLE VOLUME) SMITHSONIAN ev ole AL TABLES FIGH THA REVISED EDITION PREPARED BY BPREDERICK (Es. POWIiis ASSOCIATE PHYSICIST, SMITHSONIAN ASTROPHYSICAL OBSERVATORY ory 800g ene! (PUBLICATION 3171) CITY OF WASHINGTON PUBLISHED BY THE SMITHSONIAN INSTITUTION 1933 The Lord Baltimore Press BALTIMORE, MD., U. S. A. ADVERTISEMENT In connection with the system of meteorological observations established by the Smithsonian Institution about 1850, a series of meteorological tables was compiled by Dr. Arnold Guyot, at the request of Secretary Henry, and the first edition was published in 1852. Though primarily designed for meteoro- logical observers reporting to the Smithsonian Institution, the tables were so widely used by physicists that it seemed desirable to recast the work entirely. It was decided to publish three sets of tables, each representative of the latest knowledge in its field, and independent of one another, but forming a homo- geneous series. The first of the new series, Meteorological Tables, was published in 1893, the second, Geographical Tables, in 1894, and the third, Physical Tables, in 1896. In 1909 and 1922, respectively, two further volumes were added, so that the series now comprises: Smithsonian Meteorological Tables, Smithsonian Geographical Tables, Smithsonian Physical Tables, Smithsonian Mathematical Tables, Smithsonian Mathematical Formulae. The 14 years which had elapsed in 1910 since the publication of the first edition of the Physical Tables, prepared by Prof. Thomas Gray, made im- perative a radical revision for the fifth and sixth revised editions published in tg10 and 1914. The latter edition was reprinted thrice. The seventh revision was issued in 1919 and was reprinted thrice. The present eighth edition results from a further extensive revision. Inconsistencies that will be noted in minor points of style, such as abbrevia- tions, etc., arise from the fact that many of the tables are printed from electro- type plates; to change them to agree with present usages would involve too great expense. CHARLES G. ABBOT, Secretary, Smithsonian Institution. March, 1932. PREPACEIV®) ctu REVISED EP DiTI@nN The present edition of the Smithsonian Physical Tabies entails a consider- able enlargement. Besides the insertion of new data in the older tables, about 270 new ones have been added. Their scope has been further broadened to include many new tables relating to astrophysics, geophysics, meteorology, geochemistry, atmospheric electricity, wireless, molecular and atomic data, ete. Many suggestions and data have been received: from the Bureau of Stand- ards, the Coast and Geodetic Survey (magnetic data), the Geophysical Labora- tory, Naval Research Laboratory, Department of Terrestrial Magnetism, Harvard College Observatory, Eastman Kodak Co. (photographic data), National Research Council (International Critical Tables); from Messrs. Adams, White (Geophysical Laboratory), R. T. Birge, Briggs, Dellinger, Deming (Bureau of Chemistry and Soils), Dorsey (I. C. T.), Fleming, For- sythe, Hulburt, Lovejoy and Loomis (Eastman Kodak Co.), Kimball, Menzel, van Maanen, Russell, Shapley, St. John, Wells, Wherry, and many others whose names generally will be found with the corresponding data furnished. To all these we are indebted. The changes in the domain of physics and allied branches have been so radical and extensive that it has been difficult to do justice to the advances. Further, it has been deemed essential to keep this volume in handy size, referring the reader to the more extensive International Critical Tables or to Landolt-Bornstein’s Physikalisch-chemische Tabellen for more extensive data. It has been inadvisable to delay the tables for revision in many places. We will be grateful for criticisms, the notification of errors, and new data. FREDERICK EUGENE FowWLE. ASTROPHYSICAL OBSERVATORY, SMITHSONIAN INSTITUTION, March, 1932. PABEEZOn CONTENDS PRUEELOCIUIC LL TIe ear temo Ue Uni R DT ot fe tore Woe 4. ut a erica: aba Tebre . oe RU ISM TMC ASTIRCIITetita me wes ecules oc pre se oar ace les duels eect eieternhs, ERC Fundamental units, xxxi; derived units, xxxii. Conversion factors and dimensional formulae. ... . sca tLe OTE Geometrical and mechanical units, xxxiv; heat aie XXXVI; electric and magnetic units, xxxvii; electrostatic system, Xxxviii; electromagnetic system, Xxxix. Fundamental standards . : Standard of length, xlii; semdard of: mass, aaa andar af nie. xlii; standard of temperature, xlii. Numerically different systems of units ; Proposed Syoiems Of units (Pable, 1), xin; Ennssion ee xliii; “ practical ” electromagnetic system, xliv; the inter- national electric units, xliv. The standards of the international electrical units . . Resistance, xlvi: Mercury standards, xlvi; secondary standards: xlvii; resistance standards in practice, xlvii; absolute ohm, xvii. Current, xlviii: The silver voltameter, xlviii; resistance stand- ards used in current measurements, xlix; absolute ampere, xlix. Electromotive force, xlix: International volt, xlix; Weston normal cell, xlix; Weston portable cell, li; absolute and semi-absolute volt, li. Quantity of electricity, lii: Standards, lii. Capacity, lii. Inductance, lii: Inductance standards, lii. Power and energy, liii: Standards and measurements, lii1. Magnetic units : . The ordinary and the ampere- uid magnetic units 6 Table II), fe TABLE 1. Spelling and abbreviations of common units of weight and measure. 2. Fundamental and derived units, conversion factors (a) Fundamental units (b) Derived units Mat hfe 3. Tables for converting U. S. weights ane measures : (1) Customary to metric .(2) Metric to customary : 4. Miscellaneous equivalents of U. S. and metric iaeatae ea measures, sll . xin . xivi v1 on 35: CONTENTS Equivalents of metric and British imperial weights and measures: (1) Metric to imperial (2) Metric to imperial, multiples . (3) Imperial to metric (4) Imperial to metric, multiples MATHEMATICAL TABLES Derivatives and Ea 3 Series Nie Mathematical constants . Seer ‘ : Reciprocals, squares, cubes, square roots of meter aamabere Logarithms [4-place, 1000-2000 | i ee Antilogarithms [| 4- ries : *s [eae Saas oeeoes I penal : Circular (trigonometric) functions [arguments (° 4] ; i r : [ : Gatianan Logarithmic factorials, !, 7 =1 to 100 . Hyperbolic functions . Factorials [1 to 20] Exponential functions ; : Values of e® and e* and their logarithms. 66 ‘e “c (eC ee 6c ““ “6 e4 Cans ‘6 66 ‘“ ‘6 Va. 6 ME pie Gc 6 ‘“ Cua” e 5 ee ce ve ee er “ec e— ee ce “e | fractional | argument /iv 4/7 Least squares: Probability integral, ee oe oe oe ee Values of 0.6745V1/(n—1) “ 0.6745 V1/n(n—1) “0.8453 V1/n(n—1) “ 08453{41/nVn—1h ( Formulae ) : Diffusion integral, inverse poke inteoral ‘ “ce “ce “ce ee “e “ce ce 6é ce “ce oe Exponential integral, E7(+), ine (e“/u)du Gamma function, logarithms, m between 1 and 2 Zonal spherical harmonics [first seven, 9=0° to6=go°| . Cylindrical harmonics, oth and tst orders | 6-place values, + =0 to Al % sei? A | 4-place values, r=4to 15] (a) 1st 10 roots (Rm) of Jo(4)=0; Ji(Rm) (b) “6 15 “ec of 1,(4)= 22) =o Notes, general formulae of Bessel’s functions 10 Te 12 13 14 15 24 26 28 30 a7 40 4I 47 48 54 59 55 CONTENTS T 38. Elliptic integrals: Values of | 2 (1—sin?@ sin? 6)+!d@ , -O 39. Moments of inertia, radii of gyration, and corresponding weights . 40. Al. 2) 43- 44. 45. 46. 47. 48. 49. 50. Ble 52. 53: 54. 55- 56. 57- BrrGe’s PHYSICAL CONSTANTS Probable values of the general physical constants . The velocity of light in vacuum (c) [2.99796 cm/sec. i Newtonian constant of gravitation (G) [6.664 dyne cm?/ o] Mean density of the earth [5.522 ae Relation liter to dm* [1.000027 dm*] . Normal mole volume of ideal gas [Ry/, 22.41 ; 5 i Jeaote) Ratio international to absolute electrical units . Atomic weights of certain elements . Ep ore iie iN, At p. 62: 1 C, p83; Cin ea! Normal atmosphere, 4, [1.013249 x 10° dyne/cm? | Absolute temperature of ice-point (7,) [273.18° K.| Mechanical equivalent of heat (J) ; electrical, (/’) The faraday (F) [96489 abs. coul. | Electronic charge (e) [4.770 X 10°7° abs. e.s.u. Va Specific charge of electron (e/1) Planck constant (h) [6.547 x 10-7’ erg/sec. | Fundamental constants, Birge ROWwers! Ob (c, hye, /c-*. . Additional constants used by Binge in aancesion ane Table 40 . Miscellaneous derived physical constants, Birge . Volume of glass vessel from weight of its volume of Hg or H.O . Reductions of weighings in air to vacuo . Reductions of densities in air to vacuo . MECHANICAL PROPERTIES Introduction and definitions . ye oer care eo Ferrous metals and alloys: Iron and iron alloys . ¥ " : Carbon steels Heat treatments . Alloy steels . , Steel wire—specification males a Tf is ro les experimental values . Semi-steel “ec “cc “ce “ “ec “cc ce Plow-steel rope [specification values | 58. Aluminum Steel-wire rope—specification values. experimental values. vil lie Ww GOINT NT NaN Sy e NJ Ul wn UL tN 103 103 104 105 108 109 109 TIO Il I12 I12 rie I1l4 114 114 Drs an 115 116 Vill 39: 60. 61. 62. 63. 64. 65. 66. 68. 69. 70. od 2. 73: Ji. CONTENTS Aluminum sheet: (a) Experimental values (b) Specification values . Aluminum alloys Copper : ra ae rolled 3 pene ont values ; wire |hard-drawn |—specification maine: : , medium hard-drawn . Copper wire—soft or annealed % PlALES esta ey eae alloys [nomenclature] . “c“ “cc “ec “ce “e oe “cc : Three (or more) components . Miscellaneous metals and alloys . “ec ce “ce ee Cement and concrete: (a) Cement ..... (b) Cement and cement ese (2) Concrete: hea Stone and clay products: (a) American building byanes ‘ : Copper-zine or peassens copper-tin or Gronsee ‘ (a) Tungsten and zinc . (b) White metal bearing alloys (6) Bavarian building stones . (c) American building bricks . (d) Brick piers, terra-cotta block piers. (e) Various bricks Rubber and leather: (a) Rubber, sheet (>) Leather beltine. < Manilla rope vk Hardwoods grown in wu S. “(onettic units) : Conifers eet bes i Hardwoods “ “ “ “ (English units) Conifers “ec ee ee “ee “ce “e Rigidity modulus Variation of the rigidity modulus with the demperauire 5 Interior friction at low temperatures . Hardness . ‘ Relative hardness a thie! dlemients (Gneaceyae Poisson’s ratio ete of crystals Fbnetavlaell . [numerical results| . Wise hesnien, ee eae metal crystals, etaaic esneeiate ce “ce “ce . “ec “ec “ee cubic Relations between T, p, v, and wt. of gases [theory ] Values of factor P= (273.1/T )ipv . : Relative gas volumes at various pressures . ee Sono + lO . MZ ; rs Pee bi tc: 5 ES 5 TG) . TO , 1r9 AIG » 120 IGE A aes 125 pl 26 126 § 27 ~ £28 . 128 - £29 129 29 = 130 = LZ0 Sei = 32 - 133 - 134 - 135 =, 136 ; £320 - 137 >) 37 - 137 - 137 - 138 - 139 . 140 linear compressibility 140 140 = TA : 142 .. 142 106. 107. 108. 109. 110. Tn: E12: 113. 114. ELS: 116. EL. 118. 119. 120. Er, 522: 123. 124. 125. 126. 127%, 128. 129. 130. 03T. 132. CONTENTS ix Correcting factors: Saturated gas volume to volume at 760 mm, 0° C. 143 Compressibility of gases: At ordinary et 144 i Menai * low 144 “ ele een OMatienIN atid hit ne 145 ss emi EL CVIEN ey 4) sc Beane 145 = en en @atbonr dioxide Sa AS es «_“ ~ Physical properties of eames neaeen 146 fe So) Under hich presstiresie. 147 Gage pressure to atmospheres (absolute) . eine 147 Relation between p, T, and v, sulphur dicside ged 5 148 s sg be sammonias . . 148 Volume of gases: Values of 1+ one sh Sleuh opimenie ; 149 (a) For values of ¢t between 0° and 10° C Ey OLE: steps , 149 (b) Logs for ¢ between —49° and +399° C by 1° steps . . 150 (c) For values of t between —go° and ee C by 10° steps. 152 (d) Logs for t between 400° and 1990° C by 10° steps . 153 oe of liquids Bikg 154 and thermal expansion a pettoleans oils 155 es of solids 156 . “ crystals 157 DENSITIES Specific gravities corresponding to the Baumé scale . . . . . . . 158 Degrees A. P. I. corresponding to specific gravities at 60° /60° F eee Density of the elements, liquid or solid 159 ‘s ‘“ different kinds of wood . 161 : ‘““ various solids . 162 i me v2 alloys... 163 sy “some foreign woods . : 163 - “various natural and artificial Peale ‘ 164 4 “liquids . s ore hari es 165 - “pure water free fone anenGas Lomi ae 166 Volume of water free from air, 0° to 36° C . 167 Density and volume of water, —10° to +250° C 168 + - i mercury, —10° to a E 169 : of aqueous solutions ; 170 - “mixtures of ethyl alcohol atid water . 172 cs “aqueous methyl alcohol, cane sugar, sulphuric Hoe a Si eliget Re “cane sugar solutions, Brix and Baumé degrees . 175 a ey eases ‘ 170 i moist \att: h/'760, h fem I os 9 177 iE uae “log h/760, h from 80 to 860. 177 o eG “values of 0.378¢ 179 Maintenance of air at definite humidities . «L7@ Pressure of columns of mercury and water . . 180 ie 134. 15. 130. 17: 138. 139. 140. 41. 142. 143. 144. 145. 146. LAE 148. 140. 50. Toye 152: ges 154. 155. 156. 157. 158. 150. 160. 101. 162. nOZ 104. 165. 166. 167. 168. CONTENTS BAROMETRIC TABLES Reduction a barometric height to standard temperature 181 ‘ barometer to standard gravity, free-air altitude oa 182 ‘ Pe . oe ‘metric measures 183 ‘ - * ee “English measures 185 Correction of the barometer for capillarity . 187 Volume of mercury meniscus in mm* 187 Pressures and the boiling point of water: (a) Metric units . 188 (b) English units : 188 Determination of heights by the poramees 5 189 ACOUSTICS Velocity of sound in solids 190 : oi | ae Abe : 190 rs “ «© liquids and gases IQI Musical scales: Data for middle octave . ; : 192 as : Notes needed to transpose to other seiles - 1g2 Fundamental tone, harmonics, nearest tone of equal-tempered scale. 193 ihesbelvand: theydecihely scars 193 Loudness levels of various noises . 193 Peak power in watts of musical instruments Goninon 193 Relative strength of partials, various musical instruments . 194 Miscellaneous sound data. . 194 Audibility as dependent on sound pressure oad Heliteney 194 SECC en. can oll cclisyen vem Ese eke 195 Characteristic resonance values’ for apoken Howls : 195 Speech power (Fletcher ) 195 Phonetic powers, average conversation 195 AERODYNAMICS Velocity pressure at different air speeds 196 Corrections to Robinson cup anemometers 197 Resistance coefficient for thin flat plates normal to wind 198 Forces on thin flat plates at angles to wind 199 Forces on nonrotating circular cylinders . 4200 mf “spheres . + 2201 i * miscellaneous panties . 201 ¥ “cylinders 4 (202 Skin “friction:\\.." < fe. cs 4? aa se ee » 202 MrictiOr ~.... 9,472 Ls Guta AS es, cea “204: Bab ricants i 1.1 Gig chess Woe Cait ne aeeee ge st Rn . 204 eGbricants: for cutting toolse- act enone ame one . 204 169. 170. Ul M72: 73: 174. 175. nO: “e “ce ce ce ce “ce “cc “ec alcohol-water mixtures (temperature Pesan) and density of sucrose in aqueous solution 6c é CONTENTS VISCOSITY BEES of fluids and solids . water in centipoises (temperature variation) . * glycerol “ “cc of organic liquids . : ae Fluidities of gasolines and kerosene (eauipenaniiee a Acitioui) ee “ce (20° C) castor oil (temperature variation ) tb tb bd S) ©). Nm oun 177. Pressure effect on viscosity of pure liquids 178. Viscosity of miscellaneous liquids : Py le, 179. Specific viscosity of solutions (density and ean nerattire Na. 180. = sd $$ (various concentrations, 25° C) Tele \VAISCOSIty-OL gases and VapOrs.. 2 = fs sa Gs eve 182. i “« “ ; Variation with pressure ana eriperatare 183. Diffusion of an aqueous solution into pure water . oe “cc 184. MAPORGH Tears ae. feu BeBe ed en N25 , coefficients of, for various gases and vapors 185. 5a 186. s of metals into metals . . . Cite as 187. Solubility of inorganic salts in water (etaneriture ehetiow) 188. s “a few organic salts in water (temperature variation ) 189. x “gases in water (temperature variation) 190. “ , change of, produced by uniform pressure 191. Commonly used organic solvents, boiling points fae se NbSOnpuoMmOmeases My MQUIGS) 0 4.) 2 ag) ne eh 193. Capillarity and surface tension: Water and alcohol in moist air 194. ‘ * y Miscellaneous liquids in air 195. . % Solutions of salts in water 196. Surface tension of liquids cin a pn 197. cs “« “at solidifying point VAPOR PRESSURE 198. Vapor pressure and rate of evaporation 199. - * of elements . 200. F is * organic liquids 201. ri at low temperatures 202. ;, cS of ethyl alcohol . . 203. as “methyl alcohol . . . 204. > 2 (a) carbon disulphide . (b) chlorobenzene (c) bromobenzene (d) aniline . (e) methyl salicylate (f) bromonaphthalene (g) mercury . . bo b&b Ww WY Wb Oo b&b Ww Wb WN MS) TPS) Asi ey ©) to to tN to LS) w X11 CONTENTS 205... Vapor pressure of solutions of saltsin water...) sees es, 280 206. Pressure of saturated aqueous vapor over ice, low temperatures . . 232 207. > < i. o i “water, low temperatures. 232 208 “ee ce ‘ce “ce &é 6e “ec Oo to 374° & 232 209. Weight in grams of a cubic meter of saturated aqueous vapor . . . 234 “ce “e = cc “ce “ce “e “ce 6é 210. grains foot We 211. Pressure of aqueous vapor in une atmosphere: Various altitudes . 234 212. , i : iy ee 2 Sede Velen tain oos 213. Relative humidity, vapor pressure and dry temperature . . . . . 236 214. % a wet and. dry; thermometers, 4). i..6 4. eee ego THERMOMETRY 215; «The anternational temperatune scale gv. sement en ne ee a 210. Recommended: procedure fcr calibration) =.) sa) eee eee Pathe The standard platinum resistance thermometer. . . . . . . 242 218. Whe standard thermocouples =.) care eee et ie eee 219. Secondary calibration points ... . yaar eae 220. Directions for use of standard iictnoclement canines tions ee ae 221. Standard calibration curve for Pt-PtRh (10%Rh) thermoelement . 245 222. w . “© Cu-constantan thermoelement . . . 245 223: = * PST ate ij =, below,o" (C2246 224. Melting points of some purified salts, 400° to 1300° C. . . . . . 246 225. Standard calibration curve for chromel-alumel thermoelement . . 247 220) pticalpyTOMetny ius lowe urcpeepee see 4248 227. Correction for temperature of micreneel heerorernetes hve 2 ye 240 226. Stemcorrection for centiorade thermometers): ae fen eer 229. Reduction of gas thermometers to eae seate a vofulsly ors, PRO) 230. Practical thermoelectric scales (comparisons) . . . icy eo 231. Temperature differences between I. T. S. and various oldee seates 250 232. Cotiversion factors for units of work = 2 2 2 2 > =9 250 233. English and American horsepower at various altitudes and atiiudes: 251 234.5 Noniammable liquids for cryostats: (11.0. bea eet eee) eee MELTING AND BoILinG Points 235. Melting and boiling points of the chemical elements. . .... . 252 236. Effect a pressurevon melting “point 7.085 ee. 9 ee eee 227. - y hreezing. pomt of water... ns SeeeesG 238. aia ih DOLE PoInth et AINE oie ee se ee 239. Densities and melting and boiling points of inorganic compounds . 254 240. t ‘i i - i> organic e . 256 (a) Paraffin series .. . he BEAL ea ee eS (6) Olefines or the sthyléne ls SEriesy {42s 2 A ee ee Ce). Acetylene series tree ream “O02... ea ee eee 241. 242. 243. 244. 245. 246. 247. 248. 249. 250. 251. 252. 252: 254. 255. 250. 257: 258. 259. 260. 261. 262. 263. 264. 265. 266. 267. 268. 270. B7K: O72: 2273. CONTENTS Xili (d) Monatomic alcohols 257 (e) Alcoholic ethers “257 (f) Ethyl ethers . 257 (g) Miscellaneous i 250 Melting point of mixtures of metals : i - 2256 ? “ “alloys of lead, tin, and bismuth . . 259 * “© Jow-melting-point alloys . - 250 cs “© some refractory substances . 260 Enantistropic inversions in crystals ; 261 Transformation and melting temperatures of einer: i eutectic’ 266 Lowering of freezing points by salts in solution . : 5 267, Rise of boiling point eae by salts dissolved in water . ; 1260 Freezin@ mixtures; ~ <<. - Ae : | 270 Critical temperatures, pressures, and denenies oe gases . 27 THERMAL CONDUCTIVITIES Thermal oe of metals and alloys . han 272 s ‘““ insulators at high temperatures . : 273 4 = “various substances . $273 i e “insulating materials 2 274 - f “various insulators 276 - “water and salt solutions . “1270 s a “organic liquids 297. . - peta SCShay wenn 277. DDikiiSIVIteS. 2.0 a). Bi eeheyil eho Lie 7 ae ey, Thermal conden enauits pressure ences : 278 The unit of thermal resistance—the fourier . - 279 Factors to reduce heat flow in fouriers to other units . . 279 Conversion factors between units of current density of heat sent = 279 Thermal resistivities in fouriers . AiezG) Anti-freezing solutions (for automobile radiators, etc.) . 0279 EXPANSION COEFFICIENTS Linear expansion of the elements . nan: . 280 a cs “miscellaneous substances . 28% Cubical expansion of solids . =) 202 e - ** liquids 7/283 Thermal expansion of gases . - 204 SPECIFIC HEATS Specific heat of the chemical elements . = 205 Formulae for true specific heats . : A es 207 Heat capacities, true and mean specific heats, fatent heats at Cheon . 288 283. 284. 285. 2806. 287. 288. 289. 290. 291. 292. 293. 204. 205. 296. 207. 307. 308. CONTENTS Atomic heats and specific heats (50° K.), atomic volumes, elements. 289 Specific heat of various, solidS) Stee ees eae e200 ss ** water and of mefeury: Guaen cy ceo) 200 i “© various liquids Succes tyes eV SRE «20H ce “ce “liquid ammonia under saturation conditions . . . 291 Heat content of saturated liquidjammonia 2)). 2 <2 =). 2 4 201 Specific heat of mineralsiand roclksgsmaeteinc: aca ee eae i e silicates Aes reed vie ee, ee eae eee we 20m 5 “ “ogases and Vaporsiay picts ecteeae el oiersd ears 208 LaTeENT Heats Latent. heat of fusion: ( ait iat emer tteiee eo) eee ee ‘i “ “vaporization, eevents an) apts, SENGeio bee) Sacee nee mEEeOS ‘3 oe i liqntidlss ce4e8) Ges hea jet tetas 205 “and total heat of vaporization, formulae Syesy -oruesa eee ZOO. 5 “of vaporization, ammonia .. . a eels es 6 eee eZOe) “Latent heat of pressure variation” of liquid ammonia . . . . . 296 Thermal properties of saturated water and’steamm. <-. 2 = = = - 207 Properties of saturated steam: Metric and common units, 0° to 220i Gai e7 es 6 hate rea tch Se ee dt Co Re ate ee eee Properties of saturated steam: Common units, 400° to 700° F. . 304 . “ superheated steam: Common units, 212° to 3000° F. 305 i ** MMETCUrY VApPORs 402. tOkOOO yy) ans 0.0 ren neEsOO) re “liquid ammonia: "100" to -=250° F753. 2 2 geo Heats oF CoMBUSTION, FORMATION, ETC. Heats of combustion of some carbon compounds .... . . . 307 Bal why a miscellaneous compounds jj, 6) niet 8 S07 Heat values and analyses of various fuels: (a) Coals... .. . 308 (b) Peats and woods . 308 (ce) iqtidvtuels Sas 1305 (@)nGases tea cs See ee @hemical-and physical-properties of explosivesi9. =<) =) 3-109 (Additionalsdata on ‘explosivesii-) 3 cyeeyent-ae oe che) Ueireueees oun une Ignition temperatures of gaseous mixtures. . .. . +... . + + 310 Time of heating for explosive decomposition. . ....... - 310 Flame temperatures... . : Siig. Wels et io We eae LO, Thermochemistry: Heats of fopeecion fore femente 6 8 4a pois Se gets fe Of OMS. sa: 7 Uy hove Maes of neutralization < s' c ele it eee «dilution of sulphuric ice . aves, eae RADIATION Radiation constants and formulae for black body... . .. . « 313 - in ergs and g. cal. from a perfect radiator to absolute zero. 313 309. 310. Sr. are. 313. 314. B05. 316. B17. 318. 319. 320. ao B22: B23. 324. Bore 320. 27. 328. 329. 330. Sole 332. 333- 334- 335. 336. 3o7- 338. 339. 340. 341. 342. CONTENTS Black: body oes MESHSIEES (59),2850" to, 20000°C KK: Wns to: 600? aK: 800° to 25000° K. “e “ce “ce ce ce “ce e e “ce DERAMIECS. ites) epee -ey 6 hs . Black-body spectrum intensities, J y» Various atareence Cc Spectral energy distribution, luminosity. Relative J) Luminosity relative to maximum value at each temperature . Spectral energy distribution and luminosity. Luminosity factors - “ . 0 i: Variation with C, ‘ . Metals and oxides . ; Some intrinsic properties of tungsten [300° to 3655° mepe Spectrum emissivity of tungsten (percentage) [| 1800° to ee. Ke] Temperature scale for tungsten [1700° to 2400° K.| Radiation characteristics of tungsten [500° to 3500° K. | 3 and other properties of tantalum [300° to 3300° K. | - eee a ca “ molybdenum [273°-2895° K. |] Relation brightness and color temperatures for various substances Color minus brightness temperature for carbon . Percentage emissivities of metals and oxides . Wee Emissivities, metals [Au, Ni, Ta, Pt, Ag, Fe, nichrome] . Total radiation from bare and soot-covered nickel (watts/em*>) . CooLiInG BY RADIATION, CONDUCTION, AND CONVECTION Cooling by radiation and convection: At ordinary pressures _ 7% i % . “ different pressures ce “ce ce cc oe velope Cooling by radiation and secant Efteet ae pressure aud temp. Conduction of heat across air spaces (ordinary temperatures ) Convection of heat in air at ordinary temperatures . sat? xe and conduction of heat by gases at high temperatures (a) s as function of a/B epee Mee (b) ¢ in watts per cm as function of aiearnte temperature Heat losses from incandescent filaments (a) Wires of platinum sponge . (Oy tee 7° bright platinum THE Eve AND RADIATION Spectral variation of sensitiveness as a function of intensity Threshold sensibility as related to field brightness Heterochromatic threshold sensibility Contrast or photometric sensibility . Aetna table, J,, any tem- WW Do WW WH WH W W bOS Hw Wb Ww Platinum wire in copper en- WWW WW W W W XV ate 315 316 317 Su areas 318 “09 + 310 Radiation emissivities: Relative emissive powers for total radiation. 320 WW WwW b bw HH YN COMICS NO NON ae) by NY b AK WwW WwW Ww W bo wb wb WYN SL) CONT Ny CN ON on on bo b& w& bw bw OOO OW a00 330 OL 33! Xvi CONTENTS aa3. Glare sensibilitye a). & apRep aia) Co 15 | Ge a aie ; Ber 344. Rate of adaptation of senha : + Bak 345. Apparent diameter of pupil and flux Beech 2 at retina . . 262 346. Relative visibility of radiation (international stidard toe) B32 347. Miscellaneous eye data . A ga2 PHOTOMETRIC TABLES 348. Photometric definitions and units SIRS 349. n standards : A334 350. Waidner-Burgess standard of light . 334 351. Intrinsic brightness of various light sources : | 234 352. Brightness, Crova wave length, mechanical encivalene ee Genes 2 age5 353. Luminous and total intensity and luminous efficiency of black-body. 335 354. Color of light emitted by various sources . . 335 355. Blue brightness B, brightness in candles of ineandesrent coats Rie Rae 3506. Efficiency of various electric lights . + 337 357. Color and brightness temperatures, and bhenenese a cients » 238 358. Temperature, efficiency, brightness of vacuum lamps . > B28 359. Temperature, efficiency, brightness of gas-filled tungsten eee 1 338 300. Energy distribution for some tungsten lamps . ‘ . 1330 361. Brightness of some tungsten lamps and other sources . - 330 362. Characteristics of some miniature lamps . : = 329 363. oe “sunlight Mazda lamp (S ve Boon Wealelecuge : 340 304. re “ photoflash lamp . ; ie ome . 340 365. Visibility of white lights . - 340 PHOTOGRAPHIC DaTA 306. Sensitometric constants of type plates and films, definitions . 341 307. Formula for laboratory pyrogallol developer 341 308. Sensitometric constants of type plates and films . 342 369. eee line power, shar ase and astro gamma, definitions 342 370. ae - data 343 371. Relative spectrum sensitivity of various plates and films . 343 372. Spectrum sensitivity of photographic materials . 344 373. Relative photographic efficiency of illuminants . 344 374. Variation of resolving power with plate and developer . 345 375. Relative intensification of various intensifiers - 345 376. Reflection and transmission by photographic plates . 2345 SPECTRUM WaAvE LENGTHS 377. Wave lengths of Fraunhofer lines . i : 5 BAO 378. Primary wave-length standard. Definition of eee BAT 379. International secondary standards. Iron arc lines . Seid Bae 380. Computed wave lengths of iron arc lines . 2 349 381. 382. 383. 384. 385. 380. 387. 388. 389. 390. 301. 302. 393- 394. 395. 3096. 397. 308. 399. 400. 4ol. 402. 403. 404. 405. 406. 407. 408. 409. 410. All. 412. 413. 414. Media for determinations of refractive indices with the microscope : 415. Media for determinations of refractive indices with the microscope: CONTENTS Neon wave lengths PO Pa URIS MEET Y Standard solar wave lengths. International Angstroms . Provisional ultra-violet and infra-red solar wave lengths . Reduction of wave-length measures to standard conditions . Spectra of the elements . INDICES OF REFRACTION Index of refraction of glass: nx—mp and ng —np Cia oh “ “, effect of composition on Derivation of partial dispersions of glass from mp—“e . Index of refraction of glasses (American) ..... Dispersion of glasses of Table 389. ....... Index of refraction of glasses made by Schott and Gen, eas ‘ Mp, Dispersion and density of Jena glasses. . .. . Change of indices for 1° C [for some Jena glasses] . Index of retractions Rock-salt invaitiy. (4 4.24.) ae 6s; . Change of, for 1° C [for rock calelite Silvite (potassium chloride) in air . emacs iu Hluorite ansaim iii yieie. “6 & Change of, for 1° C [for Aueeeel eo ts Iceland spar (CaCOs) in air . « « a Nitroso-dimethyl-aniline . ac - Quartz (Si@>), 18; CC. Various alums . . solids . Index of refraction: Selected uniaxial minerals: (a) Positive . (b) Negative Miscellaneous uniaxial crystals . Miscellaneous biaxial crystals Liquefied gases, oils, fats, waxes . Liquids relative to air. . Gases and vapors... . wave lengths and frequencies in air to vacuo. . Liquids with np (0.589) =1.74 to 1.87 . Resinlike substances, mp (0.589) =1.68 to 2.10 . Selected monorefringent or isotropic minerals. Miscellaneous monorefringent or isotropic . 364 . 365 . 365 . 366 = 9367 . 368 3370 . 370 237i Selected biaxial minerals: (a) Positive . (b) Negative Relative to air for solutions of gales aed spite: XVii S349 = 350 - 353 - 354 - 355 . 356 » 356 fH . 358 . 259 + 359 - 359 359 . 360 . 360 = 360. is SOR 301 2 20K . On . 362 ~ 362 363 372 - 373 mig (Ts C76, cm); rections 80 reducing - 374 0D 0375 XVill CONTENTS 416. Media for determinations of refractive indices with the microscope: Permanent standard resinous media, mp (0.589) = 1.546 to 1.682. 375 417. Media for determinations of refractive indices with the microscope : Substances, #p == 4:86) tOUDy ae: ie ae Hh oc tst ode: eee eee RITES REFLECTING POWERS 418. a reflected when light is normal to surface. . ..... . - 376 419. i «mS near unity enrequals 1-4-dn > een ee seo A420. , Seamer Pes, oe LN Lie 81710) 421. ‘Optical:constantsiof metals, “Weer tee ve eco on cree 422. s additional edata i )"2). etter 423. ae nove Of metals) Tan FORME a (eid! Sha US eee 424. si ‘“ : Perpendicular incidence and reflection. 379 425. Percentage diffuse reflection: from miscellaneous substances . . . 379 420. ei reflection from metals, violet end of spectrum. . . . 380 427. Ultra-violet reflecting power of some metals... . . ti deseo 428. Infra-red reflectivity of tungsten (temperature Hae. 51 3380 429. Percentage reflecting power of dry powdered pigments. . . . . 381 430. Infra-red diffuse percentage reflecting powers of dry pigments . . 381 431. Reflectivity of snow, sand, etc... . Sg ne aie Meee he ae ool 432. Reflecting power of powders (white iene oe ee oe 433. Variation of reflecting power of surfaces with anble oe eae 434. The reflecting power of building materials. . . ...... . - 383 TRANSMISSIVE POWERS 435. Light filters, narrow spectrum regions . . . n45 A Oe Sao 436. Absorbing power of various materials—infra- ea ches eset 437. Transmissibility a ea eblor By GyeOS: 2," 5. eye ee ee ee OS 438. ib Jenapelasses. Guta to eee eee 439. ii > i *. o “coloned olasses Cait \leue seus oo 440. if + 2 iinoleultra=violet classes ¥-44) = eeon 441. ‘i . 4 ‘S Amiericanioelasses (2 5)... oat. eee 442. Transmission of various lights through colored glasses. . . . . . 388 443.) Witra-violet transparency, (202 saip ep cere ee eee ce tree 388 444. (a) Ultra-violet transparency atmospheric components . . . . . 389 (b) Atmospheric transparency for ultra-violet. . . .... . . 389 445. Penetration ultra-violet light into sea water... . «ay eee) 446. Transparency of the various substances of Tables 394 to ioe + ine) 3 BOO 447. Color’screens [Landolt] . ots Phy pcp seen 5 ee etal Last 20 eee ae he AAS) aa 7‘ [ Wied] oy fee's xs cceyl seeehee COE 449. Transmission percentages of en through mOist.air >). ssa soe 450. ena of water vapor pee Si tas nite axg3 ek ROS 451. TE Watery ee Me HIE ays oa. 6 oy ee OZ 452. Infra-red transmission and Aeorptions ones C7 £0. 329O i. wae SOS 453. i ve . 1 = Solids 6:70 32:8): .0 eS 454. 455. 456. 457: 458. 459. 460. Aor. 462. 463. 464. 465. 466. 467. 468. 409. 470. 471. 472. 473. 474. 475. 476. 477: 47°. 479. 481. 482. 483. 484. 485. 486. 487. 488. 489. CONTENTS inira-red refection,psolids;;22:0 and 32.8. 0s) « to ye60% co rf eee, (ti. iad nV OlES aw. seis aaiyey cae g eats @hernioclectric power; pressure elects < 2°. 5: Peltier and Thomson heats; pressure effects . . . The tribo-electric series ELECTRICAL RESISTANCE Auxiliary table for computing wire resistances... . . iesistivity of tuetals-andisomevalloys’. i, 7 «is 5 + «% Resistance “ “ under pressure (Bridgman) i “ mercury and manganin under pressure . metals, effect of tension on . . Conductivity and resistivity of miscellaneous ailoyee eae doe. Conducting power of alloys . “cc “cc XIX 393 - 393 - 394 - 394 - 394 - 395 - 395 Si 397 . 398 =. 398 a 308 308 099 . 400 1 408 . 402 . 403 =| 403 . 404 . 404 . 404 . 404 . 405 » 405 . 406 . 406 - 406 2407; 5. 407 . 408 oh Tien Ven © pmer 10) 46 P.e) fe) hse] Vel? ce . 408 . 409 . AL » #i2 3 A oe ata . 415 xX 490. 491. 492. 493: 494. 495. 490. 497: 498. 499. 500. 50l. 502. 503. 504. 505. 506. 507. 508. 509. 510. ine Fae. S12. 514. ise 516. 5Lg 518. 519. 520. 521. 522. 523- CONTENTS Allowable carrying capacity of rubber-covered copper wires . . . 416 Resistivities at high and low temperatures . : | A, Volume and surface resistivity of solid dielectrics . . . 418 Variation of resistance, glass and porcelain, with temperature . . . 419 Temperature resistance coefficients of glass, porcelain, and quartz . 419 Wire TABLES Tabular comparison of wire gages . . 420 Introduction ; mass and volume resistivity of copper ea al Wnatatieee 421 Copper wire: Temperature coefficients . - 422 is “Reduction of observations to standard Liners 422 ra ““, standard annealed: English units, B. Sa cape: eee 4 a ‘ m Metric alia! TOO Cae Se? PEE! 468 XXi1 561. 562. 563. 564. 565. 560. 567. 568. 569. 570. vale 72. 573- 574- 575: 576. 577: 578. 579: 580. 581. 582. 583. 584. 585. 580. 587. 588. 589. 590. Sol. 592. 593: 594: 595. 590. CONTENTS Magnetic pag een tes of cobalt at 0° and 100° C. nickel Samay Weenie. magnetite . ‘ Lowmoor wrought iron a: “< “ Vicker’s tool steel . Hadfield’s manganese steel . saturation values for steels . Demagnetizing factors for rods... . ce “cc “cc ce “ce ee ee ee oe ce “e “cc “ce ee “ce ce “ec Magnetic properties of iron and steel . Cast iron in intense fields . Corrections for ring specimens Energy losses in transformer steels . Magnetic properties of permalloy Wireman ace Wade Dissipation of energy in cyclic magnetization, various substances . Magnetism and temperature, critical temperature . Temperature variation for paramagnetic substances . : ' effect on susceptibility of diamagnetic elements . Seas 4 ““ paramagnetic elements . Magnetic susceptibility a te comrenien tot cehon nen temas te MAGNETO-OPTIC ROTATION Magneto-optic rotation: General discussion . oi mt é Solids, Verdet’s constant . Liquids, 5 . be m a Acids and salts in water, ender s constant. Gases, Verdet’s constant . Verdet srandseKundtxs constants ar acne ercecuete Values (of Ners’s constant 2) .0.0 te mene catenee Dispersion ot Kerr effects, ae ie ce “cc “ce ce Various MAGNETIC EFFECTS Resistance of metals: Bismuth, variation in transverse magnetic field LAN Cotas es Rerweee he neat: ste. Te Resistance of metals: Nickel, increase in transverse magnetic field. aa oi Change, in transverse magnetic field . Transverse galvanomagnetic and thermomagnetic effects . Variation of Hall constant with the temperature . Atomic DATA International atomic weights, atomic numbers and valencies . Isotopes, packing fractions . 469 . 469 . 469 . 469 . 469 . 469 . 469 . 470 . 470 Aga SAGA ARE : A72 . 472 - 473 - 474 - 474 - 474 - 474 - 475 . 476 - 477 . 478 - 479 - 479 . 480 . 480 . 480 . 481 481 . 481 . 482 . 482 . 483 . 484 597- 598. 599. 600. 601. 602. 603. 604. 605. 606. 607. 608. 609. 610. 61I. 612. 6L3: 614. 615. 6106. 617. 618. 619. 620. 621. 625. 620. 627. CONTENTS Periodic system of the elements . Atomic numbers . suhe Periodic system and the Pavonctize isotopes . Atomic structure content hane ee Electron configurations in normal atom . Effective atomic radii ATOMIC STRUCTURE (a) Electrons, protons, Rutherford atom . (b) Bohr atom, relativistic considerations (c) Hydrogen orbits, inner quantum numbers . (d) The spinning electron, summary . Energy of binding of an electron—neutral atoms . First ionization potentials of the elements . Second == r res 7 Radiation units ear: Spectrum ranges of various Fadations The mechanical effects of radiation . ATOMIC SPECTRUM SERIES RELATIONS AND NOTATIONS Normal series relations in atomic spectra . Inner quantum numbers Spectroscopic notation . . . ‘ numbers Sic : Comparison of notations : Ultimate spectrum lines, raies ultimes Persistent lines, arc spectra . = 2 ‘spark Resonance lines . ae she Electron impacts in gases ieroducine et Average life for various quantum states of excited atoms . Molecular constants of diatomic molecules, [description] . oe oe “ec oe oe | table | Various atomic and spectrum functions . RADIOACTIVITY Introduction. The uranium family Ionium-radium family Actinium family singly 1onized atoms . = 903 =. 50A Comparison series letters and SP mathal ana Bohr’s s quanta . 506 CEC Xxili ~ 485 . 485 . 486 487 . 488 . 491 . 492 - 494 - 495 . 496 - 497 . 498 - 499 500 501 501 501 502 5°95 507 509 . 510 51I 511 gee - 51g » 515 516 517 518 XXiV CONTENTS 628. Thorium family; Boe rubidium) 2 40 Se ee 629. Radioactivity units ... G aeih cera ee SnPHE Searea ts 630. Miscellaneous radioactivity constants. ..... 631. Relative phosphorescence excited by radium . 632. Vapor pressure of the radium emanation in cm of mercury . 633. ee particles: Range; velocity, ionization’ %. 9/3 Sees 634. % Relative ranges of, of RaF in gases. .... 635. c 40 ee TRaC’-in) solid elements. 635(a). ‘ = , long-range [from RaC’ and ThC’]. Relative HuMDETS. — 5.5. S Estaoiesuna a eee ness farcical ee 636. Alpha particles: Atomic stopping powers for, aE aCe 637. ss 5 Stopping powers of molecules for, of RaC’ . 638: El Jparticles: << +s Mel /sucobcuch canes ieee remem eee : 639. Relative total ionization by a rays in various gases . 640.. Delta “rays: 5. 2° (sh ai. dex ems imoehe aes eee 641. Heating effect of radium onda its emanation . O42 Jbeta aysus. -s,) sattars eta Sl ne awn 643. “ particles, work of extraction of . : C44 from Rak, effective range of, ina ea Slenieats ¢ GAGs ee absorption of, in air and CO, . 646. Gamma rays: Emission, energy and wave length, etc. . 647. = *““ Nuclear analysis, ionization . ; 648. “Scattering, comparison of sources . 649. re “Absorption of me 650. Characteristic gamma rays, wave lengths iia energies . 651. Gamma rays: Nuclear energy from spectra. . . ‘ 652. i “Wave lengths and energies by crystal Fedection : 653. ‘Quantities ini radioactive eqtilibmum’. . < +2. se eee RONTGEN Rays (X Rays) 654. Cathode rays . ae 3 655. Constants for euhode -ray eee in matter ‘ 656. X-ray emission 657. Emission lines and ee absangeon fhartie (in Angstroms) 658. Probabilities of ionization in K and L shells . : 659. Energy and efficiency of production of characteristic X rays . 660. Energy and quality of emission X rays . 661. “X-ray -specttoscopy i275. 800 2h see 662. Lattice constants of crystals . : ; 663. Absorption and scattering of X rays; adgrecrence é 664. X-ray absorption and chemical combination . 665.. Mass absorption coefiicients; u/p. = 4. sear: 666; Photographic eiiects oreerays es Ss Ss 54S fyee@ontactiGN alta)pepotentiaise 46 Ay Geka. 6 ae «548 oie. Hlectromatiinity of the elements, inivolts’. . . 20:02 % +» = = ~ "549 674. Molecular velocities .. . : Bees oss 50 675. i free paths, coieien Trequencies nad diameters ene. GO 676. Cross-sections and lengths of some organic molecules. . . . . . 551 O777eoize Ol diiitacting Unitsamenystals 2... El eee se 5D G76: lonic mobilities: 5. . 6 6 ss OE RE Sere CES, Gh 670.) Ditusion coefficients <4. 7.6 2s PEA NUR SES! ee Geos Galloids. seneral properties:or. ¢ 7.92) Ve a.) B58 681. san tno lectilak WeIohts Our Uses. he Re cee ee tense tae ee ed ee 6 ODS 682. ‘© : Brownian movement. . . Wee ee Se 683. “Adsorption of gas by finely aivided maciaiee ee he ee at 684. = Eleats or adsorption. "2. - SeGSa 685. “Molecular heats of adsorption ea Gqueiacien (F are) 554 METEOROLOGY 686. Transmission of solar radiation by earth’s atmosphere. . . . . . 555 687. Ultra-violet solar radiation at earth’s surface... ....-. - 555 688. Relative intensity of solar radiation. ....... FT Te so 689. Mean monthly and yearly temperatures... .. . = aig diene: 550 690. Temperature variation over earth’s surface (Hann) . ... . - 557 691. s 5 with depth (land and ocean) . . . . . . 557 692. Atmosphere: Miscellaneous data. Variation with latitude. . . . 558 693. a Var. percentage Seren with altitude (Hum- plireys), =. pate) PN SS sa peas ML ae . 558 694. Atmosphere: ae foe Dreeerre: i density with alee Scene PRSey Ss) VA 9e lie wen ve cual choke sf Sak oe ee 695. Atmosphere: Sinedard [ Nat. Adv. Con Peron rca i Fs so lei Ee 696. re p. in dynes/cm?, summer and winter, day and night (VaGIS Viet comet a, Noasteee teuetietpcani, foe, 8) bee: Ste Ms . 560 697. Atmosphere: Minleaulan, corciies of Weenie gases (Mfarieyi 500 698. > Geopotential, dynamic heights. . .. . . 561 699. Equivalents, in geodynamic km, of Pepneeine heente, 561 700. . : “geometric “ “ dynamic > 501 701. - Temperature variation lower 25 km with lat. and alt. 562 702. 7 Seasonal variation of tropopause at Agra and Batavia. 562 XXXVI CONTENTS 703. Atmosphere: Seasonal variation height of tropopause over Batavia. 562 704. AtmOSpheHicpozonen fo. 3 205 secee are ce Consus 705. : Mean free path, air plecuics o 2k ye Bee wees, SOR GEODESY 706. Acceleration of gravity: For sea-level and different altitudes . . . 564 FOZ. ’ s 3 Vanious world’ stations: ..7: Jt peas OS 708. ‘ % : (g)angthe: United) States’ 5.0) acai Soe 709. Some places of anomalous gravity... . 507 710. Length of seconds pendulum at sea-level and tok diflerent fatitades! 568 711. [Replaced by Table 716, which see] . ys Ne tol ne Sains aS GEOPHYSICS 712. Muscellaneous veostraphicalidata, © 903) 22) 25 ie eonene ee Oo 713. Wensitiesiand presstires ‘of earth's interion ..) -yecweeie eee SOO 714. Velocities ‘of earthquake waves: “\ Rigas chien aie Ronee ete ee OO 75. Elastic constants ot earths) Imtenons shite enemas es Om) zi. Muscellaneous geophysical data ~ 4, cass as be ena eee ee 77. Age of earthyand) its strata) reas. a Me cee ale Gal 718. (a) Geologic age determinations teem on ae ical meried a a eal (b), ‘The agevot thesearthy 2 juin osha onseucuach irs occa Sie che one ee de 7rg.. (Geochemical data 4 sr sc)-ouuutpsies. 3! cei 2 2 ates kere) eS gee 720. lhe é€arthis rotation; Its vanabtonwyc) ysis cure ie as cn mS S yon. ides, sea-level, level met ca ae ae. <4 cast en ee E ‘TERRESTRIAL MAGNETISM y722.. Magnetic and electric data forsun andearthy. 2) 2. 9 5) 2 oat 723. Niagnetic constants of the earth, sath. a en eae ee 5 724, Northtmagnetic pole..1/ 2's 12.8: Fn aes eects joe eee ne meee an 725. South 5 SEO M POI Rae, RUTTER al BS nc ey UC eS 720 aGhart+ World isogoniclines, JOS) 9. (te 2. tats) 0 ee ee i) 727. Chart: “World isoclinic lines Ia. see tie 2 ae) ee Fat oe es isodynamic lines; 7.3: ; 4 An4%) ay ics A es ea (70 ae ““ isoporic Sy MUD! Rae Saat LS Aticaaned aly Ae een terme Maes F205 © = 4 i fo Ane RAP Fn 1 RR Se, em fe a x * ED Peek, IRIS Cc hk eh EMO een 732. Annual ee inwmacnetie declination, JP*s 0) Si 2s. = eeO 733. 5 i x inclinations Fx. cas, 2A) eee 734. J “ * i‘ horizontalsintensity, Fl 929 rn 79 735. Chart: World asoporie!lines, verticalintensity). "| . 9. 2. 2usss5c8 730. ‘ s y etotabmntenisity Otis c~. ‘i ca eo 737. Mean annual values of magnetic elements at observatories. . . . 581 738. og t oes ‘ = Sw ebibliography > = 22589 739. Secular change in declination, United States [1820-1930] . . . . 590 740. 741. 742. 743- 744. 745. 746. 747- 748. 749. 759. 751. 752: 753: 754- . 754(a). Maximum electron density y, max. in the upper Perot phere : ape 756. Thea 758. 759. 701. 762. 763. 764. 765. 760. 767. 768. 769. 7/0: Wipik. 7/2 773: 77/4- 775: 770. CONTENTS XXVIII Dip or inclination, United States [ 1925, long. and lat. variation] . Secular change in dip, United States [1855-1925] . Horizontal intensity, United States [ 1925, long. and lat. variation]. Secular change in horizontal intensity, United States | 1855-1925]. Total intensity, United States [1925, long. and lat. variation] . Secular change in total intensity, United States [REAR : Agonic line, United States [1800 to 1925] . ba alae Mean magnetic character of each month, oon to mae ATMOSPHERIC ELECTRICITY Elements and constants of atmospheric electricity . Atmospheric-electric data . ‘ Tonic equilibrium in the atmosphere . Thunderstorm electricity . Charge on rain and snow . ‘ Tonization in the upper atmoepliere =f fhe ear Ion density y, in the upper atmosphere . ASTRONOMY Miscellaneous astronomical data . tae oS “and formulae . Calendar, Julian day . « perpetual ae Right ascension-declination into Palaces cognate tes : Planetary data : Satellites of the solar eystenn Diameters of the planets . Planetary and Satellite distances, Bode’ S as tafe develpeente. Albedos f Equation of time . Solar data: The solar constant é Solar spectrum energy, transmission by ean S si aanepbete ‘ Amount of solar radiation, u.-v., visual, i.-r., in calories . Distribution of intensity (radiation) over the solar disk . The solar constant, decade means . Klin coke i. monthly and yearly means 1930, 1931 : ; Wolf’s observed sun-spot numbers. Annuals means . Duration of sunshine pag lk Transmission of radiation ne moist aac acy air . Brightness of sky radiation, Mt. Wilson wee oa Flint Island (sea-level) . : : ote idle “cc “ec ce 2 592 - 592 593 593 - 594 = 994 - 395 - 595 - 596 . 596 - 597 =. 5O8 . 598 - 599 - 599 . 600 - GOL ; 602 : 602 . 603 » 5 "604 s "606 =. 606 . 606 607 = 607, ~ 607, . 608 . 608 . 608 . 608 . 609 . 609 . ‘610 . 610 . 610 Or! ‘Ort XXVill CONTENTS 777: 778. a> 779: 780. 781. 782. 783. 784. 785. 780. 787. 788. 789. 790. 7O1. 792. 793: 794- 795: 790. 797: 708. 799. 800. Sol. 802. 803. 804. 805. 806. 807. 808. 809. 810. SII. 812. 813. 814. Distribution in normal spectrum of sunlight and skylight, Mt. Wilson . GUE Air masses . : ‘ Pos ~ OFT 58 elements known in ee sun’s iene here Bee eka 's LOLS Quantitative estimates of composition of solar aimoe aber Hus Abundance of elements in sun, earth and meteorites . Gna Abbot-Priest solar-energy curve, sea-level . . 614 Constellation abbreviations (Astron. Union, 1922).............- 615 Occurrence and abundance of elements in the stars . S1Gins Stellar systems ; . 616 Stellar spectra and related Geneeidvied - OE7 The Harvard spectrum classification . . 'OL7 Log (no. stars) /(sq. degree) brighter thant! HiStOstapIie. magni- tude, m, at stated galactic latitudes . - 1618 Numbers and equivalent light of the stars . . 618 The first-magnitude stars . : : . OLO Stars known to be within five parsecs ke tea sun . . ‘616 Percentage of stars of various spectrum classes . . 620 Galactic concentration of various spectrum classes . . 620 Distribution of binaries as to spectrum class . . 620 Masses of spectroscopic binaries, Sun=1 2 1620 Russell diagram [Adams] ‘ 2 O21 Spectrum types and absolute magnitudes [Strombergils . 622 Brightness of the stars . + (622 Giant and dwarf stars .. 622 Masses and densities . ia Shock . 022 Parallax and mean apparent mastatnde ‘ . 624 Spectrum type and mean absolute magnitude . - 024 Reduction of visual to bolometric magnitude. . ....... . 624 STELLAR Motions Summary, elements of solar motion eee 1928) . 625 Elements of solar motion (Charlier, 192 Te 1625 Stars of large proper motion . 025 Spectrum class and proper motions . . 626 Equipartition of energy in stellar motions . : - 626 Stars of large space velocity, greater than 300 km . sec! . = (O27 Stars of small space velocity, 5 km/sec. or less . (627 Motions of the stars . : . 628 Known stars of radial velocity Breetes ise 100 ieee . 628 Binary STARS Visual binary stars . 626 Spectroscopic binary stars . 629 CONTENTS XX1X 815. Spectroscopic eclipsing binaries... ....... : . 629 816. Periods of known binary stars within 10 parsecs of the sun Pension 1930 | . 630 817. Masses and aboot Beenie of Gina stars SIGE tmans neal. 631 818. Mass luminosity data . HORT 819. Stellar radiation measurements (Pettit, Nicholson, 1928) . +632 820. Spectrum classes and temperatures . ; ; = (622 821. Visual and radiometric magnitudes and total Pao : (632 822. Stellar radiation measurements: Energy spectra (Abbot, oo 2, (623 823. Be * ;" Temperatures, radiation, eters 633 VARIABLE STARS 824. Variable stars, general characteristics; classification . mr OZA 825. The Cepheid period-luminosity curve . . 635 SUMP IN ONACTI Gy oo rSd ruminn cas Rates eles ssc 7-635 827. Observed maxima of spectrum lines in the giant sequence . . . . 635 828. High-density stars. White dwarfs. ..... . 636 829. Low-density stars. Giants see = 626 830. High-temperature stars. High- “luminosity ae =e . 636 STAR CLUSTERS eer. Properties and’ classification of star clusters; 4...) 63.0) «hee eis 9s 637 832. Distribution of open star clusters . fs 207. 833. Globular star clusters . «1638 834. Galactic star clusters . . 638 NEBULAE pace) Classiication of nebulae). . 2°. a -. 3 tg IIS 21 gs. the 639 Boa) ra GalachicnMepUlaG s.. iv, seucistarsy ia) ietecsagial’ s | 630 836(b). Data on six planetary nebulae . . . 639 837. Diffuse galactic nebulae, dimensions . . 040 838. Nongalactic nebulae .. . : . 640 839. The Magellanic clouds and N. G. e eee fpeatons : . 640 840. Magnitudes, radial velocities and distances of external pales OAT 841. Extra-galactic nebulae, high velocities . 642 842. Rotation of stars Dee ad . 642 843. The galaxy, its center ae rotation . ee. ss OAS 844. Transmission of Hen zeae space ; tieoreteal. . 643 845. i i ‘observed estimates . . . 643 846. Amount of matter in interstellar space . a nOAA! 847. Radii of curvature of space . . 644 XXX CONTENTS 848. . Interstellar’ gases! (calcium; sodium) gm © (ei seem ee 644 840. sTemperaturesof anterstellansspace mice. is em ee het 4 OAS 850.9 Matter and energy :. 20h wc epee aiewne =) eee ye eee - O45 Compton‘éfiect: |) 74x kth techs = 0.0610 cu. in. millimeters ) cu. decimeter (cd) iGjooccubic:-= 61.024“ centimeters ) CU. METER or stere . (1,000 cd ) cu. centimeter } me eac arse at. * —\L 1.307954 cu. yds. MEASURE, OF CAPACITY: milliliter (ml) \= 4 (.oo1 liter) == 0,0010, CU. in. if o:61e24"* ~ (0.070 gill. = 0.176 pint. “ centiliter (.o1 liter) deciliter (.1 liter) I LITER (1,000 cu. centimeters or I 1.75980 pints, cu. decimeter ) dekaliter (10 liters) = 2.200 gallons. hectoliter (100 “ )= 2.75 bushels. kiloliter (1,000 “ ) = 3.437 quarters. APOTHECARIES’ MEASURE; cubic centi- 0.03520 fluid ounce. meter (I ¢— 4 0.28157 fluid drachm. gram w't) 15.43236 grains weight. cu, millimeter = 0.01693 minim. AVOIRDUPOIS WEIGHT. 0.01543 grain. OG 1.54324 grains. 15.43236 “ 5.64383 drams. 3-52739 OZ. 2.2046223 Ib. 1 15432.3504 grains. 22.04622 lbs. 1.96841 cwt. milligram (mg) centigram (.01 gram) decigram (.1 cores) GRAM oe dekagram (10 grams) ) ) te hectogram (100 “ | KILOGRAM (1,000 “ myriagram (10 kg) quintal (Goom) millier or tonne | (1,000 kg) se Il Il I| 0.9842 ton. TROY WEIGHT. 0.03215 oz. Troy. .=4 0.64301 pennyweight. 15.43236 grains. APOTHECARIES’ WEIGHT. 0.25721 drachm. | 0.77162 scruple. 15.43236 grains. Notre.—The Meter is the length, at the temperature of 0° C, of the platinum-iridium bar deposited at the International Bureau of Weights and Measures at Sévres, near Paris, France. The present legal equivalent of the meter is 39.370113 inches, as above stated. The KrLocram is the mass of a platinum-iridium weight deposited at the same place. The Lirer contains one kilogram weight of distilled water at its maximum density (4° C), the bar- ometer being at 760 millimeters. * In accordance with the schedule adopted under the Weights and Measures (metric system) Act, 1897. SMITHSONIAN TABLES TABLE 5 (continued) EQUIVALENTS OF METRIC AND BRITISH IMPERIAL WEIGHTS AND MEASURES (2) METRIC TO IMPERIAL, MULTIPLES (For U. S. Weights and Measures, see Table 3) LINEAR MEASURE. MEASURE OF CAPACITY. Kiloliters to quarters. Hectoliters to bushels. Dekaliters to gallons Kilo- meters to miles. Liters to pints Meters Meters to feet. Millimeters | to inches 2.74969 5.49935 5.24908 10.99877 13-74846 1.75980 | 3.51961 5-27941 | 7.03921 8.79902 | 3-28084 | 6.56169 9.84253 | IS 22397, 16.40421 0.62137 [.24274 1.56412 2.48549 | 3-10686 2.19975 4.39951 6.59926 8. 79902 10.99877 13.19852 15.39828 14.07842 | 17.59803 15.83823 | 19.79778 S495 7/5 2a) 6.87423 10.31135 | 13.74846 17.18558 0.03937011 | 0.0787 4023 | oO. 11811034 | 0.15748045 0.19685056 mew we ON 3-7 2823 || 20.6226g | 4.34960 8.74891 | 4.97097 || 8 9.84253 | | 939735 | | 9 10.5582 12.31862 | 16.49815 19.24785 | 24.05981 21.997 54 | 27-49692 | 24-74723 | 30.93404 | 0.23622068 | OSD 90719 0.31496090 | 0.35433102 | 19.68 506 22.96590 26.24674 29.52755 NI SQUARE MEASURE. WEIGHT (Avorrpupots). Kilo- grams to pounds, P| : | Milli- | | | Quintals | Hectares | | Kilograms | to acres. to grains, | Square | meters to square yards. Square meters to square Square centimeters to square inches. weights. grains. 1.96841 | 3-93683 | 5:90524 7-87 365 9.84206 | 2.20462 4.40924 | 6.61387 | 8.81849 | | 11.0231T | 15432.356 | 30864.713 46297.069 61729.426 | 77161.782 2.4711 | 49421 7.4132 9.8842 12-3553) 0.15500 0.31000 0.46500 0.62000 0.77 500 I. 7.19599 2.39198 | 5.587 98 | 4.78397 | 5-97990 is 17595 37194 | | z 56794 | | 10.76393 | 0.01543 0.03086 0.04630 0.06173 0.07716 | I il 3 4 5 11.81048 13-77889 | 15-747 30 7.71572 (3.22773 | 1 5.43236 17.63698 19.84160 | 14.8263 || 6 17.2974 ||| 7 19.7685 || 8 22.2395 || 9 0.09259 | 92594.138 0.10803 | 108026.495 0.12346 | 123458.851 0.13889 | 138891.208 0.93000 1,05 500 1.24000 1.39501 | 64.58357 | MEPS SS | $6.11143 96.87 530 | | I 3 4 5 6 i 5 > 2 APOTHE- CARIES’ WEIGHT. APpoTueE- | CARIES’ MEASURE. Troy WEIGHT. CUBIC MEASURE. | ORES (cont.) Cubic decimeters to cubic inches, 61.02390 | 122.0478! 183.07171 244.09561 305.1 1952 366.14342 | 176. Cubic meters to cubic feet. 35-31476 70.62952 105.94428 141.25904 57379 211.88855 | Cubic meters to | cubic yards, | Cub, cen- |) meeters Milliers or to fluid tonnes to drachms. 0.28157 || 0.56314 |) 0.84471 1.12627 1.40784 1.30795 2.61591 3-92386 | 5.23182 6.53977 | 7.84772. | 1.68941 1.97098 I 2 5 4 5 6 7 8 427.16732 | 247.20331 | 9.15568 | 488.19123 | 282.51807 | 10.46363 9 | 549.21513. | 317.83283 | 11.77159 | Cr N MbWN 2.25255 No} Grams to ounces Troy. 0.03215 0.06430 0.09645 0.12860 0.16075 0.19290 0.22506 0.25721 0 28936 C7 | 0.64301 Grams to penny- | weights. | scruples. | ; | 0.77162 1.54324 2.31485 | 3.08647 | | 385809 | 1.28603 1.92904 4.62971 5-401 32 | 6.17294 | 6.94456 SMITHSONIAN TABLES. Io TABLE 5 (continued) EQUIVALENTS OF BRITISH IMPERIAL AND METRIC WEIGHTS AND MEASURES (3) IMPERIAL TO METRIC (For U. S. Weights and Measures, see Table 3) LINEAR MEASURE. MEASURE OF CAPACITY. ; ae milli- Pet. . |.) == eae deciliters: I inch = meters. Iepint(qscills)ie Se 0.568 liter. TefOOt} (2k) eens 0.30480 See I quart (2 pints) . .—= 1.136 __ liters, 1 YAED (3 ft.) .. 0.914399 I GALLON (4 quarts) = 4.5459631 “ I pole (St yd.) ... 5.0292 meters. impeek (2\gal;) . 2 —@ioge “ 1 chain (22 yd. or ! Bote mea 1 bushel (8 al.) . = 3.637 dekaliters. 100 links) ran se 1 quarter (8 bushels) = 2.909 hectoliters, t furlong (220 yd.) = 201.168 1.6093 kilo- 1 mile (1,760 yd.) . = } meters, a 1420210. X Cdra. I yard . (Tutton 1932) AVOIRDUPOIS WEIGHT. , ey Ges om itt SQUARE MEASURE. ah: ries ech bole ne ; grams, Ty cleanly. eee ae 1.772 grams. 6.4516 sq. cen- || 1 ounce (16 dr.). . 28:35010 timeters. I POUND (16 oz. or 4 sq. ft: (nagioqnin) Mn reg el Col, ecm) f= 045359243 ke. ca ey Re le meters. I stone (14 1b.) . . 6.350 = t Squarednehe. 1. — ; 0.836126 sq. I quarter (28 1b.) . 12.70 - meters. I ae or ae 50.80 = 25-2 . - 2 es i perch (30g sq. yd.) = cae ak etre ca a SQ. YARD (9 sq. ft.) = rood (40 perches) = IO.II7 ares. igs ACRE (4840 sq. yd.) = 0.40468 hectare. || I ton (20 cwt.) . OPO ENS sq.mile (640 acres) — 259.00 hectares. grams. TROY WEIGHT. CUBIC MEASURE. 1 Troy OUNCE (480 cu. inch = 16.387 cu. centimeters. grains av.) (0.028317 cu. me- I pennyweight (24( __ ee fool a8 aL 7 Oe | (| esa as et cu. decimeters. = 31.1035 grams. 1.5552 s cu. YARD (2 1 Note. — The Troy grain is of the same weight as = a ) of 0.76455 cu. meter. the Avoirdupois grain. APOTHECARIES’ MEASURE. APOTHECARIES’ WEIGHT. gallon (8 pints or] _ : 160 fluid ounces) =| fodagoguliters. fluid ounce, f 3 fees cubic on ‘ (8 drachms) centimeters. ; eee Basis iccr = 3.888 « 3.5515 cubic I scruple, 5i (20 centimeters. rains) =} 0.05919 cubic 8 a centimeters. Notre. — The Apothecaries’ ounce is of the same weight as the Troy ounce. The Apothecaries’ Notr.—The Apothecaries’ gallon is ot the same grain is also of the same weight as the Avoirdupois capacity as the Imperial gallon. grain. I ounce (8 drachms) = 31.1035 grams, 66 (60 minims) minim, mM (0.91146 grain weight) = 1.296 fluid drachm, f 5 t ( ) Notr.— The Yarp is the length at 62° F., marked on a bronze bar deposited with the Board of Trade. _ The Pounp is the weight of a piece of platinum weighed in vacuo at the temperature of o° C., and which is also deposited with the Board of Trade. The Gatton contains 10 Ib. weight of distilled water at the temperature of 62° F., the barometer being at 30 inches. SMITHSONIAN TABLES TABLE 5 (concluded) EQUIVALENTS OF BRITISH IMPERIAL AND METRIC WEIGHTS AND MEASURES (4) IMPERIAL TO METRIC, MULTIPLES LINEAR MEASURE. centimeters. Feet to meters. Yards to meters. Miles to kilo- meters. Te (For U. S. Weights and Measures, see Table 3) MEASURE OF CAPACITY. liters. Gallons to liters. Bushels to dekaliters. | Quarters | | to hectoliters. | | 2.539998 5.079996 7-619993 10.1 59991 12.699989 15.239987 17-779984 20.319982 22.859980 WO OND NMAWNH 0.30480 0.60960 0.91440 1.21920 1.52400 1.82880 2.13360 2.43840 2.74320 0.91440 1.82880 2.74320 3.65760 4.57200 5.48640 6.40080 7-31519 8.22959 1.60934 3-21869 4.82803 6.43737 8.04671 9.65606 11.26540 12.87474 14.48408 MO COND MNPWN A 1.13649 2.27298 3-40947 4.54596 5-68245 6.81894 795544 9.09193 10.22842 4.54596 o-29093 13.63789 18.18385 22.72982 27.27578 31.82174 36.36770 40.91 367 363677 7-27354 10.91031 14.54708 18.18385 21 82062 25-45739 29.09416 32-73093 2.90942 selon -7.2825 11.63767 14.54708 17.45650 20.30591 23-27 533 26.1847 5 SQUARE MEASURE. Square inches to square centimeters. Square feet to square decimeters. Square yards to square meters. Acres to hectares. WEIGHT (Avorrpurois). Grains to milli- grams. Ounces to grams. Pounds to kilo- grams. Hundred- weights to quintals, | 6.45159 12.90318 19:35477. 25.80636 38.70953 45.16112 51.6127 58.00430 I 2 5 4 5 6 7 8 9 0.83613 1.67225 2.50838 3-344 50 4.18063 5.01676 5.85288 6.05901 T5295 03 0.40468 0.80937 64.79892 129.59754 194.3997 5 259-19567 323-99459 388.7935 453-59243 §18.39135 583.19026 28.34953 56.69905 85.04858 113.398L1 141.74763 170.097 16 198.44669 226.79621 255-14574 0.45359 0.90718 1.36678 1.81437 2.26796 2.72155 3-17515 3.62874 4.08233 0.50802 1.01605 1.52407 2.03209 2.54012 3.04814 3.55016 4.00419 4.57221 Cubic inches to cubic centimeters. MEASURE. Cubic feet to cubic meters. Cubic yards to cubic meters. MEASURE. || Fluid drachins to cubic centi- meters. | AVvoIRDUPOIS (cont.). Tons to milliers or tonnes. Ounces to grams. Troy WEIGHT Penny- weights to grams. APOTHE- CARIES’ WEIGHT Scruples 16.38702 32-77404 49-16106 65-54808 81.93511 98.32213 IL4-70915 131.09617 147.48319 O OND MPWNH 0.02832 0.05663 0.08495 0.11327 0.14158 0.16990 0.19822 0.22653 0.25485 SMITHSONIAN TABLES. 3 0.76455 1.52911 2.29306 3.05821 3.82276 4.58732 5.35187 6.11642 6.88098 3°55153 7.10307 10.65460 14.20013 17-7 5767 21.30920 24.8607 4 28.41227 31.96380 O OND MPWN 1.01605 2.03209 3.04814 4.00419 5.08024 6.09628 7.11233 8.12838 9.14442 31.10348 62.20696 93-31044 124.41392 155-51749 186.62088 | 217.72437 | 248.82785 | 279-9313 1.55517 3.11035 4.66552 6.22070 7-77 587 9.33104 10.88622 12.44139 13.99657 1.29598 2.59196 3-887 94 5.18391 6.47989 7-77 587 9.07185 10.36783 11.66381 TABLE 6 DERIVATIVES AND INTEGRALS * I2 “ntl — , unless n=—1 Tei = logs d fe S e% dx S e%dx qm ett / rmere dx a ma x m-1 ett dr a =x log x—x =uvr—/vdu _ (a+bx)r+1 JS log x dx Judv xt (1+log, x) dx cos x dx —sin x dx d cos % d tan x = sec? x dx —csc? x dx tan « sec x dx = —cotx.cscxrdr (1—x?) —4 dx —(1—4?)—2 dx (1+x?)—! dx —(1+x?)—! dx = x1 (x?-1)—3 dx —x—! (x2—1)-3 dx cosh x dx sinh x dx sech? x dx —csch? x dx —sech x tanh dx —csch x. coth x dx = (x?+1)—-3 dx = (x?—1)—} dx = (1—x?)—! dx = (1—x?)—! dx —x—1 (1—x?)—3 dx Se GAA) ot dcotx adsecx acscx d sin—1 4% d cos—! x d tan—! x dcot—1x dsec—1 x d csc—! d sinh x d cosh x d tanh x d coth x d sech x d csch x d sinh—! x d cosh—! x d tanh! x d coth—! x d sech—! x d csch—! x JS (a+bx)” dx S (@?+x")—! dx S (a?—x?)— dx S (a2—x?)-3 dx P&C x) aide J sin? x dx JS cos? « dx J sin « cos x dx (n+1)b I % Shi = a a Mtr =—ISina 4 a Vx'+a? a+x a—-x I = 10, 2a 5 x x = sin—! ~—, or—cos—! — a a = +(a?+x7)t —} cos xsinx+i x hsin x cos x+3 4 3 sin? x J (sin x cos x)—1dx = log tan x J tan x dx J tan? x dx JS cot x dx S cot? « dz JS csc x dx Sx sin x dx J x cos x dx JS tanh x dx JS coth x dx JS sech x dx J csch x dx Sx sinh x dx Sx cosh x dx JS sinh? x dx J cosh? x dx JS sinh x cosh x dx —log cos x tan x—2% log sin x —COL ec — 7 log tan 4% sin x—x COS ¥% cosa+~ sin x log cosh x log sinh x 2 tan—! et=gd y log tanh : x cosh x—sinh x x sinh x—cosh x (sinh «cosh x—2) (sinh x cosh x+2) + cosh (2 x) * See also accompanying table of derivatives. SMITHSONIAN TABLES For example: §fcos. « dx = sin. x + constant. TABLE 7 SERIES 13 n (n—1) fis N—2 a2 A x V2 Sten arate n(n—1) : -(u—m+1 ') m! nN n= xn ues — — + an ly 4 I pT) x4 = —2)x? Wiel) ls Ttnx + Me : Je a (A) ins )x a ie (Ein! x : (n—k)! k! 3 ° 3 2) (2>x>0) (x >0) (x? <1) (2 (Gi) (a2<1) 25>) SMITHSONIAN TABLES. 14 TABLES 7 (continued) AND 8 TABLE 7 (continued) SERIES cosh x = * (e% -+ e=*) = I -- a (a?< 0) tanh x = x (x? < 11?) (a? <1) sinh-! 4+ =x oy! log 2x (a?> 1) |- 3 cosh—! x = log 2x (x2 >1) Nile ble loo IW Alin Alun Or s a Or 3 a tanhise canola. (x2 <1) I Baa J I Bia oP te tere (x small) 7 I sech3x — — sech. x — —- ———= 2 x large Bp 3 (x large) (<2) _ Wx 24x + ay Se ean eee a, +...(—c n3 \2 n 1000.3 \2 , | za 1000 | 3.1623 |} GS | 15.3846 , 4225 | 274625 8.0623 1331 | 3.3166 || 66 | 15.1515 | 43250 | 287496 8.1240 1728 | 3.4641 67 12.925¢,| 4489 | 300763 8.1854 2197 3.6056 63 14.70;9 | 4624 | 314432 8.2462 274d) | 357407 69 14.4628 | 4761 | 328509 8.3066 3375 | 3-8730 || 70 | 14.2857 | 4900} 343000 8.3666 4096 | 4.0000 71 14.0845 | 5041 | 357911 | 8.4261 4913 | 4.1231 | 72 | 13.8889 | 5184 | 373248 | 8.4853 5832 | 4.2426 | 73 | 13.6986 | 5329 | 389017 | 8.5440 6859 | 43589 | 74 | 13.5135) 5476 405224 | 8.6023 8000 | 4.4721 AS) |) 138335 uh 50250 421075 8.6603 9261 | 4.5826 70; | 13-D5700\. 5770 | 438976 | 8.7178 10648 | 4.6904 77 | 12.9870 | 5929 | 456533 | 8.7750 12167 | 4.7958 78 | 12.8205 | 6084] 474552 8.8318 13824 | 4.8990 | 79 | 12.6582 | 6241 | 493039 8.8882 15625 | 5.0000 || 80 | 12.5000; 6400} 512000 8.9443 17576 | 5.0990 81 12.3457 | 6561 531441 9.0000 19683 | 5.1962 82 | 12.1951 | 6724 | 551368 9.0554 21952) |) 15.2015 83 | 12.0452 | 6889 | 571787 g.1 104 24389 | 5.3852 || 84 | 11.9048 | 7056 | 592704 | 9.1052 27000 5:-4772 || 85 11.7647 | | 7225 614125 9.2195 29791 5.5678 | 86 | 11.6279 | 7396 | 636056 9.2730 32768 | 5.6569 87 11.4943 | 7509 658503 9.3274 35937 | 5:7446 || 88 | 11.3630 | 7744 | 681472 | 9.3808 39304 | 5.8310 | 89 | 11.2360 | 7921 | 704969 | 9.4340 42875 | 5.9161 || 9O | It.111t | 8100 | 729000 9.4868 46656 | 6.0000 QI 10.9890 | 8281 | 753571 9.5394 50653 | 6.0828 2 10.8696 | 8464 | 778688 9.5917 54872 | 6.1644 93 | 10.7527 | 8649 | 804357 9.6437 59319 | 6.2450 || 94 | 10.6383 | 8836 830584 | 9.6954 64000 | 6.3246 | 95 10.5263 | 9025 | 857375 9.7468 68921 | 6.4031 96 | 10.4167 | 9216 | 884736 9.7980 74088 | 6.4807 97 10.3093 | 9409 | 912673 9.8489 79507 | 6.5574 || 98 10.2041 | 9604 | 941192 9.8995 85184 | 6.6332 || 99 | 10.1010 | 9801 | 970299 9.9499 gtt25 | 6.7082 ||| 100 [0.0000 | 10000 | 1000000 | 10.0000 97330 | 6.782 IOI 9.90099 | 1020f | 1030301 10.0499 103823 | 6.8557 102 | 9.80392 | 10404 | 1061208 | 10.0995 110592 | 6.9282 | 103 | 9.70874 | 10609 | 1092727 | 10.1489 117649 | 7.0000 ]| 104 | 9.61538 | 10816 | 1124864 | 10.1980 | | 125000 | 7.0711 || 105 | 9.52381 |; trozs5 | 1157625 | 10.2470 132651 | 7.1414 106 | 9.43396 | 11236 | 1191016 | 10.2956 140608 ; 7.2111 107 | 9.34579 | 11449 | 1225043 10.3441 148877 7.2801 108 | 9.25926 | 11664 | 1259712 | 10.3923 157464 | 7.3485 | Tog | 9.17431 | 11881 | 1295029 10.4403 166375 | 7-4162 || 110 | 9.0go91 | r2100 | I 331000 10.4881 | P75OLO | 174833 ||| 10, | Q.oogor || T2321 | 1367631 4| 1o:.5357 185193 7.5495 112 | 8.92857 | 12544 | 1404928 10.5830 Tg5112 | 7.6158 113 | 8.84956 | 12769 | 1442897 10.6301 | 205379 | 7-6811 || 314 | 8.77193 | 12996 | 1481544 | 10.6771 | 216000 | 7.7460 || 11S | 8.69565 | 13225 | 1520875 | 10.7238 | 226981 | 7.8102 | 116 | 8.62069 | 13456 | 1560896 | 10.7703 238328 | 7.8740 || 117 | 8.54701 | 13689 | 1601613 | 10.8167 250047 | 7-9373 | 118 | 8.47458 | 13924 | 1643032 | 10.8628 262144 | 8.0000 || I19 8.40336, T4161 | 1685159 | 10.9087 i 16 TABLE 9 (continued) VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS n3 | 1 V n | 2 1000.7, V2 | 14400 | 1728000 | 10.9545 | 30625 | 5359375 | 13-2288 | | | 275 5.71429 14641 | 1771561 | 11.0000 | 176 | 5.68182 | 30976 | 5451776 | 13.2665 | 14884 | 1815848 | 11.0454 |) 177 564972 | 31329 |] 5545233 | 13-3041 3 | 15129 | 1860867 | 11.0905 | 178 | 5.61798 | 31684 | 5639752 | 13.3417 15376 1906624 (EES Se) 179 | 5.58659 Wooeue §735339 | 13-379! 8.00000 | 15625 | 1953125 | 11.1803 || 180] 5.55556 | 32400 | 5832000 | 13.4164 7.936051 | 15876 | 2000376 | 11.2250 |} 181 | 5.52486 | 32761 5929741 | 13-4536 7.87402 | 16129 | 2048383 | 11.2604 182 | 5.49451 | 33124 | 6028568 | 13.4907 7.81250 | 16384 | 2097152 | 11.3137 183 | 5.46448 | 33489 | 6128487 | 13.5277 7.75194 | 16641 | 2146689 | 11.3578 184 | 5.43478 | 33856 | 6229504 | 13.5647 7.69231 | 16900 | 2197000 | 11.4018 185 | 5.40541 | 34225 | 6331625 | 13.6015 7-63359 17161 | 2248091 11.4455 186 | 5.37634 34596 6434856 13.6382 7-57570 | 17424 | 2299968 | 11.4891 187 | 5.34759 | 34969 6539203 _ 13-6748 7-51880 | 17689 | 2352637 | 11.5326 || 188 | 5.31915 | 35344 | 6644672 | 13.7113 7.46269 | 17956 | 2406104 | 11.5758 189 | 5.29101 | 35721 | 6751269 | 13-7477 | 7-40741 | 18225 | 2460375 | 11.6190 || 190 | 5.26316 | 36100 | 6859000 13.7840 7.35294 15496 | 2515450 | 11.6619 7-29927 | 18769 | 2571353 | 11.7047 | 7-24638 | 19044 | 2628072 | 11.7473 7.19424 | 19321 | 2685619 | 11.7808 19t | 5.23560 | 36481 | 6967871 | 13.8203 192 | 5.20833 | 36864 | 7077888 | 13.8564 193 | 5.18135 | 37249 | 7189057 | 13.8924 194 | 5.15464 37636 7301384 13.9284 195 | 5.12821 | 38025 | 7414875 | 13.9642 196 | 5.10204 | 38416 | 7529536 | 14.0000 197 | 5.07614 | 38809 | 7645373 14.0357 198 | 5.05051 | 39204 | 7762392 | 14.0712 199 | 5.02513 | 39601 | 7880599 14.1067 200 | 5.00000 40000 | 8000000 14.1421 201 | 4.97512 | 40401 | 8120601 | 14.1774 202 | 4.95050 | 40804 | 8242408 | 14.2127 203 | 4.92611 | 41209 | 8365427 | 14.2478 204 | 4.90196 | 41616 | 8489664 | 14.2829 7.14286 | 19600 | 2744000 | 11.8322 7.09220 | 19881 | 2803221 | 11.8743 7.04225 | 20164 | 2863288 | 11.9164 6.99301 | 20449 | 2924207 | 11.9583 6.94444 | 20736 | 2985984 | 12.0000 | 6.89655 | 21025 | 3048625 | 12.0416 6.84932 | 21316 | 3112136 | 12.0830 6.80272 | 21609 | 3176523 | 12.1244 6.75676 | 21904 | 3241792 | 12.1655 6.71141 | 22201 | 3307949 | 12.2066 || 6.66667 | 22500 | 3375000 | 12.2474 || 205 | 4.87805 | 42025 | 8615125 | 14.3178 6.62252 | 22801 | 3442951 | 12.2882 || 206 | 4.85437 | 42430 | 8741816 | 14.3527 6.57895 | 23104 | 3511808 | 12.3288 || 207 | 4.83092 | 42849 | 8869743 | 14.3875 6.53595 | 23409 | 3581577 | 12.3693 | 208 | 4.80769 | 43264 | SgQ8912 | 14.4222 6.49351 | 23716 | 3652264 | 12.4097 ||| 209 | 4.78469 | 43681 | 9129329 | 14.4568 | 6.45161 | 24025 | 3723875 | 12.4499 || 210 | 4.76190 | 44100 | 9261000 | 14.4914 6.41026 | 24336 | 3796416 | 12.4900 6.36943 | 24649 | 3869893 | 12.5300 6.32911 | 24964 | 3944312 | 12.5608 || 6.28931 | 25281 | 4019679 | 12.6095 | 211 | 4.73934 | 44521 | 9393931 | 14.5258 212 | 4.71698 | 44944 | 9528128 | 14.5602 213 | 4-69484 | 45369 | 9663597 | 14.5945 214 | 4.67290 | 45796 | 9800344 | 14.6287 215 | 4.65116 | 4622 9938375 | 14.6629 216 | 4.62963 | 46656 | 10077696 | 14.6969 217 | 4.60829 ; 47089 | 10218313 | 14.7309 218 | 4.58716 | 47524 | 10360232 | 14.7648 219 | 4.56621 | 47961 | 10503459 | 14.7986 220 | 4.54545 | 48400 | 10648000 | 14.8324 221 | 4.52489 | 48841 | 10793861 | 14.8661 4.50450 | 49284 | 10941048 | 14.8997 223 | 4.48430 | 49729 | 11089567 | 14.9332 224 | 4.46429 | 50170 11239424 14.9066 225 | 4.44444 | 50625 11390625 | 15.0000 226 | 4.42478 | 51076 | 11543176 | 15.0333 227 | 4.40529 | 51529 11697083 | 15.0665 228 | 4.38596 | 51984 | 118 52352 15.0997 5268024 | 13.1909 || 229 | 4.36681 | 52441 | 12008989 | 15.1327 6.25000 | 25600 | 4096000 | 12.6491 6.21118 | 25921 | 4173281 | 12.6886 || 6.17284 | 26244 | 4251528 | 12.7279 | 6.13497 | 26569 | 4330747 | 12.7671 6.09756 | 26896 | 4410944 | 12.8062 | 6.06061 | 27225 | 4492125 | 12.8452 6.02410 | 27556 | 4574296 | 12.8841 | 5.98802 27859 4057463 | 12.9228 | §-95238 | 28224 | 4741632 | 12.9615 | 5.91716 | 28561 | 4826809 | 13.0000 5-388235 | 28900 | 4913000 | 13.0384 | 584795 | 29241 | 50002T1 | 13.0767 | 5.81395 | 29584 | 5088448 | 13.1149 | 5-78035 | 29929 | 5177717 | 13-1529 5-74713 | 30276 ty tN ~] SMITHSONIAN TABLES. TABLE 9 (continued ) 17 VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS L | | Br Th 1000.,, ns | = ies n® \2 | 81225 | 23149125 | 16.8819 | 81796 | 23393656 | 16.9115 | 82369 | 23639903 | 16.9411 82944 | 23887872 | 16.9706 83521 | 24137569 | 17.0000 4.34783 12167000 | 15.1658 | 4.32900 12326391 | 15.1987 | 4.31034 | 12487168 | 15.2315 | 4.29185 12649337 | 15.2643 | 4.27350 12812904 | 15.2971 || 4.25532 12977875 | 15-3297 || 4.23729 13144256 | 15.3623 | 4.21941 13312053 | 15.3948 | 4.20168 13481272 | 15.4272 4.18410 | 13651919 | 15.4596 4.16667 13824000 | 15.4919 | 4.14938 | 13997521 | 15.5242 4-13223 14172488 | 15.5563 || 4.11523 14348907 15.5885 || 4.098 36 14526754 | 15.6205 4.08163 14706125 | 15.6525 4.06504 14886936 | 15.6844 | 4.04858 15069223 | 15-7162 4.03226 15252992 | 15.7480 g1809 | 27818127 | 17.4069 4.01606 15438249 | 15.7797 92416 | 28094464 | 17-4356 4.00000 15625000 | 15.8114 Y | 93025 | 28372625 | 17.4642 3-98406 15813251 | 15.8430 : | 93636 | 28652616 | 17.4929 3-96825 16003008 | 15.8745 | 94249 | 28934443 | 17-5214 3-95257 16194277 | 15.9060 | .24675 | 94864 | 29218112 "17-5499 3-93701 16387064 | 15-9374 95481 | 29503629 | 17.5754 3-921 57 16581375 | 15.9687 .22 96100 | 29791000 | 17.6068 3-90625 16777216 | 16.0000 : 96721 | 30080231 | 17.6352 3:89105 16974593 | 16.0312 97344 | 30371328 | 17-6635 3.87597 17173512 | 16.0624 3.194 97969 | 30064297 | 17.6918 3.86100 17373979 | 16.0935 98596 | 30959144 | 17.7200 3.84615 17576000 | 16.1245 my 99225 | 31255875. | 17-7482 | 3-83142 17779581 | 16.1555 99856 | 31554496 | 17.7764 3-81679 17984728 | 16.1864 5 100489 | 31855013 | 17-8045 3-50228 18191447 | 16.2173 : IO1I24 | 32157432 | 17.8326 3-78788 | 18399744 16.2481 ; IOI761 | 32461759 | 17.8606 Gate Ga Qu 84100 | 24389000 | 17.0294 84681 | 24642171 | 17.0587 85264 | 24897085 | 17.0880 85849 | 25153757 | 17-1172 86436 | 25412184 | 17.1464 87025 | 25672375 | 17.1756 87616 | 25934330 | 17-2047 88209 | 26198073 | 17.2337 88804 | 26463592 | 17.2627 89401 | 26730899 | 17.2916 WHWYW Wowodg g0000 | 27000000 | 17.3205 go6or | 27270901 | 17.3494 91204 | 27543008 | 17.3781 Gao Ga Ge Gs N Go & Go Go 3-77358 18609625 | 16.2788 3.12500 | 102400 | 32768000 | 17.8885 3-75940 | 18821096 | 16.3095 3.11526 | 103041 | 33076161 | 17.9165 3-74532 | 19034163 | 16.3401 2 | 3-10559 | 103684 | 33386248 | 17.9444 3-73134 19248832 | 16.3707 3-09598 | 104329 | 33698267 | 17.9722 3.71747 19465109 | 16.4012 3.08642 | 104976 | 34012224 | 18.0000 3:70370 19683000 16.4317 3.07692 | 105625 | 34328125 | 18.0278 3.69004 | 19902511 | 16.4621 3.06748 | 106276 | 34645976 | 18.0555 3-67647 20123648 | 16.4924 3.05810 | 106929 | 34965783 | 18.083 | 3.66300 20346417 | 16.522 3.04878 | 107584 | 35287552.| 18.1108 3:64964 | 20570824 | 16.5529 3.03951 | 198241 | 35611289 | 18.1384 3.63636 20796875 | 16.5831 | 3.03030 | 108900 | 35937000 | 18.1659 3-62319 21024576 | 16.6132 3.02115 | 109561 36264691 | 18.1934 3-61011 21253933 | 16.6433 3.01205 | 110224 | 36594368 | 18.2209 3-597 12 21484952 | 16.6733 | 3.00300 | 110889 | 36926037 | 18.2483 3-58423 21717639 | 16.7033 2.99401 | I11556 | 37259704 | 18.2757 3:57143 21952000 | 16.7332 2.98507 | 112225 | 37595375 | 18.3030 3-55872 16.7631 | 2.97619 | 112896 | 37933056 | 18.3303 3-54610 2242 16.7929 | 2.96736 | 113569 | 38272753 | 18.3576 3:53357 | 16.8226 2.95858 | 114244 | 38614472 | 18.3848 3.52113 | 16.8523 2.94985 | 114921 | 38958219 | 18.4120 |] SMITHSONIAN TABLES. 18 TABLE 9 (continued ) VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS 1 1000.4 n | ns \ 72 : n® ns yz 2.94118 | 115600 | 39304000 | 18.4391 ; | 156025 | 61629875 | 19.8746 2.93255 | 116281 | 396051821 | 18.4662 |} ; 150816 | 62099136 | 19.8997 2.92395 | 116964 | 40001688 | 18.4932 .51889 | 157609 | 62570773 | 19.9249 2.91545 | 117649 | 40353607 | 18.5203 |} 158404 | 63044792 | 19.9499 2.90698 | 118336 | 40707584 | 18.5472 || ; 159201 | 63521199 | 19.9750 2.89855 | 119025 | 41063625 | 18.5742 ; 160000 | 64000000 | 20.0000 2.89017 | 119716 | 41421736 | 18.6011 : 160801 | 64481201 | 20.0250 2.88184 | 120409 | 41781923 | 18.6279 ; | 161604 | 64964808 | 20.0499 2.87356 | 121104 | 42144192 | 18.6548 .48 162409 | 65450827 | 20.0749 2.86533 | 121801 | 42508549 | 18.6515 ; | 163216 | 65939264 | 20.0998 2.85714 | 122500 | 42875000 | 18.7083 || 2.46914 | 164025 | 66430125 | 20.1246 2.84900 | 123201 | 43243551 | 18.7350 2.46305 | 164836 | 66923416 | 20.1494 2.84091 | 123904 |-43614208 | 18.7617 2.45700 | 165649 | 67419143 | 20.1742 2.83286 | 124609 | 43986977 | 18.7883 2.45098 | 166464 | 67917312 | 20.1990 2.82486 | 125316 | 44361864 | 18.8149 2.44499 | 167281 | 68417929 | 20.2237 2.81690 | 126025 | 44738875 | 18.8414 2.43902 | 168100 | 68921000 | 20.2485 2.80899 | 126736 | 45118016 | 18.8680 2.43309 | 168921 | 69426531 | 20.2731 2.80112 | 127449 | 45499293 | 18.8944 2.42718 | 169744 | 69934528 | 20.2978 2.79330 | 128164 | 45882712 | 18.9209 2.42131 | 170569 | 70444997 | 20.3224 2.78552 | 128881 | 46268279 | 18.9473 2.41546 | 171396 | 70957944 20.3470 2.77778 | 129600 | 46656000 | 18.9737 2.40964 | 172225 | 71473375 | 20.3715 2.77008 | 130321 | 47045881 | 19.0000 2.40385 | 173056 | 71991296 | 20.3961 2.76243 | 131044 | 47437928 | 19.0263 2.39808 | 173889 | 72511713 | 20.4206 2.75482 | 131769 | 47832147 19.0526 -39234 | 174724 | 73034632 | 20.4450 2.74725 | 132496 | 48228544 | 19.0788 ; | 175561 | 73560059 | 20.4695 2.73973 | 133225 | 48627125 | 19.1050 j | 176400 | 74088000 | 20.4939 2.73224 | 133950 | 49027896 | 19.1311 2 i | 177241 | 74618461 | 20.5183 2.72480 | 134689 | 49430863 | 19.1572 § | 178084 | 75151448 | 20.5426 2.71739 | 135424 | 49836032 | 19.1833 -36407 | 178929 | 75686967 | 20.5670 130161 | 50243409 | 19.2094 : 179776 | 76225024 | 20.5913 370 | 2. 136900 | 50653000 | 19.2354 2.352904 | 180625 | 76765625 | 20.6155 371 : 137641 | 51004811 | 19.2614 2.34742 | 181476 | 77308776 | 20.6398 372 | 2.688 138384 | 51478848 | 19.2873 2.34192 | 182329 | 77854483 | 20.6640 B73 2: 139129 | 51895117 | 19.3132 2.33045 | 183184 784027 52 20.6882 374 | 2. 139876 | 52313624 | 19.3391 2.33100 | 184041 | 78953589 | 20.7123 375 | 2. 140625 | 52734375 | 19.3649 || 2.32558 | 184900 | 79507000 | 20.7364 BUMS) || 2s 141376 | 53157376 | 19.3907 2.32019 | 185761 | 80062991 | 20.7605 B77: 142129 | 53582633 | 19.4165 32 | 2.31481 | 186624 | 80621568 | 20.7846 378 | 2. 142884 | 54010152 | 19.4422 2.30947 | 187489 | 81182737 | 20.8087 379 | 2.63852 | 143641 | 54439939 | 19.4679 2.30415 | 188356 81746504 | 20.8327 380 | 2. 144400 | 54872000 | 19.4936 2.29885 | 189225 | 82312875 | 20.8567 Bisie |) 2s T45161 | 55300341 | 19.5192 2.29358 | 190096 | 82881856 | 20.8806 BSom ime: 145924 | 55742968 | 19.5448 2.28833 | 190969 | 83453453 | 20.9045 383 | 2. 146689 | 56181887 | 19.5704 2.28311 | 191844 | 84027672 | 20.9284 384 | 2. 147456 | 56623104 | 19.5959 2.27790 | 192721 | 84604519 | 20.9523 385 | 2.59740 | 14822 57066625 | 19.6214 | 2.27273 | 193600 | 85184000 | 20.9762 386 | 2.59067 | 148996 | 57512450 | 19.6469 2.26757 | 194481 | 85766121 | 21.0000 387 | 2.58398 | 149769 | 57960603 | 19.6723 || 2.26244 | 195364 | 86350888 | 21.0238 388 | 2.57732 | 150544 | 58411072 | 19.6977 ||| 2.25734 | 196249 | 86938307 | 21.0476 389 | 2.57069 | 151321 | 58863869 | 19.7231 || | 197136 | 87528384 | 21.0713 390 | 2.56410 | 152100 | 59319000 | 19.7484 | 2.24719 | 198025 | 88121125 | 21.0950 391 | 2.55754 | 152881 | 59776471 | 19.7737 | 2.24215 | 198916 | 88716536 | 21.1187 392 | 2.55102 | 153664 | 60236288 | 19.7990 2.23714 | 199809 | 89314623 | 21.1424 393 | 2.54453 | 154449 | 60698457 | 19.8242 2.23214 | 200704 | 89915392 | 21.1660 394 | 2.53807 | 155236 | 61162984 | 19.8494 2.22717 | 201601 | 90518849 | 21.1896 SMITHSONIAN TABLES. VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE N NNN KH NbN dNYHN bv 2.15054 14592 -14133 | -13675 213 220)|2 2.12766 2.12314 11864 | 11416 | -10970 2.10526 2.10084 2.09644 2.09205 2.08768 2.08333 2.07900 2.07469 2.07039 2.06612 2.06186 2.05701 2-05339 2.04918 | 2.04499 | 2.04082 | 2.03666 2.03252 2.02840 2.02429 2.02020 2.01613 | 2.01207 2.00803 2.00401 2.00000 1.99601 1.99203 1.98807 1.98413 | 214369 n2 202500 203401 204304 205209 200116 | | 207025 207930 208849 209764 210081 211600 212521 213444 215296 216225 217150 218089 219024 NHON NN 230400 231361 232324 233289 234250 235225 230196 237169 238144 239121 240100 241081 242064 243049 244030 245025 246016 247009 248004 249001 2 50000 251001 252004 253009 254016 SMITHSONIAN TABLES. TABLE 9 (continued) OF NATURAL NUMBERS ns 91125000 91733951 92345408 92959677 93570664 9419637 5 94818816 | 2 95443993 g6071912 | 2 96702579 | 97 336000 97972181 g8611128 99252847 99897344 | 2 100544625 | 2 101194696 101847 563 102503232 103161709 103823000 104487111 | 105154048 105823817 100496424 | 107171875 107850176 108531333 109215352 BOD502239 110592000 111284641 TI1980168 112678587 113379904 114084125 114791256 T15 501303 116214272 116930169 117649000 118370771 119095488 119823157 120553784 121287375 122023936 122763473 123505992 124251499 125000000 125751501 126506008 127263527 128024064 21.8632 21.8861 | 21.9089 |} 21.9317 | 21.9545 ~) 0 Om Ne NNN N N NNN NN (al (oy Te} fey (oe) HO OL N NNN H ND NNN Nb RR eRe Ww WwW Ro wWwhN hd NNN HN ND NNN NN NNWN bo | 521 21.7945 || 21.8174 || 21.8403 ||| 21.9773 || 22.0000 | NI 505 506 597 508 509 | SIL 512 DS oe | 515 516 517 i} 518 | 519 520 522 N23 I) 524 1000.} 1.98020 | 1.97628 | 1.97239 1.96850 | 1.96464 1.96078 1.95095 | 1.95312 1.94932 | 1.94553 | 1.9417 5 1.93798 | 1.93424 | 1.93050 | 1.92678 | 1.92308 | 191939) 1.91571 1.91205 1.90840 1.90476 I.QOIl4 1.89753 1.59304 1.89036 1.88679 1.88324 1.87970 1.87617 1.87266 1.86916 1.86567 1.86220 1.85874 1.85529 1.85185 | 1.84843 1.84502 | 1.84162 | 1.83824 | 1.83486 | 1.83150 | 1.82815 | 1.82482 | 1.82149 | 1.81818 | 1.81488 | 1.81159 | 1.80832 1.80505 | 1.80180 | 1.79856 | 1.79533 | 1.79211 | 1.78891 | 260100 261121 | 262144 | 263169 264196 26522 206256 267289 268324 | 139795359 209361 270400 271441 272484 273529 274576 27 5625 276676 277729 278784 279841 280900 | 149721201 | 150508768 284089 | 285156 281961 283024 28622 289444 290521 291600 292681 293764 294849 295936 297025 298116 299209 | 300304 | 165469149 301401 302500 303601 304704 305809 300916 308025 3091 36 310249 311304 312481 128787625, | 129554216 | 130323843 | 131096512 13187222 132651000 133432831 | 134217728 135005697 | 135796744 | 13659087 5 137388096 138188413 1389918 32 140608000 141420761 142236648 143055067 143877824 PAA OB 12) 145531576 146303183 147197952 148035889 148877000 151419437 15227 3304 | 153130375 287296 288 369 153990656 154854153 155720872 | 2 | 156590819 157464000 158340421 159220088 160103007 160989184 | 161878625 162771336 163667 323 164566592 16637 5000 167284151 163196608 169112377 170031464 170953875 171879616 172808693 173741112 174676879 | 1g ROOTS — > s RN HD ANAM UuNnpp oO Go oe mn oo \O NI NwNN ND N bo iS} Co Ww XS NN Nh NNN WN ty NI - Go NS =O On tN Nb NN NNN 1G Su Oo’ ON u ‘oO ON NON to ow Wm N wN NNN NWN DBDOOUOO mmnnmnwo NInNnNN WO AL WO — NW Onwst NN NNNNN = ~I\O Wh NNN OMIM wW OMAN OWN NNN NN G2 Ga Gs Ga Go =-O0O00 NNN mw NNN NN PWWOD WHO OAHOW HHOALY Nv Oo ON 5 a) y to NR WN 20 TABLE 9 (continued) VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS 1000.3 n ns yz 1000.4 n2 m3 \2 560 | 1.78571 | 313600 | 175616000 | 23.6643 | 615 | 1.62602 | 378225 | 232608375 | 24.7992 | 561 | 1.78253 | 314721 | 176558481 | 23.6854 | 616 | 1.62338 | 379456 | 233744896 | 24.8193 | 562 | 1.77936| 315844 | 177504328 | 23-7065 || 617 | 1.62075 | 380689 | 234885113 | 24.8395 563 | 1.77620 | 316969 | 178453547 | 23-7276 || 618 | 1.61812 | 381924 | 236029032 | 24.8596 564 | 1.77305 | 318096 | 179406144 | 23.7487 | 619 | 1.61551 | 383161 | 237176659 | 24.8797 565 | 1.76991 | 319225 | 180362125 | 23.7697 1.61290 | 384400 | 238328000 | 24.8998 566 | 1.76678 | 320356 | 181321496 | 23.7908 1.61031 | 385641 | 239483061 | 24.9199 507 | 1.76367 | 321489 | 182284263 | 23.8118 1.60772 | 386854 | 240641848 | 24.9399 568 | 1.76056 | 322624 | 183250432 | 23.8328 1.60514 | 388129 | 241804367 | 24.9600 569 | 1.75747 | 323761 | 184220009 | 23.8537 1.60256 | 389376 | 242970624 | 24.9800 570 | 1.75439 | 324900 | 185193000 | 23.8747 1.60000 | 390625 | 244140625 | 25.0000 57 egg | 326041 ISO109411 | 23-8956 1.59744 | 391876 | 245314376 | 25.0200 572 | 1.74825 | 327184 | 187149248 | 23.9165 1.59490 | 393129 | 246491883 | 25.0400 573 | 1-74520 | 328329 | 188132517 | 23.9374 1.59236 394384 24707 31 52 25-0599 574 1.74216 | 329476 | 189119224 | 23.9583 1.58983 | 395041 | 248858189 | 25.0799 575 | 1.73913 | 330625 | 190109375 | 23-9792 | 630 | 1.58730 | 396900 | 250047000 | 25.0998 576 | 1.73611 | 331776 | 191102976 | 24.0000 || 1.58479 | 398161 | 251239591 | 25.1197 577 | 1-73310 | 332929 | 192100033 24.0208 1.58228 | 399424 | 252435968 | 25.1396 578 | 1.73010 | 334084 | 193100552 | 24.0416 | £.57978 | 400689 | 253636137 | 25.1595 579 | 1-72712 | 335241 | 194104539 | 24.0624 |} 1.57729 | 401956 | 254840104 | 25.1794 580 | 1.72414 | 336400 | 195112000 | 24.0832 | 1.57480 | 403225 | 256047875 | 25.1992 581 | 1.72117 | 337561 | 196122941 | 24-1039 1.57233 404496 | 257259456 | 25.2190 582 | 1.71821 | 338724 | 197137308 | 24.1247 1.56986 405769 258474853 | 25.2389 583 | 1-71527 | 339889 | 198155287 | 24.1454 1.56740 | 407044 | 259694072 | 25.2587 584 | 1.71233, 341056 | 199176704 | 24.1661 1.56495 | 408321 | 260917119 | 25.2784 585 | 1.70940 | 342225 | 200201625 | 24.1868 1.56250 | 409600 | 262144000 | 25.2982 586 1.70048 | 343396 | 201230056 | 24.2074 1.56006 | 410881 | 263374721 | 25.3180 587 1.70358 | 344509 | 202262003 | 24.2251 1.55763 | 412164 | 264609288 | 25.3377 588 | 1.70068 | 345744 | 203297472 | 24.2487 1.55521 413449 | 205847707 | 25.3574 589 | 1.69779 | 340921 | 204336469 | 24.2693 1.55280 414730 | 267089984 | 25.3772 590 | 1.69492 | 348100 | 205379000 | 24.2899 1.55039 416025 | 268336125 | 25.3969 591 | 1.69205 | 349281 | 200425071 | 24.3105 1.54799 | 417316 | 269586136 | 25.4165 592 | 1-68919 | 350464 | 207474688 | 24.3311 1.54560 | 418609 | 270840023 | 25.4362 593 | 1.08634 | 351649 | 208527857 | 24.3516 1.54321 | 419904 | 272097792 | 25-4558 594 | 1.68350 | 352836 | 209584584 | 24.3721 1.54083 | 421201 | 273359449 | 25.4755 1.68067 | 354025 | 210644875 | 24.3926 1.53846 | 422500 | 274625000 25.4951 596 | 1.67785 | 3552160 | 211708736 | 24.4131 I} 1.53610 | 423801 | 275894451 | 25.5147 597 | 1.67504 | 356409 | 212776173 | 24.4336 1.53374 | 425104 | ores 25-5343 508 | 1.67224 | 357604 | 213847192 | 24.4540 1.53139 | 426409 | 278445077 | 25.5539 599 | 1.66945 | 358801 | 214921799 | 24.4745 1.52905 | 427716 279720264 25.5734 600 | 1.66667 | 360000 | 216000000 | 24.4949 1.52672 | 429025 | 281011375 | 25.5930 601 | 1.66389 | 361201 | 217081801 | 24.5153 1.52439 | 430336 | 282300416 | 25.6125 602 | 1.66113 | 362404 | 218167208 | 24.5357 1.52207 | 431649 | 283593393 | 25.6320 603 | 1.65837 | 363009 | 219256227 | 24.5561 1.51976 | 432964 | 284890312 | 25.6515 604 | 1.65563 | 364816 | 220348864 | 24.5764 1.51745 | 434251 | 286191179 | 25.6710 605 |. 1.65289 | 366025 | 221445125 | 24.5967 1.51515 | 435600 | 287496000 | 25.6905 606 | 1.65017 | 367236 | 222545016 | 24.6171 1.51286 | 436921 | 288804781 | 25.7099 607 | 1.64745 | 368449 | 223645543 | 24.6374 1.51057 435244 | 290117528 | 25-7294 608 | 1.64474 | 369664 | 224755712 | 24.6577 1.50530 | 439569 | 291434247 609 | 1.64204 | 370881 | 225866529 | 24.6779 1.50602 | 440896 | 292754944 610 | 1.63934 | 372100 | 226981000 | 24.6982 1.50376 | 442225 | 294079625 611 | 1.63666 | 373321 | 228099131 | 24.7184 1.50150 | 443556 | 295408296 612 | 1.63399 | 374544 | 229220928 | 24.7386 1.49925 | 444559 | 296740963 613 | 1.63132 | 375769 | 230346307 | 24.7588 || 1.49701 | 446224 | 298077632 614 168806, 57h906 231475544 | 24-7790 1.49477 | 447561 299418309 SMITHSONIAN TABLES. l 1000.; n n3 1.49254 1.49031 1.48810 1.48588 | 1.48368 1.48148 1.47929 1.47710 1.47493 1.47275 1.47059 1.46843 1.46628 1.46413 1.46199 1.45985 | 1.45773, 1.45560 | 1.45349 | 1.45138 1.44928 | 1.44715 | 1.44509 1.44300 | 1.44092 | 1.43885 1.43678 1.43472 1.43206 1.43062 | 1.42857 1.42053 1.42450 1.42248 | 1.42045 | 1.41844 1.41643 | 0.41443 | 1.41243 | 1.41044 1.40845 | 1.40647 1.40449 1.40252 | 1.40056 1.39860 1.39665 1-39470 1.39276 1.39082 1.38889 1.38696 1.38504 1.38313 1.38122 445900 450241 451554 452929 454276 455625 450976 458329 459084 401041 462400 463761 405124 460489 467856 469225 470596 47 1969 473344 474721 476100 477481 478864 480249 48 1636 483025 484416 | 485809 487204 458601 490000 491401 492804 494209 495016 497025 498436 499849 501264 502681 504100 505521 300763000 BO21i7 II 303464448 304821217 306182024 307 540875 30891 5776 310288733 311665752 313040839 Besos 315821241 317214568 318611987 32001 3504 321419125 | 3228288 56 324242703 32506067 2 327082769 328509000 379939371 331373888 332812557 334255354 TABLE 9 (continued ) VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS 335702375 337153536 33860587 3 340368392 341532099 343000000 344472101 | 26.4764 | 345948408 347428927 34891 3664 350402625 351895816 899395243 354894912 | 26.6083 | 356400829 | | 357911000 506944 508 369 509796 511225 512656 514089 5t5524 516961 518400 519841 | 371694959 37 3248000 374805 361 521284 522729 524176 SMITHSONIAN TABLES. 359425431 360944128 362467097 363994344 365525875 367061 368601813 370146232 376367048 377933067 379503424 6 | | 21 26.0768 26.0960 260.1151 26.1343 26.1534 26.1725 |ll 26.1916 |} 26.2107 26.2298 || 26.2488 || 26.2679 26.2869 26.3059 | 26.3249 26.3439 | 26.3629 ||) | 26.3818 |f| 26.4008 26.4197 | 26.4386 26.4575 26.4953 26.5141 | 26.5330 | 26.5518 26.5707 | 26.5895 26.6271 | 26.6458 26.6646 20.6833 26.7021 | 26.7208 | 26.7 395 | 26.7 582 26.7769 || 26.7955 | 26.8142 ||| 26.8328 | 26.8514 26.8701 26.8887 | 26.9072 | I. I. I I I -33869 | -33690 | -33511 “33333 3793: | 37741 37552 37363 37174 36986 | 30799 | -30012 | . 36426 36240 36054 -35870 35085 | sSOSOE 35318 | 35135 | 34953 34771 34590 | -34409 34228 | 34048 | | 525625 527076 522529 529984 531441 532900 534301 535824 537259 | 538756 540225 541696 543169 544044 | 540121 547600 | 400869021 549081 550564 552049 553536 555025 | 381078125 382657176 384240583 | 385828352 387 420489 550516 559009 559504 501001 562500 | 504001 | 505504 567009 | 568516 570025 571536 573049 | 574564 — §76081 | 577600 | 579121 580644 | 444194947 582169 583696 | 440711081 442450728 359017000 390617591 392223168 393832537 395440904 397065375 398688256 | 27.1293 A003 E99 401947272 403553419 405224000 408518488 410172407 411830784 413493625 415160936 410832723 418508992 420189749 42187 5000 23564751 425259008 420957777 428661064 43036887 5 432081216 433798093 AS92952 437245479 438976000 | 445943744 585225 447697125 586756 | 588289 589824 591361 | 592900 504441 | 595984 597529 | 299 463054824 28866 | .28700 | -28535 .28370 599076 600625 602176 603729 605284 606841 449455096 451217663 | 452984532 4547 50609 456533000 | 458314011 400099048 461889917 465484375 467288576 | 469097433 470910952 | 472729139 26.9258 20.9444 20.9629 26.981 5 27.0000 27.0185 27.0370 27-595 27.0740 27.0924 27.1109 27-1477 27.1662 27.1846 27.2029 27.2208 27-2397 27-2580 27.2704 27-2947 27.3130 2/1330 NNN Nb NNN NN NNN NN NNN ND NNN NN NNN NN Die TABLE 9 (continued) VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS y2 n? n8 V2 697225 | 582182875 | 28.8964 698896 | 584277056 | 28.9137 700569 | 586376253 | 28.9310 702244 | 588480472 | 28.9482 703921 | 590589719 | 28.9655 705600 | 592704000 | 28.9828 | 707281 | 594823321 | 29.0000 | 708964 | 596947688 | 29.0172 | 710649 | 599077107 | 29.0345 | 712336 | 601211584 | 29.0517 714025 | 603351125 | 29.0689 715716 | 605495730 | 29.0861 717409 | 607645423 | 29.1033 719104 | 609800192 | 29.1204 720801 | 611960049 | 29.1376 | 608400 | 474552000 | 27.9285 609961 | 476379541 | 27-9464 611524 | 478211768 | 27.9643 613089 | 480048087 | 27.9821 | 614656 | 481890304 | 28.0000 | | — 616225 | 483736625 | 28.0179 | , 617796 | 485557656 28.0357 | | 619369 487443403 | 28.0535 | 620944 | 489303872 | 28.0713 | 622521 | 491169069 | 28.0891 ot 624100 | 493039000 | 28.1069 625681 | 494913671 | 28.1247 627264 | 496793088 | 28.1425 628849 | 498677257 | 28.1603 630436 | 500566184 | 28.1780 ee 722500 | 614125000 | 29.1548 724201 | 616295051 | 29.1719 725904 | 618470208 | 29.1890 727609 | 620650477 | 29.2062 729316 | 622835864 | 29.2233 632025 | 502459875 | 28.1957 633616 | 504358336 | 28.2135 | 635209 | 506261573 | 28.2312 | 636804 | 508169592 | 28.2489 638401 | 510082399 | 28.2666 ein iene in| 731025 | 625026375 | 29.2404 732730 | 627222016 | 29.2575 734449 | 629422793 | 29.2746 730164 | 631628712 | 29.2916 737881 | 633839779 | 29.3087 739600 | 636056000 | 29.3258 741321 | 638277381 | 29.3428 743044 | 640503928 | 29.3598 744769 | 642735647 | 29.3769 | 746496 | 644972544 | 29.3939 | 748225 | 647214625 | 29.4109 | 749956 | 649461896 | 29.4279 | 751689 | 651714363 | 29.4449 753424 | 653972032 | 29.4618 755161 | 656234909 | 29.4788 756900 | 658503000 | 29.4958 | 758641 | 660776311 | 29.5127 760384 | 663054848 | 29.5296 762129 | 665338617 | 29.5466 763876 | 667627624 | 29.5635 640000 | 512000000 | 28.2843 641601 | 513922401 | 28.3019 | 643204 | 515849608 | 28.3196 644809 | 517781627 | 28.3373 || 646416 | 519718464 | 28.3549 648025 | 521660125 | 28.3725 649636 | 523606616 | 28.3901 651249 | 525557943 | 28.4077 652864 | 527514112 | 28.4253 654481 | 529475129 | 28.4429 656100 | 531441000 | 28.4605 | 657721 | 533411731 | 28.4781 | 650344 | 535387328 | 28.4956 660969 | 537367797 | 28.5132 |} 662590 | 539353144 | 28.5307 |} | 664225 | 541343375 665856 | 543335496 | 667459 | 545338513 | 669124 | 547343432 670761 | 549353259 | 672400 | 551368000 674041 | 553357661 | 675684 | 555412248 | 677329 | 557441767 | 678976 | 559476224 2) 680625 | s61sr5625 | 5 682276 | 563559976 | 2 | 683929 | 565609283 | 685584 | 567663552 | 2 687241 | 569722789 688900 | 571787000 690561 | 573856191 692224 | 575930368 693889 | 578009537 695556 | 580093704 sO i Oe oe 765625 | 669921875 | 29.5804 767376 | 672221376 | 29.5973 769129 | 674526133 | 29.6142 770884 | 676836152 | 29.6311 772641 | 679151439 | 29.6479 774400 | 681472000 | 29.6648 776161 | 683797841 | 29.6816 777924 | 686128968 | 29.6985 779689 | 688465387 | 29.7153 781456 | 690807104 | 29.7321 a | FE) 783225 | 693154125 | 29.7489 784996 | 695506456 | 29.7658 786769 | 697864103 | 29.7825 788544 | 700227072 | 29.7993 790321 | 702595369 | 29.8161 Oe ape revereiarene 's: SMITHSONIAN TABLES, TABLE 9 (concluded) 23 VALUES OF RECIPROCALS, SQUARES, CUBES, AND SQUARE ROOTS OF NATURAL NUMBERS t000.} n n3 2 | T0004 n? | | 8329 ||| 945 | 1.05820 | 893025 | 843908625 | 30.7409 8496 || 946] 1.05708 | 894916 | 846590536 | 30.7571 -8664 || 947 | 1.05597 | 896809 | 849278123 | 30.7734 .8831 || 948 | 1.05485 | 898704 | 851971392 | 30.7896 8998 | 949 | 1.05374 | goobor | 854670349 | 30.5058 .9166 || 950 | 1.05263 | 902500 | 857375000 | 30.8221 -9333 || 951 | 1.05152 | 904401 | 860085351 | 30.8383 “9500 |] 952 | 1.05042 | 906304 | 862801408 | 30.8545 -9666 || 953 | 1.04932 | 908209 | 865523177 | 30.8707 -9833 || 954] 1.04822 | g10116 | 865250664 | 30.8869 .12360 | 792100 | 704969000 -12233 | 793881 | 707347971 | .12108 | 795664 | 709732288 | -11982 | 797449 | 712121957 -11857 | 799236 | 714516954 -11732 | 801025 | 716917375 | .11607 | 802816 | 719323136 .11483 | 804609 | 721734273 | -11359 | 806404 | 724150792 | 11235 | 808201 | 726572699 | RO NNN DN WODOWOOO OOUOWOWO NwHNHN N -IIIII | 810000 | 729000000 | 30.0000 || 955 | 1.04712 | 912025 | 870983875 | 30.9031 10988 | 811801 | 731432701 | 30.0167 |} 956] 1.04603 | 913936 | 873722816 | 30.9192 -10865 | 813604 | 733870808 | 30.0333 |] 957 | 1.04493 | 915849 | 876467493 | 30.9354 .10742 | 815409 | 736314327 | 30.0500 |} 958 | 1.04384 | 917764 | 879217912 | 30.9516 10619 | 817216 | 738763264 | 30.0666 || 959} 1.04275 | 919681 | 881974079 | 30.9677 .10497 | 819025 | 741217625 | 30.0832 || 960 | 1.04167 | 921600 | 884736000 | 30.9839 -10375 | 820836 | 743677416 | 30.0998 || 961 | 1.04058 | 923521 | 887503681 | 31.0000 10254 | 822649 | 746142643 | 30.1164 |} 962 | 1.03950| 925444 | 890277128 | 31-0161 .10132 | 824464 | 748613312 | 30.1330 || 963 | 1.03842 | 927369 | 893056347 | 31.0322 -IOOII | 826281 | 751089429 | 30.1496 || 964 | 1.03734 | 929296 | 895841344 | 31.0483 1.09890 | 828100 | 753571000 | 30.1662 ||| 965 | 1.03627 | 931225 | 898632125 | 31.0644 1.09769 | 829921 | 756058031 | 30.1828 ||| 966} 1.03520 | 933156 | 901428696 | 31.0805 1.09649 | 831744 | 758550528 | 30.1993 |] 967 | 1.03413 | 935089 | 904231063 | 31.0966 1.09529 | 833569 | 761048497 | 30.2159 ||| 968 | 1.03306 | 937024 | 907039232 | 31-1127 1.09409 835396 | 763551944 | 30.2324 || 969 | 1.03199 | 938961 | 909853209 | 31.1288 1.09290 | 837225 | 766060875 | 30.2490 ||| 970 | 1.03093 | 940900 | 912673000 | 31.1448 1.09170 | 839056 | 768575296 | 30.2655 || 971 | 1.02987 | 942841 | 915498611 | 31.1609 1.09051 | 840889 | 771095213 | 30.2820 || 972 | 1.02881 | 944784 | 918330048 | 31.1769 1.08932 | 842724 | 773620632 | 30.2985 || 973 | 1-02775 | 946729 | 921167317 | 31.1929 1.08814 | 844561 | 776151559 | 30.3150 || 974 | 1.02669 | 948676 | 924010424 | 31.2090 1.08696 | 846400 | 778688000 | 30.3315 ||| 975 | 1.02564 | 950625 | 926859375 | 31.2250 1.08578 | 848241 | 781229961 | 30.3480 || 976| 1.02459; 952576 | 929714176 | 31.2410 1.08460 850084 | 783777448 | 30.3645 || 977 | 1.02354 | 954529 | 932574833 | 31.2570 1.08342 | 851929 | 786330467 | 30.3809 || 978 | 1.02249 | 956484 | 935441352 | 31.2730 1.08225 | 853776 | 788889024 | 30.3974 || 979 | 1.02145 | 958441 | 935313739 | 31.2890 1.08108 | 855625 | 791453125 | 30.4138 || 980 | 1.02041 | 960400 | 941192000 | 31.3050 1.07991 | 857476 | 794022776 | 30.4302 || 981 | 1.01937 | 962361 | 944076141 | 31.3209 1.07875 | 859329 | 796597983 | 30.4467 || 982 | 1.01833 | 964324 | 946966168 | 31.3369 1.07759 | 861184 | 799178752 | 30.4631 || 983 | 1.01729 | 966289 | 949862087 | 31.3528 1.07643 | 863041 | 801765089 | 30.4795 || 984 | 1.01626 | 968256 | 952763904 | 31.3088 1.07527 | 864900 | 804357000 | 30.4959 ||| 985 | 1.01523 | 970225 | 955671625 | 31.3847 1.07411 | 866761 | 806954491 | 30.5123 || 986] 1.01420 | 972196 | 958585256 | 31.4006 1.07296 | 868624 | 809557568 | 30.5287 || 987 | 1.01317 | 974169 | 961504803 | 31.4166 1.07181 | 870489 | 812166237 | 30.5450 ||| 988 | 1.01215 | 976144 | 964430272 | 31.4325 1.07066 | 872356 | 814780504 | 30.5614 || 989 | I.o1112 | 978121 | 967361669 | 31.4484 1.06952 | 874225 | 817400375 | 30.5778 ||| 990 | 1.01010 | 980r00 | 970299000 | 31.4643 1.06838 | 876096 | 820025856 | 30.5941 || 991 | 1.00908 | 982081 | 973242271 | 31.4502 1.06724 | 877969 | 822656953 | 30.6105 ||| 992 | 1.00806 976191488 | 31.4960 1.06610 | 879844 | 825293672 | 30.6268 || 993 | 1.00705 | 979146657 | 31.5119 1.06496 | 881721 | 827936019 | 30.6431 ||| 994 | 1.00604 982107784 | 31.5278 1.06383 | 883600 | 830584000 | 30.6594 || 995 | 1.00503 985074875 | 31.5436 1.06270 | 885481 | 833237621 | 30.6757 ||| 996] 1.00402 988047936 | 31.5595 1.06157 | 887364 | 835896888 | 30.6920 ||| 997 | 1.00301 991026973 | 31-5753 1.06045 | 889249 | 838561807 | 30.7083 ||| 998 | 1.00200 994011992 | 31.5911 1.05932 | 891136 | 841232384 | 30.7246 ||| 999 | I.coI00 997002999 | 31.6070 SMITHSONIAN TABLES. 24 TABLE 10 LOGARITHMS SMITHSONIAN TABLES, TABLE 10 (continued) 2 5 LOGARITHMS 1 Om lonwe) Cn Ry HHN NNN N ND wRwN dN Nw NHN be COUn Gs - SMITHSONIAN TABLES, 26 TABLE 11 LOGARITHMS eH NNR NHWW WwWwwtpp NNNNN =NNNN WWWWW WwWWwWw HPHAH AUMUND DDN CO I I I I I Ce | NNHWNNN en len ile le NNNNN SS = Oe NNNNN NNNWW WWWWW WWWWW WHnowth fAAALH AU UMW ADADODA NNN OO WwWwww HAHAH HAHAH HUH UNUMUNAD DAQONN NNOWOW Ww AAPL A PANN UNuUNN DANAN BAOQNN™N NWOOCWO WOvwo te NNNNN SMITHSONIAN TABLES. 60 | 7782 7789 61 | 7853 7860 62 | 7924 7931 63 | 7993 8000 64 | 8062 8069 65 | 8129 8136 66 | 8195 8202 67 | 8261 8267 68 | 8325 8331 69 | 8388 8395 70 | 38451 = 8457 71 | 8513 8519 72 $573 8579 74 |8692 8698 POVNO75U ) 8756 76 | &308 8814 77 | 8865 8871 78 | 8921 892 79 | 8976 8982 80 9031 9036 go 82 Bae 9143 83 | 9191 9196 84 | 9243 9248 85 | 9294 9299 86 19345 9350 87 19395 9400 88 19445 9450 89 |9494 9499 SMITHSONIAN TABLES. 7796 7868 7938 8007 8075 8142 8209 8274 8338 8401 8463 8525 8585 8645 8704 8762 8820 8876 8932 8957 go42 9096 9149 9201 9253 9304 9355 9405 9455 9504 8710 8768 8825 8882 8938 8993 9047 gIOI 9154 g206 9258 9309 9360 9410 9460 9509 TABLE 11 (continued) LOGARITHMS 7810 7882 7952 8021 8089 8156 8222 8287 8351 8414 8476 8537 8597 8657 8716 8774 8831 8887 $943 8998 9°53 gito6 9159 g212 9263 9315 9365 9415 9465 9513 7818 7889 7959 8025 8096 8162 8228 $293 8357 8420 8482 8543 $603 8663 8722 8779 8837 8893 8949 9004 9058 QgII2 9165 9217 9269 9320 9370 9420 9469 9518 7825 7896 7966 8035 8102 8169 8235 8299 8363 8426 8488 8549 8609 8669 8727 8785 8842 8899 8954 goog 9063 gI17 9170 aD) 9274 9325 9375 9425 9474 9523 7832 7993 7973 8041 8109 8176 8241 8306 8370 8432 8494 8555 8615 8675 8733 8791 8848 8904 8960 9015 9069 gI22 9175 9227 279 933° | 9380 9430 9479 9528 7846 7917 7997 8055 8122 8189 8254 8319 8382 3445 8506 8567 862 8686 8745 8802 8859 8915 8971 9025 9079 9133 g186 9238 9289 9340 9390 9440 9489 9538 ee OOO F SS oe eels tile ila | “OO o0000 SS eS Oe OoOo000 Se ho el eatiilen ien ian! See ee — ey — Om et tet eee NN NwNNN NNNNN NNNNN NNNNN NNNNN ee NNN NN NNONNNHN WWWWO WWWWW WWWWW | NNNNN NNNNN NNNNN NNNNN N NNN HN NN NWW WwWwwwW Coa WW OO WW Os WW WwWWWoW WHowtf PHP HL NNNNN NNNNN 28 TABLE 12 ANTILOGARITHMS a O0000 — Lain iilen tien tien! — oe OROLOEOLO) — Oe ~ eee OFOVORORO: — | NwWH a to Oo0000 — — mn 9 I oO I O | I O° I O° I NNN Ne N NHN oo0o0°0 = = = db WH HN NNHNNN ~O0000 Nee ee LS ee WNNNN COU © Cond O NNHNN In & G2 Gs bv ee) NwNH LW NNHHNHN of Ov W Od Ga Go U2 db NHKHHHN OO OOr.O on Pm RMN hh OofhN HUN Mmnwo G2 2 Wd a Gd QW WH N RWW G2 G2 Cn G2 Go eet NNN WN be SMITHSONIAN TABLES. TABLE 12 (continued) 29 ANTILOGARITHMS | NNN WN & NNN NN ee NN HN Www nd — NNNNN WwW WW GW — OS et NNNHNN NDAAADACO DON UNnmnnmn wnfHPHf SPA AH I I I iF I OS CS a a a) ee | AANDADO NOUN Munir mp HH AA AL HWW W WwWwWwWw N™NN™N™N wR NN bY & G2 G2) G2 Go Go WWW 2 OD Muti Munim & HHH HHH Wd Wd Wd WD NNNNWN fHWWW 0O00O0OO WOOWO COO 00 CO CO COMI RN wRN NNHNN WOO CO mOMmcecon NunNNN SIS IES tonto Tonyfonanylaniton} SMITHSONIAN TABLES. 30 TABLE 13 ANTILOGARITHMS SMITHSONIAN TABLES. TABLE 13 (continued) 31 ANTILOGARITHMS SMITHSONIAN TABLES, 32 TaBLe 14 CIRCULAR (TRIGONOMETRIC) FUNCTIONS (Taken from B. O. Peirce’s ‘‘ Short Table of Integrals,’’ Ginn & Co.) COSINES. TANGENTS. COTANGENTS. Nat. Log. 7.4037 -7648 -9408 | 116 8.0658 | 145 .1627 0175 8.2419 | 0204 .3088 | 0233 .3668 0262 .4179 0291 .4637 | 0320 .5050 ‘|| 0349 8.5428 0378 .5776 || 0407 .6097 10436 .6397 0465 .6677 | | 0494 .6940 0523 8.7188 0552 = -7423 | O53r .7645 || 0610 .7857 0640 .8059 .0669 ~=.8251 ‘|| .0698 8.8436 || 0727 .8613 || 0756 .8783 | 0785 .8946 | 0814 .g1o4 0843 .9256 | 0872 8.9403 | O90L = -9545 | 0929 ~=—.g082 | 0958 .9816 0987-9945 -I0I6 9.0070 | 1045 9.0192 | 1074 .O311 | 1103 .0426 | -£132 .0539 | .1161 .0648 | .I190 .0755 || .1219 geese || .1248 .og6I .1276 .1060 Woligtols | Bielsy iggqanesl2ice2 -1363 .1345 -1392 9.1436 al42T) 0525 -1449 .1612 .1478 .1697 SO7) ealyol 15360 .1863 -1564 9.1943 | .98 I.0000 0.0000 | 1.0000 .0000 | 1.0000. .0000 | 1.0000 .0000 -9999 0000 | 9999-0000 9998 9:9999 - 9998 .9999 | 9997-9999 9997-9999 | 9996 .9998 9995 -9998 99949-9997 9993-9997 9992-9996 | 9990-9996 | 9989-9995 9988 .9995 9986 9.9994 9985-9993 | 9983-9993 -998L 9992 -9980 =.99QI 9978 .9990 9976 9.9989 9974-9989 | 9971 .9988 | 9969 .9987 9967-9986 9964 .9985 | .9962 9.9983 | 9959 .9982 9957-9981 9954 .9980 ‘995! -9979 9948 .9977 9945 9.9976 | 9942 .9975 9939-9973 -9936 .9972 -9932 .9971 9929 .9969 9925 9.9968 9922 .9966 9918 .9964 9914 — .9963 | QO9II .gg61 9907 .9959 9903 9.9958 9899 .9956 9894 .9954 9890 .9952 | .9886 .9950 .9881 —.9948 | Nat. Log. COSINES. SMITHSONIAN TABLES. .0000 .0029 .0058 .0087 .O116 0145 0175 .0204 .0233 .0262 .029I .0320 0349 .0378 .0407 0437 .0466 -0495 .0524 0553 0582 .0O12 .0041 .0670 .0699 8 .07 29 0758 0787 | .0816 .0846 .087 5 .09O4 0934 .0903 .0992 -1022 -IOSI ace -IITIO .1139 .1169 1198 1228 1257 .1287 a7 -1346 .1376 1405 1435 1465 “1495 -1524 ASSES 9.9946 | - 1584 ~o eo 343-772-5363 171.89 2352 | 114.59 0591 | 85.940 1.9342 68.750 8373 57-290 1.7581 || 49-104 .6QII 42.964 .6331 | 38.188 5819 34.368 — .5362 31.242 .4947 28.636 1.4569 | 26.432 .4221 24.542 — .3899 22.904 = .3599 21.470 .3318 20.206 = .3055 19.081 1.2806 13:07.5 25711 17.169 .2348 16.350 .2135 15.605 .1933 14.924 1739 14.301 1.1554 13°72 73 7,0 13/197. | 2.1205 12.706 .1040 12.251 .0882 11.826 .0728 11.430 1.0580 11.059 .0437 10.712 .0299 10.385 .0164 10.078 .0034 9.7882 0.9907 9.5144 0.9784 9.2553 -9664 9.0098 .9547 8.7769 .9433 8.5555 9322 8.3450 .9214 8.1443 0.9109 7-9539 -9005 7:7704 .8904 7.5958 .8806 7.4287 .8709 7.2687 .8615 7.1154 0.8522 6.9682 .8431 6.8269 .8342 6.6912 .8255 6.5606 .8169 6. nae 808 5 6.3138 0.8003 | Nat. Nat. Log. ; TANGENTS. SINES. 1564 °1593 1622 -1650 -1679 .1708 1736 1765 1794 .1822 -1851 -1880 .1908 | 1937 | «1965 -1994 .2022 -2051 2079 2108 .2136 .2104 | .2193 222I1 2250 2278 +2306 -2334 2303 .2391 -2419 2447 | .2476 .2504 .2532 “2500 -2588 2016 .2044 .2672 .2700 2728 -2756 2784 2812 .2840 .2868 2896 2924 -2952 :2979 +3007 | 3035 -3062 TABLE 14 (continued ) CIRCULAR (TRIGONOMETRIC) FUNCTIONS COSINES. 9877 2 | .9872 | 9863 9858 | 9853 | .9848 | .9843 | .9838 | 9833 | 9327 | .g822 9816 | .o81t | .9805 9799 | 9793 | 9787 9781 9775 9769 9763 -97 57 ‘9750 9744 9737-9884 | 9730 .9881 9724 .9878 9717 9875 9710 .9872 9.9869 .9866 .9863 9859 9856 9853 | 9.9849 -9846 9843 -9839 19628 .9836 | . | 9621 .9832 | 9613 9.9828 .g605 .9825 9596 .9821 9588 .9817 9580 .9814 9572 9810 .9563 9.9806 9555 -9802 | 9546 .9798 9537 -9794 9528 .9790 9520 .9786 9511 9.9782 | TANGENTS. 1584 4 | .1614 | .1644 1673 .1703 -1733 | .1763 1793 | .1823 | 1853 | 1833 | 1914 | -1944 +1974 -2004 .2035 2005 | +2095 | .2126 | .2156 .2186 .2217 | 2247 | .2278 | .2309 -2339 .2370 .2401 2432 .2462 -2493 2524 2555 2580 .2617 .2648 .2679 2931 -2962 -2994 3026 “3057 .3089 3121 “3153 23185 3217 =3249 Nat. Log. Nat. 9.1997 | 6.3138 -2078 6.1970 2158 | 6.0844 2236 | 5.9758 -2313 | 5.8708 -2389 5.7004 9.2463 | 5-6713 -2536 | 5.5764 -2009 | 5.4845 -2080 | 5.3955 927 5ON159:3 093 2819 5-2257 9.2887 | 5.1446 2953 | 5.0658 3020 4.9894 3085 | 4.9152 -3149 | 4.8430 -3212 | 4.7729 9.3275 | 4.7046 +3330 | 4.6352 +3397 | 4.5736 +3458 | 4.5107 +3517 | 4.4494 -3576 | 4.3897 9.3634 | 4.3315 -3091 | 4.2747 -3748 | 4.2193 3804 | 4.1653 3859 | 4.1120 3914 | 4.0611 9.3968 | 4.0108 .4021 | +4074 4127 4178 -4230 | 9.4281 | -433! 4381 4430 -4479 4527 9-4575 .4622 .4669 4716 4762 .4808 | 9.4853 | -4898 | 4943 | .4987 “9O3F | 3:2397 -5075 | 3.1084 9.5118 | 3-0777 \COTANGENTS. Log. 0.8003 | -7922 | -7842 | 7764 -7687 7611 | 0.7537 | -7404 -7 391 «7320 -7250 | 7181 | O701s || 6542 6483 .6424 0.6366 .6309 || 6252 -6196 .6141 || -6086 | 0.6032 O79 5926 || -5873 5022 | “577° | 0157029) .5669 5619 | -5570 5521 5473 || 0.5425 +5378 533! | 5284 5238 5192 || 0.5147 5102 || “D257 -5013 || -4969 | “4925 )) food ped Bont) lod ert Reh pmed Dae fe Sad bed Bd eh tt a stp Dr dD emt a) ed ibe Bette iS Vt RL gal EA I) Oe de ets ce COSINES. SMITHSONIAN TABLES. Nat. Nat. Log. | Nat. 0.4882 | Log. COTAN- | = GENTS. | TANGENTS. 33 34 TABLE 14 (continued) CIRCULAR (TRIGONOMETRIC) FUNCTIONS ui 1g SINES. COSINES. | TANGENTS. | COTANGENTS. i gy | <4 Ax | m4 oO Nat. Log. | Nat. Log. Nat. Log. Nat. Log. | 0.3142 | 18°00’ | .3090 9.4900 | .9511 9.9782 | .3249 9.5118 | 3.0777 0.4882 | 72°00! | 1.2566 0.3171 10 | .3118 .4939 | 9502. .9778 | .3281 «5161 | 3.0475 4839 50 | 1.2537 0:3200 20 GI45 4977-9492" O74 3BT4 (5203) 3.0178 -4797 4o | 1.2508 0.322 BOmiesi7s SOS | .9483 .9770 | .3346 5245 | 2.9887 ~ .4755 30 .2479 0.3258 4o | .3201 .5052| .9474 -9765 | .3378 .5287 | 2.9600 .4713 20 2450 0.3287 50 | -3228 .5090 | 9465 .9761 “3411 .5329 | 2.9319 .4071 10 2421 0.3316 | 19°00’ | .3256 9.5126 (+9455 9-9757 | -3443 9.5379 | 2.9042 0.4630 | 71°00! | 1.2392 0.3345 10 | .3283 5163 | 9446 .9752 | .3476 5411 | 2.8770 .4559 50 2363 0.3374 20 | 3311 «5199-9436 .9748 3508 «5451 | 2.8502 .4549 40 | 1.2334 0.3403 30 | -3338 -5235 | 9426 .9743 | -3541 -5491 | 2.8239 4509 30 | 1.2305 0.3432 4O | .3305 -5270) -9417 9739 | -3574 5531 | 2.7980 -4469 20 | 1.2275 0.3462 50 | .3393 -5306 | 9407 .9734 | -3007 .5571 | 2.7725 .4429 10 | 1.2246 0.3491 | 20°00’ | .3420 9.5341 | 9397 9-9730 .3640 9.5611 | 2.7475 0.4389 | 70°00! | 1.2217 0.3520 | 10 | .3448 .5375 | -9387 -9725 | .3673. .5650| 2.7228 .4350 50 .2188 0.3549 20 | -3475 +5409 | 9377-9721 | 3706 .5689 | 2.6985 4311 40 | 1.2159 0.3578 | 30 | 3502 -5443 | 9367 9716 | .3739 —--5727 | 2.6746 4273 30 | 1.2130 0.3607 40 | -3529 354771) -9350- 970-3772) -5700)| 20501 | 423% 20 2101 9.3636} 50 , -3557 -5510 | .9346 9706 .3805 5804 | 2.6279 .4196 Io | 1.2072 |I 0. 3665 | 21°co’ | 3584 9.5543 | -9336 9.9702 -3839 9.5842 | 2.6051 0.4158 | 69°00’ | 1.2043 0.3694 | Io | 3611 .5576| .9325 .9697 | .3872 + .5879 | 2.5826 4121 50 .2014 0.3723 | 20 | .3638 5609 | .9315 .9692 | .3906 = .5917 | 2.5605 .4083 40 1985 0.3752 | 30 | 3665 -5641 .9304 9687 | .3939 =-5954 | 2.5380 .4046 30 1956 0.3782 | 40 | .3692 .5673 | 9293 .9682 | .3973 5991 | 2.5172 .4009 20 .1926 0.3811 | 50 | 3719 .§704 | .9283 .9677 | .4006 =.6028 | 2.4960 = .3972 10 | 1.1897 0.3840 | 22°00’ | .3746 9.5736 | -9272 9.9672 | .4040 9.6064 | 2.4751 0.3936 | 68°00! | 1.1868 0.3869 10 | .3773 -5767 | -9261 .9667 | .4074 =.6100 | 2.4545 .3900 50 -1839 0.3898 | 20 | .3800 .5798 9250 .9661 | .4108 .6136| 2.4342 .3864 40 -1810 0.3927 | 30 | .3827 5828 | .9239 6.9056 | 4142 .6172| 2.4142 .3828 30 1781 0.3956 | 4° 3854 -5859 | -9228 .9651 | .4176 .6208 | 2.3945 .3792 20) ||| Malis 0.3955 | 50 | .3881 .5889! .9216 .9646| .4210 6243 | 2.3750 .3757 TO) |) LaG723 -1694 0.4014 | 23°00’ | .3907 9.5919 | .9205 9.9640 | .4245 9.6279 | 2.3559 0.3721 | 67°00’ 0.4043 | 10° | .3934 ~=-5948 | 9194 .9635 | .4279 .6314 | 2.3369 ©—.3686 50 1665 _ mee eee meee eee . ae is . apenas on 0.4072 | 20 | .3901 .5978 | .9182 .9629 | -4314 .6348 | 2.3183 .3652 40 1636 0.4102 30 | .3987 6007 | .g171 9624 | -4348 6383 | 2.2998 ~=—.3617 30 | 1.1606 0.4131 | 40 | .4014 .6036 | 915g .9618 | 4383 .6417 | 2.2817 3583 20 S77 0.4160 50 | .4041 6065 | .O147. .9613| .4417 .6452 | 2.2637 354 10 1548 0.4189 | 24°00’ | .4067 9.6093 | .9135 9.9607 | .4452 9.6486 | 2.2460 0.3514 | 66°00’ | 1.1519 0.4218 Io | .4094 .6121 | 9124 .9602 | .4487 .6520 | 2.2286 .3480 50 | 1.1490 0.4247 | 20 | .4120 .6149| .9112 .95§96| .4522 .6553 | 2.2113 .3447 40 | 1.1461 0.4276 30 | -4147 -6177 | .QI00 9590 | .4557 .6587 | 2.1943 -3413 30. | 1.1432 0.4305 40 | 4173 -6205| .g088 = .9584 | .4592 .6620 | 2.1775 .3380 20 | 1.1403 0.4334 50 | -4200 .6232 | .9075 .9579 | .4628 6654 | 2.1609 .3346 Io | 1.1374 0.4363 | 25°00’ | -4226 9.6259 | .9063 9.9573 | .4663 9.6687 | 2.1445 0.3313 | 65°00’ | 1.1345 0.4392| 10 | -4253 -6286]| 9051 .9567 | .4699 6720 | 2.1283. .3280 50 | 1.1316 0.4422 | 20) |-4279) EOzi3h| 90088. OSOU \l-a7e4, O7i52) |) 2:12 3248 40 | 1.1286 0.4451 30 | -4305 -6340| .9026 § .9555 | .4770 .6785 | 2.0965 -3215 Zo) | Ue2 57 0.4480 40 | .4331 .6366| 9013 .9549 | .4806 .6817 | 2.0809 == .3183 20 | 1.1228 0.4509 50 | 4358 -.6392| .gool .9543| .4841 .6850 | 2.0655 .3150 10 | 1.1199 |] 0.4538 | 26°00’ | .4384 9.6418 | £8988 9.9537 | 4877 9.6882 | 2.0503 0.3118 | 64°00! | 1.1170 0.4507 10 | .4410 .6444 | .8975 .9530 | 4913 .6914 | 2.0353 .3086 50 | I-1141 0.4596 20 | .4436 .6470 | .8962 .9524 | .4950' .6946 | 2.0204 3054 4o | T1112 0.4625 30 | 4462 .6495 | -8949 .9518 | .4986 ©.6977 | 2.0057 = -3023 30. | 1.1083 0.4654 40 | .4488 .6521 | 8936 .9512]| .5022 .7009| 1.9912 .299I 20 | 1.1054 0.4683 50 |.4514 .6546 | .8923 .9505| .5059 .7040 | 1.9768 .2960 10 | 1.1025 0.4712 | 27°00’ | .4540 9.6570 | .8910 9.9499 | .5095 9.7072 | 1.9626 0.2928 | 63°00’ 1.0996 | | ae rm | Nat. Log. Nat. Log. Nat. Log. Nat. Log. wn 2 |- a | oe COSINES. SINES. eoraee TANGENTS. | 9% | @< SMITHSONIAN TABLES. CIRCULAR (TRIGONOMETRIC) FUNCTIONS TABLE 14 (continued) COSINES. Nat. Log. TANGENTS. no nn YW HWW bo Ss WWNn Nh -7342 9.7361 -7380 7419 7438 -7457 -7400 | . “7513 753! 7559 -7508 9.7586 | -7604 -70622 -7640 | 5854 7875 | .5878 9.7692 | COSINES. SMITHSONIAN TABLES. 9.7476 | . -7494 | - -7657 | . .8Q10 8897 9.9499 9492 | -9486 9479 9473 9466 9.9459 9453 -9446 9439 | -9432 | - 9425 9.9418 | -O411 9404 9397 “9390 9383 99305 9368 9361 9353 | -9346 -9338 9-933! 9323 9315 9308 -9 300 .9292 9.9284 192701)|) -9208 9260 |. 9252))|\. 9244 9.9236 | . 9228 |. 9219 | SQeiTiTy .9203 ‘9194 9.9186 | 4227 98585 -6794 -103312 77 -20300 959 .062662 28 -Q9019 .7767 .102284 78 .20734 16.119 062039 .29 99453 8749 101266 79 21168 281 .061 421 2.30 0.99888 9.97 42 0.100259 2.80 1.21602 16.445 0.060810 31 1.00322 10.074 .099261 SI .22037 610 060205 32 .007 56 176 .098274 82 .22471 aT, .0 59606 33 .OTIQI 278 .097 296 83 .22905 945 059013 34 01625 1381 096328 84 .23340 17.116 058426 ails 1.02059 10.486 0.095369 2.85 1.23774 17.288 0.057844 -36 .02493 Sgt 094420 || 56 -24208 -462 .057 269 .37 02928 .697 .093481 87 24643 637 .056699 38 .03362 805 092551 88 .25077 814 056135 39 .03796 913 091630 89 25511 993 055570 2.40 1.04231 11.02 0.090718 2.90 1.25945 18.174 0.055023 41 04605 .134 08981 5 gl .26380 -357 054476 .42 .05099 .246 0838922 .Q2 .26814 541 053934 43 105534 -359 -088037 93 27248 .728 -053397 44 05908 473 .087161_— |] .94 .27683 .g16 052866 2.45 1.06402 11.588 0.086294 || 2.95 1.28117 19.106 0.052340 .40 .068 36 705 085435 .96 28551 .298 051819 47 07271 822 084585 .97 28985 492 051303 48 07705 O41 .083743 98 .29420 .688 050793 .49 .08139 =—«: 12.061 .08 2910 99 29854 886 050287 | | Zaks 1.08574 12.182 0.082085 || 3.00 1.30288 20.086 0.049787 SMITHSONIAN TABLES. logyo(e) TABLE 19 (continued) EXPONENTIAL FUNCTIONS logyo(ex) 1.30288 39723 31157 31591 -32026 32460 -32894 33328 33763 34197 34631 35006 35500 -35934 -36368 36803 °37237 37671 .38 106 38540 -38974 -39409 -39343 -40277 -40711 .41146 .41580 42014 42449 .42883 43317 “43751 -44186 .44620 45054 -45489 45923 -46357 .46792 .47226 .47660 -48094 .48529 48963 49397 .49832 .50266 50700 -S1134 “51509 1.52003 SMITHSONIAN TABLES. 33-115 0.049787 .049292 .048801 .048316 047835 0.047359 .046888 .046421 045959 045502 0.045049 .044601 04.4157 .043718 043283 0.0428 52 042426 042004 .041 586 041172 0.040762 0403 57 039955 039557 039164 0.038774 038388 .038006 .037628 -037254 0.036883 036516 0361 53 035793 035437 0.035084 034735 034390 034047 -033799 0.035373 .033041 032712 032387 032065 0.031746 .031430 -O31117 .030807 .030501 0.030197 1.52003 52437 52872 -53306 °53740 54175 -54609 -55043 -55477 «55912 . 56346 56780 57215 57049 58083 58517 -58952 -59356 -59820 .60255 .60689 61123 61558 61992 .62426 .62860 163295 .63729 64163 -64598 65032 .65466 .65900 66335 .66769 67203 -67638 .6807 2 -68 506 68941 69375 -69809 .70243 .70678 -71112 71546 -71QS1 72415 -72849 73283 1.73718 0.030197 .029897 029599 029305 029013 0.028725 028439 .028156 .027876 -027 598 0.027324 .027052 026783 026516 026252 0.025991 025733 025476 02522 024972 0.024724 .024478 024234 0235993 0237 54 0.023518 .023284 023052 .022823 022596 0.022371 022148 .021928 .021710 .021494 0.021280 .021068 020858 020651 020445 0.020242 .02004I .O19841 .019644 .019448 0.019255 .019003 .018873 018686 018500 0.018316 52 TABLE 19 (continued) EXPONENTIAL FUNCTIONS logy o(e) logyo(e*) 1.73718 0.018316 1.95433 0.011109 -74152 .018133 : 95867 9 -010998 -74586 017953 ; .96301 .010889 .7 5021 -017774 : 96735 .010781 75455 .017 597 . -97170 -010673 75889 0.017422 1.97604 0.010567 70324 017249 98038 010462 .767 58 .017077 ; 98473 010358 -77192 .016907 ; -98907 010255 77626 016739 : 99341 -O10153 .78061 0.016573 : 1.99775 0.010052 78495 .016408 : 2.00210 0099 52 .78929 .016245 3 00044 009853 79364 .016083 ‘ .01078 0097 5 79798 : 01 5923 : 01513 .00965 80232 : 0.01 5764 2.01947 0.009562 .50667 ‘ .01 5608 02381 .009466 STIOI at 015452 4 .02816 .009372 81535 é .01 5299 : .03250 .009279 81969 i 015146 ; 03684 .009187 82404 : 0.014996 3 2.04118 0.009095 82838 : .014846 ; 04553 009005 83272 3. .01 4699 : .04987 -00891 5 .83707 : 014552 : 05421 .0088 26 4141 : .014408 : 05856 .0087 39 NNN hd 84575 : 0.014264 2.06290 0.008652 85009 : .O14122 .067 24 .008 566 85444 : .013982 é .07158 .008 480 85878 2.2 013843 ‘ 07593 .008 396 .86312 : .013705__ | i .08027 .008 312 oO I 3 4 5 6 7 8 9 bb RRL 86747 : 0.01 3569 : 2.08461 0.008230 87181 .01 3434 : .08896 .008148 87615 18 013300 || : 09330 .008067 .88050 4 .O1 3168 : .09764 .007987 88484 : 013037 2 | .10T99 .007907 88918 : 0.012907 || i 2.10633 0.007828 89352 2 .012778 4 -11067 .0077 50 .89757 : 012651 . II SOI .007673 90221 838 .012525 . -11936 .007 597 90055 6 .O1 2401 : .12370 .007 521 -Q1090 : 0.012277 2.12804 0.007447 -Q1524 : 012155 ‘ 13239 007 372 91958 : 012034 : .13673 007299 .92392 : .OLIQT4 : .14107 .007 227 .92827 : .O11796 : -14541 -007155 .93261 .62 0.011679 2.14976 0.007083 93095 ; -O11 562 -15410 .007013 94130 : -O11447 |Il ; 15844 .006943 94504 : .011333 : 16279 00687 4 .94998 a2 011221 16713 .006806 1.95433 : 0.011109 : Ul) 2507047 0.0067 38 SMITHSONIAN TABLES. TABLE 19 (concluded) 53 EXPONENTIAL FUNCTIONS logio(e~) E logio(e~) 2.17147 0.0067 38 -21490 .006097 25833 .005517 30176 .004992 34519 .004517 2.17147 ; 0.0067 38 17582 : .00667 I .18016 3 .00660 5 18450 3 .006539 18884 ‘ .000474 wm 2.38862 0.004037 43205 .003698 -47548 .003346 51891 003028 56234 .002739 mn 2.19319 } 0.006409 19753 . 006346 go ; oes .20622 ; .006220 21056 2. 006158 -wWNeHO WO ON Qu ahwWNHO 2.60577 0.002479 .64920 .002243 69263 -002029 -7 3606 .001836 77948 .001662 2.21490 : aoe! 21924 ; .00603 22359 : 005976 22793 .02 005917 23227 : 005858 [ony 2.82291 0.001 503 86634 .0O1 360 .90977 2 001231 95320 OOL1I4 99663 001008 2.23062 : 0.005799 -24096 : .005742 -24530 : 005685 24905 : 005628 -25399 ; 005572 2.25833 : 0.005517 .26267 : 005462 .26702 : 005407 .27136 E -005354 .27570 : .005 300 3.04006 0.00091 2 .08349 .0008 2 5 .0007 47 .000676 -OOOOII “I NI 2.28005 3 0.005248 28439 2. 005195 .28873 : 005144 .29307 005092 .290742 .005042 3.25721 0.000553 .30064 .000 500 “344097 0004 53 38750 .000410 43093 .00037 I oo Zou : 0.004992 30610 : 004942 31045 204. 004893 31479 ; .004844 31913 : 004796 3-47436 0.000335 -51779 000304 56121 .00027 5 .60464 .000249 .64807 .000225 eo 2.32348 : 0.004748 32782 212.72 -004701 -33216 ; .004654 -33650 : .004608 34085 : 004 562 3.691 50 0.000203 73493 .000184 77836 .000167 82179 .OOOI 51 86522 0001 36 3-90865 0.0001 23 95208 .OOOT 12 99551 .OOOIOI 4.03894 : .00009I 08237 . .000083 2.34519 34953 35388 35822 36256 0.004517 .004472 004427 004383 004339 0.004296 004254 004211 004169 004128 0 4.12580 ; 0.00007 16923 : .00006 .21266 : .000061 .25609 : .000055 .29952 . .0000 50 2.36690 3/125 -37559 *3799 .3842 ROR HY RHODE 0 AnADWIHDA Pum COW 0 ODONODn ABWKHEO OONTH F£0H0NHO OBNOAH £WHHO ODN OM 2.38862 : 0.004087 _ 9° 4.34294 0.00004 5 SMITHSONIAN TABLES. 54 TABLE 20 EXPONENTIAL FUNCTIONS Values of ex” and e—~’ and their logarithms 2 log e” - ° ° COON DD UpwndEe = = COON OD Utwne 2° 5534 3.6966 5.4598 8.2269 1.2647 X 1.9834 3:1735 5.1801 8.6264 1.4656 X 2.5402 4.4918 8.1031 nN Ne NO COON OD UPHOrndH | 1.4913 2.8001 5.3637 1.0482 2.0898 4.2507 8.8205 1.8673 4.0329 8.8861 @ OOON DD HWewn eH Pop 1.9975 X 4.5809 1.0718 X 2.5582 6.2296 1.5476 X 3:9225 1.0142 X 2.6755 7.2005 SMITHSONIAN TABLES, 1.2936 X 10 1.7993 0.00434 01737 93929 06949 19857 0.15635 21280 27795 35178 43429 0.52550 62538 73396 85122 97716 -IL179 25511 40711 56780 73718 .Q1524 .IOIQ9 29742 50154 71434 2.93583 3.10601 40487 65242 90865 4.17357 44718 72947 5.02044 32011 5.62846 94549 6.27121 60562 94571 7-30049 66095 8.03010 40794 79446 9.18967 59357 10.00614 42741 85736 0.99005 96079 91393 85214 77880 0.69768 61263 52729 44486 36788 0.29820 0.77305 X 55576 39164 27052 18316 0.12155 79071 X 50418 31511 9309 0.11592 68233 X 39307 22263 12341 0.67055 X 35713 18644 95402 X 47851 0.23526 11337 53553 X 24796 11254 0.50062 X 1077 21830) 93303 X 10-8 39089“ T6052) 0.64614 X 107° 2 494 “cc 98595 X 10—! s7870° © 13888 2 log e* 1.99566 98263 96091 O8O51 89143 1.84365 78720 72205 64822 56571 1.47450 37462 26604 14878 02284 2.88821 74489 59289 43220 26282 2.08476 3-89801 70258 49846 28566 3.06417 4.83399 59513 34758 09135 582643 55282 27053 6.97956 67959 6.37154 _ 05451 7-72879 39438 05129 8.69951 _ 33995 9.96990 59206 20554 10.81033 _ 40643 11.99386 57259 14264 TABLES 21 AND 22 EXPONENTIAL FUNCTIONS 7 Tr TABLE 21,—Values of €@4*and@ * and their logarithms 8 Tr log @4” 21935 0.34109 0.45594 4.8105 .68219 .20788 1.0551 X 10 1.02328 .94780 X 2.3141 ss 36438 43214 5.0754“ -79547 19703 T0032 x0 10% 2.04656 0.89833 2.damgny |< .38766 -409538 53549“ -72875 -18674 1.1745 X 103 3.0698 5 85144 X 235,000 ies -41094 .38820 1 3 4 5 6 7 8 9 ° 56498 “ 3-75203 0.17700 1.2392 X 104 4.09313 80700 X 2.7178“ 43422 -36794 Re sicy 9 77532 .16776 1.3074 X 10° 5-11641 .76487 X 2.8675“ 5-45751 0.34873 * 6.54249 6.2893‘ -79860 ssi{ayo). | _+20140 1.3794 X 108 6.1 3969 -72495 X 7.86031 30254“ -48079 -33053 “51921 6.6356 “ 82188 .15070 17812 Vr and @ *~ and their logarithms =z Vi TABLE 22,—Values of & + 0.64203 41221 26465 16992 -10909 0.070041 .044968 .028871 018536 .OIIQOI 0.0076408 0049057 0031496 .0020222 .0012983 CODON G UbhWwWdNH 3.07907 0.00083355 HF EST .00053517 .46395 .00034360 .65639 00022060 848353 .0001 4163 SMITHSONIAN TABLES. - 56 TABLES 23 AND 24 EXPONENTIAL FUNCTIONS AND LEAST SQUARES EXPONENTIAL FUNCTIONS TABLE 23,—Values of e* and e-* and their logarithms. log e | alos: 1.0157 | 0.00679 | 0. | 1.3956 | 0.14476 .0317 FOS 7a mae | .6487 | +21715 .0045 .02714 . 21170 | .32572 HOGS |) Tdoigvis) || 34. I 7183 | .43429 all 5) |) 0402 50m 34 I 3.4903 | 54287 .1331 | 0.05429 | 0.882 | 3/2 | 4.4817 | 0.65144 a1533 00 |. COZO4 SII: } 4| 5-:7546 | .76002 eTOud ||) O72 80m laue | 7.3891 | .86859 .2214 | .08686 .8 | 9) 9.4877 | .97716 .2840 | .10857 | .77880 | 12.1825 | 1.08574 LEAST SQUARES 2 h TABLE 24,—Values of P= ie © the? J (hx). P, the probability of an observational error having a value positive or negative equal to ; oe hx 5 or less than + when / is the measure of precision, P =2 fp omiathe). h’=(4mAz”) where m=no. obs. of deviation Ax. 3 03384 -14587 -25502 35928 -45689 54646 .62705 -69810 75952 81156 85478 88997 91805 .94002 95086 -96952 97834 98558 99035 -99366 99591 -99741 -99839 -99902 | . 99941 | - -99965 | - 99980 | .99989 | -99994 -99997 T.00000 o = vO N 0 aie 2 3 4 5 6 7 8 9 0 ol 3 4 1.5 6 a 8 9 0 ol we 3 4 5 6 7 8 9 0 oO Burgess, James. Trans. Roy. Soc. Edinburgh, 39, 257, 1900. SMITHSONIAN TABLES. TABLES 25 AND 26 57 LEAST SQUARES TABLE 25 This table gives the values of the probability P, as defined in last table, corresponding to different values of «x |x where 7 is the ‘‘ probable error.’? The probable error 7 is equal to 0.47694 / 4. .00000 05378 10731 .16035 212608 .20407 31430 .36317 -41052 45618 . 50000 54188 50171 61942 | 65498 68833 yD) 74947 77528 79999 82266 84335 86216 87918 -89450 90825 92051 .Q3141 94105 94954 O 95698 509502 -99926 — rponnNovone 0 ODYDAG £Wb-> TABLE 26,—Values of the factor 0.67454, ed =v? This factor occurs in the equation 7; = o. ous | 22 for the probable error of a single observation, and other similar cate ane 0.3016 | 0.2754 | 0.2549 0.2248 | oO. 2 2 : -1803 | .1742 | .1686] .1636 1547 | . E 1438 | .1¢ , -1349 | .1323 |] .1298 W25ze (12 .12 SL O2el ; II4O | .1124 | .I109 1080 | . : -10¢ -102 ; -I005 | .0994 | .0984 0.0909 | 0.090I | 0.0893 OS7OR|| a: : -08 08 .08 08 37 .0830 | .0824 Coren | : : : 5 .0779.| .0774 | .0769 0759] . : : ; : 073? | .0727'| .0723 soyiigt|| a : : : : .0692 | .0688 | .0685 SMITHSONIAN TABLES. 58 TABLES 27-29 LEAST SQUARES 1 TABLE 27.—Values of the factor 0.67454 ert n(m—1) s : ‘| Se? : This factor occurs in the equation 7>= ons] aay for the probable error of the arithmetical mean. = 0.1947 | 0.1508 0500 | .0465 0287 0275 .0201 .O196 0155 | .O152 0.0126 | 0.0124 .0106 | .O105 .0092 .009 I .OOSI .0080 .007 2 .007 I TABLE 28,—Values of the factor 0.04634 ve n(m—1) z|v! yt (7—1) for the probable error of a single observation. This factor occurs in the approximate equation = 0.8453 TABLE 29,—Values of 0.8453 —_-— n¥n—1 ’ z|v| This factor occurs in the approximate equation 70=0.8453 i; —= for the probable error of the arithmetical mean. wYaM—T 0.1993 | 0.1220 | 0.0845 | 0.0630 0188 | .0167 | .O1SI .0136 .0078 | .0073 | .0069 | .0065 .0045 | .0043 | .0041 | .0040 0030 | .0029} .0028 | .0027 0.0022 | 0.0022 | 0.0021 | 0.0020 .OO17 .OO17 .0016 | .0016 0014 | .0013 | .0013 | .0013 .OOII .OOTT .OOTI .OOTI .0009 | .0009 | .0009 | .0009 SMITHSONIAN TABLES. TABLE 3O 59 LEAST SQUARES (FORMULAE) Observation equations : ajZj + byZ2 +... 14Zq = Mi, weight p, agZz1 + beze +... |eZq = Me. weight po anZ, + bnZe Tet esis InZq = Mp, weight Pn. Auxiliary equations: [paa] =pia? +peazZ +... pnaZ. [pab] = pyaib; + peagbe + . . ~ pnanbn. [paM] = pyaiMy + peagMe + .. . pnanMn. Normal equations : [paa]z,;+[pab]z. + .. . [pal]zq = [paM] [pab]zi + [pbb]z +... [pbl]zq = [pbM] (pla]z: + (plb ]z2 res eros " [pll]zq = [plM]. Solution of normal equations in the form, 71 = Ai[paM] + B,[pbM] + .. . Ly[pIM] Z2 = Ag|[paM] + Be|pbM] + .. . Le[plM] | 2q = An{[paM] + Bn[pbM] +. . . Ln[pIM], | gives: q weight of z] = pz; = (Ai)—!; probable error of z; ee VPA weight of zp = pzo = (By)— a Res weight of zq = Pz, = (Ln); probable error of zqg = = VPzq wherein r = probable error a observation of weight unity | = 0.6745 aes a aa - (g unknowns.) Arithmetical mean, n observations: 2 0.8 =z r = 0.6745 oe yo Pee (approx.) probable error of ob- | al amet): servation of weight unity. Be Seo Oa 5a) ar v =o0. a approx. ) = probable error easy (n— Dive nVn—1 Epon? re mean. | Weighted mean, n observations: Dpv? r _=pv r = 0.6745 \ ae ; To Sao ae Vas Probable error (R) of a function (Z) of several observed quantities z1, 22, . . . whose probable errors are eerie Wag Tow. osee ee = f ( (Z1, ZQ. + + cok (ey ae 6Z} Examples : = +2z0+ . R2 = ais St Ppa Ronee egies t Masini Z = 2 Zo. R? = z,? 12 + Za 22. See Birge, Calculation of errors by the method of least squares, Phys. Rev., 40, 207, 1932. SMITHSONIAN TABLES. 60 TABLE 31 DIFFUSION INTEGRAL 2 7 Inverse * values of v/e=1~— We e—Pdg aKa log x =log (2g) + log./4z. ¢ expressed in seconds. = log 6+ log./&z. ¢ expressed in days. = logy + log \/&¢. “ “ years. & = coefficient of diffusion.t ¢ = initial concentration. v =concentration at distance x, time 4 ae log 29 | log 6 6 logy y 0.00 +00 +00 +2 00 00 OI | 0.56143 | 3. 3.02970 | 1070.78 || 4.31098 | 20463. [O23 |e S LOM |e: | 2.98545 | 967.04 .26674 | 18481. 03 | .48699 | 3. | .95525 | 902.90 || .23654 | 17240. .04 | .46306 | 2. | .93132 | 853.73 || .21261 | 16316. 0.05 | 0.44276 | 2. | 2.91102 | 814.74 || 4.19231 | 15571. .06 | .42486 | 2. 89311 | 781.83 || .17440, | 14942. .07 | .40865 | 2.562 87691 | 753-20 || .15820 | 14395. OS nine O3725 (ne: 86198 | 727.75 14327 | 13908. 09 | -37979 | 2. 84804 | 704.76 || .12933 | 13469. 0.36664 | 2.3262 || 2.83490 | 683.75 || 4.11619 | 13067. 35414 | 2. 82240 | 664.36 || .10369 | 12697. 34218 | 2. 81044 | 646.31 09173 | 12352. 2GQ007) ||) 2: 79893 | 629.40 || .08022 | 12029. 31954 | 2. .78780 | 613.47 .06909 | 11724. 0.30874 | 2. | 2.77699 | 598.40 || 4.05828 | 11436. 29821 | I. 76647 | 584.08 .04776 | T1162, .28793 | I. 75619 | 570.41 .03748 | I0gol. .27786 | I. 74612 | 557-34 02741 | 10652. .26798 | I. -7 3624 | 544.80 01753 | 10412. s2RO25) | Te | 2.72651 | 532.73 || 4.00780 | ro18r. .24866 | 1.772 : 521.10 | 3.99821 | 9958.9 -23919 | I. ‘ 509.86 || .98874 | 9744.1 22953 | I. . 498.98 || .97937 2205 (5m eae : 488.43 .97010 0.21134 | I. 2: 478.19 || 3.96089 .20220 | I. : 468.23 || .95175 19312 | I. : 458.53 || .94266 .18407 | I. i 2} 449.08 93361 -17505 | I. . 43985 || .92460 | 0.16606 | I. 2.63431 | 430.84 || 3.91560 15708 | I. 62533 | 422.02 : 2 -14810 | I. | .61636 | 413.39 -I13Q12 | I. .60738 | 404.93 || -13014 | 1.3494 || .59840 | 396.64 | 0.12114 | I. 2.58939 | 388.50 | sitar |) dis .§8037 | 380.51 -10305 | 1.2 S57 L3te | 3g 72.00 .09396 | I. 56222 | 364.93 || .08482 | 1.2 | -55308 | 357-34 || 0.07 563 | I. | 2.54389 | 349.86 | .06639 | I. | -53464 | 342.49 || 05708 | I. 52533 | 335-22 | 04770 | I. 51595 | 328.06 || .03824 | 1. -50050 | 320.99 0.02870 | I. | 2.49696 | 314.02 || 3.77825 .O1907 | I. “497/33 | 307-53) || 76862 00934 | I. -47760 | 300.33 || .75889 9-99951 | 0. | -46776 | 293.60 || .74905 .98956 | O. -45782 | 286.96 73911 997949 | 0. | 2.44775 | 280.38 || 3-72904 | RbHbHt ty 3 4 5 6 7 8 9 bKHKK + Kelvin, Mathematical and Physical Papers, vol. III. p. 428; Becker, Am. Jour. of Sci. vol. III. 1897, p. 280. * For direct values see table 2a. SMITHSONIAN TABLES. TABLE 31 (continued) 61 DIFFUSION INTEGRAL log 29 2q | log 5 log y | 9.97949 | 9-95387 || 2.44775 | 280.38 || 3.72904 .96929 | .93I 74 -43755 | 273-87 71884 -95896 | .90983 || .42722 | 267.43 -70851 .94848 | 88313 -41674 | 261.06 .69803 -93784 | .86605 -40610 | 254.74 | -687 39 | | 9.92704 | 0.84536 | 2.39530 | 248.48 3-67659 91607 | .82426 || .38432 | 242.28 66561 -90490 | -80335 | .37316 | 236.13 || 65445 89354 | -78260 || .36180 | 230.04 -64309 88197 | .76203 -35023 | 223.99 63152 | 9.87018 | 0.74161 || 2.33843 | 217.99 3.61973 | 85815 | -72135 || -32640 | 212.03 -60770 84587 | .70124 || .31412 | 206.12 | .59541 83332 | -68126 || .30157 | 200.25 58286 82048 | .66143 || .28874 | 194.42 57003 | 3 9.80734 | 0.64172 .27560 | 188.63 3.55689 79388 | .62213 || .26214 | 182.87 54343 -78008 60266 | .24833 ] 177.15 | -52962 76590 | .58331 || .23416 | 171.46 51545 75133 | -56407 || .27959 | 165.80 50088 9-7 3634 | 0.54493 | 2.20459 | 160.17 3-48583 | 72089 | .52588 -ISQI5 | 154.58 | .47044 | 2 -70495 | -50094 || -17321 | 149.01 -45450 68849 | .48808 || .15675 | 143.47 .43804 -67146 | .46931 | +13972 | 137-95 | -42101 N Wt Om wp ON reas hw 9.65381 | 0.45062 || 2.12207 | 132.46 | 3-40336 | -63550 | .43202 -10376 | 126.99 |} .38505 -61646 | .41348 08471 | 121.54 | .36600 .§9662 | .39502 || .06487 | 116.11 || .34616 | -57590 | -37062 || .04416 | 110.70 eeozicaicg!| NN NNN me NWhi mm NW NO WON Ds NONUOD 9-55423 | 0.35829 || 2.02249 | 105.31 || 3:3037 -53150 | .34001 || 1.99975 | 99.943 || .28104 -50758 | .32180 | .97584 | 94.589 -25713 48235 -30363 | .g5061 | 89.250 -23190 45504 | .28552 || -.92389 | 83.926 |, -20518 9.42725 | 0.26745 89551 78.615 3-17680 | -39695 | 24943 | 86521 73.317 -14650 -36445 | -23145 || .83271 | 68.032. |] .11400 -32940 | .21350 || -79766 | 62.757 || .07895 | -29135 | -19559 | -75961 | §7-492 | 3-04090 9.24972 | 0.17771 || 1.71797 | 52. age | 2.99926 .20374 | .15986 | .67200 | 46.989 95329 | 15239 | .14203 || .62065 | 41.750 -QOIQ4 09423 | .12423 -56249 | 36.516 84378 9.02714 | .10645 || -49539 | 31.289 77068 8.94783. 08868 | .41609 26.067 2.69738 85082 | .07093 || -31907 | 20848 | .60036 | -72580 ae -19406 | 15.633 | .47535 | tlle -54965 | .03545 .O1791 10.421 | .29920 | coo .01773 || 0.71684 | 5.21007 || 1.99813 | —c 0.00000 SMITHSONIAN TABLES. 62 TABLE 32 VALUES OF THE EXPONENTIAL INTEGRAL -L Ei(x) = | (e-“/u)du (Taken from Glaisher, Philos. Trans., 160, 367, 1870) SMITHSONIAN TABLES TABLE 32 (continued) 63 VALUES OF EXPONENTIAL INTEGRAL Ei(x) = (ee/avta Ei(x) 15-(E9) E(x) & & + 9.933 10.626 11.367 12.161 13.012 +1.895 118 —0.219 384 2.167 378 —0.185 991 2.442 092 —0.158 408 2.721 399 —0.135 451 3.007 207 —0O.116 219 — = OWA ROHHO +3.301 285 —0.100 020 3.605 320 —0.086 3083 3.920 963 —0.074 6546 4.249 868 —0.064 7131 4-593 714 —0.056 2044 +13-925 14.906 15.960 17.094 18.315 +19.630 21.048 22.577 24.227 26.008 OU Ah PHOHHO = ss +4.954 234 —0.048 9005 5:333 235 —0.042 6143 5-732 615 —0.037 IQII 6.154 381 —0.032 5023 6.600 670 —0.028 4403 ay ° +27.933 30.014 32.263 34-697 37-332 +7.073 766 —0.024 9149 7.576 I15 —0.02I 8502 8.110 347 —0.019 1819 8.679 298 —0.016 8553 9.286 024 —0.014 8240 YP RAE PEEEE SERED HHWOY O ON DWN PwWNHO ° +40.185 +9.933 833 —0.013 0484 Ei(x) E1(—x) + 85.989 0.000 360 + 191.504 -000 II5 + 440.379 -000 037 + 1037.878 -000 O12 + 2492.228 .000 004 -++ 6071.406 .000 OOI + 14959.532 -000 000 + 37197.688 -000 000 + 93192.513 .000 000 + 234955.852 .000 000 (Taken from Glaisher, Philos. Trans., 160, 367, 1870) SMITHSONIAN TABLES 64 Taste 33 CGAMMA FUNCTION * o Value of log if e 7x" "dx +10 0 0 Values of the logarithms + 1o of the “‘ Second Eulerian Integral’’ (Gamma function) e-22"%-ldxro log I(#)+1¢ 0 for values of 2 between 1 and 2. When 2 has values not lying between 1 and 2 the value of the function can be readily calculated from the equation T(z+1) = xT) = n(w—1) . . . (x—r)T(2—7). 75287 51279 27964 05334 9.9883379 62089 41455 21469 02123 9-9783407 65313 47834 30962 14689 9-9599007 83910 69390 55440 42054 9.9629225 16946 05212 S9FOUS 33350 9.957 3211 63592 54487 45890 37798 Rae SES Nd wn oO ON DD 9-9530203 23100 16485 10353 04698 ile w SS TEENS 94800 90549 86756 83417 9.94805 28 78084 76081 74505 73382 * Legendre’s “Exercises de Calcul Intégral,” tome ii. SMITHSONIAN TABLES. TABLE 33 (continued ) GAMMA FUNCTION n O 1 2 3 4 5 6 7 8 9 1.45 | 9.9472677 | 72630 | 72587 | 72549 | 72514 | 72484 | 724590 | 72437 | 72419 | 72406 1.46 72397 | 72393 | 72392 | 72396 | 72404 | 72416 | 72432 | 72452 | 72477 | 72506 1.47 72539 | 72576 | 72617 | 72662 | 72712 | 72766 | 72524 | 72886 | 72952 | 73022 1.48 73097 | 73175 | 73258 | 73345 | 73436 | 7353! | 73630 | 73734 | 73841 | 73953 1.49 74068 | 74188 | 74312 | 74440 | 74572 | 74708 | 74848 | 74992 | 75141 | 75293 1.50 | 9.9475449 | 75610 | 75774 | 75943 | 76116 | 76292 | 76473 | 76658 '| 76847 | 77040 1.51 77237 | 77437 | 77642 | 77851 | 78064 | 78281 | 78502 | 78727 | 78956 | 79189 1.52 79426 | 79067 | 79912 | 80161 | 80414 | 80671 | 80932 | 81196 | 81465 | 81738 1.53 82015 82295 82580 | 82868 | 83161 | 83457 | 83758 | 84yo62 | 84370 | 84682 1.54 84998 | 85318 | 85642 | 85970 | 86302 | 86638 | 86977 | 87321 | 87668 | 880I19 1.55 | 9.9488374 | 88733 | 89096 | 89463 | 89834 | 90208 | 90587 | 90969 | 91355 | 91745 1.56 92139 | 92537 | 92938 | 93344 | 93753 }| 94166 | 94583 | 95004 | 95429 | 95857 1.57 96289 | 96725 | 97165 | 97609 | 98056 | 98508 | 98963 | 99422 | 99885 | 00351 1.58 500822 | 01296 | 01774 | 02255 | 02741 | 03230 | 03723 | 04220 | 04720 | 05225 1.59 05733 | 06245 | 06760 | 07280 | 07803 | 08330 | 08860 | 09395 | 09933 | 10475 1.60 | 9.9511020 | 11569 | 12122 | 12679 | 13240 } 13804 | 14372 | 14943 | 15519 | 16008 1.61 16680 | 17267 | 17857 | 18451 | 19048 }| 19649 | 20254 | 20862 | 21475 | 22091 1.62 22710 | 23333 | 23960 | 24591 | 25225 | 25863 | 26504 | 27149 | 27798 | 28451 1.63 29107 | 29766 | 30430 | 31097 | 31767 | 32442 | 33120 | 33801 | 34486 | 35175 1.64 35867 | 36563 | 37263 | 37966 | 38673 | 39383 | 40097 | 40815 | 41536 | 42260 1.65 | 9.9542089 | 43721 | 44456 | 45195 | 45938 | 46684 | 47434 | 45187 | 48944 | 49704 1.66 50468 | 51236 | 52007 | 52782 | 53560 | 54342 | 55127 | 55916 | 56708 | 57504 1.67 58303 | 59106 59913 6072 61536 | 62353 | 63174 | 63998 | 64825 | 65656 1.68 66491 | 67329 | 68170 | 69015 | 69864 | 70716 | 71571 | 72430 73293 | 74159 1.69 75028 | 75901 | 76777 | 77657 | 78540 | 79427 | 80317 | 81211 | 82108 | 83008 1.70 | 9.9583912 | 84820 | 85731 | 86645 | 87563 | 88484 | 89409 | 90337 | 91268 | 92203 1.71 93141 | 94083 | 95028 | 95977 | 96929 | 97884 | 98843 | 99805 | 00771 | 01740 1.72 602712 | 03688 | 04667 | 05650 | 06636 | 07625 | 08618 | 09614 | 10613 | 11616 173 12622 | 13632 | 14645 | 15661 | 16681 }| 17704 | 18730 | 19760 | 20793 | 21830 1.74 22869 | 23912 | 24959 | 26009 | 27062 | 28118 | 29178 | 30241 | 31308 | 32377 1.75 | 9.963345! | 34527 | 35607 | 36690 | 37776 | 38866 | 39959 | 41055 | 42155 | 43258 1.76 44364 | 45473 | 46586 | 47702 | 48821 | 49944 | 51070 | 52199 | 53331 | 54467 1.77 55006 | 56749 | 57894 | 59043 | 60195 | 61350 | 62509 | 63671 | 64836 | 66004 1.78 67176 | 68351 | 69529 | 70710 | 71895 | 73052 | 74274 | 75468 | 76665 | 77866 1.79 79070 | 80277 | 81488 | 82701 | 83918 | 85138 | 86361 7588 | 88818 | goosr 1.80 | 9.9691287 | 92526 | 93768 | 95014 | 96263 | 97515 | 98770 | C0029 | oF2g1 | 02555 1.51 703823 | 05095 | 06369 | 07646 | 08927 | 10211 | 11498 | 12788 | 14082 | 15378 1.82 16678 | 17981 | 19287 | 20596 | 21908 } 23224 | 24542 | 25864 | 27189 | 28517 1.83 29848 | 31182 | 32520 | 33860 35204 30551 | 37900 | 39254 | 40610 | 41969 | 1.84 43331 | 44697 | 46065 | 47437 | 48812 | So1go | 51571 | 52955 | 54342 | 55733 | 1.85 | 9.9757126 | 58522 | 59922 | 61325 | 62730 } 64139 | 65551 | 66966 | 68384 | 69805 | 1.86 71230 | 72657 | 74087 | 75521 | 76957 | 78397 | 79839 | 81285 | 82734 | 84186 1.87 85640 | 87098 | 88559 | 90023 | 91490 | 92960 | 94433 | 95909 | 97359 | 98871 | 1.88 800356 | 01844 | 03335 | 04830 | 06327 | 07827 | 09331 | 10837 | 12346 | 13859 1.89 15374 | 16893 | 18414 | 19939 | 21466 | 22996 | 24530 | 26066 | 27606 | 29148 | 1.90 | 9.9830693 | 32242 | 33793 | 35348 | 36905 | 38465 | 40028 | 41595 | 43164 | 44736 1.91 46311 | 47890 | 49471 | 51055 | 52642 | 54232 | 55825 | 57421 | 59020 60621 1.92 62226 | 63834 | 65445 | 67058 | 68675 | 70294 | 71917 | 73542 | 75170 | 76802 1.93 78436 | 80073 | 81713 | 83356 | 85002 | 86651 | 88302 | 89957 | 91614 | 93275 1.94 94938 | 96605 | 98274 | 99946 | 01621 | 03299 | 04980 | 06663 | 08350 | 10039 1.95 | 9.9911732 | 13427 | 15125 | 16826 | 18530 | 20237 | 21947 | 23659 25375 | 27093 1.96 28815 | 30539 | 32266 | 33995 | 35728 | 37464 | 39202 | 40943 | 42688 | 44435 1.97 46185 | 47937 | 49693 | 51451 | 53213 | 54977 | 56744 | 58513 | 60286 | 62062 1.98 63840 | 65621 | 67405 | 69192 | 70982 | 72774 | 74570 | 76368 | 78169 | 79972 1.99 81779 | 83588 | Ssgor | 87216 | 89034 | 90854 | 92678 | 94504 | 96333 | 98165 poe lie | SMITHSONIAN TABLES. 66 TABLE 34 ZONAL SPHERICAL HARMONICS * Degrees P; -+ 1.0000 9957 9830 .9620 9329 + 0.8962 8522 8016 7449 6830 + 0.6164 -5462 “4731 3980 3218 ‘Oo CON Om fWNeO + 0.2455 + .1700 + .0961 + .0248 — +0433 — 0.1072 .1664 .2202 -2680 3094 — 0.3441 3717 -3922 4053 4113 — 0.4102 .4022 -3877 -3671 +3409 — 0.3096 -2738 -2343 -1918 1470 — 0.1006 O59 — .0064 + .0398 + .0846 + 0.1271 -1667 -2028 2350 .2626 + 0.2854 * Calculated by Mr. C. E. Van Orstrand for this publication. SMITHSONIAN TABLES, TABLE 34 (continued) 67 ZONAL SPHERICAL HARMONICS Degrees P, + 0.6428 .6293 6157 .6018 5878 + 0:5736 *5592 “5446 "5299 *5150 + 0.5000 .4848 -4695 .4540 4384 + 0.4226 .4007 -3907 .3746 -3584 + 0.3420 3256 .3090 .2924 .2750 .2588 : — 0.2730 2419 ‘ . . : .2850 .2250 : : : .2921 .2079 : : : .2942 1908 : : : : 2913 + 0.1736 ; — 0.2835 1564 . . . -2708 .1392 : s .2530 1219 : Zaz : .2321 1045 ; : -2067 + 0.0872 | ' — 0.1778 .0698 : 3 8 : .1460 .0523 , ; : DLE .0349 : 3 ‘ .0755 0175 ; : : .0381 -++ 0.0000 : — 0.0000 SMITHSONIAN TABLES. 68 TABLE 35 CYLINDRICAL HARMONICS OF THE OTH AND 1ST ORDERS dJo (x) Ine) = Se {3 A eh OT eee oA . Juz) = Jd (x) = SF 2"-T' (n + 1) ~~ 22(n-+1) | 242! +1)(n+2)° °° Fac ate) FAG) Tae oe) x | Jo(x) | Sr(x) unity zero -50} .938470] .242268/|1 .00) . : ‘ 557937 .999975| .005000|| .51| .936024] .246799]| .o1| .760781] .443286]| .51/ .506241] .559315 .999900] .or0000]| .52| .933534] -251310]| -02| .756332| .446488]) .52] .500642| .560653 .999775| -.0F4998|| .53] -930998] .255803|| .03] .751851] .449658]| .53] -495028] 561951 .999600] .org996|| 54] .928418] .260277|| .04] .747339] -452794/| -54| -489403] .563208 .999375| .024992|| .55} .925793| .264732/|1 .08| .7427096] .455897||1 65) .483764) .564424 999100] .029987/| .56] .923123] .269166]| .06] .738221| .458966|| .56) .478114| .565600 .998775| -034970]| -57| -920410] .273581|| .07]| .733616] .462001|| .57| .472453] -566735 .998401| .039968]| .58] .917652| .277975]| -08] .728981] .465003]| .58] .466780} .567830 .997976| .044954|| .59| -914850] .282349]] -09] -724316] .467970]|| .59] .461096} .568883 .997502| .049938]| .60) .g12005} .286701)|1 .10) .719622) .470902/|1 .60) 455402] .569896 .996977| .054017|| .O1| .gogt16] .291032]| .11| .714898] .473800]] .61| .449608] .5 70868 .996403] .059892|| .62] .995184] .295341|| .12] .710146] .476663]) .62] .443985] .571798 .995779| .064863]| .63] .g03209] .299628]| .13] .705365] .479491|| -63! .438262] .572088 .995106] .069829]| .64| .goorg2] .303803]] -14] .700556] .482284]| .64] .432531] -573537 -994383] .074780]| .65| .897132] .308135||L .16] .695720} .485041]|1 .65) .426792! .574344 .993010] .079744|| .66] .894029] .312355]| - .690856| .487763]| .66) .421045] .575111 992788] .084693]} .67] .890885] .316551|| 17] .685965] .490449]| .67] .415290] .575836 .99IQ16| .089636|| .68} .887698] .320723]| .18] .681047] .493098]| .68} .409528] .576520 -990995]| .094572|| .69| .884470] .324871|| . -676103] .495712|| .60] .403760| .577163 .990025] .oggs5o1|| .70) .881201] .328996]|1 .20} .671133] .498289]|1 .70) .397985] .577765 .989005} .104422]| .71| .8778g0] .333096]| .21] .666137] .500830]| .71| .392204] .578326 .987937| .109336|| .72| -874539] -337170|| -22| 661116} .503334|| -72] .386418] .578845 .986810| .114241|| .73] 871147] .341220]| .23] .656071) .50580r|| .73} .380628] .570323 .985652| .119138|| .74] 867715] .345245]| -24] 651000] .508231]| -74] .374832] .579760 .984436] .124026]| .75| .864242| .349244||1 .25] .645906] .510623]|1 .75| .369033| .580156 .983171| .128905]| .76] -860730] .353216|| .26] 640788) .512979]| -76) .363220] .580511 .981858] .133774|| .77| 857178] -357163]] -27| 635647] .515296]| -77] .357422| .580824 .980496| .138632|| .78] .853587] .361083]| .28] .630482] .517577]| -78) .351613] .581096 .979085| .143481|| .709] 849956] .364976]| .29] .625295] .519819]| -79] 345801] .581327 .977626| .148319|| .80} .846287] .368842]|1 .30] .620086} .522023]|1 .80) 339986] .581517 .976110| .153146|| .81] .842580] .372681]| .31] .614855] .524189]| .81] 334170] .581666 .974563| .157961|| .82] .838834] .376492]| 32] 609602] .526317|| .82] .328353] .581773 .972960| .162764]| .83] .835050] .380275]] .33] .604320] .528407]| .83] .322535] .581840 .971308| .167555|| .84| 831228] .384029]] .34] .599034] .530458]| .84] .316717| .581865 .969609| .172334|| .85} 827360} .387755||1 .35] 593720] .532470||1 .85) .310808] .581849 .967861] .177100]] .86] .823473] -391453|| -36] .588385] .534444]| .86] .305080] .5817093 .966067| .181852|| .87| 819541] .395121|] .37| -583031| .536379|| -87] .299262| .581695 .964224| .186591|| .88] .815571] .398760]| .38) .577658] .538274]| -88] .293446] .581557 .962335| -191316]|| .809| 811565] .402370]| .39| .572206] .540131]| .89] .286631| .581377 .960398] .196027|| .90} .807524| .405950||1 .40) .566855] .5410948||1 .90) 281810] .581157 -958414] .200723]] .g1} .803447] .409499|| 41] .561427] .543726|| .91| .276008] .580896 .950384| .205403|| .92] -799334| .413018]] .42] .555981] .545464|| .92| .270201| .580595 -954306| .210069|| .93} -795186] .416507]| .43] .550518} .547162]| .93] .264397] .580252 .952183| .214719|| .94] .791004] .419965|| .44] .545038] .548821]| .94] .258596] .579870 -9§0012| .219353|| .95| .786787] .423392/|1 45) .539541| .550441||1 .95) .252799] 579446 .947796| .223970]| .96] .782536| .426787]| .46| .534029] .552020|| .96] .247007| .578983 945533] -228571|| .97| -778251| -430151|| -47| .528501] .553550|| -97| .241220] .578478 -943224] .233154|| .98] .773933] -433483]| -48] .522958] .5550590]| -98| .235438] .5779034 .940870| .237720|| .99] -769582| .436783]| 49] .517400] .556518]| .99] .229661| .577349 .938470| .242268]|1 .00] .7651098] .440051]|1 .60) .511828) .557937||2 00) .223891] .576725 SMITHSONIAN TABLES. ee TABLE 355 (continued) CYLINDRICAL HARMONICS OF THE OTH AND 1ST ORDERS Ji (x) = —Jo’ (x). Other orders may be obtained from the relation, Jn41(x) = * In(w) — Jn-1(x). J_n(x) = (—1)"Jn (x). Jo(x) Ji (x) -576725 .576060 -575355 .574011 -573827 .223891 .218127 -212370 .200620 -200878 -195143 .189418 .183701 -177993 .172295 -166607 .160929 -155262 -149607 -143963 -573003 572139 -571236 +5 702904 .569313 .568292 -567233 566134 -564907 .563821 .562607 -501354 -560063 -558735 -557368 .138330 .132711 .127104 -121509 -115929 -110362 -104810 .099272 -093749 .088242 -555963 554521 -553041 -551524 -549970 .082750 077274 -O71815 .066373 .060947 -548378 -546750 -545085 543384 -541646 -539873 538063 -536217 -534336 -532419 *055540 -O50150 -044779 -039426 -034092 .028778 .023483 -018208 .O12954 .007720 -530407 .5 28480 526458 524402 522311 : .002508 -41|—.002683 -42|—.007853 -43|—-013000 -44)—.018125 .520185 -518026 -515833 .513606 .511346 2.45|—.023227 .46|—.028306 -47|—-033361 -48|—.038393 -49|/—-043401 2.50|—.048384 509052 .506726 -504366 -501974 -499550 -497094 SMITHSONIAN TABLES. x Jo(x) Ji (x) 2.50|—.048384|.497004 -51|—-053342].494606 5 2|—-058276].492086 -53|—-063184].489535 -54|—.068066}. 486953 2.55|—.072923}].484340 .56|—.077753].481696 -57|—-082557]|-479021 -58|—-087333]-476317 -59|—-092083].473582 2.60|—.096805].470818 -61]—.101499].468025 .62]—.106165].465202 .63|—.110803].462350 -64|—.115412].459470 2.65|—.119992|.456561 -66]—.124543].453625 -67|—.129065].450060 -68]—.133557].447068 -69|—.138018|.444648 2.70|—.142440].441601 -71|—.146850].438528 -72|—.151220].435428 -73|—-155559}-432302 -74|—-159866].429150 2.75|—.164141|.425972 -76|—.168385].422769 -77|—-172597|-419541 -78|—.176776|.416288 -79|—.180922].413011 2.80|—.185036}.409709 -81|—.189117].400384 .82|—.193164].403035 .83|—.197177].399062 -84|—.201157]|.396267 2.85|—.205102/.392840 -86|/—.209014].389408 .87|/—.212890|.385945 .88|—.216733].382461 .89|—.220540|.378955 2.90|—.224312|.375427 -QI|—.228048].371879 -92|—.231740].3608311 -93|—-235414).364722 -94|—.239043].301113 2.95 —+242636|.357485 -96|—.246193 .353837 97|—-249713|.350170 -98|—.253196}.346484 -99|—.-256643).342781 3.00|—.260052].339050 x Jo(x) 3.00|—.260052 .O1|—.263424 .02/—.266758 .03|—.270055 :04|—.273314 3.05|—.276535 06|—.279718 .07|—.282862 .08/—.285968 .09|—.289036 3.10|—.292064 -II|—.2905054 -12/— 298005 .13/—.300916 -14/—.303788 3.15|—.306621 -16|—.309414 -17/—.312168 -18/—.314881 -19/—-317555 3.20|—.320188 .21/—.322781 -22)—.325335 .23|/—.327847 -24|—.330319 3.25 -20 S27 .28 .29 3.30 ar 332 33 34 3.35 -36 37 .38 39 3.40/—.3642096 -41|—.366067 -42|—.307797 -43|—-369485 -44/—-371131 —-332751 —-335142 —-337492 —.339801 —.342069 —.344296 —.346482 —.348627 —-350731 —-352793 —.354814 —-350793 —.358731 —.360628 —.362482 3.45|/—.372735 -46|—.374207 -47|—-375818 .48|—.3772096 -49|—-378733 3.50|—.380128 Ji (x) | -339059 -335319 .331563 -327789 -323998 320191 .316368 312529 -308675 .304805 300921 297023 .293110 .289184 .285244 .281291 -277326 -273348 .269358 -2605356 .261343 -257319 -253284 -249239 -245184 .241120 -237046 -232963 228871 .224771 .220663 .216548 -212425 -208296 -204160 .200018 -195870 -Ig1716 -187557 -183304 .179226 -175054 .170878 .166699 -162516 158331 -154144 -140954 -145763 -I41571 -137378 69 = x Jo(x) Ji (x) 3.50/—.380128 .51|/—.381481 .52|—-382791 -53/—-384060 -54|—-385287 3.55/—.386472 -56/—.387615 -57|—-388717 .58|—.389776 -59|—-399793 3.60|—.391760 .61|/—.392703 -62/—.393595 -63/—-394445 -64|—.395253 3.65|—.396020 -66|—.396745 .67|—.397429 .68]—.398071 .69|/—.398671 .137378 -133183 .128989 -124795 -120601 -116408 -112216 -108025 .103836 .099650: f .095466 .091 284 .087106} .082931 .078760 -074593 .070431 .066274 .062122 057975 .053834 .049699 1045571 -041450) -037336 3.70/—.399230 -71|—.399748 -72|—.400224 -73|—-400059 -74|—-401053 3.75|—.401406 -76|/—.401718 -77|—-401989 .78|—.402219 -79|—-402408 3.80|—.402556 .81/—.402004 .82|/—.402732 .83/—.402759 .84/—.402740 3.85/—.402692 .86]—.402599 .87|—.402465 .88]—.402292 -89|—.402079 3.90|—.401826 -Q1/—.401534|—.031186 -92|—.401 202|—.035115 -93|—-40083 2|—.039031 -94|—.400422|—.042933 -033229 .029131 -025040 .020958 .016885 .O1 2821 .008766 .004722 .000687 — 003337 —.007350 —.O11352 —-015343 —.019322 —.023289 —.027244 3.95)—.399973|—.040821 .96|—.399485|—.050095 -97|—-398959|—-054555 -98|—.398394|—-058400 -99|—-397791|—.062229 4.00|—.397150] .066043 TABLES 36 AND 37 CYLINDRICAL HARMONICS OF THE OTH AND 1ST ORDERS TABLE 36.—4-place Values for x —4 TABLE 37. 7O to 15 (a) Ist 10 roots (Rm) of Jo(4)= 0; Ji( Rm) ce oan ee Ae) Higher roots may be calculated to better than I part in 10,000 by the approximate 4-0/— .3972 9-5/—-1939/+-1013/} formula Rm = Rma+ 7 tl 3087 voli fo oal: eee Ri = 2.404826 — Ja (its D=4- 0.5101 .2/— .3766 .7|—.2218] .1166 R. = 5.520078 J1(R2)= — 0.3403 -3|— -30T0 “O)— 72323) 70020 Re = 8.653728 Js (Rs = +0.2715 3423 -9|— 2403] 0684 R. =11.701534 Ja (Rs )= — 0.2325 3205 .O|—.2459| .0435 Rs =14.930018 J; (R; )=-+ 0.2065 . 2961 .I|—.2490|+ .0184 Re = 18.071064 Js (Re )= — 0.1877 . 2693 .2|— .2496|— .0066 IR; =21.201637. JR) 011738 - 2404 -3|— - 2477|— -0313 Rs = 24.352472 Ji (Rs )=— 0.1617 - 2007 -4/— - 2434|— .0555 Rs = 27.403479 Ji (Rs )=-+ 0.1522 .1776 .5|—. 2366|— .0789 Rw = 30.634606 Ji (Ri)= — 0.1442 .6)— .2276|— . 1012 .7|—.2164|— .1224 .8|— . 2032|— . 1422 .Q|— . 1881|— . 1603 .O]— .1712|— .1768 -I/—.1528|—. 1913 . 2|— .1330|— . 2039 -3)—.1121|/—. 2143 .0902|— . 2225 .0077|— . 2284 .0446|— . 2320 .0213|— . 2333 .0020|— . 2323 .0250|— . 2290 -0477|— - 2234 .0097|— . 2157 .0908]— . 2060 .1108|— . 1943 .1296|— .1807 .1469|— . 1655 .1626|— . 1487 .1766|— .1307 .1887|—. 1114 .1988|— .og12 . 2069|— .0703 .2129|— .0489 1443 . 1103 .0758 .O412 .0068|—. .0270|—. -0599|— . .OgI7/—. .1220]—. .1506|—. -1773\— - .2017|—. .2238)/-. . 2433|—. .2601|—. .2740|—. .2851|—. .2931|—. .2981|—. .3001|—. .2991|+. .2951 . 2882 . 2786 . 2663 . 2516 (b) 1st 15 roots of hh(a)=— with corresponding values of maximum or minimum values of Jo(+). dJo(x) _ Me No. of root (n) Root = 2, Jo(xn) .831706 .015587 .173468 . 323692 .470630 .615859 . 760084 .903672 .046829 . 189680 . 332308 -474766 .617094 - 759319 .gor461 -402759 . 300116 - 249705 . 218359 . 196465 . 180063 .167185 .156725 . 148011 . 140606 .134211 .128617 . 123668 . 119250 .115274 I 2 3 4 5 6 7 8 9 10 tee (ects | eta et ee ta tt | Higher roots may be obtained as under (a). 1OOn B&W HHO O OU OMN RO HHO OWOVIANAWHHO O ONION . 2346 .2167|— .0271 Notes. y=J,(x) is a particular solu- . . 2154 . 2183|— .0052 tion of Bessel’s equation, .1944 .2177|+.0166 ay dy : : .1717 .2150| .0380 erat eat Ww )y=o. antl ees ieee The general formula for J,(x) is .0960 .1943]} .0984 Qo (Hr) gents .0092 . 1836 . 1165 J r(x) = er rae .O419 ALC isen or 9 .0146 .1570| .1488 (—1)%nts .7|\— .O125 .1414| .1626 = Soa ENT ..8|— .0392 .1245| .1747 Sans! (n+ sy! .0053 .1065| .1850 when m is an integer and .0903 .0875| .1934 Nase o .1142 .0679] .1999 ey Inti(x) i In(x) — In-(x), .1367 .0476| .2043|f * T(x) = Ho) .1577 .0271| .2066 LA aaa O OU AN Aw LHHO O ONAN RWHHO OWI ON AWHHO Of .1768 - 1939 .0004 15 .0]—.0142 . 2069 . 2051 J—n(x) = (-1)"Jn(x). Tables 36 to 37 are based upon Gray and Matthews’ reprints from Dr. Meissel’s tables. See also Reports of British Associa- tion, 1907-1916. SMITHSONIAN TABLES TaBLe 38 ELLIPTIC INTEGRALS 2 +} Values of is 2(1— sin? 6 sin? ¢)-* do /0 "This table gives the values of the integrals between o and m /2 of the function (1—sin?@ sin?) ** @ for different val. ues of the modulus curresponding to each degree of @ between o and go. oar. i 7 db T (ae ata yy 7(1—sin*@sin°)-adp Ee ea RTE 2 (1—sin%sin%)*dp (1—sin2@ sin? 6)? kJ 9 9 (1—sin?@ sin? ¢) 0 Number. Log. Number. Log. Number. Log. Number. Log. oO 1.5708 | 0.196120 } 1.5708 | 0.196120 1.8541 | 0.268127 | 1.3506 | 0.130541 5709 196153 5707 196087 8691 271644 | 3418 127690 5713 | 196252 | 5703 | 195988 8848 | 275267 | 3329 | 124788 5719 196418 5097 195822 goll 279001 3238 121836 5727 196649 5689 195591 g180 282848 | 3147 118836 Q fwnrHO Oo 1.5738 | 0.196947 ] 1.5678 | 0.195293 .9356 | 0.286811 |1.3055 | 0.115790 5751 197312 5065 194930 9539 290895 2963 112698 5707 197743 5649 194500 9729 295101 2870 109563 5785 | 198241 | 5632 | 194004 9927 | 299435 | 2776 | 106386 5805 198806 | 5611 193442 .0133 303901 | 2081 103169 oO COON oO h 1.5828 | 0.199438 | 1.5589 | 0.192815 0347 | 0.308504 | 1.2587 | 0.099915 5854 | 200137 | 5564 192121 0571 313247 | 2492 096626 5882 200904 5537 191 302 0804 318138 2397 093303 5913 201740 | 5507 | 190537 1047 323182 | 2301 089950 5940 202643 5476 189646 1300 328384 | 2206 | 086569 oO ra) WOON OAT FWNH 1.5981 | 0.203615 | 1.5442 | 0.188690 1565 | 0.333753 [1.2111 | 0.083164 6020 204657 5405 187668 1842 339295 201 § 079738 6061 205768 | 5367 186581 2132 | 345020 | 1920 | 076293 6105 200948 | 5326 185428 2435 350936 | 1826 | 072834 6151 208200 | 5283 184210 2754 357053 1732 069364 tO ° ° 1.6200 | 0.209522 | 1.5238 | 0.182928 .3088 | 0.363384 | 1.1638 | 0.065889 6252 210916 5191 181580 3439 369940 1545 062412 212382 5141 180168 3809 376736 | 1453 | 058937 213921 5090 178691 4198 383787 1362 055472 215533 5037 177150 4610 391112 1272 | 052020 Q PWN oO N 0.217219 | 1.4981 -175545 .5046 |0.398730 | 1.1184 | 0.048589 218981 | 4924 173876 5507 406665 1096 | 045183 220818 | 4864 172144 5998 414943 IOI 041812 222732 | 4803 170348 6521 423596 | 0927 038481 224723 4740 168489 7081 432660 | 0844 035200 oO oOo OONO a .226793 | 1.4675 | 0.166567 2.7681 | 0.442176 | 1.0764 | 0.031976 228943 4608 164583 8327 452196 0686 028819 231173 4539 162537 9026 462782 o6Il 025740 233485 | 4469 | 160429 9786 | 474008 | 0538 | 022749 235880 | 4397 158261 3.0617 485967 | 0468 019858 q@ O ONIN AN PWN .238359 | 1.4323 | 0.156031 3.1534 | 0.498777 ] 1.0401 | 0.017081 240923 | 4245 153742 2553 512591 | 0338 | 014432 243575 | 4171 | 151393 3099 | 527613 | 0278 | or1927 246315 | 4092 | 148985 5004 | 544120 | 0223 | 009584 249146 4013 146519 6519 562514 O172 007422 Oo » hwWnHO .252068 | 1 3931 | 0.143995 3.8317 | 0.583396 | 1.0127 | 0.005465 255085 3849 I41414 4.0528 607751 0086 003740 253197 3765 138778 3387 637355 0053 002278 261406 | 3680 136086 7427 676027 | 0026 | oorI2I 264716 | 3594 | 133340 5-4349 | 735192 | 0008 | 000326 » a oO 0.268127 | 1.3506 | 0.130541 oo o 1.0000 SmitHsonian TaBLes. 72 TaBLe 39 MOMENTS OF INERTIA, RADII OF GYRATION, AND WEIGHTS In each case.the axis is supposed to traverse the centre of gravity of the body. The axis is one of symmetry. The mass of a unit of volume is w. Weight. Moment of Inertia Io. Sphere of radius ~ Spheroid of revolution, po- lar axis 2a, equatorial di- ameter 27 Ellipsoid, axes 2a, 20, 2c Spherical shell, external ra- dius 7, internal 7’ Ditto, insensibly thin, ra- dius 7, thickness a7 Circular cylinder, length 2a, radius 7 Elliptic cylinder, length 2a, transverse axes 20, 2c Hollow circular cylinder, length 2a, external ra- dius 7, internal 7” Ditto, insensibly thin, thick- ness adr Circular cylinder, length 2a, radius 7 Elliptic cylinder, length 2a, transverse axes 2a, 20 Hollow circular cylinder, length 2a, external ra- dius 7, internal 7’ Ditto, insensibly thin, thick- ness dr Rectangular prism, dimen- sions 2a, 24, 2c Rhombic prism, length 2a, diagonals 24, 2¢ Ditto For- further mathematical data see Smithsonian Mathematical Tables, Becker and Van | Diameter Polar axis Axis 2a Diameter Diameter Longitudinal axis 2a | Longitudinal axis 2a Longitudinal axis 2a Longitudinal axis 2a Transverse diameter Transverse axis 2d Transverse diameter Transverse diameter Axis 2a Axis 2a Diagonal 2 4mrwre 3 qrewart 3 4nwabe > 3 4rzw(73—r’8) 3 4nwredr 2nwar2 2mwabe 2mwa(r2—r'?) | 4nwardr 2mwar? 2mwabe 2mrwa(72—r'?) 4nrwardr Swabe 4wabe | | Te 6 8rwr® 15 8rwart 15 4nwabc(b2-+-c? ) 15 8r7w(7r5—r’) 15 Srwrtdr 3 mwart mwabc(b?-+-c?) 2 mwa(74*—vr'4) 4rwarrdr mwar?(37?-+ 4a”) mwabc(3c?+-4a") 6 ; 3(74A—r’4) 1a Fag) 5 eva(2r84 "adv Swabe(P+e) 3 eat Meiee 3 2wabc(c? 20”) 3 ) Square of Ra- dius of Gyra- tion p%. 2r2 272 5 b2- 2 5 2(7°—+r') 533) art 3 72 2 +2 4 rr? 2 rz (Taken from Rankine.) Orstrand (Hyperbolic, Circular and Exponential Functions) ; Smithsonian Mathematical Formulae and Tables of Elliptic Functions, Adams and Hippisley; Functionentafeln, Jahnke und Emde (xtgx, x“tgx, Roots of Transcendental Equations, a+ bi and re, Exponentials, Hyperbolic Functions, Ee Qo 2 ze, . — e-x*dx, Pearson Function e-$7 Vr Qo Qo and Cylindrical Functions, etc.). For further references see under Tables, Mathematical, in the 11th ed. Encyclopedia Britannica. See also Carr’s Synopsis of Pure Mathematics and Mellor’s Higher Mathematics for Students of Chemistry and Physics. SMITHSONIAN TABLES. . Loo % x eae ; SUE wf £08. aw f “— du, Fresnel Integral, Gamma Function, Gauss Integral u u“ “ x Co Tv sinv evxdx, Elliptic Integrals and Functions, Spherical TABLE 40 73 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS (As of January 1, 1929) (Considerably abbreviated from paper by Raymond T. Birge published in Phys. Rev. Suppl., vol. 1, no. 1, July, 1929, which see for further details) Some of the most important results of physical science are embodied in the numerical magnitudes of various universal constants; the accurate determina- tion of such constants has engaged the time and labor of many most eminent scientists. Some of these constants can be evaluated by various methods. Each has been investigated by various persons, at various times, and each investiga- tion normally produces a result more or less different from that of any other investigation. Under such conditions there arises a general and continuous need for a searching examination of the most probable value of each important con- stant. An investigation of the values of general constants in current use reveals a surprising inconsistency, both in regard to the actually adopted values and to their origin, probably because of the fact that it is almost impossible to find a critical study of the best values, sufficiently up-to-date to be really reliable, and sufficiently detailed to explain the inconsistencies found among older tables. (1) In what follows “ each general constant has been determined from the available data, beginning with that constant whose value depends least on other constants. The value thus adopted has then been used consistently in the calcu- lation of each succeeding constant for which it is an ‘ auxiliary constant’. No attempt has been made to compare the results of different investigators until these have been made properly comparable by the use of the same value of each auxiliary constant. (2) “ Each constant has been calculated from the available data by the use, as far as possible, of formulas which involve no approximations. (3) “Each constant has been recalculated, whenever it seemed necessary, by analytic methods—usually by the method of least squares.” Attention should be directed to two important sources : (1) The International Critical Tables (1926) publish a list of nine so-called “Accepted Basic Constants,’ each with its “ Uncertainty.” A list is given of 21 constants derived from these, and also certain other conventional and ex- perimental constants. The I.C.T." list was adopted in 1923; since then im- portant work on nearly every constant has appeared. It was prepared with the aid of various scientific societies and individuals. The values are not claimed to be the best values then available, although obviously an attempt was made to obtain the best values. The chief weakness of this list is the lack of any state- ment as to their origins. By correspondence and in other ways Doctor Birge has obtained such information, and specific references to this are made in the various sections to follow. *LC.T. will be used for International Critical Tables, 1926. SMITHSONIAN TABLES 74. TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS (2) The Geiger and Scheel “ Handbuch der Physik ”* contains an article by F. Henning and W. Jaeger on “ The General Physical Constants.” There is a list of 52 constants, basic and derived, and a statement as to the theoretical t and numerical basis of each value. Many approximations and sources of incon- sistency are pointed out, but with one or two exceptions no attempt is made to recalculate data to improve the published values. The Henning and Jaeger article, written in 1926, contains more recent information than the I.C.T. Since 1926 much new material has appeared, so that practically every con- stant adopted in the present paper differs more or less in value from that given in either of these two preceding lists. In fact for the great majority of the con- stants considered the adopted value is based primarily on work which has appeared since 1926. In the case of most of the constants, the situation is now much more satisfactory than it was a few years ago. The velocity of light in vacuum (c).—An accurate summary of all numerical results to 1927, in which many errors in the literature are corrected, has been given by de Bray.’ A good recent account of the experimental methods for measuring c, as well as the numerical results, is that by Ladenburg.” The latest and most accurate direct determination of the velocity of light is that by Michelson,‘ in 1921-1926. When the various sets of results are col- lected under the five different mirrors used, the agreement is quite remarkable, all five results varying only from 299797 to 299795 with a mean of 299796 as before. c= (2.99796 + 0.00004) x 10*° cm - sec.* The velocity of electromagnetic waves may be obtained indirectly from the measured ratio of the electrostatic (es) to the electromagnetic (em) system of electrical units, according to the generally accepted electromagnetic theory of light. The best value of this ratio, which is here denoted by c’, is undoubtedly that found by Rosa and Dorsey.’ Their final result is the average of a very large number of individual results, taken at different times, under varying conditions, and of remarkable consistency. It seems to Doctor Birge that about one part in 30000 is a very conservative estimate for the probable error, giving C == 2. 90/1 0.0001. This result is in terms of international electrical units. Henning and Jaeger * show that, to obtain the true ratio between the es and the em system, in absolute units, the result of Rosa and Dorsey must be multiplied by p*/*, where one int. ohm=p abs. ohm. According to a subsequent discussion, p = 1.00051 + 0.00002. This gives a corrected value of c’ = (2.9979+0.0001 ) X 10° cm+ sec. It is in beautiful agreement with Michelson’s recent value of c. * Henceforth denoted by H.P. * Nature, 120, 602, 1927. * Handb. der Exp. Phys., 18, 1, 1928. * Astrophys. Journ. 65, 1, 1927. * Bur. Standards Bull., 3, 433, 1907. °H.P., 2, 507. SMITHSONIAN TABLES TABLE 40 (continued) 75 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS _ The Newtonian constant of gravitation (G).—The H.P.” gives a table of seven determinations of G, ranging from 6.60 to 6.70 10° dyne: cm? g~’. Henning and Jaeger adopt 6.65. In their list they omit Poynting’s value? of 6.66+0.01. The I.C.T. adopt as one of their basic constants G=6.66+0.01. Since the publication of these reviews, Heyl* has made undoubtedly the most reliable determination of G. His final result is G = (6.664 +0.002) x 10-8 dyne - cm? - g~” This result is adopted here. It is based on five separate determinations vary- ing from 6.661 to 6.667. Mean density of the earth—Assuming R =6.371 x 10° cm as the mean radius of the earth, as given in the H.P., and gs; =980.616 cm: sec’, G - 8(earth) = 30.797 X 10°° sec”, where 8(earth) is the mean density of the earth. From the H.P. result G=6.65 S(earth)=5.53 g-cm™*. With the new result G = 6.664 s(earth) — 5.522 + 0.002 g -cm-* Relation of the liter to the cubic decimeter (1000 cm*),—The liter is defined as the volume of a kilogram of air-free water at its maximum density. In other words, the maximum density of water is, by definition, one kg- 1+. The kilogram is defined as the mass of the prototype kilogram preserved in Paris. This original prototype was intended to be the mass of a cubic decimeter (dm*) of water, at maximum density. Later determinations have shown a slight discrepancy. The various experimental results are discussed by Henning and Jaeger.’ The mean of the best determinations is 1 liter=1000.027 cm°; this value has been accepted in all recent tables. Henning and Jaeger give no prob- able error for the result, but one unit in the last place seems a reasonable assumption. Hence 1 liter = 1000.027 + 0.001 cm* = 1.000027 + 0.000001 dm? The maximum density of water 6n(H2O) is accordingly 1/1.000027 = 0.999973 + 0.000001 kg - dm-* or g - cm? It should be noted in conclusion, that it is customary to define I cc as liter/1000, while 1 cm*=liter /1000.027. The normal mole volume of an ideal gas.— (vn cm? mole, or FR, liter - mole?) The normal mole volume of an ideal gas is the volume occupied by one gram mole of an ideal gas, at o° C, under one normal atmosphere pressure. This *H.P., 2, 507. 7“ Gravitation,” Encyc. Brit., XI ed. * Proc. Nat. Acad. Sci., 13, 601, 1927. Heyl’s more recent value is 6.670 X 10° cm®-g™- sec.” Bur. Standards Journ. Res., Breas, 1930, *H.P., 2 491: SMITHSONIAN TABLES 5 76 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS quantity can theoretically be determined from any real gas, correcting to reduce to an ideal gas. Actually, only oxygen is used because its atomic weight is 16.000 by definition ; there is no error in the resulting value due to error in the atomic weight. As a result of extensive investigations, the cor- rection to change oxygen to an ideal gas is known with considerable accuracy. The LCT. gives v,=22.4115 X10® cm®.’ The H.-P. gives’ 22.414, x 108 cm® or Ry= 22.4135 liters. The discrepancy must be due to different values of dn(Oz), the normal density of oxygen, or of (I—a), the factor due to the deviation of oxygen from an ideal gas.’ Thus Vn = 32(1—a) /8n(Oz) =4 32(1—a) /Ln(Oz2) $1000.027 = R,, ( 1000.027) where vy» is the normal mole volume in cm’, R,, the same in liters, §,(O.) the normal density of O2, in grams per cm*, and L,»(O,) the normal density in grams per liter. All these values correspond to normal gravity (gn=980.665). It is, however, customary among chemists to express the experimental results in terms of gs; (980.616). Such values will be denoted by v, 6, L, and R. Thus R=M(1-—a)/L where J is the molecular weight. *The most general definition of a is (1/pv) d(pv)/d(p), (temp. constant) ; it measures the change in pu, per unit change in pressure, and has the dimensions of pres- sure’. To make the numerical values more definite, it is customary to write a = [1/(pv):] d(pv)/d(p), where (pv): refers to unit pressure. In investigations on normal density or normal mole volume, it is natural to choose one atmosphere as the unit of pressure. Henning and Heuse use one meter of mercury as the unit of p, and denote a by xt (see page 85). Since the numerical magnitude of a is proportional to the size of the unit of p, we have «kt = 1002/76. Henning (H.P. 9, 528) uses the symbol xt, but states that p is measured in atmospheres. Within limits of error, the isothermal pv is a linear function of p, for the so-called permanent gases Oz, Nz, Hz, etc., for such substances a is independent of p but is a function of temperature, and is more properly written at. The linear extrapolation of pu to p=0 gives then (pv)o= (1 — a) (pv). Now in the limit p=0, any gas becomes, by definition, an ideal gas. Hence (pv)o is the constant pv of an ideal gas, and (1 — a) is the factor which converts the real (pv):, (unit pressure) into the ideal (pv)o, both at some definite temperature. (I — a) is often denoted by (1+), and (1—a) or (1 +A) may be defined as the ratio (pv)o/(pv)1. Frequently v is so chosen (in magnitude or unit) that (pv): is unity. a (or xt) is then numerically (but not dimensionally) the slope of the pv isothermal (see H.P. 9, 528 and 538). SMITHSONIAN TABLES TABLE 40 (continued) | PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Henning and Jaeger’ give as a mean value, L=1.42892 g-1I* and (1—a) =1,00092. A more recent result by Baxter and Starkweather * (L =1.42901) is omitted, but is included in the discussion by Henning and Jaeger, and raises the mean L to 1.42893. From this, and the value of (I1—a) just quoted, the H.P. gets its value of v,. The more recent values of (1—a), average 1.00086, and this, taken with the Baxter and Starkweather value of L, gives vn =22.4119 x 10° cm’, in close agreement with the I.C.T. value. Baxter and Starkweather “have recalculated their 1926 data in a more logical manner and obtain L=1.428965 grams per liter, (1 —a) =1.000927. L= (1.428965 + 0.000030) gram : liter"? (g=980.616) I —a= 1.000927 + 0.000030. R= 22.4146 + 0.0008 liter - mole (g,;—980.616) R,, = 22.4135 + 0.0008 liter - mole (g,,— 980.665) Vn = (22.4141+ 0.0008) x 10° cm? - mole“ (g,,—980.665). Ratio of international (int.) to absolute (abs.) electrical units—For prac- tical convenience, the ohm, ampere, and volt have been defined, by international agreement,’ in terms of definite physical apparatus.” These international units are to be compared with the corresponding absolute units, with which they were of course identical, within limits of experimental error, at the time of adoption in 1908. One abs. ohm=10° em units of resis- tance, the em unit, under the assumption that permeability is dimensionless, being one cm sec.-t. Measurements of the abs. ohm have been made ina variety of ways, but all methods necessarily involve the measurement of length and time. The abs. ampere is 107 em units, the em unit being one dyne’/*, again with the assumption of dimensionless permeability. The definition of the int. amp. just given is the primary definition, and Doctor Birge follows the I.C.T. in designating the int. amp. so defined, and all quantities involving it, by the symbol “(a).’’ Now let (1) I int. ohm=p abs. ohm (2) 1 int. amp. (a) =q abs. amp. then (3) I int. coul. (a) =q abs. coul. (6) 1 int. henry=p abs. henry (4) 1 int. volt (a) =pq abs. volt (7) 1int. gauss=q abs. gauss (5) I int. joule (a) = pq? abs. joule *H.P., 2, 493. * Proc. Nat. Acad. Sci., 10, 476, 1924. *Proc. Nat. Acad. Sci., 14, 57, 1928. *London, 1908. ° This book, p. xlvi et seq. SMITHSONIAN TABLES 78 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS The int. ohm can be constructed as a definite laboratory standard. This is not true of the int. amp. (a). Hence the 1908 London conference appointed a committee to determine the e.m.f. of the Weston normal cell, in terms of the int. ohm and int.amp. The final value adopted by the committee (Jan. I, 1911) was 1.0183 int. volts, at 20°C, which, to avoid ambiguity, is written 1.01830. This is effectively a new definition of the int. volt and to distinguish it, if neces- sary, from the primary definition, Doctor Birge again follows the I.C.T. in writing int. volt (v). Similarly all units involving the Weston normal cell will be designated by “(v).” Let I int. volt (v) =r abs. volt (8) as contrasted with eq. (4). It is now possible to use the int. volt (v) and the int. ohm to obtain a new (subsidiary) definition of the int. amp. Thus I int. amp. (v)=r/p abs. amp. (9) as compared to eq. (2). Finally, in many investigations, a so-called “ semi- absolute” volt has been used. This is defined as the e.m.f. required to force one abs. amp. of current through one int. ohm resistance. Hence from eq. (1) I semiabs. volt= abs. volt. (10) From eqs. (8) and (10) one obtains I int. volt (v)=r/p semiabs. volt. (11) We have now to consider the most probable value of p and of q, and the difference, if any, between 7 and pq (or between r/p and q). These questions are discussed by Henning and Jaeger in the H.P., and they conclude, q= ies pe 1.00059, r=pq= 1T.0005o. On the other hand, the I.C.T. gives G=01909003, P=—1.00052, _ 7= 1.00042; while pqg=1.00045. Hence r/p=o0.g9990q. The correct determination of the best values of p and q is a very technical and extremely involved matter. Unfortunately, as just seen, there is no exact agreement on the subject. Part of the present disagreement in the values of p and q is due to the fact that there is no standard international unit of resistance or of voltage. Each national laboratory has its own standards which differ more or less among themselves, and also may change with time. The values of p and q finally adopted here represent, as well as possible, mean values both in respect to place and to time. Fortunately the accuracy of these quantities is so great that any possible error in the finally adopted values is entirely immaterial in its effect on the many constants derived later in this paper. SMITHSONIAN TABLES TABLE 40 (continued) 79 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS The numerical relation of the int. and abs. ohm rests chiefly on two exten- sive investigations, one P=1.00052+0.00004, by Smith,’ at the National Physical Laboratory (N.P.L.) of England, and the other, p=1.00051, by Griineisen and Giebe,’ at the German Reichsanstalt. The latter estimate their probable error, as well as that of Smith, as about 3 parts in 10°. In 1925 a committee at the N.P.L. began an investigation of the relation of the int. and abs. electrical units. This work is incomplete. It was stated in 1925 ° that a comparison of various manganin with mercury resistances indicates that the former have all increased in resistance by about 2.5 parts per 10° since 1912, or that the mercury standards (defining the int. ohm) are really smaller by this amount. The latter assumption would give p=1.000495, in place of Smith’s value of 1.00052. In a recent investigation at the Reichsanstalt, Steinwehr and Schulze * evidently assume that the N.P.L. 1925 standards are 2 parts in 10° less than the older 1912 standards, giving a mean value of p in exact agreement with the 1920 Reichsanstalt value. Their own experiments in 1928 agree with this same mean value to +I in 10°. Various intercomparisons at the N.P.L.° show that the German and American standards lie between the I1g12 and 1925 N.P.L. values. It seems certain that the best value of p, at the present time, is 1.00051 (p.e. seems to be not more than 2 parts in 10°), The most probable value of g is more uncertain. In the older work, the abs. amp., determined with either a current balance or a tangent galvanometer, was compared directly with the int. amp. as measured by a silver voltameter. There was measured by means of a silver voltameter, with certain specifications, the amount of silver, in grams, deposited per sec. by a current of one abs. amp. This mass of silver was then compared with 0.00111800 gram, the defined amount deposited, under the same conditions, by one int. amp. per sec. Such a procedure determines g unambiguously, but does not necessarily evaluate the electrochemical equivalent of silver (Ea,) per abs. coul. The electrochemical equivalent of a substance is the mass actually associated with unit charge, and is independent of experimental imperfections, while the mass deposited in an electrolytic cell per unit charge—the only quantity we can actually measure—is subject to experimental imperfections. This distinction has no bearing on the value of gq, so long as one accepts the official definition of the int. ampere. It concerns only the value of electrochemical equivalents and the resulting value of the faraday. The various experimental values of g, determined as explained above, are listed by Henning and Jaeger.” *Philos. Trans., 214, 27, 1914. 7 Ann. Phys., 63, 1790, 1920. *N.P.L. Reports, p. 94, 1925. * Ann. Phys., 87, 760, 1928. °N.P.L. Reports, p. 8, 1927.. °H.P., 2, 490. SMITHSONIAN TABLES 80 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS In the later work (1906 to date) the current, measured in abs. amp., usually with a current balance, is sent through,an int. ohm resistance, using a Weston normal cell. From the known current in abs. amp. and the known resistance in int. ohms, one obtains the e.m.f. of the Weston cell in semiabsolute volts. By eq. (11) the ratio of this result to the e.m.f. in int. volt (v), (1.01830 by definition), is r/p, evaluating only r/p, and not q. The value of the e.m.f. of the Weston cell, in semiabs. volts, the assumed corresponding electrochemical equivalent of silver per abs. coul., and the true resulting value of r/p, are listed by Henning and Jaeger." Omitting a probably less accurate value by Guthe, the remaining four values range from 1.00006 to 0.99989. Henning and Jaeger give correctly as 1.01822 semiabs. volts the Rosa, Dorsey and Miller * value of the e.m.f. of the Weston cell, but misquote and use in their averages the resulting E4, and r/p, giving 0.99995 for r/p in place of the true 0.99992 ( = 1.01822/1.01830). Using 0.99992, the unweighted average of the four investigations * is r/p=0.99995. The Bureau of Standards * considers only (a) (c) and (d) of reference 3 and gives 0.99991 as the best average value of r/p. The I.C.T. value (0.99990) is based on (a) and (d) only. Henning and Jaeger? take the unweighted average of all four values, and Doctor Birge has done the same, since there seem to be differences of opinion as to the relative weighting of these four values. It is very probable that (c) should be given a relatively lower weight; the final average is fortunately not changed. The next question concerns the equality of r/p and g. Rosa, Vinal and McDaniel * determined the e.m.f. of the Weston cell as 1.01827 int. volt (a), by using a silver voltameter and an int. ohm resistance. Hence by eqs. (4) and (8), knowing 1.01827 int. volt (a) =1.01830 int. volt (v), pq/r=1.01830/ 1.01827 = 1.00003. Hence g=1.00003 r/p. These investigators naturally as- sumed r/p=0.99992, for reference 3 (d). Hence g=0.99995. This is the figure misquoted as r/p, by Henning and Jaeger. The result indicates that q differs from r/p by 3 parts in 10°, and that, to agree with the primary int. units, the Weston cell should have been taken as 1.01827 int. volts. But at the Reichsanstalt,* the corresponding quantity was found, in 1908, to be 1.01834 int. volts, and in 1922, 1.01831. The average of these three results indicates that the accepted value of 1.01830 int. volts is correct within limits of error. In other words, g=r/p, and one int. volt (a) =one int. volt (v). This agrees with the view of Henning and Jaeger.’ The relative values of g and r/p adopted by the I.C.T. are based directly on the work of the Bureau of Standards.” ° *H.P., 2, 500, Table 6. * Bur. Standards Bull., 8, 260, 1912. *(a) Ayrton, Mather, Smith, (N.P.L.) 1908, r/p = 0.99980, (b) Janet, Laporte, Jouaust, 1908, 1.00006, (c) Haga, Boerema, 1913, 0.99994, (d) Rosa, Dorsey, Miller (Bur. Standards), 1912, 0.99992. * Bur. Standards Circ. 60, 38, 1916. ° Bur. Standards Bull., 10, 475, 1914. °Z. Instrument., 28, 327 and 353, 1908; ibid., 42, 221, 1922. *H.P., 2, sor. SMITHSONIAN TABLES TABLE 40 (continued) SI PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Henning and Jaeger * consider that the variation from unity of either r/p or q is less than the experimental error, and think it more practical to assume r/p=q=1.0000. It seems best to accept the mean value of r/p=0.99995, determined in four different laboratories, with the probable error as +0.00005. Assuming then no distinction between int. volt (v), and int. volt (a), we have p=1.00051 + 0.00002 pq = 1.00046 + 0.00005 q= 0.99995 + 0.00005 pq’ = 1.00041 + 0.00010 The atomic weights of certain elements.—In evaluating some of our con- stants, it is necessary to use the atomic weights of various elements. In the ultimate analysis, only ratios of atomic weights enter our formulas for the general constants. All atomic weights are determined from ratios, but in general not directly from the particular ratios we need. Hence it is necessary to consider individual atomic weights. The present atomic weights are based on the arbitrary assumption that the weight of oxygen is 16 exactly. In choosing oxygen as a basis, it is assumed that it has always the same atomic weight; i. e., it has no isotopes. Giauque and Johnston * have very recently found an isotope of atomic weight 18, from an analysis of the atmospheric absorption bands of oxygen. H. D. Babcock states that experiments performed on absorption coefficients in these bands indicate that O,, has an abundance of only one part in 1250 (probable error some 25 per cent). Aston’s atomic weights should be greater than the chemical values by about one part in 10,000. Babcock’s determination of relative abun- dance, involves the assumption that the absorption coefficient is the same, per molecule, for- each species of molecule (Ois—Oxg and Oig—O;s), and this may not be true. The atomic weights determined by Aston, from the mass spectrograph, need not be identical with those determined by chemical means, since Aston’s atomic weights are based on the mass 16 isotope of oxygen con- sidered as exactly 16, while the chemical atomic weights are based on the ordinary mixture of the two isotopes considered as exactly 16. We shall see that Aston’s atomic weights of hydrogen, helium, nitrogen and iodine seem to agree with the chemical values within his limit of error (one part in ten thousand to one part in five thousand). Hydrogen.—Moles* lists nine results lying in the narrow range 1.00766 to 1.00783, with a mean value of 1.00777 + 0.00002, or a rounded figure of 1.0078. The final average represents the result of 223 different measurements by five different investigators, using four different methods, and seems to be the most reliable now available. Doctor Birge accordingly adopts *H.P., 2, 501. 7 Journ. Amer. Chem. Soc., 51, 1436, 1929. * Proc. Roy. Soc., 115 A, 487, 1927. * Berichte, 61 B, 1, 1928; 59, SII, (A) 1926. SMITHSONIAN TABLES 82 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS H= 1.00777 + 0.00002. Aston, from positive ray analysis, obtains H=1.00778 with a limit of error 0.00015. The recent discovery of an isotope of oxygen makes it permissible to use Aston’s value only as an indication of the relative abundance of O,; and Oy,., not as an atomic weight determination. It is in perfect agreement with the chemical value, which indicates a very low abundance of Oy,s. _ Helium.—The true atomic weight of helium must be close to Aston’s value. The chemical value is at present slightly less accurate than Aston’s, and Doctor Birge accordingly adopts his value but his assumed error as the probable error, although he considers such a procedure may be open to criticism, in view of the situation regarding the oxygen isotopes. He accordingly writes He = 4.0022 + 0.0004. Nitrogen.—The error in the atomic weight of nitrogen produces practically the entire error in the atomic weight of silver. Since the great majority of the accepted atomic weights are derived more directly from silver than from oxygen, that of silver is of the highest importance. The atomic weight of nitrogen can be obtained by direct comparison with oxygen, and also from density measurements, using the adopted value of R. According to Clarke,’ the final average of these two methods gives N=14.0076. The atomic weight can be obtained indirectly in many ways. The results of all methods, including the two just mentioned, are summarized by Clarke* and give N=14.0081, presumably the best value in 1920. Now it is generally agreed that, as in the case of helium, the atomic weight of nitrogen can be determined most accurately from its density and deviation from a perfect gas, by the use of R=M(i—a)/L where FR is 22.4146+0.0008 (see p. 77), (1—a) =1.00043 +0.00002, and L=1.25046+0.000045 * whence N=14,0083 + 0.008. Aston‘ obtains N=14.008, but his assumed accuracy is only one part in 5000. Aston gives always the limit of error, and his probable error should be much smaller. His values all agree beautifully with the chemical values; the decision as to his actual probable error may be left open. Silver.—The best atomic weight of silver is at present directly dependent on that of nitrogen. A summary is given by Moles and Clavera.’ Of the many methods for obtaining the value of Ag, the most accurate is based on the reduc- *Mem. Nat. Acad. Sci., 16, 1920. ”Z. anorg. Chem., 167, 49, 1927. *Ibid., 167, 40, 1927. * Proc, Roy. Soc., 115 A, 487, 1927. SMITHSONIAN TABLES TABLE 40 (continued) 83 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS tion of AgNO, to Ag. Since O= 16.000, by definition, the sole error is due to that in N. The proportional error is due to that in NOs, only about one fourth the probable proportional error in N. The ratio AgNO;/Ag can be determined with great precision. The most accurate ratio, by far, is that by Richards and Forbes,’ yielding also 1.57479. A very elaborate investigation by Hénig- schmid, Zintl and Thile,’ gives again exactly the same ratio. With our adopted value of N and the above value of AgNO;/Ag=r, one has NO;/(r—1) = (62.0083 + 0.0008) /(0.57479) = 107.8799 + 0.0014. The atomic weight of silver can be obtained in many ways. Clarke ®* lists 43 methods, yielding a final weighted average of 107.8804. It seems reasonable that at the present time only the AgNO;/Ag ratio results need be considered, with a final real error in Ag due merely to that in N. It seems reasonable to adopt Ag=107.880=+0,001. Iodine.—The atomic weight of iodine enters into the discussion of the value of the faraday. Clarke* lists eight methods, with a mean of 126.926. This result will bear closer scrutiny. The most accurate is the direct determination of the I/Ag ratio, assuming the atomic weight of silver as known. Among the values of this ratio, 1.176603, obtained by Baxter,’ in 1910, is the most reliable. Clarke lists all determinations. Now the four earlier results are all approximately 1.1753, while the later results run much higher. These earlier results probably are vitiated by some systematic error. They are quite self consistent, and so by Clarke are given a high weighting. With the four earlier results eliminated, we have a new weighted average of 1.176549, in closer agreement with Baxter’s 1910 result. This ratio, combined with Ag= 107.880, gives [=126.926, while Baxter’s result gives 126.932. Using the revised average value for the I/Ag ratio with Clarke’s results for the other seven methods, we obtain a final weighted average of I= 126.932, in place of Clarke’s value 126.926, and in exact agreement with Baxter’s result. Doctor Birge adopts I=126.932 + 0.002. In conclusion it is of interest to note that Aston gets I1=126.932, in exact agreement with our adopted value. Carbon.—The atomic weight of carbon can be determined directly from oxy- gen. The result of all such determinations, as obtained by Clarke,’ is 12,0000+ 0.00026. This result (written 12.000) was accepted in 1925 by the Inter- national Committee on Atomic Weights,’ and has since been used by Baxter.’ * Journ. Amer. Chem. Soc., 29, 808, 1907. *Z. anorg. Chem., 163, 65, 1927. *Mem. Nat. Acad. Sci., 16, 1920. * Journ. Amer. Chem. Soc., 32, 1591, 1910. ° Journ. Amer. Chem. Soc., 47, 507, 1925. ° Journ. Amer, Chem. Soc., 50, 603, 1928. SMITHSONIAN TABLES 84 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Thirteen methods, including the above, listed by Clarke, give a weighted mean of 12.0025+0.00019. Aston* finds C=12.0036, (limit of error 0.0012). The mean of the final Clarke value and Aston’s value is 12.003, and is adopted here. C=12.003 + 0.001. Calcium.—The atomic weight of calcium is needed for the grating space of calcite. The value of Ca, accepted since I91I, is 40.07. When readopted in 1925 by the International Committee, reference was made to the work of Richards and Honigschmid.* These investigators precipitate CaCl, by a solu- tion of Ag, and determine the amount of AgCl produced. They assume Ag=107.88 and Cl=35.457. The final result is Ca=40.075, based on four determinations ranging from 40.085 to 40.070. It seems probable that the Richards and Honigschmid value of 40.075 is the best. The probable error 0.005, is very uncertain. Ca= 40.075 + 0.005. The normal atmosphere (A,,).—The normal atmosphere is defined as the pressure due to a column of Hg 76 cm high, of normal density (o0°C, An), under normal gravity. The I.C.T. gives An = 1.013250 X 10° dyne-cm”, based on the definition of A, as the pressure of a column of a liquid of density 13.5951 g per cm®, normal gravity. The H.P. gives An=1.013253x10°, from the defining equation An=Hn- pn(Hg) + 8m(H2O) + gn, in which H,=height of normal barome- ter = 76.000 cm, pn»=normal specific gravity of Hg (at 0o°C, A,), referred to air-free water of max. density, 8,(H.2O) =max. density of water, gn =normal gravity‘ =980.665 cm-sec.-*. Henning and Jaeger,’ using the density of mer- cury in the definition, investigate the most probable value of pn, then adopt pn=13.5955. The value of 8n(H2O) is 0.999973 g-:cm™*. The product pn( Hg) - 8m(H20) = Dn = 13.5955 X 0.999973 = 13.595133 g:cm™®, agreeing with the I.C.T. value to the six significant figures given by the I.C.T., but, with the use of seven figures, leading to 4,=1,013,253, as given by the H.P. Doctor Birge adopts as the most probable value of pn, the figure calculated by Scheel and Blankenstein,’ viz. 13.59546. Dn=13.59546 X 0.999973 = 13.59509 g:-cm™’, and An=13.59509 x 76 x 980.665 = 1.013249 X 10° dyne-cm-*, This should have a probable error of not more than two or three units in the last digit, + 0.000003. The 45° atmosphere is obtained by the mere substitution of gs5(980.616) for gn. A, = (1.013249 + 0.000003) x 10° dyne - cem-. A,;= (1.013199 + 0,000003) x 10° dyne - em-?. *Proc. Roy. Soc., 115 A, 487, 1927. 7Z, anorg. Chem., 163, 315, 1927. °H.P., 2, 490, 494. *Z. Phys., 31, 202, 1925, SMITHSONIAN TABLES TABLE 40 (continued) 85 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Note.—It is evident that the definition of the normal atmosphere given by Dorsey in the I.C.T. is technically quite different from Henning and Jaeger’s inthe H.P. The I.C.T. definition makes the normal atmosphere a conventional constant, with no probable error. Doctor Birge had some correspondence on this matter with Doctor Dorsey, leading to the conclusion that the H.P. defini- tion is correct. The adopted value is therefore based on this H.P. definition. Unfortunately, an article by Burgess * was overlooked in which the “standard atmosphere ” is defined as “ the pressure due to a column of mercury 760 mm high, having a mass of 13.5951 g-cm’%, gravitational acceleration of 980.665 cm: sec.”, and is equal to 1,013,250 dyne-cm-?.” It is thus a conventional constant, with no error. This definition was adopted in 1927 by the Inter- national Commission of Weights and Measures. Fortunately, this definition makes no change in the magnitude or the error of any derived constant. It should be noted that no temperature is specified and that the word “ mercury ” is technically superfluous. This seems very objectionable, since there is thus technically no simple method for reducing to standard atmospheres an actual barometer reading at an actual observed temperature. The H.P. definition, as used by Doctor Birge, seems preferable, in spite of international agreement. The absolute temperature of the ice-point (T,).—The generally accepted value of JT, was, for many years, 273.09°K., based on Berthelot’s analysis ” of the data of Chappuis,’ and of Joule and Thomson for the porous plug experi- ment. The final average value was y=36618X10%, or T)>=273.09°. The I.C.T. gives T)=273.1 as one of its basic constants. Most extensive observations on the volume and pressure coefficients (a and 8) of certain gases have recently been made by Henning and Heuse,* at the Reichsanstalt. The value of y was obtained by two different methods.° The first method gave for the gases He, Hz, and Nz, y X 10’= 36600, 36607, and 36606, or 7)=273.224°, 273.172° and 273.179°. The mean is yx 10° = 366043 or 7)=273.190° +0.015. The second method gave for He (two determinations at slightly different Po), Hz and No, yx 107=36598, 36597, 36617, and 36604. The mean is 36604.0 or T)>=273.194°. They conclude that the best mean value of all the experiments is y X 10’= 36604. The reciprocal of this is T,=273.19°. They write it as 273.20°. In the later article * by Heuse, neon is used, and the above value of y is confirmed. The only other determination of T, of. comparable accuracy is that by Roebuck,’ using the Joule-Thomson effect in air.’ This method requires a, the volume coefficient, as well as the Joule-Thomson coefficient ». Roebuck mea- *Bur. Standards Journ. Res., 1, 635, 1928. * Tray. et Mem. Bur. intern.; 13, 12, 1907. Sinid.) vols. 6,13. --Z. Phys.,.5, 264, 1021; 5, 285, 1921; 37, 157, 1926. °H-P., 9, 527. * Proc. Amer. Acad. Arts and Sci., 60, 537, 1925. *H.P., 2, 496. SMITHSONIAN TABLES 86 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS sured p, but for a used data, mainly by Chappuis. Henning and Jaeger * note this and adopt merely the Henning and Heuse value 273.20° (which as previously noted should be 273.19°). Roebuck obtained three results, 273.18°, 273.16° and 273.12°, average, 273.15°. He lists all previous determinations, and chooses 273.17°, lying midway between his own result and that of Henning and Heuse. He gives +0.02° as the probable error. Doctor Birge feels that these two results (273.15° and 273.19°) are entitled to far more weight than any of the older work, but that the second result is probably the most accurate, being based on new determinations of a. Hence he adopts—with the probable error given by Henning and Jaeger— T,=273.18+0.03°K. (Roebuck’s +0.02° may well be more reasonable). The mechanical equivalent of heat (J) and the electrical equivalent of heat (J’).—A description of the methods for the evaluation of J, and a dis- cussion of the results, is given by Jaeger in the H.P.* The value adopted by Henning and Jaeger in the H.P.’ is one cal.4;=4.184, int. joule= 4.186; abs. joule. The I.C.T. value is one cal..4;=4.185 abs. joule. The cal.,; is defined as the amount of thermal energy required to heat one gram of pure water from EAs tout oea ce, Joule turned mechanical energy directly into thermal energy, and J was evaluated in abs. joules. In most modern work electrical energy is turned directly into thermal, thus evaluating the electrical equivalent of heat (J’, mea- sured in int. joules). Since the relation between the int. joule and the abs. joule (107 ergs) is known with considerable precision, the mechanical equiva- lent may be obtained from the electrical equivalent. The value of J adopted by the H.P. results from the work of Jaeger and Steinwehr.* They determined J’, for many different mean temperatures lying between 4.75°C and 49.60°C. This is undoubtedly the most accurate work now available. They list 67 results. These results are represented as a para- bolic function of f. On examining their data, Doctor Birge finds that a parabola is not a suffi- ciently complex function. Their residuals show pronounced trends; unfortu- ately the largest trend is near 15°C. He accordingly made a separate investi- gation of the best curve for their data. J’ = 4.21040 — 2.78958 X 1073¢ + 7.73723 X 10°? — 8.52567 x 10°78 + 3.7540 X 10-*t# (1) This gives J’1;= 4.18327 int. joules, and is the most probable value resulting from the work of Jaeger and Steinwehr. Jaeger gives two parts in 10000 (i.e., 8X 107+ joules) as the probable error. Doctor Birge therefore writes J’15= 4.18334 0.0008 int. joules. We have one int. joule=pq? oe joule, where pq*=1.00041+0.00010. Hence there results J45= (4.1833 + 0.0008) (1.00041 + 0.00010) = 4.1850+ 0.0009 abs. joules. +H.P., 2, 406. *H.P., 0, 476, *H.P., 2, 497. *Ann. Phys.,64, 305, 19at. SMITHSONIAN TABLES TABLE 40 (continued) 87 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS The most accurate direct determination of the mechanical equivalent of heat J is the work of Laby and Hercus,’ which appeared since the H.P. was compiled. They use a continuous flow calorimeter and make 23 determinations, grouped about six different temperatures, the temperature change in the calorimeter being always about 5°C. Their result is J=4.1841+0.0001 abs. joules at 16.67°C. A more precise method of reduction is first to adopt a curve for the tempera- ture variation of the specific heat of water. Such a curve is given immediately by eq. (1). If it is desired that the specific heat at 15°C be unity, eq. (1) is to be divided by 4.18327. Doctor Birge finally adopts one 15° calorie (J,; ) =4.1852 + 0.0006 abs. joules onel5° “ (J’,;) =4.1835 + 0.0007 int. joules and by eq. (1) »9 = 4.1813 + 0,0006 abs. joules J’ 59 = 4.1796 + 0.0007 int. joules The faraday (F).—The faraday is defined as the quantity of electricity carried in electrolysis by one gram equivalent of any element. It is believed to be a general constant of nature. According to modern ideas, each univalent ion carries a charge numerically equal to the electronic charge e. The Avogadro number NV, gives the number of atoms (or molecules) in one gram equivalent. Hence one may define the faraday more precisely as the product No: e. The fact that F can be most accurately evaluated from electrolysis, and No is then obtained from F and e, does not affect the validity of the definition. One electrochemical equivalent is the mass associated with unit electric charge. Like the faraday, its true value, independent of experimental condi- tions, depends only on the adopted unit of charge. On the other hand we can measure only the amount of a substance deposited or released in an electrolytic cell, per unit current per second. This is affected by experimental conditions, and may or may not equal the electrochemical equivalent. The faraday is then, by definition, the ratio of the gram. equivalent of a substance to its electrochemical equivalent. Almost universally the distinction between mass deposited per unit charge, and electrochemical equivalent is ignored. Con- siderable confusion results regarding the best value of certain electrochemical equivalents, and the resulting best value of the faraday. Nevertheless, it is convenient to assume, for the moment, that the silver deposited per unit charge in a silver voltameter, under the conditions defining the international ampere, is the electrochemical equivalent of silver (Fug). With this assumption, the value of faraday follows from constants already adopted. The gram equivalent of silver, or of any univalent substance, is numerically equal to its atomic weight in grams (Ag). The amount of silver deposited in electrolysis by one international coulomb is, by definition, 0.00111800 gram. Hence * Philos. Trans., A 227, 63, 1927, SMITHSONIAN TABLES 88 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS F = Ag/0.0011 1800 = (107.880 + 0.001 ) /0.001 11800 int. coul. =96494.+1 int. coul., (1) = 96489. + 5 abs. coul. (2) If q=1, as adopted by the H.P., F=96494 int. coul. or abs. coul., the actual value adopted by Henning and Jaeger. If g=0.99993, as adopted by the I.C.T., there results F=96487 abs. coul. The I.C.T., however, adopts F =96500+ 10 abs. coul., which with its adopted value of q, leads to F=96507 int. coul. This last value requires Ag = 107.893, in direct contradiction to facts. F=96500 +10 abs. coul. is evidently taken from Vinal and Bates,’ and to understand the seeming discrepancy, it would be necessary to examine in detail this last quoted work employing the distinction between mass carried in electrolysis and mass deposited (see Doctor Birge’s discussion, Phys. Rev., Suppl. 1, 35, 1929). Henning and Jaeger * make no distinction between mass carried and mass deposited, writing E4,=0.00111800 g per int. coul. It seems evident from Vinal and Bouvard * that there are inclusions in the silver deposit, tending to make E4, too large by 4X 10% g, and F too small by 4 coulombs. There may be small parasitic chemical reactions in the silver voltameter, tending to de- crease the value of E4, and hence to increase the value of F. It seemed best to adopt the value of F given in eqs. (1) and (2), but to assign to E4, a probable error of 5X 10°*g, 1.e., an error slightly greater than the measured effect of the inclusions. Then hy 107.880 + 0.001 ~~ (1.11800 + 0.00005) x 10-3 = 96489 + 7 abs. coul. = 9648.9+0.7 abs. em units, = (2.89270 + 0.00021) x 10** abs. es units. F = 96494 + 5 int. coul. (3) The electronic charge (e).—The values of a large number of important con- stants depend directly on the value of the electronic charge; in most cases the final probable error is due mainly to the error in e. It is desirable that it be determined in many different ways, and by many different persons. The situation has been the reverse. Only one precision method for the evaluation of e was known, and the work had been carried out by a single individual. It is very fortunate that the investigation referred to is a masterpiece. Milli- kan’s * investigations extend over more than a decade; the latest value of e was published in 1917. The great importance of e, and because higher values have recently been obtained, led Doctor Birge to investigate the matter in more than usual detail. Millikan found that if the viscosity of air is taken as constant, in Stokes’ law of fall, the apparent value of ¢ is a function of the radius of the drop and of the pressure of the air. The true value of e can be found by assuming a modification of Stokes’ law such that his observations could be plotted as a *Bur. Standards Bull., 10, 425, 1914 (p. 447). 7H.P., 2, 502. *Bur. Standards Bull, 13, 147, 1916. * Phys. Rev., 29, 60, 1909; 32, 342, I9II; 2, 109, 1913; Philos. Mag., 34, I, 1917; 19, 209, IQIO. SMITHSONIAN TABLES TABLE 40 (continued) 89 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS linear graph, its intercept on the y axis giving e?/*, and leading to the desired quantity. Millikan found that for values of 1/pa less than about 700 (p in cm Hg, a, radius of drop, in cm), the resulting graph was linear. Only that part of the curve corresponding to 1/pa less than 700 was used in precise determinations of e. The 1917 value of e was deduced from 25 oil drops, each giving one point on the graph. The 25 observations form a beautifully consistent set of data. The least squares solution, as calculated by Doctor Birge, gives for the inter- cept (61.111 +0.032) X10*; but plotted data are based on the 1913 value (0.0001824) for the viscosity of air. The value of a)(=e?/*) is proportional to the viscosity. With the improved 1917 value of the viscosity (0.00018227), €=d,*/? = (4.7721 + 0.0038) X 107? es units. Millikan stars 18 of the points, with conditions of observation as perfect as possible. These 18 drops give a)=61.121+0.038 (e€=4.7733+0.0045, IQI7 viscosity). These 18 drops deviate from the best straight line more than do the other 7. The standard deviation of the 25 drops is 0.121 x 10-8, while for the 18 drops it is 0.123 x 10%. The drops of smaller radius fall more slowly, and can be more accurately timed. Actually they are less reliable. Thus 13 smaller drops have a standard deviation of 0.134, considered as part of the 25 drops, definitely larger than the 0.121 average of the 25. A least squares solution of these 13 drops gives d)=61.143 +0.050, standard deviation of 0.132. This is so close to 0.134 that we can conclude that the 13 drops fit the graph of the entire 25 as well as a graph designed to fit them alone. On the other hand, the 12 larger drops give for the least square solution, @) =61.078 + 0.045, stand- ard deviation 0.117, thus definitely more reliable than the smaller drops. The resulting value of e, reduced to the 1917 viscosity, is 4.7759+0.0058 for the 13 smaller drops, and 4.7683+0.0053 for the larger drops. The weighted mean is 4.7718, in essential agreement with the value (4.7721) obtained from all 25 drops. This, of course, is what we should expect. The average deviation from the average for small and large drops is 0.0038, much less than the probable error of either. This is an analytic proof that the true value of e is not a function of the radius of the drop. This also indi- cates that the larger drops are, if anything, more reliable than the smaller. If the larger are given a higher weight, the resulting value of e would lie between 4.772 and 4.768. The final conclusion is that there is no particular reason for giving different weights to the different drops, and that any such weighting, if made, would slightly lower e. We therefore take 4.772 x 10° es units as the best result of the 1917 work. SMITHSONIAN TABLES go TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS In 1913 data on 58 drops were obtained. Millikan used, in evaluating e, the 23 drops (out of 58) of smallest 1/pa. These are more consistent, having a standard deviation of only 0.092. They lead to e=4.7665+0.0058 (1917 viscosity), while the entire 58 give 4.7703+0.0022. This last figure might appear more reliable than that of 1917; such a conclusion ignores other errors. In 1913 Millikan estimated four factors, each with a maximum uncertainty of 0.1 per cent. In 1917 he estimated two such factors, each with a maximum uncertainty of 0.05 per cent. His final 1917 estimate for the maximum uncer- tainty in e is 0.1 per cent, based mainly on these two factors. The above calcula- tions show, however, a probable error of 0.08 per cent (+0.0038) in the 1917 value, due to accidental errors. The final uncertainty is therefore several times as large. Doctor Birge estimates that the final probable error is about 0.1 per cent, and writes e= (4.772+0.005) X 107° es units. This value is now subject to two further corrections. In reducing the result to es units per cm, Millikan used c=2.999 x 101° cm: sec.“?, and made no dis- tinction between international and absolute electrical units. It has been shown definitely that the int. volt differs from the abs. volt by an appreciable amount. We have also now the new value, c=2.99796. The change in c is obvious, it lowers e from 4.772 to 4.770. The other change seems to have been overlooked by everyone. Because the electrical potential forces the charged drops against the viscosity of air, instead of against electrical resistance, one has only electric voltage coming into the calculations. One int. volt=1.00046+0.00005 abs. volts. The true value of F, in abs. volts, is larger and the true value of e, in abs. es units is smaller by just this ratio. Hence, the value of e is reduced’ from 4.770 to 4.768. Since the error in each of these corrections is negligible, the final result is e= (4.768+0.005) X 10°7° abs. es units. This should be the most reliable value from Millikan’s oil-drop work, Recently an entirely different method has been devised for e. The two results which have already been published are apparently less reliable than the oil-drop value. This new method measures directly the Avogadro number No, and from this and the value of the faraday, e immediately follows. It utilizes the absolute wave lengths of X-ray lines, determined with an ordinary ruled grating at grazing incidence, as compared with the wave lengths determined with a crystal grating. A=2d - sin (1) where d is the grating space. It has been pointed out by Siegbahn,* and by 1 Professor Millikan agreed, 1928. *Siegbahn, Spectroscopy of X-rays, p. 26. SMITHSONIAN TABLES TABLE 40 (continued) gl PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Compton, Beets and DeFoe,’ that, to obtain the true X-ray wave length J, it is necessary to use an effective grating space d, automatically correcting for the refraction of the X rays at the crystal surface. For first order spectra and the high frequencies of ordinary X rays, the true grating space d’ is connected with the effective space d by the relation d=d'(I—0.000135). | (2) Siegbahn uses for calcite d= 3.02904 X 10° cm, at 18°C. This is a more or less arbitrary value, assuming that d for rock-salt, at 18°C, is 2.81400 x 10-8 cm. We shall denote by dj, this 3.02904 value, and by A” the resulting wave- length. Hence Nr pet (2) NAL = GeO 18 (3) where J is the true wave length from a ruled grating, d,s the effective grating space of calcite at 18° C, A” the supposed true wave length from measures with a calcite crystal with d”;g as an assumed grating space at 18°C. dy, follows knowing d”,, and A. From (2) we obtain d’;s, the true grating space of calcite. The temperature coefficient* is 1.04 10°; d's) is accordingly 2.08 x 10% larger. This 20° value is given theoretically by the formula d' y= {nM /pNo(B) (°° (4) where n is 4, M, the molecular weight of calcite (CaCos3), p, its density at 20°C, (8), a geometrical constant depending on the crystal structure, and No, F/e; knowing d'x) we can obtain No and then e. We have M = 100.078 + 0.005 ; the best value of p is 2.7102+0.0004 g + cm=® (DeFoe, Compton *), of (8), 1.09630+0.00007 at 20°C (Beets*) whence and e= (1.7176+0.0003) X 1013 (d'99)%. (5) The two published determinations of ds, based on absolute X-ray wave lengths, are by Backlin,’ and Wadlund.° Using (3), Wadlund obtains 1.5373 +0.0008A for the Ka, line of Cu, combined with Siegbahn’s values of d”13 and Xr”, giving d,s= (3.0290+0.0016) X 10-8 cm. The corresponding value of doo is 3.02906 ; the true grating space d’.9, (30295 0.0016) x 10° cm. This value is to be substituted in (5). It gives e=(4.7757+0.0076) X 107° abs. es units. This is not as accurate as the oil-drop value. It is difficult to appraise the work of Backlin, as regards its accuracy. He gets 8.333+0.008A for the absolute wave length of the Al Ka line. Compar- ing this with an unpublished result by A. Larsson (8.3229+0.0008A ), ob- tained with a crystal, Backlin obtains djg=3.033+0.003A. This gives d'2o = 3.03347A, and e=(4.794+0.015) X107° abs. es units. This value is 0.55 per cent higher than the oil-drop result. *Phys. Rev., 25, 625, 1925. *Siegbahn, Spectroscopy of X-rays, p. 85. * Phys. Rev., 25, 618, 1925. * Phys. Rev., 25, 621, 1925. ° Upsala Dissertation, 1928. ° Proc. Nat. Acad. Sci., 14, 588, 1928; Phys. Rev., 32, 841, 1928. SMITHSONIAN TABLES g2 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Backlin’s results lead to 4.794+0.015. The investigation by Backlin is a pioneer piece of work, and it is quite likely, as such, to contain unsuspected systematic errors. If the three values of e (4.768 from Millikan’s oil-drop work, 4.776 by Wadlund, and 4.794 by Backlin) are weighted according to the apparent probable error of each, the result is still suspiciously high. The thorough examination made of the actual value of e and its probable error, from the oil-drop work, was carried out because of this inconsistency. It seems best to reject the Backlin value, and to use the weighted mean of the remaining two values, viz. 4.768+0.005 and 4.776+0.008, or 4.770; as usual adopt as its probable error the smaller of the two individual errors, rather than that given by least squares; the latter is meaningless when only two observations are concerned. The finally adopted value is then e= (4.770+0.005) x 10-'° abs. es units. The specific charge of the electron (e/m).—A very complete and critical account of all work on the measurement of e/m, up to 1919, has been given by Bestelmeyer.’ His final conclusion is that e/m= (1.76+0.02) X 10 em units. A more recent discussion is that by Gerlach,” who concludes that e/m= 1.766 x 107 em units. The question is discussed very briefly by Henning and Jaeger,” who however adopt Gerlach’s value. The I.C.T. adopts 1.769 + 0.003. The latest work greatly exceeds in accuracy all the preceding; it seems legitimate to confine the discussion to these new results. The value of e/m has been obtained with considerable accuracy by three distinct methods, (a) deflection of electrons in electric and magnetic fields, (b) Zeeman effect, (c) fine structure and relative wave lengths of H and He? spectral lines. It may be obtained also from Bohr’s theoretical expression for the Rydberg constant, R,, provided one assumes the value of e and of h. This last method is not as accurate as the preceding. A fifth involves the Compton shift. This also is as yet a relatively inaccurate method. The latest and most accurate work with method (a), that by Wolf,” is carried out with every possible refinement. The essential point is the employ- ment of a longitudinal magnetic field. The electron velocity is calculated from the potential fall. He concludes that e/m=(1.7679+0.0018) X 107 em units. 1.7679 should be corrected for the difference between the int. and abs. units. It then becomes (1.7689 + 0.0018) X 107 abs. em units. * Marx, Handb. Radiologie, 5, 1, 1919. *H.P., 22, 41. *H.P., 2, 504. * Ann. Phys., 83, 849, 1927. SMITHSONIAN TABLES TABLE 40 (continued) 93 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS The most recent accurate work, using method (0b), is by Babcock." A large number of spectrum lines (116 in all) were employed. Nearly all showed a complex Zeeman pattern. For determining e/m it was necessary to assume the Runge denominator of each line. In cases where this is small, it was known with certainty. In some cases it was large and rather uncertain. His work has been criticized, and Gerlach, in his final table,” omits Babcock’s result. It appears to Doctor Birge that the criticism is unjustified; at his suggestion, Babcock has recalculated his data, omitting all Zeeman patterns in any way doubtful. The new result,® based on 48 lines for which the Zeeman pattern is definitely established, is 1.7606+0.0012; the error is purely observational. The difference between the two values is just that produced by the change in the value of c. Doctor Birge therefore writes e/m= (1.761 +0.002) X 107 abs. em units as the best result from Zeeman effect. The latest, most accurate work using method (c), is by Houston,’ based on the Bohr-Sommerfeld model consisting of a positive nucleus and one encircling electron (moving in elliptic or circular orbits). Such atoms are H and He’. In order to determine e/m, we must evaluate the so-called Rydberg constant for hydrogen (Ry) and for ionized helium (Ruy-). Practically the entire error in ¢/m is merely the error in the difference Rue—Ru. The pioneer work was performed by Paschen.’ He obtained Ry = 109677.69 +0.06 cm, Rye=109722.14+0.04 cm™. Those give e/m=1.768+0.003, using his values and assumed errors for Ry and Rue, but the present accepted values and errors for H, He, and F. The recent investigation by Houston,’ is so much more accurate than the work just mentioned that it alone will be considered. Houston’s new experimental results are Rue=109722.403 + 0.004 cm", Ru=109677.759 + 0.008 cm-. The stated errors are purely least squares probable errors. He believes the relative values of Rye and Ry are correct to 0.02, although the absolute error in each may be about 0.05. Houston used m=5.4 X10, He=4.0001, H=1.0077, F=96470 abs. cou- lombs, and obtained e/m= (1.7606+0.0010) X 107 em units. Using his con- stants and the corrected formula the result is 1.7603. The error in his formula is therefore almost negligible. The entire probable error in e/m, due to errors in all factors, aside from (Rye—Ry), is less than 0.01 per cent and so is entirely negligible compared to the error in (Rye—Rzu). * Astrophys. Journ., 58,.149, 1923. *H.P., 22, 81. * Phys. Rev., 33, 268 A, 1929; Astro- phys. Journ., 60, 43, 1929. * Phys. Rev., 30, 608, 1927. ° Ann. Phys., 50, 901, 1916. SMITHSONIAN TABLES 94 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Using Houston’s value of Ry, and of Rue—Ru, together with the values of H, He, etc., we obtain e/m= (1.7608 + 0.0008 ) X 10° abs. em units. This value of e/m thus agrees with that obtained by Babcock. Summarizing the results we find e/m=1.769+0.002 from deflection experiments, =1.761 +o,002 from Zeeman effect, =1.761+0.001 from H and He spectra. The discrepancy between the first result and the last two is four times the probable error of the first. Theory gives only one chance in 143 of this occurring. The discrepancy seems to be real. The last two results are measurements of e/m for electrons inside of an atom, based upon the quantum theory of atomic structure. The first is the measure- ment of ¢/m for electrons 1m free space. The figures point to the conclusion that the e/m of an electron is less when it is inside an atom than when it is outside. If this conclusion seems unacceptable, then it would appear that there is some general error in the equations of the quantum theory of atomic struc- ture or there is some unknown general error in all the deflection experiments. Under the circumstances two values may be assumed of e/m—one for where atomic structure is involved, the other for free electrons. Hence e/m (spectroscopic) = (1.761 +0.001) x 10° abs. em units per g; — (5.279 +0.008) x10" abs.es “ * ro e/m (free electrons) = (1.769 + 0.002) x 107 abs.em “ ee = (5.303 + 0.006) x10 abs.es =“ oe The Planck constant (h).—The Planck constant has been evaluated in a number of ways. There is difference of opinion as to the relative accuracy of the results ; some are more or less incompatible. A satisfactory determination of this constant is difficult. The first attempt to obtain a value of h, from the results of all seven meth- ods, was made by Doctor Birge in 1919. The value found was (6.5543 +0.0025) X 10°*” erg : SEC., the error being merely the least-squares probable error. This error has been criticized by Ladenburg as far too small. It is not the final error since, as clearly stated, one must add to it an error somewhat greater than the proportional error in e. This occurs with some positive power (unity to two) in every known method for obtaining h. This makes the total probable error more nearly +0.01. Doctor Birge’s 1919 evaluation of h has been adopted by the I.C.T., but the probable error should be +0.001. In 1920 Ladenburg* wrote an article on the evaluation of h, in which several of Doctor Birge’s conclusions were criticized. His own result in that article was 6.54+0.01. In 1925 Ladenburg wrote another article on this subject, for the H.P? He then concludes that h=6.547, which value he rounds 1 Jahrb. Radioakt. und Electronik, 17, 93, 1920. *H.P., 23, 279. SMITHSONIAN TABLES TABLE 40 (continued) 95 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS off to 6.55+0.01. Henning and Jaeger * discuss the most probable value and adopt 6.55. (a) Bohr’s formula for the Rydberg Constant.—Bohr’s theory of the Hy- drogen atom leads to the equation wo = 2re®/hic2e/m (1) in which Ro is the Rydberg constant for infinite mass (cm units), e, the electronic charge (abs. es units), and e/m is in em units. Ra» is derived from the observed Ry by the equation Ro =Ry(1+m/myg) =Rait + F/(e/m) (H —m) =109737.424 em. (2) The probable error in R» is about 0.06 cm. In absolute units Ro +c = (3.28988 + 0.00004) x 10? sec.t. Substituting in (1) the spectroscopic value of e/m, since we are dealing with spectroscopic data, h=(6547=20.011) <10;*" ete.-sec. After adopting a weighted mean value of h, (1) becomes a method for calcu- lating, indirectly, the value of Rw. Or, using the directly determined value Re, (1) becomes a means for calculating e/m. (b) Ionization potentials —In 1919 Birge had available 13 values of ioniza- tion and resonance potentials. Many more such potentials have been obtained. The probable error in each is rather large. We have one really accurate de- termination obtained with electrons of carefully controlled velocity. This is Lawrence’s value* of the ionization potential of Hg. His final value equals 10.40 +0.02 int. volts. The equation for obtaining h is hv=eV; all quantities are in absolute units. The observed potential (’’) is always in int. volts. The potential in abs. es units is then VY = pqV’108/c. The spectral frequency v (in sec.*') is obtained always from the wave length A, in cm. Hence v’(cm™) =1/A, and v=c/A. The above equations lead to h/e= (pqV'10*) /(c7v') = (pqV'A10*) /c? (3) It seems quite customary to assume that V¢s=IV" volts/300 and to write this pavation h/e=V'X/300¢. (4) This is equivalent to assuming c=3 X 10° cm: sec.-1, causing an error of 0.07 per cent. Scarcely anyone uses c=3 X10'° cm: sec.* when reducing A to », and thus in the same equation it is customary to use two different values of c. The “term” of Hg corresponding to the ordinary ionization potential is 84178.5 cm™, whence 4772.5 t= (0:500-=0.015 107". The probable error in V’ is 0.2 per cent and in e, 0.1 per cent. The errors of the other factors are negligibly small. (c) X-ray continuous spectrum.—This method uses (3), A being measured by means ofa calcite crystal, i.e., \=2d sin 6 where d is the grating space, and 6 the angle at which the given wave length shows constructive interference. h/e=pq 2d(V’ sin 6) 108/c? Duane, Palmer, and Yeh * have carried out an accurate investigation. The resulting value of h is (6.556+0.009) x 10°’. Another result for which equal accuracy is claimed, is by Wagner.’ Ladenburg” gives a complete list of Wagner’s experimental results. Ladenburg, using eq. (4), with c=2.9985 X10", gets 6.529+0.01. *H.P., 2, 510. * Phys. Rev., 28, 947, 1926. * Proc. Nat. Acad. Sci., 7, 237, 1921. ‘ Phys. Mei 21, 621, 1920. °H.P., 23, 2063; : SMITHSONIAN TABLES 96 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Duane, Palmer, and Yeh used a known potential (int. volts) and measured the angle 6 at which the ionization suddenly started (or stopped). This gives the critical ionization frequency corresponding to the given voltage. Wagner used known wave lengths varying the voltage for a given wave length, until ionization suddenly began (or ceased). Both methods involve the calcite grating space d. On page 91 the absolute wave lengths of rays were used to evaluate d’, the true grating space; d’ was then used with other known con- stants to evaluate the electronic charge e. In this section we use the finally adopted value of e, (4.770+0.005) X 107° abs. es units, with these same con- stants, to evaluate d’. @ 9 =14.770 * 1079/ 1.7570 <1! (2 — (310283 + O:0010) <1; cnt This value of d’x9 includes the result of the X-ray work, since the value of e just used is the weighted average from both oil-drop and X-ray work. We might have used e= 4.768 to get a value of d’ based on oil-drop work. A second value of da’ might then be obtained from absolute X-ray measurements. The weighted average of these two values would be the value given, provided we use the data and probable errors indicated on p. 91. We obtain for the effective grating space of calcite at 20°C, for the first order Spectrult doo = (3.0279 + 0.0010) X 10°? cm. This value is to be substituted with the direct experimental value of V’’ sin 6. For the latter Duane, Palmer, and Yeh found 2039.9+1 int. volts (mean tem- perature of about 20°C). Thus we have h—\(6'550== 6.006) <10;4terg,1sec. Similarly revising Wagner’s result we obtain 6.532+0.010, in place of 6.526+0.010. It is difficult to judge what revision is required in the values of A used by Wagner ; the change is probably small. We thus have, as the two best values of h, from X-ray data, 6.559+0.008 (or 0.009) and 6.532+0.010. The work of Wagner has not yet been published in sufficient detail. For this reason in adopting a weighted average only one-half as much weight is given to Wagner. Since the two results differ by much more than the probable error of either, the regular least squares probable error is used. Hence, from X-ray data, bes h= (6.550+0.009) X 10-* erg : sec. (d) Photoelectric effect—-The most accurate determination of h, from photoelectric work, is by Lukirsky and Prilezaev." They use a somewhat different technique from that employed by Millikan,’ and obtain a simple empirical relation for the ionization current as a function of voltage. The actual curve may be transposed into a linear graph, making the extrapolation to zero current more certain. They also carry the readings very close to this zero point. 1 Zeit. Phys., 49, 236, 1928. * Phys. Rev., 7, 355, 1916. SMITHSONIAN TABLES TABLE 40 (continued) 97 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS The equation for evaluating h is that just used, except that now the energy (P) to pull an electron out of the metal is no longer negligible compared to hv. Hence we write Ve —hy— ee To eliminate P, light of varying frequencies is used, measuring for each the critical voltage V at which ionization starts. V is plotted against v; the result- ing curves should be linear, with a slope dV /dv=h/e. With V measured as V’’ int. volts, and v as »’ cm-?, we have dV /dv= (pato®dlV’")/(c?dv’) =h/e Lukirsky and Prilezaev use the metals Al, Zn, Sn, Ni, Cd, Cu, and Pt. Six curves, three with Zn, two with Al, and one with Ni, were the best. Un- fortunately these investigators give no detailed data, and no indication of the actual equation used. Their final value of h is 6.543 x 10°" erg - sec., the indi- vidual results being 6.539, 6.542, 6.540, 6.556, 6.536, and 6.546. We take h= (6.543 +0.010) X 10°*" erg ='sec. These investigators estimate their final error in h as 0.1 to 0.2 per cent. (e) Wien’s displacement law; Planck equation—h may be had from radia- tion constants in two different ways. The first is by means of cs, in the Wien displacement law, Kee G/p—A. where B=4.9651 (root of e+ 8/5—1=0). The radiation constant cz occurs also in Planck’s black-body radiation law in the form 6G1—NG/E: c=velocity of light, k( Boltzmann constant) =R,/No, Ro (gas constant per mole) =vnAn/To, and No (Avogadro’s number)=Fc/e. Substituting the values of vn, An, To, F and e previously adopted, No = (6.0644 + 0.0061 ) X 1078 mole, Ro= (8.3136+0.0010) X 10" erg - deg.? : mole7?. h=(( 1637002010014) < 107, erg. deg. In 1919 Doctor Birge asked Coblentz what in his opinion was then the best value of co. He recommended 1.433 cm: deg.; this value was adopted. In a long critical review of the radiation constants, three years later, Coblentz * gives 1.432 as the most probable value. No probable error is given but the four results, obtained by four investigators, were 1.436, 1.430, 1.430 and 1.4318, *Bur. Standards Bull., 17, 7, 1922. SMITHSONIAN TABLES 98 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS the last being Coblentz’ own value. Ladenburg* gives 1.432+0.006. The separate results which he used are 1.425 to 1.441, 1.4295+0.007, 1.435, 1.4318, 1.430. The chief error arises from the various corrections applied to the observed values. Coblentz’ original value * of 1.4456 has become 1.4318 in his latest article, Doctor Birge believes 0.003 is a much more reasonable estimate of error. Both Coblentz and Ladenburg agree on the absolute value. Hence he adopts C2= 1.432 + 0.003 cm: deg. h=(6.548+0.015) X 10°" erg - sec. The radiation constant cy. occurs in the Boltzmann factor e-*/#7, (e=energy, T =absolute temperature) in the form e-¢”/?=e-%/A?, where v in cm, or A in cm, is the quantum equivalent of e ergs. (f{) The Stefan-Boltzmann law and the Planck equation—The second method for determining h by the radiation constants is through the Stefan- Boltzmann law, E=oT*=acT*/4. h is connected with o, using Planck’s law, by the relation h= (2n°k*/15c?c)?. As in the case of ¢s, there is a difference of opinion concerning the accuracy with which o may be measured. The best value, in 1919, was that obtained by Coblentz,’ namely (5.722+0.012) X 10° erg -cm™?: deg.*: sec.-*. In his more recent discussion, Coblentz* gives all available data, and concludes that the most probable value lies between 5.72 and 5.73. Since this 1922 article by Coblentz, there have been two new determinations of o, one by Hoffman’ (method of Westphal), giving o=5.764+0.052, and the other by Kussman,’ using the modified Angstrém pyrheliometer. This latter method was used also by Coblentz * giving 5.722 as stated, by Gerlach‘ giving 5.80, and by Kahanowicz * giving 5.69 to 5.73 as corrected by Coblentz.* Kuss- man obtained o=5.795 +one per cent. Ladenburg’* quotes the four results by Gerlach, Hoffman, Coblentz, and Kussman. He adopts the unweighted mean. He agrees with Gerlach that Coblentz’ true error is more nearly 0.06 than 0.012. The experimental results of Kussman* and Coblentz* are in almost perfect agreement. The discrepancy in their results is due to the correction for the lack of complete absorption of the receiver. Michel and Kussman”* claim to prove that the correction Coblentz applied is too small. The values of o by Kussman and by Hoffman, as well as Gerlach’s earlier value of 5.80, corre- spond to impossibly low values of h. Coblentz’ result gives an h in good agree- ment with that obtained by more accurate methods. This tends to indicate the correctness of Coblentz’ correction for incomplete absorption, as opposed to Kussman’s. 7 HEP. 23/303.) = Bus. (Standards Bulli rommior4) 4 ProcyyNatiiAcadasSch, ssn soe 1917.. * Bur: Standards Bull. 17, 7, 1912," Zeit Phys., 14, 30%, 10235) -lbidy 25.65e 1924. "Ann. Phys., 50, 259, 1916; Zeit. Phys., 2, 76, 1920. * Nuovo Cimento, 13, 142, 1917. * Zeit. Phys., 18, 263, 1923. SMITHSONIAN TABLES TABLE 40 (continued) 99 PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS It appears that Coblentz’ estimated error for his own work (5.722+0.012) is too small, but that his final average of the work of all investigators up to 1922 (5.72 to 5.73) should be more trustworthy than any single value. We will choose 5.725 and 0.02 for its probable error. This result is then to be averaged with the more recent work whence T= (0735 O.OlN) X16 ere’ ciir> - deg. «sec. ae @—Ag/C—\(7,052-— 0.005) X07 > ere semi sder.* There has appeared a further determination of this quantity, by Hoare.’ He used a Callendar radio balance ; the advantage of the method is that both source and receiver are essentially “ black-bodies.’’ Hoare obtains «= 5.735, agreeing exactly with the value adopted. He lists 38 separate results, average deviation only 0.016. The inclusion of this new result leaves the average value un- changed, and Doctor Birge leaves the probable error unchanged. Objection might be made to this adopted error as too small; such an objection can hardly hold in the face of Hoare’s work. This new work also speaks against Strum’s assumption of an inadequacy of Planck’s formula. We have then R=(61539== O1:01O >< TO ere * Sec: (g) Summary—We have now six determinations of h: Rydberg constant h = 6.547 + 0.011 Power of e involved, 5/3 Ionization potentials 6.560 = 0.015 3/3 X rays 6.550 + 0.009 4/3 Photoelectric 6.543 + 0.010 3/3 C2 6.548 + 0.015 3/3 o 6.539 + 0.010 4/3 Doctor Birge adopts h= (6.547 + 0.008) x 10-°’ erg - sec. This value of h is identical with Ladenburg’s most recent estimate.” This identity is spurious, since Ladenburg assumes e=4.774X 107°. If this older value of e had been used in the present work, we should have obtained h=6.5535, in practically exact agreement with Doctor Birge’s 1919 value (6.5543). Another potentially accurate method is given by the Compton shift of X-ray lines. The theoretical equation for this is AA=(h/mc)(1—cos ¢), where m is the mass of an electron, as deduced from the values of e and e/m. Since h varies in value with e, this equation can better be used to evaluate e/m. We can in fact write AA= (h/e) (e/m) (1—cos ¢) in which ¢ as usual is in es units, and e/m in em units. Then e/m= (Ad) /(h/e)(1—cos ¢) The most accurate work on this subject has been done by Sharp,’ who obtains AX= (0.04825 +0.00017) X 10% cm, for (I—cos ¢) =(1.984+0.001). With the adopted values of h and e, we have h/e=(1.3725+0.0005) x 1072" * Philos. Mag., 6, 828, 1928. 7H.P., 23, 279. * Phys. Rev., 26, 691, 1925. SMITHSONIAN TABLES I0O TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS erg:sec:es?. Substituting, one finds e/m=(1.772+0.006) X10" abs. em units, the final error being due almost entirely to the error in AA. It seems pos- sibly significant that this value agrees better with the deflection than with the spectroscopic value of e/m, for the theory used in the derivation of the equa- tion is essentially the collision theory of classical dynamics for free electrons. e, e/m, and h* appear in many important constants. h depends for its value on e, therefore the e appears implicitly, if not explicitly, in every quantum relation. The outstanding discrepancy was between the work of Wagner and of Duane and co-workers, on the value of h from the X-ray continuous spectrum. The recent work of Feder, using this method, gives h in exact agreement with the value adopted, and explains Wagner’s low value. Doctor Birge now feels that the value of h/e listed in Table 43 can be assumed with some confidence. The real problem concerns the values of e and of e/m. The need of two values of e/m is very annoying, and fundamentally unsatis- factory. The same situation seems to be arising in regard to e. Millikan’s value has been accepted; it was the only one available. The new work on X rays opened another possibility. The value of Backlin is one-half per cent higher than Doctor Birge’s adopted value. As a final result Doctor Bearden obtains for the absolute wave length of the (unresolved) Cu Ka line, 1.5439 +0.0002A, and for the Cu KB line, 1.3940+0.0002A. These results are ob- tained under many varied conditions. The first is 0.345 per cent higher than Siegbahn’s value, the second 0.336 per cent. The relative wave lengths are in agreement with Siegbahn, but the absolute wave lengths lead to a value for calcite of d’2.5=3.0398A, and e=4.825 x 10°*° abs. es units, 1.15 per cent above Doctor Birge’s adopted value of e. It is desirable to consider the various relations that have been suggested between these constants. The most famous connects e, e/m, h, and c in Bohr’s formula for the Rydberg constant. This was used to evaluate h, and the value (6.54713) is identical to four digits with that adopted. Hence, the indirectly calculated value of e/m is also practically identical with that adopted. Thus the adopted values of e, e/m,h and c form a self-consistent system, as judged by the Bohr formula for Ro. Lewis and Adams * (theory of ultimate rational units), have obtained, with the aid of Planck’s radiation law, the relation: hc/2mre?=87(87°/15)3. The right side equals 137.348; the left side, with the constants here adopted, equals 137.29,+0.11. The left side equals the reciprocal of the fine structure con- stant a, and the value quoted is taken directly from Table 43. The numerical agreement is very striking. The present agreement shows that this method yields a value of / almost identical with that adopted. a is a dimensionless constant involving fundamental general constants ; it should be remembered that to make a dimensionless, we must include with the factor hc the unknown dimensions of specific inductive capacity. ‘Note added by Birge April, 1929 (abbreviated). * Phys. Rev., 3, 92, 1914. SMITHSONIAN TABLES TABLE 40 (continued) IOI PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Perles * has pointed out that the ratio of the mass of the proton to that of the electron (M/,/m,) is another dimensionless constant which should have some significance, and has found that (he/e*) (=2mr/a) = (M,/m,) (7-1) the left side equals 862.64+0.68, the right 858.36+0.49 or 862.26+0.99 de- pending on whether one uses the spectroscopic or the deflection value of e/m. The agreement is good for the deflection value but poor for the spectroscopic. Note.—In evaluating the constants, it has been necessary to calculate auxiliary con- stants, and also to use certain conventional quantities, such as gis and gn. All such quan- tities are listed in Table 42. In addition to constants listed in Table 42 there are many other functions of constants given on page 103 of this table and in Table 42. A number of these dcrived constants are collected in Table 43. An attempt has been made to include the more important or more frequently used values. The process for obtaining the correct probable error for many of the constants of Tables 42 and 43 is sometimes involved. The various derived constants of Table 43 (and the occasional derived constant appearing on page 103 of this table and in Table 41) are given with one and often two more digits than required by the probable error. Such digits are printed below the line, and have been added that calculations made in different ways shall not introduce any appreciable error. e/m always indicates merely the ratio of charge to mass for an electron, in em units; e indicates electronic charge in es units; mmo, electronic mass; m, the atomic weight of an electron. A more logical but less convenient nomenclature would have been (e/mo) es units, and possibly (e’/mw) em units. In the quantum relation, e=hv=eVl, each side represents energy in ergs, provided all quantities are in abs. c.g.s. units. v/V (=e/h) then measures the frequency in sec.* associated with one abs. es unit of potential. It is usually convenient to substitute the wave number (»’) or the wave length (A) in place of », and to substitute the number of abs. volts (V”) in place of V. (V’’ = int. volts, throughout this paper). The values of the various ratios, such as »’'/)’” etc., are given in Table 43. An electron which has fallen through one abs. volt of potential is termed an abs. volt- electron; its energy in ergs and speed in cm: sec.” are given in Table 43. Corresponding to any ionization potential of an atom or molecule in volts (V”), there is an energy of ionization (eV") which can be measured in units equal to the energy of a volt-electron, and is so designated. An ionization potential of 10 volts corresponds to an energy of ionization of 10 volt-electrons. Similarly, in the case of molecules, we speak of a dissociation potential of, let us say, 10 volts, and a corresponding energy of dissociation (heat of dissociation) of 10 volt-electrons per molecule. The factor by which this last quantity must be multiplied to give the heat of dissociation in calories per mole is given in Table 43. Unfortunately there has arisen the practise, to which Doctor Birge pleads guilty, of designating the heat of dissociation as 10 volts, instead of stating, more correctly, that the equivalent dissociation potential is 10 volts, or that the heat of dissociation per molecule is 10 volt-electrons. The name of the units conforms as far as possible with current practise. Difficulties arise with the unknown dimensions of magnetic permeability mu, and specific inductive capacity e. It is customary to indicate these unknown dimensions by the symbols yu and e. A given unit, such as the gauss, is applied only to quantities of a given set of dimensions, including « and e. In the present discussion we are concerned only with numerical mag- nitudes and no particular attention has accordingly been paid to this matter of dimensions. SNE Nahe SLI ene LGe I Rae no es PN reg CE eT er oe ap * Naturwiss., 16, 1094, 1928. SMITHSONIAN TABLES 102 TABLE 40 (continued) PROBABLE VALUES OF THE GENERAL PHYSICAL CONSTANTS Thus the statement that the absolute em unit of resistance is one cm- sec.” involves the assumption not only of unit permeability, but also of dimensionless permeability. In a number of the equations given in Table 43 the two sides of the equation do not check dimensionally unless one assumes u and e to be dimensionless. It follows from this that the name of the unit stated in the table applies strictly only to one side of such an equation. In such cases the unit applies to the left side of the equation, since this is the quantity being evaluated. The right side gives merely the most direct derivation of the numerical magnitude, in terms of quantities already evaluated. Since this ambiguity does not affect the numerical magnitude, it is inconsequential in the present discussion. As examples of this situation we cite the fine structure constant a, which is dimensionless. To satisfy this condition one should write a= 2me*/ehc where & is numerically unity, | and represents merely the dimesions of e. The ratio of the Bohr magneton m to the Bohr unit of angular momentum (//27) is strictly uo}(e/m), where wo is numerically unity, and represents merely the dimensions of permeability. The mole is a (variable) unit of mass, equal to the molecular weight in grams. The gram equivalent is a similar (variable) unit of mass, equal to the atomic or molecular weight in grams, divided by the valence. The various quantities appearing on page 103 of this table and in Table 42 have been discussed. No general explanation will be given of the meaning or use of the quantities appearing in Table 43; any adequate explanation would constitute a textbook of modern physics and physical chemistry. For the more specialized constants, no explanation is needed by investigators working with such constants, and it is to such persons that the data will be most useful. In conclusion, attention should be directed merely to two constants for which the formula used here differs from that normally given. It is customary to use for the speed of the electron in the normal orbit of hydrogen, as given by Bohr’s original theory, a value which refers to the nucleus considered as the center of coordinates. This is called v(=ac) in Table 43. It would seem more logical to give the speed referred to the center of mass, the quantity denoted vo’ in Table 43. There is a similar discrepancy in the case of the radius of this orbit. The electron, according to Bohr, moves about the center of mass in a circle of radius a’, as it is denoted in Table 43. This is not the same as the constant separation of the nucleus and electron, which is here denoted ao. In the literature these two quantities, ao, and ao’, are sometimes confused. The expressions for vo, vo’, do, and do’ given in Table 43 include also the factor (1 —a’)*/*, arising from the variation of mass with speed. Birge. Probable values of e, h, e/m and a Phys. Rev. 40, 228, 1932. e, (4.7688 + 0.0040) X 10°” es units h, (6.5443 + 0.0091) X 10” erg - sec. e/m, (1.7611 = 0.0009) X 10° em units - g* I/a, 137.307 + 0.048 SMITHSONIAN TABLES TABLES 40 (concluded) AND 41 103 Fundamental constants, Birge——The critical discussion of the determina- tion by Dr. R. T. Birge of theses values will be found in abbreviated form on pages 73 to 102 of this book; for full details see Phys. Rev. Suppl., 1, 1, 19209. These constants, for purposes of computation, are to be taken as exactly correct ; that is, all additional digits in each constant are to be assumed as zero. The real probable error of each value is of course that indicated in the table, and each constant has an accepted value carried only to the number of signifi- cant figures required by the adopted probable error. Beretny7OL: LIGNE. os icu Sse aviere oele'sacs ¢ = (2.99796 + 0.00004) X 10*.cm- sec.” Eeravitation constant... .).....s0.00¢ G = (6.664 + 0.002) 10° dyne - cm’ - g? ERE Ths Satu Soe eR Ph a 1 = 1000.027 + 0.001 cm* Volume of perfect gas (0°C, An)..vn = (22.4141 + 0.0008) 10° cm® - mole Volume of perfect gas (0°C, Ass)...R = 22.4146 + 0.0008 liter - mole* International ohm =>? abs. ohm....f = 1.00051 + 0.00002 International ampere = g abs. amp..g = 0.99905 + 0.00005 Normal atmosphere .............. A, = (1.013249 + 0.000003) X 10° dyne - cm MEMHINOSPNELe ...2..6.00000c0 Aas = (1.013199 + 0.000003) X 10° dyne - cm? Ice point (absolute scale)......... Tig 2731S = O03 ale Mechanical equivalent of heat..... Jis = 4.1852 + 0.0006 abs. joule - cals” Electrical equivalent of heat...... J'1s = 4.1835 = 0.0007 int. joule - cal.15* Beeta@ay *CONStANE ~ = 666+ core sisisinjesee . .F = 96404 + 5 int. coul. - g-equiv.* =: 96489 + 7 abs. coul. - g-equiv.~ = 9648.9 + 0.7 abs. em-unit - g-equiv.* Fe = (2.89270 = 0.0002) X 10% abs. es-unit - g-equiv.* Bilectronic charge * 5.:....6-ccesses e= (4.770 + 0.005) X 10°’ abs. es-units e/c-= (1.5910s + 0.0016) & 10°” abs. em-units Specific electronic charge (spectro- REET oS ee oe 5 ta Ae Site e/m = (1.761 + 0.001) X I0' abs. em-unit - g* (e/m)c = (5.2704 + 0.003) X 10” abs. es-unit - g* Specific electronic charge (deflec- BRIM Oh iss sicieins cae es Soe oe e/m = (1.769 = 0.002) X 10° abs. em-unit - g7 (e/m)c = (5.303% + 0.006) X 10” abs. es-unit - g7 Elanckeconstant «22. csgueseeoens h = (6.547 + 0.008) & 10° erg - sec. Atomic weights O = 16.0000 C = 12.003 + 0.001 I = 126.932 + 0.002 He = 4.0022 + 0.0004 H = 1.00777 = 0.00002 Ca = 40.075 + 0.005 Ag = 107.880 + 0.001 N = 14.0083 + 0.0008 TABLE 41.—Powers of c, h, e, h/c 0.012) 1078 erg-3 «sec, -% .005) 10° erg-2*sec,-2 (1.11262 + 0.00003) 10-2! cm-2 *sec.2 Se (3.33560 + .00005)10-lcm-!-sec. ae (5.77546 + .00006) 10-§cm-!/2+ sec,1/2 + .o10)10-%erg?:sec. 2 (1.73146 + .00001)105cm!/2+sec,-1/2 ; + .010)10-%erg3 «sec, 3 (8.98782 + .00024)10%cm2°sec.-2 2; i + .009)101!8¢5-units-* 5 + .0045)10-%¢s-units? + .0033)10-% es-units$ + .021)10-% ¢s-units4 + .012)10-47 e¢s-units® (2.60449 + .00011)10%!cm3:sec,-3 (8.07798 + .00043)104!cm4*sec,-4 (2.1838 + .003)10-37g:cm * Millikan, Phys. Rev., 35, 1930, takes ¢ = 4-774 X 10°, h = 6.547 X 10-27, N = 6.062 X 10-8, SMITHSONIAN TABLES 104 TABLE 42 ADDITIONAL PHYSICAL CONSTANTS Used or evaluated by Doctor Birge in Phys. Rev. Suppl., 1, 1, 1929, in connection with Table 40, p. 103. Ratio of es to em units (direct)...... c’ = (2.9979 + 0.0001) X 10°’ cm: sec. Acceleration of gravity (45°)....... gss = 980.616 cm - sec. * Acceleration of gravity (normal) ...gn = 980.665 cm- sec.” Mean’ density, of the earth... «1-111 6 = 5.522 + 0.002 g-cm™” Maximum density of water...5m(H20) = 0.999973 + 0.000001 g - cm™® Density of oxygen gas (0°C, As) L(O2) = 1.428965 + 0.000030 g - liter Factor converting oxygen (0°C, Ais) to ideal: easy Pee aes ore I — a(Oz) = 1.000927 + 0.000030 Density of nitrogen (0°C, Ass).L(N2) = 1.25046 + 0.000045 g - liter Factor converting nitrogen (0°C, Ass) tomideal@gasacmem coc socte 1 — a(N:) = 1.00043 + 0.00002 Density ‘of Hg s(0°G An): sss - Dn = 13.59509 + 0.00003 g :cm™* International volt (= pq abs. volts) ..~q = 1.00046 + 0.00005 International joule (= pq’ abs. joules) pq’ = 1.00041 + 0.00010 Electrochemical equivalent of Ag E(Ag) = (1.11800 + 0.00005) X I0™ g - int. coul.* = (1.11805 + 0.00007) 10“ g - abs. coul.** Density of calcite” (2o7@)i2-.-. 23. p = 2.7102 + 0.0004 g-cm™* Structural constant of calcite (20°C) (8) = 1.09630 + 0.00007 True grating space of calcite (20°C) d'2 = (3.0283 + 0.0010) X 10 *°cm Effective grating space of calcite (Oo CG)» Pht Sor ee eee dx = (3.0279 + 0.0010) X 10*°cm Rydberg constant for hydrogen...... Ru = 100677.759 + 0.05 cm™ Rydberg constant for ionized helium R ge = 109722.403 + 0.05 cm™ Wave length of red Cd line (15°C, An) Aca = 6438.4606 1.A. (definition of I.A. unit) Rydberg constant for infinite mass..R = 109737.42 = 0.06 cm™ cRy = (3.28988 + 0.00004) X 10” sec. Avogadro’s number ........ No = Fe/e = (6.0642. + 0.006) X 10° mole Gas constant per mole... Ro = vnAn/To= (8.31360 + 0.0010) X 10’ erg - degree” - mole* R'> = Ro/ (Jss XK 10") = 1.98643 + 0.0004 calas - deg. - mole™ Boltzmann constant ........ k = Re/No = (1.3708 + 0.0014) X 10°” erg - deg.” Second radiation constant (exp. value) C2 = 1.432 = 0.003 cm - deg. Second radiation constant (indirect ) C2 = hc/k = 1.4317; = 0.0006 cm - deg. Radiation density constant....a = 40/c = (7.651s 0.015) &K 10°’ erg -cm”™ - deg.~* Stefan-Boltzmann constant (exp. value) o="69:735 = 001) X10" ergem= “deg secig Stefan-Boltzmann constant (indirect) o = 2m k*/15c7h®'= (5.7139 + 0.006) X 10° erg: cm’ - deg.~* - sec. SMITHSONIAN TABLES TABLE 43 105 MISCELLANEOUS DERIVED PHYSICAL CONSTANTS Evaluated by Doctor Birge in Phys. Rev. Suppl., 1, 1, 1929. (See notes on page 99.) Mass of electron (spectroscopic ) mo = e/ { c(e/m) sp +} = (9.035 + 0.010) X 10" ¢ Mass of electron (deflection) mo = e/ 4 c(e/m)adeft | = (8.9042 + 0.014) XK 10” g Atomic weight of electron (spectroscopic) m = F/(e/m) sp = (5.4792 + 0.003) * 10% Atomic weight of electron (deflection) m = F/(e/m) deft = (5.4544 + 0.006) X 10“ Mass of atom of unit atomic weight Mo = 1/No= (1.64893 + 0.0016) & 10“ ¢ Mass of hydrogen atom........Mx= H/No = (1.66172 + 0.0017) X 10 “g Number of atoms per gram of hydrogen 1/Mu = (6.0170 + 0.006) X 10” g* Meassvor proton... 2.1... Mr = (H — m)/No = (1.6608 + 0.0017) X 10% ¢ Mass of oa particle....Ma= (He — 2m)/No = (6.597% + 0.007) X 10% g Charge (electrolysis) of 1 g hydrogen e/Mu = F/H = (9574.5: + 0.7) abs. em-units - g* Specific charge of proton e/Mr = F/(H — m) = (9579.73 + 0.7) abs. em-units - g* Specific charge of a particle 2e/Ma = 2F/(He — 2m) = (4823.11 + 0.6) abs. em-units - g* Ratio, mass H atom to mass electron (spec- EGOSCOPIC) «gh. skate says: (e/nt) sp/(e/Mu) = 1830.26 + 1 Ratio, mass H atom to mass electron (deflec- LOT ME Rac ae (e/m) deft/(e/Mx) = 1847.0 + 2 Ratio, mass proton to mass electron (spec- PRCISEODIG)) © iscis ote Lanes odes 6 bea os Me/msp = 1839.20 — 1 = 1838.2 1 Ratio, mass proton to mass electron (deflec- ETO) Mamede ete Sots oe oles (are eae otek Mor/imdeft = 1847.61 — 1 = 1846.1 + 2 Energy associated with unit wave number e/v’ = hc = (1.96274 + 0.0025) K 10 “erg - cm Potential (es) associated with unit frequency V /v=h/e= (1.37251 = 0.0005) XX I0 Frequency associated with 1 abs. volt »/V" = 10°e/hc = (2.43025 + 0.0009) X 10" sec.” - abs. volt™ Wave number associated with 1 abs. volt vo = v' /V" = 10°e/hc? = (8106.1 = 3) cm™ - abs. volt™ Wave length associated with 1 abs. volt No = AV" = he?/e= (123361 = 5) X 10° cm - abs. volt -™ os-units - sec. SMITHSONIAN TABLES 106 TABLE 43 (continued) MISCELLANEOUS DERIVED PHYSICAL CONSTANTS Energy of one-abs.-volt-electron hv/V" = 10°e/c = (1.5910s + 0.0016) X 10 ergs Speed of abs.-volt-electron (spectroscopic) vc = [2 X 10°(e/m) sp]*/ = (5.9346. + 0.0017) X 10’cm- sec. Speed of abs.-volt-electron (deflection) ve = [2 X 10°(e/m)deft]*/* = (5.9481: + 0.0034) X 107 cm: sec? iBsine structure constant... see ee a = 2me*/hc = 7.2830, = 0.006) X 107 Reciprocal of fine structure constant........ I/a = 137.20 £0.11 Magnetic moment, Bohr magneton (spectro- SCOPIC) trance clearer Hs =} h(e/m) sp | /4m = (0.91740 + 0.0013) X 10 erg - gauss Magnetic moment, Bohr magneton (deflection) Ma = 4 h(e/m)adeft ¢ /4m= (0.921635 + 0.0016) X 10 erg - gauss Magnetic moment per mole (1 Bohr magneton per molecule) (spectroscopic).......... baNo = 5563.5; + 10 erg’: gauss - mole* Magnetic moment per mole (1 Bohr magneton per molecule) (deflection)? scree nee MiNo = 5580.15 + II erg - gauss - mole Zeeman displacement per gauss Av'/H = (e/m) sp/4mc = (4.67438 = 0.003) X I0-° cm™ - gauss Band spectrum constant connecting wave-number (cm) and moment of inertia......... h/87*c = (27.658: + 0.04) X 10 g-cm Atomic specific heat constant....... c2/c = h/k = (4.77572 = 0.0019) X 10™ sec - deg. Reduced mass of H atom...ux = Ru(mo) sp/R » = 9.0301 + 0.010) X 10°" g Schroedinger constant for H atom..... 82 un/h? = (1.66312 + 0.003) X 10% g- erg - sec.” Schroedinger constant for electron 82 (10) sp/h? = (1.66422 + 0.003) X 10” g - erg - sec. Ionization potential for H atom.......... Ru/vo = 13.520. + 0.005 abs. volt Ionization potential for Het............ 4Rue/% = 54.141; + 0.020 abs. volt Radius of Bohr orbit in normal hydrogen, re- ferred to center of mass, using experimental Wales Gh vices. tree ao’ = a(1 — a?)*/?/4r7R op = (0.528109 + 0.0004) X 10° cm Speed of electron in normal H orbit, referred to center of massmenr. Otte vast sec Vo = acRu/R ow» = (2.18242 + 0.0017) X 10° cm - sec.* SMITHSONIAN TABLES ' TABLE 43 (concluded) 107 MISCELLANEOUS DERIVED PHYSICAL CONSTANTS Hydrogen doublet constant Ava = Rua’/16 = 0.363650 + 0.0006 cm™ Compton shift at 90° (spectroscopic) h/moc = (e/m) sph/e = (0.024170; + 0.000016) X 10“ cm Compton shift at 90° (deflection) h/moc = (e/m) defth/¢ = (0.024280 + 0.00003) X 10 cm Wave length of 1-abs.-volt-electron h/[mo(ve) sp] = (12.210) + 0.006) X 10° cm Loschmidt number ......... to = No/vn = (2.7050 + 0.003) X 10" cm™ (0°C, An) Wien’s displacement constant (indirect) A = ¢2/4.9651 = 0.28836: + 0.00011 cm - deg. Hirst radiation. constant *.....:....... 1 = 8rhc = (4.93206 + 0.006) X 10” erg -cm or hc? = (0.58842. + 0.0008) X 10-° erg - cm’ - sec. or 2mhc? = (3.6972 + 0.005) X 10° erg - cm’: sec.* Energy per mole, equivalent to I-abs. -volt-electron per molecule F (abs. coul. - g-equiv.~*) / Jss(abs. joule - calas*) = 23054.s + 4 cal.ss - mole™ Sackur-Tetrode constant (e€= base of log. = 2.71828) -1 So= Ro'ln [(2mk)?/?6/?/h°No°/?] = — 11.0533 + 0.0026 cal.ss - deg.* - mole™ Chemical constant (unit at. wt., pressure in atm.) to’ = 8 log [2rk*/*?/Noh?] — log An = — 1.58825 + 0.0004 Multiplier of (Curie constant)*/” to give magnetic moment in Bohr magnetons per molecule ......... (3k/No)*/?/pa= 2.83842 + 0.0019 erg™/” - gauss - deg.*/? - mole’/? *E = cid *(e-¢2/AT — 1)"; E) may be defined in various ways, and c: varies accord- ingly. If E\d\ denotes the energy density of unpolarized radiation in range dA, c: = 87h. If E)dX denotes the intensity of emission of linearly polarized radiation in range dk, perpendicular to a surface, per unit of surface, per unit solid angle, c:=hc*. If E, dx denotes the emission of unpolarized radiation in range dA, per unit surface, in all directions (2x solid angle), c:1 = 2mhc’. SMITHSONIAN TABLES 108 TaBLe 44 VOLUME OF A CLASS VESSEL FROM THE WEICHT OF ITS EQUIVALENT VOLUME OF MERCURY OR WATER lf a glass vessel contains at °C, P grammes of mercury, weighed with brass weights in air at 700 mm pressure, then its volume in ccm at the same temperature, 4,: V= PR = Pe, at another temperature, 4,: V= PR; =Pop/dfi+y(4-4} p = the weight, reduced to vacuum, of the mass of mercury or water which, weighed with brass weights, equals I gram; d = the density of mercury or water at ¢°C, and y = 0.000 025, is the cubical expansion coefficient of glass. WATER. MERCURY. Rigs Ly = Ol ale leap Oe : ie er One Teac 20s 1.001192 1.001443 | 1.001693 || 0.0735499 0.07 35683 0.07 35867 1133 1609 $633 5798 5982 1092 292 1542 5766 5914 6098 1068 1493 5900 6029 6213 1060 1460 6033 6144 6328 1068 1443 6167 6259 6443 1.CO1092 1.001192 1.001442 || 0.0736301 0.07 36374 0.07 30558 1131 1206 1456 6490 6674 1184 1234 1485 6605 6789 1252. | 1277 1527 6720 6904 1333 1333 1534 6835 7020 1.001428 1.001403 1.001653 || 0.0736969 0.07 36951 0.07 37135 1486 1730 7103 7066 7250 1582 1832 7236 7181 7305 1690 1940 7370 7297 7481 1810 2060 7504 7412 7590 3 1.001942 1.002193 0.07 37637 0.07 37 527 0.07 37711 2086 2337 7771 7642 7826 2241 2491 7905 7757 7941 2407 2658 8039 7872 8057 2584 2835 8172 7988 8172 1.002772 1.003023 0.07 38306 0.07 38103 0.07 38288 2970 322 8440 8218 8403 3178 3429 8573 8333 8518 3396 3647 8707 8449 8633 3624 3875 8841 8564 8748 1.004264 1.003862 1.004113 0.07 38974 0.07 38679 0.07 38864 4537 4110 4301 g108 8794 8979 4518 4366 4616 || 9242 8910 9094 5110 4632 4884 9376 9025 9210 5410 4908 5159 | g510 g140 9325 Taken from Landolt, Bornstein, and Meyerhoffer’s Physikalisch-Chemische Tabellen. SMITHSONIAN TABLES. TABLES 45 AND 46 10g TABLE 45.—Reductions of Weighings in Air to Vacuo When the weight M in grams of a body is determined in air, a correction is necessary for the buoyancy of the air equal to M 8 (1/d—1/d,) where 5 = the density (wt. of I ccm in grams =o.0012) of the air during the weighing, d the density of the body, d, that of the weights. 8 for various barometric values and humidities may be determined from Tables 128 to 130. The following table is computed for 8 = 0.0012. The corrected weight = M-+kM/tooo. Density : Density of body weighed d. Correction factor, k. Bteeins a | ee | Brass uartz or weights i i j weights | Al. weights dj=a2r.5. | 8.4. | .65. ake. 8.4. | ° ON _ + 2.34 + 1.94 + 1.66 + 1.55 + 1.44 + 1.36 + 1.28 + 1.21 + 1.14 + 1.04 + 0.94 sn 07 + .80 =er75 .56 52 -49 .46 +34 .20 16 .06 .OI |) | | ++ +++4+4+44+4+ SPS Sissies | +t+tt+t++t+++ TABLE 46.— Reductions of Densities in Air to Vacuo (This correction may be accomplished through the use of the above table for each separate weighing.) If s is the density of the substance as calculated from the uncorrected weights, S its true den- sity, and L the true density of the liquid used, then the vacuum correction to be applied to the uncorrected density, s, is 0.0012 (t —s/L). Let Ws = uncorrected weight of substance, W1= uncorrected weight of the liquid displaced by the substance, then by definition, s= .Ws/W1. Assuming D to be the density of the balance of weights, Ws {1 + 0.0012 (1/S —1/D)}and Wi {1 + 0.0012 (1/1.—1/D) \are the true weights of the substance and liquid respectively (assuming that the weighings are made under normal atmospheric corrections, so that the weight of 1 cc of air is 0.0012 gram). Ws{t + 0.0012 (1/S — 1/D) be W1 {1 + 0.0012 (i 1/D) } ‘ But from above Ws/W1=s/L, and since L is always large compared with 0.0012, S—s=ooor2 (1—s/L). The values of 0.0012 (1 —s/L) for densities up to 20 and for liquids of density 1 (water), 0.852 (xylene) and 13.55 (mercury) follow : (See reference below for discussion of density determinations). Then the true density S = Density of Corrections. subst ee a L=0.852 Water. Xylene. Density of Corrections. l | substance Sree || a Lr L=1713°55 Mercury. | Water. Mercury. 0.9 + .0ooo12 .0132 .O144 .O156 .0009 | : 0168 0180 0192 .0204 .0216 0228 | | + 0.00024 | - | | : — 0.0120 0.0000 | | | .OOT2 0024 | | 0036 | .0048 .0060— | .007 2 .008 4 .0096 .0108 tHe eb t et I. 2. Be 4. 5: 6. ie 8. 9. oO. _ Johnston and Adams, J. Am. Chem. Soc. 34, p. 563, 1912. SMITHSONIAN TABLES. IIO TABLE 47 MECHANICAL PROPERTIES: INTRODUCTION AND DEFINITIONS (Compiled from various sources by Harvey A. Anderson, C.E., Assistant Engineer Physicist, U. S. Bureau of Standards.) The mechanical properties of most materials vary between wide limits; the following figures are given as being representative rather than what may be expected from an individual sample. Figures denoting such properties are commonly given either as specification or experimental values. Unless otherwise shown, the values below are experimental. Credit for information included is due the U. S. Bureau of Standards; the Am. Soc. for Testing Materials; the Soc. of Automotive Eng.; the Motor Transport Corps, U.S. War Dept.; the Inst. of Mech. Eng.; the Inst. of Metals; Forest Products Lab.; Dept. of Agriculture (Bull. 556); Moore’s Materials of Engineering; Hatfield’s Cast Iron; and various other American, English and French authorities. The specified properties shown are indicated minimums as prescribed by the Am. Soc. for Testing Materials, U. S. Navy Dept., Panama Canal, Soc. of Automotive Eng., or Intern. Aircraft Standards Board. In the majority of cases, specifications show a range for chemical constituents and the average value only of this range is quoted. Corresponding average values are in general given for mechanical properties. In gen- eral, tensile test specimens were 12.8 mm (0.505 in.) diameter and 50.8 mm (2 in.) gage length. Sizes of compressive and transverse specimens are generally shown accompanying the data. All data shown in these tables are as determined at ordinary room temperature, averaging 20° C (68° F.). The properties of most metals and alloys vary considerably from the values shown when the tests are con- ducted at higher or lower temperatures. The following definitions govern the more commonly confused terms shown in the tables. In all cases the stress referred to in the definitions is equal to the total load at that stage of the test divided by the original cross-sectional area of the specimen (or the corresponding stress in the extreme fiber as computed from the flexure formula for transverse tests). Proportional Limit (abbreviated P-limit). — Stress at which the deformation (or deflection) ceases to be proportional to the load (determined with extensometer for tension, compressometer for compression and deflectometer for transverse tests). Elastic Limit. — Stress which produces a permanent elongation (or shortening) of o.oo1 per cent of the gage length, as shown by an instrument capable of this degree of precision (determined from set readings with extensometer or compressometer). In transverse tests the extreme fiber stress at an appreciable permanent deflection. Yield Point. — Stress at which marked increase in deformation (or deflection) of specimen occurs without in- crease in load (determined usually by drop of beam or with dividers for tension, compression or transverse tests). Ultimate Strength in Tension or Compression. — Maximum stress developed in the material during test. Modulus of Rupture. — Maximum stress in the extreme fiber of a beam tested to rupture, as computed by the empirical application of the flexure formula to stresses above the transverse proportional limit. Modulus of Elasticity (Young’s Modulus). — Ratio of stress within the proportional limit to the corre- sponding strain, — as determined with an extensometer. Note: All moduli shown are obtained from tensile tests of materials, unless otherwise stated. Brinell Hardness Numeral (abbreviated B.h.n.). — Ratio of pressure on a sphere used to indent the material to be tested to the area of the spherical indentation produced. The standard sphere used is a 10- mm diameter hardened steel ball. The pressures used are 3000 kg for steel and 500 kg for softer metals, and the time of application of pressure is 30 seconds. Values shown in the tables are based on spherical areas computed in the main from measurements of the diameters of the spherical indentations, by the following formula: B.h.n. = P + atD = P + rD(D/2— VD?2/4 — d2/4). P = pressure in kg, ¢ = depth of indentation, D = diameter of ball, and d = diameter of indentation, — all lengths being expressed in mm. Brinell hardness values have a direct relation to tensile strength, and hardness determinations may be used to define tensile strengths by employing the proper conversion factor for the ma- terial under consideration. Shore Scleroscope Hardness. — Height of rebound of diamond pointed hammer falling by its own weight on the object. The hardness is measured on an empirical scale on which the average hardness of martensitic high carbon steel equals 100. On very soft metals a ‘“‘ magnifier’? hammer is used in place of the commonly used “universal”? hammer and values may be converted to the corresponding “universal’’ value by multi- plying the reading by #. The scleroscope hardness, when accurately determined, is an index of the tensile elastic limit of the metal tested. Erichsen Value. — Index of forming quality of sheet metal. The test is conducted by supporting the sheet on a circular ring and deforming it at the center of the ring by a spherical pointed tool. The depth of impression (or cup) in mm required to obtain fracture is the Erichsen value for the metal. Erichsen standard values for trade qualities of soft metal sheets are furnished by the manufacturer of the machine corresponding to various sheet thicknesses. (See Proc. A. S. T. M. 17, part 2, p. 200, 1917.) Alloy steels are commonly used in the heat treated condition, as strength increases are not conimensinata with increases in production costs for annealed alloy steels. Corresponding strength values are accordingly shown for annealed alloy steels and for such steels after having been given certain recommended heat treat- ments of the Society of Automotive Engineers. The heat treatments followed in obtaining the properties shown are outlined on the pages immediately following the tables on steel. It will be noted that considerable latitude is allowed in the indicated drawing temperatures and corresponding wide variations in physical prop- erties may be obtained with each heat treatment. The properties vary also with the size of the specimens heat treated. The drawing temperature is shown with the letter denoting the heat treatment, wherever the information is available. TABLE 48 Tat MECHANICAL PROPERTIES Tron and Iron Alloys Ultimate strength. Ultimate strength. Sclero- Tension. Tension scope. kg/mm? Ib/in? Iron: Electrolytic* (remelt): as forged...| 34.0} 38.5) 48,500) 55,000 annealed goo® C | 12.5} 27.0] 18,000) 38,000 Gray cast{(19 mm diam. bars) .... indet. 17.5| indet. | { 25,000 ZOBIS|| == | 38,000 35,000 57,000 Malleable cast, American (after (igi 24.5 20,000 Hatfield) 31-5 40.0| 45,000 65,000 28.0 409,000) GastingspAss)) kee 1- eben 45-5 (see p. 653) Commercial wrought bares { 19. 5! (34.0 zen 48,000 | 22.5] 637.0] 32,000] (53,000 Silicon alloys|| Si 0.01: as forged...; 29.5! 31.5] 41,800] 45,200 (Melted in vacuo) ann. 970° C II.0] 24.5] 16,000] 34,900 (Note: C max. o.o1 per cent) Si 1.71: as forged 48.0] 53.5] 68,100] 76,300 annealed 970° C 25.0] 38.0] 35,800] 54,200 Si 4.40: as forged............| 66.0] 74.0] 94,000] 105,000 annealed g70° C ......| 51.0] 64.5] 72,900] 91,600 Aluminum alloys§ Al0.00:asforged) 35.5] 38.5] 50,700) 54,700 (Melted in vacuo) ann. 1000° C 12.5] 24.5] 17,600] 34,g00 (Note: C max. 0.01 per cent) Al 3.08 : as forged 48.0] 54.5] 68,200] 77,500 annealed 1o00° C 22.5] 37.5| 31,800] 53,400 Al 6.24: as forged 54.5] 60.5| 77,700] 86,000 annealed 1000° C 37-5| 49.0] 53,400] 69,800 European (after Am. Malleable i ee pees pee Composition, approximate: Electrolytic, C 0.0125 per cent; other impurities less than 0.05 per cent. Cast, gray: Graphitic, C 3.0, Si 1.3 to 2.0, Mn 0.6 to 0.9, S max. 0.1, P max. 1.2. . S. T. M. Spec. A48 to 18 allows S max. 0.10, except S max. 0.12 for heavy castings. Malleable: American ‘‘ Black Heart,” C 2.8 to 3.5, Sio.6 to 0.8, Mn max. 0.4, S max. 0.07, P max. 0.2. European ‘‘ Steely Fracture,” C 2.8 to 3.5, Sio.6 to 0.8, Mn o.15, S max. 0.35, P max. 0.2. Compressive Strengths [Specimens tested: 25.4 mm (1 in.) diam. cylinders 76.2 mm (3 in.) long]. Electrolytic iron 56.5 kg/mm? or 80,000 |b/in?. Gray and malleable cast iron 56.5 to 84.5 kg/mm? or 80,000 to 120,000 Ib/in?. Wrought iron, approximately equal to tensile yield point (slightly above P-limit). Density: lectroly tic iON +... eco 7.8 g/cm’ or 487 Ib/ft8 Malleable iron............... see page 653 MC ASETON pons cveteeeussties o. hee store 7.2 g/cm or 449 lb/ft} Wrought iron............... 7.85 g/cm or 490 lb/ft? Ductility: — Normal Erichsen values for good trade quality sheets, 0.4 mm (0.0156 in.) Thickness, soft annealed. Depth. mm in. Sheet metal hoop iron, polished...............-020000- 9-5 0.374 Charcoallsronitinned sheeth.c se cincuinee ee eens 75 0.205 Second quality tinned sheetsene eae oem eee. 6.7 0.264 Modulus of elasticity in tension and compression: Electrolytic iron.... 17,500 kg/mm? or 25,000,000 lb/in? Malleable iron... see page 653 REFS EArONS <-jocesjcve-s « 10,500 kg/mm? or 15,000,000 Ib/in? Wrought iron.... 17,500 kg/mm? or 25,000,000 Ib/in? Modulus of elasticity in shear: Electrolytic iron....... 7030 kg/mm? or 10,000,000 Ib/in? Cast iron....... 8450 kg/mm? or 12,000,000 lb/in? Wirourhtironin stem a cnen cn eer 7030 kg/mm? or 10,000,000 |b/in? : Scleroscope hardness values shown are as determined with the Shore Universal hammer. Strength in Shear: Electrolytic (remelt) Commercial wrought -limit eT te Peosiate 8.4 kg/mm? or 12,000 lb/in? Pelimit eee eee 21.1 kg/mm? or 30,000 |b/in? Ultimate strength..... 21.1 kg/mm? or 30,000 |b/in? Ultimate strength... 35.0 kg/mm? or 50,000 |b/in? Transverse strength, from flexure formula: Gray cast iron Modulus of rupture, 33.0 kg/mm? or 47,000 lb/in? “Arbitration Bar,” 31.8 mm (1} in.) diameter, or 304.8 mm (12 in.) span; minimum central load at rup- oe - neo Ee (2500 to 3300 lb.); minimum central deflection at rupture 2.5 mm (0.1 in.), (A. S. r . Spec. 48-18). * Properties of Swedish iron (impurities less than 1 per cent) approximate those of electrolytic iron. t These two values of B.h.n. only are as determined at 500 kg pressure. + U.S. Navy specifies minimum tensile strength of 14.1 kg/mm? or 20,000 |b/in?2. || From T. D. Yensen, University of Illinois, Engr. Exp. Station, Bulletin No. 83, 1915 (shows Si 4.40 as alloy of Maximum strength). 4 From T. D. Yensen, University of Illinois, Engr. Exp. Station, Bulletin No. 95, 1917. SMITHSONIAN TABLES. 112 TABLES 49 AND 5O MECHANICAL PROPERTIES TABLE 49. — Carbon Steels — Commercial Experimental Values S. A. E. (Soc. of Automotive Eng., U. S. A.) classification scheme used as basis for steel groupings. First two digits S. A. E. Spec. No. show steel group number, and last two (or three in case of five figures) show carbon content in hundredths of one per cent. The first lines of properties for each steel show values for the rolled or forged metal in the annealed or nor- malized condition. Comparative heat-treated values show properties after receiving modified S.A. E. heat treatment as shown below (Table 50). The P-limit and ductility of cast steel average slightly lower and the ultimate strength 10 to 15 per cent higher than the values shown for thesame composition steel in the annealed condition. The properties of rolled steel (raw) are approximately equal to those shown for the annealed con- dition, which represents the normalized condition of the metal rather than the soft annealed state. The data for heat-treated strengths are average values for specimens for heat treatment ranging in size from 3 to 14 in. diameter. The final drawing or quenching temperature for the properties shown is indicated in degrees C with the heat treatment letter, wherever the information is available. In general, specimens were drawn near the lower limit of the indicated temperature range. Hardness. S.A.E.| Nominal Metal. spec. | contents no. | per cent. Ultimate strength Ultimate strength Reduct. in area 3000 kg, @ Steel, carbon | roto) | See Spec. IOIO No. 1020 Ann. 1020 (Mn 0.45) Hi2zornC 1045 Ann. 1045 (Mn 0.65) H 260° C 1095 1095 §7,50¢ 88,000 59,500 I 20,000 00000000 00n00000 00000000 (Mn 0.35)|p eae $4 1 Specification values: Steel, castings, Ann. A.S.T.M. A27-16, Class B;* P max. 0.06; S max. 0.05. Ultimate tensile strength. Per cent | elong. Per cent i ew 50.8 mm reduct. kg/mm? lb/in? or 2 in. area. Yield point. o.45 ultimate 56.2 80,000 0.45 ee 49.2 70,000 “cc 0.45 42,2 60,000 Structural Steel: Rolled: S max: 0.05; P-Bess. max. 0.10; —O-H. max. 0.06. Tension: Yield Point min. = 0.5 ultimate; ultimate = 38.7 to 45.7 kg/mm? or 55,000 to 65,000 Ib/in? with 22% min. elongation in 50.8 mm (2 in.). * aretie carbon contents: steel castings, C 0.30 to 0.40; structural steel, C 0.15 to 0.30 (mild carbon or medium hard steel). TABLE 50.— Explanation of Heat Treatment Letters used in Table of Steel Data Motor Transport Corps Modified S. A. E. Heat Treatments for Steels. (S. A. E. Handbook, Vol. 1, pp. od and oe, 1015, q. v. for alternative treatments.) Heat Treatment A. — After forging or machining (1) carbonize at a temperature between 870 and 930° C (1600 and 1700° F.);_ (2) cool slowly; (3) reheat to 760 to 820 C (1400 to 1s00° F.) and quench in oil. Heat Treatment D. — After forging or machining: (1) heat to 820 to 840° C (1500 to1550° F.); (2) quench; (3) reheat to 790 to 820° C (1450 to r500° F.); (4) quench; (5) reheat to 320 to 650° > (600 to 1200° F.) and cool slowly. Heat Treatment F. — After shaping or coiling: (1) heat to 775 to 800° C (1425 to1475° F.); (2) quench; (3) reheat to 200 to 480° C (400 to 900° F.) in accordance with degree of temper required and cool slowly. Heat Treatment H.— After forging or machining: (1) heat to 820 to 840°C (1500 to 15so° F.); (2) quench; (3) reheat to 230 to 650° C (450 to 1200° F.) and cool slowly. Heat Treatment L. — After forging or machining: (1) carbonize at a temperature between 870 and 950° C (1600 and 1750° F.), preferably between 900 and 930° C_(1650 and 1700 F.); (2) cool slowly in car- bonizing material; (3) reheat to 790 to 820° C (1450 to r500° F.); (4) quench; (5) reheat to 700 to 760° C (1300 to 1400° F.); (6) quench; (7) reheat to 120 to 260° C (250 to 500 F.) and cool slowly. Heat Treatment M.— After forging or machining: (1) heat to 790 to 820°C (1450 to 1500° F.); (2) quench; (3) reheat to between 260 and 680° C (500 and 1250° F.) and cool slowly. Heat Treatment P. — After forging or machining: (1) heat to 790 to 820° C (1450 to r500° F.); (2) quench; (3) reheat to 750 to 770° C (1375 to 1425°F.); (4) quench; (5) reheat to 260 to 650° C (500 to r200° F.) and cool slowly. Heat Treatment T. — After forging or machining: (1) heat to goo to 950° C (1650 to1750° F.); (2) quench; (a) reheat to 260 to 700° C (500 to 1300° F.) and cool slowly. Heat Treatment U. — After forging: (1) heat to 830 to 870°C (1525 to 1600° F.), hold half an hour; (2) cool slowly; (3) reheat to 900 to 930° C (1650 to 1700° F.); (4) quench; (5) reheat to 180 to 290° C (350 to 550° F.) and cool slowly. Heat Treatment V. — After forging or machining: (1) heat to 900 to 950°C (1650 to 1750° F.); (2) quench; (3) reheat to between 200 and 650° C (400 and 1200° F.) and cool slowly. Epitor’s Nore: Oil quenching is recommended wherever the instructions specify ‘‘ quench,” inasmuch as the data in the table are taken from tests of automobile parts which must resist considerable vibration and which are usually small in section. The quenching medium must always be carefully considered. SMITHSONIAN TABLES. TABLE 51 113 MECHANICAL PROPERTIES Alloy Steels — Commercial Experimental Values S. A. E. heat treat- ment. SHAVES Nominal spec. contents, no. per cent. Ultimate strength Ultimate strength Elong. in 50.8 mm (2 in.). Tension Ib/in? Steel, nickel. . . | 30.0] 38.0] 42,500] 54,000 53-0] 76.0] 75,000/107,500 39.0] 48.0] 55,000] 68,000 106.0]131.0]151,000| 186,000 ] ; 44.0] 55.0| 62,500] 78,000 (Mr 0.65) 136.0|149.0|193,000] 212,000 Invar | Ni 36.0 C 0.40 , 50.0] 77.5| 71,000|I10,000| . nickel chrome... .| 3120 he r.25| Ann. 34-0] 44.0] 49,000] 62,000 3120 Cr 0.60} H 450°C | 60.0] 82.0] 85,000/116,000 3135 Ann. 40.0] 50.0] 57,000] 71,300 3135 | |((Mn 0.65)| Hor D | 88.0}/121.0/125,000]172,000 3220 Ann. 39-0] 49.0] 55,000] 69,000 3220 Ni 1.75 | Hor D | 77.0/106.0]/110,000]151,000 3250 Cri.to | Ann. 44.0] 55.0] 62,000] 78,000 3250 J |(Mn 0.45) M 134.0|183.0]190,000] 260,000 3320 Ann. 32.0] 42.0] 46,000] 59,500 3320 Ni 3.50 L 77.0|105.0|I10;000] 150,000 3340 Cr 1.50 Ann. 39-0] 52.0] 56,000] 74,000 3340 { |(Mn 0.45) iE 120.0] 163.0]1 70,000] 232,000 chromium. |51120 || Cr 1.00] Ann. 44.0] 58.0] 62,000] 82,000 51120 { |(Mn 0.35)| M or P |144.0]193.0|205,000]275,000 Cr20 Ann. 44.0] 58.0] 62,000] 82,000 M or P. ]141.0|178.0|200,000] 253,000 vanadium } : Ann. 43-0] 59.0] 61,500] 84,500 al 84.0] 115.0]120,000]163,000 Ann. 48.0] 63.0} 68,200] go,000 U 176.0] 23 2.0|250,000]330,000 silico- manganese|9250 Si 1.95} Ann. 42.0| 54.0] 60,000] 77,000 9250 Mn 0.70 V QI.0]122.0|130,000]1 74,000 Si 0.85} Ann. 48.0] 61.0] 68,000} 87,000 Mn 1.75 V 113.0|148.0]160,000] 211,000 tungsten. . W 2.4 Ann. 34.0| 59.0] 48,100] 84,200 W 09.7 Ann. 63.0] 89.0] g0,000}1 26,000 W 15.6 | Quench 1065° |158.5|175.0]225,000] 248,000 Draw 2056 e eeNeEAL Note. — Table on steels after Motor Transport Corps, Metallurgical Branch of Engineering Division, able No. 88. Maximum allowable P 0.045 or less, maximum allowable S 0.05 or less. Silicon contents were not determined by Motor Transport Corps in preparing table, except for silico-manganese steels. Compressive strengths: F 4 For all steels approx. equal to yield point in tension (slightly above P-limit). ensity: Steel weighs about 7.85 g/cm% or 490 lb/ft? Ductility, Erichsen values: 0.75 mm (0.029 in.) thick, low carbon soft annealed sheet (B. S.), depth of indentation 12.0 mm or 0.472 in. 1.30 mm (0.050 in.) thick, low carbon soft annealed sheet (B.S.), depth of indentation 12.5 mm or 0.492 in. Modulus of elasticity in tension and compression: For all steels approx. 21,000 kg/mm? = 30,000,000 Ib/in?. Modulus of elasticity in shear: For all steels approx. 8400 kg/mm? = 12,000,000 lb/in?. Scleroscope hardness values shown are as determined with the Shore Universal hammer. Strength in shear: P-limit and ultimate strength each about 70 per cent corresponding tensile values. SMITHSONIAN TABLES. 114 TABLES 52-54 MECHANICAL PROPERTIES TABLE 52.— Steel Wire — Specification Values (After I. A. S. B. Specification 3S12, Sept., 1917, for High-strength Steel Wire.) S. A. E. Carbon Steel, No. 1050 or higher number specified (see Carbon steels above). Steel used to be manutac- tured by acid open-hearth process, to be rolled, drawn, and then uniformly coated with pure tin to solder readily. American Diameter. Req’d Weight. Req’d Spec. minimum tensile strength. 5 or FP cae tance Twists EEE bends . and S. ; 203.2 mm 1 . : wire gage. . or 8 in. byace thru 90 c . {kg/mm?} Ib/in? 219,000 229,000 233,000 244,000 244,000 254,000 252,000 255,000 258,000 259,000 264,000 267,000 270,000 275,000 280,000 ° O0O000 OHH HN 284,000 Nore. — Number of 90° bends specified above to be obtained by bending sample about 4.76 mm (0.188 in.) radius, alternately, in opposite directions. % (Above specification corresponds to U.S. Navy Department Specification 22W6, Nev. 1, 1916, for tinned, galvan ized or bright aeroplane wire.) TABLE 53.— Steel Wire — Experimental Values (Data from tests at General Electric Company laboratories.) ‘‘ Commercial Steel Music Wire (Hardened).’ Diameter. Ultimate strength. kg/mm? tension lb/in? 226. 249. 253- 260. 262. 265. 386. 527. 49. 321,500 354,000 360,000 370,000 372,500 378,000 550,000 750,000 70,000 ° ° ° ° ° 5 5 ° 2 * For 4.55 mm wire drawn cold to indicated sizes. + For 4.55 mm (0.018 in.) wire annealed in Hz at 850°C. TABLE 54.— Semi-steel Test results at Bureau of Standards on 155-mm shell, Jan. 1919. : Microstructure — matrix resembling pearlitic steel, embedded in which are flakes of graphite. Composition-Comb. C 0.60 to 0.76, Mno.88, P 0.42 to0.43,$ 0.077 to 0.088, Si1.22 to 1.23, graphitic C 2.84 to 2.94. Hardness. Ultimate strength Ultimate strength Ultimate strength Ultimate strength | Brinell | ctero- : : : @ Tension Compression Compression eS CS scope. Semi-etect: xraph. C 2.85 x Comb. C 0.76 : 28,200 | 24.3 | 72.6 specie 103,000 | 176 Graph. C 2.92 - 6 oO GomUEGIENGS ‘ : 21,200 18.3 | 61.4 26,000 87,30 Tension specimens 12.7 mm (0.5 in.) diameter, 50.8 mm (2 in.) gage length; elongation and reduction of area negligible. ; 3 i Compression specimens 20.3 mm (0.8 in.) diameter, 61.0 mm es in.) long; failure occurring in shear. Tension set readings with extensometer showed elastic limit of 2.1 kg/mm? or 3000 ]b/in?. Modulus of elasticity in tension — 9560 kg/mm? or 13,600,000 Ib/in?. SMITHSONIAN TABLES. TaBLEes 55-57 I 15 TABLE 55.— Steel-wire Rope — Specification Values Cast steel wire to be of hard crucible steel with minimum tensile strength of 155 kg/mm*or 220,000 lb/in? and minimum elongation of 2 per cent in 254 mm (to in.). ; Plow steel wire to be of hard crucible steel with minimum tensile strength of 183 kg/mm? or 260,000 lb/in? and minimum elongation of 2 per cent in 254 mm (to in.). aye , Annealed steel wire to be of crucible cast steel, annealed, with minimum tensile strength of 77 kg/mm? or 110,000 Ib/in? and minimum elongation of 7 per cent in 254 mm (ro in.). i Type A: 6 strands with hemp core and 10 wires to a strand (= 6 X 19), or 6 strands with hemp core and 18 wires to a strand with jute, cotton or hemp center. Type B: 6 strands with hemp core, and 12 wires to a strand with hemp center. Type C: 6 strands with hemp core, and 14 wires to a strand with hemp or jute center. Type AA: 6 strands with hemp core, and 37 wires toa strand (= 6 X 37) or @ strands with hemp core and 36 wires to a strand with jute, cotton or hemp center. Diameter. Approx. weight. Minimum strength. Description. — oe bol aoleoto|e . 59,735 2,095 5,210 20,890 47,965 18,825 515575 4,690 8,165 32,675 69,140 | 152,430 4,540 10,000 8,750 | 19,300 32,250 71,100 83,010 | 183,000 —————— I I i 2 3 8 1 2 HHH HA bol bol co|e0 colon “ “cc ee bol a0 cor ce “ce on BPHOOWHOONHNHOOWHOOWHOO CoS gO) CARBS On CaS Po Sa One tesa) Casa On DAnvnookhnodofhdtwWHtOOdONMNndadNUnvoOod)O ee olor TABLE 56.— Steel-wire Rope — Experimental Values (Wire rope purchased under Panama Canal Spec. 302 and tested by U. S. Bureau of Standards, Washington, D. G:) Ultimate strength Diameter. Ultimate strength. (net area). Description and analysis. mm in. kg Ib. kg/mm? Ib/in2 Plow Steel, 6 strands x 19 wires C 0.90, S 0.034, P 0.024, Mn OMG ROlONn7 2. Gyre ton cece 50.8 2 137,900 | 304,000 | 129.5 184,200 Plow Steel, 6 strands x 25 wires C 0.77, S 0.036, P 0.027, Mn COM SLIONDE2 ey. sake snes: 69.9 23 314,800 | 694,000 | 151.2 | 214,900 Plow Steel, 6 x 37 plus 6x 19 C 0.58, S 0.032, P 0.033, Mn ETP SU, OSE OO actos pecs uctacancincns 82.6 31 | 392,800 | 866,000 | 132.2 | 187,900 Monitor Plow Steel, 6 x 61 plus 6 X 19, C0.82, S0.025, Po.otg, IMmVvO.22" SiOs6O8. sas 82.6 31 | 425,000 | 937,000 | 142.5 | 202,400 SS ee ee Se Recommended allowable load for wire rope running over sheave is one fifth of specified min. strength. TABLE 57.— Plow-Steel Hoisting Rope (Bright) : (After Panama Canal Specification No. 302, 1912.) _, Wire rope to be of best plow steel grade, and to be composed of 6 strands, 19 wires to the strand, with hemp center. Wires entering into construction of rope to have an elongation in 203.2 mm or 8 in. of about 2} per cent. Diameter. Spec. minimum strength. Diameter. Spec. minimum strength. | ah ke Ib. 5 Bom 164,000 50.8 280,000 63.5 458,000 69.9 | 3 550,000 3 8 1 2 3 4 SMITHSONIAN TABLES. 116 TABLES 58 AND 59 MECHANICAL PROPERTIES TABLE 58. — Aluminum Density Hardness. 24 aS 2 to to Eg eS BE : Pn n Tension, Tension, Metal, approx. i's composition, Condition. per cent. Per cent. ALUMINUM: Av. Al 99.3 Imp., Fe and Si. . . 2.57|160.5]6.0 to Broke 8,500 to|12,000 to Ke) : 10,000 | 14,000 Cast, sand and i : Z heat treated — |8.9to| — _ |12,600 to Ann. 500° C, air ; 13,600 Cast, chill 2 : : : : 13,000 Sheet, ann : : : : g, 13,500 Sheet, hard 7 Be - 3 ; 30,000 ' Bars, hard : ; B . : 33,000 Wire, hard y Ba ; i : 40,000 Compressive strength: cast, yield point 13.0 kg/mm? or 18,000 lb/in?; ultimate strength 47.0 kg/mm? or 67,000 lb/in?. Modulus of elasticity: cast, 6900 kg/mm? or 9,810,000 lb/in? at 17° C. TABLE 59.— Aluminum Sheet (a) Grade A (Al min. 99.0) Experimental Erichsen and Scleroscope Hardness Values. [From tests on No. 18 B. & S. Gage sheet rolled from 6.3 mm (0.25 in.) slab. Iron Age v. 101, page 952]. Heat treatment Thickness, Indentation, Scleroscope annealed. mm mm hardness. None (as rolled) : 6.83 @ 200° C, 2 hours : 8.86 @ 300° C, 2 hours : 10.17 @ 400° C, 2 hours : 9.40 @ 200% €Bommine eee : Hoey @ijoo; Gy soymins +s.) ee ‘ 9.80 (b) Specification Values. — (1) Cast: U. S. Navy 49 Al, July 1, 1915; Al min. 94, Cu max. 6, Fe max. 0.5, Si max. 0.5, Mn max. 3. Minimum tensile strength 12.5 kg/mm? or 18,000 lb/in? with minimum elongation of 8 per cent in 50.8 mm (2 in.). (2) Sheet, Grade A: A. S. T. M. 25 to18T; Al min. 99.0; minimum strengths and elongations. Tensile strength.| Elong. in 50.8 mm or 2 in. per cent. Gage, sheet thicknesses. Renee ING. | hardness. |————_— (B. &S.) in. kg/mm2|_ |b/in? 12,500 Sheets of temper No. 18,000 I to withstand being 22,000 / bent double in any di- 12,500 rection and hammered 18,000 flat; temper No. 2 to 25,000 bend 180° about radius 12,500 equal to thickness with- 2 Half-hard 18,000 out cracking. 3 Hard 30,000 ped be EE ee ee ee ee t Soft, Ann. 2 Half-hard 3 Hard 12 to .052 to | 0.0808 to 16 incl.| 1.293 .0509 2 Half-hard 3 Hard t Soft, Ann. 643 -0253 .574 to .0226 to - 404 -O159 152 to .0453 to eae Ann. Nore. — Tension test specimen to be taken parallel to the direction of cold rolling of the sheet. SMITHSONIAN TABLES. TABLE 60 LL MECHANICAL PROPERTIES Aluminum Alloys oo || eat 3 nS esa ASa ire ey s=) = ~ Wee S Density a 8 be E ge |G ec) 38 Hardness. a or weight. | = | 39 Bo SLO CONS erga Alloy, approx. Condition, Ay 54 Ay 53 ey Omi Wes composition per cent we ; SOR per cent. reduction. ax E a gm/ | |b/ Tension, Tension, 82/35 cm? | ft? kg/mm? - Ilb/in? Per cent. : 2) % Aluminum—Copper.| Cast, chill. . | 5.3) TORS 7,500 |15,000 |24.0 |34.0 ee Alo8 CurImp.max.1| Rolled, 19% 3o|| == — 19:0 21.0 |27,000 |30,000 4.0 — —}— { Cast, chi sel] = —— I. [13.7 |11,500 |10,500 |12.0 |2I1.0 =, || = Al96 Cu 3 Imp. max. 1 \ Rolled, 19%: i= — |25.0 |28.8 135,000 |41,000 5.5 —_ ae Cast, ch es — |10.0 |15.0 |14,500 |21,500 7.0 |14.0 —= || — Alo4 Cus Imp. max. 1 \ Rolled, be .| — | — |23.0 |27.0 [33,000 |38,000 6.0 — |) —. |, — Al 92 Cu 8: Alloy No.| Cast, sand... .|2.38 |180 7.7 to|10.5 to|11,000 to|15,000 to} 4.0 to] 3.5 to|s50 to|13 to TED ie avec apsbors etehcis aiese ais = — |10.5 |16.2 |15,000 |23,000 | None} None]65 {18 Al go-92 Cu 7-8.5 imp Smaxcuts yey war ee CaSbee sme sci 2.9 |181r — 12.7 — 18,000 1.0 _ — | — Copper, Magnesium..| Castat 700° C.| — — | 3.2to} 9.6 to] 4,500 to]13,600 to] 2.0 to] 0.5 to}74 to|17 tc Al 9.52 Cu 4.2 Mg 0.6 4:6 113.3 6,500 |18,900 ° ° 74 «+|18 Ann. 500° C...| — | — | 4.6° |17.3 6,500 |24,900 3.0 1.0 |80 |2r Duralumin or 17S { ANT cryshesstes 2.8 |174 |25.0 |42.0 |35,100 |50,500 |21.1 |29.5 —|— Alloy Al 94 Cu 4 Mg} { Rolled 70%...| — — |53.0 |56.0 175,400 179,600 4.0 |13.2 — | — Ee ec | | Rolled heat tees sus = — 123.4 130.0 |33,400 [55,300 |25.5 |26.0 —-~|— Copper, Manganese..| Cast, chill....} — — |10.0 |14.0 |14,300 [20,300 5.0 —_ —|— Alo6 Cu2Mn2.... Rolled, 2omm| — — 19.0 |27.0 |27,100 |38,200 |16.0 |28.0 —|— Al 96 Cu 3 Mnz..... Cast, chill. . — — |11.3 |19.0 |16,200 |27,000 |14.0 —_ —|— Naval Gun Factory... {eae sand....|2.8 |175 — |14.0 — 20,000 |12.0 — —}|— Algo7 Cur.5 Mni....| ( Forged....... — — |14.0 |19.0 |19,500 |27,800 |12.0 |47.0 —|— Al 4 es max. 6 Mn Perera sis Minimum f...| — _ — |12.7 —_— 18,000 8.0 —_— —|— Gener Nickel, Mg VED 5 2 ssf. sioresofatelers ce Cast at 700° C.| — — | 3.5 to|17.9 to] 5,000 to|25,500 to|6.0 to | 8.5 to|54 tolg to Al 93.5 Cu 3.5 Ni 1.5 Mg1Mno.s5..... a — | 9.8 |23.2 |14,000 |33,000 1.5 I.o |86 25 Copper, Nickel Mn.. Cast at 700° C.| — —_ — |14.5 to — 20,600 to|6.0 to |1I.0 to|50 to|g to Al 94.2 Cu 3 Ni 2 Mn OlGe eitcrae dae aejerent 21.4 30,500 1.0 20) jor | |27 Miaedietam: Magnalium Al 95 eS Cast, sand....}2.5 |156 5-6 [15.5 8,000 |22,000 7.0 8.5 —|— Al 77-08, Mg 23-2. Cast, chill. ...]2.4 to|1rsoto] — {29.5 to _— 42,000 to] — cae a 2.57 |160 145.0 64,000 Cast, chill. ...| — — | 4.0 |1I1.0 5,800 |14,900 |21.0 |36.0 —|— Nickel Al 97 Ni 2.....| } Drawn, cold..| — | — |14.0 [16.0 |19,700 |22,700 |13.0 |37-0 —|— Rolled, hot...| — — | 8.0 |13.0 |11,900 |18,200 |28.0 [52.0 —|— Cast, chill....| — | — | 6.0 [15.0 9,000 21,700 9.0 |II.0 —\|;— PALO SMNIUS ey essers cares Drawn, cold..| — | — |16.0 |20.0 22,900 {27,900 | 8.0 |24.0 —|—-— |) Rolled, hot...| — | — | 9.0 |16.0 |13,500 |22,300 |22.0 1|36.0 —|—-— Nickel Copper: Al 93.5 Nis5.5 Cur..}| Cast, chill....| — | — | 7.0 |17.0 [10,700 [24,800 | 6.0 | 80 | — | — Al or.5 Ni4.5 Cuq4.. Casts chills: -| — | — | 7.0 \18.0 9,900 |25,200 4.0 5.0 - — : rawn, cold..| — — |22.0 |27.0 |31,700 |37,800 8.0 |15.0 —|— Al 92 Ni 5-5 Cu 2.... \ Rolled, hot...| — | — |13.0 |22.0 |18,200 |31,500 |16.0 |24.0 —|— Zinc, Copper: Al 88.6 Cu 3 Zn 8.4..] Castat 700°C.) — | — | 4.7 |18.5 | 6,700 |26,300 |*8.0 |.7.5 |50 |10 Ann. 500° C. .}| — — | 4.4 |20.2 6,200 |28,800 8.0 7.5 50 |IO Al 81.1 Cu 3 Zn 15.9.} Castat700°C.}3.1 {193 9.8 |24.7 |14,000 |35,100 2.0 2.0 |74 |I5 Ann. 500° C...|_ — — | 9.8 |29.0 |14,000 |41,200 4.0 4.0 |70 |15 * Specification Values: Alloy “No. 12”: A.S.T. M. B26-18T, tentative specified minimums for aluminum, copper. t+ Quenched in water from 475° C ee heating in a salt bath. Modulus of elasticity for Duralumin averages 7000 kg/mm? or 10,000,000 |b/in?. t Specification values: Aluminum castings; U.S. Navy 49 Al, July 1, 1915 (Impurities: Fe max. 0.5, Si max. 0.5) SMITHSONIAN TABLES. 118: TABLES 61-63 MECHANICAL PROPERTIES TABLE 61.— Copper Metal and Density or weight. approx. os composition. Condition. Per cent. Ultimate strength. Ultimate strength Ib/ Tension, Tension, lb/in? Copper: 99-9: electrolytic neguee brea” Culoo!6=e eee toate at 8.85 { Hard, 40% reduct} 8.89 “ragesesaioneee \ Ann. at 500°C... .] 8.90 Drawn cold, 50% Sota e No Ann. (96% re- duction)....... Ann. 750°C after drawing cold... aie Ciotaiole Drawn hot (64% reduction)..... * Wire drawn cold from 3.18 mm (0.125 in.) to 0.64 mm (0.025 in.) Bull. Am. Inst. Min. Eng., Feb., to19. + Wire drawn at 150° C ‘from 0.79 mm (0.031 in.) to 0.64 mm (0.025 in.) (Jeffries, Joc. cit.). Cempression, cast copper, Ann. 15.9 mm (0.625 in.) diam. by 50.8 mm (2 in.) long cylinders. Shortened 5 per cent at 22.0 kg/mm? or 31,300 lb/in? load. g to “ “ 29.0kg/mm? “ 41,200 lb/in? “‘ ss 20 & € 39.6kg/mm? “ 55,400 lb/in? Shearing strength, cast copper 21.0 kg/mm? or 30,000 lb/in® Modulus of elasticity, electrolytic 12,200 kg/mm? or 17,400,000 Ib/in? s se cast 7,700 kg/mm? or 11,000,000 |b/in? ce ff “ drawn, hard 12,400 kg/mm? or 17,600,000 Ib/in? TABLE 62.— Rolled Copper — Specification Values Specification values: U. S. Navy Dept., 47C2, minimums for rolled copper, — Cu min. 99.5 “ Tensile strength. = oe earn Elong. in 50.8 Description, temper and thickness. rere eon clad enya or 2 in. — per cent. Rods, bars, and shapes: 30,000 25 Hard: to 9.5 mm (# in.) incl : 50,000 Io Hard: 9.15/mm’ to.2i5.4.mmi(G@ 1n=) see er : 45,000 12 Hard: 25.4 mm to 50.8 mm (2 in.)......... 28.0 40,000 I5 Hard moverssouciri (Zale) eect eieiciterioeiat 24.5 35,000 20 Sheets and plates: 21.0 to 28.0 30,000 to 40,000 25 to 25 35,000 18 TABLE 63.— Copper Wire — Specification Values Specific Gravity 8.89 at 20° C (68° F). Copper wire: Hard Drawn (and Hard-rolled flat copper of thicknesses corresponding to diameters of wire) Specification values. (A. S. T. M. Br-15, and U.S. Navy Dept., 22W3, Mar. 1, rors.) Diameter. Minimum tensile strength. Maximum elongation, oo per cent in kg/mm? Ib/in? 254 mm (Io in.). 49,000 51,000 52,800 54,500 56,100 57,000 $9,000 HRN NNWD in 1524 mm (60 in.) 24. .18 anal -09 06 02 Anko HON 60,100 61,200 62,100 63,000 63,700 64,300 64,900 65,400 65,700 65,900 66,200 66,400 66,600 66,800 67,000 -97 10. 9. 8. 7-3 6. Be Re 4. 4. Bs 3. 2. 2s oh 2% ae I. I. Te Te re HO OYANW ROW OHUOH ODODDDDOOH HHH HHH _ P-limit of hard-drawn copper wire must average 55 per cent of ultimate tensile strength for four largest sized wires in table, and 60 per cent of tensile strength for smaller sizes. SMITHSONIAN TABLES. TABLES 64-67 11g MECHANICAL PROPERTIES Table 64.— Copper Wire — Medium Hard-drawn (A. S. T. M. B2-15) Minimum and Maximum Strengths. Tensile strength. _ Elongation, minimum per cent in 254 mm (zo in.). Diameter. Maximum. kg/mm? Ib/in? Minimum. kg/mm? Ib/in? 49,000 3-7 5 2.50 in 1524 mm (60 in.) 56,000 1.15 575332 1.04 60,000 0.88 47,000 38.0 54,000 49,000 39-5 595330 49.5 53,000 42.0 Representative values only from table in specifications are shown above. P-limit of medium hard-drawn copper averages 50 per cent of ultimate strength. TABLE 65.— Copper Wire — Soft or Annealed (A. S. T. M. B3-15) Minimum Values. Minimum tensile Diameter. kg/mm? strength. lb/in? Elongation in 254mm (ro in.), per cent. 11.70 to 7.37 | 0.460 to 0.290 25.5 36,000 7.34 to 2.62 | 0.289 to 0.103 26.0 37,000 2.59 t0 0.53 | 0.102 to 0.021 27.0 38,500 0.51 to 0.08 | 0.020 to 0.003 28.0 40,000 Nore. — Experimental results show tensile strength of concentric-lay copper cable to approximate 90 per cent of combined strengths of wires forming the cable. TABLE 66.— Copper Plates (A. S. T. M. Br1-18) for Locomotive Fire Boxes. Specification Values. Tensile strength. Elong. in 203.2 mm Minimum requirements. (8 in.) kg/mm? \b/in? per cent. Copper, Arsenical, As 0.25-0.50 Impurities, max. 0.12 j Ba Copper, Non-arsenical: Impurities, max. 0.12 : 30 Note. — Copper to be fire-refined or electrolytic, hot-rolled from suitable cakes. TABLE 67.— Copper Alloys The general system of nomenclature employed has been to denominate all simple copper- zinc alloys as brasses, copper-tin alloys as bronzes, and three or more metals alloys composed primarily of either of these two combinations as alloy brasses or bronzes, e.g., ‘‘Zinc bronze”’ for U. S. Government composition ‘“‘G”’ Cu 88 percent, Sn 10 percent, Zn 2 percent. Alloys of the third type noted above, together with other alloys composed mainly of copper, have been called copper alloys, with the alloying elements other than minor impurities listed as modifying copper in the order of their relative percentages. In some instances, the scientific name used to denote an alloy is based upon the deoxidizer jused in its preparation, which may appear either as a minor element of its composition or not at all, e.g., phosphor bronze. te Commercial names are shown below the scientific names. Care should be taken to specify the chemical composition of a commercial alloy, as the same name. frequently applies to widely varying compositions. SMITHSONIAN TABLES. 120 TABLE 68 MECHANICAL PROPERTIES Copper Alloys — Copper-Zine or Brasses; Copper-Tin or Bronzes Metal and Density approx. or weight. composition, Condition. per cent. Ultimate strength. Ultimate strength Tension, Brass: Sand cast Cu 90 Zn rof. .| { Cold rolled, hard Cold rolled, soft.) 8.7 Sand cast _— Cu 80, Zn 20 f.| { Cold rolled, hard Cold rolled, soft. 55,000 * 37,000 * 35,000 75,000 * 42,000 * 40,000 60,000 48,000 * Cu 70, Zn 30... Cu 66Zn 34 Std. { Cold rolled, hard h Cold rolled, soft. 45,800 Cu 60, Zn 40...| Sand cast { 70,000 Muntz metal...} Cold rolled, hard CI mn Un 8.4 w H Bronze: Cu 97.7, Sn 2.3. { 28,000 48,000 Cast or Cu 90, Sn to... bronze or ‘ 33,000 Cu 80, Sn 20... 3 ‘ g 32,000 Gu 7oF Sn 30... : 5 ‘ z 7,000 Compressive Strengths, Brasses: Cu go, Zn 10, cast 21.0 kg/mm? or 30,000 lb/in? Cu 80, Zn 20, cast 27.4 kg/mm? or 39,000 lb/in? Cu 70, Zn 30, cast 42.0 kg/mm? or 60,000 Ib/in? Cu 60, Zn 40, cast 52.5 kg/mm? or 75,000 lb/in? Cu 50, Zn 50, cast 77.0 kg/mm? or 110,000 |b/in? Modulus of elasticity, — cast brass, — average 9100 kg/mm? or 13,000,000 |b/in? Erichsen values: Soft slab, 1.3 mm (0.05 in.) thick, no rolling, depth of impression 13.8 mm (0.55 in.). Hard sheet, 1.3 mm, rolled 38% reduction, depth of impression 7.3 mm (0.29 in.). Hard sheet, 0.5 mm, rolled 60% reduction, depth of impression 3.7 mm (0.15 in.). Compressive Ultimate Strengths, Cast Bronzes: Cu 97.7, Sn 2.3 to 24.0 kg/mm? or 34,000 |b/in? Cu 90, Sn 10 to 39.0 kg/mm? or 56,000 lb/in? Cu 80, Sn 20 to 83.0 kg/mm? or 118,000 |b/in? Cu 70, Sn 30 to 105.0 kg/mm? or 150,000 lb/in? i Specification value, A.S.T. M., B 22-18 T, for specimen = cylinder 645 sq. mm (1 sq. in.) area, 25.4 mm (r in.) ong. Cu 80, Sn 20: minimum compressive elastic limit = 17.0 kg/mm? or 24,000 lb/in? i; Modulus of elasticity for bronzes varies from 7000 kg/mm? or 10,000,000 lb/in? to 10,000 kg/mm? or 15,500,000 /in? * Values marked thus are S. A. E. Spec. values. (See S. A. E. Handbook, Vol. I, p. 13a, rev. December, 1913.) + Red metal. { Low brass or bell metal. : § A.S.T.M. Spec. Bro-18T requires B.h.n. of 51-65 kg/mm? @ 5000 kg pressure for 70: 30 annealed sheet Tass. Foot NoTES To TABLE 69, PAGE 121 * Tensilite, Cu 67, Zn 24, Al 4.4, Mn 3.8, Po.or compressive P-limit: 42.2 kg/mm? or 60,000 lb/in? and 1.33 per cent set for 70.3 kg/mm? or 100,000 Ib/in? load. + Compressive P-limit 20.0 to 28.2 kg/mm? or 28,500 to 40,000 Ib/in? t Compressive ultimate strength 54.5 kg/mm? or 77,500 lb/in? § Compressive P-limit 4.2 kg/mm? or 6000 Ib/in? and 4o per cent set for 70.3 kg/mm? or 100,000 Ib/in? § Modulus of elasticity 9840 kg/mm? or 14,000,000 Ib/in? || Values are for yield point. ** Minimum values for ingots. : Tt Rolled manganese bronze (U. S. N.) Cu 57 to 60, Zn 40 to 37, Fe max. 2.0, Sno.5 to 1.5; 2.9 per cent increase for thickness 25.4 mm (1 in.) and under. tt Nig per cent, B.h.n. = 130 as rolled; B.h.n. = 50 as annealed at 930° C. i 4 U. S. Navy Dept. Spec. 46S 3a, June 1, 1917: German silver Cu 60 to 67, Zn 18 to 22, Ni min. 15, no mechanical requirements. p e For Tee ore German silver alloys, see Braunt, ‘‘ Metallic Alloys,” p. 314, — “‘best”’ (Hiorns), “‘ hard Sheffield,” u 46, Zn 20, Ni 34. §§ Platinoid Cu 60, Zn 24, Ni14, W 1 to 2; high electric resistance alloy with mechanical properties as nickel brass |||| Specification Values, Naval Brass Castings, U. S. Navy, 46B rob, Dec. 1, 1917 for normal proportions Cu 62, Zn 37,501, min. tensile strength 17.5 kg/mm? or 25,000 lb/in? with 15 per cent elongation in 50.8 mm (2 in.). SMITHSONIAN TABLES, ‘ TABLE 69 121 MECHANICAL PROPERTIES Copper Alloys — Three (or more) Components Ultimate strength. Ultimate Alloy and approx. * composition Condition. per cent. Brass, Aluminum...} Cast Cu 57, Zn 42, Alr.. Cu 55, Zn 41, Alq. Cu 62.9, Zn 33.3, Alls.3. Cu 70.5, Zn 26.4, All3 | Alum., Manganese.. Gast tensilite* Cu 64, Zn 20, Al 3.1, Mn 2.5, Fe 1.2... Alum., Vanadium... Cu 58.5, Zn 38.5, Al 1.5, V 0.03 Cold drawn... 4 3 s 12.0 |14.0 Iron: Cu 56, Zn 41.5, Fet. : 72,000 to/35.0 to}35.0 to|/r09 to 84,000 |22.0 |25.0 |119 Aich’s Metal Cu 60,Zn 38.2,Fe1.8 : 2 57,300 = a Delta Metal inGastysandier. 7 45,000 |I0.0 — Cw's7,Zn 42, Fer.. \ Rolled, hard. . .2 60,000 {17.0 —_— Cu 65, Zn 30, Fes..| Rolled hard... 5. 65,000 — a Tron, Tin: Cus6.s, cnae,E Hex-5; : 49.2 to]33,000 to] 70,000 to]35.0 to|35.0 to|104 to SOM olfeeee : 52.8 |37,000 75,000 |20.0 |22.0 |119 Sterro metal: Cu 55, Zn 42.4 Fe 53.0 — 76,200 aa ae He uio8 Hard drawn. .| — 58.5 — 83,100 _— ~- Lead or Yellow brass : 23.2 to 33,000 to}30.0 to 27.5 39,000 + |26.0 Cu 60 to 63.5, Zn 35] { Sheet ann..... 25.5 — 42,000 |50.0 = to 33.5, Pb5 to3.| \ Sheet hard.... 42.9 — 61,000 |30.0 a Lead, Tin or Cu83,Zn7,Pb6,Sn4 Cu 78, Zn9.5, Pb Io, Sn 2. ase a 4| 8. 3 12,000 26,500 : 24.9 Yellow brass: o 70, Zn 27, Pb) 2, oT 42.5 — 60,500 — -- 21.0 |16,000 30,000 |17.0 |I9.0 20.7. |10,500 29,500 |25.0 |28.5 153.0 Manganese or Man- ganese bronze Cu 58, Zn 39, Mnj Cast, sand f..|8. : 49-2 to|30,000 to} 70,000 to]30.0 to]32.0 to|rog to|18 to 0.05 4 52.7 |35,000|| | 75,000 |22.0 |25.0 |119 |19 (Sn, Fe, Al, Pb.) Cast, chill... . 4 52.7 to|32,000 to] 75,000 to]32.0 to}34.0 to|r19 to|18 to 56.3 |37,000!| | 80,000 {25.0 28.0 |130 |22 Cu 60, Zn 39 Mn,| Rolled : : 52.5 |45,000 75,000 |25.0 |28.0 — |30 t r suretieation values: 16a a : coe 70,000 U.S.N.,46 B 15a) Rolledtt : .2 |35,000 | 70,000 Manganese Vana- dium: Cu 58.6, Zn 38.5, Al] Cold drawn... : : 50,600 81,400 1.5 Mno.s, Vo.03. Nickel: Nickel sil- ver, Cu 60.4, Zn StS INL 7e7 ects 3 i E 15,400 36,000 German silver, Cu 61.6, Zn 17.2, Nj 2rt ee. : ; : 18,800 40,900 Cu 60.6, Zn 11. 8, NIG 2723 arena 8 15 : Z 23,700 53,500 Fine wire: Cu 58,Zn 24, Ni18} Drawn hard. .|8. f _ 150,000 Nickel silver ff Nickel Tungsten: §§ Tin: Cnl6r Zn 38; snr-..|| Cast, sand... II.0 : Xi 42,600 Navalbrass,asabove| Ann. after roll- MG fee sare — |26.0 f ; 62,000 Tobin bronze: as be- .8.3]518)17.6 : 60,000 Cu 58.2, Zn 30.5, Sn 2:3. . -4 |524|38.0 : : 79,000 Cu ss, Zn 43, Sn 2 Cas —| — ' 68,900 For Footnotes see page 120. SMITHSONIAN TABLES. 122 TABLE 69 (continued) MECHANICAL PROPERTIES Copper Alloys — Three (or more) Components Ultimate strength Alloy and approx. composition Condition. per cent. Ultimate strength Tension, Per cent Brinell @ Brass, Tin — (continued): Rods:* o to 12.7 mm (3 in.) : : 35.0 |To bend 120° 12.7 to 25.4 mm (I in.) f i 40.0 cold about radius equal over 25.4 mm (in.) diam.. : 40.0 to diameter. Shapes, all 39.4 30.0 < Plates to 12.7 mm (} in.) 38.7 32.0 over 12.7 mm (3 in.) thick 39.4 35.0 Tubing (wall thickness) o to 3. 2smmi (Fins) jena ares : 42.2 28.0 _ 3.2 to 6.4 mm (4 in.)..... ; 38.7 32.0 _— over 6.4 mm (3 in.)...... : 35.1 35.0 —_— Vanadium: Victor bronze, V 0.03, Cu 58.6, Zn 38.5,| Cold drawn ¢ 64.5 II.5 11.5, Fer.o U.S. Navy t 49 B rb.... 8 38.7 25.0 Bronze, Aluminum. ....... See Cu Al Lead: Cu 89, Sn to, Pb1 15.5 _ — = Cu 88, Sn 10, Pb 2 21.1 to] 19,000 to] 30,000 to} 20.0 to} 26.0 to|65 to 24.6 |23,000 |35,000 |15.0 |18.0 {70 Cu 80, Sn 10, Pb 10 { Cast, sand. |8. 22.1 |15,500 |31,400 |13.5 |I2.0 163 Cast, chill.. 24.7. |18,200 {35,200 4.5 3.5 {85 Lead, Phosphor: Cu 80, Sn to, Pb 1o, P trace : 21.0 |16,000 |30,000 6.0 Sa | ey Lead Zinc, Red brass: : 18.8 |19,600 |26,800 |1ro {|II.5 — Cu 81, Sn 7, Pho, Zn3 | z 21.1 to] 19,000 to] 30,000 to} 18.0 to] 24.0 to}50 to 24.6 |20,000 |35,000 |1I5.0 |22.0 |55 Cu 88, Sn 8, Pb 2, Zn 2 Piesy Calls = 31,000 to}20.0to} — {57 to 26.0 37,000 |16.0 59 Lead, Zinc Phosphor: Cu 73.2, Sn 11.3, Pb 12.0, 2ni2-5 bt seaete 10.5 |21.4 |15,000 |30,400 4.0 3.3 Manganese: Cu 88, Sn ro, Mn 2 9.0 |19.1 |12,800 |27,200 |25.0 _ Nickel, Zinc: Cu 88,Sns5, Nis, Zn2(1)...} Cast 9.2 |28.6 |13,100 |40,700 |32.0 {28.0 Cu 89, Sn 4, Nig, Zn 3 (2)...| Cast 8.1 |27.9 |11,500 |39,700 |31.0 |31.0 Phosphor: Gatos; Snia-On bok cee ee i 28.0 |46.0 |40,000 |65,000 |30.0 _ Cwi8o"Snit0:5) Pos... 22s ee II.2 to}21.8 to] 16,000 to| 31,000 to] 6.0to} — CulSos%SnizosPimaxur cee sratets I4.I |24.6 |20,000 |35,000 |10.0 Rods and bars §§ up to 12.7 AMG (Fane) reese 42.2\|||||56.2 |60,000 {80,000 |12.0 |Required to (minimum) over 12.7 mm bend cold to 25.4 mm (1 in.)..... 28.1|||||42.2 |40,000]||||60,000 | 20.0 through 120° Over 25.4 mm (I in.)..... 21.1|||||38.7 |30,000]||||55,000 |25.0 about radi- Sheets and plates §§ spring us equal to — 163.2 90,0 a thickness. Medium temper 17.6|||||35.2 |25,000|||||50,000 25.0 e Bronze, Phosphor: spring wir2, hard-drawn or hard-rolled (U. S. Navy Spec. 22 Ws, Dec. 1, 1915). Cuoggq, Sn min. 4.5, Zn max 0.3, Fe max. 0.1, Pb max. 0.2, P 0.05 to 0.50; max. elong. in 203 mm (8 in.) = 4 per cent. Min. tensile Diameter Min. tensile Diameter (group limits). strength. (group limits). strength. kg/mm? Ib/in? mm in. kg/mm? Ib/in? Up to 1.59 mm or 0.0625 in : 3 135,000 to 6.35 to 0.250 aI II0,0co Over 1.59 mm to 3.17 mm (0.125 in.).. : 125,000 to9.52 to 0.375 74.0 105,000 * Specification Values, Rolled Brass, Cu 62, Zn 37,Sn1, min. properties after U. S. Navy Spec., ror8. | + Specification Values: Jan. 3, 1916, Vanadium Bronze Castings, Cu 61, Zn 38, Sn max. 1 (incl. V). Mimima. t Compressive P-limit 15.5 kg/mm? or 22,000 lb/in? § Compressive P-limit 10.5 kg/mm? or 15,000 lb/in? and 28 per cent set for 70 kg/mm? or 100,000 lb/in? || Ultimate compressive strength, 54.2 kg/mm? or 77,100 lb/in? (Cu 76, Sn 7, Pb 13, Zn 4). {| Compressive P-limit 8.8 to 9.1 kg/mm? or 12,500 to 13,000 Ib/in?, and 34 to 35 per cent set for 70 kg/mm? ** Compression: ultimate strength 49.5 kg/mm? or 70,500 |b/in? +t Modulus of Elasticity: (1) 12,200 kg/mm? or 17,300,000 lb/in?; (2) 10,500 kg/mm? or 14,900,000 lb/in? tt Compressive P-limit 17.6 to 28.1 kg/mm? or 25,000 to 40,000 lb/in? and 6 to 1o per cent set for 70 kg/mm? or 100,000 lb/in? load. Specification Values: U. S. Navy 46 B sc, Mar. 1, 1917, Cu 85 to 90, Sn 6 to 11, Zn max. 4: Cast, Grade 1. — Im- purities max. 0.8; min. tensile strength 31.6 kg/mm? or 45,000 lb/in? with 20 per cent elong. in 50.8 mm (2 in.). 4 Grade 2.— Impurities max. 1.6; min. tensile strength 21.1 kg/mm? or 30,000 |b/in? with 15 per cent elong. in 50.8 mm (2 in.). , §§ Specification Values: U. S. Navy 46B 14b, Mar. 1, 1916, Cu min. 94, Sn min. 3.5, P 0.50, rolled or drawn. ||| Minimum yield points specified: for P-limits assume 66 per cent of values shown. SMITHSONIAN TABLES. TABLE 69 (concluded) 123 MECHANICAL PROPERTIES Copper Alloys — Three (or more) Components >o 24 Secu eSeel sire 2S = E & 2 ad woe! 3S | Hardness. Alloy and approx oe fee a ae 83.9 E 2 an : =3 Hs I268 j composition. Condition. Aly a |e im Pa jaw | & ©. |. er cent. a ov F se a Tension, ee Per cent 29 3 3 pe pe | ke/mm? Ib/in® ( | Eola & Bronze: Silicone see tec eesteteione @astiesies ace —}—]| — 146.0 _ 65,000 — — —|— Cu 70, Zn 29.5, Sio.5..|Drawn, hard..} —}| — | — 174.0 = 105,000 —_ —_ — |— “inc *|Comp) (G77. 0. .||Cast..<: 2. -11 8.6 | 535| 8.6 |27.4 |12,200 38,900 25.0 |2I.0 64 13 Admiralty gun metal. .|Castt.........| — | — | 5-6 to}22.5 to] 8,000 to] 32,000 to}25.0 to}25.0 to] 65 tojro to Comm’c’l range... . . 8.4 |26.7 |12,c00 38,000 |10.0 |12.0 75 |20 Spec. values.......... Cast (mins.):-\.|/— | — | = {21-1 = 30,000 |14.0 — == | GimesnSnis, Zn ase | Castine. st: 8.5 |530 | 7-7 |27-5 |11,000 39,200. |30.5 |24.0 58 II Cu 85,Sn13,Zn2..... Castatece —|—] — |26.7 —_ 38,000 |2.5 es — |25 Ane UCAS facies as jorexs Cugo,Sn6.5,Zn2,Pbr.5|Cast §........ — | — | 8.4 to}23.9 to]12,000 to] 34,000 to}33.0 to|34.0 to} 50 to} — Rods and bars || up to 11.2 |28.1 |16,000 40,000 |25.0 |26.0 | 60 12.7 mm (} in.)..... — | — }]28.1 {56.2 |40,000 80,000 |30.0 |Required to bend Over 12.7 mm to 25.4 cold through MITIUN (KIN) taper cheeky — | — }j26.4 |52.7 |37,500 75,000 |30.0 120° about ra- over 25.4 mm (rin.).. — | — }24.6 {50.7 |35,000 72,000 30.0 dius equal to Shapes,|| all thicknesses —} — |26.4 {52.7 137,500 75,000 |30.0 thickness. Sheets and plates,||o to 12.7 mm (4 in.)..... — | — }27.4 |54.8 |309,000f] | 78,000 30.0 ee over 12.7 mm (#in.).. — | — |26.4 |52.7 137,500 75,000 |30.0 os AluminumTin: Cu 88.5, Al 10.4, Sn 1.2/Cast, chill....] — | — |26.0 |48.0 |36,700 68,000 4.5 5.5 |189 |32 Aluminum Titanium: Gast¥e aca. — | — |13.9 |52.0 |19,800 74,000 |19.5 |23.7 |100 |25 Wugo Altos... 042%: Quench, 800° C....] — | — }29.0 |74.0 |40,500 |105,200 1.0 0.8 |262 —_ Cu 89, Alro, Fer..... Gast iilencsese 7.58] 473 |14.1 to]45.7 to] 20,000 to] 65,000 to}30.0 to}30.0 to} 93 to}25 to 17.6 |56.2 |25,000 80,000 |20.0 |20.0 |100 |26 Lead: Cu 71.9, Pb 27.5, Sn.o.5|Cast......... —|]—] — | 4.2to _— 6,000 to] 3.0to} 4.2to] — | — 4.6 6,600 3.2 6.7 Nickel, Aluminum: Cu 82.1, Ni14.6, Al 2.5, INOW REE tSefentes ne Forged... ....- —]|— |44.5 90.0 |63,300 |128,000 |10.0 |12.0 — |—- Cu 8s5,Sn5,Zn5, Pbs5.|Cast §§....... — | — |10.5 to]19.0 to|/15,000 to} 27,000 to}20.0 to] 20.0 to] soto} — : 13.4 |23.2 |19,000 33,000 |16.0 |15.0 62 Gis3:Snit4yZni2, bbit|Gast. en. 2 — | — |ro.5 to]16.2 to|/15,000 to} 23,000 to} 4.0 to] 4.0to} — |20 13.4 |19.0 |19,000 27,000 0.5 0.5 — |24 Zinc, Phosphor (‘* Non Gran’’) Cms6, Snir, 20.3, Ptr.| Casts... < — | — |13.0 |25.0 |19,000 35,000 9.0 — — |—- Vanadium, See Brass, ; Vanadium. Copper, Aluminum or Aluminum Bronze: GiigovAlito wes. tsa Cast, sand || ||.]7-5—| 468-|13-.9 to]51.1 to}19,800 to] 72,700 to} 28.8 to} 30.0 to}102 to}25 to 7.45|465 |23.3 |60.0 |33,200 85,500 21.7 |22.4 |106 |26 @wi92:5,Al-7.2.....4..- Rolled, andj — | — | 7.0 137-5 9,600 53,500 |9I.0 |72.9 81 |19 ann. Aluminum, Iron or Sill-|Wrought..... —}]—1] 09.8 1}59.3 |14,000 84,400 |II.5 — — | — man bronze........ Castanos, —|—] 8.1 [55.5 |11,500 78,850 |14.5 — — |— Cu 86.4, Alg.7, Fe3.9..|_ Cast, sand..| — | — ]14.0 |54.0 |20,000 77,000 |24.5 |25.0 |I00 — Quenched 850° C Cu 88.5, Al 10.5, Fe 1.0. drawn 700° C....]| — | — ]|28.0 |65.0 |40,000 92,000 |14.0 |18.5 |140 — * Gov’t. Bronze: Cu 88, Sn 10, Zn 2 (values shown are averages for 30 specimens from five foundries tested at the Bureau of Standards). + Compressive P-limit 10.5 kg/mm? or 15,000 lb/in? with 29 per cent set for 70 kg/mm? or 100,000 lb/in? load. t Values from same series of tests as first values for ‘‘ 88—10-2,” averages for 26 specimens from five foundries tested at Bureau of Standards. ; Compressive P-limit 9.1 kg/mm? or 13,000 lb/in® with 34 per cent set for 70 kg/mm? or 100,000 |b/in? load. | Specification minimums: U. S. Navy 46B17, Dec. 2, 1918, for hot-rolled aluminum bronze, Cu 85 to 87, Al 7 to 9, Fe2.5 to 4.5. Specification values under P-limit are for yield point. Two and six tenths per cent increase in strength up to 762 mm (3o in.) width. \ 4) Compressive P-limit: cast, 14.1 kg/mm? or 20,000 Ib/in? with 11.4 per cent set at 70 kg/mm? or 100,000 |b/in? oad. +t Compressive P-limit: cast, 12.7 to 14.1 kg/mm? or 18,000 to 20,000 Ib/in? with 13 to 15 per cent set at 700 kg/mm? or 100,000 |b/in? load. tt Modulus of elasticity 14,800 kg/mm? or 21,150,000 lb/in? - Compressive P-limit 8.4 kg/mm? or 12,000 lb/in? with 36 per cent set for 70.3 kg/mm?, or 100,000 lb/in? load. ||| High values are after Jean Escard ‘‘ L’Aluminum dans L’Industrie,” Paris, 1918. Compressive P-limit 13.5 g/mm? or 19,200 lb/in? with 13.5 per cent set for 70.3 kg/mm? or 100,000 |b/in® load. SMITHSONIAN TABLE3. 124 TABLE 70 MECHANICAL PROPERTIES Miscellaneous Metals and Alloys Density or weight. Ultimate strength. Metal or alloy. Approx. composition, Condition. per cent. peat han seeot gm | lb. per | per cm3 | ft§ * Cobalt, Co gg. 8.8 | 550 0 99.7 8.9 | 556 Gold, Au 100 19.3 1203 Copper, Au go, Curo.... 17.2 |1073 Copper, Silver, Au 58, Cu 30 Ag 12 Drawn hard.....| — Lead, Pbt Cast 11.38] 710 Rolled hard 11.40] 711 (CommiciS) Peer oeeree = |= Antimony tPb95.5,Sb4.5 Magnesium, Mg { Drawn hard..... nN lol] J II 655 4 Coe alta NOUIIH aS on HO on ele tales? calla es leslealis Wrought, ann.... Wrought, com. Rolled hard, “ Rolled ann. ‘“ Drawn hard, D = mm | Heeltecs| lett al elie lees Viele ecw lle leet |rean| ele ellie 76,000]35.0 155,000) — Copper, iron, manganese or Monel metal: : 3 : : 70,000]18.0 Ni 67, Cu 28, Fe3, Mn2. : j 104,900|31.3 Ni 66, Cu 28, Fe3.5,Mn| Wrought........ : : 92,200] 46.3 2.5 Ni71, Cu 27, Fe2§ Drawn hard 3 160,000] — 46 Mia || Se eae ) Rolled, min., rods 46 M 7b! and bars J... . Rolled, mini- mum, sheets and plates... .. : 65,000|15.0 § |Palladium, Pd Drawn hard 39,000] — Platinum, Pt Drawn hard 53,000]18.0 Drawn ann 35,000]50.0 40,000} — 51,200] — 109,500] — 130,000] — 4,000|35.0 5,300 a 10,000); — Silver, Ag too. 4). ome ek (pen hae Copper, Ag 75,Cu2s5....| Drawn hard Tantalum, Ta Drawn hard Tin, Sn 99.8tt | Antimony, Copper, Zinc (Britannia Metal): Sn 81, Sb 16, Cu 2, Znt. Zinc, Aluminum, etc. (aluminum solder): Sn 63, Zn 18, Al 13, Cu 3, Sb 2, Phr : 14,500] 1.9 Sn 62, Zn 15, Al 11, Pb 8, Cu3, Sb1 : 13,000] 1.6 Zinc, aluminum: Sn 86, Zn g, Al 5 4 12,200|41.0 Aluminum, zinc, cad- mium: Sn 78, Alo, Zn 8, Cds. ; | 14,300]18.0 FLAS TI a Ve less) teal io tale lea LlolIS lax] | | | Antimony: Modulus of Elasticity 7960 kg/mmz2 or 11,320,000 lb/in? (Bridgman). * Compressive strength: cast and annealed, 86.0 kg/mm2 or 122,000 Ib/in? , Leek: Comm’c’l. comp., C 0.06, cast, tensile, ultimate, 42.8 kg/mm? or 61,000 lb/in?, with 20 per cent elongation in 50.8 or 2 in. Compression, ultimate 123.0 kg/mm? or 175,000 lb/in? : 3 Stellite, Co 59.5, Mo 22.5, Cr 10.8, Fe 3.1, Mn 2.0, Co.9, Sio.8. Brinell hardness 512 at 3000 kg, density 8.3 : +t Modulus of elasticity, cast or rolled, 492 kg/mm? or 700,000 Ib/in?; drawn hard 703 kg/mm? or 1,000,000 Ib/in t For compressive test data on lead-base babbitt metal, see table following zinc. § Modulus of elasticity 15,800 kg/mm? or 22,500,000 Ib/in? , eee values, U. S. Navy, Monel metal, Ni min. 60, Cu min. 23, Fe max. 3.5, Mn max. 3.5, C + Si max. 0.8, max. 0.5. , ‘| Values shown are subject to slight modifications dependent on shapes and thicknesses. ** Values are for yield point. tt Compressive strength: cast, 4.5 kg/mm? or 6,400 lb/in? ‘ Modulus of elasticity: cast av. 2,810 kg/mm? or 4,000,000 Ib/in?; rolled av. go1.0 kg/mm? or 5,700,000 Ib/in? SMITHSONIAN TABLES. TABLE 71 126 MECHANICAL PROPERTIES Miscellaneous Metals and Alloys (a) TUNGSTEN AND ZINC | Density Hardness. Metal or or weight. alloy f; approx. Condition. comp. per cent. : ae Per cent Ultimate strength P-limit. Ultimate strength Brinell @ 500 kg ( Ingot sintered, D = 5.7 mmoro.22 in. : E207 18,000 Swaged rod, D =0.7 mmoro.o3 in. 151.0 215,000 Drawn hard, D = 0.029 0.00114 in 415.0 590,000 Swaged and drawn hot 97-5% reductionf.. . 164.0 233,500 Same as above and equiaxed at 2000°C i 118.0 168,000 (Impurities Pb, Fe and Cd) Coarse crystalline... .. 2.8to| — 4,000 to Fine crystalline 8.4 12,000 Rolled (with grain or direction of rolling). d i 27,000 Rolled (across grain or direction of rolling) . E a 36,000 Drawn hard ; x 10,000 * Commercial composition for incandescent electric lamp filaments containing thoria (ThO2) approx. 0.75 per cent after Z Jeffries Am. Inst. Min. Eng. Bulletin 138, June, 1918. + Alter Z Jeffries Am. Inst. Min. Eng. Bulletin 149, May, roro. ¢ Ordinary annealing treatment makes W brittle, and severe working, below recrystallization or equiaxing tempera- ture, produces ductility W rods which have been worked and recrystallized are stronger than sintered rods. The equiaxing temperature of worked tungsten, with a 5-min. exposure, varies from 2200° C fora work rod with 24 per cent reduction, to 1350° C tor a fine wire with roo per cent reduction. Tungsten wire, D = 0.635 mm or 0.025 in. § Compression on cylinder 25.4 mm (x in.) by 65.1 mm (2.6 in.), at 20 per cent deformation: For spelter (cast zinc) free from Cd, av. 17.2 kg/mm? or 24,500 lb/in? For spelter with Cd 0.26, av. 27.4 kg/mm? or 39,000 lb/in? (See Proc. A. S. T. M., Vol. 13, pl. 19.) Modulus of rupture averages twice the corresponding tensile strength. Shearing strength: rolled, averages 13.6 kg/mm? or 194,000 lb/in? Modulus of elasticity: cast, 7,750 kg/mm? or 11,025,000 |b/in? Modulus of elasticity. rolled, 8450 kg/mm? or 12,000 000 Ib/in? (Moore, Bulletin 52, Eng. Exp. Sta. Univ. of Ill.) (6) Waite Metat BEeaArinc AtLoys (BABBITT METAL) A. S. T. M. vol. xviii, I, p. 491. Experimental permanent deformation values from compression tests on cylinders 31.8 mm (r} in.) diam. by 63.5 mm (23 in.) long, tested at 21°C (70° F.) (Set readings after removing loads.) Permanent deformation @ 21° C Hardness. Formula, , pS Se per cent. : @ 454kg @ 2268kg | @ 4536kg = = 1000 |b. = 10,000 lb. kg @ 500 @ too" C 0.000] 0.0000] 0.025 .000] .0000] .038] .0o15 .025| .OoIo] . -0045 .013] .0005 .0025 .025| .OOIO] . «0030 HU tb Qo COoO~1 SI C—O .038] . 3 «0050 <025] =. A .0050] .583 deen On405|tOn52) | 205 ulmsnEs 740 | 6.30 | 0.76] 1.95 | 2.40 | 0.42 | 0.84 | 0.42 | 365 1% (Nyssa aquatica) Gumitined er ncccocssrsitestnae 0.44 | 0.53 | 2.60 | 4.890 810 | 7.05 | 0.84] 1.70 | 1.95 | 0.32 | 0.75 | 0.36 | 285 || (Liquidambar styraciflua) Enickory;pecan nice aes 0.60 | 0.69 | 3.65 | 6.90 960 | 8.65 | 1-35 | 2.15 | 2.80] 0.63] r.04 | 0.48 | 57501 (Hicoria pecan) Hickory, shagbark........ 0.64 — 4.15 || 7.75'| pros |ro.r0 | 1.88)! 2.40 °|| 3.20 | 10.70 | (0.93 — —_— (Hicoria ovata) Holly. American as. -se1 oe 550] 0.6%, || 2.40) || 4.55 630 | 6.25 | 1.30] 1.40 | 1.85 | 0.43 | 0.80 | 0.43 | 30971mm (Ilex opaca) Laurel, mountain......... 0.62 | 0.74 | 4.10 | 5.90 650 | 7.20] 0.81 — 3.00 | 0.78} 1.18 —_— 635 | | (Kalmia latifolia) ocustyblackenemnnenn cer 0.65] 0.71 | 6.20 | 9.70 | 1300 |12.90 | 1.12 | 4.40 | 4.89] 1.01 | 1.24 | 0.54 | 7400Kmm (Robinia pseudacacia) Locust; honey2. «+... ee ce 0.69 | 0.67 | 3.95 | 7.20 910 | 8.30 | £.20 | 2.35 || 3.r0'| T.09 | 1.27 | 0.66 | 655mm (Gleditsia triacanthos) Magnolia (evergreen)......| 0.46 | 0.53 | 2.55 | 4.80 780 | 6.20 | 1.37 | I.55 | I.90 | 0.40] 0.73 | 0.43 | 3550/mm i eaealie foetida) Mapletsilveriia.cia.cic6 & | &3 | 54 ee Pe eam lise | Peja lan |e AE ——— — eta 3 50 | | 1 2 3 4 5 6 7 8 9 11 13 14 15 Cedar, incense.......... Cal. and Ore.| 108 45 24. | 3900 | 6200] 840 7300 2870 | 460] 830 | 280 (Libocedrus decurrens) Cedar, Port Orford een Ore. 52 39 31 3900 6800 | 1500 9300 3970 380 880 | 240 | (Chamaecyparis law- \ soniana) Cedar, western red...... Wash. and 39 27 23. | 3300 | 5200] gso] 7100 2500 | 310 | 720 | 210 (Thuja plicata) Mont ieedar; white.......-..- Wis. 55 28 21 2600 4200 640 5300 1420 290 620 | 240 (Thuja occidentalis) isypress, bald: 2. ss... La. and Mo. 87 48 30 | 4000 | 6800} 1190 | 8000 3100 470 | 820 | 280 . pecan distichum) 5 a REAM AILS ©. 3 c.c)wlcrelereie'= re. an Io2 47 27 3900 6300 00 800 2380 20 670 | 240 (Abies amabilis) Wash : g 2 d Z 3 f ; Bi DAISAM 5, «-1-1- veins Wis. 117 45 25 3000 | 4900 | 960] 6900 2220 210 | 610 | 180 | (Abies halsamea) Bar PYOULIaS (L)). s.)<.100 Wash. and 36 38 34 5000 7800 | 1580 9400 3400 530 gio | 200 (Pseudotsuga taxifolia) Ore. nics Douglas) (2)... 2... Mont. and 38 34 32 3600 6400 | 1180 gIoo 2520 450 880 | 350 (Pseudotsuga taxifolia) Wyo. BE ETANG ena ie clots, s,sieie's Mont. and 94 44 27 3600 6100 | 1300 8100 2680 340 700 | 230 (Abies grandis) Ore | BA NODLE ve, 4.341at + 3.460B* + 3.7717! + 2 (3.879877? + 2.85677a" + 2.39078?) 10 a = 14.88at + 16.548! + 16.4574 + 30.8987? + 40.8977" + 43-5147B? Quartz. 10 a = 12.734 (I— 7”)? + 16.693 (1 — y”)y? + 9.7057 — 8.460By (3a — B?) “a = 19.665 -F 9.06072" + 22.9841? — 16.920 [(yBit B71) (3401 — BBi) — B2y2)] * These formule are taken from Voigt's papers (Wied. Ann. vols. 31, 34, and 35). SMITHSONIAN TABLES. TABLE 87 139 ELASTICITY OF CRYSTALS Some particular values of the Elastic Moduli are here given. Under E are given moduli for extension or compression in the directions indicated by the subscripts and explained in the notes, and under T the moduli for torsional rigidities round the axes similarly indicated. Moduli in grants per sq. cm. (z) ISOMETRIC SYSTEM * Substance. E, E, BE, rT. Authority. Bluontes 0. 2.) €473 cro | To0s x 10° gto X 108 345 X 108 | Voigt.t EY TILC Me Mare etme (SSGODeL Oo | 2530 Ot 23 TOD GIO mmo 75 >< 108 Rockisalt. 2 = |) 419 xX 108 349 X 108 303 X 108 129 X 108 Rie Ee ado aoe 339 X 108 — = Koch. SVIVILCe een eA OlOeIOe 209 X 10° — — < < he ed temas 2 X 108 196 X 108 ~~ 655 X 10° | Voigt. Sodium chlorate. Boe XS1o2 Ab x 108 — ae ens | Potassium alum. , 181 X 108 199 X 108 — — Beckenkamp.§ Chromium alum. 161 X 10° 177 X 108 = _ “ Txonialumile sue es 186 X 108 (4) ORTHORHOMBIC SYSTEM || Substance. E, E, | Es | Ey | E; Es Authority. 376 X 10°} 702 X 108| 740 X 108] Voigt. 2670 X 10° | 2893 X 10° | 3180 X 108 as | Barite .| 620 X 108 ge X 108} 959 X 108 | Topaz . | 2304 X 10°| 2890 X 10°] 2652 X 108 Substance. Ty.=To T,3=Ts1 To3 = T30 Authority. WBaritel™ jo 8s Meters oie ots 283 X 108 293 X 108 I2I X10 | Voigt. MapaZzcme panne mrt n io ac 1330 X 108 1353 X 108 1104 X 108 se In the MONOCLINIC SySTEM, Coromilas (Zeit. fiir Kryst. vol. 1) gives { Enax = 887 X 108 at 21.9° to the principal axis. nine — U3 aloe ate7 os > eC ee cu: { Emax == 2213 X 108 in the principal axis. Emin = 1554 X 108 at 45° to the principal axis. Gypsum Mica In the HEXAGONAL SYSTEM, Voigt gives measurements on a beryl crystal (emerald). The subscripts indicate inclination in degrees of the axis of stress to the principal axis of the crystal. Bij — 2165 >< 10°, Eus——1790><10, ton — 2312 “10% To = 667 X 108, Too = 883 X 10°. The smallest cross dimension of the prism experimented on (see Table 86), was in the principal axis for this last case. In the RHOMBOHEDRAL SYSTEM, Voigt has measured quartz. The subscripts have the same meaning as in the hexagonal system. E9= 1030 X 105, E_45;=1305 X 10°, Eas; 650 x 10%, Eao— 785 x 108, Wins Fe SK WY, Wy = SHS So. Baumgarten § gives for calcite : Ej— 5o1-oi1e. B= 4 — 441 X 10%, he — 772 < 10°, tog — 790 xX 10° * In this system the subscript 2 indicates that compression or extension takes place along the crystalline axis, and distortion round the axis. The subscripts 6 and ¢ correspond to directions equally inclined to two and normal to the third and equally inclined to all three axes respectively. + Voigt, ‘‘ Wied. Ann.” 31, p. 474, Pp. 701, 18873 34, P- 981, 1888; 36, p. 642, 1888 + Koch, ‘* Wied. Ann.” 18, p. 325, 1882. § Beckenkamp, ‘“‘ Zeit. fiir Kryst.’’ vol. 10. || ‘he subscripts 1, 2, 3 indicate that the three principal axes are the axes of stress; 4, 5,6 that the axes of stress are in the three principal planes at angles of 45° to the corresponding axes. {| Baumgarten, ‘‘ Pogg. Ann.” 152, p. 369, 1879. SMITHSONIAN TABLES. 7 140 TABLES 88-90 MECHANICAL PROPERTIES OF SOME SINGLE METAL CRYSTALS (BRIDGMAN) All the following metals have an axis of rotational symmetry: Zn and Cd have a 6-fold axis (hexagonal system); Bi, Sb, Te, 3-fold, trigonal; Sn, 4-fold, tetragonal. The rotational axis is taken as the datum line. The notation of Voigt is used (Lehrbuch der Kristallphysik, Berlin, 1910). Bridgman, Proc. Amer. Acad. Arts and Sci., 60, 305, 1925. TABLE. 88.—Elastic Constants, Abs. c.g.s. units Constant Zn Su Sezai NO Siz +0.34 513 —6.64 533 26.38 544 25-0 VY See S11-Si2 S14 Oo 12.98 X 10%) — 5.32 X 10°2p? 1.946 15.92 6.450 16.48 5.256 — 4.137 27.48 6.719 6.022 (V/V); Pressure kg/cm? ROVS7, XO pe 29.17 26.99 50.82 18.76 3.18 SMITHSONIAN TABLES Cd Bi Sb Te Sn Ww 12.9 X 2 OI
  • is no longer true. In Table 92 4 273.1/T } pv is given as a function of the pressure. This quantity 4 273.1/T | pv is called the factor (F). Consider the 0°C isothermals. They are taken on the basis of pv at o°C and I atm. as unity. The factor for any pressure given by the table will represent the ratio of the value of pv at this pressure to the value of pv at 1 atmosphere; that is, (pv) n/ (pv)s = Fn where Fn is the factor for n atmospheres. This relation, of course, holds for all pressures, therefore, vm = vn} PnFm/PmFn |. The corrections are made as though the substance behaved as a perfect gas, and the result multiplied by the ratio of the factor at the desired pressure to the factor at the measured pressure. SMITHSONIAN TABLES 142 TABLES 92 AND 93 TABLE 92.—Values of Factor F = (273.1/T) pv. (See p. 141) v =I at I atm. pressure, 0° C Air: Holborn, Schultze, 1915 Argon: Holborn, Schultze, 1915 One 50°C 100°C 200°C o°C 50°C =100°C 200°C o°C -9950 .9995 1.0019 1.0059 -9919 .9971 .9998 1.0021 1.0043 .9875 .9985 1.0042 1.0082 -9782 .9916 .9982 1.0042 1.0117 .9780 .9994 1.0098 1.0175 -9575 -9840 .9969 1.0082 1.0233 .9720 1.002 1.0189 1.0275 -940I .9781 .9969 1.0136 1.0356 -9710 1.0075 1.0251 1.0380 .9260 .9744 .9988 1.0195 (1.0490) Helium: Holborn, Otto, 1922 Hydrogen: Holborn, 1920 Oxygen: Holborn, Otto, 1922 o°C 50°C 100°C o°C 50°C o°C 20-G) 50-@ | 100.6 1.0048 1.0040 1.0033 | I.0055 1.0055 1.0045 | .9915 .9940 .9972 1.0000 1.0127 I.0106 1.0090 | 1.0150 1.0136 1.0122 | .9778 .9842 .9915 .9987 1.0258 1.0216 1.0183 | I.03I1I 1.0280 1.0248 | .9569 .9692 .9838 .9975 1.0390 1.0327 1.0277 | 1.0475 1.0422 1.0375 | .9385 9778 .9978 1.0522 1.0438 1.0370 | 1.0640 1.0565 1.0500 | .9238 .... .9740 .9990 Nitrogen Mean tf Methane: Keyes, Smith, Joubert 0°C SOG 100°C arG s0°@ x008G, 200°C *Onnes, Crommelin, 1915. we a + Holborn, Otto, 1922, .996 1.000 1.002 .978 .989 .993 .999 Srey Daylomee as: .982 1.002 I1.OII <093 .941) 971. §.007 .982 1.013 1.028 781 .896 .951 .998 1.000 1.037 1.053 (.730) .873 .943 1.004 eee OG 7A OS2 sae -973) 6950) -1-020 TABLE 93.—Relative Gas Volumes at Various Pressures (Deduced by Cochrane, from the pv curves of Amagat and other observers) Relative volumes when the pressure is reduced from the value given at the head of the column to 1 atmosphere; see also Bur. Standards Circ. 279: Relative volume which the gas will occupy when the pressure . Gas is reduced to atmospheric from (Temp. = 16°C) Iatm. 50atm. 100 atm. 120 atm. 150 atm. 200 atm. “‘Perfect”’ gas 50 100 120 150 200 94.6 112.5 141 ty drogentmmeric steele 48.5 93.6 I11.3 136.3 176.4 Nitrogen 50.5 100.6 120.0 147.6 190.8 Air 50.9 101.8 121.9 150.3 194.8 ye Reus 106.3 127.6 161 aie 105.2 Bete Nets Oxygen (at 0°C) : 107.9 128.6 161.9 218.8 Carbon dioxide Ap 485* 498* 515* 212.6 * Carbon dioxide is liquid at pressures greater than 90 atmospheres. SMITHSONIAN TABLES TABLE 94 143 CORRECTING FACTORS: SATURATED GAS VOLUME TO VOLUME AT 760 MM HG AND O°C [Multiply observed volumes of saturated gas by factor to correct to volume of dry gas at 760 mm of mercury pressure (0°C) and o°C] (Abridged from Bur. Standards Circ. 279) Pressure mm of Hg. 725 730 735 740 745 0.935 0.942 0.948 0.954 924 .931 -937 -944 .950 920 .927 .933 -940 .946 -QLOe) .923))) 929) -936) .942 919.925.932.938 O08 1:9D5)) -921. 2928), +934 [QOAWI OI) -OL7, © -9245) .920 -900) .907)) 913)" -919) 925 “390% 902), 909) = -O15) 921 899 .905 .QII .QI7 895 .9OI1 .907 .QI3 .890 .896 .903 .909 886 .892 .898 .905 .882 .888 .894 .900 878 .884 .890 .896 : 7379) 2800) = 869 .875 .881 .887 POOR EST MS 77m EeOOs ESOOM SOO G72) move .856 .862 .868 : LOST OOS 847 .853 .859 .865 842 .848 .854 837.843 .849 838 .844 .850 : .833 .840 .823 .829 .835 .840 SOLS.) O23) O30) S835 POlZ) OLS 1-o240 S30 SOLsi CLOW O25 [SOG : so02): 814 797 - .809 27.0) eae -803 -785 5780) =: ; 7 Ae es -786 P7OSsen -779 702s Ts SMITHSONIAN TABLES 144 TABLES 95 AND 96 COMPRESSIBILITY OF GASES TABLE 95.—Compressibility at Ordinary Temperatures As a measure of the compressibility, it is customary to use a coefficient, I + A = Poo/ Pith, Po, Yo being at o°C I + A = 0.99939 + 0.00001 1.00044 0.00001 1.00094 0.000013 0.99948 0.000005 0.99951 0.000025 1.00099 0.000026 Wild, Philos. Mag., 12, 49, 1931 Rayleigh, Z. Phys. Chem., 52, 705, 1905 TABLE 96.—Compressibility at Low Temperatures pv = 1 for 0°, 1 atmosphere Table 96a.—Helium Table 96b.—Hydrogen Pp po Density tae p po Density atm. atm. 26.66 1.0146 26.28 0.00 32.313 1.0188 31.715 38.95 1.0196 38.20 Soa SrTG 1.0266 43.284 58.58 1.0294 56.91 —103.57 38.41 -6376 38.41 24.13 -6337 38.07 58 51.49 -6433 80.04 49.96 -6479 77.08 —204.70 16.75 -2404 69.68 .232 .O1I26 =20.63 M 37.00 .2316 159.7 353 -OI104I 33.92 pia 44.63 -2300 194.0 .0308 -OO9QII 3.381 — 257.26 .06698 .05783 1.1582 .0649 .00858 7.535 S1ZU53) O57 1O4N me B03 Bocke, Onnes, 1924 Nighoff, masa eg eo az a 1903; Table 96c.—Neon Table 96d.—Argon Pp po Density Pp po Density atm. atm. 23.06 1.0089 21.87 : 20.58 -9856 20.88 39.79 1.0147 30.34 31.57 -9774 32.30 84.66 1.0408 81.35 14.86 -5813 25.57 61.66 -2337 763.8 45-09 -4706 95.80 79.92 -2293 348.6 62.24 -3939 158.01 49-93 -1393 358-5 12.77 -4663 27-39 64.97 -1269 511.8 11.99 -4262 28.12 79.42 1256 632.2 I1.15 3821 29.18 Onnes, Crommelin, 1915 Onnes, Crommelin, I910 Table 96¢.—Oxygen Table 96f.—Nitrogen AC en pv Density a po Density oO 20.92 9813 21.32 33.14 .9886 33.52 66 49.79 9573 52.01 43.08 -9860 43-70 — 80.03 21.01 -6550 32.09 58.63 -9834 » 59.62 + 34.18 -6213 55.02 30.17 -6516 46.13 s 61.88 -5464 13.23 45-47 -6270 72.52 —116.01 22.30 -4835 46.12 56.71 -6109 92.84 - 43-95 -3541 124.1 22.92 -3340 68.62 55-05 -1667 330.2 30.14 .2656 113.48 36.49 1058 = 344-5 Onnes, Kuypers, 1923, 1924 Onnes, Van Urk, 1924 6c SMITHSONIAN TABLES TABLES 97-99 145 COMPRESSIBILITY OF GASES TABLE 97.—O, Air, N, and H. Relative Volumes at Various Pressures and Temperatures, the volumes at O°C and at 1 atmosphere being taken as 1 000 000 Nitrogen. Amagat: C. R. 111, p, 871, 1890; Ann. chim. phys. (6) 29, pp. 68 and 505, 1893. TABLE 98.—Ethylene po at o°C and i atm. = I Amagat, C, R. 111, p. 871, 1890; 116, p. 946, 1893. TABLE 99.—Carbon Dioxide Pressure in Relative values of po at— meters of mercury liquid 625 825 1020 1210 1405 1590 1770 1950 2135 Amagat, C. R. 111, p. 871, 1890; Ann. chim. phys. (5) 22, p. 353, 1881; (6) 29, pp. 68 and 405, 1893. SMITHSONIAN TABLES 146 TABLE 100 COMPRESSIBILITY OF GASES TABLE 100.—Some Physical Properties of Compressed Nitrogen (Abridged from Deming, Shupe, Phys. Rev., 37, 639, 1931; based on data by Bartlett and collaborators, Journ. Amer. Chem. Soc., 1927-31.) Tables published by Bartlett et al show compressibility factors po/(pv)s at the different pressures and tem- peratures. The denominator (pv); is the value of pv at S.T.P. In order to find the specific volume of the gas it is required to know the volume of 1 g at S.T.P. Birge gives 22414.1 cc as the volume of a mole of an ideal gas at S.T.P po/(po)s at I atm. is close to 1/1.00046. The gas used by Bartlett contained 0.9993 nitrogen and 0.0007 inert gas, presumably argon; the apparent molecular weight is therefore taken as 28.025. The volume adopted for I gat S.T.P. is 22414.1/1.00046 X 28.025 = 799.42 cc, and the value of RT at 0° is 22414.1/28.025 = 700.70 cc atm./g. When one of Bartlett’s compressibility factors is divided by the pressure and multiplied by 799.42 the result is the volume in cc of 1 g of the gas at the given temperature and pressure. For fugacities, see Lewis and Randall, Thermodynamics, 1923. Density Sp. vol. p cc/g g/cc 28.50 -03508 8.840 -II31 5.082 -1968 2.725 .3669 1.806 -5273 1.508 -6630 1.358 +7305 31.75 -03149 10.13 -09872 5.952 -1680 3.139 -3186 2.068 -4836 1.5901 -6284 1.408 -7103 35-75 -02798 11.66 -08578 6.950 -1439 3.645 +2744 2.287 -4372 1.605 -5901 1.473 -6789 39.67 -02521 13.11 -07627 7.886 -1268 4.139 -2416 2.510 -3984 1.798 -5500 1.543 -6481 42.74 -02340 14.23 -07027 8.604 -1162 4.524 -2210 2.603 -3713 1.880 -5318 1.601 -6248 47.33 -O2113 15.87 .06301 9.639 -1038 5.078 -1969 2.007 -3371 2.010 -4974 1.688 -5925 54.87 .01822 18.52 -05400 11.29 -08856 5.955 -1679 3.421 +2924 2.225 -4404 1.836 -5447 84.64 -OIIT8I 28.73 .03480 17.57 -05602 9.230 -1083 5.008 -1962 3.060 -3268 2.387 -4190 128.8 .007766 43.57 -02205 20.54 -03768 Dain -07264 7.409 -1350 4.234 -2362 3-177 3148 Ue fugacity atm. 19.22 53.31 83.18 152.1 319.2 976.2 2545 19.48 55-49 88.75 168.4 357.8 1063 2645 19.70 57.43 93-70 183.6 395-5 II2I 2703 19.84 58.72 97.05 194.6 424.2 1194 2732 19.92 59.41 99.06 201.0 441.5 1226 2737 20.01 60.18 100.9 207.5 459.7 1254 2719 20.08 60.87 102.1 213.7 476.8 1271 2649 20.18 61.62 104.6 219.6 487.4 1218 2306 20.15 61.36 103.9 215.8 466.9 1097 1938 PSP» fab! vp dp 1.053 1.075 1.004 +717 -403 .280 .250 1.031 1.048 1.000 “775 -472 +313 -286 1.018 1.025 .900 .830 -540 +353 -978 .850 T ad alee ar 1.162 1.530 1.806 1.564 -918 -551 -356 1.129 1.381 1.560 1.462 -937 -578 -404 1.004 1.266 1.377 1.363 -961 -608 -457 1.068 1.183 1.265 1.281 .083 -639 -503 T.055 I.140 1.199 T2232) -9904 .660 -534 1.037 1.099 1.138 I.I51 +995 .688 -506 1.023 1.052 1.078 1.078 974 -720 +597 1.003 -997 -992 .969 -804 5% -642 -995 -987 -978 -943 .801 -792 -720 ACp ML p cal./mole° °/atm. -50 1.79 3.13 5-17 5.10 SMITHSONIAN TABLES Joule- Thomson coefficient -627 -538 -408 -128 .013 -057 -074 +559 -463 +355 -136 .O12 .064 .O81 -470 -383 .298 -134 .008 .069 085 -387 -308 +247 125 -005 .O71 .084 325 -203 -211 -II4 .002 .O71 .083 -208 asvietLe TABLES 101 AND 102 147 TABLE 101.—Compressibility of Gases Under High Pressures (Bridgman, Proc. Amer. Acad., 59, 173, 1924.) Actual vols. rest upon Amagat’s doubtful values at 3000 kg/cm.” Vol. of gas = 1 cm’ at o°C, 1 kg/cm? pressure. Densities at highest pressures indicate that the molecules or atoms are very nearly in contact in the sense of the kinetic theory. (a).—Results for Hydrogen (b).—Results for Nitrogen Vol. change 2 c3/g from yes Vol. c3/mol V ep uence volun at po 3000 kg at 68°C 30°C 65°C || c3/g_ c?2/mol | c3/g_c3/mol 23.47 24.53 -000 0.00 | 1.2900 36.13 4.68 21.21 22.24 089 2.49 | 1.201 33.64 5.82 19.76 20.74 .152 4.25 | 1.138 31.88 6.80 17.88 18.73 -234) 0:56) 1-056) 205577 8.05 L655, 17212 -308 8.61 “982 27.52 II.OL 14.76 16.05 -357 10.00 -933 26.13 14.70 sas uous -382 10.70 908 25.43 16.50 (d).—Results for Argon (e).—Results for Ammonia (c).—Results for Helium Vol. Total change vol. Volume at Vol. change at Vol. change at c3/g change 65°C 2 Sieg kg/cm? 30°C 30-95° c3/g c3/g atom c3/g c3/mol 0.000 0.00 1000 —0.827 —I4.I -049 1.96 2000 — .217. — 3.70 -085 3.39 3000 .000 0.00 -134 5.34 5000 + .200 + 3.41 -180 7.18 7000 .310 5.28 -209 8.34 10000 -409 6.07 -224 8.04 12000 -461 7.85 TABLE 102,—Gage Pressure (lb./in.2) to Atmospheres (absolute) (Taken from Bur. Standards Circ., 279, 1926.) SMITHSONIAN TABLES 148 TABLES 103 aND 104 RELATION BETWEEN PRESSURE, TEMPERATURE, AND VOLUME OF SULPHUR DIOXIDE AND AMMONIA* TABLE 103.—Sulphur Dioxide Original volume 100000 under one atmosphere of pressure and the temperature of the experi- ments as indicated at the top of the different columns. Corresponding Volume for Ex- Pressure in Atmospheres for periments at Temperature — Experiments at Temperature — Pressure in 58°.0 99°.6 183°.2 9.60 TOs 11.85 13-05 14.70 16.70 20.15 23-00 26.40 30.15 35-20 TABLE 104.—Ammonia Original volume 100000 under one atmosphere of pressure and the temperature of the experiments as indicated at the top of the different columns. Corresponding Volume for Ex- Pressure in Atmospheres for Experiments periments at Temperature — at Temperature — Volume. 46°.6 99°-6 183°.6 ; 46°.6 99°.6 183°.0 Pressure in Atmos °o 9500 a 9-50 12.5; 7245 7935 : 10.45 5880 6305 11.50 13.00 14-75 16.60 18.35 18.30 bos On | | | | | FPHWW momo * From the experiments of Roth, ‘‘ Wied. Ann.” vol. 11, 1880 SMITHSONIAN TABLES. TaBLe 105 149 VOLUME OF CASES Values of 1 + .00367 ¢ The quantity 1 + .00367 ¢ gives for a gas the volume at /° when the pressure is kept constant, or the pressure at £2 when the volume is kept constant, in terms of the volume or the pressure at 0°. (a) This part of the table gives the values of 1-++.00367¢ for values of ¢ between 0° and 10° C by tenths of a degree. (b) This part gives the values of 1-+ .00367 ¢ for values of ¢ between —go° and + 1990° C_ by 10° steps. These two parts serve to give any intermediate value to one tenth of a degree by a sim- ple computation as follows :—In the (4) table find the number corresponding to the nearest lower temperature, and to this number add the decimal part of the number in the (2) table which corresponds to the difference between the nearest temperature in the (4) table and the actual temperature. For example, let the temperature be 682°.2: We have for 680 in table (4) the number . : : « 3.49560 And for 2.2 in table (a) the decimal . ; : 4 . .00807 Hence the number for 682.2 is . : : : + 3.50367 (c) This part gives the logarithms of 1+ .00367¢ for values of ¢ between — 49° and + 399° C by degrees. (d) This part gives the logarithms of 1 + .00367 ¢ for values of ¢ between 400° and 1990° C by 10° steps. (a) Values of 1+ .00367¢ for Values of ¢ between 0° and 10°C by 0.1° Steps 0.1 0.2 0.3 1.00037 1.00073 I.0O110 00404 00440 00477 .00771 .00807 .00844 01138 -O1174 O1211 01505 .O1541 01578 .01872 .01908 01945 .02239 .02275 .02312 .02606 .02642 .02679 02973 03009 03046 03340 03376 03413 WOON DW pond 0.6 1.00220 .00587 00954 .O1 321 01688 02055 .02422 .02789 03156 -03523 WOON DW pond GMITHSONIAN TABLES. 150 TABLE 105 (continued ) VOLUME OF (b) Logarithms of 14+ .00367¢ for Values 1.931051 949341 960892 .98 3762 0.000000 0.000000 .01 5053 .030762 045362 059488 0.073168 086431 .099301 -IL1S00 .123950 135768 -147274 158483 .169410 .180068 190472 .200632 210559 220265 220750 -239049 -248145 ee, .265734 274343 282735 -290969 -299049 -30698 2 314773 0:322426 329947 -337 339 344608 351758 0.358791 -305713 -372525 -379233 -385439 SMITHSONIAN T ABLES, 1920179 “947 546 965169 982104 -998403 0.001591 017188 032244 .046796 06087 5 0.074513 .087735 -100567 -11 3030 125146 -136933 .248408 159588 -170488 .181120 .191498 -201635 .211540 315544 0.323184 -330692 -338072 “340529 352466 * 0.359488 -366399 373201 -379898 -386494 1.927299 945744 +9634 38 -980440 996801 0.003176 .O18717 033721 .048224 062259 0.07 5853 .089036 101829 114257 126339 0.138094 149539 .160691 171563 182169 0.192523 .202635 212518 .222180 .231633 .240884 249942 258814 -207 510 -276034 -284395 “292597 300048 ~308 552 316314 0732394 “331435 338803 -346048 353174 0.360184 .367084 -373875 -380562 -387148 1.925410 943934 -QO1701 978769 995192 0.0047 55 020241 03519 .04964 063637 0.077190 090332 103088 115481 -127529 .139252 -1 50667 -161790 172635 183216 -193545 203034 oars, -223135 .232507 241798 250837 .259692 -208370 .276877 285222 "293409 .301445 -309334 317083 0.324696 332178 339533 -346766 353880 0.360879 367768 +374549 381225 387801 1.923513 942117 959957 -977 092 993577 0.006329 .021760 036661 051008 005012 0.078522 091624 .104344 -116701 .128716 0.140408 “151793 -162887 -173795 -184260 -194564 -204630 .214468 .224087 -233499 0.242710 251731 -260507 269228 :277719 -286048 -294219 -302240 310115 317850 325450 “332919 -340262 -347482 354585 -361573 -368451 -37 5221 .381887 -388453 Mean diff. per degree. 1884 1805 1733 1667 1605 1582 1526 1474 1426 1381 1335 - 1299 1259 1226 IIQl 1158 1129 1101 1074 1048 1023 1000 TABLE 103 (continued) I51 GASES. of t between — 49° and + 399° © by 1° Steps | Mean diff. : 5 6 7 8 9 seedeeiees — 40 1.921608 1.919695 1.917773 T.915843 T.91 3904 1926 =)30 .940292 .938460 -936619 934771 932915 1845 — 20 958205 956447 954081 952909 951129 1771 — 10 -97 5409 973719 972022 970319 .968609 1699 == 10 -991957 -990330 988697 .987058 985413 1636 +0 0.007897 0.009459 0.011016 0.012567 0.014113 1554 10 .023273 .024781 026284 .027782 029274 1 500 20 038123 .039581 .041034 042481 043924 1450 30 052482 053893 055298 .0 50699 058096 1402 40 .066382 067748 .009109 .070466 071819 1359 50 0.079847 0.081174 0.082495 0.083811 0.085123 1315 60 .092914 094198 .09 5486 .096765 098031 1281 70 105595 106843 .108088 .109329 110506 1243 80 117917 119130 .120340 121547 .122750 1210 go .129899 .131079 132256 .133430 .134601 1175 100 0.141559 0.142708 0.143854 0.144997 0.146137 1144 110 -152915 154034 -I55151 156264 SLATES TII5 120 163981 .164072 -166161 .167246 .168330 1087 130 174772 175836 176898 177958 179014 1060 140 185301 .186340 187377 188411 189443 1035 150 0.195581 0.196596 0.197608 0.198619 0.199626 IOII 160 -205024 .20061 5 .207605 .208 592 -209577 988 170 -215439 .216409 217376 218341 219304 966 180 .225038 .225986 .226932 .227876 228819 946 190 -234429 235357 236283 .237 207 238129 925 200 0.243621 0.244529 0.245436 0.246341 0.247244 906 210 252623 253512 -254400 .255287 2560172 887 220 261441 262313 263184 .264052 .264919 870 230 .27008 5 .270940 .271793 272644 273494 853 240 278559 .279398 280234 .281070 281903 836 250 0.28687 2 0.287694 0.288515 0.289326 0.290153 820 260 295028 295835 .296640 297445 298248 805 270 -303034 303827 .304618 305407 306196 790 280 310895 311673 312450 .313226 314000 776 2 318616 .319381 320144 .320906 321667 763 300 0.326203 0.326954 0.327704 0.328453 0.329201 750 310 -333659 -334397 -335135 -335871 -336606 737 320 -340989 341715 342441 343164 .343887 722 330 -348198 348912 -349624 -350337 351048 713 340 -355289 -355991 -356693 -357394 -35&093 701 350 0.362266 0.362957 0.363648 0.364337 0.365025 690 360 .3691 32 369813 .370493 37 L171 .371849 678 370 -37 5892 376562 377232 -377900 -378567 668 380 .382548 .383208 .383868 384525 .385183 658 390 -389104 -3897 54 -390403 -391052 -391699 648 SMITHSONIAN TABLES. TaBLe 105 (continued) VOLUME OF GASES 152 (c) Values of 1+ .00367¢ for Values of ¢ hetween —90° and + 2090° C by 10° Steps 00 I .OOOOO 1.00000 1.36700 1.73400 2.10100 2.46800 2.83500 3-20200 3.56900 3.93600 4.30300 4.67000 5:03700 5.40400 5:77 100 6.13800 6.50500 6.87200 7.23900 7.60600 7-97 300 8.34000 50 0.81650 1.18350 1.55050 1.91750 2.28450 2.65150 3.01850 3-38550 S275 52 4.11950 4.48650 4.85350 5.22050 5-587 50 5-95450 6.32150 6.68850 705550 7.42250 7-78950 8.15650 8.52350 SMITHSONIAN TABLES. 10 0.96330 1.03670 1.40370 1.77070 2.13770 2.50470 2.87170 3.23870 360570 3-97279 4-33970 4.70070 5-07370 5-44070 5-30770 6.17470 6.54170 6.90870 7-27570 7.64270 8.00970 8.37670 60 0.77980 1.22020 1.58720 1.95420 2.32120 2.68820 3-05 520 3.42220 3-78920 4.15620 4.52320 4.89020 5:25720 5-62420 5-99120 6.35820 20 0.92660 1.07 340 1.44040 1.80740 2.17440 2.54140 2.90840 3:27 549 3-64240 4.00940 4.37640 4-74340 5.11040 5-47749 5-84440 6.21140 6.57840 6.94540 7.31240 7-67940 8.04640 8.41340 70 0.74310 1.25690 1.62390 1.99090 2.35790 2.72490 3-09190 3.45890 3.82590 4.19290 4205992 4.92690 529390 5.66090 6.02790 6.39490 6.76190 7.12890 7-4959° 7.86290 8.22990 8.59690 30 0.88990 I.1IO1O 1.47710 1.84410 2.21110 2.57810 2.94510 3.31210 3.67910 4.04610 4.41310 4.78010 5-14710 5.51410 5.08110 6.24810 6.61510 6.98210 7:34910 7.71610 8.08310 8.45010 80 0.70640 1.29360 1.66060 2.02760 2.39460 2.76160 3.12860 3-49560 3.86260 4.22960 4.59660 4.96360 5.33060 5.69760 6.06460 6.43160 6.79860 7.16560 7.53260 7.89960 8.26660 8.63360 40 0.85320 1.14680 1.51380 1.88080 2.24780 2.61480 2.98180 3-34880 3-71 580 4.08280 4.44980 4.81680 5-18380 5.55080 5.91780 6.28480 6.65180 7.01880 7.38580 7.75280 8.11980 8.48680 PSS SPT AMG ere 90 0.66970 1.33030 1.697 30 2.06430 2.43130 2.79830 3.16530 353230 3-59930 4.26630 4.63330 5.00030 5-367 30 5:73430 6.10130 6.46830 6.83530 7.20230 7-56930 7-93630 8.30330 8.67030 TaBLe 105 (concluded) 153 VOLUME OF GASES (d) Logarithms of 1+.00367¢ for Values of ¢ between 400° and 1990° C by 10° Steps 00 0.392345 0.452553 -505421 552547 -§95055 .633771 0.669317 -702172 732715 701251 -788027 0.813247 837083 859679 881156 .go1622 0.423492 0.479791 529623 574321 .614545 .651908 0.68605 5 717712 -747218 774845 .800820 0.825329 848528 870550 891510 -QI1 504 | 10 0.3987 56 0.458139 510371 -556990 599086 .637 460 0.672717 795325 735955 -704004 .790616 0.81 5091 839396 861875 883247 .go 3616 60 0.429462 0.485040 - 57854 .618696 655446 0.689327 -720755 -7 50061 777514 803334 0.827705 850781 .87 2692 893551 “913454 20 0.405073 0.463654 515264 501388 .603079 -O41117 0.676090 -708455 738575 -766740 793199 0.818120 .541697 .864060 885327 -905602 70 0.435351 0.49022 -538938 582734 622515 -658955 0.692574 -723776 752886 -780166 805834 0.830069 853023 874824 895583 915395 30 0.411300 0.469100 520103 565742 .607037 -644744 0.679437 -711563 741475 -769459 795745 0.8205 36 843986 866234 887 398 .907578 80 0.441161 0.495359 543522 -586880 .626299 .662437 0.695797 726776 75692 782802 808319 0.832420 855253 876945 897605 917327 40 0.417439 0-474479 524889 570052 610958 -648341 0.6827 59 -714648 744350 0.446894 0.500415 548058 -590987 630051 .665890 0.698996 -7297 56 758480 785422 .810790 0.8347 58 857471 879056 899618 919251 | SMITHSONIAN TABLES. 154 TABLE 106 COMPRESSIBILITY OF LIQUIDS At the constant temperature t, the compressibility 8 = (1/I’o) (dV /dP). In general as P increases, 8 decreases rapidly at first and then slowly ; the change of 8 with ¢ is large at low pressures but very small at pressures above 1000 to 2000 megabaryes. I megabarye =10° dynes/cm* = 1.020 kg/cm* = 0.987 atmosphere. ty per Substance. Reference. megabaryes. Compres- sibility per megabaryes. Reference Pressure, megabaryes. Compres- sibili megabaryes, B X 108 OV H Ethyl ether, ctd. a4 Ethyl iodide....... me ° HHO me ° HoH HOO iS} w AH HHH NANDD HoH H NAN DW iso.. iso.. iso.. aS “ “cc iso. . Carbon bisulphide. . Lal ‘cc ef cf Nitric acid Carb. tetrachloride. Oils: Almond...... e . : @astorsa5eer Chloroform Dichlorethylsulfide. Rape-seed.... $ : Phosph. trichloride. Ethyl acetate...... si 2 : ce “ “cc “ Ethyl bromide For references, see page 156. SMITHSONIAN TABLES. TABLE 107 155 COMPRESSIBILITY AND THERMAL EXPANSION OF PETROLEUM OILS, 0-50 kg/cm?, 0-400°C (R. S. Jessup, Bur. Standards Journ. Res., 5, 985, 1930.) It was found that the compressibility and thermal expansion of two samples of the same specific gravity, but from different sources, differed more than 30 per cent at the higher temperatures, whereas oils of the same specific gravity and the same viscosity had the same compressibility and thermal expansion within rather narrow limits. In other words, with a knowledge of the specific gravity and viscosity of the oils, it was possible to represent all the measured volumes within less than 0.5 per cent over the entire range of temperature and pressure covered by the measurements. Kinematic Specific Relative volumes 7 A Pressure viscosity gravity kg/cm? I00°F., c.g.s. | 60°/60°F. 0° | 20° | 50° 100° .80 oO .0o18 : .096 “ 50 .O14 -O41 85 oO -O17 -044 oo 50 O14 .040 -90 ° -O17 .043 oe 50 .80 °O j ss 50 A .038 85 Oo 4 .O41 . 50 5 -037 -90 oO zi -040 ae 50 .85 oO : k op 50 i .036 -95 oO ; .038 ve 50 -85 ° A .038 e 50 ; -034 -95 o .036 rf 50 .85 ° “ 50 -95 oO ze 50 85 oO ee 50 -95 oO “es 50 .85 oO oe 50 -95 e ‘ 50 210°F., c.g.s. | 60°/60°F.| kg/cm? -90 “95 -00 oe -90 00 “ -90 -00 oe -90 -00 “a SMITHSONIAN TABLES 156 TABLE 108 COMPRESSIBILITY OF SOLIDS If V is the volume of the material under a pressure P megabaryes and Vo is the volume at atmospheric pressure, then the compressibility 8 = — (1/Vo) (dV/dP). Its unit is cm?/ megadynes (reciprocal megabaryes). 10°/8 is the bulk modulus in absolute units (dynes/ cm?). The following values of 8, arranged in order of increasing compressibility, are for P =o and room temperature. I megabarye = 10° dynes/cm? = 1.020 kg/cm? = 0.987 atmosphere. Compres- Compres- sion per Bulk sion per Bulk unit vol. | modulus, | Refer- Substance unit vol. | modulus, | Refer- per mega- | dynes/cm?| ence per mega- | dynes/cm?| ence barye X 1012 barye X 108 Substance Tungsten 0.27 0.3 0.32 Platinum 0.38 INickel eee er 0.43 Molybdenum 0.46 sRantalumy so. ee 0.53 Palladium 0.54 0.55 Nichrome=-3...... 0.56 0.60 0.60 0.7 0.75 0.84 0.89 0.9 0.99 Mg. silicate, crys.. 1.03 ; Mg. silicate 1.21 0.82 Aluminum TSS 0.75 1.39 0.72 1.40 0.71 1.74 0.57 1.89 0.53 2.09 0.48 Cadmium=: 4-0 2517 0.46 Thallium Antimony Quartz Magnesium Graphite Silicavelasska. ce WOONNNNNNNN Sodium chloride.. . Ca Rey pp” N Potassium chloride. Strontium Phosphorus (red). . Selenium HHORADIWMOOKHHWOAHOA HHH HHH HHH HRD HDHWWW - NNOW snr 0 Or oo a4 Ce) N AHO | NR” SOAGHLVOO SINE RYHHWHHHNN! w Nee ee ee Phosphorus (white) Potassium Rubidium Caesinmin eee ee NHR DACOOCONKOBRBINHOAHOOONS NNNNKHNITINHNONNHNOANNHOKRNHANHNND Leal nN Op Ww HOR oon Winklemann, Schott, and Straulel (Wied Ann., 1897, 1899) give the following (among others) for Jena glasses in terms of the volume decrease divided by the increase of pressure expressed in kg/mm2, Bulk Bulk ¥ moduli 7520 2154 | Kalibleisilicat 1299 | Barytborosilicat 5800 S208 | Heaviest Bleisilicat 16 | Natronkalkzinksilicat 4530 || St9o6 | Tonerdborat with sodium, baryte..| 3470 These values are in cm?/kg x 108 x Compressibility, Griineisen, Ann. der Phys. 33, p. 65, 1910. Al — 191°, 1.32; 17°, 1.46; 125°, I.70 Fe — 190°, 0.61; 18°, 0.63; 165°, 0.67 Cu— I91°, 0.72; 17°, 0.77; 165°, 0.83 Ag —I9gQI°, 0.71; 16°, 0.76; 166°, 0,86 Pt — 189°, 0.37; 17°, 0.39; 164°, 0.40 PD Olen (225) sles) (3.2) 4 References to Table 106, p. 154: (1) Bridgman, Pr. Am. Acad. 49, I, 1913; (9) Amagat, C. R. 73, 143, 1872; (2) Roentgen, Ann. Phys. 44, I, 18901; (10) Amagat, C. R. 68, 1170, 1869; (3) Pagliani-Palazzo, Mem. Acad. Lin. 3, 18, 1883; (11) Amagat, Ann. chim. phys. 29, 68, 505, 1893; (4) Bridgman, Pr. Am. Acad. 48, 341, 1912; (12) de Metz, Ann. Phys. 41, 663, 1890; (5) Adams, Williamson, J. Wash. Acad. Sc. 9, Jan. 19, (13) Adams, Williamson, Johnston, J. Am. Chem. 1919; Soc. 41, 27, 1919; (6) Richards, Boyer, Pr. Nat. Acad. Sc. 4, 389, 1918; (14) Colladon, Sturm, Ann. Phys. 12, 39, 1828; (7) Richards, J. Am. Ch. Soc. 37, 1646, 1915; (15) Quincke, Ann. Phys. 19, 401, 1883; (8) Bridgman, Pr. Am. Acad. 47, 381, 1911; (16) Richards et al. J. Am. Ch. Soc. 34, 988, 1912. References to Table 108, p. 156: (1) Adams, Williamson, Johnston, J. Am. Ch. Soc. (5) Richards, Boyer, Pr. Nat. Acad. Sc. 4, 388, 1918; 41, 39, I9IQ; (6) Voigt, Ann. Phys. 31, 1887; 36, 1888; (2) Richards, tbid. 37, 1646, 1915; (7) R. E. Gibson, L. H. Adams, unpublished; (3) Bridgman, Pr. Am. Acad. 44, 279, 1909; 47, 366, (8) Bridgman, Pr. Am. Acad., 48, 310, 1912; IQII; (9) Bridgman, Pr. Am. Acad., 58, 166, 1923. (4) Adams, Williamson, unpublished; SMITHSONIAN TABLES Crystal Quartz Hanksite Orthoclase Galena Barite Celestite Calcite Sphalerite Fluorite Apatite Jeffersonite Tourmaline (black) Cobaltite Spodumene Pyrite Andradite Topaz Magnetite Garnet * These symbols relate to the corresponding trigonal, tetragonal, hexagonal, axes respectively. TABLE 109 ES/ COMPRESSIBILITY OF CRYSTALS Trigonal Hexagonal || ale Monoclinic A ( Y Cubic Orthorhom q G Orthorhom A B C Trigonal || Alt Cubict Cubic Hexagonal || AL Monoclinic A Trigonal Cubic Monoclinic A B Cubic Cubic Orthorhom A B C Cubic Cubic Linear, L/Lo = ap — bp? 30°C a X 106 6b X 102 a X 108 || *| 0.7052 * 9764 1.1651 .624 -9944 -5490 -4599 .0765 .6122 -4940 .6695 .5660 .6268 -4476 4537 .8071 -2688 -427 -4019 -2410 -4160 -3093, +3924 -3078 -1945 -478 .163 -2519 .1801 -2459 -1997 -2474 .2243 .2210 -2145 -1486 -2393 -1799 -1793 30°C Volume, V/Vo = ap — bp? 75°C a X 106 b X 102 + Transition above 9000°. Data from Bridgman, Amer. Journ. Sci., 10, Dec., 1925; 15, Apr., 1928. Unit of pressure kg/cm?. The following additional crystal volume compressibilities have been taken from Madelung, Fuchs, Ann. Phys., 65, 305, 1921. Their unit of pressure is dynes X 108 per cm? at 0°C. 1 dyne/cm? equals 1.020 X 10-6 kg/cm?2. Sylvite, KCl..... Halite, NaCl.... CAQIN Ossie cuieisic ave Bismuthinite, BieSs3 Argentite, AgoS... Gypsum. ise acce Witherite, BaCOs Anglesite, PbSOs Cerusite, PbCOs. . Andularia, K2AleSiceOis...... SMITHSONIAN TABLES AnhyaritenCasOL-eemecie cet 1.76 Strontianite, SrCO3........ 1.74 Aragonite, €aCQz.......... 1.53 Rhodocrosite, MnCO3...... Tes Chalcopyrite, CuFeS:....... Dolomite, CaCOsMgCOs3.... 1.21 Hematite, Fe:O3........... 1.08 Siderite; FeCQav. .s6ccs03%s 0.99 ZirconnsiOsZnOaee senior 0.85 Marcasite, FeSoe. .. cic. ee 0.81 ZiniciteeZnOMemercc cette 0.77 Periclase; MgO. scien eee 0.71 Hematite (specular)........ 0.59 Rutile Di Oeste seein 0.58 Ilmenite, (FeTi)2O3......... 0.55 @assiterite; SnO)s . 5. oi. cferes 0.48 Sapphiferts cas Microcline a — Ca2SiOs art i -307 B — CaeSiOs art 3.27 -306 y — Ca2SiOs art 2.965 +3373 Calcium Metasilicates a — CaSiO; (¥ — Wollastonite) art 2.004 +3444 B — CaSiO; (Wollastonite) art 2 2.906 -3441 Diopside CaSiO3.MgSiOz 3.257 -3070 o a 3.265 -3063 Enstatite MgSiO3; art 3.166 «3159 se (MgSiOs) ss (FeSiOs)12 3.254 +3073 Hypersthene (MgSiOs) 70 (FeSiOs) 30 3.415 -2928 Forsterite Mg2SiO. 3.223 -3103 Fayalite FezSiOs art 4.28 +234 Garnet—grossularite 3.544 -2822 a almandite 4.160 +2404 Jadeite 3.328 «3005 Miscellaneous Substances Borax, Anhydrous, NazBsO; art 2.27 -440 CaCOs3; aragonite or) 2.032 -3411 CaCQOs3; calcite 2.7102 -3688 CaF>2; fluorite 3.180 -3145 3-516 -2844 NaCl; rock salt 2.1632 -4623 Na2SO,V ; thenardite art 2.664 -3754 Naz2SO,III art 2.607 -3708 KCl; fine powder art 1.984 -5040 Pyrite FeS2 5.012 -1995 Marcasite eSotinny.< so cieeis eta es Cee Ee een eee 4.873 -2052 (1) Day and Allen, 1905. (2) Day and Shepherd, 1906. (3) Allen, Wright and Clement, 1906. (4) Allen and White, 1909. (5) Larsen, 1909. (6) Bowen, 1912. (7) Johnston and Adams, tort. (8) Merwin, 19IT. (9) Allen and Crenshaw, tort. (10) Busz and Riisberg, 1913. (11) Madelung and Fuchs, 1921. (12) Adams and Williamson, 1923. (13) Rinne, 1923. (14) Pauling and Hendricks, 1925. (15) Wyckoff and Crittenden, 1925. (16) Greig (unpublished). (17) Aurousseau and Merwin, 1928. (18) Adams and Gibson, xo29: (19) Kracek and Gibson, 1929. (20) Bjeljankin, 1927. (21) DeFoe and Compton, 1925. (22) osman, 1927. a X-ray diffraction data. b Calculated from density and composition of adularia. SMITHSONIAN TABLES TABLE 118 DENSITY OF LIQUIDS Density or mass in grams per cubic centimeter and in pounds per cubic foot of various liquids. Liquid. Acetone ; Alcohol, ethyl methyl Aniline Benzene Bromine ; Carbolic acid (crude) Carbon disulphide Chloroform . ; Cocoa-butter Ether . 5 Gasoline Glycerine Japanwax . Milk : Naphtha (wood) . Naphtha (petroleum ether). Oils: Amber Anise-seed . Camphor Castor Clove Cocoanut Cotton Seed Creosote Lard Lavender Lemon Linseed (boiled) . Neat’s foot. ss Olive . Palm ; ‘ Pentane . ; “cc Peppermint Petroleum . 2 s pent ee : Popp Raped fenudeyi G (refined) Resin . , Sperm Soya-bean : Train or Whale. Turpentine. Valerian Wintergreen Pyroligneous acid Water . . 165 Grams per cubic centimeter. Pounds per cubic foot. Bie” (Or 6) 8) 8), 1016, ele") Sa) a), (8. ee). 8 eeeee ff © @ © © © © © © © © @ Og OO nO WORN Ong OO" 16) ey fertie® ier 0 Oe 10 '2) le; 58) 40) 0. 8 Oe). (a) (6) (O46) 6) Oe 6. (0) (0) (0) ce. ee. e 0..'0) 6 0) ‘0. 6: see tex (6: 50. 0) «e686, (0 1e) © 40 “6 “euse ie. 18 6 0.792 0.807 0.810 1.035 0.899 3.187 0.950-0.965 1-293 1.489 0.857 0.736 0.66-0.69 1.260 0.875 1 .028-1 .035 0.848-0.810 0.665 0.800 0.996 0.910 0.969 -04-1 .06 0.925 0.926 I.040-I.100 0.920 0.877 0.844 0.942 0.Q13-.917 0.918 0.905 0.650 0.623 0.90-.92 0.878 0.795-0.805 0.850-0.860 0.924 0.915 0.913 0.955 0.88 0.919 0.906 0.918-0.925 0.873 0.965 1.18 0.800 1.000 SCUSGO! Oe OUR OL 10 0°10" 10) Je ‘ele ey 16). Se) oe 6) ey ie. Ke. <0) Yee, (4) je. -@:-.0) -6:..6 ‘0 0) ‘e: 10.6) Je) ‘6: 0) ‘e). 0 (¢ 49.4 50.4 50.5 64.5 50.1 199.0 59.2-60. 80.6 93.0 53-5 45.9 410-43. 78.6 54.6 64.2-64.6 52.9-50. SMITHSONIAN TABLES. 6 eH 166 Tas.ie 119 DENSITY OF PURE WATER FREE FROM AIR. O° TO 41° G [Under standard pressure (76 cm), at every tenth part of a degree of the international hydrogen scale from 0° to 41° C, in grams per milliliter 1] Tenths of Degrees. 0.999 8681 887 8936 9267 9405 | 9452 9679 9769 | 9796 9922 9962 3 lee 1.000 0000 *9992 | *9986 0.999 9919 9864 9842 9682 9582 | 9545 9296 QI5I | g100 8764 8577 | 8512 8091 7863 | 7784 O ON Ou fWNHO 7282 7014 | 6921 6331 8 6020 | 5913 5248 4898 | 4780 4040 3654 | 3523 2712 2289 | 2147 1266 0809 | 0655 0.998 9705 9214, 9048 8029 7505 | 7328 6244 5686 | 5498 4347 3757 | 3558 2343 17/22 | TS in 0233 *9580 | *9359 0.997 8019 7335 | 7104 5702 4983 | 4747 3286 2 2541 | 2201 bw NNN HN CON Qn hWNnNHO 0770 *9997 | *9736 0.996 8158 7356 7087 5451 4620) 4342 2052 | 2 1793) 1505 0.995 9761 8876 | 8579 by NN NH 2 \o 6780 5869) 5564 3714 2776| 2462 o561 #9599 | *9276 0.994 7325 6338 | 6007 4007 2997 | 2659 Ww =O ~) WwW Pw et o610 *9576 | *9230 0.993 7136 6078 | 5725 38 2505| 2144 8559 | 8490 5140) 4765 Ww Our 1352) 0971 0.991 8661 1 According to P. Chappuis, Bureau international des Poids et Mesures, Travaux et Mémoires, 13; 1907. SMITHSONIAN TABLES. Tas.ie 120 167 VOLUME IN CUBIC CENTIMETERS AT VARIOUS TEMPERATURES OF A CUBIC CENTIMETER OF WATER FREE FROM AIR AT THE TEMPERATURE OF MAXIMUM DENSITY. 0° TO 36° CG Hydrogen Thermometer Scale 1.0001 32 073 032 008 000 008 032 070 124 tgI 272 367 476 596 729 873 1.001031 198 378 568 769 981 1.002203 430 679 N NNN NN O CON ON PWHRO 932 1.003195 467 749 1.004041 Rb NNN 341 651 968 1.005296 631 975 Reciprocals of the preceding table. Influence of Pressure * kg/cm? O=€ 20° C 40° C kg/cm? 20° C 40° C I I.0000 I.0016 1.0076 7,000 0.8404 0.8485 500 9771 -9808 .9873 8,000 8275 .8360 1,000 9578 .9630 -9700 Q,000 .8160 .8240 2,000 .9260 .9327 -9403 10,000 — 8149 3,000 .QOI5 -9087 -9164 I1I,000 _ .8056 5,000 .8632 .8702 8778 12,000 _ -7906 6,000 8480 8545 -8623 12,500 = -7922 * Williamson, Change of Physical Properties with Pressure, J. Frank. Inst. 193, p. 491, 1922. SMITHSONIAN TABLES. 168 TaBLe 121 DENSITY AND VOLUME OF WATER —10° TO +250° C The mass of one cubic centimeter at 4° C is taken as unity. Temp. C.| Density. Volume. Temp. C.| Density. Volume. —10° : 1.00186 | 0.99406 1.00598 —0) 8 } | 22 —8 131 || —7 108 —6 | 088 —5 0.99930 | 1.00070 | 0.99225 4 945 055 | 187 a 955 042 147 —2 970 O31 107 —I 979 O21 066 0.99987 1.00013 0.99025 1.00985 993 007 0.98982 1.01028 997 cos 940 072 999 oor || 896 116 1.00000 1.00000 852 162 + O COONOAM pwn Oo 0.99999 1.00001 |} 0.98807 1.01207 997 003 | 762 254 993 Co7 715 gfou 988 oi2 669 349 981 O19 398 0.99973 1.00027 |Ij 1.01448 963 037 || 795 952 048 | 979 940 o60 | 7 y } 1.02270 927 073 || 576 _ _ 0.99913 1.00087 |] 2 5 1.02899 397 103 1.03237 880 120 590 862 138 c 959 843 || 9553 1.04343 0.99823 1.00177 ||| y 1.0515 802 198 || : 1.0601 780 220 || r 1.0693 757 244 | 92 1.0794 733 268 | e 1.0902 0.99708 1.00293 | : -1019 682 320 || ; 1145 655 347 -1279 of) 875 .1429 404 | SZ -1590 -177 From — 10° to 0° the values are due to means from Pierre, Weidner, and Rosetti; from o° to 41°, to Chappuis, 42° to 100°, to Thiesen; r1o° to 250°, to means from the works of Ramsey, Young, Waterston, and Hirn. SMITHSONIAN TABLES. TABLE 122 DENSITY AND VOLUME OF MERCURY — 10° to + 360°C Density or mass in grams per cubic centimeter, and the volume in cubic centimeters of one gram of mercury. Mass in Volume of || Massin Volume of grams per| 1 gram in grams per| 1tgram in cu. cm. cu. cms. || cu. cm. cu. cms. | 0.0734225 13.5213 | 0.0739572 4358 5189 9705 4492 5164 9839 4626 5140 9973 4759 5116 40107 .0734893 . 5091 .0740241 5026 5066 0374 5100 5042 0508 5293. 5018 0642 5427 4994 0776 .0735560 . 4909 .0740910 5694 4725 2250 5828 4482 3592 5961 4240 4936 6095 3998 6282 .0736228 «3723 | 0.0747631 6362 3515 8081 6496 3279 50305 6629 3040 1653 6763 2801 3002 0736893 | .2563 | 0.0754°54 7030 2326 5708 7164 2090 7064 7298 || 1853 8422 7431 1617 9784 -0737565 . 1381 .O761149 7699 1145 2516 7832 ogIo 3886 7966 0677 5260 8100 0440 6637 0738233 3.0206 | 0.0768017 8367 -9972 9402 8501 9738 7090 8635 9504 2182 8768 9270 3579 -0738902 || .9036 | 0.0774979 9036 8803 6385 9170 8569 7795 9304 i) 68336 9210 9437 | 8102 80630 .0739571 || ! .7869 | 0.0782054 7635 3485 7402 | 4921 Based upon Thiesen und Scheel, Tatigkeitber. Phys.-Techn. Reichsanstalt, 1897-1898; Chappuis, Trav. Bur. Int. 13, 1903. Thiesen, Scheel, Sell; Wiss. Abh. Phys.-Techn. Reichsanstalt 2, p. 184, 1895, and 1 liter =1.000027 cu. dm. SMITHSONIAN TABLES. 170 TaBLe 123 DENSITY OF AQUEOUS SOLUTIONS * The following table gives the density of solutions of various salts in water. The numbers give the weight in grams per cubic centimeter. For brevity the substance is indicated by formula only. Weight of the dissolved substance in 100 parts by weight of the solution. Oo Substance. a Authority. co 5 10 15 20 25 30 40 | 5° 60 a K,0 . . . «| 1.047] 1.098] 1.153] 1.214 | 1.284] 1.354] 1-503] 1-659| 1.809|15. | Schiff. |KOH . .. .| 1.040] 1.082] 1.127 | 1.176] 1.229 | 1.286) 1.410] 1.538 | 1.666 5. ss |NagO . . .|1.073| 1.144] 1.218 | 1.284] 1.354 | 1.421 | 1.557 | 1-689 | 1.829] 15. a NaOH . . .|1.058| 1.114] 1.169 | 1.224] 1.279 1 33) 1.436| 1.539] 1-642] 15. " NH3. - . .|0.978|0.9§9|0.940| 0.924 | 0.909 | 0.596] —- - - |16. | Carius. |NH,C] . . .| 1.015] 1.030] 1.044] 1.058] 1.072| — ~ - -— |15. | Gerlach. [KCL .°*.. $6) Sieg |1:665))t000)| 12135) — - ~ ~ — |15. . NEKO 65 5. TOAG| rey || Hol UO| Mer Fo| Tne || = - - — |15. a LiCl 2 2 Pa) eile020 | 1.057, |(1-085)| Mann) iran) pr Om |. 2515 -— |I5. a CaClh . .*.| 2.041 |\1.086) 1.132) 1.18% | 1.232)|1.286|'1.402) = - |15 s eee omee 1.019 | 1.040 | 1.061 | 1.083] 1.105 | 1.128 | 1.176] 1.225] 1.276] 18. | Schiff. INE a> 1.030 | 1.072 | 1.111] 1.153] 1.196] 1.241 1.340) — — |15. | Gerlach. MgClo . 1.041 | 1.085 | 1.130] 1.177 | 1.226|1.278] — - — |I5. if MClo-+6ti20 1,014 | 1.032 | 1.049 | 1.067 | 1.085 | 1.103] 1.141 | 1.183] 1.222] 24. | Schiff. ZC) See 1.043 | 1.089 | 1.135 | 1-184] 1.236] 1.289 | 1.417 | 1.563 | 1-737 | 19-5] Kremers. CdClp . . «| 1.043] 1.087 | 1.138] 1.193] 1.254 | 1-319 | 1.469] 1.653] 1.887 | 19.5 & SiG@loeme.s 1.044 | 1.092 | 1.143] 1.198] 1.257 | 1-321] | — elo tise Gerlach. SrClo + 6H,0 1.027 | 1.053] 1.082] 1.111 | 1.042] 1-174] 1.242]1.317] -- |15 “ BEKEI 5 1.045 | 1.094 | 1.147 | 1.205] 1.2 = - ~ =) a) ris s§ BaClo+ 2H20 1.035 | 1.075 | 1.119| 1.166] 1.217] 1-273] — - — |21. | Schiff. WiGuGl 2S a ltodal oon |marts 5-220 T2o T(r 3O0! T5277) | — |17.5| Franz. INIE@IS) co ko) -al 0-04 8)'1-098) |ali5 7, ||1-223))1-200)|) — - - — |17.5 s¢ Ele Cp aroma ey POA | 12002)|Nne— = - - - - — |20. | Mendelejeff. FeoCle . . .| 1.041 | 1.086] 1.130] 1.179| 1.232] 1.290 | 1.413] 1.545| 1-668 |17.5) Hager. PtCla. . bo) 2 \'r046') ¥,097))1-053)| 1-204 n.285)| 1.3021 1.540) rs705 |) > rt | || Keene. SnClo + 2H20 | 1.032 | 1.067 | 1.104] 1.143] 1.185 | 1-229] 1.329] 1.444] 1-580] 15. | Gerlach. SnCl4 + 5H20 1.029 | 1.058 | 1.089 | 1.122] 1.157 | 1.193 | 1.274 | 1.365 | 1.467 | 15. “| (eB ee 1.033] 1.070] I.1I1| 1.154] 1.202 | 1.252] 1.366|1.498] — |19.5| Kremers. KBr 1. he) A 0g'5)| 1-073) |t-B 14] CPS) e208) 1.2541) 1-404 | - |19.5 NaBr . . .| 1.038] 1.078] 1.123] 1.172] 1.224 | 1.279| 1.408] 1.563] — |19.5 as MgBre . . .{1.041| 1.085] 1.135 | 1.189] 1.245] 1.308] 1.449]1.623] - | 19.5 ZnBrg . . .|1.043) 1.091 | 1.144 | 1-202 | 1.263 | 1.328 | 1.473 | 1-648 | 1.873 | 19.5 ae CdBrg . . .| 1.041] 1.088] 1.139] 1-197 | 1.258 | 1.324 1.479|1 678} - 119.5 “« CaBre . % .«|1.042) 1.087) 1.137) 1-192) 2.250] 1.313] 1-459 1-039) - — ||19-5 ef BaBrg . ~ «| 1.043] 1.090] 1.142 | 1.199| 1.260 | 1.327 | 1.483| 1.683} — | 19.5 ‘§ SrBrg . « «| 1.043] 1.089] 1.140] 1.198 | 1.260 | 1.328 | 1.489 | 1-693 | 1-953 | 19-5 ¢ KI . . . .[1.036] 1.076] 1.118 | 1.164] 1.216 | 1.269 | 1.394 | 1.544 | 1-732] 19-5 s Lil . . . .{1.036] 1.077 | 1.122] 1-170| 1.222] 1.278] 1.412} 1.573] 1-775] 19-5 as Nal . . .. .|1.038| 1.080] 1.126] 1.177 | 1.232 | 1.292 | 1.430 | 1.595 | 1.808 | 19.5 Za wee aces 1.043 | 1.089 | 1.138 | 1-194 | 1.253 | 1.316] 1.467 | 1.648 / 1.873} 19.5) “ CdIg. . . «| 1.042] 1.086] 1.136] 1.192 | 1.251 | 1.317|1.474|1.678| — | 19.5 a Mgl,. . . -|1.041| 1.086] 1.137 | 1-192] 1.252 | 1.318] 1.472] 1.666] 1.913] 19.5) Calg. . . «| 4.042| 1.088] 1.138] 1-196] 1.258 | 1.319] 1.475 | 1-663 | 1.908 | 19.5 < SrIz . . . «| 1.043] 1-089] 1.140 | 1.198 | 1.260 | 1.328 | 1.489 | 1.693 | 1-953] 19-5 ss Balz . . . .| 1.043] 1.089] 1.141 | I-199| 1.263] 1.331 | 1-493 | 1-702 | 1-968] 19.5 a NaClO3. . «| 1.035] 1.068] 1.106] 1-145] 1.188 | 1.233] 1.329] — = ||To:5)) © NaBrOg. . .| 1.039] 1.081 | 1.127 | 1-176] 1.229|1.287| — - - |19.5| “ |KNOg . . .|1.031| 1.064] 1.099/1-135| — - - ~ - |15. | Gerlach. NaNOg. . .|1.031| 1.065] 1.101 | 1.140] 1.180 | 1.222 | 1.313 1.416] —- | 20.2] Schiff. AgNO3.. . .|1.044| 1.090] 1.140] I.195| 1.255 | 1.322| 1.479 | 1-675 | 1-918 | 15. Kohlrausch. * Compiled from two papers on the subject by Gerlach in the “‘ Zeit. fiir Anal. Chim.,” vols. 8 and 27. SMITHSONIAN TABLES. TABLE 1 23 (continued) 17! DENSITY OF AQUEOUS SOLUTIONS Weight of the dissolved substance in 100 parts by weight of the solution. Substance. NH4NOz3 Zn(NOs)2 ; Zn(NO3)2 +6H2O0 Ca(NOs)e Cu(NOs)o Sr(NOs)2 Pb(NOs)2 Cd(NOs)o Co(NOs)2 Ni(NOsz)2 Feo(NOsg)¢ - Mg(NOs)2-+6H2O Mn(NOs)2+6H20 Ke C@grt: KeCO3 = BHO! NagC O310H2O (NH4)2S04 Fes(S@i)a LOSE; FeSO,+7H20 . MgSQ,'. . . MgSO4 + 7H2O . Na SO4 + 10H2O CuSO4+ 5H20. MnSO4+4H20 . ZnSO4+7H20 . Feo(SO4)3+ KeSO4 24 rIG@) ess Cro(SO4)g* K2SO4 4 24H20 . MgSO4 + KoSO4 26H.O . . (NH4)2 SO4 ot FeSO, + 6H20 KoCrO, . 4 KyCr2O7 Fe(Cy)gk4 . Fe(Cy)sK3 a) eas Pb(C2Ho0) Ep 3 : 2NaOH zs As.Os +24H,0 . . SOs SOz SC nie. C4HegO¢ . CEba@r - Cane sugar. 25 Authority. 10 20 . | 1-040] 1.084 1.013] 1.028 1.033] 1.069 1.021 | 1.047 1.018 | 1.038 . | 1.019 | 1.039 1.025] 1.050 . | 1.035] 1.073 . | 1.037 | 1.077 | 1.032 | 1.069 . | 1.040 | 1.082 a @) cs ke eke ane P.Os o 3H2O . IBN (OFE MS CoH4O2 . SmitHSONIAN TABLES. 8 . | 1.035 | 1.077 . | 1.027 | 1.057 1.028 | 1.056 1.007 | 1.014 1.179 1.063 I.141 1.096 1.079 1.082 1.101 I I I I I I 158 165 145 Bley 119 1.086 | I. 1.088 | I. 167 1.021 | 1.028 | I. “I a eae 2| Schiff. Gerlach. Franz. Oudemans. Gerlach. Franz. Kremers. Gerlach. Franz. “cc Schiff. Oudemans. Gerlach. “ce Schiff. Hager. Gerlach. Schiff. Gerlach. Schiff. Franz. Kremers. Schiff. a“ Gerlach. Schiff. Brineau. Schiff. Kolb. Gerlach. “cc Kolb. Topsoe. Kolb. Stolba. Hager. Schiff. Kolb. Oudemans. ne TABLE 124 DENSITY OF MIXTURES OF ETHYL ALCOHOL AND WATER IN GRAMS PER MILLILITER The densities in this table are numerically the same as specific gravities at the various temperaturesin terms of water at 4° C asunity. Based upon work done at U. S. Bureau of Standards. See Bulletin Bur. Stds. vol. 9, no. 3; con- tains extensive bibliography; also Circular rg, 1913. Temperatures. | by weight roo. 15o1C; ; BEG: 0.99973 | 9.99913 0.99708 785 725 520 602 542 330 426 365 157 258 195 .98954 098 032 : 817 .98946 98877 780 656 801 729 500 660 584 346 524 442 193 393 304 043 267 171 97897 145 O41 : 753 026 97914 611 “97, 9 EL 79° 472 800 669 334 692 552 199 583 433 062 473 313 96923 363 I9I : 782 10 ON Qui fWNHe O 252 068 639 139 -96944 2 495 024 818 348 -96907 689 199 787 558 048 bow NN YD OO WN 665 424 539 287 406 144 95996 844 I2 bY HNN 10 CONI Qn 686 823 524 665 357 502 186 oll 94832 650 464 273 079 193882 682 478 271 062 92852 6 SMITHSONIAN TABLES. TABLE 1 24 (continued) I 73 DENSITY OF MIXTURES OF ETHYL ALCOHOL AND WATER IN CRAMS PER MILLILITER Temperature. Per cent C,H;OH eer rol: : 20° C. ZEOles | | | 0.92162 : 0.91384 0.9098 5 160 760 -90936 534 711 397 485 079 258 89850 031 621 89803 392 574 162 344 .88931 113 699 88882 466 650 233 417 -0799) 183 763 87948 527 713 ZO 477 054 241 86817 004 S79) 340 37 100 85859 618 376 134 84891 647 493 > 158 ums Oo uns oo & Oo wr “SIO NUN SI DN NN “NI C~NIUn tv 83911 664 415 164 82913 660 40 14 81888 626 362 094 80823 549 272 fore) Oo ‘79991 706 415 117 78814 506 SMITHSONIAN TABLES. 174 TABLE 125 DENSITY OF AQUEOUS MIXTURES OF METHYL ALCOHOL, CANE SUGAR, OR SULFURIC ACID Per cent by weight 1 of substance. Methyl Alcohol. Dc. 4° Cane Sugar. 20° See p. 175 Sulphuric Acid. Per cent by weight of Methyl Alcohol. substance. 4 D 22: Cane Sugar. 20° See p. 175 Sulphuric Acid. 20 x D-5 CG: O ON OQU PWHHO 0.99913 -997 27 99543 99379 -99198 .99029 .98864 .98701 -98547 98394 98241 -98093 97945 .97802 -97 660 97 518 97377 -97 237 -97046 96955 .96814 .9667 3 90533 .96392 .96251 .96108 95963 95817 .9 5668 95518 -95366 95213 95050 .94896 -947 34 -94570 94404 94237 .94067 -93894 ‘93720 93543 93365 93185 93001 92815 .92627 .92436 .92242 .g2048 91852 0.998234 1.002120 T.00601 5 1.009934 1,01 3881 1.017854 1.021855 1.025885 1.029942 1.034029 1.038143 1.042288 1.046462 1.050665 1.054900 1.059165 1.063460 1.067789 1.072147 1.076537 1.080959 1.085414 1.089900 1.094420 1.09897 I 1.103557 1.108175 112828 17512 122231 126984 131773 .136596 -T41453 -146345 151275 156238 .161236 .166269 .171340 -176447 181592 186773 -191993 -197 247 .202540 .207870 1.213238 1.218643 1.224086 1.229567 mee tee _ 1.00506 1.01178 1.01839 1.02500 1.03168 1.03843 1.04527 1.05216 1.05909 1.06609 1.07314 1.08026 1.08744 1.09468 10199 .10936 .11679 12428 13183 -13943 -14709 15480 16258 17041 .17830 .18624 19423 20227 .21036 .21850 22669 -23492 .24320 25154 25992 .208 36 27685 1.28543 1.29407 1.30278 LeQUnisy7 1.32043 1.32938 1.33843 1.34759 1.35686 1.36625 1.37574 1.38533 1.39595 ~ mee mee * sie . . = 0.91852 91653 Q1451 -91248 ‘91044 .908 39 .90631 90421 .90210 .89996 89781 89563 89341 SOQ1I7 88890 .88662 88433 88203 87971 87739 87507 87271 87033 86792 86546 .86300 86051 85801 85551 .85300 85048 84794 84536 84274 .84009 83742 33475 83207 82937 .82667 82396 82124 81849 81568 81285 -80999 80713 .80425 80143 79859 79577 .229567 235085 240041 .246234 251866 ese ‘268980 274774 .280595 286456 "202354 298291 304267 .310282 -316334 322425 -325554 +3347 22 .340928 -347174 -353456 -359778 .3061 39 1.372536 1.378971 1.385446 1.391956 1.398505 1.405091 1.411715 1.418374 1.425072 1.431807 1.438579 1.445388 1.452232 1.459114 1.466032 1.472986 1.479976 1.487002 1.494063 1.501158 1.508289 1.515455 1.522656 1.529891 1.537161 1.544462 1.551800 Pmt et te ttt tte tt tte pay _ 1.39505 1.40487 1.41481 1.42487 1.43503 1.44530 1.45568 1.46615 1.47673 1.48740 1.49818 1.50904 1.51999 1.53102 1.54213 1.55333 1.56460 1.57595 1.58739 1.59890 1.61048 1.62213 1.63384 1.64560 1.65738 1.66917 1.68095 1.69268 1.70433 1.71585 1.72717 1.73827 1.74904 1.75943 1.76932 1.77860 1.78721 1.79509 1.80223 1.80864 1.81438 1.81950 1.82401 1.82790 1.83115 1.83368 1.83548 1.83637 1.83605 (1) Calculated from the specific gravity determinations of Doroschevski and Rozhdestvenski at 15°/15°C; J. Russ., Phys. Chem. Soc., 41, p. 977, 1909. pt (2) According to Dr, F. Plato; Wiss. Abh. der K. Normal-Eichungs-Kommission, 2, p. 153, 1900. (3) Calculated from Dr. Domke’s table; Wiss. Abh. der K. Normal-Eichungs-Kommission, , p. 131, 1900. 5 31, 19 All reprinted from Circular 19, U.S. Bureau of Standards, 1913. SMITHSONIAN TABLES. TABLE 126 175 DENSITY, BRIX, AND BAUME DEGREES, OF CANE SUGAR SOLUTIONS Degrees Brix, Specific Gravity, and Degrees Baumé of Sugar Solutions. Degrees Brix = Per cent Sucrose by Weight. 3 Specific Gravities and Degrees Baumé corresponding to the Degrees Brix are for G 145 The relation between the specific gravity and Degrees Baumé is given by Degrees Baumé = 145 — ————~2—. specific gravity ' Peerees egrees rix or SoU Baumé per cent Spee) (modu- sucrose Sean lus 145) 20°/20°C Degrees Peerecs Brix or . Degrees rix or Grant per cent Specific Baumé per cent Specific sucrose SrAVALY, on (modu- sucrose Brava Ly, oe by 20°/20' lus 145) ; 209/20 weight weight Degrees Baumé (modu- lus 145) 40. at 42. 43- 44. 45- 46. 47 48. 49. 0000000000 See ee ee Re Oe Se ee OO OO O0 ON ANHWHHO NwWWNHNHHH OO 0000000000 Se ee ee ee Oe oe 0000000000 50. Shee 52. 53- 54 55 56 57- 58. .o -o -O .o .o Oo -o Oo -O .O on ee | ©000000000 i ee | 0000000000 O00 COrI331 DOM HHH HHH HHH moe o - 0000000000 0000000000 SO Ot Ot ot we OR 0000000000 0000000000 St OO Catenin! The above table is abridged from Bureau of Standards Technologic Paper No. 115. The original table is given in steps of o.1 Degrees Brix. SMITHSONIAN TABLES. 176 TABLE 127 DENSITY OF GASES The following table gives the density as the weight in grams of a liter (normal liter) of the gas at o°C, 76 cm pressure, and standard gravity, 980.665 cm/sec.?, (sea-level, 45° latitude), the specific gravity referred to dry, carbon-dioxide-free air, and to pure oxygen, and the weight in pounds per cubic foot. Dry, carbon-dioxide-free air is of remarkably uniform density; Guye, Kovacs and Wourtzel found maximum variations in the density of only 7 to 8 parts in 10,000. For highest accuracy pure oxygen should be used as the standard gas for specific gravities. Observed densities are closely proportional to the molecular weights. The following table was prepared by the Gas Chemistry Section, Bur. Standards, 1929. yas rm Air =I 2=1 : H : pau cubic grams Gab 4 INIT ESS geacg tact ere tee sila 1.2929 1.0000 9047 ee OSO 7 mal Acetylene niats iano: &. ceuacicion C2He ren 73 -907 28208) -07322) 1 Ammonia see oo sc okie toe NH; a7 7LO) -5963 -5395 .04813 IAT ONES. crsteyepsaierueral es Ek ere A 1 O37) a AL 7 OOnN L242 a5) ae VABIITE 8.0 Wo Nello ods ee ee AsH; 3.48 2.69 2.44 27, I IBTItATIC-1SO}, ..Aiyavarrn susiecckekerehe CaHio 2.673 2.067 1.870 .1669 I Butane meee een aiesie. «Gaeta C4Hio fe aioe 2.0854") T.886s" 3157257 5,6 Garbonidioxides ... S.'cesie CO, 1:9769 | “T5200 11-3834 0812341 | Carbon monoxides..-aeeacdeee CO 1.2504 .9671 8750 .07806 I Garbonioxysulphides.e cane COS 2.72 2.10 1.90 .170 I Ghiorine 2h ee ene aaoe: Cle 3.214 2.486 2.249 .2006 I Chlorine monoxide... &..- 4. Cl,0 3.89 3.01 2.72 243 I Es thameteetoc os eee eee C.He 1.3566 1.0493 -9493 .08469 I Ethylene erst we eee sentence C.H4 1.2604 -9749 .8820 .07868 I BWOrne Sak acy oe eee ner F, 1.696 Tae 1.187 -1059 I PACIIUITIL i, Bock creas oes He .17847 .13804 ~ .1248) -O1TI42 I Fiydrogen). peels arte He .08988 .06952 .06290 .00561I I Hydrogen bromide. =. 5222. - HBr 3.6445 2.8189 2.5503 .22752 I Hydrogen chloride........... HCl 126392 9 91-2678) 0 Herd 7. 1oe 0232 eel Eiydrocensiodidesee rae a eto HI 5-78901 4.4776 4.0510 -36140 I Hydrogen selenide........... H2Se 3.670 2.839 2.568 .229 I Hydrogen sulphide.......... H2S 1.539 1.190 Te O77; .09608 iI KGryEOMs ty a oie cao Se Kr 3.7038 2.863 2.595 2315 I Miethane:. knees aoe eer eee: CH, -7163 5544 SSOlgue ee O4A75 nl Monomethylamine........... CH3NH2_ 1.396 1.080 9769 .08715 I Methylkchlonides ee. a. eon CH;Cl 2.3076 1.7848 1.6148 .14406 1 Miethylketh erence: eee an (CH:)20)))2:10908) ) 91-6318) 0r-47645 Taree ot Methyl fluortdesee. «+ sea aneoe CH;F 125452) MelO5Tan OS lsum OOG46n mmr INCOME Soccer pees ic Ae ee Ne .90035 .6963g .6300, .05620; 3 INitriCOxtdene tee ae ae NO 1.3402 1.0366 19378" -08367r Nitrogen’: (chemi)... 92"). 223% No 1.25055 .96724 .875I0 .07806) 1,4 Nitrogen (atin) =) eerie Se: 1.2568 .9721 8795 .07846 I INitrosylachlorides =. =o +e) NOG! 2.992 2.314 2.094 -1868 I INGtTOUSIOXIGEZ 7. i. s sae Ais eNO 1.9778 1.5297 1.3840 .12347 I Oxy nem cas ye ec can eve ae O, 1.42904 1.10527 1.0000 .089212 I PhoOsphinest ) seek ce Aes PH; 1.5294 1.1829 1.0702 .0954s I IPO DAM Ch nee mac parech neiecs coacheis C;Hs 2.020 1.562 1.414 -1261 I Silicon! tetrahuoride o5..s..4- 4: SiF 4 4.684 3.623 3.278 2924 I Sulphuridioxidemmnr seers SO, 219260) 2.202012 0482 S272. ELEM OIE 5 vce Cl wae edehal eieheamevar ease xX 5.851 4.525 4.094 3653 I * Both butane and air at 710 mm. . Based on densities in I. C. T., 3, 3, 1928. . Baxter and Starkweather, Proc. Nat. Acad. Sci., 14, 57, 1928. . Baxter and Starkweather, Proc. Nat. Acad. Sci., 14, 50, 1928. . Moles and Clavera, Z. Anorg. Allgem. Chem., 167, 49, 1927. Bogaert, Bull. Soc. Chim. Belg., 36, 384, 1927. . Beckers, Bull. Soc. Chim, Belg., 36, 559, 1927. QAMBWNH SMITHSONIAN TABLES TABLES 128 AND 129 17 RELATIVE DENSITY OF MOIST AIR FOR DIFFERENT PRESSURES AND HUMIDITIES TABLE 128,—Values of a from h=1 to h=9, for the Computation of Different Values of the Ratio of Actual to Normal Barometric Pressure This gives the density of moist air at pressure h in terms of the same air at normal atmosphere pres- sure. When air contains moisture, as is usually the case with the atmosphere, we have the following equation for pressure term: h=B—o.378e, where e is the vapor pressure, and B the corrected barometric pressure. When the necessary psychrometric observations are made the value of e may be taken from Table 212 and theno.378e from Table 130, or the dew point may be found and the value of 0.378e taken from Table 130. ExAMPLES OF USE OF THE TABLE. To find the value of + when hk = 75493 760 hi = 700 gives .g2105 ae 1 0.001 3158 .065739 “ 2 0026316 ; -005263 3 -0039474 -3 “* .000395 754-3 -992497 4 Oe eets: == .006 2 Sous To find the value of x when 4 = 5.73 7 Goseenes R= S5 gives .0065789 } 7) 0009210 8 .0105263 .03 “© 0000395 9 -O118421 5-73 -0075394 | TABLE 129,—Values of the logarithms of da for values of ” between 80 and 800 Values from 8 to 80 may be got by subtracting 1 fom the characteristic, and from o.8 to 8 by subtracting 2 from the characteristic, and so on. Values of log 4 9 80 | 1. : 1.03300 1.04347 | I. T.05368 | 1.05 1.06858 | go| . : .08297 0922 Tilly. 10146] . -11482 100 | f.11919| 1.12351 | 1.12779 1.13622 | 1.14038 | 1.14449 | I. T.15661 I10| .16058| .16451| .16840] . 17609] . 8| .18364} . j 19473 120] .19837| .20197| .20555] . PAO) || A .21950| . : 22978 130 | .23313} -23646 23976] . | -24629| . 2215273) .2 5 . .26220 140| .26531| .20841| .27147| .2 eee rane .28354| -2 : 29237 150 | 1.29528 | 1.29816 | 1.30103 | I. | 1.30671 | T. T3023 0s (ie ie 1.32058 160] .32331| -32601| .32870| .33137)| .33403] - 233029)|— =< . -34707 170 -34904| .35218] .35471| - 3| 35074] - .36470| . : 37204 180 | .37446| .37686| .37926| . 38400] .38 .38870| . : 39505 190 | .39794| .40022| .40249| . .40699 | . heared Tele All is : 41804 200 | 1.42022 | 1.42238 | 1.42454 | I. .42882 | T. T-4'3305)||¥. : 1.43933 | 210) .4414t| .44347| -44552| - -44960| .45162| .45364| . -45903 220| .46161} .46358} .46554] . .46943| -4713 AAB2Oile ; -47902 230| .48091| .48280| .48467| . .48840] . -49210} . Bille 49758 240 | .49940} .50120] .50300| . 50658] . sSNA) 03] 51539 250 | 1.51713] 1.51886 | 1.52059 | I. -52402 | I. BS 27a ai lle 2) itis 1.53249 260 | -53416| .53583| -53749| - -54079| - -54407 | - 54894 270 | .55055| -55216] .55376| . -550694) . -56010| . : 56479 280 | .50634] .56789| .56944] . 57250) cs SSSI : 58008 290} .58158] .58308} .58457]| . SO75SiN 59048 | . ; 59486 300 1.59631 | 1.59775 | 1-59919 | I. 1.60206 | T. 1.60491 | 1.60632 | I. 1.60914 310 | .61055| .61195! .61334/ . OTO0T |e. .61887 | .62025]| .; 62298 320 | .62434| .62569| .62704| . .62973| . .63240| . ate 63638 330 .63770| -63901 | .64032 .64293| - -64553 | -64682 -64939 | 340 | .65067} .65194]| .65321 -65574| - .65826| . 66201 1 SMITHSONIAN TABLES. 178 TABLE 129 (continued) DENSITY OF MOIST AIR Values of logarithms of 500 for values of 2 between 80 and 800 Values of log Le, 760 4 5 1.66325 | 1.66449 | 1.66573 | 1.66696 | 1.66819 | 1.66941 | 1.67064 | 1.67185 | 1.67307 | 1.67428 .67549| .67669| .67790| .67909| .68029| .68148| .68267| .68385| .68503) .68621 .68739| .68856| .68973| .69090| .69206| .69322| .69437| .69553| -69668) .69783 -69897 | .7001I | .70125| .70239] .70352| .70465| .70577| .70690| .70802| .70914 71025] -71136| .71247| .71358| .71468| .71578| .71688] .71798] .71907| .72016 1.72125 | 1.72233 | 1.72341 | 1.72449 | 1.72557 1.72664 | 1.72771 | 1.72878 | 1.72985 | 1.73091 -73197| - 73408 | -73514| -73619| .73723| -73828| 73932) -74036| .74140 -74244| . | -74450} -74553 74655 -74758| -74860| .74961| .75063| .75164 SIS ZOSi| es 75407 | -75567| -75663| .75768| .75867| .75967| .76066| .76165 -76264| . 76461) .76559| .76657) .76755| .76852| .76949| .77046| .77143 1.77240 | I. 1.77432 1.77528 1.77624 | 1.77720 | 1.77815 | 1.77910 | 1.78005 | 1.78100 -78194| . -78383 | -78477| .78570| .78664| .78757| -78850| .78943| .79036 79128] . 79313} -79405| -79496| -79588| -79679| .79770| .79861| .79952 80043] . .80223| .80313] .80403| .80493| .80582| .80672| .80761| .80850 80938 | . 81115| .81203] .81291] .81379|] .81467| .81554| .81642] .81729 1.81816 | T. 1.81989 | 1.82075 | 1.82162 | 1.82248 | 1.82334 | 1.82419 | 1.82505 | 1.82590 .82676| .82 82846] .82930] .83015| .83099| .83184| .83268) .83352| .83435 83519| . 83686] .83769] .83852] .83935| .84017| .84100] .84182]| .84264 84 346 ; 84510] .84591| .84673] .84754 848 3 3 .84916| .84997| .85076 85158 | .85238| .85319| .85309} .85479) .85558] .85638| .85717| .85797| .85876 1.85955 | 1.86034 | 1.86113 | 1.86191 | 1.86270 | 1.86348 | 1.86426 | 1.86504 | 1.86582 | 1.86660 86737 | .86815] .86892] .86969| .87047| .87123| .87200| .87277| .87353]| .87430 .87506| .87582] .87658| .87734| .87810| .87885] .87961| .88036| .88111| .88186 88261 | .88336| 88411] .88486) .88560| .88634| .88708| .88782| .88856] .88930 89004] .89077] .89151| .89224| .89297]| .89370] .89443| .89516|] .89589] .89661 1.897 34 | 1.89806 | 1.89878 | 1.89950 | 1.90022 | 1.90094 | 1.90166 | 1.90238 | 1.90309 | 1.90380 90452] -90523] .90594| .g0665} .90735] -90806| .90877]} .90947| .g1017| .g1088 -QI1158| .91228] .91298| .91367| -91437] .91507| .91576] .91645] .91715| .91784 91853] .91922] .91990] .92059| .92128| .92196| .g2264|] .92333] -92401]| .92469 92537 | -92604] .92672] .92740| .92807| .92875| .92942| -93009| .93076| .93143 1.93210 | 1.93277 | 1.93343 | 1-93410 | 1.93476 | 1.93543 | 1-93609 | 1.93675 | 1.93741 | 1.93807 -93873 | -93939| -94004| -94070| .94135| -94201| .94266/ .94331| .94396| .94461 94526] .94591| -94656| .94720| .94755| -94849| .94913] .94978| .95042| .95106 ‘95170| .95233] -95297| -95361| -95424| -95488| .95551| .95614| .95677| .95741 .95804| .95866] .95929| .95992| .96055| .96117]| .g6180| .9g6242| .96304|] .96366 1.96428 | 1.96490 | 1.96552 | 1.96614 | 1.96676 | 1.967 38 | 1.96799 | 1.96861 | 1.96922 | 1.96983 97044] .97106| .97167| .97228| .97288| .97349| -97410] .97471| .97531] .97592 97652] .97712| .97772| -.97832| .97892| .97951| .98012] .98072| .98132] .g8191 98251 | .98310] .98370| .98429| .98488} .98547| .98606| .98665| .98724] .98783 -98842 | .98900] .98959| .99018| .99076| .99134| -99193] -99251| .99309| .99367 1.99425 | 1.99483 | 1.99540 | 1.99598 | 1.99656 | 1.99713 | 1.99771 | 1.99828 | 1.99886 | T.99942 0.00000 | 0 00057 | 0.00114 | 0.00171 | 0.00228 | 0.00285 | 0.00342 | 0.00398 | 0.00455 | 0.00511 00568 | .00624| .00680| .00737| .00793| .00849| .00905| .00961| .o1017| .o1072 01128] .01184] .01239| .01295| .01350| .01406] .o1461| .01516| .o1571| .01626 .O1681 | .01736] .o1791| .01846] .o1901| .01955| .02010] .02064| .02119| .02173 SMITHSONIAN TABLES. TABLES 130 AND 131 179 DENSITY OF MOIST AIR TABLE 130. — Values of 0.378e* This table gives the humidity term 0.378e, which occurs in the equation 6 = 8 760 B — 0.378e 760 e; Jo is the density of dry air at normal temperature and barometric pressure, B the ob- served barometric pressure, and h = B — 0.378e, the pressure corrected for humidity. For for the calculation of the density of air containing aqueous vapor at pressure A ; ‘ j bh values of 560" see Table 128. Temperatures are in degrees Centigrade, and pressures in milli- meters of mercury. e e e Vapor Dew Vapor Vapor pressure i point. pressure pressure (ice). (water). (water). mm .58 .g2 29 68 IO 54 OI 51 04 61 21 85 52 .24 -99 2.79 .64 54 -49 .49 55 .66 . 84 .09 . 40 a7o .24 mm 31.86 33-74 35-72 37-78 39-95 42.2 44.62 47.13 49.76 G2asa 55-40 58.42 61.58 64.89 68.35 71.97 75-75 79.70 83.83 88.14 92.6 97. 102. 107. Lie 118. 124. 130. 130. 142. 149. mm .029 054 og6 169 288 480 53° 585 646 712 783 862 -947 .O41 .142 252 -373 503 .644 -798 .964 -144 - 340 550 778 .025 . 291 .578 .887 . 220 . 580 ° on \W Oo SIAM WNHH ODT = ee al 000 WHOIAN DAAUUNDA LE = e HHH Wh oO He eS eS oe HO COON DAMN » NS h h ty Ww ~) b = OO WONININAANUKHAHPHHPWWWWWHNHNHNHND A Hoy ° oO. O. O. O. oO. Or oO. O. O. (of oO. ° I I I I I I I I 2 2 ae 2. 3 3 3 3 4 4 HHMH HHH O00000000009009000900090000 i 4 * Table quoted from Smithsonian Meteorological Tables. TABLE 131.— Maintenance of Air at Definite Humidities Taken from Stevens, Phytopathology, 6, 428, 1916; see also Curtis, Bul. Bur. Standards, 11, 359, 1914; Dieterici, Ann. d. Phys. u. Chem., 50, 47, 1893. The relative humidity and vapor pressure of aqueous vapor of moist air in equilibrium conditions above aqueous solutions of sul- phuric acid are given below. Vapor pressure. Vapor pressure. Density of Relative Density of Relative acid sol. humidity. Vere 30° C acid sol. humidity. 20°C mm mm mm ye oie I.30 58. 17. 39. T.35 47. 16. 29. 1.40 Bie TS 28. TSO 18. 14. 25: 1.60 8. rs 22. 1.70 BI. 6 7 6 O 4 2 AW Nn Ww Pe SMITHSONIAN TABLES. 180 TaBLeE 132 PRESSURE OF COLUMNS OF MERCURY AND WATER British and metric measures. Correct ato? C for mercury and at 4° C for water. METRIC MEASURE. Pressure in grams per sq- cm. Pressure in pounds per sq. inch. Inches of Hg. 13-5956 40.7868 54-3824 67.9780 81.5736 95.1692 108.7648 122.3604 135.9560 0.193376 0.3867 52 0.580128 0.773504 0.966880 1.160256 1.353632 1.547008 1.740384 1.933760 1 BRITISH MEASURE. Pressure in grams per sq. cm. 34-533 69.066 103.598 138.131 172.664 207.197 241.730 276.262 310.795 Pressure in pounds per sq: inch. 0.491174 0.982348 1.473522 1.964696 2.455870 2.947044 3.438218 3:929392 4.420566 4.911740 Pressure In grams per sq- em. Pressure in pounds per sq. inch. Inches of 2. Pressure in grams per sq. cm. 0.0142234 0.0284468 0 0426702 0.05689 36 0.07 11170 0.08 53404 0.0995638 0.1137872 0.1280106 0.1422340 2.54 5-08 7.62 Pressure in pounds per sq- inch. 0.036127 0.072255 0.108382 0.144510 0.180637 SMITHSONIAN TABLES. REDUCTION OF BAROMETRIC HEICHT TO STANDARD TEMPERATURE * TaBLeE 133 181 Corrections for brass scale and Corrections for brass scale and Corrections for glass scale and English measure. metric measure. metric measure. Height of a Height of | a Height of a barometer in in inches for barometer in | in mm for barometer in in mm for inches. temp. F. mm. temp. C. mm. temp. C. 15.0 0.001 35 400 | 0.0651 50 0.0086 16.0 .OO1 45 410 .0668 100 .O172 17.0 00154 420 0684 150 .0258 17-5 001 58 430 .0700 200 0345 18.0 .00163 440 0716 250 0431 18.5 .00167 450 0732 300 0517 19.0 .0O172 460 -07 49 350 0003 19.5 .00176 470 | .0765 480 0751 400 0.0689 | 20.0 0.00181 490 0797 450 -| 0775 20.5 00185 500 | .0861 21.0 .OO190 500 0.0813 520 .0895 21.5 .00194 510 -08 30 540 .0930 22.0 00199 520 .08 46 560 0965 22.5 00203 530 .0862 580 0999 23.0 00208 540 .0878 2355 00212 550 .0894 600 0.1034 500 -OOLI 610 -IOSI 24.0 0.00217 570 0927 620 1068 24.5 00221 580 0943 630 1085 25.0 00226 590 0959 640 1103 25.5 00231 650 -I120 26.0 00236 600 0.097 5 660 S037 26.5 .00240 610 0992 27.0 00245 620 .1008 670 0.1154 27.5 00249 630 -1024 680 1172 640 -1040 690 1189 28.0 0.00254 650 -1056 700 .1206 28.5 .00258 660 1073 710 A222 29.0 00263 670 1089 720 1240 29.2 -00265 680 -1IOS 730 1258 29.4 .00267 690 1121 29.6 00268 740 0.1275 29.8 .00270 700 0.1137 750 1292 30.0 .00272 710 1154 7600 .1309 720 1170 770 .1327 30.2 0.00274 730 1186 780 1344 30.4 .0027 740 .1202 790 sUgOr 30.6 .00277 750 .1218 800 .1378 30.8 00279 760 1235 31.0 .00281 770 1251 850 0.1464 31.2 .00283 780 .1267 goo SURETY 31-4 .00285 790 1283 950 1639 31.6 00287 800 1299 1000 0723 * The height of the barometer is affected by the relative thermal expansion of the mercury and the glass, in the case of instruments graduated on the glass tube, and by the relative expansion of the mercury and the metallic inclosing case, usually of brass, in the case of instruments graduated on the brasscase. This relative expansion is practically proportional tothe first power of the tem- perature. The above tables of values of the coefficient of relative expansion will be found to give corrections almost identical with those given in the International Meteorological Tables. The numbers tabulated under a are the values of ain the equation Hy= Hy’ —a(t/ —¢) where H;is the height at the standard temperature, H/’ the observed height at the temperature /’, and a (¢’—7) the correction fortemperature. Thestandard temperature is 0° C for the metric system and 28°.5 F. for the English system. The English barometer is correct for the temperature of melting ice ata temperature of approximately 28°.5 F., because of the fact that the brass scale is graduated so as to be standard at 62° F., while mercury has the standard density at 32° F. EXaAMPLE.—A barometer having a brass scale gave H= 765 mm at 25° C; required, the cor- responding reading ato° C. Here the value of a isthe mean of .1235 and .1251, or .1243;.°.a(/’/—2} = .1243 X 25 =3.11. Hence Ay = 765 — 3.11 = 761.89 N. B.—Although ais here given to three and sometimes to four significant figures, it is seldom worth while to use more than the nearest two-figure number. In fact, all barometers have not the same values for a,and when great accuracy is wanted the proper coefficients have to be deter: mined by experiment. ‘ SmitHsonian TABLES: 182 TaBLeE 134 REDUCTION OF BAROMETER TO STANDARD GRAVITY Free-air Altitude Term. Correction to be subtracted. The correction to reduce the barometer to sea-level is (g1 — g)/g X B where B is the barometer reading and g and gi the value of gravity at sea-level and the place of observation respectively. The following values were computed for free-air values of gravity gi (Table 706). It has been customary to assume for mountain stations that the value ef gi = say about 3 the free-air value, but a comparison of modern determinations of gi in this country shows that little reliance can be placed on such an assumption. Where g: is known its value should be used in the above correction term. (See Tables 707 to 709. Similarly for the latitude term, see succeeding tables, the true value of g should be used if known; the succeeding tables are based on the theoretical values, Table 706.) - Observed height of barometer in millimeters. Height abvove sea-level. meters. Ico ; Correction in mm to be subtracted for 200 : height above sea-level in first column and 300 : barometer reading in the top line. 400 500 600 700 800 900 I000 IIooO 1200 1300 1400 1500 1600 1700 1800 1900 2000 2100 2200 2300 2400 2500 2600 2700 2800 2900 3000 3200 3200 3300 3400 3500 3600 3700 3800 3900 4000 LSet a ara as staat 90900000000 SIAKDDUUUP HL Hw BPH OOM NO 00 ON DUN ela leet ate TU eatcet Ghillie Tealis| RODWAY ROO KBAnRKGA 12 14 16 18 20 22 24 26 28 30 32 34 36 39 -41 o21 020 o19 o18 O17 o16 ors o14 O13 p w& HHL Conn — ie Tet tel > o n ° ar Corrections in in. to be = ; ; : ; subtracted for height above = sea-level in last column and barometer reading in bot- tom line. Height above sea-level. Observed height of barometer in inches. eel SMITHSONIAN TABLES. Taste 135 183 REDUCTION OF BAROMETER TO STANDARD GRAVITY * METRIC MEASURES From Latitude 0° to 45°, the Correction is to be Subtracted. 640 | 660 | 680 Ae eRe Ke oy fees Sea = = eS ee ipl 0* co.) 0 OHH ee Bane aetnctas SS = Re SS eS ee a tte ema (a Oo Orn- i pacer Bee aoe eee t i ee eaten ieratak b coco ooood * “Smithsonian Meteorological Tables.” SMITHSONIAN TABLES 184 TABLE 135 (continued) REDUCTION OF BAROMETER TO STANDARD GRAVITY * METRIC MEASURES From Latitude 46° to 90°, the Correction is to be Added. 580 | 600 760 | 780 mm. mm. mm. nm. mm. mm. . . . . ° mm. mm. —0.02—0.03 —0.03 —0.03 —0.03 —0.03 —0.03 —0.03 —0.03 —0.03—0.03 —0.03\—0..04) '+0.03/+0.03,+0.03 +0.03 +0.03 +0.03 +0.03 -+0.03/+0.03)+0.03|/+0.03 +0.04,+0.04 0.08) 0.08 0.08} 0.08) 0.09] 0.06] 0.00| 0.09] 0.10} 0.10) 0.10) 0.10) 0.11 0.12] 0.13|° 0.13] 0.14 ©.14| 0.15] 0.15] 0.16) 0.16] 0.17) 0.17| 0.18] 0.18 0:17| (Oc18| O10) ‘O.16| 10.20) /.0221) 6:21) 10.22) \O.23))0523)-No-eal) tos25)Ge2s 0.22) 0.23] (0.24) (0.25) ©:26) ©.26) 0.27) 0.28) (0.20) 10.30) “O.3%| (O23) joss +0.27 +0.28+0.29+0.30+0.31+0.32+0.33+0.34+0.35 +0.36+0.37+0.38+0.39 0.32| 0.33] 0.34) 0.36| 0.37] 0.38] 0.30) 0.40) 0.42) 0.43} 0.44) 0.45] 0.46 0.37| 0.38] 0.40} 0.41| 0.42) 0.44 0.45] 0.46] 0.48) 0.49) 0.51) 0.52) 0.53 0.42) 0.43} 0.45] 0.46) 0.48] 0.49) 0.51| 0.52) 0.54) 0 56 .057| 0.59) 0.60 0.46} 0.48} 0.50) 0.52} 0-53) 0-55) 0-57; 0.58 0.60) 0.62) 0.64) 0-65) 0.67 +0. 51/+0.53+0.55\+0-57+0-59+0.60 +0.62 +0.64-+0.66 +0.68 +0.70 +0-72+0.74 0.56] 0.58} 0.60) 0.62) 0.64] 0.66) 0.68 0.70) 0.72) 0.74| 0.76) 0.78) 0.80 0.60| 0.62} 0.65] 0.67) 0.69} 0.71| 0.74) 0.76) 0.78 0.80) 0.82) 0.85) 0.87 0.65| 0.67} 0.69} 0.72) 0-74] 0-77| 0.79] 0-81) 0.84) 0.86) 0.89] 0-91] 0.93 0.69} 0-72| 0.74) 0.77] 0-79] 0.82] 0.84) 0.87] 0.89) 0-92] 0.94) 0.97] 1-00, +0.73-+0.76+0.79 +0-81+0.84|+0.87 +0.89 +0.92/+0.95,+0.98 +1.00+1.03,+1.06 0.77| 0.80) 0.83) 0.85) 0.88] 0.91) 0.94) 0.97) I-00} I-02} 1.05) I-08} I.1I 0.81; 0.85] 0.88) 0-91; 0.94! 0.97) 1.00) 1.03) 1.06] 1.09) 1.12) I.15| 1.18 O65) (Oz 80] 70.92|" (0295|!) 0:08) sl OL) 04) Wa -O8| hrs mtl) ste r4 eng |) ecole 0.80] ©:93| 0:96] 0-99) 1.03] 1-06) 1-00] 1-13] 1.16 T-1O) .22) 1-26) iezo +o.93+0.97,+1.00+1.04+1-07/\+1.10+1.14/+1.17)+1.21)+1.24,+1.28+1.31+1.35 0.97) ©-00l\-t204) W-08) a. Tal. wers|, 218) ws22) “a25|| 20) Geesal e360) eae 1.00) 1.04) eS) WITT) Sbsts) < T9}) Vassily 4226) Esso] ae S4l| Sr 37 estes TAOA AOS) WSL TL! Mey LS| ets LO| sets 23) ues) eee salle ate Sele © Te LO7|) Tell) Veet5|) Geto) ee23|) ie 27) ere srl ere B5| ile SO) ele AS | elt 4 zee Silesia 5 +1.104+1.14-+1.18+1.22+1.26+1.31/+1.35/+1.30/\+1.43/)+1-47/,+1.51/+1-55+1.59 Pete) Wsr7] s22| 26)" 7230), 2394) 38) 42) saz) 5a SS) sso) Bros WzOe Mes 2O| eye 25 |) Ae 2O|| el 33) lig7 | eae) eA eres 1155] el 5O hema Os | mmm oz) Moule) oA dinztel) iosvl Atastolp ainZlidl Stor ieotfol| atalevll ino kel] (5 oO) a7 $220) 1.26) Ps 30° 1235) 2es30) aaa! e48) ands3) we57|, 62). ere O6l ia ees +1.244+1.2841.33+1.37+1.42\+1.47)+1.51/+1.56/+1.60)+1.65,+1.70+1.74,+1.79 120) “Ls 3i|. 535] 1240) Ts45|- 1240) 54) se): 163) TAGS) Te7aieoie77 | atees TZ) 33 le sol, we42| re 4z|| ale SZ aeS7 | ROL ete OO!) ate7/l| ere 76m OOS S 1230) 1235] 1.40) Weas|) T.4o) a54)) eso) a4) 60) Te73/) Ie ZS) os) aos TG2|) @e37|) We42|| WEA seS1|) E56 SreOn| 1266) eae Z|) Se 7G) seen ee SO) Ie OO! +1.33+1.38+1.43+1.48+1.53)\+1.58 +1.63/+1.68+1.73+1.78)+1.83+1.88+1.93 135) 40) WAS) ou. 50) ere55| e-60)) ar65|) 1670) a475| Se Sol) TESS ele OO areOS TO} 40 ete 40l) S50 ae SO) Ie Onl| seO7|) eate2l ale 77) ele Sz |i 7 ere Oe TRO 1237 WeAal se 48) Ts53l ee58| eos 16S) mes) ore 78)) aees| ie Scie eos EROS TAS Sines 1 1.54] 1 Te Le Tie ies Te Tks ite 7. +1.41/+1-46+1.51+1.56 * “ Smithsonian Meteorological Tables.” SM'THSONIAN TABLES. TaBLeE 136 185 REDUCTION OF BAROMETER TO STANDARD GRAVITY * ENGLISH MEASURES From Latitude 0° to 45°, the Correction is to be Subtracted. i — 19 20 | 21 22 23 24 | 25 ‘a 26a 28 | 29 | 30 | | | | Inch. Inch. | Inch. Inch. Inch. Inch. Inch. Inch. | Inch. Inch, | Inch. | Inch. ere em ee cm oh, pee 050\—0.053 —0.055—0.058—0.. 061 —0, 063—0 , 066 —0.069—0.071—0.074—0.077 —0..079) 050! 0.052 0.055 0.058 0.060 0.063 0.066 0.068 0.071) 0.073 0.076 0.079 .049| 0.052) 0.055) 0.057, 0.060 0.062 0.065, 0.068 0.070, 0.073 0.075) 0.078 049} 0°052) 0.054) 0.057; 0.059) 0.062) 0.064) 0.067; 0.070; 0.072) 0.075! 0.077 048} 0.051| (0.054) 0.056 0.059) 0.061; 0.064; 0.066) 0.069) 0.071 pea 0.076 048 —0.050—0.053—0.055 —0.058—0. 060 —0. 063 —O.066—0.068 —0.071—0.073—0 .076 047| 0.050] 0.052 0.055, 0.057, 0.060 0.062) 0.065 0.067) 0.070 0.072) 0.075 .047| 0.049] 0.051| 0.054, 0.056 0.059 0.061) 0.064 0.066, 0.069 0.071 0.074 .046 0.048 0.051) 0.053 0.055) 0.058) 0.060) 0.063) 0.065, 0.068 0.070 0.072 .045 mca 0.050] 0.052| 0.055] 0.057| 0.059] 0.062} 0.064) 0.066 a i .044—0.047 —O.049—0.051 —0.053—0.056—0, 058 —0. 060—0 , 063 —0.065—0.067 —o.07 .043, 0.046 0.048 0.050 0.052) 0.055) 0.057) 0.059) 0.062) 0.064 0.066 0.068 .042) 0.045) 0.047 0.049 0.051} 0.053| 0.056) 0.058) 0.060) 0.062) 0.065) 0.067 .041; 0.044 0.046 0.048 0.050) 0.052, 0.054 0.057; 0.059 0.061) 0.063) 0. 040) oa 5) aa 0.049} 0.051] 0.053) 0.055) 0.057; 0.059) 0.062) o, .039—0 .041 —0,043—0. 04 —0.047—0.050—0. 052-0. 054 —0. 056, —0.058—0.060—o, .038) 0.049 0.042) 0.044 0.046 0.048 0.050 0.052 0.054 0.056 0.058 o. .037, 0,039, 0.041) 0.043) 0.045, 0.047| 0.049 0.050 0.052, 0.054 0.056 O. .036, 0.038 0.039 0.041 0.043, 0.045, 0.047) 0.049) 0.05I/ 0.053, 0.054) 0. a oe eee eee 0.042) 0.043) 0.045] 0.047| 0.049] 0.051} 0.052) oO. .033—0.035 —0.037 —0 .038 —0.040—0 .042 —0.. 043 —0.045—0.047 —0 .049—0.050—o. .032| 0.033/ 0.035| 0.037} 0.038 0.040! 0.042) 0.043} 0©.045| 0.047] 0.048) o .030| 0.032) 0.033) 0.035) 0.037; 0.038] 0.040| 0.041) 0.043) 0.045| 0.046) o. .029| 0.030, 0.032) 0.033) 0.035| 0.036 0.038) 0.039] 0.041; 0.043| 0.044) Oo .027 ae 0.030) 0.032) 0.033) 0.035) 0.036) 0.037) 0.039) 0.040) 0.042) o .026—0 .027 —0.029 —0.030—0 ,031 —0.033—0.034 —0.035—0.037,—0 .038—0 .040— 0. .024, 0.026) 0.027) 0.028 0.030 0.031/ 0.032) 0.033] 0.035| 0.036) 0.037} o .023| 0.024| 0.025] 0.026; 0.028] 0.029] 0.030, 0.031| 0.032} 0 034) 0.035] o. .021| 0.022} 0.023) 0.025} 0.026) 0.027; 0.028 0.029] 0.030) 0.031|/ 0.032} o .020) 0.021) 0.022 a 0.024, 0.025) 0.026) 0.027} 0.028) 0.029) 0.030; oO .018 —0.019 —0.020—0.021 —0.022—0.023—0.024—0.025—0 .026—0.027;—0.027\—0. .O16) 0.017; 0.018} 0.019! 0.020! 0.021} 0.022) 0.022) 0.023) 0.024) 0.025) oO. .O15| 0.015) 0.016] 0.017) 0.018) 0.019] 0.019} 0.020| 0.021; 0.022| 0.022] 0. .O13| 0.014 0.014) 0.015) 0.016) 0.016} 0.017}; 0.018) 0.018) 0.019) 0.020, oO. OI a 0.012| 0.013} 0.014, 0.014] 0.015] 0.015; 0.016] 0.017| 0.017] Oo. .O10;—0. 010|/—0..011|—0.. O11 0.012 —_0..012\0..013|0.. 0130. 0140 .014,—0.. 0150. .008 0.008 0.009} 0.009 0.009) 0.010 0.010; 0.OIT) 0.011) 0.012 OLOT2! (Oo: .006, 0.006, 0.007 0.007, 0.007 0.008 0.008! 0.008) 0.009) 0.009 0.009 o. .004, 0.005} 0.005) 0.005, 0.005) 0.005] 0.006, 0.006) 0.006 0.006, 0.007 Oo. .003 Pas 0.003 0.003) 0.003/ 0.003) 0.003) 0.004; 0.004) 0.004 ae Oo. | | | -OOI—O.00I—O.00I —0.00I—0.001I —O.00I—0.001'—0 ..001I|—0.O0I —0..00I|;—_ 0. 00I —O. * “ Smithsonian Meteorological Tables.” SMITHSONIAN TABLES. 186 TABLE 136 (continued) REDUCTION OF BAROMETER TO STANDARD GRAVITY * ENGLISH MEASURES From Latitude 46° to 90° the Correction is to be Added. 0.011 0.013 0.015 0.017 0.019 0.021 0.023) 0.025) 0.026 0.028 0.030 0.032 0.033 0.035 0.036 +0.038 0.039 0.041 ota 19 20 | 21 Inch. Inch. Inch. 45 +—0.001—0.00I—0. 001 46 |+0.090:|\+0.001/+0.001 47 | 0.003) 0.003) 0.003 48 | 0.004) 0.005) 0.005 49 | 0.006; 0.006) 0.007 50] 0.008) 0.008 0.009 51 |+0.010/;+0.010-+0.011 2] 0.011; 0.012) 0.012 53 | 0-013) 0.014) 0.014! 54] 0.015} 0.015} 0.016 55 | 0.016) 0.017; 0.018 56 |+0.018-++0.019+0.020 57 | 0.020) 0.021} 0.022 58] 0.021} 0.022) 0.023 59 | 0.023) 0.024) 0.025 60 | 0.024) 0.026) 0.027 61 |+0.026/+0.027\+0.028 62] 0.027) 0.029) 0.030 63] 0.029) 0.030 0.032 64] 0.030) 0.032) 0.033 65 | 0.031) 0.033) 0.035 66 |+0.033,+0.034+0.036 67 | 0.034, 0.036 0.038 68 | 0.035) 0.037) 0.039 69 | 0.036; 0.038) 0.040 70} 0.038 0.040) 0.042 71 !|+0.039/+0.041|+0.043 72| 0.040) 0.042) 0.044 73 | 0.041} 9.043) 0.045 74] 0.042) 0.044] 0.046 75 | 0.043| 0.045) 0.047 76 |+0.044+0.046-+0.048 77} 0.044) 0.047| 0.049 78 | 0.045) 0.047] 0.050 79 | 0.046) 0.048 0.051 80] 0.046) 0.049) 0.051 81 |+0.047\+0.049-+0.052 82] 0.047| 0.050) 0.052 83 | 0.048) 0.050) 0.053 84] 0.048) 0.051) 0.053 85 | 0.049) 0.051; 0.054 90 !+0.049-+0.052/+0.055 SMITHSONIAN TABLES. 0.042 0.044 +0.045 .046 -047 .048 .049 oo0o0°o 050 O51 052 .053 054 ooo0o°o +054 -055 -056 .056 .056 ooo0o°o +0.057 23 24 | 25 26 27 28 29 30 Inch. Inch. Inch. Inch, Inch. Inch. Inch. Inch —0.001I|—0.00I—0.001,-—0.00I —O.001 —O.001|—0.001/—O.001 +0.001|+0.001)+0.001|+0.001/+0.001/+0.001/+0.001/+0.001 0.003} 0.003) 0.003 0.004 0.004 0.004 0.004 0.00. 0.005) C.006 0.006, 0.006 0.006 0.006 0.007, 0.007 0.007} 0.008 0.008 0.008 0.009 0.009) 0.009 0.01 0.010) 0.010) 0.010} O.OII| 0.011; 0.012) 0.012) 0.012 +0.012/+0.012|+0.013/+0.013/+0.014+0.014-+0.015/+0. 0.014] 0.014) 0.015) 0.015] 0.016 0.016) 0.017] oO. 0.016, 0.016, 0.017) 0.018 0.018 0.019 0.020 0. 0.018, 0.019 0.019 0.020 0.021 0.022 0.022) Oo. 0.020) 0.021) 0.021} 0.022 oo 0.024) 0.025] Oo. +0.022|+-0.023/+0.024/+0.024'+0.026+0.026;+0.027/+0 0.024' 0.025) 0.026) 0.027; 0.028 0.029 0.030; O 0.026} 0.027/ 0.028) 0.029 0.030, 0.031) 0.032) oO 0.028) 0.029} 0.030 0.031, 0.032 0.033) oO 035) O 0.029) 0.031) 0.032) 0.033 oes 0.036 0.037) Oo +0.031/-+0.033 +0.034|+0.035 +0.037 +0.038 +0.039 +o. 0.033) 0.034] 0.036) 0.037) 0.039) 0.040) 0.042) Oo. 0.035, 0.036) 0.038 0.039 0.041) 0.042 0.044 0. 0.036] 0.038 0.040) 0.041) 0.043) 0.044 0.046 o. 0.038} 0.040) 0.041} 0.043) 0.045) 0.046) 0.048) o. +0.040/+0.041|-+0.043/-+0.045/+0.047|/+0.048)+0.050-+0. 0.041] 0.043) 0.045} 0.047| 0.048) 0.050) 0.052) oO. 0.043) 0.045} 0.046) 0.048) 0.050) 0.052) 0.054) oO. 0.044) 0.046) 0.048) 0.050) 0.052) 0.054) 0.056) Oo. 0.046) 0.048) 0.050} 0.052} 0.053) 0.055) 0.057] o. +0.047/+0.049-+0.051|+0.053|/+0.055|+0.057/+0.059|/++0. 0.048) 0.050) 0.052) 0.054; 0.057) 0.059 0.061) oO. 0.049} 0.052) 0.054 0.056) 0.058) 0.060 0.062) Oo. 0.051; 0.053} 0.055} 0.057; 0.059! 0.062) 0.064) oO. 0.052} 0.054) 0.056) 0.058) 0.061) 0.063) 0.065] oO. +0.053/+0.055|+0.057-+0.060+0.062)\+0.064 0.066 o. 0.054, 0.056 0.058 0.061) 0.063) 0.065 0.068) oO. 0.055} 0.057 0.059} 0.062) 0.064) 0.066, 0.069) oO. 0.055) 0.058 0.060; 0.063) 0.065) 0.067, 0.070) oO. 0.056, 0.059 0.061) 0.063) 0.066] 0.068 0.071) oO. +0.057|+0.059 +0.062/+0.064 +0.067/+0.069,+0.072/+0. 0.057, 0.060/ 0.062) 0.065 0.067| 0.070) 0.072) o. 0.058 0.061) 0.063) 0.066 0.068 0.071) 0.073) oO. 0.059 0.061) 0.064 0.066 0.069 0.071) 0.074 oO. 0.059 0.061) 0.064, 0.067 0.069) 0.072) 0.074 O. +0.060-+0.062-+0.065 +0.068-+0.070+0.073-+0.075 +0. * “ Smithsonian Meteorological Tables.” TABLES 137 AND 138 187 TABLE 137,—Correction of the Barometer for Capillarity * 1. METRIC MEASURE. HEIGHT oF Meniscus 1N MILLIMETERS. Diameter of tube ik H 0.8 | 1.0 | 1.2 1.4 in mm. Correction to be added in millimeters. 1.54 1.98 2.37 - 0.86 1.19 1.45 1.80 .56 0.78 |! 0.98 1.21 .40 ‘53 .67 0.82 .29 3 .46 .56 .21 .28 33 .40 IS .20 125 .29 .10 14 18 21 .07 .10 “13 15 .04 .07 -10 a2 . BRITISH MEASURE. HEIGHT OF MENISCUS IN INCHES. Diameter of tube .O1 | .02 | .03 | .04 | .05 .06 in inches. Correction to be added in inches. 0.069 0.092 0.116 ~ 033 .045 059 0.078 O19 .028 .037 -047 O13 018 023 029 .008 O12 O15 018 .006 .008 , O12 003 .005 : .008 .002 .004 j .006 .OOT .002 f .004 * The first table is from Kohlrausch (Experimental Physics), and is based on the experiments of Mendelejeff and Gutkowski (Jour. de Phys. Chem. Geo. Petersburg, 1877, or Wied. Beib. 1877). The second table has been calcu- lated from the same data by conversion into inches and graphic interpolation. TABLE 138.—Volume of Mercury Meniscus in Cu. Mm Diameter of tube in mm Height of meniscus. Scheel und Heuse, Annalen der Physik, 33, p. 291, 1910. SMITHSONIAN TABLES. T88 TABLE 139 PRESSURES AND THE BOILING POINT OF WATER Useful when a boiling-point apparatus is used in the determination of heights. (A) METRIC UNITS. | Tem- perature. | Z5OR7Si30L. 362.65 374.51 | 376.02) 377. 389 .80 | 391 . 36} 302. 405.61 | 407.22] 408. 421.95 |423-61| 425. 438 .83 | 440.55 450.28] 458.06] 459. 474-31 | 476-14] 477. 492.93 | 494.82] 406. 512.15/514. 531.99| 534.01] 536. 552.48] 554.56] 556. 573-61] 575. 595-41 | 507. 2 | 617.90] 620. 641.09] 643.45]645. 665 .00| 667 . 43 | 669. 689.65 | 692.15] 694. 715.04| 717.63| 720. 741.21| 743.871 740. 768.17| 770.91 | 773.66 | 776.42 Tem- perature. 185 Inches. | Inches. | Inches. | Inches. | Inches. | Inches. | Inches. | Inches. | Inches. | Inches. 185° 117.075 |17.112|17.150| 17.187] 17.224| 17.262] 17.300] 17.337 | 17.375] 17.413 186 |17.450|17.488| 17.526] 17.564] 17.602] 17.641] 17.679] 17.717 | 17.756] 17.794 187 |17.832 |17.871117.910| 17.948] 17.987| 18.026] 18.065| 18.104 | 18.143] 18. 182 188 |18.221/18.261 . 300} 18. 340] 18.379] 18.419] 18.458] 18. 498 | 18.538] 18.578 189 |18.618] 18.658] 18.698] 18.738] 18.778] 18.818] 18.859] 18.899 | 18.940] 18.980 | 190 .02I | 19.062| 19.102] 19.143] 19.184] 19.225} 19.266] 19.308 | 19.349] 19.390 IgI -431 -473 -514| 19.556] 19.598] 19.639| 19.681] 19.723 | 19.765] 19.807 192 .849 { 19.892 | 19.934] 19.976] 20.019] 20.061 | 20.104] 20. 146 | 20. 189] 20.232 193 275 {20.318 301 .404| 20.447] 20.490] 20.533) 20.577 | 20.620 664 194 -707 | 20.751 -795 .839| 20.883 | 20.927 | 20.971] 21.015 | 21.059 .103 195 .148) 21.192 | 21.237! 21.282! 21.326] 21.371 | 21.416] 21.461 | 21.506] 21.551 196 .597 | 21.642 |21.687| 21.733] 21.778) 21.824] 21.870] 21.915 | 21.961] 22.007 197 -053 , 22-099 22.145| 22.192| 22.238| 22.284] 22.331 | 22.377 | 22.424] 22.471} 198 .517] 22.564 22.611 .658 | 22.706) 22.752] 22.800] 22.847 | 22.8905 -942 199 .990 | 23.038 | 23.085 | 23.133 | 23. 181 | 23.229] 23.277 | 23.325 | 23.374] 23.422 200 .470| 23.519} 23.568 23.616] 23.665 | 23.714| 23.763] 23.812 | 23.861 .910 201 -959|24.009'24.058) 24.108} 24. 4.207| 24.257 - 307 | 24.357 202 -457|24.507 24.557] 24.608) 24. 4.709) 24.759] 24.810 | 24.861 203 ‘ .O14 , 25.065 pO 25 ye .219| 25.271 .322)25.374 204 ‘ .530 | 25.582] 25.634] 25. .738| 25.791 | 25.843 | 25.806 205 ; .054 26.107 | 26.160) 26. 26.266 | 26.319| 26.373 | 26.426 206 3 -587 |26.641 .695 : 26.803} 26.857 | 26.912 | 26.966 207 . .130/ 27.184] 27.239] 27. 27 .349 | 27.404] 27.460] 27.515 208 |27.62 LOSTIZ7e73 727579327. 27 .904| 27.960] 28.016 | 28.073 27 209 : .242 | 28.298 | 28.355 | 28. 28.469 | 28.526] 28.583 | 28.640 210 75 .812 | 28.869 | 28.927 | 28. 29.042| 29.100} 29.158 .216 211 : 391 | 29.450| 29.508] 29. 29.626 | 29.685 | 29.744 .803 212) 120.02 .Q8I | 30.040 | 30.100 ; 30.219 | 30.279 | 30.339 -399 213 : . 580 | 30.640 | 30.701 ; 30.822 | 30,883} 30.944 .005 214 -199 | 31.250 oe Stt ‘ 31.435 | 31.497] 31-559 | 31-621 SMITHSONIAN TABLES, Taste 140 189 DETERMINATION OF HEIGHTS BY THE BAROMETER 5 —8 B+ 8B C (in feet) = 52494 [: +. Be English measures. goo Formula of Babinet: Z = C C (in meters) = 16000 [: + 2% +4) metric measures. 1000 In which Z = difference of height of two stations in feet or meters. Bo, B = barometric readings at the lower and upper stations respectively, corrected for all sources of instrumental error. %, ¢ = air temperatures at the lower and upper stations respectively. Values of © ENGLISH MEASURES. METRIC MEASURES. 4 (t) +2). G Log C 4 (4) +2). G Log C Fahr. , Meters. 10° 4-698 34 15300 4.18639 15 70339 3 15488 «19000 15016 -19357 20 4-70837 15744 -19712 25 .71330 15872 -20063 30 4.71818 16000 4.20412 35 -7 2300 16128 .20758 16256 -21101 40 4-72777 16354 45 73248 16512 50 4.73715 16640 55 -74177 2 16768 16896 4-74633 17024 75085 17152 4.75532 17280 ‘75975 17408 17536 4.76413 17064 -76847 17792 4.77276 17920 -77702 18048 E 18176 4.78123 18304 Values only approximate. Not good for great altitudes. A more accurate formula with corresponding tables may be found in Smithsonian Meteorological Tables. SMITHSONIAN TABLES. Igo TABLES 141 AND 142 VELOCITY OF SOUND TABLE 141.—Velocity of Sound in Solids The velocity of sounds in solids varies as ¥ 'E/p, where E is Young’s modulus of elasticity and p the density. These constants for most materials vary through a somewhat wide range. The numbers can be taken only as rough approximations to the velocity in any particular case. When temperatures are not marked, between 10° and 20° is to be understood. NHNNNNHRNNHNNN Ash, along the fiber... . ac across the rings. . . along the rings.... Beech, along the fiber. . ““ across the rings. along the rings. . Elm, along the fiber... . ‘““ across the rings: along the rings.. Fir, along the fiber Mahogany, along the ae ae NNNNNNNNNDND DWAWOAAN AUN Magia along the fiber. . Oak, along the fiber. . Pine, along the fiber... . Poplar, along the fiber. . Sycamore, along the NNN NW vv (1) Masson. (2) Wertheim. (3) Cast steel, Wertheim. (4) Melde. (5) Chladni. (6) Gray & Milne. (7) Stefan. 8) Warburg. (9) Ciccone & Campanile. (10) Exner. TABLE 142.—Velocity of Sound in Water Substance : Substance Water, air-free. Pik Water, sea: (continued) dust-free . Seine River eae N. Atlantic, distilled 1228m deep 10% Na Cl sol.. Carib. Sea, 15% Na Cl sol.. ‘ 338m deep 20% Na Cl sol.. Carib. Sea, Water, sea: 1771m deep 35.1% salt Pacific, 2962m deep. . nav On n wo Explosive Waves: 35% _ “ : Gun Cotton, 9 0z.... se ae Io ae ee % LS ier ce 64 “ae NNNIN (1) Dérsing, 1908. (2) Ionescu, 1924. (3) Wood, Browne, Cochran, 1923. (4) Colladon-Sturm. (5) Wertheim. (6) Heck & Service, 1924. (7) Threlfall, Adair, 1889, see Barstow’s Sound, p. 518. SMITHSONIAN TABLES TABLE 143 IgI VELOCITY OF SOUND IN LIQUIDS AND GASES For gases, the velocity of sound = ¥7vP/p, where P is the pressure, p the density, and + the ratio of specific heat at constant pressure to that at constant volume. For moderate temperature changes V; = Vo(1 + at) where a = 0.00367. The velocity of sound in tubes increases with the diameter up to the free-air value as a limit. The values from ammonia to methane inclusive, except for argon and helium, are for closed tubes. Substance Temp. C| m/sec. Alcohol, 93% Ethyl “ Methyl 1143 Ammonia, .880 1663 1166 Carbon bisulphide.... .... 1060 Chloroformeyeeec ose 983 Mercury 1407 Turpentine oil 1326 Gases: Air, dry, 1 atmosphere.... 331.7 waies 25 ~ ete 332.0 : 334-7 350.6 386 553 700 415 308 666 337-1 337-4 258.0 189 206.4 205.3 314 971 1269.5 1286.4 490.4 432 325 337-8 261.8 aI7.2 “c ‘* disulphide Chlorine Ethylene Hydrogen Illuminating gas Nitric oxide Nitrogen Nitrous oxide Oxygen Explosive waves in air: oO oO oO oO oO oO oO oO O oO oO oO oO oO O 0 336 500 931 1268 230.6 179.2 401 404.8 Authority Cisman, 1926 Busse, 1924 Dérsing, 1908 Cisman, 1926 Dorsing, 1908 Mean Bungetziam Dorsing, 1908 Mean % (Witkowski) Stevens Masson Mean ID), (Cy 12%, repr Wullner Dulong Brockendahl, 1906 Masson Martini Strecker Dulong Scheel, Heuse, 1919 Dulong Zoch Masson “c Mean Dulong Violle, Cong. Intern. Phys. 1, 243, 1900 Masson ae “ec Treitz, 1903 Supersonics: Reid, 1930:—Air, 0°C, no CO, 42 Kc/sec., 331.75 m/sec.; 20°C, sat. H2O, 333.1 m/sec.; 140 Ke/sec. 331.60, 332.92, respectively; Thompson, 1930:—109 c/sec. sat. H2O vapor, 27°C, 432 m/sec.; Poole, 1930:—Water, distilled, audio-frequency, 25°C, 1485 m/sec. SMITHSONIAN TABLES 192 TABLES 144 AND 145 MUSICAL SCALES The pitch relations between two notes may be expressed precisely (1) by the ratio of their vibra- tion frequencies; (2) by the number of equally-tempered semitones between them (E. S.); also, less conveniently, (3) by the common logarithm of the ratio in (1); (4) by the lengths of the two portions of the tense string which will furnish the notes; and (5) in terms of the octave as unity. The ratio in (4) is the reciprocal of that in (1); the number for (5) is 1/12 of that for (2); the number for (2) is nearly 40 times that for (3). Table 144 gives data for the middle octave, including vibration frequencies for three standards of pitch; As=435 double vibrations per second, is the international standard and was adopted by the American Piano Manufacturers’ Association. The ‘“just-diatonic scale’? of C-major is usually deduced, following Chladni, from the ratios of the three perfect major triads reduced to one octave, thus: 4 : 5 . 6 4 : 5 : 6 4 : 5 : 6 F A Cc E G B D 16 20 24 30 36 45 54 24 27 30 32 36 40 45 48 Other equivalent ratios and their values in E. S. are given in Table 145- By transferring D to the left and using the ratio 10: 12: 15 the scale of A-minor is obtained, which agrees with that of C-major except that D=26 2/3. Nearly the same ratios are obtained from a series of harmonics beginning with the eighth; also by taking 12 successive perfect or Pythagorean fifths or fourths and reducing to one octave. Such calculations are most easily made by adding and subtracting intervals expressed in E. S. The notes needed to furnish a just major scale in other keys may be found by successive transpositions by fifths or fourths as shown in Table 145. Disregarding the usually negligible differ- ence of 0.02 E. S., the table gives the 24 notes to the octave required in the simplest enharmonic organ; the notes fall into pairs that differ by a comma, 0.22 E. S._ The line “mean tone” is based on Dom Bedos’ rule for tuning the organ (1746). The tables have been checked by the data in Ellis’ Helmholtz’s “‘Sensations of Tone.” TABLE 144.—Data for Middle Octave Interval. Ratios. Logarithms. | Number of double Vibrations per second. Tem- pered. Tem- pered. | eS en eee 0. Just. Tem: | Just. | Just.| Just. Tem: | Tem. | Tem- Just. pered. | pered- | pered. | pered Just. -00000 -00000 | 25 258.7 | 258. -05926 -02509 || 274. .12246 -05017 291.0] 290. - 18921 -07526 | 307. -25992 - 10034 B23nANl 25 33484 | -12543 | 344-9 | 345- -41421 |} -I5051 | 365. -49831 || . -17560 | 388 -58740 20069 410. -68179 22577 -78180 . 25086 88775 +27594 | .00000 +30103 261.6 | 271. 277. 287. 293 - 304- Sari. 322. 329.6 | 341. 349. 361. 370. 383. 392. 406. 415-3 | 430 440.0} 456 466. 483 493 - 511. 523: 542- 2.04 3.86 4.98 SO CONTOQNUN CSN) AO 77 NOn OWOOK DHnN WORM ORKNRO DROW A 0 AY AS enw fF uM AN B E A D G Cc F NOON SSS wmmoododa ODOONHNHNN 5.88 76 | 5.88 3.84 5.38 nNnhpPHRL pRPPPp NNO O10 10 Tie 2.98 4-70/| 5.51 7:73 | Cycle of fifths 3.18 | 4.08 | 5.22 | 6.12 | 7.02 | 8.16 Cycle of fourths 2.94 | 3.84 | 4.98 | 5.88 | 6.78 | 7.92 Mean tone : 3.11 | 3.86 | 5.03 | 5-79 | 6.97 | 7-72 Equal 7 step 3.43 5-14 6.86 | Harmonic Series : ( es ) 3.86 ( 3 ) = Be ( es) SMITHSONIAN TABLES. TABLES 146-149 193 TABLE 146.—A Fundamental Tone, its Harmonics (Overtones) and the Nearest Tone of the Equal-tempered Scale No. of partial Frequency Nearest tempered note Corresponding frequency.... No. of partial Frequency Nearest tempered note Corresponding frequency.... CHARACTERISTICS OF SPEECH, Music, AND NOoIsE (See Kaye, Nature 128, 253, 1931; Fletcher, Rev. Mod. Phys., 3, 258, 1931.) Average ear perceives frequencies 20~20,000 cycles/sec. Upper limit less with increasing age. Ordinarily attention largely restricted to 505,000 for speech, 35~7,000 1n music. Matching of sounds.—Average ear detects 10 per cent difference of energy when two notes of medium loudness sound alternately without break; doubled if interval of silence; ordinarily 25 per cent holds. Weber-Fechner law.—When sound sensation advances arithmetically, physical intensity advances geometrically (Kingsbury). Frequencies, 700-4,000 c/sec., relation between loudness and intensity independent of frequency. Lower frequencies, loudness increases proportionally more rapidly than intensity. TABLE 147.—The Bel and the Decibel Bel, Decibel.—One bel is 10-fold increase in power or energy. Intensities differing as r to 1 differ by log 7 bels. Ra GTOMIMECNSIELES: oa 3. lors = aye oe I 10 100 1,000 10,000 108 Number decibels, 1o logr......... © 10 20 30 40 130 db Least perceptible change in loudness of a sound of medium loudness under various con- ditions = 1 db (0.2 to 9 db according to frequency and loudness). Threshold of audibility taken as zero (see Table 148). Pure sounds of medium frequency: range of audibility be- tween threshold and sensation of “‘feeling’’ of the sound about 130 db. If intensity levels of two pure sounds is the same, then if each is increased by the same amount of energy they no longer give an equal sensation of tone. Standard for mixed sounds may be taken as a pure note. Frequency about 1000 cycles/sec. Threshold value (zero) = about 1 millidyne/cm®. TABLE 148.—Loudness Levels of Various Noises Average = ate Distance decibels z istance decibels ft. above Source ft. above threshold threshold Source Quiet whisper 10 1 Lindbergh applause.. Street Onutetigardentesen | pa. 30 Pneumatic drill 20 Elevated R.R., N.Y. 20 INS Wasi wayeese: 2. Unt. Riveting Steamship siren Airplane cabin Airplane engine Ordinary talk 50 Express train 60 Steamship siren... 1,500 60 Biisy, traitic, NepYien a | oe 72 Police whistle 80 Lion roaring, Zoo.. 85 WwWNHWF AH OD (1) Davis, Journ. Roy. Aeron. Soc., 1931. (2) Free. (3) Galt. (4) Parkinson, Journ. Acoust. Soc. Amer., 1930- (5) Fletcher. (6) Kaye. TABLE 149.—Peak Power in Watts of Musical Instruments (Fortissimo) (Sivian, Dunn, White, Journ. Acoust. Soc. Amer., Jan. 1931.) 5-piece orchestra ..... 70 MrOmbONE wevetaraveicve erciers 6 Piccolo dcidistcxelenererers 0.08 arge bass drum...... 25 Piano rics ecco 0.4 BIMtet go aec fe cloleeiciers 0.06 me sougan steers citer 13 Prumpetal o.cttwecrcemoeies 0.3 Glarinetime. soc wos 0.05 SA LesAnUnie sie eee ee 12 Bassmtubaw eee ete. 0.2 Erench) norms — cacao 0.05 ymibalgy csleies les sleloclevelels 10 BAS VIO ioeisisice creer 0.16 Miriane ler e.sererciere asuetets 0.05 Peak powers, fortissimo playing. Orchestra of 75 pieces. Both peak and average powers of orchestra are about 10,000 times such for conversational speech. Violin played as softly as possible, 4 microwatts. Threefold peak power 20,000,000 times this. SMITHSONIAN TABLES 194 TABLES 150-152 TABLE 150.—Relative Strength of the Partials in Various Musical Instruments The values given are for tones of medium loudness. Individual tones vary greatly in quality and, therefore, in loudness. Strength of partials in per cent of total tone strength. Instrument. Tuning fork on box. . | | 11 HwWORH Avr of O | | 4 tb HOOF H TABLE 151.—Miscellaneous Sound Data Koenig’s temperature coefficient for the frequency (7) of forks is nearly the same for all pitches. Nt = No(1 — o.ooo11t® C), Ann. d. Phys. 9, p. 408, 1880. Vibration frequencies for continuous sound sensations are practically the same as for continuous light sensation, ro or more per second. Helmholtz’ value of 32 per sec. may be taken as the flicker value for the ear. Moving pictures use 16 or more per sec. For light the number varies with the intensity. The quality of a musical tone depends solely on the number and relative strength of its partials (simple tones) and probably not at all on their phases. The wave lengths of sound issuing from a closed pipe of length L are 4L, 4L/3, 4L/s, etc., and from an open pipe, 2L, 2L/2, 2L/3, etc. The end correction for a pipe with a flange is such that the antinode is 0.82 x radius of pipe beyond the end; with no flange the correction is 0.57 x radius of pipe. The energy of a pure sine wave is proportional to n*A*; the energy per cm® is on the average 2p7*U*A*/)*; the energy passing per sec. through 1 cm? perpendicular to direction of propagation is 2pm7*U%A*/)*; the pressure is 3(y + 1) (average energy per cm*); where n is the vibration number per sec., \ the wave length, A the amplitude, VY the velocity of sound, p the density of the medium, y the specific heat ratio. Altberg (Ann. d. Phys. 11, p, 405, 1903) measured sound-wave pressures of the order of 0.24 dynes/cm? = 0.00018 mm Hg. TABLE 152.—Audibility as Dependent on Sound Pressure and Frequency The ear detects sounds over a pressure range about 0.001 to 1ooo dynes/cm*; over much of this range it differentiates between complex sounds so nearly alike that no existing physical device can distinguish them. Plot shows minimum audibility pressures from 72 normal ears from 60 to 4000 cycles (both scales logarithmic); standard deviation indicated by dotted curves. The maximum audibility curve was obtained from 48 normal ears. A louder sound becomes painful. The AC CnSEY of pressure neces- ae is about _ required to excite the tactile nerves in the finger tips. (Wegel, » Nat. Acads Se. P- 155, 1922 CYCLES PER} SECOND SMITHSONIAN TABLES \ ‘\ 1000 ©2000 5000 10000 20000 TABLES 153-156 195 TABLE 153.—Speech (Fletcher, Rev. Mod. Phys., 3, 258, 1931.) Speech is composed of vowels and consonants. Most are continued in steady tones (con- tinuants), long vowels, a, short, i, diphthongs, ou, semivowels, 1, fricative consonants, s; others are interrupted (stops). The pure stops are p, t, ch, k; voiced, b, d, j, g. When frequencies, f, are measured in kilocycles, then the pitch P=log, F. J is the intensity of the sound passing through a cm* of the wave-front. The intensity level I =1ogio J and is expressed in bells. TABLE 154.—Characteristic Resonance Values for Spoken Vowels The larynx generates a fundamental tone of a chosen pitch with some 2o partials, usually of low intensity. The particular partial, or partials, most nearly in unison with the mouth cavity is greatly strengthened by resonance. Each vowel, for a given mouth, is characterized by a particular fixed pitch, or pitches, of resonance corresponding to that vowel’s definite form of mouth cavity. These pitches may be judged by whispering the vowels. It is difficult to sing vowels true above the corresponding pitches. The greater part of the energy or loudness of a vowel of a chosen pitch is in those partials reinforced by resonance. The vowels may be divided into two classes, — the first having one char- acteristic resonance region, the second, two. The representative pitches of maximum resonance of a mouth cavity for selected vowels in each group are given in the following table. Vowel indicated by italics in Pitch of maxi- Vowel indicated by italics in Pitch of maxi- the words. mum resonance. the words, mum resonance. father, far, add, 800 and 1840 fall, feather, 691 and 1953 rode, bait, 488 and 2461 move, pique, 308 and 3100 Pitch in octaves from one kilocycle. For the first 6 vowels high pitch region less intense (Fletcher). pool —0.3 —1.3. talk —0o.I —0.7 tap —o045 +08 tip —124+1.2 put OO. — ai. Le ston + 0.2 —0.5 ten —0oO7 +090 team —I1.4 +1.3 tone —o.2 —1.0 father +03 —03 tape —og +1.1 TABLE 155.—Speech Power (Fletcher) Average conversational speech power, 10 microwatts or 100 ergs per second. About 1/3 of time no sound is flowing (pauses), so if silent intervals are excluded these values may be taken as 15 and 150. Shouting as loud as possible increases 100-fold, whispering in- telligibly 1/10,000. The mean speech power may be defined as average over 1/100 sec. period; phonetic speech power, max. value of mean speech power of a fundamental vowel or consonant; peak speech power, max. value of instantaneous power over interval considered. TABLE 156.—Phonetic Powers, Average Conversation 0 680 6 470 ifn Sto 1 x60 ch 42 S 16 V Ti 5 GOON (1107400, i 260 sh 80 n 36) it 15 b 7 th I Oo 510 apn370 Ch220 ee e738 j 23 g 15 d oy a 4090 Cun 50) esti 210 mt 52 Zz 16 k 13 D 6 The most powerful sound is “ azwl,’—900 times the power of th in thigh. Intoned without emphasis it is about 50 microvolts. Peak powers are 10-20 times the phonetic power. In ordinary conversation 2% of time > 20 db over average level ; 42%, 6 to 16 db. Note.—For Bibliography of Acoustics of Buildings (Watson) see Nat. Res. Council, Reprint, and Circulars, No. 98, 1931, or Journ. Acoust. Soc. Amer., 2, 14, 1931. SMITHSONIAN TABLES 196 TABLE 157 VELOCITY PRESSURE AT DIFFERENT AIR SPEEDS The resistance F of a body of fixed shape and presentation moving through a fluid may be written oi Fis oR) @) in which p denotes the fluid density, » the viscosity, Z a linear dimension of the body fixing the scale, and V is the speed of the body relative to the fluid. The dimensionless ratio ues is termed the Reynolds Number R. Values of R are comparable only for geometrically bw similar bodies. The quantity (1/2)pV? is termed the velocity pressure q; it is the increase in pressure above the static pressure set up in a tube whose open end is pointed into the relative wind. The relation (1) is usually written F = CAq, A being some specifically defined area as, for example, the area of the projection of the body on a plane normal to the wind. C is usually termed the absolute resistance coefficient. It has the same value in any self- consistent system of units and is a function of the Reynolds Number R. The method of defining A and L must in every case be explicitly stated. For speeds near the speed of sound, C is also a function of the ratio of the air speed to the speed of sound. Values given in these Tables can not then be used. The table gives values of the velocity pressure qg at different air speeds. In conjunction with the values of C in subsequent tables, this table can be used for computation of the resistance under specified conditions. It is computed for standard air density: dry air, normal CO, content, 15°C, one atmosphere, standard gravity, metric slugs (Ages = 0.002378 slugs ‘ea (mass) 0.12497 maz 9.807 m3 ft-* \ 322. 156t.* For other densities the values must be multiplied by the ratio of the actual density to the standard density. Air Air Air Air Air speed Pressure,q | speed Pressure,g | speed Pressure,q | speed Pressure, q | speed Pressure, g m/sec. kg/m? m/sec. kg/m? m/sec. kg/m? m/sec. kg/m? m/sec. kg/m? 0.063 on 7.56 21 27.56 31 60.06 4I 105.1 .250 12 9.00 22 30.25 32 64.00 42 110.3 .562 13 10.56 23 33.06 Be 68.06 43 115.6 1.00 14 12.25 24 36.00 34 72.25 44 121.0 1.56 15 14.06 25 39.06 35 76.56 45 126.6 2.25 16 16.00 26 42.25 36 81.00 46 13 2"2 3.06 17 18.06 2H 45.56 37 85.56 47 138.1 4.00 18 20.25 28 49.00 38 90.25 48 144.0 5.06 19 22.56 29 52.56 39 95.06 49 150.1 6.25 20 25-00 30 56.25 40 100.0 50 156.3 COO ON ANLWN _ Air Air Air Air Air speed Pressure, qg | speed Pressure,qg | speed Pressure, gq | speed Pressure,q | speed Pressure, ft./sec. 1b./ft.? ft./sec. Ilb./ft.? ft./sec. lb./ft.? ft./sec. Ib./ft.2 ft./sec. 1b./ft.2 0.00119 II .1438 21 5243 55 3.597 105 Toa .00476 12 elle. 22 25755 60 4.280 I1IO 14.39 .O1070 13 -2009 23 .6290 65 5.024 115 15.72 .O190 14 .2330 24 .6849 70 5.826 120 Lyle .0297 15 -2675 25 -7431 75 6.688 125 18.58 .0428 16 -3044 30 1.070 80 7.610 130 20.09 .0583 17 -3436 355 2-457, 85 8.591 135. (21-67 .O761 18 -3852 40 1.902 90 9.631 140 23.30 .0963 19 -4292 45 2.408 95 10.73 145 25.00 11 SOn)) | 2O -4756 50 2.973 100 11.89 150 26.75 OO ON DAuNLWN _ SMITHSONIAN TABLES TABLE 158 197 CORRECTIONS TO ROBINSON CUP ANEMOMETERS The official Weather Bureau instrument used for measuring speed of natural winds is a Robinson type cup anemometer. Before January 1, 1928, a four-cup driving unit was used; after that date a three-cup unit, because of the large errors of the older type at high speeds. The table gives the speeds indicated by the old and new instruments at various true speeds. Indicated Indicated Indicated Indicated Indicated Indicated speed, speed, speed, speed, speed, speed, True four-cup three-cup True four-cup three-cup True four-cup three-cup speed, standard, standard, speed, standard, standard, speed, standard, standard, miles miles miles miles miles miles miles miles miles per hour perhour per hour perhour per hour’ perhour per hour per hour per hour 5 5 5 40 50 41 75 98 © 79 10 II 10 45 57 47 80 105 84 15 17 15 50 64 52 85 112 89 20 23 20 55 71 57 90 118 95 25 30 25 60 78 63 95 125 100 30 37 31 65 85 68 100 132 105 35 44 36 70 QI 73 110 145 116 Note.—Values above a true speed of 75 miles per hour are extrapolated. It must be borne in mind that problems in aerodynamics can not be idealized as easily as many problems in mechanics. The side of a building may not be regarded as a thin flat plate in computing the force of the wind, and data for a cylinder of a given length can not be directly applied for the wind force on a cylinder of some other length. Further, objects nearby exert an appreciable influence. These complications limit the strict application of a test on a particular object to geo- metrically similar objects in similar surroundings. They also cause apparent discrepancies among the results of different experimenters which are to be attributed to departure from geometrical similarity of the models, to the effects of the relative size of the body and the air stream, of the supports or other nearby objects, and to differences in the fine structure (turbulence) of the approximately steady air streams rather than to errors of measuring. The data here given are intended to apply to the ideal condition of an isolated body of exactly the shape specified in a uniform, steady air stream of infinite extent. Example of tables: Take the problem of the resistance of a sphere 1.5 cm. diam. moving at a speed 35 m/sec. (3500 cm/sec.) through still air of density 0.ooro g/cm* and viscosity 0.000173 g/cm sec. The Reynolds number is 3500 X 1.5 X 0.0010/0.000173 Or 30,347; logiR is 4.482; whence from Table 162 C is 0.50. From Table 157 the value of q for std. density is 76.56 kg (force) /m’. The ratio of the actual to std. density is 0.0010/0.0012255 or 0.816. The resistance is therefore {0.50 } { 7/4 } { 1.5/100 }?{ 76.56 } { 0.816 | =0.00552 kg (force) = 5413 dynes. SMITHSONIAN TABLES 198 TaBLE 159 RESISTANCE COEFFICIENT FOR THIN FLAT PLATES NORMAL TO THE WIND The pressure on a thin rectangular plate varies with the “aspect ratio,” a term intro- duced by Langley for the ratio of the length of the leading edge (span) to the chord length. The resistance coefficient is nearly independent of the Reynolds Number if the Reynolds Number (ZL taken as the chord length) is greater than 100. In the following table the values of C are given as a function of the aspect ratio. 4 is taken as the area of the plane, viz., product of chord and span. Values of C for circular disks are practically the same as for a square plate. Aspect ratio I 2 3 4 5 6 7 8 00 Cc I.12 1.18 1.22 1.24 1.26 1.28 1.30 1232 2.00 (2 jo ASPECT Rario 1. SQUARE PLATE. Ix - COEFFICIENTS OF RECTANGULAR PLATES, SEE P. 190. SMITHSONIAN TABLES TABLE 160 199 FORCES ON THIN FLAT PLATES AT ANGLES TO THE WIND For plates at angles, the force is usually resolved into components at right angles and parallel to the direction of the relative wind. The components, termed the lift and drag respectively, are expressed in the form of absolute coefficients, the forces being divided by the product of the velocity pressure and the area of the plate (N. B.—wnot the projected area on a plane normal to the wind). The line of action of the force is given by the inter- section of the resultant force with the plate expressed as the ratio of the distance of the intersection from the leading edge to the chord length, a quantity called the center of pressure coefficient. The lift coefficient L = lift/Agq, the drag coefficient D = drag/Agq, and the center of pressure coefficient for various angles are given for plates of aspect ratios 1, 3, and 6 in the form of graphs. (See page 198.) The following formulae indicate the use of the coefficients from the plots for the deter- mination of the forces: Fa = component of resulting wind force parallel to wind = drag = DAgq; F, = that normal to wind and width al =lift = LAg; x- (see small figure in upper set of curves) = CP: W; W is that dimension of the plane of reference which makes the least angle with wind. = area of one surface of plate. D, L, CP are independent of Reynold’s No. and tempera- ture. Authorities and the conditions of their experiments: (1) Eiffel. (2) Dines, 1890. (3) Féppl, toro. (4) Ria- bouchinski, 1912. (5) Stanton, 1903. (6) Bureau of Standards. In lower figure of previous page: Li, Féppl; Io, Lz, B. of S.; Ls, Eiffel; Di, Foppl, B. of S.; De, B. of S.; Ds, Eiffel. For more detailed information as to references and data see I.C.T. 1, 406, 1926. Aspect ratio I Aspect ratio 3 Aspect ratio 6 Authority (1) (3) (6) (6) 90} 30-5] 72] 30.5 15] 5.08 12] 5.08 . : P ROM NTe7A| vee Tunnel diam.... 1500 | 1370 | 2000 Reynold’s No...| 210 126| 64] 55 SMITHSONIAN TABLES TABLE 161 FORCES ON NON-ROTATING CIRCULAR CYLINDERS The coefficient for cylinders normal to the wind, the area A being taken as the product of length and diameter and the linear dimension L as the diameter, depends to a marked degree on the ratio of length to diameter and on the Reynolds Number, Rk. The graph shows the variation of C with R for cylinders of infinite length. The variation of C with the length-diameter ratio for a Reynolds Number of 80,000 is as follows: 200 Ratio of length to diameter I 2 a 5 10 20 40 GE 0.63 .69 75 74 83 .Q2 1.00 1.20 If the axis of the cylinder is inclined to the wind direction, the force remains approxi- mately at right angles to the axis of the cylinder, its magnitude falling off approximately as the square of the sine of the angle of the axis to the wind. Arr Forces, CIRCULAR CYLINDERS. Force = CAq. Reynold’s number = R = V Dp/u. C is taken from above plot; for q see Table 157; 4 = Area axial section of cylinder = L (length) * D (diameter) ; the plane of reference contains the axis and is perpendicular to the plane defined by the axis and the wind direction; V = air speed; p, the density of the medium and uy, its viscosity. Curve (a) is due to Wieselsberger, 1922; curve (b) to Relf. SMITHSONIAN TABLES TABLES 162 AND 163 201 TABLE 162.—Forces on Spheres For spheres the linear dimension L is taken as the diameter of the sphere D aD? and the area as . For values of the Reynolds Number between 80,000 and 300,000 the value of C depends in large measure on the turbulence of the air stream (cf. Technical Report 342 of the National Advisory Committee for Aeronautics). The curves marked S and W most clearly approximate the con- dition of zero turbulence. Arr Forces ON SPHERES. Forcee=F=CAq. A=nrD?/4. R=VDp/p. For meaning of letters see previous table. Authorities: A, Allen, 1900; B., Bacon and Reid; E, Eiffel; P, Pannell ; R, Riabouchinski, 1914; S, Bureau of Standards; W, Wieselsberger, 1914, 1922. For more detailed references see I.C.T., 1, 411, 1926. TABLE 163.—Forces on Miscellaneous Bodies The values of the shape coefficients in the following table are to be used with the area of the projection of the body on a plane normal to the wind direction. Where this projection is a circle, the diameter is used as the quantity L in the Reynolds Number. Where the projection is rectangular, the shortest side of the rectangle is taken as L. SMITHSONIAN TABLES 202 TABLES 163 (continued) AND 164 TABLE 163 (continued).—Forces on Miscellaneous Bodies Body Struts (bodies streamlined in two dimensions)......... 0.06-0.08 Streamline. bodies of revolution). cir qe. selec 1210) stelele ere 0.03-0.04 Rectangular prism, I x I x 3, normal to 1 x3 face...... 1.60 * Model of *automobiletiar cre ecieelac ie eer a at acoso toto .78 * Cone, angle 60°, diam. base 40 cm, point to wind, solid.. 51 Cone, angle 30°, diam. base 40 cm, point to wind, solid.. 34 Hemisphere; convex:-to- wind s 18.31 r: 49.31 MnSO, 11.45 eS 22.08 NaCl 7.95 se 14.31 < 23.22 NaBr 9.77 i 18.58 a 27.27 Nal 8.83 re 17.15 ns 5-47 NaClOs; seuek : 3-54 NaNO; cae pH 18.20 . 31-55 NaeSO, 4.98 M 14.03 a 19.32 NazCrO, 10.62 . 14.81 NH.Cl 3.67 i 15.68 of 23.37 NH,Br 15.97 ee 36.88 27.08 1.148 1.506 96.0 396.8 129.4 661-8 a 82.4 94.8 128.3 75-6 82:6. 4 95-9 WaRt 73.8 157.2 78.7 121.0 75-6 87.0 12-2 96.2 187.9 302.2 103.3 127.5 71-5 67.3 67.4 65.2 62.4 69.6, | 67.0 81.1 107.9 148.4 S32 229.5 90.7 76.4. 2 301.1 98.6 474-3 52.0 60.1 79-4 48.7 53:5 61.7 46.0 47-4 96.4 50.0 75:7 47-9 59-9 76.2 59-0 107.4 166.4 79-3 97.1 45.0 46.2 47-7 43.2 44.6 44-3 47-7 63.3 52-3 74.8 70.0 70.1 64.5 221.0 78.3 347-9 31.8 36.9 47-4 34-4 38.2 43.8 32-4 33-7 66.9 35-3 53.0 33.8 39-3 53-4 49.9 7 106.0 63.5 77°3 31.9 34-0 36.1 31-5 34-3 31.6 34-9 48.9 37-0 54-1 60.8 57:4 128.2 55-6 45 | Wagner 188.8 “ os 63.4 oe “ae 266.8 “ * ER Sprung “52.3 40 | Slotte 63.0 ‘ ae ee Sprung om) TABLE 180 SPECIFIC VISCOSITY OF SOLUTIONS (VARIOUS CONCENTRATIONS, 25°C) Normal solution. 3 normal. oe 3 ° = 3 p — Dissolved salt. Authority. viscosity. Density. Specific viscosity. Density Specifie viscosity. Specific viscosity, Oo ty oo 1oS} Reyher “ ° \O \O \O Acids : Cl,03 FCI o0°0 WO OW 9 9 No) HNOs HeSO4 | Aluminium sulphate Barium chloride . “nitrate _ Calcium chloride ce nitrate . Cadmium chloride . ce nitrate e sulphate. Cobalt chloride “nitrate sulphate . “ee _ Copper chloride . we nitrate “sulphate | Lead nitrate | Lithium chloride ss sulphate. Magnesium chloride nitrate . sf sulphate Manganese chloride s nitrate . - sulphate Nickel chloride coe nitrate “sulphate . Potassium chloride . se chromate nitrate sulphate Sodium chloride. cs bromide. gs chlorate nitrate Silver nitrate. . . 3 : ; : : Wagner e Strontium chloride . 5 : : F : < ce nitrate . ; 3 : : : Se Zinc chloride. . . : ; 3 Z : se Se nithatey va wae. j : ‘ z ; cs <7 sulphate. 2) 5 : : : : < * In the case of solutions of salts it has been found (wéde Arrhennius, Zeits. fiir Phys. Chem. vol. 1, p. 285) that the specific viscosity can, in many cases, be nearly expressed by the equation “=”, where p, is the specific viscosity for a normal solution referred to the solvent at the same temperature, and x the number of gramme molecules in the solution under consideration, The same rule may of course be applied to solutions stated in percentages instead of gramme molecules. The table here given has been compiled from the results of Reyher (Zeits. fiir Phys. Chem. vol. 2, Pp. 749) and of Wagner (Zeits. fiir Phys, Chem. vol. 5, p. 31) and illustrates this rule. The numbers are all for 25° C. SMITHSONIAN TABLES. TABLE 181 213 VISCOSITY OF GASES AND VAPORS The values of w given in the table are 10® times the coefficients of viscosity in c.g.s. units. | Substance. oC. Substance. oC Refer- ence. Ethyl chloride. . . . Ethyl iodide. ..... Helium' = viata Alcohol, Methyl. ... s Alcohol, Ethyl Alcohol, Propyl, “e WWwWNHN NNN ND Hydrogen OARAWIOOW e NSN ONWNH NN WCWWCKOWOH NHN NHNHONMNUNNNNW SHH Alcohol, Isopropyl. . Alcohol, Butyl,norm. Alcohol, Isobutyl. . . Alcohol, Tert. butyl. 144. 160. 96. 108. 210. 220. 224. 272k 322. 70. 79- 118. Q2. 129. 142. 145. 186. 22). 268. 163. 184. 128. 147. 95- 102. 189. RUDOUOO MOH HONWD Lal SNIONODOOOHO OR FP WORHO OR Methane Methyl chloride. . . “cc 6h O ® COW —— s+ Methyl iodide. .... Nitrogen Carbon bisulphide. . Carbon dioxide. .... 3000-7 bp ol tn © 60101010 010000 Of b eH Ooonwo ONO ON HAHN HWHHPARONNHNNONKH ADIONUMNUUNPHPWWWWW ONROD0000FHO. a co oO Puluj, Wien. Ber. 69 (2), 1874. 9 Meyer-Schumann, Wied. Ann. 13, 188r. Breitenbach, Ann. Phys. 5, 1gor. 10 Jeans, assumed mean, 1916. Steudel, Wied. Ann. 16, 1882. 11 Rankine, 1910. Graham, Philos. Trans. Lond. 1846, III. 12 Vogel (Eucken, Phys. Z. 14, 1913). For Schultze, Ann. Phys. (4), 5, 6, 1901. summaries see: Fisher, Phys. Rev. 24, Schumann, Wied. Ann. 23, 1884. 1904; Chapman, Phil. Tr. A. 211, Obermayer, Wien. Ber. 71 (2a), 1875. tg11; Gilchrist, Phys. Rev. 1, 1913. 8 Koch, Wied. Ann. 14, 1881, 19, 1883. Schmidt, Ann. d. Phys. 30, 19009. SIAN PW DNDN HH * Gilchrist’s value of the viscosity of air may be taken as the most accurate at present avail- able. His value at 20.2° C is 1.812 x 10-4. The temperature variation given by Holman (Phil. Mag. 1886) gives p = 1715.50 X 10-"(1 + .00275t — .c0000034/). See Phys. Rev. 1, 1913. Millikan (Ann. Phys. 41, 759, 1913) gives for the most accurate value pd: = 0.00018240 — 0.000000493(23 —f) when (23>f>12) whence px =0.0001809 + 0.1%. For po he gives 0.00017II. + The values here given were calculated from Koch’s table (Wied. Ann. 19, p. 869, 1883) by the formula w = 489 [1 + 746(t — 270) ]. SMITHSONIAN TABLES. TABLE 182 VISCOSITY OF GASES Variation of Viscosity with Pressure and Temperature According to the kinetic theory of gases the coefficient of viscosity m = 3(pcl), p being the density, ¢ the average velocity of the molecules, / the average path. Since / varies inversely as the number of molecules per unit volume, p/ is a constant and uw should be independent of the density and pressure of a gas (Maxwell’s law). This has been found true for ordinary pressures; below #o atmosphere it may fail, and for certain gases it has been proved untrue for high pres- sures, e.g., CO, at 33° and above 5c atm. See Jeans, ‘‘ Dynamical Theory of Gases.”’ If B is the amount of momentum transferred from a plane moving with velocity U and parallel to a stationary plane distant d, and s is a quantity (coefficient of slip) to allow for the slipping of the gas molecules over the plane, then u» = (B/U) (d+ 2s); s is of the same magnitude as J, probably between .7 (Timiriazeff) and .9 (Knudsen) of it; at low pressures d becomes negligible compared with 2s and the viscosity should vary inversely as the pressure. © depends only on the temperature and the molecular weight. ¢ varies as the VT, but u has been found to increase much more rapidly. Meyer’s formula, wt = mo(1 + at), where a is a constant and mo the viscosity at o° C, is a convenient approximate relation. Sutherland’s formula (Phil. Mag. 31, 1893), esse \s Oe rae Ge is the most accurate formula in use, taking in account the effect of molecular forces. It holds for temperatures above the critical and for pressures following approximately Boyle’s law. It may be thrown into the form T = K qT? /y2 — C which is linear in terms of T and Tt /p, with a slope equal to K and the ordinate inter-ept equal to —C. See Fisher, Phys. Rev. 24, 1907, from which most of the following table is taken. Onnes (see Jeans) shows that this formula does not represent Helium at low temperatures with anything like the accuracy of the simpler formula P= bo(L/273-1) The following table contains the constants for the above three formulae, T being always the absolute temperature, Centigrade scale. Hydrogen Krypton eH oo Y Ch Carbon mo- H ON noxden- nee 2 25a OO? ; Nitrogen Carbon dioxide 5 , : Nitrous oxide, Chloroform... Ethylene Helium Helium....... H Oo * The authorities for m are: Air, Rayleigh; Ar, Mean, Rayleigh, Schultze; CO, CO2, Na, N2O, von Obermayer; Helium, Mean, Rayleigh, Schultze; 2d value, low temperature work of Onnes; He, Oo, Mean, Rayleigh, von Obermayer. SMITHSONIAN TABLES, TABLE 183 215 DIFFUSION OF AN AQUEOUS SOLUTION INTO PURE WATER If 4 is the coefficient of diffusion, aS the amount of the substance which passes in the time a at the place x, through g sq. cm of a diffusion cylinder under the influence of a drop of concen: tration dc/ dx, then ye aS = —kq ae at. & depends on the temperature and the concentration. ¢ gives the gram-molecules per liter. The unit of time is a day. Substance. Substance. Refer- ence Bromine . Chlorine . ‘ Copper sulphate Glycerine : Hydrochloric acid . Iodine. 6 ; Nitric acid ; ; Potassium chloride . “hydroxide - Silver nitrate . ; Sodium chloride Urea Acetic acid Barium chloride Glycerine Sodium actetate “chloride Urea A j Acetic acid Ammonia f Formic acid Glycerine : : | 10.14 | 0.339 Hydrochloric acid . \ate2en | Magnesium sulphate We Potassium bromide. 10. “hydroxide . | 12. Sodium chloride “ “ _ Calcium chloride « oe “ce Magnesium sulphate “ce ae | “ “ Potassium hydroxide “ nitrate . “cc “ , es : 0.02 «hydroxide . sulphate | 0.95 se iodide & , Sugar : Sulphuric acid Zinc sulphate . Acetic acid Calcium chloride Cadmium sulphate . Hydrochloric acid . Sodium iodide Sulphuric acid Zinc acetate ac “cc Acetic acid : Potassium carbonate me hydroxide Acetic acid . ; Potassium chloride . > 0.28 ¢ . | 0.05 A - | 0.02 Silver nitrate . mS 6 6 - f 0.9 [igs rh : - | 0.02 | Sodium chloride /8 : /8 8 /8 ae “ce 4 6/ 10 14/8 9.85 4.85 2.85 0.85 | 0.35 | 0.005 | WOADNDW!IOO NANO DHO DAWNW YN DOP QWNN QW NUWFHPWNNNNN Nw nd 1 Euler, Wied. Ann. 63, 1897. 5 Kawalki, Wied. Ann. 52, 1894; 59, 1896. 2 Thovert, C. R. 133, I901; 134, 1902. 6 Arrhenius, Zeitschr. Phys. Chem. ro, 1892. 3 Heimbrodt, Diss. Leipzig, 1903. 7 Abegg, Zeitschr. Phys. Chem. 11, 1893. 4 Scheffer, Chem. Ber. 15, 1882; 16, 1883; 8 Schuhmeister, Wien. Ber. 79 (2), 1879. Zeitschr. Phys. Chem. 2, 1888. 9 Seitz, Wied. Ann. 64, 1898. Compiled from Landolt-Bornstein-Meyerhoffer’s Physikalisch-chemische Tabellen SMITHSONIAN TABLES, 216 TABLE 184 DIFFUSION OF VAPORS Coefficients of diffusion of vapors in C. G. S. units. The coefficients are for the temperatures given in the table and a pressure of 76 centimeters of mercury.* ; kee for vapor | Ae for v. c 0 Vapor. Temp. C. diffusing aaa Hien aot | eo hydrogen. air. carbon dioxide.) Acids: Formic : . : 5 0.0 0.5131 0.1315 0.0879 Ss : ; : ; 65.4 0.7873 0.2035 0.1343 ea : : : : 84.9 0.8830 0.2244 0.1519 Acetic j ‘ ‘ ‘ 0.0 0.4040 0.1061 0.0713 s : ; ; : 65-5 0.6211 0.1578 0.1048 cman . . ; 98.5 0.7481 0.1965 0.1321 Isovaleric . : : E 0.0 0.2118 0.0555 0.0375 ee . : . ; 98.0 0.3934 0.1031 0.0696 Alcohols: Methyl . : ‘ : 0.0 0.5001 0.1325 0.0880 SSS) BAH Ped : : 25-6 0.6015 0.1620 0.1046 hs ‘ : : : 49.6 0.67 38 0.1809 0.1234 Ethyl . : 3 2 0.0 0.3806 0.0994 0.0693 7 : : ‘ 2 40.4 0.5030 0.1372 0.0898 ge : ; : : 66.9 0.5430 0.1475 0.1026 Propyl . : : z 0.0 0.3153 0.0803 0.0577 a : : : : 66.9 0.4832 0.1237 0.0901 a : . : : 83-5 0.5434 0.1379 0.0976 Butyl . : : , 0.0 0.2716 0.0681 0.0476 s : ; : ; 99.0 0.5045 0.1265 0.0884 Amyl . : 7 : 0.0 0.2351 0.0589 0.0422 ss : ; : : 99.1 0.4362 0.1094 0.0784 Eexy lair : : : 0.0 0.1998 0.0499 0.0351 : ; 2 . 99.0 0.3712 0.0927 0.0651 Benzene . : . : : : 0.0 0.2940 0.07 51 0.0527 “ : : : ; 2 : 19.9 0.3409 0.0877 0.0609 6 ‘ ; ; : : : 45.0 0.3993 O.IOII 0.0715 Carbon disulphide . ; : : 0.0 0.3690 0.0883 0.0629 ss 5 ; . . 19.9 0.4255 O.1OT5 0.0726 s & : : : 5 32.8 0.4626 0.1120 0.0789 Esters: Methyl acetate . . : 0.0 0.3277 0.0840 0.0557 x e : ; , 20.3 0.3928 0.1013 0.0679 Ethyl ; : . 0.0 0.2373 0.0630 0.0450 ce ce : 2 : 46.1 0.3729 0.0970 0.0666 Methyl butyrate. : : 0.0 0.2422 0.0640 0.0438 es « ; : ; 92.1 0.4308 0.1139 0.0809 Ethyl < ; : : 0.0 0.223 0.0573 0.0406 s of : 2 : 96.5 0.4112 0.1064 0.07 56 «valerate .- : : 0.0 0.2050 0.0505 0.0366 cs es : : C 97-6 0.3784 0.0932 0.0676 Ether : ; ; ; : : 0.0 0.2960 0.0775 0.0552 “ : : : : : : 19.9 0.3410 0.0893 0.0636 Water . : : : 5 2 0.0 0.6870 0.1980 0.1310 ‘6 j : : : : : 49.5 1.0000 0.2827 o.18TI ss : : : E ; : 92.4 1.1794 0.3451 0.2384 * Taken from Winkelmann’s papers (Wied. Ann. vols. 22, 23, and 26). The coefficients for 0° were calculated by Winkelmann on the assumption that the rate of diffusion is proportional to the absolute temperature. According to the investigations of Loschmidt and of Obermeyer the coefficient of diffusion of a gas, or vapor, ato° C and a pressure of 76 centimetres of mercury may be calculated from the observed coefficient at another temperature and as - pressure by the formula k= Fn) e where 7 is temperature absolute and ¢ the pressure of the gas. The exponent is found to be about 1.75 for the permanent gases and about 2 for condensible gases. The following are examples: Air—CO., »=1.968; CO.—N.O, x=2.05; CO,—H, x=1.742; CO—O, x=1.785: H—O, = 1.755; O—N, x=1.-792. Winkelmann’s results, as given in the above table, seem to give about 2 for vapors diffusing into air, hydrogen or carbon dioxide. SMITHSONIAN TABLES. TABLES 185 AND 186 217 DIFFUSION OF GASES, VAPORS AND METALS TABLE 185,—Coefficients of Diffusion for Various Gases and Vapors * Gas or Vapor diffusing. | Gas or Vapor diffused into. a Pvt Authority, PAN TM aroun keene Tay = Hydrogen be 0.661 Schulze. 0.1775 Obermayer. 0.1423 Loschmidt 0.1360 Waitz. 0.1405 Loschmidt. 0.1314 Obermayer. 0.5437 ey 0.1465 . 0.0983 Loschmidt. 0.1802 s 0.0995 Stefan 0.1314 Obermayer. 0.101 “ 0.6422 Loschmidt. 0.1802 #6 0.1872 Obermayer. 0.0827 Stefan. 0.3054 * 0.6340 Obermayer. 0.5334 : 0 6488 0.4593 0.4863 0.6254 0.5347 0.6788 0.1787 OES 57 0.7217 Loschmidt. 0.1710 Obermayer. 0.4528 Loschmidt. 0.2390 Guglilemo. 0.2475 oo 0.8710 cs ee eee OSV CD Carbonrdioxides 45. 4) Air sf Se oe Carbon monoxide eee ebydrogen w tery bets Methane . se Se eee ee Nitrous.oxide x: : cone Oxygen Carbon disulphide . . . A enue spe cae Carbon monoxide .. . Carbon dioxide os erie Ethylene . mas Hydrogen Oxygen IAN Ings), Lcuuae Hydrogen : ATs loin oeenon tt Carbon dioxide ss monoxide Ethane Ethylene . Methane . Nitrous oxide Oxygen Nitrogen ese eas eer ONSFREM Gg Bea to Woe ioy t Carbon dioxide oS Cities ae Hydrogen Wee teak tee ks Nitrogen . Sulphur dioxide . . : Hydrogen EMITS Gc Redrse ee INP Ge “cc “ec Ce GolOC' On) © O)'O!0! 0) .©5 60) © (OOO) OF O):O80) (O10) 0) 0:0) 0) ©1080 0) OOO — Hydrogen * Compiled for the most part from a similar table in Landolt & Bornstein’s Phys. Chem, Tab. TABLE 186.— Diffusion of Metals into Metals dv __,d*v_ where x is the distance in direction of diffusion; v, the degree of concentration of at dx’ the diffusing metal; 4, the time; 4, the diffusion constant = the quantity of metal in grams diffusing through a sq. cm_ in a day when unit difference of concentra tion (gr. per cu. cm ) is maintained between two sides of a layer one cm thick. ; : Dissolving | Tempera- we , ; : : fates Tempera- Diffusing Metal. Meat Wate Ncs Diffusing Metal. | Maral. haa: Lead . | 492 Wit oo I} RE Readies 550 Gold’ = - = Wee SS5 Platinum . Sl at eee El eed Oz f JFead@aeaae 251 Rhodium. 165 Lead 100 Zinc. 555 | Sodium : 15 oe. 555 : || Potassium : 15 Silver. . cae 555 Goldie. cb escent | 15 ee oh 15 Sie 9 15 | | 200 donee Mercury | 15 From Roberts-Austen, Philosophical Transactions, 187A, p. 383, 1896. * These values are from Guthrie. SMITHSONIAN TABLES. 218 TABLE 187 SOLUBILITY OF INORGANIC SALTS IN WATER (TEMPERATURE VARIATION) The numbers give the number of grams of the azhydrous salt soluble in 1000 grams of water at the given temperatures. Temperature Centigrade. | | | | 50° | 60° | 80° | go? | 100° | | 40° | nee ADIN Osyn-parcniesmes | | 3350 4000 | 4700 0502 | 7600 | | 9100 AIS(SOZ) sence chee | | 521 | 5Qt 2 731 | 808 | 891 AlgKo(SO4)4 SW iestgh ze a j a 248 = 1540 Alo(NH4)e(SO4)4- | 124| 159 211 352) - - BIOs acme Ronee: | ao eliue oe OZ) = 157 ERMC 5 a to Oc | | 436 | 464 524! 5560] 588 BEUNKOA 6 oa c | ) tae)! elas 270 | 306 (CalGiby ak ts: 5, det {1153} — | 1368 1470 | 1527 COO oc o 6 6 « | | 650; 935 | 940 960) - CsCley i ates: | | ; 2080 | 2185 | 2290 | 23 2500 | 2601 CEN Op ue ees ce ogc. | | 230 | | 472| 644 | 838 70 | 1340; 1630 CsoS OW eet 5 1899 | 1949 | 1999 | 2 | 2103 | 2149 | Cul(N@s)o0 ean | = | 1598! — | 1701 2078 | = CuS Omer are | 295] 336 | 390 535 |. 62 BEC IS a fale a - | - $20 | = - 1040 | 1050 | INAH Ge boo. cia 4 | lee (Ta Te | }5258| — FeSO ae ee 264 | | 402| 486 | 550 | 506 HigGloy i sahesess | (90) ins a e139 243] 371 KSB 1 Peyatet orem iod ae Sea | | 760; - | 860 OSS) teal KsCOs. eka s. - | 1170 | 1210 | 1270 1400 | 1470 | KG ee eet rope: 401} 429 | 455 510} 533 ICNOS So oa 6 145] 197 | 260 396 | 475 | KoCrOus seeds | in 16708| CGO |ae7.10 750 || “aaa ACGIH OG) 3) 8 fon | - 202) SOS 730) KHCOs a ete | 453 | 522 | 600 Pf - | = Kee cee h cane 5 1600 | 1680 | 1760 | 1920 | 2010 | KEN @ oacycu ancien | 6 | 639 | 855 | 1099 1690 | 2040 KOT Sey oe eet | 20 | 12 1360 | 1400 | 1460 1590 | 1680 | Keet@leru-amsmesmes 18 22 26 38} 45 KoSOg "2 vals. | 148| 165 | 182 214| 228 161) eee 133) 138 153 MIKO 5° G 5 5s S75 ni Gey || = 660 | E MgSO4 hy Oo 2 | = | = = | s ae ) | 504 | 550 642 | INEGI ey es rea anos | | 504 552 656 INJshilalClORNs 6 to 6 | - | | INMSYINKOR Go ol Gc | 2 2970 3540? | 43002 | (N H4)eSOq. a Pinte tate 5 810 844 | IN ABTS sh iiciiren eos 45 | | - | 1058 | 1160 E ee T1865 | Nas BiO7 Ae aaa =) il | - 105 | 200 2 314 | NagCO3. . (10aq) | } = - | - — | See 74g) ze: | }(taq)| 475 | 464 452 NAGI a 6 ee eee | | | 360} 363] 367 | B7len| 380 INaClO xia emet nOZOn| pas Siete | 1750 Na CrOAme cma g60 1050 | II50 | 1240 | Nas@rm@7 1.) ewes 2200 | 2480 | 2830 | 3 3860 | NaliGO atest ce pene | 2 127| 145 | 164 | — el : Gaotlet— iene AQ) || Ss 2050 | 2280 | 2570 - | 2950 1049 | I140 | 12 | 1480 | | | we Cun VP al eaticots eal 2 ° Compiled from Landolt-Bérnstein-Meyerhoffer’s Physikalisch-chemische Tabellen. SMITHSONIAN TABLES. TABLES 187 (continued)=-189 219 TABLE 187 (continued).—Solubility of Inorganic Salts in Water (Temperature Variation) The numbers give the number of grams of the azAydrous salt soluble in 1000 grams of water at the given temperatures. Temperature Centigrade. 10° | 20° 30° | 40°) ROD 60° INA@EUNT eh ter co 515 | 1090 1190 | 1290 | 1450 | 1740 | 3130 | Nag PSO ai ict ser aos 3 39|- 621 99:|-135\| 174 |) 220 300 | a . . | | | oO | arene oe | ce | 482 468} 455 | 437 NagSeO03. . | 610 | 1697 | 2067 | | 2488 | Ne oie ien oe sal Melnas | | 760) 810 | ~ INTIS © oar maces 02 48 | 4| 632 sie G of oh 8s yo ea Bs | a | BD UNI@s)\om ments) le: | | | 787| 880} 977 | 1076 | ARDC Metso) de von ° | 8 | 1093 | 1155 | 1214 | 1272 IRIN 5 Go a | 1556 | 2000 | 2510 | 3090 | IR SKOhe ig. os oF case 64 | 5 631| 674]! 714] 750 SCI Te ee 6 4| 831] 896| 924 | SVAby sco) Tom O Wow 0 WE | 21 A || eto Sr(NOs)2_ 940 | 950) 972 Th(SO4)o = Seta ace “ 16 | ICU co eae 2 Sila a5 10 AIN@ss Joes es ) 462 SOse Ts eee 7 | ues) Yb2(SO4)3 : | Zn(NOs)2 ZnSO, lst(COMy 6 98 o © 36 53 | 102 635 978 Ho(CHy.COg)2 .§ .- 28 45 69 511 | 708 Tartaric acid . . . {| I150/ 1260 | 1390 30 | 2440 | 2730 Racemic “95% 92] 140] 206 999 | 1250 Ke(HIC Os) Wee 2900)! =a s3ise = 57/50 KEEN(@aizOe) 2 3 4 6 Bo neds TABLE 189,—Solubility of Gases in Water (Temperature Variation) The table gives the weight in grams of the gas which will be absorbed in tooo grams of water when the partial pressure of the gas plus the vapor pressure of the liquid at the given tempera- ture equals 760 mm. .0263 .0221 00129} .0o118| .O12I Compiled from Landolt-Bérnstein-Meyerhoffer’s Physikalisch-chemische Tabellen. SMitHsonian TaBLes. TABLES 190 AND 191 Table 190.—Change of Solubility Produced by Uniform Pressure* CdSO,8/3 H,O at 25° Pressure Conc. of satd. soln. gs. CdSO, per Percentage change. Conc. of satd. soln. gs. ZnSO, per 100 gs. H,O. ZnSOq.7H20O at 25° Percentage change. Mannite at 24.05° NaCl at 24.05° Cone. of satd. soln. gs. monnite per 100 gs. H,O. Percentage change. Cone. of satd. soln. gs. NaCl. per too gs. H.O. Percentage change. S) 9 aD O bo OE © O * E. Cohen and L. R. Sinnige, Z. physik. Chem 67, p. 432, 1909; 69, PD C. Euwen, 7é7d. 75, p. 257, 1911. 102, 1909. E. Cohen, K. Inouye and These authors give a critical résumé of earlier work along this line. Table 191.—Commonly Used Organic Solvents Arranged in the order of their Boiling Points (Table by Dr. J. W. H. Randall, reprinted with permission of Chemical Catalog Co.) Boiling Name point Ethyl ether Carbon disulphide Methyl acetate Chloroform Methyl alcohol Carbon tetrachloride Ethyl acetate Ethyl alcohol Benzol lsopropylalcohole ess aaaei eee Ethylene dichloride Trichlorethylene Ethyl propionate Butyl alcohol (n) Ethyl butyrate Methyl cellosolve Diethyl carbonate Butyl acetate Tetrachlorethane Cellosolve Ethyl benzene Amy] alcohol (n) Boiling Name Xylene (0) Amy] acetate Cellosolve acetate Ethyl lactate Cyclohexanone Buty! cellosolve Ethyl acetoacetate Diethyl oxalate Ethylene glycol Benzyl alcohol Ethyl benzoate Butyl stearate Butyl carbitol Diethylene glycol Triphenyl phosphate Triacetin Diacetin Dimethyl phthalate Diethyl phthalate Dibutyl phthalate Diamyli phthalates st.os eer 344 For producers of solvents, see the following pages of Chemical Engineering Catalog: 1017, I018, 1020, 1023, 1024, 1027, 1028-9, 1030, I03I, 1032, 1033, 1036-7, 1038, 1039, 1041, 1043, 1046-7, 1048, 1050, 1052, 1056, 1060, 1063, 1066, 1068-9, 1072-3, 1077, 1078, 1082-3, 1084, 1087, I09I, 1004, 1095. SMITHSONIAN TABLES TABLE 192 Dont ABSORPTION OF CASES BY LIQUIDS * ABSORPTION COEFFICIENTS, a;, FOR GASES IN WATER Temperature 2 =: Centigrade. ; Nitric Nitrous oxide. oxide, NO NO Carbon Carbon dioxide. monoxide. Hydrogen. | Nitrogen. ~ ss H N CO, CO Oxygen. oO 1.797 0.0354 0.021 10 0.02399 0.0738 1.048 0.04925 1.450 0315 .02022 .021 34 .0646 0.8778 04335 1.185 .0282 -01944 01918 .0571 0.7377 03852 1.002 0254 01875 01742 0515 0.6294 034.56 0.901 .0232 01809 01599 .0471 0.5443 .03137 C.772 .0214 01745 .O1 481 0432 ~ .02874 - .0200 -O1690 01370 .0400 - .02646 0.506 0177 01644 OLIQS 0351 02316 - .O161 01608 .O1074 0315 .02080 0.244 .OI4I .01600 .OIOII 0263 01690 Temperature Centigrade. Ammonia. | Chlorine. Ethylene. Methane. Hydrogen Sulphur 7 . sulphide. dioxide. NH; Cl C,H, CH, HS SO. 0.02471 1174.6 3.036 0.2563 0.05473 02179 971.5 2.808 2153 .04889 01953 840.2 2.585 1837 .04 367 01795 756.0 2.388 L615 03903 .O1704 683.1 2.156 1485 03499 = 610.8 1.950 - 02542 79:79 67.48 56.65 47.28 39:37 32°79 PYQwQs ABSORPTION COEFFICIENTS, a4, FOR GASES IN ALCOHOL, C.H;0H Temperature Centigrade. Caton : , : Nitric Nitrous | Hydrogen} Sulphur dioxide. aires ond Ey dresen: Neen oxide. oxide. sulphide. | dioxide. : C0; NO To H,S SO. 0.5226 | 0.0092 0.1263 | 0.3161 5086 : 1241 | .2998 4953 : 1228 | .2861 -4828 : 1214 | .2748 .4710 .o€ 1204 | .2659 4598 .066 -1196 | .2595 17.89 | 328.6 14.78 | 251.7 11.99 | 190.3 9-54 | 144-5 7.41 5-62 42329 3.891 3-514 37199 2.946 2.756 Qn ty Oo WR ROGo& ~ BS Mw N QwsMN mn oO SI Pow qg + * This table contains the volumes of different gases, supposed measured at 0° C and 76 centimeters’ pressure, which unit volume of the liquid named will absorb at atmospheric pressure and the temperature stated in the first column. The numbers tabulated are commonly called the absorption coefficients for the gases in water, or in alcohol, at the temperature ¢ and under one atmosphere of pressure. The table has been compiled from data published by Bohr & Bock, Bunsen, Carius, Dittmar, Hamberg, Henrick, Pagliano & Emo, Raoult, Schénfeld, Setschenow, and Winkler. The numbers are in many cases averages from several of these authorities. Note. — The effect of increase of pressure is generally to increase the absorption coefficient. The following is approximately the magnitude of the effect in the case of ammonia in alcohol at a temperature of 23° C : { Pe —A5CMs 50 cms 55 cms 60 cms 65 cms G53 = 69 74 79 84 88 According to Setschenow the effect of varying the pressure from 45 to 85 centimeters in the case of carbonic acid ir water is very small. SMITHSONIAN TABLES. TABLES 193-195 CAPILLARITY AND SURFACE TENSION OF LIQUIDS Table 193.—Water and Alcohol in Contact with Moist Air 222 Table 195.—Solutions of Salts in Water Values represent means. See I.C.T. and L. and B. for more elaborate tables. Tension (vy) in dynes/cm. °C H:2O C:H;sOH —5 76.4 °C H:O C:H;OH 79.3 69.5 68.7 67.9 67.0 66.1 67.0 64.3 2IEO 20.6 20.2 19.8 19.4 19.0 18.6 18.2 Oo 75.6 5 74.8 24.0 23-5 2ant D2e7, 223, 21.8 21.4 LOVE 74:2 15. 73-4 2072.7 25 71.9 2007 1st Table 194.—Miscellaneous Liquids in Contact with Air i ¥ C Dynes per cm Liquid Aceton, (CH3)2CO.... 20 on, 23-7 Acetic acid, CH;CO.H. 20 27.6 Amy] alcohol, C5H120. Aniline, CsH;N Benzene, CsHe Bromoform, CHBr3... Butyric acid Carbon disulphide... . Carbon tetrachloride. . Chloroform, CHCl;. .. Ether, C,H yO Ethyl chloride Glycerine Methyl alcohol Petroleum Phenol, CsH-O Propyl alcohol Silicon tetrachloride, SiCl, Toluene, C;Hs Turpentine SMITHSONIAN TABLES 24 43 : 27. Richards ’21 28.9 Sudgen '24 41.5 Mean 26.7 CH3(CH:2).CO2H 32.3 CS: 26.8 CCl, 27.2 Mean 17.01 16.2 CH;Cl 63 C3Hs(OH)s 22.6 CH;0H Baer 26 41.0 23 CH;3(CH:2),;OH 17.0 Ramsay ’93 28.4 27 TABLES 196-198 TABLE 196.—Surface Tension of Liquids * 223 | Surface tension in dynes per cen- timeter of liquid in contact with — Liquid. Specific te } gravity. Air. Water. Mercury. Water . : : : : . : : 1.0 75:0 0.0 (392) Mercury : . : : ; : : 13-543 513.0 392.0 ° Bisulphide of carbon . 5 7 ; 6 : 1.2687 30-5 41.7 (387) Chloroform . A : A ; - 1.4878 (31.8) 26.8 (415) Ethyl alcohol : : : : : 0.7906 (24.1) - 364 Olive oil : : : ; : : 5 0.9136 34.6 18.6 Bly Turpentine . ; “ : ' : ; 0.8867 28.8 11.5 241 Petroleum. ; : : : ; : : -7977 29.7 (28.9) 271 Hydrochloric acid : : : 1.10 (72.9) - (392) Hyposulphite of soda solution 1.1248 69.9 - 429 TABLE 197.—Surface Tension of Liquids at Solidifying Point t Tempera- Tempera- Surface Substance. Platinum Gold Zinc Tin Mercury Lead Silver ture of solidifi- cation. Cent.° tension in dynes per centimeter. ture of solidifi- cation. Cent.° Substance. Surface tension in dynes per centimeter. 2000 1200 360 230 330 1000 1691 1003 877 599 588 457 427 Antimony Borax Water Selenium Sulphur Carbonate of soda Chloride of sodium . - 432 1000 1000 249 216 210 116 87.91 71.8 42.1 ‘ : ° 217 III Bismuth Potassium Sodium 8 Phosphorus . : : 43 : 5 371 WWiaxtae : : : 68 34-1 ; go 258 1390 42.0 * This table of tensions at the surface separating the liquid named in the first column and air, water or mercury as stated at the head of the last three columns, is from Quincke’s experiments (Pogg. Ann. vol. 139, and Phil. Mag. 1871). The numbers given are the equivalent in dynes per centimeter of those obtained by Worthington from Quincke’s results (Phil. Mag. vol. 20, 1885) with the exception of those in brackets, which were not corrected by Worthington ; they are probably somewhat too high, for the reason stated by Worthington. The temperature was about 20° C. + Quincke, “‘ Pogg. Ann.” vol. 135, p. 661. ; + It will be observed that the value here given on the authority of Quincke is much higher than his subsequent measurements, as quoted above, give. | ‘‘ Proc. Roy. Soc.” 1877, and “ Phil. Trans. Roy. Soc.”’ 1881, 1883, and 1893. Norte. — Quincke points out that substances may be divided into groups in each of which the ratio of the surface tension to the density 1s nearly constant. Thus, if this ratio for mercury be taken as unit, the ratio for the bromides and iodides is about a half: that of the nitrates, chlorides, sugars, and fats, as well as the metals, lead, bismuth, and antimony, about 1; that of water, the carbonates, sulphates, and probably phosphates, and the metals platinum, gold, silver, cadmium, tin, and copper, 2; that of zinc, iron, and palladium, 3; and that of sodium, 6. TABLE 198.—Vapor Pressure and Rate of Evaporation Evaporation rate. g/cm?/sec Platinum. 1200 1400 1600 . 014260 -O1401 E 09966 1800 07667 2000 ; 05195 4180 — Langmuir, MacKay, Phys. Rev. 2, 1913; 4, 1914. Order of vacuum, 0.001 mm. -O101 44 09798 . 07236 06429 -05523 . 04467 03769 00000000 Oo. °. Oo. °O. oO. oO. oO. OF p = K.T~te-do/RT dynes/cm?. Zn, Axo = 3-28 X 104; K = Hg, Xo = 1.60 X 104; SMITHSONIAN TABLES. Egerton, Phil. Mag. 33, p. 33, 1917. T.17 x to (Cd kee 2577 * 10% K = 6.27 x10" = 3.72 X 108 (Knudsen) 224 TABLE 199 VAPOR PRESSURE OF ELEMENTS (Over liquid unless otherwise noted) 4-9 4.20 3-52 Onnes, 1923 Onnes, I915-6 Onnes, 1917 Travers, 1902 Niton K Oxygen mm SKS mm 62.37 68.57 Uefa 77-59 86.18 90.13 377-5 62 364.4 53 321.7. 26.4 290.3, 13.2 262.8 6.6 212.4 202.6 9.59 36.1 64 162.2 493 1.05 .66 Gray, Ramsay, 1909 Cath, 1908 Ozone mm 120 162 89.94 86.01 83.24 81.36 34 760 042 .O152 Spangenburg, Ton Horiba, Reisenfeld 1923 Fischer, Alt., Arsenic, solid o atm. Chlorine Nitrogen ake: atm. mm +100 + 20 6.62 fo} 3.66 33.6 760 DO oOo 7On nL TS 80 62 760 700 500 400 300 200 77-33 76.65 74-03 72-39 70.42 67.80 41.7 Knietsch, 1902 1890 Bismuth Ae atm. Cadmium Xe 793 1000 feo oaL 350 Greenwood, 1910 Copper Ae Gallium mm 5 mm 20 100 257 926 .0004 1009 .003 1875 1980 2180 Greenwood, IOII sc T1155 1985 2315 Gold mm 808 .08 996 1.75 1178 16.8 1275 73 .00007 17 130 Harteck, Ruff Wartenberg, 1913 252 .279 1315 105 210.5 41240 201.5 31620 170.9 11970 Li2:7, 387, 88.6 17a 9 287.7 44110 255-6 21970 244.2 15870 231.4 11130 237-4 13500 183.2 2020 Ramsay, Travers, I901 Bromine Me mm +58.75 760 51.95 600 40.45 400 23.45 200 8.20 100 — 7.0 —12.0 45 30 Young, 1886 Calcium a mm 1028 23 1049 4I 1085 99 1129 287 Hartmann, IQI4 Lead mm 1410 266 1325 760 6 atm. Greenwood, IQII Iodine 2c mm 55 50 45 40 35 3.084 2.154 1.498 1.025 -699 Baxter, Hickey, Holmes, 1907 Caesium sG mm Magnesium a mm 623 742 20 986 211 1080 751 9 Hartmann, 1924 Rubidium ce mm -00006 -0004 98 115 250 759-8 783 Gray, Ramsay, 1909 19 SMITHSONIAN TABLES Flock, Redebust, various Ruff, Silicon ° Silver mm 1038 1368 1660 1758 Konschak, 1926 .82 103 200 various TABLE 200 225 VAPOR PRESSURE OF ORGANIC LIQUIDS The vapor pressures on this page are in millimeters over a liquid phase unless distinguished by the subscript ;. They are generally means from various determinations. Carbon | Carbon Ethyl °C Acetone | Benzine | Cam- bisul- tetra- | Chloro- | Ethane | Ethyl bro- Turpen- CsHsO CeHe phor phide | chloride| form CoHe ether mide tine CioHisO CSe CCls CHCls CsHiO | CoHsBr} CioHe —60° \ —100°| —101.3° \. sy 8 390 O58: 4.8 — 90°| — ash 10 700 { 4 Leia 19 — 80°|\ — a 59 : 1180 f 19 102 610 — 75° 186.1 166 : 1500 ae 207 100 ete 201.8) 6257 oe mete te B17 160 Oe 442.4 386 247 Siels 648 564 370 eiors g2I 802 540 stere 1276 III3 750 ele 1728 I510 eee 204 2015 sas 2991 2640 1120 aoe 3840 3400 1460 500 Lkels%o) 4310 1880 : Siow Are 5390 2390 sere 7500 6660 3000 oasis ere 8120 3700 ele ea 9780 160° 4500 15800f ° ims teeaeee Ethylene Glycerine Met beds Methyl ether Naphthalene eae chloride 4 ( 2H, C3HsO 3)2 10H 2Hs5 se mm 3 mm Tc mm cc mm Xe mm cc mm —I50 14.9 24) —180) 119) — 67 78 oO .02, —30 —190 45.6 6.5 —175 212 — 60 120 20 .06; —20 —145 26.7 13 —170 353 — 41.4 326 50 815 —10 —135 74.4 32 —165 559 — 30.9 524 79 4.0s oO —130 I17.2 100 —160 848 —241 782 80 10 10 —120 260 385 —155 1229 O 2.52atm. 90 13 20 —IIO 519 —150 1720 254 (Oy (ar3 20 30 —103 792 AO sees 29 50 SOT) 1 223Tes 43 75 00.ON Seen a 119 100 7250 St Ss 490 SMITHSONIAN TABLES 226 TABLES 200 (continued) AND 201 Table 200 (continued).—Vapor Pressure of Organic Liquids Nap- | Sulphur Hy- Methyl Am- | Carbon] Ethyl Ethyl thalin tence 2 ; esis omen drogen chlo- NH. eaai ea acetate |sulphide} ride Hes | CH:c1 | CeHs mm mm °c Sie So 6 86 —9QI.9 579 ate 286 —81.7 TES Pert 379 —77-4 SSaF worse 474 —67.5 . 1079 06 j25 =—57:7) » .060 NaNO). Sse 760 —38.0 . D5 7 Qe wectete sel) nA 2) WAY, 1891 Sats 1155 — 2.9 5.72 2250 eqs eke oO 6.86 PANTO SIS 1714 +15.0 16.8 B13 AS Me leley ois --- 725.8 28.7 3667 Boo 2460 Cha ayy Ongie 4267 eyes sis 4940 aa 3420 5700, Ac 5 Gh Sade ole 6650) 7 o5- 4650 Drucker, US Bens Soe: Jumen, 8510 Bie 6210 I9I5 10900 aE 8150 Barker, 14300... 10540 I9IO 16800 9:6" a8. 21000 TOs saree 25800 19. 27.8 atm. fees fee eee 53600 | 490 \71.4 “ Table 201.—Vapor Pressure at Low Temperatures Many of the following values are extrapolations made by Langmuir by means of plots of log p against 1/T. Gen. Elec. Rev. 23, 681, 1920. 1 bar = 0.000000987 atm. = 0.000750 mm Hg. .0023 4:3°X 40% 2.2 etom SMITHSONIAN TABLES TABLES 202 AND 203 ODF TABLE 202.—Vapor Pressure of Ethyl Alcohol * Vapor pressure in millimeters of mercury at 0° C | TANG) WS CON G.20 || 17.3% 18.46 55-50 | 58.86 |] 62.33 97-21 | 102.60 | 108.24 49-47 | 52-44 87.17 | 92.07 148.10 | 155.80 | 163.80 | 172.20 | 181.00 242.50 | 253-80 | 265.90 | 278.60 | 291.85 383-10 | 400.40 | 418.35 | 437-00 | 456.35 588.35 | 613.20 | 638.95 | 665.55 | 693.10 | 1 27.94 | 28.67 | 30.50 | 32.44 | 34-49 From the formula log =a + /a’ + cB’ Ramsay and Young obtain the following numbers.t | 30° | 40° | 50° 60° 70° | 80° | 90° Vapor pressure in millimeters of mercyry at 0° C 133-42] 219.82] 350.21 40.91} 811.81) 1186.5 5686.6 |7368.7 |9409.9 |11858. |14764. | 18185. TABLE 203.—Vapor Pressure of Methyl Alcohol + Vapor pressure in millimeters of mercury at 0° C 0 I 2. 40.2 71.4 22.7 9 3 7 ok = NIOnWw to Aono BNI SIG * This table has been compiled from results published by Ramsay and Young (Jour. Chem. Soc. vol. 47, and Phil. Trans. Roy. Soc., 1886). + In this formula @= 5.0720301; log = 2.6406131; log ¢ =0.6050854; log a= 0.003377538; log B= 1.99682424 (c is negative). + Taken from a paper by Dittmar and Fawsitt (Trans. Roy. Soc. Edin. vol. 33). SMITHSONIAN TABLES. 298 TABLE 204 VAPOR PRESSURE * Carbon Disulphide, Chlorobenzene, Bromobenzene, and Aniline (a) CARBON DISULPHIDE. 0°| 127.90 | 133-85 | 140.05 | 146.45 | 153-10 | 160.00 | 167.15 | 174.60 | 182.25 | 190.20 10 | 198.45 | 207.00 | 215.80 | 224.95 | 234-40 | 244.15 | 254-25 | 264.65 | 275.40 | 286.55 20 | 298.05 | 309.90 | 322.10 | 334-70 | 347-70 | 361-10 | 374:95 | 389.20 | 403.90 | 419.00 30 | 434-60 | 450.65 | 467.15 | 484.15 | 501-65 | 519.65 | 538.15 | 557-15 | 576-75 | 596.85 40 | 617.50 | 638.70 | 660.50 | 682.90 | 705.90 | 729.50 | 753-75 | 778-60 | 804.10 | 830.25 (b) CHLOROBENZENE. 20°} 38.65 9.14 9.66 ove 10.79 | 11.40 | 12.04 | 7la|| oS Aen LA ey 30 | 14.95] 15-77 16:63, |) 17-584) 15:47) || 1O.45, ||) 20:48 1.56 | 22.69 230 Aon ||) Parente) 26.30) 2767220. Ten!) 30.50 |) .32alOn ll 43:00. 35 | 37.08 | 38.88 I 3 50} 40.75 | 42-69 | 44.72 | 46.84 | 49.05| 51.35 | 53:74 | 56.22 | 58.79 | 61.45 60 | 64.20 |. 67.06 | 70.03 | 73.11 | 76.30 | 79.60 | 83.02 | 86.56] 90.22 | 94.00 70 | 97.90 | 101.95 | 106.10 | 110.41 | 114.85 | 119.45 | 124.20 | 129.10 | 134.15 | 139.40 80 | 144.80 | 150.30 | 156.05 | 161.95 | 168.00 | 174.25 | 181.70 | 187.30 | 194.10 | 201.15 go | 208.35 | 215.80 | 223.45 |* 231.30 | 239.35 | 247-70 | 256.20 | 265.00 | 274.00 | 283.25 100 | 292.75 | 302.50 | 312.50 | 322.80 | 333-35 | 344-15 | 355-25 366.65 | 378.30 | 390.25 ITO | 402.55 | 415.10 | 427-95 | 441-15 454-05 468.50 | 482.65 | 497.20 | 512.05 | 527.25 i120 | 542.80 | 558.70 | 575.05 | 591.70 | 608.75 | 626.15 | 643.95 | 662.15 680.75 | 699.65 TOMES: 59730-0500 750-COn lh eas - - - (c) BROMOBENZENE. 40° z= = = = - 12:40) 1310" eL3\7 5a d=4 7m elo 22m 50 | 16.00| 16.82) 17.68 | 18.58 | 19.52 | 20.50 | 21.52 | 22.59 | 23.71 | 24.88 60 | 26.10 | 27.36) 28.68 | 30.06 | 31.50 | 33-00] 34.56] 36.18 | 37.86] 39.60 vo | 41.40 | 43-28 | 45.24 | 47.28] 49.40 | 51.60] 53.88) 56.25 | 58.71 | 61.26 80 | 63.90 | 66.64 | 69.48 | 7242] 75.46| 78.60 | 81.84 | 85.20 | 88.68 92.28 90 | 96.00} 99.84 | 103.80 | 107-88 | 112.08 | 116.40 | 120.86 | 125.46 | 130.20 | 135.08 100 | 140.10 | 145.26 | 150.57 | 156.03 | 161.64 | 167.40 | 173.32 | 179.41 | 185.67 | 192.10 110 | 198.70 | 205.48 | 212.44 | 219 58 | 226.90 | 234.40 | 242.10 | 250.00 | 258.10 | 266.40 120 | 274.90 | 283-65 | 292.60 | 301.75 | 311-15 | 320-80 | 330.70 | 340.80 | 351-15 | 361.80 130 | 372.65 |} 383-75 | 395-10 ; 406.70 | 418.60 | 430.75 | 443-20 | 455.90 468.90 | 482.20 140 | 495.80 | 509.70 | 523.90 | 538.40 | 553.20 | 568.35 | 583-85 | 599.65 | 615.75 | 632.2 150 | 649.05 | 666.25 | 683.80 | 701.65 | 719.95 | 738-55 | 757-55 | 776-95 | 796.70 | 815.90 (ad) ANILINE. 80°, 18.80 | 19.78 | 20.79 | 21.83 | 22.90 | 24.00 | 25.14 ASC) || Ayfouvin || Assis QO! || 30:10) || 31-A44el 32.8351 34-27 35.76 | 37-30 | 38-90 | 40.56 | 42.28! 44.06 100 | 45.90 | 47.80] 49.78 | 51.84] 53-98 | 56.20] 58.50 | 60.88 | 63.34 | 65.88 110 | 68.50 | 71.22 | 74.04 | 76.96] 79.98 | 83.10 | 86.32 | 89.66 | 93.12 96.70 120 | 100.40 | 104.22 | 108.17 | 112.25 | 116.46 | 120.80 | 125.28 | 129.91 | 134.69 139-62 130 | 144.70 | 149.94 | 155-34 | 160.90 | 166.62 | 172.50 | 178.56 184.80 | 191.22 | 197.82 140 | 204.60 | 211.58 | 218.76 | 226.14 | 233-72 | 241.50 | 249.50 | 257.72 266.16 | 274.82 150 | 283.70 | 292.80 | 302.15 | 311-75 | 321-60 | 331.70 | 342.05 352-65 | 363-50 | 374.60 160 | 386.00 | 397.65 | 409.60 421.80 | 434.30 | 447-10 460.20 | 473-60 | 487.25 | 501.25 170 | 515.60 | 530.20 | 545.20 | 560.45 | 576.10 | 592.05 | 608.35 | 625.05 | 642.05 659-45 180 | 677.15 | 695.30 | 713-75 | 732-65 | 751-90 | 771-50 - - - * These tables of vapor pressures are quoted from results published by Ramsay and Young (Jour. Chem. Soc. vol. 47). The tables are intended to give a series suitable for hot-jacket purposes. SMITHSONIAN TABLES. TABLE 204 (continued) VAPOR PRESSURE Methyl Salicylate, Bromonaphthalene, and Mercury (e) METHYL SALICYLATE. Hb Coo ee ° ° Oo Dn OO nw N 2.97 5-44 9.06 14.47 22.55 34-21 50.96 74-38 106.10 148.03 202.49 271.90 359-95 467.25 600.25 761.90 3.18 5:74 O52 15-15 23-53 35-63 52.97 (f) BROMONAPHTHALENE. Se eee Oo NN 4. 6.2 9:7 4.9 (g) MrERcuRY. 3-40 6.05 9-95 15.85 24-55 37-10 55:05 80.00 113-60 157.85 215.10 287.80 375.90 A/S 630.15 798.10 4.40 6.80 10.60 16.20 24.00 34-40 48.05 66.10 89.75 120.20 158.85 207-35 267.55 342-75 434-45 545°35 677.85 4:79 7-42 Ow xe co Od WNN Ss me ON Os SO Copy eee DAL td to Go Oo0oOnN as un wm 126.97 161.07 202.53 381.18 | 463.20 558-87 | 669.86 SMITHSONIAN TABLES. 252.18 | 31T.30 | 164.86 207.10 257.65 317.78 388.81 472.12 569.25 681.86 no- = m= QO mm SoG. Sip QW Or tn OW CO n OO SOMONE Ce) SEH bb CWO Q™N “I oy Xo) a ° a 136.50 172.67 216.50 268.87 331.08 404-43 490.40 590.48 706.40 230 TABLE 205 VAPOR PRESSURE OF SOLUTIONS OF SALTS IN WATER * The first column gives the chemical formula of the salt. The headings of the other columns give the number of gram-molecules of the salt in a liter of water. The numbers in these columns give the lowering of the vapor pressure produced by the salt at the temperature of boiling water under 76 centimeters barometric pressure. Substance. 0.5 1.0 2.0 3.0 4.0 5.0 6.0 8.0 10.0 Alp(SO4)s 12.8 | 36.5 AlCls . 22.5 | 61.0 | 179.0 | 318.0 BaSoOg 6.6 ie, | BY Ba(OH)2 12.3 22.5 | 39.0 Ba(NOs)o - iehis || 2770 Ba(ClOs)o .« 15:07 1) 33-Sual) a7. C= 5h | eLOo:2 BaCle . 3 16.4 | 36.7 77-0 BaBry . 16.8 | 38.8 | 91.4 | 150.0 | 204.7 CaS-Os 9.9 | 23.0] 56.0 | 106.0 Ca(NOs)2 16.4 | 34.8] 74.6 | 139.3 | 161.7 | 205.4 CaCl . 172On|) 39:08 5.aii| 1 OO-Onleza Tease | aiOns Cabre . 1727) | 442) | 1O5:55| PIO L-Oul 253135 30Ss6 CdSO4 4.1 8.9 18.1 Cdlg HAS || whey || SeEG |) Gey CdBrp . SiON eres. | sOs7n |e 557m OOO CdCl, . : O10} PTS Sr |tgOs74 |S 7Onlln 77238 9:0 Cd(NOs)eo . 15-9 | 36.1 78.0 | 122.2 . Cd(C1Os3)2 : 17-5 CoSO4 , Spl Kap | 2a: 45-5 CoCle . 15-0 | 34.8 83.0 | 136.0 | 186.4 Co(NOs)e 17:3 |' 39:2) | 89:0 |) 152.0: | 218.7""|)-282:0 133270 FeSQ4 5.0 al) LOs7.| me 24-On |) 42-4! H3BOg3 GOW 2 -aull ee 25 alll g0-0 au) aS Te H3PO4 6.6] 14.0] 28.6] 45.2 | 62.0] 81.5 | 103.0 | 146.9 | 189.5 HsAsO4 73 15.0 | 30.2 46.4 | 64.9 H2SO4 12.9] 26.5} 62.8 | 104.0 | 148.0 | 198.4 | 247.0 | 343.2 | KH2PO4 10.21) Sigics!) 23:30 47-Onle OO Gul e7 a ial eros KNOs. 1Os3))| 20a |) 4 Oar 57-0) || 74-5 | (88.2 |) 102.1 126.351 948.0 KC1O3 10.6 | 21.6 220) ||| O2aT 80.0 KBrOg 10.9 | 22.4 | 45.0 IES Ons eae : sil) LO:ON | ez Qu] 43-3) O5-sull woSa5 ue LO7-o nt 2O:201 mt O0 KNOg : ; ea eeaLi Lek 22.8} 44.8 | 67.0] g0.0 | 110.5 | 130.7 | 167.0 | 198.8 KC1O4 ° : oa lea) 225g KCI: : 7 = ||) b222 )) 24-4) 48:81 74-03) LOO:Ou ne h25.5. |) 152.2 KECOs : Fy) tN Heya Gover ||) Yayo) Werks |) 1eeHe) || ikSeHe).|| Bitover || AEG SIG. : ; =) [es le2s 5a means 2:2) 82:05 |) l2.2 04s) | 071.9. | ee2itcn| areas KeCoO4 St : wi LS -Oh| 2823) le SO:on | O4-2u leo 2 KoWOq_.. : ai) LS:On i) saeco 73-0 123.8 | 175.4 | 226.4 KC Og «| T4.a"l” (3n-ofl #683) 105-5 4, 1s2:0 | 200.0) || 258:5)|\ atoro KOH . : ; -| 15.0] 29.5 | 64.0] 99.2 | 140.0 | 181.8 | 223.0 | 309.5 | 387.8 KoCrO, : -| 16.2 | 29.5 | 60.0 LiNOg : : S|) UAE BEG) ire || tetsio) || hear I | 188.0 | 253.4 | 309.2 LiCl . : : 2 |Pet2%, | (256 ocr |) OR Onlens2.g0) Tims. ch| 219.5) |) ols Oans Libr. : . - | 12.2 | 26.2 | 60.0 | 97.0 | 140.0 | 186.3 | 241.5 | 341.5 | 438.0 LigSO4 ° 5 S| aieben i cise Kosei toe LiHSO, . i oii gL250))} 7127-0). 57-0 Q3.0nleT30:0) flOs-O Ga ls eat : : ‘ 13.6 | 28.6] 64.7 | 105.2 | 154.5 | 206.0 | 264.0 | 357.0 | 445.0 | LigSiFlg . 2 , 15-4 | 34.0] 70.0 | 106.0 LiOH . : : el eLIS AO oT Aalst Lip€rOny 3 : 16.4 | 32.6] 74.0 | 120.0 | 171.0 pe eee * Compiled from a table by Tammann, ‘‘ Mém. Ac. St. Petersb.’’ 35, No. 9, 1887. See also Referate, ‘‘ Zeit. f Phys.” ch. 2, 42, 1886 SMITHSONIAN TABLES. TABLE 205 (continued) 231 VAPOR PRESSURE OF SOLUTIONS OF SALTS IN WATER Substance. 0.5 1.0 2.0 3.0 4.0 | 6.0 6.0 8.0 10.0 MgSO, : : : 6.5 | 12.0] 24.5 | 47.5 MgCl. : : -| 16.8] 39.0 | 100.5 183.3 277.0 | 377-0 Mg(NOs)o . . : 7G! 42.0n|) TOTO} 174. Mgbr2 . : SL Onl eAzOn | Uhs.50|| 205-3) 205.5 MgH2(SO4)2 ‘ : 18. 46.0 | 116.0 MnSO4 : : | MOON) rors | aen.O| MnCl. : : af) 5-0. 34-08 7.0:0 | 122-3 | IG7:0m 200;0 NaHePO, . : Bf) HOLS | | 20.0. |) $36.54) 51-7) | (66:8) | 82.0) OG:5 | 26:7" |) r57-1 NaHSO, . : : 10.9 | 22.1 4753)|) 75:07) 100:25 |b r26:1) (4825) 189.7) 231-4 NaNOg : : STieeLOsOy| 22s 46:2") 68.1 |! -90:g) | 141.5 | 2317)| 167.8 | 198:8 NaClOg : ee toss f° 23-07} 4 8ige lores “98s5 "|r 2 3538 (raz -Heh 19625" |-223:5 (NaPOs)g_ .- : ; 11.6 NaOH : : eB elon 22:Onlmea O20 lea 7.20| LO7. Su enaQuin et 2eGnle2da.aulat4.O NaNOg . j : 11.6 | 24.4 50-0 | 75.0 | 98.2 | 122. 146.5 | 189.0 | 226.2 NagHPQ, . : 5 || tee |) ene || Zgxer ||) Wexen|| 7isk47 ||) Geka |) eeen NaHCOg 1210) Aer 48.2 | 77.6 | 102.2 | 127.8 | 152.0 | 198.0 | 239.4 NagSO4 WHS) |] | oy || itso) |] Gil NaCl . E2090), 252.) G2. |, SOOb| VI TL-On 1430) 176.5 NabrOg T2502 GON || esd otal Oleg) LOS:onl 0:0 Nabr . 12.6 || 25.9) 57:0 | 89.2: |) 124.2 | 10:5 || 197.5 | 268.0 Nale =: : : : 12.1 21516) || 00:2 OOa5u EU 3647 4) 177-55 |s 220-0) || BOI-5) |/9370:0 NagP2O7 .. 5 ; 13.2 22.0 NagCOg_ . : S| Bee) ee Gens) |) eter imix) NaoCsO4, .. ; i 14.5 30.0 | 65.8 | 105.8 | 146.0 NagWO,4 . : : TALS eS -ON ee leOnlULIS.75)|) 10216 NagPO,_ : +) CHS |) sfekey |) Gas (NaPOs)3 . , a Ue || Sion NH4NO 3 . ; ‘ 12.8 22.0 42.1 62.7 82.9 | 103.8 | 121.0 | 152.2 | 180.0 (N H4)eSiFl¢ : : Pies || 25:0" 54455 NH,Cl . ; e |) 20") 23-70) <45.1 |) X60:34|" 94:28) B1S:55/en30-25 | 179.0) 213.0 NH,4HSO, . : ; 11.5 22.0 | 46.8 7A.O)\ O4258 |e LlGs 139.0 | 181.2 | 218.0 -(NH4)2SO4. . S| LON! 24-0),|F 4635) |) 60:59) O3:0) VT 17-0) pare NH4Br : : 3] Dro} £239 |) 48.5°| 74210) -90:4 || 121-5. 145-5 | 190-2 | 228.5 NHgl . : : -| t291 25.1 | 49.8 | 78.5 | 104.5 | 132.3 | 156.0 | 200.0 | 243.5 NiSO4 : ° : FOn| pe LOs2a|e2res NiCle . 37.0 Ni(NOsz)z BIS Pb(NQs)o 23-5 ae 20.3 Sr(NOs)o 31.0 131.4 SrClo . 223.3 SrBre . 267.0 ZnSO4 66.2 ‘7nCle . 107.0 | Zn(NOs)2 223.8 ee SMITHSONIAN TABLES. 232 TABLES 206-208 PRESSURE OF SATURATED AQUEOUS VAPOR The following tables for the pressure of saturated aqueous vapor are taken princi- pally from the Fourth Revised Edition (1918) of the Smithsonian Meteorological Tables. TABLE 206.—At Low Temperatures,—69° to 0° C over Ice NHOOOOO mm mm mm mm L079) | TeO20) | LAOSA 550 |p e14'20 4.255 | 3-952 | 3-669 | 3.404 | 3.158 Onw pp Aunnn f& Annn & DANN fp Dan fp On Ov an Aw vO Oo COn~INI OD 0 C~ISNI DD ConINI OD moons a Co CONTI NI OO COnn nn te H HOF ae O° nn HW comsy NO NN AR NH O SMITHSONIAN TABLES. TABLE 208 (continued) 233 PRESSURE OF SATURATED AQUEOUS VAPOR For Temperatures 0° to 374° C over Water NNN N 0 eA ®WSNHNNN WNHNNN w 130. 136. 164. oz ie 179. 5 Aig 205. 214. 254. 266. 277. a3 : 314. 307. 385. 400. AL ; : 468. 487. 567. 588. 611. 3 : 682. 707. 815.9 845.0 875.1 ‘ j 970.5 ; 1004.2 1149 1187 1227 2 1353 1307 1585 1636 1687 1850 1907 2140 2214 2280 2487 2559 2866 2947 3030 3290 3381 3793 3864 3967 4290 4402 4873 4097 5123 525 é 5518 5654 6228 6378 6532 7009 W174 7865 8046 8230 8802 890909 9823 10040 10260 10940 III7o 12140 12400 12650 13450 13730 14870 15160 15470 5 16400 16720 18050 18390 18740 19820 20190 21720 22120 22520 2 f 23770 24190 25950 26410 26870 28290 28780 39790 31310 31830 33450 34000 36280 | 36870 | 37470 39300 | 39920 42500 43160 43840 5 45900 46600 49500 50250 51000 53320 54110 57360 58190 59040 61620 62510 66130 67060 68000 70890 71870 75910 7694¢ 77990 81200 $2290 86760 87910 89070 92630 93840 98790 | 100060 ! 101350 i 105280 | 106600 II2I00 | 113500 | I14900 119200 | 120700 126800 | 128300 | 129900 | 131400 | 133000 | 134600 | 136300 142900 | 144600 | 146300 | 148100 | 149800 | 151600 | 153400 158800 | 160700 | 162600 | 164400 SMITHSONIAN TABLES. 234 TABLES 209-211 TABLE 209.—Weight in Grams of a Cubic Meter of Saturated Aqueous Vapor -797 10. 664 -348 : . 832 -635 19. 430 578 . .049 | 24.378 33.812 .656 , -599 | 41.706 For higher temperatures, see Table 290. COMNPWNHHOO 4 H COW ONNWNHHHO COP ONINWNHHHO HHH ee NSWONNWNHHO PHONnPNHHOO AH ONnENNHOO HH NH love} wr Ow wn Hp Tables are abridged from Smithsonian Meteorological Tables, fourth revised edition. TABLE 211.—Pressure of Aqueous Vapor in the Atmosphere For various altitudes (barometric readings). The first column gives the depression of the wet-bulb temperature t, below the air temperature t. The value corresponding to the barometric height at the altitude of observation is to be subtracted from the vapor pressure corresponding to the wet-bulb temperature taken from Table 208. The temperature corresponding to this vapor pressure taken from Table 208 is the dew ae The wet bulb should be ventilated about 3 meters per second. For sea-level use Table 212. Example: ¢ = 35°, t; = 30°, barome- ter 74 cm. Then 31.83 — 2.46 = 29.37 mm = aqueous vapor pressure; the dew ate IS—2816O-7 G: Abridged from Smithsonian Meteorological Tables, 1907. Barometric pressure in centimeters. eH OO iS) WWNNnH WOWNNH 2. 2 2 A 2 3 3. 2 3 3. 3 4 3- 3 PhHRWW WNHNHNH anp pw ufh pw Ann APR wWW WNHNNH nan PhRWW WNHNNH NNN Anu > INN Aunt NAD ANH NAD UMNpPppp ADAH UMNPHEs Ane PPAOWW Dan NDown ann SMITHSONIAN TABLES. TABLE 212 235 PRESSURE OF AQUEOUS VAPOR IN THE ATMOSPHERE; SEA-LEVEL This table gives the vapor pressure corresponding to various values of the difference ¢ — 4, between the readings of dry and wet bulb thermometers and the temperature f: of the wet bulb thermometer. The difference ¢ — h is given by two-degree steps in the top line, and 4 by degrees in the first column. Temperatures in Centigrade degrees, vapor pressures in millimeters of mercury are used throughout the table. The table was calculated for barometric pressure B equal to 76 centimeters. A correction is given for each centimeter at the top of the columns. Ventilating velocity of wet thermometer about 3 meters per second. Corrections for B per cm 10.0; B = 74.5 cm $1 = 77.2 From table: 6.17 — 12 X 0.050 For B, 1.5 X .048 Hence p Qa CO O NNNHN HR 99900 PRCT OES Hnopu NAAR eR #0000 90900 bHHOO oro ° ° an pf Oo 1 uo a NHHOO Ooo NO o0o0o000 © CONT Qu hwNHO oo o~ISI OV Out BWW Www DAoupp fPwWwWdb th nn w Hes OH Iw NUN 2. 2. 2). 2. Be an Be 4: 4. Se Si 6. 6. 7 mi 8. 8. 9. oO. °. COON AD UMnpww WNNHH DAouk WRNHH re I at OO Onn oo INITAUMN HLHWNDNHD ODO MID UNfwo 00 cox 99000 He RRS, DHHNHN Auwnoao o0o0000 nN o nw no ROHN ND oo0000 OW Ww Oo aL oo ODOR N 9909090 ° SMITHSONIAN TABLES. 10 236 TABLE 213 RELATIVE HUMIDITY, VAPOR PRESSURE AND DRY TEMPERATURE Vertical argument is the observed vapor pressure which may be computed from the wet and dry- bulb readings through Table 211 or 212. The horizontal argument is the observed air temperature (dry-bulb reading). Based upon Table 43, p. 142, Smithsonian Meteorological Tables, 3d Revised Edition, 1907. | Vapor F Air Temperatures, dry bulb, ° Centigrade. Pressure. | mm. —6° —7o —8° —9° —10° —1]° —12° —13° —14° —15° —200 | LG pL7e) eS SOM SAT AES 7 AGA SOe TSS 61; 67474 76 84 92 92 100 mm. 3.50 3.75 4.00 4.25 4.50 QOQWHONNNN FRPP OOS UNOIYGUND NUNS Nb OUuSuons Bwous aon | Vapor Air Temperatures, dry bulb, ° Centigrade. Pressure. mm. go 10° 11° 12° 13° 14° 4 8 iS 17 2I i Sno Qn 25 ey Rb Nhe es elon tea Tete es iinet = 0.5 1.0 1.5 2.0 2.5 3.0 3.5 4.0 4.5 5.0 5:5 6.0 = 6.5 - 7.0 - 7.5 ~ 8.0 85 9.0 9.5 0.0 10 2.0 3.0 40 5.0 .O .O Hee ep HH “0 | SMITHSONIAN TABLES. TABLE 213 (continued) 27] RELATIVE HUMIDITY, VAPOR PRESSURE AND DRY TEMPERATURE Vapor Air Temperatures, dry bulb, ° Centigrade. Pressure. mm. ° 26° 27° 28° 29° 80° 31° 382° 33° 34° ONINHDH PONE Nw dee ~ me OO MWONF mO OW Np lo bWWwo out COAL Ww O ¥ aE Aun t Orn he oh ale in NON Pe el ay oO’ Wn Lila [lial Peet | alt oko SMITHSONIAN TABLES. 238 TABLES 213 (concluded) AND 214 TABLE 213 (concluded) —Relative Humidity, Vapor Pressure and Dry Temperature (Data from 20° to 60° C based upon Table 208.) Air Temperatures, dry bulb, ° Centigrade. | 40° 41° 42° 43° 44° 45° 46° 47° 48° 49° 60°? 51° 52° 53° 64° 65° 56° 57° 58° 69° 60° ONES RID 7a we 17 aelOm NS ees 13 As) 2 2B BP 20 34 33 31 2 26 43 39) 37, 33 3 7 10 Noe ee ODn OF ete tet Piet Cn en et ofr ONS SI 46 44 40 60 Ga i 46 68 62 59 53 77 69 66 59 86 TS 66 85 81 93 88 IN & SD Gok Ny hw Nh Onur Our AR > OONn Of ° Munn & WoW Nt afodn Cin SO Onn Of Ww boy by vy SOS an Ovo mn me NOD 0 oO’ 2 oo nn Wo ow MN G2 0 TABLE 214.—Relative Humidity, Wet and Dry Thermometers This table gives the relative humidity direct from the difference between the reading of the dry (t ° C) and the wet (ti ° C) thermometer. It is computed for a barometer reading of 76cm. The wet thermometer should be ventilated about 3 meters per second. From manuscript tables computed at the U.S. Weather Bureau. Depression of wet-bulb thermometer, t9-t,°. DDO ACS God 822.02 44 35 25 54 39 62 50 69 59 74 66 78 71 81 75 SMITHSONIAN TABLES. TABLE 215 239 THE INTERNATIONAL TEMPERATURE SCALE (Adapted from G. K. Burgess, Bur. Standards Journ. Res., 1, 635, 1928.) The Thermodynamic Centigrade Scale, on which the temperature of melting ice, and the temperature of condensing water vapor, both under the pressure of one standard atmosphere, are numbered 0° and 100°, respectively, is recognized as the fundamental scale to which all temperature measurements should ulti- mately be referable. The experimental difficulties incident to the practical realization of the thermodynamic scale have made it expedient to adopt for international use a practical scale designated as the International Temperature Scale. This scale conforms with the thermodynamic scale as closely as is possible with present knowledge, and is designed to be definite, conveniently and accurately repro- ducible, and to provide means for uniquely determining any temperature within the range of the scale, thus promoting uniformity in numerical statements of temperature. Temperatures on the international scale will ordinarily be designated as “°C,” but may be designated as “°C (Int.) ” if it is desired to emphasize the fact that this scale is being used. The International Temperature Scale is based upon a number of fixed and reproducible equilibrium temperatures to which numerical values are assigned, and upon the indications of interpolation instruments calibrated according to a specified procedure at the fixed temperatures. The basic fixed points and the numerical values assigned to them for the pressure of one standard atmosphere are given in the following table, together with formulas which represent the temperature (t,) as a function of vapor pressure (p) over the range 680 to 780 mm of mercury. Basic Fixed Points of the International Temperature Scale oC. (a) Temperature of equilibrium between liquid and gaseous oxygen at the pressure of one standard atmosphere (oxygen point). — 182.97 tp=tz60 + 0.0126( p — 760) —0.0000065 ( p — 760)? (b) Temperature of equilibrium between ice and air-saturated water ai normal atmospheric pressure (ice point)i. 5 .5.544---. - 0.000 (c) Temperature of equilibrium between liquid water and its vapor at the pressure of one standard atmosphere (steam point).. 100.000 tp=tre0 + +0.0367 ( p — 760) — 0.000023 (p— 760)? (d) Temperature of equilibrium between liquid sulphur and its vapor at the pressure of one standard atmosphere (sulphur FIOM Me eer ree ea eater a5 Wie 6 2 siece MSR nea eT hs he 444.60 tp =tz60 + 0.0909 ( p — 760) — 0.000048 ( p — 760)” (e) Temperature of equilibrium between solid silver and liquid silver at normal atmospheric pressure (silver point)...... 960.5 (f) Temperature of equilibrium between solid gold and liquid gold at normal atmospheric pressure (gold point)..,.......... 1,063 SMITHSONIAN TABLES 240 TABLE 2155 (continued) THE INTERNATIONAL TEMPERATURE SCALE Standard atmospheric pressure is defined as the pressure due to a column of mercury 760 mm high, having a mass of 13.5951 g/cm’, subject to a gravita- tional acceleration of 980.665 cm/sec.” and is equal to 1,013,250 dynes/cm?. It is an essential feature of a practical scale of temperature that definite numerical values shall be assigned to such fixed points as are chosen. It should be noted, however, that the last decimal place given for each of the values in the table is significant only as regards the degree of reproducibility of that fixed point on the International Temperature Scale. It is not to be understood that the values are necessarily known on the Thermodynamic Centigrade Scale to the corresponding degree of accuracy. The means available for interpolation lead to a division of the scale into four parts. (a) From the ice point to 660° C the temperature t is deduced from the resistance FR, of a standard platinum resistance thermometer by means of the formula R,=R.(1+4,4+Bt?) The constants R,, A, and B of this formula are to be determined by calibration at the ice, steam, and sulphur points, respectively. The purity and physical condition of the platinum of which the thermometer is made should be such that the ratio R,/A> shall not be less than 1.390 for f—T00- and! 2.645 for t=A24410"- (b) From —190° to the ice point, the temperature t is deduced from the resistance FR, of a standard platinum resistance thermometer by means of the formula R,=R,[1+At+BHP+C(t—100)¢] The constants Ry, A, and B are to be determined as specified above, and the additional constant C is determined by calibration at the oxygen point. The standard thermometer for use below 0° C must, in addition, have a ratio R,/Ro less than 0.250 for t= — 183°. (c) From 660° C to the gold point, the temperature ¢ is deduced from the electromotive force e of a standard platinum v. platinum-rhodium thermo- couple, one junction of which is kept at a constant temperature of 0° C while the other is at the temperature ¢ defined by the formula C=4-" bi Gt" The constants a, b, and ¢ are to be determined by calibration at the freezing point of antimony, and at the silver and gold points. (d) Above the gold point the temperature ¢ is determined by means of the ratio of the intensity J, of monochromatic visible radiation of wave length A cm, emitted by a black body at the temperature ty, to the intensity J, of radia- tion of the same wave length emitted by a black body at the gold point, by means of the formula ia 7 = 4a - I | Se ve Nel. e36 (t+273) The constant cy» is taken as 1.432 cm degrees. The equation is valid if A(t+273) is less than 0.3 cm degrees. SMITHSONIAN TABLES TABLE 216 241 THE INTERNATIONAL TEMPERATURE SCALE Recommended Procedure for Calibration I. OXYGEN The temperature of equilibrium of liquid and gaseous oxygen has been best realized experimentally by the static method, the oxygen vapor-pressure ther- mometer being compared with the thermometer to be standardized in a suitable low temperature bath. ZIOCE The temperature of melting ice is realized experimentally as the temperature at which pure, finely divided ice is in equilibrium with pure, air-saturated water under standard atmospheric pressure. The effect of increased pressure is to lower the freezing point to the extent of 0.007° C per atmosphere. 3. STEAM The temperature of condensing water vapor is realized experimentally by the use of a hypsometer so constructed as to avoid superheat of the vapor around the thermometer, or contamination with air or other impurities. If the desired conditions have been attained, the observed temperature should be independent of the rate of heat supply to the boiler, except as this may affect the pressure within the hypsometer, and of the length of time the hypsometer has been in operation. 4. SULPHUR For the purpose of standardizing resistance thermometers, the temperature of condensing sulphur vapor is realized by adherence to the following speci- fications relating to boiling apparatus, purity of sulphur, radiation shield, and procedure. The boiling-tube is of glass, fused silica, or similar material, and has an internal diameter of not less than 4 nor more than 6 cm. The vapor column must be sufficiently long that the bottom of the radiation shield is not less than 6 cm above the free liquid surface and its top is not less than 2 cm below the top of the heat insulating material surrounding the tube. Electric heating is preferable, although gas may be used, but the source of heat and all good con- ducting material in contact with it must terminate at least 4 cm below the free surface of the liquid sulphur. Above the source of heat the tube is surrounded with insulating material. Any device used to close the end of the tube must allow a free opening for equalization of pressure. The sulphur should contain not over 0.02 per cent of impurities. Selenium is the impurity most likely to be present in quantities sufficient to affect the tem- perature of the boiling point. The radiation shield is cylindrical and open at the lower end, and is provided with a conical portion at the top, to fit closely to the protecting tube of the thermometer. The cylindrical part is 1.5 to 2.5 cm larger in diameter than the protecting tube of the thermometer and at least I cm smaller in diameter than the inside of the boiling tube. The cylinder should extend at least 1.5 cm SMITHSONIAN TABLES 242 TABLES 216 (continued) AND 217 THE INTERNATIONAL TEMPERATURE SCALE TABLE 216 (continued).—Recommended Procedure for Calibration beyond each end of the thermometer coil. There should be ample opening at the top of the cylindrical and below the conical portion to permit free circula- tion of vapor. The inner surface of the shield should be a poor reflector. The shield may be made of sheet metal, graphite, etc. In standardizing a thermometer the sulphur is heated to boiling and the heating so regulated that the condensation line is at least I cm above the top of the insulating material. The thermometer with its radiation shield is inserted in the vapor, and when the line of condensation again reaches its former level simultaneous observations of resistance and barometric pressure are made. In all cases care should be taken to prove that the temperature is independent of vertical displacements of the thermometer and shield. 5. SILVER AND GoLpD For standardizing a thermocouple, the metal to be used at its freezing point is contained in a crucible of pure graphite, refractory porcelain, or other ma- terial which will not react with the metal so as to contaminate it to an appre- ciable extent. Silver must be protected from access of oxygen while heated. The crucible and metal are placed in an electric furnace capable of heating the contents to a uniform temperature. The metal is melted and brought to a uniform temperature a few degrees above its melting point, then allowed to cool slowly with the thermocouple immersed in it as described in the next paragraph. The thermocouple, mounted in a porcelain tube with porcelain insulators separating the two wires, is immersed in the molten metal through a hole in the center of the crucible cover. The depth of immersion should be such that during the period of freezing the thermocouple can be lowered or raised at least I cm from its normal position without altering the indicated e.m.f. by as much as I microvolt. During freezing, the e.m.f. should remain constant within I microvolt for a period of at least five minutes. As an alternative to displacing the couple, as a means of testing the absence of the influence of external conditions upon the observed temperature, both freezing and melting points may be observed and if these do not differ by more than 2 microvolts, the observed freezing point may be considered satisfactory. TABLE 217.—The Standard Platinum Resistance Thermometer The diameter of the wire should not be smaller than 0.05 or larger than 0.2 mm. The platinum wire of the thermometer must be so mounted as to be subject to the minimum of mechanical constraint, so that dimensional changes accom- panying changes of temperature may result in a minimum of mechanical strain being imposed upon the platinum. The design of the thermometer should be such that the portion, the resistance of which is measured, shall consist only of platinum, and shall be at the uniform temperature which is to be measured. This may be accomplished by either of the accepted systems of current and potential, or compensating leads. After completion, the thermometer should be annealed at a temperature of at least 660°. SMITHSONIAN TABLES TABLES 218 AND 219 243 THE INTERNATIONAL TEMPERATURE SCALE TABLE 218.—The Standard Thermocouple The platinum of the standard couple shall be of such purity that the ratio R:/Ro is initially not less than 1.390 for t= 100°. The alloy is to consist of 90 per cent platinum with Io per cent rhodium. The completed thermocouple must develop an electromotive force, when one junction is at 0° and the other at the freezing point of gold, not less than 10,200 nor more than 10,400 international microvolts. The diameter of the wires used for standard thermocouples should lie between the values 0.35 and 0.65 mm. The freezing point of antimony, specified for the standardization of the thermocouple, lies within the range of 0° to 660° where the international scale is fixed by the indications of the standard resistance thermometer, and the numerical value of this temperature is therefore to be determined with the resistance thermometer. In the appendix the result of such determinations is given as 630.5°, but the temperature of any particular lot of antimony which is to be used for standardizing the thermocouple is to be determined with a standard resistance thermometer. The procedure to be followed in using the freezing point of antimony as a fixed tempera- ture is substantially the same as that specified for silver. Antimony has a marked tendency to undercool before freezing. The undercooling will not be excessive if the metal is heated only a few degrees above its melting point and if the liquid metal is stirred. During freez- ing the temperature should remain constant within 0.1° for a period of at least five minutes. TABLE 219.—Secondary Calibration Points These points and their temperatures on the international scale are listed below. The temperatures correspond to a pressure of one standard atmosphere. The formulas for variation of vapor pressure with temperature are for the range from 680 to 780 mm. 2G Baling hy Grog en) yep ten =15101 0044 |(pi— 760) ae acc eens «lapse oye sieve cpereyeiene ers olor — 252.75 Equilibrium between solid and gaseous carbon dioxide tp = treo + 0.1443 ere 827719) MLO Bran 7 OO) Manaieineie sista cule ale eeetsteh idee Aists (sei Sieve cemnstan eo eueiais oboe — 78.5 SRE CZ 101 SIT CT CUI yperret ge anaes tent cre aes eA Tose lore ole aie eels eceb sie sar cye SO Srspoieeoe Sievaasicke — 38.87 Mas EON) Oly SOGIUIM ASU pMave ays ure sys: 4.5| clckete gree cla ds elvis o Sein she care tej ale elals aur oleha dere ace 32.38 Condensing naphthalene vapor tp = treo + 0.208 (tp + 273.2) logi (p/760)....... 217.096 MME a RUIN YS Se Ese Pyar s ae recreate TI wialele rap ale ait oly Wao SRA ame beatae eaue Oo orale 231.85 Condensing benzophenone vapor tp = tro + 0.194 (tp + 273.2) logio (p/760).... 305.9 re COZITT Ra CTTITINTUM tap rte era siees eh asics tual Sue CEA POC oeGT Gs ais a alee Ua Sle eco SONS ee eck sbi 320.9 Baier T SS ALC GLE Fos aust se P St och 5 SY. Re ete be 6 he ae eee lakes SS REDS, Se SR cy BRAM che el chavs es 327.3 Freezing zinc ...... PATE REST pee be ats s choot eet yA SUSE NS. oy TAGES SEA PIE Ue ees beets 419.45 ICC ZING ATICITMOL Vas Mele ease loci niles BO lac idis celle hee wales kad drtalen( do sarate be 630.5 Beeczine copper itl a reducing atmosphere... 2.6500. Gos eee sees ccs ees te os 1,083 Beer a AlIACIil a sy..e Sele. Geter cere os wien s lace ts ea. eee a ne 1,553 Be ted GPa CELEY US LEU date raver tes ev che cnc tagmenn epee aeaey tier: ranaita ada lneNeaas Several dnc nee Se 3,400 BEMEMTANE! cc c0000cssecieesecs — 159.6 {* Ete S Orme on arc ees ak 1202) sala}; PATON) GIOKICE oo05 0 ccec cess — 111.6 f INGCkel Perit reece ce 1455. m,f PEEREE cis ccalesec.senceecees —o5.1 f Cobaltsrer ceo ae costes 1490. m,f HIV ACELALC sees cece ess < — 83.6 f Ga SE@ eaten oe sohs ohae 1555. m PRUGLOVOTTT- 0... 5 sods os Sone. — 63.5 f ‘Blatinummesstneir asec one 1755. m Carbon tetrachloride ......... — 22.9 f *f, freezing. jm, melting. SMITHSONIAN TABLES 244 TABLE 220 DIRECTIONS FOR USE OF STANDARD THERMOELEMENT CALIBRATIONS Deviation curves.—Standard tables such as are given on pages 245-247 have no absolute significance; they are reference curves that, while representing fairly well the e.m.f. functions for certain couples, are intended for use with an appropriate deviation curve. The correction curve is determined for each element by calibration at several fixed points—preferably three or more—given in the tables. It is constructed by plotting AF as ordinate (AE=E observed minus F standard) against E,s. In order to obtain the temperatures corre- sponding to the measured e.m.f., the appropriate value of AE (obtained from its deviation curve by inspection) is subtracted algebraically from the observed value of E before the latter is converted into degrees by means of the table. The required accuracy may be secured by plotting the deviation curve on a small scale; coordinate paper 20 by 20 cm is ample. There need be no fear of error with this method even with deviations of several hundred pv, especially if sufficient calibration points are taken. Fixed-junction correction.—Thermocouples have two junctions. The “ busi- ness end ” is usually called the hot junction, and the other, the cold junction. The calibration tables are made on the assumption that the fixed junction is maintained at o° C. The standard method is to use a vacuum-jacketed flask filled with ice into which is inserted the junction protected by a glass tube closed at one end and partly filled with kerosene. If it is not feasible to have the fixed junction at 0°, a fixed-junction correction must be applied. This correction, in general, is not equal to the temperature of the fixed junction and depends on both the temperature TJ) of the fixed junction and the tem- perature T of the variable junction. It may be applied by either of the follow- ing two methods. (1) The e.m.f. corresponding to T) may be added directly to the e.m-f. Er-ro and the resultant e.m.f. Ey, converted into degrees by means of the proper table (Tables 221-225). Thus if a platinum-platinrhodium couple gives a reading of 6000nv (microvolts), T) being 50°, the value of E7o, according to Table 221, is 298uv which added to 6000 gives 6298 as the value of Ez, which by referring to the table corresponds to T=.703.6°. This method of correction is mathematically exact. (2) Multiply the fixed junction tempera- ture by a factor, f= (dE/dt) )/(dE/dt), the ratio of the mean e.m.f. tempera- ture gradient between 0° and ¢; to the gradient at ¢, and add the product to /’, the uncorrected temperature, or t=?t’+ft;. The e.m.f. temperature gradients may be obtained by taking the reciprocals of the numbers corresponding in successive vertical difference of the numbers in the vertical columns. SMITHSONIAN TABLES TABLES 221 AND 222 246 TABLE 221,—Standard Calibration Curve for Pt—PtRh (10% Rh) Thermoelemenat Giving the temperature for every 190 microvolts. For use in conjunction with a deviation curve determined by cali bration of the particular element at some of the following fixed po‘nts: Water boiling-pt. 100.0 643mv. Silver melting-pt. 960.2 QOIrmmvy. Naphthalene re eS 217.95 1585 Gold - “ 1062.6 10296 Tin melting-pt. 231.9 1700 Copper <6 ss 1082.8 10534 Benzophenone boiling-pt. 305.9 2365 Li,SiO3 ae s¢ 1201. T1941 Cadmium melting-pt. 320.9 2503 Diopside s? £ 1391.5 14230 Zinc ne s 419.4 3430 Nickel sf ae 1452.60 140973 Sulphur boiling-pt. 444.55 3672 Antimony melting-pt. 630.0 5530 Palladium sf s 1540.5 16144 Aluminum a of 658.7 5827 Platinum we ie 1755. 18608 3000. | 4000. | 5000. TEMPERATURES, °C. 374-3 478.1 578.3 | 675.3 | 769.5 | 861.1 950.4 384.9 488.3 588.1 684.8 778.8 870.1 959.2 395-4 408.4 597-9 | 604.3 | 788.0 | 870.1 968.0 405.9 508.5 607.7 703.8 797.2 888.1 976.7 416.3 518.6 617.4 713.3 806.4 807.1 985.4 426.7 528.6 627.1 722.7 815.6 | go6.1 994.1 437.1 538.6 636.8 72000 824.7 915.0 1002.8 447.4 548.6 646.5 741.5 833.8 923.9 IOII.5 457-7 558.5 656.1 750.9 842.9 932.8 1020.1 467.9 568.4 665.7 760.2 852.0 941.6 1028.7 478.1 578.3 675.3 760.5 861.1 950.4. 1037.3 13000. | 14000. | 15000. | 16000. 17000. | 18000. TEMPERATURES, °C. 1289.3 1372.4 1454.8 1620.9 | 1704.3 1207.7 1380.7 1463.0 1629.2 | 1712.6 1306.0 1389.0 1471.2 1637.6 1721.0 T314.3 1397-3 1479.4 1645.9 1720.3 1322.6 1405.6 1487.7 1654.3 1737.7 1330.9 1413.8 1496.0 1662.6 1746.0 1339.2 1422,0 1504.3 1670.9 1754.3 1347-5 1430.2 1512.6 1679.3 1355.8 1438.4 1520.9 1687.6 1364.1 1446.6 1520.2 1696.0 1372.4 1454.8 1537-5 1704.3 TABLE 222.—Standard Calibration Curve for Copper—Constantan Thermoelement For use in conjunction with a deviation curve determined by the calibration of the particular element at some of the following fixed points: ; Water, boiling-point, 100°, 4276 microvolts; Naphthalene, boiling-point, 217.95, 10248 mv.; Tin, melting-point, 231.9, 11009 mv.; Benzophenone, boiling-point, 305.9, 15203 mv.; Cadmium, melting-point, 320.9, 16083 mv. 3000. 4000. | 5000. | 6000. if 7000. | 8000. | Qooo. TEMPERATURES, °C. 0.00 25.27 49.20 72.08 94.07 115.31 135.91 155-95 175.50 | 104.62 2.60 27.72 51.53 74.31 96.23 117.40 137-04 157-92 177.43 | 1096.51 Sony 30.15 53-85 76.54 98.38 119.48 139.96 159.89 179.36 | 1098.40 Tas 2.577 56.16 78.76 100.52 121.56 141.98 161.86 181.28 | 200.28 10.28 34.98 58.46 80.97 102.66 123.63 143.90 163.82 183.20 | 202.16 12.81 37.38 60.76 83.17 104.79 125.69 146.00 165.7 185.II | 204.04 15.33 39-77 63.04 85.37 106.91 127.75 148.00 167.73 187.02 | 205.91 17.83 42.15 65.31 87.56 109.02 129.80 150.00 169.68 188.93 | 207.78 20.32 44.51 67.58 89.74 II1I.12 131.84 151.99 171.62 190.83 | 2009.64 22.80 46.86 69.83 QI.or 113.22 133.88 153-97 173.56 192.73 | 211.50 25.27 49.20 | 72.08 04.07 Ur5.30) |) 135.08 | 155.95 175.50 194.62 | 213.36 10000. | II000. | 12000. | 13000. | 14000. | 15000. 16000. | 17000. | 18000. TEMPERATURES, °C. 213.36 249.82 267.60 285.13 302.42 319.49 336.36 215.21 251.61 269.36 286.87 304.14 321.19 338.04 217.06 253-40 271.12 288.61 305.85 322.88 339.72 218.91 255.18 272.88 290.35 307.56 324.57 341.40 220.75 256.96 274.64 292.08 309.27 326.26 343-07 222.59 258.74 276.40 293.81 310.98 327.95 344.74 224.43 260.52 278.15 205.54 312.69 320.64 346.41 226.26 262.29 279.90 297.26 314.39 331.32 348.08 228.09 264.06 281.65 298.98 316.09 333.00 349-75 229.92 265.83 283.39 300.70 317-79 334.68 351-42 231.74 267.60 285.13 302.42 319.49 | 336.36 353.00 Cf. Day and Sosman, Am. Jour, Sci. 29, p. 93, 32, P- 51, ; thid. R. B. Sosman, 30, p. I. SMITHSONIAN TARLES. 246 TABLES 223 AND 224 TABLE 2238.—Standard Calibration Curve for Copper—Constantan Thermoelement, Temperatures Below 0°C — 124.46 é —55.81 4.01 ; 3.05 — 128.47 : — 58.86 4.09 — 132.56 4.18 3-51 — 136.74 98.25 4.28 3-57 — 141.02 —101.82 4.39 3-63 — 145.41 — 105.45 4.50 3.68 —149.91 — 109.13 4.61 3-74 —154.52 — 112.87 4-73 3.80 —159.25 — 116.67 4.87 3.86 — 164.12 —120.53 5.02 3-93 3-37 —169.14 —124.46 — 87.86 TABLE 224.—Melting Points of Some Purified Salts, 400-1300°C (Roberts, some new standard melting points at high temperatures, Phys. Rev., 2d ser., 23, 386, 1924, which see for technique of their use.) Potassium dichromate 397.5°C | Sodium chloride 45 KCl + 55 NaeSO, by wt..... 517.1 Sodium sulphate 30.5 NaCl + 69.5 Na2SOu by wt. 627.0 Potassium sulphate * Potassium chloride Dicalcium borate (Ca2B20s5) ....1304 * Potassium sulphate has sharp inversion point at 583° +1. SMITHSONIAN TABLES TABLE 225 247 STANDARD CALIBRATION CURVE FOR CHROMEL-ALUMEL THERMOELEMENT * 4.0 4-5 5.0 5:5 6.0 6.5 7.0 7:5 8.0 8.5 9.0 9-5 10.0 12.6 12.6 12.4 25.0 12.3 37-3 £252 49.5 12.2 6re7, L255 73-8 T2.1 85.9 12.2 98.1 E2ve 110.3 12.4 T2247 12.5 135.2 12.6 147.8 12.6 160.4 12.7 Tyger 12.7 185.8 12.8 198.6 12.8 211.4 12.9 224.3 12.9 BRED aot) 250.1 250.1 13.0 263.1 12.9 276.0 27) 288.7 12.5 301.2 12.3 313-5 I2.1 325.6 I1I.9 337-5 11.6 349.1 II.5 360.6 II.5 Bea II.7 383.8 11.8 395-6 11.8 407.4 11.8 419.2 11.8 431.0 11.9 442.9 II.9 454.8 II.9 466.7 II.9 478.6 I1I.9 490.5 586.6 I2.1 598.7 I2.1 610.8 I2.2 623.0 12.2 635.2 I2.2 647-4 I2.3 659.7 I2.3 672.0 12:3 684.3 12.3 696.6 12.4 709.0 12.4 721.4 12.4 733-8 847.4 12.8 860.2 12.9 873.1 12.9 886.0 13.0 899.0 13.0 Q12.0 I3.1 925.1 I3.1I 938.2 I3.2 951.4 13.2 964.6 13-3 977-9 13-4 991.3 (1220.0) I5.0 (1235.0) 16.0 (1251.0) 16.0 (1267.0) 16.0 (1283.0) * Standard calibration curve for chromel-alumel (Hoskins) thermocouple giving the temperature and temperature differences for every 0.5 millivolt. Fixed junction is at 0°. For use in conjunction with a deviation curve determined by calibration of the particular couple at some of the following fixed points: S, boiling point Sb, melting point Al, melting point Degrees C Ag, melting point........ SMITHSONIAN TABLES Milli- volts Au, melting point Degrees € Cu (in air), melting point Milli- volts mo 1063.0 42.60 1065.0 42.68 Cu (pure), melting point. 1082.8 43.31 248 TABLE 226 OPTICAL PYROMETRY (The following discussion is abbreviated from Dushman, Rev. Mod. Phys., 2, 387, 1930.) Data on various substances are now available by which accurate determina- tions may be made of the temperature of an emitting surface. For a compre- hensive review see Lax and Pirani, Handb. Phys., 19, 1-45; 21, 190-272, Julius Springer, Berlin, 1929. Data on total radiation from various bodies have been summarized by Coblentz (I.C.T. 5, 238-245, 1929). Undoubtedly the most accurate method consists in determining the brilliancy (candles/cm?). The temperature coefficient (dB/B)/(dT/T) where B= brightness in international candles/cm?, for W varies from 22.75 at 1000° K, to 8.45 at 3000° K. (Jones, Langmuir, Gen. Elec. Rev., 30, 310, 354, 408, 1927). With the exception of electron emission and the rate of evaporation, the candlepower shows the greatest temperature variation. While the values of B as a function of T are available for several substances, a fair approximation is possible to the true T of a substance for which the average luminous emissivity is unknown by the following methods. (Average luminous emissivity means the ratio of the total normal brightness to that of a black-body at the same T. For W this value is from 0.464, T=1000° K. to 0.440, T=3000° K., Forsythe, Worthing, Astrophys. Journ., 61, 126, 1925). With a photometer determine the temperature T, at which substance emits light of the same color as a black-body—a value higher than the true tempera- ture. The following table is due to Worthing-Forsythe : Tc (tungsten) True T (Te —T)/T Ts (tungsten) 1000° K. 1000° K. 0.006 966° K. 1517 1500 .OIl 1420 2033 2000 .0165 1857 2557 2500 023 2274 30904 3000 .031 2673 The brightness may be compared with a standard lamp for a given wave length, usually 0.6654. The temperature found is called the brightness tempera- ture, 7, lower than the true temperature, increasingly so with decrease in e), the emissivity for this wave length, and increasing with the temperature. Thus for w, e, for A=0.665p varies from 0.456, T=1000° K. to 0.415, T=3000° K. and the observed values T; are given in the preceding table. From these determinations of T, and T; fairly approximate values of T may be deduced. It is possible to determine the actual value of e, by methods described by both Langmuir, Worthing and Forsythe, then calculate 7, the true tempera- ture from optical pyrometer measurements of JT. See Forsythe, Journ. Opt. Soc. Amer., 16, 307, 1928; Journ. Amer. Ceram. Soc., 12, 780, 1929; Foote, Fairchild, Symposium on Pyrometer, Amer. Inst. Mining and Metallurg. Eng., 338, 324, 1920; also loc. cit., p. 291, 367, 285. At temperatures below 1100-1200° K. optical methods become impractical, and radiation in watts radiated per unit area or resistance must be used. Data on energy radiated as a function of the temperature have been summarized by Lax and Pirani, Handb. Phys., 21, 236-240, for W, Mo, Ta, Pr, Os, Au, Ni, Fe, Cy Ag, Cujjand Zz. SMITHSONIAN TABLES TABLES 227-229 249 TABLE 227.—Correction for Temperature of Emergent Mercurial Thermometer Thread When the temperature of a portion of a thermometer stem with its mercury thread differs much from that of the bulb, a correction is necessary to the observed temperature unless the instrument has been calibrated for the experimental conditions. This stem correction is proportional to n§(T —t), where n is the number of degrees in the exposed stem, 8 the apparent coefficient of expansion of mercury in the glass, T the measured temperature, and t the mean temperature of the exposed stem. For temperatures up to 100° C, the value of 8 is for Jena 16!1 or Greiner and Friedrich resistance glass, 0.000159, for Jena s9!I1, 0.000164, and when of unknown composition it is best to use a value of about 0.000155. The formula requires a knowledge of the temperature of the emergent stem. This may be approximated in one of three ways: (1) by a “‘ fadenthermometer ’”’ (see Buckingham, Bulletin Bureau of Standards, 8, p. 239, 1912); (2) by exploring the temperature distribution of the stem and calculating its mean temperature; and (3) by suspending along the side of, or attaching to the stem, a single thermometer. Table 228 is taken from the Smithsonian Meteorological Tables. TABLE 228.—Stem Correction for Centigrade Thermometers Values of o.ooo155n(T —?). Oo. ° Oo. ° oO. ° oO. ° °. ° 90000 CuO 6,076 TABLE 229.—Reduction of Gas Thermometers to Thermodynamic Scale The final standard scale is Kelvin’s thermodynamic scale, independent of the properties of any substance, a scale resulting from the use of a gas thermometer using a perfect gas. A discussion of this is given by Buckingham, Bur. Standards Bull., 3, 237, 1907: ‘‘ The thermodynamic correction of the centigrade constant-pressure scale at the given temperature is very nearly proportional to the constant pressure at which the gas is kept’’ and “the thermodynamic correction to the centigrade constant- volume scale is approximately proportional to the initial pressure at the ice point.’’ These two rules are very convenient, since from the corrections for any one pressure, one can calculate approximately those for the same gas at any other pressure. é ; The highest temperature possible is limited by the container for the gas. Day and Sosman carried a platinum-rhodium gas thermometer up to the melting point of palladium. For most work, however, the region of the gas thermometer should be considered as ending at about 1000° C (1273° K.). Note: All corrections in the following table are to be added algebraically, 273.1° C (ice point) For a discussion of the various values and for the corrections of the various gas thermometers to the thermodynamic scale see Buckingham, Bull, Bureau Standards, 3, p. 237, 1907. Scale Corrections for Gas Thermometers. Constant pressure = 100 cm Constant vol., pp = 100 cm, tg = O°C H N +o.18 .06 O10 .004 .000 .000 .000 +4+4+4++ | [+ SMITHSONIAN TABLES 250 TABLE 230 PRACTICAL THERMOELECTRIC SCALES (Comparisons) (Adapted from Roeser, Bur. Standards Res. Paper 99, 1920, which see for details of use.) Prior to the adoption of the International Temperature Scale, the Pt-Pt1o% Rh ther- mocouple was almost universally used for scales 450° to 1100°C, and defining equations were quadratic or cubic depending upon the number of calibration points. The scale based on the work of Holborn and Day was calibrated at the freezing point of Zn (419.0°C), Sb (630.6°C) and Cu (1084.1°C) and a quadratic equation, E = a + vt + cf, for interpolation. This was almost universally used from 1900-1909. Work of Waidner, Burgess, 1909, and Day, Sosman, 1910-1912, necessitated a readjustment. In 1912 the Bureau of Standards redefined its scale, assigning values determined with the resistance thermometer to the Zn and Sb points, while the freezing point of Cu was taken as 1083.0°C. This 1912 scale, used from 1912-1916, will be called the Zn,Sb,Cu temperature scale. A scale proposed by Sosman and revised by Adams (Journ. Amer. Chem. Soc., 36, 65, 1914) was realized by using a standard reference table, giving the average #,e.m.f. relation for thermocouple used by Day and Sosman. A deviation curve, determined by any other couple by calibration at several points would be plotted relating the difference between observed e.m.f. and the e.m.f. from the reference table against the obs. e.m.f. of the couple. This scale, although very convenient, is not completely defined and no comparison is made here. In 1916, the Physikalische-Technische Reichsanstalt adopted a scale with the couple calibrated at the Cd point (320.9°C), Sb (630°C), An (1063°C) and Pd (1557°C). No com- parison will be made here. A scale adopted by the Bureau of Standards in 1916 was defined by calibration at the Zn and Al points with a Cu point (1083.0°C). This was used from 1916-1926 and is here designated the Zn,Al,Cu scale. The scale adopted by the P.T.R. and the Bureau of Standards in 1924 was calibrated at Zn and Sb points (determined by resistance thermometer) and the Ag point (960.5°C) and the Au point (1063.0°C). It will be designated the Zn,Sb,Ag,Au scale. The 1927 7th Annual Conference of Weights and Measures (31 nations) unanimously adopted what is between 660° and 1063°C the Zn,Sb,Ag,Cu scale with the Zn point omitted. The table below shows a comparison of the various scales. The following values for the freezing points were used: Zn 419.47°C Al 659.23°C Au 1063.0°C Sb 630.52°C Ag 9g60.5°C Cu (reducing atm.*) 1083.0°C Table 231 gives the corresponding difference of temperature. Comparison of #°C—e.m.f. relations with International Temperature Scale. (Comparisons with two thermo-couples are given.) E.m.f. in microvolts for temperature scales, E.m.f. in microvolts for temperature scales, Thermocouple A Thermocouple B Tempera- ae Interna- Interna- ture (°C) n, Sb, tional Zn, Sb, tional Zn, Sb, Zn, Al, Ag, and | tempera- Zn, Al, Ag, and | tempera- and Cu and Cu Au ture and Cu Au ture scale scale 3438.2 3438.2 3438.2 3447.5 3435-6 3435-6 3444.7 3732-9 3732-8 3733-4 3740.5 3729.6 3730.2 3737-2 4222.6 ~4222.204A 223739 WA22 7-6 4218.2 4219.3 4223.5 4720.9 4720.4 4721.6 4723.7 4715-4 4716.6 4718.7 5227.9 5227.2 5228.2 5228.8 5221-2) 5222°4) 5222.9 5541-6 5540.9 5541.6 5541.6 5534-2 5535 5535 5743-5 5742.8 5743-3 5743 5735-7) 5730-3 - 5736 5839.7. 5838.9 5839.3 5838.9 5831.6 5832.1 5831.6 6267.8 6267 6267 6266.1 6258.8 6258.8 6258 6800.8 6800 6799.3 6798.3 6790.6 6790 6789 7342-5 7341-7 7349-3 7339-4 7331 7329.8 7328.9 7892.8 7892.1 7890.2 7889.6 7880.1 7878.4 7877.7 8451.8 8451.2 8449.1 8448.8 8437.8 8435.8 8435.5 9019.5 9019 9017 9016.9 9004.2 9002.3 9002.2 9139-8 9139-3 9137-4 9137-4 9124.2 9122.4 9122.4 9595-8 9595.5 9594 9594.1 9579-2. 9577-8 9577-9 10180.8 10180.7 10180.3 10180.3 10162.8 I0162.5 10162.5 10334.4 10334.3 10334.2 10334.2 10316 10316 10316 LO5 7147 LO57147) 10572.3, 1057251 10552.8 10553.4 10553-3 10774.5 10774.6 10775.8 10775.5 10755.2 10756.4 10756.1 SMITHSONIAN TABLES TABLES 231-234 251 TABLE 231.—Temperature Differences between I.T.S. and various Older Scales Neeiee emt | kedeesss— | PLe tls s= Bilyss5s—)1| eledeaSem| elas: = Tee le ees 0 | lebees= ZnSb- | ZnAl- | ZnSb- ce - | ZnAl- | ZnSb- ZnSb- | ZnAl- | ZnSb- Cu J c Cu AgAu Cu Cu AgAu TABLE 232.—Conversion Factors for Units of Work o British thermal units Kilowatt- hours Foot- Kilogram- 15 Joules pounds meters Calories I 0.73767 | 0.1020F | 0.2391 |0.0009486|0.2778 XK 10% a5 Om i 0.1383 | 0.3241 *|0.001286*|0.3767 X 10%* 9.807 * Wee I 2.345* |0.009302*|2.724 X 10°%* 4.183 Be oBst 0.4267 T I 0.003965 |I.162 X 10% 1 Foot-pound.. I Kilogram- -meter 1 15° Calorie. 1 British thermal 1054. 777.51 Oras || DS) I 0.0002928 3 600 000.|2 655 000. t/367 200. t|860 800.} 3415. I 1 Kilowatt-hour.. The value used for g is the standard value, 980.665 cm. per sec. per sec. = 32.174 feet per sec. per sec. * The values thus marked vary directly with ‘‘g.”’ + The values thus marked vary inversely with ‘‘g.’’ For values of ‘“‘g’’ see Tables 706-709. TABLE 233.—Value of the English and American Horsepower (746 watts) in Local Foot-pounds and Kilogram- meters per Second at Various Altitudes and Latitudes Kilogram-meters per second Foot-pounds per second Latitude Latitude o km 76.275 | 76.175 | 76.074 | 75-973 | 75-873 || 551-70 | 550.97 | 550-24 | 549-52 | 548.79 1.5 76.297 | 76.197 | 76.095 | 75.995 | 75-895 || 551-86 | 551-13 | 550-41 | 549.68 | 548.95 3 76.320 | 76.220| 76.119 | 76.018 | 75.918 ]| 552.03 | 551-30] 550.57] 549.85 | 549.12 ae TABLE 234.—Nonflammable Liquids for Cryostats (Taken from Kanolt, Bur. Standards Sci. Paper, 520, 1926.) CCL GHG. 42 Goi; eres 2 39* No. rai ae point —23 —63 -—8I1 —II9 —139 —145 —I150+ *Compositions: No. 4; CCla, 49. 455; CHCl, 50.6%. No. ber, GEE: 19. oe C:H; Br, 44.9%; C.H2Cl, 13.8%; C.HCl,, 21.6 No. 39; CHCls, 14. a CoHsBr, 33.4%; CoH2Ch, 10.4%; CeHCls, 16. 4%; CHCl, 2 5-3/0 No. 40; CHCl, 17. 9%, GHC, 9.3%; CoHsBr, 40.7%; CoHeClhe, 125%; C;HCls, 19.6%. —80°C —90° —100° ~—110° ~—120° —130° —140° —145° —I150 Wiscositiesin” GSH Br "1.81 “2:25 2:89 3:86. 5.6... ee SCenrIpoisess= MING! S2he)..-) 13.03 4.57 7.46 496.7. 20.3. 81 vale ruse Nor34° 1:97 2.57 3-69 : 10 22°35 nos 242 1480 Nax400 4:2 2.88" 3.85 : ROL 2a 2 2-5 70 170) nO3t ° * Because of volatility and oxidation of some, these liquids should be kept in well stoppered bottles when not in use. SMITHSONIAN TABLES 252 TABLE 235 MELTING AND BOILING POINTS OF THE CHEMICAL ELEMENTS Symbol Melting Boiling Symbol Melting Boiling Element and point point Element and point point atomic no. iG 2 atomic no. | 2c Aluminum..| Al 13 659.7 1800 Molybdenum..| Mo 42 2620 3700 Antimony...| Sb 51 630.5 1380 Neodymium. .| Nd 60 840 ATOM eee. el AY eS || — sto. 2k T85s7 INeoneew ee Ne 10] — 248.67| — 245.9 Arsenice....- |) Asi 33 (820) 615.s Nickelsi2 ss. Ni 28 1455 2900 Barium, . 5300) Bismuthye sa) bie 83 278 1450 Oxygen...... O 8 | — 218.4 | — 183 Borans eta. B 5 2300 Ozone. .| Og Ee Sian || alae Bromine ae Byes we 72 58.8 || Palladium...| Pd 46 1553 2200 Cadmium....}| Cd 48 320.9 766 Phosphorus...| P15 44.1 280 Galeimmeas oor Ca 20 810 1170 Platinum....| Pt 78 1773s 4300 Carbone eal 6 | >3500 (4200) Potassium....} K 19 62.3 760 Cerium, a. 42 (Ce758 640 T400 Praseodymium] Pr 59 940 Ceasiimaarins aie sues 5 26 670 Radian. 4. 4c Ra 88 Q60 II40 Chlorine...... Chea 7 MOL On|; =) aqua Radom. .Su0.on Rn 86 | — I1o Chromium er 2 1615 2200 Rhenium..... Re 75 (3000) Cobaltaee aa. Con27, 1480 3000 Rhodium..... Rh 45 1985 >2500 Columbium...} Cb 41 1950 2900 Rubidium. ...| Rb 37 38.5 700 Copper...... Cu 29 1083 2300 Ruthenium...} Ru 44 2450 >2700 Dysprosium...| Dy 66 Samarium....| Sm 62 | >1300 Erbium) a.. Er 68 Scandium....| Se 21 1200 (2400) Europium....| Eu 63 Selenium..... Se 34 220 688 HilWorine so. g | — 223 — 187 Silicons. ce cen Si 1d 1420 2600 Gadolinium...| Gd 64 Silwerscoscre Ag 47 960.5 1950 Gallium. .... Cast 29.7 | >1600 Sodium. ..... Na II 97-5 880 Germanium Ge 32 958.5 (2700) Strontiom!, 7 =|"Ssrr3s 800 IIso Goldin. t.3 Au 79 1063 2600 Sulphur. ence S 16] 113-119 444.6 Hainium ..-. - Elim (1700) (> 3200) Mantalums =.) hae 73 2850 (> 4100) elise pe He 2 |<—272 — 268.94 || Tellurium....| Te 52 452 1390 Holmium..... Ho 67 Merbininyiwos Tb 65 Hydrogen....| H I | — 259.14 | — 252.8 || Thallium..... ley Sin 303.5 1650 Indiumi.cas |) Ins 149 155 >1450 Thorium..... Th 90 1845 > 3000 lodines. ks: T ¥S3 113.5 184.35 || Thulium..... Tm 69 Iriditum>s Nia 2350 (> 4800) Aine eaeeo ROD SO 231.80 2260 LEGO nhe nee Fe 26 1535 3000 Mitanium\.s..|) ie 22 1800 (> 3000) Keypronee ce Kr 36 | — 169 — 151.8 Tungsten..... W 74 3370 5900 Lanthanum...| La 57 826 T800 Uranium. UP 62> | P1850 Lead... 25. % Pb 82 327.4 1620 Vanadium;.25) V. 23 1710 (3000) Lithium sc. A es 186 > 1200 ENONES doco. Xe 54] — 140 — 109.1 (uteciumen . eee 7a Ytterbium.. Wo 70) Magnesium...| Mg 12 651 II00 Mittra: cq Wins 39 1490 (2500) Manganese. ..| Mn 25 1260 1900 ZANC csc Zn 30 419.47 907 Mercury..... Hg 80 | — 38.87 356.00 || Zirconium....| Zr 40 1900 >20900 (Metals in heavy type are often used as standard melting points.) SMITHSONIAN TABLES TABLES 236-238 253 TABLE 236.—Effect of Pressure on Melting Point Highest 4s | Melting point experimental dt/dp At (observed) | at 1 kg/sq. cm pressure: at 1 kg/sq. cm kg/sq. cm for Reference} tooo kg/sq. cm Substance. go: 59. 12,000 2,800 12,000 12,000 2,000 2,000 2,000 2,000 N mn ODD 0 An wo WwwwWw PPD * At (observed) for 10,000 kg/sq. cm is 50.8°. + Na melts at 177.5° at 12,000 kg/cm?; K at 179.6°; Bi at 218.3°; Pb at 644°. Luckey obtains melting point for tungsten as follows: 1atme, 3623° K; 8, 3504; 18, 3572; 28, 3564. Phys. Rev. 1917. References: (1) P. W. Bridgman, Proc. Am. Acad. 47, pp. 391-96, 416-19, 1911; (2) G. Tammann, Kristallisieren und Schmelzen, Leipzig, 1903, pp. 98-99; (3) J. Johnston and L. H. Adams, Am. J. Sci. 31, p. 516, 1911; (4) P. W. Bridgman, Phys. Rev. 6, 1, 1915. A large number of organic substances, selected on account of their low melting points, have also been investigated: by Tammann, loc. cit.; G. A. Hulett, Z. physik. Chem. 28, p. 629, 1899; F. KGrber, ibid., 82, p. 45, 1913; E. A. Block, ibid., 82, p. 403, 1913; Bridgman, Phys. Rev. 3, 126, 1914; Pr. Am. Acad. 51, 55, 1915; 51, 581, 1916; 52, 57,1916; 52,91, 1916. The results for water are given in the following table. TABLE 237.—Effect of Pressure on Freezing Point of Water * Pressure: T ke/sq: cm Freezing point. Phases in Equilibrium. Ice I — liquid. Ice I — liquid. Ice I — liquid. Ice I— ice III — liquid (triple point). Ice III — liquid. Ice III — ice V — liquid (triple point). Ice V — liquid. Ice V — liquid. Ice V — ice VI — liquid (triple point). Ice VI — liquid. Ice VI — liquid. Ice VI — liquid. Ice VI — liquid. * P. W. Bridgman, Proc. Am. Acad. 47, pp. 441-558, 1912. 7 1 atm. = 1.033 kg/sq. cm. TABLE 238.—Effect of Pressure on Boiling Point * Metal. Pressure. 10.2 cm Hg. : 2 20.6 cm Hg. Assy (eotk) g kes ; 6.3 atme. 6.3 atme. ; 11.7 atme. I1.7 atme. ; : TE acme: 16.5 atme. : 5 21.5 atme. 10.3 cm Hg. ! ; 53-0 atme. * Greenwood, Pr. Roy. Soc., p. 483, 1910. SMITHSONIAN TABLES. 254 DENSITIES AND MELTING AND BOILING TABLE 239 POINTS OF INORGANIC COMPOUNDS Substance. “c sulphate... phosphite. . Antimony trichloride. . . t pentachloride Arsenic trichloride Arsenic hydride Barium chloride y enitrate perchlorate. ... Bismuth trichloride... . Boric acid “ce cc “ Borax (sodium borate).. Cadmium chloride Calcium chloride rf chloride Mitrateee eee Carbon tetrachloride... = estrichlondess: .. ce “ce ce Chloric(per) acid Chlorine dioxide Chrome alum Chromium oxide....... Cobalt sulphate Cupric chloride Cuprous chloride Cupric nitrate Hydrobromic acid Hydrochloric acid Hydrofluoric acid Hydriodic acid Hydrogen peroxide * phosphide. .. sulphide..... Tron chloride * nitrate sulphatesess: caer Lead chloride ‘* metaphosphate.. . Magnesium chloride... . ce “ oe “f nitrate sulphate... Manganese chloride... . * nitrate sulphate. ... Mercurous chloride... .. Mercuric chloride “ Chemical formula. Al(NOs)3 + 9H2O 1,03 NH; NH,NO; (NH4)2SO4 NH,H2,PO3 SbCl; SbCl; AsCl AsHg BaCl, Ba(NOs) 2 Ba(ClOx) 2 BiCl; H3BOs3 Cd(NO3)2 + 4H20 CaCl, CaCl. + 6H.O Ca(NOs)2 Ca(NOs)2 + 4H20 CaO CCl C2Cle CO CO, CS. HCI1O, + H,0 ClO, KCr(SQ,)2 + 12H,0 Cro(NOs)¢6 + 18H,0 CroO3 CoSOx4 CuCl, CueCle Cu(NOs3).2 + 3H20 HBr HCl HFI HI H,02 PH3 H2S FeCl; Fe (NOs)3 + 9H,0 FeSO, + 7H20 PbCl, Pb(POs3)2 MgCl, MgO Mg(NOs)2 + 6H20 MgSO, + 5H.0 MnCl, + 4H.O Mn(NOs)> + 6H,O MnSO, + sH.O Density, = Melting point ce Boiling about point c Authority. Authority. eV Uae St 1 = 15S) eel al Sal See cere a een ena ee | | nw Ww a R Nw tS 4 Hh Nov Swe lo me eH Cnr H nN COO 0 AN leon tN H oO 1 (lisse inte AISI] Sesel sel ooton lel ieent (1) Friedel] and Crafts; (2) Ordway; (3) Faraday; (4) Marchand; (5) Amat; (6) Olszweski; (7) Gibbs; (8) Baskerville; (9) Carnelly; (10) Carnelly and O’Shea; (11) Ruff; (13) Wroblewski and Olszewski; (14) Anschiitz; (15) Roscoe; (16) Tilden; (21) Schacherl; (28) Kanolt. 6mMITHSONIAN TABLES, (17) (22) Tammann; * Decomposes. (18) Ladenburg; Thorpe; (23) Staedel; (24) Bruhl; Day; (20) (27) (19) Clarke, Const. of Nature; Ramsay; (25) Lorenz; (26) Morgan; TABLE 239 (continued) 255 DENSITIES AND MELTING AND BOILING POINTS OF INORGANIC COMPOUNDS 'Density,| Melting 2 Boiling | Pres- 2 Substance. Chemical formula. | about point & point Sures|mee 20°C C 3 mm | ¥ PRC ee Ba < Pees Nickel carbonyl....... NiC.sO, 1.32 —25. I 43.° | 760 | — ameTNIEGACE aes acgot: Ni(NO3)2 + 6H2O | 2.05 On ial2 136.7 || 760], 2 ORAM E etic h geen oc NiO 6.69 oo — — — |— SeESUl phates tee NiSO, + 7H,0 1.98 99. Bi — — |— INTGRIChaCIdemer er ee HNO; Dys2 —42.. 4 86. 760 | 16 Pe eankydrides. «34: N20; 1.64 30. 5 48. 760 | 9 ee MOXIGE aa eee ‘ NO 1.27 | —167. — | -153. 760 | 6 Meh peroxider a. 4e- N20, 1.49 —9.6 | 8 21.6 | 760 | — Nitrous anhydride. .... N2O3 1.45 | —II1. 7 3.5 | 760 | — ee Gxideaet.eeee NO oa —102.4 8 —89.8 | 760 8 Phosphoric acid (ortho). H3PO,4 1.88 40 + | — — — |— Phosphorous acid...... H;PO3 1.65 De — — — |j— Phosphorus trichloride... PCl; reo || aeieie teh |) aM) 76. 760 | 19 ‘“* oxychloride . . POC]; 1.68 41.3) — 108. 760 | — “disulphide... . P3S¢ — 297. 12 — 760 | — “« pentasulphide PSs — 275. 13 522. 760 | — ‘* ~~ sesquisulphide P4S3 2.00 168: |/— 400. 760 | — “« trisulphide... P2S3 — 290 + | 14 490. 760 | 25 Potassium carbonate.. . K,CO; 252 909. — — = | = oa schiorate. 44% KCIO; 2.34 B57 15 — = > =) chromate «24: K.2CrO, 2.72 975. 17 — ane oF cyanide)... KCN T52) |) redahit. |) — — ett ie ‘perchlorate ... KCIO, Dae 610. 15 410.f | 760 | — » eMchloride <': 32: KCl 1.99 772. |— | 1500. 760 | — SaMMitrater: ..t47 KNO; 2.10 341. | — A@oqi} || || “acid phosphate KH,2PO, 2.34 96. 2 — rn ee ‘** acid sulphate. . KHSO, 2.35 2O5N dec ai ears Silver chloride......... AgCl 5.56 451. 15 — — |— ech Danitrateca.s+.:. ee: AgNO; 4.35 218. — dec. — | — = perchlorates... 2 .. AgClO, — 486. 18 — anal + “phosphate... --- Ag3PO, 6237 840. 15 — =. |= ‘* ~~ metaphosphate.. . AgPOs — 482. 15 — a SeeESulphateneee nee: AgeoSOg Baas 655 = | — "|| ro8ssh is) Sodium chloride. ...... NaCl 27 800. II 1490. 008) a Se ehydroxidesyse- NaOH 2a 318. 27 —_ — | = ~ eamitratess 45. NaNOsz 2.26 2050 OCs ieee | eae ra eechlorates=4 445 NaClO; 2.48 248. 28 t li & ee perchlorate= a. NaCloO, — } 482. 18 — == || == = acatbonates....- Na.CO; 2.48 852. = tT — | — PmcaTbonatensees NaeCO3 + 10H2O | 1.46 34. 3 — — | — “« phosphate. ....| NazHPO, + 12H2O | 1.54 38. | — = —= | — “« metaphosphate. NaPO; 2.48 617. 15 — — |— “pyrophosphate . Na4P207 2.45 970. 30 — = | = os phosphite...... (H,NaPO3)2 +5H2O — 42. 20 — 1; — | — a sulphate... .... NaeSOu 2.67 884. Il —— — |— eeeSUl phates Na,SO, + 10H2O | 1.46 32.38] 17 Sa = |= “« hyposulphite...| Na2S:0; + 5H2O 1.73 48.16] — t — |— Sulphur dioxide........ SO. — —76. — —I0. 760 | — Sulphunelacides mrs oer H.SO,4 1.83 10.4 I 338. 760 | 22 i AGIUEA Se tecaae 12H.SO,4 + H,O — —0.5 — = |= Bs ACIG4 a. cee H.SO,4 + H,0 ad 8. So Saad ame == e acid (pyro)... H2S20; 1.89 B5E 22 T = |= Sulphur trioxide....... 3 1.91 16.3 | — Aiatay || yfeXe) || —= Tin, stannic chloride. .. SnCh 2.28 —33. 23 TAs 760 | 19 «« stannous chloride. . SnCly — 250. 24 605. 760 | — Zinc chlovides seer ZnCle 2.91 3605. 29 710. fore) || = pachloridete ane eae ZnCl, + 3H20 —_ 6.5 { 26 — ee oe fo) omitrateten <4) /:.822 Zn(NO3)2 + 6H2O | 2.06 36.4 3 131 760 2 pe Sulphate joceer ZnSO, + 7H2O0 2-02 50. 3 = | References: (1) Mond, Langer, Quincke; (2) Ordway; (3) Tilden; (4) Erdmann; (5) R. Weber; (6) Olszewski; (7) Birhaus; (8) Ramsay; (9) Deville; (10) Wroblewski; (11) Day, Sosman, White; (12) Ramme; (13) Meyer; (14) Lemoine; (15) Carnelly; (16) Mitscherlich; (17) LeChatelier; (18) Carnelly, O’Shea; (19) Thorpe; (20) Amat; (21) Mendelejeff; (22) Marignac; (23) Besson; (24) Clarke, Const. of Nature; (25) Isambert; (26) Mylius; (27) Hevesy; (28) Retgers; (29) Griinauer; (30) Richards and others. * Under pressure 138 mm mercury. +t Decomposes. SMITHSONIAN TABLES. 256 TABLE 240 DENSITIES AND MELTING AND BOILING POINTS OF ORGANIC COMPOUNDS Authority or pres- sure for boiling Chemical Temp. Cc point if not 760 mm Melting Boiling formula i Substance point point Density (a) Paraffin Series: CnHony2. Normal compounds only Miethanes =. .2-1.. CH, —164 |0.415 ||—184 C3He¢ — 88 .546 ||—172.0 CsHs |— 44 | .595 ||—189.9 CH oO 6011 || —135.0 CsHi2 20 .631 CcoHis 20 .660 C7 Hie 20 -684 CsHig -707 CoH ale CoH» -747 Undecane Cy Hos -741 Dodecane CoH .768 iiridecaness neee Ci3Ho e757) Tetradecane CysH30 .765 Pentadecane CisH32 ie Hexadecane 16H 34 775 Heptadecane CizH36 778 Octadecane CisHs 777 Nonadecane Ci9H a0 Srlafal Eicosane CooH a2 .778 Heneicosane CorHas 775 : 215 Docosane Coo His .778 4 224.5 Tricosane Co3Hag -779 é 320.7 dietracosane wasn: CosH 50 -779 324 Pentacosane CosH 52 -779 284 Hexacosane CopHs4 -779 296 Heptacosane Co7Hs6 -779 270 Octacosane Cos He -779 318 Nonacosane CopHe0 .780 348 Triacontane C3oH ee .780 70 235 Hentriacontane....} Cs:Hes 781 302 Dotriacontane C32Hee ls 75 310 15 mm Tetratriacontane...| CssHzo 781 76.5 255 1.0 mm Pentatriacontane . . C35H 72 .782 74.7 331 15 mm Hexatriacontane... C3sH74 .782 76.5 265 1.0 mm ateste siege eleel (6) Olefines or the Ethylene Series: C,H2n. Normal compounds only Ethylene CoH, —102 .566 ||—169.4 |—103.8 Propylene C3He — 47 .609 ||—185.2 |— 47.0 Butylene C,Hs — 13.5] .635 Sieben Amylene. 3. 3240 2|) GsElis 20 651 ||—139 + 36.4 Hexylene CesHie oO 76 69 Wreden or Znatowicz Heptylene CrHis 20 703 96-99) Morgan or Schorlemmer Octylene CsHie 17 -722 123 MoOslinger Nonylene Co His 15 -754 149.9 Decylene CyoH oO -763 172 Undecylene CH» 20 iO 188 Dodecylene CypH 15 -762 , 96 15 mm Tridecylene Ci3H oO .845 232.7 Tetradecylene CyuH TTS 246 Pentadecylene H 814 247 Bernthsen Hexadecylene c .789 274 Octadecylene...... CisH 791 179 15 mm Eicosylene C 871 395 Beilstein Cerotene Cx7H Bernthsen Melene ec : 380 SMITHSONIAN TABLES TABLE 240 (continued) 267 DENSITIES AND MELTING AND BOILING POINTS OF ORGANIC COMPOUNDS Melting | Boiling | AURotoS voile. point point | point if not 760 mm Chemical Temp. Substance ve formula Density (c) Acetylene Series: C,H2n-». Normal compounds only Acetylene.........| CoHe —80 .613 ||— 81.8 |— 83.6 | Villard Allylene C;H, —13 .660 ||—104.7 |— 27.5 Ethylacetylene....| CyH¢ oO .668 ||—130 + 18.5 Propylacetylene. ..| CsHs oO .722 ||— 95 + 40 Butylacetylene....] CsHio —150 71.5 Amylacetylene....| C;Hie 103) .738 ||— 70 110.5 Hexylacetylene....] CsH,4 oO .770 125 Undecylidene 213 Bruylant Dodecylidene .810 105 Krafft, 15 mm aD wake Tetradecylidene. .. + 6.5} .806 |l+ 6.5 134 erate Hexadecylidene.... 20 .804 20 160 Octadecylidene.... 30 .802 30 184 (d) Monatomic alcohols: CpH2.4,;0H. Normal compounds only Methyl alcohol... .| CH;0H 20 -792 ||— 97.8 64.5 Ethyl alcohol C,H;OH 20 .789 ||—117.3 78.5 Propyl alcohol.....| Cs;H;OH 20 .804 ||—127 97.8 Butyl alcohol C,H,OH 20 810 ||— 89.8 TAL 7-77 Amyl alcohol......} CsH1OH 20 817 ||— 78.5 137.9 Hexyl alcohol C.eH:30H 20 .820 ||— 51.6 155.8 Heptyl alcohol... .| C7;H,;OH 22 817 ||— 34.6 175.8 Octyl alcohol......| CsH:;OH 20 .827 ||— 16.3 194 Nonyl alcohol CyHigOH 20 828 ||— 5 215 Decyl alcohol CyoH»OH 20 829 ||+ 7 22h Undecvl alcohol. . .| Ci;H230H 20 .833 ||+ 19 146 Dodecyl alcohol. ..} Ci2H2;0H 20 831 24 259 Tridecyl alcohol...) Ci3H2,OH 31 .822 30.5 156 Tetradecyl alcohol.} CisH290H 38 .824 38 167 Pentadecyl alcohol.| CisH;,0H 46 Cetyl alcohol Ci6H330H 79 798 49.3 344 Octadecyl alcohol. .| CigsH3,OH 59 812 58.5 210.5 (e) Alcoholic ethers: CyHon 420 Dimethyl ether... .| C2H sO 20 .6606 || —138 Diethyl ether CyHyoO 20 -714 ||—116.3 ; B=123'3 bs pt. Dipropyl ether. ...| CsHisO -747 ||—122 Di-n-butyl ether. ..} CsHigs0 .769 Di-sec-butyl ether.. oe -756 Di-iso-butyl ether. . i .762 Diamy] ether CioH 220 774 Di-iso-amyl ether. . a -783 Dihexyl ether Cy2H 260 Diheptyl ether... .| CisH300 815 Dioctyl ether CisH340 .820 (f) Ethyl ethers: C,Hon420 Ethyl-methyl C;Hs0 20 .697 + 7.9 ‘“ -propyl C5H120 20 732 ||I<_—79 61.4 -isopropyl.... oO -745 54 -n. butyl CsHi4O 20 SAGE QI.4 -iso-butyl.... = 20 -751 80 Wurtz -iso-amyl....| C;HisO 18 -764 II2 nN. hexyl CsH,30 -n. heptyl....| CyH2O 16 -790 : -n. octyl CioH20 17 -794 z Méslinger Where no reference is given the data were compiled from the International Critical Tables. SMITHSONIAN TABLES 258 TABLE 240 (concluded) DENSITIES AND MELTING AND BOILING POINTS OF ORGANIC COMPOUNDS (g) MiscELLANEOUS Density and Melting Boiling Substance Chemical formula. temperature. Sonu ointte Authority. Acetic acid CH;COOH Acetone CH;COCH; Widehydes. ace C.H.O Aniline C.sH;NH>2 IBEESWAKE Sas ace Benzoic acid. .... Benzene CeHe Benzophenone.. . (CeHs)2CO Sauls 16.7 : Young, ’og .812 —94.6 iSOr . 806 —120. +20. .038 1 8! 183. .960) + 62. 293 E20 249. .879 5.48 80. Richards . 090 48. 305. Holborn- Henning HOH OH OOH Butter Camphor Carbolic acid.. .. C,H;OH Carbon bisulphide CS2 “ ~ tetrachlor- 86-7 30+ 99 176. 209. o60 43- 182. 292 —IIo. 46. HHOO CCL 582 —30. 76. Chlorbenzene... . C,H;Cl eaten —40. Chloroform CHC1; -4989 -63. 61. CoNo ae ie Ethyl bromide... C.H;Br 45 —II7. 38. 5 chlondes C.H;Cl g18 Ate C,Hi.O 736 —118. C2HsI 944 aa Formic acid..... HCOOH 242 8. Gasolene 68 + — Glucose CHO(HCOH),CH,OH 56 Glycerine C3HsO3 269 20. Iodoform CHI, or H Me oe PHHOR HAH OOH 29 Methyl chloride. . CH;Cl Methyl iodide... CH:;I Naphthalene .... CeHy- Cs 992 285 —64. : 152 80. - Holborn- Henning HNO Nitrobenzene .... Ce>H;02N Nitroglycerine.. . C3H;N309 Oliveros. Oxalic acid C,H20,: 2H2O Paraffin wax, soft. 350-390 is ‘¢ hard 390-430 Pyrogallol....... CeH;(OH)s; 293. Spermaceti Sc H OHH CeHio0; Sugar, cane CyoHo2On Steanines.- ..- 24. (CisH3502)3C3H5 Tallow, beef Seem uttonien santaniciaciduess: CyHeO¢ ‘Toluene C.>HsCHs3 C.H4(CHs3)> CcoHa(CHs)2 C.eH4(CHs3)2 Richards ©COO0OHOOOHHOH SMITHSONIAN TABLES TABLES 241-243 259 MELTING POINTS TABLE 241,.—Melting Point of Mixtures of Metals Melting-points, °C Metals. Percentage of metal in second column. Reference. 30% | 40% | 50% | 60% | 70% 262 240 220 190 185 = 179 145 126 168 880 917 760 600 480 590 620 650 705 775 400 370 330 290 250 925 945 95° 955 985 330 395 440° 49° 525 925 945 950 9792 1000 560 540 580 610 755 800 855 gI5 970° 1025 600 | 590 580 575 570 600 580 560 530 510 1145 1145 1220 1315 620 605 590 570 575 555 54° 520 47° 520 500 505 545 450 430 395 35° 540 57° 565 540 525 1235 1290 1305 1230 645 690 720 730 285 325 330 340 700 760 805 850 262 258 245 230 313 327 340 355 995 925 975 1000 1054 1049 1039 1025 1320 1380 1455 1530 5 11 26 4l - go 110 135 205 215 220 240 1320 1335 1380 1410 gio 870 830 788 725 680 630 580 goo 880 820 780 690 660 630 610 550 495 450 | 420 ae eee ” N 0 CON DNWO CON 60 22 55 1 Means, Landolt-Bornstein-Roth Tabellen. II Heycock and Neville, J. Chem. Soc. 71, 1897. 2 Friedrich-Leroux, Metal. 4, 1907. 12 ss Phil. Trans. 202A, 1, 1903. 3 Gwyer, Zs. Anorg. Ch. 57, 1908. 13 Kurnakow, Z. Anorg, Chem. 23, 439, 1900. 4 Means, L.-B.-R. Tabellen. a Fe 30, 86, 1902. 5 Roberts-Austen Chem. News, 87, 2, 1903. iM ve £s 30, 10g, 1902. 6 Shepherd J. ph. ch. 8, 1904. 78 Roland- Gosseli in, Bul. Soc. d’ 'Encour. Sere 1896. 7 Kapp, Diss., Konigsberg, rgor. 17 Gautier, (GS) 8 Fay and Gilson, ‘Trans. Am. Inst. Min. Eng. Nov. 18 Le Chatelier, Sen ase + (4) 10, 5735 190t. 1895 9 Heycock and Neville, Phil. Trans. 189A, 1897. 19 Reinders Z. Anorg. Chem. 25, 113, 1896. 10 ““ 194A, 201, 1900. 20 Erhard and Schertel, Jahrb. Berg-u. Hiittenw. Sachsen. 1879, 17. TABLE 242.—Melting Point of Alloys of Lead, Tin, and Bismuth Per cent. 10.7 50.0 35-8 20.0 | 70.9 2 f 23-1 33-0 52.1 60.0 "| g.t Bismuth . Sikes i ‘ aya 33 66.2 17.0 12.1 20.0 | 20.0 | Solidification at 148° 161° 181° 182° | 234° Charpy, Soc. d’Encours, Paris, rgor. TABLE 243.—Melting Point of Low-melting-point Alloys Per cent. Cadmium . shing. Lead Bismuth i Solidification at Drewitz, Diss. Rostock, 1go2. All compiled from Landolt-Boérnstein-Meyerhoffer’s Physikalisch-chemische Tabellen, SMITHSONIAN TABLES. TABLE 244 MELTING POINT OF SOME REFRACTORY SUBSTANCES (Compiled by F. C. Kracek, Geophysical Laboratory, Carnegie Institution, 1930.) Symbols: m, melting point; r, reaction temperature, resulting in the break up of a compound into another and liquid; Compound BINARY SILICATES 2BaO.SiO» BaOmsiOiae sane ABaOsSiOs. .)... BaOZSiOw... 5-28 BeOlSiOos ane oe ACH OLSHOns cdot old GCAO LSIOse0... (CAOSOhasonosiope 2CdO.SiO» (ColOISHORe Ss Bc olbt KGO!SiOssee ee. K,0.2Si02 K,0.4Si02 icetowe seks LizO.SiO2 LiO.2Si0>2 2Mn0O.SiO, Min @2Si@snenr ee 2MgO.Si0> Mg0.SiO, 2Na20.SiO» Na,0.SiO, NazO.2SiO2 2EebOMSsiO weer rb @ SiO sae Ae 2SrO.SiO, 27 nO SiOss nee ZnO SiOsn mak DO SiGe sess) he | tre 2050 + 10 1240 1923 ==310 2400 + 50 2572 +10 1692 I4i9 1560 1540 1900 + 20 27 30)==)20 1475 +5 1540 +2 2420-12 1242 +2 976 1036 = 1 765 40.5 1256+5 I20I +2 103245 1323 1273.-=15 1890 + 20 1557 +2 1120+ 5 1088 + 2 875 41 746 + 10 766 + 10 ASS 1580 + 4 5 2r==e 5 1437 2550 + 50 Type Bess8a8 < » ° < ~ Q 353300 Susi Ses aes m m m m m ie m Tj m m m m m m r m fy r m m r r m m m m m m m r? m Ref. 21 II th 21 40 Compound BINARY ALUMINATES 3Ca0.Al,O; 5CaO0.3Al03...... CaO.Al-O3. elena iLOLALOy. see MgO.AI.03 Na2O.AI.03 ALUMINO- SILICATES BaO.Al.03.2SiO». ab 2CaO.AI203.SiO». . : CaO.Al.03.2Si0Ox. . ; K20.A1203.2SiO». . . K20.A1203.4Si0Os. 35 K.0.A]203.6Si0Osz. . . LigO.Al203.2Si10>». . . iO. ALO.4siOl.., Na,O.AI.03.2Si0». E Na20.A1203.6Si0O». . SrO.AI,03.2Si0.2. one 2Si02.3Al,03 TERNARY CALCIUM SILICATES BaO.2CaO.3Si0Oz. . K,0.CaO.SiO2.. .. 2K,0.Ca0O.3SiOs.. . 4K20.CaO.10Si0... 2K2,0.CaO.6S10... . K,O.2Ca0.6SiO».. . K,0.2CaO.9SiO>. . : MgO.CaO.SiOz.... MgO.2CaO.2SiO. . 2Mg0.5Ca0.6Si0O». MgO.CaO.2SiO... . 2Na20.Ca0.3SiOz... Na,0.2CaO.3SiOz».. Na2O.3CaO.6SiOn. . MISCEL- LANEOUS COMPOUNDS 2CaO.Fe,0; CaO.Fe.03. cheweel eY cfs 2CaO.B.O3 K,0.2Ti02 Na2O.Fe203.4Si0». 5 d, compound decomposes before melting with evolution of gas; vac, melting in vacuo. II00 +10 >1700 1810 +10 1320 +4 1oI0o+5 TOr§ = 5 946 +1 959 £1 EE Syst) 5 10o25+5 1498 + 5 TAS Sit 2 1365+ 5 139I +2 D4 = 5 1284+ 5 1047 1436 + 5 1216+5 1304 +5 2350 + 25 980 990 + 10 Type| Ref. ASBeHeSus sen Se Bape: HBxwrs tS ssa ea if is m m m r Author List (References may be located in Abstract Journals): (1), Bowen, 1913. (2) Bowen, tor4. (3) Bowen, Andersen, 1914. (4) Bowen, 1917. (5) Bowen, Greig, 1924. (6) Bowen, Schairer, 1929. (7) Bunting, 1926. (8) Cooper et al, 1909. (9) Day, Shepherd, Rankin, Wright, 1909-15. (10) Day, Sosman, Allen, 1911. (11) Eskola, 1922. (12) Ferguson, Merwin, 1919. (13) Ferguson, Buddington, 1920. (14) Friedrich, Sitting, 1925. (15) Goeke, 1o11. (16) Greig, 1927. (17) Jaeger, torr. (18) Jaeger, Simek, ror4. (19) Jaeger, van Klooster, 1914. (20) Jaeger, van Klooster, 1916. (21) Jaeger, van Klooster, 1919. (22) Kanolt, 1914. (23) Kracek, 1930. (24) Kracek, Bowen, Morey, 1929. (25) Matignon, 1925. (26) Morey, 1917. (27) Morey, Bowen, 1922. (28) Morey, Bowen, 1924. (29) Morey, Bowen, 1925. (30) Morey, Kracek, Bowen, 1930. (31) Niggli, 1916. (32) Rankin, Merwin, 1916. (33) Roberts, 1924. (34) Ruff et al, 1916. (35) Ruff et al, 1929. (36) Schumacher, 1926. (37) Slade, Higson, 1919. (38) Sosman, Merwin, 1016. (30) Tiede, Birnbrauer, 1914. (40) Washburn, Libman, 1920. SMITHSONIAN TABLES TABLE 245 261 ENANTISTROPIC INVERSIONS IN CRYSTALS (Arranged by F. C. Kracek, Geophysical Laboratory, Carnegie Institution, 1931.) Values are given, for the more important crystals, of the inversion temperature in °C, the heat of inversion in cal./g and the inversion volume change in cm*/g. No monotropic inversions have been included. hi, i inversion temperature on heating; m, metastable inversion temperature; e, estimated; g, gradual inversion (not to be confused w ‘ith slow retarded inversions). Inversion volume change cm3/g Inversion heat cal./g Reference =i Substance Phases eon Pressure atm. 158 98.5 tee 99.4 99.4 99.4 175 133 412 159.5 70 EE 275 red-black 267 red-yellow 170 : 704* 924 284 1149 811 & 982 Leis —35 diamond- 25 B graphite g 22s g — 252.7 g —II2 L-I Ss 48.5 115 II-III I-III I-II I-III II-III L-I-II L-II-III I-II-1V II-III-1V I-II I-III II-III © CON ANHRWWWW DN ase Ft aa ona a elisa mee nn _ FE OO re WO ONO GH OHA on cof ate 2 - O CH;COOH.. CH;CON Ho. (Acetamide) (CH3)2COF.. ae ONIN NT RD RWW WWW WWW WWW WWW WD * Third modification at room temperature. + Acetone. SMITHSONIAN TABLES 262 TABLE 245 (continued) ENANTISTROPIC INVERSIONS IN CRYSTALS Inversion volume | Refer- change ence cm$s/g Inversion heat cal./g Inversion Pressure °, Substance Phases eC naa CoCle I-II 6.93 0.0280 (Perchlor ethane) II-III : 2.63 -0097 : 40.7 -0599 C;H7NO, (Urethane) L-I 37.9 .0253 t 35-9 0355 L-Il 34.4 -0184 Tesla | 40.6 .0640 LU 2.07 .O102 1.64 -0092 E 6.12 -0456 II-III 5.50 .0482 I-III Spal -0574 : : .O105 CsHe (Benzene) I-II 7.73(e) .0132(e) LI 2 30.2 3T7 33-25(e) .0369(e) L-II 25:5(€) pcre) C.HsOH (Phenol) L-I o18 hope . ea 30 -0825 I-II ae nee 33: .083 CH3CsH,OH (0.Cresol) L-I 34.2 .0317 L-II : 35 0555 I-II 8 .0238 I-II E 25 .00187 I-II 9.38 NNNNNN NNN NN I-II high CO; > = i: Jess 1190 + 10 Bee Casion” sae 2CaO.SiOz ae 1420, 675 ae soee) LO%, 675 Co Curie point ~ 1100 Be tar Te eae -II IOI5 II-III 400 CoO Ape 350 + 10 CoOH Scare 223 CsCl Pte 460 CsClO, ore 219 CsoSO4 ars 2 660 CsNO3; Pee 153-5 Cs,Ca2(SOx)3 Syevohe 722 CuoBre I-IT-III 390, 470 Curl I-I]-III 402, 440 II-III 200 II-III 100 CueS ee gI CuzSe ee TIO CurTe cae 351, 387 Fe Curie point 730 B-y 920 7-6 1400 Fe;0, Curie point 570+ FeO; II-III —163 to —148 I-II 500+ FeS ica 140 FeS, pyrite, marcasite SH * Five other modifications; not accurately located. + Cyclo-hexanol. § Very beautiful for demonstration purposes. SMITHSONIAN TABLES TABLE 245 (continued) 263 ENANTISTROPIC INVERSIONS IN CRYSTALS ——<$<—<—<—<<$<—<—<—<——_—<————— $<‘ —_— Inversion volume | Refer- change ence em3/g Inversion heat cal./g Inversion Pressure EC atm. Substance Phases 80 440 pane 215 eat ae Bis hs red-yellow 127.5 tee Tes 0.00342 gre ee Aisle Sees 524 bar cinnabDar \metacinnabar 386+ ruby-brown ard: aye aay. Stee 248 eR sks 27k I-II 255 Cisse II-III P = 5500 a 10. ot do, = 0.02510 — 2.2 X 10" Ahz = 0.165 at 0° 0.281 at 200° 3 mae 295 = : Tent Bae 4 765 00095 = 146.4 i! ecise B LIl ae 7 I : .00484 128 81 : -0049 I-III 128 81 ; .0138 128 81 : -0089 II-III 21.3 2840 : -O156 III-IV 2108 2840 : .0284 II-IV 21.3 2840 : .0440 588 rae sj ate L-Il 180.5 I ; -00066 198.6 1773 ‘ -00197 164.2 I : -00566 IT-1T 118.2 2810 ‘ .00570 198.6 1773 : -OO113 II-IV {118.2 2810 .I34 .OOII0 I-IV 198.6 1773 ; -00310 III-IV 118.2 2810 : .00680 KPO; ae 450 fi tee f Ae K,P207 eiaers 278 K,CO; Beate 410 Stee Ses Ce KCNS ae 143 : -00306 K.CdlI4 ewe 215 K,CrO, 50690 666 KeyCr,0; Shas 243 K,MoO, Scohte 327, 454, 477 K,WO, eet? 388 575 K»Ca2(SOx)s or. 937 KoSr(SOx4)3 oie 775 KLiSO, Poe 435 KNO, { me KO (SiO»)> Eyer 290 2K,0(Al.03) (SiO»)4* eit 714 LiClO; yt 41.5, 99 LipSO, Sos 580 (MgO)«(B203)sMgCl aioe 266 MgO.SiO2t ses ae Mn cals: 742, II9QI MnSO, eet ie 860 MnO, Ns —185 to —175 MnO Beh —153 to —163 N> Bagen — 237.6 NH,Cl i — 30.5(g) 184.3 *Leucite. + Probably pentamorphic, inv. at 1150 and 1300°. SMITHSONIAN TABLES 264 Substance NH,Br NHagl NH,C10, NH,HSO, (N H4)3H (SO,)2 NH,CNS NH,NO; NaOH NaClO, NaClO; NasSO, NaF.Na2SO, NasCO;3 NaNO; NasAlF es NasMoO, Na2sWO, NaAISiO, NaC.H;0.* Ni Ni3Se NisAse Oxygen Phosphorus PbO PbSO, PbCrO, PbWO, RbOH RbC1O, Rb2SOg RboCay (SOx) RbLiSO, TABLE 2455 (continued) ENANTISTROPIC INVERSIONS IN CRYSTALS Inversion : Inversion Inversion Pressure © volume Phases 1°C ere —38 (g) ; fee Bae 137.8 ; 0.0647 —42.5(g) ‘ SE hice eaheve —17.6 4.80 -0561 bi Sua 240 sie Seda I-II-III 126.2 II-ITI-IV 176.9 er 134 I-I] 120 a rags sr oe II-III S77. 10.36 .0409 L-I 169.5 LO OST LI oe 12.9 01351 186.7 12.6 -00475 I-VI 186.7 1233) .00855 169.2 227 .00309 II-VI 186.7 aaa .00380 84 4 .00758 IT-IT 63.3 2.48 .00925 “Tv 32 4.67 .02026 TH-IV 63.3 4.03 .02135 II-IV 63.3 6.51 .OI210 169.2 11.84 .01267 IV-VI 169.2 r250 .00958 IV-V —18 1.6 .O17 aici 300 Bee Ake, 308 Si Suede ee 248 oan Saveht spate IV-III 185 ate 8.6 ,-0034 III-I 241 ees 15.5 .0070 eee 105 fA 4 sere vee 430 rat einen) Mt aca 275(g) Jone (GhekA) (Geos) 68 su S3 59 sae Hie 424, 585, 623 Sea I-IT 588 wd ee RAs I-III 586m Seas 4.4 III-II m See 29.2 neph.—carn. 1250 \Ae,3 Ae eas carnegicite 226, 650-690 snek cal a Sess 198 Curie pt. 355 see 545 38 ei 970 I-IT II-III L-I I-II red-yellow * Acetate. t+ Sluggish. SMITHSONIAN TABLES ENANTISTROPIC INVERSIONS IN CRYSTALS TABLE 2455 (concluded) 265 Substance RbNO3; RbCl RbBr RbI Sulphur Sb Sb.O3 SbCl; Si02* SiO.t SiO.§ Phases Inversion heat cal./g Pressure atm. Inversion Xe I-II II-III I-II L-I-II expl.-common rhomb.-reg. I-II-III I-II I-II I-II II-III 219 164.4 218.6 50 50 50 95-5 155 7.12 5:93 570 65, 69.5 573 215 150h 1o4gh Inversion volume change cm3/g 0.00688 -00434 Refer- ence SiO. *_§ 870 *_f 1250 §—t 1470 Sn Sera 161 eel 18 SnO, Bae 430; 540 SrSO, ores 1152 SrCO3; 925 TICIOg 226 TII 173 TINO; 144.6 7 44 ey : nie 230 He 3+ pha Rutile, anatase, brookite, stability relations unknown —15 t 2400 175, 300 1020 ca 1000 small 00244, .00073 .O18 2.86 .89 I-IT II-III TI picrate Neneh wl TiO; TiBr, (1) Vorlander, 1923. (2)Reedy, 1921. (3) Bridgman, 1915. (4) Rinne, 1924. (5) Bellatti, 1889. (6) Nacken, 1907. (7) Bridgman, 1916. (8) Kendall, 1923. (9) Rushton, Daniels, 1926. (10) Borodorvski, 1906. (11) Guertler, 1903. (12) Yortisch, 1914. (13) Grahmann, 1013. (14) Boeke, 1913. (15) Lewis, Schumacher, 1929. (16) Roth, 1925. (17) G. N. Lewis, 1923. (18) Clusius, 1929. (19) Kelley, 1929. (20) Latimer, 1922. (21) Bridgman, 1914. (22) Tammann, 1903. (23) Wallerant, 1915. (24) Backstrom, 1921, 1925. (25) White, ror9. (26) Day, 1906. (27) Various. (28) Hendrichs, 1930. (29) Emmett-Schulz, 1930. (30) Hevesy, 1910. (31) Zemcuzny, Rambach, toro. (32) Miiller, 1910. (33) Tubandt, 1028. (34) Bellati, 1889. (35) Chicaschigé, 1907. (36) Baudisch-Welo, 1925. (37) Millar, 1928. (38) Rinne, Boeke, 1907. (39) Allen, 1912. (40) le Chatelier, 1909. (41) K6nigsberger, 1910. (42) Varet, 1896. (43) Stortenbeker, 1889. (44) Kracek, 1930. (45) Kracek, 1931. (46) Amadori, 1913. (47) Brand, 1912. (48) Hare, 1924. (49) Van Klooster, 1914. (50) Rinne, toro. (51) Kraus, Burgess, 1927. (52) Kroeker, 1802. (53) Allen, White, 1900. (54) Perrson, Ohmann, 10929. (55) Friedrichs, toro. (56) Eucken, 1924. Clusius, 1920. (57) Simon, 1927. (58) Vorlander, 1923. (59) Fischer, to11. (60) Vresnevsky. (61) Retgers. (62) Kracek, Gibson, 1929. (63) Roth, 1929. (64) Jaeger, Germs, 1921. (65) Bowen, Greig, 1925. (66) Friedrichs, 1914. (67) Friedrichs, 1907. (68) Hare, 1924. (69) Schwarz, 1892. (70) Bridgman, 1928. (71) Mondain, Monval, 1926. (72) Cohen, rors. (73) Fenwick, 1927. (74) Fenner, 1913. (75) White, 1900, 1919. (76) Wietzel, t921. (77) Werner, 1913. (78) Bronsted, 1913. (79) Gernez, 1904. (80) Cohen, 1920. (81) Baltz, Jelp, 1927. (82) Becker, 1928. (83) Saldan, 1930. (84) Bo6hm, 1925. * Quartz. f+ Cristobalite. + Zincblende and wurtzite. § Tridymite. SMITHSONIAN TABLES 266 TABLE 246 TRANSFORMATION AND MELTING TEMPERATURES OF LIME-ALUMINA- SILICA COMPOUNDS AND EUTECTIC MIXTURES The majority of these determinations are by G. A. Rankin. (Part unpublished.) | Substance. % CaO Al,O3 SiO, ‘Transformation. Temp. | | | CASTOR soe a c 48.2 = 51.8 Melting . . Bet haere. ee TEA0e 1e2ca LMCASOKR 9 go ¢ 48.2 — 51.8 @ toyB and reverse! . 20.) =). une) I | th (Gan Si@4u 4) to. |, 265: as BiG: Melting = pic =} Soh Mpoh as be chaedl ee Oe rtm | “« ats tllipaoee == 2. 5Y to) fab tinGl EWES 5 o 6 5 « 675 +5 | | “ ec cdlnose — BG. B to a and reverse 1420 2 i e@asSinOr iu 58.2 — 41.8 Dissociation into CagSiOg and liquid . . wriigy Iee| CasSiOrnea 73-6 — 26.4 Dissociation into " CagSiOg and | (Ca Oj mueae 1900 +5 | | CagAlgOg . 62:2 37:8 oa Dissociation into CaO and liquid TSS Sees b (GarAlgOi. == 47.8 52.2 — Melting oR GER. uses lates isc: Je | GatlOwe 35-4 64.6 = Melting.) reese od ion ee 1600 15 | CagAl1oO1g 24.8 75.2 os Melting Sl er teed Nina dee ee Eee 1720 10 | Al2SiO5 — 62.8 Byal Melting . «ieee - = « © + ||, §6167Eroy CaAlg pSigOan. oH lee2Os0 OL 43-3 MICS 5 oo yo oo 6 Oo |) Be) Gee Cas AlsSiO; sl) 40.8) 372 22.0 Melting PC eaten |G OOM? CagAleSiOg . . 50.9 30.9 18.2 Dissociation into CagSiO4+ CagAl2SiO; and liquid . .| 1335 +5 EUTECTICS. EUTECTICS. | Crystalline Phases. | % CaO Al,03; SiOz, eee | Crystalline Phases. | % CaO Al,O3; SiO, Tee Cet, 37: — 63 | 1436° Il CaaS: : = z DPE, 3C20,28i0, tf} ses — 455 | tassel Csi,” | oe Ae ile ee ‘ CagSi0O4 a oye Bee all CaAleSigOg | CaO, or 3?°5 205 =e CagAloSiO; 29.2 39. 31.8 | 1380 | AlgSiOs,SiOeg = wes 87. 1610 AlzO3 \ | AlpSiOs,Al,03 = Oi 36. | 1810 CagSiO, | CaAleSizg0g U sti fheae CaAlO4 AOS aA Sez, 6.8 | I | SiO, 20128 ¢| 105 195 70. | 1359 | | CaAleSig0g a “ QUINTUPLE POINTS. | Si0.,CaSiOg (| 232 14.8 (625 \/1T6s5 CagAlgSiO7z 5 I Casio, AQIS: REIT 420-71 ES ASN ete Aeon | euleo. IG:gi, F083) ae ALAM radi Clos (| 48.2 11.9 39.9 | 1335 CaAleSigOg t CagAloSiO7z AlzSi05,SiO2 98 19.8 (79-4 | 1345 CaaSiOs 48.3 42. 9.7 | 1380 a 6 CaMROR (ih S5s) meso wera eels? CaAl,SisOs / | Cag aor 378 52.9 9.3. | 1512 ae ( 15:6 36:56 “47.98 ersi2 | aArlg4 ; 29105 | CagAleSiOz CagAloOj1g Con aya. eh 9.3 | 1505 Cae BL.2n edd h ee 24 .oenaS a3filj0V18 203 CaAleSigO | CaAlpSiO, SOs ON as CagAl,SiO7z QUADRUPLE POINTS. CagSigO7 ATR een AL. 1310 | CaSiOg ; CagAleSiO CaO.2SiO | Casio, i 45:7 13.2 41.1 | 1316 3C20.SiOx. } SSNs 44.5 | 1475 The accuracy of the melting-points is 5 to 10 units. Geophysical Laboratory. See also Day and Sosman, Am. J. of Sc. xxxi, p. 341, 1911. SMITHSONIAN TABLES. is therefore the product of these two columns. TABLE 247 LOWERING OF FREEZING POINTS BY SALTS IN SOLUTION In the first column is given the number of gram-molecules (anhydrous) dissolved in 1000 grams of water; the second contains the molecular lowering of the freezing point ; the freezing point After the chemical formula is given the molecular weight, then a reference number. 267 Molecular Pb(NO;)., 331-0: 1, 2. 0.000 362 : .OO1 204 .002805 005570 -017 37 5015 Ba(NO,)., 261.5: 1. 0.000383 001259 .002681 005422 .008352 Cd(NO,),, 236.5: 3. 0.00298 .00689 -01997 04873 AgNOs,, 167.0: 4, 5. 0.1506 .5001 8645 1.749 2.953 3.856 0.0560 1401 3490 KNOs, to1.g: 6, 7. 0.0100 .0200 .0500 -100 200 .250 500 -750 1.000 NaNO, 85.09: 2, 6, 7 0.0100 .0250 -0500 -2000 .500 5015 1.000 1.0030 NH,NOs, 80.11: 6, 0.0100 0250 5 5 5 &. 5. 5 5 5 5 3 an 1 I Bt Be a 3. 3: 3. 3. 3. 3: 2 Ge Ga 9 GY Ge Ga Ga GW Go He Wm Cun VA CODOb WO’ mMonknnina one QD Doo Lowering. OrFnnNaA eww ° | Oo OHWhiUnH One COO He OFWnHWHL WwuwidOfpR LRH O nn ie. <. in OV OO g. mol. 1coo g H,O Molecular 0.0500 .1000 .2000 .500 1.000 LiNOsg, 69.07: 9. 0.0398 -1671 .4728 1.0164 me Noh pp RY GY Ge FAW WY Wo ww Oo bo | Alo(SO4)3, 342-4: 10. 0.0131 .0261 0543 .1086 217 CdSO,, 208.5: 1, rr. 0.000704 .00268 5 OLISI .03120 -1473 4129 -7501 1.253 YNQW HEPA MOWnO OO K,SO4, 174.4: 3, 5,6, 10, 12. ° 0.00200 00398 .00865 .0200 .0500 .1000 .200 -454 €uSO,, 159-7: 1, 4; 0.000286 .000843 002279 .006670 01463 -IOSI 2074 4043 De 8898 17 MgS0O,, 120.4: 1, 4, 11. 0.00067 5 002381 01263 .0580 2104 5-4 5:3 4.9 Lowering. WOumtn oO ° Go Ww 4-76 | 4.60 4.32 4.07 | 3-87 | 1.95 | 84 6 3.29 3.10 2.72 2.65 | 2.23 g. mol. 1000 g- H,O Molecular Lowering. | 0.4978 8112 15-33 BaCl.,, 208.3: 3,6, 13. 0.00200 .00498 .0100 .0200 04805 .100 .200 .500 586 -750 || CdCl, 183.3 0.00299 .00690 .0200 0541 0818 214 429 858 1.072 3) CuCl,, 134.5: 0.0350 -1337 -3380 7149 CoCl,, 129.9: 0.0276 1094 2369 -4399 538 CaCl,, 111.0: 0.0100 .05028 -1006 -5077 .946 2.432 | 3-469 3.829 0.0478 — | MgCly, 95.26: 6, r4. LiCl, 42.48: 9, 15. AIBr;,, 267.0: 9. g. mol. _ 1000 g. H,O Molecular Lowering. 0.0100 .0500 .1500 » 3000 .6099 5 KCl, 74.60: 9, 17-19. 0.02910 05845 pe 3139 476 12000) — 1.989 3.269 NaCl, 58.50: 3, 20, 0.00399 -O1000 202211 04949 -T081 2325 4293 -700 NH,Cl, 53-52: 6, 1 0.0100 -0200 .0350 - 1000 -2000 .4000 7000 of tb bw d&bhAAU Ui oe m= Go oO WW GW WW 5 WOW wu HWP Riu ON” WN N COsetiNnN oF ur Oo ON WY GW Qo HO Ur OV mOWOW O ° 0.00992 0455 09952 -2474 -5012 7939 BaBr,, 297.3: 0.100 -150 -200 -500 N ows > G2 Gs Gd Ga G2 Ga — = 0.0078 0559 Ts4° 2 || 4355 1.07 1.07 1971 tr Kahlenberg, J. Phys. Ch. 5, rgor. 12 Abegg, Z. Phys. Ch. 20, 1896. 13, Jones-Getman, Am, Ch. J. 27, rgo02. 14 Jones-Chambers, Am. Ch. J. 23, 1900 15 Loomis, Wied. Ann. 60, 1897. 16 Roozeboom, Z. Phys. Ch. 4, 1889. 17 Raoult, Z. Phys. Ch. 27, 1808. 18 Roloff, Z. Phys. Ch. 18, 1895. Hausrath, Ann. Phys. g, 1902. Leblanc-Noyes, Z. Phys. Ch. 6, 1890. Jones, Z. Phys. Ch. 11, 1893. Raoult, Z. Phys. Ch. 2, 1888. Arrhenius, Z. Phys. Ch. 2, 1888. Loomis, Wied. Ann. 57, 1896. 7 Jones, Am. Chem. J. 27, 1902. 8 Jones-Caldwell, Am. Chem. J. 25, 1901. c 9 Biltz, Z. Phys. Ch. 40, 1902. 19 Kistiakowsky, Z. Phys. Ch. 6, 1890. to Jones-Mackay, Am. Chem. J. 19, 1897. : 20 Loomis, Wied. Ann. 51, 1894. Compiled from Landolt-Bornstein-Meyerhoffer’s Physikalisch-chemische Tabellen. SMITHSONIAN TABLES. Il Aunt WN | 1000 g. H,O | Molecular | Lowering. TABLE 247 (continued) LOWERING OF FREEZING POINTS BY SALTS IN SOLUTION Molecular Lowering. __ g. mol 1000 g. H,O Molecular Lowering. Molecular Lowering. CdBr., 272.3: 3, 14. 0.00324 .007 18 .03627 -0719 p22 .220 .440 .800 | | CuBr., 223.5: 0.0242 .OS17 2255 6003 | CaBr., 200.0: 0.0875 . 1742 -3484 5226 | MgBr,, 184.28: 0.0517 103 .207 | 517 KBr, 119.1: 0.0305 .1850 6801 250 | .500 | Cdl., 366.1: 0.00210 .00626 .02062 .048 57 .1360 ° Wb POwotu UisIO WH COO ° Cuomo Chee \o w oO’ WO Gog inst oo NOow 35 5) 22- PRP oORS MN SWNT OM SAWwwWwMN OW ° KI, 166.0: 9, 2. 0.0651 2782 .6030 1.003 SrI., 341.3: 22 0.054 .108 216 +327 | NaOH, 40.06: 0.02002 05005 -IO01 oO GG) GaGa ° OU SI ° Muni inWw WN = RUN Kee HDWMKO \o KOH, 56.16: | CH,OH, 32.03: 1, 15, 23+ 0.00352 3.60° .00770 3-59 .02002 3-44 .05006 3-43 -1001 3-42 2003 3-424 230 3-50 465 3-57 24, 25- 0.0100 Hesse .0301 1.82 .2018 1.811 1.046 1.86 34 1.88 6.200 1.944 iz »H,OH, 46.04: I, 12, 17, 24-27 0.000402 1.67° 004993 1.67 -O100 1.81 02892 1.707 0705 : .1292 2024 5252 1.0891 1.760 3-901 7.91 VI.11 18.76 0.0173 .0778 K,CO,, 138.30: 6 0.0100 .0200 0500 .100 .200 Na.COs,, 106.10: 6. 0.0100 .0200 0500 1000 -2000 Na.SOg, 126.2: 28 0.1044 29507, -7080 Na,HPO,, 142.1: 0.01001 02003 .0 5008 .1002 4.93 4.71 4.54 4.39 Sere 4.93 4.64 4.42 4.17 | Na,SiO,, 122.5: 15 0.01052 505239 -1045 -2099 5233 HCl, 36.46: 1-3, 6, 0.00305 -00095 -O100 .01703 -0500 1025 -2000 +3000 -464 -516 1.003 1.032 1.500 2.000 2 eT 3-000 3:053 4.0065 4.657 | HNO,, 63.05: 0.02004 OSOI5 0510 1004 1059 2015 1250 .500 1.000 2,000 3.000 H;PO,, 66.0: 29. 0.1260 2542 5171 1.071 H3POsz, 82.0: 4, 5+ 0.0745 1241 2482 1.00 H;PO,, 98.0: 6. 22. 0.0100 .0200 .0500 .1000 2000 °o 6.4 5.86 | 5.28 4.66 3:99 Wa pls eee 68° fey) ON SHRPRPHHHWOROKQOHY YW MOL FON DAnUUU OV NN WR OWMO CaS OO 0 AND OOo Oo N OW 6.19 3) 13, 15- | Levulose, 180.1: | (COOH), 90.02: 4, 15. 0.01002 02005 .O5019 -1006 2022 366 .648 C;H;(OH)s;, 92.06 : 24, 25. 0.0200 1.56° -1008 186 -2031 1.85 535 I.O% 2.40 1.98 5-24 2513 (C,H5).0, 74.08: 24 0.0100 .0201 -IOIT .2038 Dextrose, 180.1: 0.0198 .0470 .1326 .4076 1.102 1.67 1.72 1.702 24, 30. 1.84° 1.85 1.87 1.894 1.921 24, 25 1.87° 1.871 2.01 0.0201 .2050 554 1.354 2.32 2.77 3:04 C,.H»201;, 342-2: 1, 24, 26. 0.000332 1.90° -OOI410 1.87 .009978 1.56 .0201 1.88 1305 1.88 H,SO,, 98.08 : 13, 20, 31-33. 0.00461 4.8° .O100 4.49 .0200 4.32 .O461 4.10 100 3-96 -200 3-85 -400 3.98 1.000 4.19 1.500 4.96 2.000 5.65 2.500 6.53 1-20 See page 217. 21 Sherrill, Z. Phys. Ch. 43, 1903. Chambers- Frazer, Am. Ch Noyes-Whitney, Z. Phys. Ch. 15, 1894. . J. 23, 1900. 24 Loomis, Z. Phys. Ch. 32, 1goo. SMITHSONIAN TABLES. Abegg, Z. Phys. Ch. 15, 1894. Nernst-Abegg, Z. Phys. Ch. 15, 1894. 27 Pictet-Altschul, Z. Phys. Ch. 16, 1895. 28 Barth, Z. Phys. Ch. 9, 1892. 29 Petersen, Z. Phys. Ch. 11, 1893. 30 Roth, Z. Phys. Ch. 43, 1903. 31 Wildermann, Z. Phys. Ch. 15, 1894. 32 Jones- Carroll, Am. Ch. J. 28, 1902. 33 Jones-Murray, Am. Ch. J. 30, 1903. TABLE 248 269 RISE OF BOILING POINT PRODUCED BY SALTS DISSOLVED IN WATER * This table gives the number of grams of the salt which, when dissolved in 100 grams of water, will raise the boil- ing point by the amount stated in the headings of the different columns. The pressure is supposed to be 76 centimeters. Salt dS ° " 5° 7° 10° 15° BaClg + 2H20 . CaCls . cae Os)2 2 2H:0 (71.6 gives 4°.5 rise of temp. 32.0) -41.5|" '55-5\|| .69:0 84.5 IO1.0| 152-5} 240.0] 331-5] 443-5 26.4] 34:5) 47-0} 57-5) 67.3 44.0 03:5, 98.0] 134.0] 171.5 tN Go NOM & OWMmun = _ RHO N OO -& SIO mG NAOROO NANO KC.H0, : INCIRe K2COg 7.4 gives a rise of 8°.5) Sasi P1O3+5)| 12755 | 5255 36.2) 48.4] (5 60.5] 7 | 99.5 . | 185.0 |(220 gives 18°.5) | 120.5] 188.5] 338.5 b ObUN Fey Oat On 00 Guin WwWNN DANAE vv ON OM) a) UmnW BO KeC.H,O, + 4H,0 KENaAGZHZOg |. KNaC4H4O¢ + 4H, O eiCliae : LiCl + 2H2O | 126.5 .O| 284.0 119.0 .O| 272.5] 390.0 266.0 .0 | 5510.0 20.0] 26. B5Ollaedeas 44.0] 62. 92.0] 123.0 nN =e DYN mum OWwodod Nee O™N Av G0 OnNon7O MgCly+6H20 . NaOH : : : : .4| 30-0; 41.0] 51.0 NaCl . : ; : : ; ; 1s ca .5 | (40.7 gives 8°.8 rise) NaNOg S 5 0} 99.5] 156.0| 222.0 NaCeH302 + 3H20 . k 194.0| 480.0 | 6250.0 NagS203SC«j , : : : ; : ; .0| 104.0] 152.0] 214.5 NagHPO, . ‘ : s : . ) ) NagC4H4Og¢ + 2H20. | 21. x 2) ORs 3.0 | (237-3 gives 8°.4 rice) NaeS203 + 5H20 ‘ : : ;. .3,| 216.0 | 400.0 | 1765.0 NagCOg -+- 10H2,0 . 309. s NapB4O7 + aka? : } .2 | 254.2 | 808. 5 gives 4°.5 rise) NH,Cl : 2 Sy aus : 3 |) SeuOl| Ger2|) Glebs NH4NOz . ; : .O | 20. : .O| 74.0| 108.0! 172.0 (NH4)2SO4 : : : : 4. : 8] 99.1 | (115.3 gives SrClp + 6H2O . ; : : : : 3.0 | 150.0 Sr(NOs)z ‘ ‘ é : Soe : : Y - 4 3 : .O | 123.0 H2O,4 + 2H,O : .0 | z 5 2.0 | 169.0 | CHO! + H,0 . | 29.0] 58.0 | s : .O | 208.0 TO .O| 170.0| 241.0 HOR Oy wood w mn & mn ° Cals - ‘ ‘ 2 .0 | 4. QE : : 5 : 8 | ; : 444.4 | 623.0 NaOH : : .3 | 800. .0| 2353-0] 6452.0] — NH,4NOs . : 1370.0 2400.0 CyHeOe¢ : : 37740, (infinity gives 3) * Compiled from a paper by Gerlach, ‘‘ Zeit. f. Anal. Chem.”’ vol. 26. SMITHSONIAN TABLES. 270 TABLE 249 FREEZING MIXTURES * Column 1 gives the name of the principal refrigerating substance, A the proportion of that substance, B the propor. tion of a second substance named in the column, C the proportion of a third substance, D the temperature of the substances before mixture, Z the temperature of the mixture, # the lowering of temperature, G the temperature when all snow is melted, when snow is used, and & the amount of heat absorbed in heat units (small calories when A isgrams). Temperatures are in Centigrade degrees, Substance. | NaCgH302 (cryst.) NH,Cl. F : NaNOs. : | NagS2O0s3 (cryst.) KI » On One CaCle (cryst.) NH4NO3 . (NH4)2SO4 . INTBIACH ‘ CaCle KNO3 . NaeSO4 NaNO3. : KoSOx4 . ‘ ‘ Snow 100 ~ NagC Qs (cryst.) ‘ a KNO3 CaCle ° NH,Cl . NH4NOg NaNOs. NaCl NNN & NEON UCONN Core NH,NO3-25 nN won on} ce 6 N H4Cl-25 rs 9 ° ww nw tN me ORO 00 oe oo No at sh wo oO + ‘oO Wink NW WOM Oo _ H2SO4+ H20 (66.1 T H2SO4) ee | CaCly + 6H20 “ 73 COgzg solid “é “c i Alcohol at 4° Chloroform Ether . Liquid SOs H20-.75 6 94 ac me * Compiled from the results of Cailletet and Colardeau, Hammerl, Hanamann, Moritz, Pfanndler, Rudorf, and Tollinger. + Lowest temperature obtained. SMITHSONIAN TABLES. TABLE 250 27K CRITICAL TEMPERATURES, PRESSURES, AND DENSITIES OF GASES Substance Acetylene Alcohol (C2H,O) Alcohol (CH,O) Allylene Benzene Bromine iso-Butane Carbon dioxide Carbon disulphide Carbon monoxide Chlorine Ether (ethyl) Ethyl chloride Ethylene Hydrogen Hydrogen bromide Hydrogen chloride Hydrogen iodide Hydrogen sulphide Nitric oxide Nitrogen Nitrous oxide Phosgene Propane Propylene Sulphur dioxide _ HO OOo (a) ‘Plait point.” (b) *‘Critical point of contact.” 1. Pickering, Bur. Standards Sci. Paper No. 541, 6. Ramsay and Young, Trans. Philos. Soc., London, 1926. 177, 123, 1887. 2. Lowry and Erickson, Journ. Amer. Chem. Soc., 7. Young, Journ. Chem. Soc., 590, 903, 1891. 49, 2720, 1927. 8. Ramsay and Young, Trans. Philos. Soc., London, 3. Mathias, Crommelin, and Watts, Compt. Rend., 178, 313, 1888. 185, 1240, 1927. 9. International Critical Tables, 3, 248, 1928. 4. Cardoso and Fiorentino, Journ. Chim. Phys., 23, 10. Ramsay and Young, Trans. Philos. Soc., London, 841, 1926. 178, 57, 1888. 7 5. Cardoso and Sorrentino, Journ. Chim. Phys., 24, 11. Young, Proc. Roy. Soc., Dublin, 12, 374, 1910. 77, 1927. (Table prepared by Gas Chemistry Section, Bur. Standards, Feb. 19, 1929.) SMITHSONIAN TABLES 272 TABLE 251 THERMAL CONDUCTIVITY, METALS AND ALLOYS The coefficient k is the quantity of heat in small calories which is transmitted per second through a plate one centimeter thick per square centimeter of its surface when the difference of tempera- ture between the two faces of the plate is one degree Centigrade. ‘he coetticient k is found to vary with the absolute temperature of the plate, and is expressed approximately by the equation ki = kot + a(t — to) ]. ko is the conductivity at to, the lower temperature of the bracketed pairs in the table, &; that at temperature ¢, and ais aconstant. k; in g-cal. per degree C per sec. across cm cube = 0.239 X k; in watts per degree C per sec. across cm cube. Substance Substance. ts Aluminum... .|—16o0/o. Mercury.... ojo. i 18|o. 7 eps 50}o. 1oo|o. : Molybdenum] 17J/o. 200|0. —I16o0]o. 40o|o. Se atoes 18]o. “ce , yellow.. ee RLeG es nas 500]|0. Cadmium,pure|—16olo. oc “ce “cc Constantan. Pe. (60 Cu+4o Ni) Copper,* pure. ce “ German silver. Tron,f pure... “ce “cc Iron, wrought. “cc ce 18|o. IOo|O. 2 18|o. Too]o. —I60|r. 18]o. Too|o. olo. T7Il0. 17/0.0: I7|O. 18]o. Ioo|o. —I6olo. 18]o. Too|o. 18lo. Too}o. ..|—I6olo. Magnesium... Manganin.... “* (84 CU+4 Ni 12 Mn) 18jo. Too|o. otol O°. 100§ —I60]o. 18lo. Too|o. Palladium... Platinum. ; . [ PiTooZulne Pt 10% Rh. Platinoid ... Potassium. . 5 Rhodium... Silver, pure.. Tungsten.... Tungsten.... ‘ j 2000 2400 ....| 2800 Wood’s alloy| — Zinc, pure. ..|—160 i sate 18 “cc “ce Ioo ce “cc -145 .192 .476 oo 090000 249 272 204 313 319 278 2653 \|_ 2610 | .00016 References: (1) Lees, Phil. Trans. 1908; (2) Jaeger and Diesselhorst, Wiss. Abh. Phys. Tech. Reich. 3, 1900; (3) Angell, Phys. Rev. 1911; (4) Lorenz; (5) Macchia, 1907; (6) Barratt, Pr. Phys. Soc. 1914; (7) H. F. Weber, 1879; (8) Hornbeck, Phys. Rev. 1913; (9) Worthing, Phys. Rev. 1914; (10) Worthing, Phys. Rev. 1917. * Copper: 100-197° C, kt = 1.043; 100-268°, 0.969; 100-370°, 0.931; I00-541°, 0.902 (Her- ing; for reference see next page). t Iron: 100-727° C, kt = 0.202; 100-g12°, 0.184; r100-1245°, 0.191 (Hering). SMITHSONIAN TABLES. TABLES 252 AND 253 273 TABLE 252.—Thermal Conductivity of Insulators at High Temperatures (See also Table 251 for metals; & in gram-calories per degree centigrade per second across a centimeter cube.) Tempera- Material. ture, G Material. Reference. Reference | Brick: Carborundum] 150-1200 | .0032-.027 Amorphous carbon... 37-163 .028-. 003 Building | 170-330 -027—.004 240-523 .020-.003 283-507 .OII—.004 100-360 -089 100-751 .124 100-842 -129 Graphite (artificial)...] 100-390 -338 100-546 +324 100-720 -300 100-914. . 291 30-2830 -162 2800-3 200 .002 QO-II0 -55--45 180-120 -44-.34 500-700 p3i—.22 ner ecattal I5-II00 | .co18—-.0038 Fire-clay....]| 125-1220 | .0032-.0054 Gas-retort...] Io0o-1125 | .0038 Graphite. ...] 300-700 .024 Magnesia....| 50-1130 | .0027—.0072 ili IO0-1000 | .002 —.0033 Granite 100 .0045—. 0050 200 .0043-.0097 500 . 0040 Limestone 40 .0046—.0057 100 .0039-.0049 350 . 003 2—. 0035 Porcelain (Sévres)..]| 165-1055 | .0039-.0047 Stoneware mixtures.| 70-1000 | .0029~-.0053 HHHHHNRNHNNNNKNHHHH WARDHA HARWOWWHW WW References: (1) Hansen, Tr. Am. Electrochem. Soc. 16, 329, 1909; (2) Hering, Tr. Am. Inst. Elect. Eng. 1910; (3) Bul. Soc. Encouragement, I11, 879, 1900; Electroch. and Met. Ind. 7, 383, 433, 1909; (4) Poole, Phil. Mag. 24, 45, 1912; see also Clement, Egy, Eng. Exp. Univers. Ill. Bull. 36, 1909; Dewey, Pro- gressive Age, 27, 772, 1909; Woolson, Eng. News, 58, 166, 1907, heat transmission by concretes; Richards, Met. and Chem. Eng. 11, 575, 1913. The ranges in values under 1 do not depend on variability in ma- terial but on possible errors in method; reduced from values expressed in other units. TABLE 253.—Thermal Conductivity of Various Substances Substance, temperature. kt Substance, temperature. Naphthalene MP 79° C, —160.. 0013 Naphthalene MP 79° C, o -Ooo8I Naphthol — 8, MP 122° C, —160..| .00068 Naphthol, o .00062 Nitrophenol, MP 114° C, —160....] .0o106 Nitrophenol, o .00065 Paraffin MP 54°C, —160 . 00062 Parafhin, o - 00059 Porcelain -0025 .0586 .O173 .0133 Quartz’ || to axis, o .0325 Rock salt, o .0167 Rock salt, 30 .O150 Rubber, vulcanized, . 00033 Rubber, o . 00037 Rubber, para . 00045 Sand, white, dry . 00093 Sandstone, dry .0055 . 00012 Slate | to cleavage .CO34 slate '|[itoicleavages.......-.--.-..|, 0060 Snow, fresh, dens. ; . 00026 Snow, old . OO12 Soil, average, sl’t moist .0037 Soil, very dry . 0037 Sulphur, rhombic, o . 00070 Vaseline, 20 .00022 Vulcanite . 00087 Aniline BP 183° C, -QOOII2 Carbon, gas..... -O10 Garbonttgraphite si... cares « «/='s'- -O12 Carborundum .00050 Concrete, cinder . 00081 .0022 Diatomaceous earth..............| .00013 Earth’s crust -004 Fire-brick.... .00028 Fluorite, —190 -093 Fluorite, o -025 Glass: window -0025 crown, 03572, —190 -oo118 crown, 03572, O .00280 crown, 03572, LOO .00324 h’vy flint o165, —190 . 0008 h’vy flint o165, o .OO170 h’vy flint o165, 100 .OO18r Glycerine, —160 .00077 Granite¢ .0053 .0006 .0050 Iceland spar, —190..............| .038 Iceland spar, o - 0103 .00029 Limestones, calcite | .0047 to Marbles, dolomite J .0056 Mica .0o18 Flagstone _|_ to cleavage . 0063 Micaceous || to cleavage -0044 ISN DAIL AOD UnnMnNUMnnnn | HHH HHA A ADIL ADRUMNHHOAHUMNANN [ane [RW Iw I IH © com | References: (1) Lees, Tr. R. S. 1905; (2) Lorenz; (3) Norton; (4) Hutton, Blard; (5) Eucken, Ann. d. Phys., 1911; (6) Herschel, Lebour, Dunn, B. A. Committee, 1879; (7) Jansson, 1904; (8) Melmer, rorr; (9) Stefan. SMITHSONIAN TABLES. 274. TABLE 254 THERMAL CONDUCTIVITY OF INSULATING MATERIALS (Compiled from the International Critical Tables, which see for more complete data.) Conductivity Material joule/cm?/sec. | g-cal./cm?/sec. Air, 76 cm Hg ‘ .00023 .000055 Asbestos wool : .00068 .000162 ‘i a .00090 .000215 .OOIOI .00024 with 85 percent MgO..|_ . .00075 .000179 Brick, very porous, dry 5 .OO174 .00042 ‘machine made, dry 3 .00038 -00009I ae “ce “ec ae -00096 -00023 Calorox, fluffy mineral matter...| . .00032 -000076 Celluloid, white : .00021 -000050 Cement mortar j -0055 -0013 -0092 .0022 Charcoal j .00055 .00013 Coke dust 5 .OO15 .00036 Concrete : -008 -002 -00032 -000076 -O00041 .000098 -OOO6I -0001 46 -00079 -0001 89 -00038 -OOO09I .00056 -000133 IIe 5 Pe OS : -00076 .00018 Cotton wool, tightly packed i .00042 .OOOTO Diatomite, (binders may increase 100%) : .00052 .OOOI2 Diatoinite, ditto ; .00094 .00022 _ a .00086 .00021 : .OO157 .0003,7 Ebonite , .00138 .00033 . .OO157 .00038 .00160 .00038 .00047 .OOOIT -00036 -000086 .00063 .OOOI51 .00052 .OOO1 24 Fuller’s earth ‘ -OOIOI .00024 Glass, lead .0060 .001 43, 2 .0072 .0O172 .0076 .00182 .00042 .0OOT00 .00050 .0001 20 -00065 -OOO155 .00081 -OO0O195 ; .0018 -00044 40 Sted RAPS PA : .0038 -00093 20 to 40 mesh : .O129 -0031 Horsehair, compressed ; .00051 .0001 22 .022 .0053 Leather, chamois .00063 .OOO1 51 i cowhide .00176 .000421 .OO16 .00038 .00086 -00021 Linoleum, cork 4 .00080 .OOOIQI Mica, average .0050 .OO12 ‘cc ae cc “eo ‘c ae 4c “e SMITHSONIAN TABLES TABLE 254 (continued) 275 THERMAL GONDUCTIVITY OF INSULATING MATERIALS Conductivity Material Density EE joule/cm2/sec. | g-cal./cm?2/sec. Micanite 30 .0021— .000050-— .0042 .0OOIO Mineral wool 3 .00042 .OOOTO sf a -00052 .OOOI2 Paper, rice .00046 -OOOTI ‘blotting .00063 .OOOT 5 Paraffin wax ‘ .0023 .00055 .00052 .OOO12 .OO17 .00041 Porcelain .O104 .0025 Rubber, rigid sponge, hard : .00037 .000088 5 sponge, vulcanized. . alone .00054 .00013 commercial, 40% rubber. .0028 .00067 < % -OO16 -00038 .00060 -0001 43 .0023 -0006 .00040 .OOOTO 00023 .000055 -00037 -000088 -000495 .00O118 -00056 -OO01 34 -0O16 .00038 -00080 -OOOTQI .00090 .00022 .00036 -000086 very loose packing...|_ . .00042 .OOOTO Woods: Ash | to grain : .OO17 00041 ae .0031 .00074 Balsa | to grain : .00045 .000084 Boxwood : .OOT5 .00036 Cedar | to grain ‘ .OOIT .00027 Cypress | to grain ‘ .00096 .00023 Fir | to grain 5 ¢ .OOT4 .00033 “|| to grain ; .0035 .0008 I Lignum vitae : .0025 .00060 .0030 .00072 Mahogany, ale tO GTAIN)..a1|\- .0O16 .00038 [ito grain | 7 0031 .00074 Oak, | to grain : 0021 .00050 +. |(to;grain 3 .0036 .00086 Pine, pitch, | to grain. . .OO15 .00036 “Virginia, ditto ‘ .OO14 .00033 ‘white, ditto : .OOII .00026 ca ; || to grain..} . .0026 .00062 Spruce, | to grain t .OOTT .00026 Teak, | to grain ; .OO175 .00042 - || to grain : .0038 .OOO9T Walnut, | to grain 3 -OO14 .00033 .020 .0048 .0092 .0022 : .022 .0053 Limestone, very variable.| 2. .O1O .0024 Slate, | to cleavage .O14 .0033 “|| to cleavage 025 .0060 Sandstone, air-dried : .O13 .00031 - freshly cut....] 2. .O17 .00041 “e ae 108 Running numbers arranged in order of increasing conductivity at room temperatures: .0002: 10, 1, 16, Onsen 775 71 03; 09, 30).55,.78; OL, 37, 31) 50) 72, 61; -00052 46, 24,56, 34, 60, 64, 13, 21, 67, 28. 33, 58s -00075: 5, 52, 26, 51, 3, 76, 84; .001: 35, 83, 97, 85, 94, 100, 14, 82, 93, 30, 50, 66, 74, 89, 61, 79, 6, 43, 08, 54, 91, 50, 68; .0025: 87, 65, 80, 90, 86, 44, 36, 92, 90, 54; .005: 53, 36, 37, 15, 12, 102; .010: 104, 45, 107, 108, IOI, 47, 103. SMITHSONIAN TABLES 276 TABLES 255 AND 256 TABLE 255.—Thermal Conductivity of Various Insulators kt is the heat in gram-calories flowing in 1 sec. through a plate 1 cm thick per sq. cm for 1°C drop in temperature. Substance. Density.| °C k, Substance. k, Authority. peas | Asbestos fiber 0.201 500 .00019 Asbestos paper 0.00043 Iecase@horle | 8207 magnesia asbestos Se eee .00016 Blotting paper. . -O0015 ‘an 5/0 mag Coe sae \ 500 .00017 Portland cement . 00071 : Cottonteii-n set) o- .021 100 -OOOIII Corky toga. .0007? Forbes. | east oc aP an Sis a= 101 ce .000071 Chalk . ane 0020 ! EG les De | Eiderdown .... .» -0021 150 -00015 Ebonite, t, 49° - .00037 see p. 205. es ou) Woy oy eect eon -109 sh -000046 Glass,mean .. -002 Various. : § 100 00007 4 COV Hepner +0057 Neumann. Lampblack, Cabot number 5 T93 | 1 soo -000107 Leather, cow-hide 00042 | | Quartz, mesh 200 ; 1.05 500 .0002 4 igi chamois . .00015 | Lees-Chorl- ee f 200 .00009I Linen . . -0002 1 imtol: | Poplox, popped Na,SiOs 0-093), || sco .000 160 Silk = a) «|, .000095))|)) | Wool fibers .O15 100 ooo 118 Caen stone, limestone | .0043 HeLa | re Ee .054 « .000085 Free stone, sandstone | .oo21 ead mage S “ .192 fy .000054 See eee eee eee ed Left-hand half of table from Randolph, Tr. Am. Electroch. Soc. XXI., p. 550, 1972; k, (Randolph’s values) is mean conductivity between given temperature and about 10°C. Note effect of compression (density). The following are from Barratt Proc. Phys. Soc., London, 27, 81, 1914. Nae ce k, ky Substance. Density. Substance. Density. at 20°C | at 100°C at 20°C | at 100°C Brick, fire . 1.73 .OOTLO .00109 Boxwood . 0.90 .00036 .00041 Carbon, gas 1.42 -0085 -0095 Greenheart 1.08 .OO112 -OO11O Ebonite 1.19 .OOO14 -00013 Lignumvite . 1.16 .00060 .00072 Fiber, red 1.29 -OOTI2 -OOT19 Mahogany 0.55 00051 -00060 Glass,soda . . 2.59 -00172 -00182 Oak. 0.65 .00058 -00061 Silica, fused. . 2.17 00237 -00255 Whitewood 0.58 .0004 I .00045 The following values are from unpublished data furnished by C. E. Skinner of the Westinghouse Co., Pitts- burgh, Penn. They give the mean conductivity in gram-calories per sec. per cm cube per °C when the mean I 10.6 temperature of the cube is that stated in the table. Resistance in thermal ohms (watts/inch2/inch/CC ) = conductivity. Conductivity. Grams. per cm’ 100° C 200° C 300° C 400° C 500° C Safe Substance. temp. Air-cell asbestos . 0.232 0.00034 0.00043 0.00050 — — 320 Cork, ground . -168 .O0015 .00019 _ _— — 180 Diatomit Ae RCy Ms 326 -00028 -00032 -00037 0.00042 0.00046 600 Infusorial earth, natural . . . +506 -0003 4 .00032 .00040 — -- ss ‘*h’d pressed blocks 321 -00030 .0002G .00033 .00036 _ 400 Magnesium carbonate . : -450 .00023 .00025 00025 a _ 300 Vitribestos. . . Ss .362 .00049 .00066 .00079 .00090 +O00102 600 °C Substance. k, Authority. Solution in water. Density. SE k, ° It 25 20 0.00150 -OO147 -00136 +001 43 SMITHSONIAN TABLES. Goldschmidt, ’11. Lees, ’98. Milner, Chattock 98 .160 -026 -178 +054 +180 +134 +136 0.00118 -OO116 ,OOTIS .00135 +00126 -00130 -o0118 -OO1I5 Authority. H. F. Weber. Graetz. H. F. Weber. Chree. } H. F. Weber. \ j TaBLEs 257-259 277 TABLE 257.— Thermal Conductivity of Organic Liquids Carbon disulphide.| o 5|.03472 Chloroform. .....}]9-15]. 0352 - 0346 - 03345 Aniline 03434 Benzene - 03333 ae Glycerine .03 Vaseline Oils: petroleum... 2 Xylene. “turpentine. . 03325 Hw 1LONKRH wWnwthp References: (r) H. F. Weber; (2) Lees; (3) Goldschmidt; (4) Wachsmuth; (5) Graetz. TABLE 258.—Thermal Conductivity of Gases The conductivity of gases, kt = }(ovY — 5)uCv, where y is the ratio of the specific heats, Cp/Cv, and p is the viscosity coefficient (Jeans, Dynamical Theory of Gases, 1916). Theoretically kt should be independent of the density and has been found to beso by Kundt and Warburg and others within a wide range of pressure below one atm. It increases with the temperature. kt : : 5. kt . 0000180 .0000566 . 0000719 . QCOOOT 42 .0000388 . 0000509 . 0000542 .0000219 . 0000332 .0000406 . 0000395 .000T 46 000344 000398 000133 . 000416 - 060499 . ©0007 20 .0000185 .0000183 0000568 0000718 0000172 0000570 0000743 000046 0000353 oo00000000 RHR Re RR ee 000000000 BHR HH RH DH 000000000 NOH HH RH HD References: (1) Eucken, Phys. Z. 12, 1911; (2) Winkelmann, 1875; (3) Schwarze, 1903; (4) Weber, 1017. * Air: ky = 5.22 (10-5) cal. cm ~! sec.-! deg. C-1; 5.74 at 229; temp. coef. = .oo2zg ; Hercus-Laby, Pr. R. Soc. Ags, 190, IgIQ- TABLE 259.—Diffusivities The diffusivity of a substance = fh? = k/cp, where k is the conductivity for heat, ¢ the specific heat and p the density (Kelvin). The values are mostly for room temperatures, about 18° C. Material. Diftusivity. Material. Diffusivity. archaea’ oralatetey Sepereiarahas, eaeeels .82 SPRL StaCaL Me Laer eCoTCHeTSI CI ee reve mists, Srel die ake IANLIMONY Bitton sion etovarto recto eee : lngyy. |i| (Caprese (Gielen s agnotoueoneouasobe Be eect pe kalsvanliatecssten weer oe POO Gall) oncreten(StOne) biascinciece emis scorer IBrASSaY ELlOW)h.: 0 erence ieicrs onisersisinee -339 Woncrete (lightislag) pea eee ole oe Gadmnimiy. Gaia an cea eens .467 Gorki(ground) Perec ieee cin SPR eerste arco vA Sin neers ae Fran | See pete feos re Rete cies RAS tee toe Eee Ft een ee .182 |) 1Glassi (ordinary) sour omin. Soecnme cn. Tron (wrought, also mild steel).......... e173; sal Granite seyerpe terry. toro cs tras sa ie task: Iron (cast, also 1% carbon steel)........ .121 Ce seieareter aero ais eee ate rule ees Re eee re mat denen cperet, india antacids . 237 EERE Te nea Sie Mets ca BN RSM Sei eee aioe ec . 883 abe rehsiaiavarcr asin acerae austere Be srcrronevaral Srocatclovetel Sroiea ete crs chats Wecane .0327 RAW ey evaytay eo cwvaie sicia) claverone coaches IPS ie Cia ea eVects SUR one ae Dies .152 Rock material (earth aver.)........... Re een oir alin .240 Rock material (crustal rocks).......... Byte NERO eet rhe 0.243 SandsStoncemmacen sees one eto: SPT ate nah Srakore ere Run thor aerials a7 SNOWACLECSHN Mice oe cisiatcie reais ana cam ts LIN ate Se eye eR arene up eo eaieaeaale ©. 497 Soil (clay or sand, slightly damp). .... . Pa sesh tates HO Siete cera euahe teks, Siar on elel Setehe .402 Soilil(verveary. es. eye ee a Gig utecilcjee See PE Nera el ede hehe ete cate terete ete hale .179 IWiailermp rere rer aantaelkeiaceaia wucicaphelete FASDEStOST LOOSE) sen aon oe iene on .0035 || Wood (pine, cross grain).............. Bricka(average dire) aciciewrcieccemiee arete .0074 Wood (pine with grain)............... Brick (average building)............... .0050 Taken from An Introduction to the Mathematical Theory of Heat Conduction, Ingersoll and Zobel, 1913. SMITHSONIAN TABLES. 278 TABLE 260 THERMAL CONDUCTIVITY—LIQUIDS, PRESSURE EFFECT (P. W. Bridgman, Proc. Amer. Acad., 59, 158, 1923.) Conduc- Conductivity relative to unity 0 kg/cm? as function of Liquid tivity at pressure in kg/cm? 0 kg/cm? 1000 2000 4000 6000 8000 10000 11000 12000 201 1.342 1.557 1.724 1.864 1.986 2.043 2.097 .212 1.365 1.601 1.785 1.939 2.072 2.133 2.191 .221 1.363 1.574 1.744 1.888 2.014 2.070 2.122 -233 1.400 1.650 1.845 2.007 2.152 2.217 2.278 .205 1.352 1.570 1.743 1.894 2.028 2.091 2.150 .230 1.399 1.638 1.812 1.962 2.093 2.154 2.211 .18I 1.307 1.495 1.648 1.780 1.900 1.955 2.008 .218 1.358 1.559 1.720 1.859 1.985 2.043 2.099 .184 1.320 1.524 1.686 1.828 1.955 2.013 2.069 .207 1.348 1.557 1.724 1.868 1.998 2.063 2.126 .305 1.509 1.800 2.009 2.177 2.322 2.388 2.451 313 1.518 1.814 2.043 2.231 2.394 2.469 2.537 184 1.315 I.5I1I 1.659 1.786 1.900 Freezes -I8I 1.325 1.554 1.738 1.891 2.024 2.083 2.137 .174 1.310 1.512 1.663 1.783 1.880 1.923 1.962 .208 1.366 1.607 1.789 1.935 2.054 2.107 2.154 .193 1.327 1.517 1.657 1.768 1.858 1.895 1.928 .230 1.390 1.609 1.772 1.907 2.022 2.073 2.121 .125 1.232 1.394 1.509 1.592 1.662 1.694 1.724 148 1.265 1.442 1.570 1.671 1.757 1.799 1.837 .058 I.113 1.210 1.293 1.366 1.428 1.456 Freezes .065 1.123 1.225 1.308 1.379 1.445 1.476 1.506 I I Methyl .000505 .000493 Ethyl .000430 .000416 Isopropyl .000367 .000363 Normal butyl .000400 .00039I Isoamyl .000354 -000348 .000329 .000322 .000429 .000403 Carbon .000382 bisulphide. . .000362 Ethyl .000286 bromide.... .000273 Ethyl .000265 .000261 Waters 5. .OO144 .00154 Molwoleers ee .000364. .000339 Normal .000322 pentane-..- -000307 Petroleum .000312 ethers .000302 Kerosene .000333 .159 1.286 1.470 1.604 1.716 (2%2025) .210 -355 1.573 1-738 1.872 1.987 2.039 2.089 .281 1.483 1.777 1.987 2.163 2.325 2.404 2.481 .319 1.534 1.855 2.112 2.335 2.543 2.642 2.740 266 1.460 1.752 1.970 2.143 2.279 2.333 2.379 .268 1.466 1.780 2.026 2.232 2.409 2.488 2.561 .185 1.314 1.502 1.654 1.792 1.925 I.990 2.054 OO OOO OO OO OO OO OR OO OO OR OO OO OO Oot I, 2, 6, 8, 12, 13, extreme purity; 3, 4, 5, 7, 9, 10, II, very pure; 14, 15, commercial. * Toluol freezes at 9900 kg/cm? at 30°. The figure at 11000 is for the solid. SMITHSONIAN TABLES TABLES 261-265 279 TABLE 261.—The Unit of Thermal Resistance—the Fourier The fourier is defined as that thermal resistance which will transfer heat energy at the rate of one joule per sec. (one watt) for each degree (centigrade) temperature difference between the terminal surfaces (equivalent roughly to a prism of Ag or Cu 4.cm long by 1 cm? cross section). (Harper, Journ. Wash. Acad. Sci., 18, 469, 1928.) TABLE 262.—Factors to Reduce Heat Flow in Fouriers for a cm’ to Other Units To watts/cm? cal./sec./cm? kilocal./hr./m? hp./ft.2 hp./ft.2 hp./ft.2 watts/in.? Gradient °C/cm °G/em Ream Cy ree itachi Ani aac /110) Multiples I 4.18 .O116 4.14 44 3.67 394 TABLE 263.—Conversion Factors Between Units of Current Density of Heat Flow. Quantity of Heat Energy Transferred Through Unit Area per Unit Time Joules/ sec. cm? Cal./sec. cm? |Kilocal./hr./m? Hp./ft.? Watt/in.? watts/cm? I watt /cm? 1 cal./sec. /cm? 5 5.211 1 kilocal./hr./m? .OOOI1 162 .0000278 .0001448 .0007497 1 hp. /ft.? .8027 -I9I9 I 5.178 I watt /in.? .I550 .03705 .1931 The calorie is taken as 4.183 absolute joules. TABLE 264.—Thermal Resistivities at 20°C Expressed in Fouriers for a Centimeter Cube Silveh sana ee ake 0.239 Water.. wes, 17.0 Rubber* (over Copperie. chet .258 Mica* ean to GOT ens. 700 Aluminum...... -49 laminations).. 200 Wood (Virginia Brass (30% Zn). 93 irebnick= a. sr 200 pine across MEONOE sete cs ae 1.6 [Firebrick 25°C rain) asco 710 sNickella si Aros Ter7) 10) 1K OOAC 45 Clo Papertic akc 1000 Steel (7% ©)s,... 2:1 Brick masonry*. 250 Asbestos* (wool) 1100 Constantan..... 4.4 Weather*. 35.05. 600 Corley ee Saas 2000 Mercury. ...... 12.0 Hydrogen. -.... 600 Cotton batting ice at o°G] -h...... 45 Hard rubber.... 610 (loose)y. <5... 2500 Glass sheen. 133 elim) eee ee O90 Wool (loose)... .2500 @Concrete*; , 54" 140 PANTS en ee ete gns Cia 3 4100 Carbon dioxide. .6700 * Substances marked with the asterisk vary widely in thermal conductivity according to composition. For limits of such variation, consult International Critical Tables, Vol. 2. The figure listed above for any such material represents the author’s estimate of the ‘‘best guess’’ for use in those cases where the composition of the material is not specified. In preparing this table, the author has consulted Vol. 2, I.C.T. and has courteously been furnished advance values for some other materials by the editors of I.C.T. For still other materials, grateful acknowledgment is made to the staff of the Bureau of Standards, for advice in selecting most probable values in the light of present information. TABLE 265.—Anti-Freezing Solutions (for automobile radiators, etc.) (From Bur. Standards Letter Circulars No. 29, 1925.) Per cent by vol. in water with freezing points and specific gravities. Per cent by vol Denatured alcohol (90% by vol.) * Wood alcohol tf Distilled glycerine§ (95% by vol.) Ethylene glycol§ (oso Dy Vole ones et * 90 % by vol. indicates quality of alcohol (180° proof); if 188 proof (that is containing only 6 % water) amount required will be about 4% less. + The vapor from wood alcohol is harmful, §Glycerine and ethylene glycol are practically nonvolatile and noncorrosive. SMITHSONIAN TABLES 280 TABLE 266 LINEAR EXPANSION OF THE ELEMENTS C is the true expansion coefficient at given temperature; R indicates reference to notes and authority, see page 282; M is the mean coefficient between given temperatures; where one temperature is given the true coefficient at that temperature is indicated; a and B are coefficients in formula /; = Jy) (1 + at + Bé); Jo is length at 0° centigrade (unless otherwise indicated, when if x is standard temp.,/; = J, (1 + a(t — tz) + B(t — tr)?); Jr is length at £°C. Element “cc Lead (99.9).... Magnesium.... Manganese Molybdenumf.. Nickele occ cc. Palladium Platinum Potassium Ruthenium.... Selenium Silicone een. vee Silver Steel, 36.4 Ni... Tantalumt Tellurium...... ahallinmiee a. Tungstent TALKS BO Ge ED * For references, see page 282. t Molybdenum, t300° to 2500° /: = /s00[1 + 5.00 X 10-8 (t — 300) Tantalum, 300° to 2800° lt = l30[1 + 6.60 X 10-6 (t — 300) range | M X ro! 100°| .235 .080 R || Temp. range} @ X 104] B X 108 a + 10.5 X 10-9 (¢ — 300)?] Worthing, 1926 + 5.2 X 10-10 (t — 300)2] Worthing, 1926 Tungsten, 300° to 2700° loge = ls00[1 + 4.44 X 10-6 (t — 300) + 4.5 X 10-10 (¢ — 300)2] Worthing, 1926 SMITHSONIAN TABLES TABLE 267 281 LINEAR EXPANSION OF MISCELLANEOUS SUBSTANCES The coefficient of cubical expansion may be taken as three times the linear coefficient. ¢ is the tempera- ture or range of temperature, C the coefficient of expansion, and A. page 282. Substance. 71.5 Cu+ 27.7 Zn + 0.3Sn+o0.5Pb... 71 Cu+ 29 Zn Bronze: 40 o-100 16.6-100 6 66 ba ee oe 16.6-350 oc 4 353 Cu + 9.7. Sn at 16.6-957 40 o-80 ts 0.2P Caoutchouc Constantan 4-29 Fluor spar: CaFe.... German silver Gold-platinum: o-100 Gold-copper: 2Au+1Cu. Glass: Tube.........e+-e. Jena ther- | roll mometer | normal nt eo sae $s “ ....|— 191 to+16 Gutta percha....... 20 NCGS akc. ceecce ce | ‘—20tO— Iceland spar: Parallel to axis Perpendicular to axis Lead-tin (solder) 2Pb + 1'Sh.c. se... Magnalium Manganin Marble..... o-80 “ Platinum-iridium TO Peal TLE. yercternisve Duralumin, .94 Al,...... 20-100°, Steel, .14 GC, 34.5 Ni. ..... 25-1007, Monel metal, 25-100°, ° ° °. . 1930 .1783-. 193 .1859 °. . 2116 .1782 .1713 .1708 .770 .1523 .842 .1950 . 1836 1552 .0833 .0828 .o891 .0897 0054 .0788 .o81 Substance. Platinum -silver: 1 Pt+ 2Ag Porcelain Quartz: 1906 Parallel toraxis:)... Perpend. to axis... Quartz glass 1844 “c “ -1737 Speculum metal. ... Topaz: Parallel to lesser horizontal axis.. . Parallel to greater horizontal axis... Parallel to vertical 7-0. 686 Tourmaline: Parallel to longi- tudinal axis Parallel to horizon- . 1523 Type metal Vulcanite Wedgwood ware... Wood: Parallel to fiber: .058 -424 -983 -51 . 2631 0544 . 2508 . 238 . 181 NIL .0662 - 3030 7707 .0884 .000023 -0000037 -OOOOI4 25-600", 25-600, Insulating materials, Souder-Hidnert, 1919: Bakelite, bleached, .... 20-60°, SelM OLs eter reretolaleters) voi 20-7 0, amestone, ..ceeeeee se 25-LO0-, SMITHSONIAN TABLES -000022 -000100 -000009 Marble, Porcelain, Hard rubber, .. the authority. For reference see OFOTO 1000-1400 o-80 —190 to + 16 o-80 —190 to + 16 16 to 500 16-1000 40 °° 0000000000 —160 o-100 900000000 Ab WO 0000000 Ca Hidnert, “ «000025 -0000136 .0o00016 10 — 16 x 1078 3— 11x 1078 .00008 ° 25-100°, 20-200", 20-60°, 282 TABLE 268 CUBICAL EXPANSION OF SOLIDS If v2 and wv: are the volumes at f2 and t; respectively, then v2 =v: (1 + CAt), C being the coefficient of cubical expansion and At the temperature interal. Where only a single tem- perature is stated C represents the true coefficient of cubical expansion at that temperature. The coefficient of cubical expansion may be taken as three times the linear coefficient. Substance. Antimony Beryl . Bismuth . Copper . Diamond Emerald . Galena o cat Glass, common tube. OG hard. a ne Jena, borosilicate 59 ILI ss pure silica . Gold . 3 Ice. Iron ead: Paratfin . Platinum : Porcelain, Berlin . Potassium chloride . ss nitrate & sulphate . Quartz omer Rock sait Rubber Silver . Sodium . Stearic acid. Sulphur, native Tin ahs Zinc Authority. Matthiessen Pfaff Matthiessen iT) Fizeau ee Pfaff Regnault Scheel Chappuis Matthiessen Brunner Dulong and Petit Matthiessen Russner Dulong and Petit Chappuis and Harker Playfair and Joule “sé “é “ee Tutton Pfaff Pulfrich Russner Matthiessen E. Hazen Kopp Matthiessen “cs References to Table 266, page 280: (1) Uffelmann, 1930. (2) Mean. (3a) Bridgman, 1924-5, parallel to axis. (3b) ditto, perpendicular to axis. (4a) Griineisen, paral. axis, hexag. (4b) ditto, perpendicular. (5) Fizeau. (6) Disch, 1921. (7) Tutton, 1809. (8) Dittenberger, 1902. (9) Uffelmann, 1930. (10) Grtineisen, 1910. (11) Miller, 1916. (12) Dewar, 1902. (13) Benoit, 1889. (14) Holborn, 1897. (15) Le Chatelier, 1899. (16) Holborn, Day, 1900. (17) Hidnert, Sweeney, 1930. (18) ditto, 1928. (19) Scheel, 1921. (20) Hidnert, Shad, 1919. (21) Scheel, 1907. (22) Hagen, 1883. (23) Valentiner, Wallot, 1915. (24) Dorsey, 1908. (25) Spring, 1881. (26) Matthiessen. (27) Worthing, 1917. (28) Hidnert, Sweeney, 1925. (29) Schulze, 1921. (30) Hidnert, 1931. References to Table 267, page 281: (1) Smeaton. (2) Various. (3) Fizeau. (4) Matthiessen. (5) Daniell. (6) Benoit. (7) Kohlrausch. (8) Pfaff. (9) Deluc. (10) Lavoisier and Laplace. (11) Pulfrich. (12) Schott. (13) Henning. (14) Russner. (15) Mean. (16) Stadthagen. (17) Frohlich. (18) Rodwell. (19) Braun. (20) Deville and Troost. (21) Scheel. (22) Mayer. (23) Glatzel. (24) Villari. (25) Kopp. (25) Randall. (27) Dorsey. Note: Crucibles of thorium oxide may be used for t<3000° C; magnesium oxide, <1800° C; beryllium oxide, <2000° C. Swanger, Caldwell, Bur. Standards, Journ. Res., 6, 1131, 1931, which see for further information about use of crucibles. SMITHSONIAN TABLES TABLE 269 283 CUBICAL EXPANSION OF LIQUIDS If VY, is the volume at o° then at ¢° the expansion formula is Vy; = V, (1 + af + Be + 7). The table gives values of a, 8 and y and of C, the true coefficient of cubical expansion, at 20° for some liquids and solutions. A¢ is the temperature range of the observation and A. the authority. Liquid. y 108 | | | Acetic acid | 1.0630 2 1.0876 | Acetone 1.3240 8 —0.87983 _ Alcohol: | Amyl 30 «| ~0.goo1 1.18458 Ethyl, 30% by vol. ye S— | 0.2928 —11.87 | 50% ai 0.7450 : 0.730 | 99.3% “ : 2 | sion - | 500 atmo. press. : | 0.866 - p~ 3000 se Fs | o 524 ma i Methyl Hae Pe De Be eerste 363 0.8741 MBenzenerrr., « oe fF - | 1.17626 2 0.80648 | Bromine. . Boh | 1.06218 . —0.30854 | Calcium chloride : 58% solution . . . 38-25 | 0.07878 4.2742 - 40.9% is Rey ee =24 | 0.42383 ' a Marton disulphide . . .}| —34- 1.13980 ; 1.91225 500 atmos. Bicssnse : 0.940 = - B000 ae“ : | 0.581 - = Carbon tetrachloride : | 1.18384 1.35135 Shioroform: |) ws. . |. | 1.10715 : 3 —1.74328 MeL CheIdhogncs es ors | wo te - 1.51324 | 2.35918 4.00512 'Glycerine . . oHeee es - | 0.4853 .48 = | _ Hydrochloric acid : foo 277 Solution «= = )- 0.4460 | Mercury . Se tee Be | 0.18182 | mOlveroiley © 5. | 0.6821 |Pentane. . sds 1.4646 Potassium chloride: Peeve SOWCIN & 5 5 C 2 0.2695 ehenoOl@ aces cia ee 7 | 0.8340 Petroleum : Density 0.8467. . . .| 24-12 0.8994 Sodium chloride : 20.6%, solution. . . . 2 0.3640 1.237 | Sodium sulphate : 247 solution: © =) i.) : - 0.3599 1.258 ' Sulphuric acid : TO:GY ;SOUPON = ss a5 0.2835 2.580 - iCOyeWA ot id oe poo ae 0.5758 | —0.432 - MRUKPEHtINE «<<. a> — 0.9003 1.9595 | —o.44998 MRNIALCYS iS Prey ies is —0.06427 8.5053 SOC SL IEE (ENEMIES Ww | | | | AUTHORITIES. Ama cat. Cai. 105, Pp. ll20);) 1Oo7- g. Marignac: Lieb. Ann., Supp. VIII, p. 335; . Thorpe: Proc. Roy. Soc. 24, p. 283; 1876. 1872. . Zander: Lieb. Ann. 225, p. 109; 1884. . Spring: Bull. Brux. (3) 3, p. 331; 1882. . Pierre: a. Lieb. Ann. 56, p. 139; 1845. . Pinette: Lieb. Ann. 243, p. 32; 1888. b. Lieb. Ann. 80, p. 125; 1851- . Frankenheim: Pogg. Ann. 72, p. 422; . Kopp: a. Lieb. Ann. 94, p. 257; 1855. 1847. b. Lieb. Ann. 93, p. 129; 1855. . Scheel: Wiss. Abh. Reichsanstalt, 4, p. 1; . Recknagel: Sitzber. bayr. Ak. p. 327, 2 1903. Abt.; 1866. 4. Thorpe and Jones: J. Chem. Soc. 63, | . Drecker: Wied. Ann. 34, p. 952; 1888. P- 273; 1893. . Emo: Ber. Chem. Ges. 16, 1857 ; 1883. SMITHSONIAN TABLES. TABLE 270 THERMAL EXPANSION OF GASES Pressures are given in centimeters of mercury. Coefficient at Constant Volume. Coefficient at Constant Pressure. Pressure Substance. ae Reference. Argon Carbon dioxide © 0°=20° o0°—40° 0°-100° o0°—20° * 0°-100° 0°-100° | Carbon monoxide . | Helium . | Hydrogen 16°-13 37° Se ~132° 12°-185° 0°-100° Nitrogen 13°-132° “ Nitrous oxide Sulph’r dioxide SO, 1 Meleander, Wied. Beibl. 14, 1890; Wied. Ann. 47, 1892. 2 Chappuis, Trav. Mem. Meas. 13, 1903. 3 Regnault, Ann. chim. phys. (3)5, 1842. 4 Keunen-Randall, Proc. R. Soc. 59, 1896. Bur. Intern. Wts. Carbon dioxide | | Nitrous oxide | Water- | 1 Atm. pressure. Coeffi- Pressure cient Substance. cm. Reference. 100. 76. 257. 100.1 100.0 200 Atm, AN) Gooy Soomme 76. 51.8 51.8 .3071 3693 -367 28 30600 222 -332 -295 .261 .242 3710 37128 37100 -37973 -37602 -37410 -37972 37703 1097 ‘6574 .3069 “S79 -3903 3980 .4187 .4189 .4071 3938 -3799 Ww “ of-100° Hydrogen 0°-100° “ “cc o0°—20° o°=40° 0°100° 0°-20° 0°—100° 0°—20° o0°—100° 0°-7.5° 64°-100° Carbon monoxide . Sulphur dioxide “ce ad 0°-119° o0°-141° o0°-162° 0°-200° 0°-247° vapor _ the following for the calculation of the ex- | constant pressure: Thomson has given, Encyc. Brit. “ Heat,” pansion, E, between o° and 100°C. Expansion is to be taken as the change of volume under .3062(1 — cea V /v), Hydrogen, & = ( ee 3662( ( ( Air, Oxygen, Nitrogen, £ = .3662 COs Le = .3662(1 — at V’/z is the ratio of the actual density of the gas at o° C to what it would have at o° C and E = .3662 5 Chappuis, Arch. sc. phys. (3), 18, 1892. 6 Baly-Ramsay, Phil. Mag. (5), 38, 1894. 7 Andrews, Proc. Roy. Soc. 24, 1876. 8 Meleander, Acta Soc. Fenn. 19, 1891. g Amagat, C. R. 111, 1890. 10 Hirn, Théorie méc. chaleur, 1862 , 1862. SMITHSONIAN TABLES, TABLE 271 285 SPECIFIC HEAT OF THE CHEMICAL ELEMENTS When one temperature is given the true specific heat is given, otherwise the mean specific heat between the given limits. See page 289 for references. Element : Element toc Aluminum....... 3 Carbon, graph... —183 — 66 II 85 896 Oo — et et C, diamond : 223 823 Cerium —253, —196 20, 100 Chlorine 0, 24 Chromium....... —150 OO Antimony* Arsenic yd HpRoNI Cobalt Barium Beryllium Bismuth * 2 2 3 4 I I 7 I 5 6 * 4 4 4 7 8 9 Oo I I I I * * xe Hee OV Xe *¥ ¥R A Caesium Calcium h Iodine Ioo 300 600 Carbon, graph.. —191,—79 7 OO SMITHSONIAN TABLES 286 TABLE 271 (continued) SPECIFIC HEAT OF THE CHEMICAL ELEMENTS iC Sp.ht. é Element tC Sp.ht. —256.2 0.00067 Molybdenum.... — 34.5 0.0561 —240.7 .00355 O -0589 —214.0 .0194 + 5.3 .0589 —172.6 .O512 +100 .0612 — 67.5 .0939 250 .0632 oO LOA saan Nickel —258 .0008 100 -II5 —247.9 .0024 500 -163 —201.2) 0303 760 -320 —150 .0660 1000 .162 — 100 .0817 100 27, — 50 .0940 700 -157 oO .1032 -162 100 -1146 -0448 500 .1270 -OOOOI 800 -1413 -00086 Osmiuni..-:..... _19,-08 40311 .0073 Palladium —180,+18 .0528 .0279 O .0538 -0283 100 .0564 .0289 500 -0653 -0297 900 .0717 .0320 1500 .0766 .0356 Phosphorus,yellow —136 .124 .0375 — 40 -165 .0370 =O) .189 3 (red)Re e136 -107 .600 -182 .96 -190 374 Platinum 6 .00123 .1767 af OO78) .2025 I nc O2 ar .2228 il O20 .2316 8 .0307 -257 .03162 -279 -0349 Sailer .0365 650,775 .284 .0381 Manganese....—188,—79 .0820 -0400 -I0QI .0319 S12 -0346 SSS 4.022 a2 Tele 8.045 .0979 STeAO .1072 sh gil -1143 ‘4.177 Mercury (s) .3 .00552 .200 .00620 .196 .00783 Rhenium .035 .O172 .058 .0255 Rubidium (s).... .0298 (ise .0324 Ruthenium .0337 Selenium .0338 -0335 .03 Molybdenum.... coe .0034 -0300 -0399 SMITHSONIAN TABLES TABLES 271 (concluded) AND 272 TABLE 271 (concluded).—Specific Heat of the Chemical Elements Element Silicon 0.029 .087 .126 .168 -181 18.0, 900.6 .210 —238 —150 —100 Silver .046 .050 -053 Sp.ht. .0146 I 5 7 Oo -0557 100 300 goo 20-900 20-1200 —256.1 — 238.5 a LOO:) 100 .060 .026 .108 +245 na -137 .220 .176 .18I I1I5, 160 15, 96 0, 52 —201.7 +380 900 1100 1400 —188,+18 15, 100 15, 200 monochin hantalun’ ssi - -035 .036 -043 -044 -047 .288 .0564 I .0685 .0650 .0880 .0205 .0483 .0487 Element Thorium Zc Sp.ht. —253,—196 0.0197 0, 100 .0276 —203.5 .0385 —186.7 .0422 —150 .0450 —100 .0483 — 50 -O512 O .0536 + 25 0548 100 -0577 1100 .0758 Titanium......—185,+20 .082 0,100 .1125 —247.I .0012 —218.4 .0098 —173.I .0205 pau Toee .0288 + 26.9 .0321 .0320 -0344 .0367 .0390 .0280 .1153 -095 .0071 -0573 .0740 Tungsten TABLE 272.—Formulae for True Specific Heats Element Antimony Bismuth Chromium Cobalt Copper Iron 0.0493 .0292 -1055 -1000 -O915 .1060 -0295 .2370 .1020 Lead Magnesium Nickel Platinum Silver Tin Zinc a. 4 — a a. a a ole — 0.000012 t -OOOOI2 ¢ -OOOIO f — -000067 ¢ -000024 f -000096 ¢ 00002 f -O00142 f — -.ooorr8 t — .00000617 # + 2.33 X 10%f .000008 ¢ -000052 ¢ -000044 f 0.00000015 ?? .oooooo! 2 -00000006 ?? Pt from Jaeger & Rosenbaum, 1928. Others recalculated by Dr. W. P. White (1931), mainly from Schiibel. SMITHSONIAN TABLES 288 TABLE 273 HEAT CAPACITIES, TRUE AND MEAN SPECIFIC HEATS, AND LATENT HEATS AT FUSION (SEE PP. 285-287) The following data are taken from a research and discussion entitled “‘ Die Temperatur- Warmeinhaltskurven der technisch wichtigen Metalle,” Wiist, Meuthen und Durrer, For- schungsarbeiten herausgegeben vom Verein Deutscher Ingenieure, Springer, Heft 204, 1918. (a) There follow the constants of the equation for the heat capacity: W=a-+ bt+ c?#’; for the mean specific heat: s==at* + b + ct; and for the true specific heat: s’ =b + act: also the latent heats at fusion. Much greater faith should be given to tables on pages 285 to 287. Tempera- é Tempera- Ele- ture - ture ment range. se O-I500 é ‘ .05725| 5.48]26.0 O-1500 .06162 : g61-1300 : -00710]28.30} — O-1500 .03325 ; o-1064 .O3171] 1.30/15.9 O-1500 .O3121 ‘ 1064-1300] 26.35/0.01420} 8.52] — G-220 .00829 8. O-1084] — |9.10070] 3.05]41.0 232-1000 , .07020 d 1084-1300] 130. 74/—.04150]65.6 | — 0-270 0.03141 ; ; ©-1070] — _ |0.12037/25.41] 36.6 270-1000 ; .03107 : 1130-1210] —7.41/0.17700] — |24.14* 0-321 £05550 : 1230-1250| 3.83|0.19800} — a 32I-1000 5 .00952 f i 0-320 — jo. 10950/52.40! 56.1 0-327 .03591 : ; 330-1451] 0©.41]/0.12931| 0.11 1.33" 327-1000 .07|/0.02920 I45I-1520] 50.21j0.13380] — o-419 .08777| 43. 48 23.0|| Co 0-950 — |o.o9119|40.77| 58.2 419-1000 : .13340|—16. 10} — IIOO-1478] 22.00/0.11043]14.57 14-7 70* 0-630 -O5179] 3.00/38.9 1478-1600] 57.72/0.14720| — 630-1000 : .05090| 2.96] — |] Fe 0-725 — |o0.10545|56.84/ 49.4 0-657 .22200| 38.57/94.0 785-919 | —1.63]0.1592 | — | 6. 56° 657—1000]102.39]0. 21870] 24.00! — QIg-1404] 18.31]0.14472] 0.05 6.67" 1405-1528|—77.18]0. 21416] — 1.94" 1528-1600] 70.03/0.15012| — * Allotropic heat of transformation: Mn, 1070-1130°; Ni, 320-330°; Co, g50-1100°; Fe, 725-785°; 919° 13 1404.5° + 0.5. (6) TRuE Sprectric HEATS Cu .0573]0. . 1008}o. .0583 10. IOI4|O. 12 0504 . 1020 .0605 . 1026 . 0616 . 1032 |0.0627 . 1038 .0638 . 1045 .0049 . 1051 .0060 . 1057 .0671 . 1063 .0637 . 1069 .0094 . 1028 .0750 . 1159 .0807 . 1291 I055|0.0912} — . T168]0.0993]0. 2372 1282/0. 1073/0. 2416 1396/0. 1154/0. 2460 T509|0.1235/0. 2504 1623]/0. 1316/0. 2548 1737|0. 1396/0. 2592 1850|0.1477|0. 2636 1592/0. 1558)0. 2680 1592/0. 1639/0. 2724 1448] — |o.2768 1448|0.1424/0. 2812 1448]0.1454/0. 2856 1449/0. 1483]0. 2900 1449|0. 1512/0. 2944 2142|0.1472]/0. 2988 _ 1500-1472 0000000000000 © 9000000000000 9909009000000000000 For more elaborate tables and for all the elements in upper table, see original reference. SMITHSONIAN TABLES. TABLE 274 289 ATOMIC HEATS (50°K.), SPECIFIC HEATS (50°K.), ATOMIC VOLUMES OF THE ELEMENTS The atomic and specific heats are due to Dewar, Pr. Roy. Soc. 809A, 168, 1913 Specific | Atomic . Specific | Atomic é 7 Specific Ele- Atomic || Ele- Atomic]| Ele- e eat heat volume ea heat Weerenes heat ment. —223°C. |—223°C. — 223°C. —223°C. Sn Sb I Te Cs Ba ea 0286 0240 03601 0288 0513 0350 0322 .0330 0095 0078 0099 O135 o160 0232 0235 0240 0218 O197 0138 O142 0229 0175 0208 0207 0245 0384 0258 .0361 0453 .O7II .0550 .0262 .OI4I .O10Q 0134 O190 0242 0308 1924 0137 0212 0137 0028 1519 0713 -O413 .0303 .0303 Oo. °. Oo. Oo. O°. Oo. °. ° ° ° OOnHwW OOOOH boise eon 2 bv 0774 0431 0546 0967 1280 o714 .0205 099900000090900000000 Coie ROOST etn HO Gow Ginores, Sonne WOE Somat Sls 999999090900090009000 QRAARAG HH HHERAR AWE Dw er eieeeuiaboaiy a exocceren evo aca nies 090000 * Graphite. { Diamond. t Fused. § Crystallized. {{ Impure. References to Table 271: * Values derived from formulae recalculated by Dr. W. P. White from Schiibel’s results. The Pt formula is from Jaeger and Rosenbaum. (1) Schimpff values interpolated by White. (2) Eastman, William Young, 1924. (3) Magnus, 1910. (4) Anderson, 1930. (5) Ewald, 1914. (6) Linnavuori, 1922. (7) Nordmeyer, Bernoulli, 1907-8. (8) Simon-Rubemann, 1927. (9) Humpidge, 1883. (10) Nilson, Pettersson, 1880. (11) Magnus and Danz, 1926. (12) Kosef, 1911. (13) Moisson, Gautier, 1896. (14) Suhrmann, Liide, 1924. (15) Andrews, 1848. (16) Lange, Simon, 1928. (17) Eckardt, Graefe, 1900. (18) Eastman, Rodebush. (19) Nernst, Lindemann, r1o11. (20) Magnus, Hodler, 1926. (21) Dewar, 1913. (22) Hirsch, 1912. (23) Kneitsch. (24) Schiibel, 1914. (25) Adler, 1903. (26) Eucken, Werth, 1930. (27) Richards, 1893. (28) Griffiths, 1894. (29) Clusius, Harteck, 1928. (30) Jaeger, Diesselhorst, 1900. (31) Bunsen, 1870. (32) Lange, 1924. (33) Estreicher, Straniewski, 1912. (34) Behn, 1900. (35) Kleinkhardt, 1927. (36) Hillebrand, 1876. (37) Keesom, 1927. (38) v. d. Eude. (39) Bidwell, 1925. (40) Laemmel, 1905. (41) Zulinski, 1928. (42) Simon, 1922, 1923. (43) Carpenter, Stoodley, 1930. (44) Simon, Zeidler, 1926. (45) Cooper, Langstroth, 1929. (46) Regnault, 1849, 1861. (47) White, 1918. (48) Dixon, Rodebush, 1927. (49) Noddeck, 1928. (50) Rengade, 1913. (51) Tammann. (52) Gronow. (53) Anderson, 1930. (54) Magnus, 1923. (55) Umino, 1926. (56) Mondain, Monval, 1926. (57) Dewar, 1905 (58) Wilgard, 1906. (59) Pirani, 1912. (60) Tilden, 1904. (61) Schmitz, 1903. (62) Wilson, 1883. (63) Rodebush, 1923. (64) Pionchon, 1886. (65) Zwikker, 1928. (66) Jaeger, Rosenbaum, 1930. (67) Bliimcke, 1885. (68) Mache, 1897. (69) Clusius, Harteck, 1928, References to Table 276: R, Regnault. L, Lorentz. T, Tomlinson. JD, Jaeger, Diessel- horst. M, Mazotto. S, Schtiz. P, Person. W, Wachsmuth. Z. Zouloff. HM, H. Meyer. B, Batelli. GT, Gee and Terry. RW, R. W. Weber. SMITHSONIAN TABLES 290 TABLES 275 AND 276 TABLE 275.—Specific Heat of Various Solids Temperature Specific | Authority sc heat See p. 289 Alloys: Bell metal 15-98 0.0858 Brass, red oO -08991 ‘* yellow oO .08831 80 Cu + 20 Sn 14-98 .0862 Constantan, 60 Cu, 4o Ni 18 .0977 “ ~ 100 -1018 German silver 0-100 .09464 Lipowitz alloy: 24.97 Pb + 10.13 Cd + 50.66 Bi + 14.24 Sn 5-50 -0345 Lipowitz alloy 100-150 .0426 Manganin: 84 Cu, 4 Ni, r2 Mn 18 .0973 “é “ec “e “eé I0O 4 1004 20-1300 27, -0356 0552 Wood's alloy: 25.85 Pb + 6.99 Cd + 52.43 Bi + 14.73 Sn 3 .0352 Wood's alloy: (fluid) .0426 Miscellaneous alloys: 17.5 Sb + 29.9 Bi + 18.7 Zn + 33.9 Sn .05657 37.1 Sb + 62.9 Pb .03880 39.9 Pb + 60.1 Bi .03165 63.8 Bi + 36.2 Sn .04001 46.9 Bi + 53.1 Sn -04504 3145 Glass, normal thermometer 16!! -1988 ‘French hard thermometer .1869 -I61 -117 -350 -434 -465 .487 481 10 .3768 5251 -6939 -622 a 7A EB 27, TABLE 276.—Specific Heat of Water and of Mercury Specific Heat of Water. Specific Heat of Mercury. Barnes- ||| Temper- Barnes- || Temper-| Specific Specific Regnault.|| ature,°C. ')Regnault.| | ature,°C.| Heat. Heat. ‘Temper- ature,°C. Barnes. | Rowland. I.0155 - 60 0.9904 0.03346 0.03277 1.0001 1.0004 65 1.0004 -03340 -03260 1.0050 1.0053 70 I.0015 -03335 -03262 1.0020 1.0023 80 1.0042 -03330 -03255 1.0000 1.0003 90 1.0070 -03325 -03248 0.9987 0.9990 100 I.OI1OI .03320 -03241 .9978 -9908I 120 1.0162 -03316 -0324 0973 .0976 I40 1.0223 .03312 +0322 9971 -9974 160 1.0285 -03308 -0320 -9971 9974 180 1.0348 -03300 .0319 -9973 -9976 200 I.0410 -03204 - -0977 -9980 220 1.0476 -03289 - 9982 9985 - - .03284 - Barnes’s results: Phil. Trans. (A) 199, 19023 Phys. Rev. 15, 19023 16, 1903. (H thermometer.) Bousfield, Phil. Trans. A 211, p. 199, 1911. Barnes-Kegnault’s as revised by Peabody ; Steam Tables. The mercury data from o° C to 80, Barnes-Cooke(H thermometer); from go® to 140, mean of Winklemann, Naccari and Milthaler (air thermometer); above 140°, mean of Naccari and Milthaler. SMITHSONIAN TABLES. TABLES 277-279 291 TABLE 277.—Specific Heat of Various Liquids Liquid. Temp.| Spec. | Au- Liquid. Temp.| Spec. | Au- ec heat. |thority. C. | heat. |thority. Alcohol, ethyl 2 - 5053 Ethyl ether R se a eA Galan Glycerine ; i 648 KOH + 30H20 .590 + I00 “ .601 NaOH + 50H:0 .514 tei ebaces .520 i NaCl + 10H.O 529 + 200 “* .340 | E Naphthalene, CioHs... .|& Sete tar cre -423 cs . Gelee ee ok .482 CaCle, sp. gr. I. . 764 - ONO means eel Shas 775 Oils: castor . 787 CltrONneee er tie 695 Olivetermac see sate 712 sesame a7 2I5 funpeneine eee ae .651 Retroleumbereneeeecee. .663 Sea water, sp. gr. 1.0043. .676 “ce ce oe “ce CuSo, + 50 H20 .848 Cae ie eeeees 7 5 200.5 .Q51 + 400 “ 975 Diphenylamine, “Swi ™I ty OOo onmnn rs dy uu AAO “ ce .464 | B ZnSO, + 50 H20... 482 | 200m o0000000000000000000000000 References: (A) Abbot; (B) Batelli; (E) Emo; (G) Griffiths; (DMG) Dickinson, Mueller, and George; (H—D) de Heen and Deruyts; (Ma) Marignac; (Pa) Pagliani; (R) Regnault; (Th) Thomsen; (W) Wachsmuth; (Z) Zouloff; (HW) H. F. Weber. TABLE 278.—Specific Heat of Liquid Ammonia under Saturation Conditions Expressed in Caloriesx) per Gram per Degree C. Osborne and van Dusen, Bul. Bureau of Standards, 1918. Ri a ies Sa a aa PER er rear Wel eee as HRS ae a Mee ee ety cane ctr Ce ache ee EN CURR ike Deen ceo aera rege Ae ce ee ene Bee Se ee Oe Oe OR Oe SS Se Se ee ae RS ee SS SO OOOO Ot TABLE 279.—Heat Content of Saturated Liquid Ammonia Heat content = H = € + pv, where € is the internal or intrinsic energy. Osborne and van Dusen, Bul. Bureau of Standards, 1018. Temperature. ..| —50° | —40° | —30°} —20° | —10°| 0° | +10° | +20° | +30° | +40° | +50° —5§3-8|/-—43.3}-32.6]/—21.8 acl alperse +22.4|-33.9/-45-51—57-4 SMITHSONIAN TABLES 292 Substance. Andalusite Anhydrite, CaSOy Apatite . Asbestos Augite . Barite, BaSO, Beryl Borax, Na2B Or fused Calcite, CaC : “ “ Cassiterite SnOg Chalcopyrite Corundum . Cryolite, AlpF¢. 6NaF Fluorite, CaF Galena, PbS. Garnet . ; : Hematite, Fe2O3 . Hornblende . Hypersthene Labradorite . Magnetite . Malachite, CuyC O4Ha0 Mica (Mg) ; it3 (K) Oligoclase Orthoclase . Pyrolusite, MnO... : Quartz, SiO ; 400-1200 | TABLES 280 AND 281 TABLE 280.—Specific Heat of Minerals and Rocks 0-100 0-100 15-99 20-98 20-98 10-98 eee 16-98 0-50 0-100 0-300 16-98 pecific Refer- Tempera- | Speci ture °C, Heat. | 0.1684 1753 ence. COM OI DAdNwwwn QuWwNwnN NUP HP HP Ree HPWOWNEH | 4 Regnault. Substance. Rock-salt Serpentine . Siderite Spinel . Talc Topaz . : W ollastonite x“ Zinc blende, ZnS . Zircon . : Rocks: Basalt, fine, black “ “ “ce 13-45 7 0-100 19-51 0-100 21-51 12-100 20-470 470-7 50 750-880 880-1190 Dolomite Gneiss “ 20-98 me Granite Kaolin Lava, Aetna 6s “ 12-100 20-98 23-100 31-776 25-100 15-100 0-100 20-98 Kilauea Limestone . Marble Quartz sand Sandstone . “cc 1 Lindner. 2 Oeberg. 3 Ulrich. 6 Kopp. 7 Joly. 8 Pionchon. 5 Tilden. 10 R. Weber. Tempera- ture °C, 17-213 | Compiled from Landolt-Bérnstein-Meyerhoffer’s Physikalisch-chemische Tabellen. TABLE 281.—Specific Heat of Silicates Silicate. Albite ReeeeOesSpan Amphibole, Mg. silicate glass Andesine | sf glass Anorthite 6 x glass Cristobalite Microcline “e glass | Pyroxene Quartz Silica glass Wollastonite . glass pseudo . “ Oo 100° | 500° | Mean specific heats. to goo° |. 1948 -1977 |. 2033 . 2040 .1925 . | -1934 . 1901 - [1883 . 1883 |. 1924 . 1939 .1871 '. 1919 . 2039 . | 1868 1845 .1852 |. 1844 . 2363 .2410 .2461 - 2474 |. 2330 . 2296 . 2305 |. 2426 .2314 |.2332 |.2262 . 2321 . 2484 - 2379 . 2302 . 2206 .2170 |. .2561 . 2640 3 Specific |Refer-| Heat. 0.219 -2586 1934 “194 -2092 | True eiceiic heats. 500° | 1000° 204 *0°-1100°3 SMITHSONIAN TABLES. t0°-1250°; Taken from White, Am. J. Sc. 47, 1, 1919. ence. APN OV WO OWUOUUONY D DAH AHW 11 Bartoli. 12 Morano. 9 Roberts-Austen, Riicker. TABLE 282 293 SPECIFIC HEAT OF GASES AND VAPORS Sp. ht. Range Mean | Range of constant ‘Authorit of ratio. oF temp. ° C pres- oe 19) sure. Substance. temp. ne .3468 | Wiedemann. .2377 | Regnault. 20 : Moody. A238 75 ra —79.3|1.405 | Koch, 1907. .2366 | Holborn and | —79.3|2.333 ** 200 atm 2429 | Austin. ° : Su DES” 20-800 2430 5 500 |r. Fiirstenau. 108-220 4534 | Regnault. 53 i Jaeger. ce = cael 10o |I. Stevens. 101-223 |o.4580 | Regnault. 100 He 23-100 5202 | Wiedemann. ° : Wiillner. 27-200 5350 i 100 i 20-90 1233 | Dittenberger.| o : Niemeyer. 34-115 2990 | Wiedemann. 20 : Pagliani. 35-180 3325 ? 60 e eee ee le LO 2nS 3754 | Regnault. : Stevens. Bromine 83-228 0555 HY : Strecker. Carbon dioxide, CO2...| —28- +7 1843 s Lummer and * f | MITs=T00 2025 - Pringsheim. ye errno 2169 a Moody, 1912. | monoxide, CO..| 23-99 2425 | Wiedemann. ; Willner. | cs “a 26-1098 2426 . ‘disulphide, CS2.| 86-190 1596 | Regnault. ' Beyme. Chlorine 16-343 1125 | Strecker. : Martini. Chloroform, CHCl... . 27-118 .1441 | Wiedemann. ; Beyme. sais} 28-189 1489 “ Stevens. Ether, CsHioO 69-22 4797 | Regnault. ’ Miiller. a Se 25-111 |o.4280 | Wiedemann. Low, 1894. = aad — : Mean, Jeans. 13-100 1940 | Strecker. : Strecker. | 22-214 1867 | Regnault. ce 3 28-+9 |3.3996 . Lummer and 12-198 |3.4090 + Pringsheim. 21-100 .4100 | Wiedemann. : Hartmann. 20-206 .2451 | Regnault. : Capstick. al od ; Ramsay, ’12. | Mercury — — ; Kundt and Warburg. Methane, CH, Regnault. Miiller. == Ramsay, 712 Regnault. : Cazin. Holborn and ; Masson. Austin. “ce 26-110 —30—--LO 0-200 20-440 20-630 oo0o0o000 0 “cer “ce ce OLONONON ONO) ONONONORO) OVMOKOVO TORO TOO OWwWwWw Od ° ce Nitric oxide, NO 1 ( Regnault. Nitrogen tetroxide, NOs. “ce “ “ee Berthelot and : Natanson. Olger. “ce “ec “cc Nitrous oxide, N.O.... “ “ a“ Regnault. : Wiillner. Wiedemann. s Leduc, ’98. Regnault. i Lummer and Holborn and Pringsheim. Austin. Regnault. 4A |I. Miiller. Thiesen. : Beyme. rs Jaeger. ae Makower. Xenon . Ramsay,’ 12. Sulphur dioxide, SO... Water vapor, H,O “ “ce DOOD TODO DODOHHOOON0D . SMITHSONIAN TABLES TABLE 283 LATENT HEAT OF FUSION The values indicated by * were chosen by Dr. W. P. White of the Carnegie Geophysical 294 Laboratory. Temp. Element 2¢ Al Sb Cal./g 657 630 —190 269 a 321 285 809 1600 1489 1083 1063 — 249 1528 327 93 39 6.64 12.8 16 12.8 3.8 78 70 64 49-3 15.9 14 49.3 6 * Via Dr. W. P. White. Temp. He 650 SOT 1450 —2I10 —219 58 39 217 960 98 II5 232 420 w 5, — * OV wm oro % bE FCO ty * wa 26.6 + Mean of several. (1) Eucken-Hauck, 1928. (2) Regnault. (3) Rengade, 1913. (4) Zalesinski, Zulinski, 1928. (5) Umino, 1926. (6) Thun. (7) White, 1921. (8) Monval. Compound BaCl, Cac KCl NaCl SrCly Cal./g 28 54 86 124 26 Ref. Plato, 1906 Compound Anorthite Albite Diopside Quartz Cristobalite Cal./g 104 48.5 100 50 305 Ref. Bowen, 1922 eé ae White Sosman Kracek, 1930 Substance Alloys: 30.5Pb + 69.5Sn 36.9Pb + 63.1Sn 63.7Pb + 36.3Sn 77.8Pb + 22.2Sn Britannia metal, gSn + 1Pb Rose's alloy, 24Pb + 27.3Sn + 48.7Bi 5 25.8Pb + 14.7Sn Wood's alloy ie 52.4Bi + Ae Ammonia Benzole oe ‘““ (from sea water) Naphthalene Potassium nitrate Phenol Paraffin Sodium “nitrate ‘* phosphate Spermaceti Wax (bees) 1 Total heat from o°C. C Composition Cal./g Authority PbSn, PbSn 3 PbSn Pb.Sn 3 CeHe HO “cc H20 + 3.53 of solids CioHs KNO; CsH,O Na NaNO; NasH PO,\ 12H.O 2 —8.7 79.8 333-5 25-3 52.40 97 305.8 36.1 43-9 61.8 17, 15-5 11.6 9-54 28.0! 6.85 8.40 108 30.6 79-63 79-59 54.0 35-62 48.9 24.93 35.10 31.7 64.87 66.8 36.98 42.3 7 7 Spring sa Ledebur Mazzotto “c Massol Mean Dickinson, Harper, Osborne? Smith? Pettersson Pickering Person Pettersson Batelli Joannis ae Batelli Mean 2 Bureau of Standards, 1013, in terms of 15° calorie. : $1903, based on electrical measurements, assuming mechanical equivalent = 4.187, and in terms of the value of the international volt in use after 1911. SMITHSONIAN TABLES TABLES 284 AND 285 TABLE 284.—Latent Heat of Vaporization of Elements Element tC Sb 755 A I atm. Ba, | 1537 Bi 920 Br 60+ Cd 778 (Ca 143.9 Ol — 63 Fl —188.2 He —271.3 He —253 Zn o + DN HD BH HW ND Element I Kr Pb Li Mg Hg N Or Sr xX Zn + Mean; (1) Tait, 1914. (2) Eucken, 1916. (3) Hartmann, Schneider, 1929. (4) Egerton, 1917. (5) Cady Hildebrand, 1930. (6) Dana, Onnes, 1925. (7) Favre, Silbermann (old). (8) Peters, Weil, 1930. (9) Alt, 1906. (10) Peters, Weil, 1930. TABLE 285.—Latent Heat of Vaporization of Liquids Substance Alcohol: Ethyl ac “é Methyl Aniline Benzene Carbon dioxide, solid “ae ae liquid “ee disulphide “e Chloroform Ether Ethyl bromide ‘chloride ‘« iodide Heptane Hexane Octane Pentane Sulphur dioxide Toluol Turpentine SMITHSONIAN TABLES Authority Wirtz Regnault “ie Wirtz Ramsay and Young Mean Wirtz Favre Cailletet and Mathias Mathias Wirtz Regnault Wirtz Regnault Wirtz Regnault Mean Young ae Cailletet and Mathias Mean Brix 296 TABLES 286-288 TABLE 286.—Latent and Total Heat of Vaporization, Formulae 7 = latent heat of vaporization at °C; H = total heat from fluid at o° to vapor at #?C. T° refers to Kelvin scale. Same units as preceding table. 0.5 + 0.36644! — 0.000516 —3° to 147° -23356f + 0.000553582 —3 147 ’ Acetone, C3H6O 4 3 30. .27287t + 0.00015717 —3 147 ° .24420f — 0.00013157 7 215 18. 485(31 — t) — 0.4707(31 — t)? 25 31 .o + 0.14601! — 0.0004123f —6 143 -5 + 0.16993t — o.ooror161f + 0.05342/3 —6 143 -5 — 0.06530 — 0.0010976f + 0.053423 —6 143 .o + 0.14625t — 0.0001722 163 ° ° Benzene CgHg.... Carbon dioxide Carbon bisulphide, CS2... . Carbon tetrachloride, CCl. .9 + 0.17867 -0009590% + 0.0537338 163 9 — 0.01931 .ooto05o0s5 + 0.0537338 163 .O + 0.1375! 159 .o + 0.14716 0.0000937/2 1590 .0 — 0.08510 0.0001444f 159 .O + 0.45000! — 0.0005556/ I2I 94.0 — 0.07g900f 0.0008514f 121 177000 — 2.57 (cal/g-atom) 68.85 — 0.2736T 131.75(36.4 — tl) — 0.928(36.4 — #)? 69.67 — 0. 2080T 128000 — 2.57 (cal/g-atom) 91.87 — 0.3842t — 0.0003 40/7 ° 217800 — 1.87 (cal/g-atom) — oO Chloroform, CHCl3........ Ether, CsHi00 Molybdenum Nitrogen, Ne Nitrous oxide, N20........ Oxygen, O2 Platinum Sulphur dioxide........... Tungsten Water, H20 20 638.9 +.0.3745(t — 100) — 0.00099(t — 100)? = 94.210(365 — #)31249 (See Table 290) MUMS POP AWssWssnesnoOnssn I0o R, Regnault; W, Winkelmann; C, Cailletet and Mathias; A, Alt.; D, Davis; H, Henning; L, Langmuir. TABLE 287.—Latent Heat of Vaporization of Ammonia CALORIES PER GRAM © COWWO HO COOH CO Co Don RAO aN Osborne and van Dusen, Bul. Bureau Standards, 14, p. 439, 1918. TABLE 288.—‘‘ Latent Heat of Pressure Variation’? of Liquid Ammonia When a fluid undergoes a change of pressure, there occurs a transformation of energy into heat or vice versa, which results in a change of temperature of the substance unless a like amount of heat is abstracted or added. This change expressed as the heat so transformed per unit change of pressure is the “latent heat of pressure variation.”’ It is ex- pressed below as Joules per gram per kg/cm?. Osborne and van Dusen, Joc. cil., p. 433, 1918. Temperature° C]| —44.1 39. : : 5 +26.5 +35.4 + 40.3 Latent heat.... .055 .O5 : : : —.123 —.140 —.150 SMITHSONIAN TABLES. TABLE 289 THERMAL PROPERTIES OF SATURATED WATER AND STEAM 2o7 (Osborne, Stimson, Fiock, Bur. Standards Journ. Res., 5, 411, 1930.) Accuracy: It is estimated that there is only one chance in 100 that the values given for H differ from the truth by as much as one part in 2000; it is equally unlikely that the values for L and H' are as much as 1.5 joules/g from the truth in the range of the experiments, 100°-270°C. Heat con- tent of Temperature, °C liquid, 1 Int. joules/g oO 42.02 83.83 . 125.59 167.34 209.11 .. 250.90 202.75 334-66 .. 376.65 . 418.75 460.97 . 503.36 545-93 588.71 631.75 675.06 718.66 a8 702572 ne OO7eL5 . 852.02 SMITHSONIAN TABLES Latent heat, L Int. joules/g 2494.02 2472.26 2450.17 2427.73 2404.90 2381.64 2357-91 2333-65 2308.32 2283.38 2257-24 2230.35 2202.65 2174.04 2144.44 2113.76 2081.89 2048.72 2014.10 1977-89 1939.93 1900.00 1857.89 1813.33 1766.02 1715-59 1661.60 1603.51 Heat con- tent of vapor, H' Int. joules/g 2494.02 2514.28 2534.00 2553-32 2572.24 2599.75 2608.81 2626.40 2643.48 2660.03 2675-99 2691.32 2706.01 2719.97 2733-15 2745-51 2756.95 2767.38 2776.82 2785.04 2791.95 2797-35 2801.13 2803.08 2802.99 2800.56 2795-47 2787.83 Entropy— of liquid d Int. joules/g°C Oo -I511 .2962 4363 -5719 -7032 .8305 9543 1.0746 1.1918 1.3064 1.4177 1.5268 1.6335 1.7381 1.8407 1.9416 2.0406 2.1384 2.2348 2.3299 2.4239 2.5169 2.6091 2.7007 2.7919 2.8828 2.9746 of vapor gpl Int. joules/g°C 9.132 8.884 8.656 8.446 8.253 8.074 7-999 7-756 AOL 3) 7.480 7-356 7.240 7.130 7.027 6.929 6.837 6.749 6.664. 6.584 6.506 6.430 6.357 6.285 6.213 6.143 6.072 6.000 5-927 298 TABLE 290 PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C Reprinted by permission of the author and publishers from ‘‘ Tables of the Properties of Steam,’’ Cecil H. Peabody, 8th edition, rewritten in 1909. Calorie used is heat required to raise 1 Kg. water from 15° to 16°C. B. T. U. is heat required to raise 1 pd. water from 62° to 63° F. Mechanical Equiv. of heat used, 778 ft. pds. or 427m. Kg. Specific heats, see Barnes-Regnault-Peabody results, p. 227. Heat of Liquid, q. heat required to raise 1 Kg. (1 Ib.) to corre- sponding temperature from 0° C. Heat of vaporization, r. heat required to vaporize 1 Kg. (1 lb.) at corresponding tem- perature to dry saturated vapor against corresponding pressure; see Henning, Ann. der Phys., 21, p. 849, 1906. Total Heat, H ena, see Davis, I'r. Am. Soc. Mech. Eng., 1908. Heat of the Heat of Heat Rauivaieae Vaporization. Titernal Wane Pressure. Liquid. Degrees Centigrade. Degrees Fahrenheit. Temperature | ‘Lemperature Mm of Kg Pds. ~ . - 2 : 5 : Mercury. per sq. cm | per sq. in. Calories. |B. T. U.|Calories.| B. T. U. |Calories.| B. T. U. p- p. ; q- q- ie r. p- p. 4.579 | 0.00623 | 0.0886 0.0 | 595-4 | 1071.7 | 565.3 | 1017.5 6.541 | .00889 1265 592.8 | 1067.1 | 562.2 | Io1l.9 9.205 | .01252 1780 590.2 | 1062.3 | 559.0 | 1006.2 12.779 | .01737 -2471 587-6 | 1057.6 | 555-9 | 1000.5 17.51 .02381 -3386 36.1 | 584.9 | 1052.8 | 552.7 | 994.8 23.69 03221 4581 582.3 | 1048.1 | 549.5 | 989.1 31.71 04311 .6132 . 579.0 | 1043-3 | 546.3 | 983.4 42.02 05713 8126 ‘ 576.9 | .1038.5 | 543-1 977-6 55-13 07495 1.0061 | 40. © | §74.2 | 1033-5 | 539-9 | 971.7 71.66 .09743 1.3858 $70.3) |) oz8-4..1 636.5) | NeOs.7. 92.30 .12549 1.7849 568.4 | 1023.2 | 533-0 | 959.6 117.85 .16023 2.279 8 : 565.6 | 1018.2 | 529.7 | 953-5 149.19 .20284 2.885 562.8 | 1013.1 | 526.4 | 947-5 187.36 2547 3.623 .98 559-9 | 1007.8 | 523.0 | 941.3 233:53 “3175 4.516 556.9 | 1002-5 | 519.5 | 935-0 289.0 +3929 5-589 554-0 | 997-3 | 516.0 | 928.8 355-1 4828 6.867 551.1 | ‘991.9 | 512.6| . 922.6 433-5 5894 8.383 548.1 | 986.5 | 509.1 916.3 525-8 .7149 10.167 544-9 | 980.9 | 505-4 | 909.9 546.1 7425 | 10.560 544-3 | 979.8 | 504.7 | 908.5 567-1 -7710 10.966 Jal S43:7) | 97047 || 504-0) 007.2 588.7 .8004 11.384 : 543-1 977-6 | 503-3 | 906.0 611.0 .8307 Ir.815 542.5 | 976.5 | 502.6 | 904.7 634.0 .8620 12.260 541-9 | 975-4 | 501-9 | 903.4 657-7 8942 12.718 541-2 | 974.2 | 501.1 | 902.1 682.1 .9274 13.190 8:| 540.6 | 973.1 | 500.4 | 900.8 707-3 -9616 539-9 | 971-9 | 499.6 | 899.4 733-3 9970 539-3 | 9708 | 498.9 | 898.2 760.0 1.0333 : 538-7 | 969.7 | 498.2 | 896.9 787.5 1.0707 , 538.1 968.5 : 895.5 815.9 1.1093 , Baraat || Cisne 3 894.1 845.1 1.1490 : 530.8 | 966.2 5 892.9 875.1 1.1898 : 530-2 | 965.1 ; 891.6 906.1 1.2319 : 535-6 | 964.0 3 890.3 937-9 1.2752 . 534-9 | 962.8 s 889.0 970.6 1.3196 : 534-2 | 961.6 : 887.6 1004.3 1.3653 : : Bt 960.5 : 886.3 1038.8 1.4123 : Be: 959-3 d 885.0 958.1 i 883.6 956.9 : 882.3 955-7 : 880.9 954-5 7 | 879.5 953-3 878.2 1074.5 1.4608 Te Tey 1.5106 1148.7 1.5017 1187.4 1.6144 122790 1.6684 NO NSN tN Ove COON mo WOn+f ON NNN Wk ITO GNHHAO 1267.9 1.7238 1309.8 1.7808 1352.8 1.8393 1397.0 1.8993 | 119 | 1442.4 1.9611 952.1 876.8 950.8 ; 875.4 949-5 ‘5 | 873-9 948.4 : 872.6 947-2 871.3 td NHN N SMITHSONIAN TABLES. TABLE 290 (continued) PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C 299 If a is the reciprocal of the Mechanical Equivalent of Heat, p the pressure, s and o@ the specific volumes of the quid and the saturated vapor, s —.o, the change of volume, then the heat equivalent of the external.work is Apu = Ap(s —¢). solute temperature T. Heat equivalent of internal work, p = r — Klebe, Mitt. tiber Forschungarbeiten, 21, p. 33, 1905. Apu. for temperatures above 205° C corrected from Regnault. : For experimental sp. vols. see Knoblauch, Linde and Entropy = S dQ/T, where dQ = amount of heat added at ab- For pressures of saturated steam see Holborn and Henning, Ann. der Phys. 26, p. 833, 19083 Heat Equivalent of External Work. Degrees Centigrade. Temperature Calories.| B.T.U. Apu. Entropy of the Liquid. Entropy of Evapo- ration. Specific Volume. Cubic Meters per Kilo- gram. Cubic Feet per Pound. Ss s 55.2 50.1 57.1 > 59.0 59-9 60.9 61.8 62.7 Ko Go Go Wa HW Coa 6 64.6 65-6 66.5 67.4 hopOD W Gs Oo WO 69.3 70.2 71.0 71-5 71.6 71.8 t YEQwrp ppny nw wv O CO Dur = “Im BO 9 COM] 206.3 147.1 100.3 TE 57.8 3394: 2356. 1703. 1248. 926. 43-40 92:95 25.25 19:57 ae 12.02 9.56 7.66 6.19 5:04 4.130 3-404 2.824 2.358 2.275 2.197 2.122 2.050 1.980 1.913 1.849 1.787 1.728 1.671 1.617 1.564 1.514 1.465 1.419 1.374 1.331 1.289 1.248 172 . /- -136 101 1.068 Density. Kilograms per Cubic Meter: i s 0.0048 5 .00680 00941 01283 O17 30 02304 03035 03960 .OSII .0656 .08 32 .1046 .1305 L615 -1984 .2421 .2938 3541 4241 4395 4552 471 487 °505 523 Pounds per Cubic Foot. 1 ial 0.000303 .000424 .000587 .OOCSOI .0O1T080 001439 001894 00247 I .003190 004092 00519 .00053 .00814 .01008 .01239 .O1510 01835 02211 .02648 02743 .02842 .02941 03043 03149 .03260 03375 03492 .03611 103734 .03861 .03990 .04124 .04261 .04400 04543 04692 04845 .0500 0516 -0$33 .0550 .0507 0585 .0603 .0622 0641 .0659 .0679 SMITHSONIAN TABLES. To Temperature Degrees Fahrenheit. 300 TABLE 290 (continued) PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C = === eo. Heat of H f Heat Equival Eo ess a 5 gg Pressure the ieee Vac uneaiors ceaiwore A 3 BE Fae BES | Qos Mm Kg Pds. : , SI EQS of per sq. per sq. | Calories. |B T. U. | Calories. | B. T. U. | Calories | B. T. U. EQ's | LY |Mercury cm in. Be t. P- P. P- q q: r r. p p. | 120 1489 2.024 28.79 12014 alee O.7 525-6 | 946.0 | 483.4 | 870.0 | 2 121 1537 2.089 29.72 121.4 218.5 524-9 944.5 482.6 | 868.6 | 2 122 1586 | 2.156 30.66 122.5 -220:4.a| 52422. | 04325) || 480-8) | MOOzaEa ima | 123 | 1636 | 2.224 31.64 P2gt5 wiecao.e: + 52315 9) 042.3" 4OT-O hh GO5.01 nln i2 | 124 | 1688 | 2.294 Be2'O4u||| el2dshn lezen 522.8 | 941.0 | 480.2 | 864.3 | 2 | 125" |) 07400)|).2-366 33-66 | 125-5 | 225.9 | 522-1 | 939.9 | 479-4 | 863-0 | 257.0 126 | 1795 | 2.440 34.71 12625) 227-7 521.4 | 938.6 | 478.6 | 861.6 | 258.8 | 127 1850 | 2.516 36.78 || T2725.) 229.5) | 520-7) || 987-35 || 477-0 ||) G00-251|) 260-6 128 | 1907 | 2.593 36.88 | 128.6 | 231.4 | 520.0 | 936.1 | 477.0 | 858.8 | 262.4 129 | 1966 | 2.673 38.01 129.6 | 233.3 | 519-3 | 934.8 | 476.3 | 957-4 | 264-2 130 | 2026 | 2.754 39-17 | 130.6 | 235.1 | 518.6 | 933-6 | 475.5 | 856.0 | 266.0 | 131 2087 2.837 40.36 | 131.6 | 236.9 | 517-9 | 932-3 | 474-7 | 854-6 | 267.8 | 1320 2U5Ons 2.923 Ale G7) il 032-08| 280+7) al 5 loll OR Mal 474.0 | 853.2 | 269.6 133) ||) 2204 \\" Zoro 42.81 133-7 | 240.6 | 516.6 | 929.8 | 473.3 | 851.8 | 277.4) 134 | 2280 | 3,100 44.00. | 134.7 | 242.4 |) 515.9..| 928:5 ||| 472151) S§0:45)|| (2732 | 135 | 2348 | 3.192 45:30) [13570 | 244.2 |) 55-0 1927-24) 471.6) | a4e:oniizne om 136 2416 3.285 46.73 136.7 246.0 | 514.4 | 925.9 | 470.8 | 847.5 | 276.8 | 137 2487 3-382 48.10 137-7 247.9 513-7, | 924:6 | 470.0 | 846: | 278:69) 138 | 2560 3-480 49.50 | 138.8 | 249.7 513.0 | 923-3 | 469.3 | 844.6 | 280.4 139 | 2634 | 3.581 50.93 | 139.8 | 251.6 | 512.3 | 922.1 | 468.5 | 843.3 | 282.2 |, 1401 2710 3-684 52-39 140.8 253.4 511.5 | 920.7 | 467.6 | 841-8 | 284.0 141 | 2787 | 3-789 | 53.89 | 141.8 | 255.3 | 510.7 | 919.3 | 466.8 | 840.2 | 285.8 | | 142 | 2866 | 3.897 BAB ue U42-0 m | eaiczar 510.1 | o18.1 | 466.1 | 838.9 | 2876 | liens 2948 | 4.008 57.00 143-9 259.0 509.3 | 916.7 465.3 | 837-4 | 289.4 291.2 | 144 | 3030 | 4.121 58.60 144.9 | 260.8 508.6 | 915.4 464.4 | 835.9 | digs @SEES, i 42230 60.24 145.9 262.7 507-8 | 914.1 463.6 | 834-5 | 146 3202 4.354 61.92 146.9 264.5 507.1 912.8 462.8 | 835-1 | 147 3291 4.474 63.64 148.0 266.4 506.4 | o1t.5 | 462.0 | 831.6 | 148 | 3381 | 4.507 65.39 | 149.0 | 268.2 | 505.6 | 910.1 461.2. | 830.1 | 149 | 3474 | 4-723 67.18 150.0 270.1 504.9 | 908.8 | 460.4 | 828.7 150 | 3569 | 4.852 69.01 mgt) || Zito) || Hoyle | Coyatl |) AGG || wee I51 | 3665 | 4.984 70.000 |e L521 273.8 | 503.4 | 906.1 | 458.7 | 825.7 152 | 3764 5.118 72.79 153-1 275-6 502.6 | 904.7 457.9 | 824.2 153 | 3865 | 5.255 | 74-74 | 154-1 | 277-4 | 501-9 | 903-3 | 457-1 | 822.7 154 | 3968 | 5.395 76.73 155-1 279.2 501.1 901.9 | 456.3 | 821.2 155 | 4073 | 5-538 Te |) TiO || eeritel 500.3 | 900.5 | 455.4 | 819.6 156 | 4181 5.684 | 80.84 Tig 7e2 283.0 | 499.6 | 809.2 454.6 | 818.2 157 | 4290 | 5.833 82.96 | 158.2 284.8 | 498.8 | 897.8 | 453.8 | 816.7 158 | 4402 | 5.985 85.12 TSQi3)4 |) 280.7 ||) AOS) So6:5) ||| 453-0) || Siis33 159 | 4517 | 6.141 87.33 | 160.3 | 288.5 | 497-3 | 895.1 | 452.1 | 813.7 160 | 4633 | 6.300 89.59 161.3 || 2090:4.' 496;5 || 893.7, || 451-2 ,| Siz.2 161 4752 6.462 91.89 162.3 292.2 495-7 $92.3 450.4 | 810.7 162 4874 6.628 94.25 163.4 294.1 494.9 | 890.9 449.5 | 809.2 163 | 4998 | 6.796 96.65 164.4 295.9 | 494.2 889.5 | 448.7 | 807.7 164 5124 | 6.967 99.09 165.4 297.7 493.4 | 888.1 447.9 | 806.2 165 5253 7.142 | 101.6 166.5 299.6 492.6 | 886.7 447.0 | 804.7 166 5384 | 7.320 | 104.1 167.5 301.5 | 491.9 | 885.4 | 446.3 | 803.3 LOZ |S SUS 725020 OO. 168.5 | 303-3 | 491.1 | 883.9 | 445.4 | 801.7 168 | 5655 | 7.688 | 109.4 169.5 | 305.1 | 490.3 | 882.5 | 444.6 | 800.1 NOON MG ZOA Ml 7RO7 TU ele. 170.6 | 307.0 | 489.5 | 881.0 | 443-7 | 798.5 mw WN th Pu Oe G2 Go God Gd GD i G2 Gd G2 G2 Gd SMITHSONIAN TABLES, TABLE 290 (continued) 301 PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C | Heat Equivalent . : of External Work. Specific Volume. Density. Entropy Entropy of the of Evapo- ; SF Liquid. ration. Cubic Cubic Kilograms|} Pounds Calories.| B. T. U. Meters per} Feet per | per Cubic! per Cubic Kilogram. Pound. Meter. Foot. Temperature Degrces Centigrade. Temperature Degrees Fahrenheit. Ss 14.28 13.86 13.46 I 3.07 12.69 HHH NNN NL 12.33 11.95 11.64 11.32 11.00 10.70 10.40 10.12 9.839 9.569 9.309 9.060 8.820 8.587 8.360 8.140 7.926 7-719 7-519 7.326 7-139 6.957 6.780 Noh & ROO toh 2.885 259 3-032 3.108 3-185 3.265 3-345 3:425 S255 3-582 WWW OW NWNNN SMUwW = 0 3.664 3-75" 3.842 3-937 4.032 baw WO AEROS N+ OCO | Ww WW Od NNHNN }inkWW N SMITHSONIAN TABLES. 302 TABLE 290 (continued) PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C Heat of Heat of Heat Equivalent Pressure. the Liquid. Vaporization. of Internal Work. Mm Kg of per sq. . | Calories. | B. T. U. | Calories. | B. T. U. | Calories. Mercury. cm in. p p- q- q- ie : p- Temperature Degrees Centigrade. Temperature Degrees Fahrenheit. 5937 : 171.6 | 308.9 | 488.7 ; 442.8 6081 ; : 172.6 | 310.7 | 487.9 | 878. 441.9 6229 : 2 173 7aalG le. 0. | 4oza0 376. 441.1 6379 A 3: L74s7e 304.5 |) 480:3 : 440.2 6533 : Zon 75 7ea ng LO-3) 4535 : 439-4 6689 : ; 176.8 | 318.2 | 484.7 3 438.5 6848 ; : 177.8 | 320.0 | 483.9 5 437-7 7010 : i 178.8 ON 483.1 5 | 436.8 7175 : : 179.9 g 482.3 436.0 7343 98 ; 180.9 : 481.4 ! 435.0 7514 : 181.9 : 480.6 : 434.2 7688 : 183.0 | 329. 4798 7866 os 184.0 : 479.0 8046 4 185.0 478.2 8230 ’ 186.1 : 477.4 8417 : 187.1 ; 476.6 8608 ; 188.1 ‘ 4757 8802 : 189.2 : 474.8 8999 «22 A. 190.2 s 474.0 g200 4 191.2 ; 473-2 9404 : 192.3 : 472.3 g612 193-3 ‘9 | 471-5 9823 : ; 194.4 ; 470.6 10038 4 4 195-4 ; 469.8 10256 3 ; 196.4 : 468.9 10480 ‘ 202. : , 468.1 10700 : : : ‘ 467.2 10930 3 ‘ : : 466.4 11170 : i ; : 465.6 II410 ; 20. : ; 464.7 463.8 462.9 462.1 461.2 460.3 11650 11890 12140 12400 12650 NN HH NN DOW how dvd vd On OLR Ee NOI cn CR RHO C}O NN OON 12920 13180 13450 13730 14010 459.4 458.6 457-7 456.8 455-9 455.0 454.1 453-2 452.4 451-5 450.6 449.6 448.7 447.8 446.9 NNHN HN “J 14290 14580 14870 15170 1$470 ybybnn Oo COCon!I by Dow | ONE NOM al os SOC ICO 15780 16090 16410 16730 17060 NR NH WN WN Se WW WW WD = Con Go HH tm Ne nN bo 17390 446.0 w | Go Go SMITHSONIAN TABLES. Heat Equivalent | 200 47.3 | 85.1 201 47.3 85.2 202 47-3 85.2 203 47-4 85.3 204 47-4 85.3 47-4 | 85.4 47-5 | 85.4 47-5 | 85.5 47-5 | 85.5 47-5 | 85.5 47-5 | 85.5 47.5 | 85.5 47-5 85.6 47-5 85.6 47-5 85.6 47-5 85.6 47-5 85.6 47-5 | 85.6 47-5 | 85.6 47-5 85.6 47-5 85.6 5 ug | of External Work. eos Bee EA § |Calories.| B. T. U. H YU t. Apu. Apu 170 45:9 $2.6 171 46.0 82.7 172 46.0 82.8 173 461 82.9 174 40.1 $3.0 175 | 46.2 | 83.1 176 46.2 83.2 177 46.3 83.3 178 AGcl Osa: 179 | 46.4 | 83-5 180 46.4 83.6 181 40.5 83.7 182 46.5 | 83.8 183 46.6 83.8 184 46.6 83.9 185 46.7 84.0 186 46.7 | 84.1 187 46.8 84.2 188 46.8 84.3 189 46.9 | 84.3 190 46.9 | 84.4 IgI 47.0 84.5 192 47.0 84.6 193 47.0 84.6 194 47.0 84.7 Entropy of the Liquid. TABLE 290 (concluded) PROPERTIES OF SATURATED STEAM Metric and Common Units 0° to 220° C Specific Density. 323 Volume. 4 Entropy 2 32 BAF vaRys Cubic Cubic Kilograms Pounds 3 bo © . Meters per | Feet per | per Cubic | per Cubic E A= Kilogram. | Pound. Meter. Foot. a = s Ss 1 Ss it. |p 8 8 1.1029 0.2423 3.883 4.127 0.2575 338.0 1.0987 .23608 3.794 4.223 .2630 339.8 1.0944 2314 3.709 4.322 2696 341.6 1.0901 2262 3.626 4.421 2758 343-4 1.0859 2212 3-545 4.521 2821 345.2 1.0817 2164 3.467 4.621 2884 347.0 1.0775 2117 | 3-391 4.724 -2949 | 348.8 1.0733 2072 3.318 4.826 3014 350.6 1.0691 2027 | 3.247 4.933 3080 | 352.4 1.0649 1983 | 3-177 5.04 3148 | 354.2 1.0608 1941 3.109 5-15 3217 356.0 1.0567 -1899 3.041 5-27 3288 357-9 1.0525 1857 | 2.974 5-3 3362 | 359.6 1.0484 1817 2.911 5-50 3435 361.4 1.0443 1778 2.849 5-62 3510 363.2 1.0403 1740 2787 5:75 3588 365.0 1.0362 1702 2.727 5.88 .3067 360.8 1.0321 .1666 2.669 6.00 .3746 368.6 1.0280 1632 2.614 6.13 3826 370.4 1.0240 1598 2.560 6.26 3906 372.2 1.0200 1565 2.507 6.39 3989 3740 1.0160 1533 2.456 6.52 4072 | 375-8 1.0120 1501 2.405 6.66 4158 377.6 1.0080 1470 22255 6.50 4246 379-4 1.0040 1440 2.300 6.94 4336 381.2 7.09 8 7:23 354. 7:38 7-53 7-69 .9804 1274 2.041 7.84 .4900 392.0 9765 1249 2.001 5.00 .4998 393-8 9727 122 1.962 8.16 510 395-6 .g688 1201 1.923 8.33 520 397-4 .9650 L167 1.885 8.50 531 399.2 O61 1153 1.847 8.67 541 401.0 .9572 1130 1.810 8.85 SIS 402.8 9534 1108 1.774 9.03 504 404.6 .9496 1086 1.739 9.21 G75 406.4 .9458 1065 1.705 9.39 597 408.2 -9420 1044 1.673 9.58 598 410.0 9382 102 1.640 9:77 -610 411.8 9344 1004 1.608 9.96 .622 413.6 .9307 0984 1.577 10.16 634 415.4 9269 0965 1.546 10.30 .647 417.2 9232 0947 1.516 10.56 .660 419.0 9195 .0928 1.486 10.78 .673 420.8 9157 Ogto 1.458 10.99 .686 422.6 9120 0893 1.430 11.20 699 424.4 gos 4 .0876 1.403 11.41 713 420.2 0860 1.376 11.62 428.0 SMITHSONIAN TABLES. TABLE 291 PROPERTIES OF SATURATED STEAM Common Units, 400° to 700° F. 304 Abridged from Steam Tables and Mollier’s Diagram by Keenan. Printed by permission of the publisher, The American Society of Mechanical Engineers. For detailed discussion see Mechanical Engineering, Feb., 1929. v, specific vol., ft.3/lb.; h, total heat, enthalpy, B.t.u./Ib.; s, entropy, B.t.u./°F./lb. The strict definition of total heat (internal energy + 144/J) is adhered to; zeros of both # and s are arbitrarily placed on the sat. liq. line at 32°F. No internal energy values are tabulated but may be easily found by subtracting 144 pu/J from the total heat. The energy unit, the B.t.u., is 778.57 ft.-lb. (J) is 1/180 of the change in total heat along the saturated liquid line between 32° and 212°F. (Osborne, Fiock, Stimson.) ae Temp. Abs. ? _ Specific Volume _ Total Heat _ Entropy F. ~~" ** Sat. liq. Evap. Sat. vapor Sat. liq. Evap. Sat. vap. Sat. liq. Evap. Sat. vapor t lb./in.? of Ufg 09 hy hto a Sf Sha 400 247.25 0. 1.8421 1.8608 375.0 826 1200 s 0.9602 405 26167." 7: 1.7428 1.7615 380.4 821 1201 : -9491 410 2764720) ae 1.6493 1.6681 385.9 816 1202 : .9381 415 20240 1.5615 1.5804 391.3 811 1202 ; -9271 420 208.82) |. 1.4792 1.4982 396.8 806 1203 : -QI61 425 225.010) ie 1.4022 I.4212 402.4 801 1203 : -9052 430 BA ae ae 1.3295 1.3486 407.9 796 1203 : .8942 435 262.27) 0: 1.2610 1.2802 413.5 790 1204 : .8833 440 381.59 1.1965 1.2158 419.1 785 1204 : .8724 ie 1.1550 424.7 779 1204 : .8616 450 422101) 9: 1.0782) 1.0977, ) 430) 97.74 1204 : .8507 455 444.35 « 1.0241 1.0436 436° 768 1204 : .8398 460 466.94. 9730 .9927 442 762 1204 : 465 490.40 . -9249 .9446 447 756 1204 : .8180 470 iZle7koy ic .8793 .8991 453 750 1204 : .8071 475 540.04 . .8361 .8560 459 744 1203 d -7962 480 566:26) 7: 7951 .8151 465 738 1203 é 4 .7852 485 503-47. - 503) L704) 47 731 i202 . 7742 490 620-67 Obes BOS (AT 7aee 2 Le O2 : -7632 495 650:87/ 5: 6847 .7050 483. 718 1201 2 eu 500 68iOO) 6516 .6721 489 7II 1200 : -7410 1.4314 505 712AO) We 6201 .6408 495 704 I199 : -7299 1.4266 510 TAA TAL Ve 35903) -OLLOis) 5020) 5007, sIOS : .7187 1.4218 515 Ggkseilo) -5018 .5826 508 690 II97 : -7075 1.4170 520 SI2572) We. 5347-35557 514 682 S196 : .6963 1.4121 525 848.43. .5090 :5301 52I 675 1195 ‘ -6851 1.4073 530 Ss5ean ae 4845 .5058 527 4667 I193 ‘ .6738 1.4024 535 923-39 .- -4614 .4828 533 659 1192 . -6625 1.3975 540 962-72) 7: 4394 .4610 540 £651 IIQI ; .6512 1.3926 545 1003.4 . -4184 .4401 547 643 1189 . -6399 1.3877 550 1045.4 : .3982 .4201 553 634 1188 : .6285 1.3828 555 1088.7 : -3789 .4010 560 626 1186 : .6170 1.3778 560 1133.4 d -3605 .3828 567 618 1184 : -6056 1.3728 565 1179.7 . 3429-3654 574 609 1182 . -5940 1.3677 570. | 5227.6 : -3261 .3488 580 600 1180 : -5825 1.3626 S75 L277, 007) : 3 LOL B30) 587.5 OL ents : -5709 1.3576 580.) 1327-2 : -29049 .3180 594 581 1176 : .5592 1.3524 585)" 1379:2 .0232 28040-30377) GO2N me5 72) il ‘ -5474 1.3472 590 1432.7 : .2664. .2900 609 £562 II7I ; -5356 1.3420 595 1487.8 : 2530) -2760)) (O16; p e552) 168 ‘ .5237 1.3368 600 1544.6 : 2AOT 22642591623) 542) 166 j -5118 1.3316 610 1663.2 : -2159 .2406 638 521 1160 ; .4875 1.3208 620 ~=1788.8 -025¢ .1933 .2186 653 499 I153 : -4623 1.3093 630 1921.9 2 L720 |) LOSZ mG 7OMmn4 7/5 auld: : .4358 1.2970 640 2062.8 : 522) el 7OL 687 448 1135 : -4073 1.2836 650 2211.4 , 33h | -LOLON ss O54, 22 ‘ -3764 1.2688 660 2368.6 : LIAS) | 4a 725 ees od) LOO : -3426 1.2523 670)8 253452 : 0966 .1269 748 344 1092 : -3049 1.2336 I I if Mis 445 401.70 1356 680 2709.7 : O71 | .TTO2 Wie 299) 1072 : .2619 1.2119 690 2896.8 : -0589 .0936 1044 : -2098 1.1852 700 3096.4 2 -0353 .0747 1003 : 1354 1.1471 1102 1.0785 705) 3202.0 ‘ .0135 .0597 73) (962 : .0630 706.1 3226.0 : oO .0522 O 925 oO SMITHSONIAN TABLES TABLE 292 PROPERTIES OF SUPERHEATED STEAM Common Units, 212° to 3000°F. 305 (Abridged from Steam Tables and Mollier’s Diagram by Keenan, 1930. Printed by permission of publisher, The American Society of Mechanical Engineers.) Abs. P. at pSate ase 200°F. 300°F. 400°F. 500°F. 600°F. 700°F. 800°F. 900°F. 1000°F. OL02N 26182 27-167 930552) ) 34:65) 9 38575) 942283)" 46.91% 50:97 55:03 59:09 14.696 LSOO MSO MeUT SA. eo? seeT2304. T2860n Iss4e 882; ) 4325" 14835) 0535: ir200)) 0.3119 1-7564 1.762 1.815 1.873 1.925 1.972 2.016 2.057 2.096 2.133 0.017 8.514 v SH, One OO: OOM lil Ol D255 Cian alia 7/Ane iA OGi me STONn As ln7234. 50 250.0 1173.5 h TSA 224202) sei olen 4ST 048255 534. (281.01) 0.4111 1.6580 S 1HO7 2 e734 e787.) IES sOle IeSSOn 81-922) | 1:96 12998 0.018 4.426 Uo) Waser: © 4.93 5.58 6.21 6.83 7.44 8.04 8.64 100 298.3 1186.6 ne [227 127, S68 SON Ie Oem TAZON SUAS Te | T533. (327.83) 0.4742 1.6022 Sho | ans T-O5 a 9) 1: OO ume SA et Ol Il O4A aL OOAN O27 0.018 3.010 Orr ol eoits s.: aaa 3.68 4.11 4.53 4.94 5.34 5-75 150 330.4 1194. eh eee I2TOs 1272. eee eT ONe TAZ 7A UAT Ol 6 532. (358.43) 0.5140 1.569 Sy) fatten T5000 | 1-050 lO le 7/50 81-7909 ose | 0.870 0.018 2.285 Ua uh iectensa: 2.258 23722 3.06 3.38 3.69 4.00 4.30 200 355- 1198. Dea Wesocer WANOS | WA IAG Bey IAS ante (381.82) 0.543 1.545 Sei. alisietns 1559) 12022) | 1hO7ON 17235 81.766, 0-806) 1.6438 0.0189 1.541 DOM Westeeiare

    (ed? — 1)71dr where J, represents the intensity at wave length *c, = (3.697 + 0.005) X 10° erg-cm*sec,!, unpolarized radiation over solid angle 27. = (3.194 + 0.004) erg:cm? day"! = (8.832 + 0.01) X 1078 g cal.15 cm? deg. = (3.697 + 0.005) X 10°” watts:cm? Co = (1.432 + 0.003) cm-deg. Wimax — 35D x 10s 1° A max T = ©/4.9651 = (0.28836 + 0.00011) cm-deg. *c, = 2nhc? = 3.697 X 10° erg-cm*sec.-! when E)dd denotes the emission of unpolarized radiation in range dd, per unit surface in all directions (27 solid angle). €, = 8rhc = 4.932 X 10°% cm-deg., when £,dd denotes energy density of unpolarized radiation. (, = hc® = 0.5884 X 10° erg-cm*sec.“!, when Ed) denotes intensity of linearly polar- ized radiation in range dX, perpendicularly to a surface, per unit surface, per unit solid angle. TABLE 308.—Radiation in ergs (R x 10") and gram-calories (R* >< 10") per cm? per sec. from a perfect radiator at ¢°C to absolutely cold space (— 273°C) Computed from Stefan-Boltzman formula, ¢ = 5.73 X 10-5 erg. cm.- 2deg.-4 erg/cm?/ cal./cm?/ erg/cm?/ | cal./cm?/ sec. sec. : R n | Ri n 5.29 —3] 1.27 —I10 1.61 3.86 —7 1.64 3:94 —5 2.73 655i 5 4.31 1.03 —4 9-37 2.25 —4 i geil 3.14 —4 1.82 4-37 —4 2.40 570) 4 3-15 7-56 —4 4-05 9-72 —4 5.15 1.24 —3 6.44 TS 7:97 LOT amo 9-74 2.34 —3 1.18 2.83 —3 1.42 3.41 —3 1.69 4.06 —3 2.00 4.80 —3 2-35 5:64 —3 2.74 6.58 —3 2.83 6.79 —3 2.92 7.01 —3 3.00 7.20 —3 3-09 7-42 —3 3.19 7.66 —3 3.28 West 1 3 AMNannanannnnnaPpPpPPPPAHPPRWWWW ANnAAnAAAnannanrnnanannnnwni nn wn wi Ut Ut Note: Above table correct probably to one per cent. SMITHSONIAN TABLES 314 TABLE 309 BLACK-BODY SPECTRUM INTENSITIES (J\), 50° TO 20000°K. Values of J\ using for C1, 9.23 X 10%, C2, 14350., X in mw. If the figures given for J\ are plotted in cms as ordi- nates to a scale of abscissae of 1 cm to 1 ws, then the area in cm? between the smooth curve through the resulting points and the axis of abscissae is equivalent to the radiation in calories per sec. from 1 cm? of a black body at the correspond- ing temperature, radiating to absolute zero. The intensities when radiating to a body at a lower temperature may be obtained by subtracting the intensities corresponding to the lower temperature from those of the higher. The nature of the black-body formula is such that when AT is small, a small change in C2 produces a great change in J); e.g., when C2/AT is 100 or 10, the change is 100 and ro fold respectively; as AT increases, the change becomes proportional; e.g., when C2/ AT is less than 0.05, the change in J is proportional to the change in C2. 000000 +00220 . 00201 .OO157 -OOIT7 . 0387 . 03653 «05403 000000 .03258 - 03146 .04558 -04255 . 05580 . 05197 000000 ° a 1000° | 1500° | 2000° 3000° 4000 K. x 5 c K. 5000° | 6000° 8000 K. K K. -0115 | 0.0624 | 0.0331] 0.038 T5i0 . | 7IO000. .OOI2 0.46 15.4] 184. 3660. . | 820000. -44 24.2 263. | 13r0. 9640. . | 382000. rs TTKS 690. | 2280. |10300. . | 180000. 226. 952. | 2490. 8400. : 92300. 301. Iooo. | 2240. 6290. ; 51460. 328. 925. | 1860. 4590. ‘ 30700. 321. 800. 1490. 3350. , 19400. 205. O7 Tee | Lez 2470. : 12820. .0548 Jo. .0408 |o. .00045]0. .00183]0. 090000000% © ON ANUARWN HF me Hooo0000 262. 554. 928. 1842. i 8800. T2268 210. 300. 527. : 1980. Wie go. 125. 198. ‘ 668. 20. 43. 58. 90. 284. 16. 23). 30 46. : I40.7 13. 17. 26. ha .00538|0. .0848 - 221 -305 «320 . 296 ODROKM® BHR WO nonounod howuwon .256 .178 -1IQ .o81t .0562 .0398 .59 ° 9 .81 81 .84 42 .40 348 .88 808 .20 513 +709 “165 .653 - 416 OHnNS COO 99000 OD0OOHND OOHNSH Oo ONAN WWHNHHH oo00000 .0288 Jo. .o160 |o. .0096 |o. .00606]o. .00400]|0. .00275]0. 342 -470 168 .230 0921 oe 0546 | 0.0742 0344 0406 0227 .0307 000000 090000 990000 0900900 990000 .QOI 22 . 03019 °. 00941] 0.0127 °. . 03209 Jo. O°. O. oO. 00455| 0.00616 .00146] 0.00197 .03603 .03808 .03120 .O3161 .04381 -04510 04888 .04184 -05598 000000 9909000 9009000 000000 9099000 See Forsythe, J. Opt. Soc., 4,331, 1920, relative values, 0.4 to 0.76 @ (steps 0.01 #4), 12 temperatures, 1000 to 5000° K, SMITHSONIAN TABLES, TABLE 310 Bus BLACK-BODY SPECTRUM INTENSITIES (Jr), 25° to 600°K. Values computed by editor using for Ci, 3.703 X 10° erg:cm*sec.-!, Cz 1.433 cm:°K, Jy = tabular Jy X I0”. 3-7 —234 | 1-3 —109 4-9 —152| 4.9 —69 3.9 —111 | 6.8 —49 9.9 —87|6.4 —37 1.6 —70|5.0 —29 Ope 9) 1-9 S23 2.1 —50|2.8 —19 1.9 —38/1.5 —13 1.6 —30|8.6 —I10 6.1 —25 =F 8.6 —2I —5 14) o— 07 —4 ° oe “NI Se OU Ow COI OMd a ME DON ORHOOwB® WH 2.19 2 aril 2.87 3.81 4.15 4.06 3-73 3-31 AT tS 2.7 —II It —8 9.8 —7 2.90 —5 4.14 —4 4.18 —2 7.68 —I RAN OO OW ‘2.28 1.52 7:24 3-71 9:77 3-54 —I I 2 Ss 3 4 4 5 5 5 5 6 6 6 5 5 5 NANO AGW WOO IM wBOdOAansA YN ADN WoO G0 00 00 CO CO CO Co CO COOONTINI wm ANINTN 0O 00 60 CO CO CO 00 GO CO CO CO CO CO CON DAunw Nd wm ANININI 00 00 CO CO CO CO'\O 0000 C0 ONIN OL NA ANINT NT 00 00 CO CO'O 0 © 10.00.00 0 \O © CONT QU OQ ONIN 00 00 cm mMOOOO OOOO Ov”) won onu NaAANNN mn OANNN SMITHSONIAN TABLES 316 TABLE 311 BLACK-BODY SPECTRUM INTENSITIES (JX), 800° to 25000°K. (Same origin and data as Table 310.) ro0o°K. 1200°K. 1400°K. 1600°K. 1800°K. 2000°K. 2200°K. IRNe J» Xe ee Nae Lt a 2.1—42 5. 1.3—24 4. I.O—I4 2.8—I1 1.9 —8 6.9 —4 4. O10) 8183.2 ayo. s ane 253 ; A570) (6:5 eet eo 2.8 : 8:2) 18) 16:00) 69) 3-08mr0 2.67 ; Aek7@ 19) 2-45 1.04 II 1.53 : TAA LOM 7p LON 2. OO)smr 6.1 : 2 CO MlOumILO2 man 1.86 : 8:2) LOPE sO Gr 4.61 : Te QL <2 Tale 9.9 6. 2a5 3) Lie 7-@ lane 1.90 1.84 Skioley thie Lg iit 10 Beil 3.14 1.55 5.39 II 1.46 KOS TO!) 7-21 2.99 9.03 II 2.19 : 2A TOM ESS 4.78 1.29 12 2.86 2.4610) BIE 70) Ti 85.30 1.25 2.43 12 4.15 8.96 10 2.96 I1 6.98 1.33 2420) 12) F353 Te 23a oe 2 ee OLA 1.08 E204) 2) 2°20 3.03 12 ON e229 OM IE 5:20 8.11 a5, L252 1.96 1 OAL ie Os atte 63:03 4.31 572) Tile 8.83 Fel 5 el OMe le © ee talann ler. © QE, 2:02 lease 7a 4.42 [-LOe LO) i Ole TO} 2:08 2.56 3.04 10 3.54 4.03 2.74 1.08 3.36 8.6 OO CONN DAULW O00 MOON ANU FO 4000°K, 5000°K. 6000°K. 8000°K. 1o0000°K. 15000°K. 20000°K. 25000°K. Jy n Jy n Jy n Jy n Jy n Jy n JN n Jy n 7.02) 5. 112328 1257 sO. G2) 212" 2:27 eA ® 2163167 2:06 t7amincoers 1.92.11) (6.9. 12. 47-5. 1130 1:49) 5) (8:95 5) 9384 16 73-3817 FOS sr, 9:9), 12. $1-08) 14 15:32 314) (379005) (1.30716) 16558 TO tt 5217 - OA? 4.66 13 2.80 14 9.25 14 4.16 TeOZwRON 3 O02 On 7-24 elOmeel aml, 7200) 13) 13-45 149y.9:98) 1493-82 S67 15) 52-73 0lO! 5-13 alone On LO 9.16 13 3.85 14 1.00 15 3.39 7 TSS 2:OOM On Sele Ome 5152 900 1.09) 14) 44-04) 14) 97.2004) 2°05 SS 7A Se lsd Zar hOn 92-74 OMA OO MO 1.22 14 4.05 14 9.06 14 2.53 A.80) LS) 1-22) 16) 2:07elO 2-98 er6 TeGOeTA 13.O3n TAS aleenA ee 2elO Z1960 D5) O53. 5 eo Ome 2-200110 1.32 dees 7A Ae 75 te Aa OF. 260015) 755ml Sn les Lome 73) Lo 1S 2E TANS. 4 981467 4e TAs s56 27 5a OOO Mise Oy7ON lS) eso) lo 130) TAs 3-230 14) 0-008 TANS A! 2.26 AOL 5) 72605 Ose TQ) T4227 14) AL Std 1OLO3) UA 1-60 2232) 50 Sult5) U5 -O4uwrS 1206) TAN 2-235 TA 3570 4 7-4 t 1.16 2225 35405) 47m AESS) 1Qe 6S: 4i/a 13 alee Ay eee 22 3.04 5.48 14 7.96 14 1.04 15 PA? 13 3-025 L350 3) 77-99 1.10 1.88 14 2.68 3.48 14 Holts), 103) Tig7Ao) 3) BB, 1B Bho 4.90) 13) Sol 5913) 1.4! 1.47 14 Gr63 12) 19.5329 tee 5) ors 1.86 2.48 ALO), 13 EOS WS) 9/241, 13 250M 12m 450 L2 need 22) Os4.0 8.40 ISAs ele O4) 132. 34s TAZ 5S 2s OS ew2 5 e275 3257; O22 N77, 9.76 12 SG) WO) Mg ie “shee, sy anette} 2.40 3:66 Ti 4.98) 10 16:28) 10 SMITHSONIAN TABLES TABLES 312 AND 313 317 TABLE 312.—Black Body Spectrum Intensities Auxilliary table for J, at any temperature (Menzel, Harvard Observatory) Let Jo = intensity for TJ) = 10,000° K.; for another temperature T° K., we have the relationship Ff Jo = |X, (e® = 1) |/[sce2? — 1) |. Let \ = AoZ0/T.Then Jo (T/T>)®. e. g., to find Jx for 0.54, 6000°K., we take 0.54 = Ao X 10,000/6,000 or do = 0.3u, Jo for 0.3u = 1.2977 X 10!8, whence J = 1.2977 X 10 X (6000/10000)' or 1.01 X 10%, In the following table J, is for 10,000° K.; Jx X 10" is intensity at wave length Xu. A is given in » but in plotting it should be used in cm (one » = 10cm) that the area under curve be in ergs. hc/k = 1.43187; 27hc? = 3.69728 c.g.s. units. A change in c, may be allowed for by a con- stant factor, in ce by taking a different value for T so that 1.4319 X 10,000 = @7J. One erg-cm:~-sec.-! = 2.389 X 10° cal.15: cm~: sec. Jy (ergs) 2 Jy (ergs) n Jn (ergs) 2 Jn, (ergs) n 2.4131 —37 A 2.9673 4 5.8731 5.3480 4.7932 —26 2 3.4824 : 4.8153 3.5080 9.3330 . 4.5367 . 3.9579 1.7645 5.0592 : 5.7244 : 3.2677 9.6897 2.8437 i 6.8702 : 2.7735 5.7562 1.2032 : 7.9607 3 2.2620 3.6208 I.0261 5 8.9902 ; I.Q165 2.4018 3.0403 A 9.9008 A 1.6018 Deu 27 4.3245 3 T.O711 ‘ 1.3596 6.3824 3.6280 : 1.1387 1.1601 3.7652 2.0556 : -1938 8.5810 2.3634 8.6361 ; -2365 6.4670 : 1.5569 2.8766 4 .2680 4.9587 6.4241 7.9649 ; -2883 3.8600 3.1121 I.9021 ; -2996 3.0472 1.6858 4.0261 : .3023 2.2038 9.9057 7.7120 ‘ +2077 1.9702 6.1974 1.3598 : -2700 1.6096 4.0718 2.2355 5 .2246 1.3276 2.7860 3.4037 ‘ -1673 1.1046 1.9697 5.1028 é I.1031 7.8206 1.3083 7.1944 . 1.0358 . 5.6907 1.0643 9.7255 f 9.9002 4.2361 6.2476 1.2839 ‘i 9.0036 3.2185 3.9036 1.6394 ; 8.3551 2.6973 2.5640 “I~I~I COOH MMMM OO 2.0414 : 7.7401 1.3927 2.4858 7.1589 8.3888 TABLE 313.—Values of J, for Various Temperatures Centigrade Ekholm, Met. Z. 1902, used C; = 8346 and C, = 14349, and for the unit of time the day. For 100°, the values for JA have been multiplied by 10, for the other temperatures by 100. ~ 15°C} 0° C | —309 C | —80° C 0 ON’ Quipw wv F 23 24 25 26 28 SMITHSONIAN TABLES. TABLES 314 AND 315 SPECTRAL ENERGY DISTRIBUTION AND LUMINOSITY DATA For use in computing light transmissions and relative brightnesses from spectrometric data. Range of color temperatures 2000°K. to 3000°K. Considerably abridged from Skogland, Bur. Standards, Misc. Publ., No. 86; see also No. 56, 1925, range, 1000° to 28000°K. Planck’s formula used with C:, 14330” deg. The constant of Wien’s displacement law has 318 been determined as 2886.3 deg. that at 0.59 is 1.6361. TABLE 314.—Relative J), based on J at \ = 0.59, or 590 my EXAMPLE: At color temperature 2296°K. and X, 0.65u, the energy radiated relative to r in » 2000°K.'2100°K. 2200°K. 2300°K. 2400°K. 2500°K. 2600°K. 2700°K. 2800°K. 2900°K. 3000°K 32 0.0007 21 50 -O1I0 218 402 690 SLL22 +1735 -2571 .3067 -5058 -6773 -8835 -00007 1.1256 1.4044 1.7195 2.0608 2.4534 2.8679 3.310 3-777 4.205 0.0012 31 73 .OI51 287 507 841 .1321 -1981 -2852 -3964 -5336 .6986 -8923 .00013 1.1148 1.3657 1.6435 1.90468 2.2727 2.61890 2.7986 3.360 3.748 0.0019 47 -O102 203 369 628 -1006 -1533 -2235 -3136 -4254 -5602 -7186 .9006 .0002 I.I051 1.3314 1.5773 1.8410 2.1199 2.4110 2.7120 3.020 3-332 0.0029 67 .0139 204 463 762 -1185 +1755 +2404 +3420 -4538 -5850 +7373 -9080 .0004 .0963 -3009 -5193 -7498 -9895 2.2361 2.4872 2.7403 2.9931 0.0042 92 -0184 336 571 910 -1376 1988 .2760 .3701 -4815 -6100 -7549 -9148 .0006 1.0885 1.2734 1.4680 1.6699 1.8770 2.0860 2.2072 2.5068 2.7126 0.0059 .0124 239 420 601 -1073 -1580 -2228 .3028 -3981 -5085 -6333 -7714 -9213 -0008 .0810 -2486 .4223 -5998 -7792 1.90584 2.1357 2.30905 2.4786 0.0080 .O164 303 517 826 -1248 -1794 -2477 -3208 -4257 -5347 -6550 -7871 9272 0012 0743 -2263 .3815 -5378 -6034 .8468 1.9065 2.1413 2.2801 0.0108 211 378 626 973 -1435 -2019 -2731 +3570 -4531 -5002 -6739 .8017 -9327 -0O17 1.0681 1.2060 1.3449 1.4824 1.6177 1.7493 1.8757 1.9966 2.1105 0.0141 267 463 747 -1134 -1634 p2252 20901 -3843 -4800 -5849 -6973 -8156 -9379 .0024 1.0624 1.1875 I.3114 1.4329 1.5505 1.6633 1.7704 1.8710 1.9647 0.0182 333 561 882 -1306 -1844 +2404 +3254 -4116 -5006 -6090 -7170 -8289 -9428 .0032 -O571 .1704 .2812 .3882 -4905 1.5872 1.6776 1.7614 1.8380 0.0230 409 6690 .1029 +1492 -2060 +2743 +3520 -4388 +5320 -6322 -7356 8413 -9473 -0043 .0523 1.1549 1.2537 1.3479 1.4366 1.5193 1.5955 1.6648 1.7272 TABLE 315.—Luminosity Relative to Maximum Value at Each Temperature ExampLe: At color temperature 2680°K. and \ = 0.55u, the luminosity relative to that at 0.5720p is 0.8874. 2000°K. -0000 .0002 .002T .0087 -0314 -1079 -3383 -6270 .8758 -9988 -9231 -6054 -3910 -1641 -0542 .0153 .0045 -OO12 .0003 10.464 -5818u Sum Max. at 2200°K. .0000 .0003 .0029 -0123 .0397 -1292 -3853 -6816 -9120 -9994 .88097 -6473 -3524 -1433 20460 .0126 .0035 .0010 .0003 10.503 -5788 2400°K. .0000 -0005 .0040 -O149 -0480 -1495 4274 7275 -9390 9950 -8585 -6066 .3212 -1273 +0399 -O107 0030 .0008 .0002 10.535 -5758 2600°K. .0000 .0006 .0050 .O182 .O5601 -1683 -4645 -7655 -9584 -9873 .8209 -5722 -2960 -1148 .0352 .0093 .0026 .0007 .0002 10.550 -5730 2800°K. .OOO1 .0008 0062 -0215 .0640 .1859 -4977 -7972 .9726 -9780 -8035 -5422 -2751 .1048 .0316 -0082 .0022 0006 -OOOL 10.572 -5705 SMITHSONIAN TABLES 3000°K. .OOOI .OOI1O .0074 .0248 .0716 -2021 -5209 .8239 -9826 -9676 -7796 -5166 -2570 .0966 -0287 .0073 .0020 -0005 .OO01 10.581 -5682 Equal energy = visibility .0004 -004 -023 .060 -139 “23 -710 -954 -995 .870 -631 -381 175 -O6O1 -O17 .OOAI .0010 .0002 .OOOI 10.686 -555 TABLES 316 AND 317 319 SPECTRAL ENERGY DISTRIBUTION AND LUMINOSITY DATA (concluded) Factors proportional to the values of Table 315 adjusted so that the area of each complete curve of minosity factors between 0.40 and 0.76y is equal to unity. To obtain the light transmission of a screen, ultiply the spectrum transmission at each \ by the corresponding tabulated or interpolated factor, taining in each case an element of light transmission for the wave-length interval \ — .oIu tod + .OIn. he integral light transmission is obtained as the sum of these elements. The same process is followed r spectrum reflection. TABLE 316.—Luminosity Factors Ain pu 2000°K. 2100°K. 2200°K. 2300°K. 2400°K. 2500°K. 2600°K. 2700°K. 2800°K. 2900°K. 3000°K. 0.40 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000 -42 .0000 .0000 .0000 .0000 .0000 .0000 .0000 .0OO0OI .O000I .OOOI .OOOI -44 .0002 .0002 .0003 .0003. .0004 .0004 .0005 .0005 .0006 .0007 .0007 46 .0008 .0OOIO0 .OOII .0OI2 .00O14 .00I6 .0OI17 .O00I9 .0020 .002I .0023 .48 .0030 .0034 .0038 .0042 .0046 .0049 .0052 .0056 .0061 .0064 .0067 -50 (O103) | .OLIA 40023) |-0133) -0142) 01511) C160, 20168) 0176-0184 -O1O1 52 .0323 .0347 .0367 .0386 .0406 .0424 .0440 .0455 .0471 .0486 .0498 54 .0599 .0627 .0649 .0669 .0690 .0710 .0725 .0740 .0754 .0768 .0779 56 .0837 .0855 .0868 .0880 .0891 .0901 .0908 .0914 .0920 .0925 .0929 .58 0954 -0954 .0954 .0949 .0944 .0939 .0935 -.0930 .0925 -0919 .09I4 .60 .0882 .0863 .0847 .0832 .0815 .0799 .0786 .0773 .0760 .0747 .0737 .62 .0664 .0638 .0616 .0596 .0576 .0558 .0542 .0527 .0513 .0499 .0488 -64 0374. .0352 .0335 -.0320 .0305 .0292 .0280 .0270 .0260 .0251 .0243 .66 .0157. .0145 .0136 .0129 .OI12I .OI1I5 .O109 .0104 .0099 .0095_ .O009I .68 .0052 .0047 .0044 .0041 .0038 .0035 .0033 .0032 .0030 .0028 .0027 .70 .0OI5 .0013 .OOI2 .OOIIT .OOIO .0009 .0009 .0008 .0008 .0007 .0007 ae .0004 .0004 .0003 .0003 .0003 .0003 .0002 .0002 .0002 .0002 .0002 aT: .0OOOIL .0OOOI .000I .000I .00OI .OOOI .O0OOI .O000I .000I .0000 .0000 .76 .0000 .0000 .0000 .0000 .0000 .0000 .0000 .0000 .0000 .0000 .0000 Max. value .0956 .0953 .0952 .0950 .0949 .0948 .0947 .0947 .0946 .0945 .0945 Max. at uw = .5818 .5802 .5788 .5774 ESW5O eS TAS. 5740" a-57LO 05705. 5093 =5083 Cantroid » = .5830 .5814 .5800 .5786 .5770 .5757 -5742 -5730 -5717. -5705_— 5695 TABLE 317.—Percentage Change in J for Change of + 30 in Planck’s C, (14830) EXxAmPLe: At color temperature 2300°K., the value below for 0.44u is 0.8%, due to a change of 30 in ». For a change of 20 in C, the change in Jo.4 is 24 of 0.8 = 0.5%; for a change of 15 in Cx, % of 0.8 70.4%, etc. Algebraic sign of tabulated values: Tabulated values , Ist 6 col. Next 6 col. Change in C,—Increase 7 avinin elisha) alyrallettedcatya |e) ,e)t@is! ate, eels) .a)(eive.tel/e)yeice (ey elisicaice) =) = TD) CEKEASE hay secs Sroeperreee rae bests erent \oud thon a eioions + ad In line “‘all \” are given values for adjustment of the percentage values above in Table 315 to obtain he % change in the luminosity factors of Table 316. Each of these constants applies to all values given bove it in the table; that is, one constant for each temperature. Combine the given constant by algebraic ddition with the individual values at each wave length. ExampLe: Color temp. 2600° K.; \ = 0.52u; C2 changed from 14330 to 14310. At 0.52u, 2600°K., 0.3% s tabulated. Its sign is +, and C, is decreased. The corresponding constant in line ‘“‘all \’’ is —0.07, the linus sign corresponding to a decrease in Cy. For a change of —30 in C, the % change for Table 317 is .3-0.1%. For the assigned change of —20 in (2, the required adjustment to the value in Table 316 is %4 £0.2 = 0.1%. At \ = .71n, the adjustment would be 24 (—0.3 — 0.1) = — 0.2%, etc. hin 2000°K. 2300°K. 2600°K. 2900°K. 3200°K. ding 2000°K. 2300°K. 2600°K. 2900°K. 3200°K. 0.32 BOG GEO%e) Tate 15064. 1-3%. 0:60 | a «1.8 1.6 Te 1.3 Ear i620 Pere ete. s4Or1 0.1 0.1 36 1.6 1.4 m3 Holt 1.0 -64 as 0.2 2 Be me 38 1.4 1.2 Ti 9 9 .66 0.3 er r2 : .68 3 3 23 2 2 | -40 12 1.0 9 8 8 -42 1.0 9 8 A] oF, -70 4 3 “3 3 2 | 44 9 8 .7 6 6 72 4 4 4 3 3 | 46 7 6 5 5 5 -74 5 4 4 4 3 | 48 6 A 4 4 4 .76 6 5 4 4 4 -50 5 4 4 x4) 48 all > 04 .06 07 O07 O07 52 oa oa 3 2 S A 54 2 .2 a2 2 ee -56 aD ail aD aT an 58 .0 .O .O .O .O 'MITHSONIAN TABLES 320 TABLES 318 AND 319 RADIATION EMISSIVITIES TABLE 318.— Relative Emissive Powers for Total Radiation Emissive power of black body = 1._ Receiving surface platinum black at 25°C; oxidized surfaces oxidized at 600 + °C. Randolph and Overholzer, Phys. Review, 2, p. 144, 1913. Temperature, Deg. C Platinum (1) Oxidized zinc Oxidized aluminum Calorized copper, oxidized Cast iron Oxidized nickel Oxidized monel Calorized steel, oxidized Oxidized copper Q@xidizedbrassi,seee oe Ociieioe soe Oxidized lead Oxidized cast iron Oxidized steel Black body HOO0000000000 Remark: For radiation properties of bodies at temperatures so low that the radiations of wave length greater than 204 or thereabouts are important, doubt must exist because of the possible and perhaps probable lack of blackness of the receiving body to radiations of those wave lengths or greater. For instance, see Tables 455 and 460 for the transparency of soot. TABLE 319.—Enmissivities of Metals and Oxides Emissivities for radiation of wave-length 0.55 and 0.65 uw. Burgess and Waltenberg, Bul. Bureau of Standards, II, 501, 1914. In the solid state practically all the metals examined appear to have a negligible or very small temperature coeffi- cient of emission for AX = 0.55 and 0.65 sz within the temperature range 20° C to melting point. Nickel oxide has a well-defined negative coefficient, at least to the melting point. There is a discontinuity in emissivity, for X = 0.65 uw at the melting point for some but not all the metals and oxides. This effect is most marked for gold, copper, and silver, and is appreciable for platinum and palladium. Palladium, in addition, possesses for radiation a property analogous to suffusion, in that the value of emissivity (A = 0.65 4) natural to the liquid state may persist for a time after solidification of the metal. The Violle unit of light does not appear to define a constant standard. Article con- tains bibliography. Metals €v, 0.55 psolid.... 0.55 @ liquid.. 0.65 mw solid... liquid... Metals eA, 0.55 m solid... : ; : ; é 0.77 liquid... | 0.65 m solid... j : ‘ .61 : 2 ; ‘ ; 0.54 liquid... ©. 40 : ‘ 61 : °.39 0.34 Oxides: 0.65 uw NiO | Co304] FesOs |MnzO4} TiOz | ThOz | Y20O3 | BeO Cr203 | UsCs- e), solid ‘ : . 6; — -52 ; : m2 : “ 0.60 | 0.30 — |-.0.3r SMITHSONIAN TABLES. TABLE 320 321 SOME INTRINSIC PROPERTIES OF TUNGSTEN (Jones, Langmuir, Gen. Electr. Rev., July-August, 1927 ) Power . Vapor Thermal : Resis- | radi- Bright- Ef- | Electron | Evapora- | pressure P abst expan- ule eee ° tivity | ated NESS) | 222 | emission tion SDSS sion [°K. f 7 ciency p baryes | Sivity ‘ Y pExXnLo! W int. cand./ ital black in cal./g- cal-10-2 ohm.cm| watts/ | 1” yan fia) Si LOB |X LOR |e ehORnes eae = 1|Per cent Jatom./°C] ‘atom cm? | a lpe M | > | 2 y ly at 293° amp./cm? | g/cm? sec. | dynes/cm? 300 5.65 |3 X 10% .O17 .003 6.0 I2 400 8.06 |2 X 10-3 | -024 -044 6.0 18 500 | 10.56 |I X 10% .032 .086 6.1 24 600 | 13.23 -030 -043 -130 6.1 30 700 | 16.09 .076 -057 -175 6.2 36 800 | 19.00 .169 | .072 .222 6.2 42 900 | 21.04 -322 .088 -270 6.3 48 1 n M n P n 1000 | 24.93 EOO2 |e tie LOM i703) || t-O'7n——L5a 05.320 —3 4) |. OS) — 20) .105 -320 6.4 54 II00 | 27.94 1.027) 1 >< 10-5 | 15.6 | 1.52 —13 | 2.17 —30 | 1.22 —25 -124 -371 6.4 60 1200 | 30.08 1.66 | 6 X 10-3 | 14.2 | 9.73 —I2 | 3.21 —27 | 1.87 —22 -141 -424 6.5 66 1300 | 34.08 2.57 3 X 10-2 | 13.1 | 3.2t —IO| 1.35 —24]| 8.18 —20 .158 -479 6.7 75 1400 | 37.19 3.83 | I X 107! | 12.0 | 6.62 —9] 2.51 —22 | 1.62 —17 -175 +535 6.8 82 1500 40.36 5.52 0.33 | II.I | 9.14 ——8| 2.37 —20]| 1.54 —15 .192 -593 7.0 89 1600 | 43.55 7.74 0.93 | 10.3 | 9.27 —7|1.25 —18 | 8.43 —14 .207 -652 FOE 96 1700 | 46.78 10.62 2.33 | 9.5 | 7.08 —6] 4.17 —17 | 2.82 —12 .222 -713 7.2 103 1800 | 50.05 14.19 5.12 | 8.8 | 4.47 —5 | 8.82 —16| 6.31 —II £237 Tens 7.4 IIo 1900 | 53.35 18.64 £0503) 8:2) | 2:28) — 4 AL —TAul fOr 6—0 .250 .839 7.6 118 2000 | 56.67 24.04 20.66 7.6 | 1.00 —3]| 1.76 —13] 1.33 —8 .263 -904 Her 125 2100 | 60.06 30.5 37-75 Tok I Bh 83 || AC) an | ey -274 -O71 7.8 133 2200 | 63.48 38.2 64.0 6.7 | 1.33 —2] 1.25 —11 | 9.88 —7 -285 1.039 8.0 I4I 2300 | 66.91 47.2 103.7 6.2 | 4.07 —2]| 8.00 —11 | 6.47 —6 -2905 I.109 8.2 149 2400 70.39 57-7 164.4 | 5.8 | 1.16 —I| 4.26 —I0O |] 3.52 —5 .304 1.180 8.3 157 2500 | 73.91 60.8 248 5.5 | 2.08 —1] 2.03 —9|]1.71 —4 —su2 1.253 8.4 166 2600 | 77.49 83.8 364 5.1 | 7.16 —1] 8.41 —9] 7.24 —4 .320 1.328 8.6 174 2700 | 81.04 99.6 532 4.8 | 1.63 0} 3.19 —8| 2.86 —3 R327 1.404 8.7 183 2800 | 84.70 | 117.6 732 4.5 | 3-54 0| 1.10 —7|9.84 —3 -334 1.479 8.9 192 2900 | 88.33 | 137.8 087 4.2) e723 One3t30)) —75|3:00i 5 —2 .340 1.561 9.0 201 3000 | 92.04 | 160.5 1326 4.0 | 1.42 +1] 9.95 —7| 9.20 —2 -346 1.642 9.2 210 3100 | 95.76 | 185.8 1745 3.7 | 2.64 +1 | 2.60 —6] 2.50 —1 -352 1.724 9.4 219 3200 | 90.54 | 214.0 2252 3.5 | 4.78 +1 | 6.38 —6]| 6.13 —I -357 1.808 9.5 228 3300 | 103.3 245.4 2803 3.3 | 8.44 +1 | 1.56 —5 | 1.51 oO .362 1.893 9.6 238 3400 | 107.2 280.0 3660 3.1 | r.42 —--2)\\ 3°47, —5 | 3.45 oO -366 1.980 9.8 248 3500 | III.1 318.0 4540 2.9 | 2.33 +2] 7.54 —5 | 7-52 ° -370 2.068 9.9 258 3600 | II5.0 360.0 5530 I 2:86 0373) 2) |p — Au rss I -374 2.158 10.1 268 3655 | 117.1 382.6 6163 I 2s Ae7Ole =1-2) (228.0 —A" |Pais3 Tals 70 2.200 10.2 273 ITHSONIAN TABLES 322 TABLES 321-323 TABLE 321.—Spectrum Emissivity of Tungsten (Percentage) Weniger and Pfund (Phys. Rev., 14, 427, 1919) verified Drude’s formula for tungsten, 100 — Ry = e, = 3650 Vp/x, valid for \ > 2u, where R)\ = reflectivity, \, the wave length in u, p, the specific resistance at the temperature considered. The following u.v. data is from Hulburt (Astrophys. Journ. 45, 149, 1917, via Forsythe, Christison, Gen. Electr. Rev., p. 622, 1929), from which the data for 0.2 to 4.24, 2800° are taken. TABLE 322.—Temperature Scale for Tungsten Hyde, Cady, Forsythe, Journ. Franklin Inst. 181, 418, 1916. See also Phys. Rev. 10,395, 1917. The color temperature = temperature of black body at which its color matches the given radiation. Color Black-body True True _True= temperature temperature temperature temperature brightness 1763°K. 1627°K. 1729°K. 1700° 100° IQI7 1753 1875 1800 115 2025 1840 1976 1900 128 2109 1909 2056 2000 142 2179 1967 2125 2100 158 2237 2017 2184 2200 175 2290 2062 2238 2300 I9I 2338 2102 2286 2400 208 2383 ' 2140 2332 ae ae 2425 2174 2373 OO ON AUHW ND ~ TABLE 323.—Radiation Characteristics of Tungsten (Forsythe, Worthing, Astrophys. Journ., 61, 146, 1925.) Emissivity Temperature °K Average Color Brightness enone 0.665u Color Radiation 0.6654 0.467" 0.466 0.498 et eyhs ait are alas Ae .456 .486 0.464 0.396 966 1006 581 -445 -476 -457 -383 1420 1517 991 -435 -469 -452 -370 1857 2033 1428 -425 -462 -446 -356 2274 2557 1859 415 -455 -440 343 2673 3094 2286 (.405) (.449) (.434) (.329) 3053 (3646) | (2704) SMITHSONIAN TABLES TABLES 324-327 323 TABLE 324.—Radiation and Other Properties of Tantalum (Worthing, Phys. Rev., 28, 190, 1926.) Resis- tivity Radi peice, adia- tion Tdn fol att ATLIS= Radiation eee Wert/ sivity Emissivity Temperature Bright- 3) mite Pe ce een ee ete CO 00 00 CO COCO OO. ere OLS ORONO! Ole eer = TABLE 325.—Radiation and Other Properties of Molybdenum (Worthing, Phys. Rev., 28, 190, 1926.) Resis- Emissivity Temperature fae Brighness a Luminous normally |. A efficiency Bright- 5 : candles/ ane lumens/ ness : cm? erie 0.0001] 0.55 .089 3.18 -765 6.30 4.13 Tels 15.9 19.2 48.5 30.7 123) 47.0 270 69.5 540 98 18.4 730 116 DOL TABLE 326.—Relation between Brightness Temperature and Color Temperature for Various Substances Corresponding color temperature for— Brightness temperature | Untreated Nernst Platinum glower Osmium Tantalum | Tungsten TABLE 327.—Color Minus Brightness Temperature for Carbon (Hyde, Cady, Forsythe, Phys. Rev. 10, 395, 1917.) Brightness temp. °K..... 1600° | 1700° | 1800° | 1g00° | 2000° | 2100° Color —brightness....... 7 I2 16 22 28 SMITHSONIAN TABLES 324 TABLES 328-330 TABLE 328.—Percentage Emissivities of Metals and Oxides Emissivity of black body taken as 100 True temperature C, 60 FeO.40 Fe2O3 = Fe heated Platinum: True temp. C...... 750 | 1000 1600 | 1700 App.* temp. C..... — — _— 486 780 930 | 1005 Total emiss. Pt.....} 3. : : 6.05} 7.0) | Su01 ||| ton) ||r2.4 D5 5) | LOeo) | an7ze5: Tungsten: True temp. K (abs.)....... 200 | 600] I000 | 1400 | 1800 | 2200 | 2600 | 3000 | 3400 | 3800 4 51.8 | 50.8] 49.8 | 48.9 | 47.9 | 47.0 | 46.0 | 45.0 | 44.1 — 4 47.2| 46.3 | 45.3 | 44-3 | 43-3 | 42-4 | 41-4 |] 40.4 |] 390-5] 4 * As observed with total radiation pyrometer sighted on the platinum. References: (1) Burgess and Foote, Bul. Bureau of Standards, 12, 83, 1915; (2) Burgess and Foote, Joc. cit. II, 41, 1914; (3) Foote, loc. cit. 11, 607, 1914; (4) Worthing, Phys. Rev. 10, 377, 1917. TABLE 329.—Emissivities, Metals (Black body — 1) (Worthing, Phys. Rev., 28, 174, 1926.) t°C 0.460u 0.535u 0.665u TKS 0.460u 0.535u 0.665u eleUvonetoratetetelc 20 0.635 0.352 0.062 Bie ieee eich Neel ve OLO3 21 OLA A Om Oa © te 245 WARES 3758 S200 —LO SO ate seycere Bas Chey Siena. 4 Om Ul SLAOOU vs bron toaiae setters 442 5 Avra fees eeeysl So ale(ianaie Sao Umeha REALS Se elt, Mei ne SOO “cc ‘antalutctates errs Platinum |0.665 |1100°K. 0.292| 1300° 0.297 | 1500° 0.302 | 1700° 0.307 | 1900° 0.312 463 [500° .370'| T7007 .381 | £900" 9.302 Total radiation = C’T” watt/cm’, nichrome values poor. Suydam, Phys. Rev., 5, 497, I915. Ag 610°— Pt 640°— Ni 463°- Fe 700°— Nichrome 325°— 980°K. 1150°K. 1280°K. 1300°K. 13 TO ge (Cl 2.) X< iO Dis xox 2 TO 1074 BP xeon! 1S) oe LOs MAST 5.0 4.65 5.55 4.1 Specific values are given in this paper for various temperatures of both radiator and absorber. Also for electrical resistances. TABLE 330.—Total Radiation from Bare and Soot-Covered Nickel (Watts/cm?) (Barnes, Phys. Rev., 34, 1026, 1929.) °K: 400 500 600 700 800 900 I000 1200 £1400 Soot-covered Ni..........0.096 0.28 0.59 1.87 3 B ABE Accs Polished! Na initial heat. 5. <0092) 4032) 2079) 5-166) 1-30, 1-55 9-91 2°17, 4.49 sé 4c after above.... .0066 .023 .058 .123 .24 .44 .76 2.04 4.49 SMITHSONIAN TABLES TABLES 331 AND 332 325 COGLING BY RADIATION AND CONVECTION TABLE 331.—At Ordinary Pressures TABLE 332.— At Different Pressures According to McFarlane* the rate of loss of heat by a sphere Experiments made by J. P. Nicol in Tait’s Labo- placed in the centre of a spherical enclosure which has a ratory show the effect of pressure of the en- blackened surface, and is kept at a constant temperature of closed air on the rate of loss of heat. In this about 14° C, can be expressed by the equations case the air was dry and the enclosure kept at about 8° C. € = .000238 + 3.06 X to—%t — 2.6 X 10-872, whe the surface of the sphere is blackened, or Polished surface. Blackened surface. @ = .000168 -+ 1.98 X 10-64 — 1.7 X 10—8/2, whe the surface is that of polished copper. In these equa- et et tions: ¢ is the amount of heat lost in c. g.s. units, that is, the cuantity of heat, small calories, radiated per second per square centimeter of surface of the sphere, per degree differ- ence of temperature #, and ¢ is the difference of temperature between the sphere and the enclosure. The medium through ; .00987 61.2 .01746 which the heat passed was moist air. The following table FL .00862 50.2 .O1 360 gives the results. : .007 36 41.6 .01078 .00628 34.4 .00860 00562 : .00640 00438 : .00455 .00378 - .00278 - -O0O2TO ad PRESSURE 76 CMs. OF MERCURY. Differ- Value o: e. ence of | tempera- Ratio. ture t Polished surface. | Blackened surface. 000178 0002 52 PRESSURE 10.2 RCURY. .000186 .000266 O FIO 67.8 01298 .O1158 .01048 .00898 .00791 .00490 00492 61.1 00433 55 00383 .000193 .000279 49.7 | .00340 | | .00020I .000289 44.9 .00302 .00020 .000298 7 7 40.8 00268 pA RUM nOnnun 00021 2 .000306 -000217 | -000 313 PRESSURE 1 CM. OF MERCURY. -00C22C -000319 | OV nN .o1 182 .O1074 01003 .007 26 .00639 .00 569 .00446 00391 .00388 00355 00256 00219 00157 .OO1 24 .000223 .000323 .00022 000326 -000226 000328 NNWoOAUIN SE U5EN NM OMUN NUN 000220 000328 * * Proc. Roy. Soc.” 1872. t “ Proc. Roy. Soc.’’? Edinb. 1869. See also Compan, Annal. de chi. et phys. 26, p. 526. SMITHSONIAN TABLES 326 TABLES 333 AND 334 COOLING BY RADIATION AND CONVECTION TABLE 333.—Cooling of Platinum Wire in Copper Envelope Bottomley gives for the radiation of a bright platinum wire to a copper envelope when the space between is at the highest vacuum attainable the following numbers : — t= 408° C, ef = 378.8 X 10~4, temperature of enclosure 16° C. ss ss D7 IG. It was found at this degree of exhaustion that considerable relative change of the vacuum produced very small change of the radiating power. The curve of relation between degree of vacuum and radiation becomes asymp- totic for high exhaustions. The following table illustrates the variation of radiation with pressure of air in 2 C050 Cr eh— 720 ten Ome enclosure. Temp. of enclosure 179 C, ¢= 505° C. Temp. of enclosure 16° C, ¢= 408° C. Pressure in mm et Pressure in mm et 740. 8137.0 X 10-4 0.094 1688.0 X 10~# 440. I40. 42. 4. 0.444 .070 7971.0 “ 053 7875-0 7591.0 “ “ee “ 5O3 a 013 .0046 00052 .OOOTg 1255-08 oe 1126.0 920.4 831.4 767-4 740.4 “ee 034 7. Lowest reached .O12 but not measured .005 1 .00007 726.1 TABLE 334.—Effect of Pressure on Loss of Heat at Different Temperatures The temperature of the enclosure was about 15° C. The numbers give the total radiation in therms per square cen- timeter per second. Pressure in mm Temp. of wire in C° About O.I 77 0.025 100° | 0.01 0.005 200 . : ‘ .02 0055 300 . : : -O4 -O105 400 : : : .07 .025 509 : : 613 .055 600 : : 23 ag, 700 .37 24 Soo .56 .40 goo : - 61 Nore. — An interesting example (because of its practical importance in electric light- | ing) of the effect of difference of surface condition on the radiation of heat is given on the authority of Mr. Evans and himself in Bottomley’s paper. The energy required to keep up a certain degree of incandescence in a lamp when the filament is dull black and when it is “flashed ” with coating of hard bright carbon, was found to be as follows : — Dull black filament, 57.9 watts. Bright “ ge 39-8 watts. SMITHSONIAN TABLES. TABLES 335 AND 336 327 TABLE 335.—Conduction of Heat across Air Spaces (Ordinary Temperatures) Loss of heat by air from surfaces takes place by radiation (dependent upon radiating power of surface; for small temperature differences proportional to temperature difference; follows Stefan-Boltzmann formula, see p. 313), conduction, and convection. The two latter are generally inextricably mixed. For horizontal air spaces, upper surface warm, the loss is all radiation and conduction; with warm lower surface the loss is greater than for similar vertical space. Vertical spaces: The following table shows that for spaces of less than 1 cm width the loss is nearly proportional] to the space width, when the radiation is allowed for; for greater widths the increase is less rapid, then reaches a maxi- mum, and for yet greater widths is slightly less. The following table is from Dickinson and van Dusen, A. S. Refrigerat- ing Engineers J. 3, 1916. HEAT CONDUCTION AND THERMAL RESISTANCES, RADIATION ELIMINATED, AIR SPACE 20 CM HIGH Heat conduction. Thermal resistance. Cal./hour/cm?2/° C, Same units. Temperature difference. Temperature difference. Variation with height of air space: Max. thermal resistance = 4.0 at 1.4 cm air space, 10 cm high; 6.0 at 1.6 cm, 20 cm high; 8.9 at 2.5 cm, 60 cm high. TABLE 336.—Convection of Heat in Air at Ordinary Temperatures In very narrow layers of air between vertical surfaces at different temperatures the convection currents, in the main, flow up one side and down the other, with eddyless (stream-line) motion. It follows that these currents trans- port heat to or from the surfaces only when they turn and flow horizontally, from which fact it follows, in turn, that the convective heat transfer is independent of the height of the surface. It is, according to the laws of eddyless flow, proportional to the square of the temperature difference, and to the cube of the distance between the surfaces. As the flow becomes more rapid (e.g., for a 20° difference and a distance of 1.2 cm) turbulence enters, and the above Bann begin to change. For the dimensions tested, convection in horizontal layers was a little over twice that in vertical. Taken from White, Physical Review, 10, 743, 1917. Heat Transfer, in the Usual C.G.S. Unit, i.e., Calories per Second per Degree of Thermal Head per Square Cm of Flat Surface, at 22.8° Mean Temperature. Wh re two values are given, they show the range among determinations with different methods of getting the tem- perature of the outer plate. It will be seen that the value of the convection is practically unaffected by this difference of method. 8 mm gap. 12 mm gap. 24 mm gap. Thermal head. Total. Convection. Convection Total. Convection. .000 065 ao ° | 2 J .000 OOT HO .000 090 .000 003 .000 106 000 O40 003 vy .000 126 .000 060 Fwy .000 007 SMITHSONIAN TABLES. 328 TABLE 337 CONVECTION AND CONDUCTION OF HEAT BY GASES AT HIGH TEMPERATURES * The loss of heat from wires at high temperatures occurs as if by conduction across a thin film of stationary gas adhering to the wire (vertical and horizontal losses very similar). Thickness of film is apparently independent of temperature of wire, but probably increases with the temperature of the gas and varies with the diameter of the wire according to the formula b-log)/a = 2B, where B = constant for any gas, b = diameter of film, a, of wire. The rate of convection (conduction) of heat is the product of two factors, one the shape factor, s, involving only a and B, the other a function @ of the heat conductivity of the gas. If W = the energy loss in watts/cm, then W = s(¢2 — $1). s may be found from the relation =e Ss = 5) b=4.19 [7 kdt, where & is the heat conductivity of the gas at temperature T in calories/em °C. dz is taken at the temperature T2 of the wire, di at that of the atmosphere. The following may be taken as the conductivities of the corresponding gases at high temperatures: For hydrogen Tape Pagshelsia ati k= 28X 1O°V TI (1 + .0002T)/(t + 77T7)} Bh yee k=4.6X 10 *VT I(r + .0002T)/(1 + 124T-)} mercury vapor........ k=2.4X TONED (x fe 960T-1)}. To obtain the heat loss: B may be assumed proportional to the viscosity of the gas and inversely proportional to the density. For air (see Table 338(6)) B may be taken as 0.43 cm; for He, 3.05 cm; for Hg vapor as 0.078. Obtain s from section (a) below from a/B; then from section (5) obtain ¢2 and ¢1 for the proper temperatures; the loss will be s(@2 — di) in watts/cm. (a) s AS Function oF a/B HHHHHHOOOOO ononounounonod e©o000O0OnN 0000 O00 WHIAIDAUUH OnONdDNUN DON ONO NIN OAUUNEPHWNHNH UbBBRWWNHNHHHOO H (b) TABLE oF ¢@ IN WATTS PER Cm AS FUNCTION OF ABSOLUTE TEMP. (°K.) * Langmuir Physical Review, 34, p. 401, 1912. SMITHSONIAN TABLES. TABLE 338 329 HEAT LOSSES FROM INCANDESCENT FILAMENTS (a) Wires oF PLATINUM SPONGE SERVED AS RapIATORS TO ROOM-TEMPERATURE SUR- ROUNDINGS, HARTMAN, PHYSICAL REVIEW, 7, Pp. 431, I9Q16 (A) Observed heat losses in watts per cm. Diameter Absolute temperatures. 1400° | 1500° | 1600° | 1700° 6.18 | 7.70 . 12315 4.29 | 5-33 . 8.25 3.23 | 3-91 : 5-72 2.54 | 3.04 : 4.32 radiation, watts per cm (A-C). T.23 BSN |e ces Bere ce ssae |e .00 Tel) O30) |\exg2 BAS ali cree y70 |inee .08 I.05 22 ena SS 7A ake OMe .67 0.89 FOZ) |ieln5 2 Sul Scan pe -47 (C) Computed radiation, watts per cm, 0 = 5.61 X 10 12.* B20 | c7o4) 2520) 4.47.1 | 407 | Onr6) Il 7078) LosLs 7S LOO etes3 |) 2k |) 204) Su-74ei| e4o4: 6.17 PAS On7ie etOLe iene son |r. OO) 2a450eseuny 4.05 N34) MONSON On7 Cul Oey) lke Gu |eLe7smiNeee4: 2 (D) Conduction loss by silver leads, watts per cm. 0.61 | 0.75 | 0.88 | I.00 | 1.07 0.28 | 0.35 | 0.43 | 0.48 | 0.55 ||. 0.57 0.08 || ©.09) || O- £4 || (0.12) | (0.14 | 0.15 Convection loss by air, watts per cm. 0.45) || 0: ‘ 0.70 | 0.67 | 0.57 | 0.59 | 0.69 0.62 : ; 0.87 | 0.92 | 0.89 | 0.91 | 0.93 .07 0.64 | o. ; OnOA | SiOs ate aen eet | |er 25 . 29 * This value is lower than the presently (1919) accepted value of 5.72. (b) Wires OF BriGHT PLATINUM 40-50 CM LONG SERVED AS RADIATORS TO SURROUNDINGS AT 300° K. LAncmutr, PHYSICAL REVIEW, 34, Pp. 401, 1912 Observed energy losses in watts per cm. Diameter wire, Absolute temperatures. cm. ° .02508 .01262 . 00691 . 00404 NNKRWUN Energy radiated in watts per cm.* .049 0.137 -323 .024 0.067 -159 .O12 0.034 .080 - 007 0.019 -O44 . 004 0.oIl .026 “Convection” losses in watts per cm. 0.85 0.66 0.52 0.47 0.41 Thickness of theoretical conducting air film. .0510 .02508 .01262 . 00691 . 00404 Means. WNHwWLWwWbd H~I HNO CO * Computed with a = 5.32, black-body efficiency of platinum as follows (Lummer and Kurlbaum): 0.039; 654°, 0.060; 795°, 0.075; 1108°, 0.112; 1481°, 0.1543; 1761° K., 0.180. t Weighted mean. ‘ SMITHSONIAN TABLES. 330 TABLES 339 AND 340 THE SENSITIVITY OF THE EYE Definitions: A meter-candle is the intensity of illumination due to a standard candle at a meter distance. The millilambert (0.oor lambert) measures the brightness of a perfectly diffusing (according to Lambert’s cosine law) surface diffusing .oor lumen/cm2. A brightness of 10 meter-candles equals 1 millilambert. o.oor ml corresponds roughly to night exteriors, 0.1, to night interiors, 10 ml to daylight interiors and tooo, to daylight exteriors. A bright- ness of 100,000 meter-candles is about that of a horizontal plane for summer day with sun in zenith, 500, on a cloudy day, 4, rst magnitude stars just visible, 0.2, full moon in zenith, .oor, by starlight; in winter the intensity at noon may drop about 4. TABLE 339.—Spectral Variation of Sensitiveness as a Function of Intensity Radiation is easily visible to most eyes from 0.330 m (violet) to 0.770 uw (red). At low intensities near threshold values (gray, rod vision) the maximum of spectral sensibility les near 9.503 m (green) for 90% of all persons. At higher intensities, after the establishment of cone vision, the max. shifts as far as 0.560 uw. See Table 346 for more accurate values of sensitiveness after this shift has been accomplished. The ratio of optical sensation to the intensity of energy increases with increasing energy more rapidly for the red than for the shorter wave-lengths (Purkinje phenomenon); i.e., a red light of equal intensity to the eye with a green one will appear darker as the intensities are equally lowered. This phenomenon disappears above a certain intensity (above ro millilamberts). Table due to Nutting, Bulletin Bureau of Standards. The intensity is given for the spectrum at 0.535 (green). Intensity - (meter-candles) = feels 38 i 6) ; i : aaa 590-4 Ratio to preceding step = a ; 4 i Wave-length, A. o -430 Me .450 47° 490 5°05 520 535 -555 575 599 605 625 .650 .670 \, maximum sensitiveness GEO} O FORGO O10) OROFOROS) 90990000099H09000 o000000000H 9000 ©C000000000HDOO ©0900000000HGONOO 999009990009000 TABLE 340.—Threshold Sensibility as Related to Field Brightness The eye perceives with ease and comfort a billion-fold range of intensities. The following data were obtained with the eye fully adapted to the sensitizing field, B, the field flashed off, and immediately the intensity, T, of a test spot (angular size at eye about 5°) adjusted to be just visible. This table gives a measure of the brightness, 7, necessary to just pick up objects when the eye is adapted to a brightness, B. Intensities are indicated log intensities in milli- lamberts. Blanchard, Physical Review, 11, p. 81, 1918. +2.0 1+3.0 7|—4.17| —3.30] —2.59]—2.02 —o.75|+0. 28 Las oO. .13} .068 | .050 | .026 | .c096 .0018 | .corg .|—6.70] —6.38]—5s. ‘ —4.23] —3.46| —2.70]—2.18 ’ — Log T, green —6.42|—6.20]—5. .00| —4.23| —3.39] —2.60] —2.08 Log T, yellow 4.61] —4.03| —3.33|—2-.57]—1. Log T, red A. .00| —3.47| —2.96| —2.43]—1. SMITHSONIAN TABLES, TABLES 341-344 331 THE SENSIBILITY OF THE EYE TABLE 341.—Heterochromatic Threshold Sensibility The following table shows the decrease in sensitiveness of the eye for comparing intensities of different colors. The numbers in the body of the table correspond to the line marked 7/B of Table 340. The intensity of the field was probably between 10 and 100 millilamberts (25 photons). Comparison color. 0.693 M | 0.640 M | 0.575 M | 0.505 M | 0.475 uM | 0.430 Standard color: red yellow TABLE 342.—Contrast or Photometric Sensibility For the following table the eye was adapted to a field of 0.1 millilambert and the sensitizing field flashed off. A neutral gray test spot (angular size at eye, 5 X 2.5°) the two halves of which had the contrast indicated (3 transparent, 3 covered with neutral screen of transparency = contrast indicated) was then observed and the brightness of the transparent part measured necessary to just perceive the contrast after the lapse of the various times. One eye only used, natural pupil. Blanchard, Physical Review, 11, p. 88, 1918. Values are log brightness of brighter field in millilamberts. Time in seconds. | Hi wWW Ww TABLE. 343.—Glare Sensibility When an eye is adapted to a certain brightness and is then exposed suddenly to a much greater brightness, the latter may be called glaring if uncomfortable and instinctively avoided. Observers naturally differ widely. The data are the means of three observers, and are log brightnesses in millilamberts. The glare intensity may be taken as roughly 700 times the cube root of the field intensity in millilamberts. Angle of glare spot, 4°. Blanchard, Physical Review, oc. cit. Log. glare... | TABLE 344.— Rate of Adaptation of Sensibility This table furnishes a measure of the rate of increase of sensibility after going from light into darkness, and the values were obtained immediately from the instant of turning off the sensitizing field. Both eyes were used, natural pupil, angular size of test spot, 4.9°, viewed at 35 cm. Blanchard, Joc. cit. Retinal light persists only 10 to 20 m when one has been recently in darkness, then in a dimly lighted room; it persists fully an hour when a subject has been in bright sunlight for some time. A person who has worked much in the dark “gets his eyes” quicker than one who has not, but his final sensitiveness may be no greater. Logarithmic thresholds in millilamberts after Sensitizing field. osec. | 1 sec. | 2 sec. | 5 sec. |10 sec. |20 sec. | 40 sec. }60 sec. | 5 min. |3omin. White, o. os iS | ty CO | ° a | Ds * 5 : “ 5 : —4.82]—5. Io. : : : 3. 3.! .94] —4.31| —4. I0o. ; ; , ; ‘ . 88] —3. 20] —3. Blue o. i ; : : : .53| —5. 68] —s. Green o. ! F a ; Le ie .43/—5. Yellow o. , 3 E : : ; .02]—5. Redo. : ; : : . 65 .73|—3- | Anan aan HERA An ALRUUH | On oD | | OW On INU D NO OW An SMITHSONIAN TABLES. 13 332 TABLES 345-347 VARIOUS PROPERTIES OF THE EYE TABLE 345.—Apparent Diameter of Pupil and Flux Density at Retina Flashlight measures of the pupil (both eyes open) viewed through the eye lens and adapted to various field intensities. For eye accommodated to 25 cm, ratio apparent to true pupil, 1.02, for the unaccom- modated eye, 1.14. The pupil size varies considerably with the individual. It is greater with one eye closed; e.g., it was found to be for 0.01 millilambert, 6.7 and 7.2 mm; for 0.6 ml, 5.3 and 6.5; for 6.3 ml, 4.1 and 5.7; for 12.6 ml, 4.1 and 5.7 mm for both and one eye open respectively for a certain indi- vidual. At the extreme intensities the two values approach each other. The ratio of the extreme pupil openings is about 1/16, whereas the light intensities investigated vary over 1,000,000-fold (Blanchard and Reeves, partly unpublished data), Field (1.14/1.02) Effective Flux at retina, millilamberts Observed x Obs 0.00001 mm area lumens per mm? .96 mm 64 mm? Be Ox Soil 57 JO Ome .28 42 5) IOS -48 16 ; mle OES a 4.3 aoe LORS DoOANOOO TABLE 346.—Relative Visibility of Radiation (International Standard—Geneva, 1924) (See Gibson, Tyndall, Bur. Standards Sci. Paper 475, 1923; Judd, Journ. Opt. Soc. Amer., 21, 267, 1931.) This table gives the relation between luminous sensation (light) and radiant energy. Data determined for intensities above Purkinje effect. See Table 339. Ratio of light unit (lumens) to energy unit (watt) at .554, 0.00162 (Ives, Coblentz, Kingsbury). +710 .0021 5 .0015 *720 .O0I105 5 .00074 -730 .00052 5 .00036 740 .00025 5 .00017 -750 .00012 5 .00008 -760 .00006 5 .00004 +770 .00003 TABLE 347.—Miscellaneous Eye Data Light passing to the retina traverses in succession (a) front surface of the cornea (curvature, 7.9 mm); (b) cornea (equivalent water path for energy absorption, .o6 cm); (c.) back surface cornea (curv., 7.9 mm); (d) aqueous humour (equiv. H20, .34 cm, m = 1.337); (e) front surface lens (c, ro mm); (f) lens (equiv. H20, .42 cm, m = 1.445); (g) back surface lens (c.,6 mm); (#) vitreous humour (equiv. H2O, 1.46 cm, m = 1.337). An equivalent simple lens has its principal point 2.34 mm behind (a), nodal point 0.48 mm in front of (g), posterior principal focus 22.73 mm behind (a), anterior principal focus 12.83 mm. in front of (a), curvature, 5.125 mm. At the rear surface of the retina (.15 mm thick) are the rods (30 X 2) and cones (to (6 outside fovea) w long). Rods are more numerous, 2 to 3 between 2 cones, over 3,000,000 cones ineye. Macula lutea, yellow spot, on temporal side, 4 mm from center of retina, long axis 2mm. Central depression, fovea centralis, .3 mm diameter, 7000 cones alone present, 6 X 2 or 3m. In region of dis- tinct vision (fovea centralis) smallest angle at which two objects are seen separate 1s 50” to 70” = 3.65 to 5.14u at retina; 50 cones in roo here; 4 between centers, 344 to cone, ru to interval. Distance apart for separation greatet as depart from fovea. No vision in blind spot, nasal side, 2.5 mm from center of eye, I5 mm in diam. Persistence of vision as related to color (Allen, Phys. Rev. 11, 257, 1900) and intensity (Porter, Pr. Roy. Soc. 70, 313, 1912) is measured by increasing speed of rotating sector until flicker disappears: for color, .4M, .031 S€C.; .45u, .020 SEC.; .5[l, O15 SEC.3 .5 7M, .OT2 Sec.; .68u, .o14 sec.; .76u4, .o18 sec.; for intensity, .o6 meter-candle, .028 sec.; 1 mc, .020 Sec.; 6 MC, .O14 SeC.; IOO MC, .OIO SEC; 142 MC., .007 SEC. - ; ; Sensibility to small differences in color has two pronounced maxima (in yellow and_ green) and two slight ones (extreme blie, extreme red). The sensibility to small differences in intensity is nearly independent of the intensity (Fechner’s law) as indicated by the following data due to KGnig: I/Io I,000,000 | 100,000 | 10,000 | 1000 SMITHSONIAN TABLES. TABLE 348 333 PHOTOMETRIC DEFINITIONS AND UNITS Radiant flux = © = rate of flow of radiation as energy, measured as ergs per second or watts. Luminous flux = F or ¥ = rate of flow of radiation measured according to power to produce visual sensation. Although strictly thus defined, for photometric purposes it may be regarded as an entity, since the rate of flow for such purposes is invariable. Unit is the /wmen, the flux emitted in a unit solid angle (steradian) by a point source of unit candle power. Visibility of radiation of wave-length \ = Ka = ratio of luminous to radiant flux for that A, = Fa/®a. Mechanical equivalent of light = ratio of /F for the \ of max. visibility expressed in ergs/sec /lumen or watts/lumen; it is the reciprocal of max. visibility. See p. 335. Luminosity at wave-length A = (Ka) (®a). Spectral luminosity curve expresses this as a func- tion of d and is different for various sources. Luminous efficiency = F/® expressed in lumens/ watt. Luminous intensity of (approximate) point source = I = solid-angle (w) density of luminous flux in direction considered = dF/dw, or F/w when the intensity is uniform. Unit, the candle. Illumination on surface = E = flux density on surface = dF/dS (S is surface area) = F/S when uniform. Units, meter-candle, foot-candle, phot, lux. Lux = one lumen per m2; phot one lumen per cm?. Brightness of a luminous surface may be expressed in two ways: (1) br = dI/dS. cos @ where @ is the angle between normal to surface and the line of sight; normal brightness when @ is zero. (2) br = dF/dS’ assuming that the surface is a perfect diffuser, obeying cos. law of emission or reflection. Unit, the lambert. Specific luminous radiation, E’ = luminous flux density emitted by a surface, or the flux emitted per unit of emissive area, expressed in lumens per cm?. For surfaces obeying Lambert’s cosine law, E’ = mby. The lambert, the cgs unit of brightness, is the brightness of a perfectly diffusing surface radiat- ing or reflecting one lumen per cm?. Equivalent to a perfectly diffusing surface with illumination of one phot. A perfectly diffusing surface emitting one lumen per ft? has a brightness of 1.076 millilamberts. Brightness in candles per cm? is reduced to lamberts by multiplying by 7. A uniform point source of one candle emits 47 lumens. One lumen is emitted by .07958 spherical candle power. One lumen emitted per {t? = 1.076 millilamberts (perfect diffusion). One spherical candle power emits 12.57 lumens. One lux = 1 lumen incident per m? = .ooor phot = .1 milliphot. One phot = x lumen incident per cm? = 10,000 lux = tooo milliphots. One milliphot = .oot phot = .g29 foot-candle. One foot-candle = 1 lumen incident per ft? = 1.076 milliphots = 10.76 lux. One lambert = 1 lumen emitted per cm? of a perfectly diffusing surface. One millilambert = .929 lumen emitted per ft? (perfect diffusion). One lambert = .3183 candle per cm? = 2.054 candles per in?. One candle per cm? = 3.1416 lamberts. One candle per in? = .4868 lambert = 486.8 millilamberts. Adapted from Reports of Committee on Nomenclature and Standards of Illuminating Engineer- ing Society. 1916 to 1918. SMITHSONIAN TABLES. TABLES 349-351 TABLE 349.—Photometric Standards 334 In Germany the Hefner lamp is most used; in England the Pentane lamp and sperm candles; in France the Carcel lamp is preferred; in America the Pentane and Hefner lamps are used to some extent, but candles are largely employed in gas photometry. For the photometry of electri¢ lamps, and in accurate photometric work, electric lamps, stand- ardized at a national standardizing institution, are employed. The “International candle” designates the value of the candle as maintained by co- operative effort between the national laboratories of England, France, and America; and the value of various photometric units in terms of this is given in the following table (Circular No. 15 of the Bureau of Standards). 1 International Candle =1 Pentane Candle. 1 International Candle =1 Bougie Decimale. 1 International Candle =1 American Candle. 1 International Candle = 1.11 Hefner Unit. 1 International Candle = 0.104 Carcel Unit. 1. Standard Pentane Lamp, burning pentane.......... ... 10.0 candles. 2. Standard Hefner Lamp, burning amyl acetate........ . 0.9 candles. 3. Standard Carcel Lamp, burning colza oil............ . 9.6 candles. 4. Standard English Sperm Candle, approximately........ 1.0 candles. TABLE 350,—The Waidner-Burgess Standard of Light The Waidner-Burgess standard light consists in immersing a hollow inclosure in a bath of molten platinum and observing the light from the inclosure during the period of freez- ing. The exceptionally pure Pt was in a thorium oxide crucible heated by an induction furnace. At all times before and after test the Pt was 99.997% pure. Reproducible to 0.1% the brightness is 58.84 International Candles per cm* (Wensel, Roeser, Barbrow, Caldwell, Bur. Standards Journ. Res., 6, 1103, 1931.) TABLE 351.—Intrinsic Brightness of Various Light Sources National Electric Ives & Luckiesh. Lamp Association. C. P. per Sq. In. of surface of light. Barrows. C. P. per 5q. In. of surface of light. C. P. per Sq. In. of surtace of light. P. perS Sin: of ea face of light. 600,000 - = 200,000 84,000 130. 10,000-50,000 = ss 5,000 = = 600,000 200,000 10,000-50,000 5,000 Sun at Zenith . Crater, carbon arc Open carbon arc Flaming arc Magnetite arc . . . ; . = Nernst Glower . : 800-1,000 Tungsten incandescent, 1.15 w. p.c: > 1,000 Tungsten incandescent, 1.25 Ww. p. c- 1,000 1,000 ‘ 875 Tantalum incandescent, 2.0 w. p. ¢. 75° 580 5 750 Graphitized carbon filament, 255 W.p. Cc. . : 625 750 : 625 Carbon incandescent, Zatsweiphic.) 9. 480 485 480 Carbon incandescent, 3.5 W.p.c. . 375 400 ; 375 Carbon incandescent, 4,0 .We)ps Cc. © 300 325 : - Inclosed carbon arc (d. c.) 100-500 - 100-500 4,000 6.2 = (115v.6 amp. d.c.) 3,010 (1.5 W.p.c.) 2,200 Acetylene flame (1 ft. burner) . dl 75-100 Acetylene flame (34 ft. burner) 2 - Welsbach mantle . = : | 20-25 Welsbach (mesh) . : = Cooper Hewitt mercury veper lamp 16.7 Kerosene flame , 4-8 Candle flame . 5 . . 3-4 Gas flame (fish tail) . ‘ . : 3-8 Frosted incandescent lamp. Moore carbon-dioxide tube lamp Inclosed carbon arc (a. c.) : ‘ =» - 53-0 33-0 31-9 56.0 14.9 g-0 a7 Taken from Data, 1911. SMITHSONIAN TABLES 75-200 75-100 20-50 17 3-8 3-4 3-8 2-5 0.3-1.75 TABLES 352-354 335 BRIGHTNESS OF BLACK BODY, CROVA WAVE-LENGTH. MECHANICAL EQUIVALENT OF LIGHT. LUMINOUS INTENSITY AND EFFICIENCY OF BLACK BODY The values of Z, the luminous intensity, are given in light watts/steroradian/cm? of radiating surface co r . woth . ' a . . = (1/7) nif V) Ey 4A, where } r 3s the visibility of radiation function. Mechanical equivalent. The unit of power is the watt; of lumininous flux, the lumen. The ratio of these two quan- tities for light of maximum visibility, \ = 0.556 mw, is the stimulus coetticient Vm; its reciprocal is the (least) mechanical equivalent of light, i.e., least since applicable to radiation of maximum visibility. A better term is ‘luminous equiva- lent of radiation ot maximum visibility.” One lumen =o.001406 watts (Hyde, Forsythe, Cady); or 1 watt of radia- tion of maximum visibility (A = 0.556 u) = 668 limens White light has sometimes bee : defined as that emitted by a black body at 6000° K. The Crova wave-length for a black body is that wave-length, X, at which the luminous intensity varies by the same fractional part that the total luminous intensity varies for the same change in temperature. ee i ’ W: es 7 i Treas: og Reeds Coan TABLE 353.—Luminous and Total Intensity and Equivalent of Light * Radiant Luminous Efficiency of Black Body * Bright- Crova Mech. ness, wave- equiv. candles length, watts per cm? per /. Radiant Total intensity | luminous oo T+ watt/cm? | efficiency. Luminous intensity L watt/cm? T, degrees absolute. .001478 .OOIT4QI . 001408 .001498 . 001407 -34 X 10° .45 X 10°23 .46 X I074 .88 X 102 .85 X Io 2 -34 X Io 4 7 32nG 10m .26 X 10 4 .69 X 101 -79 X 101 Ti Lon -29 .66 105) Oe LO .36 X 102 .26 XK 102 .03 X 102 -59 X 102 .84 X 10% NRA Rw aie 6 3 +3 si a “3 .O eek: 7 6 . 001406 .©0O1T 407 .001407 On Ou Ww CORWWHOALHRNHNODIAOKHUNOWONHA - 001502 .OOI5iI 90000000000000000000 HAOMMWBWO OHI NO DOH OD SPNDHHLUOR™TONOOWUNUNO ND HO DWHWE HAH OOMNW DN HNIW HOW ND HIRD HR H -OCT496 * Hyde, Forsythe, Cady, Phys. Rev. 13, p. 45, * Coblentz, Emerson, Bul. Bureau of Standards, 14, p. 255, IQIgQ. IQI7. Nore. — Minimum energy necessary to produce the sensation of light: Ives, 38 X 107%; Russell, 7.7 X 10719; Reeves, 19.5 X 1029; Buisson, 12.6 X 101° erg. sec. (Buisson, J. de Phys. 7, 68, 1917.) Color temperature (temp. black-body same color) 500 w. gas-filled lamp (22 1/w) 3082°k; 900 w. gas-filled movie lamp, 22.7 1/w, 3086°k, crater 65v. 10 amp. arc, solid carbon, 3780°k; cored carbon 3420°k. Priest, 1922. TABLE 354.—Color of Light Emitted by Various Sources * Color, Color, Source. per cent : Source. per cent white. white. Sunlight N-filled tungsten, 0.50 wpc Average clear sky N-filled tungsten, 0.35 wpc Standard candle Mercury vapor arc Hefner lamp Helium tube Pentane lamp Neon tube Tungsten glow lamp, 1.25 wpc..... Crater of carbon arc, 1.8 amp...... Carbon ,low lamp, 3.8 wpc........ Crater of carbon arc, 3.2 amp Nernst glower, 1.50 wpc Crater of carbon arc, 5.0 amp N-filled tungsten, 1.00 wpc Acetylene flame (flat) * Jones, L. A., Trans. Ill. Eng. Soc., Vol. 9 (1914). SMITHSONIAN TABLES. 336 TABLE 355 RELATIVE BLUE BRIGHTNESS, B, AND BRIGHTNESS IN CANDLES PER CM.’ C, OF SOME INCANDESCENT OXIDES AT VARIOUS RED (0.665,z) BRIGHTNESS TEMPERATURES, Sp Material Black body Tungsten Urania, gas air and oxy-gas... Ceria, pure: Oxy-gas eee yellowes 5 , brown: Oxides of Ce group: Oxy-gas. Neodymia: Oxy-gas Lanthana: ti Erbia: < Yttria, pure: Oxy-gas © 37 059e, pure: “ “ce 6“ Zirconia: Oxy-gas Thoria : " Alumina: Beryllia: Magnesia: Thoria 1% ceria: Oxy-gas... “cc “cc ‘ urania: trace urania: 1% neodymia: SS = eVinvoxides ce “ 6c oe Note.—1 microcalorie through 1 cm* at I m= 0.034 sperm calorie = 0.0385 Hefner unit (no diaphragm) = 0.043 Hefner unit (diaphragm 14 X50 mm). Coblentz, Bull. Bur. of Stds., 11, 87, 1914. SMITHSONIAN TABLES TABLES 356 EFFICIENCY OF VARIOUS ELECTRIC LIGHTS 337 Bryant and Hake, Eng. Exp. Station, Univ. of Ill. Regenerative d.-c., series arc Regenerative d.-c., multiple arc Magnetite d.-c., series arc Flame arc, d.-c., inclined electrodes Mercury.are, d.-c., multiple Flame arc, d.-c., inclined electrodes Flame arc, d.-c., vertical electrodes Luminous arc, d.-c., multiple Open arc, d.-c., series Magnetite arc, d.-c., series Flame arc, a.-c., vertical electrodes Flame arc, a.-c., inclined electrodes Open arc, d.-c., series Tungsten series Flame arc, a.-c., inclined electrodes Inclosed arc, d.-c., Series Luminous arc, d.-c., multiple Tungsten, multiple Nernst, a.-c., 3-glower Nernst, d.-c., 3-glower Inclosed arc, a.-c., series Inclosed arc, a.-c., series Tantalum, d.-c., multiple Tantalum, a.-c., multiple Carbon, 3.1 w. p. c., multiple Carbon, 3.5 w. p. c., series Carbon, 3.5 w. p. c., multiple Inclosed arc, d.-c., multiple Inclosed arc, d.-c., multiple Inclosed arc, a.-c., multiple Inclosed arc, a.-c., multiple - Terminal Watts. Lumens. Amperes. 385 605 528 55° 395 440 OP OOH O Dur AOOMNO Ain HO oO’ 9 9 eM o0o°o Kw-hours for 100,000 Lumen- hours. 33 5.18 7.16 6.37 15.92 7.16 7.16 9.85 9-55 11.15 8.75 8.75 I1.15 12.0 9-55 14.32 15.32 6 _ nN tN we AWD =m m0 NE ONO 4 BR WO td WWNHNNN I Total cost per 100,000 Lumen-hours at 10 cts. per Kw-hour. 0.339 0.527 0.729 Ives, Phys. Rev., V, p. 390, 1915 (see also VI, p. 332, 1915); computed assuming 1! lumen = 0.00159 watt. Open flame gas burner Petroleum lamp Acetylene Incandescent gas (low pressure) Incandescent gas (high pressure) Nernst lamp Moore nitrogen vacuum tube Tungsten incandescent (vacuum) Carbon arc, open arc Mazda, type C Mazda, type C Magnetite arc, series Glass mercury arc Quartz mercury arc Enclosed white flame carbon ‘ “c ““ “cc ‘ arc “ce Openiarces “* inclined oe ve “ “ Enclosed yellow flame carbon arc “e “ “ “i “ Open arc, “ g “cc “oc “cc “cc , inclined “ Carbon incandescent (treated filament) | 4-watts per mean hor. C. P. Commercial Rating. Bray 6’ high pressure 1.0 liters per hour .350 lumens per B., t. u. per hr. .575 lumens per B. t. u. per hr. | 220-v. 60-cycle, 113 ft. 1.25 watts per hor. C. P. g.6 amp. clear globe 500-watt multiple .7 w. p. c. 600 C. P. -20 amp. .5§ w. p. c. 6.6 amp. direct current 40-70 volt; 3.5 amperes 174-197 volt; 4.2 amperes Io ampere, A. C 6.5 ampere, D. C. 10 ampere, A. C, 10 ampere, D. C. 10 ampere, A. C. 6.5 ampere, D. C. 10 ampere, A. C. 10 ampere, D. C. SMITHSONIAN Tarnirs Lumens per Watt. av N Cnunkne _ AR Av CON RIOR ASH HOM umn PPWWN HW KHAN N HR Nab AE Luminous Watts Flux — Watts In- put or True Efficiency. 0.00035 .0004 .OOIT 0019 .0031 .0076 .008 3 0041 .013 O19 024 .031 034 .036 .067 042 057 .046 1044 .050 054 .066 .07 1 338 TABLES 357-359 TABLE 357.—Color Temperature, Brightness Temperature, and Brightness of Various Illuminants Brightness Source S (A = .665) c/cm?2 Gas flame Batswing Candle shape about 10 cm high Hefner as a whole Candle Sperm Paraffin Pentane 10-cp. std. Kerosene Flat wick 1.27 Round wick 1.51 4 w p. c. carbon 54.9 3.1 w p. c. treated carbon 70.6 2.5 wp. c. gem 78.1 2 w p. c. osmium 60.8 2 wp.c. tantalum 53.1 Acetylene as a whole One spot 6.69 Mees burner 10.8 1.25 w p. c. tungsten 125 ao w p. c. Nernst 258 un Outside atmosphere 224000 At earth’s surface 165000 TABLE 358.—Temperature, Efficiency, and Brightness of Vacuum Lamps Maximum Maximum temperature, brightness K. candles/cm? Lumens per watt 50-watt carbon 2115° 50-watt gem ‘ 2180 50-watt tantalum 2160 10-watt tungsten : 2355 25-watt tungsten ; 2450 40-watt tungsten 2460 60-watt tungsten : 2465 TABLE 359.—Temperature, Efficiency, and Brightness of Gas-Filled Tungsten Lamps Average Maximum color brightness of temperature, filament K. candles/cm?2 Maximum Lamp Lumens temperature, per watt Regular gas-filled lamps: BRO RAN gee Tua spleen eu aye 2685° 2670° 469 Bratey Melee teeel chavs ke caso ayaa eyercoets 4 2735 2705 563 TOO=Warttc..;., sat be veredoutcuctetrstos fe hemes 2760 2740 605 ZOOS WALEED Kanth sestetoneeierohors ete ales : 2840 2810 781 ZOOsWACl rete crsrereieceeno ec one clbuossutae ‘ 2870 2840 862 BOO=Waltrnrercserotetcnenedsnenedccsrote conelia: sete 2930 2920 IOI5 TOOO=WaAtE.,< cussclatte ee tebelowenelieaniane ene atk 2990 2080 1225 ZOOO= Watts arcpnrsithaienetous ere verdefolene folcels A 3020 3000 1350 Special lamps: 1000-watt stereopticon............ 3185 3175 2065 QOO=watl MOVICbee rie se cer sie ee ere a 3290 3220 2660 es Biel Qaaaes orokareihenstetsiers 9 aaah 3350 3300 3050 SA SR cd TR ore amuse 3350 3300 3050 Daylight lamps: e ZOO-“WAUE facta cee raciorsiersteas tetera cshoxtet 2860 HOO=WaALts hae tugs hel ole tints loaneeie sre 5 2960 Photographic: TE O=WAtU aac setese dic-o ghey Senctegans eterereca: ae 3065 D5 O0-WeacGanteyretetetsretonelohcueheter cic stedeKehone Sale 3105 ——— SMITHSONIAN TABLES TABLES 360-362 339 TABLE 360.—Energy Distribution for Some Tungsten Lamps (Taken from Forsythe, Christison, Gen. Electr. Rev., p. 662, 1929.) 500 w, 1000 hr. 500 w, 100 hr. 900 w movie tungsten arc* oF. milli- o milli- oF milli- of milli- ne watts | Ao watts ae watts {0 watts 0.31—-0.29u O0.0II 0.00044} 0.015 0.006 0.030 0.0028 0.095 0.0108 below 0.325 032 .0013 042 .0017 .083. .0076 .26 .030 O35 ye .08 -003 -10 .004 .18 .O17 52 .059 OAOn ee SL .O12 .38 .O15 63 .058 153 a7, 0.40-0.76.... ; pe 16.7 .67 19.4 1.8 27.0 Bul 4.0 9.2 11.4 * Calculated for cm? of molten tungsten. TABLE 361.—Brightness of Filaments and Bulbs of Some Tungsten Lamps and of Some Other Sources for Comparison Brightness Brightness measured at— candles/cm? Kerosene flame Flat wick Tye 4-watt per candle carbon lamp Filament 55.0 40-watt vacuum tungsten lamp Filament 206 40-watt vacuum tungsten lamp Buib-frosted 40-watt golden Mazda Bulb 50-watt white Mazda Filament 50-watt white Mazda Bulb 75-watt white Mazda sprayed Filament 75-watt white Mazda sprayed Bulb 2000-watt gas-filled Mazda Filament 2000-watt gas-filled Mazda Between coil 2000-watt gas-filled Mazda Bulb-frosted Sun as observed at earth’s surface 165,000 Clear sky, average TABLE 362.—Characteristics of Some Miniature Lamps (Forsythe, Watson, Gen. Electr. Rev., 34, 734, 1931.) Automobile Mazda lamps Flash-light lamps Max. Watts Service and is : . Volts eeu per sph. Dower candle Rear, instrument bd. : F : 282 1225) 0519) 4500 Step, aux. headlight... : : 2 225 40" 1-30 Dome, panel ; : : 223 eA Gaels Signal : : : 2AO) MEAS 1235 Dome, panel : : PATA 5 Anet Ad Headlight, depres. beam 6. 5 : ; BeAr 1.39 Head and See ee Senos i : at7 un we: Tou 6 SAO) the 1.06 Headlight...... 13 Motor coach Side and headlight Ford 2 fil. headlight. . Spotlight 5. 5 Headlight, depres. beam 6 * Surgical (grain-o'-wheat) 2 mm diam., 8.7 mm long, 0.06 g. +RCA_photophone photo-tube exciter. | R C A recorder. § Western Electric sound-picture photo-tube exciter. ** Radio 4o. Feb., 1932. Gen. Electr. Rev., 50 K watt; 120 v; 3300°K.; 1,400,000 lumens; max. candle power 166,000 24 lumens/watt. 10 K watt; 120 v; 3300°K.; 280,000 lumens; max. candle power 33,000; 24 lumens/watt. SMITHSONIAN TABLES 340 TABLES 363-365 TABLE 363.—Characteristics of Sunlight Mazda Lamp (S1) 300 Watts a.c. Combined Incandescent Tungsten, Mercury Arc, Special High Transmission Bulb For more detailed data see Taylor, Journ. Opt. Soc. Amer., 21, 20, 1931; Forsythe, Barnes, Easley, loc.cit. p. 30, Gen. Electr. Rev., 33, 358, 1930. Characteristics of S1 lamp: distance between electrodes 5.4 mm. Current 31 + amp., voltage 11 volts; light output ee speciat 5670 lumens. Efficiency, 17.6 lumens/watt; % light from mercury arc, 20; light from filament 100 lumens ; max. temp. suncsten. Clectrodes 3200° K, of filament 2330° K: Temp. of Hg ELECTRODE 285° C, pressure of Hg vapor, 177 mm Hg. TUNGSTE POOL OF FILAMENT MERCURY Transmission of I mm of glass used: Nein wAnestromsmseeeecce 2500 2600 2700 2800 2900 3100 3300 3500 4000 5000 To transmissible se. cers 10 20 33 52me G7A5 88 89 90 g2 92 Energy Flux in Microvolts/cm? Sunlamp Quartz Unit * 7 Hg Arc * § Below 2000 A : 2.6 37 2900-3000 : WA, I2 2800-3100 : 41. 39 2900-3200 ; 103. 70 * im from center of arc. + 3.75 amp. 72 vy in lamp, no reflector. § In center of beam. + Directly overhead. Per cent Total Energy Flux in various Spectrum Regions <3200A 3200—-4000A | 4000—7600A | 7600-17000A|} >17000A Continuous spectrum... . Line spectrum * Includes Hg red lines. TABLE 364.—Characteristics of Photoflash Lamp (Forsythe, Earley, Journ. Opt. Soc. Amer., 21, 685, 1931.) G. E. Photoflash lamp burns electrically ignited 65 mg Az foil, .oo004 cm thick in closed glass bulb with excess of 02. ; ; Light output, 47,000 lumens, sec. Max. intensity 4,500,000 lumens Light equals that of 100-watt Mazda for 37 sec. | Over 3,000,000 for 0.005 sec. Flashes start in 0.01 sec. with 110 v. Flash lasts 0.066 sec. Time to max. 0.014 sec. TABLE 365.—Visibility of White Lights Candle Power Range 1 Paterson, Dudding. 2. Deutsche Seewarte. SMITHSONIAN TABLES TABLES 366 AND 367 341 TABLE 366.—Sensitometric Constants of Type Plates and Films, Definitions Ordinates are density (D) ; abscissae, logs of exposure (log £). Density (D) is the absorbing power of the silver deposit. If Fo is the luminous flux incident upon — the deposit, F, the luminous flux transmitted, T, the transmission, O, the opacity, D, the density, then Te — eyo Ola / age D—No gO — logio 1/T = logio Fo/F1 Typical Characteristic Curves Exposure (E): E=IJt (expressed in meter-candle seconds, mcs), J = illumination (meter-candles, mc) incident on the photographic material during exposure, t = exposure time in seconds. Speeds given in the following table were obtained with a light approximately equivalent to mean noon sunlight in spectral composition. Gamma (7): Gamma is defined as the tangent of angle alpha (a). Gamma infinity (7,): y,» is defined as a theoretical limiting value to which gamma _ approaches as the development time is increased.” aA ‘% Yes Fea a Aa 21° Time of Development for Gamma of Unity (t=1.0): A convenient practical specifi- cation of development rate. Fog (F): Fog is the density produced when material is developed without exposure. Values in the table are when development is carried to a gamma of unity. Latitude (1): L=length of the projection (expressed in exposure units) of the straight line portion on the logi E axis, assuming development to a gamma of unity. Inertia (i): i=the value of exposure where the straight line portion of the char- acteristic curve extended cuts the logis E axis. The inertia is in general a function of the extent to which development is carried. Values of 7 given in the table were determined for a gamma of unity. Speed (S): Sa 10. In the determination of the values given in Table 368 a developing solution made up according to the following formula was used: Velocity Constant of Development (K): K = = loge TABLE 367.—Formula for Laboratory Pyrogallol Developer Solution A Solution B Pyrogallol .... Water to 1 liter Temperature 20° C. For use, mix equal volumes of A and B. 1 Sheppard and Mees, Investigations on the theory of the photographic process. London, Longmans, 1907. SMITHSONIAN TABLES 342 TABLES 368 AND 369 TABLE 368.—Sensitometric Constants of Type Plates and Films Material Motion picture film: Extra fast Panchromatic Positive Portrait extra fast Portrait normal Amateur fi “Focal plane’’ plate Commercial ordinary Commercial orthochromatic Commercial panchromatic........ Process ordinary Process panchromatic Lantern slide plate 4 6 ‘6 ui 4 8 8 8 2 2 2 .O .O 2 HO HM DOM DO G0 CUMUNnNnnNnownnodow I Ee I 2 I I Bee I 2 2 2 3 3 3. TABLE 369.—Resolving Power, Sharpness, and Astro Gamma, Definitions Resolving Power. (R). The capacity of a photographic plate or film to render fine detail is known as its resolving power. It is usually found by photographing a series of gratings of alternate parallel transparent and opaque lines, each line of a width equal to the space between the lines. The grating constant, (width of line plus width of space), is variable for different line groups over a relatively wide range. Resolving power is specified by stating the number of lines per mm resolvable by the material.'? Resolving power depends upon exposure, development time, the developing solution, the spectrum composition of the exposing radiation, and the contrasts in the test object. The values of resolving power given are for the optimal exposure values and optimal time of development in a particular developing solution (laboratory pyrogallol). The exposing radia- tion used had a spectral composition close to that of average daylight and the contrast between the elements of the test object was very high (greater than 10,000). Sharpness. The sharpness characteristics of a photographic material is defined as the differential of density (D) with respect to distance (s) in a direction perpendicular to the edge of the image; sharpness (S) = dD/ds, where s is expressed in microns (0.001 mm). Images used are obtained by making a contact print of a very carefully prepared knife edge. The exposing radiation is carefully collimated and incident normal to the surface. Sharpness of the developed image depends upon the extent to which development is carried and this is specified by one value of gamma (y), dD/d log E. It is dependent upon the quality of radiation. The values given in the table were obtained by exposure to light, approximately equivalent to average daylight, and the exposure was so adjusted that development to a gamma of unity in pyrogallol at 20°C gave an image density of unity. These values of sharpness express the diffuse-density gradient (dD/ds) of the straight line portion of the sharpness curve obtained by plotting diffuse density (D) as a function of the distance (s) from the geometrical edge of the image. Astro gamma. Astro gamma is defined as the coefficient (6) of logy E in the Scheiner equation, which gives the relation between the diameter (D) of a stellar image and the exposure (£). =a+ bd logy FE Since exposure (£) = intensity (/) - time (t) this equation offers a means of determining the relative brightness of stars by measurement of the diameter of the stellar images ob- tained under known conditions of exposure and development. In the table are given values of astro gamma for a group of typical photographic ma- terials. These values were determined by photographing with a highly corrected lens, using a magnification of 0.05, a circular aperture (diameter of 0.56 mm). Exposing radiation was of daylight quality, and intensity was so adjusted that an exposure of 1 second was just above the threshold value. Keeping the intensity factor constant, the exposure time was increased by consecutive powers of 2 from I to 512 seconds. The exposed plates were de- veloped to a gamma of unity in standard pyrogallol at 20°C. 1 Mees, Proc. Roy. Soc. (London), 83, 10, 1909. | 2 Ross, Physics of the developed photographic image, New York, Van Nostrand, 1924. SMITHSONIAN TABLES TABLES 370 AND 371 343 TABLE 370.—Resolving Power, Sharpness, and Astro Gamma Material Resolving Sharpness Astro Power gamma Motion picture film extra fast 50 0.080 35 Motion picture film normal 55 .085 35 Motion picture film panchromatic............. 50 .080 Motion picture film positive 80 .120 Portrait extra fast 50 .065 Portrait normal 60 .070 Amateur film 65 .090 “Focal plane’”’ plate 55 .080 Commercial ordinary 65 | .092 Commercial orthochromatic 65 .097 Commercial panchromatic 60 .085 Process ordinary go .130 Process panchromatic 75 .IIO Lantern slide plate -140 TABLE 371.—Spectrographs Showing Relative Spectrum Sensitivity of Various Plates and Films Ordinary, blue sensitive. ola ton bagpfadustn Orthochromatic, blue and green sensitive. Panchromatic. Dicyanine sensitized. Kryptocyanine sensitized. Neocyanine sensitized. Nrrladae da dasa) dua 40 50 cO TO 80 90 (See following page) SMITHSONIAN TABLES 344 TABLES 372 AND 373 TABLE 372.—Spectrum Sensitivity of Photographic Materials The spectrum distribution of sensitivity may be shown qualitatively by wedge spectro- grams. These (see preceding page) are made with a spectrograph over whose slit is mounted a wedge of neutral gray glass, the transmission of which increases logarithmically from the thin to the thick end. The boundary of the exposed area outlines approximately a curve which is the resultant of the spectral sensitivity function of the material and the spectral distribution of energy in the radiation emitted by the source illuminating the slit of the instrument. The source used is an acetylene flame operating at a color temperature of 2360°K. All plates had the same exposure. By the application of a correction based on the spectral emission of a black body at 2360°K., an approximation to the actual spectral sen- sitivity of these materials may be obtained, The neutral glass wedge, while fairly non- selective in absorption for radiation of wave lengths longer than 450 mu, increases in density for radiation of wave lengths shorter than 450 mu. The apparent falling off in sen- sitivity at wave lengths less than 450 my is therefore due to excessive absorption of the neutral wedge rather than to a decrease in the spectral sensitivity of the materials. (Mees, Journ. Franklin Inst., 201, 525, 1926. Walters and Davis, Bur. Standards Bull., 17, 353, 1921.) Note: Photo plates for spectroscopy and astronomy. Mees, Journ. Opt. Soc. Amer., 21, 753, 1931. TABLE 373.—Relative Photographic Efficiency of Illuminants C = luminous efficiency of source (lumen/watt). E, = relative pherosrapbic efficiency of source evaluated on basis of equal visual intensities, sunlight = 100%. E, = relative photographic efficiency of source evaluated on basis of equal energy consumption by the source, sunlight = 100%. (Jones, Hodgson, and Huse. Trans. Illum. Eng. Soc., 10, 963, 1915.) Photographic material Ordinary Orthochromatic} Panchromatic E, Ee Ey Ee IO0O |IO0O 155 Acetylene : & 4 44 Acetylene (screened) * ; : 85 .040 Pentane y : 28 Mercury arc in quartz y 500 |132 Mercury arc in nultra glass ‘ 195 | 46 Mercury arc in crown glass : 275 | 68 Carbon arc, ordinary XG Te 9 Carbon arc, white flame { 5 234 | 45 Carbon arc, enclosed k II Carbon arc, ‘‘Aristo”’ : 86 Magnetite arc Carbon glow lamp Carbon glow lamp Tungsten (vacuum) Tungsten (vacuum) Tungsten (gas filled) Tungsten (gas filled) Tungsten (C3) Tungsten (C3) Mercury vapor * Screened with Wratten No. 79 filter. SMITHSONIAN TABLES TABLES 374-376 345 TABLE 374,—Variation of Resolving Power with Plate and Developer The resolving power is expressed as the number of lines per millimeter which is just resolvable, the lines being opaque and separated by spaces of the same width. The developer used for the comparison of plates was Pyro-soda; the plate for the comparison of developers, Seed Lantern. The numbers are all in the same units. Huse, ip Opt. Soc. America, July, 1917. Plate. Albumen. | Resolution. Process. Lantern. Medium High speed. Resolving power 81 67 62 Resolving Resolving Resolving Developer . Developer. Developer. Pyro-caustic Pyrocatechin , Glycin Pyro-metol Process hydroquinone. . Hydroquinone.... Eikon.-hydroquinone .. . Ortol Ferrous oxalate....... Caustic hydroquinone. . X-ray powders Eikonogen Kachin TABLE 375,.—Relative Intensification of Various Intensifiers Intensi- Bleaching solution. Blackening solution. Reference Restion: Mercuric Dromidceneeiteeerenaicne Amidol developer Eee pote (Monckhoven sol. A). Mercuric chlorides sce.cec elec cielelees Bleach according to Ben- nett; blackener.* Potassium bichromate + hydro- GHIOTIGHACIG pegs «sp eis?s eictorrler ie eels Amidol developer Piper. * Mercure nodides = ericic cetera Schlippe’s salt Debenham, B. J., f p. 186, ’17. Weadiferricy amides -1ssy<( < Deon r RDWKHRONW 5820.155 5852.488 5881.895 5944-834 5975-534 | 6029.997 | 6074.338 6096.163 6143.062 6163.594 Wave length — OUWROS DOR UA Wave length 6217.280 6266.495 6304.789 6334-428 6382.991 6402.245 6506.528 6532.883 6598.953 6678.276 Inten- sity AIHA WUW KWSCwon International Units (Angstroms). Burns, Meggers, Merrill, Bull. Bur. Stds. 14, 765, ro18. SMITHSONIAN TABLES 6717.043 Wave length 6929.468 7024.049 7032.413 7059.1II 7173-939 7245.167 7438.902 7488.885 7535-784 350 TABLE 382 STANDARD SOLAR WAVE LENGTHS. INTERNATIONAL ANGSTROMS Adopted at the Leyden Meeting of the International Astronomical Union. See Trans. Int. Astron. Union. 3, 93, 1929. The solar wave lengths in the Rowland Revision by St. John (and others) are based upon the former arc standards and require the folllwing corrections to reduce them to the scale of the following adopted lines: dX 3592 to \ 5625 A. —o.002 A. at \ 6350 A. —o0.007 A. at 2850 — .003 6500 — .008 5950 — .004 6700 1-009 6050 — .005 6850 — .OLI 6200 — .006 7100 — Old. In the following table the + sign following the designation of an element indicates the state of ionization; an indication like Fe—, solar line too strong to be due to iron alone; Fe, Co, coincidences of like order; Fe Co, coincidence closer for preceding element; Fe-Co, Fe line to the red, Co, to the violet; an italicized element indicates predominence of that element. Asolar Elements Int. Asolar Elements Int. Asolar Elements Int. |f 3.592.027 4079.843 Fe 4439.888 Fe 3635-469 4082.943 4451.588 3650.538 4091.557 4454.388 3672.712 4094.938 4459-755 3695.056 4107.492 4470.485 3710.292 4120.212 4481.616 3725.496 4136.527 4502.221 3741.065 4139-936 4508.289 3752-418 4154.814 > 4512.741 3760.537 4163.654 Ti1+Cr—Fe 4517-534 3769.994 4525.146 3781.190 4531.631 3793-876 4534-785 3804.015 4541.523 3821.187 4547-853 4548.770 4550-773 4563.766 4571.102 4571.982 4576.339 4578.559 4587-134 4589.953 4598.125 4602.008 4602.949 4607.654 4617.276 4625.052 NHWW 4168.620 Fe 4178.859 Fe+ 4184.900 Fe, Cr 4191.683 Fe 4198.638 V—Fe 3836.090 3843-264 3897-458 3906.752 3916.737 3937-336 3949-959 3953-861 3960.284 3963.691 3977-747 3991.121 4003.769 4016.423 4029.642 4030.190 4037.121 4053.824 4.062.447 4073-767 4208.608 4220.347 4233.612 4241.123 4246.837 4257.661 4266.968 4267.680 4282.412 4291.472 4318.659 4331.651 4337-925 4348.947 4365.904 4389.253 4398.020 4416.828 4425-444 4430.622 NUNWN GUN AWW WWHWH HF AAH ULPWOLW AunFPNN WNHHNUN WWHNH NN NL 4630.128 4635-853 4637.510 4638.017 4643.470 BUOWNN UNWWAD WHWOUMWH UPN NHN HPONWOHL HOHPWOHO TWNHN HAMNH NW DW WWNHWN wR NAN SMITHSONIAN TABLES TABLE 382 (continued) 351 STANDARD SOLAR WAVE LENGTHS. INTERNATIONAL ANGSTROMS = 5 ss Asolar Elements Int. Asolar Elements Elements I: 4647.442 Fe 5415.210 4656.474 Ti 5432.955 4664.794 —CrNa? 5445-053 4678.172 5462.970 4678.854 5473-910 4683.567 5487.755 4690.144 5501-477 4700.162 5512.989 4704.954 5525-552 4720.999 5534-848 4728.552 5546.514 4733-598 5590.126 4735-848 5601.286 4736.783 5624.558 4741-535 5641.448 4745-807 5655-500 4772-823 5667.524 4788.765 5679.032 4789.658 5690.433 4802.887 5701.557 4824.143 5731-772 4832.719 5741.856 4839-551 5752-042 4939.694 5760.841 4983.260 5805.226 4994.138 5002.798 5014.951 5028.133 5979-745 5090.782 5109.657 5150.852 5159.065 5198.718 5225-534 5242.500 5253-468 5273-389 5288.533 5300.751 5307-369 5322.049 5332.908 5348.326 5365-407 5379-581 5389.486 5398.287 54099.799 Ss o Asolar 6003.022 Fe 6008.566 Fe 6013.497 Mn 6016.647 6024.068 ay 6027.059 6042.104 6065.494 6078.499 6079.016 6082.718 6085.257 6086.288 6089.574 6090.216 6093-649 6096.671 6102.183 6102.727 6111.078 6116.198 6122.226 6127.912 6128.984 6136.624 NHR W DWwnwt HNNHPUWwW WWFH HUN NUNwPhP NADAS NAPWW HD Ot a A ae! NwWOWwWFPHL WAWFH NO DW Ww 6137.002 6137.702 6141.727 6145.020 6149.249 6151.623 6154.230 6157-733 6161.295 6162.180 5809.224 5816.380 5853.688 5857-459 5859-596 N NNN W DHW Of 5862.368 5866.461 5867.572 5892.883 5898.166 5995.680 5916.257 6165.363 6166.440 5919.054 6169.564 5919.644 6170.516 5927-797 6173-341 5930.191 5932.092 5934-665 5946.006 5952.726 5956.706 5975-353 5976.787 5983.688 5984.826 NNNNN WNHA NU HLNWNH WWWWW NUH HFPNWOD USCUMMF HNN LHOWNN 6175-370 6176.816 6180.209 6186.717 6187.995 6191.571 6200.321 6213-437 6215.149 6216.358 HOM DANAO HPNUUH NONUMWH UAFPUNL Powwow LPWWN Dnfwk HOUND SMITHSONIAN TABLES 352 TABLE 382 (concluded) STANDARD SOLAR WAVE LENGTHS. INTERNATIONAL ANGSTROMS Agolar Elements Int. Asolar Elements Int. Agolar Elements Int. 6301.508 Fe 6302.499 Fe 6302.764 Atm.O2 6305.810 Atm.Oz 6306.565 Atm.O2 6309.886 Atm.O2 6315.314 Fe 6315.814 Fe 6318.027 Fe 6322.694 6482.809 6493.788 6494-994 6498.945 6499.654 6516.083 6518.373 6569.224 6592.926 6609.118 6643.638 6677.997 6717.687 6810.267 6858.155 6219.287 6226.740 6229.232 6230.736 6232.648 Nn NUMA 6240.653 6244.476 6245.620 6246.327 6247.562 N COR NW W OHH D Aunnvvds we OAH 6327.604 6330.852 6335-337 6336.830 6344-155 6355-035 6358.687 6378.256 6380.750 6393.612 6252.565 6254.253 6256.367 6258.110 6258.713 6870.946 6879.928 6918.122 6919.002 6923.302 6924.172 6928.728 6934.422 6959.452 6961.260 6978.862 6986.579 6988.986 7022.957 7923-504 7027.478 7034.910 7122.206 6265.141 6270.231 6279.101 6279.896 6280.393 6280.622 6281.178 6281.956 6283.796 6289.398 NNWwWWMN WN Aus 6400.009 6400.323 6408 .026 6411.658 6419.956 me NeW 6421.360 6430.856 6449.820 6455-605 6456.391 6290.221 6292.162 6292.958 6295.178 6295.960 6297-799 6299.228 Sn a POWNFO OOO DM NWUUM WwW 6471.668 6475.632 Nn WNAUN ANUWN CO NYARNHALP PUAN H PAKNN wu RWwWWNN PN Za SMITHSONIAN TABLES TABLE 383 359 PROVISIONAL ULTRA-VIOLET AND INFRA-RED SOLAR WAVE LENGTHS Suggested at the 1928 meeting of the International Astronomical Union for further measurements leading to the use of them as standards. Trans. Int. Astron. Union, 3, 101 and 102, 1929. Wave lengths in International Angstroms. Asolar Elements ; Agolar Elements Int. Agolar Elements Int. 2990.421 Fe 3199.528 3389.749 2998.815 3210.226 3396.982 3005.061 3217.393 3401.531 3021.067 3.225.805 3.412.350 3935-745 3232.291 3419.705 3046.676 3243-415 3425-584 3061.825 3254.762 ? 3431.587 3070.266 3.262.289 3.445.126 3086.788 3273-053 3450-335 3094.898 3278.296 3455-246 3109.334 3293-150 3.462.359 3121.161 3295.825 3.466.505 3126.208 3301.226 3477.866 3140.758 3318.032 3485.903 3142.471 3323-753 3509.126 3152.263 3333-396 3161.775 3344-524 3162.571 3355-231 3170.345 3365-774 3187.714 3381-354 7905-903 7583-796 7O11.323 7676.563 7052.776 7677.618 7068.423 7682.756 7090.390 7696.868 7130.925 7714-309 7181.509 7727.616 7195-044 7742-722 7204.306 7780.567 7216.527 7797-587 7227-493 7807.915 7236.136 7832.207 7245-676 7849.984 7265.594 7887.117 7303-197 7901.780 7323-972 7918.383 7326.164 7937-149 7335-334 7945-857 7355-893 7984.343 7369.208 8012.940 7383.722 7389.391 7393-610 7495-790 7411.158 7422.286 7445-755 7491.652 7511.030 7525-115 8194.835 7555-608 8212.132 7568.906 I 8223.990 NWwWNHW+ 3517-307 3540.127 3549-873 3564.127w Fe—Co 3583.340w Fe— HNNHPOM UAWUMPWH PpAWWU YJOWDHD NAPNNH WAKADAN UNWUNs 8233.905 8252.727 8272.041 8289.533 8300.406 NNR ND CWE H 8327.060 8329.682 8342.289 8357-041 8367.333 8387.783 8426.518 8439.583 8468.420 8514.081 NW NWW Nod NW HNOCOW NH HWHD WHEHDU UPOMNW NUPWOH ANP H NU®WHN NUN WwW Ween 8515.121 8556.795 8582.271 8611.813 8621.619 — eS eS Oe ms me NG e ae ee O 8648.472 8674.756 8688.642 8699.459 8717.832 8736.043 752.024 8763-974 8793.346 8806.768 8034.293 8046.056 8085.175 8107.841 8125.444 8139.718 8158.019 8176.976 8186.371 m= me NN & me NN ee OomN eH =m Ne De _ Nm©ONDN ny Ree ee ty 8824.233 n> SMITHSONIAN TABLES 354 TABLE 384 REDUCTION OF WAVE-LENGTH MEASURES TO STANDARD CONDITIONS The international wave-length standards are measured in dry air at 15° C, 76 cm pressure. Density variations of the air appreciably affect the absolute wave-lengths when obtained at other temperatures and pressures. The follow- ing tables give the corrections for reducing measures to standard conditions, viz.: 6 = Ao(mo — mo’) (d — do)/do in ten-thousandths of an Angstrom, when the temperature ¢° C, the pressure B in cm of Hg, and the wave-length A in Angstroms are given; and d are the indices of refraction and densities, respectively; the subscript 0 refers to standard conditions, none, to the observed; the prime ’ to the standard wave-length, none, to the new wave-length. The tables were const.ucted for the correction of wave-length measures in terms of the fundamental standard 6438.4606 A of the cadmium red radiation in dry air, 15° C, 76 cm pressure. The density factor is, therefore, zero for 15° C and 76 cm, and the correction always zero for \ = 6438 A. As an example, find the correction required for \ when meas- ured as 3000.0000 A in air at 25° Cand 72 cm. Section (a) of table gives (¢ — do)/do = —.085 and for this value of the density factor section (b) gives the correction to \ of —.0038 A. Again, if A, under the same atmospheric condi- tions, is measured as 8000.9000 -A in terms of a standard \’ of wave-length 4000.000 A, say, the measurement will require a correction of (0.0020 + 0.0008) = +.0028 A. Taken from Meggers and Peters, Bulletin Bureau of Stand- ards, 14, p. 728, 1918. (a). — 1000 x (d— do)/do (6). — 6 = do(Mo—No’) (d— do) /do, in Ten-thousandth Angstroms Wave-lengths in Angstroms. 1000 X d —d0} 2000 | 2500] 3000] 3500 | 4000 | 4500 | 5000 | 5500 | 6000 |6509 | 7090 | 7500 do Corrections in ten-thousandth Angstroms. —61 Sod —52 —47 —42 =28 Oo —28 —24 —I19 —I4 =39 SS ° +5 +9 —18 —17 —15 = —13 ral TO —3 / —6 =e a3 at —§ Sh SMITHSONIAN TABLES. +1 jar +1 mn th ooOnt ++t++ ++++ one + TABLE 385 35 Wn SPECTRA OF THE ELEMENTS The following figure gives graphically the positions of some of the more prominent lines in the spectra of some of ihe elements. Flame spectra are indicated by lines in the lower parts of the panels, arc spectra in the upper parts, and spark spectra by dotted lines. <— violet — blue greenXyellowX orangex——_red——_> ae oO Line spectra of the elements. For bibliography see Gibbs, Rev. Mod. Phys., 4, 205, 1932. The following wave lengths are in Angstroms 5889.065 4202 5895.932 4216 4044 5048 4047 5724 5802 6207 7668 6299 7702 5351 4132 4102 4602 4511 6104 4046. 6707 4078. 4555 4358.: 4593 4916. 5664 4959. 5945 5460. 742* 6011 5769. 508* Zn 6213 5790. 659* 6724 6152 6074 6232 For other elements, see Kayser’s Handbuch der Spectroscopie. * Fabry and Perot. + Merrill. SMITHSONIAN TABLES. TABLES 386-387—INDEX OF REFRACTION OF GLASS TABLE 386.—Relationship between nx — np and no’ — np 8 5 3 3 3 3 3 3 8 a Abscissae are 2x —Mp, 4=2.4, 2.2, 2.0, 1.8, 1.6, 1.4, 1.2, 1.0, 0.8, .768, .656, 589, .535, 509, 486, 480, 468, .434, .361, .347, -327, 313, 1308, .208, .288, 284, 276. Ordinates 1g:— Mp for glasses measured by Rubens and Simons. Various Schott glasses included: O10g2, light barium crown, (mp=1.51698) ; S204, borate glass, (%p=1.51007) ; O1 143, dense barium crown, (mp=I. 57422); O1151, high-dispersion crown, (mp=1.52002); O451, light flint, (np =1.57524); O469, dense flint, (mp=1.64985); Os5o0, dense flint, (mp = 10751 30) 5 S103) extra dense flint (mp=1 88995). TABLE 387.—Effect of Composition on Index of Refraction 2.00 Lxteume | | fe |p fs fommuofecnr | | | | tet | | | Tol clad His q se el eh a ea ae Se SS [Tea hs ei Ui a eeeal eal ala | | | Pst, [et 719 | Bees eT Sts fs +++ na es ca Ee sas CRO i lek OROSILICATE Leal al esol FETT HEE PHOSPHATE| CROW [ Hae SMITHSONIAN TABLES TABLE 388 357 DERIVATION OF PARTIAL DISPERSIONS OF GLASS FROM n,-n, (F. E. Wright, Journ. Amer. Ceramic Soc., 3, 783, 1920; Journ. Opt. Soc. Amer., 4, 148, 195, 1920; 5, 380, 1921.) The optical constants of a glass are generally stated as the index of refrac- tion mp, and the partial dispersions between the A (.768), C (.856), D (.589), F (.486) and G’ (.434») lines and its v value, (mp —1)/(np—nc). The reciprocal of y is called the average dispersive value. The following table is computed from ny—nx=a(np—nc) —b. The mean indices of refraction of two sets of glasses from which a and b were derived are: Ma Nec Zp ie, ie’ Nc—Na Np—NcC NE—-Nyp Ne’ —NF 1.539909 1.543168 1.545958 1.552616 1.557004 @ =.288936 .272167 727833 ~—- 658443 1.588807 1.503505 1.507767 1.608201 1.616995 & = .000529 .000219 —.000219 —.000843 NE—Nc Nc—Na No—Ne NF—Nyp Nc’—NF NE—Nc No—NA NpD—Nc NE—Np NG’—NF .0050 .00197 .00158 .00342 .00245 : .00486 .00430 .01070 .000903 55 212 172 378 278 492 436 1084 O17 .0060 226 185 415 311 498 441 1099 930 65 241 199 451 344 504 446 1114 943 .0070 255 212 488 BU; 500 452 1128 956 75 270 226 524 410 ; .00515 .00457 .OI1143 .009690 .0080 284 240 560 442 521 463 1157 082 85 208 253 507 475 527 468 1172 996 . 0090 313 267 633 508 533 474 1186 1009 -O100 .00342 .00204 .00706 .00574 538 479 1201 1022 348 300 720 587 ; .00544 .00485 .O1215 .01035 353 305 735 600 550 490 1230 1048 359 310 750 614 556 495 1245 10061 365 316 704 627 561 501 1259 1075 .0037I .0032I .00779 .00640 567 506 1274 1088 B77 327 703 653 . .00573 .00512 .01288 .orIOI 382 332 808 666 5: 587 525 1325 1134 388 338 822 679 2 602 539 1361 1167 304 343 837 693 616 GB) | BISO7/ ey 2.0) .00400 .00349 .00851 .00706 : 631 566 1434 1233 405 354 866 719 645 580 1470 1266 411 359 881 W32" © 660 503 1507 1208 417 365 895 745 674 G07, 1543; 1331 423 370 910 759 ‘ 689 621 1579 1364 .00429 .00376 .00924 .00772 703 634 1616 1307 434 381 939 785 ; VAY | 648 1652 1430 387 953 708 732 661 1689 1463 392 968 811 ; 746 675 1725 1406 397 983 824 761 6860) | 1768, | Ts20 .00403 . .00838 3 a5 702 1708 1562 408 851 790 716 = 1834-1505 414 864 : 804 730 1870 1628 419 877 819 743. $1907 1661 425 890 3 .00833 .00757 .01943 .01693 SMITHSONIAN TABLES 358 TABLES 389 AND 390 TABLE 389.—Index of Refraction of Glasses (American) Indices of refraction of optical glass made at the Bureau of Standards. Correct probably to o.ccoor. The com- position given refers to the raw material which went into the melts and does not therefore refer to the composition of the finished glass. Ordinary Rercrill Barium barium t pa crown. | i flint. int. Se crown. crown. crown. Medium Wave-length. flint. Hg : - 53189 53817 58351 59137 : 63675 65788 Hg : - 53147 1.53775 . 58701 - 59084 : 636190 65692 H 3 . 52818 . 53468 - 58327 - 58698 i 63189 64973 Hg : 52798 - 53450 - 58209 - 58674 F 63163 64931 - 52326 - 53008 - 57046 . 58121 : .62548 - 63041 Hg : . 52283 - 52907 -57587 . 58071 ‘ .62492 - 63854 . 51929 . 52633 . 57105 57657 . 62033 63143 asa . 52484 1.56894 - 57473 . 61829 - 62834 . 51760 - 52475 1.56881 . 57460 1.58112 . 61817 . 62815 . 51714 . 52430 1.56819 - 57400 I. 58038 .61756 .62725 - 51573 - 52207 1.56634 -57242 I.57818 . 61576 .62458 -51458 . 52188 1.56482 . 57107 1.57638 . 61427 .62241 . 51412 -52145 1.56423 - 57054 1.57567 . 61369 .62157 . 51160 . 51908 I. 56100 . 56762 I. 57183 . 61047 . 61701 (Percentage composition) a #uanododod | [mo [oR eos Co ies) |~ ° w 100% Het al -lleeees: 000 ote || | moSpant ||| |xSes > HOL o0o°o 1.51714 I. 52430 % 1.57406 1.58038 0.00868 0.00820 : o.o1ol4 0.01391 ; 0.01700 0.01904 59.6 63.9 : 56.6 Ate, : 36.9 34.4 0.00612 0.00578 0.00715 0.00991 00’ 0.01216 0.01363 0.00492 0.00460 0.00681 0.00577 0.00831 j 0.01032 0.01168 0.00256 0.00242 0.00337 0.00299 ©.00400 0.00320 0.00484 0.00541 SMITHSONIAN TABLES. TABLES 391-393 359 TABLE 391,—Index of Refraction of Glasses Made by Schott and Gen, Jena The following constants are for glasses made by Schott and Gen, Jena: 7a, 0, 2p, 7p, %a, are the indices of refraction in air for A=0.76824, C=0.65634, D=0.5893, F=0.4861, G’=0.4341. V=(zp—1)/(#r—nc). Ultra-violet indices: Simon, Wied. Ann. 53, 1894. Infra-red: Rubens, Wied. Ann. 45, 1892. Table is revised from Landolt, Bornstein and Meyerhoffer, Kayser, Hand- buch der Spectroscopie, and Schott and Gen’s list No, 751, 1909. See aiso Hovestadt's ‘‘ Jena Glass.” Catalogue Type = O 546 O 381 O 184 | O 102 O 165 S57 Higher Dis- | Light Silicate | Heavy Silicate | Heavy Silicate! Heaviest Sili- persion Crown.) Flint. Flint. | Flint. cate Flint. Melting Number= 1092 1151 451 469 500 | 163 v = 60.7 51.8 41.1 33-7 27.6 Designation Zinc-Crown. Cd 0.2763 .56759 io = = Cd -2837 56372 - - - Cd_ .2980 -55723 ; 1.65397 - - 3403 -54369 4 1.63320 -71968 1.85487 3610 53897 ; -61388 70536 1.83263 »4340! -52788 . -59355 -67561 -78800 1.94493 -4861 -52299 : -58515 -66367 -77091 1.91890 -5893 -5 1698 . 57524 -64985 *75130 1.88995 -6563 -51446 : 57119 .64440 -74368 1.87893 +7682 +51143 . - 50669 -63820 *7353° 1.86702 800K -5103 : .5659 -6373 -7339 -8650 1.200 -5048 : 5585 | -6277 +7215 -8481 1.600 .5008 ; 5535 6217 7151 -8396 2.000 -4907 5487 -O171 +7104 -83 16 2.400 = -5440 -O131 = -8286 Kind of Light and Wave-length. Percentage composition of the above glasses: O 546, SiOz, 65.4; K20, 15.0; NagO, 5.0; BaO, 9.6; ZnO, 2.0; Mn2Os, 0.1; AseQOs, 0.4; BoOs3, 2.5. O 381, SiOz, ea) PbO, 13.3; NapO, 15.7; ZnO, 2.0; MnOg, 0.1; AseOs, 0.2. O 184, SiOs, 53.7; PbO, 36.0; KO, 8.3; NagO, 1.0; Mn2O3, 0.06; AseOs, 0.3. O 102, SiOz, 40.0; PbO, 52.6; K20, 6.5; Na2O, 0.5; Mn2Osz, 0.09; AseOs, 0.3. O 165, SiOz, 29.26; PbO, 67.5; K20, 3.0; MnegQO3, 0.04; AseQOz, 0.2. S157, siOx, 21.9; PbO; 78!0; AszOs, 0.1. TABLE 392.—,,, Dispersion and Density of Jena Glasses ae fi No. and Type of Jena Glass. — = | —n, | ty— Cae Weight! O 225 Light phosphate crown . . .007 37 : O 802 Boro-silicate crown. . . . 3 0765 | : Say oges UV 3199 Ultra-violet crown . . . 5035 0781 : 0432 O227 Barium-silicate crown . . . . 0909 | 3 o514 Orrg Soft-silicate crown. . . . 3G + og1o0 | : | 2 0521 O 608 High-dispersion crown . . : 0943 ear é 0543 UV 3248 Ultra-violet flint. . . . : 0964 | ne | ; 0553 O 381 High-dispersion crown. . 5 1026 : 0596 O6o2 Baryolizht flint, 2-2 27. 5 1072 | 53. 59 | 0618 SisSoBorateflint 25 5. . 1102 6 | | 0629 O 726 Extra light flint... . .- ; 1142 : 8 0669 O 154 Ordinary light flint. . . . ; 1327 | : 2 0791 O 184 ie Seine” Ming wabliciy 3 “5 1438 : 2 o861 Omasibarvitintes 0% re 14 a: .62 1599 | : | 0965 O 102 Heavy flint . . sae 648 1gtg | O41 S Seikctrct cs * Sean Le. 2434 Ones) Ss Rex gene ae cen : 2743 S 386 Heavy flint. . . tl Gh ite 3 4289 Spy beleraneciniltits 5 “o sobs Gop .9626 | 4882 No. and Designation. Temp. $57 Heavy silicate flint . . . 58.8° : ; 0.0166 O 154 Light silicate flint .. . 58.4 | a : 0.0078 O 327 Baryt flint light . . . . 58.3 .o8 2 0.0079 O 225 Light phosphate crown . Feb | ‘ | : 0.0049 Pulfrich, Wied. Ann. 45, p. 609, 1892. SMITHSONIAN TABLES. 360 TABLES 394-396 TABLE 394.—Index of Refraction of Rock Salt in Air | Obser- ver. | A(z). i | a 1.89348 | M |i 0.88396 : | 32. | 1.516014 1.76964 (072290) Nel | 1.515553 1.61325 + .98220 1.513628 | 1.57932 1.036758 | 1.513467 | 1.55962 5 1.1786 | 1.511062 1.55339 i | 1.508318 1.553406 | 1.555137 2 | 1.506504 1.553399 P .7080 2 1.502035 1.544340 | L 27 1.494722 1.544313 1 26 1.481816 1.540672 iF 25¢ 1.471720 1.540702 | Ie, 2584 1.460547 1.538633 | P 24 1.454404 1.536712 | P 23 1.447494 1.53666 M 2164 1.441032 1.536138 iB 21 1.3735 1.534011 iP 18 1.340 pos MM, VGN AG Sma Gna el Me M; a2 loans ae kre — hr or=6 aaa x2) age AP—at where a?= 2.330165 Ao? =0.02547414 62= 5.680137 M,=0.01278685 & =0.000928 5837 M3=12059.95 A17=0.0148 500 i = 0.000000286086 A3?= 3600. (P) Mz=0.005343924 TABLE 395.— Change of Index of Refraction for 1° C in Units of the 5th Decimal Place Mi || C line | —3. 0.202 | 43-134 | Mi |} 0.441m | —3.425 7 “cc D iT een 6 oA MO || Seite) |) 508 | —3.5 3.6 L Annals of the Astrophysical Observatory P Paschen, Wied. Ann. 26, 1908. of the Smithsonian Institution, Vol. I, r900. Pl Pulfrich, Wied. Ann. 45, 1892. M Martens, Ann. d. Phys. 6, rgor, 8, 1902. RN Rubens and Nichols, Wied. Ann. 60, 1897. Mi Micheli, Ann. d. Phys. 7, 1902. TABLE 396.— Index of Refraction of Svlvite (Potassium Chloride) in Air NGa): aa | Obser- || ; ei | Obser- || eae re) eset) est Prd eet cl ati] seg Ve 4 a ver. 0.185409 1.82710 ‘ 1.478311 | ; | 1.462726 -200090 1.71870 1.47824 1.46276 -21946 1.64745 : 1.475890 | 8.8398 1.460858 257317 1.58125 § 1.47589 ill 1.46092 -251640 1.558306 | i 1.474751 | 1.45672 308227 1.54136 aC 1.473834 | : 1.45673 358702 1.52115 1.47394 : | 1.44919 -394415 | 1.51219 | 3-5 1.473049 | “| 1.44941 .467832 | 1.50044 ‘ 1.47 304 | 1.44346 508606 1.49620 714 1.471122 | | 1.44385 58933 1.49044 ‘ 1.47129 | | 1.43722 .67082 1.45669 A 1.47001 3 1 42617 .78576 1.483282 op | ayOon 3 We | 1.41403 .88 398 1.481422 8932 | 1.468804 | i} | 1.3882 .98220 1.480084 | s 1.40880 ; MM, My : 2 MM, Mp Mz eT NE A pa AO) 8 AN oer fi Aaljupsesseschee eS ae tai 2 kr? — hr* or =1 T38—a2t ap Age ae a® = 2.174967 Ag? =0.0255550 0? = 3.866619 M, =0.008344206 &=0.000513495 Ms= 5569.715 A1?=0.0119082 A=0.000000167 587 A3?= 3292.47 (P) Mz =0.00698 382 W Weller, see Paschen’s article. Other references as under Table 395, above. SMITHSONIAN TABLES. 1S, See Ee eee ee TABLES 397-400 361 INDEX OF REFRACTION TABLE 397,—Index of Refraction of Fluorite in Air | Obser- ver Iw SHH OO 40855 P -40559 me 40238 39898 -39529 39142 357 19 37819 1.50940 5 4733 1.496029 | “ jf} 1.5715 1ASA@2 || ess el .6206 eA 777 O2m8)|| a lls T7680 1.46476 | 9153 1.44957 . 9644 1.446097 : 2.0626 L.44214 | ; 2.1608 1.43713 2.2100 30805 1.43393 | 2-3573 | | | 1 35680 1.43257 | S | 2.5537 1.42088 8.2505 -34444 1.43200 | | 2 1.42016 | | 8.8308 | 1.33079 1.43157 Nene: 1.41071 | 9.4291 | 1.31612 1.43101 | 2.¢ 1.41826 51.2 Bry, | 34 .63 RO. On Oo COMOWN™N pPARAKRARAARA A WN ND LN WL WRN iO COM = = Aine bo pa \O 1.42982 i), 3 1.41707 | 61.1 1.42787 Be 1.41612 ee ed 20907 Ne willl eSs5C5¢ 1.41379 | : a 1.42641 | | .5 306 I.41120 | | References under Table 33r. ip 9 AT, 9 = 9 Ms M3 n* = q? + ——~— — ea? — fd or = 624 —=*—+ — ny ZAP ; J aceon ESET 02 where a? = 2.03882 J = 0.000002916 M;3= 5114.65 My, = 0.0062183 6? = 6.09651 A, = 1260.56 Ay? = 0.007706 My = 0.0061 386 A, = 0.0940u € = 0.0031999 A,? = 0.00884 Ar = 35-54 (P) TABLE 398.— Change of Index of Refraction for 1°C in Units of the 5th Decimal Place C line, —1.220; D, —1.2060; F, —1.170; G, —1.142. (PI) TABLE 399,—Index of Refraction of Iceland Spar (CaCO.) in Air Obser- C Carvailo, J. de Phys. (3), 9, 1900. Pl Pulfrich, Wied. Ann 45, 1892. M Martens, Ann. der Phys. (4) 6, 1901, 8, 1902. RA Rubens-Aschkinass, Wied. Ann. 67, 1899. P Paschen, Wied. Ann. 56, 1895. S Starke, Wied. Ann. 60, 1897. TABLE 400.— Index of Refraction of Nitroso-dimethyl-aniline (Wood) Nitroso-dimethyl-aniline has enormous dispersion in yellow and green, metallic absorption in violet. See Wood. Phil. Mag 1903. SMITHSONIAN TABLES. 362 TABLES 401 AND 402 INDEX OF REFRACTION TABLE 401.—Index of Refraction of Quartz (SiO), 18°C Wave length Index Ordinary Ray Index Extra- ordinary Ray Wave- length Index Ordinary Ray Index Extra- ordinary Ray Kb 0.185 -193 .198 .206 B2 IA! .219 1.67582 -65997 .65090 .64038 .63041 62494 -61399 .59622 .58752 -56748 -55815 .55050 -54968 -54424 1.68999 67343 .66397 .65300 .64264 .63698 .62560 .60712 .59811 57738 .56771 .56600 -55896 1.55334 Le 0.656 .686 .760 1.160 1.54189 “54099 -53917 -5329 .5216 -5156 -9939 -4944 -4799 -4679 -4569 417 274 Wolt(oy7/ 1.55091 54998 54811 Rubens : Except Rubens’ values,—means from various authorities TABLE 402.—Index of Refraction for Various Alums* Temp. C.° Index of refraction for the Fraunhofer lines. Aluminium Alums. RAM(SO4)o+12 H,0.t Na NH3(CHg) K 17-25 a I4-15 7-21 15-25 15-20 10-23 LAS 492 -45013 45226 45232 45437 “45509 49226 1.43563 | 1.43653 45177 -45398 “45417 45018 -45093 49443 45062 Ogos 45325 Aon “45599 295 "/, 1.43884 -45410 45045 -45060 45856 45939 -49748 1.44185 45091 45934 -45955 -40141 -46234 50128 Chrome Alums. 6-12 6-17 2.043 1.817 1.946 | 12-17 1.719| 7-18 2.386] 9-25 1.47627 -47642 .47660 47911 51692 1.47732 -47738 -47756 48014 51798 1.47836 | 1.48100 -47865 .47868 48125 51923 -48137 48151 48418 52280 RCr(SO4)o+12H.O.F 1.48434 -48459 -48456 -487 44 -52704 1.44412 “459041 46181 .46192 1.44231 “45749 -45996 45999 46203 .46288 50209 .46481 50463 1.48723 -487 53 -48775 -49040 53082 1.48491 48513 48522 -48794 52787 46386 1.45640 1.44804 40363 -46609 .46618 .46821 46923 51076 Tron Alums. R¥e(SO,)>+12H.0.+ 1.806 1.916 2.061 1.713 1.47706 47770 47921 .48029 51790 1.48169 -48234 .48378 .48482 52365 1.48580 48054 -48797 48921 -52859 1.47837 -47594 .48042 .48150 51943 1.47639 -47700 -47825 -47927 -51674 7-11 7-20 20-24 7-20 1.48670 | 1.48939 .48712| .49003 .48867 | .49136 .48993 | .49286 -52946| «53254 * According to the experiments of Soret (Arch. d. Sc. Phys. Nat. Genéve, 1884, 1888, and Comptes Rendus, 1885). + & stands for the different bases given in the first column. 5 For other alums see reference on Landolt-Boérnstein-Roth Tabellen. SMITHSONIAN TABLES TABLE 403 363 INDEX OF REFRACTION Selected Monorefringent or Isotropic Minerals The values are for the sodium D line unless otherwise stated and are arranged in the order of increasing indices Selected by Dr. Edgar T. Wherry from a private compilation of Dr. E. S. Larsen of the U. S. Geological Survey. Index of Mineral. 5 refraction, A = 0. 589M. Villiaumite NaF Cryolithionite 3NaF.3LiF.2AlFs Opal oars nH20 Fluorite Ko. *AlzOs. 4S03.24H20 Sodalite 3Na,0.3 Al,0;.6Si0,.2NaCl Cristobalite SiO: Analcite Na,O, Al,O3.4S105.2 HzO oars Gi Noselite 5Na,0.3A1,0;.6SiO,.2SO3 Hauynite Like preceding + CaO Lazurite 4Na.0.3Al,03.6Si0O.. NayS¢6 i K,0.A1,03.4Si0, Pollucite 2Cs50.2AloO3.9Si02.H»O i NaCl Bauxite Os. nH,O Pharmacosiderite.... €203.2As.O5.3K,0.5H2O Gpinclieah ee Jeon. M0 Aico, Berzeliite feo Mg, Mn)O.As205 3Ca0. Al2O3.3SiO2 3(Mn, Fe)O.3Be0.3Si0O2.MnS ) 3Mg0.Als03.3Si02 Arsenolite As203 Hessonite 3CaO.(Al, Fe)203.3SiO2 Pleonaste (Mg, Fe)O.Al2O3 Almandite 3FeO.Al203.3Si02 Hercynite Gahnite Spessartite 3Mn0. Alz203.3Si02 i CaO Uvarovite 3CaO.Cr203.3Si02 Andradite 3CaO.Fe203.3Si02 Microlite 6Ca0.3Ta20s5.CbOFs3 Nantokite CuCl | Pyrochlore Contains CaO, Ce203, TiOz, etc. Schorlomite.........| 3CaO.(Fe, Ti)203.3(Si, Ti)Oe2 Percylite PbO.CuCle.H20 Picotite (Mg, Fe)O.(Al, Cr)203 Eulytite 2Bi203.35iO2 Cerargyrite AgCl Mosesite Contains Hg, NHs, Cl, etc. Chromite -328 - 339 . 406-1. 440 434 -450 483 . 486 .487 - 490 -495 . 490 . 500 509 525 544 .570 .676 723 727 -736 - 736 -739 -745 -755 - 763 -770 -778 . 800 800 .8ir .830 . 838 857 -925 -930 .960-2.000 - 980 -050 .050 .050 . O61 .005 .070 .087 ATO) . 160 .18 (Li light) . 200 200 -253 . 330 S10 .360 (Li light) .370-2.470 .380 PerOUe® | . 490 (Li light) . 690 (Li light) .700 (Li light) 849 Senarmontite. . SbeOs Embolite Ag(Br, Cl) Manganosite........| MnO Bunsenite Lewisite 5CaO.2TiO2.3Sb205 Miersite Bromyrite gBr Dysanalite Contains CaO, FeO, TiOs, etc. Marshite Cul Franklinite (Zn, Fe, Mn)O.(Fe, Mn)20z Sphalerite (Zn, Fe)S Perovskite CaO.TiO2z i Cc Welestonites 52505575 HgO.2HgCl Hauerite...........| MnSe Aijiabandite.........| MnS ne A NREL Cu0 SMITHSONIAN TABLES- RDNHNHKHHHNHNHNHNNDKHNHNNNKHNKNHKNNDNRNH AHHH HRA RR RRR RH RH HR RRR RRR ROH RRR RRR RRR 14 364 Substance. Anorthite glass Asphalt Bell metal Boric Acid, melted oe ae “e Borax, melted “cc “oe “ “ Fuchsin oe ce Gelatin, Nelson no. 1 Gum Arabic Obsidian Phosphorus Pitch Colophony Copal TABLE 404 INDEX OF REFRACTION Miscellaneous Monorefringent or Isotropic Solids Spectrum line. ° 4 SuyomyanyaysoouY 23 pOmQnwW> yous Index of refraction. Authority. . 4890 Larsen, 1909 . 546 Miihlheim 6422 Grailich -5755 Larsen, 1909 -635 E. L. Nichols -621 See > .0052 Beer . 4623 Bedson and Williams : 4637 “ “a “c - 4694 -4624 . 4630 . 4702 - 532 Kohlrausch - 5462 Miihlheim 530 Mean .66 Ayrton, Perry -03 Mean .19 “ -33 -97 32 - 530 Jones, 1911 I. 516-1. 534 ? a 1.480 Jamin 1.514 Wollaston . 482-1. 406 Various .1442 Gladstone, Dale Saar Wollaston - 5593 Topsée, Christiansen -6574 = 3 . 6666 SF i Jamin -528 Wollaston - 548 Jamin 528 . 535 Wollaston 593 Baden Powell 61 Wood -68 3 73 “ 93 “ “cc “ ““ MH HN NN AO Oe Oe OOO OO OOO OO Dussaud Fock HAHN NNN HH ERE SMITHSONIAN TABLES. TABLE 405 30 5 INDEX OF REFRACTION Selected Uniaxial Minerals The values are arranged in the ordex of increasing indices for the ordinary ray and are for the sodium D line unless otherwise indicated. Selected by Dr. Edgar T. Wherry from a private compilation of Dr. Esper S. Larsen of the U. S. Geological Survey. Index of refraction. Mineral. Formula. ; : | Ordinary Extraordinary ray. ray. (a) Untaxtat Positive MINERALS. Chrysocolla CuO.SiO2.2H20 Laubanite 2CaO. AloO3.5Si02.6H20 Chabazite (Ca, Naz)O.Al203.4Si02.6H20 Douglasite 2K Cl.FeCle.2H20 Hydronephelite 2Na20.3Al203.6Si02.7H20 Apophyllite K20.8Ca0.16Si02.16H20 SiOz Coquimbite Fe20s. soe 9H20 i Mg0O.H ] K.0.3 Ais, 4S03.6H20 Penninite 5(Mg, Fe)O.Al203.35i102.4H20 Cacoxenite 2i°e203.P205.12H20 Eudialite 6Na20.6(Ca, Fe)O.20(Si, Zr)O2.NaCl Dioptasite CuO.SiO2.H20 Phenacite 2BeO.SiO2 Parisite 2CeOF.Ca0.3CO2 Willemite 2Zn0.SiO2 Vesuvianite 2(Ca, Mn, Fe)O.(Al, Fe)(OH, F)O.2Si02 Xenotime Y203.P205 ; i 20CuO.SOs3.2CuCls.20H20 BaO.TiO2.3SiO2 6PbO. Ne Mn)O.6SiO2.H20 CaO.W rua .718 .816 .746 . 804 945 -934 . 968 -978 .650 . 093 .029 .140 . 210 220 .420 (Li light) 378 . 510 (Li light) - 520 - 903 697 .- 201 Cassiterite O Phosgenite PbO.PbCle.CO2 Penfieldite PbO.2PbCle lodyrite AglI Tapiolite FeO.(Ta, Cb)20s n Derbylite Greenockite Moissanite Cinnabarite NNHNHNNNKHNHNKNN ND HH WAR OW ORO eH Oe ROR OH OR ROR OW Oe OR OR OW OW OW OW OW OW OH ORO WHNHHNHNKHNNNNKHNRNH HHH HHH HHH RRR RRR OR OOOO OO OOO (b) UntaxtaL NEGATIVE MINERALS. Chiolite 2NaF.AIF3 Hanksite 11Na20.9SO3.2CO2.K Cl Thaumasite 3CaO.CO2.Si02.SO3.15H20 Hydrotalcite 6Mg0O.Al2O3.CO2.15H20 Cancrinite 4Na20.Ca0.4Al203.2CO2.9SiO2.3 H20 Milarite K20.4CaO.2Al203.24Si02.H20 Kaliophilite K20. AlsO3.2SiO2 Mellite Al2O3.C1209.18H20 Marialite “Ma” = 3Na20.3Al203.18Si02.2NaCl Nephelite Na2O.Al203.2SiO2 HHH HR HHH BHR ROR RHO SMITHSONIAN TABLES 366 TABLES 405 (continued) AND 406 INDEX OF REFRACTION TABLE 405 (Continued). — Selected Uniaxial Minerals Index of refraction. Mineral. Formula. 3 5; Ordinary | Extraordinary ray. ray. (b) Untaxtat NEGATIVE MINERALS (continued). Wernerite MeiMai + Beryl 3 BeO.Al203.6Si02 Torbernite CuO.2U03. P205.8H20 Meionite “Me” = 4Ca0.3Al203.6Si02 Melilite Contains Na2O, CaO, AleOs, SiOz, etc. Apatite 9CaO.3P20s.Ca(F, Cl)2 Calcite CaO.COz Gehlenite 2CaO.Al203.SiO2 Tourmaline Contains Na2O, FeO, AlzO3, B2Os, SiOz, etc. Dolomite CaO.Mg0O.2CO2 Magnesite Pyrochroite Corundum FeO.CO2 Pyromorphite 9PbO.3P20s.PbCle Barysilite 3PbO.2Si0O2 Mimetite oPbO.3As205.PbCle PbO.PbClez PbO.WOs (Mg, Fe)O.TiO2 Vanadinite 9PbO.3V20s.PbCle Wulfenite O, Octahedrite Massicotite Proustite 3AgeS.AsoSs3 Pyrargyrite 3Ag2S.Sbe2S3 Hematite 9 (Li light) (Li light) WWHNHKHNNNNNHNNNKD HHA AR RRR RRR RHR RA NPHNHNNKHNHNNHNNNHHHHHHHH HH RRR RRA TABLE 406.— Miscellaneous Uniaxial Crystals Index of refraction. Crystal. Spectrum Authority. a) line. Ordinary |Extraordinary 4 ray. ray. . 5766 . 5217 T. and C.* .6588 .6784 Mean . 769 .760 Osann . 308 313 Meyer - 207 - 304 = -539 541 Kohlrausch .5762 - 5252 LyandiG: 5074 -5179 “ck “ - 5632 . 5146 -457 . 466 Mean . 586 -336 te 447 -453 . 5173 - 4930 T. and C. ios 1873 ccUMTCUMRM -5078 .4844 f .614 -599 Martin Ammonium arseniate NHsHeAsOx Benzil (CeHsCO)2 Corundum, Al2O3, sapphire, ruby Ice at —8°C “aL ~ Ivory . Potassium arseniate KH,AsOy “ “ec “ ce “ec Sodium arseniate NasAsO4.12H2O ct nitrate NaNOs “phosphate NasPO4.12H2O Nickel sulphate NiSOs.6H20 Strychnine sulphate ““c “ce “cs Does oepoeASHoeesys * Topsde and Christiansen. SMITHSONIAN TABLES TABLE 407 367 INDEX OF REFRACTION Selected Biaxial Minerals The values are arranged in the order of increasing 6 index of refraction and are for the sodium D line except where noted. Selected by Dr. Edgar T. Wherry from private compilation of Dr. Esper S. Larsen of the U. S. Geological Survey. Mineral. Stercorite Tridymite Thenardite Carnallite Alunogenite Melanterite Natrolite Arcanite Struvite Mascagnite Aibite Hydromagnesite Wavellite Kieserite Copiapite Whewellite Variscite Labradorite Gibbsite Wagnerite Anhydrite Colemanite Fremontite Vivianite Pectolite Calamine Chondrodite Turquois Topaz Celestite Prehnite Anthophyllite Sillimanite Forsterite Enstatite Euclasite SMITHSONIAN TABLES. (a) BrAxtaL PositrvE MINERALS. Index of refraction. nq | 1B Formula. NazO.(NH4)20.P20s.9H20 AleOs.SO3.9H20 SiOz Na20.SO3 KCl. MgCls.6H20 Al2O3.3S03.16H20 FeO.SO3.7H20 Naz0.Al203.3Si02.2H20 20.SO3 (NH4)20.2Mg0.P20;.12H2O CaO.Al203.6Si02.3 H2O0 (Naz, Ca)O.A!203.2Si02.3H20 (Ke, Ba)O.Al203.5SiO2.5H20 LizO.Al203.8SiO2 2CaO.P205.H20 2MgQ.P205.7H20 CaO.SO3.2H20 (NH4)20.SOs “Ab” = NaoO.Al203.6SiO2 4Mg0.3CO2.4H20 3Al203.2P20s.12(H20, 2HF) Mg0O.SO3.H2O0 2Fe203.5SO03.18H20 CaO.C203.H20 Al2O3.P205.4H20 AbsAn3 Al203.3H20 3MgO.P205.MgF2 CaO.SOs 2CaO.3B203.5H20 Na2O.Al2O03.P205.(H20, 2HF) 3FeO.P205.8H20 Na2O.4Ca0.6Si02.H20 2ZnO0.Si0O2.H20 4Mg0O.2Si0O2.Mg(F, OH): CuO.3Al203.2P205.9H20 2AlOF.SiO2 SrO.SO3 2CaO.Al203.3SiO2.H20 O.SQ3 nan bHHO bat to OwnuUn~InHtO 5 35 es) “5 “5 -5 WNNNN > oO H UN Dur no AHR He RHR RHR OR RR OR OR OR OR ROR RR ROR OR ROR OR OR ROR OR OR OR OR OR OR ROR OR OR OR OR ROR OR OR OR OR Oe OR OR Oe Oe wn on } oO mn S c So H ¢ RAR A Oe OW OR OR OR OR OR OR OR OR OR OR OR OR OR OR OR ORR ROR OR OR OR OR OR OR RW OR OR ROR OR ROR OR OR ORO OR ROR OR OR Oe Mg0.SiO2 2BeO.Al203.2Si02.H20 3Mn0O.P20;.MnF2 LigO. Al2O3.4Si02 CaO.MgO.2Si0O2 2(Mg, Fe)O.SiO2 LizO.2(Fe, Mn)O.P205 HHHHH HHH RRR RRR ARR RRR ARR OA OR OW OR ORR OW ROH OH HHO RRO OOOOH OA OA OO 368 TABLE 407 (continued) INDEX OF REFRACTION Selected Biaxial Minerals Index of refraction. Mineral. Formula. "a. | eB EI mn (a) BraxtaL PosiTIVE MINERALS (continued). -706 -745 -750 .746 -757 - 838 -797 . 863 - 804 -034 -o10 - 240 . 260 2320 Gee - 530 (Li) . 300 -310 . 430 (Li) . 460 (Li) .660 (Li) .420 (Li) AS Tae .650 (Li) 741 .710 Zoisite 4Ca0O.3Al203.6Si02.H20 Strengite Fe203.P205.4H20 Diasporite AlsO3.H2 Staurolite 2FeO.5Al203.4Si02.H20 Chrysoberyl BeO.AlsO3 3CuO.2CO2.H20 Fe203.As20s.4H2O0 4CuO. As205.H20 Anglesite PbO.SOs3 Titanite CaO.TiO2.SiO2z Mendipite Tantalite (Fe, Mn)O.Ta20s Wolframite (Fe, Mn)O.WOs Crocoite PbO.CrOz 2Fe203.3TiO2 Sb203.Ta20s HgO NNNNKHNHNNHNNHNKNNNNN WN ND HH HRW RRR I. Ti Te rT. I. pn I. I. I. I. qr. I. 2. 2. 2. 2. 2. 2. 2. 2. 2. 2. 2). 2. 2. (6) Braxtat NEGATIVE MINERALS. Mirabilite Na2z0.SO3.10H20 Thomsenolite NaF .CaF2.AlF3.H2O Na20.CO2.10H20 Ke20.Al203.4SO03.24H20 Epsomite MgO.SO3.7H20 Sassolite B203.H20 NazO.2B203.10H20 ZnO.SO3.7H20 Pickeringite MgO. Al203.4SO3.22H20 Bloedite Na2O.MgO.2SO3.4H20 3Na20.4CO2.5H20 Na2O.CO2.H20 (Ca, Naz)O.Al203.6Si02. 51120. K20.N205 MgO.SO3.K Cl.3H20 Gaylussite Na2O.CaO.2COz.5H20 Scolecite CaO. Al2O3.3Si02.3H2O CaO. Al203.4Si02.4H20 K20.Al203.6SiO2 Same as preceding (Na, K)20.Al203.6Si02 NaszO.CaO.2SOs 4(Mg, Fe)O.4Al203.10SiO2.H20 RR HR RH HR RHR HH RH HR ARH HR RRR RRA ROR ORO OOO oe SMITHSONIAN TABLES. TABLE 407 (Concluded) 369 INDEX OF REFRACTION Selected Biaxial Minerals Index of refraction. Mineral. Formula. na ng (b) BraxtAL NEGATIVE CRYSTALS (continued). Beryllonite Na20.2BeO.P205 Kaolinite AlO3.2Si02.2H20 Biotite K20.4(Mg, Fe)O. 2Al203.6Si02.H20 Autunite CaO.2UO3.P205.8H20 Anorthite “An” = CaO.AleO3.2SiO2 Lanthanite La203.3 CO2.9H20 Pyrophyllite Al2O3.4Si02.H20 3Mg0.4SiO2.H20 Hopeite 3ZnO0.P205.4H20 Muscovite K20.3Al203. eos 2H20 Amblygonite Al2O3.P205.2LiF Lepidolite AlzO3.3SiO2.2(K, Li)F Phlogopite K20.6MgO.Al203.6Si02.2H20 Tremolite CaO0.3Mg0.4SiO2 Actinolite Ca0.3(Mg, Fe)O.4Si02 Wollastonite CaO.SiO2 Lazulite.... a (Fe, Mg)O.Al203.P205.H20 Danburite CaO. B203.2SiO2 Glaucophanite NazO.2FeO.Al203.6Si0O2 Andalusite Al203.SiO2 Hornblende Contains Na2O, MgO, FeO, SiOs, etc. i 2CaO.2SiO2. B2O3.H20 Erythrite 3CoO.As205.8H20 Monticellite CaO.MgO.SiO2 SrO.CO: O.CO2 6(Ca, Mn)O.2A1203. aA 8Si02.H20 Dumortierite 8Al203. B203.6SiO2.H Cyanite Al2O3.SiO2 Epidote 4Ca0.3(Al, ee Atacamite 3Cu0.CuCle.3H: Fayalite 2FeO.SiO2 Caledonite 2(Pb, Cu)O.SO3.H20 Malachite 2Cu0, COz.H20 Lanarkite 2PbO.SO3 Leadhillite 4PbO.SO3.2CO2.H20 Cerussite PbO.CO2 Laurionite 2 Matlockite PbO.PbCle Baddeleyite rO: Lepidocrocite Limonite 2Fe203.3H20 in part Goethite... . : tone Valentinite Sb203 i 2Fe203.H20 in part a Terlinguaite Hutchinsonite ae OS S-PbS.2AseSs Stibnite fc BON KHNNNHNHNNHNHNNNHHH HHH HHH HH HHH HHH RRR RRR RRR RRR RRR 5 ¢ aie ‘ BRWNNHNHNNHNNHDNKHNNKNNNNRHHHHHH HHH HH HH HHH RHR HRA RRR RRR WOWONNHHNHKHNHNRNNHHHHHHHHH HH HHH HHH HHH RRR RR HARRAH RA t ‘ “ SMITHSONIAN TABLES. 370 TABLES 408 AND 409 INDEX OF REFRACTION TABLE 408.—Miscellaneous Biaxial Crystals Index of refraction. Crystal. re — Authority. - 4381 k : Brio . 5188 Ammonium oxalate, (NH4)2C204.H20. .. Ammonium acid tartrate, (NH4)H(C4H40¢) Ammonium tartrate, (NH4)2CsH4Oc..... Antipyrin, CuHi2NO2 Citric acid, CsHsO7.H2O0 Codein, CisH21NO3.H20 Magnesium carbonate, MgCO3.3H20.... £ sulphate, MgSO4.7H20 T. and C* Cloisaux Liweh Schrauf Grailich Genth Means Borel Dufet Te and GC} Mallard Schrauf TandiC. “ “ce “ 5607 4032 - 5390 - 495 -432 - 4990 - 4307 7202 b rs an :~ Potassium bichromate, K2Cr2O7 chromate, K2CrO« HHH HAHA guol sebbbi xy 6873 - 3346 -4976 4932 - 4911 4 oO Q. nitrate, KNOs sulphate, K2SO4 HH WH He Groth Dufet Brio Calderon “ Racemic acid, CsaHeOc.H20............ Resorcin, C6H6O2 Sodium bichromate, NazCr207.2H2O0 “acid tartrate, NaH (C4H40s). 2H20 Sugar (cane), Cr H20un “ec Tartaric acid, CaHeOc (right-)............ Zinc sulphate, ZnSOs.7H20 . 6610 . 5422 5397 - 5379 4953 . 4620 - 4568 4544 “cc Means T. and C. cep yecin ce HHH HHH HHH HRA ODO rUss puboURd = * Topsée and Christiansen. TABLE 409.—Miscellaneous Liquids (see also Table 410), Liquefied Gases, Oils, Fats and Waxes Temp. Index for D Refer- Temp.| Index for D Refer- Substance. oC 0. 589. ee Substance. °C 0. 580}. ence, Liquefied gases: Oils: 650 Lavendar. size SN . 464-1. 466 . 367 . 4820-1. 4852 -195 Maize. . ence , -4757-1.4768 -325 Mustard seed... : -4750-1.4762 . 180 Neat’s foot .4695-1.4708 - 384 Olive : -4703-1.4718 . 205 . 4510 325 4723-1 .4731 . 330 . 464-1. 468 194 : 4770 . 221 HORDOr es. aoe .4677 . 350 Rape (Colza). ne 8 : -4748-1. 4752 .252 Seal . ; tea -4741 325 4742 . 466 Soja bean ; .4760-1.4775 Sperm 5- . 4665-1. 4672 Sunflower....... Gi .4739 - 503 - 4649 coma ctegacooooe HH HH HHH RRR RRR 5 -4728-1. 4753 - 4799-1 . 4803 -47-1.48 . 5301-1. 5360 4587 - 4790-1 . 4833 -4737-1.4757 -4757-1. 4768 - 460-1. 467 -4702-1.4720 COh*ADAOAADAAAe AAO Oo Citronella Clove. Cocoanut... . Codiliver.s.- Cotton seed. . Fats and Waxes: Beef tallow -4552-1.4587 Beeswax. . ae 5 - 4398-1. 4451 Carnauba wax... -4520-1. 4541 Cocoa butter... .. .4560-1. 4518 Lard / . 4584-1. 4601 Eucalyptus . . Mutton tallow... - 4510 arden HH eee HR AormMeanaegaonog COoORDrrVrDAa References: (a) Martens; (b) Bleekrode, Pr. Roy. Soc. 37, 330, 1884; (c) J iveing, Dewar, Phil. Mag., 1892-3; (d) Tolman, Munson, Bul. 77, B. of C., Dept. Agriculture, ro05; (e) Seeker, Van Nostrand’s Chemical Annual. For the oils of reference d, the average temperature coefficient is 0.000365 per ° C. SMITHSONIAN TABLES. TABLE 410 371 INDEX OF REFRACTION Indices of Refraction of Liquids Relative to Air Indices of refraction. Substance. 0. 589¢ D Acetaldehyde, CHsCHO Acetone, CH3COCHs3 Aniline, CeHs.NH2 Alcohol, methyl, CH3.OH ethyl C2Hs.0OH “e “oe dn/dt s n-propyl CoH. OH. Benzene, C,.H,- Game ahi apa in Bromnaphthalene, Spee Br... Carbon disulphide, CS2 “tetrachloride, CCl... .. Chinolin, CogH7N Chloral, CCls.CHO Chloroform, CHCb Decane, CioH22 Ether, ethyl, CoHs.0.C2Hs ean /aie Ethyl nitrate, CoHs. O.NOs. . Formic acid, H.COoH.. Glycerine, CsHsOs. . rete Hexane, CHs(CHe)«CHs . Hexylene, CH3(CH2)3CH.CH2. . Methylene iodide CH,I, dn/dt . Naphthalene, CioHs Nicotine, CioHisNe Octane, CH (CH2)sCHs Or almond rites eel lelale eraser anise seed - 3593 - 5863 . 3290 . 3695 .3618 . 0004, 3854 . 5012 .0006 .6582 -6433 .6276 . 4607 .6245 -4557 -4467 . 4108 3538 . 0006 - 3853 -3714 -4739 -3754 - 3945 - 7417 . 0007 - 5823 - 5239 . 4007 .4782 -5572 -5475 ees tte Ue eae ere tte eet) et et eel peauspe ehasvcae eee eI Pe eT ea acon vA tiene 0s) SD SPL alee ete et Se aie meat cts call eee eRe eine etd . 6104 . 6026 .6188 4763 +4573 4744 -4721 - 3581 -5425 CUTpPENitiNe rere nasil se Pentane, CH3(CH2)3CHs : 3645 Phenol, CsHsOH : ; - 5684 Styrene, CsHsCH.CHe ; : . 5816 Thymol, CioHisO : —- Toluene, CH3.CeHs : .5170 Water, H20 -3435 - 3404 i 3444 - 3413 . 3411 - 3380 .3332 . 3302 HHH HHH HRA H 5485 -4955 - 3330 3338 . 3307 - 3230 et nM SIMI RIG Ainieieie oIoieNeuriiiel sala eeeneeeit larieietepabatred! ai lPURpI er ehay eer HH HHH HR RR RHR RRR RRR RRR References: 1, Landolt and Bérnstein (a, Landolt; b, Korten; c, Briihl; d, Haagen; e, Landolt, Jahn; {, Nasini, Bernheimer; g, Eisenlohr; h, Eykman; i, Auwers, Eisenlohr); 2, Korten; 3, Walter; 4, Ketteler; 5, Landolt; 6, Olds; 7, Baden Powell; 8, Willigen; 9, Fraunhofer; ro, Brihl. SMITHSONIAN TABLES. 372 TABLE 411 INDEX OF REFRACTION Indices of Refraction for Solutions of Salts and Acids Relative to Air Indices of refraction for spectrum lines. Substance. Density. | Temp. C.| Authority. (a) SoLutrons In WaTER. Ammonium chloride | 1.067 | 27°.05 | 1.37703) 1.37936| 1.38473] —- | 1.39336) Willigen. ae fas 025 | 29-75 | 34850) .35050) .35515] - | .36243) “ Calcium chloride . 39 25-65 | -44000] .44279| .44938 ~ .46001 s ‘ « 2UG al 22.0 39411] .39652| .40206) — 41078 ff ee « SEAR 25 .o 37152] .37309] .37876} — - 38666 He Hydrochloric acid .| 1.166 | 20.75 |1.40817/1.41109]1.41774 — |1.42816 i Nitric acid. . .| .359 | 18.75 | .39893] .40181| .40857 - 41961 Ue Potash (caustic) . Seog On er TO ~40052 -40281| .40808 ~ 41637 | Fraunhofer. Potassium chloride .|normal solution | .34087] .34278| .34719] 1.35049 — |Bender. & a double normal | .34982| .35179) .35645] -35904 - ss ie x triple normal | .35831| .36029| .36512| .360890| — | Soda (caustic) . .| 1.376 | 21.6 |1.41071|1.41334 1.41936 — |1.42872|Willigen. Sodium chloride. .| .189 | 18.07 | .37562| .37789| .38322|/1.38746, -— |Schutt. - ce -109 18.07 -3575!| -35959, 36442 36823 - ss et - 035 18.07 | .34000] .34191| .34628] .34969 = S Sodium nitrate 1.358 | 22.8 |1.38283]1.38535]1-39134 — |1.40121| Willigen. Sulphuric AGL gal) aati i8.3 -43444| .43669| .44168 - .44883 sf < .632 18.3 -42227| .42466| .42967 - 43094 ys s ne e220 18.3 36793] .37009] .37468 - 38158 ‘¢ Kc se 028 | 18.3 .33063| .33862| .34285) —- 34938 s¢ Zinc chloride . . .| 1.359 26.6 |1.39977| 1.40222] 1.40797 - 1.41738 ss ‘6 - 5 3 “oll pasts) || alent -37292| .37515] .38026 ~ 38845 - (b) SoLutions In EtHyt ALCOHOL. Ethyl alcohol . . .| 0.789 | 25.5 |1.35791|1.35971| 1-36395| - |1.37094| Willigen. of se 932) || 27:6 -35372| -35550| -35986| — .36662 rs Fuchsin (nearly sat- urated) ; : 3918 | .398 361 - -3759 Kundt. Cyanin (saturated) : .3831 = -3705 = 3821 seh Nore. — Cyanin in chloroform also acts anomalously ; for example, Sieben gives for a 4.5 per cent. solution w44—= 1.4593, Ms = 1.4695, wr(green) = 1.4514, we (blue) = 1.4554. For a 9.9 per cent. solution he gives 41= 1.4902, ur (green) = 1.4497, we (blue) = 1.4597. (c) SoLuTions oF PoTass1uM PERMANGANATE IN WATER.* Wave Wave- Spec- | Ind Ind Ind Ind Spec- | Inde) Ind Ind Ind leet | ee | Mr’ | Ue’ | ioe’ | Mort iene] Siig | Tages | Use | Me™ | Mae ; : sol. | 2 % sol. | 3 % sol. | 4 % sol. ; . | 1 %sol.|2%sol.| 3 % sol. | 4 % sol. 6357s Pumas 2oneneA2 = 1.3382 | 51.6 — | 1.3368 | 1.3385 - - 65.8 C | -3335 | 3348 1.3305 e | 3374 -3383 | 1.3386 1.3404 1.7 a 3343 | -3395 | -33°1 -3377 = = -340 59-4} - | -3354 | -3373 | -3393 — | -3381 | -3395 | -3398 | -3413 58-9 | D 3353 | -3372 a = +3397 | 3402 | -3414 | -3423 50.8 - SG O2MINaGo7 ln -B4ne - -3407 | .3421 | .3426 | .3439 55-3| = | -3306 | -3395 | -3417 9 eC aN ee se) 3452 ea ae eee — | .3431 | -3442 | -3457 | -3468 52.2 - BRI || e : - - - - * According to Christiansen. SMITHSONIAN TABLES. TABLE 412 INDEX OF REFRACTION Indices of Refraction of Gases and Vapors 373 A formula was given by Biot and Arago expressing the dependence of the index of refraction of a gas on pressure and No bao P_, where , 1 + at 760 n, is the index of refraction for temperature 7, 7, for temperature zero, a the coefficient of expansion of the gas temperature. More recent experiments confirm their conclusions. The formula is #,—1 = with temperature, and / the pressure of the gas in millimeters of mercury. For air see lable 413. (a) Indices of refraction. te 3 yo8(n=2) (n=1 ) 103. Air. Spectrum line. Spectrum Wave- 103 (n=1) line. Air. 2905 2911 2914 2922 -2038 -2943 .2962 .2978 .2980 .2987 OFAAOO WS CAR 2993 -3003 3015 3023 *3031 *3043 3053 3004 +3075 GHanoveZzs length. el we -4861 5461 5790 6563 .43600 5462 .6709 6.709 8.678 .2951 .2936 .2930 2919 .2971 .2937 2918 .2881 2888 O. -2734 S27 2710 2698 -2743 .2704 2683 2643 -2650 N. Hi: .1406 gO -1393 1387 1418 CUS 1385 -1361 .1361 .3012 .2998 .2982 CO, 4506 4471 .4804 -4579 | First 4, Cuthbertsons; the rest, Koch, Igoo. Pp: 25-27). Kind of Substance. light. Acetone’. « . D Ammonia sc AA D JAVON 9 A161 Uc D Benzene . : D Bromine. . . D Carbon dioxide | white “ “ D white Carbon disul- D phide white white white Carbon mon- } oxide . Chlorine . Chloroform Cyanogen Ethyl alcohol Ethyl ether . Helium Hydrochloric acid . Indices of refraction and authority. I.001079-I.001 100 1.000381-1.00038 5 ,000 37 3-1.000379 .000281 Rayleigh. .001700-1.001823 .001132 Mascart. .000449—1.0004 50 .000448-1.0004 54. .001 500 Dulong. 001 478-1.001 485 .000340 Dulong. .009335 Mascart. .000772 Dulong. .000773 Mascart. .001436-1.001 464 .000834 Dulong. -000784—1.000825 .00087 I-1.00088 5 OOI 521-1.001 544 .000036 Ramsay. .000449 Mascart. -000447 Zi Substance. Hydrogen Hydrogen sul- phide Methane . “ Methyl alcohol. Methyl ether Nitric oxide. ee “ce Nitrogen . “ce Nitrous oxide “cc “cc Oxygen “ce Pentane : Sulphur dioxide Water. “ec SMITHSONIAN TABLES. Kind of light. white D D D D D D white D white D white D white D D D D (b) The following are compiled mostly from a table published by Briihl (Zeits. fiir Phys. Chem. vol. 7, The numbers are from the results of experiments by Biot and Arago, Dulong, Jamin, Ketteler, Lorenz, Mascart, Chappius, Rayleigh, and Riviére and Prytz. of one observer the name of that observer is given. When the number given rests on the authority The values are for 0° Centigrade and 760 mm pressure. Indices of refraction and authority. 1.0001 38-1.000143 1.000132 Burton. .000644 Dulong. 1.000623 Mascart. 1.000443 Dulong. .000444 Mascart. .000549—1.000623 .000891 Mascart. .000303 Dulong. .000297 Mascart. .00029 5-1.000300 .000296-1.000298 .000503-1.000507 .000516 Mascart. .00027 2—1.000280 .00027 I—1.00027 2 .0o1711 Mascart. .000665 Dulong. .000686 Ketteler. .000261 Jamin. .000249-1.000259 TABLE 413 INDEX OF REFRACTION TABLE 413.—Index of Refraction of Air (15°C, 76 cm) Corrections for reducing wave lengths and frequencies in air (15° C, 76 cm) to vacuo. 374 The indices were computed from the Cauchy formula (m — 1)107 = 2726.43 + 12.288/(A2 X 10-8) + 0.3555/ (A4 X 10°16). For o° C and 76 cm the constants of the equation become 2875.66, 13.412 and 0.3777 respectively, and for 30° C and 76 cm, 2589.72, 12.259 and 0.2576. Sellmeier’s formula for but one absorption band closely fits the observations: 2 = 1 + 0.00057378A2/(A2 — 595260). Ifm — 1 were strictly proportional to the density, then (n—1)o/ (n — 1)t would equal 1 + at where a should be 0.00367. The following values of a were found to hold: 0.85 0.75 0.65 0.55é 0.45 -¢ 0.35M¢ 0.25 M @ 0.003672 0.003674 0.003078 0.003685 0.003700 0.003738 0.003872 The indices are for dry air (0.05 + % COs). Corrections to reduce to dry air the indices for moist air may be made for any wave-length by Lorenz’s formula, + 0.000041(m/760), where m is the vapor pres- sure in mm. The corresponding frequencies in waves per cm and the corrections to reduce vwave-lengths and frequencies in air at 15° C and 76 cm pressure to vacuo are given. E.g., a light wave of 5000 Angstroms in dry air at 15° C, 76 cm becomes 5001.39! A in vacuo; a frequency of 20,000 waves per cm correspondingly becomes 19994.44. Meggers and Peters, Bul. Bureau of Standards, 14, p. 731, 1918. Wave- length, A Dry air X 107 (Ce 76 cm Ang- stroms. Vacuo for \ in air (nX — A). Add. 009000 00000 oO. oO. °. Oo. °. HHHA He HHH HA HHHHO HHHHH SMITHSONIAN TABLES. Fre- quency cm I IN in air. 50,000 47,019 45,454 43,478 41,666 40,000 38,461 37,037 35,714 34,482 33,333 32,258 31,250 30,393 20,411 28,571 27,777 27,027 26,315 25,041 25,000 24,390 23,809 23,255 22,727 22,222 21,739 21,276 20,833 20,406 20,000 19,607 19,230 18,867 18,518 Vacuo correction (n — 1) |correction|Waves per} ¢). I ope ee nn 2X Subtract. 16. Te TA Tio7 I2. I2. Ir. LOS Io. Io. NUNN OH MWOOO Anan ANnNAD Annan Wave- length, Av Ang- stroms. Dry air X 107 Toe 76 cm Vacuo for A in air (nX — A) Add. NN NNNNNNNN Fre- quency — ion | Wav r Tis). 82 (n I) |correction €s Per |fo- = in air cm I A in air. 18,181 17,857 17,543 17,241 16,049 16,666 16,393 16,129 15,873 15,625 15,384 15,151 14,925 14,705 14,492 14,285 14,084 13,888 13,608 . 13,513 13,333 13,157 12,987 12,820 12,658 12,500 12,345 12,121 11,764 11,428 II,1II 10,810 10,526 10,256 10,000 Vacuo correction A Gaon): Subtract. CFS ph) hae a GR ee eo WR WW WW NHN NHWWWW Ww WWWWwW TABLES 414-417 375 MEDIA FOR DETERMINATIONS OF REFRACTIVE INDICES WITH THE MICROSCOPE TABLE 414,—Liquids, np (0.5891) = 1.74 to 1.87 In 100 parts of methylene iodide at 20° C the number of parts of the various substances indicated in the following table form saturated solutions having the refractive indices specified. When ready for use the liquids can be mixed to give intermediate refractions. Commercial iodoform (CHIs) powder is not suitable, but crystals from a solution of the powder in ether may be used, or the crystalized product may be bought. A fragment of tin in the liquids containing the SnI, will prevent discoloration. TABLE 415.—Resinlike Substances, np (0.589) — 1.68 to 2.10 Piperine, an inexpensive alkaloid, comes in very pure straw-colored crystals. Melted it dissolves the tri-iodides of Sb and As very freely. The solutions are fluid at slightly above 100° and when cold, resinlike. Three parts antimony iodide to one part of arsenic iodide with varying proportions of piperine are easier to manipulate than one containing either iodide alone. In preparing, the constituents, in powder of about 1 mm grain, should be weighed out and then fused over, not in, a low flame. Three-inch test tubes are suitable. Per cent Iodides. Index of refraction 1.683 | 1.700 | 1.725 | 1.756 | 1.794 | 1.840 | 1.897 | 1.968 | 2.050 TABLE 416.—Permanent Standard Resinous Media, np (0.589) — 1.546 to 1.682 Any proportions of piperine and rosin form a homogeneous fusion which cools to a trans- parent resinous mass. On account of the strong dispersion of piperine the refractive indices of minerals apparently matched with those of mixtures rich in this constituent are 0.005 to 0.01 too low. To correct this error a screen made of a thin film of 7 per cent antimony iodide and 93 per cent piperine should be used over the eye-piece. Any amber-colored rosin in lumps is suitable. Per cent Rosin. Index of refraction 1.670 | 1.657 1.604 | 1.590 | 1.575] 1.560 | 1.544 All taken from Merwin, Journ. Washington Acad. Sci. 3, 35, 1913. TABLE 417.—Substances, np — 1.39 to 1.75 n-Heptane p-Xylene ; o-Toluidine ‘ a-Chloronaphthalene Octylene 4 Chlorobenzene 1. o-Bromophenol 1.5 a-Bromonaphthalene Cyclohexane Eugenol 2 Bromoform ‘ a-Iodonaphthalene d-Limonene Nitrobenzene : Quinaldine : Methylene iodide Anethole P Todobenzene SMITHSONIAN TABLES 376 TABLES 418-420.—THE REFLECTION OF LIGHT According to Fresnel, the amount of light reflected by the surface of a transparent medium Rk eel sin? (i — r) tan? (¢ — r) = # AB) 2) eae tan? (i + 7) dence; B is that polarized perpendicular to this; 7 and r are the angles of incidence and refraction. TABLE oe reflected when i=O° or Incident Light is Normal to Surface (2 -1)2/(m-+1)2 ; A is the amount polarized in the plane of inci- ‘B(A+B). | : (A+B). | es ae | 4 (A+B). 4.00 : : | : 50.00 66.67 96.08 |e : 2.78 || : : : 44.44 | 100.00 | | 4(A+B). 1.000 ‘ | 1.000 é The values for A and B 1.015 : 1.000 ; are strictly (dn2/4) sect i 1.063 .039 1.001 : and (dn?/4) (1— tan? i); 1.149 .862 1.005 : In columns 2, 3, and 4 | 1.282 S752 1.017 y dn2/4 is omitted. | 1.482 612 1.047 | 1.778 -444 Teleae 2.221 .260 1.240 : 2.904 .088 1.496 : | 4.000 .000 2.000 5-857 176 3.016 9-230 1.081 5.160 16.000 4.000 10.000 31.346 12.952 22.140 73-279 42.884 57-981 222.85 167.16 195.00 1099.85 Q71.21 1035.53 17330.64 16808.08 17069.36 oe) PEb hppa RES NNO ON AADAA DOnw Onan w omg YNUM who Angle of total polarization = 57° 10/.3, A = 16.99. * This column gives the degree of polarization + Columns 5 and 6 furnish a means cf determining A and BS for other values of x. They represent the change in these quantities for a change of x of 0.01. Taken from E. C. Pickering’s ‘‘ Applications of Fresnel’s Formula for the Reflection of Light.” SMITHSONIAN TABLES. TABLE 421 eT OPTICAL CONSTANTS OF METALS Two constants are required to characterize a metal opticaily, the refractive index, 2, and the absorption index, 4, the latter of which has the following significance: the amplitude of a wave after travelling one wave-length, A! measured in the metal, is reduced in the ratio! 1 :e—27k or for A 2mdk ees é ; 2mdnk any distanced, 1:e—~y; ; for the same wave-length measured in air this ratio becomes 1:e ——),_, nk is sometimes called the extinction coefficient. Plane polarized light reflected from a polished metal surface is in general elliptically polarized because of the relative change in phase between the two rectangular components vibrating in and perpendicular to the plane of incidence. Fora certain angle, ¢ (principal incidence) the change is 90° and if the plane polarized incident beam has a certain azimuth y (Principal azimuth) circularly polarized light results. Approximately, (Drude, Annalen der Physik, 36, p. 546, 1889), sin ¢ tan (i +2) (1 + 4 cot? ¢). For rougher approximations the factor in parentheses may be omitted. R—=computed per- centage reflection. k=tan 2y (1 — cot 24) and n= (The points have been so selected that a smooth curve drawn through them very closely indicates the characteristics of the metal.) Computed. k nk Authority. Cobalt : Minor. “ec HH rn WO Orn w Ingersoll. Onw uno Minor. eé vv w “c w Ingersoll. Gold Deurnoorbe On> Iridium Non aD OWwWD Da Tool. Drude. Ingersoll. Nickel nn a “ Platinum : c : ’ ‘ Forst.-Fréed. ROE EOS Teer UT tre ee OG PS ON OOS) Silver Ingersoll. ‘ ee Forst.-Fréed. oc “ce Minor. ae “ “ee Ingersoll. “ Drude, Annalen der Physik und Chemie, 39, p- 481, 1890; 42, p. 186, 1891; 64, Pp. 159, 1898. Minor, Annalen der Physik, 10, p. 581, 1903. ‘Tool, Physical Review, 31, p. 1, 1910. Ingersoll, Astrophysical Journal, 32, p. 265, 1gt0; Férsterling and Fréedericksz, Annalen der Physik, 40, p. 201, 1913. SMITHSONIAN TABLES. TABLES 422 AND 423 TABLE 422.—Optical Constants of Metals (Additional Data) Ir* Fe.§ Pb.* Mg.* Mn.* Hg. (ligq.) wn oh HHRAARHAAWHA AAW HE HPHAWEARRRWW HD HH -400 -490 589 -760 589 125 yale 559 -579 589 -579 -579 oi, 441 668 | 2.94 Bale 2.93 2.60 4.18 | 3-67 3°53 -004 2.05 1.48 2.76 3-93 0.55 CO3E 1.93 2.62 4.67 2.31 1.49 0.45 0.06 0.09 0.08 0.08 2.61 2.31 5:25 27 3-51 0.61 3:19 4.66 5.08 w 2 FPP BPWW HW FH DDOAUUUwW as film in vacuo. A= wave-length, n refraction index. k = absorption index, R = reflection. (1) Drude, see Table 421 ; (2) Kundt, prism used, Ann. der Physik und Chemie, 34, p. 477, 36, p. 824, 1889; (3) v. Wartenberg, Verh. | deutsch. Physik. Ges. 12, p. 105, 1910; (4) | Meier, Annales der Physik, 10, p. 581, 1903; (5) Wood, Phil. Mag. (6), 3, 607, 1902; (6) Ingersoll, see Table 421. * solid, t electrolytic, { prism, § deposited Wave- length Bb ~ NEO SE ieee as 000000 Bn _ TABLE 423.—Reflecting Power of Metals (See page 379) Coblentz, Bulletin Bureau of Standards, 2, p. 457, 1906, 7, p. 197, 191T. samples were not perfectso that the corresponding values have less weight. The methods for polishing the various metals are described in the original articles. The surfaces of some of the The following more recent values are given by Coblentz and Emerson, Bul. Bur. Stds. 14, p. 207, 1917; Stellite, an exceedingly hard and untarnish- able alloy of Co, Cr, Mo, Mn, and Fe (C, Si, 8S, P) was obtained from the Haynes Stellite Co, Kokomo, Indiana. Wave-length, “, «1 “20 | -30:, 250) .75)) 0.09) (2.00) §3500) )44/.008 5.007) 9-00 Tungsten, - _ =i eS Omer sa 576 .900 .943 .048 .953 _ Stellite, Smale 42 500 OSs O7, -689 .747 .792 .825 -848 .880 SMITHSONIAN TABLES, TABLES 424 AND 425 379 TABLE 424.—Reflecting Power of Metals Perpendicular Incidence and Reflection (See also Tables 426-428) The numbers give the per cents of the incident radiation reflected. ys + 5Fe. Steel. Untempered, zercially Pure, Gold. Electrolytically Deposited. Brass. (Trowbridge), Silver. Chemically Deposited. Wave-length, p. Silver-backed Glass, Mercury-backed Glass. Mach's Magnalium. 69A/+ 31Me, Ross’ Speculum Metal. 68.2Cu + 31.857, Nickel, Electrolytically Deposited. Copper. Platinum. Electrolytically Deposited, Copper. Electrolytically Deposited. Comm Brandes-Schiinemann Allo 32Cw+ 3452+ 29Ni fe ee Wet Go Gs Go ty & 00 nw = Paes em eset FuUM ON KN ff Ww ele ols tey es Goo CONuW = ow ON in OV Mmnh PPL LP =~ eOON OUMMWW nnd ON oO ty Sok OOH -. -N OOOO OONNNI gu GGS) A GOO INO FMUM COO™NO W Based upon the work of Hagen and Rubens, Ann. der Phys. (1) 352, 1900; (8) I, 1902; (11) 873, 190%. Taken partly from Landolt-Bérnstein-Meyerhoffer’s Physikalisch-chemische Tabellen. TABLE 425.—Percentage Diffuse Reflection from Miscellaneous Substances Lamp-blacks. Wave- length Acetylene Camphor. Pt. black electrol Green leaves. Lead oxide. Al. oxide. Zinc oxide. White Paper. carbonate. | Asphalt. Black velvet. Black felt. Red brick. Paint. ow Unga V1 Co 2 e CO ty 00 00 CNB RCS Ro N™N PHOWHW fh Onk NN *Not monochromatic (max.) means from Coblentz, J. Franklin Inst. rgr2. Bulletin Bureau of Standards, g, p. 283, 1912, contains many other materials. SMITHSONIAN TABLES. 380 TABLES 426-428 TABLE 426.—Percentage Refleotion from Metals, Violet End of Spectrum (Coblentz, Stair, Bur. Standards Journ. Res., 2, 343, 1020.) Wave length in w......... ‘ Ni electroplated vac. fused Ag (min. 7%, 334) Stellite (Co, Cr, Mo) “ Stainless steel, 13% Cr.... Cobalt Speculum Rey fe Rae ae Beryllium (08.7%) (Oy) | 5G) Chromium on steel 71 TABLE 427.—Ultra-violet Reflecting Power of Some Metals (Coblentz, Stair, Bur. Standards Journ. Res., 4, 189, 1930.) 0.250u .300 Aluminum, cast, polished. -45 of lled ; 28 Rhodium : 537 Tin, polished : .38 Duralumin .24 aol “ tarnished to . 20 TABLE 428.—Infra-red Reflectivity of Tungsten (Temperature Variation) Three tungsten mirrors were used, — a polished Coolidge X-ray target and two polished flattened wires mounted in evacuated soft-glass bulbs with terminals for heating electrically. Weniger and Pfund, J. Franklin Inst. Per cent increase in reflectivity in Absolute reflec- going from room temperature to tivity at room temperature in per cent. 7 = - 2056° K. Bg “0 -O 3 5 5 See also Weniger and Pfund, Phys. Rev. 15, p. 427, 1919. SMITHSONIAN TABLES. TABLES 429-431 381 TABLE 429.—Percentage Reflecting Power of Dry Powdered Pigments Taken from “The Physical Basis of Color Technology,” Luckiesh, J. Franklin Inst., rot7. The total reflecting power depends on the distribution of energy in the illuminant and is given in the last three columns for noon sun, blue sky, and for a 7.9 lumens/watt tungsten filament. _ Spectrum color. 's 3 Green. Yellow. Orange. Sky light. Tungsten Wave-length in uw jo. 44/0. 46]0. 48] 0. 50/0. 52/0. 54] 0. 56]0. 58] 0. 60/0. 62/0. 64]0. 66/0. 68/0. 70 American vermilion.... Venetian red Tuscan red... Indian red NH NNO PNY CUM Chrome yellow ochre. . . Yellow ochre Chrome yellow medium. iS} op, Chrome yellow light... . Chrome green light.... Chrome green medium.. Cobalt blue * Non-monochromatic means from Coblentz, Bul. Bureau Standards 9, p. 283, 1912. For the REFLECTING (and transmissive) power of ROUGHENED SURFACES at various angles of incidence, see Gorton, Physical Review, 7, p. 66, 1916. A surface of plate glass, ground uniformly with the finest emery and then silvered, used at an angle of 75°, reflected 90 per cent at 4u, approached too for longer waves, only ro at ry, less than 5 in the visible red and approached o for shorter waves. Similar results were obtained with a plate of rock salt for transmitted eneiny when roughened merely by breathing on it. In both cases the finer the surface, the more suddenly it cuts off the short waves. TABLE 431.—Reflectivity of Snow, Sand, Etc. (Hulburt, Journ. Opt. Soc. Amer., 17, 23, 1928.) Sodium ¢ White Maine Fla. Crushed Plaster White carbon- Sodium cotton sand* sand quartz Snow of paris paper ate chloride cloth § tONOAL ccc 15 40 35 40 8 14 38 tC. O:Sile tooo 25 40 50 40 53 30 28 49 COL 2Opb cee ee 33 50 53 60 30 35 54 COZ Uscdecse Gt 30 28 63 15 18 55 wcvcvccccses 4 ee ee ee ee ee ee * Yellow white grains of many kinds. 7 Very white. + Anhydrous, § Handkerchief. SMITHSONIAN TABLES 382: TABLES 432 AND 433 TABLE 4382.—Reflecting Power of Powders (White Light) Various pure chemicals, very finely powdered and surface formed by pressing down with glass plate. White (noon sunlight) light. Reflection in per cent. Nutting, Jones, Elliott, Tr. Ill. Eng. Soc. 9, 593, 1914. Aluminum oxide............ 83.6 Magnesium carbonate...... 86.6 Sodiumichlondes....2 ee 78.1 Barium sulphateriyee siti: 81.1 mG a (block) 97.5 Sodium sulphate............ 17-9 BOraK yao Sate 81.6 Magnesium oxide.......... 85.7 Starch 42) esters 80.3 Boriciacid sh tebe once cone 83.2 Rochelle‘’salt-" 5. vache 79.3 SUfal a ec oe ere one 87.8 Calcium carbonate.......... 83.8 Salicylictacideemaaenaieceee 81.1 artarictacid=nc-peeeeiceae 79.1 Gitrietacidys 5.3 ses ost cele 81.5 Sodium carbonate.......... 81.8 | Wave-length of max. energy of Nernst lamp used as source about 2. TABLE 433.—Variation of Reflecting Power of Surfaces with Angle Illumination at normal incidence, 1} watt tungsten lamp, reflection at angles indicated with normal. Ill. Eng. Soc., Glare Committee, Tr. Ill. Eng. Soc. 11, p. 92, 1916. Angle of observation. Magnesium carbonate block............... 0.88 — — 0.88 | 0.88 | 0.87 | 0.83 | 0.72 | 0.68 Mapnesiumroxides. aecnnn ipeitees anor nine 0.80 — — 0.80 | 0.80 | 0.80 | 0.77 | 0.75 | 0.66 Matt photographic paper................ .| 0.78 — — 0.78 | 0.78 | o 78 | 0.78 | 0.76 | 0.72 Wihiteiblotterc és. ates atin waneoeh ae 0.76 — — 0.76 | 0.76 | 0.76 | 0.73 | 0.70 | 0.67 Rotiopalseroundise sete mee neces 0.69 | 0.69 | 0.69 | 0.69 | 0.69 | 0.69 | 0.68 | 0.66 | 0.64 Blashed opal, notizround!s)s.).0).0, sace ese. Diese |trese ieL-s 0.31 | 0.22 | 0.21 | 0.20 | 0.20] 0.18 Glass fineyerounder. aA eee eee ee 0.29 | 0.29 | 0.29 | 0.29 | 0.27 | 0.20 | 0.14 | 0.13 | 0.12 Glass#coursesproundmasce eine oe eee 0.23 | 0.22 | 0.2r | 0.20 | 0.19 | 0.16 | 0.14 | 0.11 | 0.12 Matt warnishronstoileas. se seen eeiee omen 0.83 — 0.78 | 0.72 | 0.62 | 0.49 | 0.28 | 0.21 | 0.16 IMnrroniwathigrounditacelans setae cere 4.9 — — 4.55 | 3.86 | 3.03 | 0.78 | 0.42 | 0.35 The following figures, taken from Fowle, Smithsonian Misc. Col. 58, No. 8, indicate the amount of energy scattered on each side of the directly reflected beam from a silvered mirror; the energy at the center of the reflected beam was taken as 100,000, and the angle of incidence was about 3°. Anglerofsreflections 32 =e eerie sie 3’ 8’ 10’ TS, 20/ 30° ae 60’ 100! ISN Vinoe feat te ee Te oes 100,000 600 244 146 107 66 33 22 Il SMITHSONIAN TABLES TABLE 434 383 THE REFLECTING POWER OF BUILDING MATERIALS Filter I (1.78u), Chance’s blue-green contrast filter No. 6, 3.3 mm thick, with their orange contrast filter No. 4, 2.7 mm thick. Filter II (0.844), 2 cm water-cell, Chance’s orange contrast filter No. 4, and cobalt-blue glass, 1.8 mm thick. Filter III (0.614), 1 cm Ky Crp O; sol. (72 g/l) and 1 cm cell CuSO, sol. (57 g of hydrated salt/1). Filter IV (0.50u), 2 cm cell CuSO, sol. sat. at 14.2° C. Gold film: radiation from ‘ ‘pointalight ’’ through a thin gold film can be used in place of sunlight (compare with computed values). (Beckett, Proc. Phys. Soc., 43, 227, 1931.) Description Magnesium carbonate CUAY TIEES Dutch: light red Machine-made: red Ef lighter red . dark purple Hand-made: red ro red-brown CONCRETE TILES Uncolored Brown: very rough SLATES Dark gray: smooth * fairly rough rough Greenish gray: rough sc Blue-gray Silver-gray (Norwegian) OTHER ROOFING MATERIALS Asbestos cement: white Enamelled steel: Galvanized iron: ne very dirty whitewashed Special roofing sheet: brown i green “cc Bituminous felt Aluminized felt Weathered asphalt Roofing lead: old BRICKS Gault: cream Stock: light fawn Fletton: light portion a dark portion Wire cut: red Sand-lime: red Mottled purple Stafford: blue Lime-clay (French) SMITHSONIAN TABLES I II III IV (1.784) (0.84u) (0.61u) (0.50) 0.99 0.98 0.66 0.56 +34 -31 32 -19 -37 .28 384 TABLES 435 AND 436 For classification of various light and radiation filters with bibliography, plots, and dis- cussions, see Gibson, Spectral Filters, Journ. Opt. Soc. Amer., 13, 267-280, 1026. Filters for the reproduction of sunlight and daylight and the determination of color temperatures, see Davis, Gibson, Bur. Standards Misc. Publ. 114, 1931. TABLE 435.—Light Filters, Narrow Spectrum Regions (Jones, Journ- Opt. Soc. Amer., 16, 259, 1928. Filters from the following components : Distilled HzO; Ag. sol. CuSOs-5H20; NiSOs-7H20; Glasses, Corning G 986A, G 586 G 980A; dyed gelatin, Wratten filters 88A, 25, 61, 49.) ; Concentration Wave lengths Transmissi p : sion Filter and Absorbent thickness imits Max. .720— 1.400 ee .720— 1.380 .800 .720— 1.020 : .590— .690 .630 .490— .690 530 .380— .500 .460 .330- .430 380 .200— .360 de HENNNNDNDD , 5%, AO, bi => 5%, G 586, hear ee tevshere es .32 cm; 10%, G 986, NiSO,-7H.0..... .32 cm; 50%, TABLE 436.—Absorbing Power of Various Materials—Infra-red. (Cartwright, Phys. Rev., 35, 415, 1930.) The absorptive power is an integrated effect over the entire far infra-red. Litharge, powdered glass, white lead, copper sulphide, celestite, and red phosphorus were the best absorbers beyond sou. A very thin coat of the absorbing material in most cases was an inefficient absorber of the extreme infra-red waves. A very poor absorbing material in most cases such as copper or platinum will absorb if the surface is sufficiently rough. For radiometers, the absorbing material is better when mixed with turpentine and alcohol and painted on the vanes. For thermocouples, the absorbing material is better if it is mixed with lacquer. 60-fold sensitiveness and better steadiness comes from evacuation. The high absorption of glass in the near infra-red suggests its use as a source of radia- tion. Two Pt wires separated by 4 mm and covered with glass were heated by an electric current; the hot portion of the glass between the wires served as a source of extreme infra- red radiation. A convenient method of filtering out the near infra-red is to grind the windows with emery so that the pits are about 4u deep. The apparatus may be adjusted with visible light by covering the rough surface with turpentine. Radiation absorbed for A<5M ADS5o0u V LST Radiation absorbed for A<5u@ A>Ds50Lu V TT V Substance Substance Mithareee rn. 6 tee 10.8 4.3 .40 Silver sulphide ..... 12.8 4.4 .34 Ground glass ....... TG) Ay, eo Copper sulphate crys- Powdered glass .... I1.7 5.0 .43 tals from solution. 15.0 4.1 .27 White lead 2 Pb Wellsbach mantle COE b COR) see l4:Onr4-One-33 MILO Loonoonooc So) 3535 White lead in lacquer 14.3 4.4 .31 Platinum: black |... 2: 18.2 4.4 .24 Red phosphorus .... 18.3 5.0 .27 Tartaric acid and Red phosphorus from SURAT ond tre eres 16.0 3.9 .24 al matches Doseseee 1707) eS 20 Mall CM ets eoxs oy ahetekous ators 121593. one 30 Celestite, powdered Wiatertclassir sin 12 Ta ae SrS@Gtra scree « TA7, 46 31 Tellurium, powdered. 19.2 3.3. .17 Brucite, powdered Nracliaiertaleresteteletelereners 1G:8) 310) 20 Wike((Ols\a wacooos TA) PACA 37, Lacquer ...-.-.-+++- 8.6 3.0 .35 Angelsite, powdered Gastorsoilleaeraratcerel SiSeaisarae PHSOR Gs: Aeeces 1422) 402) 30 Glycerine 2... Mca saeco Copper sulphide .... 17.1 5.2 .30 Turpentine ......... 8:1, 02 o2 Copper oxide ...... 13:8 44) 32 Clean receiver ...... AO (OF 07/ Ss SMITHSONIAN TABLES TABLE 437 385 TRANSMISSIBILITY OF RADIATION BY DYES Percentage transmissions of aqueous solutions taken from The Physical Basis of Color-Technology, Luckiesh, J. Franklin Inst. 184, 1917. Spectrum color —> Violet. Blue. Wave-length in u — Carmentruby, Optecs,).. sn Amido naphthol red Coccinine Erythrosine Hematoxyline Alizarinered Acid rosolic (pure) Rapid filter red Aniline red fast extra A...... | Pinatype red fast Tele ISPAVESSsas elie al PS aecel sie lel aleismens lies Rose bengal Cobalt nitrate Ha w NOR b oo tor | liens eal iat mol liens IT) Sell lleunal || w Tartrazine Chrysoidin ; Aurantia Aniline yellow phosphine Fluorescein Aniline yellow fast S Methyl orange indicator nn nN Vee w | wl ls KH mn Uranine naphthaline Orange B naphthol Safranine Martius gelb Naphthol yellow Potassium bichromate, sat... . Cobalt chromate Teel fal es lecsualbal Selec ele lle ienel sl] Sloullaxwtlst lit. Sal TIM Veleerale literal tele | H _ Naphthol green Brilliant green Filter blue green Malachite green Saurgriin Methylengriin Aniline green naphthol B Neptune green Cupric chloride Turnbull’s blue Victoria blau Prussian blue (soluble) Wasser bl Resorcine blue Toluidin blau Patent blue Dianil blue Filter blue Aniline blue, methyl Pes Tete ees & len | Wallies coals ° ~ tb w Sy |[lfsrsocsp lect Nv Ql enulo ls x3 eles lea H oo wn no 8 | L118le lund la laliistsyrretes H kan H Ear H NO Oo CO 1c) Rb Ann On E~ | op,n~r H Magenta Gentiana violet Rosazeine Iodine (dense) ! Rhodamine B | Acid violet Cyonine in alcohol Xylene red Methyl violet B - nw [4 1F8lass lata lH | BRL wo Ls wr l118alllel L1 180118 || | For the infra-red transmission (to 124) and reflection powers of a number of aniline dyes, see Johnson: and Spence, Phys. Rev. 5, p. 340, 101s. Scientific Paper 440 of the Bureau of Standards, 1922, gives spectrum transmission curves (0.24 to 1.36 #) for the following dyes. Napthol Yellow S, Orange I, Amaranth, Erythrosine, Indigo Disulpho Acid, Ponceau 3R, and Light Green S F Yellowish. SMITHSONIAN TABLES. 386 TABLES 438 AND 439 TABLE 438.—Transmissibility of Radiation by Jena Glasses Coefficients, a, in the formula I; = Joa‘, where Jo is the Intensity before, and J; after, transmission through the thickness ¢. Deduced from observations by Miiller, Vogel, and Rubens as quoted in Hovestadt’s Jena Glass (English translation). Coefficient of transmission, a. 375 B | 390 # +434 & | +436 K| -455¢@ |. Unit ¢=1 dm, O 340, Ord. light flint 388 | .456 569 | .680 O 102, H’vy silicate flint - | .025 .502 | .566 O 93, Ord. se ae - — | .714 ©2035, a 583 .667 | .806 O 598, (Crown) = = Unit t=1 cm. S 204, Borate crown S 179, Med. phosp. cr. O 1143, Dense, bor. sil. cr. O 1092, Crown ©) reaBrig O 451, Light flint O 469, Heavy “ O 500, “c “ce S 163, “ “ TABLE 439.—Transmissibility of Radiation by Jena Colored Glasses Taken from Catalog 4213, 1931, Schott and Gen, (41 glasses). R is reflection factor yellow light for two surfaces. Values of transmission are for I mm thickness. Ordinary figures refer to wave lengths in yp, .281 to .775, black-faced to infra-red. -700 Glass Density] .281 .302 : -366 -436 .480 | .546 | .578 | .644 -850 -950 ae 1.30 1.60 2.00 2.20 2.40 2.60 2.80 durability R WiGar 217) he S50 -OOnm OO a OONP OOM = OO mmol .00 222) Pell: 04 .03 .04 .06 11 15 86.19 LOA AON ae O77 SON eAAL 9-O40m OS tn- Olas iL 30 er-O Suee 258-40) 7 2500 59-694 ae 00) BOO. AW Meo 70) eS Ce Olen Olen a OOM O7] 2 atl Ges oh 2) 4 2145 59) 6345 {00} OO) 164) 7203) 405) 04) 288)" 275 o2 col 25) eS 47, On OOM DON DOMMES, -00)) 00) 1: 100) 2020) 47a Ti/aeee 5 O) ane uaee OO 2055 5-09 ee: ents ams OD meer caer OD e/ ae OF) :00), 4.00 64 :99 1.00) 1:00 1-00, {1.00 “oo .00 1.00 00 1.00 .99 .99 .98 .94 .84 Or QO ¢ 201) 67a 92) 97) 90K O40. O6 0 o oo ae -99) 99) 7399) 299) 98) 9485 (oo) Holy) cl {OO Ole 2405-90) 90) 0009 Ooo Ole 99 Oe 97 De Oe 200) 00. =: 100) | 00) 00) 00) OONO2msmE.O5 BET Ay i IS eh aay PF Salil LOON 00) © = £00) 00) OO) 00) 00 025-00 98 .98 . A) A A Pry) 2008 7-001) 20) 59003) -OOR r-OSsues7OMmna 7 O {Ol hg Hie) 6783 ths) oh) 7h Do U G 1 dark purple (u. v., extreme red). B G 1 blue (u. v., extreme red). B G 4 blue (i. r.). B G 10, light blue green, i. r. absorption. V G 1 yellow-green. G G 2 colorless, u. v. absorption. G G 4 almost colorless, strong u. v. absorption. G G 11 dark yellow for contrast filters. R G 2 pure red. RG 5 dark red. N G 5 light neutral. & i] aN 4 ° Nd mn - Nv . Pe on % G 3 BG 5 BuG X% V Gt 2 GG 3 GG 2 GG 2 RG 2 RG 2 NG I on SMITHSONIAN TABLES TABLES 440 AND 441 387 TABLE 440.—Transmissibility of Radiation by Jena Ultra-violet Glasses No. and Type of Glass. | Thickness. | 0.397 @ | 0.383 M | 0.361 M | 0.346 m@ | 0.325 UV 3199 Ultra-violet 0.99 : 0.90 se ! ; 0.89 E 0. 36 UV 3248 : s 1.00 g 0.98 cs fe 0.98 | 0.92 0.78 s6 ! : 0.79 s 0.08 TABLE 441.—Transmissibility of Radiation by American Glasses The following data giving the percentage transmission are selected from Coblentz, Emerson and Long, Bull. Bureau Standards, 14, 653, 1918. Thick- Wave lengths in p Glass or substance, manufacturer | ness, mm. Purple fluorite... . Gold film on Crookes’ ‘glass “crown glass. . Molybdenite Cre(SOx4)3:18 H2O Chrome alum, 10g to 100g CoCi:, 10 g to 100 g HO... GLASSES: Copper ruby, flashed G24, Corning, red, No. 243 Schott’s red, No. 2745 G34, Corning, orange, No. 349. . Pyrex, Corning, No. 774... Noviol, B, Corning, yellow. Novieweld 3, Corning, dark-yellow Schott’s 43111, green G17I0N, green, Corning.. G174J, Corning, heat absorbing G124JA, Corning Cobalt blue Schott’s F3086, blue G4o13, Corning, blue G584, Corning, blue, blue- green, No. 428 G1711Z, Corning, pale- blue-green Amethyst, G172BWs, Ny sHouN oOon ww iN) NPRONDD wWOn BNH _ _ ~I G172BWs5, Corning, red-purple Crookes’ A, A. O. Co Crookes’ sage green 30, iN. ©. Co Lab. 58, A. O. Co Fieurzal B, A. O. Co.. Akopos green, J. K. O. “Co. ONNW nan _ Manufacturers: Comming Glass Works, Corning, N. Y.; A. O. Co., American Optical Co., South- bridge, Mass.; J. K. O. Co., Julius King Optical Co., New York City. For other glasses see original reference. See also succeeding table, which contains data for many of the same glasses. For Corning Filters: Journ. Opt. Soc. Amer. 17, 40, 1928; Coblentz, Stair, Bur. Standards, Tech. Pap. 369, 1928; Sci. Pap., 113, 1929. Corning, Heat Transmitting, no. 254, 1 mm, transmits over 30%, 0.8 to 4); Sextant red, 2 mm. over soe 0.8 to 4.24; Red Corex A, Gg86A, 3 mm., U. V. freely, visible to 0.4u, it. with max. at 0.7 and 2.64. SMITHSONIAN TABLES 388 TABLES 442 AND 443 TABLE 442.—Transmission of the Radiations from a Gas-filled Tungsten Lamp, the Sun, a Magnetite Arc, and from a Quartz Mercury Vapor Lamp (no Globe) through Various Substances, especially Colored Glasses. Transmission, per cent. Trade name. Quartz Mag- Solar mercury | netite Tadia- Fieuzal, B Fieuzal, 63 Fieuzal, 64 Euphos Euphos, B Akopos green Hallauer, 65 Hallauer, 64 Smoky green G 124, IP Yellow-green Noviweld, 30% Ou .3u; < .28u about that due to molecular scattering. Air transmission reduced by 1/100: 22 km at .28u; 5 at 25u; 0.57 at .22u; 20 km at .205u. (Dawson, Granath, Hulburt, Phys. Rev., 33, 1073, 1929.) (6).—Atmospheric Transparency for Ultra-Violet (Zenithsun, Fabry, Buisson, C. R. 175, 156, 1922; Astrophys. Journ., 54, 297, 1921; joined to Abbot’s, Annals Astrophys. Obs. Smithsonian Inst., 2, 112, 1908, via Forsythe-Christison, Gen. Elec. Rev., 662, 1929.) Wave length, u...... 2QN EBON eal 32) aoe a4 a5 ea Ona ed aS % transmitted : CO, 20, Be seh 2h 7G Fi Gas Cop Ge TABLE 445.—Penetration Ultra-Violet Light into Sea Water (Hulburt, 1928.) The transparency of sea water declines rapidly with decreasing wave length (A) in the u. v., becoming quite small below 3000 A. \ 3400 to 3000 A, CaSO, gives % the absorption, H:0 1%; 3000 to 2500 A, MgCle, CaSO., H2O each about %. I = Io1o-*, x in cm. 366 436 5406 578 612myu distilled water i : f : i .OOI .00005 .00OI5 .00028 .oo1O tap water : g : 3 ; : .OOI . sea water : ; ; : i .0OI3 .OOOIO .00015 .0003 .OOIO SMITHSONIAN TABLES 390 TABLE 446 TRANSPARENCY OF THE VARIOUS SUBSTANCES OF TABLES 394 TO 402 Alum: Ordinary alum (crystal) absorbs the infra-red. Metallic reflection at 9.05 and 30 to 40. Rock-salt : Rubens and Trowbridge (Wied. Ann. 65, 1898) give the following transparencies for ar cm. thick plate in %: r 9 10 | 12 13 14 15 16 18 | 19 20.7 | 23.7 fo | 99-5 | 99-5 | 99.3 97-6 | 93.1 | 84.6 | 66.1 | 51.6 27.5 | 9.6 0.6 oO. Pfliiger (Phys. Zt. 5. 1904) gives the following for the ultra-violet, same thickness: 280mm, 95.5% ; 231, 86%; 210, 77%; 186, 70%. Metallic reflection at 0.110u, 0.156, 51.2, and 87y. Sylvite: Transparency of a 1 cm. thick plate (Trowbridge, Wied. Ann. 60, 1897). d 9 10 Ii 12 13 at | ie 16 17 | 18 | 19 | 20.7 23.76 99:0 | 99-5 | 99-5 Metallic reflection at 0.114p, 0.161, 61.1, 100. Fluorite: Very transparent for the ultra-violet nearly to 0.1m. Rubens and Trowbridge give the following for a 1 cm. plate (Wied. Ann. 60, 1897) : | | | r SHV Siem | | ho | 84.4 | 54.3 | I Metallic reflection at 24m, 31.6, 40m. Iceland Spar: Merritt (Wied. Ann. 55, 1895) gives the following values of & in the formula — heme (Ginucms)s For the ordinary ray : 97-5 | 95-4 | 93-6 98.8 15. 2) 86. | 76. | 58. | 10 | ar T2u | ° 6.4 | 1.0 2.65 | 2.74m 1.74 | 2.36 | | | | 2.90 | 2.95 | 304 | 3: ndqe ||| (3:02 ait: : 4.35 | 4.52 | 4.83p ss eee . | | 0.70 | 1.80 | 4.71 | 22. : 1On | 6.6 | TACSi | PmOst | 3:38 | 3-59 | 3-76 | 3.90 | 4.02 | 4.40 | 4.674 0.89 | TeL7) ||| 10:80) | 107 d | gor | 5.04 | 5.34 | 5-5om 21 Wek hn i tet hk 1.25 | 2.13 | 4.41 | 12.8 Quartz: Very transparent to the ultra-violet; Pfliiger gets the following transmission values for a plate 1 cm. thick: at 0.222u, 94.2%; 0.214, 92; 0.203, 83.6; 0.186, 67.2%. Merritt (Wied. Ann. 55, 1895) gives the following values for £ (see formula under Iceland Spar) : For the ordinary ray : r 2.72 | 2.83 |m2:05 | 3.07 | Bel im|ines | 0.20 | © R 0.20 | 0.47 | 0.57 | Ogi ||| ty oO For the extraordinary ray : X_12"74. |). 2:89) 93:60) 53-08)|/ 13:26 3-64 | 3-74 Otomo oe 0.26 | O.01 | -0:5 04) 50-7014) 3-59 1.88 | 3-91 | 4.19 4-36 1.83 | 1.62 | 2.22 3-35 | 8.0 k 0.0 OMT) |||FO:33 For A>7 mw, becomes opaque, metallic reflection at 8.sou, 9.02, 20.75-24.4u, then trans- parent again. The above are taken from Kayser’s ‘‘ Handbuch der Spectroscopie,”’ vol. iii. SMITHSONIAN TABLES. TABLES 447 AND 448 391 TABLE 447,—Color Screens The following light-filters are quoted from Landolt’s “ Das optische Drehungsvermogen, etc.” 1898 Although only the potassium salt does not keep well it is perhaps safer to use freshly prepared solutions. | Grammes of Optical cen- | Water solutions of _Substance | tre of band, Transmission. in 100 ¢.cm, B&B \ begins about 0.718u. Crystal-violet, 5BO | 0.005 0.6659 ) ends sharp at 0.639. Potassium monochromate IO. Nickel-sulphate, NisO4.7aq. 30. 0.5919 | 0.614-0.574m, Potassium monochromate ie aos Potassium permanganate 0.025 Copper chloride, CuCly.2aq. 60. 0.5330 | 0.540-0.505u Potassium monochromate 10. i a anil Double-green, SF 0.02 0.488 5 NersZ ea Copper-sulphate, CuSO4.5aq. | 15. Wao o-a 52H Crystal-violet, 5BO 0.4482 0.478-0.410¢ Copper sulphate, CuSO 4.5ay. | 15. TABLE 448.—Color Screens The following list is condensed from Wood’s Physical Optics : Methyl violet, 4R: (Berlin Anilin Fabrik) very dilute, and nitroso-dimethyl-aniline transmits 0,365y. Methyl violet + chinin-sulphate (separate solutions), the violet solution made strong enough to blot out 0.4359, transmits 0.4047 and 0.4048, also faintly 0.3984. Cobalt glass + aesculin solution transmits 0.4359u. Guinea green B extra (Berlin) + chinin sulphate transmits 0.491 6m. Neptune green (Bayer, Elberfeld) + chrysoidine. Dilute the latter enough to just transmit 0.579¢ and 0.5461; then add the Neptune green until the yellow lines disappear. Chrysoidine + eosine transmits 0.57904. The former should be dilute and the eosine added until the green line disappears. Silver chemically deposited on a quartz plate is practically opaque except to the ultra-violet region 0.3160-0.3260 where 90% of the energy passes through. The film should be of such thickness that a window backed by a brilliantly lighted sky is barely visible. In the following those marked with a * are transparent to a more or less degree to the ultra-violet ° * Cobalt chloride: solution in water, — absorbs 0.50-.534; addition of CaClz widens the band to 0.47-.50. It is exceedingly transparent to the ultra-violet down to 0.20. If dissolved in methyl alcohol + water, absorbs 0.50-.53 and everything below 0.35. In methyl alcohol alone 0.485- 0.555 and below o.4ou. Copper chloride: in ethyl alcohol absorbs above 0.585 and below 0.535 ; in alcohol + 50% water, above 0.595 and below 0.37. Neodymium salts are useful combined with other media, sharpening the edges of the absorption bands. In solution with bichromate of potash, transmits 0.535-.565 and above o.60u, the bands very sharp (a useful screen for photographing with a visually corrected objective). Praseodymium salts: three strong bands at 0.482, .468, .444. In strong solutions they fuse into a sharp band at 0.435-.485u. Absorption below 0.34. Picric acid absorbs 0.36-.424, depending on the concentration. Potassium chromate absorbs 0.40-.35, 0.30-.24, transmits 0,23u. * Potassium permanganate: absorbs 0.555-.50, transmits all the ultra-violet. Chromium chloride: absorbs above 0.57, between 0.50 and .39, and below 0.334. These limits vary with the concentration. Aesculin: absorbs below 0.363u, very useful for removing the ultra-violet. * Nitroso-dimethyl-aniline: very dilute aqueous solution absorbs 0.49-.37 and transmits all the ultra-violet. Very dense cobalt glass + dense ruby glass or a strong potassium bichromate solution cuts off everything below 0.70 and transmits freely the red. Iodine: saturated solution in CSg is opaque to the visible and transparent to the infra-red. SMITHSONIAN TABLES, 392 TABLES 449-451 TABLE 449.—Transmission Percentages of Radiation Through Moist Air The values of this table will be of use for finding the transmission of energy through air containing a known amount of water vapor. An approximate value for the transmission may be had if the amount of energy from the source between the wave lengths of the first column is multiplied by the correspond- ing transmission coefficients of the subsequent columns. The values for the wave lengths greater than 184 are tentative and doubtful. Fowle, Water-vapor Transparency, Smithsonian Misc. Coll., 68, No. 8, 1917; Fowle, The Transparency of Aqueous Vapor, Astrophys. Journ. 42, 394, 1915. Range of wave lengths. Precipitable water in centimeters. mn * Te I ts 2. 3 4 5 6 7 8 9 ooocoll!IIlooll || cooooolllIllooll/| * These places require multiplication by the following factors to allow for losses in COz gas. Under average sea-level outdoor conditions the COz (partial pressure = 0.0003 atmos.) amounts to about 0.6 gram per cu.m. Paschen gives 3 times as much for indoor conditions. 2p, to 3, for 2 grams in m? path (95); for 140 grams in m? path (93); 4 “cc ae “ ae “cc “ce “ae (93); “ “ce “ee se ce “ee (70); more CO2 no further effect; 13 “ 14, slight allowance to be made; 14 “ 15, 80 grams in m path reduces energy to ZeIO; “ce 16, “oe ‘ “ee “ce ‘ ‘ ‘ “ce + These places require multiplication by 0.90 and 0.70 respectively for one air mass and 0.85 and 0.65 for two air masses to allow for ozone absorption when the radiation comes from a celestial body. TABLE 450.—Transparency of Water Vapor (steam) (Hettner, Ann, Phys., 55, 476, 1918, places of greater absorption. Original article gives plot of absorption throughout range of wave lengths.) Absorp- Absorp- Wave ‘ tion tion length Absorp- Wave tion length Steam Steam Steam 32.4 cm 80% : 80% 104 15 : 22 104 30 104 55 50 32.4 55 80 TABLE 451.—Transparency of Water Values of a in I = Ipe*4, d in cm Ip, I, intensity before and after transmission. Wave length p, | .186 a .0688 |. Wave length yp, | .430 a -00023 } .0002 | .OOOI First 9; Kreusler, Drud. Ann. 6, t901; next Ewan, Proc. R. Soc. 57, 1894, Aschkinass, Wied Ann. 55, 1895; last 3, Nichols, Phys. Rev. 1, 1. y See Rubens, Ladenburg, Verh. D. Phys. Ges., p. 19, 1909, for extinction coefs, reflective power and index of refraction, 1 w to 18 4“. SMITHSONIAN TABLES TABLES 452-455 393 INFRA-RED TRANSMISSION AND ABSORPTION TABLE 452.—Per Cent Transmission, Gases, 6.7 to 32.8y (Strong, Phys. Rev., 37, 1565, 1931, restrahlung.) Length of cell, 4 inches. Material Pressure 6.7 20.75 22.0" 760mm 24 79 93 760 99 IOI 760 98 97 760 7 58 96 102 99 114 97 99 361 100 86 200 99 98 526 61 45 Material Description 8.74 20.75¢@ 22.0u 27.36 20.44 32.8u Lacquer film +.55u thickness 93 98 99 99 +100 Mica 10u thickness 22 00 35 44 Soot on lacquer Opaque to visible 22 60 60 Quartz, fused 10u thickness 02 68 Glass 3h thickness 07 56 Cellophane 25u thickness 04 26 MgO Deposit from burning Mg ribbon 8 86 87 ZnO Deposit from Zn arc 80 80 Description of reflector Deposit of MgO from burning Mg ribbon Reflection B-MgO Pencil mark on paper Soot coating. MgO coating ZnO coating Optical black Gold foil blackened with bismuth KBr + 1.5u CaF: deposited by evaporation KI + 1.5u CaF, deposited by evaporation Silver covered with TABLE 455.—Per Cent Transmission, Various Substances, 20 to 130z (Barnes, Phys. Rev., 39, 562, 1932, which see for special technique used for analysis in this region.) 120 130u Fused quartz.... Py ae e nae : Q 5 22s Cry staleeaeeel eee ‘ (Oe Sulphur, rhombic| o. mee 58 38 Ne natee Ss cone : 76 70 ease eA 5 Sa! (55) (55) Cellophane...... 30 42 Celluloidy....... 99 99 Black paper..... ay, 28 30 Camphor soot... : 89 90 Pfund Bi black. . : Siw 5 60 63 Lampblack, water glass... . : : 5 OmaesO * On celluloid 1” thick. + For Rubens, Hoffmann, lampblack-water-glass mixture see Berliner Ber. 424, 1922. For Pfund’s Bi Black see Rev. Sci. Instr., 1, 397, 1930. A considerable number of bands appear in some of the curves from which the above values were read. SMITHSONIAN TABLES 394 TABLES 456-458 FAR INFRA-RED, 20 TO 150, (John Strong, Phys. Rev., 38, 1818, 1931.) TABLE 456.—Restrahlung bands Filter Number of Crystal (3 mm _paraffin Wave length Frequency reflections mirrors in each case) in uw in ~/cm Quartz Icm KCl 20.7 483 Fluorite 5 mm KCl 23 435 Metal Fluorite 3 mm KBr Be 366 Calcite 20.4 340 Fluorite 0.4 mm quartz 32.8 Metal 1.2 mm KBr Aragonite 0.4 mm quartz 41* Ff Metal NaCl 2 mm quartz 52 “ 63 83 94 117 152 BPPPRRRARHHOHOWERN HOLE * The use of a paraffin window about 3 mm thick stops the short wave length restrahlung of quartz at 8.7u and of calcite at 6.7. + Weak reflection at 41. TABLE 457.—Reflecting Power = 20h ~/cm = 500 Rough brass “ Zincite 8 magnesia, fused Stibnite Sphalerite Corundum Cuprite (1) Ground with No. 60 carborundum. (2) Ditto No. 220. (3) Ditto No. 400. (4) Surface | to cleavage plane, highly polished. (5) Natural crystal. (6) Qualitative only. TABLE 458.—Transmission A = 204 25 663 100 150 ~/cm = 500 400 150 100 66% 61 83 Amorphous SiO: ...... “3 27 62 CChk liquid 63 74 97 80 (7) No corrections for reflections. (8) Evaporated on lacquer film. SMITHSONIAN TABLES TABLES 459 AND 460 395 REFLECTION AND ABSORPTION OF LONG-WAVE. RADIATIONS TABLE 459.—Long-wave Absorption by Gases Unless otherwise noted, gases were contained in a 20 cm long tube. Rubens, Wartenberg, Verh. d. Phys. Ges. 13, P. 796, Iort. Percentage absorption. Percentage absorption. Long J, Hg lamp. Long X. Hg lamp. N w ics n nN it Pressure, cm Pressure, cm Fil- tered, 314M NH3... > | 83. 2 : Brg 66. CHare a : 100 CoHe...} 7 ‘ md “13 , 100 CoH. .. : ; 100 can ae ale mt! 100 CoO . 5-4 Be 52. C4H100. i 3 . a CsHiies. ) 5 ao 84. CHsCl.. ; 04. H20 *.. 30. ; , , 49. * Steam 100° C passed through tube 4o cm long, 150° C; 0.06 cm ppt. H2O. t+ Pentane vapor, pressure 36 cm. TABLE 460.—Properties with Wave-lengths 108 + yu Rubens and Woods, Verh. d. Phys. Ges. 13, p. 88, tort. With quartz, 1.7 cm thick: 60 to 80, absorption very great; 63M, 00%; 82M, 97.5; 97M, 83. (a) PERCENTAGE REFLECTION. Wave-length. Iceland Marble. Ror Sylvite a ; ass. ‘ater. | Alcohol. A = 82y*.. A = 108" t.| 47.1 43.8 * Restrahlung from KBr. + Isolated with quartz lens. (6) PERCENTAGE TRANSPARENCY. Uncorrected for reflections. Thickness precipi- table liquid. Thickness. |Transparency. Liquid. Thickness. Benzene Ethyl alcohol Ethyl ether a0 ao Quartz || axis Quartz, amorph Rock salt Fluorite FHI NHOOWNO OW ON OR WWOH -025 mm thick.} 0.11 mm thick.] 0.4 mm thick. Spectrometer Fluorite ‘ ‘reststrahlen ” Rock salt ‘‘ reststrahlen ” Quartz lens isolation | i ed TRANSPARENCY OF BLACK ABSORBERS. Black silk | Opaque black | Black card-_ | Candle lamp- Method and wave-length. paper, paper, board, aC, SMITHSONIAN TABLES. 15 396 TABLES 461-462 ROTATION OF PLANE OF POLARIZED LIGHT TABLE 461.—Tartaric Acid; Camphor; Santonin; Santonic Acid; Cane Sugar A few examples are here given showing the effect of wave length on the rotation of the plane of polarization. The rotations are for a thickness of one decimeter of the solution. The examples are quoted from Landolt & Bornstein’s ‘‘Phys. Chem. Tab.” The following symbols are used:— p = number gramis of the active substance in 100 grams of the solution. c= ve a solvent s ee a “ q= ts cc active Right-handed rotation is marked +, left-handed —. “e “ce cubic centimeter ‘* Wavelength] Tartaric acid,* CsHs6Oc, Camphor,* CioHi6O, Santonin,f CisHisO3, Line of | according to dissolved in water. dissolved in alcohol. dissolved in chloroform. spectrum | Angstrom in q = 50to95, q = 50to 95, q =75to 96.5, cm X 106 temp. = 24°C temp. = 22.9°C temp.) —/20-6 68.67 i —140°.1 + 0.2085 ¢ 65.62 +2°.748 + 0.00446 q 38°.549 — 0.0852 q —149.3 + .1555q 58.92 +1.950 + .13030q 51.045 .0964 q —202.7 -3086 q 52.69 + .153 + .175149 74.331 1343 q —285.6 + .5820q¢ 51.83 ae ea is ie —302.38 + .65574 51.72 — 1632 + 19147, ¢ 79.348 — .1451q ef: = 48.61 —3.598 + .239774 99.601 — .I912q —365.55 + .82844 43.83 —9.657 + _-314374 149.696 — .23464 —534.98 + 1.5240 q Santonin, f CisHisO3 Seen Gane ‘ $$ acid, Santonin,f CisH1sOs,* dissolved in | dissolvedin | C1sH 20x, pouzats dissolved in alcohol. alcohol. | chloroform. | dissolved in | 4; 2 oe pes ave c = 4.046 |c = 3.1-30.5| chloroform, [CSO Vee In emp. = 20 : t : c = 27.192 |, Wa 5 temp. = 20°C TOOLS ne CHATTHOOW 1088 —105 1053 1148 —IiI2 me 1323 1444 TS, 2011 2201 —197 2381 2610 —230 * Arndtsen, Ann. Chim. Phys. (3) 54, 1858. + Narini, R. Acc. dei Lincei, (3) 13, 1882. t Stefan, Sitzb. d. Wien. Akad. 52, 1865. RAO*MToMAOIOW Supplementary to Table 461 Values obtained at the Bureau of Standards for the rotation of sucrose are given below. Light é Light Rot. Source ine Source Rot. \ = 5461 5 a $$ | 1.644 1.786 eS | eee Hg 4047 1.95 —————— ee ES The above values are for a near normal solution, i.e. approximately 26 g of sucrose per 100 cc. TABLE 462.—Sodium Chlorate; Quartz Sodium chlorate (Guye, C. R. 108, 1889) || Quartz (Soret & Sarasin, Arch. de Gen. 1882, or C. R. 95, 1882)* Spectrum}| Wave Temp. Rotation Spectrum| Wave Rotation |} Spectrum} Wave Rotation line length line length line length per mm 7164A | 15°.0 : : Cdo 3609 63°.628 6870 17.4 3582 64.459 : N 6563 20.6 z Cdio 3465 69.454 5802 18.3 ‘ O 3441 70.587 5270 16.0 4861 Il.9 : : cee 3401 72.448 4340 10.1 2 3360 74.571 4308 14.5 . QO 3286 78.579 AIOI 13.3 : Cdi2 3247 80.459 3820 14.0 3728 10.7 t ; 3180 84.072 3581 12.9 : 2747 121.052 3361 TET " ; 2571 143.266 3287 II.9 : : 2312 190.426 3180 13.1 3021 12.8 : 2264 201.824 2747 12.2 : é 2103 220.731 2571 11.6 5 , 2143 235.972 * The paper is quoted from a paper by Ketteler in Wied. Ann. vol. 21, p. 444. SMITHSONIAN TABLES TABLE 463 397 ELECTRICAL EQUIVALENTS Abbreviations: int., international; e.m.u., electromagnetic units; e.s.u., electrostatic units ; C.g.s., centimeter-gram-second units. (Taken from Circular 60 of U. S. Bureau of Standards, 1916, Electric Units and Standards, but made consistent with Birge’s values, p. 77 et seq.) RESISTANCE: CAPACITY : I international ohm = I international farad = 1.00051 absolute ohms 0.99949 absolute farad 1.0001 int. ohms (France, before 1011 ) * a 1.00016 Board of Trade units (England, z apsolute iaiad “aa 1903) 1.00051 ates Ss 1.01358 B. A. units I practical e.m.u. 1.00283 “legal ohms” of 1884 10 Co Sg 1.06300 Siemens units S027 GUN Sere s ee 1 absolute ohm = INDUCTANCE: 0.99949 int. ohms Tega pLacticall:\je:m-ss 10° C.g.s. €.m.u. Tet 2029X6 The GOES aiesS. 11. absolute henry = aan REE SGuSESRTEREEET ERE aa aus henry : Te pLActicalsanestn: ts Se 10” e.m.u. Teh b202. OONO NH ADONIS HO +o4+o444 | bo * + t¢ § Same significance as in preceding table. SMITHSONIAN TABLES. 408 TABLES 482 AND 483 TABLE 482 THE TRIBO-ELECTRIC SERIES In the following table it is so arranged that any material in the list becomes positively electrified when rubbed by one lower in the list. The phenomenon depends upon surface conditions and circum: stances may alter the relative positions in the list. Asbestos (sheet). 13 Silk. 24 Amber, Rabbit’s fur, hair, (Hg). AS Nie Zn i eCdeiCr atelt: 25 Slate, chrome-alum. Glass (combn. tubing). | hand, wash-leather, 26 Shellac, resin, sealing-wax. Vitreous silica, opossum’s Filter paper. 27 Ebonite. fur. Vulcanized fiber. 28 Co, Ni, Sn, Cu, As, Bi, Glass (fusn.). Cotton. Sb Aga eds Gites bus Mica. Magnalium. reka, straw, copper sul- Wool. 19 K-alum, rock-salt, satin phate, brass. Glass (pol.), quartz (pol.), spar. 29 Para rubber, iron alum. glazed porcelain. Woods, Fe. 30 Guttapercha. Glass (broken edge), Unglazed porcelain, sal- 31 Sulphur. ivory. ammoniac. 32 Pt, Ag, Au. Calcite. K-bichromate, paraffin, 33 Celluloid. Cat’s fur. tinned-Fe. ; 34 Indiarubber. Ca, Mg, Pb, fluor spar, Cork, ebony. borax. I 2 3 4 5 6 Zi 8 Shaw, Pr. Roy. Soc. 94, p. 16, 1917; the original article shows the alterations in the series sequence due to varied conditions. TABLE 483 AUXILIARY TABLE FOR COMPUTING WIRE RESISTANCES For computing resistance in ohms per meter from resistivity, p, in michroms per cm. cube (see Table 484, etc.). ¢..g. to compute for No. 23 copper wire when p= 1.724: I meter = 0.0387 + .0271 + .0008 +- .0002 = 0.0668 ohms; for No. 11 lead wire when p= 20.4; I meter =0.0479 + 0010 = 0.0489 ohms. The following relation allows computation for wires of other gage num- bers: resistance in ohms per meter of No. N = 2(2— 3) within 1 %: ¢. g. resistance of meter of No. 18 =2 X No. 15. p in micro-ohms per cm. cube. Diam. . in | Section : & 6) | 6. | 7. 2 mm*. mm. Resistance of wire 1 meter long in oh 03280 | .03373 | .03466 +0560 03653 -03445 | -03593 | 03742] .03890| «00104 | +03707 | .03943 | .09118 -Oo14t +0165 +OgI12| «OoI50| .09187 109225 09262 109179 | +02239| 05298 #09358 +00417 +0284 | 09379] +02474| +02569| -02664 +0452} .02603] -00754 #09904 0106 +02719| .02959] .0120 0144 .0168 -OIT4 -O152 -OIQL +0229 -0267 -0182 +0242 +0303 +0364 10424 -0289 +0385 .0482 -0578 | .0674 +0460 0613 .0766 +0919 -1072 -0731 .0974 | .1218 +1462 | «1705 +1162 +1549 +1936 22324 -271f -1847 | «2463 +3079 +3695 +4310 +2938 | .3918 4397 5377 -6856 +4671 .6228 | .7786 9343 1.090 ©7428 +9904 | 1.238 1.486 1.733 1.181 1.575 1.968 2.362 2.750 1.879 | 2.505 | 3-132 3-757 4.383 2.985 | 3-980 | 4.975 5.970 6.965 4.748 | 6.331 7.914 9-497 11.08 5.988 | 7.984 | 9.980 | 11.98 13.97 SMITHSONIAN TABLES, TABLE 484 RESISTIVITY OF METALS AND SOME ALLOYS The resistivities are the values of p in the equation R = pi/s, where R is the resistance in microhms of a length 7cm of uniform cross section s cm®. The temperature coefficient is a, in the formula R; = R,{1 + a.(¢ — t,)]. The information of column 2 does not necessarily apply to the temperature coefficient. See also next table for temperature coefficients 0° to 100°C, also page 413 for values on metals of high purity. 409 Temperature coefficient Tempera-|,,- Microhm-|Refer- Substance Remarks ture cm ence see constantan +0.0039 + .0034 + .0040 + .0050 + .0036 wW Arsenic Beryllium..... w OO ONOO HH DAIDOWWWWWH -0 -002 [Soe ha drawn ‘6 “ liquid solid \ liquid Calcium.......] 99.57 pure see constantan Chromium..... = Glimaxin eee es 99.8 pure 60% Cu, 40% Ni + ae Tes least own annealed hard-drawn electrolytic eit lltalielken pure very pure, ann’ld see constantan H Ow 20 German silver..} 18% Ni Germanium.... al 99.9 pure H Ann 20 WwW tN 20 roo ann'ld 500.“ 1000 : pure, drawn 99.9 pure see constantan +t++ + + 4444441144 4 folks el “IOHN N NH cow Ag 1.468 Mn 5. Pd 10.21 Ga 53 Cu 1.59 Mo (5.3) Pt 10.96 Os 56 Au 2.22 Zn 5.75 Rb 13 Hg 94.07 Al 2.6 Ir 6.10 Sn 13 Bi IIo Cr 2.6 K 6.1 Ta 14.6 Graphite 8 X I0? ay 3.2 Ni 6.93 Tl 17.6 Carbon 3 X 103 Na 4.3 Cd 7.04 Cs 19 Te 2 X 105 Ca 4.3 In 8.37 Pb 20.4 ig trol? Mg 4.35 Li 8.55 Sry) (23.5) B 8 X 1012 Rh 4.69 Fe 8.8 As 35 Se trols WwW 5 Co 9 Sb 39 Ss rol” SMITHSONIAN TABLES 410 TABLE 484 (continued) RESISTIVITY OF METALS AND SOME ALLOYS Temperature coefficient Tempera-|,,- Substance Remarks ture MERE Refer- Refer- ence 99.98% pure pure, soft “6 “ “ac “ “ “ac electrolytic Bieber ee Bib: Siemens-Martin manganese 35 % Ni, “‘invar.”’ piano wire temp. glass, hard “, yellow blue U5 foie NN aeaadlaunusael! | 11] 11] | | Suaneaaalaaaadal |) 11) 1 | lwal& led launal | laaaata cold pressed ++ + ++ +444 ac “a “ “ ““ “ solid ATG liquid Magnesium... . ae E 20 st ...| free from Zn E ° i cies 25 100 500 ra eee pure Manganese... — Manganin 84 Cu, 12 Mn, 4 Ni I2 -000006 os — 25 .000000 100 -000042 250 475 500 20 jf 0 6 Ra Rit + e -o008ot + .000001??) “a Molybdenum. .| very pure “ Monel metal... — Nichrome..... = very pure pure “ce oo | Sooo mnnn | | +4444 $4+4444+ SMITHSONIAN TABLES TABLE 484 (concluded) 4! I RESISTIVITY OF METALS AND SOME ALLOYS Temperature coefficient Tempera- : Substance Remarks ture, Microhm Refer- °C cm ence Refer- ence 20 20 —183 — 78 oO 08.5 oO — 203.1 — 97-5 oO 100 400 ee oO 55 —186 — 78.3 oO 100 —190 oO 35 40 20 99.98 pure 18 electrolytic —183 “ — 7B oO 98. 192. 400 —180 Sand) oO 55 116 I 20 2 20 15.5 19.6 200,000 —183 4.08 — 78 11.8 to} 17.60 98.5 24.7 20 47 20 TI-5; —184 3.40 — 78 8.8 oO eesel till ooco°o Pw aa Sve esl ela eieelbat + + abt Se oo alate ssllil oO NS mH ol. 20 1000°K 727 1500°K 1227 2000°K 1727 3000°K 2727 3500°K 3227 trace Fe —183 1.62 rae tere 3.34 oO 5-75 92.45 8 IQI.5 10.37 440 37.2 evel (Steals) H o - wn ttt ooo ooo oun on Rous WOO HUW COW ORRWARKDK [| | Fla [Oa ells Tocete ell esescrash [et1WOL al Ratenere 10 ele alvecxe leslie core Teele icexeasopscerny UplecUiIe Wcibeoralig ti tiedyewmalt He Ne Viren ah | exter | H1 itty ll 183et 111 Pht tl References to Table 484: (1) See page 421. (2) Jager, Diesselhorst, Wiss. Abh. D. Phys. Tech. Reich. 3, p. 269, 1900. (3) Nicolai, 1907. (4) Somerville, Phys. Rev. 31, p. 261, 1910; 33, p. 77, 1911. (5) Circular 74, Bureau of Standards, 1918. (6) Eucken, Gehlhoff. (7) Dela Rive. (8) Matthiessen. (9) Jager, Diessel- horst. (10) Lees, 1908. (11) Mean. (12) Guntz, Broniewski. (13) Hackspill. (14) Swisher, 1017. (15) Shukow. (16) Reichardt, 1901. (17) Dewar, Fleming, Dickson, 1898. (18) Wolff, Dellinger, 1910. (19) Erhardt, 1881. (20) Broniewski, Hackspill, 1911. (21) Dewar, Fleming, 1893, 1896. (22) Circular 58, Bureau of Standards, 1916. (23) Strouhal, Barus, 1883. (24) Vincentini, Omodei, 1890. (25) Bernini, 1905. (26) Glazebrook, Phil. Mag. 20, p. 343, 1885. (27) Grimaldi, 1888. (28) Fleming, 1900. (29) Lang- muir, Gen. Elec. Rev. 19, 1916. (30) Eucken-Gehlhoff, 1912. (31) Wenner-Lindberg, I. C. T., 1929. (32) Bidwell, 1922. (33) Mean. (34) Gumlich. (35) Worthing, I. C. T., 1929. (36) Blau, 1905. * See note to Table 467. SMITHSONIAN TABLES 412 TABLES 485 AND 486 TABLE 485.—Resistance of Metals under Pressure (Bridgman) The average temperature coefficients are per ° C between o° and 100°C. The instantaneous pressure coefficients are the values of the derivative (1/ r){dr/dp}, where 7 is the observed resistance at the pressure p and temperature ¢. The average coefficient is the total change of resistance between o and 12,000 kg/cm? divided by 12,000 and the resist- ance at atmospheric pressure and the temperature in question. Table taken from Proc. Nat. Acad. 3, p. 11,1917. For coefficients at intermediate temperatures and pressures, see more detailed account in Proc. Amer. Acad. 52, p. 573, 1917. Sn, Cd, Zn, Kahlbaum’s “K” grade; TI, Bi, electrolytic, high purity; Pb, Ag, Au, Cu, Fe, Pt, of exceptional purity. Al better than ordinary, others only of high grade commercial purity. Pressure coefficients. Average temperature coefficient Instantaneous coefficient. 4 rr 0° to 100° C Average coefficient /em?2 AtoeC Neen cela o to 12,000 kg/cm’ At ° ° 12,000 kg Ato At 100 srayavellsdhyea rove isles 2 — .041226] — .oat016 .o4t510f| —.o41072{] —.o4ro2t|—.osr131 ft Aare acts ree : . 00¢ -041044] .040936 .041062 -040973 .040920| .040951 seca wlshicl ene lanauatere , . .O41319] .O41180 -041456 -041 200 -O41I51I| .041226 We aaovaleisiohe lode: : : .041063] .040837 .041 106 -040887 .040894| .040927 sbeneyeitver eters ‘ : .041442| .041220 -041 483 041 237 .O41212| .041253 Lhaveustehs eterseee : : .040540] .040425 .0405 24 .040407 -040470| .040454 bebe ceo pahatens fuses j ; .040416] .040365 -040307 -040373 .040382| .040377 iain tarereatoe . 004 : -040358] .04032T -040355 -040331 - 010333] .040336 seat chars reteeenete ‘ : 4 .040312| .010286 -040304 -040292 .040287; .040292 eieiter tele chererers ‘ ; 040201] .040179 -040184 -O40175 .040183| .040177 i ae .O40158] .040142 .040163 -040156 -040147| .040158 Biostar ateyecosee : : .040094| .040081 .040076 .040070 .040087}] .040073 aereneys .040241| .040218 .040247 -040230 .040226} 040235 oe Dy Gench operators A : .040198] .010190 .040189 .040187 .O40190| .040186 de .040198| .osor8I -0401.90 -040182 .040187]} .040184 wisteteichs (eierereyele : ‘ .040133] .040126 -040130 -O401 25 .O40129} .040126 LET See pethsets ; ; .040149| .040139 -O401 53, -0401 47 040143] .O40149 Recep a eos veash ore : -003216| -040128] . 040127 -040130 -0401 23 .040123] .040126 Rie eteiey ren ameliad= : = -04055 = = ae -04055 aad Raiclats tetas cigaraiee .00473 .00403 |+.041220] +.041064]| +.040768 | +.040723 | -+.041220]+ .040768 i ‘ eee +.00395 |+.04154 |+.040213]| +-04152 § | +.041895§] -+.042228]+ 041980 § ras erditteiare — — .03129 _- — = | * ©° to 20°. + 0° to 24°: t Extrapolated from 50°. § Extrapolated from 75°. Additional data from P. Nat. Acad. Sc., 6, 505, 1920. Data are 10,000 X mean pressure coefficient, o — 12,000 kg, and 10,000 X instantaneous pressure Coefficient ato kg. 1= liquid; s =solid. Li, s, 0° + .0772, + .068 (Caroe + .106 + .129 atts Ge + .oo1? Li, 1, 240° -+.093 + .093 Sr, 0° + .680 + .502 Zr, 0° —.0040 — .004 Na, s, 0° | =-345 O03 Higa SHOS — .236b Bis e75c — .101C arena Na, 1, 200° — .436 O22 Hg, 1, 25° i219 — .334 WwW, 02 — +0135 Old K, s, 25° — .604 — 1.86 Ga, s, 0° — .0247 aero? — .0331 — .039 K, 1, 165° — .80ga —1.68 Gaylezoe — .0531 — .064 P, black, 09 —.81 — 2.00 a, 0 — 9,000 kg; b, 7,640 — 12,000 kg; c, o— 7,000 kg. The Ga, Na, K, Mg, Hg, Bi, W, P, of exceptional purity. TABLE 486.—Resistance of Mercury and Manganin under Pressure Mercury, pure and free from air and with proper precautions, makes a reliable secondary electric-resistance pres- sure gauge. For construction and manipulation see ‘*’lhe Measurement of High Hydrostatic Pressure; a Secondary Mercury Resistance Gayge,”’ Bridgman, Pr. Am. Acad. 44, p. 221, 1919. 500 I000 | 1500 | 2000 | 2500 | 3000 | 4000 | 5000 | 6000 | 6500 0. 9186/0. 9055]0. 8930/0. 8818]0. 8714]0. 8582]0. 8478]0. 8268]0. 8076/0. 7896}0. 7807 . |1.0000]0. 9836/0. 968210. 9535/0. 9304]0.9258/0. 9128]0. 8882]0. 8652}0. 8438]0. 8335 I .0000]0. 9854/0.9716/0.9588]0. 9462/0. 9342/0. 9228]0. goIO|O. 8806)0. 8616]0.8527 I.0970|1.0770/1.0580] I .0400|1.0230/1.0070/0.9Q908]0. 9614/0.9342]/0.9086|0. 8966 * This line gives the Specific Mass Resistance at 25°, the other lines the specific volume resistance. The use of mercury as above has the advantage of being perfectly reproducible so that at any time a pressure can be measured without recourse to a fundamental standard. However, at o° C mercury freezes at 7500 kg/cm2. Man- ganin is suitable over a much wider range. Over a temperature range o to 50° C the pressure resistance relation is linear within 1/1o per cent of the change of resistance up to 13,000 kg/cm?. The coefficient varies slightly with the sample. Bridgman’s samples (German) had values of (AR/pRo) X 10% from 2295 to 2325. These are + instead of —, as with most of the above metals. See “The Measurement of Hydrostatic Pressure up to 20,000 Kilograms per Square Centimeter,’ Bridgman, Pr. Am. Acad. 47, p. 321, 1911. SMITHSONIAN TABLES. TABLE 487 413 EFFECT OF TENSION ON THE RESISTANCE OF METALS (Bridgman, Proc. Amer. Acad. Arts and Sci., 57, 41, 1922.) Generally hydrostatic pressure decreases the electrical resistance of metals. A few are abnormal (see Table 485)—Bi, Li, Ca, Sr, Sb. Unit stress, kg/cm’. The tension coefficient of specific resistance is obtained by subtracting (1 + 20)/E from the coefficient of observed resistance. Sb i Mang. Therlo Co Recip. Young’s MOGs >< LOose= «| 20 4.75 7.5 1.25 4.2 0.72 0.69 0.5 Poisson ratio. ... .42 .30 36 30? 127 233) na .30 Tens. coef. spec. resist. X 108...|/+11 + 8 |—21.2 |+3.0 |—3.65 |— .60 |— .73 |+ .19 Supplementary Values to Table 484 Resistance temperature coefficient for a number of metals and alloys of high purity due to J. R. Caldwell (1931). Metal — (Rioo-—Ro) /100Ro Alloy (R1o0—Ry) /100Ry 0.00667 95 Pt— 5 Rh 0.00215 . 00419 90 Pt—10 Rh 0.00169 .00423 80 Pt—20 Rh 0.00140 .003925 60 Pt—40 Rh 0.00144 . 00436 40 Pt—60 Rh 0.00194 20 Pt—8o Rh 0.00260 Note to Table 491, p. 417: Superconductivity. Apparent only below about 10° K. (— 263°C). The following metals are known to show it below the indicated temperatures. A low current density is necessary. AMerenbhl Goooocc De75) IS. IpaXohibsed, gon ooaodoc 3°37 K. Mhallivimimeeseieiere ect 2°37) Ke Gallistimigennyerclete- 1.05 Tin’ Qaveusve cate vero Bray. Wea gaaters cis syetsrererc 7.2 Niobium, ..1.< <2. 8.2 antaltirnia meryeye yer 4-4 Alera Shogo o0c D5 Molybdenum .... 1.? Mierctiteys telus ne 4.22 Some alloys Zn, Cd, Ge, Al, Pt, Na, Li do not show it. McLennan, Nature, 130, Dec. 10, 1932. Hill, Rev. Scientific Instr., 4, 3, 1933. SMITHSONIAN TABLES 4l4 TABLE 488 CONDUCTIVITY AND RESISTIVITY OF MISCELLANEOUS ALLOYS TEMPERATURE COEFFICIENTS I nductivity in mhos or ———————— = = yo(I —at bt?) and resistivity i i - Condu y Bis erica yt = yo + bt?) and resistivity in microhms —cm = pt = poi + at — 5). Metals and alloys Composition by weight uthor- ity | A Gold-copper-silver. .| 58.3 Au + 26.5 Cu + 15.2 Ag Brae & us “..| 66.5 Au + 15.4 Cu + 18.1 Ag 6.83 520T ss ..| 7-4Au + 78.3 Cu + 14.3Ag | 28.06 1830f 2000 Welding iron ¢ 6000 Woods metal 1.93 2900 52 12.2-15.6|1-2 X 10% 6.4-8.4 ca 8.2 hard drawn... annealed German silver Various 60.16 Cu + 25.37 Zn + 14.03 Ni + .30 Fe with trace 3.33 of cobalt and manganese “eo NWWN HOO SSS > Aluminum bronze Phosphor bronze Silicium bronze Manganese-copper. . Nickel-manganese- 3 Ni + 24 Mn + 73 Cu...... 18.46 Ni + 61.63 Cu + 19.67 Zn + 0.24 Fe + 0.19 Co + 0.18 Mn 25.1 Ni+ 74.41 Cu + 0.42 Fe + 0.23 Zn + 0.13 Mn + trace of cobalt 53-28 Cu + 25.31 Ni + Rheotan 16.89 Zn + 4.46 Fe + 0.37 Mn Rheotan 53 Cu,25Ni,17Zn,5Fe Copper-manganese- i 91 Cu+7.1 Mn+1.9Fe....| 4.98 Copper-manganese- i 70.6 Cu + 23.2 Mn + 6.2 Fe. 1.30 Copper-manganese- i 69.7 Cu + 29.9 Ni + 0.3 Fe.. 2.60 85 Cu,13Mn,2Al E Manganin 84 Cu + 12 Mn+ 4 Ni : 44 Constantan 60 Cu + 40 Ni A 49 1 Matthiessen. 4 Feussner and Lindeck. 7 Feussner. 107 Grae. 2 Various. 5 Van der Ven. 8 Jaeger-Diesselhorst. 11 Weber. 3 W. Siemens. 6 Blood. 9 LeChatelier. 22 Niccolai. *, t, f, b X 109 = 924, 93, 7280. SMITHSONIAN TABLES TABLE 489 415 CONDUCTING POWER OF ALLOYS This table shows the conducting power of alloys and the variation of the conducting power with temperature.* The . . . . of . . values of C, were obtained from the original results by assuming silver = Ee mhos. The conductivity is taken as C,= C, (1—at+é2"), and the range of temperature was from 0° to 100° C. The table is arranged in three groups to show (1) that certain metals when melted together produce a solution which has a conductivity equal to the mean of the conductivities of the components, (2) the behavior of those metals alloyed with others, and (3) the behavior of the other metals alloyed together. It is pointed out thar, with a few exceptions, the percentage variation between o” and 100% can be calculated from the Z : : ° formula P = P, 7? where Z is the observed and / the calculated conducting power of the mixture at 100° C and /, is the calculated mean variation of the metals mixed. Weight % | Volume % Variation per 100° C. of first named. Observed. |Calculated. Group 1. DSUGEO Mi ny la : 7-57 Siig © Clem neini tne er. 9.18 SZ nies. ccalice™ 10.56 BbSie -.) kilee 6 iweuees 6.40 NG da FM he) the 16.16 SC Cane 13.67 GcdlR beware wh ee 5-78 Group 2. Lead-silver (PbgoAg) . : 5.60 Lead-silver (PbAg) . : 8.03 Lead-silver (PbAgy) . 32: : 13.80 Tin-gold (Sny2Au). . : 5-20 Sonn (TNE cA) rene ' 3-03 phin-cOppels wisn -nee : 7.59 s § aoe ; 8.05 325%, 6.41 7-64 12.44 39-41 UMN 6 6 ooo : 7.81 Sam MN ee | to Bose oe : 8.65 t 13-75 ieee : 13-70 ile ee ose Ne : 3.44 T : t Zinc-copper “ce “oc 29.01 38.09 Nore. — Barus, in the ‘“‘ Am. Jour. of Sci.’’ vol. 36, has pointed out that the temperature variation of platinum oie ° n : alloys containing less than 10% of the other metal can be nearly expressed by an equation y = es where y is the temperature coefficient and + the specific resistance, 7 and 7 being constants. If a be the temperature coefficient at o° C and s the corresponding specific resistance, s (a + #2) =x. For platinum alloys Barus’s experiments gave #2 = — .000194 and 2— .0378. For steel #72 = —.000303 and 2 = .0620. Matthiessen’s experiments reduced by Barus gave for Gold alloys 7 = — .o00045, 7 = .00721. Silver “* 9#=—.o000112, 2 = .00538. Copper ‘* #2 = — .000386, 7 =.00055. * From the experiments of Matthiessen and Vogt, ‘‘ Phil. Trans. R. S.” v. 154- + Hard-drawn. SMITHSONIAN TABLES. 416 TABLES 489 (continued) AND 490 TABLE 489 (continued).—Conducting Power of Alloys Group 3. Weight % | Volume % Variation per 100° C. Alloys. a aS ce a X 108 & X 109 of first named. Observed. |Calculated. Gold-copper iti on O9:23 98.36 35-42 2650 _ 4650 21.87 23.22 sf Crea Pease sterol [OOS Gy 51.66 10.16 749 SI 7-41 788 Gold-silver Tf . 87-95 79.86 13 46 1090 793 10.09 9.65 se Soares aerial 2O)5 79.86 13-61 1140 1160 10.21 9.59 ss SOME Rabat os OAESO 52.08 9.48 673 246 6.49 6.58 s¢ Eee tote he neuer a OALOO. 52.08 9-51 721 495 6.71 6.42 «s t B38 19.86 13.69 885 531 8.23 8.62 ss eee 31.33 19.86 13.73 908 641 8.44 8.31 | Gold-coppert . . .| 34.83 19.17 12.94 864 570 8.07 8.18 s eo ilies 37 Sage 1.52 0.71 53-02 3320 7300 25-90 25.86 Platinum-silvert . .| 33.33 19.65 4.22 330 208 3-10 3.21 a Hoag ns oe 9.31 5:05 11.38 774 656 7.08 7.25 s Sdiert ite: 5-00 2.51 19.96 1240 1150 11.29 11.88 Palladium-silver | . . | 25.00 23.28 5-38 324 154 3-40 4.21 Copper-silvert . . .| 98.08 98.35 56.49 3450 7990 26.50 27-30 fe CO Tio) eye Oded O 95-17 51.93 3250 6940 21S) 25-41 ss CART NG 76.74 77.64 44.06 3030 6070 24.29 21.92 ‘s Set aoe 42.75 46.67 47-29 2870 5280 22.75 24.00 ss co Belin 7.14 8.2 50.65 2750 4360 23-17 25-57 << ST ee 1.31 1.53 50.30 4120 8740 26.51 29-77 Iron-gold f=. - . =|) 13:59 27.93 173 3490 7010 27.92 oS Se Canora vac 9.80 21.18 1.26 2970 1220 17.55 Ae aes Td ety cor Peo 4.76 10.96 1.46 487 103 3.84 Iron-copper tf). «- 0.40 0.46 24.51 1550 2090 13-44 Phosphorus-copper f . 2.50 ~ 4.62 476 145 ~ oot 0.95 - 14.91 1320 1640 - Arsenic-coppert . . 5-40 - 3.97 516 989 - ce Soa weal i cere: 2.80 - Sol | gO 446 - “ ea eee ee CLACe - 38.52 | 2640 4530 - * Annealed. }+ Hard-drawn. TABLE 490.—Allowable Carrying Capacity of Rubber-covered Copper Wires (For inside wiring — Nat. Board Fire Underwriters’ Rules.) 5 alese nea ° 00 ~=6| ~(©000 | | | Amperes : : 65 | 76 | 90 | 107) £27) || DEO | 210 | | | 500,000 circ. mills, 390 amp.; 1,000,000 c. m., 650 amp.; 2,000,000 c. m., 1,050 amp. For insulated al. wire, capacity =84% of cu. Preece gives as formula for fusion of bare wires [ =ad?, where d = diam. in inches, a for cu. is 10,244; al., 7585; pt., 5172; German silver, 5230; platinoid, 4750; Fe, 3148; Pb., 1379; alloy 2 pts. Pb., 1 of Sn., 1318. SMITHSONIAN TABLES. TABLE 491 417 RESISTIVITIES AT HICH AND LOW TEMPERATURES#* The electrical resistivity (p, ohms per cm. cube) of good conductors depends greatly on chemical purity. Slight con- tamination even with metals of lower p may greatly increase p. Solid solutions of good conductors generally have higher pthan components. Reverse is true of bad conductors. In solid state allotropic and crystalline forms greatly mod- ify p. For liquid metals this last cause of variability disappears. The + temperature coefficients of pure metals is of the same order as the coefficients of expansion of gases. For temperature resistance (t, p) plot at low temperatures the graph is convex towards the axis of t and probably approaches tangency to it. However for extremely low temper- atures Onnes finds very sudden and great drops in p. e.g. for Mercury, 3.6K <4x10-10 p, and for Sn., P3.9k <10-po. The t, p graph for an alloy may be nearly parallel to the t axis, cf. constantan ; for poor conductors p may decrease with increasing t. At the melting-points there are three types of behavior of good conductors: those about doubling p and then possessing nearly linear t, p graphs (Al., Cu., Sn., Au., Ag., Pb.); those where p suddenly increases and then the + temp. coefficient is only approximately constant; (Hg., Na., K.); those about doubling p then having a -, slowly changing to a + temp. coef. (Zn., Cd.); those where p suddenly decreases and thereafter steadily increases (Sb., Bi.). The values from different authorities do not necessarily fit because of different samples of metals. The Shimank values (t given to tenths of ©) are for material of theoretical purity and are determined by the a rule (see his paper, also Nernst, Ann. d Phys. 36, p. 403, tg11 for temperature resistance thermometry). The Shimank and Pirrani values are originally given as ratios to py. (Ann. d. Phys. 45, p. 706, ror4, 46, p. 176, 1915.) Resistivities are in micro-ohms per cm. cube unless stated. Italicized figures indicate liquid state. Silver. Pt 0.014 0.009 ; -252.9 -016 5 -O14 —200. -028 a -334 < -IgI.1 +163 7 +357 . —150. -249 -638 : 100. -567 -g16 q - 77.8 .9O4 1.040 : = 50. 1.240 1.212 2 o. 1.578 : 1.506 ; 100, 2.28 2.15 300. 2.96 j 2.80 415. 5.08 ; 3.46 427. 7-03 ‘ : 6.65 450- 9-42 2 : 8.4 ; 500. 10.20 : ; 16. 600. 21.30 ; 17.01 700. 22.30 : 19.30 r 800. 23.86 : : 21.72 : 850. 24.62 fi 23.0 Mercury. Potassium. Sodium. Pe : Pt ys Pr 5-38 | : 1.720 246 ; 0.605 * : 0.011 10.30 : . 2.654 +379 . 1.455 - : 2.27 15-42 b 3-724 532 : 2.380 ; : -844 21.4 z 5 5.124 +732 3-365 5 5-92 QI-7 7.000 1,00 : : 4.40 ‘ 6.43 04.1 . 7-116 1-016 . 4.873 . 8.15 08.3 i 8.7G0 1.256 : 6.290 : 10.68 103.1 : I3.gO 1.014 9.220 : 16.61 114.0 ; 15.31 2.187 ' 9.724 : 24.50 127.0 ; 16,70 2.386 ; 10.34 : 43.29 4.052 Manganin. German Silver. Constantan. 90 % Pt. 10% Rh. ce Prt Au. below 0°, Niccolai, Lincei Rend. (5), 16, p- 757; 906, 1907; above, Northrup, Jour. Franklin Inst. 177, p. 85, 1914. Cu. below, Niccolai, ]. c. above, Northrup, ditto, 177. p. 1, 1914. Ag. below, Niccolai, ].c. above Northrup, ditto, 178, p. 85, 1914. Zn. below, Dewar, Fleming, Phil. Mag. 36. p. 271, 1893; above, Northrup, 175, P. 153, 1913. | Hg. below Dewar, Fleming, Proc. Roy. Soc. 66, p. 76, 1900; above, Northrup, see Cd. K. below Guntz, Broniewski, C. R. 147, P- 1474, 1908, 148, p. 204, 1909. Above, Northrup, Tr. Am. Electroch. Soc. p. 185, 1911. Na, below, means, above, see K. Fe., Manganin, Constantan. Niccolai, l.c. German Silver, 90% Pt. go% Rh., Dewar and Fleming — Phil. Mag. 36, p. 271, 1893. * See also page 413. SMITHSONIAN TABLES. 418 TABLES 491 (continued) AND 492 TABLE 491 (continued).—Resistivities at High and Low Temperatures (Ohms per cm cube unless stated otherwise.) Platinum. Bismuth. Cadmium. Pt Carbon, Graphite.* Fused silica. Alundum cement. p in ohms oC in ohms, cm. cube. : = megohms cm. , Pp & cm. cube. Carbon Graphite ; >200,000,000. ; >9x 106 0.0035 0.00080 ' 20,000,000. : 30800. .0027 .00083 b 200,000, 2 13600. -0021 -00087 7 b 7 7600. -OO15 -00090 3 3 6500. -OOIT OOTOO . . . 2300. .0009 .OOLT j about 20. : 190. Pt. low, Nernst, l. c. high, Pirrani, Ber. Deutsch. Phys. Ges. 12, p. 305, Pb. low, Schimank, Nernst, 1. c. high. Northrup, see Zn. Bi. low, means, high, Northrup, see Zn. Cd. low, Euchen, Gehlhoff, Verh. Deutsch. Phys. Ges. 14, p. 169, 1912, high, Northrup, see Zn. Sn. low, Dewar, Fleming, high, Northrup, see Zn. Carbon, graphite, Metallurg. Ch. Eng. 13, p. 23, 1915. Silica, Campbell, Nat. Phys. Lab. 11, p. 207, 1914. Alundum, Metallurg. Ch. Eng. 12, p. 125, 1914. * Diamond 1030° C, p >107; 13809, 7.5 x 105, v. Wartenberg, 1912. TABLE 492,—Volume and Surface Resistivity of Solid Dielectrics The resistance between two conductors insulated by a solid dielectric depends both upon the surface resistance and the volume resistance of the insulator. The volume resistivity, p, is the resistance between two opposite faces of a cen- timeter cube. The surface resistivity, 7, is the resistance between two opposite edges of a centimeter square of the surface. The surface resistivity usually varies through a wide range with the humidity. (Curtis, Bul. Bur. Standards, If, 359, 1915, which see for discussion and data for many additional materials.) a, megohms a; megohms ao; megohms p 50% humidity. | 70% humidity. | go% humidity. Megohms-cms. Material. Aim be ramen o. Mewite Beeswax, yellow . Celluloid Fiber, red Glass, plate. . ‘So Kavalier a. Hard rubber, new IQWOGs Belo. lao Khotinsky cement Marble, Italian Mica, colorless Paraffin (parowax) Porcelain, unglazed . Quartz, fused Rosin . Sealing wax Shellac Slater eat Awe is Sulphur eee Wood, parafined mahogany . 109 10# 103 To! 109 1012 102 109 10? 1010 108 109 10)? x 102 toll To! 10° 108 108 102 10 108 To3 10 10? 10 103 109 Io 102 108 107 108 10 108 103 108 108 tot foe IO 103 108 10° 108 102 10? 109 10° 108 108 108 10° 10 10? 10° 108 108 104 1ot rot 108 109 10° 108 103 10" 109 10° 10° 10° 109 107 10 109 10° CHMNN WN MntinwWw = Ne by NH KK KKK KK XK OK OK OK KOK XK OK XK WmP WW QW NNNS NW HH Bh QW DN ON xx«K KKK KKK KKK KK KKK KK XK NB BNON NUN DONUWW NHN N NU | XxX KK KKK KK KK KK KKK KK KOK 6x 6 xX OS 2X 5 x 4X 3X 5x TX 3x 2X 9X 6 xX 3x 6X 2x 6x 9X Few 4X pH ee SMITHSONIAN TABLES. TABLES 493 AND 494 419 TABLE 493.—Variation of Electrical Resistance of Glass and Porcelain with Temperature The following table gives the values of a, 6, and c in the equation log R =a-+ &t-+ ct, where & is the specific resistance expressed in ohms, that is, the resistance in ohms per centimeter of a rod one square centimeter in cross section.* Range of Kind of glass. Density. temp. Centigrade. | Test-tube glass rane: ‘ 13.86 000065 | 0°250° peace Sis ; : 5 5 ; | 14.24 : .OOOI | 37-131 | Bohemian glass 3 : : ; 3 | 16.21 .0000 394 60-174 Lime glass (Japanese manufacture) . ; 13.14 . —.000021 10-85 ‘“ «“ “ «“« ; 14.002 | —. —.00006 | 35-95 Soda-lime glass (French flask) : 14.58 | —.049 .00007 5 Potash-soda lime glass. : ; 16.34 | —.0425 .0000364 Arsenic enamel flint glass ; : ‘ 18.17 | —.055 .000088 Flint glass (Thomson’s electrometer jar) . : : : : ; : :8.02I | —.036 | —.c0o000g9I | 100-200 Porcelain (white evaporating dish) . 15.65 | —.042 .0000 5 68-290 a CoMPOSITION OF SOME OF THE ABOVE SPFCIMENS OF GLASS. Number of specimen = Silicay | : : ; 61.3 Potash . ; 22.9 Sodan Lime, etc. | Lime, etc. Lead oxide. : ; . | by diff. by diff. Limes. : : : ; 15.8 16.7 Magnesia . 3 : : - - Arsenic oxide Alumina, iron oxide, etc. * T. Gray, ‘* Phil. Mag.’’ 1880, and “‘ Proc. Roy. Soc.” 1882. TABLE 494.—Temperature Resistance Coefficients of Glass, Porcelain and Quartz dr/dt Temperature. Glass Porcelain. Quartz. Somerville, Physical Review, 31, p. 261, 1910. SMITHSONIAN TABLES. 420 TABLE 495 TABULAR COMPARISON OF WIRE GAGES ; ; sea Birming- ; American| American : : Stubs’ | (British) : Gage wire gage| wire gage Steel VIS Seer eee steel wire| standard ham. ate Gage No. (B.&S.) | (B.& S.) eee ee gage |wire gage (Stubs’) No. mils.t mm.t : 5 mils. mils. ioe i 7-0 | 490.0 12.4 500. 6-0 461.5 Tey 464. 5-0 430.5 10.9 432. 4-0 460. TY.7 393.8 10.0 400. 3-0 410. 10.4 362.5 9.2 Be 2-0 365. 9.3 331.0 8.4 348. Oo 325. 8.3 306.5 7.8 324. I 2809. wag 283.0 Wee 227. 300. 2 258 6.5 262.5 6.7 219. 276 3 229. 5.8 243.7 6.2 Oi. 252 4 204 5.2 225.3 5.7 207. 232 5 182. 4.6 207.0 5.3 204. 212 6 162. 4.1 192.0 4.9 201. 192 7 144. 3-7 177.0 4-5 199. 176 8 128 B33 162.0 4.1 197. 160 9 114. 2.91 148.3 ar 194. 144 10 102. 2.59 135.0 3-43 I9l. 128 II gl. 2.30 120.5 3-06 188. 116 12 81. 2.05 105.5 2.68 185. 104 13 HX 1.83 QI.5 2.32 182. 92 14 64. 1.63 80.0 2.03 180. 80 15 Bis 1.45 72.0 1.83 178. 72. 16 Sire 1.29 62.5 1.59 175. 64. 17 45- 1.15 54-0 1.37 172. 56. 18 40. 1.02 47.5 1.21 168, 48. 19 36. 0.91 41.0 1.04 164. 40. 20 32. OI 34.8 0.88 161. 36. 21 28.5 LB 31.7 81 Tie 32. 22 25.3 -62 28.6 Hie 155. 28. 23 22.6 °57 25.8 -66 15S 24. 24 20.1 -51 23.0 58 TiSiTe 22. 25 17.9 “45 20.4 ers 148. 20. 26 15-9 -40 18.1 -46 146. 18, 27 14.2 36 1763 +439 143. 16.4 28 12.6 Be 16.2 “411 139. 14.8 29 11.3 .29 15.0 +381 134. 13.6 30 10.0 25 14.0 +356 M27 12.4 31 8.9 227) 13.2 +335 120. 11.6 32 8.0 .202 12.8 +325 IIS. 10.8 33 met 180 11.8 +300 112, 10.0 34 6.3 -160 10.4 -264 110. 9.2 35 5.6 +143 9.5 -241 . 108. 8.4 36 5.0 127 9.0 .229 106. 7.6 37 4.5 113 8.5 .216 103. 6.8 38 4.0 IOI 8.0 +203 Iol. 6.0 39 365 090 7:5 +191 99. 5.2 40 3.1 080 7.0 .178 97. 4.8 6.6 .168 95. 4-4 6.2 057, 92. 4.0 6.0 -152 88. 3-6 5.8 +147 85. 3-2 55 -140 81. 2.8 5.2 .132 79. 2.4 5.0 .127 Pre 2.0 4.8 .122 Fl 1.6 4.6 SLL, Eds 1.2 4.4 -112 69. 1.0 * The Steel Wire Gage is the same gage which has been known by the various names: “ Washburn and Moen,” “ Roeb- ling,” “American Steel and Wire Co.’s.” Its abbreviation should be written “Stl. W. G.,” to distinguish it from “S.W. G.,” the usual abbreviation for the (British) Standard Wire Gage. + The American Wire Gage sizes have been rounded off to the usual limits of commercial accuracy. They are given to four significant figures in Tables 499 to 502. They can be calculated with any desired accuracy, being based upon a simple mathematical law. The diameter ot No. oooo is defined as 0.4600 inch and of No. 36 aso.oosoinch. The , 39 ratio of any diameter to the diameter of the next greater number “Are = I, 1229322. +005) Taken from Circular No. 31. Copper Wire Tables, U.S. Bureau of Standards which contains more complete tables. SMITHSONIAN TABLES. TABLE 496 421 Introduction to Wire Tables; Mass and Volume Resistivity of Copper and Aluminum The following wire tables are abridged from those prepared by the Bureau of Standards at the request and with the codperation of the Standards Committee of the American Institute of Electrical Engineers (Circular No. 31 of the Bureau of Standards). The standard of copper resistance used is ‘“ The International Annealed Copper Standard” as adopted Sept. 5, 1913, by the International Electrotechnical Commission and represents the average commercial high-conductivity copper for the purpose of electric conductors. This standard corresponds to a conductivity of 58 X 10° c.g.s. units, and a density of 8.89, at 20° C. In the various units of mass resistivity and volume resistivity this may be stated as 0.15328 ohm (meter, gram) at 20° C. 875.20 ohms (mile, pound) at 20° C. 1.7241 microhm-cm at 20° C. 0.67879 microhm-inch at 20° C. 10.371 ohms (mil, foot) at 20° C. The temperature coefficient for this particular resistivity is a2—= 0.00393, Or ao = 0.00427, The temperature coefficient of copper is proportional to the conductivity, so that where the conductivity is known the temperature coefficient may be calculated, and vice-versa. Thus the next table shows the temperature coefficients of copper having various percentages of the standard conductivity. A consequence of this relation is that the change of resistivity per degree is constant, independent of the sample of copper and independent of the tem- perature of reference. This resistivity-temperature constant, for volume resistivity and Centigrade degrees, is 0.00681 microhm cm, and for mass resistivity is 0.000597 ohm (meter, gram). The density of 8.89 grams per cubic centimeter at 20° C, is equivalent to 0.32117 pounds per cubic inch. The values in the following tables are for annealed copper of standard resistivity. The user of the tables must apply the proper correction for copper of other resistivity. Hard- drawn copper may be taken as about 2.7 per cent higher resistivity than annealed copper. The following is a fair average of the chemical content of commercial high conductivity copper: Copperas.) eee. 99.91% Sulphur esses cee 0.002% Silvery cere cess oe 03 Tri aercde serene eres .002 Oxygen en cece 052 Nickel ea sansa Trace AGSEMC ME icc. ke oes .002 Lead So dsdkot, soe: $ ATLIMONYs eee eee .002 Zine soa ere eee oe The following values are consistent with the data above: Conductivity at 0° C, in c.g.s. electromagnetic units.......... 62.969 X 107° Resistivity at Ome Comin michonin=CimiSynaciec ceieteleiee cecil 1.5881 Densityaat Op Gur’. = cnet BE Mio So tlhe Randa ene eee 8.90 Coefficient of linear expansion per degree C................ 0.000017 “Constant mass” temperature coefficient of resistance at 0° C. 0.00427 The aluminum tables are based on a figure for the conductivity published by the U. S. Bureau of Standards, which is the result of many thousands of determinations by the Aluminum Company of America. A volume resistivity of 2.828 microhm-cm and a density of 2.70 may be considered to be good average values for commercial hard-drawn aluminum. These values give: Conductivity at o° C in c.g.s. electromagnetic units............ 38.36 X 10° Mass resistivity, in ohms (meter, gram) at 20° C............. 0.0764 “ of z; eS Gaavles Farereretal)) Ehe ZO" (So cconescoooee 436. Mass per cent conductivity relative to copper................ 200.7 Yo Volume resistivity, in microhm-cm at 20° C................. 2.828 a ool, S(SAOavoaerbalooy che AO (Co seaocaccccacee 1.113 Volume per cent conductivity relative to copper............. 61.0% Density, in grams per cubic centimeter........-1.s+....-<+- 2.70 Density, in pounds per cubic inch.......... Merce reine « 0.0975 The average chemical content of commercial aluminum wire is NU LITTLUMNITT y woven eRe slor «66 sre Be Spo RTO e io. eios ese eure os 99.577 Sil iC Ones rons Piso in ks ea weirs 0.29 ASOT aeate de opto ner MI ee Pan Toke aie soso ee ce okunin o> 0.14 SMITHSONIAN TABLES . 422 TABLES 497 AND 498 COPPER WIRE TABLE 497,—Temperature Coefficients of Copper for Different Initial Temperatures (Centigrade) and Different Conductivities Ohms (meter, gram) at 20°C. Per cent conductivity. ars a30 0.161 34 05% 0.004 03 0.003 80 0.C03 73 0.003 60 .159 66 96% .004 08 -003 85 .003 77 -003 64 -158 02 07% -004 13 .003 89 .003 81 .003 67 -157 53 97-37% .004 14 -003 90 .003 82 .003 68 -156 40 98% .004 17 -003 93 .003 85 .0C3 71 154 82 99% .004 22 003 97 .003 89 .003 74 .153 28 100% .004 27 .004 OI .003 93 .003 78 -151 76 101% -004 31 -004 05 .00 397 .003 82 Nore. — The fundamental relation between resistance and temperature is the following: Rr=Re(t ta, [t—t,]), where a¢, is the “‘temperature coefficient,” and t, is the “initial temperature’’ or “temperature of reference.” The values of a in the above table exhibit the fact that the temperature coefficient of copper is proportional to the conductivity. The table was calculated by means of the following formula, which holds for any per cent conductivity, m, within commerctal ranges, and for centigrade temperatures. ( is considered to be expressed decimally: e.g., ii per cent conductivity = 99 per cent, m = 0.99.) 7 I t; = 3 1 I n(0.00393) “1 7°) TABLE 498.—Reduction of Observations to Standard Temperature (Copper) i Corrections to reduce Resistivity to 20° C. Factors to reduce Resistance to 20° C. Temper- F 2 : os 2 . __ | For 96 per | For 98 per | For roo per ature C. |Ohm (meter,| Microhm Ohm (mile, | Microhm Raieane Gant Gore eentieode Sra OO pound). inch. ductivity. | ductivity. | ductivity. Temper- ature C. 68.20 +0.053 58 1.0816 1.0834 .c853 51.15 .040 18 1.0600 1.06013 .0626 34.10 .026 79 1.0392 1.0401 .0409 +0.011 94 +0.1361 .008 96 + .1621 .005 97 0681 .024 II 1.0352 1.0359 .0367 .02T 43 1.0311 1.0318 .0325 .018 75 1.0271 1.0277 .0283 30.69 27.28 23.87 -o612 -0544 .0476 -005 37 .004 78 .004 18 .016 C7 .0232 1.0237 1.0242 .O13 40 .O192 1.0196 1.0200 .010 72 .O153 1.0156 1.0160 20.46 17.05 13.64 .0408 .0340 .0272 .003 58 .002 99 .002 39 .008 04 .O1I4 I.C1I7 1.0119 .005 36 .0076 1.0078 1.0070 .002 68 .0038 1.0039 1.0039 10.23 6.82 3-41 .OOI 79 -OO1 19 .000 60 .0204 .0136 .0068 +++ 444+ 44+ ++ +++ +++ 44+ + 44+ $44 44+ +++ +++ 44+ +++ 4+ ° ° ° 1.0000 1.0000 1.0000 .000 60 .0068 Be .002 68 0.9962 c.9gQ62 0.9961 .OOI 19 .0136 5. .005 36 -99025 -9924 -9Q22 .OOT 79 .0204 2 .008 04 .9888 .9886 -9883 .002 39 .0272 ae .O10 72 .9851 -9848 -9845 .002 99 -0340 : .O13 40 -9815 -Q8I1 .9807 .003 58 .0408 é -016 07 -0779 -9774 -9770 .004 18 .0476 z .018 75 -9743 -9737 -9732 .004 78 .0544 £ -O21 43 -9707 -Q701 .96905 .005 37 |. .0612 7 .024 II -9672 .9665 .9058 .005 07 .0681 iS .026 79 -9636 .9629 .9622 .008 96 -102I % .c40 18 -9464 -0454 -90443 -OII 94 -1361 : -053 58 .9298 -9285 .9271 .O14 93 .1701 i .066 98 -9138 -9122 -QIOS -O17 92 -2042 a .080 37 .8983 .8964 -8045 .020 90 -2382 35 .093 76 8833 .881r2 .8701 .023 89 .2722 36.4 .107 16 .8689 .8665 8642 .026 87 .3062 ‘ -120 56 -8549 8523 .8407 .029 86 -3403 4 -133 95 8413 -8385 .8358 .032 85 3743 : -147 34 .8281 SMITHSONIAN TABLES. ENGLISH TABLE 499 423 WIRE TABLE, STANDARD ANNEALED COPPER American Wire Gage (B.&S.). English Units , Cross-Section at 20° C. Ohms per rooo Feet.* Diameter in Mils. at 20° C. | Circular Mils. | Square Inches. ae (ies 211 600. 0.1662 0.049 OI 0.054 79 167 800. .1318 .061 80 133 100. 1045 077 93 105 S00. .082 89 : .098 27 83 690. .065 73 : .1239 66 370. 052 13 ‘ 1563 52 640. : : .1970 41 740. .032 . 2485 33 100. : : SBS 26 250. .020 62 : .3951 °20 820. : : .4982 16 510. : : .6282 13 0go. : : 7921 10 380. 008 155 : 9989 8234. .006 467 1.260 6530. | .005 129 1.588 5178. .004 067 2.003 4107. .003 225 2.525 3257- .002 558 3-184 2583. .002 028 4.016 2048. .0O1 609 5.064 1624. .OOI 276 ; 6.385 1288. .OOI O12 8.051 1022. .000 $02 3 10.15 810.1 .000 636 3 12.80 642.4 .000 504 6 16.14 509-5 .000 400 2 20.36 404.0 .000 317 3 25.67 320.4 .000 251 7 22537 254.1 .000 199 6 40.81 201.5 .000 158 3 51.47 159.8 000 125 5 3 64.90 126.7 000 099 53 81.83 100.5 .000 078 94 103.2 79.70 | .000 062 60 130.1 63.21 .000 049 64 164.1 50.13 | .000 039 37 206.9 39.75 | -000 031 22 260.9 31.52 | .000024 76 329.0 25.00 | .000019 64 414.8 19.83 | .000 015 57 523-1 15.72 | .000 O12 35 659.6 12.47 | .000 009 793 831.8 9.888 | .000 007 766 1049. * Resistance at the stated temperatures of a wire whose length is rooo feet at 20° C. SmitHSONIAN TABLES. 424 TABLE 499 (continued) ENGLISH WIRE TABLE, STANDARD ANNEALED COPPER American Wire Gage (B. & S.). English Units Feet per Ohm.* Diameter Pounds é in Mils. per p o° G 20°C 50° C Aso Cae 1000 Feet. i = ; (=68° F.) (=122°F.) | (—167° F.) 640.5 3 2 : 20 400. : 16 780, 507.9 .968 | 17 : 16 180, ; 13, 300. 402.8 2.482 ; 12 830. ; IO 550. 319.5 : 40. 10 180. ; $367. 253-3 é : 8070. 219. 6636. 200.9 : : 6400. : 5262. NRO 159-3 : 5075. : 4173. 120.4 : é 4025. : 3309. 100.2 : s 3192. ‘ 2625. 79.46 ; j 2Eaie j 2081. 63.02 d ' 2007. : -S1OGn. _ 49.98 20. ; 1592. : 1309. ONO Uf 39.63 ; : 1262. ; 1038. 31.43 31.82 t 1001. $23.2 24.92 : : 794.0 19.77 “5 : 620.6 15.68 : ; 499-3 12.43 : 29. 396.0 9.858 td: oa i 314.0 - 7.818 : ; 249.0 6.200 : 214. 197-5 156.6 124.2 98.50 78.11 61.95 49-3 4.917 3-899 3.092 ONN NWO W DY 2.452 1.945 1.542 RN hd SE ico was Te22 38.96 0.9699 ; : 30.90 -7692 ie 26. 24.50 tb Ny ht .6100 ; 3 19.43 .4837 : : 15.41 3836 , : 12.22 +3042 287. : 9.691 2413 : é 7.085 1913 : : 6.095 any : ; 4.833 .1203 ; : 3.833 095 42 | ; .2 3-040 WNnR NowN hw bh Oo oN WIRE TABLE, STANDARD ANNEALED COPPER Diameter in mm atezOcee. 11.68 10.40 9.266 8.252 7-348 6.544 5.827 American Wire Gage (B. & §.). Cross Section in mm ate 20 .C, | 107.2 85.03 67-43 53-48 42.41 33-63 26.67 2 Tens 16.77 13-30 Metric Units Ohms per Kilometer. * 20°1G3 0.1608 -2028 -2557 222 “j-- .4066 5127 SOcICs 0.1798 .2267 2858 . 3604 “4545 -573! aT .Q113 1.149 1.449 1.827 *Resistance at the stated temperatures of a wire whose length is 1 kilometer at 20° C. SMITHSONIAN TABLES. METRIC TABLE 500 (continued) WIRE TABLE, STANDARD ANNEALED COPPER Diameter Kilograms 1 er .P Kilometer. in mm at 209 C. American Wire Gage (B. & §.). Metric Units Meters per Gram. Meters per Ohm.* 20° C. 50° C. 11.68 953-2 0.001 049 | : 6219. 10.40 1.55:9 001 323 . 4932- 9.266 599-5 .0O1 668 : 3911. 8.252 475-4 .002 103 5 3102. 7.348 377.0 002 652 : | 2460. 6.544 299.0 | .003 345 : 1951. 5-827 237 al .004 217 : 1547. 188.0 .005 318 : 1227. | 149.1 .006 706 118.2 ecOOORAIS 7 93-78 | .010 66 74-37 O13 45 58.98 .016 96 46.77 O28 37-09 | .026 96 .034 00 .042 87 .054 06 .068 16 085 95 .1084 .1367 1723 ; 37-86 30.02 23.81 18.88 14.97 bd wh 11 87 9-417 7.408 Onez WNH wn bv \O ON win WwW = Oo oo @} =v COW \O nbn mont mms nN nb: ANI mt — Sn WNN Nb Oo £ | 8.879 [OSONZie ue LL. 2O 070 83 | 14.12 | 056 17 | 17.80 044 54 | 22.45 * Length at 20° C of a wire whose resistance is 1 ohm at the stated temperatures. SMITHSONIAN TABLES. 16 TABLE 500 (concluded) WIRE TABLE, STANDARD ANNEALED COPPER American Wire Gage (B. & §.). 428 METRIC Metric Units Diameter in mm Ohms per Kilogram. Grams per Ohm. at 209 C. 20° CG, SOG: 11.68 10.40 9.266 8.252 7-348 6.544 5.827 5.189 4.621 4.115 3-665 3.264 RN QW Ne tN be aun SMITHSONIAN TABLES. 0.000 155 4 000 247 2 .000 393 0 .000 624 9 .000 993 6 .OOI 580 .002 512 005995 .006 352 .010 10 .016 06 1025 53 .040 60 .064 56 .1026 .1632 22505 -4127 6562 1.043 1.656 2.638 4.194 6.670 10.60 16.86 2681 0.000 168 7 .000 268 2 000 426 5 000 678 2 .OO1 078 .OOT 715 .002 726 204 355 .006 893 .O10 96 O17 43 027 7 .044 06 -070 07 1114 0.000 188 6 .000 299 9 -000 476 8 000 758 2 .OOI 206 OO! QI7 003 048 .004 846 .007 706 O12 2 O19 48 .030 98 049 26 078 33 1245 1980 “3149 .5007 7961 1.266 2.013 3.201 5.089 8.092 12.87 20.46 32°53 73 baer 130.8 207.9 330-6 525:/ 836.0 1329. 2114. 3361. 5344. 8497. 13510. 21480. z 34160. 54310. 86360. ENGLISH TaBLe 501 429 WIRE TABLE, ALUMINUM Hard-Drawn Aluminum Wire at 20° C (68° F.) American Wire Gage (B. & S.). English Units Cross Section. Gage | Diameter ; : e per per No. in Mils. Creclar Sauer TCoaiB eer lirccoidieet: per Ohm. per Ohm. Ohms Pounds Ponds Feet 0.166 0.0804 195. 12 400. .132 Lor | 4. 9860. .105 : y 7820. .0829 3 7 , 6200. 0657 . : 4920. 0521 7 z ; 3900. .0413 : : : 3090. .0328 4 : : 2450. .0260 : : : 1950. .0206 : . ; 1540. .O164 : | : : 1220. .O130 : : ; 970. to ° 0103 008 15 .006 47 770- 610. 5 454. SIO + Mun. Nun 005 13 .004 07 .003 23 QED wa .002 56 .002 03 .0O1 OI mp Cw \O CON \O .0o1 28 10.5 : 143 .OOF OI .000 802 ; | 0.93 0504 .000 636 .000 505 .000 400 0355 0222 0223 .O140 NNN by tv Nui OO DWN SEO mo .008 82 005 55 -003 49 to ° al - .000 317 000 252 .000 200 Qn & Ww hv STO or No tN .000 158 .000 126 .000 099 § .002 19 OO! 38 .000 868 — = CO wo PAR SN \o .000 546 .000 343 .000 216 .000 078 9 .000 062 6 .000 049 6 to be a= SOIC .000 039 4 : .000 136 .000 O31 2 : 000 O55 4 .000 024 8 : .000 053 7 | Ow .000 019 6 : 000 0338 .000 O15 6 Gees .000 O21 2 .000 O12 3 \ aes .000 O13 4 Ono | .000 009 79 : .000 008 40 .000 007 77 i .000 005 28 mn Qe £EN WON SMITHSONIAN TABLES. TABLE 502 METRIC 430 WIRE TABLE, ALUMINUM Hard-Drawn Aluminum Wire at 20° C (68° F.) American Wire Gage (B. & S.). Metric Units Gage Diameter | Cross Section Ohms per Kilograms per Grams per Meters per No. in mm, in mm.? Kilometer. Kilometer. Ohm. Ohm. 0000 TE 107. 0.264 289. I 100 000. 3790. 000 10.4 $5.0 e888 230. 690 000. 3010. 00 9.3 67.4 .419 182. | 434 000. 2380. ° 8.3 53-5 -529 144. | 278 Oorer 1890. I 7.3 42.4 -667 114. 172 000. 1500. 2 6.5 33-6 841 90.8 108 000, I1Qo. 3 5.8 26.7 1.06 72.0 67 goo. 943. 4 5-2 Zee 1.34 57-1 42 700. 749. 5 4.6 16.8 1.69 45.3 26 goo. 593. | 6 4.1 133 2513 35-9 16 900. 470. 7 Bu 10.5 2.68 28.5 10 600. 373- 8 B33 8.37 3.38 22.6 5680. 296. 9 2.91 6.63 4.26 17.9 4200. 235- 10 2.59 5.26 5-38 2 2040. 186. II 2.30 4.17 6.78 Tite 1660. 148. 12 2.05 B31 8.55 8.93 1050. tye ng 1.83 2.62 10.8 7.08 657. 2.8 14 1.63 2.08 13-6 5-62 413. 73.6 15 1.45 1.65 We 4.46 260. 58.4 16 1.29 1.31 21.6 3553 164. 46.3 17 1.15 1.04 27.53) 2.80 103. 36.7 18 1.02 0.823 34.4 2.22 64.7 29.1 19 0.91 653 43-3 1.76 40.7 23.1 20 SI 515 54-6 1.40 25.6 18.3 21 72 411 68.9 1.11 16.1 14.5 22 64 326 86.9 0.879 10.1 lito 23 oy) 258 IIo. .697 6.36 9.13 24 51 .205 138. 553 4.00 7.24 25 45 .162 174. -438 2.52 5:74 26 .40 .129 220. .348 1.58 ASS} 27 .36 .102 277% 276 0.995 3-61 | 28 32 0810 349. .219 .626 2.86 29 .29 .0642 440. 7B -394 2.27 30 25 FOSOO ||) 555: .136 .248 1.80 3) 222 .0404 | 700. 109 .156 1.43 32 .202 .0320 883. 0865 0979 Teale 33 .180 0254 IT 10. .0086 .0616 0.899 34 .160 .0201 1400. 0544 .0387 712 35 143 .0160 1770. 0431 .0244 565 36 S25) .O127 2230. 0342 0153 .448 37 or3 .0100 2820. {| ,027.1 .009 63 +355 38 .TO] 0080 | 3550 0215 .006 06 +262 | 39 .09O .0063 4480. O17 .003 81 223 40 .080 0050 5640. 0135 .002 40 ay SMITHSONIAN TABLES. TABLE 503 ELECTROCHEMICAL EQUIVALENTS Every gram-ion involved in an electrolytic change requires the same number of coulombs or ampere-hours of electricity per unit change of valency. This constant is 96.494 coulombs or 26.804 ampere-hours per gram-hour (a faraday) corresponding to an electrochemical equivalent for silver of 0.00111803 gram sec. amp.*!. It is to be noted that the change of valence of the element from its state before to that after the electrolytic action should be considered. The valence of a free, uncombined element is to be considered as 0. The same current will clectrolyze ° ‘chemically equivalent” quantities per unit time. The valence is 431 then included in the ‘‘chemically equivalent”’ quantity. Change of valency 3 I 3 5 a if 2 I 3 I I 2 4 I 2 Mg per coulomb 0.09317 -36746 .12249 -07349 -05249 .6588 -3294 2.044 6813 .0104442 2.1475 1.07375 .53688 2.0790 1.0395 Coulombs per mg 10.731 2.7213 8.1649 13.606 19.049 1.5179 3.0358 -4893 1.468 95-747 .46565 -93130 1.8626 -48100 -96200 Grams per amp. hour 0.3354 1.3229 -4410 .2646 .18891 222717, 1.1858 7-357 2.452 -0375991 7-7310 3.8655 1.9328 7-4844 3-7422 Change of valency Mg per coulomb Coulombs Grams per amp. hour NPN RR HOP NS NWN HY 0.6082 -3041 .20273 .082909 -041454 1.01165 .50582 -33722 .4052 1.11803 .23833 .61505 -30752 -33875 1.6442 3.2884 4-9326 12.0611 24.1222 .98848 1.97696 2.9654 2.467 -894430 4.1958 1.6259 3.2518 2.9520 2.1895 1.0948 -7298 .298500 .149250 3-6419 1.8210 1.2140 1.4587 4.02491 -85799 2.2142 1.1071 1.21950 The electrochemical equivalent for silver is 0.00111803 g sec.-! amp.- For other elements the electrochemical equivalent = 1/96494 g/sec./amp. or g/coulomb. Note.—The change of valency for O2 is usually 2, etc. SMITHSONIAN TABLES (atomic ie divided by change of valency) times 432 TABLES 504 AnD 505 TABLE 504.—Conductivity of Electrolytic Solutions This subject has occupied the attention of a considerable number of eminent workers in molecular physics, and a few results are here tabulated. It has seemed better to confine the examples to the work of one experimenter, and the tables are quoted from a paper by F. Kohl- rausch,* who has been one of the most reliable and successful workers in this field. The study of electrolytic conductivity, especially in the case of very dilute solutions, has fur- nished material for generalizations, which may to some extent help in the formation of a sound theory of the mechanism of such conduction. If the solutions are made such that per unit volume of the solvent medium there are contained amounts of the salt proportional to its electro- chemical equivalent, some simple relations become apparent. The solutions used by Kohlrausch were therefore made by taking numbers of grams of the pure salts proportional to their elec- trochemical equivalent, and using a liter of water as the standard of quantity of the solvent. Tak- ing the electrochemical equivalent number as the chemical equivalent or atomic weight divided by the valence, and using this number of grams to the liter of water, we get what is called the normal or gram molecule per liter solution. In the table, # is used to represent the number of gram molecules to the liter of water in the solution for which the conductivities are tabulated. The conductivities were obtained by measuring the resistance of a cell filled with the solution by means of a Wheatstone bridge alternating current and telephone arrangement. The results are for 18° C, and relative to mercury at 0° C, the cell having been standardized by filling with mercury and measuring the resistance. They are supposed to be accurate to within one per cent of the true value. The tabular numbers were obtained from the measurements in the following manner : — Let A,,— conductivity of the solution at 18° C relative to mercury at 0° C. «¥, = conductivity of the solvent water at 15° C relative to mercury at 0° C, Then &A,, —A%, =4,, = conductivity of the electrolyte in the solution measured. “1s — 4 — conductivity of the electrolyte in the solution per molecule, or the “specific mM molecular conductivity.” Value of 7, for a few Electrolytes This short table illustrates the apparent law that the conductivity in very dilute solutions is proportional to the . amount of salt dissolved. KC,H,0, am 1 nN ~ Se = 0.00001 0.939 boon 0.00002 1.856 0.00006 5-610 0.0001 9.34 NN RS bum WO nhWwnN _ _~ TABLE 505.—Electro-Chemical Equivalents and Normal Solutions The following table of the electro-chemical equivalent numbers and the densities of approximately normal solutions of the salts quoted in Table 506 may be convenient. ‘They represent grams per cubic centimeter of the solution at the temperature given. Salt dissolved. Grams nS Density. | Salt dissolved. ee 4 Density. per liter. y KG en ea 74259 INSET Cle yea 53°55 NaCI aan o350 TiC lies epee 45 4BaCl, . .| 104.0 4ZnClp . .| 68.0 Keg 6. 6 || LORE KEN Osh 28 oe | ROM, NaNOg . .| 85.08 AgNO 3 . . | 169.9 4Ba(NOs)2 : 65.28 KClOs ey a Ol29 0457 | #K2SO4 .| 87.16 | 1. 9 | 1.0658 0152 | 4NagSOg . | 71.09 : 1.0602 0391 | $LigsO4 «| 55-09 1.0445 0227 | 4MgSO, .| 60.17 1.0573 .0888 | 4ZnSO, . | 80.58 | I. 1.0794 0592 | 4#CuSO4g . | 79.9 1.0776 1183 | }KgCOg . | 69.17 1.0576 .o601 | 3NagCOg . | 53-04 | I. 1.0517 542 | Oia sey. | 56:27 1.0477 - ENC] | 30255 1.0161 _ to - JSUNKO oh oul) Rate) 1.0318 : .0367 | 4H2SO4 . | 49.06 1.0300 KC,H302 .| 98.18 : .0467 ORO RIB aarp abril ere mMmnAooooododoan * “Wied. Ann.” vol. 26, pp. 161-226, 1885. SMITHSONIAN TABLES. SPECIFIC MOLECULAR CONDUCTIVITY OF SOLUTIONS MERCURY = 108 TABLE 506 433 Salt dissolved. TGSOg). Salt dissolved. LK2SO, . Keel rai NH,Cl KNO3 1BaCle KClOg_ . 4 BaN2O¢g 4CuS O4 . AgNOg . 17nSO, . IMgSOg . ENagSO, 2ZnCle NaCl NaNOs3 . KC2gH 302 4NagCOz LH SO, . C2H4O HCl HNO, LHsPO, . KOH oy NHs SMITHSONIAN TABLES. * Acids and alkaline salts show peculiar irregularities. 434 TABLES 5O7 AND 508 SPECIFIC MOLECULAR CONDUCTIVITY OF SOLUTIONS TABLE 507.—Limiting Values of u This table shows limiting values of 4» = z .108 for infinite dilution for neutral salts, calculated from Table 305. i Salt. Salt. Salt. Salt. 4KeSO4 . 4+BaCle . 1150 4MgsO4 . 4H2SO4 IMGiigt a 4KClO3. . 1150 4NagSOg . HCl Re iy cece 4BaN20¢,¢ .| 1120 4ZnClo. . HNOs. NECle nel) a2 AcCusO, || “arco NaCl os 1H5POq KNO;s. . 2 AgNO3 .| togo NaNO3 . 980 KOH 4ZnSO4 .| 1080 KsCoH30o 940 tNaeCOz . If the quantities in Table 507 be represented by curves, it appears that the values of the specific molecular conductivities tend toward a limiting value as the solution is made more and more dilute. Although these values are of the same order of magnitude, they are not equal, but depend on the nature of both the ions forming the electrolyte. When the numbers in Table 508 are multiplied by Hittorf’s constant, or 0.00011, quan- tities ranging between 0.14 and o.1o are obtained which represent the velocities in milli- metres per second of the ions when the electromotive force gradient is one volt per millimetre. Specific molecular conductivities in general become less as the concentration is in- creased, which may be due to mutual interference. The decrease is not the same for different salts, but becomes much more rapid in salts of high valence. Salts having acid or alkaline reactions show marked differences. They have small specific molecular conductivity in very dilute solutions, but as the concentration is in- creased the conductivity rises, reaches a maximum and again falls off. Kohlrausch does not believe that this can be explained by impurities. H3PO,4 in dilute solution seems to approach a monobasic acid, while HzSOq4 shows two maxima, and like H3PO4 approaches in very weak solution to a monobasic acid. Kohlrausch concludes that the law of independent migration of the ions in media like water is sustained. ee pp ES, TABLE 508.—Temperature Coefficients The temperature coefficient in general diminishes with dilution, and for very dilute solutions appears to approach a common value. The following table gives the temperature coefficient for solutions containing o.o1 gram mole- cule of the salt. Temp. Coeff. Salt. IK 6 : 1 Bees bee te 4K oS : : 4KoCO3 INGEIG @ lias x TINO goer ae : 2SC ; 4NaeCOz . | NaCl oly te le NaNOgs . KOH 1 Clearer : AgNOs. . : 5 3] © Cle HNO; . 4+BaCle of a 4Ba(NO3)2 b S . 4H2SO4 | 7nCly aoe | cot CIOs. +H2SO4 l 4MgCk .| o. I CASELOR A150) for m= .oo1 § SmitHSONIAN TABLES. TABLE 509 435 THE EQUIVALENT CONDUCTIVITY OF SALTS, ACIDS AND BASES IN AQUEOUS SOLUTIONS In the following table the equivalent conductance is expressed in reciprocal ohms. The con- centration is expressed in milli-equivalents of solute per liter of solution at the temperature to which the conductance refers. (In the cases of potassium hydrogen sulphate and phosphoric acid the concentration is expressed in milli-formula-weights of solute, KHSO4 or HgPOx, per liter of solu- tion, and the values are correspondingly the modal, or “formal,” conductances.) Except in the cases of the strong acids the conductance of the water was subtracted, and for sodium acetate, ammonium acetate and ammonium chloride the values have been corrected for the hydrolysis of the salts. The atomic weights used were those of the International Commission for 1905, referred to oxygen as 16.00. Temperatures are on the hydrogen gas scale. Concentration in sramieduivaleniy 1000 liter reciprocal ohms per centimeter cube grant equivalents per cubic centimeter Equivalent conductance in Equivalent conductance at the following ° C temperatures. Substance. 18° | 25° 100° | 128° | 156° | 218° | 281° | | Potassium chloride . 130.1 |(152.1) ; -5)| 414 |(519)| 625 | 825 vee ‘ “ a 126.3 | 146.4 | | Se ese00 779), 930 | 122.4 | 141.5 | : : | | 560 | 741 | 874 MES:5¢[ sll 2| — | 498 | 638 | 723 | 112.0 | 129.0 | : 490 | Sodium chloride. . | 109.0) - | 555 | 760 a re AS weal 105.6 | | WS saul 722 8qc: | le 102.0 | 511 | 685 | 93 5 | | aOR SCOR ae 92.0 | | 442 | Silver nitrate . . . | 115.8) | 570 | 780 | 965 as ec St 112.2 | S3On| 27 | 877 ; on eae 108.0 | | SO7mlmO78 105.1 | | 488 | 639 | 462 | 599 | 96.5, | 432 | 552 | 94-6 78.1 | | 450 | 660 | | 421 | 578 | 396 | 542 349 | 452 690 | 1080 | 377 | 260 | 241 | 143 | | 195 | 110 PLCSn oo 139 75 | 126 cl AB TE | | | | I0Q | Ammonium chloride | 131.1 | 152.0 | | (628) | (841) | oe essa 126.5 | 146.5 | 6o1 | 8or | ep as 122.5 | 141.7 573 | 758 tration. BO HR RU &inta ONO 4 QNN OnRON DHL HW HE wMOWN ce 118.1 - | (99.8) 91.7 | 88.2 | Ammonium acetate. | “ “ “cc “cc | | | From the investigations of Noyes, Melcher, Cooper, Eastman and Kato; Journal of the American Chemical Society, 30, P+ 335, 1908. SMITHSONIAN TABLES. 430 THE EQUIVALENT CONDUCTIVITY OF SALTS, ACIDS AND BASES IN Substance. Potassium hydrogen ) sulphate Phosphoric acid ‘ ay Acetic acid . “cc 6c Ammonium hydrox- idey.. mars SMITHSONIAN TABLES, TABLE 509 (continued) AQUEOUS SOLUTIONS Equivalent conductance at the following ° C temperatures. 116.9 109.7 101.0 88.7 81.6 | 79.1 132.8 124.5 115-7 104.2 97.2 | 95-0 379-9 373-6 | 368.1 | | 353:0 | 350.6; - 377-0 | 421.0 | 371.2 | 413-7 | 559 305.0 | 406.0, 548 | 353-7 | 393-3, 528 340.4 | 385.0| 516 383-0 | (429) | (591) | 390.8 | 501 | 337-0, 406 | 27/301 323 251-2 | 300 | 506.0 | 661.0 | 318.3 | 374-4 283.1 | 329.1 | 376 | 510 311.9 | 401 222.0))|) 27-30 | 132.6 | 157.8 | [ane2 27 57° OR ee OOF tod bv 389 liane ans eo 235 | 342 215.1 | 308 | 204.2 | 201 8) | (271) 256 —~r edn HN LY (404) | | 706 | 826 | (520 | 449 | 373 | 443 | 75° 128° | 156° 385 600 352 | 536 322 451 | 280 412 | 258 | 372 249 | 455 | 719 402 | | 605 365 537 | | 320 | 455 204 415) 286 850 : 1085 $26 | 1048 | 807 | 1016 | 762 946 | 754 | 929 | 20 | 1047 $06 | TO12 | 786 | 978 649 | 750) 8 917 632 | 728 | 880 (746) 891 | 1176 | 561 | 571 530 | 435 | 446 481 356 | 384 | 448 336 | 369 435 | 754 | 784 754 403 | 422 477 354 | 375) 435 631 | 73¢ | 93° 464 | 498 489 300 308 2 274 16S Oe 142 129.9 | 128 | 12 108 = .|(773) | (980) 25.1 | 22.2 14.7 13.0 | 9.05 | | 8.00 | | 8.10 (ie | | 594 835 | 1 | §82 | S14 559 lira 2 690 676 = | $40! = Jeo738 | 0) | O45 (760) 847 ee 664 | 722 | | 478 | 549 | 593 503 | 53! (526) (647) (764) (908) 399 - |13.6| - | 13.0 (1230), 2.9 | 22.3 22.2) |e 6.70 a ply * These values are at the concentration 80.0, 218° | 281° 840 | 1120 715| 828 615 | 658 507 | 593 449 | 430 1065 | 1460 806 | 893 672 | 687 545| 519 482) 448 1265 | 1380 T2107) | 1322 1168 | 1226 1044 | 1046 1006 1166 306° 1300 24 61 44 867 637 466 TABLE 510 437 THE EQUIVALENT CONDUCTIVITY OF SOME ADDITIONAL SALTS IN AQUEOUS SOLUTION Conditions similar to those of the preceding table except that the atomic weights for 1908 were used. : | Equivalent conductance at the follawines C temperature. Concen- a Substance. ation: | = cs 7 Seen eLOOS 128° 156° | | | | 126.3 I} 219 | 299 | 384 | 485 580 122.5 . 212.7 | 289.9 | 370.3 | 460.7 Ct | a7=2 f 202.9 | 276.4 | 351-5 | 435-4 | 520.4 | | 109.7 : 189.5 | 257-4 | 320.1 8 476.1 104.5 ; 180.2 -L | 308.5 127.6 aCe 30 419 119.9 ; 215.9 399.3 111.1 29.2 | 199.1 354-1 101 5 | 178.6 Bl22 94.6 | : 107 288.9 88.4 | 102. 155 265.1 to —_ + =] 2 Qo Ow’ ne™N Ono = tN ONE NN HN WW W237 .6 | 202 25 369 107.1 191.9 | 260. 346. 5 98.6 a5 170.2 88.6 | 102.6 | 157.2 82.6 | 5. 146.1 76.7 | 88.8 | 135-4 | 159.6 | 288 | un OS tn CODE Aon QON™N FOMmWOMN bv Wo kU Qo Mm bn NWG NOs NH ¢ S sy SS oO | 137 113.4 93-7 34.9 | 77.8 72.1 to Qo ae t N-O _ Barium ferrocyanide . “ “ “ “ce Calcium ferrocyanide “cr NNWWwfUN C0 From the investigations of Noyes and Johnston, Journal of the American Chemical Society, 31, p. 287, 1909. SMITHSONIAN TABLES. 438 TaBLEes 511 AND 512 TABLE 511.—The Equivalent Conductivity of the Separate Ions From Johnson, Journ. Amer. Chem. Soc., 31, p- 1010, 1909. TABLE 512.—Hydrolysis of Ammonium Acetate and Ionization of Water Hydrogen-ion concen- tration in pure water. | Equivalents per liter. Percentage Ionization constant Temperature. hydrolysis. of water. KywxX 1ol4 . CyX 107 0.089 0.30 0.46 0.68 0.91 6.9 14.9 Noyes, Kato, Kanolt, Sosman, No. 63 Publ. Carnegie Inst., Washington. SMITHSONIAN TABLES. TABLES 513 AND 514 439 DIELECTRIC STRENGTH TABLE 513.—Steady Potential Difference in Volts required to produce a Spark in Air with Ball Electrodes R=o0 =o. : os | tet R=0 Points. . j set : - P Plates. Based on the results of Baille, Bichat-Blondot, Freyburg, Liebig, Macfarlane, Orgler, Paschen, Quincke, de la Rue, Wolff. For spark lengths from 1 to 200 wave- lengths of sodium light, see Earhart, Phys. Rev. 15, p. 163; Hobbs, Phil. Mag. 10, p. 607, 1905. TABLE 514.—Alternating Current Potential required to produce a Spark in Air with various Ball Electrodes The potentials given are the maxima of the alternating waves used. Frequency, 33 cycles per second. Spark length. Ripe cm. 3770 4400 5990 7510 9045 10480 11980 13300 14770 16140 18700 21350 23820 26190 28380 32400 35550 38750 40900 42950 Based upon the results of Kawalski, Phil. Mag. 18, p. 699, 1909. SMITHSONIAN TABLES. 440 TABLES 515 AND 516 DIELECTRIC STRENGTH TABLE 515.—Potential Necessary to produce a Spark in Air between more widely Separated Electrodes Steady potentials. Steady potentials. Alter- Alter- nating current. Ball electrodes. Cup electrodes. Ball electrodes. Spark length, cm. nating current. Projection, R= acm} || R==2.5\Chy: sees | | 4.5mm. 1.5mm. | R=2.5cm. Spark length, cm. Dull points. Dull points. Ps = - 11280 3 61000 86830 17610 | 17620 - 17420 i = = | 23050 - 22950 : 67000 90200 30240 | 31390 | 31400 | 31260 7 3000 91930 33800 | 36810 = 30700 82600 93300 8/980) © || 44310 44510 92000 94400 42320 | 56000 56500 | 56530 | - 94700 45000 65180 | - 68720 || 101000 101000 46710 71200 80400 | 81140 : 119000 - 75300 92400 z 140600 49100 75600 103800 : 165700 - 81540 114600 190900 50310 | 83800 126500 3 =o 135700 ANP EOWNDH A= O09 MmONnNdOMdOMdOMNbn ONWMwW This table for longer spark lengths contains the results of Voege, Ann. der Phys. 14, 1904, using alternating current and ‘‘dull point’? electrodes, and the results with steady potential found in the recent very careful work of C. Miik ler, Ann. d. Phys. 28, p. 585, 1909. TRUE PT The specially constructed elec- mavens trodes for the columns headed | “cup electrodes’? had the form of AL : a projecting knob 3 cm in diame- : _— "4 : : ter and having a height of 4.5 mm i€— 2%om — >! andr.5 mm respectively, attached : a : to the plane face of the electrodes. : @cm > : These electrodes give a very satis- | factory linear relation between the spark lengths and the voltage throughout the range studied. TABLE 516.—Effect of the Pressure of the Gas on the Dielectric Strength Voltages are given for different spark lengths /. Pressure. cm Hg This table is based upon the results of Orgler, 1899. See this paper for work on other gases (or Landolt-Bornstein- Meyerhoffer). : : ; ; For long spark lengths in various gases see Voege, Electrotecha. Z. 28, 1907. For dielectric strength of air and CO, in cylindrical air condensers, see Wien, Ann. d. Phys. 29, p. 679, 1909 SMITHSONIAN TABLES: TABLES 517 AND 518 441 DIELECTRIC STRENGTH TABLE 517.—Dielectric Strength of Materials Potential necessary for puncture expressed in kilovolts per centimeter thickness of the dielectric. Kilovolts | | Kilovolts per cm | Substance. : per cm. Substance. Substance. Kilovolts Ebonite . . . .| 300-1100 || Oils: Thickness | Papers : Empire cloth . .; 80-300 | Castor 0.2mm | 190 || Beeswaxed i ePApeTE = ASOnn | es 1.0 “ | 130] Blotting . EBibre yeeystats 3) 20 ~+||| ~=«Cottonseed . oP oll) Manilla’ Fuller board . .| 200-300 Lard 0.2 | 140 || Paraftined Glass.) . <4 ..| 300-1500} . 1.0 | 40] Varnished Granite (fused). go =o: t}_—=Sf Linseed, raw 0.2 | 185 || Paraffine: Guttapercha. . .| 80-200 a a 1.0 | gol] Melted . . .| Impregnated jute . 20 boiled 0.2 190 |] Melt point. | Leatheroid . . .| 30-60 s| constant. | Alcohol: | Alcohol : Amyl Wace’ fe frozen Methyl ——1OO ity “cc Propyl Oo Acetone , “ Be CO NEN COONS an “ RwNH&O eh to NEON OW’ O “cc | Acetic acid “ “ NNNN NWN — SIO CaS Oa Coca ta eet TON TOON OTE DAO OF WW Qn Amy] acetate | | Amylene I References on page 444 N On OWNN COOQOOW Wb CONN bt Oorwon mn OO NN DON Qui hd HH eNO ee Saas Oo N mee RODIN DN HH Re eRe DD Be OO un go ° SMITHSONIAN TABLES Substance. | Aniline : Benzol (benzene) . | “ “ | Bromine . Carbon bisulphide Chloroform . Decane Decylene Ethyl ether Hexane : Hydrogen perox- ide 46 % in H2O Drude, 1896. Marx, 1898. Lampa, 1896. Abegg, 1897. Thwing, 1894. Drude, 1898. Francke, 1893. Lowe, 18908. © ON AnfW DN Abegg-Seitz, 1899. Temp. Poe 18 18 19 23 20 17 18 17 14 17 ' (frozen) 15 16 TABLE 523 (continued) DIELECTRIC CONSTANT OF LIQUIDS A wave length greater than 10000 centimeters is designated by 00. Wave- lenge = too NG to PREP HEAP WE! WAMDONWOO NH AD tv ° =N ON ODO Re DAfun 10 Landolt-Jahn, 11 Turner, 1900. 12 Schlundt. 13 Tang], 1903. Substance. Nitrobenzol . a Octane || Oils : Almond Castor . Colza Cottonseed Lemon . Linseed Neatsfoot. Olive Peanut. Petroleum Petroleum ether | Rape seed Sesame Sperm . ‘Turpentine Vaseline . Phenol Toluene se “ Meta- xylene . “ ay a | Wave- | oC length cm. ' (frozen) | -|/——-IO |! ao 20 Own 13.4 | 20 20 | 48 sage 19 18 17 Za | eal Nh he tN No N n - WWW wmM Ah NN SW = CONTI OO Water for temp. coeff. see Table 524. 1892. 18 14 Coolidge, 1899. 15 v. Lang, 1896. 16 Nernst, 1894. 17 Calvert, 1900. 0 ° N | Hasenohrl, 1896. Arons-Rubens, 1892. Hopkinson, 1881. Salvioni, 1888. Tomaszewski, 1888. Heinke, 1896. Marx. Fuchs. | 900g Ceo aN SMITHSONIAN TABLES TABLES 524 aND 525 445 DIELECTRIC CONSTANT OF LIQUIDS TABLE 524.—Temperature Coefficients of the Formula: D6 Substance. Amy] acetate. Aniline . Benzene. . : Carbon bisulphide : Chiesa Ethyl] ether Methyl alcohol Oils: Almond Castor . Olive . Parattine . Toluene . Meta -xylene 0.0024 0.00351 0.00106 0.000966 0.000922 0.00410 0.00459 0.0057 0.00163 0.01007 0.00364 0.0007 38 0.00092 I 0.000977 0.004474 0.004583 0.004 36 0.000817 = D,[1—a(¢— 6) + B(¢ — 6)?] Hers al | Tange, ©.0000087 0.00000060 0.00001 5 0.000026 0.000007 2 0.00000046 0.0000117 Authority. | } TeeeRauel | Ratz. Tangl. | Ratz. | Drude. | Hasenohrl. Heinke, 1896. Hasenohrl. Ratz. | Tangl. Heerwagen. Drude. Coolidge. Tangl. (See Table 520 for the signification of the letters.) TABLE 525.—Dielectric Constant of Liquefied Gases A wave-length greater than 10000 centimeters is designated by oo. Substance. length cm. Air “oe Ammonia . “a Carbon dioxide . “ “ Cyanogen . : Hydrocyanic acid Hydrogen sulph. Diel. Cone ata Substance. Authority. | || Nitrous oxide mbhwn eR | Critical . Diel. constant. ) Wave- length cm. Authority. 1 v. Pirani, 1903. 2 Bahn-Kiebitz, 1904. SMITHSONIAN TABLES. 3, Goodwin-Thompson, 1899. 4 Coolidge, 1899. 5 Linde, 1895. 6 Eversheim, 1904. 7 Schlundt. rgor. 8 Hasenohrl, 1900. 9 Fleming-Dewar, 1896. 446 TABLES 526 AND 527 DIELECTRIC CONSTANT TABLE 526.—Standard Solutions for the Calibration of Apparatus for the Measuring of Dielectric Constant Drude. Nernst. Diel. const. Acetone in benzene at 19°. A=75 cm. Ethyl alcohol in Substance. 8°. water at 19.5°. | A=, Per cent D | Dielectric | Temp. by weight. | constant. | coefficient. Benzene... . ; Per cent |Dielectric| } Meta-xylene | a ~ ||by weight.| constant. Ethylicther . = - ‘ 0.885 2.26 Aniline. : 2 0.866 5.10 . roa BGS 0.847 8.43 : ‘ Ethyl chloride . . : 90 20.3 O-nitro toluene. : 0.830 12.1 : 86 Nitrobenzene . . 36. 0.813 16.2 5 70 Water (conduct. 10-6) A 0.797 20.5 . 6 ensity 16°. Water in acetone at 19°. 0.797 20.5 0.856 31.5 0.903 43-5 0.940 57-0 0.973 70.6 0.999 80.9 . | Wave- ° seal 7 - | Wave- Condi- length Dielectric Suetance: ondi- length, | Dielectric tion. constant. | . constant. | cm. cae | | cm. Asphalt .. 20 Barium — sul- Iodine (cryst.) . phate! =~ 75 Lead chloride . Caoutchouc . 0 (powder) Diamond . . eas “nitrate = aver 75 “sulphate . Ebonite . . 0 ““ molybde- a f nate . as Marble Glass * Density. (Carrara) Flint (extra | Mica . heavy) .]| 4.5 sD mee te Flint (very Madras, brown ligihit) woes | 2:87 "| 3 green Hard crown | 2.48 | : ss rub IMGUTCOIE 5 |b - | | 6. .46 | | Bengal, yellow ai } whites aes | ruby Lead (Pow- Canadian am- ell). Si|/2!0=2) 4-8. bers. geaee Jena | | South America Boron) 5-8. || Ozokerite (raw) Barium . i 8-8. Paper (tele- Borosili- phone) cate . ON OF “ (cable) Gutta percha. | 3.3-4. Paraffine . i a t Co PRU DLO wm NE oN “c “cc | | | “cc b Rs ny 0 mn AfONDA.,. Melting | point. Tce. 5. avo. Ie Bios ee anes eee eR ( -3rOun| ee esa 50 Sees cae | | 1.76-1. - + + | 74-76) NN to N N Heep References on p. 447- * For the effect of temperature, see Gray-Dobbie, Pr. Roy. Soc..63, 1898; 67, 1900. “* wave-length, see K. F. Lowe, Wied. Ann. 66, 1898. SMITHSONIAN TABLES. TABLES 527 (continued) AND 528 DIELECTRIC CONSTANT 447 TABLE 527 (continued).—Dielectric Constant of Solids Condi- Substance. han. Paraffine Phosphorus: Yellow Solid . Liquid Porcelain: Hard (Royal B’I’n) SER hams BI SUTe he oe Selenium . “ Shellac. “ i Amber . Wave- length, cm. Diel. Substance. | constant, ity. Condi- tion. Wave- length, cm. Diel. | constant. | | Author- Sulphur Amorphous NN ar Cast, fresh oe “ bm bw ty Liquid . \ | Strontium sulphate | Thallium carbonate nitrate Wood Red beech . “se Nd bo CoO Mt fw N =~ near | melting: | point I fibres lo eo) Oo 0 On Mmumh Oo =) ~ NY OOW COM N & Vo REY = = I vy. Pirani, 1903. 2 Schmidt, 1903. 3, Gordon, 1879. 4 Winklemann, 1889. 5 Elsas, 1891. 6 Ferry, 1897. 7 Hopkinson, 1891. 8 Arons-Rubens, 189. g Gray-Dobbie, 1598. 10 Lowe, 1898. 11 (submarine-data), 12 Thwing, 1894. 13 Abegg, 1897. 14 Behn-Kiebitz, 1904. 15 Starke, 1897. 16 E. Wilson. 17 Campbell, 1906. Fallinger, 1902. Boltzmann, 1875. Zietkowski, 1900. Hormell, 1902. Schlundt, 1904. Willner, 1887. Donle. nN nS eS MPO Ne OW OC N HNN NK WN Y Vonwiller-Mason, 1907. TABLE 528.—Dielectric Constant of Crystals Da, DB, Dy are the dielectric constants along the brachy, macro and vertical axes respectively. SMITHSONIAN TABLES. 3 Curie, 1889. 6 Ferry, 1897. Wave-| Diel. const. | 5 || Wave- | Diel. const. % : Substance. length, | => Substance. length, sb cm. | Axis. || Axis. 2°77 roe eo Dg Dy a UNIAXIAL: | RHOMBIC: | | Apatite 75 | 9-50 | 7-40) 1 || Aragonite . co, | On4 | — | 7.03) 4 Beryl . CON 7-5 elh7 44a) p24 ‘ 75 | 9.80] 7.68) 6.55] 1 SO A on eel ois se 7.10 | 6.05] 3 ||| Barite oo 6.97 |10.09 | 7.00] 4 ries BAe bn 8 heyy GrO 55-520 ot : WSmi 7-05, | 2.205727. Calcite 5 all es 8.49 | 7.56] 4 || C elestite 7 7e7O) |) LOssal Oss I ss : s 8.78 | 8.2 5 || Cerussite Sea Sail 2 54a 232 ytO.2, 1 Dolomite 75 | 780 |680| 1 || MgSOut+7H2O .| oc | 5.26] 6.05 | 8.28 | 7 Iceland spar 75 | 3.50 | 8.00} 1 os Osiris “| 6.09 | 5.08 | 4.48 | 7 Quartz 0 4.69 | 5.06] 4 | | Rochelle salt* < 6.70 | 6.92 | 8.89} 7 | Sonmen Oss tom ey ¢ 4-38 | 4.46) 6 || Sulphur : 3-80 3:97 14:77. 18 eh eres OOS 144.27 )1.4.34 |. fe “ | 3.65 | 3-85 | 4.66| 7 Rubye( Siam), hw jel— eleiaea, Wearesy| 4 it | ie 13:62) 3.85 | 4.601) (2 Rutile (TiOg) . 75 89 | 1.73] 1 || Topaz soo oll ZR || G95|| O77 || OO] 2 Tourmaline. © Foi oy || (hiyital RPA “< colorless . - 6.25 | 6.54 | 6.44] 4 z 75 | 6.75 | 5.65) 1 Zircon 75 12.8 | 12.6 I * See page 448. 1 Schmidt, 1903. 4 Fallinger, 1902, 1919. 7 Borel, 1893. 2 Starke, 1897. Cave Pirani, 1903. § Bolztmann, 1875. 448 TABLES 529 AND 530 ELECTROSTRICTION. PIEZO-ELECTRICITY | Electrostriction is a phenomenon observed when an isotropic dielectric is placed in an | electrostatic field (F), the form and volume of the dielectric altering. Similar effects | occur in anisotropic materials but are obscured by piezo-electric effects. Piezo-electricity | occurs when a crystal dielectric is mechanically strained becoming electrically polarized. The magnitude and direction of the polarization (P) depends on the crystal used, the amount of strain and its direction relative to the axes of the crystal. Pyro-electricity is of the nature of a temperature-coefficient dp/dt. For fuller discussion and more extensive data see I.C.T., 6, 207, 1918 (Cody), Glass Paraffin Ebonite Rubber (vulcanized) AI/1E? .4 xX 10” 90 X 10°” 600 X 10°” 6000 X 10°” cm?/c.g.s.e" These values divided by 1.11 X 10° for values in cm’/volt’. TABLE 530.—Piezo-electricity Rochelle salt, KNaC:H:O.-4H2O di:= 17 X 10°°(es/cm’)/(dyne/cm’) — 70° C e . 8100 + 20 f 1100 + 30 : 400 + 40 Benzil, CisH10O2 du = 24 oD OC LiNas(MoOs)2 -6H20 dss Rb. tartrate, Rb:CsH:O6c di Tartaric acid, CsHeOc dis “ “ dis dos dat d32 das de Tourmaline dss 6 dis 14 “cc ‘ Patchouli camphor, CisH2sO Diamond, C Quartz, SiO. Sodium chlorate, NaClO; Fenchoneoxene, CioHusNO Ll ll Addenda to Table 528, p. 447, Dielectric Constant of Rochelle Salt: The polarization of the Rochelle salt dielectric in an electric field is somewhat analagous to the behavior of the magnetization of iron in a magnetic field, showing both saturation and hysteresis. The dielectric constant D depends on the initial and final fields and the hysteresis. Initial field, 765 v/cm; Final field, 690 v/em; Average D (23° C), 40 765 153 205 765 = 705 157 0 880 86 The last value may be fair value for ordinary purposes. The electrodes were tinfoil at- tached with shellac. The field was applied perpendicular to the a axis. Like piezo-electric properties, the dielectric constant varies with different crystals. It depends on the tempera- ture as follows: (field 0 to 880 v/cm) — 70° C, D=12; — 40°, 14; — 20°, 48; 0°, 174; + 20°, 88; + 30°, 52. (Data from Valesek, University of Minnesota, 1921.) SMITHSONIAN TABLES TABLE 529.—Electrostriction (Means) TABLE 531 449 THE CALCULATION OF THE HIGH-FREQUENCY RESISTANCE OF CONDUCTORS (By Dr. F. W. Grover, Consulting Physicist, Bur, Standards, 1931.) The resistance of a conductor to high frequency alternating currents is not the same as it offers to direct or low frequency currents. The linkages of flux with the inner portions of the conductor are more numerous than with the outer portions. That is, the reactances of the inner filaments are greater than those of the outer filaments. Consequently, the current density decreases from the outside toward the center of the conductor. This tendency of the current to crowd toward the outer portions of the cross section becomes more pronounced the higher the frequency, and at very high frequencies the current density is sensibly zero everywhere except in the surface layer of the conductor. This phenomenon is called the “skin effect.” It causes an increase in the effective resis- tance of the conductor over its resistance to a direct current. Whai is of interest in the calculation of the high frequency resistance is the resistance ratio, the quotient of the resistance at the given frequency by the direct current resistance. The resistance ratio depends upon the distribution of current density in the cross section, and this is a function of the frequency and the shape of the cross section. In general, J , in which f is the fre- Ro quency, and R is the direct current resistance per unit length. In what follows Ro will be taken as the direct current resistance per 1000 ft. of conductor. The distribution of current in the cross section is affected by a neighboring conductor carrying high frequency currents. This proximity effect finds an explanation in that the value of the mutual inductance of any filament A of one conductor on a filament B of the other conductor depends upon the positions of A and B in their respective cross sections. The proximity effect may be very appreciable for conductors nearly in contact; falling off rapidly as their distance is increased, it is negligible for moderate ratios of distance apart to cross sectional dimensions. In such cases the resistance is sensibly the same as for an isolated conductor. Beside the spacing factor of the conductors, the proximity effect depends upon the frequency, and in lesser degree upon the shape of the cross sections. Quantitatively, the proximity effect may be expressed by the proximity factor, which is the quotient of actual resistance of the conductor by the resistance which it would have if removed to a great distance from the disturbing conductor, both values of resistance being referred to the same frequency. hat is, i however, the resistance ratio is a function of the parameter Ro = the direct current resistance 1 = the resistance of the conductor when isolated, frequency f R:= the resistance in the presence of the disturbing conductor at frequency f ees 3 R ; ons Laven then the proximity factor is P =p and the resistance ratio RB,’ in the presence of the 1 0 disturbing conductor, is obtained from the resistance ratio —- when isolated by the rela- Ro j R R j i : : : ; ‘ tion R =P RP . Resistance ratio may be obtained in any case if the resistance ratio 0 0 when isolated is known, together with the value of the proximity factor. Formulas for the high-frequency resistance ratio have been developed in only a few simple (but important) cases, and even then very complicated formulas result. For prac- tical work tables are necessary for simplifying the calculations. The following tables cover the most important cases, Formulas have been derived for the high-frequency resistance ratio of single-layer coils wound with round wire. Generally, these differ from one another and from measured values, because, simplifying assumptions are made which are not sufficiently realized in practice. No tables of values for coils such as are met in practical radio work are available. As a rough guide, the high-frequency resistance ratio for a single-layer coil is often from two to five times as great as the resistance ratio of the same wire stretched out straight and carrying current of the given frequency. The experimental work available indicates that this factor due to the coiling of the wire, that is, the total proximity effect of the turns of the coil, is largely dependent upon the frequency and the ratio of wire diameter to pitch of winding, and in lesser degree to the ratio of length to diameter. SMITHSONIAN TABLES 450 TABLES 532-534 (Calculated by Dr. F. W. Grover, Consulting Physicist, Bur. Standards, 1931.) TABLE 532.—Resistance Ratio ‘“‘F’’ for Isolated Round Wires _Resistance ratio F of isolated round wire, asa function of the square root of the frequency divided by the direct current resistance per 1000 ft. of conductor. Vf/Ro 0 Io 20 30 40 50 60 70 80 90 100 F 1.000 I.000 1.0005 1.0025 1.008 1.019 1.038 1.069 I.1I4 1.173 1.247 q Vf/Ro 100 120 140 160 180 200 250 300 350 400 500 | F 1.247 1.427 1.631 1.836 2.036 2.231 2.715 3.201 3.688 4.176 5.152 TABLE 533.—Values of Resistance Ratio for Isolated Tubular Conductors t, thickness of wall of tube; d, outer diameter of tube. TABLE 534.—Coefficients in Formula for Proximity Factor of Equal Parallel Round Wires The proximity factor of two equal parallel conductors may be calculated by the formula P=1+4+([G.@/s)/[Fa — Hd?/s*)] in which the coefficient F is to be obtained from Table 532 for the given value of f/Ro and the coefficients G and H are to be taken from the table below for the given value of f/Ro. In the table below the values of H apply to currents in the same direction; in the case of currents in opposite directions H' is to be used. In the above formula d is the diameter of the wires and s their axial spacing. The proximity factor for two equal parallel tubular con- ductors does not differ much from the value for two solid wires with the same axial spacing and a value of f/Ro one-half the value for two solid wires of the same diameter, except for conductors very close together. +0.0417 -0395 -O109 .0659 -1379 -1685 .1776 .1839 SMITHSONIAN TABLES TABLES 535 AND 536 451 TABLE 535.— Ratio of Alternating to Direct Current Resistances for Copper Wires This table gives the ratio of the resistance of straight copper wires with alternating currents of different frequencies to the value of the resistance with direct currents. Frequency f = Diameter of wire in millimeters. OunHO an as eh oof ° * I NIOPWNHOOOO n ° Q C BR HHH HH ee NN QU 8 He AA HaUhO} COARhWNHHHHEA OonO0- oH He wi CON WMnNWNND BHR RH OHH Values between 1.000 and t.oor1 are indicated by *r.oor. The values are for wires having an assumed conductivity of 1.60 microhm-cms;_ for copper wires at room tempera- tures the values are slightly less than as given in table. The change of resistance of wire other than copper (iron wires excepted) may be calculated from the above table by taking it as proportional to dvV/f/p where d = diameter, f the frequency and p the resistivity. If a given wire be wound into a solenoid, its resistance, at a given frequency, will be greater than the values in the table, which apply to straight wires only. The resistance in this case is a complicated function of the pitch and radius of the winding, the frequency, and the diameter of the wire, and is found by experiment to be sometimes as much as twice the value for a straight wire. TABLE 536.—Maximum Diameter of Wires for High-frequency Resistance Ratio of 1.01 Frequency + 10°... . Wave-length, meters Material. Diameter in centimeters. OIrI2 . O10Q . 0133 0354 0836 0564 0508 o614 .O125 .O122 o149 0396 0936 0631 0664 0692 271 -O145 .O14I .O172 -0457 . 1080 .0729 .0772 0792 - 312 Manganin Constantan German silver Carbon Tron .00263]0. .OO131|0. .00094/0.00083]0. . 00059 .00373/0.002 .00187/0. 00132/0. 0OO118]0. OOTOS/o. 00084 K 73 Le .00838]0. 00590]0. 00418]0. 00340/0.00295|0. 00264)0.00241/0.00215/0.00186] 0. 00152 CO99050000 OO0DTT0000 COTOOD0000 0909990000 oO. O°. Oo. oO. °. °. Oo. oO. Oo. ie 0000000000 O000000000 ‘ ‘ Bureau of Standards Circular 74, Radio Instruments and Measurements, 1918. SMITHSONIAN TABLES. TABLES 537 AND 538 WIRELESS TELEGRAPHY TABLE 537.—Radiation Resistances for Various Wave-Lengths and Antenna Heights 452 The radiation theory of Hertz shows that the radiated energy of an oscillator may be repre- sented by K constant (h?/a?) I?, where h is the length of the oscillator, A, the wave-length and I the current at its center. For a flat-top antenna E = 1600 (h?/ A?) I? watts; 1600 h?/A? is called the radiation resistance. (h =height to center of capacity of conducting system.) 160 Ft. | 200 Ft. 40 Ft. | 60 Ft. | 80 I't. | 100 Ft. 300 Ft. 600 Ft. | 1200 Ft. Wave- Length A ohm ohm ohm 13.4 6.0 3-4 1.5 0.54 0.54 0.37 0.24 | 0.13 | Austin, Jour. Wash. Acad. of Sci. 1, p. 190, 1911. TABLE 538.—The Dielectric Properties of Nonconductors — Phillips Thomas, J. Franklin Inst. 176, 283, 1913. Results of tests at unit area and unit thickness of dielectric. At 1000 cycles. Mica. Paper. Celluloid. Max. breakdown volts per cm. 1.06X 108 | 0.71 X 108) 1.05 X 108 Specific induc; capacity-q. sap sis hy Max. absorbable energy, watts-sec/cm* go°-angle of lead SU be ath ak Equiv. resistance ohms/cm* X 10” Conductivity per cm, cubeXI071" Percent change in cap. per cycleX 10' Percent change in resistance per cycle At 15 cycles. Specific inductive capacity . . . .- Max. absorbable energy, watt-sec/cm®. Percent change in capacity per cycle 4.00 0.198 ° Om Sy., 4 (3291 5 oEo 2.18 . (0.258 4.90 0.108 2a 9.84 1.02 14.31 0.146 13.26 0.640 3° 40’ 48.3 0.207 30.7 0.106 5-77 0.126 0.306 On direct current. Conductivity per cm* 2.4210" 2.27 X10"* 71-5 10714 163. 10-11 SMITHSONIAN TABLES. TABLE 539 453 POWER FACTOR AND DIELECTRIC CONSTANT (See also Table 540 on page 454.) From the range of the values given, an approximate figure can be taken for a particular material and its relative position with respect to other materials seen. Data of this kind are much effected by the condition and past treatment of the samples, and by the conditions of the tests. The power factor and dielectric constant of dry air may be taken as zero and 1.00. Fused quartz has the lowest power factor among the solid insulating materials, and is used for supporting the insulated plates of standard air condensers. TABLE 539.—Values for Power Factor in Per Cent for Several Electrical Insulating Materials at Radio-Frequencies e Frequency Measurements reported by— Material ee r 3 187.5 0.459 300 .476 600 -495 1000 513 30 es 600 0.040—-0.653* Cobalt glass 500 shige 0.70 Flint glass 500 See 42 890 sa Te -40 Plate glass 14 ayes ae 100 eae mene 500 ere -70 635 1000 Pyrex glass 14 bet Bete Seis 30 ee Seer: .... 0.56and 0.26 100 : Br 420 500 759 Photographic 100 235 0.35-2.98° Hard rubber "(88 1.05 ak oxen oes ee 0.35 —4.72 .O17 Mee Mrs ee .007— .93! 3.85-7.35 Ae: eras 2.62— 8.0 4.20-6.65 Sage ae ore 3.85- 5.6 Laminated phenolic insulation oo sat Spas sity Aisa le Soy 1.64-10.9 phenolic 6— 8 insulation eral el le oe) .e 8: O85 6 “eee T.5 4 Wood (oak) ane 3.68 y4ns bh tats 13.8, 2.94° oe 3.85 See sets 10.1, 3.24° 4.20 tag Seta aan: 3-33 sdetege 8 3.63 6.48 eats atikaks See 2 3.76 (baywood).... 870 dies oye Paraffin 14 aren Saal .042 ‘ eNsiRe 100 scabs eee .031 staid .O17 500 Soe 1, very small but positive, kK = 10 * to 10%: oxygen, especially at low temperatures, salts of Fe, Ni, Mn, many metallic elements. (See Table 580.) Diamagnetic substances, w<1, K negative. Most diamagnetic substance known is Bi, —14 x 10, Volume susceptibility (see Table 580). Paramagnetic substances show no retentivity or hysteresis effect. Susceptibility independent of field strength. The specific susceptibility for both para- and diamagnetic substances is in- dependent of field strength. Tor Hall effect (galvanomagnetic difference of potential), Ettinghausen effect (galvanomagnetic difference of temperature), Nernst effect (thermomagnetic difference of potential) and the Leduc effect (thermomagnetic difference of temperature), see Tables 593 and 504. Magneto-strictive phenomena: Joule effect: Mechanical change in length when specimen is subjected to a magnetic field. With increasing field strength, iron and some iron alloys show first a small increment Al// = (7 to 35) X 10”, then a decrement, and for H = 1600, A//l may amount to —(6 to 8) x 107%. Cast cobalt with increasing field first decreases, A//] = —8 x10-*, H = 150, then increases in length, A//l = + 5 x 10 *, H = 2000; annealed cobalt steadily ccntracts, A//l = —25 x 10 *, H = 2000. Ni rapidly then slowly contracts, Al/l = —30 x 10 *, IJ = 100; —35 X 10°*, H = 300; —36 x 10 *, H = 2000 (Williams, Phys. Rev. 34, 44, 1912). A transverse field generally gives a reciprocal effect. Wiedemann effect: The lower end of a vertical wire, magnetized longitudinally, when a current is passed through it, if free, twists in a certain direction, depending upon circumstances (see Williams, Phys. Rev. 32, 281, to11). A reciprocal effect is observed in that when a rod of soft iron, exposed to longitudinal magnetizing force, is twisted, its magnetism is reduced. Villari effect; really a reciprocal Joule effect. The susceptibility of an iron wire is increased by stretching when the magnetism is below a certain value, but diminished when above that value. SMITHSONIAN TABLES. 464 TaBLes 550-552 TABLE 550.—Magnetic Properties of Various Types of Iron and Steel From tests made at the Bureau of Standards. B and H are measured in cgs units. Values of B 2000 | 4000 | 6000 | 8000 | 10,000] 12,000} 14,000] 16,000] 18,000] 20,000 Annealed Norway iron} H .81| 1.15) 1.60) 2.18) 3.06) 4.45) 7.25) 23.5) 116.) — BK | 2470] 3480] 3750] 3670] 3270] 2700] 1930] 680] 150 | — Cast semi-steel...... H | 2.00} 2.90) 4.30) 6.46) 9.82/15 .1 |24.9 | 50.5) 135.) 325. HL | 1000] 1380] 1400] 1240] 1020] 795] 563] 317 | 133 | 62. Machinery steel...... H | 5.0 | 8.8 |13.1 |18.6 |25.8 |35.8 |50.5 | 76.0 oo 455| 460] 430] 390] 340] 280] 210 TABLE 551.— Magnetic Properties of a Specimen of Very Pure Iron (.017% C) From tests at the Bureau of Standards. B and H are measured in cgs units. Values of B 2000 | 4000 | 6000 | 8000 | 10,000] 12,060] 14,000] 16,000] 18,000] 20,000 H | 3.30] 4.48] 6.35] 9.10/13 .0 |18.9 |28.8 | 47.0/103. | 240. | B | 606) 893} 945) 880) 770} 635) 486) 340) 175 | 83 H be Very pure iron as received 46) «6 .80| 1.02) 1.38) 2.00) 3.20) 11.3) 72.0) 194. 4350| 6670] 7500] 7840] 7250] 6000] 4380] 1420] 250 | 103 So Annealed in vacuo from goo°® C As received: Hmax 150 After annealing: Hmax 150 Bmax 18,900 Bmax 19,500 B, 7,050 _— Elie 2.8 Ei ONS 3 TABLE 552.— Magnetic Properties of Electrical Sheets From tests at the Bureau of Standards. B and H are measured in cgs units. Values of B 6000 } 8000 | 10,000} 12,000} 14,000] 16,000] 18,000} 20,000 Dynamo steel 3.10) 4.95) 9.20 3220] 2420] 1520 Ordinary trans- \ Z 2.28] 3.85/10 .9 former steel 4380] 3120] 1280 High silicon trans- 5 . 1.99) 3.60) 9.80 former steel 5020] 3340] 1430 SMITHSONIAN TABLES. TaB_Les 553-556 465 TABLE 553.—Magnetic Properties of Two Types of American Magnet Steel From tests at the Bureau of Standards. B and H are measured in cgs units. Values of B 2000 | 4000 | 6000 10,000 | 12,000 | 14,000 | 16,000 | 18,000 Tungsten steel. BSLOMIESS EG OSeSu ll 72eo| O34. 57 75 95 120 Chrome steel. . . SAE AORON 103.5) ||) Oona. 143 58 82 95 gl 7° Percentage composition: Tungsten steel, C 0.67 W 5.1 Mn 038 S1 0.26 Chrome steel, C 0.81 W 0.96 Cr 2.09 Si 0.25 Tungsten steel: Hmax 200 Bmax 14,000 Chrome steel: Hmax 200 Bmax 11,050 H, 62.5 B, 10,400 H, 45-7 B; 7,030 TABLE 554.— Magnetic Properties of a Ferro-Cobalt Alloy, FezCo (35% Cobalt) From tests at the Bureau of Standards. Band H are measured in cgs units. Values of B 12,000 | 14,000 As received..... Annealed at \ TOOO ss Cm s! Quenched \ from 1000° C { As received 15,000 22.0 7750 | 3-79 Annealed at 1000° C Bmax;415,000 Hmax, 18.3 B, 4 7460 He} 3-95 Quenched from 1000° C 15,000 130 8240 (14.3 TABLE 555.— Magnetic Properties of a Ring Sample of Transformer Steel in Very Weak Fields From tests made at the Bureau of Standards. B and H are measured in cgs units. Values of H : ©.002 | 0.004 | 0.006 | 0.008 | 0.010 | 0.012 | 0.014 | 0.018 Values of B : 0.91 1.85 2.87 |} 3-94 5.05 6.30 7S Tal LOLS | Waluestofie ascent set. 5 455 462 478 492 505 525 536 566 TABLE 556.—Magnetic Properties of Iron in Very Weak Fields The effect of very small magnetizing forces has been studied by C. Baur and by Lord Rayleigh. The following short table is taken from Baur’s paper, and is taken by him to indicate that the susceptibility is finite for zero valucs of H and for a finite range increases in simple proportion to H. He gives the formula k = 15 + 100H, or J = 15H -+ 100H? The experiments were made on an annealed ring of round bar 1.013 cms radius, the ring having a radius of 9.432 cms. Lord Rayleigh’s results for an iron wire not annealed give k = 6.4 + 5.1H, orl = 6.4H + 5.1H2. The forces were reduced as low as 0.00004 cgs, the relation of k to H remaining constant. First experiment. Second experiment. SMITHSONIAN TABLES. 466 TABLE 557 COMPOSITION AND MACNETIC This table and Table 558 below are taken from a paper by Dr. Hopkinson * on the magnetic properties of iron and steel which is stated in the paper to have been 240. “ Coercive force’ is the magnetizing force required to reduce the magnetization to zero. revious magnetization in the opposite direction to the ‘f maximum induction ”’ stated in the table. P g pp by 47. which, however, was only found to agree roughly with the results of experiment. The maximum magnetization is not tabulated; but as stated in the The “ demag- The “‘ energy Oo ON AnfWN eH Description of specimen. Chemical analysis. Total Carbon. | | Manga- nese. Sulphur. | Silicon Phos- ‘| phorus. Other substances. Wrought iron Malleable cast iron Gray cast iron . Bessemer steel . ‘ Whitworth mild steel “ “ Hadfield’s manganese | steel Manganese steel “cc Silicon steel “ “cc “ “ Chrome steel “ “ “ “a (French) . “ “ Gray cast ijon Mottled cast iron Wihite sso ae Spiegeleisen Annealed a Annealed { Oil-hard- tl ened Annealed § Oil-hard- 1 ened As forged Annealed Oil-hard- ened As forged Annealed Oil-hard- } ened As forged Annealed Oil-hard- } ened As forged Annealed { Oil-hard- ened As forged Annealed Oil-hard- ened As forged Annealed Hardened in cold water ( Hardened in tepid ) water { Oil-hard- ) ened Very hard * Phil. Trans. Roy. Soc. vol. 176. SMITHSONIAN TABLES. None “cc 0.042 t Graphitic carbon. TABLE 557 (continued) PROPERTIES OF IRON AND STEEL 467 The numbers in the columns headed “‘ magnetic properties” give the results for the highest magnetizing force used, paper, it may be obtained by subtracting the magnetizing force (240) from the maximum induction and then dividing netizing force” is the magnetizing force which had to be applied in order to leave no residual magnetization after dissipated’? was calculated from the formula: — Energy dissipated = coercive force X maximum induction + Description of specimen. Temper. Specific electri- cal resis- tance. Maxi- mum in- duction. Residual induc- tion. Coer- cive force. Magnetic properties. Demag- netizive | Energy dis- | Sipated per cycle. force. Wrought iron . z Malleable cast iron . Gray cast iron . Bessemer steel . Whitworth mild steel ‘ “ee Hadfield’s manganese | steel : Manganese steel Silicon steel a“ “ec “ce “ Chrome steel “ (French) . Gray cast iron : Mottled cast iron. \ivlente, Spiegeleisen Annealed 6b Annealed § Oil-hard- | ened Annealed Oil-hard- ened As forged Annealed { Oil-hard- {ened As forged Annealed { Oil-hard- 1 ened As forged Annealed Oil-hard- ened As forged Annealed § Oil-hard- ) ened As forged Annealed Oil-hard- ened As forged Annealed Hardened in cold water Hardened in tepid water § Oil hard- ) ened Very hard .01378 .03254 .10560 .O1050 -O1080 .01446 .01 390 01559 01695 06554 .05368 03928 05556 .06993 .06316 .07066 .06163 06185 06195 .02016 01942 .02708 .O17Q1 01849 .0303 5 .02249 02250 .02274 18251 12408 10783 18196 19840 18736 18796 16120 16120 310 4623 10578 4769 747 1985 733 15148 14701 14696 15778 14848 13960 14680 193233 12868 15718 16498 15610 14480 12133 9148 10546 9342 385 7248 7479 3928 7860 7080 9840 11040 10740 8736 2202 5848 2158 540 11073 8149 8084 9318 7579 8595 7568 6489 7891 IOI 44 11008 Oot ao Nm Wh SN Wo CN Be 34-70 64.46 70.69 17.03 20.40 SMITHSONIAN TABLES. 13356 34742 13037 17137 10289 40120 65786 42306 99401 34567 113963 41941 15474 45740 36485 sg619 61439 42425 169455 85044 64842 167050 78568 80315 149500 216864 197660 39789 41072 36383 468 TABLES 558-560 TABLE 558.—Permeability of Some of the Specimens in Table 557 This table gives the induction and the permeability for different values of the magnetizing force of some of the spect mens in Table 557- The specimen numbers refer to the same table. The numbers in this table have been taken from the curves given by Dr. Hopkinson, and may therefore be slightly in error; they are the mean values for rising and falling magnetizations. ; : . Specimen 8 Specimen g (same as Specimen 3 Magner Specimen r (iron). (annealed steel). 8 tempered). (cast iron). ing force. =~ : rate w ; 4 B 265 709 1625 3000 5000 6000 6500 7100 7359 AID 8500 9509 IOIgO Tables 559-563 give the results of some experiments by Du Bois,* on the magnetic properties of iron, nickel, and cobalt under strong magnetizing forces. ‘The experiments were made on ovoids of the metals 18 centimeters long and 0.6 centimeters diameter. The specimens were as follows: (1) Soft Swedish iron carefully annealed and having a density 7 $2. (2) Hard English cast steel yellow tempered at 230° C; density 7.78. (3) Hard drawn best nickel containing 99 Yo Ni with some SiO, and traces of Fe and Cu; density 8.82. (4) Cast cobalt giving the following composition on analysis: Co= 93.1, Ni= 5.8, Fe=0.8, Cu=o.2, Si==o0.1, and C=o.3. The speci- men was very brittle and broke in the lathe, and hence contained a surfaced joint held together by clamps during the experiment. Referring to the columns, 7, B, and m have the same meaning as in the other tables, S is the magnetic moment per gram, and / the magnetic moment per cubic centimeter. A and S are taken from the curves published by Du Bois; the others have been calculated using the densities given. TABLE 559.—Magnetic Properties of Soft Iron at 0° and 100° C Soft iron at 0° C. Soft iron at roo° C. I B s ~ 33 eee, B 1408 1521 1627 16085 1705 1709 | m= NOON Quay AX Of NRO me NUON COO Ma ous Ao ONO Nd Steel at c° C. | 7; 1283 1408 1500 1552 1583 1595 1650 _ Hero OO AS O 9 OOXO Mm™OO Hu * “ Phil. Mag.’’ 5 series, vol. xxix. + The results in this and the other tables for forces above 1200 were not obtained from the ovoids above referred to, but from a small piece of the metal provided with a polished mirror surface and placed, with its polished face nor- mal to the lines of force, between the poles of a powerful electromagnet. The induction was then inferred from the rotation of the plane of a polarized ray of red light reflected normally from the surface. (See Kerr’s “ Constants,.’* p. 480.) SMITHSONIAN TABLES. TABLES 561-567 46g MAGNETIC PROPERTIES OF METALS TABLE 561,—Cobalt at 0° and 100° C TABLE 562.—Nickel at 0° and 100° C —— fe 6 Ss 200 | 106 848 | 10850 ’ | 3980 300 | 116 928 | 11960 : 4966 500 127 1016 | 13260 | 26.5 . 5399 700 | 131 | 1048 | 13870 8 | : 6043 1000 | 134 | 1076 | 14520 Si 6409 1500 | 138 | 1104 | 45380 ; | 687 5 2500 | 143 | 1144 | 16870 ; Re. 7707 4000 | 145 | 1164 18630 : 3. 8973 6000 147 1176 | 20780 : : 10540 gooo ! 149 | 1192 23980 : 12501 At o° C this specimen gave the fol- : 15595 lowing results : : 526 | 18606 7900 | 154 | 1232 | 23380 | 3.0 C this specimen gave the lowing results : | 67.5 | 595 | 19782 | Hm DDO, wm es OO ~ Oo TABLE 563.—Magnetite The following results are given by Du Bois * for a specimen of magnetite. Professor Ewing has investigated the effects of very intense fields on the induction in iron and other metals.t The results show that the intensity of magnetization does not increase much in iron after the field has reached an in- tensity of 1000 c. g. s. units, the increase of induction above this being almost the same as if the iron were not there, that is to say, @B/d@H is practically unity. For hard steels, and particularly manganese steels, much higher forces are required to produce saturation. Hadfield’s manganese steel seems to have nearly constant susceptibility up to a magnetizing force of 10,000. The following tables, taken from Ewing’s papers, illustrate the effects of strong fields on iron and steel. The results for nickel and cobalt do not differ greatly from those given above. TABLE 564.—Lowmoor TABLE 565.—Vicker’s TABLE 566.—Hadfield’s: Wrought Iron Tool Steel Manganese Steel To oB. Bia ares Figen Zieh ves =: 0 WOOOW 1680 | 24130 1740 | 28300 1730 | 32250 1720 | 35200 1630 | 36810 1680 | 39900 1730 | 49730 6210 | 1530 | 25480 | 4.10 1930 | 55| 2620 9970 | 1570 | 29650 | 2.97 2350| 84] 3430 12120 | 1§50| 31620 | 2.60 3350, 84) 4400 14660 | 1580 | 34550} 2-36 5920/11} 7310 15530 | 1610 35820 | 2.31 6620 | 187} 8970 ee 7890 | 191 | 10290 8390 | 263 | 11690 9810 300 | 14790 WU Od. Wn nN NWN os . ww ~ wn TABLE 567.—Saturation Values for Steels Bessemer steel containing about 0.4 per cent carbon . Siemens-Marten stee] containing about 0.5 per cent carbon | 18000 Crucible steel for making chisels, containing about 0.6 per cent carbon) = a0). : Wn RP S002. 5) os ie acy a . | 19470 | Finer quality of 3 containing about 0.8 per cent carbon. . 1833 Crucible steel containing 1 per cent carbon . . . . . ~ | 19620 Whitworth’s fluid-compressed steel. . . . . «. . « «| 18700 | Ow * “ Phil. Mag.’’ 5 series, vol. xxix, 1890. 7 + “ Phil. Trans. Roy. Soc.”’ 1885 and 189. SMITHSONIAN TABLES, 470 TABLES 568 AND 569 DEMAGNETIZING FACTORS FOR RODS TABLE 568 7/7 = true intensity 0. ee field, H’ = intensity of applied field, 7=in- tensity of magnetization, 4H = #’/—/V/. Shuddemagen says: The demagnetizing factor is not a constant, falling for highest values of / to about 1/7 the value when unsaturated; for values of B (=A+477) less than 10000, V is approximately constant; using a solenoid wound on an insulating tube, or a tube of split brass, the reversal method gives values for V which are considerably lower than those given by the step-by-step method; if the solenoid is wound on a thick brass tube, the two methods prac- tically agree. Values of VX 104. Cylinder, ae Step Method. a eee c Magneto- Dubois: Shaddemacent ee Range of Dianeer Elhipsoid. Mosca | metric yess Practical Constancy, ‘ zation, | Method : (Mann). Diameter, 0.3175 cm, | 1.111 cm,| 1.905 cm, 1960 1075 671 343 209 149 106 63 41 21 II 99m NaNO Cw CO 0O WIN ‘oO ON! C. R. Mann, Physical Review, 3, p. 3593; 1896. H. DuBois, Wied. Ann. 7, p. 9423 1902. Cale B: Shuddemagen, Proc. Am Acad. Arts and Sci. 43, p. 185, 1907 (Bibliography). TABLE 569 Shuddemagen also gives the following, where 7 is determined by the step method and A—//’— KB. See hee Values of KX ro4, Ratio of Diameter Diameter 0.3175 cm. | 1.1 to 2.0cm, 15 20 25 30 40 50 60 80 OAwm NN A wm ONS BCA CANOE NE COON 150 G SMITHSONIAN TABLES, TaB_Les 570-572 471 TABLE 570.—Magnetic Properties of Iron and Steel en a TY | Electro- Good Poor Electrical Sheets. lytic Cast Cast Steel. Cast Tron: Steel. Steel. Iron. Ordinary panel Silicon —_ - = | |— {C 0.024 0.044 | 0.56 0.99 3.11 0.036 | 0.036 : Si 0.004 0.004 | ‘0.18 0.10 B27, 0.330 3-90 Chemical compost: } y4, | .oc8 0.40 0.29 0.40 0.56 0.260 | 0.090 Song Pee cut i 0.008 0.044 0.076 0.04 | 1.05 0.040 | 0.009 Ss 0.001 0.027 0.035 0.07 0.06 0.068 0.006 a? 2.83 1.51 7.1 16.7 lige: | eorreie force aaa: 4 {o.36] | [0-37] | (44-3) | (52-4) | [46] | [1-30] |_[o.77] ; | 11400 | 10600 | 10500 | 13000 |. 5100 | | Residual B+ + + §| [10800] | [11000] | (10500) | (7500) | [5350] | [9400] _| [9850] oe 1850 | 3550 | 700 | 375 240 | | ceo perce tl hibiadeot | Teeoa) (170) | (110) | [600] | [3270] | [6130] fs 19200 | 18800 | 17400 | 16700 | 10400 | | Sn c } [18g00] | [19100] | | (15400) | (11700) [11000] | [18200] | [17550] ; ; 21620 | 21420 | 20600 | 19800 | 16400 — 4nI for saturation [21630] | [21420] | (20200) | (18000) | [16800] | [20500] | [19260] E. Gumlich, Zs fiir Electrochemie, 15, p. 599; 1909- Brackets indicate annealing at 800° C in vacuum, Parentheses indicate hardening by quenching from cherry-red. TABLE 571.—Cast Iron in Intense Fields Soft Cast Iron. Hard Cast Iron, B I B I 782 7860 614 846 2 9700 752 1070 2. | 10850 836 1200 21. | 13050 983 1280 | E | 14050 1044 1300 | 579 | 15900 1138 1465 2s 202 16800 1176 1475 : 26540 1245 1488 ; 28600 1226 1472 : 30200 1226 No oN Ny OO B. O. Peirce, Proc. Am. Acad. 44, 1909. TABLE 572,—Corrections for Ring Specimens In the case of ring specimens, the average magnetizing force is not the value at the mean radius, the ratio of the two being given in the table. ‘The flux density consequently is not uniform, and the measured hysteresis is less than it would be for a uniform distribution. This ratio is also given for the case of constant permeability, the values being applicable for magnetizations in the neigh- . borhood of the maximum permeability. For higher magnetizations the flux density is more uni- form, for lower it is less, and the correction greater. Ratio of Ratio of Average H to | Ratio of Hysteresis for Uniform Radial H at Mean Radius. | Distribution to Actual Hysteresis. Width to = SS Diameter Rectangular | _ Circular | Rectangular Circular of Ring. Cross-section. a3 Cross-section. ; Cross-section. CS section. 1.0986 MO7TO) || Reishee I 084 0397 1.0294 1.045 1.033 .0137 1.0102 I.015 1.011 0094 1.0070 1.010 1.008 0069 1.0052 1.008 1.006 1.0052 1.0040 1.006 1.004 T0033.) |. ,1.0025 1.003 1.002 1.0009 | 1.0007 1.001 1.001 lig Me 1.0216 1.0162 1.024 1.018 I Ie te M. G., Lloyd, Bull. Bur, Standards, 5, p. 4353; 1908. SMITHSONIAN TABLES. 472 TABLES 573 AND 574 TABLE 573.—Energy Losses in Transformer Steels Determined by the wattmeter method. Loss per cycle per cc—= 4A4*+6nB, where 4 = flux density in gausses and = frequency in cycles per second. x shows the variation of hysteresis with B between 5000 and 10000 gausses, and y the same for eddy currents. Ergs per Gramme per Cycle. Thick- ness. cm. 10000 Gausses. |} 5000 Gausses. Designation. Hyste- Hyste- resis. resis. Eddy Cur- rents at 60~ Eddy Cur- rents at 60~ Unannealed A 0.0399 B 0326 C .0422 D .0381 562 384 356 353 1.51 1.59 1.51 1.52 2.02 |0.00490 1.89 | .00358 1.79 | .00319 1.94 | .00312 Annealed 246 220 193 138.5 GINS 130 125 116 127 105 .0476 .0280 0304 .0307 .0318 0282 0346 0338 0335 .0340 1.58 1.60 1.54 ee 1.62 1.61 1.61 1.61 1.55 1.62 1.64 .00227 .00206 .0O174 .0O1 27 .OO105 .00122 .OO1T8 .OOLIO .OOTTS .00099 00103 Silicon steels 1.63 1.64 1.63 1.68 1.66 Bh 108 12.4} 1.67 16.6| 1.65 .00094 .00089 .00086 .00077 .00084 .00078 .00061 .00062 MadqHnxzo * a * German. + English. Eddy Current Watts per Pound at 60 Cy- cles and 10000 Gausses. + + Hyste- resis. |- Total. Loss for Gage No. 29. ¢ In order to make a fair comparison, the eddy current loss has been computed for a thickness of 0.0357 cm (Gage No. 29), assuming the loss proportional to the thickness. Lloyd and Fisher, Bull. Bur. Standards, 5, p. 4533; 1909- Note. —For formulm and tables for the calculation of mutual and self inductance see Bulletin Bureau of Standards, vol. 8, p. 1-237, 1912. TABLE 574.—Magnetic Properties of Permalloy (Yensen, Nickel-Iron Alloys, Journ. Franklin Inst., 199, 340, 1925; Arnold, Elmen, Permalloy, loc. cit., 195, 621, 1923.) Permeability Hys- Satura- | teresis tion Ba 4l 10000 (gausses)| Erg/C3 /cycle Reten- tivity Initial gausses a H=0O Fe, 3 mm thick 4G Si, 35pm thick 4 50% Ni, .35 mm thick*. 78% Ni, .35 mm thick. . * Permalloy. SMITHSONIAN TABLES TABLE 575 473 DISSIPATION OF ENERCY IN THE CYCLIC MACNETIZATION OF VARIOUS SUBSTANCES C. P. Steinmetz concludes from his experiments * that the dissipation of energy due to hysteresis in magnetic metals can be expressed by the formula e = a4, where ¢ is the energy dissipated and a a constant. He also concludes that the dissipation is the same for the same range of induction, no matter what the absolute value of the terminal inductions may be. His experiments show this to be nearly true when the induction does not exceed ++ 15000 c. g.s. units per sq. cm. It is possible that, if metallic induction only be taken, this may be true up to saturation ; but it is not likely to be found to hold for total inductions much above the satura- tion value of the metal. The law of variation of dissipation with induction range in the cycle, stated in the above formula, is also subiect to verification. Values of Constant a The following table gives the values of the constant @ as found by Steinmetz for a number of different specimens. The data are taken from his second paper. Number of Kind of material. Description of specimen. Value of specimen. a. iron. . Norway iron. : Son's ; Wrought bar ; Commercial ferrotype plate Annealed ss Thin tin plate Medium thickness tin plate Soft galvanized wire Annealed cast steel . Soft annealed cast steel . Very soft annealed cast steel . F Same as § tempered in cold water Tool steel glass hard tempered in water «tempered in oil . . annealed . s Same as 12, 13, and 14, after havi ing “been subjected / to an alternating m. m. f. of from 4000 to 6000 ¢ | : : ) ampere turns for demagnetization j Cast iron . Gray cast iron . se ane “ <)-s containing 4 % aluminium “ “ F “ec “e “ec 4 b “ce OO ON Quftwh = — ~ “cc “cc cA square rod 6 sq. cms. section and 6.5 cms. ‘long, ( Magnetite . from the Tilly Foster mines, Brewsters, Putnam County, New York, stated to be a very pure soe J Nickel . Soft wire . A § Annealed wire! calculated by Steinmets ‘from | Ewing’s experiments Hardened, also from Ewi ing ’s experiments Cc § Rod containing about 2 % of iron, also calculated | obalt \f rom Ewing’s experiments by Steinmetz Fe of thin needle-like chips obtained by (3d “ milling grooves about 8 mm. wide across a pile of thin sheets clamped together. About 30 % by vol- ume of the specimen was iron. Ist experiment, continuous cyclic variation of m.m. | f. 180 cycles per second . : : : ‘ Si 2d experiment, 114 cycles per second ss 79-91 cycles per second . Tron filings * * Trans Am. Inst. Elect. Eng.’’ January and September, 1892. +t See T. Gray, ‘* Proc. Roy. Soc.’’ vol. lvi. SMITHSONIAN TABLES. < 474 TaB_Les 576-579 TABLE 576.—Magnetism and Temperature, Critical Temperature The magnetic moment of a magnet diminishes with increasing temperature. Different specimens vary widely. In the formula Mt/Mo = (1 — at) the value of a may range from .0003 to .oor (see Tables 559-560). The effect on the permeability with weak fields may at first be an increase. There is a critical temperature (Curie point) above which the permeability is very small (paramagnetic?). Diamagnetic susceptibility does not change with the temperature. Paramagnetic susceptibility decreases with increase in temperature. This and the succeeding two tables are taken from Dushman, ‘‘ Theories of Magnetism,” General Electric Review, 1916. Critical Critical Refer- Substance: tenieere Refer- Curie point. Substance. temperature, : : ence. Curie point. ence. tron nou LONI ersten eee DS foMlans Anaeyamooco0 AV OLD crore sence ois eeee Magnetite (FesO4)........ WWNHHAHHH AnubHL HH & References: (1) P. Curie; (2) see Williams, Electron Theory of Magnetism, quoted from Weiss; (3) du Bois, Tr. Far. Soc. 8, 211, 1912; (4) Hilpert, Tr. Far. Soc. 8, 207, 1912; (5) Gumaer; (6) Stifler, Phys: Rev. 33, 268, ro1r. TABLE 577.—Temperature Variation for Paramagnetic Substances The relation deduced by Curie that x = C/T, where C is a constant and T the absolute temperature, holds for some paramagnetic substances over the ranges given in the following table. Many paramagnetic substances do not obey the law (Honda and Owen, Ann. d. Phys. 32, 1027, 1910; 37, 657, 1912). See the following table. Substance. Cex5.8 1522 e Becquerel. ce —14.9 1.22 « Rayleigh. it —17.1 1.73 Becquerel. +: Teli 480 TABLES 587-589 TABLE 587.—Values of Kerr’s Constant * Du Bois has shown that the rotation of the major axis of vibration of radiations normally reflected from a magnet is algebraically equal to the normal component of magnetization multiplied into a constant AK. He calls this con- stant AX, Kerr’s constant for the magnetized substance forming the magnet. Kerr’s constant in minutes per c. g. s. unit of magnetization. Spectrum Z go ee ee ee line. Color of light. Cobalt. | Nickel. Iron. Magnetite. Red . sagt i | ; 0.0208 | —0.0173 —0.01 54 +0.0096 TNC Camera remote : —0.0198 —0.0160 —o.0138 -+0.0120 WENN 5 fo 54 2 : —0.0193 —0.01 54 — 0.0130 +0.0133 (magn 5 co 6 of 6 : —0.0179 —0.0159 —O.OIII -++0.007 2 Bluey crs aol ; —o.0180 —0.0163 —0.OIO1 +0.0026 Wiolete sas 4 vc : —o.0182 | —0.0175 —0.0089 - *H. E. J. G. Du Bois, ‘‘ Phil. Mag.’ vol. 29. TABLE 588.—Dispersion of Kerr Effect Wave-length. Steel Cobalt . Nickel Field Intensity= 10,000 C.G.S. units. (Intensity of Magnetization =about 800 in steel, 700 to 800 in cobalt, about 400 in nickel). Ingersoll, Phil. Mag. 11, p. 41, 1906. TABLE 589,.— Dispersion of Kerr Effect Mirror. Iron Cobalt . Nickel . Steel Invar . Magnetite Foote, Phys. Rev. 34, p- 96, 1912. See also Ingersoll, Phys. Rev. 35, p- 312, 1912, for ‘‘The Kerr Rotation for Transverse Magnetic Fields,” and Snow, 1. c. 2, p. 29, 1913, ‘‘ Magneto-optical Parameters of Iron and Nickel.’’ SMITHSONIAN TABLES. TABLES 590-592 481 RESISTANCE OF METALS. MAGNETIC EFFECTS TABLE 590.—Temperature Variation of Resistance of Bismuth, Transverse Magnetic Field Proportional Values of Resistance. +18° NR eee Oe ee oe See ee ee Oe OO Dm mmm BPNOIUKANKOO WNHNN DN HH HHH HR Oe LaONKOORANKLWHHO WAN OAWONIB WH NHH OO TABLE 591.—Increase of Resistance of Nickel due to a Transverse Magnetic Field, expressed as % of Resistance at 0° and H—0O F. C. Blake, Ann. der Physik, 28, p. 449; 1909. TABLE 592.—Ohange of Resistance of Various Metals in a Transverse Magnetic Field. Room Temperature Field Strength Per cent . Metal. in Gausses. Increase. Authority. Nickel 10000 —1.2 Williams, Phil. Mag. 9, 1905. c ~ —1.4 Barlow, Pr. Roy. Soc. 71, 1903. —1.0 Dagostino, Atti Ac. Linc. 17, 1908. 3 —1.4 Grummach, Ann. der Phys. 22, 1906. Cobalt —0.53 Ss Cadmium +0.03 Zinc +0.01 Copper +0.004 Silver +0.004 +0.003 +0.002 Palladium +0.001 Platinum +0.0005 Lead +0.0004 Tantalum +0.0003 Magnesium +0.01 Dagostino, l. c. Manganin +0.01 a Tellurium +0.02 to 0.34 Goldhammer, Wied Ann. 31, 1887. Antimony i +0.02 to 0.16 ss Different specimens show very Grummach, l. c. diverse results, usually an in- Barlow, l. ¢. crease in weak fields, a decrease Williams, l. c. in strong. Nickel steel Alloys behave similarly to iron. Williams, I. c. Iron SMITHSONIAN TABLES. TABLES 593 AND 594 TABLE 593,—Transverse Galvanomagnetic and Thermomagnetic Effects 482 Effects are considered positive when, the magnetic field being directed away from the observer, and the primary current uf heat or electricity directed from left to right, the upper edge of the specimen has the higher potential or higher temperature. £ = difference of potential produced; 7=difference of’ temperature produced ; 7= primary at current; 7 > = primary temperature gradient; 4—= breadth, and D= thickness, of specimen #7 = intensity of field. C. G. S. units. : ; if Hall effect (Galvanomagnetic difference of Potential), # = Re : HI Ettingshausen eftect ( “ ss “ Temperature), 7= ] ar : 2 at Nernst effect ((hermomagnetic “ “ Potential), “ = OF, Fi at Leduc effect ( % op ‘“ Temperature), 7 = SHB. Substance, | Tellurium Antimony Steelers 5 Heusler alloy Iron Cobalt Zinc Cadmium Iridium Lead alsin. Platinum Copper Gold ; Constantine. Manganese . Palladium Silver . Sodium Magnesium . Aluminum Nickel Carbon Bismuth . German silver , Values of R. +400 to S00 + 0.9 “ 0.22 --.012 “0.033 +.o10 “ 0.026 +-.007 “ 0.011 +.0016 “ 0.0046 +.00055 -++.00040 +.00009 —.00003 —.0002 —.00052 —.00054 —.00057 to .00071 —.0009 —.00093 — 0007 to .0o12 —.0008 ‘ .0O15 —.0023 —.00094 to .0035 =—OOOR 0 0037) ——,OOA5 a: O24: —.017 up to 16. | -++ 360000 | | +9000 to 18000 | 700 “ 1700 | +1600 “ 7000 —1000 “ 1500 +1800 “ 2240 —54 “ 240 | | up to —5s.o —5.0 (?) —4.0 (?) —g0 to 270 +50 to 130 —46 “ 430 +0.04 to 0.19 | +2000 “ gooo +5. | -++ 100 +3to4o | + up to 132000 TABLE 594,—Variation of Hall Constant with the Temperature —go°? Bismuth. —23 ° 28.0 2 “ 5.0 Antimony ? —196° | —79° +21.5° +58° 0.263 0.252 0.245 0.249 0.243 02.35 0.211 | 0.217 | 0.209 | 0.203 Bismuth. 189° 2122 269° 1.42 I 259° | 24 0.97 | 0.83 1 Barlow, Ann. der Phys. 12, 1903. 2 Everdingen, Comm. Phys. Lab. Leiden, 58. 3 Traubenberg, Ann. der Phys. 17, 1905. * Melting-point. Both tables taken from Jahn, Jahrbuch der Radioactivitat und Electronik. 5, p- 166; 1908, who has collected data of all observers and gives extensive bibliography. : SMITHSONIAN TABLES. ATOMIC DATA 483 TABLE 595 INTERNATIONAL ATOMIC WEIGHTS, ATOMIC NUMBERS AND VALENCIES Quoted from the Ist Report of the Committee on Atomic Weights of the International Union of Chemistry (Journ. Amer. Chem. Soc., 3, 1637, 1931). pauee Boe Symbol eeu Ais weight Valencies Element Ree weight |Valencies oxygen OxVECM number =e number aa Element Aluminum....| Al 26.97 Molybdenum. . 96.0 Antimony....| Sb 121.76 Neodymium. .| | 144.27 Argon A 39-944 20.183 Arsenic As 3: 74.93 vi 58.69 Ba 137-30 Nitrogen ‘ 14.008 Beryllium....| Be . 9.02 ° Osmium 190.8 Bismuth.....] Bi 83 | 209.00 16,0000 IBYOVRONN. ga coc) 18 10.82 Palladium.... 106.7 Bromine Br 35 79.916 Phosphorus. . . 31.02 Cadmium,....| Cd 112.41 Platinum 195.23 Calerumbeer a: 40.08 Potassium. ... 39.10 12.000 Praseodymium 140.92 140.13 225.97 132.81 I 222 35-457 | I 186.31 Chromium.... 52.01 . 58.94 Columbium.. . 93.3 ; 63-57 Dysprosium. . 162.46 102.91 Rubidium. ... 85.44 Ruthenium... IOI.7 Samarium.... 150.43 Scandiumls.44|pS¢ 45.10 167.64 Europium.... 152.0 Rlworine = ee 19.00 Gadolinium.. . 157-3 Gallium 69.72 Selenium 79.2 Silicon i 28.06 Silver 107.880 22.997 Strontium.... 87.63 Germanium. . 72.60 32.06 197.2 Tantalum.... 181.4 178.6 eh Tellurium.... 127.5 4.002 Terbium 159.2 Holmium 163.5 Thallium 204.39 > WW WW Wren hN WwW Oo Hydrogen.... 1.0078 Indium 114.8 126.932 Iridium 193.1 55-84 Krypton 4 82.9 Lanthanum.. . 138.90 207.22 erehruiT. 4. led 6.940 Lutecium.... 175.0 Thorium 2B2rT2 Thulium 169.4 i 118.70 Titanium) - 9 8 6 ee 2 BA RRRAABECRBRRSAS ERs 3 2 1 9 | a Most Abundant Isotope {> A AAAI ZA CUP" od Eee Cer RUAN ek SAS SG Sa Toe RN ESAS SRN yy ag ica Gua wedaraea tat Ee PA Recently Discovered Isotope of Coa Abundance © Ly een as Bee ae = =3CG9HVoOLR co oyvddervd 25 8n0z0n SES aH nT cK SGE> SELCCSONGSLHSESHENGLSZEPIOEGGL-LGSISES OFAIINOH HOS=NNIOGE PAVeVITLESLASHABHVSSSSISS VIOUS I IBIAS HVS AAZ Atomic Number Feb., 1930 tium/ 4QtTon Pure species even atomic number ” ” odd ” Mean value even ” ” ” SMITHSONIAN TABLES 488 TABLE 601 ELECTRON CONFIGURATIONS IN NORMAL ATOM Individual electrons in an atom may be designated by two quantum numbers, “‘azi- muthal”’ and “‘total’’. The first is expressed by s, p, d, etc.; the last numerically in specific cases, by n in general. Designation of quantum numbers: Azimuth quantum: literal,s; number, 0; Bohr, k, 1; The total quantum number is equal to p I 2 or greater than 1 +1, i.e, 1, 2, 3, d 2 3. .— tor s electrons, 2) 3,\4,— for p f 3 4 electrons, etc. g 5 h etc. 6 An electron is called, e.g., a 6p electron, 6 for the total quantum number, p implying an | value of 1. Note that 4p, 5s, 3d, etc., electrons are equivalent to Bohr’s 4, 51, 33 electrons. The number of electrons for a given type in an atom may be expressed by an exponent, e.g., 3d°. For more detailed connection between configurations and spectroscopic terms see Hund’s book. The lower-case letters n, 1, s, j, m should be used for the quantum numbers of an electron, and the capitals L, S, J, M for the quantum numbers of a term (or level) of an atom, ionized or neutral. A specification of atomic structure would include all the inner electrons, e.g., for Fe in its normal state 1s?2s?2p°3s?3p°3d®4s%. For short only those electrons “outside” an inert gas shell need be considered. A complete np® group, and all the groups which are normally completed earlier in the periodic table, can be neglected. Thus the notation for the normal state of Fe becomes 3d‘4s?. Examples of the notation for a level and the configuration from which it arises is 3d® 4s? 5D,, the normal state of the iron atom; 2s? 2p 45°; 1,2, the low level of O II. The total quantum numbers may be omitted when they are the lowest which the particular sort of electron can have if not belonging to already completed shells. For example, 4s, 4p, 3d, 4f in spectra from K I to Zn [ and Ca II to Ga II, etc., are the s, p, d, andf electrons of lowest quantum numbers not belonging to completed groups. The 3p® group is completed and the 3s? and all the groups of smaller n have been previously completed, leaving 4s, 4p, 3d, 4f still to be added. These last can therefore be represented by s, p, d and f. The normal state of Fe I would thus be designated as d®s? °D,, that of O IT as s*p? 48%, 1,2. For Ge I, in which the electron groups 3d!° and 4s? may be regarded as completed, the elec- trons to be represented by the letters alone would be the 5s, 4p, 4d, and 4f electrons; and so on. Odd terms arise when the sum of the | values for all electrons is odd, even terms from con- figurations for which the | sum is even. Since the | sum for completed groups is always even, only outer uncompleted groups need be considered. Even (odd) terms are those in which the number of p and f electrons together is even (odd). In the parts of the periodic table where sand d groups are being completed the lowest terms of all the atoms are even. Where p groups are being completed (and also in the rare earth f-group) the lowest terms are alter- nately odd and even. Except in the rare earth group the only spectra for which the normal state corresponds to an odd term are BI, NI, F land Cll, OI], Ne II etc. and the homo- logous spectra in later periods. Permitted transitions are those in which the | of one electron changes by one unit, (and the 1 of another electron by o or 2 units, if two electrons change) so that all such transitions are between even and odd terms. ; Electron Configurations! K M N a (07 3)Ie al aa On A renames NNNNNNNN N# Same as for neon ae I 2 2 2 2 2 2 2 1 Based by permission upon table by Ruark and Urey. Atoms, molecules, and quanta, 1930. SMITHSONIAN TABLES TABLE 601 (continued) 489 ELECTRON CONFIGURATIONS IN NORMAL ATOM Ay 2 A535 30) sk 552 6,0 4f 5s Atomic No. BH NNNNHNNNDND & COON HAMMwWNH: - NNNNNNN : — om ee NN ON in 2 4 5 (6 7 8 Oo -_ NNNNNNN AS SMITHSONIAN TABLES 490 TABLE 601 (concluded) ELECTRON CONFIGURATIONS IN NORMAL ATOM N O 4,0 4,1 4,2 4,3 DOpsrlmisaze 573 6,0 Element Atomic No. 4s 4p 4d af | Bes) sd 56 6s Xenon configuration. .. Shell Shells tsto4dcon- .. 5s tain 46 electrons. .. to “ec 5p con- tain 8 elec- trons “ce “e a“ © OND W NH Io TT 2 13 14 O OVW A Quis oo Ne a eee eS ese oe See ee . I 2 2 2 2 2 2: 2 2 2 2 Zz 2 2 2 2 2 2 2 2 2 I 2 I ze I I I 2) 2 2 2 2 2 2 oe = = oO Radon configuration. Shells 1s to 5d contain 78 electrons ee shells = 6s to 6p contain 8 electrons NNNNNNNNe: SMITHSONIAN TABLES v vu Atomic Radius neutral pa Radius positively Atomic Radius neutral ey Radius positively no.; atom BS charged ion no.; atom iS charged ion element Angstroms oO Angstroms element Angstroms oO Angstroms IH 42 Mo | 1.36 6 | 0.62 2 He | (0.93) Mo 4 | 0.66( —0.83) Bg) Li (1.50 —)I.56 I | 0.60—0.78( —o0.82) 44 Ru 1.27-1.34 4 | 0.63-0.65 4 Be I.05(—1.15) 2 | 0.31-0.34 45 Rh 1.34-1.35 3 | 0.60 5 B 3 | 0.20 46 Pd 137 onc: (0.45 —)0.77 4 | 0.15 47 Ag | (1.17—)1.44 I | (0.79 —)1.13-1.26 aN (0.65 —)0.71 5 | 0.11 48 Cd | (1.47 —)1.490(—1.60) | 2 | (0.78 —)0.97-1.03 8 O 0.60( —0.65) 6 | 0.09 49 In I.45—-1.62 3 | 0.81-0.92 oF 0.67 7 | 0.07 50 Sn (1.27 —)1.40 4 | (0.64 —)0.71( —o.8r) ro Ne | (1.12) 51 Sb (1.22 —)1.34(—1.44) | 5 | 0.62 11 Na 1.77 —)1.86 1 | 0.95-0.98( —1.00) Sb 3 | 0.90 12 Mg 1.42 —)1.62 2 | 0.65-0.78( —0.85) 52 Te I.33-1.43 6 | 0.56 13 Al I.16 —)1.43 3 | 0.50-0.57( —0.66) Te 4 | 0.81-0.89 14 Si (1.12 —)1.18 4 | (0.22 —)o.39-0.41 53) 1 1.36-1.40 7 | 0.50 T5 P 0.93 5 | 0.34 I 5 | 0.94 16 I.02-1.04 6 | 0.29-0.34 54 Xe (1.90) r7 Cl I.05-1.07 7 | 0.26 55 Cs (2.37 —)2.55 I | 1.65-1.69( —1.75) 18 A (1.54) 56 Ba 2.10 2 | 1.35-1.43(—1.49) I9 K (2.07 —) 2.23 I | 1.33(—1.84) Be] ALE 3 | 1.15-1.22 20 Ca (1.70 —) 1.97 2 | 0.99-1.06( —1.50) 58 Ce 1.82-1.83 4 | 1.01-1.02 2r Sc I.51 3 | 0.81-0.83 Ce 3 | 1.18 22 Tl (1.40 —)1.490(—1.53) | 4 | (0.58 —)0.64-0.68 59 Pr 4 | 0.92-1.00 23 V I.32(—1.43) 5 | 0.59 Pr Bh et. wo! V 4 | 0.59-0.61 60 Nd Bie larars 24 Cr (1.17 —)1.25(—1.54) | 6 | 0.52-0.65 62 Sm Bh |erers 25 Mn | (1.17—)1.20(—1.59) | 7 | 0.46 63 Eu 3) eels: Mn 4 | 0.50-0.52 64 Gd eee Mn 2 | 0.80-0.91 65 Tb 3 | 1.09 26 Fe (1.21 —)1.26(—1.45) | 3 | (0.49 —)0.67 66 Dy SulL.O7 Fe 2 | 0.75-0.83 67 Ho 37 | 1.05 27 Co 1.26(—1.39) 3 | 0.29-0.47 68 Er 20) 1.04! Co 2 | 0.72-0.82 69 Tm 3) ||) 1:04) 28 Ni 1.24( —1.39) sy lorss 70 Yb 3 -00 Ni 2 | 0.69-0.78 72 1.66 29 Cu | (1.22—)1.27(—1.37) | 2 | 0.70 73 Ta | 1.42-1.44 Cu I | (0.58 —)0.96 74 W Te37 6 | 0.88 30 Zn I.3I-1.34 2 | 0.74-0.83 Ww 4 | 0.66-0.68 31 Ga | (1.28—)1.33(—1.45) | 3 | 0.62 76 Os I.30-1.34 4 | 0.65-0.67 32 Ge | 1.22 4 | 0.44-0.53 7 ly T35 4 | 0.64-0.66 33 As (1.04 —)1.16(—1.26) | 5 b 78 Et 1.38( —1.43) - As 3 }) 0.69 79 Au I.40-1.44 Delle oe, 34 Se I.I3-I.17 6 | 0.42 80 Hg | 1.46-1.49 2 | 1.10—-1.12 35 Br 1.19 7 | 0.39 (he anil (1.71-)1.99( —2.25) 3 | 0.95-1.05 36 Kr | (1.69) al 1 | I.44-I.51 37 Rb | (2.25 —)2.36 t | 1.48-1.49( —1.88) 82 Pb 1.74( —1I.90) 4 .84 38 Sr 1.95 2 | 1.13-1.27(—1.45) Pb 2 | (0.98 —)1.21-1.32 39 Y 3 | 0.93-1.06 83 Bi (1.34 —)1.46(—1.55) | 5 | 0.74 40 Zr 1.60-1.62 4 | (0.68 —)0.80-0.89 90 Th | 1.80-1.82 4 | 1.02-1.10 41 Cb 1.43(—1.50) 5 | 0.69-0.70 92 U 4 | 0.97-1.05 Cb 4 | 0.67-0.69 —NH4 1 | 1.42-1.59 o vo ovo vo Bo Radius po Radius eo Radius 2 Radius | 2 negative & negative g negative aS negative | O ion Oo ion O ion oO ion ee eee eet eee ———————— EuIED —I | (1.27); 2.08 || 14 Si —A) |! (@.98)); 2-71 || 32° Ge i) —4 |) 2.72 50 Sn | —4 | (2.15); 2.94 15 P —3 | 2.12 33 As —3 | 2.22 51 Sb —3 | 2.45 6C —4 | 2.60 16S —2 | 1.74-1.84 34 Se —2 | 1.91-1.98 52 Te | —2 | 2.03-2.21 7N =3 || 1.71 TCs — Ta test 35 Br | —1 | 1.95-1.96 53 I —tr | 2.16-2.20 8 O —2 | 1.32-1.40 | 9 F —I | 1.33-1.36 82 Pb —4 | 2.15 TABLE 602 EFFECTIVE ATOMIC RADII Goldschmidt, on the basis of reasonable though empirical assumptions, has calculated effective radii f atoms in various charged conditions; Pauling, on the basis of wave-mechanics, has presented theoretical alues for most of the elements, the two series agreeing well in many cases. The latter values are printed 1 bold-faced type; the values considered nontypical are in parentheses; e.g., for silicon we have: Sit: 9.22 —) 0.39-0.41. Si? (1.12—) 1.18. Si-* (1.98); 2.71, signifying silicon, carrying 4 + charges, has pparent radius between 0.22 and 0.41; but the lower values relate to compounds where the atoms ppear to be deformed; so Goldschmidt gives 0.39 as most significant. Wave-mechanics yields 0.41. leutral, the radius ranges from 1.12, in abnormal compounds, to 1.18 in those typical; when carrying — charges, the value is 1.98, according to calculations deemed faulty, 2.71 according to theory. In applying the data to replacements, halides and oxides are usually ionized, and the values in the uter columns apply. Thus in fluorite the value for Cat? should be added to that for F-!, giving between 32 and 2.42, or 2.37 as a mean; and the observed Ca-F distance in the crystal is 2.36 Angstrom units. n the remaining types of compounds the atoms appear to be largely neutral and the first column should e used. The units are Angstroms. Wherry, Amer. Mineralog., 14, 54, 1929. 491 IMITHSONIAN TABLES 18 492 TABLE 603 (A) ELECTRONS, PROTONS, ATOMIC STRUCTURE Free negative electron (corpuscle, J. J. Thomson).—Mass, spectroscopic (bound) 9.035 X 10°” g; free, 8.9004 K 10 g; atomic weight, 5.479 and 5.454 X 10% respectively, probably all electrical, due to inertia of self-induction. Theory shows that when speed of electron = 1/to velocity of light, its mass should be appreciably dependent upon that speed. If 10 be the mass for small velocity, m, the transverse mass for v, and v/ (velocity of light, c) =8 then m= mo (1 — B’)? (Lorentz, Einstein). B, 0.01 0.10 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 m/mo, 1.00005 1.005 1.02 1.048 1.001 1.155 1.250 1.400 1.667 2.204 Radium ejects electrons with 3/1to to 98/100 of c. m, due to charge = 2E?/3a, where E = charge, a, radius, whence radius of electron is 2 10° cm = 1/50,000 atomic radius. Cf. (radius earth/radius Neptune’s orbit) = 1/360,000. Collisions with a particles show diameter of electron must be less than 4 X 10° cm (Chadwick, Bieler, Philos. Mag., 1921). Positive electron or proton.—Heavy, extraordinarily small, never found associated with mass less than that of the H atom; mass, 1.6609 X 10 g. Specific charge, 9579.7 abs-em- units-g™. Ratio mass proton to mass electron, 1838 (spectroscopic), 1847 (deflection). If mass is all electrical, radius must be 1/2000 that of electron. No experimental evidence as with the latter since high enough speeds not available. Penetrability of atom by B particle (may penetrate 10,000 atomic systems before it happens to detach an electron) and a particle (8000 times more massive than negative electron, passes through 500,000 atoms without apparent deflection by nucleus more than 2 or 3 times) shows extreme minuteness. Upper limit of nucleus not larger than 10°’ cm for Au (heavy atom) and 10 cm for H (light atom) (Rutherford). Cf. (radius sun)/(radius Neptune’s orbit) = 1/3000 but sun larger than planets. Hg atoms by billions may pass through thin-walled, highly-evacuated glass tube without impairing vacuum, therefore massive parts of atoms must be extremely small compared to volume of atom. Rutherford atom.—Atoms of all elements are somewhat similarly built. At the center a charged nucleus of minute dimensions, responsible for most of the mass of the atom; this is surrounded by a distribution held in equilibrium by the force from the nucleus. Resultant nuclear charge = atomic or ordinal no., varies from 1 for H to 92 for U. These atomic nos. represent the number of planetary electrons which surround the nucleus. By the action of light, the electric charge, bombardment by a particles, one or more of the planetary electrons may be driven away from the nucleus; by X rays or the swift 8 rays some of the more strongly bound may be removed. New electrons are generally soon captured to replace these. The nucleus is much more stable and when disrupted (radio- active changes, bombardment with a particles) shows no tendency to revert to original state. : Moseley (Philos. Mag., 26, 1912: 27, 1914) photographed and analyzed X-ray spectra, showing their exact similarity in structure from element to element, differing only in frequencies, the square roots of the frequencies forming an arithmetical progression from element to element. Moseley’s series of increasing X-ray frequencies is with one or two SMITHSONIAN TABLES TABLE 603 (A) (continued) 493 ELECTRONS, PROTONS, ATOMIC STRUCTURE exceptions that of increasing atomic weights, and these exceptions are less anomalous for the X-ray series than for the atomic-weight series. It seems plausible that there are 92 elements (from H to U) built up by the addition of some electrical element. Moseley assigned successive integers to this series (see Table 598) known now as atomic numbers. Moseley’s discovery may be expressed in the form m/N2 = E/E, or do/ Ad = E?/E2? where E is the nuclear charge and \ the wave length. Substituting for the highest fre- quency line of W, »=—0.167 X 1o°em (Hull), 22=74=Nw, and £:=1, then = highest possible frequency by element which has one + electron; 1 = 91.4myu. Now the H ultra-violet series highest frequency line = 91.2muz (Lyman); i. e., this ultra-violet line of H is nothing but its K X-ray line. Similarly, it seems equally certain that the ordinary Balmer series of H (head at 365mp) is its L X-ray series and Paschen’s infra-red series its M X-ray series. The application of Newton’s law to Moseley’s law leads to E:1/E:= a2/a:, where the a’s are the radii of the inmost — electronic orbits, i. e., the radii of these orbits are inversely proportional to the central charges or atomic numbers. There are other negative electrons on the nucleus with corresponding + charges to make the atom neutral electrically. The negative nuclear charges may serve to hold the positive ones together. He, atomic no.= 2, has two free + charges, on nucleus; the nucleus has 4+ protons held together by 2— electrons with 2— electrons outside nucleus. H_ has one + proton and one — electron. If the — electron is designated as e (charge — I, mass negligible) and the + proton as p (charge + 1, mass 1 except in H) then the formula for the nucleus of any element from He to U may be written as (pf2e)w(pe)n where N is the atomic number and » has values from 0 to 54. If n be taken as — 1, then H may be included. (Masson, Philos. Mag., 41, 1921.) If brackets are used to designate the nucleus then the complete element becomes [ (pe) v(pe)njewv. In the formation of ions only the part exterior to the brackets is affected. For the a-transformation (emission of + charged He nucleus) 2(p:e) = (fre)2/, the subchemical equation may be written [(p.e)w(pe)nlew = [ (pre) x — 2(pe)nlev + (pre) 27 (He nucleus); the new elements upon discharge of its — charge becomes [ (f2e)y — 2(pe)nlex — 2 showing the characteristic a-ray change with the atomic weight lowered by 2 and the mass by 4. The 8-ray 2(pe) = (poe) +7 gives the equation [ (poe) w (pe) nler = [ (poe) + I(pe)n-2 + e7 mass unchanged and forms the singly — charged ion of an isobar. From the emission of nuclear a particles, 2(p2e) = pse2, it seems probable that the nuclei are compounds of He and I nuclei. By the bombardment of the nuclei of atoms up to atomic number 40 with a particles Rutherford has obtained H but only where H and He nuclei should both occur in the nucleus (Bo, N, Fl, Na, Al, P, see Table 638), Harkins has SMITHSONIAN TABLES 494 TABLES 603 (A) (concluded) AND 603 (B) TABLE 603(A) (concluded).—Electrons, Protons, Atomic Structure developed this idea (Journ. Franklin Inst., 194, 213 et seq., 1922) and shown the much greater frequency in nature of the even-atomic numbered elements (97.6 per cent in stony meteorites, 99.2 Fe meteorites, 85.6 lithosphere, 5 unknown elements all odd, even radioactive most stable). Elements below atomic number 30 make up 99.99 per cent of all meteorites, 99.85 igneous rocks, 99.95 shale, 99.95 sandstones, 99.85 lithosphere. The stability of the He nucleus may be judged by the energy set free in the formation of He from H. According to “relativity” 1 g-mass = 9 & 10” ergs (E = mc”). The change of mass involved in the formation of 1 g-atom of He (4,000 g) from 4 g-atoms of H2(4 X 1.0078 g) = 2.81 X 10” ergs = 6.71 X 10" calories. 1 Ib. H. changed to He equals heat from 10,000 tons coal. The nuclei of light even numbered atoms (most abundant isotope) up to Fe (26) almost wholly of He nuclei. To a Ist approximation the a particle behaves in collision like an elastic oblate spheroid, semi-axes, 8X 10? and 4 * 10 cm (Chadwick, Bieler, Philos. Mag. 1921). TABLE 603(B).—Atomic Structure, Bohr Atom Bohr atom.—Bohr postulated electrons rotating in circular nonradiating orbits about a central body according to the laws of celestial mechanics and its consequent energy rela- tions. He added the idea that these electrons could jump between different orbits emitting light of a frequency v which depended upon the relationship E,2— E:= hy where the E’s denote the energies (according to classical conceptions) in the two orbits and h, Planck’s “quantum of action” of the nature of a moment of momentum. In going from one possible orbit to another the moment of momentum of the electron must progress by steps, each a multiple of h/27. Balmer’s formula is consistent with such a process: »= N(1/ns" — 1/n*) where y is the frequency, N, a constant, and mm: for the visible series (Balmer’s) has the value 2, 1, the successive integral values, 3, 4, 5, ...3 33 lines in the Balmer series have been observed in stars where orbits of greater radius are possible (small gas density) than in the laboratory (12 lines). With m=1, n, 2, 3, 4, ..., Lyman’s ultra-violet series results; 11= 3, ”, 4, 5, 6, ..., Paschen’s infra-red series; m= 4, n, 5, 6, 7, ..., Brackett’s series of even greater wave lengths. No mechanism was described to show how the energy of rotation was transferred into energy of radiation nor why only certain orbits could be occupied. He evidently used non- radiating orbits at variance with Maxwell’s equations. Two independent predictions from these assumptions were verified: the predicted and observed values of Rydberg’s constant within 4% and the differences in v for the H and the He + lines due to the 4-fold mass of the He + nucleus. Relativistic considerations——Sommerfeld (1916) applied Einstein’s relativity con- siderations together with the variation of mass with the speed of the revolving electrons and brought further support to the idea of orbits through prediction and the verification of the “ fine structure of spectrum lines.” Bohr considered only circular orbits in which the speed of rotation is constant, but elliptical orbits are possible with the same h/27 as the circular and in them the speeds of revolution of the electrons change in different por- tions of the orbit as with classical mechanics but these speeds are such that a relativity SMITHSONIAN TABLES TABLES 603 (B) (continued) 495 TABLE 608(B) (continucd).—Atomic Structure, Bohr Atom correction to the mass is necessary. Their quantization brought another quantum number ; the so-called total quantum number, 1, now becomes the sum of two since both the radii (r) and azimuth (¢) of the electron vary. The orbit is usually designated by two quantum numbers, the total, n, and the azimuthal (¢) viz: 1.1, 2.3 (p orbit, circular), 2.1 (s orbit, elliptical)... 353t-gi2, (3.15). ST, The following figure illustrates the first four sets of orbits of the hydrogen atom. The table indicates the modes of the quantum numbers (az radius inner orbit, a, b, varying), total azim. radial nk n k Nr a/do b/ai I.1 I I Oo T I 25 2 I I 4 2 22 2 2 Oo 4 4 3.1 3 I 2 9 3 BP 3 2 I 9 6 3.3 3 3 0 9 9 The resonance potentials for the circular orbits are (hydrogen atom) : Te OLpit tO) > ee 3.3 4.4 5.5 6.6 Ge; Bone 00 Volts observed FOS 1205," 0270) BOO) Tskh7 = 1327 aes. 5a » Lyman series, u 1216 .1026 .0972 .0950 a ae eet. OOI2u “ Balmer 2.2 orbit Wee sil h-0503, 0" PASO 1) -4a400 UieAnO2s ae3O70) ke) i36d0u “ Paschen 3.3 orbit Hea «see l6750) 2821s OGgO Ny OOS2) 4... 2031 “ Brackett 4.4 orbit at eee as heer, -46O5 2.63 2.16 Sooo iertoyn The remarkable prediction and consequent observation of the “ fine-structure of spec- trum lines resulted from this postulate.” Thus all the lines of the Balmer series, con- sisting of jumps into the state of total quantum 2, possessing 2 orbits, a circle and an ellipse, should show a fine structure due to energy differences of these circular and elliptical orbits. Approximately they should be all doublet lines of wave length predictable from laws of orbital mechanics. The separations should be .365 cm™; actually .36 cm (Houston) was found. The separation should vary as the 4th power atomic no. Paschen (1916) actually found for He +, 16 X .365 cm”. Further remarkable results came from Epstein’s (Ann. Phys., 50, 480, 1916) work on the Stark effect and ,the prediction of the separation of the so-called L doublets of X-ray spectra. If actually a relativity doublet, one must multiply the H separation by 71 millions (92*) ; also checked with experiment. Inner quantum numbers.—It became necessary (1920, Sommerfeld, Ann. Phys., 63, 221, 1920) to account for further fine structure. e. g.: In X rays the L orbits or levels correspond to n= 2, permitting only two different orbits, 2.2 (circle) and 2.1 (ellipse) ; but lines of 3 close wave lengths were observed—two being the regular expected doubtlet whose frequency varies with 2* as expected. These two levels are indicated by the two diverging lines, Lz, Ls in the following figure. * Millikan, Proc. Amer. Philos. Soc., 66, 211, 1927, from which much of the accompany- ing description is condensed. SMITHSONIAN TABLES 496 TABLES 603 (B) AND (C) TABLE 603(B) (continucd).—Bohr Atom The third level L: is seen to follow an entirely different law: it runs parallel to Le. two orbits of the same shape but different orienta- 1, tions, something different in the central field giv- ing these orbits slightly different energies. A so-called inner quantum number, J, was intro- 36 duced. The difference in the frequencies of the familiar doublets in Li was supposed due to jumps to a common orbit (s orbit) from 2 orbits differ- 30 ing only in the “inner” quantum number, i. e, orbits of different orientations but same shapes, in this case circles, or 2.2 orbits, known as the Pip2 orbits. The s orbit into which the 2 electrons Vr Bohr and Sommerfeld introduced the idea of g 40 = jumped to form the Li doublet was the third pos- sible of total quantum 2, the 2.1 orbit. The two circular (p orbits) differed slightly in frequency, 20 but the changes from either p to the s orbit was 6577 760 74 78 83 9092 2 too large for the relativity effect. Bohr (Ann. Phys., 71, 228, 1923) suggested that the anomaly was due to the penetration of orbits of outer electrons within the field of action of inner orbits. TABLE 603(C).—The Spinning Electron and Summary The spinning electron.—A disconcerting element existed in that the difference of energy between two circular psp. orbits varied with the atomic number precisely as demanded by the relativity consideration, though it could not be due to relativity since the pips orbits had no difference in shape but only of orientation. A new conception by Uhlenbeck and Goudsmit (Nature, 117, 264, 1926) came to the rescue assuming that every electron rotates upon its axis. Two possible directions of spin are assumed 180° apart, but the moment of momentum is assumed always the same, exactly 4 unit or 4 h/2m. This intro- duces exactly the right amount of energy difference between the prp2 circular orbits. It is superposed upon the relativity effect, making the fine structure (even in H and He+ without inner electronic orbits) somewhat more complex. In the case of each individual electron there are four moments of momentum—four elements to describe an electron’s orbital motion: (1) The size of its orbit—the total moment of momentum characterized by its total quantum number » (Bohr) fixing the major axis of orbit. (2) The azimuthal quantum number, k, which with a given » or major axis, fixes the shape (minor axis). It has been found expedient to reduce by unity all values of k heretofore assigned. Since we are not ready to discard entirely the old interpretation, this reduced value of k is for convenience denoted by a new letter, /, so that =k —1I. Thus for ans orbit /=0; p orbit, 1; d orbit, 2; etc. (3) The projection of the moment of momentum 7 upon any fixed direction, which, in considering the Zeeman effect is the direction of the external magnetic field, is quantized (m1). The projection fixes the orientation in space. The significance that this projection is quantized is that only certain definite orientations are possible (Stern, Gerlach ex- periments ). (4) The projection of the moment of momentum of spin upon this fixed direction is designated by the symbol mr. In each atom only two possible directions of spin 180° apart are taken so that mr determines in what direction the electron is spinning. mi and mr are usually called magnetic quantum numbers because of their use in connection with magnetic fields. (Most of the above is abbreviated from Millikan, Proc. Amer, Philos. Soc,, 66, 211, 1927.) SMITHSONIAN TABLES TABLE 604 497 ENERGY OF BINDING OF AN ELECTRON—NEUTRAL ATOMS (Adapted from paper by Henry Norris Russell, Astrophys. Journ., 70, 1920.) The electrons in an atom, neutral or ionized, are bound in different states (a preferable term to ‘‘orbits’’). The more firmly bound inner ones which form parts of the completed shells concern the spectroscopy of X rays but not of ordinary light. The two following tables give a study of the energy of binding of an electron, in different atoms, in the same state, the state characterized by the same total and azimuthal quantum numbers, denoted in Bohr’s notation by 11, 21, 31,—} 22) 32) 42,—3 33, 43;—; 41, —, OF More commonly at present, IS, 2S, 38,—3 2p, 3p, 4p,—3 3d, 4d,—; 4f,—. The energy in volts is given required to remove an electron in the given state from the atom or liberated when it returns. Among the energy levels resulting from different space quantizations of the same electronic configuration, that with the greatest binding energy is given regardless of the multiplicity. Most values are derived from spectrum series and are fully reliable; those in ( ), two decimals, are extra- polations from series formulae and should be substantially correct; those in ( ), one deci- mal and in [ ] are interpolated and should be accurate to 0, to 0.2 v. El. Is 2s 3d 4s 4p JBL Tigyby Shasks) gaate' : 1-50) 0:81) (OLS He 24.48 4.75 3.61 : ‘ 1.51 .99 .87 IL. 5-36 3.40 ‘ I.5I 1.05 .87 9.29 6.57 : MO 2be eG 2. uate Les (O29 : ; 1525 dG) 11.22 E Te 7h eno 14.50 ‘ : i 5) OO eae 2 : cee Da 50 : ; 1-52) 0-77.) 01-32 s 95 eee a 723) : Tee eA ae aie MANS | Ri ee: 21.47 : ' 52) 2-86) W-4a : 1.00 dieses : 50 94) tS ‘ 1.02 TeCOMe eyo lie7O : 1.21 1295) 2:83) 1-89 : 1.31 Sen TA BROS) iene , Tez ite teedl (GG) ak test prem eee tcc ee? scr hes See tere (@zg8))) 3582)" 2:48 ae (1.59) 1.19 ee se a(3LO)" [20] eo eee eee eeee (293) 4:19)" )2: : 1.69 1.29 TOS Ass : : n/a ei7, 3.57 6.09 : 2 OW els 5 7, 5.13 6.57 : 2A Om aistore 5.95 6.80 : : 222 6.68 7.04 : Sea 2535 8.24 7.28 i : 2.43 5-76 7.40 : 2.54 6.98 7.83 od 2.55 7282 68.25 f 2.62 8.63 8.65 2.55 10.41 2.69 2.72 2.92 3.26 (3.4) (3.4) (3.6) (3-9) 4.13 5-65 6.40 1.19 TORN Aa Ocaitab SMITHSONIAN TABLES TABLE 605 ENERGY OF BINDING OF AN ELECTRON—SINGLY IONIZED ATOMS (Adapted from Henry Norris Russell, Astrophys. Journ., 70, 1929.) 498 This table companions the preceding one. A number of entries have been derived in various ways and may be in error by .5 volt; Li +, 3-4 v. The lines of a diagram made from the data of these two tables, with atomic numbers as abscissae and energy of binding as ordinates, a separate line for each state, are strikingly similar. The familiar “‘displace- ment law’’ applies not only to the multiplicities present in the spectrum, but also to the energy relations—the spark spectrum for any element resembling in both respects that of the arc of the preceding element. The energy of binding, for a given state, increases with the atomic number. For the s states the increase is steady; for the p and d states it is interrupted by fluctuations remark- ably similar. The increase of energy is most rapid (1) when electrons of a given type are building up a complete shell; (2) when s electrons are being added. The fluctuations are most conspicuous when a shell is half full (half of the 6p electrons in N, P, As, Ot, St, and of the rod electrons in €r, Mn*). Energy of Binding of an Electron—Singly Ionized Atoms El. Is 2s 2p 3s 3d 4s Ap 4d Het 54.16 13.54 13-54 6.02 2388 3.38 16.58 14.70 6.83 : 6:02) 13:72) 3-48 NOs LAL OMe) GL0200 3.88) 3:47 23 20.41 9.00 Ora 52a ees 24-25) OOO 6:35 294.87, 4-22 29.50 II1.10 6:45 5222) -. 34:94 12.09 9. 6.37 5-44 - a4co] (3st) aay es see 40.89 13.74 6.33 5.98 47.02 14.31 3 CWO) GRINS sou 14.97 Oni 16:33) 5.01 18.74 S850Q) 17.4810 5-73 ayaa 6.46 8.24 6.25 6:95) O30 17-08 9.70 9.80 7.51 10.25 10.56 7.98 II.23 I1.00 8.42 II.50 I1.62 9.07 NOWMAY Tale S2 a O-72 12.19 12.80 9.58 ee nh3e4 5) 3-600 9:98 se Gh4uy) A(4nAy) (10:3) 6413 3613.86 D3 —4F4) y pees 3710.30 1 295.30 3349.41 3B, —5Gs5 4h; —1G6 foot Zr ? 3391.96 V 5632.47 3003.10 45 —*Du, 6Ge? 5F5 —5Ge Cb ? 3004.20 Cr : 4254.34 2835.64 7S, —7P, &D5 —®F¢ 3798.26 2816.16 5394.68 2576.12 6S3—8P4 7S3—7P4 er 5166.20; 4375.93 2382.04 DD 5 bs : 6D5 —8F5 . ? == 2388.03 4F5—5R¢, 6Ge (®F5 —5Ge) ? 2416 16 ? (Fs —5Fs, 5Gs) (4Fs —4Ge) TABLE 620.—Electron Impacts in Gases (Langmuir, Jones, Rev. Mod. Phys., 2, 233, 1930.) Probabilities that an electron, while going through gas at 1 mm pressure, 20°C, will collide inelastically, Px, elastically, P., so as to produce Ist excited state, P,, or so as to ionize P;’ Gas Volts Px Hg 30 48.0 50 49.1 roo 50.3 250 32.0 100 : 250 ee 75 20.2 100 16.2 “ v'd HHN'D UO OWHA 0” iP Oo. Te I 2 4 9 1 I HAHN Db NPOR, Hanh COM CHO HUH NHHUHH I I RRA WOAO TABLE 621.—Average Life for Various Quantum States of Excited Atoms Theoretical values of ionized helium (Maxwell, Sugiura, Stack.) Average Life Mean av. life Levels T(n, 1,) (sec.) T(n), (sec.) 20, 21 ———— 1.02 X 10-10 T-30) eq nO-0 30, 31, 32 OL X 10-8, 3.38 X 10-19, o. 6.4 ”3 4o, 41, 42, 43 -46 ahs 7209 sz é : : 213 Ge LOR 50, 51, 52, 53, Sarr 2. ; - 1.45 X 108 5.4 X 10-9 60, 61, 62, 63, —, 65 3. Bos . : 5 f Pi LarS ecu Os8 70; 71, 72) 7335 76 5- , - “ The values for H are 16 X those for He (Sugiura, 1927, 1929). It is to be noted that the average life is longer for progressively higher quantum states. Maxwell 1931 obtains 1.1 + 0.2 X 10% sec. for av. life 6th quantum state (cf. 1.18 X 10°8) given above. Maxwell’s qualitative observation on first four lines of 4686 He + series, 4>3, 5>3, 6>3, 7>3, show definitely the longer life for higher quantum states. | Poole ae Rev., 33, 22, 1929) metastable Hg atom (Z’Po), max. time 4.2 X 104 sec. 6.8 mm). : See Ann. Phys., 83, 294, 1927, for early summary, including following: O spark, 467, 459uu, 1.53 X 10% sec. Ca spark 3933A, 3968A, 0.65 X 10° sec. Oarc, 6158, 4368A, 14.9 i Catare» 42264, 3.4 a Koenig, Ellett. (Phys. Rev., 39, 576, 1932) give for 23P1 state Cd, 2.5 & 10-6 sec. SMITHSONIAN TABLES 512 TABLE 622 MOLECULAR CONSTANTS OF DIATOMIC MOLECULES (From manuscript by E. D. McAlister, 1932.) Energy levels for molecules can be evaluated from their spectra, just as for atoms. Widely spaced levels in molecules correspond roughly to those known for atoms, are similarly designated (see “ Notation for Spectra of Diatomic Molecules,’ R. S. Mulliken, Phys. Rev., 36, 611, 1930). and are said to be related to the electronic configuration. A system of bands arise from transitions from one (often multiple) electronic configuration to another. Diatomic molecules have two other sets of levels in addition to the electronic. One is due to the energy of mutual vibration of the two nuclei and the other to the energy of rotation of the molecule as a whole. A distinct set of vibrational levels is associated with each electronic state. The energy difference corresponding to each level of such a set from that of the associated electronic state is obtained (approximately) by giving successive positive integral values to n in the expression n(wo — w X n+...) 3; 4 a positive constant. The frequency of vibration (w) is obtained by differentiating this with respect to n; w= (I —2n-+...). At the lowest level where the amplitude and energy of vibration are vanishingly small, »=o0 and ww». A transition from one vibrational level to another gives rise to a single band. A distinct set of rotational levels is associated with each vibrational level. The presence of large numbers of these closely spaced rotational levels gives rise to the many individual lines of the band. The rotational energy, relative to the associated vibrational level is ; ; : 2B ; given (approximately) by Bm?(1 — m’u*+ ...); where w= and m is a parameter 0 which is zero for zero rotation. Usually BI =h/8m°c = 27.70 x 10° g. cm, where = moment of inertia of the molecule about an axis through its center of mass and per- pendicular to the line joining its nuclei. For multiple levels this relation is not accurately true. J varies with the vibrational energy, and becomes J) when it is zero; the correspond- MoM M2 (m+ me) ~ unit atomic weight = 1.650 X 10™ g. mu, m2 are the atomic weights of the two atoms composing the molecule. ing nuclear separation is Yo= V/Jo/u where » = mo = mass of an atom of . . . No . The heat of dissociation is pe=| wdn, where mo is the value of » for wo. If the 0 bands can be experimentally followed to w =o, D” can be determined from spectroscopic data. Usually this cannot be done but Birge and Sponer (Phys. Rev., 28, 259, 1926) have found that, for the normal state of certain types of molecules, fairly trustworthy values of D” can be obtained by assuming w= wo(I — 2X) throughout the range »=0 to %=; then D=w'/4w.x. In the accompanying table D is D” plus the electronic energy for the particular state in question. Each horizontal line in the table is for one electronic state. The second column labelled energy (volts) is the electronic energy above the normal level which is assumed to have zero electronic energy. The heat of dissociation is tabulated in the same units which is the number of volts potential change an electron must undergo in order to acquire the corresponding energy. One electron volt per mole- cule = 2.306 & 10° g — cals per g-mole = 8100 cm™ per molecule. The data in the table are taken from compilations by Birge, Nat. Res. Council Bull. 57, “ Molecular Spectra in Gases” and Mulliken, Phys. Rev., 32, 206, 1928, and ibid., 33, 738, 1929, and are calcu- lated with the “ old mechanics ” formulae, SMITHSONIAN TABLES TABLE 623 513 MOLECULAR CONSTANTS OF DIATOMIC MOLECULES Io Energy (g cm? X State vo wo wo X Dv D Molecule (volts) (em X 108) 1040) (cm-1) (cm-!) (volts) (volts) Ag H oO 1.630 4.38 (1690) 3-69 1.665 4-57 (1490) Al H oO 1.658 4.41 (1625) 2.90 1.690 4.58 (1082) 5.51 1.65 (1326) o 1.54 3-93 2249.4 34.0 2037, 1.69 : 1630 79 4.72 evar (1548) oO 1253 10.2 4.10 1156 8. oO 1.35 2026 1.34 2053 0.33 1465 1.36 1354 Te 15.68 1874 1.36 20.03 1249 Tea 18.53 1270 Tid 17/03) 1630 e277 15.84 1773 1.776 5.201 1.674 4.65, 4.59 Tals 1.95 (2806) Leder 1.90 (2851) 1.20 Dei (< 2806) Mely7i 14.65 2056 13.8 1.23 1729 13.5 1.15 14.14 2144 23 15 14.9 2155 127, 1725 14.5 1173 9 24 17S 1499 Lyfe (2214) 12 14.26 2132 50 (2133) (2134) 1914 19.8 2197 15.2 1550 14.1 1698 24.3 J rm SMITHSONIAN TABLES $14 TABLE 623 (continued) MOLECULAR CONSTANTS OF DIATOMIC MOLECULES Energy yo (g 2 wo woX Dv D Molecule (volts) (cm X 108) (cm-}) (cm-}) (volts) (volts) Cu H oO 1.471 : 190357 3 7G0 3.02 3.02 2.88 1.582 Al 1655.7 44.63 1.89 BOTT. 5-51 1.50 He oO .76 ; 4262 113.5 4.42 4.42 1.55 : 1325 15.9 ‘97 . 2390 73 052 (1731.8) -047 (1790.1) .O71 3.784 .763 5-143 1308 104 4.22 _ (1938.7) 593 (4:23 }2025.7 43.8 102 (1940) ‘74 4.86 1462.2 31.25 -70 4.62 1568.7 34.75 -79 (1622) 2345 14.4 1446 13.9 1679 13.8 1718 14.4 2019 26.0 2187 16.3 2392 22.8 Rh apo fon com Om NI NAO DANO WO NN 1565 1415 708 on oO’ 1926 855 1026 1180 (3568.4) 3084.7 97.8 (1552) NOS Se bO SRR DAO & onsINIU Ne) G0 “I SMITHSONIAN TABLES TABLE 624 VARIOUS ATOMIC AND SPECTRUM FUNCTIONS Hi calories = Conte VN, /4./86 +10 rt HH FA 7 = Jemperature in F of an electron HH having K.E.=hv from hv = 2 AT- = = aries $ Puy Fao ‘de Broglie wave length of electron having energy hv. L=hVi-B2/mov- ea (4) First fonization potentials 4 1 t] Speed v =Rc i cm sec’ of an electron having] K.E. Speed of an electron @ expressed as a fraction of c; calculated from 28 Solar Radiation af the earths surface fF Coat AATEC oi Cy z /0 1. In black body unpolarized radiation the energy transmitted per sec per sg.cm per unit solid angle per unit frequency band /s, by Planck's radiation formula, My, =(hv7c)/(e AV/KT_}) 5 per unit wave-length band it is E,=(heYAfleP/A'T-/). The values hv/kT= 2.82/44 = 2 and hc/AkT = 4.96511 = b make My and Ey, take their maximum values, whence the femperature of the radiation that has its maximum My or E, af 2 particular frequency or wave length can easily be computed. 2. Electron speed ~ 1846 = speed of a proton having the same energy, with negligible error_at low energies. This holds to within 0.1% up to V=3%/0", but becomes 1.8% low at V=3%10'% 12% low at V=3%10"2 and should not be used at a// for higher frequencies. For , convenience, .6968 + 18462 =.0/622; 20.89 + 18462 =.9863; 66.07 + 1846” = /.538; .2203 + 1846/2 = 005/29 Compiled by W. Edwards Deming Drawn by Mrs. C. Sherry Revised, August 1929 SMITHSONIAN TABLES Shortest possible WL, from an oscillating electron (classical rreory) cy Cos/ition of electron and | |. proton, A.0000/F/5 A Y Ti Bil fo” yo!” jo® 0? 10” 0% j07 3. Frequency is used as the fundamental quantity with Birge’s values (Physical Review Supplement 1, 1, July 1929) of the physical constants, and the final calculation rounded off fo four figures. i Speed of light c= 2.99796 *10'°cm sec” Electronie charge, @ = 4.770 « 10°abs esu Electronic mass (by deflection), My = 8.994 «108g Planck's constant, h = 6.547 */0°°7erg sec Molecular gas constant k= 1.3708 x/0""° erg deg”! 299.796 abs volts =/abs esu of potential 1 15° calorie, Jig = 4.1852 abs joules . Avogadro's number, N,= 6.064 «/0**?mole~! Atomic weight of helium = 4.0022 Atomic weight of hydrogen = 1.00777 4. Corresponding to First ionization potentials, Cs 3.88 V, He 24.48 V. U. S. Department of Agricu/ture Bureau of Chemistry & Soils Washington, D.C. TABLE 625 RADIOACTIVITY INTRODUCTION. THE URANIUM FAMILY 516 (References: Kovarik, McKeehan, Nat. Res. Council, Bull. 51 (reprint 1929); Andrade, Structure of the atom, 3rd ed., 1926; Rutherford, Radiations from radioactive substances, 1930; Kohlrausch, Radioactivitat, 1929; Radioactive constants of 1930, Report International Radium-Standards Commission, Rev. Mod. Phys., 3 427, 1931.) Certain elements (about 40) of high atomic weight (also slightly K and Rb) are unstable in that they spontaneously change to elements of lower atomic weight with the production of heat and the emission of a, 8, or y rays. Radioactivity is an additive property of the atom, dependent only on the particular element and not on the chemical compound into which this element enters nor on the physical conditions controlling ordinary reactions—tem- perature, whether solid, gaseous or liquid, etc. The lives of these elements vary from 10” yrs. to, 10" sec: (See Table 625.) TABLE 625.—The Uranium Family, T, i, r At. Wt. = atomic weight; P. No. = proton number; At. No. = atomic number; yr = years; d = days; h = hours; m = minutes; s = seconds: T = half-period; + = average life; \ = decay constant. Rays and r 2: end product Uranium I Uranium X, At. Wt. At. No. P. No. At. No. P; No: 1.6-10-yr-4 y 5.0-:1078s-1 2.83:10-°d-! 2128 TOMS 2.90:10-*d"! 3.37:10-%st 6.3:10°%yr 2.0:10"%s 35-4d 3.05:10°s 34.4d* 2.97-10%s* a, UX, UZ .0035 0.61m-4 6, UII I.01-:10~%s-t Uranium X, (Brevium) ca 99.65% At. Wt. At. No. 91 P. No. 234 At. No. 91 Pe Nowe 234) At. No. 92 Ps Nos 234 a At. No. 90 P. No. 231 or 230 0.103h"! B, UII 2.87-10%s7} Uranium Z ca 0.35% a,lo .970 UY .030 2°3-1Oe yh 7.4° 1o-i4s-1 Uranium II 9.4:10s 24.6h 2.82-107h"! 1.03d 0.675d"! 8.88-1o4s |7.81-10-st B, Ac. Uranium Y cara, 1.48d 1.28-10°s * Earlier values still in use. Notes on Decay Constants: For U; the calculation is based on Z = no. of @ particles from 1 g Ra per sec. = 3.70 X 10"; Ra/U = 3.40 X 107; ; Avogadro’s No. = 6.064 X 10%; no account is taken of the branching Ac series. The values given are for T and 7, upper, for A lower limits. For UX, the lowest value T = 23.8 is mentioned as well as the one preferred by the Commission. UII. The adoption of 3 X 10° yr. is recommended. ThC’. Mme. Curie has recently calculated \ = about 10%sec"!. (Geiger-Nuttal Law). In view of the uncertainty of the values, T< 10° sec. has been proposed. AcC”. 150 curves give T = 4.71 min., 9, T = 4.76 min. Both values are given. SMITHSONIAN TABLES TABLE 626 RADIOACTIVITY IONIUM—RADIUM FAMILY T, X, 7 517 (Taken from 1930 Report International Radium Standards Commission, Rev. Mod. Phys., 3, 427, 1931.) Ionium Radium Radon Radium A Radium B Radium C Radium C’ 99.96% (99.97 %) Radium C’” Radium D Radium E Radium F Polonium Radium G (Uranium lead) T PN Rays and 5 end product RaF (Po) At. No. 84 P. No. 210 RaG At. Wt. 206.016 At. No. 82 P. No. 206 * Earlier values still in use. SMITHSONIAN TABLES 8.3-104yr 2.6:102s 1590 yr 5.02-10%s 3.825d 3,305:10°s 3.823d 3.303-10°s 3.05m 183s 26.8m 1.61-10%s 19.7m 1.18-10%s calo-§s 1.32m 79.28 22yr 6.94:108s 4.9d 4.26:10°s 5.0d 4.32:10°s 140d 1.2T-10’s 8.3:10-6yr-} 2.6-107183-1 4.36:10-4yr-! 1.38-10-Us-t 0.1812d°! 2.097-10-6s"} 0.1813d7! 2.098 -10®s} 0.227m71 267 O° 1On Se 2.59:10°n"! 4.31-10-4s"} 3.51-:10°m! 5.86-10-4s"! To®s-t 0.525m-! 8.7-10-%s"} 0.0315yr7} T.00:10-%s"! o0.141d7! 1.63:10-6s7} 0.139d7! 1.61-10-6s"} 4.95:10-%d"1 5.73:10-8s"! I.2-10°yr a, Ra 3.8:10"s 2295 yr 7.24:10!s 5.518d* 4.768-10°s* 5.515d* 4.765-10°s* 4.40m 264s 38.7m 2.32-10%s 28.5m I.17°10°%s B, @, .9996 RaC’ .0004 RaC” 10-65 a, RaD 1.9m B, RaD II5s 31.7yr B, RaE 1.00-109%s B, RaF 7.07d* 6.13-10°s* od 6.22-10°s* 202d 1.75:°10's a, RaG 518 TABLE 627 RADIOACTIVITY ACTINIUM FAMILY (Taken from 1930 Report International Radium Standards Commission, Rev. Mod. Phys., 3, 427, 1931.) Actinium Uranium Uranium Y (see Uranium Family) Protactinium Actinium Radio- actinium Actinium X Actinon Actinium A Actinium B Actinium C Actinium C’ 0.327% Actinium C’” 99.68% Actinium D Actinium Lead Pb207 At. Wt. 207.016 ? At. No. 82 P. No. 207 2.07, O yi 6.86-10-#8s"t 5.15:10°yr-! 1.63:10-%s-1 3.4:107yr-1 Tate Ones = 3.66-102d"! 4.24-107%s1 6.17-10-2d-1 7.14:10-%s71 6.08-107d7} 7.06:107%s1 0.177871 37481 1.93:10°m"! 2:2 1-TOmse 0.32Im-t 5-35:1073s-t ca14os1 0.145m-7! 2rAZ Ons = 0.146m-7! 2.44:10-8s-1 * EFarlier values still in use. SMITHSONIAN TABLES Rays and end product a, Ac B, RaAc a, AcX a, An a, AcA a, AcB B, AcC a, B, .9984 AcC” .0016 AcC’ a, AcD B, AcD TABLE 628 519 THORIUM FAMILY: POTASSIUM, RUBIDIUM Rays and Tr » t end product Thorium Mesothor- ium I Mesothor- ium 2 Radiothorium Thorium X Thoron Thorium A Thorium B Thorium C Thorium C’ 65% 65.7% Thorium C” 35% 34.3% Thorium D Thorium lead Pb208 Th 1.8-10yr] 4.0-1oMyr! | 2.5-10yr| a, MsTh, At. Wt. 232.12 5 OOS) || 1. 2-TOss52 8.0-10"s At. No. 90 P. No. 232 MsTh, 6.7yr 0.103yr7! 9.7yr B, MsTh» At. No. 88 2.1-:108s | 3.26-10-%s-} 3.05-108s P. No. 228 MsThe 6.13h 0.113h 8.84h B, RdTh At. No. 89 2.21-104s| 3.14-10-°s"! 3.18-104s P. No. 228 RdTh I.goyr 0.365yr7} 2.74yr a, ThX At. No. 90 6.0-:10’s | 1.16-10-8s~! 8.65-107s P. No. 228 Thx 3.64d 0.190d"! 5.25d a, Tn At. No. 88 3.14:10°s| 2.20-10-6s*} 4.54:10°s P. No. 224 Tn At. No. 86 P. No. 220 ThA 0.14s 4.9587 3 a, ThB At. No. 84 P. No. 216 ThB 10.6h 6.54:107h*! ‘ Bathe At. No. 82 3.82-104s| 1.82-10-*s"! P. No. 212 ThC 60.5m I.15:10°m ‘ B, a, .65ThC’ At. No. 83 3.63-10%s| 1I.91-10-4s"! 24: 25iDhe% P. No. 212 ThC’ 10-9s(?) 10°s-!(?) 10%s(?) | a, ThD At. No. 84 <10s SOs ¢ P. No. 212 sbhe7 3.1m 2.24:10'm! ; B, ThD At. No. 81 186s 3.73:10°3s"! P. No. 208 ThD At. Wt. 208.016 ?) At. No. 82 P. No. 208 54.58 1.27-:10°s! | 78.78 a, ThA Potassium (Krg) and rubidium (Rb37) emit 6 rays; the 6-ray activity of rubidium is 1/15 that of uranium; T is about 10" years. Cesium (55Ce) has been found to have an activity less than 1/90 of potassium. Hoffman considers neither sodium nor cesium radioactive. Be, av. period ro" years, (Langer, Raitt, 1933). Note—The following data is from Holmes, Lawson, Nature, 117, 620, 1926: N, atoms per g.. Ur Th kK Rb a5 ee O-a ne 72 OO Oz T, half-value period, years. . aoe ae iG Sh rO2 | 10" A, disintegration constant, years 4.6 X 1078 69 i t92) | 1-46 153 SMITHSONIAN TABLES 19 524 TABLE 638 RADIOACTIVITY H PARTICLES Marsden first observed the long-range particles due to the impact of a particles on matter, now known to be H particles, i.e., hydrogen nuclei or protons set in motion by a rays. Rutherford made a thorough study of this phenomenon, measured the ranges in H: of H particles due to a particles of various speeds, counted the relative number of a and H particles by the scintillation method; measured the magnetic and electrostatic deflection of the H particles and proved them to be hydrogen nuclei (protons) in motion. He was able to produce them by bombardment of substances rich in Hz. When the a particles have a 7 cm air range, the H particles have a maximum air range of 29 cm. H Particles from Atomic Nuclei Bombarded by a Particles from RaC’ (Taken from Kovarik, McKeehan, Nat. Res. Council Bull. 51, 1925.) RANGES IN CM IN AIR AT 15° C 1n Directions INCLINED TO THE a Rays Nucleus Ze ns Symbol J 5 °° 90° Li 10 Be 18 B 58 C 40 65 oN An fh W 16 58 13 (18-30) 12 (18-30) 31 32 18-30 35; 37, 39 18-30 36, 40 18-30 39, 41 18-30 * Kirsch-Pettersson, 1924. * Rutherford-Chadwick, 1924. * Rutherford-Chadwick, 1922. * Rutherford-Chadwick, 1921. SMITHSONIAN TABLES ———_ — I nclination—— ———, 180° Ref., Remarks I, (2, doubtful ) I, (2, doubtful ) > 3 I, (2, none) 3 3 2, very few 3 I, (2, very few) 4 I, (2, very few) 3 2, very few 2, very few 2, very few 2, very few TABLES 639-641 525 RADIOACTIVITY TABLE 639.—Relative Total Ionization by q Rays in Various Gases (After Bragg, Taylor, Laby, Hess-Hornyak.) Mean relative Mean relative Mean relatiue total ionization Gas total ionization Gas total ionization 100 CH. 122 CH, 117.3 99.5 C.He 130 CH.O 122 96.3 Cs His 134.8 C.H2 126.5 112 C.H.O 123 CH:I 133 101.5 CsHivO 132.3 C.H:I 128 107 CoHe 129 CHCl: 129 go CH.O 105 C.H;Cl 120.5 102 HBr 129 CCl 132 137.5 HI 129 CH:Br 132, 103 HCl 129 TABLE 640.—Delta Rays Delta rays are electronic rays (8 rays) produced by bombarding a substance with a particles, an ionization of a comparatively infrequent type. 6 rays are of various velocities, some corresponding to a few volts; others have a velocity, 3 10° cm/sec. (2400 volts) ; the number of 6 rays produced by bombarding metals is of the order of 8 to 10 per a particle. The existence of swift 6 rays in hydrogen gas has been proved by Bumstead (cloud- track method). From the wide column of droplets (a-ray track) there are short, narrow tracks nearly at right angles. Wilson obtained similar 6-ray tracks in air near the begin- ning of the a-ray tracks. These experiments show that some 6 rays are capable of ionizing air along a path of considerable length. Bianu (ionization method) was able to show that 5 rays ionize the gas and determined the velocity of the swiftest 5 rays as 2.9 X 10° cm/sec. This velocity corresponds to 2400 volts. C. T. R. Wilson suggests that the 6 rays may be due to expulsion of electrons from inner orbits of the bombarded atoms, which would agree with Kapitza’s observation that the average energy lost by an a particle in producing a pair of ions is greater at high velocities than at low. Bianu shows that the number of low-speed 5 rays produced is 40 times as great as the number of high-speed 6 rays and that each a ray from RaF produces, on the average, 10 of the more numerous class. His work also shows the 5-ray emission to be independent of the nature of the metal bombarded, an observation in agreement with earlier investigations. The usual explanation offered for the production of 6 rays is that an a particle entering a substance loses energy in ionization and that some of the electrons liberated possess speeds which enable them to escape. TABLE 641.—Heating Effect of Radium and Its Emanation (Rutherford and Robinson, Philosophical Magazine, 25, p. 312, 1913.) Heating effect in gram-calories per hour per gram radium. @ rays. B rays. y rays. Radium . ; - - 25.1 Emanation . ; : 28.6 RadiumA_, 5 ° 30.5 Radium B+C . 39-4 Totals . ; e 5 123.6 Other determinations: Hess, Wien. Ber. 121, p. 1, 1912, Radium (alone) 25.2 cal. per hour per gram. Meyer and Hess, Wien. Ber. 121, p. 603, 1912, Radium in equilibrium, 132.3 gram. cal. per,hour per gram. See also, Callendar, Phys. Soc. Proceed. 23, p. 1, 1910; Schweidler and Hess, Ion. 1, p. 161, 1909; Angstrém, Phys. ZS. 6, 685, 1905, etc. SMITHSONIAN TABLES. 526 TABLE 642 RADIOACTIVITY BETA RAYS @ rays are negatively charged particles (electrons) of the same nature as other electrons. It seems settled that the 8 particle is emitted first; the y ray is emitted from the atom re- sulting after the disintegration of the nucleus caused by the emission of the @ particle. In emitting B rays (random in direction) the original element is shifted one place to a next higher atomic number. Therefore one emitted electron is nuclear. Recent work proves some to be extra-nuclear. The velocity of the 8 particles is such that it is necessary in dealing with them to consider the Lorentz-Einstein equation, m = mo (1 — 6?)-/?; mo being the mass of a very slowly moving electron, 8, the ratio of the velocity of the particle to that of light, Vo. The @ and y rays are best designated by their spectra. A complete compilation of these would be beyond the scope of these tables. See Kovarik and McKeehan, Nat. Res. Council, Bull. 51, 1929; or Rutherford, Chadwick, Ellis, radiations from radioactive substances. The absorption coefficients (u) are not precisely defined by the relation J = Jo e-#*, but they are of great value in practical work and for the rapid diagnosis of a radioactive sub- stance. It appears desirable to include them and to give also the limits of velocity of the B-ray spectra. Magnetic spectrum Type of B D velocity Accompanying decay limits in y Tays ro0l0 cm/sec. Substance 1.44-1.74 No nuclear 3:40=2-88 B Weak nuclear 1.56-2.04 I nuclear line 1.08-2.47 9 nuclear lines D I.14-2.96 II nuclear lines .96-1.20 I nuclear line 2.05—2.84 Weak nuclear ? 126 : EATo2:35 3 nuclear lines 175 d -66-2.3 10 lines ? ? .88—-2.22 5 lines ca 1000 ‘ 1.49 ? FRRRBRB/WB + 3 nuclear lines ? I.09—2.90 8 lines I.19-1.53 2 lines 1.88—2.99 2 nuclear lines -QI—2.87 Ir nuclear lines Weak * B = band, L = line. Bands originate in the primary (nuclear) rays; lines in the photo-electrons of the gamma rays. u/p is the mass absorption coefficient (p = density); D is the thickness in which the radiation is reduced to half value and = 0.69315u. All data refer to aluminum as the absorbing material. SMITHSONIAN TABLES TABLE 643 527 RADIOACTIVITY WORK OF EXTRACTION OF BETA PARTICLES (After Bohr-Coster. Taken from Kovarik, McKeehan, Nat. Res. Council Bull. 51, 1929.) Works of extraction Vi in volts xX 10°; Vi=E(T/R); they have been interpolated assuming linear-variation of (T/R)2 with z in values given. In computing Vi, logo E = 6.13129 — 10; values not depending on interpolation italicized. M values, average of Mr and My; to get M: add, My, subtract correction term. Similarly with N, mean of Nix and Nyir; O, mean of O; and Oy. Atomic Levels No. . Lin M N O 92 QI 90 89 88 87 86 mel e1en . 1666 1624 .1582 .1540 . 1499 .1458 .1418 1378 . 1339 . 1330 .0453 = 100 0438+ 96 0424+ 93 0410 = go 03906 + 86 0382+ 83 0368+ 80 0354 77 0342 74 0330 + 70 0316 = 68 0305+ 66 .02903 = 63 0282 = .0270 = .0090 = 54 0.0022 14 0086 + 52 0082 = 50 0078 + 48 0074 = 47 0071 + 45 0067 = 44 0064 + 42 0060 + 41 0057 + 39 0052 = 37 0.0008 £6 85 84 83 82 . 1263 . 1226 .0049 = 36 0.0008 +6 .0046 = 35 0043 = 34 0.0006+ 5 0039 = 32 0.0006 5 . 1189 .IT53 GO somS) 6 OnG! 6) oO Co ONS 6) So SS (Gn O) GS) ONOn oo Om 6m o 7S, 6G Sf OO Cn C1 1OmOr OmiG! Ome Ou Sac) > GiO! Om SE On CmO gO 20) "6! (OO G50 6 SOS. Oo Cm On Ol or COMO CycmG BC SMITHSONIAN TABLES 528 TABLES 644 anpD 645 RADIOACTIVITY TABLE 644.—Effective Range of Beta Particles from RaE in a Few Elements (After Gray-Douglas. Taken from Kovarik, McKeehan, Nat. Res. Council Bull. 51, 1920.) Element Effective range, g/cm” TABLE 645.—Absorption of Characteristic Beta Particles in Air and co, (After Kovarik.) Air Cos Source (u/p)cm2/g (u/p)em?/g UX, 100 é 126. UX: 5.43 6.26 UX, UX, (Friman) RaD SMITHSONIAN TABLES TABLE 646 529 RADIOACTIVITY GAMMA RAYS rays are extremely penetrating, nondeviable by electric and magnetic fields, produce ionization of gases, act on the photographic plate, excite phosphorescence. Like X rays, they are similar to light. yy rays are merely X rays produced in the radioactive atoms. The reflection of X rays and y rays from crystals leaves no doubt that the wave theory of light is applicable. There are to be solved the same problems, as indicated by Bragg for the corpuscular theory of X rays. The same difficulties exist as in the case of visible radiation. Theoretical investigations on y rays, based on the electromagnetic theory, lead to conclusions not very different from those of a corpuscular theory. Emission of gamma rays.—The number of y rays per sec. from RaB and RaC in equilibrium with 1 g of Ra, is 1.43 X 10” and 1.49 x 10" (Hess-Lawson). The mean value obtained by Kovarik for the number of y rays per sec. from Ra(B + C) in equilibrium with 1 g of Ra was 7.28 X 10”, which is nearly (within 2%) one y ray per atom dis- integrating. The random emission in time of penetrating y rays from radium has been proved. Energy and wave length of gamma rays.—The energies and wave lengths of y rays have been obtained variously; much further research is required. The direct experimental determination of y-ray wave lengths by reflection from a crystal (NaCl) was first made by Rutherford-Andrade for the y rays of RaB and RaC. Both surface planes and internal planes were utilized. They showed that certain strong lines of the RaB y-ray spectrum are identical with characteristic X rays (L series) of nonradioactive lead. The shortest wave length measured was that of a y ray of RaC reflected at a grazing angle of 44’ having a wave length of about 70 X.U. (1 X.U.=10"%cm=107A.U.). The counting method was applied by Kovarik to high frequency y rays of RaC reflected from calcite. The shortest measured wave length was about 28 X.U. The determination of y-ray wave lengths from mass absorption is made on the supposi- tion that the relation between mass absorption and wave length found for X rays may be applied to y rays. For X rays, outside regions of selective absorption, u/p = kX” where \ is the wave length and m has a value 2.5 to 3. Rutherford found that as the mass absorp- tion coefficient, «4/p, of y rays approaches the order of magnitude of the mass scattering coefficient 7/p, it varies more slowly with \, probably as the first power; from his X-ray data he concluded that the very penetrating ~ rays have most probably a wave length between 20 and 7 X.U. Minna Lang applied her work on the absorption of hard X rays to the y rays of all known radio-elements and found that many are probably characteristic X rays (K, L, and M series). The energies of y rays have been obtained also by measuring the energy of 8 rays “excited” by them in various elements. The velocity of the f particles emitted by the 7 rays from the atom of any element depends upon the frequency of the 7 rays and upon the work necessary to separate the emitted electron from the rest of the atom. The photoelectric equation E =h»y—W, is applicable. (E is the energy of the “excited” 8 ray measured outside the atom, » is the frequency of the exciting y rays and W is the work of separation.) The energy E is the value of Hr in magnetic deflection experi- ments, the work W, the energy corresponding to the appropriate absorption edge in the X-ray spectrum of the atom in the electronic structure of which the 8 ray arises. The work of separation WV will have different values for different energy levels in the same atom and different values for the same energy level in different atoms. The soft y rays of RaB are the L-series X rays of Pb. Some of the y rays of radio-elements belong to the K, L, M, or other series of X rays of the atoms concerned in the f-ray disintegration con- sidered. Evidently, some of the y rays are of extra-nuclear source. The most penetrating y rays can not be so accounted for and must therefore be of nuclear origin. Connection between gamma rays and beta rays (or alpha rays).—The more recent work has established: (1) some of the @ rays are of photoelectric origin (extranuclear) “excited” by the y rays; (2) some of the y rays originate in rearrangements of electrons in the same part of the atom (ordinary X-ray types); (3) the change in nuclear charge requires some f rays in disintegration to be of nuclear origin; (4) some of the y rays, all of the very penetrating rays, are of nuclear origin. The principal point in dispute is whether emission of nuclear 8 rays precedes or follows the emission of nuclear y rays. SMITHSONIAN TABLES 530 TABLE 647 RADIOACTIVITY GAMMA RAYS Nuclear analysis—Analysis of nuclear y rays show evidence for energy levels in the nucleus analogous to those in the extra-nuclear structure as found by X-ray analysis. When instability arises in the nucleus an electron occupying a level of higher energy falls to a level of less energy, the excess energy being emitted as a y ray; since several changes of this kind are possible, y rays of several different but definite frequencies may be emitted from this nucleus; further, different groups of frequencies may be emitted from different individual nuclei. Some of the y rays cause (photo-electric) emission of electrons from various extra-nuclear levels, thus producing the S-ray lines in the B-ray spectrum, and rearrangement of the extra-nuclear electrons produces the 7 rays which correspond in frequency to characteristic X rays. The nuclear electron finally arrives in a stationary state in which it is not permanently stable and it flies out from the nucleus. The nuclear electrons, one per atom disintegrating, thus leave the atom with different energies and form the continuous 8-ray spectrum. The absorption of 7 rays by gases has not been studied at all exhaustively. Chadwick investigated the absorption of the y rays from radium, ie., from RaC, in air and in CO2 by varying the gas pressure, and in air by varying the distance from the source. Hess made measurements in air by varying the distance. Chadwick’s value for uw in air, reduced to atmospheric pressure and 15° C, is 6.0 X 10°/cm and Hess’ value is 4.47 X 10” cm. Ahmad and Ahmad-Stoner find that the absorption coefficient per atom can be ex- pressed as the sum of two terms, aZ + bZ*, which corresponds to a similar expression for the absorption of X rays, aZ + 8d*°Z*, the first term representing scattering and the second term true absorption. Ionization by gamma rays.—With the development of the theory of atomic structure by study of X rays and vy rays, of ionizing potentials, and by applications of the quantum theory, views on ionization by y rays have become more definite. When an X ray or a + ray traverses matter its energy hy may be absorbed (hy = E + W), an electron requir- ing energy W to remove it from the atom being ejected with residual kinetic energy E. Such an electron has generally been called a secondary 8 ray. It in turn may react with another atom, losing energy equivalent at least to the ionizing potential of a particular energy level in the atom ionized, repeating the process until its energy is dissipated, and leaving electrons and positive ions in its trail. Each of the ejected tertiary electrons if possessing sufficient energy, loses energy in the same manner. Moseley-Robinson’s values for the total number of pairs of ions produced per sec. in air at n.p.t. by y rays from quantities of RaB and RaC in equilibrium with 1 g of Ra are 0.84 X 10% and 11.34 X 10”, respectively. From Chadwick’s value for the coefficient of absorption in air the mean “range” is 1/u=1.6 X 10‘ cm. This gives as a mean value 7.5 < 10” pairs of ions/sec./cm of path in air for all the penetrating y rays from 1 g of radium in equilibrium, and, taking one y ray per atom of RaB and RaC disintegrating (Kovarik), this means about one pair of ions per cm of path in air for each penetrating y ray. SMITHSONIAN TABLES TABLE 648 531 RADIOACTIVITY GAMMA RAYS It is evident from the quantum relation, hy = E+ W, that y rays of given frequency will cause the emission of 8 particles of definite velocities, one for each energy level that can be ionized, from an atom of a given element (including all its isotopes). This has been proved experimentally and has been used in determining the energy of the exciting + rays. A discussion of the subject of photoelectron emission by X rays has been given by A. H. Compton. When vy rays pass through thin layers the 8 radiation leaving the layer on the side where the X ray beam emerges is more intense than that on the side where the X ray beam is incident. The asymmetry of this 8 radiation was more marked for light atoms than for heavy atoms; also for hard than for soft y rays. Scattering of gamma rays.—When y rays are incident on matter 7 rays may be detected on all sides of the piece as if emitted by it. y rays so re-radiated were called “secondary ” y rays. These secondary y rays appear to be really a mixture of two types: (1) scattered primary y rays; (2) fluorescent or characteristic X rays produced in the atoms of the secondary radiator by high velocity electrons liberated photoelectrically by the primary y rays. Ishino’s values of the mass scattering coefficient for Al, Fe, and Pb are respectively, 0.045, 0.042, and 0.034 (cm’/gm). The softening of the “secondary” y rays is undoubt- edly due to (1) the production of fluorescent radiation which may be in part (Compton) similar to the general “ white” radiation emitted by an X-ray tube, and (2) a modification of the true primary scattered radiation. The scattering of y rays by thin sheets indicates that the scattering per atom is nearly proportional to the atomic number, and that each electron appears therefore to act as an independent center for scattering whether it is one of a small number of electrons (Al) or one of a larger number (Pb). The scattered radiation on the emergent side is greater in amount than that on the incident side. Comparison of ganima-ray sources.—The relative ionizing powers of different types of y radiation need to be known if the quantity of any y-ray emitter is to be determined by comparison with a radium standard. The amount of MsThz in equilibrium with 1 g of Th, e.g., one month after separation of MsThn, gives a y-ray ionization equivalent to that from 0.524*X 10° g Ra in equilibrium with its y-ray products. The amount of ThC” in equilibrium with 1 g Th gives a y-ray ionization equivalent to that from 0.956 X 10% g Ra in equilibrium with its y-ray products. Since MsTh: and Ra are isotopes, chemical separation is impossible, and since the y rays compared are of nearly the same quality the detection and estimation of mesothorium impurities in radium by y-ray measurements (usually used for standardization) is somewhat difficult. Hahn and Bothe have shown how to distinguish between these materials by absorption experiments. Mme. Curie has shown that the ratio of the total heating effect to the y-ray activity is also characteristic of the proportion of mesothorium in a mixture of the two. SMITHSONIAN TABLES 532 TABLE 649 RADIOACTIVITY ABSORPTION OF CHARACTERISTIC GAMMA RAYS Source and type of decay assumed UX, B UX2 B loa Raa RaB B RaC + C” a, B RaD Bg Rak B RaF g RdAC a AcB B AcG7B MsTh, B RdTh ThB Bp The” 6 Level Riehl at * * L K Po enine ecm * Cee ents — YN * In Aluminum Half value Absorption thickness coefficient K em-t 24 .70 .140 1088 227, 41 354 16.3 “27 230 40 57 230 40 .230 .0043 160 .022 2 1.9 36 oP .090 Mass absorption coefficient / L/p cm?/gm 8.9 .26 .052 400 8.35 Sith 130 I 85 15 21 85 15 -085 047 16.7 37 16.7 37 -092 215 9.3 .070 44 11.5 .167 -073 9.6 .043 59 11.9 33 .036 Potassium, B rays, Myer 0-19; Mp), 0-14; 44), 0.065,* 0.14%. * Nucleus. SMITHSONIAN TABLES In Lead A Mass Absorption absorption coefficient coefficient n u/p em-! cm?/gm 2.3 0.20 WZ .064 TABLES 650 AND 651 533 RADIOACTIVITY TABLE 650.—Characteristic Gamma-Ray Wave Lengths and Energies Estimated from Absorption and Scattering (Taken from Kovarik, McKeehan, Nat. Res. Council Bull., 51, 1929.) Energy r ee Source cm X 1o-l volts X 105 ergs X 10-7 Reference 90 UI 903 0.137 Ozanne, 27 220 .562 .894 Ds g1 U 115 1.069 1.701 go Ra 4140 .030 .047 880 -140 .223 176 -699 A 88 Ra 2640 .047 .074 Hii -160 -260 150 .822 308 82 Ral 2230 .055 .088 IIIO ST 577 202 -610 -970 83 Ral 141 .877 395 rer noun .769 27.5 4.483 135 Compton, ’21 20 6.165 .810 Owen-Fleming, Fage, ’24 17 7.252 54 Ahmad, ’24 82 Rall 1160 .106 .169 Lang, ’21 1063 .116 SS Oe 24) 252 .489 778 Lang, ’21 290 -425 .677 Meitner, ’22 RaF 84 Ralll 3230 .038 061 Pang, 21 RdAc go Ac 918 .134 .214 130 -946 .506 AcB 82 AcI 1720 .072 .114 1000 .123 .192 184 .670 .066 ACeYy 81 Ac 132 .93I .481 MsTh,2 89 Th 932 132 .210 107 .153 .834 ThB 82 Thl 1930 .064 .102 IOIO .122 194 168 733 1.166 The” 83 Th 99 1.243 1.978 TABLE 651.—Nuclear Energy Deduced from Gamma-Ray Spectra (Kovarik, McKeehan, Nat. Res. Council Bull., 51, 1925.) No. of y rays No. of y rays Been ere ee leg ee cote || varie ieee eee actrees twice) twice) RaB O 4 ine? oO 7/ -537 6 41 5 .625 (0.628) 4 .56 2 2.571 (2.572) 4 2.28 2 2.942 3 2.48 4 4.048 3 2.54 3 5.31 4 2.74 3 RaC oO 2 Sen 5 “59 4 9.02 3 -70 I 3-07 2 3-30 2 4-45 I Ellis, Skinner, 1924; values in 3rd column of TnC” supplied by Kovarik, McKeehan. SMITHSONIAN TABLES 534 TABLE 652 RADIOACTIVITY GAMMA-RAY WAVE LENGTHS AND ENERGIES MEASURED BY CRYSTAL REFLECTION (Taken from Kovarik, McKeehan, Nat. Res. Council Bull., 51, 1929.) PART 1 Reflection from (100) Planes of Rock Salt (d = 2.814 X 10-8cm) nN Energy Energy Source 6 cm X 10-7 volts X 105 ergs X 10-7 =) 3 ie RaB 82 Ral 14°—o2’ 1365 0.0903 0.1437 1332" 1349 .0914 -1455 FB 3d 1315 0937 -1492 13°—14' 1288 .0957 1523 13°—00’ 1266 -0974 .1550 r2°—31' 1220 .IOII .1609 12°—16' 1196 .1031 -1641 12°—03’ 1175 .1049 .1670 rI°—42! II4I .1080 -I719 11°—17' IIOI .1120 .1782 11°—oo’ 1074 .1148 .1827 10°—48' 1055 .I169 .1860 10°—32’ 1029 .1198 .1907 10°—18' 1006 .1225 .1950 10°—03’ 982 1255 .1998 9°—45" 953 -1294 .206 Oo resy 918 -1344 214 5°43, 853 -1446 -230 8°—34 838 1471 234 8°—16' 809 .1524 .242 8°—06" 793 -1555 .247 4°—22' 428 .288 458 4°—o0’ 393 314 .500 3°—18! 324 381 .606 3°—00’ 294 419 .666 2°—4o’ 262 471 -749 HH SRSB RRS eR%5e44255 2°—28’ 242 .509 .810 2°—z20’ 229 538 .856 2°—oo’ 196.4 .628 -999 1°—q3’ 168.6 73 1.164 1°—37’ 158.8 -776 1.236 1°—24’ Raye5 .897 1.427 RaC 83 Ral 1°—10’ 114.6 1.076 tpt 1°—o0’ 98.2 1.255 1.998 0°43" 70.4 1.752 2.79 PART 2 Reflection from (111) Planes of Calcite (d = 3.028 X 10-8cm) RaC 83 Ral o°—q1’ 72.2 1.707 2.716 66.1 1.866 22712 2.121 Bra 75 2.545 4.050 3-333 5-304 4.374 6.961 - ° ° ° ~ NNNNNNNNNNNNNDN WBWWWWWWWWW WWW W NotEe.—Possibly second order. References: 1 Rutherford-Andrade (s. strong, m. medium, w. weak), '14. 2 Rutherford-Andrade, '14. 3 Rutherford, '14. 4 Kovarik, '22. SMITHSONIAN TABLES TABLE 653 RADIOACTIVITY QUANTITIES IN RADIOACTIVE EQUILIBRIUM (Taken from 1930 Report International Radium Standards Commission, Rev. Mod. Phys., 3, 427, 1931.) 535 SMITHSONIAN TABLES i M (mass units) for Rayo for UI =1 1.39-10!"s 2.12-108 (2.06) 108 68.4 2.4:104 9.4:10” 8.88-104 2.6:10s 5.02-101° 3.303-10° 183 1.61-10% 1.18-10 Capos’ 79-2 6.94-108 4.26-10° (4.9d) 4.32:10° (5.0d) 1.21-10" 1.01 -10!s 4.23108 (6.3-108 = 20 yr) 1.6310 9.7105 3.92 2-103 2.16-107% 130 Ga 105° 286 (283) 5.6-:10"%s 2.1-108 2.21-104 6.0-107 3.14:105 54-5 4 3.82-10! 3.63103 Caos? or 10-6 186 2.94-108 4.4:10°5 (4.3) 10° 1.4°10°% 1.7-10°8 2.0:10? 5.6-:108 52-7 1.00 6.47-10-6 Be52enOre 3.04:108 2523.1Os ca 2:10-1 6-107 1.28-10? 7.9:10°6 8.0-10°% 2.24-10-4 1.00 1.5:10- 51016 6-10-16 6.7:10° 1.9:1074 for Ra = 1 and 3% branching fraction .62 2.5:10°4 (3-7-1074) 9.8-107 5.8-:107 2.27 21Ops 1.14:10°% 120 - TO! 7 2NOee ca 2-1078 1.57-10-1 1.55:10°% Lote er 1.00 3.68-10-1 3.88-10-14 TOS One 5-41-10°8 9.23107! 2.32:10-19 6.23-10-14 5.92:10715 Cayo," To-14 1.04-10-16 for MsTh, =I 2.7-109 1.00 1.05:10-4 .286 1.47:10°%% 2.50:107 6.31 -10-10 1.69-10-4 1.61-10°% ca 3-1078 2-10;25 2.83-107 536 TABLE 654 CATHODE RAYS Prepared by W. W. Nicholas, Bur. Standards Cathode rays are swiftly moving electrons, and thus are of the same nature as B rays (see tables on radioactivity, pages 526 to 528). They are produced in gas discharge tubes. At comparatively low pressures the cathode rays thus produced have a nearly uniform velocity. Free electrons are emitted from hot bodies (Table 667), especially if the heated substance is coated with barium, calcium, or strontium oxide (Wehnelt cathode). These electrons can be given any desired speed if the heated substance (usually in the form of a wire) be enclosed in an evacuated tube and the difference of potential (17) applied between the wire (cathode) and another electrode (anode, anticathode, or target). The speed (v) of the cathode rays, expressed as a fractional part (8) of the speed of light (B= v/c, where c is the speed of light), when they have fallen through the entire potential differ- ence, is given by the formula (corrected for the relativity change of mass) V = 508.141 (1— p?)?— 1} where V is in absolute kilovolts. The equivalent power series, V = 254.01 B+ (4)6*+ ($)6°+ (82)8.... F, is useful for calculations at low and intermediate speeds (error is about 1% for 8 = 0.60, using terms given here). A tabulation of the corresponding values of ” (absolute kilo- volts) and 8 follows. An electron speed of 0.2 cm/sec. is spoken of, e.g., as a 10.5 kilovolt electron, or as having an equivalent voltage of 10.5 kv. V 0.1017 -4070 -9170 1.634 2.560 3.699 5.054 6.631 8.436 10.48 Cathode rays whose direction of motion is perpendicular to the direction of a uniform magnetic field (H7) describe a circular path of radius (r) according to the formula (cor- rected for relativity change of mass of electron) Hr = 1695 { B(1 — B’)* + where H is expressed in gauss and x in cm. When they impinge on matter, cathode rays are deflected from their original direc- tion of motion. These deflections grade all the way from 180° “reflections” to the “diffusion” corresponding to deflections through very small angles. The large-angle deflections are ordinarily comparatively infrequent. However, when the substance struck by the cathode rays is crystalline, certain directions may be preferred by the deflections. Here the beam of cathode rays behaves as though it consisted of a train of waves of wave length \e = 0.02428/8, where Xe is in Angstroms. The preferred directions for the “reflected” cathode ray beams may be calculated from the Bragg formula (see Siegbahn’s “X-ray Spectroscopy”’). The simple Bragg formula is quite limited in application here, however, since refraction in the crystal is very appreciable for the cathode ray beams. In general, the cathode rays which have been deflected by matter will have lost speed, but the rays which have undergone these “preferred” deflections remain of the same speed as the primary cathode beam. Cathode rays lose speed on penetrating matter. The losses of speed by individual cathode particles grade from complete stoppage to no loss of speed. The majority of the cathode particles, however, lose speed according to the relation (Thomas-Whiddington- Bohr law) Bo! eet _— ax where > is the initial speed, and 8 the speed after traversing a path length x in the material (+ to be measured in cm along the actual curved path), and a is a constant roughly equal to 6.59 where p is the density of the material in g/cm®. A convenient form for the expression is the following. Note that the two forms are not equivalent except at very low speeds (experiment has not yet decided between the two) : Vo -V= bx where Vo and V are the initial and final “equivalent voltages” (see above) of the cathode rays, in ky, and b is a constant roughly equal to 40 X 10‘p. A tabulation of experi- mental values of a and b for various materials follows: SMITHSONIAN TABLES TABLES 655 AND 656 537 RONTGEN RAYS (X RAYS) TABLE 655.—Constants for Cathode-Ray Speeds in Matter Material Beryllium Aluminum TABLE 656.—X-Ray Emission X Rays are generated whenever and wherever swiftly moving electrons (cathode rays) strike matter. This process occurs in gas discharge tubes at moderately low pressures (about 0.001 to 0.01 mm Hg); the gas-filled X-ray tube is based on this principle. The Coolidge tube, in which the gas pressure is so low (less than 10° mm Hg) as not to play a part, is superior for most purposes: the electrons, supplied by a hot filament incorporated in the cathode, are given a high velocity by the application of a high potential (as high as 300,000 v, in certain types) ; these cathode rays are directed against an area (“focal spot”) on the anode (“ target,” “anticathode”) where the X rays are generated. These X rays are of two types: continuous spectrum rays (“ heterogeneous, or “white” radiation) and characteristic rays (line spectra). Continuous spectrum X rays are a direct result of the acceleration of the cathode rays due to their close contacts with the atoms of the anticathode. The spectrum energy dis- tribution of this radiation, from a tube whose electrodes are maintained at a constant potential difference (I”), is described very roughly by the formula (for a more accurate type of formula, see the I.C.T. vol. 6) 9 66 general,” J dv = C(m — v)e~¢/¥ dv v= (1) for an energy-frequency graph, or by Jydd = (K/X*) 4 1/\0 — 1/d b edd A= No (2) for an energy-wave length graph. In these two formulae, Jy or J, is the energy between frequencies, vy and »+ dy, or wave lengths \ and + dX, respectively, ec, the base of natural logarithms, and » and \» the highest frequency and shortest wave length, respec- tively of the spectrum (“high frequency limit,’ “short wave-length limit,’ ‘“ spectrum limit’’). For X rays generated inside the anticathode c and k are zero; this simplifies the formulae, the exponential term becoming unity. For the X ray obtained outside the tube, c and k have values, estimates of which are tabulated in Table 660. The factor, c or k, determines the energy of the X rays; the convenient way to evaluate this energy is, instead of assigning numerical values to c or k, to evaluate E: and Ji (Table 660). 0 and Xo depend only on the voltage (I”), the relations being : No = 12.336/V (3) Yo 243-0 1One (4) (A and Xo are expressed throughout this section in Angstrom units, 10° cm, and wv and vo are in sec.”, and I’ is in kilovolts absolute.) The energy of the continuous spectrum X rays, fi, produced in the anticathode ordinarily comprises a major fraction of the total X-ray energy generated; the energy of the characteristic rays, E2, comprises the minor fraction. (£:1-+ E:) is only an exceed- ingly small fraction of the electrical energy, Es, supplied to the tube. E:/Es is called the efficiency of production of continuous spectrum X rays, and is closely represented by the formula E/E; = LV < 13 >< 107. where Z is the atomic number of the material of the anticathode, and V is expressed in kilovolts. On account of losses by absorption in the anticathode and in the walls of the tube only a small part of this energy generated inside the anticathode gets outside the tube. Table 660 supplies some numerical values of this “usable” energy, for tubes similar to the standard commercial types. Characteristic X rays result from the ionization of atoms, either (1) by direct cathode ray impact, or (2) by absorption of X rays. In the anticathode ‘of an X-ray tube both these processes occur. With a silver anticathode, for example, at any voltage between 35 and 80 kv, process (1) accounts for about 65% of the energy of the characteristic rays. SMITHSONIAN TABLES 5 38 TABLE 657 RONTGEN RAYS (X RAYS) EMISSION LINES AND CRITICAL ABSORPTION LIMITS (in Angstroms) The characteristic rays group themselves naturally into several groups, K, L, M, etc.; for any given element the lines in one group differ from each other in wave length by amounts which are small compared with the differences between separate groups. The wave lengths of the characteristic rays vary only with the material of the anticathode; these wave lengths, for some of the more prominent lines are given in the table below. Xa is the wave length of the critical absorption limit associated with the emission lines listed in the same subgroup. Taken by permission from Compton, ‘‘X-rays and Electrons.” Atomic number, Element O ON DuFWN He 5.36090 4.71821 3-73368 3-35169 3.02503 2.74317 2.49835 2.28484 2.09732 1.93230 18.37 11.8836 9.86775 8.31940 7.10917 6.14171 5-36375 4.72136 3:73706 3-35495 3.02840 2.74681 2.50213 2.28895 1.93651 Group Sub-group © ON AMUHWN * The values in italics are observed values. Other critical absorption limits are computed or interpolated. SMITHSONIAN TABLES TABLE 657 (continued) 539 RONTGEN RAYS (X RAYS) EMISSION LINES AND CRITICAL ABSORPTION LIMITS (in Angstroms) Group Atomic number, ah : Sub-group emen 2.08045 1.90591 1.75272 1.61713 1.49703 1.38933 1.29260 -20591 .12671 .05518 -99027 93085 .82703 -78151 -73932 -70048 -66449 .63124 -57143 -54470 .51972 -49630 -47428 -45373 -43439 -41624 -39924 -38341 352 343 329 .314 301 -292 -21973 -21345 .20131 -19550 - 19004 -18483 17466 -17004 -16525 .13095 SMITHSONIAN TABLES 540 TABLE 657 (continued) RONTGEN RAYS (X RAYS) EMISSION LINES AND CRITICAL ABSORPTION LIMITS (IN ANGSTROMS) L (continued) Group Atomic number, Sub-group Element 2A 5 19.17 1727, 11.951 9.3940 8.7172 8.1076 7.0604 5.8228 : ee yehe : 5-5734 5.4796 : 5:7113 : 9:2253 5.1658 . 5.3943 4.9092 4.61100 Wee 4.83567] 4.84367 | 4.3619 4.1221 ‘ 4.58778] 4.59556 | 4.1221 4.13730 4.35850] 4.36660 | 3.9007 3-92664 4.14564] 4.15382 | 3.69383 3-73008 3-94782] 3.95636 | 3.5064 3-54783 || ---- | 3-76367| 3.77242 | 3.3312 3.37792 3.59218] 3.60108 | 3.1679 3.21836 3.43177] 3.44075 | 3.0166 3.06997 3.28199] 3.29100 | 2.8761 2.93093 3.14166] 3.15087 | 2.74608 2.67784 2.88610] 2.89560 | 2.5064 2.56224 2.76964] 2.77904 | 2.3993 2.45330 2.65968| 2.66893 | 2.2980 2.35100 2.55600] 2.56511 | 2.2041 2.25390 2.45770| 2.46763 | 2.1148 2.16221 2.36531] 2.37563 | 2.0314 1.99357 2.19501| 2.20568 | 1.8781 1.91631 2.11633] 2.12733 | 1.8082 1.84246 : 2.04193] 2.05262 | 1.7419 1.77268 i 1.97149] 1.98231 | 1.6790 1.70658 1.90460] 1.91564 | 1.6198 1.64350 1.84098] 1.85206 | 1.5637 1.58344 1.78040] 1.79140 | 1.5106 1.5268 ; 72200) te 7339 1.4602 1.4725 1.66779] 1.6789 1.4128 1.4207 1.61551] 1.62636 | 1.3672 eS y7Alie 1.56607| 1.57704 | 1.3235 1.32354 1.51825] 1.5294 1.2810 -27917 1.47348] 1.48452 | 1.24191 -19459 1.38816] 1.3982 1.16838 -15495 1.34834] 1.35939 | 1.13287 L722 1.31008] 1.32121 | 1.09950 .08093 1.27355| 1.28489 | 1.06775 .0458 1.2385 | 1.2497 er .01266 1.20471| 1.21603 | 1.00786 -97990 , 1.17202] 1.18352 -97990 -94930 .9210 { T.14115| 1.1533 -95293 .76259 : -95342| .96524 -79108 -71807 : .90833| .92014 -75268 SMITHSONIAN TABLES TABLES 657 (concluded) AND 658 RONTGEN RAYS (X RAYS) 54 TABLE 657 (Concluded).—Emission Lines and Critical Absorption Limits (in Angstroms) Aa is the wave length of the critical absorption limit associated with the emission lines listed in the same subgroup. The italicized values are observed; other critical absorption limits are computed or interpolated. Atomic number, Element Al ||1100 79 24.2 122 6.042 5-797 5.567 5.151 4-963 4-746 4-557 4-392 3-746 3.605 3-329 22213 3.081 2.388 92 U 2.228 2300 190 29.9 14.16 6.699 6.403 6.190 5.621 5-427 5.216 5.038 4.827 4.083 3-895 3-597 Group Sub-group 3-477 3-333 Beet, 2.385 TABLE 658.—Probabilities of Ionization in K and L Shells An atom ionized, in the K shell, say, by one of the two processes described, can either (a) radiate a quantum of K characteristic radiation, or it can (b) convert an equivalent amount of energy into an ionization (with photoelectric emission) of its own outer shells L, M, etc. (compound photoelectric effect). The probability (w) of occurrence of process (a) subsequent to the ionization of an atom depends on the atom, and on the particular shell ionized. Some numerical values for the probability wu are given in the table below. Values in parentheses are comparatively uncertain. Ionization in the K shell Element, Ay /Cr Heys io Ni. Cu Zn, Se \ Bogwiikn Sr i Mo Ag I u 107) 1: 2345-25)(630) 1.30 2.38, -Al ..54u1-SOml Gaby £02 -08).1(-86)1 175) BS Ionization in the L shell Element Kr Xe u (13) (.25) SMITHSONIAN TABLES 542 TABLES 659 AND 660 RONTGEN RAYS (X RAYS) TABLE 659.—Energy and Efficiency of Production of Characteritsic X Rays The energy, E:, of the characteristic rays, as produced inside the anticathode for a given tube and a given type of characteristic ray, varies with the material of the anticathode and the voltage applied to the tube. The rays in a particular subgroup (see Table 657) do not appear at all until a certain critical voltage, Vo, is reached, then all the rays of the sub- group appear at once. Vo is given by the formula: Vo = 12.336/Aa, where Vo is in absolute kilovolts and \q in Angstroms. In Table 657 values of \. associated with the various sub- groups of emission lines are tabulated to the left of the particular lines with which they are associated. The efficiency of production of the characteristic rays, which may be taken as E,/E;, is given roughly by the formula: E,/E; = G[(V — Vo)?/V] V>Vo where G is a constant whose dependence on the anticathode material and type of charac- teristic ray has not yet been broadly investigated. For a silver anticathode and a tube voltage of 50 kv, E,/E3 for the K rays is about 0.48 X 10-3. Due to losses by absorption in the anticathode and walls of the tube only a part of the energy generated in the anticathode reaches the outside of the tube. The following table supplies some estimates of this ‘“‘usable”’ energy for tubes similar to the standard commercial types. J2, which is a measure of the useful characteristic ray energy, varies with voltage in a different manner than F&, on account of the variation with voltage of the absorption in the anticathode. For Vo< V<2Vo, I, is roughly proportional to (V — Vo)", where m is usually between 3/2 and 2; but at higher voltages some measurements indicate that J, increases more slowly with voltage, approaching a limiting value in the neighborhood of V = 6V. The relative intensities of the lines in a particular subgroup are independent of voltage for a given element; the variation from element to element is often negligible over long ranges of atomic number. In the K series, and at least for atomic numbers greater than 30, about 5/6 of the energy is contained in the two a lines; of these two, a; is the more intense in the ratio 2:1. In the L series of tungsten, at 22.75 kv, the ratio of the intensities a:a2 is 10:1; B1:82:83:84 have relative intensities 100:55:15:1; and yi:7y27v3:74 have 100:14:18:6. TABLE 660.—Energy and Quality of Emission X Rays I Iz Ey (£2)k at one m ergs/sec. erg/sec. cm? 1.23) Oo RO sigs! “é 3.66 a al 7.20 .20 1728 25 Silver See eae Norte: V is the constant direct current potential difference maintained across the ter- minals of the tube. For varying voltages (as with a tube supplied directly from a trans- former, or with a mechanical rectifier), where V is the peak voltage and 2 is the average current as read by a milliameter, all the values tabulated are decreased by an extent de- pendent on the voltage and current wave forms for the particular outfit used, and therefore difficult to specify here. 7 is the milliamperage tube current for tubes of the Coolidge type, but not for gas-filled tubes, where there are complicating factors. E; is the energy converted per sec., inside the anticathode, into continuous spectrum X rays. (E2)x is a similar quantity for the K characteristic rays. SMITHSONIAN TABLES TABLES 660 (continued) -663 543 TABLE 660(continued).—Energy and Quality of Emission X Rays I, is the intensity in the continuous X rays obtained outside the tube at a distance of I meter from the focal spot, supposing no filtration other than the unavoidable filtration due to the walls of the tube (assumed equivalent to 1.23 mm of Al), anticathode, etc. For practical purposes, until more thorough data is at hand, J: may be assumed proportional to the atomic number of the material of the anticathode. It is expressed in ergs per sec. falling on a 1 cm’ surface perpendicular to the X-ray beam. The orientation of the tube is supposed to be the usual one, with X rays taken off perpendicular to the cathode stream, and target face inclined at 45°. J: is a similar quantity for the K characteristic rays. c and k are quantities contained in p. 537, which describe the spectrum distribution of the intensity J1. E, and £2 are probably within 5% and 10%, respectively, of their correct values. I, and J, depend on the tube walls, the roughness of the target surface, etc., and on such accounts an estimate of accuracy is difficult to make; for a smooth target surface, inclined at 45°, and tube walls of 0.7 mm soda glass, the above values of J; and J: are probably correct to within 20%. TABLE 661.—X-Ray Spectroscopy When an X-ray beam is incident on a crystal in such a manner as to make a glancing angle @ with certain sets of parallel planes within the crystal (adjacent planes, containing large numbers of atoms, for best efficiency), these planes having an interplane spacing d, components of the beam of wave lengths A, 4/2, A/3,.... A/n will be diffracted (or “reflected.””) according to the relation (Bragg law): A=2dsin6. The angle between the directions of the original beam and the deviated beam is 26. Refraction in the crystal would introduce an additional factor in the above formula, but the effect is negligible for all ordinary work. Values for d, the “lattice constant,” for some of the commonly used crystals are tabu- ‘lated below. TABLE 662.—Lattice Constants of Crystals d in Angstroms Crystal Surface at 18° C Carborundum (111) 2.49 Rock salt Cleavage face 2.814 Calcite Cleavage face 3.029 Quartz Prism face 4.247 Gypsum .... Cleavage face 7.577 KsFeCN, (100) 8.408 Cleavage face 9.993 10.57 11.23 For an extensive tabulation of X-ray data on crystals see the I. C. T., vol. 1. TABLE 663.—Absorption and Scattering of X Rays; Fluorescence A beam of X rays loses energy as it traverses matter. For monochromatic rays, this loss of energy is given by the formula: ///J,=c-#* where J. and J represent respectively incident and emergent intensities of a parallel beam normal to a plate of absorbing material of thickness x, e is the base of natural logarithms, and uw is a constant depending only on the wave length of the x rays and the material of the plate. For the most used range (wave lengths 0.1 to 1.4 Angstroms, and atomic numbers greater than 5; outside this range there are systematic deviations from the formulae) u is approximated to about 5% or better by the formulae: (See next page.) SMITHSONIAN TABLES 544 TABLES 663 (continued) AND 664 RONTGEN RAYS (X RAYS) TABLE 663 (continued).—Absorption and Scattering of X Rays; Fluorescence p/p =(1/A) (0.01362*X* + 0.322) N< p/p =(1/A) (0.00202'X* + 0.322) MAX Ady p is the density, Z, the atomic no., A, the atomic weight of the material of the plate, 4, the wave length of the X rays, Angstrom units; x is in cm. Values for \x and Az, wave lengths at which materials have “ critical absorption discontinuities,” are listed in Table 657 under “ X-ray Emission” as Aa. Numerical values for «/p, the “mass absorption coefh- cient,’ (A. H. Compton “ X-rays and Electrons”) are given in Table 665. The first term in the brackets represents energy losses from “ fluorescent,’ or “ true,” absorption; this first appears as energy of ionization of atoms and of photoelectrons. The ionized atoms then either emit characteristic X rays or use their energy for the photo- electric process; the quantitative relations between these are described in Table 660 under “X-ray Emission.” The second term is the energy lost by the X-ray beam by scattering. Except for the (usually small) amount of energy which goes into the production of “recoil electrons,” it remains as X-ray energy which is simply redistributed as to direction of propagation, being radiated in all directions from the plate. The scattered radiation is of two parts, an “unmodified” (or “unshifted”) part, and a “modified” (or “shifted”) part. The former has the wave length of the original beam. The wave length of the modified part is longer (‘‘ Compton shift”) than that of the original beam by an amount 6A which varies with ¢, the angle between the direction of the primary beam (of wave length A), and the direction of that portion of the modified rays of wave length \+ 6A, The relation between 6\ and @ is 6\ (Angstrom units) = 0.02428(I — cos ¢). TABLE 664.—X-Ray Absorption and Chemical Combination The wave lengths of the critical absorption limits of an element depend, to a very small extent, on the chemical combination of the “absorbing” element. The K absorption limit for phosphorus follows for various chemical combinations: R stands for any one of several metals. Wave lengths, \, in Angstroms (RN)sPO (RC) 3PS RO(RC)(H)PO (RO)sP (RO) 2(RC)PO (RO)(RC)2PO O ) (RO)sP,CuCl (RN) (RO) (Cl) PO . : P (violet) (RN) (RO) 2PO . d P (black) (RN) 2(RO)PO : c P (white) There result some conclusions probably of general application: (AA) in its value for some particular compound, depends only on what atoms are directly attached to the absorbing atom (e.g., the phosphorus limit (RO):P does not depend on what metal is used for R). Ad depends on the kind of atom directly attached (compare (RO);sP with (RC):P) and on the number of these atoms (compare (RO):P with (RO)sPO). If any addition (any kind of atom) is made to a given set of atoms directly attached to the absorbing one, the limit is shifted toward a shorter A (cf., (RC)sP with (RC)sPO). Further, the wave length for the element when uncombined is usually greater than when at- tached chemically to other atoms (true for all of 11 elements investigated except sulphur). A variation of wave length is also usually shown for allotropic modifications of an element. SMITHSONIAN TABLES TABLE 665 545 MASS ABSORPTION COEFFICIENTS (u/p) Atomic Wave lengths in Angstroms number, Element | 0.017 0.057 0.080 0.100 0.125 0.150 0. 175 0.200 0.250 OMny wit wee. O18 50.4, O-4e 10.4 0.39 .060 ee 0.140 0.146 1152 .160 Mise wists McK Kole eter LOG LOSON noe a 4 One OS O57 bt aoe se ts 9 O21 .075 .058 0. SAS LOAwe lt .op-2On OH soo cli allel 620 058 . 1232) 205, 92399 FO5O erence cOla 3206475 SOV neo elR Be Uo O5 Miri GOSmE So OO Pee Ue 1G Rea 5 WH) soo of8 orl} io"/ (O56) =o) 70) £10), 2.00 = 5 AS SLO Griz FOGS) 27) 2:40) 3-60) 15.70 Pet ve, 2239) 3-04) 5:37-4 .068 .50 2.47 3.78 LO7 OME 44578 ; LOSE ate ae LOOM Wes K limit 162.170 .184 177 ~—--193 sli =222 .269 .42 1.07 Tey, 0.500 0.600 0.700 0.800 0.45 0.44 O.51 0.57 0.63 245 .306 .403 Eo OMe 54 Onnry72 1.00 I. AQSme 4 Om taLOMt- 55) 2-12) | 2: 1.56 5-9 9-5 30 45.0 tens 118 [S:9)) 31-0) 40:2 seh 133 Bye 116 we 133 | Vv L limit SMITHSONIAN TABLES iOS EB 5.c0 7-501 10-3 13. ee 23530 30:3) 57 09-6) (95 I Xo Api ST meee 6 8 20.0 126 159 181 540 TABLE 666 PHOTOGRAPHIC EFFECTS OF X RAYS X rays affect a photographic plate (or film) in much the same way as does light, except that that part, Dx, of the photographic density which is due to the radiation depends on radiation intensity, J, and the time of exposure, t, in a simpler way. The relation for mono- chromatic X rays is De=D—D=kUi—et), CO D4 (1) where ¢ is the base of natural logarithms, and k and a are constant for a given plate and given X-ray wave length. D and Do are the photographic densities of the exposed and unexposed parts of the plate. These densities are measurable with a photometer, photo- graphic density being defined as the common logarithm of the reciprocal of the transmission T, i.e., density =logio(1/T), where T is the ratio (transmitted light) / (incident light) for a beam of light normal to the developed plate. The limits of applicability of formula (1) probably depend on the characteristics of the plate used and on the development, as well as on the wave length of the X rays. Experi- mental tests indicate that the relation holds within a few per cent up to a density of at least 4, for X-ray plates, if the plate is fully developed and if the wave length of the X rays is between 0.4 and 1.1 Angstroms. Effects due to intermittency, and to the failure of the reciprocity law are negligible in the X-ray region. SMITHSONIAN TABLES TABLES 667-669 547 Note: The phenomena of electron emission, photoelectric effect and contact (Volta) potential treated in the following tables are extremely sensitive to surface condition of the metal. The most consistent observations have been made in high vacua with freshly cut metal surfaces. (See Dushman, Rev. Mod. Phys., 2, 381, 1930.) TABLE 667.— Electron Emission from Hot Solid Elementary Substances (Most of the following is taken from Dushman, loc. cit., 1930.) Among the free electrons within a metal some may have velocities great enough to escape the surface attraction. The number reaching the surface with velocities above this critical velocity = N = (RT/21M)'” e-v’"t where N = no. of electrons/cm? of metal, R the gas constant (83.14 X 10° erg-dyne), 7, the absolute temperature, M, the atomic weight of an electron (.000545, O = 16), w the work done when a gram-molecule of electrons (6.06 X 1023 electrons or 96,500 coulombs) escape. It seems probable that this work is done against the attraction of the electron’s own induced image in the surface of the conductor. When a sufficiently high + field is applied to escaping electrons so that none return to the conductor, then the saturation current has been found to follow the equation i=aNVT-e’’” (Richardson's equation) assuming NV and W constant with T. This is equivalent to the equation for just given. The equation I = AT°e-'/T (Laue’s equation) is just as valid theoretically and Dushman (Phys. Rev., 21, 623, 1923) considers A should be a universal constant (60.2 amp./cm?/deg.?/and by dependent upon the emitter. The data is not accurate enough to distinguish between the two formulas. 0 or bo isa measure of the latent heat of evaporation of the electrons, i. e., the energy needed to get the electrons through the surface. While used in °K. in the above equation, it is customary to express it in volts by the relation bok = ¢oe where k = Boltzmann's constant, e, the electronic charge, and @» is known as the work function, whence ) = Biew >< 10do (volts) The experimental values of A do not seem to be independent of the substance. Element | ) X 10-4 Dushman, 1925 DuBridge, 1928 Dushman, 1925 Zwikker, 1926 Average Zwikker, 1929 (Above table of best authenticated values is from Dushman, loc. cit., p. 394, 1930. His table contains values for G, Ca; Gs) Hf, Ni. See'also 1-/C:T.) TABLE 668.—Electron Emission from Thorium-Coated Filaments (Monomolecular), f (6) Values given for Dushman with W filaments coated with monomolecular films of thorium. 6 = (bo — bw) /(btn — by) where bo, brn and b,, represent values of bo in the emission equation for partly covered, completely covered, and pure tungsten surface. I) and ¢o refer to 1900°. TABLE 669.—Emission Current, J, Emission Efficiency I/W, Diffusion, D, J, for Zero Field, Completely Activated Surface, Th on W I (amp./cm?) aaa D (cm?2/sec.) E (atoms/ 8.0 5.3 5-4 3-5 1.8 7.9 2.9 9.5 2.8 SMITHSONIAN TABLES 548 TABLES 670-672 TABLE 670.—Electron Emission from Other Than Th-Coated Filaments Monatomic films of other rare earths (and alkaline earth metals absorbed on tungsten and molybdenum). D cm’*/sec.* for T= 2000. Qp, heat of diffusion (g cal./g-atom), E, the rate of evaporation in atoms/cm’sec. at 2000° K. A, bo refer to formulas on page 547. Emitter bo 31,500. 31,500. ett: 33,000. , 100,000 31,300. : 78,000 36,500. ; 62,000 30,500. ‘ 94,000 30,000. ; 2,000 TABLE 671.—Photoelectric Effect A negatively charged body loses its charge under the influence of ultra-violet light because of the escape of negative electrons freed by the absorption of the energy of the light. The light must have a wave length shorter than some limiting value Xo characteristic of the metal. The emission of these electrons, unlike that from hot bodies, is independent of the temperature. The relation between the maximum velocity v of the expelled electron and the frequency » of the light is (4)mv*—=hvy— P (Einstein’s equation) where h is Planck’s constant (6.58 X I0- erg. sec.) ; hy sometimes taken as the energy of a “ quanta,” P, the work which must be done by the electron in overcoming surface forces. (4)mv is the maximum kinetic energy the electron may have after escape. Richardson identifies the P of Einstein’s formula with the w of electron emission of the preceding table. The minimum frequency » (corresponding to maximum wave length \») at which the photo- electric effect can be observed is determined by hy =P. P applies to a single electron, whereas w applies to one coulomb (6.062 X 10” electrons) ; therefore w= NP = .00399% ergs. @= (12.4 X 10°) volts. See Millikan, Proc. Nat. Acad. 2, 78, 1916; Phys. Rev. 7, 355, 1916; 4, 73, 1914; Hennings, Phys. Rev. 4, 228, 1914. TABLE 672.—Contact (volta) Potentials Pt Fe Cu Au Ag Al Mg Zn Pb Sn SiO; ... +2.22 -+1.99 -++1.60 -+1.60 -++1.42 +-.93 -+.93 -+-.45 -+.16 — .30 Glass ..+1.15 +1.15 +058 -+0.58 +058 +.14 +.14 —.29 —.60 —I.14 Cu Cr lta Mo Ni +.08 +.11 —.38 —.2I —.17 Polednik, Z. Phys 66, 610, ee Kosters, “ e 66, 807, 1930. (This Table Supplements Table 677.) 2:35* 4.50 3.90 3-55 3.20 2.80 2.80 2.65 2.80 ne 3 4 6 7 8 9 0 I _ * Outer electron shell. + Cr, “electronegative,” 2.35; Mn., ditto, 2.35. Broughall (Phil. Mag. 41, p. 872, 1921) computes in the same units from Van der Waal’s constant ““b” the diameters of He, N, A, Kr, and X as 2.3, 2.6, 2.9, 3.1, and 3.4. These inert elements correspond to Langmuir’s completely filled successive electron shells. The corresponding atomic numbers are 2, 10, 18, 36 and 54. For Langmuir’s theory see J. Am. Ch. Soc., p. 868, 1919, Science 54, p. 59, 1921, SMITHSONIAN TABLES TABLES 672 (continued) AND 673 549 TABLE 672.—Contact (Volta) Potentials There has been considerable controversy over the reality and nature of the contact differences of potential between two metals. At present, due to the studies of Langmuir, there is a decided tendency to believe that this Volta differ- ence of potential is an intrinsic property of metals closely allied to the phenomena just given in Tables 667 to671 and that the discrepancies among different observers have been caused by the same disturbing surface conditions. The following values of the contact potentials with silver and the relative photo-sensitiveness of a few of the metals are from Henning, Phys. Rey. 4, 228, 1914. The values are for freshly cut surfaces in vacuo. Freshly cut surfaces are more electro-positive and grow more electro-negative with age. That the observed initial velocities of emission of electrons from freshly cut surfaces are nearly the same for all metals suggests that the more electro-positive a metal is the greater the actual velocity of emission of electrons from its surface. Fe | Brass} Sn Zn Contact potential with Ag : .19 12 .27 -590 Relative photo-sensitiveness 5 65 45 70 80 From the equation w = RT log(N 4/N pg), where w is the work necessary per gram-molecule when electrons pass through a surface barrier separating concentrations V 4 and Nz of electrons, it can be shown (Langmuir, Tr. Am. Eletroch. Soc. 29, 142, 1916, ef seq.) that the Volta potential difference between two metals should be — w 1 — v= 5 {wa — wi + RT log(V 4/N p)} = — =¢d2— Gi (see Table 671 for significance of symbols), since the number of free electrons in different metals per unit volume is so nearly the same that RT log (N_4/N p) may be neglected. The contact potentials may thus be calculated from photo- electric phenomena (see Table 671 for references). They are independent of the temperature. The following table gives a summary of values of ¢ in volts obtained from the various phenomena where an electron is torn from the attrac- tion of some surface. In the case of ionization potentials the work necessary to take an electron from an atom of metal vapor is only approximately equal to that needed to separate it from a solid metal surface. TABLE 673.—(a) The Electron Affinity of the Elements, in Volts te me electric Photo- : ingle- . and electric. piiseel: line scjusted contact. |(Richardson) * | spectra. : (Millikan.) Contact. |Thermionic. (Henning.)| (Langmuir.) uN =. Roop linea un =a Since IF lievoulltss cose QA Marc Magnesium Titanium HHH KHWWWWWkWAHRH HLH LHL COWL TOR HI C71 OH HWWEN nn (b) It should not be assumed that all the emf of an electrolytic cell is contact emf. Its emf varies with the elec- trolyte, whereas the contact emf is an intrinsic property of a metal. There must be an emf between the two electrodes of such a cell dependent upon the concentration of the electrolyte used. The following table gives in its first line the electrode potential e; of the corresponding metals (in solutions of their salts containing normal ion concentration) on assumption of no contact emf at the junction of the metals. The second line, @ — Fy volts, gives an idea of the electrode potentials (arbitrary zero) exclusive of contact emf. Metal SMITHSONIAN TABLES. 550 TABLES 674 AND 675 TABLE 674.—Molecular Velocities The probability of a molecular velocity x is (4/ Vr) xe, the most probable velocity being taken as unity. The uwumber of molecules at any instant of speed greater than c is 2N(hm/1)2 Senne dc + ce~hmc2 \ (see table), where WN is the total number of molecules. The mean velocity G (sq. rt. of mean sq.) is proportional to the mean kinetic energy and the pressure which the molecules exert on the walls of the vessel and is equal to 15,800 /T/m cm/sec, where T is the absolute temperature and m the molecular weight. The most probable velocity is denoted by W, the average arithmetical velocity by Q. G=W V3/2 = 1.225W; Q =W V4/m = 1.128W; G =2 V37r/8 = 1.0862. The number of molecules striking unit area of inclosing wall is (1/4)NQ (Meyer’s equation), where N is the number of molecules per unit volume; the mass of gas striking is (1/4)pQ where p is the density of the gas. For air at normal pressure and room temperature (20° C) this is about 14 g/cm?/sec. See Langmuir, Phys. Rev. 2, 1913 (vapor pres- sure of W) and J, Amer. Ch. Soc. 37, 1915 (Chemical Reactions at Low Pressures), for fertile applications of these latter equations. The following table is based on Kinetic Theory of Gases, Dushman, Gen. Elec. Rev. 18, 1915, and Jeans, Dynamical Theory of Gases, 1916. Sq. rt. mean sq. Arithmetical average velocity, Molec- | G X 107 cm/sec. Q X 107? cm/sec. ular eight. weight 273° | 203° | 373° | 223° ° | r000° | 1500° | 2000° | 6000° .96 | 485] 502 | 567] 404] 447 | 463] 522 | 855 | 1047 | 1209 | 2094 633 | 655 | 740] 527 | 583 | 604] 681 | I115 | 1367 | 1577 | 2734 413 | 428 | 483} 344] 381 | 305] 445 | 720 | 892 | 1030 | 1784 493 | str | 576] 410] 454 | 471 | 531 | 870 | 1065 | 1230 | 2130 303 | 408 | 459] 327] 362 | 376] 434 | 604 | 850] 981 | 1700 1311 | 1358 | 1533 | 1092 | 1208 | 1252 | 1412 | 2300 | 2840 | 3270 | 5680 Hydrogen........ : 1838 | 1904 | 2149 | 1534 | 1696 | 1755 | 1980 | 3241 | 3070 | 4583 | 7040 Keryptoneenciecciee ; 286 296 335 238 263 272 308 502 618 712 | 1236 Mercury : 184 Igl 215 154 170 176 199 325 308 4590 796 Molybdenum...... : _— — = _— — _— — 469 575 664 | I150 : 584 605 683 486 538 557 629 | 1030 | 1260 | 1460 | 2520 Nitrogen : 403 511 577 410 454 471 531 869 | 1064 | 1229 | 2128 46t | 478 | 539] 384] 425 | 440] 407 | 813 | 906 | 1150 | 1992 Mungstens erates : — a == cl od = 339 416 480 832 Water vapor ; 615 637 720 512 566 587 662 | 1084 | 1317 | 1533 | 2634 228 236 207 190 210 218 246 400 493 570 986 Free electron, molecular weight = 1/1835 when H = 1; G= 1.114 X 107 at o° C and Q = 1.026 X 107 at o° C. TABLE 675.—Molecular Free Paths, Collision Frequencies, and Diameters The following table gives the average free path L derived from Boltzmann’s formula p (. 3502p), u being the vis- cosity, p the density, and from Meyer’s formula u(.3097pQ). Experimental values (Verh. d. Phys. Ges. 14, 596, 1912: 15, 373, 1913) agree better with Meyer’s values, although many prefer Boltzmann’s formula. As the pressure decreases, the free path increases, at one bar (ordinary incandescent lamp) becoming 5 to 1o cm. The diameters may be deter- mined from L by Sutherland’s equation {1.402/-V 20 NL (1 + C/T)}3, N being the number of molecules per unit vol. and C Sutherland’s constant; from van der Waal’s }. {3b/2NVar 35 from the heat conductivity k, the specific heat at constant volume cv, {.146pGcv/Nk 3 (Laby and Kaye); a superior limit from the maximum density in solid and liquid states (Jeans, Sutherland, 1916 and an inferior limit from the dielectric constant D, {(D — 1)2/mN}3s or the index of refraction 7, {(n2 — 1)2/7N 3. The table is derived principally from Dushman, l.c. L X 108 (cm) 103 X Molecular diameters (cm): Average free path.* Collision frequency. Limiting From L| From From ae (vis- | van der cosity) | Waal’s Sees es / 20° C ie bis Ma ane Boltzmann. Meyer. Min. Dorn .08 04 12 328 65 34 . 69) .OL ars .Q2 .02 6.60 5.83 .Q7 9.88 : 88 Q. 23 .16 .19 6.15 44 34 27.45 S -99 17.44 I5.40 -40 .87 oi -35 .98 .40 qo) bd a soles beeresede| ; Argon : | Carbon monoxide. s6" *dioxide=.> Hh Oo anM COON Hydrogen Krypton —_ Mercury (14.70) (13.0) _- Nitrogen 9.29 8.21 as Oxygen 9.93 8.78 2.98 XENON Me ncilar ee — = WnRnHW -rnoaoond w w Sy SPNwOWKNHNHWWNHW moO oo w * Pressure = 108 bars = 108 dynes + cm? = 75 cm Hg. SMITHSONIAN TABLES. TABLES 676 AND 677 5s TABLE 676.—Cross-Sections and Lengths of Some Organic Molecules According to Langmuir (J. Am. Ch. Soc. 38, 2221, 1916) in solids and liquids every atom is chemically combined to adjacent atoms. In most inorganic substances the identity of the molecule is generally lost, but in organic com- pounds a more permanent existence of the molecule probably occurs. When oil spreads over water evidence points to a layer a molecule thick and that the molecules are not spheres. Were they spheres and an attraction existed be- tween them and the water, they would be dissolved instead of spreading over the surface. The presence of the -COOH, —CO or —OH groups generally renders an organic substance soluble in water, whereas the hydrocarbon chain decreases the solubility. When an oil is placed on water the —COOH groups are attracted to the water and the hydrocarbon chains penelied but attracted to each other. The process leads the oil over the surface antil all the —COOH groups are in contact if possible. Pure hydrocarbon oils will not spread over water. Benzene will not mix with water. When a limited amount of oil is present the spreading ceases when all the water-attracted groups are in contact with water. If weight w of oil spreads over water surface A, the area covered by each molecule is AM/wN where M is the molec- ular weight of the oil (O = 16), N, Avogadro’s constant. The vertical length of a molecule / = M/apN = W/pA where p is the oil density and a the horizontal area of the molecule. Cross Cross section | / in cm section | / in cm Substance. in (length) Substance. in (length) cm? X 108 cm? X 108 X rolé X rol6 | Palmitic acid CisHs1COOH......... 24 19.6 Cetyl alcohol CisH330H.......... 21 21.9 Stearic acid Ci7HssCOOH........... 24 21.8 Myricy] alcohol CsoHsi1OH........ 29 35-2 Cerotic acid C2sHsi1\COOH.......... 25 29.0 Cetyl palmitate CisHs1COOCisHas . 21 44.0 Oleiciacid’Gr;7HssGOOH pa. c-ce-: 48 10.8 Tristearin (CisH3sO2)3CsHs........ 69 23-7 Linoleic acid Ci7H3i1COOH.......... Aza |e LO Trielaidin (CisH3302)3C3Hs........ 137 II.9 Linolenic acid Ci7H22COOH.........| 66 7.0 Triolein (CisH3302)3C3Hs.........-| 145 II.2 Ricinoleic acid Ci7H32(0H)COOH....| 90 5.8 Castor oil (C17H32(0H)COO)3C3Hs.| 280 5.7 ° Linseed oil (Ci7Hsi1COO)sCsHs.. . . 7 143 II. TABLE 677.—Size of Diffracting Units in Crystals ] __The use of crystals for the analysis of X-rays leads to estimates of the relative sizes of molecular magnitudes. The diffraction phenomenon is here not a surface one, as with gratings, but one of interference of radiations reflected from the regularly spaced atomic units in the crystals, the units fitting into the lattice framework of the crystal. In cubical crystals {zoo} this framework is built of three mutually perpendicular equidistant planes whose distance apart in crystallographic parlance is dioo. This method of analysis from the nature of the diffraction pattern leads also to a moowledee of the structure of the various atoms of the crystal. See Bragg and Bragg, X-rays and Crystal Structure, 1918. Molecules or Elementary : . . Crystal. diffracting clement. Side of cube. atomsyin unit cm RGU fears crete serchetercvs Face-centered cube * 6.28 X108 4 molecules INaCl Rea sccnont é ce & 5.628 X 10°8 oe LS Sete sare atereretee ee ss fe ST 5-43 X 108 ie Cabatrotarscer ig oe Sect 5.46 X108 ss ReSg sree ee racetnve “ ee a 5.38 X108 sf Bee terciionc sete: Body-centered cube 2.86 X 10°8 2 atoms LAU crete rte eee lets Face-centered cube 4.05 X 10 8 Ata ss IN Gia Se teccraste ccvaiors Body-centered cube 4.30 X 10 8 Dee Nive ren cr oe SS ee 257 Ob eLOne Biers = Face-centered cube Bus are Lome Ane * Each atom is so nearly equal in diffracting power (atomic weight) in KCI that the apparent unit diffracting element is a cube (simple) of } this size.. Elementary body-centered cube, — atom at each corner, one in center; e.g., Fe, Ni (in art), Na, Li? Blemientary face-centered cube, — atom at each corner, one in center of each face; e.g., Cu, Ag, Au, b, Al, Ni (in part), etc. Simple cubic lattice, — atom in each corner. Double face-centered cubic or diamond lattice —C (diamond); Si, Sb, Bi, As?, Te?. t+ Diamond lattice. t Cubic-holohedral. § Cubic-pyritohedral. Metals taken from Hull, Phys. Rev. 10, p. 661, 1917 ¥ See page 543 for best values of calcite and rock-salt grating spaces. Note : — (Hull, Science 52, 227, 1920). Ca, face-centered cube, side 5.56 A, each atom 12 neighbors 3.93 A distant. Ti, centered cube, cf. Fe, side 3.14 A, 8 neighbors 2.72 A. Zn, 6 nearest neighbors in own plane. 2.67 A, 3 above, 3 below, 2.92 A. Cd, cf. Zn, 2.98 A, 3.30 A. In, face-centered tetragonal, 4 nearest 3.24 A, 4 above, 4 below, 3.33 A. Ru, cf. Zn, 2.69 A, 2.64 A. Pd, face-centered cube, side 3.92 A, 12 neighbors. 2.77 A. Ta, centered cube, side 3.27 A, 8 neighbors 2.83 A. Ir, face-centered cube, side 3.80 A, 12 neighbors, 2.69 A (A =1078 cm). Note : — (Bragg, Phil. Mag. 40, 169, 1920). Crystals empirically considered as tangent spheres of diameter in table, atom at center of sphere. When lattice known allows estimation of dimensions of crystal unit. Table foot of page 548 (atomic numbers, elements, diameter in Angstroms, 10 8 cm). SMITHSONIAN TABLES. 552 . TABLES 678 AND 679 IONIC MOBILITIES AND DIFFUSIONS The process of ionization is the removal of an electron from a neutral molecule, the molecule thus acquiring a result- ant + charge and becoming a + ion. The negative carriers in all gases at high pressures, except inert gases, consist for the most part of carriers with approximately the same mobilities as the + ions. The negative electrons must, therefore, change initially to ions by union with neutral molecules. The mobility, U, of an ion is its velocity in cm/sec. for an electrical field of one volt percm. The rates of diffusion, D, are given in cm3/sec. U = DP/Ne, where P is the pressure, V, the number of molecules per unit volume of a gas and e the electronic charge. Nature of the gas and the mobilities: (1) The mobilities are approximately proportional to the inverse sq. rts. of the molecular weights of the permanent gases; better yet when the proportionality is divided by the 4th root of the dielectric constant minus unity; (2) The ratio U +/U — seems to be greater than unity in all the more electro- negative gases. Mobilities of Gaseous Mixtures: Three types: (1) Inert gases have high mobilities; small traces of electro negative gases make values normal. (2) Mixed gases: lowering of mobilities is greater than would be expected from simple law of mixture. (3) Abnormal changes produced by addition of small quantities of electro-negative gases: e.g.: normal mobility U + =1.37. U —1.80 Wellisch, Pr. 6 mm CoH;Br gave 1.37 1.80 Roy. Soc. 82A, 6 mm CoHsl a 237, 1.80 p. 500, Igog. Iomm C2H;OH ‘* 0.91 I.10 ommC3HO “ Ts 237 Temperature Coefficient of Mobility: There is no decided change with the temperature. Pressure Coefficient of Mobility: Mobility varies inversely with the pressure in air from 100 to 1/10 atmosphere for — ion, to 4/1000, for + ion; below 1/to atmosphere all observers agree that the negative ion in air increases abnormally rapidly. Free Electrons: In pure He, Ar, and N, the negative carriers have a high mobility and are, in part at any rate, free electrons; electrons become appreciable in air at 10 cm pressure. TABLE 678.—Ionic Mobilities Mobilities. Mobilities. Sean Observer. ' ——— Observer. .000273 Nitrous oxide : ! .OO107 . 000074 Ethyl alcohol : : . 00940 . 000I00 CCla .30 3 . 00426 . 000590 Ethyl chloride Bae ; -O1550 .000540 Ethyl ether E \ .00742 .000960 | Wellisch Methyl bromide... .]| o. E .01460 .00770 Ethyl formate. .....] 0.3 : .00870 .000590 | Mean Ethyl iodide : ; — ~y cous te Oo om HOAWAT0 O Franck, Jahr. d. Rad. u. Elek. 9, p. 2, 1912; Wellisch, Pr. Roy. Soc. 82A, p 500, 1909. The following values are from Yen, Pr. Nat. Acad. 4, 19 8. SOz CsHie 2He CoH4.O | CeH;Cl CHal CoHsI -385 -451 tr. 27 TABLE 679.—Diffusion Coefficients __The following table gives the observed and computed (D = 300UP/Ne = very nearly 0.0236U) values of the diffusion coefficients. The diffusion coefficients are given for some neutral molecules as actually determined for some poe into gases of nearly equal molecular weight. Table taken from Loeb, “The Nature of the Gaseous Ion,” J. Franklin nst. 184, p. 775, 1917. D + for ions. Gas diffused Gas, diffusing. into molecules. Beyossraete botepene eevee voVs He DSL ayia pers aie a eke No ID an Seed oop eG Oo Ne ath epee eer ot N2O D natty en OnIA CO SS enccofhatades shone CO2 ANT ee A eee ererae Ethyl acetate NNN L}IT1I888sl * Or SWwBwW MOOnNWODO LUNNORHNAITUHNO | * CO2 into CO. + Ethyl formate. } Estimated. ¢ SMITHSONIAN TABLES TABLES 680-682 553 COLLOIDS TABLE 680.—General Properties of Colloids For methods of preparing colloids, see The Physical Properties of Colloidal Solutions, Burton, 1916; for general properties, see Outlines of Colloidal Chemistry, Journ. Franklin Inst. 185, p. 1, 1918 (con- tains bibliography). The colloidal phase is conditioned by sufficiently fine division (1x10-* to 10-7 cm). Colloids are suspensions (in gas, liquid, solid) of masses of small size capable of indefinite suspension; suspensions in water, alcohol, benzole, glycerine, are called hydrosols, alcosols, benzosols, glycerosols, respectively. The suspended mass is called the disperse phase, the medium the dispersion medium. Colloids fall into 3 quite definite classes: 1st, those consisting of extremely finely divided particles (Cu, Au, Ag, etc.) capable of more or less indefinite suspension against gravity, in equilibrium of somewhat the same aspect as the gases of the atmosphere, depending as in the Brownian movement upon the bombardment of the molecules of the medium; 2nd, those resisting precipitation (hemoglobin, etc.) probably because of charged nuclei and which may be coagulated and precipitated by the neutralization of the charges; 3rd, colloidal as distinguished from the crystalloidal condition, the colloid being very slowly diffusible and incapable (unlike crystalloids) of penetrating membranes (gelatine, silicic acid, caramel, glue, white of egg, gum, etc.). Lyophile, marked affinity between two phases. c.f., hydrophile. Lyophobe, “ S absent. c.f., hydrophobe. Smallest particle of Au observed by Zsigmody (ultramicroscope) 1.7% 10-7 cm. S i visible in ordinary microscope about 2.5X10-° cm. s & «« ~~ **ultramicroscope, with electric arc 15 X Lo-" cm. = cs ssany lcs fe with direct sunlight IX 10-7 cm. Viscosity of Lyophile Sols Gelatine 20° C., concentration I, viscosity 0.021 Silicieacid =; 1.00, ss 0.016 “e “ce “ec ; “e 2.00, “ec 0.035 TABLE 681.—Molecular Weights of Colloids Determined from freezing Determined from diffusion point Particle wt. Svedberg Gumiarabics soso eres) 1L750N | Glycogen | @162)*) . 00) 8to2s5 Egg albumen ........ 34500 Mannie acid (322)*... 2730 Tungstic acid (250)*. 1750 Hemoglobin Egg albumen 7420 Gum 1800 Phycoerthin Garamelendenrieieiericteetg 200m vAlbumose 2400 (Due to Graham) Ferric hydrate (107)*. 6000 Egg albumen 14000 Starch(G62) sic. seine 5 000 * Formula weight. TABLE 682.—Brownian Movement The Brownian movement is a microscopically observed agitation of colloidal particles. It is caused by the bom- bardment of them by the molecules of the medium and may be used to determine the value of Avogadro’s number. Perrin, Chaudesaignes, Ehrenhaft and De Broglie found, respectively, 70, 64, 63 and 64 X 10% as the value of this constant. The following table indicates the size and the dependence of this movement on the magnitude of the particles. Velocity =4 Material. Diameter | Medium. Yat xX 105 Observer. i. cm/sec. Zsigmody “ce “ce Svedberg, 1906-9 Henri, 1908 Perrin, Dabrowski, r909. Chaudesaignes, 1908. The movement varies inversely as the size of the particles; in water, particles of diameter greater than 44 show no perceptible movement; when smaller than .1, lively movement begins, while at 10 mp the trajectories amount up to 20m. MITHSONIAN TABLES. TABLES 683-685 554 COLLOIDS TABLE 683.—Adsorption of Gas by Finely Divided Particles Fine division means great surface per unit weight. All substances tend to adsorb gas at surface, the more the higher the pressure and the lower the temperature. Since different gases vary in this adsorption, fractional separation is possible. Pt black can absorb roo vols. H2, 800 vols. %2, Pd 3000 vols. Hz. In gas analysis Pd, heated to 100°, is used to remove He (higher temperature used for faster adsorption, will take more at lower temperature). Pt can dissolve several vols. of Hz, Pd. nearly roo at ordinary temperatures; but it seems probable that the bulk of the roo vols. of He taken by Pt and the 3000 by Pd must be adsorbed. In 1848 Rose found the density 21 to 22 for Pt foil, but 26 for precipitated Pt. The film of adsorbed air entirely changes the behavior of very small particles. They flow like a liquid (cf. fog). With substances like carbon black as little as 5 per cent of the bulk is C; a liter of C black may contain 2.5 liters of air. Mitscherlich calculated that when CO2 at atmospheric pressure, 12° C, is adsorbed by boxwood charcoal, it occu- pies 1/56 original vol. Apparent densities of gases adsorbed at low temperatures by cocoanut charcoal are of the same order (sometimes greater) as liquids. Cm? of Gas Adsorbed by a Cm! of Synthetic Charcoal (corrected to 0° C, 76 cm?) (Hemperl and Vater). See Langmuir, J. Am. Ch. Soc. 40, 1361, 1918; Richardson, 39, 1829, 1916. TABLE 684.— Heats of Adsorption Adsorber. Carbon disulphide. Fuller’s earth * 27.3 Bone charcoal * Loe 5 | exons Kaolin * 8. Fuller’s earth ft DO of HOD * Small calories liberated when 1 g of the adsorbent is added to a relatively large quantity of the liquid. + Volume adsorbed from saturated vapor by 1 g of fuller’s earth. Gurvich, J. Russ. Phys. Ch. Soc. 47, 805, rors. TABLE 685.—Molecular Heats of Adsorption and Liquefaction (Favre) Adsorber. Platinum Palladium (Gharcoallecnace “ce SMITHSONIAN TABLES. Molecular heats of adsorption. lique- 46200 a 18000 —_— 5900-8500 (5000) 6800-7800 6250 7100-10900 4400 faction. Adsorber. Molecular heats of lique- adsorption. faction: 10000-10900 5600 9200-10200 (3600) 15200-15800 (4000) 21000-23000 (4400) TABLES 686 AND 687 555 TABLE 686.—Transmission of Solar Radiation by Earth’s Atmosphere (Kimball, Monthly Weath. Rev., 56, 393, 1928; 58, 43, 1930.) Upper curves give transmission (sea-level) by the general scattering by dust-free moist air summed over all wave lengths (w= precipitable water in beam); lower curves, the added fractional depletion in the selectively absorbing water-vapor bands. No allowance is indicated for dust. (See also Table 767.) Air Mass. m. (Pressure-760 cm) Sk =EETS cy rere rs ys ss Atmospheric Transmission Water Vapor Absorption TABLE 687.—Ultra-Violet Solar Radiation at Earth’s Surface Average ultra-violet solar radiation of wave lengths <313 mp on the clearest days in Washington during 1930-31. Data in g-cal./cm*/min. X 10° (Coblentz, Stair, Bur. Stand- ards Journ. Research, 6, 971, 1931). 1930: 1931: Jan. Feb. Mar. Apr. May June July Aug. Sept. Oct. Nov. Dec. Jan. Feb. Qua tn= 5 10 3 12 22 35 41 42 41 33 16 2 oO ° I TOU se Il 24 37 49 58 63 63 59 50 35 21 II II 29 UTeace 23 37 49 60 70 76 76 71 61 48 32 19 22 42 12 noon 30 43 57 67 76 82 81 76 66 53 38 22 30 51 0.0008 cal./cm’/min. = 56 microwatts. Data are also given for greater elevations. At high elevations the spectrum quality of the u.-v. region is richer in the shorter wave lengths than at sea-level; but owing to sky-scattering, the total amount of u.-v. light less than 313 my at sea-level, on the clearest days, is almost as large as at high elevations. SMITHSONIAN TABLES 556 TABLES 688 AND 689 RELATIVE INTENSITY OF SOLAR RADIATION TABLE 688,— Mean intensity J for 24 hours of solar radiation on a horizontal surface at the top of tho atmosphere and the solar radiation 4, in terms of the solar radiation, 4., at earth’s mean distance from the sun. ReEvaTive MEAN VERTICAL INTENSITY ( Motion of the sun . in LATITUDE NORTH. longi- tude. 10° | 20° | 30° | 40° | 50° 70° 0.265 0.169 |0.117 |0.066 s202)h|e .200 | .150 | .100 SQOsiilns | .245 | .204 | .158 SLO ee -295 | .269 | .235 eSTOmin 329 | .320 | .302 SO a: 34 5m MeO meO ao eo2allee YG) || e852 | 35H SOM le: $334.1 2330) || 318 ; 305 | .285 | .256 261 | .225 | .183 POT |e KOA eae 175i al2Avn O72 0.268 |0.241 Average annual solar energy received per square dekameter of horizontal surface in kilowatt hours. U. S.: Lincoln, 160,906; Mt. Weather, 148,824; Washington, 145,403; New York, 106,460; Chicago, 97,856. Other countries: Toronto, 139,523; Johannesburg, 175,696; Davos Platz, 174,043; So. Ken- sington, 78,569; Stockholm, 79,267. (Kimball, Monthly Wea.her Rev., Apr. 1927.) TABLE 689.—Mean Monthly and Yearly Temperatures Mean temperatures of a few selected American stations, also of a station of very high, two of very low temperature, and one of very great and one of very small range of temperature. Jan. | Feb. | Mar.| Apr. | May. | une.| July. | Aug. | Sept.| Oct. | Nov.| Dec. | Year | es he ol ° 1 Hebron-Rama (Labr.)]—20.7|—20.9|—15.6|— 6.9|-+ 0.2\+ 4.5 i 7-6|+ 8.0|-+ 4.5|— 0.8|— 6.2 —16.2|— 5.2 2 Winnipeg (Canada) .|—21.6|—18.8|—11.0|++ 1.9|-+10.9+17-1|--18.9|-+17.6|+11-6|-+ 4.1/— 7-6|—15.7|-+ 0.6 3 Montreal . : .|—10.9/— 9.1/— 4.3|+ 4.8 +12.6/--18.3 +20.5|+19.3 pz 7.8|— 0.2|— 7.1/5.5 4 Boston : 6 .|— 2.8/— 2.2|-+ 1.2/-+ 7.3 13-6 + 19.1 +21.8|-+20.6 16.9|-F11.1|-- 4-8|— 0.5|+ 9.2 | 5 Chicago . , .|— 4.8/— 2.9|-+ 1.2|-+ 7.9|+-13.4|+19.7|-+22.2|+21.6 17-9) Itt + 3.6\— 1.5\+ 9.1 6 Denver : ' -|— 2.1|-+ 0.1/4 3.8/4 8.3|-+13.6|+19.1 +22.1/+21.2 +16.6)-+30.3/+- 3.3 0.0 -+ 9.7 7 Washington . «| 0.7/-+ 2.1\+ 5 2|+11.7|-+17.7/-4-22.9|+24.9|+23.7|+19-9|+13.4/+ 6.9|-+ 2.3|4+12.6 8 Pikes Peak. 5 .|—16.4|—15.6|—13.4|—10.4|— §.3|-+ 0.4/+ 4.5/4 3.6|— 0.3|— 5.8)—-11.8|—-14.4|—— 7-1 g St. Louis. c .|— 0.8) 1.7/-+ 6.2|-13.4|+18.8)+-24.0 +26.0|-+-24.9/--20.8 14.2 6.4|+ 2.0-+13.1 1o San Francisco. : +-10.1|-F10.9 +12.0|/+12.6|+13.7/+14.7 114.6/714.8 +15.8/--15.2|--13.5|--10.8 13.2 rr Yuma . ; : -|tr2.3)-+14.9/-+18.1|+21.0)-+25.1/+-29.4 +33-1|-32.6 129-1) 7-22.8)+-16.6|+-13.3 +22.3 12 New Orleans. . | 412.1|+14.5|+16.7|4+20.6|-+-23.7/+26.8 +27.9|+-27-5|+25-7|+21.0 +15.9|\-+13.1\-+20.4 |13 Massaua . : .| +25.6|+-26.0|-+-27.1|-+-29.0/-+31.1 +33-5|+34.8|-+34.7|+33-3|--31-7|1-29-0 +27.0-+30.3 14 Ft. Conger (Greenl’d) |—39.0|—40. 1|—33.5| —25.3|—10.0 + 0.4|+- 2.8/4 1.0|— 9.0|—22.7|—30.9|—33.4|——20.0 15 Werchojansk «| —51.0|—45.3|—32.5|—13-7|- 2.0|--12.3 +15.5|--10.1|-+ 2.5|—15.0|—37.8|—47.0|— 16.7 16 Batavia : ; .|+25.3) +25 4/+25.8|+26.3|+26.4/+26.0 Gh25-7|128-9)71- 26-3) 20-4) -1-20:2 125.6-125.9 | Lat., Long., Alt. respectively: (1) + 58°.5, 639.0 W, —; (2) +.49.9, 97.1 W, 233m. ; (3) +45.5, 73-6 W, 57m.; ) + 42.3, 71.1 W, 38m.; (5) + 41.9, 87-6 W, 251m.; (6) +39.7, 105.0 W, 1613m.; (7) +38.9, 77.0 W, 34m.; (8) 8.8, 105.0 W, 4308m.; (9) + 38.6, go.2 Ww, 173m.; (10) +37.8, 122.5 W, 47m.; (11) +32.75 114.6 W, 43m. ; + 30.0, go.1 W, 16m.; (13) + 15.6, 37-5 E, 9m.; (14) +81-7, 64.7 W.,—} (15) +67.6, 133.8 E, 140m.; (16) —6.2, 8 E, 7m. Taken from Hann’s Lehrbuch der Meteorologie, 2’nd edition, which see for further data. Note: Highest recorded temperature in world = 57° C in Death Valley, California, July 10, 1913. Lowest recorded temperature in world = —68° C at Verkhoyansk, Feb. 1892. SMITHSONIAN TABLES. TABLES 690 AND 691 557 TABLE 690.—Temperature Variation over Earth’s Surface (Hann) Temperatures ° C Latitude. | July. Oct. North pole +80° 70 60 50 40 30 20 +10 Equator —I0 20 30 40 50 60 70 OOHHOO HwWOUNKHORO ° ° . . . . . Sy COMO OINO FH ONIOCWWHO PUWOOANNHHHD WOUO ODADOKROP ONW OW HOON Hy 3 Od 63:61 0 OOM to Oo HINO) Goma wa Noo ~ = . a 2, 2s 2, i © =F TC -9°CN OC ie 4 278%, SCP tem | 28005 ao as . 3 O74 C78 > Ke 2 wa oie =< ne \ - 2E9°A. 290 29 LECT aPC. “ = 2859 07 0-*—o—0o SCONL _ LoSL N “4 ae COT. 289 “4 ow oN. eri ie 2939 2915 “9 | s-+ Joo”? = » | ae 2a/0°C\ ye ¢ ¢ 0 0 29999 29997 T= Lem 4) IC ° ' oO (aes ¢ i o” we = e—9_1iN ft Oo XN ELLENORLE GROESBECK GROESBECK ELLENDALE OREXEL BROKEN ARROW BROKEN ARROW DREXEL SUMMER WINTER TABLE 702.—Seasonal Variation of Tropopause at Agra and Batavia Jan. Feb. Mar. Apr. May June July Aug. Sept. Oct. Nov. Dec. Batavia °K. 184 185 186 187 188 1092 193 194 193 I90 187 184 Agra 203 203 203 203 200 195 193 193 193 194 200 204 TABLE 703.—Seasonal Variation Height of Tropopause over Batavia (km) (Bemmelen, Proc. Roy. Acad. Amsterdam, 20., 1313.) Jan. Feb. Mar. Apr. May June July Aug. Sept. Oct. Nov. Dec. 17.8 4A7.6 2 173 997.0. “16:5 “16S; MoO 16:5 - T7207. TA 1716) “a7 *In the Figure, °A is used equivalent to °K. SMITHSONIAN TABLES TABLES 704 AND 705 563 THE EARTH’S ATMOSPHERE TABLE 704.—Atmospheric Ozone This table shows the variation of atmospheric ozone (layer about 40 to 50 km above the earth’s surface), with latitude and time of the year, from measures in long-wave portions of Hartley ultra-violet band 0.230 to 0.310 », by Doctor Dobson and his associates (Proc. Roy. Soc. 110A, 660, 1926 and 122A, 456, 1929); prepared partly from unpublished data. Measures are in cm of ozone at n. t. p. As only one year’s observations are available for most stations these figures must be regarded as approximate. Latitude Jan. May July Sept. Nov. 60°N. 0.305 0.350 0.285 0.250 0.255 40 N. .260 .280 270 .250 225 .220 20 N. .205 .220 .225 .220 .205 -200 oO .I90 195 -200 -205 205 .200 20K: 210 -205 -210 215 -220 220 40 S. .240 -230 .250 .290 310 .280 Values are very steady from day to day in equatorial regions; in temperate latitudes large variations occur (up to 0.1 cm) which are apparently associated with meteoro- logical conditions (Dobson). TABLE 705.—Mean Free Path, Air Molecules (Mavis, Terr. Mag., 1928-20.) Values of mean free path, X, of air molecules, at different heights, for the density condi- tions of Table 697, col. 9. Winter Night 6.04 X 10° 1.09) X 104 2.48 X 1073 5.02 X 107% 9.41 X 107% 1.95 3.81 X 10? Te1OL XX LOS Teo hOe 2225 Xl Oe 2.65 X 107 SMITHSONIAN TABLES 564 TABLE 706 ACCELERATION OF GRAVITY For Sea-Level and Different Altitudes Calculated from U. S. Coast and Geodetic Survey formula, p. 134 of Special Publication No. 40 of that Bureau, g = 9.78039 (1 + 0.005294 sin? @ — 0.000007 sin? 2) m & = 32 08783 (1 +: 0.005294 sin? @ — 0.000007 sin? 2) ft. g Latitude g g ft./sec? p cm/sec? log g ft. /sec2 Latitude ? 978. -9903562 32.0878 981. -9Q17004 .1873 9903735 . 0891 : - 9917394 . 1902 9904254 -0929 : -9917784 1931 -9904552 .OQ51 ; - 9918177 1960 -9904898 0977 ‘ -9918558 .1988 -9905004 .OQQI ; . 9918934 . 2016 -9905298 . 1007 ‘ - 9919310 2044 -9905520 . 1023 2 - 99196077 . 2071 -9905759 . 1040 3 . 9920040 2008 -9905985 -1057 : - 9920403 .2125 . 9906234 .1076 F -9Q920752 . 2151 - 9906500 . 1095 é - 9921073 . 2176 -9906775 . 1116 : .9921424 . 2201 -9907050 .1136 3 - 9921756 .2225 -9907348 .1158 4 : - 9922079 . 2249 -9907649 - 1180 : - 9922388 32.2272 . 9907960 . 1203 : - 9922689 . 2205 - 9908275 .1227 z -9922981 . 2316 - 9908603 .1251 é -9923268 . 2338 .9908940 .1276 ; -9923542 - 2358 .9909286 . 1302 : - 9923803 - 2377 - 9909632 1327 . 9924055 - 2306 9900087 -1353 . -9924208 - 2414 - 9910350 .1380 : - 9924528 - 2431 .9910718 . 1407 $ - 9924749 - 2448 - 991095 -1435 : 9924052 . 2463 .QOII472 .1463 . -9925147 -2477 -9911853 - 1491 _ - 9925332 . 2491 -9912238 .1520 Z -9925500 - 2503 -9912628 -1540 : -99256055 .2515 .9913018 .1578 : -9925706 .2525 9913417 . 1607 : -9925029 2535 .9O13812 - 1636 3 -9926043 - 2544 - 9914210 . 1666 : -9926149 -2552 - 9914613 . 1696 : -9926242 -2558 -QQIS5OIL .1725 j - 9926321 . 2564 9915410 -1755 : - 9926379 2569 -QQIs814 .1785 : - 9926432 .2572 -9Q16212 1814 e - 9926467 “2575 . 9916606 .1844 j -9926404 -2577 To reduce log g (cm. per sec. per sec.) to log g (ft. per sec. per sec.) add log 0.03280833 = 8.5159842 — Io. The standard value of gravity, used in barometer reductions, etc., is 980.665. It was adopted by the International Committee on Weights and Measures in 1901. It corresponds nearly to latitude 45° and sea-level. FREE-AIR CORRECTION FOR ALTITUDE —0. 0003086 cm/sec?/m when altitude is in meters. —o.000003086 {t/sec?/ft when altitude is in feet. | . ; Altitude. Correction. Altitude. Correction. —o.0617 cm/sec? 200 ft. —o.000617 ft./sec? .0926 300 . 000926 .1234 400 . 001234 .1543 500 - 001543 .1852 600 001852 . 2100 700 .002160 . 2469 800 .002469 2777 goo 002777 SMITHSONIAN TABLES. TABLE 707 565 ACCELERATION OF GRAVITY, VARIOUS WORLD STATIONS The following more recent gravity determinations (Potsdam System) serve to show the accuracy which may be assumed for the values in Table 706, except for the three stations in the Arctic Ocean. The error in the observed gravity is probably not greater than o.o10 cm/sec?, as the observations were made with the half-second invariable pendulum, using modern methods. In recent years the Coast and Geodetic Survey has corrected the computed value of gravity for the effect of ma- terial above sea-level, the deficiency of matter in the oceans, the deficiency of density in the material below sea-level under the continents and the excess of density in the earth’s crust under the ocean, in addition to the reduction for elevation. Such corrections make the computed values agree more closely with those observed. See special publica- tion No. 40 of the U. S. Coast and Geodetic Survey entitled, “Investigations of Gravity and Isostasy,”’ by William Bowie, 1917; also Special Publication No. 1o of same bureau entitled, ‘‘ Effect of Topography and Isostatic Compen- sation upon the Intensity of Gravity,” by J. F. Hayford and William Bowie, 1912. Gravity, cm/sec? Elevation, Latitude. ae A Reduced to Observed. cealevell 7.645 978.366 ; -735 -427 Madras, India 3 6 .279 . 281 Jamestown, St. Helena 5 712 -715 Cuttack, India .659 978.668 Amraoti, India f 8.609 714 Jubbulpur, India -719 .856 Gaya, India 884 .g18 Siliguri, India 2 . 887 -923 Kuhrja, India .082 .143 Galveston, Texas 272 -273 Rajpur, India .002 Pains Alexandria, La 24200 -436 St. Georges, Bermuda . 806 .807 McCormick, S. C .624 .674 Shamrock, Texas e ST 705 Cloudland, Tenn 383 966 Mount Hamilton, Cal . 660 .056 Kala-i-Chumb, Turkestan 462 .877 Denver, Col . 609 .1T4 Hachinohe, Japan -359 -365 Chicago, Ill .278 334 Albany, N. Y -344 363 Florence, Italy - 491 -548 Minneapolis, Minn 597 676 Simplon Hospice, Switzerland............. . 202 .819 Fort Kent, Me 5 . 765 .814 Sandpoint, Idaho 680 877 Medicine Hat, Canada . 865 .070 Field, Canada -745 .127 Magleby , Denmark . 502 81.506 Copenhagen, Denmark ‘ -559 563 St. Paul Island, Alaska .726 729 Fredericksvarn, Norway : .874 877 Christiania, Norway -927 936 Ashe Inlet, Hudson Strait 105 .110 St. Michael, Alaska -192 .192 Hatnarfjordr, Iceland . 266 . 267 Niantilik, Cumberland Sound 273 275 Glaesibaer, Iceland ; .342 345 Sorvagen, N. .622 628 Umanak, Greenland d - 590 -593 Danes Island, Spitzbergen .078 .079 Arctic Sea . 109 -109 Arctic Sea -174 174 Arctic Sea aT5s -155 HH HHWNHWOHNWD HAHN HHNNNHNNHNNNNHNDNDNHNHNNHNNNNNNHDNHNNNNDNDDN HE References: (1) Report 16th General Conference International Geodetic Association, London and Cambridge, 1909, 3d Vol. by Dr. E. Borrass, 1911; (2) U.S. Coast and Geodetic Survey, Special Publ. No. 40; * (3) U.S. Coast and Geodetic Survey, Report for 1897, Appendix 6.* * For references (2) and (3), values were derived from comparative experiments with invariable pendulums, the value for Washington being taken as 980.112. For the latter, Appendix 5 of the Coast and Geodetic Survey Report for 1901, and pages 25 and 244 of the 3d vol. by Dr. E. Borrdss in 1or11 of the Report of the 16th General Conference of the Intern. Geodetic Association, London and Cambridge, 1909. As a result of the adjustment of the net of gravity base stations throughout the world by the Central Bureau of the Intern. Geodetic Association, the value of the Wash- ington base station was changed to 980.112. SMITHSONIAN TABLES. 566 TABLE 708 ACCELERATION OF GRAVITY (g) IN THE UNITED STATES The following table is abridged from one for 219 stations given on pp. 50 to 52, Special Publication No. 40, U. S. Coast and Geodetic Survey. The observed values depend on relative determinations and on adopted value of 980.112 for Washington (Coast and Geodetic Survey Office, see footnote, Table 707). There are also given terms necessary in reducing the theoretical value (Table 565) to the proper elevation (free-air) and to allow for topography and isostatic compensation by the Hayford method (see introductory note to Table 707). : ; To a certain extent, the greater the bulk of material below any station, the less its average density. This phenomenon is known as isostatic compensation. The depth below sea-level to which this compensation extends is about 96 km. Below this depth any mass element is subject to equal (fluid) pressure from all directions. Correction. Eleva- | Observed Station. Latitude. Longitude. tion, g Topography meters. | cm/sec? | Elevation, | and com- cm/sec? pensation, Key West, Fla New Orleans, La Austin, Tex. university BP aso hexseeericn cetera Yuma, Ariz @harlestonsiS: Cijencee anit Birmingham, Ala Arkansas City, Ark Atlanta, Ga. capitol Beaufort, N. C Little Rock, Ark Memphis, Tenn Charlotte, N. C asi Vegas Ne Mex.) near Knoxville, Tenn Grand Canyon, Ariz Cloudland, Tenn Mount Hamilton, Cal., Obs’y. Richmond, Va Sane rancisco, ales sn aetee St. Louis, Mo., university... . Pike’s Peak, Col Colorado Springs, Col........ Washington, D. C., Bur. St’ds. Wallace, Kans Green River, Utah Cincinnati, Ohio, obs’y...... Baltimore, Md., university. . . Terre Hautewindss ss ssn Denver, Col., university obs’y. Philadelphia, Pa., university. . Wheeling, W. Va Princeton, N. J Pittsburg, Pa Salt Lake City, Utah New York, N. Y., university. Winnemucca, Nev Cleveland, Ohio Chicago, Ill., university...... Worcester, Mass Cambridge, Mass. observatory Ithaca, N. Y., university.... Fort Dodge, Iowa Grand Rapids, Mich Madison, Wis., university... . Boise, Idaho Mitchell, S. Dak. university. . Wancaster Ne Hunger Grand Canyon, Wyo......... Minneapolis, Minn Calais, Me Miles City, Mont Seattle, Wash. university. ... Pembina, N. Dak H oo ‘o H OW f OW COOOKHKE Bla latet tal eect ctatstatat st lst atest tyb stated tal be) BO BO) 0 OOP 0 COU HH DOW CAN IO KHWHWOROOONRIH DRO I+ o. eas SUAS Vettel latcar ah atiet ae Ow SMITHSONIAN TABLES. TABLE 709 567 SOME PLACES OF ANOMALOUS GRAVITY With their longitudes, latitudes, and heights above sea-level (See Borrass, Verh. 16 allgem. Konferenz der Intern. Erdmessung, Berlin, 1911, 1914. The departures are from the values of gravity normally expected from Table 706.) Altitude Departure : above Gravity from Latitude sea-level cm/sec.2 value m of table Longitude east of Greenwich / 14 59-9 2943 979.350 +287 Etna 43.8 10 978.682 +260 St. Helena 51.8 4 978.960 +243 Honolulu 8 2877 979-779 +233 Pic du Midi 14.4 II 979.431 +223 Santa Cruz 52 4807 979.401 +188 Mont Blanc 27.9 3 2346 977-645 +164 Kodaikanal 4.5 978.520 +155 Fort de France 4 20.6 : 19 980.118 +152 Ponta Delgada 37 2 1140 981.015 +136 4.7 43 980.065 +-127 Catania 56.6 35 980.348 Ischia 44.6 1604 980.761 Schneekoppe 4 978.756 Santiago de Cuba 2825 977.281 Quito 50.8 104 980.270 Fukuoka 1282 979.648 Lick Observatory 33 980.109 5 980.111 Messina 27. 982.114 1050 980.323 49 980.802 176 980.562 Milan-Brera 478 980.082 Tashkent 56 981.697 Tobolsk 683 979.065 Dehra-Dun 576 980.570 Innsbruck —26 980.280 Derbent 58 979.378 Perth 26 980.441 Forli 979.131 Roorkee 980.726 Seattle 51 980.450 Bologna 82 978.924 SMITHSONIAN TABLES 568 TABLES 710 AND 711 TABLE 710.—Length of Seconds Pendulum at Sea-Level and for Different Latitudes Length in inches. Length Log. in Log. inches. Length in cm 99.0961 | 1.996056 | 39.0141 . 591222 1.997401 | 39.1351 - 592566 . 1000 .996074 .O157 - 5912390 : -997594 -1525 - 592760 .IIIQ .996126 .0204 - 591292 - -997770 - 1689 - 592041 .1310 -996210 .0©279 + 591375 5 -997939 . 1836 - 593104 570 - 996324 .0382 «591490 : - 998081 . 1964 - 593246 . 1894 -996465 .0509 - 591031 S - 998196 . 2068 «593301 . 2268 .996629 .0056 - 591794 A - 998280 . 2144 - 593446 . 2081 .996810 .o819 - 591976 5 , - 998332 . 2191 - 593498 . 3121 -997002 .0992 - 592168 : - 998350 . 2207 - 593515 -3577 997201 -I171 - 592367 == Calculated from Table 706 by the formula / = g/m?. For each 100 ft. of elevation subtract 0.000953 cm Of 0.000375 in. or 0.0000313 ft. This table could also have been computed by either of the following formu- lae derived from the gravity formula at the top of Table 706. ©.990961(1 + 0 005294 sin? — 0.000007 sin?2@) meters 0.990961 + 0.005246 sin? — 0.000007 sin?2@ meters 39.014135(1 + 0.005294 sin? — 0.000007 sin?2@) inches 39.014135 + 0.206535 sin? — 0.000276 sin?2q@ inches TABLE 711.—Miscellaneous Geodetic Data (Replaced by Table 716) SMITHSONIAN TABLES- TABLES 712-715 569 TABLE 712.—Miscellaneous Geographical Data (see page 650) (The data on this page were compiled by R. W. Goranson, Geophysical Laboratory, Carnegie Institution, 1930.) Land area, 148,847,000 km?; Ocean area, 361,254,000 km?. Mean elevation land above sea-level, 825 m. Mean depth oceans, 3,680 m. Highest known mountain, Mt. Everest, India, 87° E., 28° N., 8840 meters. Greatest known sea-depths: Mindanao deep 10,430 meters, <10° N., 127° E.; Puerto Rico deep 8,525 meters, 19°35’ N., 67°43’ W. hermal gradient: Not well-known; from Van Orstrand’s data average is 30°C per km depth but may be very different; variations observed are from 9 (Johannesburg, S. Africa) to 54 (Queensland) degrees C per km depth. Max. depth measured, 2,286 m. TABLE 713.—Densities and Pressures of Earth’s Interior Density Pressure Rock type 2.7 g/cm? Granitic 2.7 0.0027 X 108kg/cm? .0067 Basaltic .OI7I Peridotitic .0381 131 .30 “47 .68 .84 1.135 Tes Transition layer 17 2.8 Ni-Fe core 2.0 (Below 800 km, due to Adams, Williamson.) TABLE 714.—Velocities of Earthquake Waves V, is the velocity in km/sec. of the primary or condensational wave, V., of the secondary or distortional wave. Turner speaks of them as the push and shake waves. Layer: Vy, km/sec. V., km/sec. o to 20 + 10 km depth, depending on | 5.4 to 5.6, depending on locality. locality May reach 6.1 20 + 10 to 45 + 10 km depth, 6.25 to 6.75*, depending on depending on locality locality Between 45 + 10 and 2900 km depth: 45 +10 8.0 + 0.1 1300 12.5 + 2400 13.5 + <2900 3315p Core, 2700 to 6370 km (center): > 2900 Sime 6000 10.9 + * B. Gutenberg, H. Jeffreys, K. Suda, A. and S. Mohorovicic, V. Conrad. TABLE 715.—Elastic Constants of Earth’s Interior Bulk modulus Rigidity Bulk modulus Rigidity < 10-12 > 4 Io-12 >< 10-12 x Io-1l2 dynes/cm2 dynes/cm2 dynes /cm2 dynes/cm2?2 2.2 + 0.3 Defeat 4.0 + I.0 Smaller than at surface, perhaps zero. SMITHSONIAN TABLES 570 TABLE 716 MISCELLANEOUS GEOPHYSICAL DATA Equatorial radius of earth, a, 6,378,388 m + 18. Ellipticity, flattening, (a-b)/a, 1/297 or 0.003,367,003,4. (Adopted at International Geodetic and Geophysical Union, 1924.) Polar radius, b, 6,356,911.946 m. Square of the eccentricity, e*, or (a°-b*)/a’, 0.006,722,670,0. Quadrant of equator, 10,010,148.4 m; ditto of meridian, 10,002,288.3 m. Area of ellipsoid, 510,100,934 km*; volume of ditto, 1,083,319,780,000 km*. Radius of sphere having same area, 6,371,227.7 m. Radius of sphere having same volume, 6,371,221.3 m. Difference between geographical latitude, @, and geocentric latitude: ®’. & — & = 6056635 sin 26 — 171731 sin4g® + 070026 sin 6® = 6956635 sin 28’ + 171731 sin 4#/ + 00026 sin 6%" Newtonian constant of gravitation, G, (6.664 + 0.002) X 10° dyne cm*g” (Heyl). Mean density of the earth, 5.522 (Lambert). Continental surface density of the earth, 2.67. } Mean density outer 10 miles of crust, 2.40. (Harkness. ) Rigidity, u, 8.6 X 10” c.g.s. units. Michelson, Astrophys. Journ., Viscosity, 10.9 X 10” c.g.s. units (comparable to steel). 39, 105, 1914. Moments of inertia of the earth, the principal moments being taken as 4, B, and C, and C the greatest (De Sitter, 1924) : A = B=0'33235 < Ea: C= 0.33344 X Ea’ C — A =0.0010921 X Ea’. (C — A)/C = 0.0032774, from precession. Mass of the earth = E = 5.983 X 10% kg; a= equatorial semidiameter. Formulae for theoretical gravity at the surface of the ellipsoid (which is assumed to be an equipotential surface) : Y = ve (1 + 0.005288 sin® — 0.000006 sin* 2&) cm/sec’. = ;(1 + 0.002637 cos’ + 0.000006 cos*2®) cm/sec”. ‘Ye = sea-level gravity at equator yss = sea-level gravity at lat. 45° = 978.038 cm/sec”. Bowie * == 980.621 cm/sec’. Bowie .052 Helmert .629 Helmert .052 Heiskanen .630 Heiskanen There is a systematic difference between gravity determinations over land or over sea, the latter being greater; this leads Bowie to favor a value of 978.52 = .oo8 for the value above. This systematic difference has led to the formula: g = 978.0524 1 + 0.005288 sin’ ¢ — 0.000006 sin* 2 + 0.000023 cos’ cos 2(X + 5°) f, where \ = east longitude. This longitude term has appeared to be indicated by the results of several observers.—Clarke, 1878, Helmert, 1915, and Heiskanen, 1928. It could be taken as indicating that the earth had three unequal axes, Mean linear velocity of the earth in its orbit, 29.77 km/sec. Mean linear velocity of rotation of earth at equator, 0.465 km/sec. Rotational energy lost by tidal friction, 1.1 < 10” erg/sec. (Jeffreys). Angular velocity of rotation, 72.921 X 10° radians/mean-solar-second. Rotational energy, 2.160 X Io” ergs/sec. (See Lambert, Science, 63, 242, Mar, 5, 1926; Journ. Wash. Acad. Sci., 18, 571, 1928.) SMITHSONIAN TABLES TABLES 717 AND 718 571 TABLE 717.—Age of Earth, Moon, and Strata (See The Earth, by Jeffreys, 1920.) The age of the earth is probably from (1.3 to 3) X 10° years (radioactive data). Its liquefaction was probably complete within 5000 years, solidification within 15,000 years from start. The age of the earth’s crust may be taken as roughly 2000 million years. AGES OF GEOLOGIC STRATA Late Oligocene 37,000,000 yrs. Late pre-Cambrian(?) . 587,000,000 yrs. Cretaceous (?)... 59,000,000 “ Upper pre-Cambrian .. 640,000,000 “e “ce Permian-Carboniferous . 204,000,000 “ Middle pre-Cambrian .. 987,000,000 to Permian to Devonian... 239,000,000 to 1,087,000,000 yrs. 374,000,000 yrs. Lower pre-Cambrian ..1,257,000,000 “ Note (Science 73 (Suppl.), 10, Mar. 13, 1931): An age of the earth of at least 2,000,000,000 years was adopted by a committee (Kovarik, Holmes, Knopf, Brown, Lane) appointed by the National Research Council; the age of the oldest rock, a uranite from Sinyaya Palo, Carelia, Russia, 1,852,000,000,_- TABLE 718(a).—Geologic Age Determinations Based on the Lead Method (Knopf, Nat. Res. Council Bull. 80, 1931.) Age (Millions of years) Based on Based on Tu =4.56X 10? Tu=4.56 109 Geologic age. Mineral. Locality. Tth =1.28xX10!° = Tpn=1.65 Xx 102° Paleozoic; Devonian or Thorite Norway 310 Carboniferous. Latest Cambrian Pre-Cambrian Bréggerite ..Norway 910 Pre-Cambrian Cleveite Norway 96 964 Pre-Cambrian Cleveite Norway 065 Pre-Cambrian Uraninite) .. 29: Dakota =o. 1,462 Pre-Cambrian Uraninite ... Russia 1,852 TABLE 718(b).—The Age of the Earth (Taken from Nat. Res. Council Bull. 80, 1931.) Radioactive disintegration presents the only reliable measure. No trace of a beginning can yet be found. ‘“ The oldest rocks have everywhere been made from preexisting and therefore still older materials of which no other relics now survive. .... The earth is older than the oldest granitic intrusion. It is impossible with the data available to know whether the highest reliable lead ratio so far obtained (Keystone uraninite, Black Hills, S. Dak.) represents the oldest granitic rocks. Accepting a ratio of 0.216 as an index of its age this is 1460 million years old. Before the oldest granites were intruded into the crust at least one cycle of denudation and sedimentation occurred indicated by the rocks into which the granites were injected. To the 1460 we should add perhaps 140, giving as the age some 1600 million years, as indicated by above mean. An upper limit assuming all rock lead of radioactive origin is 1600 million. The estimate of the total life of the earth (Russell, Holmes, loc. cit. p. 8) is some 3000 million years. Strata accumulated: Max. since beginning of Cambrian from America data—260,000 ft. ; 111,000 of this deposited during Paleozoic time, 86 are Mesozoic, 61,000 during Cenozoic. SMITHSONIAN TABLES ne TABLE 719 GEOCHEMICAL DATA Eighty-three chemical elements (86 including Po, Ac and UrX,) are found on the earth. Besides the eight occur- ring uncombined as gases, 23 may be found native, Sb, As, Bi, C, Cu, Au, Ir, Fe, Pb?, Hg, Ni, Os, Pd, Pt, Kh, Ru, Sz, Ag, S, Ta?, Te, Sn?, Zn?. Combined the elements form about 1ooo known mineral species. Rocks are in general aggregates of these species. Some few (e. g., quartzite, limestone, etc.) consist of one specie. We have some knowl- edge of the earth to a depth of to miles. This portion may be divided into three parts: the innermost of crystalline or plutonic rocks, the middle, of sedimentary or fragmentary rocks, the outer of clays, gravels, etc. 93% of it is solid mat- ter, 7% liquid, and the atmosphere amounts by weight to 0.03% of it. Besides the g major constituents of igneous rock (see 7th col. of table) 3 are notable by their almost universal occurrence, TiO,, P2O;, and MnO. Bo, Gl, and Sc are also widely distributed. The density of the earth as a whole is 5.52 (Burgess); continental surface, 2.67 and outer ro miles of crust, 2.40 (Harkness). Computed from average chemical composition: outer ten miles as a whole, 2.77; northern continents 2.73; southern, 2.76; Atlantic basin, 2.83; Pacific basin, 2.88. ; Data of Geochemistry, Clarke, Bul. 616, U. S. Geological Survey, 1916; Washington, J. Franklin. Inst. 190, P- 757) 1920. AVERAGE COMPOSITION OF KNOWN TERRESTRIAL MATTER. Average composition. Average composition of lithosphere. Atomic A Average | ] number Litho- | Hydro- | includ- Sa Igneous Sh 4 and sphere, | sphere, ing Compound. | rocks, element. 7% ape Sand- | Lime- stone, | stone, 70 | 0.75% | 0.257% Weighted ale, q average. he 8. ve 4. Be 2. Pe 2h °. (pet esl sh leet AVERAGE COMPOSITION OF MeETEorRITES: The following figures give in succession the element, atomic number (bracketed), and the percentage amount in stony meteorites (Merrill, Mem. Nat. Acad. Sc. 14, p. 28, 1916). The “iron” meteorites contain a much larger percentage of iron and nickel, but there is a tendency to believe that with such meteorites the composition is altered by the volatilization or burning up of the other material in passing through the air. Note the greater abundance of elements of even atomic number (97.2 per cent). O (8) S (16) Na (11) CHr(6) (a) Ru (44) SMITHSONIAN TABLES. TABLE 720 573 THE EARTH’S ROTATION: ITS VARIATION (Jeffreys, The Earth, Macmillan, 1929. Innes, Changes in the Length of the Day, Scientia, 42, 60, 1927; Brown, Nature, 119, 200, 1927; Journ. Roy. Astron. Soc. Canada, 24, 177, 1930.) From eclipses, occultations, Fotheringham (M. N., 81, 104, 1920) deduces as the best value of the apparent solar acceleration 3.0"/ (century )?; lunar 21.6’ ‘/ (century )*. Lunar theory predicts 12.2”/(century)* leaving part attributable to tidal friction 9”/(century )’. Estimates of tidal friction losses (Jeffreys, Philos. Trans. A 221, 239, 1920) : Trish Sea 0.6X to% erg /sec. So. China Sea —x 1035 erg/sec, Hudson Str. 0.2101 erg/sec. Eng. Channel 1.1 Okhotsk ee MO Ae ee ay Se ee North Sea 178 Bering SSE RC. Oe s¢ Fox Strait eben “s Yellow Sea Tree eee Mallacca Str. Te Tes os Bay Fundy Obs ES (Ee Other contributions are small. Total for spring tides 22 & 10” erg/sec. 1.1 X 10°’ erg/sec. average, corresponding to about 7” secular acceleration per century per century. If Q is earth’s angular velocity of rotation, dQ/dt=—2.5 X 10”/sec. Q=7.3 X 10°/sec. Q changes by 10” of its amount in 3 X 10” sec. or 10° years. The day should have lengthened by I sec. in 120,000 years. The fluctuations in the earth’s rate of rotation indicated by astronomical evidence are of a quite greater order of magnitude. Moreover the changes vary in sign whereas fric- tional effects should not. The observations come from deviations of the sun and moon from their gravitational orbits, the transits of Mercury, and eclipses of Jupiter’s satellites. Changes in the speed of rotation of the earth rotation seem the only explanation. This may be due to shifts of matter within or on the earth. The following figure by Brown indicates that in 1928 the earth was about 25 sec. ahead of its average rotational motion during the last three centuries. The greatest apparent change is the loss or gain of one sec. in a whole year, (I part in 30,000,000. ) TRREGULARITIES IN THE EARTH’S RoraTION DERIVED FROM THE Moon’s Motion. Tidal friction should make the earth rotate more slowly and the moon recede from the earth. The rate of dissipation of energy by friction is about 1.4 * 10” * erg/sec. The earth’s rotation from this cause should have slowed by 4 hours during geologic time. The moon should continue to recede until its period of revolution and that of the earth’s rotation are equal to 47 of our present days. The moon should then gradually approach the earth, ultimately coming within Roche’s limit (about twice the earth’s radius) breaking up possibly into a ring like Saturn’s. SMITHSONIAN TABLES 574 TABLES 721 AND 722 TABLE 721.—Tides, Sea-Level, Level Net (Nat. Res. Council Bull. 78, 1931.) Spring tides: When moon (new or full) is in line with sun (large). Neap tide: When moon is in quadrature with sun (small). Generally two high and two low each day. Variation in heights of two high and two low = “ diurnal inequality.” River type tide, steep short period graph for flood, more inclined and longer for ebb. Extreme case = “bore,” tide rises so rapidly it assumes form of wall several feet high. Most famous bores, Tsientang Kiang, China; Turnagain Arm, Alaska; Severn and the Wye, England; Seine in France; Hoogly, India; Petitcodiac, Canada. Mean sea-level (geodetic): The equipotential surface which the oceans would assume if undisturbed by the tides and effects of wind and weather. Starting with mean sea-level at any given initial point the geodesist can determine by precise spirit leveling, the equipotential surface. Mean sea-level (geographic): Determined by averaging actual tidal heights over a sufficient period. It is a local or geographic value. It is much disturbed by prevalent winds and local contours. Note difference between average of hourly readings (mean sea-level) and half-tide point (because of the shape of thé tide height as related to time). On Atlantic coast 4 tide level lies below mean by about I/10 ft.; on Pacific above by 1/20 ft. Mean tide near rivers varies with rainfall. Nineteen years’ observation used for full tide cycle. A fundamental level net has been connected with mean sea-level at Portland, Me., via Boston, Mass., Ft. Hamilton, N. Y., Sandy Hook and Atlantic City, N. J., Old Point Comfort and Norfolk, Wak: Brunswick, Ga., Fernandina, St. Augustine, and Cedar Keys, Fla., Biloxi, Miss., Galveston, Tex., San Diego, San Pedro, San Francisco, Calif., Ft. Stevens, Oreg., and Seattle, Wash. The accuracy of high precision leveling is measured by the correction necessary to close circuits, about 0.00063 foot/mile. Mean sea-level differences: Portland 16.94 cm higher than Ft. Hamilton. Vancouver 10.28 cm higher than Seattle. Galveston 24 cm higher than St. Augustine. San Diego 40 cm higher than Galveston. Fort Stevens 79 cm higher than San Diego. Isthmus Panama, Pacific coast 20 cm higher than Atlantic. Peat Valley is 276 ft. (84.1 m) below sea-level, Mount Whitney 14,406 ft. (4418.4 m) above TABLE 722.—Magnetic and Electric Data for Sun and Earth (Chapman, Cosmical magnetic phenomena, Nature, 124, 19, 1929.) Sun’s magnetic field too small to be measured by direct effects on earth; measured by Zeeman effect on spectrum lines. Earth’s magnetic axis inclined 12° to rotation axis. Sun’s magnetic axis inclined 4° to rotation axis. Polarity of both same relation to direction of rotation. Earth’s field rotates at same speed as nearly rigid earth. Sun’s field and magnetic axis rotate more slowly than solar surface (31, 26 days, respectively ). Earth: Polar intensity of field 3 gauss. Sun: Estimated 50 gauss in reversing layer. Intense local fields frequent, 3000 gauss. The magnetic field of spots reverses each cycle (Proc. Astron. Soc. Pacific, 41, 136, 1920). The polarity of leading spot in a bipolar group in N. hemisphere is opposite that in the S. hemisphere—relationship reverses each new sun-spot cycle -’. complete magnetic cycle is double sun-spot cycle. Specific resistances: Earth Sun (Chapman loc. cit.) Heaviside layer, 10° Reversing layer, 3 X 10” Dry earth, 10° to 10° + Photosphere, 10°, 7, 10000° K. Sea water, 2 xaOws Center, 3X 10> fA x TOs 200-600 m deep, 3 X 10” Drift currents in sun, + ions easterly. Further characteristics of spots: (Milne, M. N. 90, 487, 1930; Russell.) Umbra (dark center), 800 (very small) to 80,000 km across: penumbra may reach 240,000 km. Gen- erally short-lived. A few last several (3) rotations, very rarely 6; one in 1840, 18 months. Most occur in 2 belts 5° to 4o° N. and S. latitudes, often occur in pairs (see above). Umbra temperature 4ooo° K. Evershed gives velocity of outburst from spot 2 km/sec. SMITHSONIAN TABLES TABLES 723-738 575 TERRESTRIAL MAGNETISM TABLE 723.—Magnetic Constants of the Earth (Prepared by J. A. Fleming, Department of Terrestrial Magnetism, Carnegie Institution of Washington. ) If V be the magnetic potential of the earth, then V/R=Zcm"Pm" sin ¢ cos (mdr + am”) where = earth’s mean radius (6.37 X 10°cm), ¢ = latitude, X= east longitude, » varies from I to », and m from 0 to n. The field-components of total intensity F designated, X positive towards geographic north, Y positive towards geographic east, and Z positive towards nadir, are V X= —(1/R) () = — em" (OPm"/O¢) cos (md + am”) Y=-— (1/R cos ¢) (OV/OX)=(1/cos ¢) Zmem"Pm” sin (md + am”) Z=—=(n+1)cem"Pm”" cos (mdr + am”) Tuy AY Bauer (Terr. Mag., 28, 1-28, 1923) made an analysis based on the latest values of the magnetic elements, epoch 1922, between the parallels 60° N. and 60° S. He found the following for the uniform portion of the earth’s X, Y, and Z magnetic systems: Epoch saa c.g.s. units. Quantity x M/R* -- 31626 + . 30699 Mp/R +. 30992 + .30084 Me/R® + .06303 : + .06113 where M is the earth’s moment, and Mp and Me are its axial and equatorial components. For the same date Bauer deduced the following values in magnetic units: M = 8.04 X 10” c.g.s. Mp = 7.88 X 10” c.g:5. Me = 1.60 X 10” c.g.s. The magnetic field of the earth approximates that of a uniformly magnetized sphere, its magnetic axis inclined to that of geographical rotation. The equivalent axis intercepts the northern hemisphere in latitude 78° 32’ N. and longitude 69° 08’ W. The intensity of the earth’s magnetic field above the surface may be expressed as a first approximation (according to Schmidt) by F(1 — 3h/R) where h is the elevation and R the earth’s radius ; that is, for each 2 km the field diminishes by approximately 0.1 per cent while the direction is practically unchanged. If the earth’s magnetism were distributed uniformly throughout its volume, the average intensity of magnetization would be 0.074 c.g.s. The equivalent intensity of magnetization has been steadily diminishing during the past 80 years at the average annual rate of about I/1,500 part. A. Nippoldt (Veroff. Preus. Meteor. Inst., Berlin, no. 372, 137-143, 1930) gives the following positions based on observations: TABLE 724.—North Magnetic Pole Latitude. Longitude. Source. / oO / oO FO) Oa IN 96. 53.5 W. Ross 70 30 N. 95 30 W. Amundsen TABLE 725.—South Magnetic Pole Latitude. Longitude. Source. o / oO / 7s) Os Sb TSA OS nels Ross We AT ABS 150 25) VRE Ist British Antarctic expedition V2 aye TSA OOmeita 2d British Antarctic expedition The magnetic poles are not diametrically opposite, each being approximately 2300 kilometers (Gutenberg, Lehrb. Geophys., 400, 1929) from the antipodes of the other. These poles are defined as the points at which magnetic lines of force are normal to the earth’s surface, and are to be distinguished from the extremities of the magnetic axis derived from analysis. SMITHSONIAN TABLES TABLES 726 AND 727 (charts) TERRESTRIAL MAGNETISM 576 | 120° 150 180° 150" 120° 20" ANNesiea aT. NOS i Vo VE, eB es aN \\/ NAL Wy OL = Ue et DX RE \ \ A Vee UE = “SNA ase “A Zee wo, |W a i SX Me HAN Go SENNA 150 80 50 TABLE 726.—World Isogonic Lines, Epoch 1930 (Lines of Equal Declination (D)) 27 ERY, UAH ee < PR LAL SAL eer eS \\ ROFL Eee RS F USS SSE See ae A (APSE 30 ou 90 0 DAES IN Cs: 7 ata 0 cil TABLE 727.—World Isoclinie Lines, Epoch 1930 (Lines of Equal Inclination (/)). Solid Lines Indicate North End Dipping; Broken, South End Dipping 120 rf al aca ee Bt oc ea ee | LETT PN ell Liar] NG [Sade Ee lfacl eee at ASRS Ty AL 2 os — Ae Bio Need year) ital cE ERE CORI fel RIE jae SNS, Pit TA ANN VA oar | Cae SNe Ae rat tt, Pe eee See ees Sa eee aS eee ae aay a, (Seto >s— eer a eee eee ESSE ha eC faethe esl ls 2 s| POST gai adc de TR 180 L » SMITHSONIAN TABLES TABLES 728 AND 729 (charts) 577 TERRESTRIAL MAGNETISM TABLE 728.—World Isodynamic Lines, Epoch 1930 (Lines of Equal Horizontal fs ac (H)) Pies ee eae 150 -ES ia ats Boe ae BH an aN Auld Bier an eG oy) rp pets <2 oi SY P| iy a RA et ie Mi \ (Ri (i Gest Ji Lh LV YZ | ve Wy 7 AP oes SAS a ep] Lt hs 4 Bed Te ee Tf P| | BN, i 3 : TLL / i | ( A i I aA ANUMELCT WAY Tf ZA \\ Le tt P te ‘ 1X TA ge WUE: AN Nica ONS ISN NS Wahss! | eH rs nh E ! | AN \\ ‘i \ NN (aN Hf i x ys " Ke zat i \A\ a \ i | PLA ARB feeAait eer IC. at The annual changes in position of isomagnetic lines shown in Tables 726-728 are most conveniently represented by the isoporic charts, Tables 729-731. To these are added also similar charts showing lines of equal annual change in vertical force (Z) and total force (F), Tables 735 and 736. The difficulty of securing data suitably distributed over the entire surface of the earth is such that only approximate positions of isopors are known, although there is sufficient evidence to show that these positions change with relative rapidity especially near the foci of change. The rates of change of the magnetic elements and the accelerations in those rates can be derived for regions where there are magnetic observatories by reference to Table 737, “ Mean annual values of magnetic elements at observatories.” TABLE 729.—World Isoporic Lines for D (Lines of Equal Annual Change) Approximate Epoch 1920-1925 SHU oe S \ AXES ACNE Sp SSS ERATE AAS RS Ze Ae awe) |} ian a Sony Coote Se BN Wy ae i Pari LLyun Hey WN Nip 2 Se anue 4 SEPT Nt WN CH EY SMITHSONIAN TABLES 578 TABLES 730 AND 731 (charts) TERRESTRIAL MAGNETISM TABLE 730.—World Isoporic Lines for J (Lines of Equal Annual Change) Approximate Epoch 1920-1925 ZZ SS Pe & ee Ly Ss. SEE ERASE RES PRR ETE DEIN DH EZ SS SSS. ie (TIS INA TIGL AAS SoS CECE ERENCES aE Re iA CIO AS Ap Ser NREL eer (oe GST TAG erst 8 ERE RONIAREET VGN AOR? RENN TABLE 731.—World Isoporic Lines for H (Lines of Equal Annual Change) Approximate Epoch 1920-1925 SS FEL FES res Se CRAFT Age Sos FONE: Sac Nr ABE SESS RRR LXX¥B Nee SOA LATE, Me SEES [i ESS es SE eS kf -AS ATKIN, ABTS INAS SARA SGORSMEGS ye V [ott ae AG ean NY) We \ DVN DV OA NENSReeSSS 22572 or pe) AAR LAY MA |S 0 ge ee See |_| PSST p es eect x Ce ETRE Sore eee 3 = ZEST een tae Soe Wiese! aay ery Ti ee ete ede a peor iiss \EXLEZ EY, QZ SMITHSONIAN TABLES TABLES 732-734 579 TERRESTRIAL MAGNETISM APPROXIMATE VALUES FOR ANNUAL RATES OF SECULAR CHANGE IN THE MAGNETIC ELEMENTS DECLINATION (D), INCLINATION (7), AND HORIZONTAL INTENSITY (#) FOR THE EPOCH 1925! (Because of the different intervals covered by available data and the known large accelerations in some yarts, the values given for the annual secular-changes at intersections of parallels and meridians indicated re approximate except for those localities near magnetic observatories; in some cases there is great un- ertainty and the values for these are enclosed in parentheses. The signs of the values given are in the Igebraic sense for extrapolation considering east declination, north inclination, and horizontal intensity s positive and west declination and south inclination as negative. TABLE 732.—Annual Change in Magnetic Declination (D) Longitude east of Greenwich -f - + + Se +f NOWNNHO ~ ~ ~ +1 —I —I +2] +1 ai Aa eat —2 +4) +2 WW sae QwoyhHHN [1 t++++ ee HHOOAW ON ap mM VU Of ai NX af UU / oY vy cy, Y a oY ny, Y i cy 60 N.| —10} —30] —45]} —60] —50 | —40]}] —25 o |}+10]-+10 0|/—I10]}— 5 o|+10}+20]+20/+ 5 40 N.| + 5] —10}] —25 |] —35 | —35] —20] —I0 oO 0 | —10}—I5 | —20|—25 | —30| —40}]—25|+ 5|+25 20 N.| +10] +15 o} + 5] +35] +30] +15] +10 0 | —20 | —30 | —35 | —45 | —60 | —90 | —60 0}+20 °O —25 | -—15| —I10 o} +25] +25] +10 o |—10] —I10 | —1I5 ] —25 | —30| —35]—25|— 5 o|—I5 20 S.| —55 | —70|] —50 | —40} —30]| —20 | —25] —25 |—25]|—20]—15]—15|—15 | —20| —20] —25 | —30 | —4o BOWS | —O5n|--LEOW OS mie— 70) 50 —450\) — 35) 30)|(—3 0) 250 2On|—2 58251-3015 O lS 5ill—70)) —70 60 S. |(—70)}( —80)|( —80)|( —70)|( —60)}( —35)}( —30)|}( —30)} —30 | —15 | —20 | —20 | —20 | —30 | —45 | —50 | —60 | —65 1 Prepared by H. W. Fisk, of the Department of Terrestrial Magnetism, Carnegie Institution of Washington. MITHSONIAN TABLES 580 TABLES 735 AND 736 (charts) TERRESTRIAL MAGNETISM WORTH_M. TABLE 735.—World Isoporic Lines for Vertical Intensity (Lines of Equal Annual Change) Approximate Epoch 1920-1925 ae oo eS ee —=. ZEEE \ EES ARES DES HER ROR IS Lgl FCS PEN eae SPOOR LPR Noe SS IG PPS AEN “S : AY SAAS Ra A aS Fey Pe ainsi ENG Ae AL FTE a SE (ie As UE NS OMAR 27 Bh aN b PVA Tey CK Cis Eee Be Gas COR 77 FERS Sea A Aelih DANY Hoe SZ apy = Gp Ss W/Z Qe WT sani aE RO TABLE 736.—World Isoporic Lines for Total Intensity (Lines of Equal Annual Change) Approximate Epoch 1920-1925 LSS. A ces ae PERRET BE AN NS ENO) SEAN STL PERC CSE We ATTA LTT FL INGEN SSS Ae ta ee ere WSO SS ARS S BS hak SEAS me ATE ES mess Fae aS Ae REN SMITHSONIAN TABLES TABLE 737 581 MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES In order to show the change of the annual rates of secular variation with geographical position and with time and the accelerations in those rates without unduly extending the tables, the values of the elements have been given for each fifth year beginning with 1900, and for consecutive years from 1925 or 1930. When the observatory was established sub- sequent to 1900, values obtained during the first year of the operation are given. The lack of uniformity in the distribution of magnetic observatories should be taken into account. The satisfactory computation of the so-called magnetic constants of the earth, the investigation of the laws of secular variation and daily variation, the study of the manner of propagation of magnetic storms and their relation to other world-wide phenomena, require additional observatories in the southern hemisphere, specifically in Africa, and on favorably located islands in the southern Pacific and Atlantic oceans. Intensity Declination Inclination (D) (1) Hor. (#) | Ver. (Z) / / 37-5 D7ae 04.1 53.2 35-5 45.0 28.4 44.5 ST 02.8 Te2 59.6 37.6 59.8 30.0 06.8 42.7 25.3 42.6 50.2 57-4 18.6 08.3 pret 59.1 16.4 23.2, 28.2 27.0 Observatory Latitude | Longitude ° / Matotchkin Shar ; 56 24 E. Sodankyla , 26 30 E. i Gress Cupas: 05.4 N. 09401 -54326 22°51 3 -12853 -49232 35-8 N. -12638 -492I11 48.4 N. -12440 -49186 02.4 N. -12228 -49216 05.0 N. -12188 -49220 34.7 N. -08259 -55788 33.6 N. -14655 -46650 -14621 -46712 -14618 -46609 -14527 -46624 -I4517 -46623 -16548 -47050 -16540 -46975 -16420 -46882 -16210 -46850 -15978 -46807 -15770 -47000 -15675 -47068 -15630 -47106 -15586 -47145 -15617 eae -15584 -46344 -15441 -50822 -15404 -56719 -15577 -56312 -15593 -56008 -15574 -55662 -15528 -55491 -15485 -55357 (.15465) | (.55307) (.15448) | (.55255) (.15454) | (.55190) -17789 -50718 -17692 -50819 -17476 -50786 -17142 -50707 -16812 -50843 -16513 -50974 -16389 -51053 (.16285) | (.51145) -17423 -447605 -17375 -44648 -17257 -44591 -17124 -44506 -17025 -44631 -17803 -44747 -17879 -44747 -178290 47635 -17530° | .47650¢ .17260 -47951 -16082 -48238 -16053 -48279 -17905 -46442 -17875 -46545 -16830 -45307 -16836 -45343 -16786 -45173 .16706 -45062 -16665 -44943 -16585 -44881 -16583 -44808 no NNHHOO ° Godhavn : W. Lerwick : W. Pavlovsk (Sloutzk) SPP PPM MMMNSSSesesenany = NON HHH HR OCOWWWWWWNNHOOWRUUN Qe ww ww 000000 15.6 3.0 Katharinenburg 5 : 04.0 (Swerdlovsk) 27.2 48.7 a5 Rude Skov A a — aa Kasan (Saimistsche) Koutchino Eskdalemuir HH HHH PRM AMBDMHAHOO DMHMOUN AAI MOO ® See also tables for previous and intermediate years in Terr. Mag., 4, 135; 5, 128; 8, 7; 12, 175; 16, 200; 20, 131; 22, 160; 23, I91; 25, 179; 26, 147; 27, 157; 29, 149; 31, 27; 32, 27; 33, 95; and 35, 165. Unless otherwise Indicated values are from continuous magnetograph records. Preliminary values, pending final reductions, are Indicated by parentheses. Observatories marked by an asterisk (*) are in regions of local disturbance. » Values from absolute observations only. ¢ No observations in February and March. 4 Absolute observations during June and July only. SMITHSONIAN TABLES 582 TABLE 737 (continued) MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity Declination Inclination (D) (1) Hor. (H) | Ver. (Z) Observatory Latitude | Longitude Year ‘amy, , i Cc g--8; Cy 28s Meanook 54 37 N. 46.7 E. 55-2 -12944> | .60481> 38.6 E. 53-6 .129235 | .60246> 10.7 E. 53.8 -12852>b | .59934b 04.2 E. 53.8 .12832> | .59844> 48.5 E. 54.6 -12790 -59719b 39.2 E. 56. -12755 -59675> Stonyhurst y 10.9 W. 50.3 -17312 | .44720 53.5 5 46.5 -17368 -44718 20.0 W. 42.2 -17407 -44605 38.0 W. 41.4 -17342 -44457 52.9 W. 43.5 17303 -44433 53-4 , 42.2 -17263 -44282 39.7 : 44.6 -17240 -44316 260.5 : 43.5 -17231 -44251 14.5 4 46.5 .17200 -44310 46.2 -17201 -44275 47.8 -I71908 | .44311> ‘ 47.3 -171818 | .44271b Wilhelmshaven : ‘ 4 : : 44.0 -18095 -44103 40.2 -18169 -44235 30.5 -18124 -43773 30.7 -I8I1I0 -43747 02.5 -19306 -50463 06.6 -19277 -56337 15.6 -19070 -50212 16.8 -19025 -560141 17.8 - 19061 -56303 19.2 -19038 -56310 24.2 -18844 -43138 19.3 -18879 -43050 19.7 -18828 -42048 -18726 -42899 -18606 -42012 -18532 -429051 -18503 -42082 -18480 -43012 .18467 -43010 -18442) | (.43049) -18890 -42074 -18866 -42033 -18765 -42885 -18645 -42809 -18570 -42038 -18539 -42968 -18526 -42087 -18505 -42005 -18480 -43034 -18456 -43072 -18450) | (.43108) -20129 -56053 .2001T +50250 -19824 -56203 -1962I -56228 -19458 -56081 -18712 -43185 -18620 -43339 -18584 -43369 18563 -43390 -18536 | .43464 -18507 -43517 -18463 -43608 -18508 -4349 .18560 -4332 -18541 -43208 -18481 -43117 18397 -43056 -18359 -43026 -18337 -43040 -18330 -43041 -18313 +43953 -18300 -43063 .18282 -43084 -18278 -43089 rrervrocrcrorrrorererrooreoese co Irkutsk* (Zouy) Potsdam Y ~~ Irkutske (Old site) Swider® I I 0 0 oO oO 9 9 9 8 7 6 6 6 5 5 9 9 8 7 6 6 6 3 5 5 5 2 I I I I 3 2 2 2 2 2 I De Bilt AAAAAAAAALAAALALALAAAAAAAZAAALZLALAAALLZLAZALZALZALZALLZAZALZALZAZZLZAZLZALZZLZZZZAZLZLZZZZ24 HHH HH ARR WODODDDCOOHNNWW © Last 4 months only. {No values in September. £ 1915, New site at Zouy; values for 1915, 1920 deter- mined from Zouy by applying corrections, D, +0’.5(E); J, —14’.7; H, +181y. » Built in 1914; World War prevented operation until ro21. SMITHSONIAN TABLES TABLE 737 (continued) 583 MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity i Declination Inclination (D) (1) Hor. (H) | Ver. (Z) Valenciab 5 10 15 W. 30.0 29.6 (Cahirciveen) 10.4 19.2 44.6 13.0 03.8 07.9 17.9 22.4 27.6 16.8 47.2 27.2 56.4 08.9 19.9 25.9 35-2 23.8 52.7 32.9 03.2 18.4 31.0 45.1 20.0 09.9 4I.2 56.5 08.6 09.9 227, 10.4 58.4 47.0 35.8 24.6 13.7 13.6 Observatory Latitude | Longitude Cx 208; c. g. Ss. -17765 -45082 117848 -44803 -17892 -44771 -17869 -44519: -17840 -44353 LLZZZLZZZ Bochum Greenwich* Abinger sdddddedasaececececceacessaceecassessece 50.6 52.7 54.6 13.6 55.0 23.9 = 4ageaacaaasee Hermsdorf Beuthen Beuthen-Mikilow Falmouthe Prague Cracow HR HH RH HHH RH RRR RHR RRR RRR HHH HR RR RRND AUUUU DAI 00 © WIT DON NWWWWAKDRRUATWTIBOO OHNWWENNNNHNWWWRAUADWARUAAAWWO ON HN NAINWOOO itz months, no observations in May. i Mean values from magnetograms at 85 and 145 daily; other values given are means of all hourly scalings. * Because of electric railway, superseded in 1926 by observatory at Abinger. ! Means, 10 months, February to November, ™ Mean, 10 months, January to October. ® Mag- netograph for D only. ° Discontinued in 1912. SMITHSONIAN TABLES 584 TABLE 737 (continued) MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity Declination Inclination (D) Hor. (H) | Ver. (Z) , Observatory Latitude | Longitude Geiss Cog .8- -19680 -42167 -19728 -42008 -19738 -41789 -19715 -41607 -19666 -41591 -19659 -41485 -19631 -41529 -19636 -41584 -20314 -40817 -20279 -409063 .20288 -41022 Val Joyeux Maisach Munich 0-Gyalla (Pesth) 0-Gyalla . (Stara Dala) Nantesp Otomari> Odessa Pola Agincourt Karsani 41 50 N. 44 42 E. (New site) Tiflis 41 43 N. 44 48 E. (Karsani, old site) 8 8 7 6 7 7 6 5 5 4 4 3 3 3 13 13 12 12 12 12 II 8 8 8 8 8 8 4 3 I 9 9 8 Us 7 6 6 5 5 6 6 6 df 7 7 7 7 ti 7 4 4 4 4 2 2 2 3 P Electrical disturbances, especially in Z. 9a No observations during 1920 to August, 1921; values for 1921 are for four months, September to December. SMITHSONIAN TABLES TABLE 737 (continued) 585 MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity Declination Inclination (D) (1) Hor. (H) | Ver. (Z) Capodimonte 4 : 32) Wie | 50235 (Naples) .3 W. | 5615. Wi 50 Da. .7 W.)|(57 02. Ebro i ‘ .o W. | 58 07. (Tortosa) d a De, esa 47 Observatory Latitude | Longitude CLUS: Caras. -24133 -36318 -24164 -30164 .24160 -36088 -23705) |(.36563) -23230 | .37359 .23251 -37145 -23277 | .36041 -23291 -30781 -23367 | .36642 -23386 -36633 -23401 -360621 -23415 -30616 .22708 -38506 .22900 -38273 -22986 -38006 +23053 -37734 -23087 | .37496 -23143 | .37368 -23179 | .37001 -23106 -30031 - 21931 -55890 -21821 .50016 -21644 | .55908 -20195 -50586 -20064 -50418 -19806 | .56200 -I9417 | .55604 -I9118 -55285 -18874 | .54824 -18501 -54402 18539) |(.54317) -18485) |(.54247) -26063 -33514 -260140 -33598 -20107 -336013 -23059> | .41283> -23059> | .41282b -23123> | .40759> -23256> -23310b -23351> ~~ AUN Nn NNW Anwonna Coimbra Annnnnn monmonorn~r~l NWUOAONNN Baldwinr Cheltenham NIA HHOOO00 OM) COMNBWNHHAUAWH —_~—a PAMTIAADADAWNUUN CO 00 LY Athens nan NN oo San Miguel* (Ponta Delgada) DP HOSGHONAOHSNGAUUM OWEN AWN S OREN CONNANIANWONAORAUNHONNHO DIHARWHWA ORE HD ADOO& ~ ALAAZLLLAZZZZLLLLLZLZAZLLLLZZZLLLLZZZZLLZZ Na oo pp Coo ooo n ° N a Zinsenb +20071 -290005 -20923 -20831 -29866 -24631 -24762 -24879 24978) ||. .25021 -33969(?) -25032 | .34035 -25072 -33881> -25106 | .33885> -20749 | .34851 -29783 -34868 -29752 | .34863 -20743 | .348590 -29708 | .34774 -20716 | .34740 -290694 | .34721 -29707 | .34721 -20713 | .34746 -30842 | .30644 .30817 -39010 -30831 -39603 -30868 -39673 -30880 | .30646 San Fernando © Kakioka" UbpBDL NOOOO ONNNN Tsingtao na nN o AQAIIIIIIWOR HOON HOD OHO ON MHI DODO ONHHDN: nn N ° an AALZAZAZAAAAALZZAZALZAZLZAZZLZZZAZZ2: HH HH HH OOO PARHAAUMNUNUNNANANMNNANNWRRUNMNADAAUUUAMBOONO r Superseded by Tucson, October, 1909. *% Means, 10 months, January to October. * Means, 6 months July to December. " Destroyed by earthquake, September 1, 1923; all records, January, 1917 to August, 1923. lost by fire. SMITHSONIAN TABLES 586 TABLE 737 (continued) MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES h tieg' sidit: Intensity Observatory Latitude | Longitude Declination Inclination Hor. (#) | Ver. (Z) Tokyov Tucson -) | (6.26432) | (.45081) -) | (6.26398) | (.45038) -33187 -33879 -33201 -33883 -33190 -33839 -33155 -33773 5 -33160 -33709 -)b} (.33264)»| (.33753)> -)>} (.33313)>] (.33751)> : -32859 -33741 -33009 -33729 -330560 -33768 -33430 -31420 -33383 -31572 -33257 »32019 Nana Lukiapang Zikawei¥ Dehra-Dun -33083* | .32522* -32951 +32949 -32048 +33353 -32963 -33631 ) | (33001) | (.33698) -30209 «25819 -30159 -25852 -30029 -25806 -30012 .26009 -29950 -26236 -290086 -26463 (.30078)>| (.26827)> (.30126)>} (.26898)> = SCODDDDDDDDDDODDOOOHHNNHNNNHHPOTOHNNWWHHHHN ~~ N. N. N. N. N. N. N. N N N N. N. N. 'N. N N N N N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. Taihoku> Barrackporey Au Taub,z Hong Kongbb AAAAS APO Seesaw wNNsseseeeseeeeesenonys eb esassaeesecnnneasas v, ¥ Because of electric car disturbances, superseded in January, 1913, by Kakioka and in 1908 by Lukiapang, respectively. * New constants determined in 1914, used thereafter, gave for that year smaller values in H by 31yand in Z by 317 than those based on the constants previously used. y¥ Observations discontinued Apr. 26, to15, New site of Hong Kong observatory. Corrections to reduce Au Tau values to the Hong Kong series from 1884 are +0/.8 in D (i.e., west D is numerically less), —2’.5 in 7, —15soy in H, —191yinZ. 93 Means, 10 months, March to December. > Original observing hut replaced in 1921; values from 1925 reduced to basis of original hut; superseded by Au Tau in 1927, SMITHSONIAN TABLES TABLE 737 (continued) 587 MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity Declination Inclination (D) (1) Hor. (H) | Ver. (Z) ° ’ / ° / Honoluluce . | 158 04 W. 19.1 40 14.5 40 05.8 39 47.2 39 29.1 39 39 (39 (39 Observatory Latitude | Longitude G88; Cgese +20255 -24758 -201907 -24583 -29132 -24259 29005 -23807 -28847 23711 .28714 .23606 -28542) |(.23516) -28551) | (.23458) -28545) | (.23405) ~~ ZALZAAAAAA Teoloyucan o (33375) -16394 -16498 VY o ~ o Toungoo4d CN a ah a ta do tah CODD ODOOMO -39005% | .16653¢e -39114 -16707 -39132 -16704 -39156 BLOW Ty, -39207 -16725 -37438 -14652 -37377 15083 -36882 -15588 -36872 -15671 Colabase (Bombay) Alibag HHOOCOCOO0C9 -36845 .16143bh .36870 -16688 -36922 -17147 o o 370051 | .17527%1 -37253 -17777 (.37323) | (.17806) -27743 -35737 (.27644) | (.35824) (.27551) | (.35795) (.27403) | (.35813) (.27451) | (.35780) 20336 -33946 -29221 -33952 -28834 -34202 .28270 -34630 -27827 -34832 -27632 -34900 +27571 -34907 -38072 -III40 -38095 -II057 .38100 -11065 ' .382I1 -10925 -)b | (.38244)> | (.10812)> -) San Juanii Vieques!! Antipolo b | (.38270)> | (.10832)> -38029 -I11005 -38215 -10960 -37307 .02013 -37403 -O2142 -37485 +02459 -3761422 | .o281700 -37787 -03042 -37832 -03071 -37878 -03003 -37950 .O3Z112 Manila™™ Kodaikanald4 SSO OOOOOD OO OSSWWNHH N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N. N N N N N. N. N. N. N. N. N. N. N. NHHHEH HHAHHR WWW ce 1913, change of earth inductors; the values with the inductor used previously appear to be 3/.0 too high. dd Discontinued 1923. e¢ New constants determined in 1014, used thereafter, gave for that year smaller values in H by 18y and in Z by 77 than those based on the constants previously used. ‘f Means, 9 months, January to September. 8 Superseded by Alibag in 1906. 4» In 1909 an earth inductor replaced the Kew dip-circle; observations of 1909-11 appear to show that the old values of J are about 2’ and of Z about 307 too low. ‘iNew 1923 constants make a change of —21y and —10y, respectively, necessary for values of H and Z given from 1904-22. ii Superseding Vieques Observatory. ** Five months means, January to May. !! Discontinued October 31, 1924; values for 1903, means for 9 months, April to December and those for 1924, 10 months, January to October. ™™ Superseded by Antipolo because of electric car disturbances, ™= I1914,newconstants, thereafter used, gave for that year larger values in H by 33y and in Z by 37. SMITHSONIAN TABLES 21 588 TABLE 737 (continued) MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES Intensity Declination Inclination (D) Hor. (H)| Ver. (Z) / Observatory Latitude | Longitude ° ° , Palaub 2 NY. | 134 29 E. 00.5 00.2 59.9 59.8 02.4 55.0 48.7 46.1 47.0 53-2 51.6 52.5 53.0 59.1 55-5 50.7 Batavia- 5 106 49 E. Buitenzorg Huancayo 3 75 20 W. Apia 3 171 46 W. (Samoa) OOONNINNINNIOOOCOOOOOHHHNN ov Tananarive*> Mauritius 2 2 —.3083394 —.30278 —.20867 —.29849 +2970I'T(?) DNDN NNNHHNHHOHHNON —.20934 —.29803 3 —.29750 (.22673) |(—.29696) -26621 —.05979 -26435 | —.05848 -26266 -05774 -26256 -05763 -24700 -06406 -24404 .06728 -2433389 -07007 -242903 | —.07205 .24276 | —.07265 .24221tt | —.07308 -2504 —.0592 La Quiacab 65 35 W. HMnnsees dedce decdddsceae SPP Vassouras 43 39 W. Rio de 43 Ir W. Janeirovr °0 Means, 6 months, July to December. »P Means, 8 months, May to December. 494 The D values from 1912 to be decreased by 5’.1 for comparison with values in previous years; in 1914 an earth inductor replaced the dip circle on another pier and values are referred to dip-circle pier. 1 Trouble experienced with galvanometer; earth inductor replaced by dip circle in 1928; the values of J and Z for 1927 are indicated as only approximate. *s No data in June, and only 4 days in May and 7 daysin July. **Nodatain January. Superseded about 1913 by Vassouras. SMITHSONIAN T438LES TABLES 737 (concluded) AND 738 589 MEAN ANNUAL VALUES OF MAGNETIC ELEMENTS AT OBSERVATORIES } , Intensity Observatory Latitude | Longitude Year Declination Inclination Ver. (Z) Watheroo Santiago> Melbourne?,vv Toolangi (—.56232) -55252 -552406 =.55277 —.55348 —.55485 —.55465 —.55486 —-55525 —.55522 —-55570 —.32808 —.32536 —.32114 —.31619 Amberley Christchurch¥w New Year's Island Orcadas ° 4 4 4 4 4 4 4 4 4 9 9 8 8 7 7 6 6 14 14 13 8 8 8 8 8 (8 17 17 16 16 16 16 16 CT, 17 17 15 15 15 15 15 5 4 SPUD UNN NS SSSA SSM RPMN MMMM NMMMBNNN cee a DNDN vy Superseded in1920by Toolangi. ¥¥ January I, 1923, the variation observatory was transferred to Amberly but all results subsequently are referred to basis of the old station at Christchurch. ** Means, 10 months, March to December in 1902 for all elements, and 9 months, January to September in 1910 for Z. yy Mean, II months, February to December. 2% Mean, 10 months, March to December. TABLE 738.—Bibliography Gauss, K. F. 1839. Theorie der Erdmagnetismus. Resultate des Magnetischen Vereins. Gesammelte Werke, vol. 5, Gottingen, 1867. Lamont, J. 1849. Handbuch des Erdmagnetismus. Giinther, S. 1897. Handbuch der Geophysik, vol. 1, pt. 1, Stuttgart. Schmidt, A. 1898. Der magnetische Zustand der Erde. Archiv der Deutschen Seewarte, Hamburg. Mascart, E. 1900. Traité de magnétisme terrestre. Paris. Chree, G) I91l. Terrestrial magnetism. Encyclopedia Britannica, 11th ed. 1912. Studies in terrestrial mag- netism. London. Schmidt, A. 1917. Erdmagnetismus. Encyklopddie der mathematischen Wissenschaften, vol. 6, Leipzig. Auerbach, F. 1920. Magnetismus. Graetz, Handbuch der Elektrizitat und Magnetismus, vol. 4. Nippoldt, A. 1921. Erdmagnetismus, Erdstrom, Polarlicht. Sammlung Géschen, no. 175, Berlin. Chapman, S. 1922. Theories of terrestrial magnetism. Dictionary of Applied Physics, London. Angenheister, G. 1927. Erdmagnetismus. Geiger und Scheel, Handbuch der Physik, vol. 15, Berlin. Nippoldt, A. 1928. Der Erdmagnetismus. Miiller-Pouillets Lehrbuch der Physik, vol. 5, Braunschweig. Angenheister, G., and Bartels, J. 1928. Das Magnetfeld der Erde. Wein und Harms, Handbuch der Experi- mentalphysik, vol. 25, pt. I. Bartels, J. 1929. Erdmagnetismus, Erdstrom und Polarlicht. Gutenberg, Lehrbuch der Geophysik. Hazard, D. L. 1929. The earth’s magnetism. U. S. Coast and Geodetic Survey. Nippoldt, A. 1929. Erdmagnetismus und Polarlicht. Einfiihrung in die Geophysik II. Hazard, D. L. 1930. Directions for magnetic measurements. U. S. Coast and Geodetic Survey. Journal of Terrestrial Magnetism and Atmospheric Electricity, Baltimore, from 1806, vol. 38 in progress. Zeitschrift fiir Geophysik, Braunschweig (from 1924). Caractére magnétique de chaque jour, De Bilt (from 1906); Caractére magnétique numérique des jours, De Bilt (from 1930). Atlas des Erdmagnetismus, Neumayer, Gotha, 1801. Reports and publications of Department of Terrestrial Magnetism, Carnegie Institution of Washington, and of individual observatories (see table of mean annual values). Isomagnetic charts, Deutsche Seewarte, 1920; British Admiralty, 1927; U. S. Hydrographic Office, 1930. SMITHSONIAN TABLES 590 TABLE 739 SECULAR CHANGE OF MAGNETIC DECLINATION Changes in the magnetic declination between 1820, or the date of the earliest observations, and 1930, based on tables in ‘‘Magnetic Declination in the United States in 1925” publishéd by the U.S. Coast and Geodetic Survey (Special Publication No. 126) in 1926. Lat./Long.} 1820 1830 1840 1850 1860 1870 1880 1890 1900 1910 1920 1930 ° ° ° ° ° ° ° ° ° ° ° ° 12.2W 13.0W 13.8W 14.6W 15.4W 15.8W 16.2W 16.5W 16.8W 17.5W 18.3W 19.1W 14.8W 15.6W 16.4W 17.3W 18.0W 18.5W 18.9W 19.0W 19.3W 20.0W 20.7W 21.3W 17.6W 18.5W 19.4W 20.2W 21.0W 21.5W 21.8W 21.9W 22.1W 22.7W 23.2W 23.8W 5.0W 5.5W 6.2W 6.90W 7.6W 8.2W 8.7W 9.2W 9.7W 10.6W 11.3W 12.2W 6.5W 7.0W 7.7W 8.4W 9.1W 9.7W 10.3W 10.8W 11.3W 12.1W 12.9W 13.7W 8.3W 8.9W 9.6W 10.4W 11.1W 11.7W 12.3W 12.7W 13.2W 14.0W 14.8W 10.9W 11.5W 12.2W 13.0W 13.7W 14.3W 15.0W 15.3W 15.8W 16.6W 17.3W 1.2E o0.0E 0.4E 0.2W 0.8W 1.4W 2.0W 2.6W 3.1W 3.7W 4.2W 0.2E 0.2W 0.6W 1.2W 1.8W 2.5W 3.1W 3.6W 4.2W 4.8W 5.4W 0.4W o.8W 1.3W 1.90W 2.5W 3.2W 3.8W 4.4W 5.0W 5.6W 6.3W 1.6W 2.0W 2.5W 3.1W 3.7W 4.4W 5.0W 5.6W 6.2W 7.0W 7.6W 3.4W 3.8W 4.3W 4.0W 5.5 6.2W 7.0W 7.5W 8.1W 8.9W 9.6W 4.7W 5.1W 5.7W 6.3W 7.0W 7.6W 8.5W 9.0W 9.6W 10.4W 11.2W 5A Sate Ase Aton Se ee eset 2.08, SOK ries ers 3 Eee Al ioe VAG ~43E) 3:8 93:3 2-7 2k ase 2.02 ose ove A00E Ase 93:0 a5 20 923k 1.72) te oOl6E 03k 70.28 400K 28H. s4b sok) (2-4) 1-8) 51.2) "0:6 0:0 0.3W 0.5W 37. 342 SrE> 26E 20k r4Ee o:8E. 0:2 of4W..0:sW) rr 208 2:46 208" Tsk 21.0E “o:3E (0:4W) 1.0W. 1-5We 2:0W.. 2.4Wi 2.00E 1.8E 1.4E 0.0E 0.3E 0.3W 1.0W 1.6W 2.2W 2.7W 3.2W 0.90E o0.7E 0.3E 0.2W 0o.8W 1.4W 2.1W 2.8W 3.4W 4.0W 4.5W 0.6E 0.4E 0.0 0o.5W 1.1W 1.8W 2.5W 3,2W 3.8W 4.4W 5.1W 0o.8W 1.1W 1.5W 2.0W 2.6W 3.3W 4.1W 4.8W 5.4W 6.1W 6.8W 62h) (Ore sob e sik 95.0 45 93:0) s-26) 2:Sh 2 7b sor: yd) Oe AAO, RYN CES < 4.5 X ron HO Hw ANNHDYDNOOO OH HN HW WWW XXX KK KK KKK 10 10 10 Io 10 10 10 10 10 10 10 a 6 p. m. or 6a. m. O53 enna 86 8 8 8 anrtodsoe8d 8 8 an on COWHYUYYYN xxXxKXXKK KKK Oe tt Our OlO1 O10, ONO Cota FUR a Sir OTS ROOYWNUNNY xX KK KK KK SOOO tt GOL) O10) 6,010 COON HUH HHH HO SMITHSONIAN TABLES 600 TABLES 754 (continued) AND T54A TABLE 754 (continued).—Ion Density y, in the Upper Atmosphere 2 170 km 160 150 140 130 120 IIS 110 100 90 80 STINT XxX ~ = a a oa a a on WHUNHNOOOHHO a CwWwokhN PHOWDOHHOOO KOXOOCK aS eae He eS GROKOROnO HO Wy w SS Se O1ONCNO XXX X Midnight 170 km 160 150 145 135 125 II5 IIO 100 90 80 NO xX se OOS a HW Ue XxX XX a) CIO SN o5 a WRANOONHOOS fb MOWHWOOONNO DAN ADS KOKO 170 km 160 150 145 135 12 II5 110 100 90 80 o x 10 x< 10 ° 5 5 Se Oo aan NORHOOODOSOCO 0 Tp T: 0 Oo 0 2. 1 3. 5. ite NERC EE OTS WMHwWum XXX X HH ee 000080 on 0° i 60° Lie Ve Max. Le ) xe Line Ye max. Noon 195 km : i 195 km M 175 km 46 aro? 3 p.m. 195 4 é 195 2 ; 175 BIOs 6 p.m. 144 : . 140 i i 140 0.6 X 10° 9 p. m. 165 £1 DG 108 145 : 145 Midnight 165 : ; 145 145 3 a.m. 165 : r 145 145 6 a.m. 144 ‘ 140 f Y 140 9 a.m. 195 A 195 : 175 SMITHSONIAN TABLES ASTRONOMY 601 TABLE 755 MISCELLANEOUS ASTRONOMICAL DATA Tropical (ordinary) year { 365.24219879 — 0.0000000614 (t — 1900) fae Sidereal year + 365.25030042 + 0.0000000011 (tf — 1900) +¢ days. Anomalistic year 365.25964134 + 0.0000000304 (t — 1900) a Eclipse year 346.620000 -+ 0.00000036 (t¢— 1900) +} days. Synodical (ordinary ) month 29.530588102 — 0.00000000294 (t — 1900) } days. Sidereal month 27.321660890 — 0.00000000252 (ft — 1900) + days. Sidereal day (ordinary, two successive tran- sits of vernal equinox, might be called equi- noctial day ) = 86164.09054 mean solar seconds. = 23 h. 56 m. 4.09054 mean solar time. Two successive transits of same fixed star 86164.09966 mean solar seconds. 1930, Julian Period = 6643. January 1, 1033, Julian-day number = 2427074. See p. 603. Solar parallax = 8.7958” = 0.002” (Weinberg). 8.807 += 0.0027 (Hincks, Eros). 8.799 (Sampson, Jupiter satellites; Harvard observations). 8.80 Paris conference; 8.8032” + 0.0013.* Lunar parallax = = 3422, 636572 030 (Newcomb). Ta Sue = 0.009 (De Sitter) .* Mean distance earth to sun = 149500000 kilometers = 92900000 miles. Mean distance earth to moon = 60.2678 terrestrial radii. = 384411 kilometers = 238862 miles. Light traverses mean radius of earth’s orbit in 408.7 sec. Velocity of light (mean value) in vacuo, 299796 + 4 km/sec. (Michelson). Constant of aberration = 20.4874” + 0.005”. 20.47 Paris conference (work of Doolittle and others indicates value not less than 20.51). Light year = 9.5 X 10” kilometers = 5.9 X I0” miles. Parsec, distance star whose parallax is 1 sec. = 31 X 10” km = 19.2 X 10” miles. General precession = 50.2564” + 0.000222 (ft — 1900)” (Newcomb). General precession 50.2486” + 0.0010 (De Sitter, 1927). Planetary precession =—\ — 0.12287 ==,00012) (De Sitter, 1927). Lunar-solar precession =D) 150.3714. == 010016) (Del SitterO27))e Of this o.o191”, Einstein, orbital motion earth.* True lunar-solar precession = p= 50.3523, sun, moon, earth’s attraction.* Obliquity of ecliptic = 23° 27’ 8.26” — 0.4684 (t — 1900)” (Newcomb). Constant of nutation = 9.21” (Paris conference) ; 9.208” + 0.003.* Constant in long. = Ag = ( — 17.234” — .017” T) sin \ Jackson, Constant in obliquity = Ae= ( + 9.218 + .0009T ) cos 2 Pin N., 1930. Latter has relativity correction; T centuries from 1900. Gravitation constant = (6.670 + 0.002) X 10° dyne cm’ g” (Heyl, 1930). Eccentricity earth's orbit =e —=0.01675104 — 0.0000004180 (t — 1900) — 0.0000000000126 (¢t — 1900)”. Eccentricity moon’s orbit = e,=0.05490056 (Brown). Inclination moon’s orbit = = 5° 8) 43:5. @brown): Delaunay’s y = sin 4/ = 0.04488716 (Brown). Lunar inequality of earth =2=6.454”"; 6.459 = 0.005.* Parallactic inequality moon = Q = 124.785” (Brown). ets ee eee = — 19° 21’ 19.3838” + 0.001294 (ft — 1900)”. Pole of Milky Way =R. A., 12h. 48 m.; Dec., + 27°. See p. 604. d (lunar perigee) i Os SOne d (lunar node) = — 5.077. * De Sitter, Bull. Astron. Inst., Netherlands, 4, 57, 1927. SMITHSONIAN TABLES 602 TABLE 756 MISCELLANEOUS ASTRONOMICAL DATA AND FORMULAE If 6=declination, t, hour angle measured west from meridian, h, altitude, ¢, latitude and A, azimuth measured from S. point through W. Then sinh = sin ¢ sind + cos ¢ cos 5 cos ¢ cos h cos A = — cos ¢ sind + sin ¢ cos 5 cos t rgiven 6, t, p cosh sin A = cos 6 sint sind = sing sinh — cos ¢coshcos A cosdcost=cos¢sinh+sing@coshcos A pgivenh, A,¢ cos 6sint = cos h sin A Refraction.— y in (”) = [983 X (barometer in in.)/(460 + ¢° F.)] tanZ, where Z = zenith distance. Error <1”, Z << 75°, ordinary ¢ and pressure. Twilight.—Considered to end when Ist mag. star is visible in zenith. Lasts until sun is about 18° below horizon; lat. 40°, equivalent to about 14 to 2 hr.; latitude > 50°, lasts until midnight. Dip of horizon.—In minutes of arc = Velevation in ft. Horizon.—Distance at sea is approximately, miles = V (3)h in feet; no account taken of refraction, actual distance greater. Date line.—180° from meridian of Greenwich. Ships crossing it from the east, skip a day; going east, count same day twice. Velocity, equatorial point on earth.—Because of rotation: 1000 mi./hr. = 1500 ft./sec. = 1600 km/m= 450 m/sec. In orbit: 18.5 mi./sec. = 30 km/sec. Latitude variation.—Direction of axis of the earth in space is invariable but a variation in latitude is caused by a shift of the earth’s body about this axis. There are two com- ponents, one, annual (narrow ellipse, varying in form and position, about 10 m long on the earth’s surface) probably meteorological in origin; the other, circular, about 8 m in diameter, period 433 days, due to noncoincidence of axis of figure and of rotation. Magnitudes.—(Apparent, m). The light of an average Ist magnitude star was found to be physically 100 times as intense as that of a 6th. Y/ 100 or 2.512 has been adopted as the light ratio between two stars differing in magnitude by unity (logs 0.400 = 2.512). If Im = approximate brightness of star of magnitude m, In of n, then, In/lm = (2.512)™™ whence m—n=2.5 (log In — log Im); if l—=brightness 0 mag. star log (logm/logo) = — 0.4 m. Magnitudes.—(‘“ Absolute,” J7.) The “absolute” magnitude of a star is its magni- tude reduced to a standard distance, 10 parsecs (Int. Astron. Union, 1922). M—m=2.5 (log amt. light rec’d)/(log amt. if at unit distance) = 5 log p— 5 log po where fp, po are observed parallax and that for standard distance; po =0.1--M=m+5-+5 log p. 8 Orionis, M = — 5.5 is brightest star. Color index.—We have visual, photographic, and bolometric (radiometric) magnitudes. The zero of the photographic scale is taken so that both the photographic and visual scale coincide, on the average, for stars of spectrum class AO and m=5.5 to 6.5. Difference of magnitudes on the two scales is the color index, photovisual is + for red, — for blue stars and may amount to + 2.0 mag. Heat index.—Radiometric (heat or bolometric), zero taken to agree with Class AO, (radiometric — visual magnitude) = head index, + for red stars. Purkinje effect—Two colored lights appearing equally bright at a certain brightness, when brightness decreased equally physically, the bluer appears brighter. SMITHSONIAN TABLES TABLES 757 AND 758 603 CALENDARS TABLE 757.—Julian Day Calendar Proposed by Scaliger, 1582. Days are numbered consecutively from Greenwich mean noon on January I, 4713 B. C. Advantage: difference between two dates becomes merely difference between two Julian day numbers. As our civil and astronomical days begin at midnight, the numbers from the table must be increased by one after noon of date. Julian Day No. = 2420000 + no. in table. Jan. 0, etc., at head of col. means Jan. o until noon, then Jan. 1, etc. Feb. 0| Mar. 0} Apr. 0} May o} June o} July o| Aug. o/Sept. 0] Oct. 0 |Nov. 0 2810 2902 3175 3267 3540 3632 3906 3998 4271 4363 4636 4828 5001 5903 5367 5459 5732 | 5 5824 6007 6180 6462 2 6554 6828 6920 7193 7285 7558 C 7650 7923 8015 8280 8381 8654 8746 9019 QIIl 0384 | « 0476 9750 9842 TABLE 758.—Perpetual Calendar To find the calendar for any year, e.g., 1924, divide century part of year (19) by 4 and with the remainder (3) enter Dominical Letters table. Use line (3) of lower sections of table corresponding to value of remainder, taking the Dominical Letter corresponding to the column in upper parts of table containing the last two figures of the year in question (24). This being a leap year we find two letters (F) to be used with Jan. and Feb., (E) with the rest of the year. In the second part of the table this Dominical Letter indicates which schedule of week days is to be used with the month in question. E.g., Jan. 1, 1924, comes on Tuesday; July 4 on Friday. 24 52 80 BA DC KE GF Month Dominical letter Jan., Oct. Feb., Mar., Nov. Apr., July M WOMWOOS Sat. i. Wed. Sun. ; Thurs. Mon. Sun. Fri. Tues. Sat. Wed. Ss. Sun. Thurs. re Mon. Fri. Thurs. Tues. NoteE—For general discussion of calendars, see British Nautical Almanac, p. 734 et seq., 1931. SMITHSONIAN TABLES 604 TABLE 759 RIGHT ASCENSION, DECLINATION INTO GALACTIC COORDINATES Condensed from Tavole calcolate dal Emanuelli (1929), Secretario della Specola Vaticano. Galactic pole, R. A., 191.1°, dec. +26.6° (Newcomb, 1904). The zero point of the tables takes the longitude of the solar apex as 0° (R. A., 270°, dec., +30°, 1900). To reduce the galactic longitude as reckoned from the intersection of the galactic plane with equator, add 23.6° to ‘‘Long.’’; as reckoned from a Cygni (proposed by Int. Astron. Union, 1925), add +27.9, 1900, (+23.7, 1930). ob Long. Lat. Long. 66.4 +26.8 66.4 64.4 +17.0 67.1 62.6) 97.1 167.7 60.9 — 2.7 68.4 59.2 —12.6' 69.0 57-2 —22.4 69.7 55.0 —32.2 70.4 52.3 —42.0 71.4 48:6 51.6 9472-8 42.9 — 61-1 75.0 32-4 —70.2 79-5 7-3 —77:8 94.9 Suan mod 278.5 —73-9 263.6 —65.3 256.3 —55-9 251.9 —46:3 248.8 —36.6 246.4 —26.8 N. B.—The reductions for plus and minus 90° are independent of the right ascension and declination and respectively: 66°.4, +26°.8 and 246°.4, —26°.9. The Galactic pole has been variously taken: Newcomb 12244™, +26°.6; Gould, 12542™, +32°; Searle, 12440™, +28°, for tables of conversion see Harvard Annals, 56, 1912; Kapteyn, 12'41™, +27°.3; Van Rhijn, 12"56™, +25°, for tables, see Gréningen Publications, 43, 1929. SMITHSONIAN TABLES TABLE 759 (continued) RIGHT ASCENSION, DECLINATION INTO GALACTIC COORDINATES +80 +70 +60 +50 +40 +30 +20 oO 740) rob Long. Lat. ° ° 74-3 134-1 83.7 +40.8 95:0 + 46.6 108.6 +51.1 124.5 +53-6 141.4 +53-9 157-7 151.8 171.9 +47.8 183.7 +42.3 193-5 135-7 201.7, a-28-5 208.9 +20.9 Pires ate 0) 221-3) sie) 5-0 227.2 a 233-2) le? 23055) 1950 15h ° ° 59.6 +34.9 "51.4 +42.6 40.9 +49.5 27-4 155-3 10.3 +59.0 350.6 +60.1 B3L-Se aig 5Oe2 315-2 +53-9 302.6 +47.8 292.8 +40.6 285.0 +32.8 278.5 +24.6 27.2. Om Nour 207 Ome a5 262-00 —— al. 257-0 — 6:8 252.3 —18.4 12h Long. Lat. 68.8 +36.6 71.9 +46.3 76.3. +55-9 83.6 +65.3 98.5 +73-9 135-7 79.7 187.8 +77.8 212 Aw 70s 222.9 +61.1 228.6 +51.6 232.3 +42.0 2A 5 (OM aoe 23722 122-4 239.2 +12.6 ZAO:ON 27, 242.60" 720 244.4. —17.0 17h 54-8 +31.2 44-7 133-9 32-7 135-9 2053) -|- 3647; 7-9 +36.2 355-8 +34-4 344-4 131.5 333-8 +27-7 B24°On-2aen Long. 65.6 64.5 62. 60.1 53-6 20.3 274-9 259-5 255-0 252.8 251-4 250.4 249.7 249.0 248.4 247-7 247.1 18h ° ° 55-3 +28.3 43-9 +28.9 32.5 +28.5 2a 27d 10.4. +24.9 OL08 =-22:0 350.5 --18-4 277-4 —17-7 207.5 lee ZEA 2ah ° °o 56.1 23.2 46.4 +19.0 27-2 28:4, .-|- 9:2 19.8 + 3-9 Ile ==" Tiel 2.9 — 6.8 354.2 —I1.9 345.2 —16.8 335-7 —21.3 325.7. —25.2 315.1 —28.4 303-9 —30.7 292.3, —32)1 280.5 —32.3 268.7 —31.5 257-3 —29.6 SMITHSONIAN TABLES ses VA SIGUA WNaO OO NS | BOW DH AN NwohRUN pao ral oa NS ae NIUINTOW®W NN | 351-9 —47.8 337-7 —51.8 321.4 —53-9 304.5 —53.6 288:6 —51-1 275-0 —46.6 263.7 —40.8 254-3 —34-1 | ++ eNwHHfPHeuwn ad SO COCR OIC SO Oo eS WOhWOUNNN OO al — 60.2 346.7 —65.1 322-3)) 0019 298.4 —64.7 280.1 —59.4 2607-51525 258.6 —44.3 251.8 —35.7 606 TABLES 760-762 TABLE 760.—Planetary Data Mean distance Sidereal from the sun. period. Mean days Mean Gravity density. at surface Reciprocals Inclination of masses of orbit RON 6000000 87.97 5.61 408000 244.70 3-393 5.16 329390 149 365.26 Sem 5-52 3093500 228 686.98 1.850 3.95 778 4332.59 1.308 1.34 2 1426 10759.20 2.492 .69 Uranus 2869 30685.93 7B 1.36 Neptune 4495 60187.64 1.778 1.30 Heclee 5900 908.85 yall abter’ Moon 781.45 38 X 10% DTERD 5.145 3.36 * Earth and moon. ft Relative to earth. Inclination of axes: Sun 7°.25; Earth 23°.45; Mars 24°.6; Jupiter 3°.1; Saturn 26°.8; Neptune 27°.2. Others doubtful. Approximate rates of rotation: Sun 2544; Moon 274, Mercury 884; Venus 225%; Mars 245 37™; Jupiter 9 55™; Saturn 105 14™. Asteroids (planetoids) : Sept. 28, 1931, 1183 had been numbered, inclination Pallas orbit 34° 43’, Hidalgo 43°; e, Albert, 0.54; Hidalgo 0.65. Heaviest meteorite (So. Africa) 50 tons. TABLE 761.—Satellites of the Solar System Mean distance Sidereal period Diameter 384,400 km 274 7 43™ 11.58 9,380 7 39 13.85 : 23,460 6 17, 54:9 Jovian: 5th 181,200 Ty e572 oO Ds MOeae op bs Shaler aes eeene 421,300 27 aaa 2, Europa 670,500 13 42.05 3, Ganymede.......- 1,069,300 42 33.35 4, Callisto 1,881,000 Gay Thien 11,450,000 11,730,000 23,500,000 9 24,100,000 Saturnian: 7, Mimas 185,700 6, Enceladus 237,900 294,500 377,200 526,700 1, Titan 1,220,000 8, Hyperion 1,480,000 3, Iapetus 3,558,000 9, Phoebe 12,930,000 Uranian: 1, Ariel 191,700 2, Umbriel 267,000 av IMEVEN, ooo oo ac 438,000 4, Oberon 586,000 Neptune’s: I 354,000 PT ETN ORS LPR) OR A a Oa ome) ere) eA eO Le * Motion retrograde. Notes: Jovian; 1st 4 called Galilean; eccentricity 6, 7, 8, 9; 0.15, 0.21, 0.38, 0.25; masses I, 2, 3, 4; 1.00, 0.65, 2.10, 0.58 of moon. 6, 7 orbits angle 29° and 28° to Jupiter's; 8, 32° or more properly, 148°. 9, inclination of orbit 156° to planets. Saturnian; Hyperion, mass., 1.86 X moon; Phoebe, eccentricity 0.17; inclination 5°3’ or 174°7’. Uranus; orbits inclined 82°.2 to ecliptic, in that plane revolve backward = 97°.8 to ecliptic and direct motion. Neptune; inclination, 40°. All other satellites are small eccentricity, mass and inclinations. The mass of Saturn’s ring < 1/1000000 Saturn’s mass. TABLE 762.—Diameters of the Planets From critical review by Rabe, Astron. Nach., 234, 154, 1928. Solar parallax taken as 8” 800, earth’s radius 6738 km. Order of p.e. + 0.04 for planets. Diameter At Diameter km earth Object sass = =I parent Mercury f 5140 0.403 Saturn: Equat... 9.539 17.44 120600 Object km earth 12620 -989 Polanac ve 15.77. 109000 12756 1.000 Outer ring 40.29 278500 Mars: Equat... 6860 -538 Crepe ring 20.83 144000 Polars2- 6820 -535 Uranus 19.19 3.84 53400 Jupiter: Equat. 5.203 143600 11.26 Neptune. ...... 30.06 2.28 49700 Polar. . 134800 10.57 SMITHSONIAN TABLES TABLES 763-765 607 TABLE 763.—Planetary and Satellite Distances as Connected by Bode’s Law; Later Developments It is notable that the planetary and satellite distances from their primaries approximately follow Bode’s law or some modification thereof. Bode’s law: Write a series of fours; to the 2nd add 3; to the 3rd, 3 X 2 or 6; to the 4th, 6 X 2, or 12; etc., doubling the added number each time. Jeans states: ‘It is nore than likely that Bode’s law isa mere coincidence” (1929). Penniston (Science, 71, 513, 1930) suggests ridding to the square of the integer the integer itself, thus assuming that the terms differ from the square of the integers by a progressively changing amount. See also Caswell, Science, 60, 384, 1929; Armellini, Scientia, 12, I, 1918; 1, 1922.* Cas- well’s System Satellite law Cas- well’s law Relative] New | Bode’s distance| law law Relative] New | Bode’s distance] law law System Satellite Mercury 3.87 4 3.82 || Saturn Mimas 10.0 10 10.6 Venus 7.23 77 6.80 y Enceladus 12.8 ee Sane ee Earth 10.0 10 10.6 be Tethys 15.8 15 15.3 Mars 15.2 16 15.3 es Dione 20.3 21 3 20.8 Ceres 27.7 28 27ea re Rhea 28.0 28 Tee Jupiter 52.0 52 51.4 : Titan 66.0 66 61.2 Saturn 95-3 95.6 Themis 78.1 78 83.1 Uranus I9I.0 187.0 Hyperion 79.0 78 83.1 Neptune 300.0 310.0 Iapetus 190.0 190 196 187.0 “Pluto” ehte 408.0 Phoebe 698.0 703 772 712.0 oieus 435.0 Uranus Ariel 10.0 10 10 10.6 Mars Phobos 1.00 1.70? s Umbriel 14.1 15 16 15.3 oe Deimos 3.22 3.82 ce Titania 22.8 21 sae 20.8 Jupiter V 2.71 3.82 ‘ Oberon 30.4 28 28 27.2 ES I 6.27 6.80 II 10.0 10.6 III T1523 * See also Narlicker, Philos. Mag. 12, 67, 1931, with 27.2 note by Larmor. Sir G. Darwin was inclined to regard VI 170.0 Bode’'s Law a subject for serious discussion. See Turner, VII 170.0 Blagg, M. N. R. A. S. 73, 414, 1913. See Pruett, Pop. VIII 357.0 Astron. 39, 360, 1931. Ix 382.0 TABLE 764.—Albedos The albedo, according to Bond, is defined as follows: ‘‘Let a sphere S be exposed to parallel light. Then ts albedo is the ratio of the whole amount reflected from S to the whole amount of light incident on it.” n the following table, m = the stellar magnitude at mean opposition; g = magnitude it would have at ull phase and unit distance from earth and sun; o = assumed mean semi-diameter at unit distance; ) = ratio of observed brightness at full phase to that of a flat disk of same size and same position, illumi- ated and viewed normally and reflecting all the incident light according to Lambert’s law; g depends n law of variation of light with phase; albedo = pq. Russell, Astrophys. Journ., 43, 173, 1916. Albedo of the earth: A reduction of Very’s observations by Russell gives 0.45 in close agreement with he recent value of Aldrich of 0.43 (see Aldrich, Smithsonian Misc. Coll., vol. 69, no.10, 1919). os Photo- : Visual Color : Object m g o p q s : graphic albedo index Albedo ROO ere yehe ss .crteys col cae ae ch auexepecee —12.55 +0.40 2.40"" 0.105 0.694 0.073 +1.18 0.051 MM ERCULY An lycris ee eee —2.94 — .88 3.45 -164 -42 -069 Pars BBS BLM Actas 8 kts apts s ene fauey aide —2.12 — .06 3-45 .077 .72 -055 eeaite Behe. BRPRINS sce a ete ciatens te emcee —4.77 —4.06 8.55 +492 1.20 +59 + .78 -60 NVPCATS Byere shen ner orotic ate citie eos —1.85 —1.36 4.07 -139 Toor 154 +1.38 .090 BPEL STs oh vetoes 0d, = craters ecco —2.20 —8.99 05.23 -375 D5 -50: + .50 2735 Set eee ote yet Se men Sere + .89 —8.67 77.95 .420 Tease 203: +1.12 AT RO GATH US fapev ssc cic 2 fe, 5. hae canes +5.74 —6.98 36.0 -42 1.5: 203): ae Shes Sette Oe ee, aL: A g 34.5 -49 Ti58 We TABLE 765.—Equation of Time The equation of time when + is to be added to the apparent solar time to give mean time. When the lace is not on a standard meridian (75th, etc.) its difference in longitude in time from that meridian just be subtracted when east, added when west to get standard time (75th meridian time, etc.). The quation varies from year to year cyclically, and the figure following the + sign gives a rough idea of his variation. IMITHSONIAN TABLES 608 TABLES 766-769 SOLAR RADIATION TABLE '766.—The Solar Constant Solar constant (amount of energy falling at normal incidence on one square centimeter per minute on body at earth’s mean distance) = 1.932 calories = mean 696 determinations 1902—12. Apparently subject to variations, usually within the range of 7 per cent, and occurring irregularly in periods of a week or ten days. Computed effective temperature of the sun: from form of black-body curves, 6000° to 7000° Absolute ; from Amax. = 2930 and max. = 0.470, 6230° ; from total radiation, J = 76.8x10-¥ x T4, 5830°. TABLE 767,—Solar spectrum energy (arbitrary units) and its transmission by the earth’s atmosphere. Values computed from em == €oa™, where em is the intensity of solar energy after transmission through a mass of air m; m is unity when the sun is in the zenith, and approximately = sec. zenith distance for other positions (see table778) ; ¢9 =the energy which would have been ob- served had there been no absorbing atmosphere; a is the fractional amount observed when the sun is in the zenith. Transmission coef- Intensity Solar Energy aubicary ficients, a One mile Mount Wilson Washington (altitude 1675 m) | (sea-level) Wave length ML Whitney nearest earth ‘lransmission coefficients are for period when there was apparently no volcanic dust in the air. * Possibly too high because of increased humidity towards noon. 7 Altitude 4420 m. TABLE 768.—The amount of Solar Radiation in different sections of the spectrum, ultra-violet, visual infra-red. Calories Wave length. Mount Whitney. Mount Wilson. Washington. Bb TABLE 769,—Distribution of intensity (Radiation) over the Solar Disk (These observations extend over only a small portion of a sun-spot cycle.) Wave BM | B be Mm | B BR | Me Mw Me M length. D 323 | 0.386 | 0 433 |0.456 | 0.481] 0.501 0.534 | 0.604 | 0.670 | 0.699 | 0.866 0.55 | 120 | 289 | 395 | 455 | 456 | 437 | 417 | 365 | 308 | 284 | 163 0.65 112 267 368 428 430 | 414 396 | 348 295 273 159 0.75 240 333 390 | 394 380 | 366 | 326 281 258 152 - (0.00 | 144 | 338 | 456 | 515 | str | 489 | 463 | 399 | 333 | 307 | 174 | 99 Be 86 | 214 | 206 | 351 | 358 337 | 304 | 262 | 243 | 145 | 0.40 128 | 312 423 486 | 483 463 440 382 320 295 169 0.875 76 188 266 317 | 324 312 284 | 247 229 138 0.92 64 163 233) 19277 al 290 281 | 259 | 227 | 212 130 L0.95 49 141 205 | 242 | 255 254 | 237 | 210 | 195 122 un ae s cS % < ° 5 o « - ce Taken from vols. II and III and unpublished data of the Astrophysical Observatory of the Smithsonian Institution. Schwartzchild and Villiger: Astrophysical Journal, 23, 1906. SmiTHSONIAN TABLES. TABLES 770 AND 771 609g TABLE 770.—The Solar Constant,* Decade Means (See Tables 771 and 772) Decade 1918 1919 1920 19021 1922 1923 1924 1925 1926 1927 1928 1929 1.968 I. 1.924 1.946 1.937 1.945 1.944 1.939 I.941 1.925 1-967, 0. 1.946 1.939 1.943 1.938 1.931 1.941 1.959 1.952 1.933 1.931 1.942 1.939 1.958 I.QII 1.934 1.938 1.938 I. 1.947 1.937 1.954 I. 1.947 1.951 1.943 I. 1.939 I. 1.941 1.925 1.956 I. 1.948 1.923 1.938 I. 1.929 1.934 1.925 1.959 I. 1.949 1.929 1.947 I. 1.941 1.950 1.932 1.948 I. 1.939 1.936 1.944 I. 1.948 I. 1.945 1.931 1.932 1-92201-030 1.042)e 1.932 i. 1.945 1.932 1.948 I. 1.930 1.934 1.942 I. 1.927 1.946 1.932 1.956 1.941 1.937 1.928 1.948 I. 1.937 1.940 1.942 1.952) 0. 1-925) D-O34 IL O47ke 1.939 1.945 1-940 1.938 1.950 I. 1.924 1.934 1.944 I. 1.937 1-947 1.943 1.936 1.961 I. 1.935 1.948 1.950 1.938 1.944 1.951 1.941 1.950 I. 1.937 1.950 I. 1.942 1.944 1.949 1.937 1943) 1. : 1.918 1.957 I. 1.939 1.950 1.947 1.938 1.9340. 3 1.934 1.956 I. 1.946 1.943 1.948 1.932 1.938 I. : 1.933 1.953 I. 1.945 1.945 1.951 1.932 1.945 I. .904 1.934 1.946 1.952 1.942 1.949 1.943 1.935 1.940 I. i 1.928) 1.951 1: 1.949 1.942 1.942 1.931 1.950 I.95I I. : 1.944 1.942 I. 1.944 1.946 1.940 1.935 1.961 1.930 I. q 1.942 1.950 I. 1.945 1.942 1.943 1-931 1.942 1.927 ; 1.940 1.940 I. 1.942 I.94I 1.937 1.932 1.955 1.932 ; 1.941 1.933 I. 1.942 1.941 1.930 1.938 1.951 1.948 1.941 I. 1.942 1.940 1.926 1.942 1.944 : 1.947 1.950 I. 1.940 1.942 I. 1.928 1.937 1.944 I. : 1.945 1.946 I. 1.943 1.950 I. 1.929 1.947 1.942 I. : 1.942 1.953 I. 1.938 1.945 I. 1.928 1.949 1.950 I. : 1.944 1.949 I. 1.937 1.944 I. 1.934 1.960 1.943 I. 1.940 1.948 I. 1.929 1.943 I. 1.926 1.958 I.951 I. : 1.935 1.948 I. 1.93I 1.945 1.924 1.932 1.951 1.946 I. F 1.945 1.951 I. 1.926 1.943 1.932 1.936 1.948 1.945 I. : 1.945 1.945 I. 1.930 1.944 I. 1.939 1.944 1.957 I. 3 1.942 1.942 I. 1.935 1.949 I. 1.941 1.949 1.957 I. : 1.942 1.947 I. 1.931 1.935 I. 1.939 1.958 : 1.921 1.939 I. 1.935 1.939 I. 1.940 I91I9 1920 1921 1922 1923 1924 1925 1926 1927 1928 1929 1.964 1.955 1.948 1.946 1.942 1.943 1.941 1.938 1.940 1.938 1.956 1.956 1.943 1.930 1.939 1.943 1.938 1.943 1.943 1.929 1.945 1.949 1.938 1.932 1.945 1.939 1.939 1.942 1.946 1.931 1.952 1.944 1.931 1.932 1.946 1.947 1.934 1.944 1.942 1.937 I.953 1-943 1.925 1.936 1.948 1.950 1.939 1.945 1.947 1.938 1.939 1.939 1.914 1.928 1.956 1.945 1-944 1.946 1.948 1.934 1.945 1.956 1.912 1.936 1.946 1.951 1.944 1.945 1.942 1.933 1.954 1.953 1.930 1.944 1.919 1.941 1.940 1.945 1.944 1.941 1.937 1.931 1.944. 1.939 1.947 1.969 1.923 1.947 1.946 1.950 1.942 1.944 1.927 1.928 1.939 1.953 1.944 1.962 1.927 I.942 1.949 1.946 1.934 1.944 1.930 1.929 1.941 1.953 1.948 1.951 1.929 1.942 1.948 1.946 1.929 1.944 1.929 1.936 1.962 1.950 1.957 1.953 1-915 1.933 1-942 1.945 1.932 1.942 1.926 1.940 1.948 1.952 1.927 1.937 1.946 1.946 1.938 1.943 1.938 1.934 * In calories/cm2/min. at earth’s mean distance from sun (Smithsonian Astrophysical Observatory). SMITHSONIAN TABLES TABLES 772-774 TABLE 772.—The Solar Constant, 1930, 1931 610 Jan. Feb. Mar. Apr. May June July Aug. Sept. Oct. Nov. Dec. 1.938 1.933 1-940 1.941 1.945 1.949 1.945 1.946 1.942 1.939 1.943 1.945 1.937 1-939 1.937 1.938 1.948 1.944 1.949 1.947 1.929 1.941 1.943 1.948 Year 1.942 1.942 1.941 1930 I Decades 2 3 _|_ 1-929 1.942 1.940 1.941 1.942 1.941 1.947 1-943 1.939 1.939 1.949 1.945 Means 1931 I Decades 2 Means 1.936 1.938 1-939 1.940 1.944 1.943 1.947 1.945 1.937 1.940 1.944 1.947 1.944 1.942 1.932 1.948 1.936 1.943 1.954 1.944 1.945 1.945 1.948 1.948 1.948 1.949 1.941 1.948 1.936 1.947 1.946 1.943 1-944 1.943 1-944 1.945 1.944 1.946 1.949 1.948 1.946 1.939 1.943 1-945 1.948 1.948 1.941 1.943 1.948 1.943 1-945 1-939 1.949 1.945 1.946 1.946 1.940 1.944 1.947 1.942 1.943 1.946 1.944 1.945 TABLE 773.— Wolf’s Observed Sun-Spot Numbers. Annual Means Sun-spot number = k(10 X number of groups and single spots observed + total number of spots ir groups and single spots). k depends on condition of observation and telescope, equaling unity for Wol with 3-in. telescope and power of 64. Wolf’s numbers are closely proportional to spotted area on sun 100 corresponds to about 1/500 of visible disk covered (umbras and penumbras). Periodicity: mean 11.13, extremes, 7.3 and 17.1 years. Terr. Magn. 30, 83, 1925, monthly means 1749-1924. See A. Wolfe: in Astronomische Mitteilungen and Zeitschrift fiir Meteorologie, daily and monthly values. See als Bull. for Character Figures of Solar Phenomena, Int. Astron. Union, Eidgen, Zurich, for spots and othe solar phenomena. Also, Terr. Magn. and Atm. Elec., 33, 223, 1928, for central spots, 1917 to 1927. NotE—The sun’s apparent magnitude is —26.5, sending the earth 90,000,000,000 times as much light as the star Aldebaran. Its absolute magnitude is + 4.8. Ratio of total radiation of sun to that of moon about 100,000 to oe 1 ae ac “é light ae ae ae “ec “ec ae ae 400,000 to I ang. ey. TABLE 774.—Duration of Sunshine : +10° Sus Seo |) ares 27) Approx. Mar. 21 Apr. 16 May 1 May 20 date: Sept. 23 Aug. 28 | Aug.13 | Jan. 24 Latitude hy em h m h hem 0° 12) 07a 2 O72 | 2 I2 07 10° 21 29 43 Bri 52 20 55 19 05 Declination] —23° 27’ of sun: Dec. 22 June 21 LF, 53 OI 48 40 23 09 13 23 36 57 52 15 OI 03 15 50 aa 05 oe For more extensive table, see Smithsonian Meteorological Tables SMITHSONIAN TABLES TABLES 775-778 611 ATMOSPHERIC TRANSPARENCY AND SOLAR DATA TABLE 775.—Transmission of Radiation Through Moist and Dry Air This table gives the wave-length, A; a the transmission of radiation by dry air above Mount Wilson (altitude = 1730 m. barometer, 620 mm.) for a body in the zenith ; finally a correction fac- tor, ay, due to such a quantity of aqueous vapor in the air that if condensed it would form a layer Icm. thick. Except in the bands of selective absorption due to the air, a agrees very closely with what would be expected from purely molecular scattering. ay is very much smaller than would be correspondingly expected, due possibly to the formation of ions by the ultra-violet light from the sun. The transmission varies from day to day. However, values for clear days computed as fol- lows agree within a per cent or two of those observed when the altitude of the place is such that the effect due to dust may be neglected, e. g. for altitudes greater than 1000 meters. If B= B the barometric pressure in mm., w, the amount of precipitable water in cm., then ap —=a™ ay. w is best determined spectroscopically (Astrophysical Jeumealy 35, P- 149, 1912, 37, P- 359, 1913) other- 1 wise by formula derived from Hann, w= 2.3ewio 70, ey being the vapor pressure in cm. at the station, h, the altitude in meters. See Table 449 for long-wave transmission. Fowle, Astrophysical Journal, 38, 1913. TABLE 776,—Brightness of (radiation from) Sky at Mt. Wilson (1730 m.) and Flint Island (sea-tevel) 108 X mean ratio sky/sun “Mt. Wilson 1500*| 400 | 520] 610 660 Joo 720 Flint Island . : 115 122 128 150 185 210 460 Ditto X area of zone Mt Wilson . # | Sync)! 5828))|| oxes, || 87220) to4sg) |) 11726) tests «6 a gs Flint Island . : 329) t7-on | 22sei|ened 29.2 35-3 | 80.0 | Zenith dist. of zone . : : | 0-15°| 15-35°|35-50°|50-60° 60-70°| 70-809) 80-g0°| Sun's brightness, cal. perc cm.? 2 per min. - =533))|) GOO) r-233n|er-355) || naps Ditto on horizontal surface \\) = .046 | .233 524 -780 | 1.041 | Mean brightness on normal surface sky x 108/sun - 423 403 385 365 346 | Total sky radiation on horizontal cal. per cm.? . per m. : , : - ; - - .056 | .110 162 189 .205 | Total sun + sky, ditto < ; ; : ; - 102 | .343 686 .969 .246 Altitude of sun . ‘ . : | | co Merce 25° B50 Ane * Includes allowance for bright region near sun. For the dates upon which the observation of the upper portion of table were taken, the mean ratios of total radiation sky/sun, for equal angular areas, at normal incidence, at the island and on the mountain, respectively, were 636 X 1o—8 and 210 X 10— 5, on a horizontal surface, 305 X 1o—8 and 77 X 10-8; for the whole sky, at normal incidence, 0.57 and 0.20; on a horizontal surface o. 27 and o.07. Annals of the Astro: physical Observatory of the Smithsonian Institution, vols. [I and III, and unpublished researches (Abbot). TABLE 777.,—Relative Distribution in Normal Spectrum of Svnlight and Sky-light at Mount Wilson Zenith distance about 50°. Place in Spectrum Intensity Sunlight Intensity Sky-light Ratio at Mt. Wilson Ratio computed by Rayleigh Ratio observed by Rayleigh TABLE 778.— Air Masses See Table 767 for definition. Besides values derived from the pure secant formula, the table contains those derived from various other more complex formula, taking into account the curva- ture of the earth, refraction, etc. [he most recent is that of Bemporad. Zenith Dist. Secant Forbes Bouguer Laplace Bemporad — NNN NN The Laplace and Bemporad values, Lindholm, Nova Acta R. Soc. Upsal. 3, 1913: the others, Radau’s Actino- metric, 1877. SMITHSONIAN TABLES. 612 TABLE 779 SOLAR DATA 58 Elements Known in the Sun’s Atmosphere Taken, with additions and corrections, from St. John’s Revision of Rowland. Papers of Mount Wilson Observatory, vol. 3 (Carnegie Inst. Publ. 396, 1928). Atomic state At. no., Reversing layer. element No. Max. lines int No. lines Max. int. mw nh cournu Ho OuOr SRE On EOE miOo *) 5875.618 He often present (absorption) over disturbed regions of disk. § Possibly TiO: in red. chromosphere. {Only in chromosphere or spots. SMITHSONIAN TABLES Chromosphere or spots.{ Molecular state Band lines No. lines Max. ae Source OH; NH VCH | -DyS>|| 30 100 Chr { MgH; CaH Spots 30 40 Chr I 4 Spots BO CN GHEa(E—) NH; CN OH; TiO § MgH + 4685.81 He+1N, present in || Present in disk and spots. TABLE 780 613 SOLAR DATA Quantitative Estimates of Composition of Solar Atmosphere (Taken from Russell, Astrophys. Journ., 70, I1, 1920.) In the chromosphere a deep layer of gases is held up by radiation pressure. The (gas) pressure, », and density, d, increase slowly downwards as gravity gradually balances the radiation pressure. At the base p may be about 107 atmosphere. At lower levels is the reversing layer in which gravity is dominant, p increases rapidly, and temperature remains nearly constant at 5000° K., as long as the gases are trans- parent. When p < 0.01 atm. general absorption by electron collisions make gas hazy. Opacity gains greatly with p, passes rapidly to the photosphere. When opacity important, temperature rises (radiative equilibrium, Schwarzschild, Eddington). Observed photospheric temperature = mean value of the radiating layers (Russell, Stewart, Astrophys. Journ. 59, 197, 1924). The presence and absence of lines of different elements depends on the excitation potential. Almost all the elements for which this is less than 5 volts appear. There are very few other lines except the strong ones of H. The level of ionization in solar atmosphere is such that those of 8.3 volts are 50% ionized. Na, Mg, Si, K, Ca, and Fe are 95% of the whole mass. Number of metallic atoms above cm? of surface = 8 X 10°. 80% are ionized. Mean atomic weight = 32, total mass 42 mg/cm. Even atomic weights 10 times as abundant as odd. Heavy metals (Ba onwards) little less abundant than those beyond Sr. Hypothesis that heavy metals sink below photosphere thus not confirmed. Metals Na-Zn far most common. Most elements not appearing in the table would hardly be expected to show spectral lines under solar conditions. Nonmetal abundance difficult to estimate. O is as abundant by weight as all metals together. Atmosphere = 60 H by vol., 2 He, 2 O, 1 of metallic vapors, 0.8, free electrons. Temperature of reversing layer = 5600° K.; pressure at its base 0.005 atm. In the following table, S, = whole no. neutral atom/cm?2; Sj, no. ionized; T, total no. both stages of ionization; Q, total mass/em? = T X at. wt. :, ::, indicate less accuracy; ?, origin doubtful. El. logSo logSi log T log@Q El. log So log Si log T El. logSo log Si log T Tl 5: e553 Cul) 4.3 | 4:9). 55:0 2nd : Zn 4.9 3.8 — 4.9 0.6: 0.6: Ga Oe AWS | AOE 210) | 2:0 Ge 2ES 2 Sesto Testy es5 As 0.6 —0.7? 0.6? req 14's Rb e255) Wize Peli eli: Sr O10 4373nes HAdR — FI(Se Vt O18), 926) 82:6 me Opis Zr O19 255) 255 Place | Oyu saynl Cb —0.2: 1.0: 1.0: —0.I —O.I 0.2 MOL O:5 4. 11-44 ed —0.5? —0.5? —0.2? Ru 1-ON) MeO) Ie Te5)) leO) 1-6 Rh —osy 40:5 | 0:5 —0.8? 1.4? Pd OL OG) ih Ou ale2 1H OO) : 1.0 CdR 2s aieG seo In —2.0: 0.0: 0.0: Sn OrialeoP eho Sb Or: 10172) O13: Ba —o0.2 ‘ 353 a! : ; 1.8 2 co is oN t co a NI Wee © Wee _ TNO NN D DY G0 cont CONI.O KO CDN DAW CO DY bv hONHL ANO oo YNNNWWWWE 3.2 E:3 3.0 2.1 3.0 1.4 CAREY EOO NE HORA DAY "Wee AAMANAAAMAN IW NAW ANN + ox NP ONION ON OD OBRN NW DAAIAAAAO NAMM ANNWON Tt ONDNON ON AN ONWRONORD Oh ODRUOHOL bb DOK DHNUG OROWBHHKHOHAY 4.0 7.0 4.6 7.0 5-7: 2.8): 4.6 1.9 3.6 1.9 4-4 5.1 6.7 5.1 5-7 CWO HUD Comparison of above values with values of Payne by a very different process show good agreement except for H (Payne 12.9, Russell, 11.5, the latter uncertain) and K, (Payne 5.3, Russell 6.8; the former probably too low). SMITHSONIAN TABLES 614 TABLES 781 AND 782 SOLAR DATA TABLE 781.—Abundance of Elements in Sun, Earth, and Meteorites (Taken from Russell, Astrophys. Journ., 70, 66, 1929.) Sun Earth D i ee el. Sun Earth E—S 8.6 : : i Ni , : — 1.0 2 — 0.5 — 08 — 3.2 — 1: = Te Oirtrcncys — 0.5: ©)ZA@)jae Quis + 0.1 SHO TN NAN © 9 DON110 bo RODRNOWH i Coo} CUO SE ENGO. S91 00 COO NOR Com HOH Ee 5 indicates less accuracy. 23 2 ? indicates doubtful origin. TABLE 782.—Abbot-Priest Solar Energy Curve (Sea-Level) 380 400 420 440 460 480 500 520 540 560 580 600 620 640 660 680 700 720 eo ELECT aa ETT tele ee HLT TT Tei te ger rat eye Pee tat Tt tt tT oot tlt Ti xaet | att ae eet te TTT a Zoot tt tte tela loli Tt | Ty eee ae 2 COAT ree wg ET TT ia i a a I I eT SE SVS TST ATA aS eee Ae ee ae R eR aaa es NOT Te) SER CTT) SO A a weg Spee SG is igo ase ileal Smnitsoien Gere High Atmos. Trans., Summer Sol. Washington Summer Sol. (Abbot et al: Ann.Astrop. 4) Av. Atmos. Trans. ore Sol. 30 Petes (a (a eepencr Fol wt te o o e Bureau of Standards) [Low Atmos. Trans.,Winter Sol. » 2» 0.S.A. Colorim. Com. “Mean” of x 20 Smithsonian Data (J.0.S.A.6, p. 563) ep a STANDARD PROPOSED BY PRIEST } 6-6-6) (Artificial Sunlight for Colorimetric Use Oo 380 400 420 440 460 480 500 520 540 560 580 600 620 640 660 680 700 720 WAVE LENGTH my SMITHSONIAN TABLES | TABLES 783 AND 784 615 STELLAR DATA | TABLE 783.—Constellation Abbreviations (Astron. Union, 1922) | | Andromeda Gircinus#ee /aNaud bea 2 6 BeegkOeeer Ant Coma Beren. . Aquarius....... Corona Aust. . Reticulum. ... Corona Bor... ibrar Lei Sagittane ane es 5 Cornvusyoa ee ; Sagittarius....S Gratera 4-2 © te Crue yt: Cyonusras! aun @aelumi arr Delphinus.... Microscopium. Mic Camelopardalis. Doradon. 55 Monoceros . . . Mon Gancenye eee ce Draco ee Wiisedeeea ess Canes Venatici.. Telescopium. . Canis Major.... ct. «6 Triangulum... eee Vin Ota See Ophiuchus.... ae AUStiE ly Capricornus.... ee uCanans. lec Garinaer een Pavowmener Ursa Major... Cassiopeia Hercules... . Pegasus Centaurus Horologium... Cenheus. «i. 7 ce Elvdtaie eens” Phoenix...... Phe Ebydiusmaere. oiivie bicton eee enIc Chamaeleon... . Indus Pisces Vulpecula.... TABLE 784.—Occurrence and Abundance of Elements in the Stars (Shapley, 1931. Payne, Stellar atmosphere, 1925. I, II, III, IV denote the occurrence of the neutral, once, twice, and thrice ionized atom. For the sun see Tables 780 and 781.) 10.2 1.9 [ II III 6.4 II II Iai id 8.0 © ON AUF WN Pe ed Elements of higher atomic number than 68 have not been noted. * Abundance 3.5. +t Abundance, 3.0. SMITHSONIAN TABLES 616 TABLE 785 STELLAR SYSTEMS (See Shapley, Harvard Reprint 68, 1931, Harvard Explorations, Science, 74, 207, 1931.) The solar neighborhood distance of 50 light-years, explored chiefly through the motions of nearby stars. A large majority are of less than solar luminosity, most below naked eye visibility. Only 40% of the stars known to be nearer than 16 light-years are brighter than the 6th magnitude. Exploring the solar neighborhood therefore involves a search for - telescopic dwarf stars. Any body 1/100 of sun’s mass within 1,000 astronomical units (.o15 light year) would be detected by its disturbance on Neptune and Uranus even if invisible (Russell). Nearest known star is 4 light-years distant (Proxima centauri, TY Vian est ye Region of brighter stars extending 500 light-years. The great majority of naked-eye stars lie in this region, though some of unusually high intrinsic luminosity are farther away. It includes probably 500,000 telescopic stars. Studied by proper motions, trigono- metric and spectroscopic parallaxes, and photometry. The local system.—Its diameter is several thousand light-years. There is good but not incontrovertible evidence of a localized star cloud in our part of the galaxy. Its popula- tion is in the tens or hundreds of millions of stars. Shapley considers it may be comparable in dimensions and composition with Magellanic clouds or a typical spiral nebula. In- vestigated principally statistically by spectra, magnitudes, and positions, and explored by spectroscopic parallaxes, star counts, and structure of variable stars and galactic clusters. The Milky Way with a radius much greater than 5000 light-years. The stars within 5000 light-years of the sun are a trifling part of the galactic system outlined by the globular clusters and Milky Way clouds. The stars are so remote that proper motions and spectroscopic analyses hopelessly fail. Statistical counts are of some help in the nearer parts. But most of our knowledge comes from eclipsing binaries, long-period variables, and Cepheids. The period-luminosity relation for Cepheid variables is the key to practically all distances > a few 1000 light-years. The Clouds of Magellan, nearly 100,000 light-years distant, nearest of all external galaxies and the most easily studied. Great advantage; all of its varied manifestations are seen at practically the same distance. These phenomena include gaseous nebulae, star clusters, giant and supergiant stars, some 1500 known Cepheids in the Larger Cloud. In this cloud 750 stars brighter than — 5.0 abs. mag. and over 200,000 brighter than the 0.0 have been estimated. The following gives an indication of the classes of stars measured in and in front of the Larger Cloud and adjacent field. G Kk M 771 768 385 206 172 77 565 506 308 The Super-Galaxies, 7,000,000 to 100,000,000 light-years distant. Composed of clusters of extra-galactic nebulae. The relative diameters and brightnesses have been determined for some of the super-galaxies. The most conspicuous is the Coma-Virgo cloud A, a stream of several hundred bright spiral, spheroidal, and irregular galaxies, about 10° light- years distant; its greatest length about 4 this. One of the richest and most distinct super- galaxies is in Centaurus. The Meta-Galaxy.—Great irregularity is found in the distribution of the objects exterior to our galaxy—perhaps partly due to obscuring clouds in our system but much attributable to aggregation of galaxies into super-systems and large indefinite streams. We find no evidence that we have approached the limits of a populated universe—no falling off in the number per cubic million light-years. The red-shift in the spectra of distant galaxies may be taken as an observational, relativistic indication of an expanding finite universe, “ but so far as the present census of the meta-galaxy goes, the total number of galaxies and the radius of space may both be infinite” (Shapley), SMITHSONIAN TABLES TABLES 786 AND 787 617 TABLE 786.—Stellar Spectra and Related Characteristics The spectra of almost all the stars can be arranged in a continuous sequence, the various types connected in a series of imperceptible gradations. With one unimportant exception, the sequence is linear. According to the now generally adopted Harvard system of classifica- tion, certain principal types of spectrum are designated by letters—O, B, A, F, G, K, M, R, S, N, P, and Q—and the intermediate types by suffixed numbers. A spectrum halfway between classes B and A is denoted B5, while those differing slightly from Class A in the direction of Class B are called B8 or Bg. In Classes M and O the notation Ma, Mb, Mc, etc., is employed. Classes R and N apparently form a side chain branching from the main series near Class K. The colors of the stars, the degree to which they are concentrated into the region of the sky, including the Milky Way, and the average magnitudes of their peculiar velocities in space, referred to the center of gravity of the naked-eye stars as a whole, all show important correlations with the spectral type. In the case of colors, the correlation is so close as to indicate that both spectrum and color depend almost entirely on the surface temperature of the stars. The correlation in the other two cases, though statistically important, is by no means as close. Examples of all classes from O to M are found among the bright stars. The brightest star of Class N is of magnitude 5.3; the brightest of Class R, 7.0. About 1% show bright lines. TABLE 787.—The Harvard Spectrum Classification Principal spectral lines Number | Per cent . Effective Mean Class (dark unless otherwise Example brighter In Color surface peculiar stated) than 6.25,] galactic index tempera- | velocity, mag. region ture, K. km/sec. O Bright H lines, bright spark lines of He, ING@). SMITHSONIAN TABLES 7 Er oe : na & wv ma n oho as LA a a a < mm = +6 622 TABLE 797.—Spectrum Types and Absolute Magnitudes (Strémberg, Mt. Wilson, Astrophys, Journ., 72, III, 1930; 73, 40, 1931; 74, 110 and 342, 1931. See also Wilson, ¢ : Astron. Journ., 41, 169, 1932.) Statistical discussion of distribution of absolute magnitudes among the various spectrum groups. Figures marked** relate to supergiants,* normal giants, + dwarfs,*} normal giants and dwarfs, and refer to the groups of which the numbers thus marked are maxima. The subscripts are the percentages in the various groups. The first line of the table shows the number of stars used in the discussion for the column, but the figures in the columns are reduced so that the distribution is for 1000 stars in each group. 1058 375 A2to | Foto Go to Ko to | K3 to K2 K x » a te * * Como NHN H * * 43 32 53:5** 50.7** 53 50 16 26 O 2 16 4 VAX). |fniCoys? 228 23233* 22950* |219 10 125 ce LST 23 64 86 99 19 37 34 88 23 2 1 132 23849*. |2697* 1 6 189 9 133 III I 19255*t|120.5* | 30 24 ie 160 109 10 7; 98 46 32 14 28 38 48 15 8 100 5303,9* Tt 18,}* 13967} 5 14 III 52 19 5 oO O 14 20 RE Cait ot a toad JALAN Oe tieeT i OOOO OONG) BON DOR DON DAO ON ACH OW 25 264** 23 6 WUWHODODOOOW DMM IW: HOANIDWNOOOCOCOOWN Pei Ooo) UCC acres ODN ON OO COHR BWHOOOF Summary (mean abs. magnitude) No. Super- Bright Normal Faint Spectrum stars giants giants giants giants Dwarts Mo to Mg 247 —4.5(9) eae —0.2(91) coin trader Kom Kg 378 —4.5(7) Sat —0.1(91) gt eget +6.7(2) Komen: ike 1058 ee —2.5(14) +0.3(78) +2.7(7) +6.1(1) Go “ Gg 601 —3.0(19) -0:4(49)\ 2,6 (28) 5 tea) Fo! “Vo 622 —3.0(9) +1.2(25) +3.2(46) NT ames Ny 478 —3.2(15) +1.2(85) The small percentage of dwarf stars is due to the fact that their apparent magnitudes in most cases are fainter than the set limit of 6.0. SMITHSONIAN TABLES TABLES 798-800 623 TABLE 798.—Brightness of the Stars Stellar magnitudes give the apparent brightness of the stars on a logarithmic scale,—a numerical increase of one magnitude corresponding to a decrease of the common logarithm of the light by 0.400, and a change of five magnitudes to a factor of 100. The brightest objects have negative stellar magni- tudes. The visual magnitude of the Sun is — 26.7; of the mean full Moon, — 12.5; of Venus at her brightest, — 4.3; of Jupiter, at opposition, — 2.3; of Sirius, — 1.6; of Vega, + 0.2; of Polaris, + 2.1. (The stellar magnitude of a standard candle 1 m distant is — 14.18.) The faintest stars visible with the naked eye on a clear dark night are of about the sixth magnitude (though a single luminous point as faint as the eighth magnitude can be seen on a perfectly black background). The faintest stars visible with a telescope of aperture 4 in. are approximately of magnitude 9 + 5 logio A. The faintest photo- graphed with the 10o0-inch reflector at Mt. Wilson are of about the 22nd magnitude. A standard candle, of the same color as the stars, would appear of magnitude + 0.8 at a distance of one kilometer. The actual luminosity (absolute magnitude) is the stellar magnitude which the star would have if placed at a distance of ten parsecs. The faintest star at present known (Innes), a distant companion to a Centauri, has the (visual) absolute magnitude + 15.4, and a luminosity 0.00006 that of the sun. The brightest so far definitely measured, 8 Orionis, has (Kapteyn) the abs. mag. —5.5 and a luminosity 13,000 times the sun’s. Canopus, and some other stars, may be still brighter. Note 1931: S. Doradus abs. mag. probably > — 8. The absolute magnitudes of 6 planetary nebulae average 9.1; average diameter, 4000 astronomical units (Solar system to Neptune = 60 astr, units), van Maanen, Proc, Nat. Acad. Sci. 4, P. 394, 1918, TABLE 799.—Giant and Dwarf Stars The stars of Class B are all bright, and nearly all above the absolute magnitude zero. Stars of com- parable brightness occur in all the other spectral classes, but the inferior limit of brightness diminishes steadily for the “later’’ or redder types. The distribution of absolute magnitudes conforms to the superposition of two series, in each of which the individual stars of each spectral class range through one or two magnitudes on each side of the mean absolute magnitude. Absolute magnitude supergiants — 2 to — 8; giants roughly o to + 1; dwarfs A, 1 to 2; F, 2 to 4; G, 4 to 6; K, 6 to 9; M, 9 to 11. The two series overlap in Classes A and F, are fairly well separated in Class K, and sharply so in Class M. Two very faint stars of Classes A and F fall into neither series. The majority of the stars visible to the naked eye are giants, since these, being brighter, can be seen at much greater distances. The greatest percentage of dwarf stars among those visible to the eye is found in Classes F and G. The dwarf stars of Classes K and M are actually much more numerous per peice volume, but are so faint that few of the former, and none of the latter, are visible to the naked eye. TABLE 800.—Masses and Densities Stars differ less in mass than in any other characteristic. The most massive star known is the brighter component of the spectroscopic binary B.D. 6°1309, 86 times the sun’s mass, 113 times its luminosity, and spectrum Oe. The smallest known mass is that of the faint component of the visual binary Krueger 60, whose mass is 0.15, and luminosity 0.0004 of the sun’s, and spectrum M. Note: Plaskett notes giant double star 184 sun’s mass. : ; The giant stars are in general more massive than the dwarfs. According to Russell (Publ. Astron. Soc. America, 3, 327, 1917) the mean values of Binary systems are: Spectrum B2 Ao F5 giant Ks giant F2 dwarf G2 dwarf K8 dwarf Ratio of mass to Sun 12 6.5 8 10 3.0 I.2 0.9 The densities can be determined only for eclipsing variables. Stars of Classes B and A have densities averaging about one tenth that of the sun and a relatively small range; Classes F to K show a wide range in density, from 1.8 times that of the sun (W Urs. Maj.) to 0.000002 (W Crucis). The surface brightness probably diminishes by at least one magnitude for each step along the Harvard scale from B to M. It follows that the dwarf stars are, in general, closely comparable with the sun in diameter, while the stars of Classes B and A, though larger, rarely exceed ten times the sun’s diameter. The redder giant stars must be much larger, and a few, such as Antares, may have diameters exceeding that of the earth’s orbit. The densities of these stars must be exceedingly low. ’ ‘ Arranged in order of increasing density, the stars form a single sequence starting with the giant stars of Class M, proceeding up that series to Class B, and then down the dwarf series to Class M. Star : iam. Density Brightness Diameter (km) | -OO0001O0 1600. 440,000,000 -OO00001 2 1450. 378,000,000 -0000020 710. 330,000,000 -OOO17 30. 53,000,000 .0007 78. 37,000,000 .OO12 13500. 40,000,000 .006 78. 13,000,000 -21 86. »200,000 -62 26. 2,300,000 -60 5. 2,300,000 Tr Er 1,391,000 4.0 580,000 4.0 333,000 4.0 249,000 Antares Betelgeuse a Hercules Aldebaran Arcturus Rigel Capella Vega Sirius Procyon Our Sun Krueger 60 Prox. Cent. Barnard’s | H SEO TON OREO LO LORON ECs Ort NTOKAADAHHOKAAODLH Computed by Plaskett, Publ. Ast. Soc. Pac. 1922; Interferometer measurements, Antares, 0.024”, 30,600,000 km; Betelgeuse, 0.047”, 386,000,000 km. (1921). SMITHSONIAN TABLES 624 TABLES 801-803 TABLE 801.—Parallax and Mean Apparent Magnitude (Reprinted by permission from Russell, Dugan, and Stewart, Astronomy, Ginn & Co., 1927.) Magnitude Mean parallax I 0.083 .056 .038 .026 .018 TABLE 802.—Spectrum Type and Mean Absolute Magnitude (Trumpler, Bull. Lick Obs., No. 420, 1930.) Mean absolute magnitude Mean absolute magnitude Dwarf branch Dwarf branch Giants. Vis. Phtgr. Vis. Phtegr. Vis. Phtgr. 250) apa +2.3 +2.5 = 2EQ 3:2 +0.5 +0.9 +3.2 +3:5 3.6 +4.0 5 --1.0 +4.2 +47 +4.5 ae 5 tie +5.0 Seri 5 +1.4 Ko +6.2 -+-7.0 5 +1.6 A2 ; Based on Adams, Joy, Mt. Wilson Contr. 199, 244, 262; Lundmark, Publ. Astron. Soc. Pacific, 34, 1922; Malmquist, Meddel. Lund. II, 32, 1924; Hess, Seeliger Festschrift, p. 265, 1924. TABLE 803.—Reduction of Visual to Bolometric Magnitude Eddington (M. N. 177, 605) gives the corrections from visual to bolometric magnitudes for the cooler stars. For the hotter stars the data are not so certain. The values are to be added algebraically to the absolute visual magnitudes. SMITHSONIAN TABLES TABLES 804-806 625 TABLE 804.—Summary, Elements of Solar Motion (Campbell, 1928) (Publ. Lick Obs., vol. 16, 1928.) Charlier a, 269.3° 50, +30.8° vo, 19.0 km/sec. 1986 r. v.; 4182 p. m.; 6467 Strémberg 27 Dat +29.5 20.6 Space veloc. 1026, A6-M. Wilson 270.8 +27.1 19.0 2748, 2305, Fr. v. and p. m. Campbell, Moore 270.58 +29.24 19.65 2149 r. v. B-M stars Mean 270.70 +29.16 19.55 Dwarf stars decidedly higher space velocity than giants (Strémberg). Class : (O05-B5) vo=22.7 km/sec. K=+4.9 K (G5-K4) vo=18.0 km/sec. K = be : A (B8-A3) 18.6 +1.7. M (Ks5-Mb) 22.1 F (A5-F4) 19.7 a 3 B-M 19.7 ca 26 G (F5-G4) 18.6 — 2 | Dwarfs appear only in classes F, G; remove 3 from G, vo = 16.6 km/sec. TABLE 805.—Elements of Solar Motion (Charlier, 1926) (Charlier, The motion and the distribution of the stars, Mem. Univ., California, vol. 7, 1926 ) Radial velocities lead to conclusion stars are receding. Galactic coordinates of apex. Galac. No. Galac. Galac lat. Mag. stars long. lat. atoilified 5 0-5-9 renee 454 20 -+-22 +22.8 6.0=6.9 5355 doe 1003 +16 +20.4 . 7.07 One 1239 +17 +28.6 3:0—5. Oe err: 811 +24 : +17.8 S65 eee ae 276 --23 x see 5 +20.6 TUSU 3, 2 Sree RRLOS +24 1986 fat v.), 646 (parallax oe sun’s velocity = 19.0 km/sec. (4 astr. units/yr. ). 1986 (rad. v.), 646 (par. stars), 4182 (p. m. stars) give as apex. Galac. long., 24°.3, latitude, 4+-22°.44: a = 269.3, 6 = +30°.85 TABLE 806.—Stars of Large Proper Motion Mag. p.m. spect. = > Barnardhse see ose, 3 9.7 10.2 Ms | O, Eridani (triple)....... 450 4-1 (G5 IeNpEGy NSE. eine Sears ac O20N8:8) Mor MWolfe4souseaee ae ene 13 3toP a: Gir SO ur ats eons 6:5707:0). (Gye | !PromiCentaurie.a ene 10.5 3.8 M? acaillergsseermrr cen ae 7A 16.9) MO) |e. Gassiopelaeeer aaa 5a) 3 caeGs Cordoba 32416 86 a 6 as 8.3. 6.1 M3 | @ Centauri (double). 22uae7 GO | 61 Cygni (double)....... 6.3 5.2 K8 | Washington 5584 ( (double) 8:90 357, GO WViolita5Ofery. aeereaabecr 13 4.8) 22 | Cordobas2onolee eee 6.6 3.5 Mo alandemrsSan eee FdO figs) INIA GIB E NN 4 oooogosdsose Anat 33 2G Sina In case of multiple stars the magnitudes and spectra of the brightest star are indicated. See Lick Obs. Bull. 344; Harvard Circular 283; also Luyten, Astronom. Journ. 42, 69, 1932. List of stars, p.m. > 0”.5 annually. The following stars, Van Maanen’s, 3”.01, Ross 619, R. A. 8806™, Dec. + 92, annual p. m. 5”.40, may be added to the above el SMITHSONIAN TABLES | | 626. TABLES 807 AND 808 TABLE 807.—Spectrum Class and Proper Motions (Reprinted by permission from Russell, Dugan, and Stewart, Astronomy, Ginn & Co., 1927.) Limits of p. m. 0”.00 to .02 to .04 to .10 to .20 to .45 to 80 to 2. Over 2”.00 £ Meant pais iysteicis tim re One Percentage of stars with TABLE 808.—Equipartition of Energy in Stellar Motions (Jeans, Nature, 122, 689, 1928.) ; Corresponding Mean mass. Mean velocity. Mean energy. temperature. 19.8 X 10” 14.8 X 10° cm/sec. (O55@10; 12:0) ee i) is ~ 24.5 272 20.9 35-9 47-9 64.6 77.6 79.4 74.1 77.6 COIS CoO Oo1) Cone MBN MmOMN UN OD OMONNNa Bp Oty Ww “ This equality of energy can be attributable only to the gravitational interaction of the stars. For if it were produced by any physical agency, such as pressure of radiation, bombardment by molecules, atoms, or high-speed electrons, this agency, as the last column shows, would have to be in thermodynamical equilibrium with matter at a temperature of the order of 2X 10" °K. Since no such temperatures are known the observed equality must be due to gravitational interactions over millions of years. Such evidence suggests a general age of the stars of 5 to 10 million-million years.” SMITHSONIAN TABLES TABLES 809 AND 810 627 TABLE 809.—Stars of Large Space Velocity, Greater Than 300 km/sec. Apex of / Apex of motion Wes Right / motion Right ascension ee Paral- mreeennen| 1aciey, ascension Sa and : lax Right cay and ~ Right declination ascension Bed declination ascension and ax 1900 and declination declination ° ° ° ° ° ° + 2.6 +23 223.6 —21.6 145 —45 +61.0 —46 | 369 || 226.2 —16.0 189 —69 a alt7) 3) |, 302)!" 22672) #159 187 —69 2 2an — 4 | 448 || 227.1 +109.7 1242 +34.1 —II | 465 || 234.4 —10.6 123 — 8 +30.9 —64 | 333 || 245.4 +19.1 205 —69 —31.2 +27 | 786 || 246.9 +48.2 220 —42 -— 6:1 —59 | 799 zeae i a r43 37 263.5 +18. 167 —5I +23-4 sawn vs 264.1 +37.3 302 —35 +34.8 + 6 | 501 ||) 304.4 —21.7 92) AT Sie —50 | 787 || 308.6 +42.5 90 +44 +20.4 239 —27 | 420 || 314-8 -F (2.6 228 —5I +38.4 243 —49 | 346 || 341.6 +13.4 78 +28 — 1.0 92 + 7 | 617 || 355.0 +29.0 80 + 6 +10.6 256 —58 | 408 —18.0 27 Oye eA +19.2 55 +66 | 444 DOOHHNHDHNAORHHHON (pS eee OC eT ON OS C2 OS ESSE ON Oo COL OO SOIT! OCWBORDKH HD HS ORL OOhL Ob 00 20 DOM G9 HO HMI SMIMIOO This and the following table are taken from Katalog von 1937 absoluten Sterngeschwindig- keiten, Klumak, Hecht, Astron. Nachr. no. 5696-7, 238, 116, 1930. See also Wilson, Ray- mond, Astron. Journ. 40, 121, 1930, 4233 stars. TABLE 810.—Stars of Small Space Velocity, 5 km/sec. or less Same reference and designations as for preceding table. Apex of Apex of Right motion ra Right motion ascension Sana lecity, ascension . ; and . Right iein/ and Right declination 7 ascension ae declination ascension 1900 and Sec 1900 and declination declination ° ° ° ° ° ° ° ° 8.7 +56.0 345 +34 185.2 +39.6 180 + 9 16.0 +35.1 OSs ZO 7a ath ood: L207, 18.1 —69.4 Br 5a 10 224.6 —24.9 193 41.0 +26.9 299 —57 241.4 +45.2 41 66.6 +42.8 306 —6I 255-8 +54.6 157 +22.8 Te iA 268.9 +16.8 125 +60.3 284 + 9 27 Aa 3 OLO 146 +46.4 243 —26 277-9 152-3 197 +25.2 230 +26 207-3 ao -5 16 cot O 17 Ae © 207-4 ci OLe oO +56.0 228 — 6 299.3 27-5 121 +-33-7 274 +41 305.0 +31.9 353 +81.0 2714 —44 325-45 — 10.6 245 +28.7 355 — 70 349.0 +37.6 330 AERA CO ANTON W OWLAN AWPU UU unin & DANA ABH ABUNN MCANORNMNNW CONORWM SMITHSONIAN TABLES 628 TABLES 811 AND 812 TABLE 811.—Motions of the Stars The individual stars are moving in all directions, but, for the average of considerable groups, there is evidence of a drift away from the point in the heavens towards which the sun is moving (solar apex). The best determinations of the solar motion, relative to the stars as a whole, are given in Table 804. In round numbers this motion of the sun may be taken as 20 km/sec. towards the point R. A. 18 h. o. m., Dec. + 30.0°. After allowance is made for the solar motion, the motions of the stars in space, relative to the general mean, present marked peculiarities. If from an arbitrary origin a series of vectors are drawn, representing the velocities of the various stars, the ends of these vectors do not form a spherical cluster (as would occur if the motions of the stars were at random), but a decidedly elongated cluster, whose form can be approximately represented either by the superposition of two intermingling spherical clusters with different centers (Kapteyn’s two-stream hypothesis) or by a single ellipsoidal cluster (Schwarzschild), the actual form, however, being more complicated than is indicated by either of these hypotheses. The direction of the longest axis of the cluster is known as that of preferential motion. The two opposite points in the heavens at the extremities of this axis are called the vertices. The components of velocity of the stars parallel to this axis average considerably larger than those parallel to any axis perpendicular to it. The preferential motion varies greatly with spectral type, being practically absent in Class B, very strong in Class A, and somewhat less conspicuous in Classes F to M, on account of the greater mean velocities of these stars in all directions. The positions of the vertices are nearly the same for all. Numerous investigators, from the more distant naked-eye stars, find substantially the same position for the vertex, the mean being R. A. 6 h. 6 m., Dec. + 9°. The nearer stars, of large proper motion, give a mean of 6h. 12 m., + 25°. (See Strémberg’s discussion, cited above.) In addition to these general phenomena, there are numerous clusters of stars whose members possess almost exactly equal and parallel motions,—for example, the Pleiades, the Hyades, and certain large groups in Ursa Major, Scorpius, and Orion. The vertices, and the directions toward which these clusters are moving, are all in the plane of the galaxy. The greatest known p. m. star is Barnard’s 9th m. in Ophiuchus, 10.3” per year, position angle 356°, parallax 0.52”, radial velocity about —117 km/sec. The average radial velocity of the globular clusters is 100 km/sec. The globular clusters as a class are approaching the sun. The spiral nebulae are receding. A general card catalogue of radial velocities is kept at the Lick Observatory. See Camp- bell, Radial velocities of 2600 stars, Lick Obs. Publ., vol. 16, 1928; of 741 stars, Adams, Joy, Stromberg, Sanford—Astroph. Journ. 70, 1929. TABLE 812.—Known Stars of Radial Velocities Greater Than 100 km/sec. Spectrum| R.A. 3 Proper | Velocity h . ¢ Star class motion | km/sec. (1) RZ Lyrae (2) Washington 5583 g iis (3) Washington 5584 Ou InG: ise Pe 3.68 (4) S Carinae faa Ses (5) Kapteyn’s star : ore aes 8.76 (6) Van Maanen No. 2 4 3.01 (7) MCordie5 243" aoc cmeh eon Sue 3 8 ae (8) R Pictoris eae (g) A G Wash. 3498 Wd .56 (10) 41312 Boss 1511 5 ae (11) w Pavonis a ee (12) Luyten 680 : 73 (13) BD +34° 2476 54 (14) V Urs. Min ae (15) BD +35° 3659 56 (16) BD +6° 2932 93 (17) AGC 27600 (18) Barnard star (19) « Columbae (20) BD —3° 3746 (21) B GC 10404 br (22) Cin. 2750 (23) 172 G Puppis (24) y 31 Aquilae (25) Boss 4188 (26) 6 Leporis "69 "146 PANAMA © WOMOWNO © HO OFPNA MAN NHNWUNUNW SMITHSONIAN TABLES TABLES 813-815 629 (Tables abridged by permission from Russell, Dugan, and Stewart, Astronomy, Ginn & Co., 1927.) TABLE 813.—Visual Binary Stars Burnham's General Catalogue, 1906, 3,665 pairs. Card catalogue kept by Aitken at Lick Observatory. Of stars brighter than 6.5 mag., one in 9 visual double. See also Aitken, The binary stars, McMurtrie, 1918, and New General Catalogue, Carnegie Institution, 1932; Innis, Southern double star catalogue, 1927. e is eccentricity, a major axis in seconds of arc, A in astronomical units of orbit. Magnitude Spectra Period e a A Pies mi, m2 Abs. mag. QUAI 255 0:9.) ote | Go; Fs 0¥.285| 0.01 | 0.054] 0.85] 7.5 253-3) ||——0.2. Our oh al Meise or eee 57a | Ei 5.70 39 0.27 4.5 | 2.8 ANE Anis AaG a CMi Os5ip 1.33 F5 39.0 23 ACOS) eae One| aes Osten; 24 BrO eT Sas a CMa —1.6, 8.4 | Ao, Fo 50.0 .60 Hesve |) Zot ||) xv 2.44, .96 Tate —& UMa efily Zio) || Iie), (EA 59.8 AI 25 allele gd ours, a Sn SET) ao. Cene... :,.. O33, we7 || (GO, ISS 78.8 51. |[Pl7cO5 0 '23- Su le2 OA ietOW a O4ul eae 7 ecoan & Boo. ....-. ASO GO) || 152.8 51 4.83 | 29 1.0 Bauer 5-9, 7.8 Oa EaTl aces: 0:7, 1-40) Ao; MG: || 248 .40 6.89 | 34 0.64 Sf Ay 1 2On Ml Ae eO) a Gem DOWN On| AOs AO! |) 306 56 6.06 | 80 55 pes fil « Ble masta... Be EEA al ios NOM |) 346 2220 TON 55 1.4 By 6) 5-0, 8.7 TABLE 814.—Spectroscopic Binary Stars Stars so close not yet visually double. Discovered and studied through shift of spectrum lines (Doppler effect). 7 is inclination of orbit to “plane of sky,’’ m, masses of components. The percentage with periods <10 d:71 for O and B stars; 64, A; 52, F-G; 16, K-M; periods >100 d, percentages are 12, 6, 18, 61. See Lick Obs. Bull. No. 355. App. (Glass Period Eccen- Orbital Asin i my sindi mag. ; days tricity velocity 10® km m2 sin*i m sinsi Abs. (m1 + m2)? mag. ei eacpane rs aa B3 1.45 0.05 480 9. shot eo NEE PAK 2.87 -004 44 red Sita tear: gi BR 688 a3 10 93 erties 2.8 203 OL 32 1.28 Seu vais 2.0 O22" 50 13.6 1.49 Te 4.01 =1O) 5026) 208) 16:0) 4e4 9: 6.4 14-41 .04 41,49 7 euererore 2.4 20.54 .54 16.4 Meee geist 0.2 104 OI Bite ite ateuskeie 4.4 665 -41 eager cee 3.2 1375 44 5 16.5 7 wee 6, 5.8 6, 63 1.66 2, 0.9 The —2°2, —1-8 0.025 Ou -070 -0097 -OO15 ae —2.6, —2.2 13.2 ye 41 1.4 .18 one 018 1-13 TABLE 815.—Spectroscopic Eclipsing Binaries Some 200 known. Last column, distance between center of two stars = radius of relative orbit. See Shapley Contr. 3, Princeton Univ. Obs. | ef Name Mea | ane mee BA) Ways pee I siete SWilact) 38-6 Gap 0:22) 0:78 72340 10425040" sO, lee WU Ma.. 7.9 Go Ae 76 ON ETS Zul elas SpantinOrs Fo OS 75 62 Teles aires S aGemC. 9.0 M BS oko 86 2500 58 25 ALS VELA eee Ae Bip 1.45 .88 74 SEA Tiey, .04, .06 @blensea- 426 B3 2:05) -.93 74 AO ey .09, .02 WEiGepe nee -0:9 Ao 22AQm 96 86 20,0 27 sie) OR GiBesiy. 42462.3 B8 2187 1-99 82 Pilg ay 3 Os exe Casi 29:3 B3 2.93 .93 88 Se Onl .006, .02 BeAr eae: 1 Aop 3:96 .99 77 2842'S Ving ole RS MVull 6:9 B8 4.48 .98 79 43355 5.0 FOO ON S Cine. o “Ce Ao 9.48 1.0 85 STOW Om “1OW OL WiGrues. 9.857 Gop 198 OI 76 (Oleg de mn (TeelOn ese ZO phi 9:7, cGo 262 ae 87 Eady Oy, of lis * Radii in terms of the relative orbit as unit. + Radius of relative orbit. MITHSONIAN TABLES | Masses | ro&km 0.69, 0.49 1-53 Ty c4e 2.30 52 ee 2.58 19 19 8.83 Hei. Ae) 10.3 2.4, 24) sie ALOy eed. 14.5 1X 10%) ee {O0N,7.00G03) es. 630 TABLE 816 PERIODS OF KNOWN BINARY STARS WITHIN 10 PARSECS OF THE SUN There is no reliable evidence (1930) for favored orientation of planes of double-star orbits. Kepler ard law gives (p, period in yrs.)? = (a, major axis, astr. units)*/(M, in solar masses). There is an apparer statistical relation between eccentricity and period, viz.: IDA 4 554cagsucee BON ess 5 ae ALO 4 eS ONES eS EGO Reriod) (logs) eae eee 162) 60) 97 OMe COM OS EES Using the mass-luminosity law (see p. 631) Luyten obtains: Log period in yrs. = 1.460 log d — 0.4§ log (M, in solar air-masses) + 0.168 + 0.35 where d is observed distance between stars at right angl to line of sight in astronomical units. From the data of the following groups the median-mean log of the periods (median-geometrical mea of actual periods) is probably about 2.5 (a little more than 300 yrs.). Half of the binaries in space ma be expected to have periods between the limits of 20 and 4000 yrs. Paral- | Mass . Paral- | Mas : Star d tax sun car aa sates Star d lax sun ae d co FiQOte he oP @:72 |0.100 | 1.0 | 11.43 ||| 26.7 || w@'Cen AB? || 7-02" |0:757 || 2:04) || T90)|) s8oun ¢ Her (2 2084)...| 1.2 SLU2 2: Teal e543 4e5cl|70)| Ophn ee |os500|peno4el mike 1.94 | 87.7 QC Mis to sc: |, 3 || 2307 | r:O4| 1.604) 40201) rsh’ pa 5) sooule m46 As} || Asiciy |e ieeyou NU bYACAIS eer 1-204 |Pe04 Ou |eien |eteo2nA2-2ull en bOORm aes 2-Ol eels tenn | a2 aon sn Wal leruls Coe eeee 7a |elO7, 290 | 1-63) |543-008|| AUS) (piri). 92225) e165) 02)32) |p 2senialeoTo KeriliGorn bee 1360255 .45| 1.65 | 44.3 || o2 Eri Be...] 4.52 | .200 04, |/)2:298 19248 on MasA Bierce. 10:6), '||.366" | 3.47)" 1-70 | 50.071) Cases 3. |S. 14) hOOn|s Foam ae mesons -UMarAB-CD Mi i6r W214 5, ered) 17809509 Spectroscopic |} 6 Tri log p: —1.57 | p: 0.0272 || 7 Boo log p: +0.13 | p: 1.36 binaries &€ UMa CD —1.56 .027-+ || £ UMa AB 0.26 1.82 x Drac —O.II -769 Paral- es : Mass Log Period Star d lex nomial Abs. magnitudes oun period years units IDRC ARS (CID Vs Sy Sacco ey if oie Toles eS SoCs Olne koko ence Reed: TAOS MESS 38 Brsrsn (B34 iy.) peewee ae 1-57) -100 Tee BOO Oleg es chun epee 1,00))|) TO 82 She2zASvABe nee ia oe Ano eal 7a: 24.8 O25), O25is snasth wove one 1.36 | 2.14 138 ING SS 77s Be Beant ls 2 Oval selene 20 TOM wel een susie eee eS ASHE || Dag 204 Kemi ce Asn (haa23))innee. eile | eelolie AG S| 52 ay cA Bae cnc es a5 OM eS il 324 eS 178 eos. WER Ce: 9 243 27 FEDS 2. timers cer lickseee ee OMI 2251 324 LU PTal'2 Siok eae eae 5.0 | .104 48 5 Oy EAC eo chs cnscciy eee .99 | 2.62 417 OES A 72 Na erent te 4.8 | .100 48 OES AO Ace ee S77) \\ doe 480 2B O Siar asc iensin erie 16 .294 SA | AT 7c meeps 2 1s 55 | 2.83 680 ALA SOL ists hea eee 5 27a| OO: 52 Sa7 EON py cos). elevaskewss SSO mez 0 500 GiiGyciC27/58) pee alee .300 70 Stor BS 7 Eettaeraoe aoe “205 2:97% 740 Shelgomsrae nee tee D424) s8a 78.8 TcsDy pel Oe rswrapic eonchswewirsn sy hee .94 | 2.95 890 OR Sx) INGs opooose oo oe 7.8 | .095 87 FR MO emake pease tee 295) | 3-01 1020 OWRD Lee, Srousy teste eesti: 19.4 | .163 119 Quik HO SRtaate ec iteus bor .84 | 3.24 1740 BOS 7a se ee eee 39 281 139 TOV4 UG Om oid lense: ra eee Sle scAe 2700 MilbYAUAIB “Gaerne 31 Ada ees Tied = Massy Tel pee 1A On| east 3200 pebler A= Caps eee 32 .105 305 2.7) = Wass) O:Q.. s 2. 2.20 | 3.64 4400 OysE ri ACS Gano eee 83 OO aus 6.0, + mass 0.64...... eS CmieaeO2 8300 aygIE epi (EV 5 0) eee 95 .149 639 I METRO M dite tnt Sacco 1.59) |e a7: 15000 Chrie1USe ae a ee 63572095 670 Bro LO check cin cuter -76 | 4.35 22000 IepZ WoC eae ee 150 .I42 | 1060 OrO8 12720. ee ee -QI | 4.60 40000 Ke Tuc-Lae 353°AB-CD? |) 3ne4y|) -1r? 2875 =|! Wiser gene 78 28 8 ee 2.53 | 5.02 | 105000 URE HUTA NEE See ener ot 310 lee 3 NOON 52a S aS ie vae cease 1.8 5.13 | 135000 OD SA7eAB- Ce are 330 .I00 | 3300 9125, 19-45 TO:2h ee a Det 165-285 el OOO0G 36 Oph-30 Sco AB-C. . .| 730 .174 | 4200 6553) (Os 7. 8 eee 1.89 | 5.32 | 210000 WEOtEIS Sine ae 512 .160 | 3210 [O21 2Aw 9. eee .56 | 5.41 | 260000 a Cen AIBS Gee Shen iise 6740 .760 | 8860 15.5, + mass 2.04...... 2.20 | 5.77 | 590000 Luyten, W. J. (Harvard College Obs., Proc. Nat. Acad. Sci., 10, 252, 257; 1930. SMITHSONIAN TABLES TABLES 817 AND 818 631 TABLE 817.—Masses and Absolute Magnitudes of Binary Stars (Pitman, Astron. Journ. 39, 57, 1929.) This paper contains a discussion of the orbits of 104 binary stars and of the relationship between stellar masses and luminosities (Eddington, M. N., March, 1924). In the following table of averages the magnitudes are visual. Values in blacker type are averages of greater weight. Six planetary nebulae give in average mass of 16.7, absolute magnitude 8.1. Visual binaries Eclipsing binaries Spectroscopic binaries Trig. Spec. Trig. Spec. Trig. Spec. Mass | Mag. | Mass Mag. Mass Mag. Mass Mag. M. 5 Mag. 70.1 |—4.26 eZ : ‘ —4.36 35-0 |—2.68 , : 3 5 15.24 | —1.54 a ; : —1.73 7.62 |— .81 : : : — .84 700: |— OL. 3 ‘ — .80 3.59 1.04 5 3 25 4.61 51 5 ‘ -56 2.36 1.52 : : ; 1.92 4.29 1.30 ; : : 1.42 2.15 : ‘ F : 2.43 ol 7, 53 : 5 : 1.26 58 1.30 ; : ‘ 2.00 2.76 BiDT WW: : 2.23 1.59 2.83 : : 3.02 1.26 5.13 : ‘ 2.27 1.08 5 ; : ‘ aeilicy Ses Soe 4.50 5-41 ous aap see Ors iS x Se WRU mI OD: Ame BOO Ron: me Re QR: Aa wONPPNHEB VRIES: - NUE wo Se ob: NSPUN OIA RO Reece eae Ce Tt re wn ema ee ae ee ee ees Sese ie ar ie ies ad Gee me TABLE 818.—Mass-Luminosity Curve (Prepared by Doctor Shapley, 1931.) Masses are stated as logarithms of masses in terms of the sun’s mass; the magnitudes absolute bolo- netric. Log mass Abs. mag. Log mass Abs. mag. Log mass Abs. mag. 1.6 —5-5: 1.0 —2.92 0.0 + 4.41 1.4 —4.6: 8 Te 7 —0.2 + 6:22 1.2 me a 6 ee Ord) + 8.19 Bras 4 -+- .72 —0:6 +10.20 2 +2.57 —0.8 +12.29 Notes added in press.—(Aitken, M. N., 92, 596, 1932.) At least one star in every 18 to 9th mag. isa lose visual double; I in 4 or 3, a spectroscopic binary; 1495 of latter known, surely physical doubles. Irbits known for 120 pairs. spectrum B A F G K M B A F G K M ssun Riaistmpution 1.7 20.4. 15's) 33. 15.6 154 masses 10.6 5.2: 2:6) 2:4..2.2 “Om see Spectroscopic Visual Periods, 2°7d 7.64 14-150 30¢0% 102.5 -3:2y |:16:8y 37.1 73: 138 2000 5000 e 5O5 aul Omee2 35 30m a0 EASE AO) B53 : : .61 .76 SMITHSONIAN TABLES TABLES 819-821 TABLE 819.—Stellar Radiation Measurements (Pettit, Nicholson, 1928) Radiometric magnitude = apparent magnitude of an Ao star which will give same radio- metric deflection. Heat index = visual — radiometric magnitudes. Heat index — color index = zero for Ao star. Water-cell-absorption is fraction of radiation eliminated by water- cell expressed in magnitudes. Giants, F5-Mo, have greater heat indicesthan dwarfs of same classes. Red stars deviate from black-body conditions. The radiation received at earth’s surface at Mount Wilson from star in zenith of zero radiometric magnitude, 17.1 X 10°? cal./cm?/min. Radiometric magnitude Hefner lamp at I meter is —20.00; International candle is 1.11 Hefner unit = —20.11; its heat index is 5.82 mag. (1900°K.). (All measures reduced to zenith at Mount Wilson, 2 reflections from fresh silver in tele- scope; rock-salt window over thermocouple.) TABLE 820.—Spectrum Classes and Temperatures 632 Observed Temperature Spectral Heat index type Water-cell absorption Water-cell absorption Color index* X0.555H | X0.520p Mag. 0.20 23 23000° 15000 11200 8600 7400 6500 5500 4700 4100 3300 3050 7500" 6200 5450 4700 4140 3750 3130 2980 2810 2550 2390 2250 2350 1830 5350 4920 4460 3550 3260 2780 * Russell, Dugan, and Stewart, Astronomy, 2, 734, 1927. + Payne, Stellar atmospheres, 1925. Note—Hottest known stars 20,000 to 30,000 °K, O type, abs. mag. —4, masses 10-80 suns, (Plaskett). TABLE 821.—Visual and Radiometric Magnitudes and Total Radiations Brightest stars— Total radiation reaching the solar system Brightest stars— Visual magnitude Brightest stars— Radiometric magnitude Cal. cm-2 min-! 1022 Vis. mag. Rad. mag. Rad. mag. Vis. Type mag. Type M2 Mr A2s |—1.58]—1.27 Sinise ee Betelgeuse. Antares... @ Centauri. Canopus... y Crucis... Betelgeuse. . —1.67|-+-0.92 Antares.... ieee ie? 7 5o —1.09/— .86 S110) |[Sru ton .98|-+ .24 F3 |— .86/—1.09 G6 |+ .33/— .08 K4 |+1.70}+ .70 Ats|+ .14|-+ .10 Go .21|— .38 Canopus... . vy Crucis... . Arcturus... a Centauri. { Vera ence Capella.... Arcturus... Procyon... Achernar. . 8B Centauri. SMITHSONIAN TABLES .24| — -34| + 48] ++ -60} -+ .86}-+ .98 .23 2D .60 .8I Aldebaran. . Capella.... o Ceti max.. a Centauri. . -60|-+1.06 38/4 .21 alate oe .08}+ .33 -70| + 1.70 Arcturus... Achernar. . Spicawgun TABLES 822 AND 823 633 STELLAR RADIATION MEASUREMENTS TABLE 822.—Energy Spectra of the Stars (Abbot, 1929) Measures made with radiometer at the Coudé focus of the Mt. Wilson 1oo-inch reflecting telescope (arbitrary units). Astrophys. Journ., 69, 293, 1929. Stellar energy spectrum distribution; normal scale, outside the atmosphere. Place in wave lengths, microns Object 0.520 | 0.589 | 0.700 | 0.905 1.316 POrionis*sha4. ¢7- 584"('233) 1) Son)! *21 fw 334 | 644 | 287 | 91 Wh 4 367) \WSiz7 || 2074 2005 17 any Onis cmie oe 434 | 455 | 277 | 121 86 ae 267 | 266 | 297 | 206 172 267 | 355 | 247 | 121 17 a Canis Min...... Bp 167 | 277 | 436 | 149 17 a, 234 | 189 | 267 | 231 159 ; a: 184 | 244 | 228 | 177 We SAY SME rere et aye Boe 434 | 244 | 208 | 149 125 a Aurigae ae: 284 | 388 | 455 | 369 202 eet Fee lest elesOOw le ss7ale25o 206 134 | 178 | 238 | 241 95 ee eS Slee O7a|eeOs' ae 166 | 198 | 298 116 33 | 109 | 199 168 200 | 228 | 37 404 Bae Srey ean 255m ce saleA4or 456 a Orionis sgh ey ee el een ed SS IO1O 6 Andromedae... . ee eS Seri t Seri |eeT SO 189 Aue SrtA LOS 202 ete oid MS 89 d 17 6 Sagittae ane Ss lass ab | eed 9 120 ; ve yaa eee auaerculisneerernc a Ses lPaacioe ees 166 387 166 331 67 396 144 185 * Additional observations for 8 Orionis: 0.4234, 505; 0.454u, 738; 0.404u, 827. + The dates refer to August 25, 26, and September 13, 10928, respectively. TABLE 823.—Stellar Temperatures, Radiation, and Diameters Sun’s diameter = 1t fort: N* Parallax °K ee ae Radiometer inbererer: Russell eat eds eee 6,000° ee Seat rae: 8 ie aye BLOrionis! 2 ne. 16,000 3.20 0””.007 20 ete 28 aulbyrae. eae 4,000 6.10 .130 2D 3 @ (Carne Wleyis5 5 5 4|| ran etoro: 6.60 -370 12 2 te mGan* Mink. s.., :. 8,000 1.24 125 II 1.6 a Aurigae....... 5,800 2.20 .O71 13 aoe Gauri ee 3,000 2.54 .053 70 39 Gekerasiquenri: 2,850 1.10 .026 94 82 BiOxioniss sea 2,600 7.90 .O17 510 280 cublerculisee a.) 2,500 3.60 { ee A 230 * Ratio of stellar to solar radiation outside earth’s atmosphere. | E ; i + To express in kilometers, multiply by 1.42 X 105; to express in miles, multiply by 0.865 X 10°. SMITHSONIAN TABLES 634 VARIABLE STARS TABLE 824 VARIABLE STARS—GENERAL CHARACTERISTICS (See Russell, Dugan, and Stewart, Astronomy, 1927; Ludendorff, Stratton, Das Stern- system, Handb. Astrophys., 6, Berlin, 1928; Payne, Stars of high luminosity, Chap. 14, 1930. ) Perhaps 5% of all stars are variable; number known, over 5000. Astronomische Gesell- schaft acts as central bureau; when a variable star is confirmed it there receives a definite designation, e.g., R. T. Persei. Most recent list Astron. Nachr., 244, 82, 1931, contains 873 additional thus named variables. The Harvard College Observatory (Doctor Shapley, Cambridge, Mass.) keeps a record of variable-star data. A yearly list of stars with known periods is published by the Berlin-Babelsberg Observatory. Note added in press: 5826 in 1933 volume. CLASSIFICATION I. Periodic Variables. (1) Eclipsing variables: Generally B and A stars. Not true variables. See Table 815. (2) Short period: 100 to 10,000 sun’s luminosity, large mass. Types B to M. Preferably F and G. (a) Period range about 4 day; about 10% of variables of regular period. Generally called cluster variables; quick rise in light, slow decline, visual range generally less than 1.5 mag.; photographic range averages 50% greater; 4} day generally of class A; peculiar velocities average 70 km/sec.; variable radial velocity range small, proportional to range in mag. Max. of approach invariably near max. mag., max. of reces- sion near min. mag. Galactic concentration small. Shortest period known (10932), 0.69746 days, 15 mag., range 1 mag. (8" 19™ 38° R. A., 18° 45’ S. dec. van Gent). ; (b) Periods 1 to 32+ days; 15% of regular variables. Cepheids. Much like (2a) but periods 4 d, class F5; 8d, Go; 20d, G5. Peculiar veloci- ties average about 12 km/sec. Galactic concentration strong. About 120 known. Long-period Cepheids are among the brightest stars known, 20,000 times brightness of sun. The following table 825 is due to Shapley, 10931. (3) Long-period variables: Nearly all red stars 87% class M, 6% class N, 5% class S, a few G and K. o Ceti typical. Abs. mag. — 2.0 (Oort, 1927) ; periods 100 to 150d, M=— 2.3; 250 to 340, M=—1.1; > 340, +03 (Gerasimovi¢, 1928). Periods often irregular, proper motions small (0.03”), radial velocities large (mean 35 km/sec.). For S Librae, 385 km/sec. Heat radiation diminishes by 1 or 2 mag. while light by 5 or so. Il. Irregular variables. (1) R V Tauri: Resembles Cepheids somewhat irregularly. 12 known (Gerasi- movic, 1929). 19 given by Ludendorff (1928). (2) R Coronae Borealis: About 11 known. Typical R. Cor. Bor. remains often for years of 6th mag.; then may rapidly drop 6 mag. for indefinite period then returns to original mag. Ludendorff gives 11. (3) U Geminorum (type): Normally faint but brighten up at irregular intervals to drop back to original magnitude. Some analogy to Novae. Ludendorff gives 20. (4) T Pyxidis: Resemble Novae. Ludendorff gives 5. SMITHSONIAN TABLES TABLES 825-827 635 TABLE 825.—The Cepheid Period-Luminosity Curve Absolute Absolute Logarithm Mean photographic bolometric of period. spectrum.* magnitude.** magnitude. 0.0 F 2.5 — 0.31 — 0.82 0.2 F 5.5 — 0.61 — 1.25 7 — 0.93 — 1.67 — 1.22 — 2.16 — 1.53 — 2.65 — 1.89 — 3.15 — 2.26 — 3.71 — 2.68 — 4.34 = oy) = OsL3 — 3.81 — 6.11 — 4.60 — 8.2: on x | ON OMALNO oan SARAAMAO| * Shapley, Harvard Bull., 861, 1928. ** Shapley, Harvard Monogr., 2, 1930. TABLE 826.—Novae Novae (temporary stars): Between 10 to 20 brighter than the oth app. mag. occur ina year (Bailey). Numerous in spiral nebulae. More than 80 in Andromeda nebula (Hubble) ; 30 per year estimated. Mean parallax of five, 0.01”; abs. mag. + 8.5 to — 3.1 (Russell). Nova Aquilae, 1918, class A before outbreak; then appears as rapidly expand- ing gas 1700 to 2300 km/sec.; fades to Wolf-Rayet, class O (T Coronae Bor. changed finally to gM); gaseous envelope visible 1918 to 1926, reached diameter 16”; abs. mag. + 3 to — 8.8; distant 1200 light years. Nova Persei: Diffuse cloud faint light expanding 6’ to 7’ in 7 months. Six weeks later moved 35” to 65”—apparently due to illumination of dark nebulous matter near star by outgoing light (Russell). See Milne, Nature, 128, 715, fg31. If after outburst it has dwindled to previous magnitude but spectrum shows a higher temperature, then radius must have decreased, say 10-fold, and the density would be much greater (compare white dwarfs, Table 828), TABLE 827.—Observed Maxima of Spectrum Lines in the Giant Sequence ( Shapley.) Ionization Excitation No. of effective potential potential Maxi- atoms at max. volts. volts. mum, per cm? surface Source. 13.54 10.15 Ao A210" Contour of line Fs * 1.9 >< 10= Contour of line 24.41 20.81 : Estimate 14.97 8.83 Estimate 11.82 0.0 2 ' Contour of line Contour of line 13.6 1.16 : : Line depth 16.5 2.82 : Line depth 10.98 0.0 : Line depth 9.96 0.0 fo: Estimate * Data for the supergiant sequence. SMITHSONIAN TABLES 636 TABLES 828-830 TABLE 828.—High-Density Stars. White Dwarfs Visual abs. mag. Density Sirius B 11.3 0.5 X 10° g/cm* o, Eridani B Procyon B Van Maanen’s* ..... * Smallest star known, about the size of the earth. TABLE 829.—Low-Density Stars. Giants Visual 4 abs. mag. Density a Scorpii A — 4.0 32 Om a Orionis — 2.9 Operon —14 2 Ton — 0.1 2x 10° (Taken by permission from Russell, Dugan, and Stewart, Astronomy, Ginn & Co., 1927.) TABLE 830.—High-Temperature Stars. High-Luminosity Stars (Plaskett, M. N. 90, 616, 1930. Payne, Stars of high luminosity, 1930. Pearce, Pub. Dom. Astron. Obs., 3, 302, 1926.) Draper Catalogue, 0.1% O; 0.3% Bo to B2; 1% B3-Bs5. Stars of highest temperature, greatest mass, highest luminosity, greatest distance from sun. Masses 5, O type, 43. sun's; 10, Bo to B2, 15 <'sun's; 12,83, B5, © x sun's, Surface Temp. brightness. M,—M, Density. 35,000° K. — 415M 3.61 M 33,000 — 4.10 3.41 31,000 — 4.03 3.20 29,000 — 3.96 2.98 27,000 — 3.88 2.76 25,000 — 3.78 2.52 22,000 — 3.61 19,000 — 3.38 16,000 — 3.08 14,000 — 2.80 Nore.—See Russell, The Constitution of the Stars, Science, 77, 65, 1933. SMITHSONIAN TABLES TABLES 831 AND 832 637 TABLE 831.—Properties and Classification of Star Clusters Star clusters fall into two distinctly different types: Globular: Typical, Messier 13; open, Messier 4; elongated, Messier 19. Have strong central condensations, rich in faint stars. Scattered widely in latitude, restricted in longitude. Many variables—nearly 900 in 45 clusters. Radial velocities > 100 km/sec. All distant > 10,000, 4 > 100,000 light-years. Very few new ones found—about 103 known. Very definitely part of galaxy. Although concentrated towards its plane, only 2 within 4° of it (cloud obstruction probably). Diameters about 35 parsecs. Many stars, tens and hundreds of thousands. Many giants and supergiants. Max. luminosity about — 2.5. Galactic: Very varied: rich, M 11; irregular, M 35; nebulous, Pleiades, M 16; accidental, M 103. Almost exclusively in Milky Way, all longitudes; apparently no variables. Radial velocities rarely > 40 km/sec., generally less. Almost all < 4000 light-years distant. Almost exclusively in galactic region devoid of globulars. Tens and hundreds, rarely thousands of stars. Hyades type, yellow stars as dominant as A type. Pleiades type, almost all B’s and A’s, on Russell’s main branch. TABLE 832.—Distribution of Open Star Clusters (Trumpler, Bull. Lick Obs., no. 420, 1930. Contains classification in diameters, distances, and distribution of 334 open clusters.) The plane of symmetry of open clusters is inclined 2°3 to the adopted galactic plane. Its pole lies at R. A. 12"50™. Dec. 27°7 (1900). Forms much flattened disklike system 1000 parsecs thick, diameter 10,000 parsecs. In plane Lto plane of concentration. In galactic latitude. No. per layer Long. Long. Mean distance 100 parsecs 90°-270°. 270°-90°. parsecs. thick. — 850 2 tO) oO — 650 — 550 — 450 — 350 — 250 — 150 sie 50 + 150 + 250 =iaoo0 + 450 + 550 + 650 + 750 + 750 Total 33 8 6 4 2 0 12 sia = 6 ae + 10 a5 + 20 1-30 + 90 I I 2 3 9 No HRU DO _ oo In galactic plane. In galactic longitude. Ring limits No. of Density per Long. No. Long. 5 parsecs. clusters. 10° parsecs?. 0°-40° 12 160°-200° 0-1000 88 28 40 -80 34 200 -240 1000-2000 108 12 80 -120 40 240 -280 2000-3000 77 5 120 -160 28 280 -320 3000-4000 38 (48) 2 320 -360 4000-5000 16 (36) I > 5000 7 SMITHSONIAN TABLES 638 TABLES 833 AND 834 TABLE 833.—Globular Star Clusters Table contains those distant greater than 40,000 and less than 10,000 parsecs. For com- plete list see Shapley, Star clusters, p. 224, McGraw-Hill, 1930. 1 kiloparsec = 31 X 10% km = 3 X 103 light-years. Proper motions: M13, R.A. -++0.0005”, dec. +0.0008; M56, —0.0013, +0.0066; M2, +0.0082, +0.0026; Van Maanen, 1927 Galactic Angular diam- No. eter , . Distance vari- kilo- Long. Lat. ables parsecs 6397 (A366) 304.5 —I2.5 19.0 TOs) (47 7Duc;)). 3. : 272 —45 23 5139 (w Gen.).... 277 23 6656 (M22) 337 9 17-3 6121 (M4) . 319 14.0 6752 (A295) : 303 “Die 23:5 6809 (M55) 336 10.0 6541 (A473) 8 317 6.3 3201 (A445) 244 Wa 269 12.0 27 333 328.5 327-5 347 334 335 on DO) 00/00/00 1 1ON NON WO Ob Lk DODD = ° ° HR ONU < Ny BAU NON DUN ee 347 32 [tittit! Nd = TABLE 834.—Galactic Star Clusters _ Selected as having ture best determined distances from list of 248 clusters in Shapley, Star clusters, p. 228, McGraw-Hill, 1930. 1 kiloparsec = 31 X 10 km = 3 X 103 light-years Galactic Diameter Dis- No. tance stars kilo- Long. Lat. Ang. Linear parsecs kps. 98 ; II 2 0.79 : 3265) 820: aie Eieete 103 : 36 6. 2 Pleiades.... : e 10: Hyades.... 147 f a 10: LOGOMaet tere = 143 : 12 4 AQ) sino be F : 145 : 8.4 SMITHSONIAN TABLES TABLES 835, 836A AND 836B 639 TABLE 835.—Classification of Nebulae (Hubble, Astrophys. Journ., 64, 321, 1926; Contr. Mt. Wilson Obs., no. 324.) Symbol e. g. I Galactic nebulae— A Planetaries N.G.C. 7662 ) Predominantly luminous DL N.G.C. 6618 (2) wv obscure DO Barnard 92 (3) Conspicuously mixed... DLO N.G.C. 7023 II Extra-galactic nebulae—A Regular N.G.C. 3379 Eo (1) Elliptical 4 - 221 E2 1 to 7 shows ellipticity 4611 E5 : 2177, (2) Spirals (a) Normal spirals (1) Early.... 5 .G.C. 4594 (2) Intermediate... . 2841 (3) Late. . Sc 5457 (b) Barred spirals (1) Early N.G.C. 2859 (2) Intermediate.... ak 3351 me 1419 B Irregular N.G.C. 4449 Extra-galactic nebulae too faint to be classified, ‘‘Q”’ TABLE 836a.—Galactic Nebulae (Russell, Dugan, and Stewart, Astronomy, 1927; Russell, Atkinson, Nature, 127, 661, 1931.) Dark nebulae: Detected by obscuration of stars. Diffuse “Irregular of outline and shape—probably owing their detection to reflected light from nearby stars. Roundish, sharply defined, almost always with a central star; less than 150 known. Gerasimovié (1929) gives mean distance about 790 parsecs. The largest parallax is for N.G.C. 7283 in Aquarius, 12’ in diameter. Russell gives mean parallax 0.008”, mean diameter 54”. Nuclear star absolute mag. + 7 to + 8 (Russell, Menzel), + 5 (Gerasimovié). Classes O, Oe (ordinary isolated O type stars abs. mag. —4). Proper motion, mean of 9, 0.022’’; av. radial veloc. +37 km/sec.; 6 > 100 km/sec. Zanstra gives temperatures 30,000 to 100,000° K. for 20 of these objects; radius perhaps 1/43 our sun’s; density 100,000 g/cm?, pos- sibly, 10° or 107 g/cm?. Apparently upper end of a white dwarf sequence probably parallel to main dwarf sequence, viz.: Planetary nuclei... 4 Sirius B A5 o Ceti B Van Maanen’s o2 Eridani B Wolf 489 13 Observed velocity of rotation 1.4 to 18, av. value 5.3 km/sec. at an apparent distance of 5.7” from center. Period of rotation must be large, 4,000 to 15,000 years. “cc Planetary TABLE 836b.—Data on Six Planetary Nebulae (Van Maanen, Proc. Nat. Acad. Sci., 4, 394, 1918.) Diameter Magnitude Abs. M N.G.C. Parallax App. m Angular Astr. units Light-years 2392 -+-0.022 -+10.0 + 6.7 46” 2100 0.03 6720 + .008 +14.7 + 9.2 80 10000 16 6804. O22 +13.4 +10.1 32 1450 -02 6905 + .015 +14.5 +10.4 47 3100 .05 7008 + .o16 +12.8 + 8.8 95 5900 .09 7662 + .023 -+12.9 + 9.7 31 1350 .02 Mean abs. mag. +9.1. Mean radial velocity 29 km/sec. (Campbell, Moore, Proc. Nat. Acad. Sci., 1, 496, 1915.) (Diameter Neptune = 60 astr. units.) SMITHSONIAN TABLES TABLES 837-839 TABLE 837.—Diffuse Galactic Nebulae, Dimensions (Trumpler, Proc. Astron. Soc. Pacific 43, 255, 1931.) 640 N.G.C. 2237 I Orion 661 (Mes. 16) er Pleiades 6523 (Mes. 8) 6514 Distance parsecs. ee as. Diameter (’) i parsecs 1090 2050 35 * 55’ 20’ Tle ouiy7, 12 540 , 150 360/ 1340 60’ TABLE 838.—Nongalactic Nebulae (Hubble, Astrophys. Journ., 64, 1926.) Some 400 considered. Distribution of magnitudes appears uniform throughout sequence. For each stage in the sequence the total magnitude (M7) is related to the max. diameter (d) by the formula: M/p = C-5 log d. When minor diameter is used, C approx. constant throughout sequence (C = 10.1). Mean absolute visual magnitude —15.2. The statistical expression for distance in parsecs is log D = 4.04 + 0.2 Mr. Masses appear to be of the order of 2.6 X 108 X our sun’s. Apparently nebulae as far as measured are distributed uniformly in space, one to 10” parsecs? or 1.5 X 10“ in C.G.S. units. Corresponding radius of curvature of the finite universe of general relativity is of order of 2.7 X 10" parsecs, about 600 times the distance at which normal nebulae can be detected with the Mt. Wilson 100-inch reflector. TABLE 839.—The Magellanic Clouds and N.G.C. 6822, Dimensions (Hubble, Astrophys. Journ., 62, 400, 1925.) Total Core Total Core Core Angular size: App. luminosity: Surface brightness: Distance Linear dimensions: | Total Core Total Core Total Core Total Core Volume: Absolute luminosity: Mean density: Large cloud Small cloud Towa BUS Digs 1.2 1.9 21.0 34,500* 4,300§ 2150 X715 4.2 X10 9.2 X 108 —16.5§ —15.8 —10.0 6.6 BIGOT 320s They” SOLO)” 2.0f D7] 21.0 31,600T 2,000 II00 X 500 4.2 X 10° 2.3108 —15.5 —14.8 8.5 6.1 * Harvard Coll. Obs. Circ. no. 268. SMITHSONIAN TABLES + loc. cit. 255. tloc. cit. 260. N.G.C. 6822 20’ X 10’ Soar 9.0 9.7 221 214,000 1250 X625 500 X 190 3.8 X 108 1-7 <0" —12.7 —12.0 8.8 6.1 phtg. mags. mag. /(’’)? parsecs 4“ 6c (parsecs)® ae phtg. mag. abs. mag./parsecs? ae “é § Harvard Coll. Obs. Bull. no. 816. TABLE 840 641 MAGNITUDES, RADIAL VELOCITIES, AND DISTANCES OF EXTERNAL GALAXIES The following table is due to Shapley (Proc. Nat. Acad. Sci., 15, 565, 1929). The velocities (mainly Slipher data) are from Hubble (loc. cit., 15, 169, 1929); the velocities are also given corrected for the sun’s motion towards the apex A, 277°, D, +36°, and a velocity of 280 km/sec. (Hubble, loc. cit.), i.e., corrected for ‘galactic rotation”. Color indices are not very reliable but the mean values for various groups serve to indicate negligible absorption of light in space. Mean difference phtg.-vis. mag., +-0.23; Hubble’s 7619, the faintest, fastest, probably most remote, shows the largest color index, +-2.8. Apparent photo- , graphic Visual Distance Radial magnitude mag. in mega- velocity Vo mean Holetschek parsecs Class N.G.C. h km/sec. km/sec. (Harvard) corrected (Hubble) Peculiar. . 205 — 300 ; 10.0 221 — 135 : : 0.275 224 : 220 4 ‘ 5275 278 + 650 404 eS 584 7 +1800 598 Tao 936 +1300 300 1068 920 1700 800 2681 700 2683 400 2841 3031 3034 3115 +AHEFEAFHEHEFHFE HE | FH+H+44 9.7 9:5 9.1 g.2 10.3 10.4 9.4 9.8 8.8 9.3 See fetes es recteteaieate st HOS WAND FO WO V op, NOROR OF OR a) = © SMITHSONIAN TABLES 642 TABLES 841 AND 842 TABLE 841.—Extra-Galactic Nebulae, High Velocities (Hubble, Humason, Astrophys. Journ., 74, 43, 1931.) Velocity (km/sec.)=(Distance in parsecs) /1790 Object. Distance. Mean velocity. Notes. Virgo cluster .... 1.8 million parsecs 890 km/sec. Several nebulae, 12° & 11° Pegasus “ 7.25 3800 100 + nebulae Pisces ¥eroup) eerie 7 4630 25 Cancer cluster ... 9. 4800 150 Perseus sew tLLs 5200 Coma en stG 7360 Urs. Maj. “ se 11800 sr ae 2) 19600 “ Extra-galactic nebulae.—(Analysis of 900 plates with 60- and 100-in. Mt. Wilson reflectors, Hubble, Science, 75, 24, 1931.) (1) None found in low galactic latitudes; avoidance zone irregular, 10° to 40° width—apparently due to known obscuring clouds in Taurus, Cassiopeia, Ophiuchus, etc. Inclined belt of bright B stars and diffuse nebulosity reaches highest latitude in Taurus and Ophiuchus. (2) Avoidance zone bordered by partial obscuration to — 40° in general direction of center of galactic system (long. 330° to 340°) ; very limited in opposite direction (except in Taurus) long. 140°, lat. — 35° to — 40°. (3) Lat. > 40° (and in lower lat. towards anti-center) nebulae approx. uniform distribu- tion log number per sq., degree = 2.375. Variation with exposure time indicates uniform distribution also in depth. (4) Appreciable absorption of light in extra-galactic space appears inadmissible. (5) Mean abs. phtg. mag. — 13.8. Density one neb./6 X 10 parsec®. Mean mass 5 X 10° sun’s. Mean density in observable space 5 X 10 g/cm®. (6) It may be hazarded that clustered nebulae (in 1 hr. plates) may be expected one per square degree, TABLE 842.—Rotation of Stars Values derived for the components, in the line of sight, of the equatorial velocities of rotation for single stars, 0 to 250 km/sec. Assuming that the axes of the stars having the largest rotational velocities are at right angles to the line of sight, it appears that these stars are still stable. ‘Our analysis of the spectra of giants and dwarfs shows that all single stars belonging to the later spectrum classes show little rotation. On the other hand, a number of spectroscopic binaries of late type, such as W Urs. Maj. have a very rapid rotation. In fact, Adams and Joy have in a number of cases successfully predicted that stars of spectrum classes F or G showing diffuse lines are close spectroscopic binaries. It is probable that we have here a real difference in behavior: in the early spectrum types rapid axial rotation is observed in single stars about as frequently as in spectroscopic binaries; while in the later types rapid rotation occurs only in close binaries. This may have a bearing on the problem of the origin of double stars. (Struve-Elrey, M. N. 26, 91, 663, 1931.) SMITHSONIAN TABLES TABLES 843-845 TABLE 843.—The Galaxy, its Center and Rotation The center of the galaxy lies apparently among the dense clouds in Sagittarius 40,000 light-years (13,000 parsecs). About this center the sun revolves with a period of about 250,000,000 years, an orbital speed of 200-300 km/sec. Amount of matter within sun’s orbit must have mass about 200 billion times our sun’s. In following table based partly on Redman, M.N. 92, 113, 1931, y = mean distance in parsecs from center of objects. A = about .017 km/sec. /parsec. /) longitude galactic center. The sun is about +33 parsecs from galactic plane (Gerasimovi¢, Luyten, Proc. Nat. Acad. Sci., 1927). 643 Approx. No: : . objects - Source dis- tance 290° | Plaskett, Pearce 300 ae ac 346 ae ae 345 | Oort, B.A.N., 1927 237 ‘f ae oe 334 | Lindblad, M.N., 1930 346 % ae ae 319 “c é “ac 17 | Redman, loc. cit., 1931 321 | Pearce, 1931 325 | Gerasimovié, Struve 330 | Astrophys. Journ., 1929 J | 250 135 330 180 210 160 190 160 230 Ny COON NANI CON N = CO NO CO me nN No un o + n © S OSB Reed a ae Interstellar Ca. Same stars.... OWWO O 4 ~sJ _ aS ro NUP AWW N ONWHN * These values seem consistent on the supposition that the Ca is more or less evenly distributed between the stars and us, so that r for Ca should be % that for the stars. Lindblad (Scientia, 61, 325, 1932) gives a more recent summary of various workers. With Plaskett’s A = +o.0155 km/sec./parsec, time of revolution = 200,000,000 years; Jo = 327°. With a linear speed of 275 km/sec. our distance to center is 9,400 parsecs (about 30,000 light-years). Total mass of stellar system = 16 X 101 solar masses. TABLE 844.—Transmission of Light Across Space; Theoretical (Russell, Proc. Nat. Acad. Sci., 8, 115, 1922; Nature, 110, 81, 1922.) Let radius of particle = 7’, density, p, (random distribution); quantity of matter per unit vol. = d. The extinction of a beam of light will be e stellar magnitudes per unit distance where e = 0.814 gd/pr. gis a numerical factor independent of physical units, taking account of complications when 27 becomes near the wave length, A, of the light; when 27 = 2 or 3A, q = sensibly unity. q increases for small particles to a max. 2.56, when circumference = 1.12 X A; then rapidly decreases, = nearly (14/3) X 2zr/M for particles less than 1/2 this diameter. g/r is max. 2.42, when circumference = . Clouds, same mean density, d, opacity reaches sharp max. when particles of this size, at the same time becomes selective (1/A*). Visual max. when 7 = 0.086p. A cloud of this size dust, (density 2.7), absorbs 1 magnitude if 1/86 mg./cm? regardless of cross section. If 1/2 this or smaller, selective absorption almost as complete as for a gas. Best size particles for opaqueness also best for light pressure. Rayleigh’s formula for gas is J = Jp e* 32° (nm — 1) : : : ee oS = a Mk where v is the index of refraction, N, Loschmidt’s number. TABLE 845.—Transmission of Light Across Space; Observed Estimates Kapteyn, 1904...0.0016 mag./parsec Van Rhijn, 1928....0.000035* mag./parsec Seeliger, IQII.... .0003 e Shalen, 1929 .0005 E ae Halm, 1917 < Lundmark, 1925... .00000007 Shapley, 1929...... .000000007 * Equivalent to 4.7 X 10-14 g/cm2. Bull. Astron. Soc. of Netherlands, 4, 123, 1928. Eddington computed 0.00007 per 100 parsecs as scattering coefficient. For Ca Gerasimovié, 1929, obtained 1.1 X 10-% as the scat- tering coefficient. ‘ Absorption and space reddening in the Galaxy as shown by the colors of globular clusters. Steb- bins, Proc. Nat. Acad. Sci. 19, 222, 1933. SMITHSONIAN TABLES 644 TABLES 846-848 TABLE 846.—Amount of Matter in Interstellar Space (Eddington, Proc. Roy. Soc., A3, 424, 1926. Note also Table 848.) Whether or not matter exists in space is important in estimating absolute magnitudes (Cepheids), and, as a resisting medium, for its dynamical effects. Density at average point, 10 g/cm* (Eddington, dynamical reasons, star velocities). (Gerasimovié, Struve, Gaseous substratum of galaxy, Astrophys. Journ., 69, 7, 1929.) Interstellar density of Ca probably about pca = 3.6 X 10 g/cm® For all gases TO%ss 3 Assuming matter of about atomic weight 20, doubly ionized so that there will be about ° one free electron per cm, then Free path for ions, roughly 10° km, duration 1 year. Free path for electrons, roughly 5.2 & 10° km, duration 10 days. An ion encounters and deflects an electron once in 5 days. Central density of typical diffuse nebula, estimated, 10°” g/cm*. Hubble (Astrophys. Journ., 1926) estimates if all matter within 100 light-years uniformly distributed, density of order 10 g/cm*. Eddington (Nature, 128, 702, 1931), 10” electrons and protons in universe. TABLE 847,—Radii of Curvature of Space Radius of curvature of the finite universe of general relativity is of the order of 2.7 < 10° parsecs (Hubble, Astrophys. Journ., 64, 1926). Radius of Curvature of de Sitterian space time: 460 stars 3.63 X Io” astr. units = 5.74 X 10° light-years = 1.8 X 10° parsecs 29 Cepheids 3.0 ni “ 35; Oxstars 3:2 “cc “c “cc (Silberstein, Nature, 9, 50, 1930.) TABLE 848.—Interstellar Gases (Calcium, Sodium) Since excited atoms are exceedingly rare, the only strong absorption lines will be the principal lines. Na, Ca, and Ca-+ have principal lines in the observable spectrum. If we take a 12000° K. temperature for the interstellar medium, ionization potential may be taken as 20 volts =y. For electrons of ionization potential Y the fraction ionized is x/(1— x) = eY—¥O/KT For Na, Y= 5.1 v. and 30.35 v., T= 12000, Ri =30.35v- whence x/(1 — x) =2 > 10° for Ist ionization; 107° for 2nd ionization. Thus the Na+ (which is undetectable) is but one part in 2,000,000 of Na. For Ca with ionization potential 6.1 and 11.8 v. we have nearly all Ca as Ca++ +, but one part in 3000 of Ca-+, one in 2 X 10° of Ca. Certain brighter stars show these lines of Ca (fewer those of Na), which when cor- rected for solar motion indicate a stationary (relative to sun) absorber, whereas other lines indicate a definite radial velocity for the star (Plaskett). Struve gives the following table indicating definitely the increase of this absorption with the distance: 0-100 parsecs 22 stars K intensity 2.1] 400-600 parsecs 30 stars K intensity 4.2 100-200 101 2.2 | 600-800 26 4.6 200-300 62 3.1 | 800 33 3.1 300-400 47 3-3 Note.—Max. intensity K corresponds closely to outside boundary of local cluster (He B stars). The interstellar Ca apparently shares in the rotation of the galaxy (see Table 843). Note added 1933.—Plaskett, Pearce consider best value of interstellar density of matter as 10°’ g/cm’. SMITHSONIAN TABLES TABLES 849 aNnD 850 645 TABLE 849.—Temperature of Interstellar Space (Eddington, Proc. Roy. Soc., A3, 424, 1926.) Total light from stars equivalent to 1000 Ist (visual) mag. or heat from about 2000 (bolometric) Ist mag. stars. Star abs. mag. 1 radiates 36 X sun = 1.37 & 10” erg/sec. At std. distance 10 parsecs (3.08 X 10" cm) gives flow of 1.15 X 10° erg/cm*/sec. Energy density due to star app. bolometric mag. 1.0, is 3.8 < 10°” erg/cm® or energy of starlight =7.7 X 10 erg/cm’. The effective temperature of space from Stefan’s law is 3°.2 K. Ina region away from prepondering influence of a star a black body will take up a tem- perature 3°.2 K.; then its radiation will balance that which it absorbs. But if the receiving matter be a strongly selectively absorbing gas, higher temperatures may result. See Fabry., Astrophys. Journ., 45, 264. Then the temperature will be governed by 4 considerations: (1) Line absorption (excitation of atoms) ; energy held about 10° sec. and then lost by reradiation. An atom meets an electron only once in 5 days. So negligible chance (107°) of thermal agitation by an encounter. (2) Scattering of free electrons ; retards an electron I mm/sec./yr.—not cumulative and negligible. (3) Continuous absorption during en- counters of electrons with atoms (orbit switches). (4) Photoelectric effect (ionization of atoms). Velocity depends on quality and not intensity of radiation. Forms an electron gas with temperature determined by the mean energy of expulsion. The temperature defined by the mean molecular speed is of the order 10,000° K.* The temperature of the electron gas will be the same in space as close to the star. The rate of production of electrons but not their speed will be diminished. The heat of the electrons will be continually renewed and the atoms will gradually be brought to the same temperature. This high temperature is a typical quantum effect. * 15,000° K. is considered a better value from more recent data. Plaskett, Pearce, The problems of the diffuse matter in the galaxy, Publ. Dominion Astrophys. Obs., 5, 167, 1923. TABLE 850.—Matter and Energy (Donnan, Nature, 128, 290, 1931. Dushman, Gen. Elec. Rev., 33, 327, 1930; Eddington, Nature, May 1, 1926.) Jeans proposed the annihilation and transformation of an electron and a proton into radiation to account for the immense output of radiation from the stars. Einstein’s special relativity theory gives as the energy corresponding to a mass of m grams of matter mc* ergs (c=velocity of light). If H=energy in ergs, then this transformed to matter =E/c* grams. The mass of a proton + electron= 6.06 X 10” g. Applying Einstein’s development of Planck’s quantum theory, then the coalescence of a proton and electron produces one quantum of monochromatic radiation (photon); and since mc*= hy», y= 2.2 X 10° or N= 1.3 X 10 cm. Formerly such short waves were not known but the discovery of cosmic rays shows their possibility. Now the reaction P + E = radiation can occur only under unusual conditions. Imagine a proton-electron gas, only photons of v2.2 X 10% could change into a matter pair. Donnan shows that the black-body temperature of a hohlraum radiation necessary would be 2.2 X 10°%°K. By another method (equation for variation with the temperature of the SMITHSONIAN TABLES 646 TABLE 850 (continued) MATTER AND ENERGY equilibrium constant of an ideal gas reaction, d-log K/dT = Q/RT”) he derives a T of 10” °K. Milne yields another solution. If n= no, of protons (electrons) present per cm* at statistical equilibrium, then 1 = 0.96 X 10% T?X 107 (2:35*10")/T. pm(g/cm*) pr(g/cm*) [658000 ~ 0.85 x 10° MOG ><:1Om 0.85 X 10° 1.34 X 10° 0.85 < 10° We have the following picture: As 7 rises, molecules will be ionized and finally all dissociated to atoms; then the atoms become ionized with finally a proton-electron gas. At some very high temperature P + E — radiation sets in. Milne’s equation shows that at T = 10" this reaction is practically complete. As T rises yet higher the birth of matter will commence and we see that JT = 10”, the equilibrium density of matter becomes equal to 1.34 X 10” g/cm*®. T= 10” corresponds to enormous densities for both matter and radiation. Enormous voltages (9 X 10° volts) may give the attainment of such reactions. Compton effect.—X rays are supposed to consist of streams of energy quanta. While each quantum carries the energy equivalent to hy, one may also specify each of these photons (light units) by the momentum which, according to the theory of quanta, is equal to hv/c. When this photon collides with a free or loosely bound electron there is an inter- change of both energy and momentum in accordance with the laws of conservation of energy and of momentum. Consequently the photon suffers a recoil in one direction with loss of momentum, while the electron moves off in another direction with added momentum. The decrease in momentum of the scattered X-ray photon corresponds to an increase in wave length. (Dushman, Gen. Elec. Rev., 33, 334, 1930.) De Broglie phase waves.—De Broglie was led to the conception that associated with a particle of mass mo (rest mass, zero velocity) and velocity v, there is a wave motion of 12 wave length given by A=AVI—V/ Cc /mov = h/mov for small values of v; c is the velocity of light. The theory of relativity gives as the total energy, E, of a particle of mass mo E = me?/V 1 —v"/c? = mc” with m the mass for velocity v. According to the quantum theory, the frequency associated with E is given by E/h. Hence the phase velocity or velocity of the individual waves con- stituting the group is given by u = vA= mc?/mv = c’/Vv. The value of h is 6.55 X 107 erg/sec. For a mass of I g moving at 1 cm/sec. the asso- ciated wave length is 6.55 X 10°” cm—too small to be measured at present. Wave lengths 10’ to 1077 cm are measurable with crystal lattices. With de Broglie’s assumption we would expect corpuscular motion to exhibit phenomena like those associated with light waves under conditions where the momenta of the particles are of the order of magnitude SMITHSONIAN TABLES TABLE 850 (concluded) 647 MATTER AND ENERGY mv =h/10™ to h/to; ie., for mv ranging from 6.55 X 10” to 6.55 & 10°. According to kinetic theory a Hz molecule (m= 3.7 X 10) has a v of about 2 & 10° cm/sec. at room temperature. mv is then 6.6 X 10”, within the above-mentioned range. An electron fall- ing through 100 volts acquires a v of 5.9 X 10° cm/sec. and mv= 5.3 * 107” and A= 1.24 X 10° cm. For cathode rays of 25,000-volt velocity, \ comes out 0.75 < 10° cm, approxi- mately. Several observers have found for diffracted electrons values of X in accordance with De Broglie’s relation, (Dushman, Gen. Elec. Rev., 33, 335, 1930.) Neutrons.—Bothe and Becker (1930) bombarded various elements with Po a particles (range 3.9 cm in air, 76 cm, O° C, initial kinetic energy 5.25 X 10° electron volts). Mg, Al, give trace of a resulting radiation, Li, Bo, Fe, notable effects, Be tremendous results—a very penetrating radiation. Joliot and Curie-Joliot (10931) detected it through 30 cm Pb. First considered photons but finally neutrons. Speed of neutrons from Be, 7 to 35 < 10° cm/sec. Curie and Joliot found two groups 29 and 38 & 10° cm/sec. Becker and Bothe found Be to eject 19 photons to 1 neutron. Mass of neutron = B”™ + Het — N*“ = 1.0051 0.005 (O=16). (Darrow, Rev. Sci. Instr., 4, 58, 1933, contains bibliography.) May be considered element of atomic number 0; close combination of electron and proton. Effective collision radius 1.31 X 10 cm. (Rabi, Phys. Rev., 43, 828, 1033.) Positron.—Positive electron (Anderson, 1932) + charge < 2e, probably exactly equal to e and a mass comparable to a free negative electron. Probably results from the dis- integration of atomic nuclei (in Anderson’s case by cosmic rays). Out of total of 25,000 exposures, I,450 cosmic ray photographs were obtained: particles of + and — charge occur in about equal numbers. Energies range > 10° volts down to few million. Mass probably less than of proton. Anderson < 20 times mass of electron (Anderson, Science, 77, 494, 1933; Darrow, Rev. Sci. Instr., 4, 263, 1933, bibliography ). SMITHSONIAN TABLES 648 ; TABLE 851 PACKING FRACTIONS (ASTON) (See Table 506.) A reason for the failure of the additive law within the nucleus in atom building is because the protons and electrons become so closely packed that their electromagnetic fields interfere and a certain fraction of the mass is destroyed and appears as an electromagnetic radiation. The greater this loss, the more stable is the resulting nucleus. A convenient and informative expression for this loss is the “ packing fraction,’ the mean gain or loss of mass per proton when the nuclear packing is changed from that of oxygen to the atom under consideration. These are given in Table 596 as parts per 10,000, and their run is indicated in the following plot (ordinates). It is a measure of the forces binding together the protons and electrons of the nucleus. The abscissae are mass numbers. It is to be noted ' that the more stable (even atomic numbers) lie on the lower of the two lines drawn. (See Millikan, Phys. Rev., 32, 535, 1928, for the following use of this curve.) oo ° ° oO ae Aston’s curve indicates that only very heavy elements can evolve energy by disintegration and there are no abundant elements above at. wt. 80 (less than 1% of all matter). The condition necessary that even a heavy atom may liberate energy through the emission of an a particle may be seen at once from Aston’s curve. Such liberation can happen only where the curve is rising so rapidly with increasing atomic weight that nAy > 4 X (0.00054 — yn). n is the at. wt. of the active atom, Ay, the difference in ordinate between (n — 4) and n, yn, the ordinate for the at. wt. m, and 0.00054 the value of y for He., i.e., it is the mass of the H nucleus within the a particle. Therefore, not only very heavy atoms alone can disintegrate with the ejection of a rays and the evolution of energy, but we can compute the max. hardness, or penetrating power, of any radiations producible by radioactive disintegration. When thorium, e.g., throws off an a particle (7 = 232, yn = 0.00031), the increase in the mass of the a particle per gram-atom, because it has escaped from the nucleus, is 4(0.00054-0.00031 ) = 0.00092. The loss in mass of the residue of the Th atom nAy — 0,000034 X 228 = 0.007752. Therefore the total loss in mass through the emission of the a ray is 0.00775 — 0.00092 = 0.00683 grams per gram-atom. By Einstein’s equation the energy available for emission from this loss of mass is 0.00683c” ergs/g-atom. The total energy from each ejection of an a particle is this divided by the Avogadro number or 1.004 X 10° ergs. The highest speed a ray known to be given off from Ra has an energy of 8.800,000 volts (1.2 X 10° ergs). ThC’ ejects in one instance an a ray with 14% more energy than this. Similarly the “upper limit” for the speed of a 6 ray ejected by any of the disintegration products of Th or Ra is 7,540,000 volts or again 1.2 X 10° ergs. Einstein’s equation predicts quite within the limits of reliabilty of Aston’s measurements of mass, the maximum energy available in the radioactive process. SMITHSONIAN TABLES TABLE 852 649 TABLE 852.—Cosmic Rays (Millikan, Cameron, Phys. Rev., 31, 921, 1928; 32, 533, 1928. ) The measurements on the absorption coefficients for the cosmic rays indicate a complex set of entering rays which may be analyzed into separate rays with mean absorption coefficients (u) per meter of water of 0.02, 0.04, 0.08, and 0.30. Formation of He nucleus from hydrogen: From Einstein’s equation and Aston’s curve (Table 851) the loss of mass in the formation in a single act of the nucleus of He from four + electrons and two — electrons is 4 < 1.00778 — 4 X 1.00054 = 0.029 g/g-atom, and the radiant energy released each time this act occurs is (0.029 X 9 X 10”) / (6.062 X 10%) = 4.3 X 10” ergs. v= (4.3 X 10°) /(6.547 X 10°") = 6.57 X 107, A= 0.00046 A. From Dirac’s relativity- quantum-mechanics formula ~ = 0.30 per meter H.O. Oxygen from hydrogen: 16 X 0.00778 = 0.1245 g/g-atom #4 = 0.074 per m H.O. Nitrogen “ ar 0.108 g/g-atom =0.086. Mean of these two corresponds to 0.08. Silicon gives w= 0.041. Tron = v= o0l0re: So that the observed mu of the cosmic ray may correspond to the creation from hydrogen of He (u= 30), O (.08), Si (.04) and Fe (.02). Cosmic rays (A. H. Compton, Phys. Rev., 43, 387, 1933).—Intensity vs. altitude curves indicate not only a rapid increase in ionization intensity with altitude but also that at each alt. the intensity is greater for high lat. than near the Equator. At sea-level the intens. at high lat. is 14% greater than at Equator; at 2000 m alt., 22%, at 4360 m, 33% greater. With arbitrary constants corresponding to 1.605 ions due to rays unaffected by the earth’s magnetic field (neutral rays or electrons of energies > 4X 10” electron-volts), and a band of electrons approaching the earth with energies between 0.5 X 10” and 1.3 X 10” electron-volts reaching the earth at lat. > 50° and producing 0.235 ion, but failing to reach the earth at the Equator, Compton’s observations will bear out the theory of Lemaitre and Vallarta (Phys. Rev., 42, 914, 1932). The extra component appearing at high lat. is more rapidly absorbed than the main body of rays. This would be anticipated if rays unaffected by earth’s magnetic field were of electrons of greater energy; or a uniform background due to neutral rays such as photons, neutrons, or high speed, neutral atoms. Average intensity lat. 0° to 22°, sea-level, 1.620 0.006 ions per cm per seC.; lat. > 48°, 1.839 + 0.006 ions. Cosmic rays (Millikan, Etat actuel de nos connaissances sur le lieu et la mode de pro- duction des Rayons Cosmiques, Congrés international d’Electricité, 1932; Phys. Rev., 43, 661, 1933; 43, 695, 1933; Science, 77, 494, 1933; 77, May 5, 1933)—Most distinctive results: (A) Ionization-altitude curve (to 18 km or 92% through the atmosphere) does not rise exponentially clear to top with apparent absorption coefficient about 0.6 per m H:O (all observers get this, say 5 to 9 km) but shows a marked decrease 9 km to top (about 12 km), actually becoming concave downward. This is inconsistent with (1) incoming rays primarily of charged particles, (2) photons in complete equilibrium with their secondaries, (3) rays of the penetrating power of y rays or rays between these and the least energetic cosmic rays. They show non-ionizing primary entering rays not yet in equilibrium with secondaries. The rays show a rapid softening with altitude (essentially the same in temperate and equatorial latitudes) ; best interpreted by cosmic photon bands of widely differing pene- trating powers as from the production of He, O, Si, Fe, etc. More than } of the cosmic rays at 7.6 km have energy < 350,000,000 volts. Millikan considers that the “cosmic rays” found at low altitudes are secondaries formed in the earth’s atmosphere by collisions of photons with air atoms. Anderson has caught the cosmic rays, which cannot themselves be photographed, in the act of smashing atoms, setting loose + and — charged particles. So all but a small fraction of the cosmic rays at sea-level are secondaries produced in the earth’s atmosphere. SMITHSONIAN TABLES 650 TABLES 853-856 OCEANOGRAPHY (See Nat. Res. Council Bull. 85, 1932.) TABLE 853.—Area of Ocean Depths (Littlehales) Area of total water surface is about 365,500,000 km*, (Land surface about 153,500,000 km’. ) Meters: (hte cca sections 0-200 200-1000 1000-2000 2000-3000 3000-4000 4000-5000 5000-6000 > 6000 Nextt OS eh ayeeers eet = 30.60 16.40 18.05 36.45 79.01 112.72 66.88 5.38 Gow at dcnsreccane ee ae ie 8.4 4.4 4.9 9-9 21.7 30.8 18.4 Tas The continental shelf dips gradually (depth contour about 200 m) ; then a steeper con- tinental slope (talus), the seat of many deposit slips, seismic disturbances. Insular shelves and taluses, then troughs, trenches, basin deeps. TABLE 854.—Oceanic Gradients Ocean bottom gradients, Atlantic Ocean between Equator and 47° N. latitude. Zane N eo slatacrm gs rer O-10° 10-20° 20-25° 25-30° 30-35° 35-40° 40-47° Gradient ch: asian meer 20'.7 28'.7 28'.7 23'.9 24’.1 36'.2 37'.1 Island gradients often great; St. Helena, up to 40°; St. Paul (Atlantic Ocean), 62°. Gradients for volcanic and coral islands also great, generally in upper 300 m. Great Caldera of Santorin > 50°. S. of Cuba, 76° W., to depth 2625 m, 35° 30’. Compare Fujiyama, Japan, fine volcanic peak, 35°; 12° at base. Steep gradients (Alpine conditions) westward of British, French, Iberian coasts (av. angle 13° to 14°) and W. of continental slope of California (San Diego to Point Conception) 14° between 2000 and 4000 m isobaths. TABLE 855.—Atlantic Ocean Basin. Areas and Depths (Littlehales) Depths! Mmm ween cette 0-2 2-4 4-6 6-8 Over8 Total area INTCRIL OY Ia? Sopa eoooese ZOvO) 19.50 50.60 7.38 0.039 107.014900 To OLEWHOlene haan eee ene 27.6 18.2 47.3 6.9 0.4 100 Remarkable feature: Mid-Atlantic Rise, of median course and continental extent, from Iceland to S. polar border; throughout its more than 13 km, the general rise of its crest is some 3 km above the basin bottom on each side. W. Atlantic trough 6 km deep over large area of N. portion; other troughs and basins of similar depth. European isolated depth of 6 km. Near Equator lessened depth, 1.9 km, and extension along Equator 34° to 15° W. long., cut by narrow gap 18° W., 4 to 5 km deep. Passage through gap leads to Brazilian basin, 7.4 km deep. Ridge <1 km deep leads from Greenland (Iceland is a volcanic rise) to British Isles. Greatest depths: 54° 30’ S., 28° 30’ W., 8.050 km; 19° 36’ N., 66° 26’ W., 8.351 km; 19° 35’ N., 67° 43’ W., 8.525 km; 19° 38’ N., 68° 17’ W., 8.198 km. See also page 651. Greatest depth in Mediterranean, 4.400 km at 35° 45’ N., 21° 46’ E.; Black Sea, entire central basin below 2 km; North Sea < 200 m throughout. TABLE 856.—Indian Ocean Basin. Areas and Depths (Littlehales) Depths skimmer cerita ok 0-2 2-4 4-6 Over 6 Total area Aceas, UiOrskinie aise autores gens oe 8.192 18.569 44.560 4.656 75.986000 Toot Wwholes ace cereale ke 10.8 24.4 58.7 6.1 100 Compared with Atlantic the bottom relief of the Indian Ocean is much simpler. 7 km deep 250 km S. of Java 10° 1’ S., 108° 65’ E. Persian Gulf, order of 0.09 km deep. Red Sea, about 2 km. SMITHSONIAN TABLES TABLES 857-858 651 OCEANOGRAPHY (See Nat. Res. Council Bull., 85, 1932.) TABLE 857.—Pacific Ocean Basin. Areas and Depths (Littlehales) WMepthswkerm) 8 km near land, off S. A., Aleutian Is., Kurtle Is., Japan, etc. There are numerous isolated volcanic formations, e. g., Hawaiian chain. The largest and deepest depressions are in the gigantic Pacific basin. Tuscarora deep, 8.513 km; 3 elongated tracts 45°, 38°, 31° lat. > 8 km for 38 km®. Manchu deep, 31° N., 142° E., 9.435 km for 4 km’; Fleming deep, 23° 48’ N., 144° 6’ E., 8.650 km deep; Tonga deep, 23° 39’ N., 175° 4’ E., 9.184 km; Aleutian deep > 6 or 7 km near S.A., 25° 42' S., 71° 31’ W., 7.635 km. These deeps are as a rule not associated with the pits of great basins but are nearer land. Note: The Arctic basin is about 4 of Atlantic Ocean in extent; greatest depths about 4km. The Antarctic Ocean basin falls steeply from its continent to 2 km. TABLE 858.—Physical Properties of Sea Water (Thompson) Temperatures.—Tropical, surface up to 28°C, an 652 TABLES 858 (continued) AND 859 OCEANOGRAPHY (See Nat. Res. Council Bull., 85, 1932.) TABLE 858 (continued).—Physical Properties of Sea Water (Thompson) Adiabatic cooling for sea water, chlorinity 19.29%, 2° C, when brought from various depths to the surface (Ekman, Schott, Amer. Hydrogr. 321, 1914) : Depth, meters ....... 1000 2000 4000 6000 8000 10000 Cooling Gace 0.06 .14 . 36 63 .96 Pays Color and transparency.—(See Atkins, Journ. Conseil, 1, 99, 1926.) Optically pure water becomes bluer with depth. Green tints due to suspended matter. A rough measure may be taken as the depth where a white immersed disk becomes just invisible; coastal water, 5 to 25 m, often 45 to 60 m. Max. record 66 m (Sargasso Sea). Density taken as So, sp. gr. at o° referred to distilled water at 4°. Density expressed as go = (So—1)1000. o = — 0.069 + 1.4708 Cl — 0.00157 Cl? + 0.0000398 Cl’. Chlonittitys, jscrceo. cee: 5% 10% 15% 20% Density reeeuton: One 5.45 10.90 20.35 25.81 iid bikisncidretstboe Gee 20m€ 5.00 10.40 15.75 25.15 IMaxcaidensitya iocee ct AG Zar +0.1 —1.9 —3.8 Breezes! “aca. cement Ie 0.5 —1.0 —1.5 —2.0 Conductivity’ 4... o71€ .0085 .0160 .0235 .0305 Reciprocal ohms agile Seg Aor (E .O140 .0205 .0385 .0500 ° Refractive index ..0° C 1.3358 1.3376 1.3394 1.3412 ss f AAO? (C 1.3347 1.3364 1.3381 1.3397 Spiheat.s:,. scisee <- 17 251C .9971 9954 .9942 .9930 Atm. pressure Conductivity ....17°5 C 1370. 1356. 1348. 1341. Thermal, all < 10° Surface tension......0° €# —77:3 77.5 BEG, 77.85 Dynes/cm ‘i REE 208: A737 73-9 74.1 74.3 oy es Sp» ViSCOsity, 4... 3. one 1.015 1.030 1.045 1.060 ) Referred to dis- : sl pt Paataed 3 10° C 74 755 705 78 tilled H.O, 1.00 ‘S od ne Maat ae 201 57 58 59 .605 atiOme Velocity of sound: Chlorinity, 19.37%; salinity, 35.00% Depth) smetersieace acca O 0 2000 4000 6000 8000 Velocity, mi/SeC.rvi.casiemens [1630]20° C [1560 1590 1625 1660 1695]o° C TABLE 859.—Chemical Composition of Sea Water (Thompson, Robinson) Concentration as millimols or milligram atoms per kilogram Cl 535.0 CO: 212500 B 0.037 | Cu 0.002 Zn 0.00003 Na 454.0 Br {Sie ies .o15 | Ba .0o15 | Hion .oooo1 Sulphate 82.88 Sr 15 | Nitrate Q m, 14. 150 m long not uncommon; some up to 300 m. Swell.—As waves pass from disturbed area they degenerate to a gentle swell; not im- portant in mid-ocean but may be dangerous to exposed coasts and harbors. Periods (Morocco coasts) 7 to 20 sec., height 0.45 to 4.5 m. Waves in shallow water are considerably different. If depth of water greater than length of wave, water deep; less, shallow. Wave of translation (Russell, Rep. British Assoc., 8, 417, 1838; 14, 311, 1845).—All the water is above the undisturbed level; there is actual translation of the water particles; due to sudden addition of water, as with breaking of a wave. Wave pressure may be as great as 3.3 X 10° dyne/cm’. Seismic waves: Lisbon tidal wave, 1755, 18.3 m; Krakatoa, 1883, 21 m at Telok Betong. SMITHSONIAN TABLES 654 ; APPENDIX TABLES 861-863 TABLE 861.—Properties of Carboloy (Hoyt, Hard metal carbides and cemented tungsten carbides, Trans. Amer. Inst. Metals, Inst. of Metals Division, p. 9, 1930.) Carboloy is a cemented tungsten carbide; WC + 13% Co. At. vol. of the C atoms indi- cates that they assume the structure of the diamond. Especially adapted to high-speed cut- ting tools—long life, great hardness and strength. Per cent cobalt 9 13 20 Density, g/cm® F : 14.56 14.10 12.54 Rockwell A hardness, C scale, 60 kg. 87 Vicker Brinell number * 1365a 1255b 755b Elec. resistance, michroms/cm‘*, 20° C. 3 ; 22.3 19.6 20.2 Ditto stemp)coei=120-30e Greenacre 3 : .0043 .0044 +0038 * (a) 10 kg load. (b) 30 kg load. Carboloy : Modulus of rupture, cross bending, 20° C, about 225000; 800° C, 183000; 850°, 170000; 900°, 141000 1b./in’. Expansion coefficient per °C, 20 to 400° C, .000006 Thermal conductivity, watts/cm/°C, .65. Specific heat, cal./g, .052. Wiedermann-Franz constant (watts/ohm/°C) x 10°, 20° C, 12.2. Hardness at high temp. Brinell, r100° C, 36; 1300° C, 2.7. Magnetizing force, gilberts/cm...... 100 200 300 500 700 900 1000 Induction, kilozauss” Sirs..saesinsieene O50, . tO", L50) 217 207, este 3.29 TABLE 862.—Properties of Dekhotinsky Cement Dekhotinsky cement for air-tight joints. Sp. resistance 2 10° ohm-+cm and inductive capacity higher than of mica; adhesion great. For cementing glass and metals. Nitric, sulphuric, hydrochloric acids, bisulphide of carbon, benzene, gasoline, turpentine do not attack it. Very little affected by ether, chloroform, caustic alkalies, etc. TABLE 863.—Properties of Fused Quartz (Vitreous Silica) Fused quartz (vitreous silica). Can be used to a working temperature of 1000° C. Softens about 1400°, melts about 1756° C. Can be used intermittently to 1700° but above 1000° devitrification commences. Thermal expansion low, .0000005 per ° C up to 1000°. Invar, .0000009. Chemical pyrex, .0000032. Jena glass 50, .0000057. Expands on continued cooling to 80° C. Specific gravity: clear fused, 2.21, translucent, 2.1. Hardness, Moh’s scale, fused, 4.9, crystal, 6.3. Modulus of elasticity, 9,400,000 Ibs./in.? Tensile strength, 7,000 lbs./in.” Compression strength, 190,000 lbs./in.” Impermeability. Not porous to common gases at high T and ordinary pressures. Helium diffuses through even at low T. Non- hygroscopic. Transparent to radiation about . 1850 to Iu. Thermal conductivity at 20° C .0024 for clear fused quartz, increases rapidly with rise in temperature. Resistivity electrical, 5 < 10° ohm - cm e5uG. Dielectric constant, 100000 cycles, 25° C, 60% humidity = 4.4. Most acids, neutral salts, refractory oxides, either no chemical action or less than with glass, Pt, or porcelain. Hot solutions and fusions of the caustic alkalies readily attack. (Vitreous silica, Sosman, 1927; Fused quartz, Gen. Elec. Co., 1928.) SMITHSONIAN TABLES TABLES 864-865 TABLE 864.—Properties of Phenol-Resinoid Products 655 Molded Laminated Pure Quality poteae Wood fl Fabri Jeo haan eae a ae ete pac eee oP Banca a eet Molding qualities............ none excellent good fair sheets, tubes, : rods, etc. BStter MOlGINg. sree f-t-i6.o|h il ee o permanently infusible permanently ey ‘ infusible EE CANIEIIT) eld auniesocchsiaicnacauelsinyecs good fair | fair fair fair fair RB Ol eflO Wiig cy cel ese assis oncteveces Gs none none none none none none ransSpAaLrency: cei kee eile - transparent opaque opaque translucent Petractivelindext sri). .<2)-)<%: - I.56-1.70 opaque opaque BPECIIO PEAVIEY : « . sacle sie Mais T2038 1.31.4. |, F-3-1-4) | 7-8-2:0))| 1-3-1 4.5) 1aa—tea Tensile strength Ib./in.?....... 5,000 to 6,000 to | 6,000 to | 3,500 to | 8,000 to | 8,000 to Fig. 8 test piece 11,000 12,900 12,000 5,000 20,000 12,000 Monpaomene. ke rte negligible negligible negligible Modulus of elasticity..... LO 2 SN ties lle cept el Gee cn | transverse lbs. /in.? Oe eae as. | Rene ean nee el Oe ee Pe ae eee Modulus of rupture.......... 12,000 to | 10,000 to} 8,000 to | 8,000 to flat or edge-wise transverse lbs. /in.? 20,000 20,000 15,000 20,000 75,000 to 30,000 | to 25,000 Hlectrical resist. w:cm3........ 10 to 10” |10" to 10/10" to ro"! 108 to 109 }10"" to 10" 109 to 101 Breakdown volts,* V/mil..... 250-700 300-500 | 20-500 | 150-4001] 500-1300] 200-500 Power factor 1o® cycles....... 4.5 to 7 4.5to8 | 4.5to7 | 5to20 | 4.5to6 | 4.5to7 Thermal conductivity.........] 3-4 4-6 4-6 12-20 5-8 5-8 cal./sec. cm° C X 10-4 x< tO X 10-4 x 10-4 X 1074 X 10-4 SMNED Erde aye tala ota ns cs RA 3-230" 9. he, 5: 30-40 ces .30-.40 MUNI oR taexs capa sate ee x5 extremely low nonflamable extremely low Instantaneous at 60 cycles. 7 Mica filler. nimal, vegetable, mineral oils, hydrocarbons, esters, ketones, no effect; alcohols, practically none; k alkalies, slowly softened, strong, disintegrates; decomposed by strong nitric and sulphuric acids by hydrochloric and hydrofluoric which attack fillers. Withstands 250° F. (Data from Mory and lor, Bakelite Corporation, 1920.) TABLE 865.—High Vacuum Technique eferences: Dunoyer, Vacuum practice, London, Bell and Sons, 1926; Newman, The production measurement of low pressures, New York, Van Nostrand, 1925; Kaye, High vacuum, Longmans, en & Co., 1927; Dushman, High vacuum, Gen. Elec. Rev., 1922; Goetz, Physik und Technik der hvakuums, Vierveg und Sohn, Akt. Ges., Braunschweig, 1926; Langmuir, Phys. Rev., 2, 450, 1930; s. Zeitschr., 15, 516, 1914. he following is taken from Dushman, Rev. Mod. Phys., 2, 381, 1930, whence the above references. stop-cocks, greased joints, etc., should be avoided in connection with the exhaust and preparation ibes containing cathodes for which electron emissivity are to be determined. While the evaporation V with the bulb immersed in liquid air was used by Langmuir, other “getters” have come into use. Ca, Ba, and alloys of rare-earth metals have been used. Ba cleans up practically all residual gases rdinary temperatures, while Mg is ineffective for H, and Ca does not take up N to any great extent. ‘emely low pressures may be obtained with a side tube containing charcoal (which has been well usted) immersed in liquid air. Care should be taken that the liquid air is maintained at constant | during the series of measurements. THSONIAN TABLES 656 TABLES 866-869 TABLE 866.—Relative Viscosity of Water; High Pressure Variation (Bridgman, 1925.) I 500 1000 2000 4000 6000 8000 10000 1.000 0.938 0.921 0.957 I.I1II 1.347 755) 3743) Nee: POA2E OOM mies 2 .500 .514 .550 (O55) ye 7CON L923 NeLO5S 2222300258 -3O20 4 O/mee 445 TABLE 867.—Viscosity of Mercury; High Pressure Variation (Bridgman, 1927.) Pressure kg/cm? I 2000 4000 6000 8000 10000 +=12000 Abs. visc. 30° 0.01516 0.01588 0.01663 0.01742 0.01825 0.01913 0.02008 is 3 01341 .01399 .01463 .01528 .01599 .01675 .01757 oO 5.1 9.9 15.2 20.0 26.3 33.5 4.6 9.6 14.4 18.8 24.7 a1 ar TABLE 868.—Viscosity of Some Glasses at High Temperatures (Washburn, Shelton, Libmann, Bull. Univ. Illinois, 140, 1924.) Composition Surface tension Viscosities dynes/cm2 SiOz NazO CaO 1206° 1454° 1000° 1200° AOVG,, On oc sei BP eee: 1.62 0.93 GOO 4OlOn We 156 149 : ; 3.04 2.05 7kOK0) Z{0KO) Go c 164 154 , 3.64 2.62 82:60) al 7-4o6 oie sey 154 seers 5-4 3.69 54.25 38.0 7.75 Se 4: ee 3.42 1.64 60.0 30.0 10.0 Se sie srt 3.02 60.0 20.0 19.5 160 128 j 630s) Wis Oin 2354 164 159 19.3. 15-75 159) 539 15-5 17.0 159 145 21.9 10.0 50} 146 20.0 154 140 10.0 156 15.1 152 16.5 159 12.0 ah: S Ne) n 2.63 2.58 2.78 3-84 3-03 3.26 fea CC Cre > BOW. ONW Or — DADs WAN OD TABLE 869.—Some Possible Accuracies, 1928 (Journ. Wash. Acad. Sci., 18, 503, 1928.) Pienkowsky : 30 national prototype kgm (and probably the international kilogram) are remaining constant within 0.02 mg or less. 10° kg measurable to 1 part in 10’. 6c ‘ S I a 10. WOuse S ae: sah alneaLOK With one type of microbalance 100 mg to I mg, I part in 10° to 10°. Curtis: I ohm, 1 to 2 parts in 10°; 1 millimicrohm with 10%, also megamegohm. I volt, 1 in 10’; 1 microvolt, 1%; 1 megavolt, 10%. I ampere, I in 10°; micromicroampere 10%; kiloampere I in 10°. 1 millihenry, I in 10°; millimicrohenry, 10%; kilohenry 1%. I microfarad, I in 10°; micromicrofarad, 1%; millifarad 1%. SMITHSONIAN TABLES TABLE 870 657 PROPERTIES OF MALLEABLE CAST IRON (From Proc. Amer. Soc. for Testing Materials, 31, pt. 2, 1931; Malleable Iron Research Institute. ) Malleable iron is the product produced by the annealing or graphitization of “ white iron” castings in which all carbon should be present in the combined form, such that the final structure of the malleable casting consists of ferrite and free carbon (temper carbon) with practically no combined carbon as free cementite or pearlite. Where strength, ductility, machineability, and resistance to shock are important, malleable iron castings are of wide application. Chemical composition: C 1.00 to 2.00; Si 0.60 to 1.10; Mn < .30; P<.2; S .06 to .15%. Density: 7.15 to 7.45. Thermal expansion: 20°-400° C, about 0.000012 per °C. Sp. Ht.: Mean 20°-100° C, 0.122 per g per °C; 20°-200°, 0.125; 20°-500°, 0.139; 20°-700°, 0.150. Thermal conductivity: Kt, 50° C, 0.145 g. cal./sec./°C/em; 100° C, 0.137; 200° C, 0.115. Tensile strength: 54,000 lbs./in.*; range 45,000 to 63,000; yield point 36,000 Ib./in.* Elongation in 2 in. 18%. Modulus of elasticity in tension 25,000,000 !b./in.* Compressive strength: Material flows indefinitely. “ Special” tensile 57,690; yield point 38,000; elongation 25% in 2 in. Ultimate shearing strength 48,000 1b./in?; yield point 23,000 Ib./in.?; elasticity mod. 12,500,000 lb./in.” Modulus rupture in torsion 58,000 Ib./in.?; yield point in torsion 24,000 1b./in.” Brinell hardness 115, range 100 to 140. Charpy impact value 7.75 ft. Ib. Note: If malleable iron is heated above its lower critical point (about 760° C), carbon redissolves and the character of the iron changes. Resistivity: 28 to 37 microhms-cm* Rioo/Ro = 1.1 Rs00/ Ro = 2.3. Magnetizing force, H, gilberts/cm...... 2c er 10 15 20 30 Induction) B,-causses (mean)).-.5.-6.- 5800 7600 9200 10000 II000 I1400 11900 Comparative machineability. Relative power required (means of planing, drilling, and milling) : Dow metal, type E.... 19 Gunemetal meee 55 Copper annealed ..... 131 Bearing bronze ....... 36 Gast inone oeceeeree ee 60 Tool steel 1.03% C... 145 Aluminum alloy no. 31. 37 Manganese bronze ... 61 Stainless Cr, iron, ann, 158 Redebrassaee pesos 38 Malleable cast iron.. 70 Monelimetalieeeiee 165 Sheetaubrasse ecm acc. 4I Unleaded! brass ~.... 85 INiekel “CAMO. Seas 193 SMITHSONIAN TABLES 658 TABLE 871 DEFINITIONS OF UNITS ACTIVITY. Power or rate of doing work; unit, the watt. * AMPERE. Unit of electrical current. The international ampere, “ which is one-tenth of the unit of current of the c.g.s. system of electromagnetic units, and which is repre- sented sufficiently well for practical use by the unvarying current which, when passed through a solution of nitrate of silver in water, and in accordance with accompanying specifications, deposits silver at the rate of 0.00111800 of a gram per second.” The ampere =1 coulomb per second=1 volt through 1 ohm = 107 e.m.u. = 3 X 10° €.S.U. Amperes = volts/ohms = watts/volts = (watts/ohms)+. Amperes X volts = amperes” X ohms = watts. ANGSTROM. Unit of wave length = 107° meter. ASTRONOMICAL UNIT. Mean distance earth to sun, 149,500,000 km. ATMOSPHERE. Unit of pressure. English normal = 14.7 pounds per sq. in. = 29.929 in. = 760.18 mm Hg. 32° F. French *.= 760, mm of Hg.07C —'20.922 in, = 14-70 Ibs. per sq. ins AVOGADRO NUMBER. Number of molecules per mole 6.064 * 10” mole”. BAR. International unit of pressure 10° dyne/cm’, g = 980.616 cm/sec’. BARYE. c.g.s. pressure unit, one dyne/cm’. BRITISH THERMAL UNIT. Heat required to raise one pound of water at its tem- perature of maximum density, 1° F.= 252 gram-calories. ) CALORIE. Small calorie = gram-calorie = therm = quantity of heat required to raise one gram of water at its maximum density, one degree Centigrade. Large calorie = kilogram-calorie = 1000 small calories = one kilogram of water raised one degree Centigrade at the temperature of maximum density. For conversion factors see page 251. CANDLE, INTERNATIONAL. The international unit of candlepower maintained jointly by national laboratories of England, France and United States of America. CARAT. The diamond carat standard in U. S.= 200 milligrams. Old standard = 205.3 milligrams = 3.168 grains. The gold carat: pure gold is 24 carats; a carat is 1/24 part. CIRCULAR AREA. The square of the diameter = 1.2733 X true area. True area = 0.785308 & circular area. CIRCULAR INCH. Area of circle one inch in diameter. COULOMB. Unit of quantity. The international coulomb is the quantity of electricity transferred by a current of one international ampere in one second = 10” e.m.u. a TO mes Ue Coulombs = (volts-seconds) /ohms = amperes X seconds. CUBIT = 18 inches. DALTON. Unit of mass, 1/16 mass of oxygen atom. 1.65 & Io™* g. DAY. Mean solar day = 1440 minutes = 86400 seconds = 1.0027379 sidereal day. Sidereal day = 86164.10 mean solar seconds. DIGIT. # inch; 1/12 the apparent diameter of the sun or moon. DIOPTER. Unit of “power” of a lens. The number of diopters =the reciprocal of the focal length in meters. DYNE. c.g.s. unit of force = that force which acting for one second on one gram produces a velocity of one cm per sec. = Ig ~ gravity acceleration in cm/sec./sec. Dynes = wt. in g X acceleration of gravity in cm/sec./sec. ELECTROCHEMICAL EQUIVALENT is the ratio of the mass in grams deposited in an electrolytic cell by an electrical current to the quantity of electricity. SMITHSONIAN TABLES TABLE 871 (continued) 659 DEFINITIONS OF UNITS FOOT-POUND. The work which will raise one pound one foot high. For conversion factors see page 251. FOOT-POUNDALS. The English unit of work = foot-pounds/g. For conversion factors see page 251. EQUATION OF TIME. Excess of mean time over true time. ERG. c.g.s. unit of work and energy = one dyne acting through one centimeter. For conversion factors see page 251. FLUIDITY. Reciprocal of viscosity. g. The acceleration produced by gravity. GAUSS. A unit of intensity of magnetic field = 1 e.m.u.= 4 10° e.s.u GRAM. See page 6. GRAM-CENTIMETER. The gravitation unit of work=g. ergs. GRAM-MOLECULE = » grams where + = molecular weight of substance. GRAVITATION CONSTANT = G in formula G a = 666.4 X 10° dyne-cm? - g~, HEAT OF THE ELECTRIC CURRENT generated in a metallic circuit without self- induction is proportional to the quantity of electricity which has passed in coulombs multiplied by the fall of potential in volts, or is equal to (coulombs X volts) /4.181 in small calories. The heat in small or gram-calories per second = (amperes* & ohms) /4.181 = volts?/ (ohms X 4.181) = (volts X amperes ) /4.181 = watts/4.181. HEAT. Absolute zero of heat = — 273°18 C. HEFNER UNIT. Photometric standard; see page 334. HENRY. Unit of induction. It is “the induction in a circuit when the electromotive force induced in this circuit is one international volt, while the inducing current varies at the rate of one ampere per second” = 10” e.m.u. = 1/9 X I0™ e.s.u. HORSEPOWER. The English and American horsepower is defined by some authorities as 550 foot-pounds per second and by others as 746 watts. The continental horsepower is defined by some authorities as 75 kilogrammeters per second and by others as 736 watts. See page 251. JOULE. Unit of work = 10' ergs. For electrical Joule see page xlv. Joules = (volts? & seconds) /ohms = watts & seconds = amperes” X ohms sec. For conversion factors see page 251. JOULE’S EQUIVALENT. The mechanical equivalent of heat. See page 86. KILODYNE. to00 dynes. About 1 gram. KINETIC ENERGY in ergs= grams X (cm/sec.)?/2. LITER. See page 6. LOSCHMIDT NUMBER. Number of molecules per unit vol. ideal gas at 0° C and normal pressure, 2.705 & 10” cm™. LUMEN. Unit of flux of light-candles divided by solid angles. MEGABAR. Unit of pressure = 1,000,000 bars = 0.987 atmospheres. MEGADYNE. One million dynes. About one kilogram. METER. See page 6. H METER CANDLE. The intensity of lumination due to standard candle distant one meter. MHO. The unit of electrical conductivity. It is the reciprocal of the ohm. MICRO. A prefix indicating the millionth part. : : MICROFARAD. One-millionth of a farad, the ordinary measure of electrostatic capacity. MICRON. (u) = one-millionth of a meter. MIL. One-thousandth of an inch. MILE. See pages 5, 6. MILE, NAUTICAL or GEOGRAPHICAL = 6080.204 feet. MILLI-. A prefix denoting the thousandth part. MOLE. Mass equal to molecular weight of substance, SMITHSONIAN TABLES 660 TABLE 871 (concluded) DEFINITIONS OF UNITS MONTH. The anomalistic month = time of revolution of the moon from one perigee to another = 27.55460 days. The nodical month = draconitic month= time of revolution from a node to the same node again = 27.21222 days. The sidereal month = the time of revolution referred to the stars = 27.32166 days (mean value), but varies by about three hours on account of the eccentricity of the orbit and “ perturbations.” The synodic month=the revolution from one new moon to another = 29.5306 days (mean value) = the ordinary month. It varies by about 13 hours. OHM. Unit of electrical resistance. The international ohm is based upon the ohm equal to 10° units of resistance of the c.g.s. system of electromagnetic units, and “ is repre- sented by the resistance offered to an unvarying electric current by a column of mer- cury, at the temperature of melting ice, 14.4521 grams in mass, of a constant cross section and of the length of 106.3 centimeters ” = 10” e.m.u. = 1/9 X 10 e.s.u. International ohm = 1.01367 B. A. ohms = 1.06292 Siemens’ ohms. B. A. ohm = 0.98651 international ohms. Siemens’ ohm = 0.94080 international ohms. PARSEC. Distance of star whose parallax is 1”. PENTANE CANDLE. Photometric standard. See page 334. PI =z=ratio of the circumference of a circle to the diameter = 3.14159265350. POUNDAL. The British unit of force. The force which will in one second impart a velocity of one foot per second to a mass of one pound. RADIAN —180°/ 7 = 5720578) = S7aail7 345, = 2002057. REAMUR. Thermometric scale. 0° C=o0° R. 100° C= 80° R. SECOHM. A unit of self-induction = 1 second & 1 ohm. SLUG. Unit of mass. Mass acquiring acceleration 1 ft./sec.” when continuously acted upon by 1 lb. wt. SLUG. (Metric) ditto accel. 1 m/sec.’, 1 kg weight. TENTH-METER. 10-° meter =1 Angstrom. THERM = small calorie = (obsolete). THERMAL UNIT, BRITISH = the quantity of heat required to warm one pound of water at its temperature of maximum density one degree Fahrenheit = 252 gram- calories. VOLT. The unit of electromotive force (e.m.f.). The international volt is “the electro- motive force that, steadily applied to a conductor whose resistance is one international ohm, will produce a current of one international ampere. The value of the e.m.f. of the Weston Normal cell is taken as 1.0183 international volts at 20° C= 10° e.m.u. = 1/300 e.s.u. See page 80. VOLT-AMPERE. Equivalent to Watt/Power factor. WATT. The unit of electrical power = 10’ units of power in the c.g.s. system. It is represented sufficiently well for practical use by the work done at the rate of one Joule per second. Watts = volts X amperes = amperes” X ohms = volts’?/ohms (direct current or alter- nating current with no phase difference). For conversion factors see page 251. Watts & seconds = Joules. WEBER. A name formerly given to the coulomb. WORK in ergs = dynes & cm. Kinetic energy in ergs = grams & (cm/sec. )?/2. YEAR. See page 601. Anomalistic year = 365 days, 6 hours, 13 minutes, 48 seconds. Sidereal Se 305) aah Om ae 9 SECO TA Ordinary “ = 365 “ 5 “ 48 ‘“ 46 + “ Tropical “same as the ordinary year, SMITHSONIAN TABLES INDEX (References in parentheses marked I.C.T., followed by volume and page number, are to the first edition of the International Critical Tables.) PAGE a particles: atomic stopping powers.......... aioe 23 TVA ON” oosoeoonouDdboDbeOUEOOS 522 in various gases.......... 525 masses, 6.60X10-%g each ........ 105 miscellaneous data ..............+. 521 molecular stopping power............ 523 TANZE; CASES) Wie ialerele ae hteclayerare¥ st «1 sus 522-523 MONS=NANE Ol MPsrcere chasse swisie. chess 523 SOMOS eietenercketeteteraleetensnet «12 <1. 523 stopping powers, atomic, molecular.... 523 velocities ..... ehckelnte/eVeleicieisieleres cele 522 Abbot-Priest sea-level solar energy, (CA) eteyerei © onsy eve 614 Abbreviations ..... miateietclelcletetetelevelelelcveretelicic: ciciers 2 PATER LOM Ie CONSE AN Gite relcheleletata: alefeleloiole\eehelelee!=1 eels 601 Absolute international units ...............-- 77-81 magnitudes (M) to apparent (m), to re- LUCE eratenererer erectile teinielelelclersrelersiele vores 602 OL rerctatavelatetetctetcratovefatereicieveiciniciebeletsisj cfs xlvii TWh. osacoon PMT ehetete tere osstsitekal Mares li zero, —273°.18 Cc. Beier ater teiclsts erate 85-86 Absorption: air, moist and dry, for radiation..... 611 AMD IY 6 GospempmdoacHace 522-523 atmospheric for radiation .......... 608 , ultra-violet, for radiation. 389 beta particlesmeeysetc i eerste wile ) = 518 AMM, Ginn ogesdon douoogbdeoupoaboBoe 658 Ndaptabilityeor eye, Fate Olean ees - 6cc e's 0 210 331 Adsorption: gases by particles................- 554 HEALS reer trensteeraleheiskerersintaternieieiere 554 MOAT THAIS 6 addaanapooéapoooe 554 Aerodynamics: (general) (I. C. T., 1, 402)...195-203 air forces on cylinders ...... fs 200 Hateiplatess ee,-.2< 198-199 miscellaneous . 201-202 SAS) Gosodoapddas 201 resistance on flat plates....198—199 SHUR ICULON gaereteraeVelersfetedere ls. cs0) + eps 203 velocity pressure vs. air speed..... 195 Aeronautics, standard atmosphere for...........- 559 AGG MERLUNIN a ateaterisieelacisisiee Sfefeteleietaisteleleisiersiercie 578 NTO MHD. co decaccomo see Siotctelatsteleteroierstafal=l= 595 Air: (see also atmosphere) conditioning with moisture (I. C. T., 2, 321). 179 convection, conduction, thermal............ 327 MASSES spat (AIDIUMGE)) s coretel stats ere iejeteleie| Dis alelensieisl cieeiniine< JOSS Curvature sol eSPACE Maier oe cicteteiciersleketereloheoneteloloisis 644 Dilution; heats of; HoSOcya-c.ctocicece cece ste Cylindrical harmonics ..........0...esseeees 68-70 Dimensional formulae: (general) ..........Xxxi, 3, 4 > ROOK! oa obdo comodo aieletvicmn7.O) GLECUNIC UNITS ree yelselele late Xk RRND electromagnetic units .....XXxxix 6 TAYS eoccccccccccsessssssceserncesseseces 525 electrostatic units .... _XXXVii PUSIUOMM pce crete tele oinjataloleie afalelesalle 'e) eye! s}el ele win cel eLolelisiieials 658 geometrical units . Soe ele ees XxxiV HES: LINO aca ielelelelareiererers\nicie¥enale(e)efereretalaieoleuelelelels 602 heat sunitst (Ac tots ees Day #101 ese wielelejeie/eielsie/o\e) eins») eie\s wie oleicieie/s)eie\0.e:8 658 magnetic units eS ENY TT 7 sidereal Rialote whalelchel ae cisioKe el syetereler=teleieisie 158 globular’ Ginats caer 638 Cane! SULA AQUEOUS sivielsicietelsisicneyais cle 174, 175 OP ah eS SN RE 637 castor Oil, f(t). ..seeeeeeeeseeeeereee 206 stars!" aeons ince as eke dave ciepeene eis 619 critical, of gasesS..........2. eee eee ees 271 sun from center of galaxy.............- 643 earth, 5.522 (Birge) ..-.-+-+-++++--: Z5 | Dominical letter ..........-.- ERG steele cle 603 TEODOR AN sets tnjoyavanelesele\ieresaceietelaloivie 569 | Doublet H constant.......... boi g aie seaveleetears 107 elements, chemical ..............-..- 159 Drying agents (I. C. T., 3, 385). aS Ce etetcbekkel nator RDN eR aces ner ees 176 | Dyes, transmission of light............eeee000s 385 glycerol, aqueous solution.............. 206 Dyne, definition 658 inorganic compounds ..............-.. 254 SiN eae ota eRe ale LET OND CREO NIGUi dS ieteet a cetera enereloie< ieteketcucieasy cueteteinvens 165 e, base of natural logarithms, 2.71828.......... 14 mercury —1o0° to 360° Ce orien 169 e, elementary charge, 4.770 x 1077° abs. es Minerals) ecierteroelei ee SSS en ce ries 164 UNLESIe e\eStereiereve 016 ahaa setays alelouateve-aeletedecerereiete 88, 92 miscellaneous sSOLIGS| ic jerereteraictote ciel syectelsyel« 162 Es. DOWEES: (Of (ADOVE iis iciazetoneverocistaheioicss ie oo oiaiee eevee 103 MOISHMAI te rere Bycloveteictateistensnshoiciciare 177, 178 e/m, bound, 1. 761X107 ‘abs. em/g. ays areysietase-3 93, 94 ONZANICTCOMPOUNGS i apeteheterel ole loys rcieletenel 256-258 Pree le 7OOE< EO Ur ADSANE IU /Giieer leds eleraiets 02,04: HEE Skecadoc afeieietsteleveistetarerelskers sees OOO C265" and theirs logssaa;— oncom Olpeleielelertaitel 48-53 ponds, VaALOUS Meerctereltatsterehehsiaieterchetatencvoter> 162 : ; @, fractionalyc).-j-ticietelere 56 SOLULIONS, pm WALEI) raleleieielshoievelelelelalereleas 170-175 627. C= Mors. F=Ovm tO ibsOmoere eevee on arene Stars .....cceceeee stent eee eens «2+ 623 wx/4 aaa 1 ve aa sucrose, aqueous solution........... T7745 175 e Ee » logs, o=1 tO 20........-..--- 55 sulphuric acid, aqueous solution..... LFA LS om ia/4 emit /4 logs, w=1 to 20. ee MSS water, 0° to 41° Gries saree atehere ate musta 08 Batis a eat ea —— Oe HOM 25 On Cui ctaicieysiorelepeveiarets 16 SS ‘ s woods ..... Bie eioetots leane sialateres oye reise 161-163 aia 2 OES ee an Developersmnyrocalloln-yaterateisvetetskers)sieterskevelevetoretaverers 341 Panel ASAI a eiavelal slareteleieleiovelelels/«lelolatonaiereleiololalsletsiseeai7al Developments phHotozraphics vsjcjcyeleieiel= icicle cic! clcielel sieve 341 ANE ULAR WOLOCIEVA ctelcvo:cletovetelaieloicrsheisivcterets BS 70 Diamagnetism ...... Mrataselehelslelerovelstatctetets\crels 463, 474 Rinse | Songdooadoseoos0cad 2. + -558-568 Diameter melemencswurercrctctel cle elelelavalere sieteleterehelsiaile 548 atmospheric electricity ..... Fisboreqshekeere 596-600 molecules) picsrs crete Ricloieleterelelsierelctshy 5 O sal sink COMPOSILION sere areyereroiator ahowsgatevevereietersts Ses S72 Dielectric constants: (general) ........----.e-- XXxxii conductivity, thermal .............. gaco sy Cry stialsiaerevareireleieccieieeisueicrorsic 447 CONSUANESsIVADIOUS i evorejetclaeveksterereictere Pieisieletee 570 TASESs Ll ((D5p ab) eekarneiemeeeetevers 442 GONNA oR Gaddadooaada aicleteleere S}OOMSIZO) Viquefied) /Serereccye efer-ie 445 depths, ocean ..... sais taishersietevcisialersrsieisi ae OOO) liquids, pressure effect ..... 443 GOES So5éonoccccnc0beoccobsonoDS 570 temperature effect .. 445 distance to sun, to moon........... Ot OOr radio-frequencies .......... 454 elastic constants ......... Bectevereneloieterenerele 569 Rochellemsaltiarercyereleterersieiatcisrs 444 electricity, atmospheric ............. 596-600 SOMOSaerree te etetenorcvsiiiorcie svavete 446 elements, % composition ...... Serare ye 572, 614 standard solutions ......... 446 ELEVATIONS eM OUNGAIN tee oreletel-totcieteloioheleterls 569 strength (see also sparking Ener ys, KOLALIONAL s)c:5) 666 INDEX PAGE PAGB Eye and radiation: (general) ...........+330 et seq. Functions: <2amma 1. 5-s7a)seravatecc (arto here Ieee eee 64 adaptation rate ............ 331 hyperholie sie tsrete arvaliclels uctciee reer: 41 blind spot, vision in.’..... aistees ae probability ...... evetielseveveloysp st eile 56-61 CONES Wapetersteretemicteacre eyeeiieete ISS trigonometric, circular” (has se reese 32 contrast sensitivity .........- 331 (radians) ..... 37 dimensions of points......... 332 ZONAL NATMONICS) wei efsiaiaiers sie = ; wargecccts ce eee ocr 561 Fi REOMEGMICH ctyeie vere eieitate Boodoanscabess 561 h, 6. SNOT 2 TM ETE Iay SEC PSR ayes a eR ELLY, be 311-312 ositive ... 367 LOLS Matetslersisiale'e )acoieiclcic/sieis\= - 312 monorefringent Ra and emanations.......+++ 525 (isotropic) ..... 363 668 INDEX PAGE PAGE x, of refraction: crystals: uniaxial: miscel- Ionization potentials, first ..........226-.+490, 614 cade laneous. 366 H, Hert A/oisislevaicrarnctne Brae OG negative .. 365 Rl Goo daacouasennocos Sow positive .. 365 ie AWN spo scssopoOosDp DCO UGCar 644 doubly refractive min- Ions: alpha particles, production iy lMadoooas 522, 525 erals cc es aes - 366 et seq. almosphericy Uppenine 1-1) ety ers ++ +++599-600 fat sieeceeeersterene terror rate Saas (370 equilibrium, atmospheric electricity........ 597 TLOMARLE bn cece eee 61 gamma TayS .:....0.... afeiersiovere era oerorere 530 Pa Uae Sot a a heat wots tormationnrecereisieyseierieieiieeiree eioeiee 312 eace TS eas PNT A he 356, 358 YOM Sopooadooseaue eieretelekelereietete sere 552 Schott-Jena, f(t) 359 Iron: alloys, mechanical PLOPELbIES relorererel-te sere eee z ‘ al are Lines’ 2 anet Kilocycle-meter conversion table (radio)...... 456-460 Be AOE BOL ae ae ett aera + U7 || MalOd yn 5 oa ebacctncehtieaeen wat oe Nees 659 _ Photographic ........ Stel che) Sti || Kinetic senergyetiiciestn. seule ae aon eae ee 659 Inorganic compounds: boiling points .......-..-- eh) |! IinGHS COMING oob0oddocannoccoeocuc Rear densities weet eee ee eee 254 melting points ........--- Zot as eal exe rayglserlesmetaereeieceee veers ressseeets 838-539 solubilities .......++.+++- 218° || gambert; definition ..650..00cuc0meccenee ae -= 333 Insulators: break-down potentials ........... 439-441 Lamps: brightness in candles/em?2 afevarinuse 338, 339 dielectric properties ...439-441, 442-447 energy, distribution, of tungsten......... 339 resistance, electrical ..... eet 5, 409 miniature, characteristics: automobile ae3aO thermal ....273, 274, ee 279 movie aoe "330 Integral?\diffusion 25. cose eee 0, I SUrZICalweueretersrers 339 elliptic gene Aas toce see iis eos 71 photoflash, characteristics ....... Rol eteare - 340 Exponentially rere ore yc sis oie Crteietere wists 623) 163 photographic efficiency of some.......... 344 FOrMUlae ties Sercieteee mg cts rete secie onsnercaseeteneLS 12 sunlight mazda, characteristics........... 340 SAM MaAeHUNCLLON! sarrererekerecoierenersieiet rote reers 64 Bandwanea Ol, (Carthi-:-perereiete eterotaleleteveVelotetere ayatetetors 569 PLOWADII yee crreccrste ererelol heuer ete 5O—57, Landé’s interval rule (Spectra); .t.:toters eerie ee 503 Intensification of photographic plates............ 345 Latent heat of fusion: elements ........ 288, pia Intensity, horizontal magnetic: f(lat., long), U. S., Fee eatin peat Se vsleseteen oe ane EO 2 15 ierevelsy ee terare 593 > AMMONIA oe oe ee ie annual change. 579 elements ee cee ec eee gap isodynamic lines, Heutda tte eee eee Be WODLGN terereretereieiete 577 tote te ee eeee isoporie lines, ‘ eee Bpaooencc Sree WOTLy . crenerensuaiste 7 x i eee eee : secular change, 3 Latitude, photographie ereheisccts saobaécggasounsos 34 s USS eeeletenier ate! 593 ‘ i aie olelalaielalcicts eietnye aie =f\=/-/e(-'iele total magnetic: f(lat., long.), U. S., rane ee Sees aera EMISSION ert retererere rere of G25 priclexKehokohepatsisvercte 594 | Least squares: formulae ............+eseeeeeee isoporie lines, world.... 580 probaliiltty integral, arg. ha ..... 56 secular change, U. S... 594 Z/T sss a vertical magnetic: annual change ...... 580 inverse .....- 9° isoporic lines, world.. 580 0:6745V T/T) eee aces Laker 15m International electrical units .................. au 0.6745V1/n(n—=1) KO awe BLandards seine xlvi ce eee eee at he eo to absolute units Tae eS a wiggevensusiadous atete a Ol teeters teisiaetoe etter xlix 0.8453[1/nVn—I1] ...... eieletejaket= Lemperauremscalewerr yc ieincieteusietere 239 Probable xerrorseepstvarcneve letdeonetetelk 57-59 Interstellaracalciumie eer ieee ccinciteionion 644 Leather belting, mechanical properties......... Caer sO MATEO ereheterne seater orayaie ose vevoxonevrekes ete 644 Leduc thermomagnetic effect................--- 482 SACO Mrcttoneyssererer spare vote coseresare he scicnore rears 644 Legal electrical UNLGS syefols is) ofeieresejeleselerst aint teetTeie ts xlvi BEMPehaLUnen cspapcreycueveeckotere le evcrarionerote 645 engthy standards: << slejarerosteiars sjels sye\e/asstaveseys XXxiv, 5 Intrinsic brightness, various light sources........ 334 Light: flux weet cece cece re nnecetearcnsacics 333 Inversions, enantistropic, of crystals ........ 261-265 intensity on various days........... --556, 608 heats of..261-265 AM DERE eeretaterete ce tejeteletclettelolerrtarets esas Tonium=radium family iy cicissiewisiecieieieieeieecisse ce) SG, TIMI) rc eyesovelerciototere’sieietelentVercieleleteiereretentelen SSG INDEX 669 PAGE PAGE Light: luminosity ......eeeeeeee seers e reece 333 Logarithms, anti, four-place .....-.- piete steeco= oe Aseeniereuels Bejoiee ts Ree total et ctaleralet efeleleyelsiisi's) s:'9 333 four-place, 100-999 «seereeeereee 26-27 mechanical equivalent .....-eeeeeeeeeees 333 1000-2000) cceeecerees 24-25 photometric standards ..++++++eeeeee ees 334 Longitudes of selected stations..... 565-567, 581-589 UNITS ..cceeecreceeererrers 333 Long-wave transmissions of energy.....-+++-++ - 393 polarized, reflection of ...+-++-2.-+s-00- 376 Loschmidt’s number, 2.705 X 107” em-*....... 107, 659 rotation of plane by substances.. 396 | Loudness level, musical instruments .....--++-++ 194 (magnetic) 476-480 MOLRES eens cele verketere 193 reflecting power, metals ..+.++++++++> 377-380 | Lowering of freezing points by salts........-- 267, 268 pigments ....-++-+--++-- 381 Lubricants (I. C. T., 2, 164)..---+eeeseeeerees 204 powders .....+-+++-- 381-382 | Lumen .......-- Spe on ee penctcieisistahereNeceretasze 333 scattered light ......... 379 Luminescence (I. C. T., 5, 386) temperature variation W.. 380 | Luminosity ......----eeseere reer rset 333 reflection of, f(index of refraction)....... 376 HACKEDOAY usin costs chersileiere/seelalelele 335 et formulae, Fresnel ......---- 376 molybdenum ....----+eeeeeereeeeee 323 sensitivity of eye to ......-- Drevosecetes 330-332 tungsten, .6654, .467M..-seerrerees 322 minimum energy ..--- 335 vs. color temperature.......+-+++ 318-319 standards: Bougie decimale ..........--- 334 Lunar parallax .....20eeeeeseeseeer eerste? 601 candle, American ...-++--++-+: 334 rotation (history) ....--+ssseeeesseeree 373 Hefner ...-++e+++-ee 334 INK. BtoooOC Ry SPU eR Pe ee tale reise aetaoaS international! .....2...- 334 pentane ..-..+++++see- 334 | M X-ray spectrum ....eeecerceeesscrsereerers 541 sperm, English ....--- . 334 | Mache radioactivity unit .....--+-seeseere rere 520 Carcel unit ....----++--+---- 334 Machinability of various materials......++++++++ 657 Waidner-Burgess So 334 Maclauren’s theorem .....--+++eerrereerrere 13 transparency to: air, moist ......--+++-- 392 Magellan, clouds of.....-.--+-- Rasta hin ocvaterevers 616 atmosphere. 389, 392, 555, 608 | Magnalium: mechanical properties...-.++++++++++ 117 crystals ..+.+eseee reese 390 | Magnetic constants of SUN......++seeeeerreeees 574 dyeS os. ese esse eee eres 385 permeability ....--+++seeeeeereesees XxXii gases, infra-red .......--. 393 poles of earth....-..++++++5 Asin ierecs 575 glasses ....--+++-.-- 384-388 properties: (general) ..-.+++eeereeres 403 colored ....- 386, 388 atomic, definition .......--- 463 ; ultra-violet ....-- 387 cobalt, 0°, 100° C....---+- 469 solids, infra-red ........- 393 ALLOYS) ayeteiereleisielaielel= 465 steam ....+-ee eee ee eeee 392 corrections for ring specimens. 464 water ....cee eee eeeeeee 392 critical temperatures .....-- 474 SCA wee ree eee eee 652 Curie point ....-.-+++eees 474 2 ultra-violet 389 demagnetizing factors, rods.. 470 velocity of (2.99796 101° em/sec.).....- 74 diamagnetic elements ...---- 474 wave lengths: cadmium standard .......-- 347 diamagnetism, definition .... 463 CLOM EME Sieetenelele evererereest sie) =) ie 355 temp. variation. 474 Fraunhofer lines .......--- 346 elements 2cciccesnmseineeer 474 neon lines ....- proteleereioleneter= 349 Ettinghausen effect ....-- S482 solar standards ......-.3507 standard, iron Lights: (see also under lamps) brightness in candles/em? of various. .338, efficiency of various electric........-.--- photographie efficiency of some.......---- temperature, brightness ......-.+--+++5 COLOLMT A ekere siete er eho volie sole rel= ei visibility of white..... P Light-year .......-+eeees Limits, spectrum series. . Miateieteleieiexs| 34 /an O49) SULIPMN eterno 35 Ons 4 353 339 337 Lines, resonance (spectroscopy) ....-+++++++++ 504 ultimate DREN SSL sonieveie'e Eee 504 Liquids: absorption of gases.........++++++ee+- 221 capillarity of ....-.-..----+eeeees 222-223 combustion heats .......-.--++++:: 307-308 compressibilities ........-+-+++++-+0- 154 conductivity, thermal ...........-- 276-277 Gensityi ee ieieterr- Beer Peisiessyeteke 159, 165, 166 Baumé scale .........---+0--- 158 mercury, f(t) .........--+---+> 169 water, De EO SSO OCOD 166, 168 dielectric constants ..........-+-+: 443, 445 SUNENEEAS eetetenetsnareiclere veleloie * cere « 441 diffusion, aqueous solutions.........-+-- 215 expansion coefficients ........+++++++-> 283 magnetic optic rotation .......-++-++> 478 susceptibility, .......+----++- 475 potential differences with substances. . 399-400 refractive indices .....--+++++++++> 370-372 sound velocity .........+--++++e+: 190, 191 sea water ........----9> 652 specific heats ........-----++++++-290-291 surface tensiong ......----++e+ers 222, 223 thermal conductivity .......---++-+> 276-277 cubical expansion ......--++-> 283 vapor pressures ....--+++eeeeee ees 225-230 viscosities, absolute ......-+--+-+++-++- 205-209 specific ....+.esseeeees 210-212 Liter, equals 1.000027 dm’.......-.-+eeeeeree 75 Logarithmic factorials .....+++++++e> mraioiey stele Se 40 ferromagnetism, definition ... 463 flux, flux density, definition... 463 galvanometric ...---+++++++> 482 Hall effect, f(t).....-- 463, 482 hysteresis ..... .»-463, 479-473 induction .......+- --463 et sed. jron and steel ...----+++++> 464 EDULE! seiclsvexehaisieiere Sea 404 soft, o°, too” C.....- 468 very weak fields......- 465 wrought (Lowmoor) ... 469 ST OULE MIE oe elotele eleloreratekarisvelel™ 463 Leduc effect ....-++-e+eees 482 magnet steel ......-+--+++> 405 magnetic resistance ...-++-- 481 magnetite ...----e-ee eee ee 469 magneto-optie rotation, defini- iN. soaccocoood 476 strietion, definition.. 463 maxwell, definition ....---- 403 molecular ....--e+ee+eeeee? 463 Nernst effect ......---+++> 482 nickel, 0°, 100° C......--- 469 paramagnetism : definition ... 463 elements, f(t) 474 permalloy’ ....----+s++seee: 472 permeability... .xxxii, 463 et sed. definition ...... 463 ring specimens, corrections.. 471 sheets, electrical ....-.-+--- 464 steel: 0°, 100° C....+--.-- 468 magnet .....-2-seee% 465 manganese, Hadfield’s.. 469 saturation values ...-- 469 tool, Vicker’s ......- 469 transformer, weak fields. 465 Steinmetz constant ......-- 473 striction, magneto-, definition. 463 susceptibility ........- 474, 475 definition .... 463 temperature changes. 468, 469, 475 OAD peioac 475 thermomagnetic effects ....- 482 670 INDEX PAGE PAGB Magnetic properties: Villari effect .........++-+ 463 Magnitudes: absolute, cepheids .............+2> 635 Wiedemann effect .........- 463 CWADh Stans irrtsleersle/eltereterate 636 LITIES) Soslarerateraeeietenelotetaveloicliohelelerelerefelote lii, liv first magnitude stars....... 619 equivalents ...--+sseeseeeeecs + 397 giant stars ............-- 636 Magnetism, terrestrial: agonic line, U. S8., high-density stars ........ 636 DSOO=0.92 5) eislalatelsteisvore 595 high-temperature stars ..... 636 charts: isoclinic, I, world.. 576 Car AEE So sdigoddwobes 619 isodynamic, H, planetary nebulae ........ 623 WONLCS Wessferereislere 77 Russell diagram .......... 621 isogonic, D, world.. 576 De. Arallaxe Meera nt 624 isoporic: spectrum class.621, 622, 624 Py elicieictercieieiele 577 apparent: binaries ............ 629, 630 EL Fe sioistaleumierereters 577 bolometric, visual to....... 24 Te ceihaiccteees 5738 Gefinitioneys sa-inreotaree 602, 623 total intensity .. 580 first magnitude stars....... 619 vertical intensity. 580 Magellanic clouds ........ 640 constants of earth....574, 575 MOON seo sie.n or ereraretetee oreiercve 623 declination: nebulae, planetary ........ 639 annual change, world.. 579 radial velocity stars....... 628 isogonic lines, ames “are TAQIOMELYICH oyeyeteletelereleeretare 632 isoporie “‘ - 577 space al velocity stars. 627 secular change, U. S.. 590 (small) ey 627 dip: annual change, world. . 579 Stars; Meare sun we sryeeiee iors 619 f(lat., long.), U. S... 592 per magnitude ..... 620 isoclinie lines, world. - 576 SUN RSS ieletorreisefita accor 623 isoporic “ ons 7S Venus: Sennen iccionermine 623 secular change, U.8.. 592 aes parallax, ) Ween e morte 624 horizontal intensity: spectrum class ....... 620 annual change, orld a As) visual to bolometric, correc- f(lat., long.), U. 593 PIONS Pe wrevoncioxcrerererercreter atte 624 isodynamie lines, ‘vorld 577 astronomical, definition ......... 602, 623 isoporic s 578 Malleable cast iron, physical properties.......... 657 secular change, U. 8S... 593 Masss alpha particles cyrercjetatsveleteraleiereleteievetetereteteters 105 inclination (see dip) electroniey oo sero sen iereciietetereeeneere 105 isoclinie lines, I, world DUGatomipereracrcrerstencte cetetstsin cle shancreiettereronet 105 CHALtIM tee ekeleisleneiesaitetet= 576 PROTON Myer tereredetatelatetereicverele ekctaheltereveloncister 105 isodynamie lines, H, world relativity correction ........ Lin rekesvekeletohetore 492 Chart . cc nccesecccces 577 Masses: spectroscopic, binaries ........---eeess 620 - jsogonie lines, D, world SUCLIAI aes core ole arevecs siete 619, 623, 629-631 Chantemer eee tote 576% | Mathematicaluconstantsi sacs eee ees 14 isoporie lines: tables: antilogarithms, 4-place ....28—30 D, world chart...... Bird Bessel’s functions ......... 70 Pe Secretly vere 578 circular Se acevettate 32-40 I, Gh SC OP Ney etete vere 78 CONSHANUS Mrcteyeveratoleterereterreneyere 14 intensity, total, world.. 580 Clibes! . 659 Macro; s Gefin ition’ vere <, fare ateiee)oler-rsietoveleteheleiet=telet -» 659 Microny ss eH atti OMireysiejeieateletatstcteletetey tele tslelets! 659 MULLS definibioninarcteye sto eletele rst ais ielcteisherercialer fete tetere -- 659 Mile, geographical, nautical.................+. - 659 Milky way Ae haan e ce ee eee . 616 DOLE) ays etetatcters aects, szevaternatercteretetatater eters 601 Minerals*sdensities\@ a cmcmecew cetieiateine cece tas 164 refractive indices, biaxial ........- 367-368 TGOULODICNe eine totes 363 Uniaxial “Joe -ei0 365 specificsheats, cctaceuaiieerideseitriacisiere 292 transformation, melting temperatures. 261-266 Miniature electric light characteristics........... 339 Minimum energy light sensation......... eivisini rete eGo Mobilitiesst1onity 2) .)-tsicleleleis)s ereislevatoiainloleisis Olefa rs ee Moistyair, (Gensity cof erecteesietetetestate Sik hayatetere 177-178 , humidity term ....-...-- “fhe maintenance of .......-.. aieretalnte ters (ols = £79 transparency to radiation, <360t0) We Were coe GOs Sse kos.) Umd to 204 sleheletuleiuteistelapmieleral~iate « 392 SUCAIN Cl 2570561025) 107 Oils: compressibility, petroleum ............... 155 Loschmidt’s, 2.70510! em-*. 107 films, s.thickness; cyemeenc nn tee 551 organie cross-sections ....... mrerefereneiers 551 thermal expansion, petroleum.............. 155 spectra: diatomic molecules, viscosity,-,castoniy yer ee cae eeieeree ion 206 GUCEINIS, So donanou6bde 512-513 fasolinenskeroseney cease ee eee 207 energy levels ............ 512-513 Optical constants of metals................. 377-378 heats of dissociation....... 512-513 PYLOMELT Ys -o cara See ee cio oes ee 248 rotational levels ......... 512-513 rotary power (I.@.7T., 2, 153, 334; 7, VElOCILIES Mei etre scree cetera a eiee rade erolene 550 3169) ia a eR RR ere ns ee Tn ee 396 LOHAN Oy GulliGkiooososdoccodsuc0s 553 rovationse magnetics sec eme cere eee 476-480 Momentswof sinerbia > earthieacterstert ctor ele elsstere 570 ThHErMOMELTy: = eee see ee 248 O. formulae ...............-- 724\ Orbital velocitysoimeattheaeeiace cece erates 570 Month, definition Feet eee eee ee eee eee eens 660 Organ pipes, DICE reread eeietene ee ran ee See 194 SLGEnealy SyNOCICAl meteretetevetatete etree telat 601 | Organic compounds: boiling points .......... 256-258 Moonzvalbedoy seacvern scree Aotcvovetarototaietelenercyero sis} = 607 densities ee ees 256-258 distance from earth.......-..........-- 601 melting points ......... 256-258 history ((tidaly e6C:)/-ycirciaveye +s cle ines « =1+1 0101 573 molecules, cross-sections ............... 551 magnitude, —12.5 seeeeeeeeseeeeeeeees 623 salts SSOLUDIIIGICS Meryarerereqeeustetstekenertetoieiece 219 tides ..... espe rolelelsielaisl oekeses iid eacdcicks 573-574 | Oscillation constants, wireless telegraphy......... 460 Mountain, highest .......-.ccsessscceres-eee 569 times of wires, temperature variation... 137 Movieslights;scharacteristics) (iss elerietartetalerere) ote 339 0 AIGIEIAU Rites enecte © . vertones@ (Sound) '™ iy-rye cle cpeiectseetcrero ereiereieiels 193 ultiplicity, spectrum series.......+.+-.+-. 502, 503 , musical instrumentaneety: See 194 Musical instruments: loudness .............+++: 194 Speeches a J SORNRR IO ots as ieee te 195 a Sus esehhe eke iege Fake oi8 wen Oxides: brightness, incandescent ............... 336 peak ower aes ones 194 emissivities (radiation) ............ 320, 324 SCATES I eretora scchevoleie dus evita s cletnineretatelers 192 I; RT ATEOBO RAR ONS TIAL Men occ 14, 660 Nebulaczaclassificaplonuereilaeie iit ieee asians 639 | P limit, mechanical property.............. 110 et seq. GAL Wee nt peril) oe, Cla ep ees 639 Packing sirachionsmey-yeretcle/aleratetotere) oleversl=aclolsletel= 484, 648 GIMUSES een een ee ee ec aes 639 Parallax, first magnitude Starsah, > 57-59 wave-length limits of various types...... 501 Probability integral ........ Par eN cicero raleis scones) 56-57 Radiations, wave lengths of various.............. 501 ; ATIVENSE!: fs loveria/s\eieeverere’s wise vere 60 Madore eyration’s As, %, tecsts aletevale eva,evvsicaversia « 519 radioactive equilibrium — Bsistsverseseraicre 534 radium and products (see ionium PaAIily,)On waa eiotetereveretolors clctouercieterctts 517 TACONM Mater aihelelchetetote tetera oieteterciclels 520 LUD UGIUIN ie yeteteleieteelelntstelelaolclete/ehelars 519 thermal activity “(Ra-+Em) ajerctohe cts 525 thorium: average life ............ 519 GecayalConsbantisieerrse revere 519 periods, 4 values......... 519 units, miscellaneous, constants. .520—521 uranium family: average life ...... 516 decay constants ... 516 periods, } values... 516 vapor pressure, Ra emanation...... 521 Radium: average life, decay constants, } period.... 517 emanation, vapor pressure.............. 521 heat generated (plus emanation)........ 525 DHOSDHOLESCENCO Mar tecrsiierelororarachelereiotsnsione 521 Radiusnoficunvaturevotespacels.cscv.tersrcrte) -lelsretererers 644 IRAGOLs dntetoterslavererovalotatereretevel oe bpelsseicrescisisieterafonclatate 520 (RAL ESMULEIM ES? Ys ievcvele cie eto rslevensvererel elevel ove 504, 507-508 Rain electricalsichargewons ciiieisiereiereretercrere areicierle 598 Range mtablews (wireless) mieretoeisssreveievedeyerererene starsvorers 462 REAM UPD cevehotevoteratoretcreret tein) eVallsy stelctetael sro ckctotehetokete 660 IRECIDLOCAISH way sceteyencucne tere t tevchons efevel hevave evolehclenerel sit 15-23 Reflection: angle, variation with................ 382 building materials) cha haie-s tee te craters - 364 standard, media «scccccere cee 375 sylvites KCL cca cnenorees een 400 VADOTS? er slatererercy ccrerrere ater tae s 373 Wabensues@aliion kane aoeties aioom f sensitivity to light and colors........330-332 glare. eee serge ects pieee ao Right ascension, declination to at ean ee 602 mann energy for “li ght nates ......604—605 Sensation) Wiarets siectetetee oe BOS Rigidity modull Rlsialaleleveleleleleleteisiete)ofels/elele sie) 00) EL SEC. Pe Reese Se GiMRCHN LM mrateleletelelatolelelalefetelets sleieicisleretelnie 6 5OQ) || 1 Mier h eee alin setter sere ao eer aed Rise of boiling point by salts in solution.......... 269 See Tebsa + +++343-344 Robinson cup anemometer, corrections.........-- 197 | Series: mathematical (i p I Ae eet cn coco ee ooe Rock salt, refractive index, f(t).......eseeeeseee 300 : at are ) ere eiocls pho ceree Samet HELE T iMRI es. aoa spectrum: atomic relat ODS 206 molecular \-ice sm sciele sis alolelelclstetate ye gules Solvents, organic, boiling points................ 220 diatomic constants ......512-513 Sound: ;audibilitys eee eee eee eee 194 energy levels ...... sie Le Sus Delle cisyerasitvacicteretane atten iether tone 193 sensitivity, photographie plates and decibel ehalatelatelaloteioteleieicteicherteraicversioleicieieis 193 films? Shes he ees, se eterese sees e343, 344 arm ONICS? e003; ss eee ene eres 193 series; atomic:/‘arc) ines!) ; 010 c/elecleleielen (504 loudness levels, musical instruments ...... 194 atomic relations ....... 502 NOISES yyaaiets eres isiestliaeieyers 193 Bohr-Hund notation ... 502 muiscellaneousidata ener eerie ere 193, 194 combinations, interseries. 504 musicalsinstrumentsmereee eee eee 194 configuration, electron .. 505 SCALES) | MEAP lacinohis « ecammmenn oe 192 displacement law ..... - 503 NOIS€S! 2y.)-. 61. erakesosclolelatateters lous ckevelensieeicievene 193 electron configurations .. 505 OverConesi Meriter itis ei Pre sos 193 volts ........ 502 SDECCHI: rs. ciaysreeinere eis LEER one 195 forbidden combinations... 355 SUPEFSONICS: © j.crere ca cee eee eee 191 Hund quantum numbers.. 504 thresholds: v.j5.0. canoer ene Meee 193 hydrogen series ....... 495 Velocity. crete cee oR sare 190, IQI inner quantum num- WENGE “GUITay WSs dodbooontooucdnod sets O3 7 DENS Mateneeyer-nekercyars 503, 504 Space: amount of matter, interstellar............ 644 Landé’s interval rule.... 503 CayNay ini interstellar) miteyrereieien eee ce en 644 life, average, of some charge, atmospheric electricity............ 597 TENMS | sicteveicicisceisieiereren SHEL temperature; dnterstellans cersrie- ire ceicee 645 limits ..... seeeeees 502 transparency, Real 2) Carts Maks APR a aie 643 lines, average lifes yc 511 Sparking potentials: alternating, in air........... 439 metastable terms ...... 505 ball electrodes .......... 439-440 multiplicity ..502, 503, 504 ex Oseneiiuirsuscciescra eae 441 normal relations ...... 502 large spark gaps, f(pressure).. 440 Notation .....cecesceee 504 Steadyainiyaireeenel ene ane 439 , Bohr-Hund ... 502 various materials ........... 441 parity notation ....... 504 Specificiicharze ampanniclewsse: see eee eae 105 persistent lines, are, MON GeoogongogcooandobeL 105 SDA, Seteveress selec 509, 510 gravity (see also densities)........ . 158-179 quanta and term type TOA Pol Sal Oi cet seen ce 158 (nd) ierereererre err 504 Baume) air tere reve foe ome 158 quanta, inner .....503, 504 Heabseammoniayesataelig see eee 291 rales) UlbIMEeS! Sarre -)eiels) 504: Me, CONSENS Saoaonoesaocaune 108 resonance lines .... 504, 511 clementisparysnincra astra 285-287 Rydberg ...........-. 502 formula for true LGU Gaeicogpoodoodan GOR gases: also Cp/Cy ultimate lines ........ 507 liquids volts; electron’ Jcjccteces) 502 MEGAN siete etcreleteleie WAVE) NUMDENS! eres 634 SUPE Ka ct icuepouekerete <2 /terei= ici, sve. 0(s:e e018 622 Harvard spectrum classes.............2++- 617 cin GICHS COLO beter yeusnereieieieie cVelsie.o\s)ers.04 wo. 617 ACE UL DMV AAD Le meme Neta rates teveborsesve «les ecco rahe 634 IPH COL alan era ratte cminicvec cls exe. + 6 0) eTe.ei0 645 Juminosity., definition eae (O32 meta-galaxy .....-2ssccrccecsccssceee® 616 MILKY; | WAY 6 teen wietelo ete ehelsiels’ o(alelstelaiasirretel= 616 nearer than 5 parseCS.......---seeereees 619 nearest approaches to suUN......-.+-+-+-+++5 620 TOVAG IN vole she veretatmolel ate Bicksorerarst avaketerepetece 634, 635 NNUDIDEM, | srcleforeretahe wietelo ele etoreneke'alavelslmiate minis 61 per square degree.......-+++++e% 618 parallax vs. mean apparent magnitude...... 624 period vs. luminosity, cepheids.......---+-- 635 periodic variables ....-..--+-+-eeeeeee8% 634 proper motion .......-+seeeseeeeereees 628 Dare ec ey cioisve sayeioionerl visio 625 vs. spectrum class......-+-- 626 Purkinje effect .......---eeeereeerrreee 602 radial velocity, great......------+-++++-+% 628 TAMLALIONN, cisicie tieelete oheieienlclclekanaevolond= 632, 633 radiometric magnitudes ......----+++++++s 632 TOAGIONL Of, clcetetersicistetelete aieie\olerelsuniat-rsinls 642 GALAXY eievsle nisi wiovetminlelalexrdoietnints - 643 SIZG teat ics erates cs wer dtate valle velo ielielernte eloiekelnieveiegn Be O2g) space, temperature Of....--+-+-+-++e++00 645 spectra: binaries ....--++++++eeeeeseeee 629 ENOL) Off s-jatove ole aja ola! laine inrekeienee 633 first magnitude stars.......--+++- 619 Harvard notation ........-+--++- 617 magnitudes as related to.....----+- 620 TCALED. sete dc eechevelouck=taker= snlsiateln as Bey (LG proper motion as related to....--- 626 temperature as related to.....---- 632 stellar systems ....-------++eeeesseres 616 sun (see also under SUN)...-+++-+++- 608-614 super-galaxies ....----++2+-+eeseres 616, 642 temperatures ...--.+-+-+++-- ..2-617, 632, 633 HUeh Peete set cie ete sveyete sfotenete raza 636 stellar space ....-----+-+-+5 645 temporary, MOVA€ ....-. eee eee eee 634, 635 variable: cepheids .....---+++++-> eeeee 634 period vs. luminosity... . 635 Classification .....----- eee eee == 634 cluster ...-- RE yrcrceuapeh keke eletetere 634 eclipsing ...-eeeeee cess erties 629 irregular ......-es+eeeeereecees 634 TOVEO ee etcterakeletalelekolenonensysiminte 635 periodic ....-.++eeeeee ees 629, 634 temporary ..-e-ee ee eee reece ees 634 wolocities ....secsceer aces erretees 617, 628 proper motions, large .....--+-+ 625 vs. spectrum class. 626 radial, >1oo km/sec. ...---++-- 628 space, > 300 km/sec. ..----++-- 62 <5 km/sec. ....----++- 627 SUM, corclete evevctetere 'atecavetwiaholelal esis 625 visual vs. radiometric magnitudes......---- 632 Steam tables: 0°-222° C, saturated......... 298-303 400°-700° F., saturated........-- 304 212°-3000° F., superheated....... 305 tramsparency ...--.seeee cere eeeeeceeee 392 Steel: alloys, mechanical properties.......-.----+ 113 carbon, . sf heat treatments. 112 castings, “ o Neate ta otekacevelela weeks 112 magnetic properties ....... Miers tataicte -463-473 semi, mechanical properties........-+-+-+++ 114 wire, = AEE™ PL SE cata ndiereo° C. Pt-PtRh stellar . Tension, surface, liquids... Tenth-meter-angstrom series (spectroscopy) spectra see ee oe Terms: metastable ......... <0 Ce ee ener eee ee ee ed Terra cotta, mechanical propertieS.....sseceeees Terrestrial magnetism: agonic line, U. S., 1925 charts: isoclinic, I, world..... isodynamic, H, < ‘ 1800- eee e were eeeenece isogonic, D, isoporic: annual change, , 1G “ DY MOREE Gaooddsos H “ae eeeercerere eens total intensity, world. vertical intensity, world constants of earth....574, declination, D, annual, world .....ee. isogonic lines, world... isoporic ‘“‘ oe secular change, U. 8... dip, I, annual change, world. f(lat., long.), U. S., 1925 isoclinic lines, world. isoporic © secular change, U. S. horizontal intensity, H, see eeeeeee eee eceeees “ ‘ world. . fi(lats, Ong.) eUceNieteters isodynamic lines, world. isoporic é secular change, U. S.e. inclination, I (see dip) . isoclinie lines, I, world chart . aie isodynamie lines, H, world chart “e ‘ eee e eer eee isogonie lines, D, world chart eee isoporic lines, D, world Chartitercistelalste “e I, , “ “ee eeoeeeeee 241 243 339 243 244 247 245 246 245 a Oy, wae222—223 . 660 505 506 502 129 595 576 577 576 ae 77 578 580 580 575 579 576 577 590 579 592 576 578 592 579 593 577 578 593 576 577 576 577 578 578 INDEX PAGE isoporic lines, intensity, total, world.. 580 vertical, world. 580 mean annual observatory ele- Terrestrial magnetism: IGILUS He rarareeeterevevere etal sje 581 mean annual observatory ele- ments, bibliography 589 mean monthly magnetic char- acteristic ....... 595 mean yearly magnetic * char- acteristic ....... 595 observatories, mean annual elements Mavetataieieteiaia os SOL observatories, mean annual elements, bibliography ... 5890 poles, magnetic .......--- 575 secular changes, declination, U. S., 1820- UC)\SiO) “Gao ono doo 590 dip, U. S., 1855-1925. 592 horizontal intensity, U. S., 1855-1925... 593 ae U. S., 1855- Ci marciistatearetleiaen SOS total Gaecneiee) f(lat., long.), U. S., MOREE tereisleterstatarate! oat 04" isoporie lines, world Chantmerrae tier. 1500 secular change, U. §S., TB55-1925 .cceceve 594 MPI GN Tete Tatevee fe perersyio =) eet eel is se si clsiciezex\e 0) eevee . 660 Thermal conductivity : AIT ret ene Veet Nclevclc occleverecels 327 SDACES ACTOSS) wc /cieles e 276 Get me eve te tetersyforaioral cleric we OS2 couples: e.m.f. calibration ......... 244-247 chromel-alumel ......... 247 copper-constantan, >o° C. 245 techniqueofahicheer--) occ onesies 655 electrical equivalents ..............0. 397 Malencieswof sthemelementsS tec jeretele cicrereielebete 234 Zn=Pt sjtciests ner eoeee 404 Vaporization, latent heat of ............. 295 et seq. tnibo-electric seniesmrcrcrerieitelst-rrenteletonele 408 AMMONIA rayeiatersyelelerele 206 WOLERIC COLIS er reveycrereies oetioter clo teteretcnere 398, 400 elements, theoretical.. 295 Weston cells ..... J ghasan eae xlix-li HOLMULAGT Fyn ciel eveheferele 296 | Voltameter, silver ....... Jeeloee ee Xlvilioney 7) ebnsed: Mercury ....2-..-6- 306 Volts, electrical equivalents. eae sai Yanaieceuens’e sveceus ++ 397 steam tables . 297-306 international yea)clsleie!<)-)-flel> piedstenstenetoke xliv, 397 ALC Olmraprierkereietereiey helertereNetelerciciere 223 Volume, atomic .... mote erckerietebetsrerets a 289 Waporsidensitiesismsccccera svctelerers ate -176, 298-306 critical, for gases. Rrencneloieealaiehehoiekeienet=netets 271 Gifusiongofemernsesete eee ete ee 2065 207, gases, f(t) with logs........ «149-152, 155 heats of vaporization ...... 295-296, 298-306 glass vessels, determination of........ aeeOS SPECI ichiactaceie cutee oni see 203 mercury, —10° to +360° C.......... -. 169 pressures (see vapor pressures)..... 223 et seq. Perfect, GaSeesie-.t. ntayaic aio tevs terete eters stele nens 103 Retrachivepindicesiacmietsi-aatercletsieletsiene eierae 373 resistance of dielectrics........ Sereno 418 Specifics heatsparrecsi aes erence 293 Waters nl (tA) He caetetere crete on chelenere olererekereie 167 viscosities) Mspiratte cic cneaaeinence 213 ——=i(0 WO, GRO Cooncconescocec 168 water, transparency to radiation......... 392 Vowels, resonance of spoken.............. Goooo MO)S Variable stars (see under stars)............ 634-635 Velocities: earth: linear, rotation ............ ++ 570 Waidner-Burgess standard light............. ease. Onbitale ey somite leitsiucicre sets errors 570 Water: boiling point, f (pressure) Bieicieyeteta totes 188, 253 light, 2+» 997961019 cm/sec. ....... 74 density: f(t) o° to, AT CaO) tre sense ences . 166 molecules sneer: RR AEEIL SLU NOD 550 _—to0° to +250° C........ 168 SOUNG) eee ee aie deetanntenetotele 190-191 maximum, 0.999973 g/cem* .....- 75 IN| PSeaAMWALEIN sen cence etets cere ar 652 sea water .......2-e+eeeeeeees 652 stellar: greater proper motions........ 628 solutions: alcohol, ethyl ....172, 173 MEAnjieey ett aris aici 617 methyl ....... 174 radial>1oo km/sec. ........ 628 glycerol ...0...----00 206 space v., large and small...... 627 sucrose ....++++++174, 175 SUM cw yait\nreicasoteave es veo eaten Tee Balen 625 sulphuric acid ....... » 174 Merdetsierconstant ame eeee tie eerie 478-479 freezing point, f(pressure).............- 253 Vertical intensity, earth’s magnetic field (world ONAN Bona conadeoncoouDGoDedadSaD 438 chart) ener eae Se atere SOO 580 melting point, f(pressure),severerereeees 253 INDEX 681 i PAGE PAGE Water: pressure, hydrostatic, of columns of....... 180 : wi 2 SEAS ACIADAVICH COOMNE Maser ieinisisicieeiciercle\¢ 652 Rete oe oe We STC ST ae poe, eee chemical composition .............. 652 numbers ee sos Soe eee O2 eilavinity MeaMe oe ee Bier ees weet ees eee cece ereeeeceeeeness 502 Coltrane oe Eee CUELEN h le aca Crate erat rales a diete ters 105 lee etek man nha nko axe 52 VElOCILY jm CANCHONEKES te c¥atercieielatelersyele cle lelelsrets 569 concentration ....--....-.+-+s+e0e 651 Waves: SCismici inte veteroce teva nelerdtetelciereraem enters 653 conduction, electrical, thermal....... 651 FMAM. GuGhiay (in gadoucedene du cen ntroL 194 CS 652 Swell cee yhe ee ae Oe Oe, ene Oe ee freezing es VOM Ur fertlelete telco s1~ <= 652 translationi o-ceyscteyaiee crore ieiimels te eat 653 ANdexX OfremrActiONijec cicrlelcls «<< « © 652 Withd 7 ret ON se Ae Ee, rae a 653 PIESSUTE oe eee ee eee eee ee eee eee 651i) | FWeber’. gasncon cs Aa eR ERG ea oe ae EUR Senge ast 652 Weighings, reduction to vacuo............-..++- 109 SAMMY ow acinia seve ee eee ee ee tee 651 | Weights and measures: customary to metric....... 5 SQUNOMVCLOCIUY) retereisterstee sicveisl~ <1+ie 190, 652 imperi: tri Sees Z nperial to metric....... 10-I1 eneciie Hen pada sae ie, erin sus: £¢ee oe metric to customary ..... 6 LEMDEL AUN G memtertetetekereieteleferolster 62 I capes : URENMOy oooadosonacouaoan 89, 652 ; P sao VELOCIE VA Of SOUNG clear leleiansisicless.c16 = i 626 MSN, eae VISCOSLOV es aiainerieilccrelclelsisicnsce.cicieiecce.« 652 BROT GS te ee OS Cera: a solubility of gases (I. C.T., 3, 255)..... 221 Here: Se ieee ee ieeiaibe Ccricirtinentrates e 5 ce columns water ot mercury....++.+++++++ 180 GUMS WN soscencooodagconogd 215 Weisstmarneton (i CT ae EA ae aa 7 electrolytic conduction ........ AS2 mil loreeton 7 CoariSrgay) xlix athe points at ete p ee eAe ieee Sees 367 White lights, visibility of........... sleleie ie 340 Sh Ree amc rieis alae rat t ces 651 Wiedermann magnetic effect (1. C. T., 6, 6 viscosities ...........206, 210-212 : : SEES Cree £ 439) +42. 463 sound svelocity, ofan vac nacwoecece oes 190 Wien displacement constant........+eeeeeees set O7, SeARWAter” Glcucwe ce 652 Wind pressures ......+-.+++e+ee- paleteisleiteikOo—202 thermal conductivity .................-% 276 Wire gages, comparison Of.....+.+++eeeeeeeeees 420 transparency to radiation .............. 392 mechanical properties of copper ......- 118-119 Sea tar ees! 389 ual Grcigsecacndc 114 Steanitee aeise as 392 : re rope and cable. 115 VADOLRE eR oe ea resistance, auxiliary table for computing..... 408 vapor: atmospheric, relative humidity i es tables: aluminum (see also introduction to wet and dry bulb ther- wire tables) ........- 421 mometers ....- 234, 235 English measures .....- os 429 determination, sea level, via wet and metric measures .....-- ++ 430 dry bulb thermom- copper (see also introduction to wire CLES Sects 234-235 tables) e) ake: ntejiese .eleessla\wlaiers 421 various altitudes, via English measures ..... sfeleitere 423 wet and dry bulb metric Soe Mee cnetsveriars be 420 thermometers 234 temperature coefficients ..... 422 in atmosphere, f(altitude)..... 558, 560 reduction to stand- DIessunemee a ee ie hie 232-233 ‘ . ard .....--- » 422 relative humidity via dry and yapor Wireless telegraphy: absorption factors in propaga- pressure 236 tion _teeeeeee *: + «+454, 455 wet and dry.. 238 absorption factors in propaga- transparency, ordinary temperature... 392 tion over land.........-.- 455 SUOAM)Mierctater ele sciera sieves 392 absorption factors in propaga- Welehtnarriertere ne ceericche; ciclo ecavassic.s 234 tion over S@2...++.+++++++ 455 saturated, per m® and ft.*... 234 antenna heights vs. wave viscosity, f(temperature) ............... 205 Length cijclele erslee et 452 high-pressure) saccc cess 6:2 «0s 656 resistances .......++ 452 volume, f(t, p), 0° to go°C............. 167 wave lengths ......- 452 —— TO MUO at 2.5.02) [Cieyere) oxeleiers cos 910i 168 dielectric constant ....... nasa weight sonacolumnsp Olin seiiecicers cero < 180 properties, noncon- Wap Ovaretsreretersiovatcieneseloley <) civescicioteeryetolestye nerterateee acretre 601 characteristic ........... 537-538 Yearly means: magnetic character ...........-.. 595 efficiency of pro- solar (constants) . daccmiateenient 609-610 duction ..... 542 SUN “SPOUS! 7. Areperepere cues faeuatetereveretereae 610 chemical combination, effect of. 544 LEM PCNabUne’ a tercyerercyencheuectery matelorarers 556 continuous spectrum ........ 537 Yield point, mechanical property.......... 110 et seq. critical absorption limits. .538—541 Young’s modulus, mechanical property...... 110 et seq. crystals, lattice constants..... 543 efficiency in production of char- Zeeman ‘displacement —.\.:sje.0 cueiacisincrevoriolesteyeiee 106 MCHETIStICH Neteverereets atoletelelstere 542 effect) (EGS essp Amo ucrtertercteretelensiels 503 EMISSION wetetoteiciercletatetsyoteretet=tats 537 Zero; sapsOlutes ——2. 7.32 Lede cere eile teil etersiere 85-86 energy in continuous spectrum. 537 Zine, mechanical properties................ 124, 125 relations ...sesessee 543 Zonal spherical harmonics..........+..+eeeee 66, 67 —— == — —$—= es SS CS —————— . —— ————— > —_— 3 —_= ————— bE ——= 6 SSS== ._—_—— =——— ¢< Sa 2a (0 _— 0 —= sd _ > — I ———— beeen