obviously therefore g2,-)=4X (an integer relative to “) + Von.
Hence
(—1)"B,=(an integer relative to w) — 5
: 1
= (an integer relative to w) + a
pe
* Yor » being a prime number greater than 2, if we put T(r) (the coeffi-
cient of ¢” in e«t—1) under the form of (an integer gud ») Xp’, we have
r r r
i=r—E-—E- > —E7;- &e,
pe lH
va T : 2
= Of ty Oe >1 when r > 2; also when r=2, (=-2—-h
When p=2, this would be no longer true; and in fact it is easily seen that
in this case, whenever r is a power of 2, z will be only equal to J.
For the benefit of my younger readers, I may notice that the direct proof
of the theorem that the product of any 7 consecutive numbers must con-
tain the product of the natural numbers up to 7, or, in other words, that
ih oh, IIn : :
the trinomial coefficient Fp 4,7 Where »+»'=2 is an integer, is drawn
from the fact that this fraction may be represented as an integer gud mp (any
prime) multiplied by p#, where
A y p\ as n y yp!
oes — hee | he hs = — i
i=(2 —E 1D ae 7 -E=-E :)+ &e
(Ez meaning the integer part of x), so that 2 is necessarily either zero or
positive, because the value of each triad of terms within the same paren-
thesis is essentially zero or positive. This is the natural and only direct
procedure for establishing the proposition im question,
and a new Theorem concerning Prime Numbers. 133
And this relation obtains for any value of yu other than 2, which
(or a power of which) could be contained in 2n. When p=2,
the & series wiil nof all of them be the doubles of relative inte-
gers to 2; but the v series, on account of the factor I1(2n), will
obviously, up to v2,—, inclusive, all contain 2 and ».,=13; conse-
quently go, will be twice (an integer gud 2)+1, and B,, will still
be (an integer relative to ~) + : as before. Hence it follows from
the lemma that (—1)"B,,=an absolute integer + 2 or
1
B,= an integer +(—)”"= ie
which is the equation expressed by the Staudt-Clausen theorem*.
My researches in the theory of partitions have naturally in-
vested with a new and special interest (at least for myself) every-
thing relating to the Bernoullian numbers. I am not aware
whether the following expression for a Bernoullian of any order
as a quadratic function of those of an inferior order happens to
have been noticed or not. It may be obtained by a simple pro-
cess of multiplication, and gives a means (not very expeditious,
it is true) for calculating these numbers from one another with-
out having recourse to the calculus of differences or Maclaurin’s
theorem, viz.
Be. igo B, Biot . 2 Pat et
Ten ~~) irey’ Tren—s tray enw
Bos B.
Qn—4 At LM Se tae 2S
et... + (2 —)it@n—4) 114
+ (227-2 1) Bra =i
Tl(2n—2) 112’
in which formula the terms admit of being coupled together from
end to end, excepting (when n is even) one term in the middle.
To illustrate my law respecting the numerators of the num-
bers of Bernoulli, and its connexion with the known law for
the denominators, suppose twice the index of any one of these
* I ought to cbserve that in all that has preceded I have used the word
imteger in the sense of positive or negative integer, and the demonstration -
I have given holds good withcut assuming B, to be positive. That thisis
the case, or, in other words, that the signs of the successive powers of ¢
. et—] ate
at alternately positive and negative, may be seen at a glance by
z 4
putting t=2’/ — 16, and remembering that all the coefficients in the series
for tan @ in terms of 6 are necessarily positive, because (a) tan 6 obvie
ously only involves positive multiples of powers of (tan @) and (sec 6).
134 Prof. Sylvester on the Numbers of Bernoulli and Euler,
numbers to contain the factor (p—1)p*, where p is any prime;
then this number will contain the first power of p in its deno-
minator; but if the factor piis contained in double the index in
question, but (p—1) not, then p‘ will appear bodily as a factor
of the numerator.
It has occurred to me that it might be desirable to adhere to
the common definition of “ Bernoulli’s numbers,” but at the same
time to use the term Bernoulli’s coefficients to denote the actual
os
coefficients in — ; so that if the former be denoted in
2(e!
general by B,, and the latter by @,, we shall have
Bon= (—)"'B,,
comin —! 0
In the absence of some such term as I propose, many theorems
which are really single when affirmed of the coefficients, become
duplex or even multifarious when we are restrained to the use
of the numbers only.
Postscript.—The results obtained concerning Bernoulli’s num-
bers in what precedes, admit of being deduced still more suc-
cinctly; and this simplification is by no means of small im-
portance, as it leads the way to the discovery of analogous and
unsuspected properties of Huler’s numbers (namely the coeffi-
cients of
in the expansion of sec @), and to some very re-
n
markable theorems concerning prime numbers in general.
In fact, to obtain the laws which govern the denominators and
numerators of Bernoulli’s numbers, we need only to use the fol-
lowing principles :—(1) That « being a prime, 2u”=0, or = —1
to the modulus jz, according as ~—1 is, or is not, a factor of m,
—the second part of this statement being a direct consequence
of Fermat’s theorem, the first part a simple inference from its
inverse. (2) That e“*—1 is of the form pt-+p72?T, where T is
a series of powers of ¢, all of whose coefficients are integers rela-
tive to ~, except for the case of ~=2, when e“*—1 is of the form
2¢+2T. We have then (u2”—1)(—)"~"B, = —II(2n) x coeffi- _
ele Wey e(h—2)t 4 wn &
ett — ]
virtue of principle (2)) =I— , where I is an integer relative to
cient of ¢?”-! in a by actual division (in
#, containing n, and —R= -< (Vt Oe +(e — 1)
Hence (—)"B,= an integer relative to w or to such integer +
and a new Theorem concerning Prime Numbers. 135
according as 2n does not or does contain (w—1), which proves
the law for the numerators; and so if pw‘ is a factor of n, but
(u—1) not a factor of 2n, x will vanish, and 2”—1 will not con-
tain “; hence (u?”—1)B,, and consequently B,, will be the pro-
duct of «* by an integer relative to ~, which proves my nume-
rator law.
So by extending the same method to the generating function
ef +
Q4 Q2n
secO=H,+E + Baya ga te t En pa gay t he
6?
IT, 2° +E
every prime number yp of the form 4n+1, such that (u—1) isa
factor of 2n, will be contained in H,,; and every such factor, when
p is of the form 4m—1], will be contained in H,+(—)"2.
I call the numbers E,, E,,... HE, EHuler’s Ist, 2nd,...nth
numbers, as Kuler was apparently the first to brmg them into
notice. In the Institutiones Caleuli Diff. he has calculated their
values up to H, inclusive: in this last there isan error, which is
specified by Rothe in Ohm’s paper above referred to; had Kuler
been possessed of my law this mistake could not have occurred,
as we know that H,+2 ought to contain the factors 19 and 7,
neither of which will be found to be such factors if we adopt
Kuler’s value of Ky, but both will be such if we accept Rothe’s
corrected value. But in still following out the same method, I
have been led, through the study of Bernoull’s and the allied
numbers, and with the express aid of the former, to a perfectly
general theorem concerning prime numbers, in which Bernoulli’s
numbers no longer take any part. Fermat’s theorem teaches us
the residue of g“~! in respect to w, viz. that it is unity; but I
am not aware of any theorem being in existence which teaches
, : #— lo] aia
anything concerning the relation of Fe Be ty (or, which is
the same thing, of the relation of gu—-1 to the modulus ?). I have
obtained remarkable results relative to the above quotient, which
[I will state for the simplest case only, viz. that where q¢ as well
as # is a prime number. I find that when q is-any odd prime,
Lo a
be w—l
where ¢,, Co, Cs). --Cy—1 are continually recurring cycles of the
numbers 1, 2, 3,...7, the cycle beginning with that number 7!
Co C3 Cu—1
Sy se ae aes ks 3
136 On a new Theorem concerning Prime Numbers.
which satisfies the congruence pr! =1(modr). Since we know
1 i! pie :
maa ae aa wine eee — — . ]
that aa Danger a pra +9 = 0 (to mod. yw) in place
of the cycle 1, 2, 3,...7, we may obviously substitute the re-
duced cycle
r—l r7—o
“9? ae “9? @oe
r—3 r—l
—1,0,1,..— “==
2 2
oodies
Thus, ea. gr., , when pw is of the form 6n+ 1,
aia 1 1 1
Fay 8 + a go ee
and when wp is of the form 6n—1,
—1 1 1 1
tee ee) Maen ae Ee
When g is 2, the theorem which replaces the preceding is as
.—1,to mod. p.
Q-1_]
follows: » when p is of the form 4n +1,
: po
1 1 1 1 a 1
See eg eb fad ae ee ee
foal pk p—d poo 5
i} 1 1
and when p is of the form 4n—1,
a0), dalton oan Be aT ac
— por lo pp? pd ph pS
1 | sa il
+ eae + re, + &c., to mod. p.
When q is not a prime, a similar theorem may be obtained by
the very same method, but its expression will be less simple.
The above theorems would, I think, be very noticeable were it
only for the circumstance of their involving (as a condition) the
primeness as well of the base as of the augmented index of the
familiar Fermatian expression g#~1,—a condition which here
makes its appearance (as I believe) for the first time in the
theory of numbers.
ptise:. 4
XXI. On a new Method of arranging Numerical Tables. By
W. Dirrmar, Assistant in the Laboratory of Owens College,
Manchester*.
[ With a Plate. |
HE use of numerical tables constructed in the ordinary
manner is, for obvious reasons, inseparably connected with
interpolation calculations. Such calculations, although by no
means difficult, involve, as every practical mathematician knows,
much loss of time, and often give rise to mistakes. This is
especially the case when, from a given value of a dependent vari-
able, the corresponding value of the independent, or of another
dependent variable has to be found. It is obvious that all inter-
polations could be avoided by giving all the values which can
possibly be required; this, however, is in most cases practically
impossible, as the tables w ould thus become inconyeniently volu-
minous, and the chance of typographical error would be greatly
increased. I believe that the completeness thus attainable can
be arrived at by the use of the following graphical method,
- while at the same time the size of the table will not extend
beyond the ordinary limits. Let it be required to construct
a table giving the values of several functions y, z,w...of a
variable x. Draw a system of vertical parallels, and call them
respectively the zw, y, z,w... line. On each of the verticals
construct a scale, and let every point on each of the scales be the
symbol for a number equal either to the number of divisions (and
in general cne fraction of a division) contained between the
origin and that point, or to a simple multiple of this number ;
so that the marks on each scale represent the terms of an arith-
metical series. These several scales must be so constructed that
the corresponding values of all the variables are found in one
and the same horizcutal line. It is true that, strictly speaking,
this can only be the case when all the functions are linear ones ; it
is, however, easy to show that, practically speaking, the problem
can always be solved with any degree of exactitude required,
provided that the functions are continuous. The mode of con-
struction and use of such tables will perhaps be best explained
by an example.
Tig. 1, Plate III. represents the commencement of a Table of
logarithms and. reciprocals, which is intended to afford about the
same degree of exactitude as a common 4-place logarithmic table.
Calumn UH. contains. the logarithm-scale; each of the divisions
is 4 millims. in length, and represents a logarit thmic increment
of 0-001; each point in this scale has a twofold meaning ; it
stands, namely, both for the mantissa v=), and for the (posi-
* Communicated by the Author.
138 On anew Method of arranging Numerical Tables.
tive) mantissa of : which equals 1—d. When this scale had
been drawn, the integral numbers from 100 to 1000 were marked
on the other two columns by drawing horizontal lines opposite
to the corresponding logarithms; the numbers up to num.
(mant. =*5000) were placed in column I. beyond this number
in column III, Lastly, the interval between every two such
marks was divided into ten equal parts. Since, now, within the
intervals « = 100 to e= 101, e=101 to x=102, &c. the
A (log x)
Aw
quotients may in our case safely be taken as a con-
stant, any Alog@ within such an interval may, together with its
Az, be graphically represented by one and the same straight
line, as is in fact done in the Table. It is now clear that any
horizontal line will cut the verticals. in points which (whether
they coincide with marks or not) are symbols for respectively a
certain number z, log #, and a number having the same succes-
sion of figures as = The above will afford complete informa-
tion for the AOA use of the Table*. The division of the
spaces between the marks on the scales 1s to be made by the eye.
With some practice an error greater than one-tenth of an interval
in the logarithm-scale will rarely be made; the position of the
marks themselves may be by far more accurately determinedt ;
the error accompanying any logarithm taken out of the Table
will therefore scarcely ever exceed 0: 0001, and. any number
found by its help will be correct within about S000 Of its value.
The reliability of the results is not so dependent upon the exacti-
tude of the drawing as one might at first sight be disposed to
think, as only that 4 portion of every number is really graphically
determined which in an ordinary 4-place table is found by compu-
tative interpolation. ‘The Table is particularly handy for finding
the values of reciprocals, as these may be obtained directly with-
* Let us suppose the logarithm and the reciprocal of 1°0653 were to be
found. Divide the interval between the marks 106°5 and 106°6 on the
a-scale (in your mind) into ten equal parts, and through the third point
from 106°5 draw a horizontal line, which is best done by bringing a straight
line etched on one side of a piece of plate-glass into the right position. This
line will cut the log-scale in the point ‘0274 = mant. 10653, and the
] 1 1
77scale in the point 938°7=1000 x T9G53- At the same time log 7-pgRy
may be read off directly, the point of intersection in the log-scale standing
also for mant. 10653 = 9/26.
+ When great exactitude is required, the figure may be drawn on a cop-
per plate by help of a dividing engine, and copies printed from the copper.
‘
,
’
«
‘
"
es he
Mr. W. Dittmar on Graphical Interpolation. 139
out the intervention of logarithms. It will therefore be especi-
ally useful in chemical calculations, as, for instance, in converting
specific grayities into specific volumes, for reducing per-centage
compositions to the unit of weight of one constituent, &c. The
general applicability of this method is evident. For the sake of
illustration I append figs. 2 and 8, giving respectively the be-
ginning of a general interpolation- and of a densimetric Table.
The mode of construction and use of these Tables will be under-
stood from the description given of the Table of logarithms.
XXII. On Graphical Interpolation. By W. Dittmar, Assistant
in the Laboratory of Owens College, Manchester*.
et principles laid down in the preceding article for the
construction of numerical tables may also be employed for
the purpose of carrying out graphical interpolations. Let us
suppose that the corresponding values x¥o, 2)Y1 %eYo-++ be-
longing to an unknown function y=/(z) are given by obser-
vation, and that it is required to complete the series of vari-
ables. It is clear that the direct results of observation may be
registered in a graphical table in the manner described above.
For this purpose itis only necessary to draw a straight line, and
to construct on one side of it a scale with a constant unit of
length, the points of which are considered as representatives of
the values of y, while on the other side of the line marks made
opposite to the points 7, ¥;, Ya,--. are taken as symbols of the
respective values of 2, 1. €. %, 2, Zq,...&c. The question now
is, how can the gaps on the w-scale be filled up by graphic inter-
polation? This may be accomplished in the following way :—
When there are reasons for supposing that f(z) does not differ
much from a linear function, all the divisions on the x-scale may
be made equal to one another, and each so long that the points
corresponding to 2%, #,, &c. coincide as nearly as possible with
those signifying respectively 7, y,, &c. on the y-scale. This is
best done by dividing the distance between the two furthest
points on the z-scale into the requisite number of equal parts,
drawing lines from the points thus obtained to one point situated
at some distance, and by moving the y-scale along in this system
of lines parallel to the line dividedy, till a position is found in
which the points of intersection of the radu with the y-scale
yield an w-scale which agrees as closely as possible with the
observed values.
* Communicated by the Author.
7 A sharp-edged drawing measure is most conveniently employed for
this purpose.
140 Mr. W. Dittmar on Graphical Interpolation.
If a satisfactory result cannot be obtained im this way, it is
best to try whether /(z) can be practically represented by an
expression of the form A+ Bz+Ca?, where A, B, and C signify
constants. If this be the case, we have*
Y=AS BOTs ee ies ss. 8 oc
y— Ay=A-+ B(@—Az) + C(e#—Az)?.
Ay=BAz-—C(Az)?+(2CAz)z.. . . . » (IL)
Ax Yen —BAx—C(Aa)?+ (2CAz) G + = (IIL)
2,—X, 2
Comparing equation (III.) with (II.), we see that In In Nz
Lx,
is equal to this Ay, the graphical representative of which is con-
tained between the two points in the 2-scale corresponding to
x +x, + Az Bidets tenn At _ A,
—— ease :
the numbers
From the equations (II.) and (III.) the following method for
constructing the z-scale may be found :—Combine the observed
pairs of variables by twos, and find from every combination, with
the help of equation (III.), a certain Ay, the graphical represen-
tative of which is contained between the two points which in the
z-scale mean z—~Az and x ‘Then construct a rectangular
system of coordinates, and represent the values of x thus obtained
(with an arbitrary unit of length) as abscissc, the corresponding
values of Ay as*ordinates, using for the latter that length as unit
which represents Ay=1 in the y-scale. Next draw a straight
line which passes as nearly as possible through the extreme
points of the ordinates. The ordinates of this line correspond-
ing respectively to Aw, 2Az, 3Az,..., when put together in the
right order, give the required z-scale. In order to obtain exact
results, it is advisable to choose first such a large value for Ax
that only a few points of the w-scale are obtained, and to deter-
mine the intermediate pomts by new constructions. As soon as
so many points are determined that two successive intervals do not
differ perceptibly in length, the subdivisions of each interval may
be made equal to one another. Should the indications of a scale
thus obtained not agree quite satisfactorily with the observed
data, it may often be improved by slightly changing the unit of
length used in the construction, and by altering its position with
respect to the y-scale. A convenient method for doing this has
been already described.
* g and y mean any values of the variables belonging together; xp, yp,
and @n, Yn mean particular pairs of variables; Av stands for the constant
numerical difference corresponding to one division in the a-scale; Ay for
the corresponding variable increment of y.
Royal Society. 141
If an interpolation of the second degree proves to be insufli-
cient for representing the observations, the series of values given
is divided into several intervals, and each of these is then treated
in the manner described.
In some cases it will be advisable to represent, not y, but some
function of y like y”, logy, &c., on a scale with equal divisions.
The advantages which the method of graphical interpolation
described appears to me to possess, as compared with the usual
one of drawing a curve in a rectangular system of coordinates,
are the following :—
1. All the lines drawn are straight lines; the personal error in
the drawing is therefore reduced to a minimum.
2. The drawing can be executed with less trouble and greater
exactitude, and it takes up less space than in the ordinary way.
3. When the drawing is finished, the value of y belonging to
any given z may be read off at once, and vice versd.
XXIII. Proceedings of Learned Societies.
ROYAL SOCIETY,
{Continued from p. 79.]|
March 22, 1860.—Sir Benjamin C. Brodie, Bart., Pres., in the Chair.
HE following communications were read :—
** Qn the Theory of Compound Colours, and the Relations of
the Colours of the Spectrum.” By J. Clerk Maxwell, Esq.,
Professor of Natural Philosophy, Marischal College and University,
Aberdeen.
Newton (in his ‘ Optics,’ Book I. part ui." prop. 6) has indicated a
method of exhibiting the relations of colour, and of calculating the
effects of any mixture of colours. He conceives the colours of the
_ Spectrum arranged in the circumference of a circle, and the circle so
painted that every radius exhibits a gradation of colour, from some
pure colour ef the spectrum at the circumference, to neutral tint at
the centre. The resultant of any mixture of colours is then found
by placing at the points corresponding to these colours, weights
proportional to their intensities; then the resultant colour will be
found at the centre of gravity, and its intensity will be the sum of
the intensities of the components.
From the mathematical development of the theory of Newton’s
diagram, it appears that if the positions of any three colours be
assumed on the diagram, and certain intensities of these adopted as
units, then the position of every other colour may be laid down from
its observed relation to these three. Hence Newton’s assumption
that the colours of the spectrum are disposed in a certain manner in
the circumference of a circle, unless confirmed by experiment, must
be regarded as merely a rough conjecture, intended as an illustration
of his method, but not asserted as mathematically exact. From the
142 Royal Society :—
results of the present investigation, it appears that the colours of the
spectrum, as laid down according to Newton’s method from actual
observation, lie, not in the circumference of a circle, but in the
periphery of a triangle, showing that all the colours of the spectrum
may be chromatically represented by three, which form the angles of
this triangle.
Wave-length in millionths of Paris inch.
DeHPlebe Hak Sere 2328, about one-third from line C to D,
Green........ 1914, about one-quarter from E to F,
Blue ........ 1717, about half-way from F to G.
The theory of three primary colours has been often proposed as
an interpretation of the phenomena of compound colours, but the
relation of these colours to the colours of the spectrum dees not
seem to have been distinctly understood till Dr. Young (Lectures on
Natural Philosophy, Kelland’s edition, p. 345) enunciated his theory
of three primary sensations of colour which are excited in different
proportions when different kinds of light enter the organ of vision.
According to this theory, the threefold character of colour, as perceived
by us, is due, not to a threefold composition of light, but to the
constitution of the visual apparatus which renders it capable of being
affected. in three different ways, the relative amount of each sensation
being determined by the nature of the incident light. If we could
exhibit three colours corresponding to the three primary sensations,
each colour exciting one and one only of these sensations, then since
all other colours whatever must excite more than one primary sensa-
tion, they must find their places in Newton’s diagram within the
triangle of which the three primary colours are the angles.
Hence if Young’s theory is true, the complete diagram of all colour,
as perceived by the human eye, will have the form of a triangle.
The colours corresponding to the pure rays of the spectrum must
all lie within this triangle, and all colours in nature, being mixtures
of these, must lie within the line formed by the spectrum. If
therefore any colours of the spectrum correspond to the three pure
primary sensations, they will be found at the angles of the triangle,
and all the other colours will lie within the triangle.
The other colours of the spectrum, though excited by uncom-
pounded light, are compound colours; because the light, though
simple, has the power of exciting two or more colour-sensations in
different proportions, as, for imstance, a blue-green ray, though not
compounded of blue rays and green rays, produces a sensation com-
pounded of those of blue and green.
The three colours found by experiment to form the three angles
of the triangle formed by the spectrum on Newton’s diagram, may
correspond to the three primary sensations.
A different geometrical representation of the relations of colour
may be thus described. ‘Take any point not in the plane of Newton’s
diagram, draw a line from this point as origin through the point
representing a given colour on the plane, and produce them so that
the length of the line may be to the part ent off by the plane as the
intensity of the given colour is to that of the corresponding point on
Prof. Maxwell on the Theory of Compound Colours. 148
Newton’s diagram. In this way any colour may be represented by
a line drawn from the origin whose direction indicates the quality of
the colour, and whose length depends upon its intensity. The
resultant of two colours is represented by the diagonal of the paral-
lelogram formed on the lines representing the colours (see Prof.
Grassmann in Phil. Mag. April 1854).
Taking three lines drawn from the origin through the points of
the diagram corresponding to the three primaries as the axes of
coordinates, we may express any colour as the resultant of definite
quantities of each of the three primaries, and the three elements of
colour will then be represented by the three dimensions of space.
The experiments, the results of which are now before the Society,
were undertaken in order to ascertain the exact relations of the
colours of the spectrum as seen by a normal eye, and to lay down
these relations on Newton’s diagram. The method consisted in
selecting three colours from the spectrum, and mixing these in such
proportions as to be identical in colour and brightness with a constant
white light, Having assumed three standard colours, and found the
quantity of each required to produce the given white, we then find
the quantities of two of these combined with a fourth colour which
will produce the same white. We thus obtain a relation between the
three standards and the fourth colour, which enables us to lay down
its position in Newton’s diagram with reference to the three standards.
Any three sufficiently different colours may be chosen as standards,
and any three points may be assumed as their positions on the
diagram. The resulting diagram of relations of colour will differ
according to the way in which we begin; but as every colour-diagram
is a perspective projection of any other, it is easy to compare diagrams
obtained by two different methods.
The instrument employed in these experiments consisted of a dark
’ ehamber about 5 feet long, 9 inches broad, and 4 deep, joined to
another 2 feet long at an angle of about 100°. If light is admitted
at a narrow slit at the end of the shorter chamber, it falls on a lens
and is refracted through two prisms in succession, so as to form a
pure spectrum at the end of the long chamber. Here there is
placed an apparatus consisting of three moveable slits, which ean be
altered in breadth and position, the position beimg read off on a
graduated scale, and the breadth ascertained by inserting a fine
graduated wedge into the slit till it touches both sides.
When white light is admitted at the shorter end, light of three
different kinds is refracted to these three slits. When white light is
admitted at the three slits, light of these three kinds in combination
is seen by an eye placed at the slit in the shorter arm of the instru-
ment. By altering the three slits, the colour of this compound light
may be changed at pleasure.
The white light employed was that of a sheet of white paper, placed
on a board, and illuminated by the sun’s light in the open air; the
instrument being in a room, and the light moderated where the
observer sits.
Another portion of the same white light goes down a separate
144 Royal Society :—
compartment of the instrument, and is reflected at a surface of
blackened glass, so as to be seen by the observer in immediate contact
with the compound light which enters the slits and is refracted by
the prisms.
Each experiment consists in altering the breadth of the slits till
the two lights seen by the observer agree both in colour and brightness,
the eye being allowed time to rest before making any final decision.
In this way the relative places of sixteen kinds of light were found by
two observers. Both agree in finding the positions of the colours to
lie very close to two sides of a triangle, the extreme colours of the
spectrum forming doubtful fragments of the third side. They differ,
however, in the intensity with which certain colours affect them,
especially the greenish blue near the line F, which to one observer is
remarkably feeble, both when seen singly, and when part of a mixture;
while to the other, though less intense than the colours in the
neighbourhood, it is still sufficiently powerful to act its part in com-
binations. One result of this is, that a combination of this colour
with red may be made, which appears red to the first observer and
green to the second, though both have normal eyes as far as ordinary
colours are concerned; and this blindness of the first has reference
only to rays of a definite refrangibility, other rays near them, though
similar in colour, not being deficient in intensity. Foran account of
this peculiarity of the author’s eye, see the Report of the British
Association for 1856, p. 12.
By the operator attending to the proper illumination of the paper
by the sun, and the observer taking care of his eyes, and completing
an observation only when they are fresh, very good results can be
obtained. The compound colour is then seen in contact with the
white reflected light, and is not distinguishable from it, either in hue
or brilliancy ; and the average difference of the observed breadth of a
slit from the mean of the observations does not exceed =), of the
breadth of the slit if the observer is careful. It is found, however,
that the errors in the value of the sum of the three slits are greater
than they would have been by theory, if the errors of each were
independent ; and if the sums and differences of the breadth of two
slits be taken, the errors of the sums are always found greater than
those of the differences. This indicates that the human eye has a
more accurate perception of differences of hue than of differences of
illumination.
Having ascertained the chromatic relations between sixteen colours
selected from the spectrum, the next step is to ascertain the positions
of these colours with reference to Fraunhofer’s lines. This is done
by admitting light into the shorter arm of the instrument through
the slit which forms the eyehole in the former experiments. A pure
spectrum is then seen at the other end, and the position of the fixed
lines read off on the graduated scale. In order to determine the wave-
lengths of each kind of light, the incident light was first reflected
from a stratum of air too thick to exhibit the colours of Newton’s
rings. The spectrum then exhibited a series of dark bands, at
intervals increasing from the red to the violet. The wave-lengths
Prof. Maxwell on the Theory of Compound Colours. 145
corresponding to these form a series of submultiples of the retarda-
tion ; and by counting the bands between two of the fixed lines, whose
wave-lengths have been determined by Fraunhofer, the wave-lengths
corresponding to all the bands may be calculated ; and as there are
a great number of bands, the wave-lengths become known at a great
many different points.
In this way the wave-lengths of the colours compared may be
ascertained, and the results obtained by one observer rendered
comparable with those obtained by another, with different apparatus.
A portable apparatus, similar to one exhibited to the British
Association in 1856, is now being constructed in order to obtain
observations made by eyes of different qualities, especially those
whose vision is dichromic.
PosTscRIPT.
Account of Experiments on the Spectrum as seen by the Colour-blind.
The instrument used in these observations was similar to that
already described. By reflecting the light back through the prisms
by means of a concave mirror, the instrument is rendered much
shorter and more portable, while the definition of the spectrum is
rather improved. The experiments were made by two colour-blind
observers, one of whom, however, did not obtain sunlight at the
time of observation. The other obtained results, both with cloud-
light and sun-light, in the way already described. It appears from
these observations—
I. That any two colours of the spectrum, on opposite sides of the
line “ F,” may be combined in such proportions as to form white.
II. That all the colours on the more refrangible side of F appear
to the colour-blind “ blue,”’ and all those on the less refrangible side
appear to them of another colour, which they generally speak of as
*‘yellow,”’ though the green at E appears to them as good a repre-
sentative of that colour as any other part of the spectrum.
Ii. That the parts of the spectrum from A to E differ only in
intensity, and notin colour; the light being too faint for good experi-
ments between A and D, but not distinguishable in colour from E
reduced to the same intensity. The maximum is about 2 from D
towards EK.
IV. Between E and F the colour appears to vary from the pure
“yellow”? of E to a “neutral tint”? near F, which cannot be distin-
guished from white when looked at steadily.
V. At F the blue and the “yellow” element of colour are in equi-
librium, and at this part of the spectrum the same blindness of the
central spot of the eye is found in the colour-blind that has been
already observed in the normal eye, so that the brightness of the
spectrum appears decidedly less at F than on either side of that line ;
and when a large portion of the retina is illuminated with the light
of this part of the spectrum, the limbus luteus appears as a dark
Spot, moving with the movements of the eye. The observer has not
yet been able to distinguish Haidinger’s “‘ brushes’ while observing
polarized light of this colour, in which they are very conspicuous to
the author.
Phil. Mag. 8. 4. Vol. 21. No. 183. Feb. 1862. =
PAB re 0 bury BRagal Baeidly Been TT Rot
- VI. Between F anda point 4 from F towards G, the colour appears
to vary from the neutral tint to pure blue, while the brightness in-
creases, and reaches a maximum at 2 from F towards G, and then
diminishes towards the more refrangible end of the spectrum, the
urity of the colour being apparently the same throughout.
VII. The theory of colour-blind vision being “‘ dichromie,”’ is con-
firmed by these experiments, the results of which agree with those
obtained already by normal or “ ¢richromic’’ eyes, if we suppose the
‘red’ element of colour eliminated, and the “green” and ‘ blue”
elements left as they were, so that the “red-making rays,” though
dimly visible to the dichromic eye, excite the sensation not of red
but of green, or as they call it, ‘‘ yellow.”
VIII. The extreme red ray of the spectrum appears to be a suf-
ficiently good representative of the defective element in the colour-
blind. When the ordinary eye receives this ray, it experiences the
sensation of which the dichromic eye is incapable; and when the di-
chromic eye receives it, the luminous effect is probably of the same
kind as that observed by Helmholtz in the ultra-violet part of the
spectrum—a sensibility to light, without much appreciation of colour.
A set of observations of coloured papers by the same dichromic
observer was then compared with a set of observations of the same
papers by the author, and it was found—
1. That the colour-blind observations were consistent among them-
selves, on the hypothesis of two elements of colour.
2. That the colour-blind observations were consistent with the
author’s observations, on the hypothesis that the two elements of
colour in dichromic vision are identical with two of the three elements
of colour in normal vision. |
3. That the element of colour, by which the two types of vision
differ, isa red, whose relations to vermilion, ultramarine, and emerald-
green are expressed by the equation
D=1-198V +0:078U—0:276G,
where D is the defective element, and V, U and G the three colours
named above.
April 26.—Sir Benjamin C. Brodie, Bart., President, in the Chair.
The followmg communication was read :—
** Note on Regelation.”” By Michael Faraday, D.C.L., F.R.S. &e.
_ The philosophy of the phenomenon now understood by the word
Regelation is exceedingly interesting, not only because of its relation
to glacial action under natural circumstances, as shown by Tyndall
and others, but also, and as I think especially, in its bearmgs upon
molecular action ; and this is shown, not merely by the desire of dif-
ferent philosophers to assign the true physical principle of action,
but also by the great differences between the views which they have
taken.
Two pieces of thawing ice, if put together, adhere and become
one ; at a place where liquefaction was proceeding, congelation sud-
denly occurs. ‘The effect will ke place in air, or in water, or in
vacuo. It will occur at everypoint where the two pieces of ice
Pxof. Faraday on Regelation. 147
touch ; but rot with ice below the freezing-point, 7. e. with dry ice,
or ice so cold as to be everywhere in the solid state.
Three different views are taken of the nature of this phenomenon.
When first observed in 1850, I explained it by supposing that a
particle of water, which could retain the liquid state whilst touching
ice only on one side, could not retain the liquid state if it were
touched by ice on both sides; but became solid, the general tem-
perature remaining the same*. Professor J. Thomson, who dis-
covered that pressure lowered the freezing-point of water‘, attributed
the regelation to the fact that two pieces of ice could not be made
to bear on each other without pressure ; and that the pressure, how-
ever slight, would cause fusion at the place where the particles
touched, accompanied by relief of the pressure and resolidification of
the water at the place of contact, in the manner that he has fully
explained in a recent communication to the Royal Society{. Profes-
sor Forbes assents to neither of these views ; but admitting Person’s
idea of the gradual liquefaction of ice, and assuming that ice is
essentially colder than ice-cold water, 7. e. the water in contact with
it, he concludes that two wet pieces of ice will have the water be-
tween them frozen at the place where they come into contact$.
Though some might think that Professor Thomson, in his last
communication, was trusting to changes of pressure and tempera-
ture so inappreciably small as to be not merely imperceptible, but
also ineffectual, still he carried his conditions with him into all the
eases he referred to, even though some of his assumed pressures
were due to capillary attraction, or to the consequent pressure of the
atmosphere, only. It seemed to me that experiment might be so
applied as to advance the investigation of this beautiful pomt in
molecular philosophy to a further degree than has yet been done;
even to the extent of exhausting the power of some of the principles
assumed in one or more of the three views adopted, and so render
our knowledge a little more defined and exact than it is at present.
In order to exclude all pressure of the particles of ice on each
other due to capillary attraction or the atmosphere, I prepared to
experiment altogether under water ; and for this purpose arranged a
bath of that fluid at 32°F. A pail, surrounded by dry flannel,
was placed in a box; a glass jar, 10 inches deep and 7 inches wide,
was placed on a low ‘tripod in the pail; broken ice was packed be-
tween the jar and the pail; the jar was filled with ice-cold water to
within an inch of the top ; a glass dish filled with ice was employed
as a cover to it, and the whole enveloped with dry flannel. In this
way the central jar, with its contents, could be retained at the un-
changing temperature of 32° F. for a week or more; for a small piece
of ice floating in it for that time was not entirely melted away. All
that was required to keep the arrangement at the fixed temperature,
was to renew the packing ice in the pail from time to time, and also
* Researches in Chemistry and Physics, 8vo. pp. 373, 378.
+ Mousson says that a pressure of 13,000 atmospheres lowers the temperature
of freezing from 0° to —18° Cent.
~ Phil. Mag. vol. xix. p. 391.
-§ -Proceedings of the Royal Society of Edinburgh, April 19, 1858. —
L 2
148 Royal Society :—
that in the basin cover. A very slow thawing process was going on
in the jar the whole time, as was evident by the state of the indi-
cating piece of ice there present.
Pieces of good Wenham-lake ice were prepared, some being blocks
three inches square, and nearly an inch thick, others square prisms
four or five inches long: the blocks had each a hole made through
them with a hot wire near one corner ; woollen thread passed through
these holes formed loops, which being attached to pieces of lead,
enabled me to sink the ice entirely under the surface of the ice-cold
water. Each piece was thus moored to a particular place, and, be-
cause of its buoyancy, assumed a position of stability. The threads
were about 13 inch long, so that a piece of ice, when depressed
sideways and then left to itself, rose in the water as far as it could,
and into its stable position, with considerable force. When, also, a
piece was turned round on its loop as a vertical axis, the torsion
force tended to make it return in the reverse direction.
Two similar blocks of ice were placed in the water with their
opposed faces about two inches apart; they could be moved into
any desired position by the use of slender rods of wood, without
any change of temperature in the water. If brought near to each
other and then left unrestrained, they separated, returning to their
first position with considerable force. If brought into the slightest
contact, regelation ensued, the blocks adhered, and remained ad-
herent notwithstanding the force tending to pull them apart. They
would continue thus, even for twenty-four hours or more, until they
were purposely separated, and would appear (by many trials) to
have the adhesion increased at the points where they first touched,
though at other parts of the contiguous surfaces a feeble thawing
and dissecting action went on. In this case, except for the first
moment and in a very minute degree, there was no pressure either
from capillary action or any other cause. On the contrary, a
tensile force of considerable amount was tending all the time to
separate the pieces of ice at their points of adhesion ; where still, I
believe, the adhesion went on increasing—a belief that will be fully
confirmed hereafter.
Being desirous of knowing whether anything like soft adhesion
occurred, such as would allow slow change of position without sepa-
ration during the action of the tensile force, I made the following
arrangements. The blocks of ice being moored by the threads
fastened to the lowest corners, stood’ in the water with one of the
diagonals of the large surfaces vertical; before the faces were
brought into contact, each block was rotated 45° about a horizontal
axis, In opposite directions, so that when put together, they made a
eompound block, with horizontal upper edges, each half of which
tended to be twisted upon, and torn from the other. Yet by placing
indicators in holes previously made in the edges of the ice, I could
not find that there was the slightest motion of the blocks in rela-
tion to each other in the thirty-six hours during which the experi-
ment was continued. This result, as far as it goes, is against the
necessity of pressure to regelation, or the existence of any condition
like that of softness or a shifting contact; and yet I shall be able to
, ee ee ee SS lS Se
© od i te ee
Prof. Faraday on Regelation. 149
show that there is either soft adhesion or an equivalent for it, and
from that state draw still further cause against the necessity of pres-
sure to regelation.
Torsion force was then employed as an antagonist to regelation.
The ice-blocks, being separate, were adjusted in the water so as to be
parallel to each other, and about 1} inch apart. If made to ap-
proach each other on one side, by revolution in opposite directions
on vertical axes, a piece of paper being between to prevent ice con-
tact, the torsion force set up caused them to separate when left to
themselves; but if the paper were away and the ice pieces were
brought into contact, by however slight a force, they became one,
forming a rigid piece of ice, though the strength was, of course, very
small, the point of adhesion and solidification being simply the con-
tact of two convex surfaces of small radius. By giving a little
motion to the pail, or by moving either piece of ice gently in the
water with a slip of wood, it was easy to see that the two pieces were
rigidly attached to each other; and it was also found that, allowing
time, there was no more tendency to a changing shape here than in
the case quoted above. If now the slip of wood were introduced
between the adhering pieces of ice, and applied so as to aid the
torsion force of one of the loops, 7. e. to increase the separating force,
but unequally as respects the two pieces, then the congelation at the
point of contact would give way, and the pieces of ice would move
in relation to each other. Yct they would not separate; the piece
unrestrained by the stick would not move off by the torsion of its
own thread, though, if the stick were withdrawn, it would move
back into its first attached position, pulling the second piece with it ;
and the two would resume their first associated form, though all the
while the torsion of both loops was tending to make the pieces
separate.
If when the wood was applied to change the mutual position of
the two pieces of ice, without separating them, it were retained for a
second undisturbed, then the two pieces of ice became fixed rigidly
to each other im their new position, and maintained it when the
wood was removed, but under a state of restraint; and when suffi-
cient force was applied, by a slight tap of the wood on the ice to
break up the rigidity, the two pieces of ice would rearrange them-
selves under the tersion force of their respective threads, yet remain
united ; and, assuming a new position, would, in a second or less,
again become rigid, and remain inflexibly conjoined as before.
By managing the continuous motion of one piece of ice, it could
be kept associated with the other by a flexible point of attachment
for any length of time, could be placed in various angular positions
to it, could be made (by retaining it quiescent for a moment) to
assume and hold permanently any of these positions when the ex-
ternal force was removed, could be changed from that position ito
a new one, and, within certain limits, could be made to possess at
pleasure, and for any length of time, either a flexible or a rigid attach-
ment to its associated block of ice.
So regelation includes a flexible adhesion of the particles of ice,
and also a rigid adhesion. The transition between these two states
150 Royal Society :—-
takes place when there is no external force like pressure tending to
bring the particles of ice together, but, on the contrary, a force of
torsion is tending to separate them ; and, if respect be had to the
mere point of contact on the two rounded surfaces where the flexible
adhesion is exercised, the force which tends to separate them may
be esteemed very great. The act of regelation cannot be considered
as complete until the junction has become rigid; and therefore I
think that the necessity of pressure for it is altogether excluded.
No external pressure can remain (under the circumstances) after the
first rigid contact is broken. All the forces which remain tend to
separate the pieces of ice; yet the first flexible adhesions and all the
successive rigid adhesions which are made to occur, are as much effects
of regelation as those which occur under the greatest pressure.
’ The phenomenon of flexible adhesion under tension looks ver
much like sticking and tenacity ; and I think it probable that Pro-
fessor Forbes will see in it evidence of the truth of his view. I
cannot, however, consider the fact as bearing such an interpretation ;
because I think it impossible to keep a mixture of snow and water
for hours and days together without the temperature of the mixed
mass becoming uniform; which uniformity would be fatal to the
explanation. My idea of the flexible and rigid adhesion is this :—
Two convex surfaces of ice come together; the particles of water
nearest to the place of contact, and therefore within the efficient sphere
of action of those particles of ice which are on both sides of them,
solidify ; if the condition of things be left for a moment, that the
heat evolved by the solidification may be conducted away and dis-
persed, more particles will solidify, and ultimately enough to form
a fixed and rigid junction, which will remain until a force sufficiently
great to break through it is applied. But if the direction of the
force resorted to can be relieved by any hinge-like motion at the
point of contact, then I think that the union is broken up among the
particles on the opening side of the angle, whilst the particles on the.
closing side come within the effectual regelation distance ; regelation
ensues there and the adhesion is maintained, though in an apparently
flexible state. The flexibility appears to me to be due to a series of
ruptures on one side of the centre of contact, and of adhesion on the
other,—the regelation, which is dependent on the vicinity of the ice
surfaces, being transferred as the place of efficient vicinity is changed.
That the substance we are considering is as brittle as ice, does not
make any difficulty to me in respect of the flexible adhesion ; for if
we suppose that the point of contact exists only at one particle, still
the angular motion at that point must bring a second particle into
contact (to suffer regelation) before separation could occur at the
first ; or if, as seems proved by the supervention of the rigid adhesion
upon the flexible state, many particles are concerned at once, it is not
possible that all these should be broken through by a force applied
on one side of the place of adhesion, before particles on the opposite
side should have the opportunity of regelation, and so of continuing
the adhesion. |
It is not necessary for the observation of these phenomena that a
earefully-arranged water-vessel should be employed. The difference
Prof. Faraday on Regelation. 151
between the flexible and rigid adhesion may be examined very well in
air, _ For this purpose, two of the bars of ice before spoken of, may
be hung up horizontally by threads, which may be adjusted to give
by torsion any separating force desired ; and when the ends of these
bars are brought together, the adhesion of the ice, and the ability of
placing these bars at any angle, and causing them to preserve
that angle by the rigid adhesion due to regelation, will be rendered
evident ; and though the flexible adhesion of the ice cannot in this
way be examined alone, because of the capillary attraction due to the
film of water on the ice, yet that is easily obviated by plunging the
pieces into a dish of water at common temperatures, so that they are
entirely under the surface, and repeating the observations there. All
the important points regarding the flexible and rigid junction of ice
due to regelation, can in this way be readily investigated.
It will be understood that, in observing the flexible and rigid state
of union, convex surfaces of contact are necessary, so that the contact
may be only at one point. If there be several places of contact,
apparent rigidity is given to the united mass, though each of the
places of contact might be in a flexible and, so to say, adhesive con-
dition. It is not at all difficult to arrange a convex surface so that,
bearing at two places only on the sides of a depression, it should
form a flexible joint in one direction, and a rigid attachment in a
direction transverse to the former.
it might seem at first sight as if the flexible adhesion of the ice
gave us a point to start from in the further investigation of the prin-
ciple of pressure. Ifthe application of pressure causes ice to freeze
together, the application of tension might be expected to produce the
contrary effect, and so cause liquidity and separation at the flexible
jomt. This, however, does not necessarily follow ; nor do I intend to
consider what might be supposed to take place whilst theoretically
contemplating that case. I think the changes of temperature and
pressure are too infinitesimal to go for anything; and in illustration
of this, will deseribe the following experiment. Wool is known to
adhere to ice in the manner, as I believe, of regelation. Some wool-
len thread was boiled in distilled water, so as thoroughly to wet it.
Some clean ice was broken up small and mixed with water, so as to
produce a soft mass, and, being put into a glass jar clothed in flan-,
nel that it might keep for some hours, had a linear depression made
in the surface, so as to form alittle ice-ditch filled with water ; in this
depression some filaments of the wetted wool were placed, which,
sinking to the bottom, rested on the ice only with the weight which
they would have being immersed in water; yet in the course of
two hours these filaments were frozen to the ice. In another case, a
small loose ball of the same boiled wool, about half an inch in
diameter, was put on to a clean piece of ice ; that into a glass basin;
and the whole wrapped up in flannel and left for twelve hours. At
the end of that time it was found that thawing had been going on,
and that the wool had melted a hole in the ice, by the heat conducted
through it to the ice from the air. The hole was filled with the
water and wool, but at the bottom some fibres of the wool were
frozen to the ice. :
152 Royal Society :—
Is this remarkable property peculiar to water, or is it general to
all bodies? In respect of water it certainly seems to offer us a glimpse
into the joint physical action of many particles, and into the nature
of cohesion in that body when it is changing between the solid and
liquid state. I made some experiments on this point. Bismuth was
melted and kept at a temperature at which both solid and liquid
metal could be present; then rods of bismuth were introduced, but
when they had acquired the temperature of the mixed mass, no adhe-
sion could be observed between them. By stirring the metal with
wood, it was easy to break up the solid part into small crystalline
granules ; but when these were pressed together by wood under the
surface, there was not the slightest tendency to cohere, as hail or
snow would cohere inwater. The same negative result was obtained
with the metals tin and lead. Melted nitre appeared at times to
show traces of the power; but, on the whole, I incline to think the
effects observed resulted from the circumstance that the solid rods
experimented with had not acquired throughout the fusing tempera-
ture. Nitre is a body which, like water, expands in solidifying; and
it may possess a certain degree of this peculiar power.
Glacial acetic acid is not merely without regelating force, but
actually presents a contrast to it. A bottle containing five or six
ounces, which had remained liquid for many months, was at such a
temperature that being stirred briskly with a glass rod crystals began
to form in it; these went on increasing in size and quantity for eight
or ten hours. Yet all that time there was not the slightest trace of
adhesion amongst them, even when they were pressed together ; and
as they came to the surface, the liquid portion tended to withdraw
from the faces of the crystals ; as if there were a disinclination of the
liquid and solid parts to adhere together.
Many salts were tried (without much or any expectation),—cerystals
of them being brought to bear against each other by torsion force,
in their saturated solutions at common temperatures. In this way
the following bodies were experimented with :—Nitrates of lead,
potassa, soda; sulphates of soda, magnesia, copper, zinc; alum; borax;
chloride of ammonium; ferro-prussiate of potassa; carbonate of soda;
acetate of lead; and tartrate of potassa and soda; but the results with
all were negative.
My present conclusion therefore is that the property is special for
water; and that the view I have taken of its physical cause does not
appear to be less likely now than at the beginning of this short
investigation, and therefore has not sunk in value among the three
explanations given.
Dr. Tyndall added to one of his papers*, a note of mine “On ice
of irregular fusibility ”’ indicating a cause for the difference observed
in this respect in different parts of the same piece of ice. The view
there taken was strongly confirmed by the effects which occurred in
the jar of water at constant temperature described in the beginning
of the preceding pages, where, though a thawing process was set up,
it was so slow as not to dissolve a cubic inch of ice in six or seven
days. The blocks retained entirely under water for several days,
* Philosophical Transactions, 1858, p. 228.
Prof. Faraday on Regelation. 153
became so dissected at the surfaces as to develope the mechanical
composition of the masses, and to show that they were composed of
parallel layers about the tenth of an inch thick, of greater and lesser
fusibility, which layers appear, from other modes of examination, to
have been horizontal in the ice whilst in the act of formation. They
had no relation to the position of the blocks in the water of my ex-
periments, or to the direction of gravity, but had a fixed position in
relation to each piece of ice.
ADDENDUM.
The following methed of examining the regelation phenomena above
described may be acceptable. Take a rather large dish of water at
common temperatures. Prepare some flat cakes or bars of ice, from
half an inch to aninch thick ; render the edges round, and the upper
surface of each piece convex, by holding it against the inside of a
warm saucepan cover, or in any other way. When two of these pieces
~ are put into the water they wiil float, having perfect freedom of motion,
and yet only the central part of the upper surface will be above the
fluid; when, therefore, the pieces touch at their edges, the width of
the water-surface above the place of contact may be two, three, er
four inches, and thus the effect of capillary action be entirely removed.
By placing a plate of clean dry wax or spermaceti upon the top of a
plate of ice, the latter may be entirely submerged, and the tendency
to approximation from capillary action converted into a force of
separation. When two cr more of such fioating pieces of ice are
brought together by contact at some point under the water, they
adhere ; first with an apparently flexible, and then with a rigid adhe-
sion. When five or six pieces are grouped in a contorted shape, as
an S, and one end piece be moved carefully, all will move withi
rigidly ; or, if the force be enough to break through the joint, the
rupture will be with a crackling noise, but the pieces will still adhere,
and in an instant become rigid again. As the adhesion is only by
points, the force applied should not be either too powerful or in the
manner of a blow. I find a piece of paper, a small feather, or a
camel-hair brush applied under the water very convenient for the
purpose. When the point of a floating wedge-shaped piece of ice ig
brought under water against the corner or side of another floating
piece, it sticks to it like a leech; if, after a moment, a paper edge be
brought down upon the place, a very sensible resistance to the rupture
at that place is felt. If the ice be replaced by like rounded pieces of
wood or glass, touching under water, nothing of this kind occurs, nor
any signs of an effect that could by possibility be referred to capillary
action ; and finally, if two floating pieces of ice have separating forces
attached to them, as by threads connecting them and two light pen-
dulums, pulled more or less in opposite directions, then it will be seen
with what power the ice is held together at the place of regelation,
when the contact there is either in the flexible or rigid condition, by
the velocity and force with which the two pieces will separate when
the adhesion is properly and entirely overcome.
154 _ Geological Society :—
GEOLOGICAL SOCIETY.
[Continued from vol. xx. p. 486.]
November 21, 1860.—L. Horner, Esq., President, in the Chair.
The following communication was read :—
“On the Geology of Bolivia and Southern Peru.” By D.
Forbes, Esq., F,R.S., F.G.S. With Notes on the Fossils by Prof.
Huxley, F.R.S., Sec.G.S. . and J. W. Salter, Esq., F.G.S.
After some observations on the previous researches by others, and
on the general features of the region, the author proceeded to de-
scribe the Post-tertiary formations of the maritime district. ‘These
beds, containing existing species of shells, occur at various heights
up to 40 feet above the sea-level. Guano deposits are frequent
along the coast, and deposits of salt also in raised beaches a little
above the sea. ‘The author could not verify Lieut. Freyer’s state-
ment of Balani and Millepore being attached high up the side of the
Morro de Arica, a perpendicular cliff at the water's edge ; indeed,
from the state of old Indian tumuli along the beach, and other cir-
cumstances, the author believes that no perceptible elevation has.
here taken place since the Spanish Conquest, although such an alter-
ation of level has occurred in Chile. The sand-dunes of the coast,
and their great mobility during the hot season, were noticed. From
Mexillones to Arica the coast is steep and rugged, formed of a chain
of mountains, 3000 feet high, consisting of rocks of the Upper Oolitic
age. At Arica the high land recedes, leaving a wide plain formed
of the débris of the neighbouring mountains; and in the middle of
this area was observed stratified volcanic tuff contemporaneous with
the formation of the gravel.
The saline formations were next treated of as three groups, ac-
cording to their height above the sea-level, and were shown to be
much more extensive than generally supposed, extending over the
rainless regions of this coast for more than 550 miles. They are
mostly developed, however, between latitudes 19° and 25° South.
These salines are supposed to have originated in the evaporation of
sea-water confined in them as lagoons by the longitudinal ranges of
hills separating them from the ocean. ‘The nitrate of soda had, in
the author’s opinion, resulted from the chemical reactions of sea-salt,
carbonate of lime, and decomposing vegetable matter (both terrestrial
and marine). The borate of lime, occurring with the nitrate, is
connected with the yolcanic conditions of the district, and was pro-
duced by fumaroles containing boracic acid. Where the highest
range of salines extend bey ond the rainless region, they are much
modified in the rainy season, and generally take the form of salt
plains encircling salt lakes or swamps.
The great Bolivian plateau, having an average elevation of 13,000
or 14,000 feet above the sea, consists of great gravel plains formed
by the spaces between the longitudinal ranges of mountains being
filled up by the débris of these mountains. The most western
of these consists of Oolitic débris with volcanic tuff and scorie;
it bears the salines above-mentioned, and is nearly destitute of
water. The central range of plains, formed from the disintegration,
Mr. D. Forbes on the Geology of Bolivia and Southern Peru. 155
of red sandstones and marls, with some volcanic scoriz, is well
watered. ‘The third range consists of plains made up of the débris
of Silurian and granitic rocks, and is auriferous. The thickness
of this accumulation of clays, gravel, shingle, and boulders is,
at places, immense. At La Paz it is more than 1600 feet. Con-
temporaneous trachytic tuff was found also in these deposits. In
freshwater ponds on this plateau, at a height of 14,000 feet (lat.
15° 8.), Mr. Forbes found abundance of Cyclas Chilensis, formerly
considered to be peculiar to the most southern and coldest part of
Chile at the level of the sea (lat. 45° to 50° S.).
_ The volcanic formations were next noticed. Volcanic action has
continued certainly from the pleistocene age to the present. The.
line of volcanic phenomena is nearly continuous N. and S$. Cones
are frequent, some of them 22,000 feet high and upwards; but
craters are rare. Volcanic matter, both in ancient times and at
present, has in a great part been erupted from lateral vents, often of
great longitudinal extent; recent trachytic lavas from such orifices
have covered in some cases more than 100 miles of country. Be-
sides trachyte, there are great tracts of trachydoleritic and felspathic
lavas. On the whole, in these South American lavas silex abounds,
and it las been the first element in the rock to crystallize; whereas
apparently in granite quartz is the last to crystallize and form the
state of so-called ‘‘ surfusion.” Diorites (including the so-called
«« Andesite”) occur in force along two parallel N. and S. lines of
eruption in this region, reaching through Chile, Bolivia, and Peru,
for more than 40 degrees of latitude. These diorites, and more espe-
cially the rocks which they traverse, are metalliferous; and the
author looks upon the greater part of the copper, silver, iron, and
other metallic veins of these countries as directly occasioned by the
appearance of this rock. |
Shales and argillaceous limestones, with clay-stones, porphyry-
tuffs, and porphyries, form the mass of the Upper Oolite formation
of Bolivia, equivalent to Darwin’s Cretaceo-Oolitic Series of Chile,
At Cobija these are traversed in all directions by metallic veins,
chiefly copper, and which, as before mentioned, appear to emanate
from the diorite. :
Red and variegated maris and sandstones, with gypsum and cu-
riferous and yellow sandstones and conglomerates, come next in
order; they have a thickness of 6000 feet, and are much folded and
dislocated. ‘These are considered by the author to resemble closely
the Permian rocks of Russia. Fossil wood is not uncommon in some
of these strata, which extend for at least 500 miles N. and 8.
Carboniferous strata occur chiefly as a small, contorted, basin-
shaped series of limestones, sandstones, and shales, with abundant
characteristic fossils. Cle
The quartzites which are generally supposed to represent the De-
vonian formation in Bolivia, but which the author is rather disposed
to group as Upper Silurian, are really not of very great thickness,
but are very much folded, and perhaps are about 5000 feet thick. ~
The Silurian rocks (perhaps 15,000 feet thick) are well developed
over an area of from 80,000 to 100,000 miles of mountain coun-
bd *
156 Geological Society.
try, including the highest mountains of South America, and giving
rise to the great rivers Amazon, &c. These slates, shales, grau-
wackes, and quartzites yield abundant fossils even up to the highest ©
point reached, 20,000 feet. ‘The problematical fossils known as
Cruziana or Bilobites occur not only in the lower beds, but (with
many other fossils) in the higher part of the series.
Lastly, the differences between the sections made by M. D’Or-
bigny, M. Pissis, and the author were pointed out, though for the
most part difficult of explanation. D’Orbigny makes the mountain
Illimani to be granite; it is slate according to the author. M.
Pissis describes as carboniferous the beds in which Mr. Forbes found
Silurian fossils,—and so on.
* On a New Species of Macrauchenia (M. Boliviensis).” By Prof.
By ot. Huxley. vor, wet, re. ce.
Some bones, fully impregnated with metallic copper, which had
been brought up from the mines of Corocoro in Bolivia were sub-
mitted to Prof. Huxley for examination. ‘The mines referred to are
situated on a great fault; and the bones were probably part of a
carcass that had fallen in from the surface,—the copper-bearing
water of the mines having mineralized them. A cervical and a
lumbar vertebra, an astragalus, a scapula, and a tibia show com-
plete correspondence in essential characters with those bones of the
great Afacrauchenia Patachonica described by Prof. Owen in the
Appendix to the ‘ Voyage of the Beagle ;’ but the relative size and
proportions of the vertebra, the tibia, and the astragalus indicate a
distinct species, much smaller and more slender ; and in some points
of structure this new form (M. Boliviensis) approaches more nearly
to the recent Auchenide than to the larger and fossil species. The
fragments of the cranium show some peculiarities of form, but, on
the whole, it has many resemblances to that of the Vicugna.
Prof. Huxley pointed out that this slender and small-headed Ma-
crauchenia may have been the highland-contemporary of the larger
M. Patachonica ; just as now-a-days the Vicugna prefers the moun-
tains, whilst its larger congener the Guanaco roams over the Pata-
gonian plains.
Lastly it was remarked that as Macrauchenia was an animal com-
bining, to a much more marked degree than any other known recent
or fossil mammal, the peculiarities of certain artiodactyles and perisso-
dactyles, and yet was certainly but of postpleistocene age, it presents
a striking exception to the commonly asserted doctrine that ‘ more
generalized”’ organisms were confined to the ancient periods of the
earth’s history. For similar reasons, the structure of the Macrau-
chenia is also inimical to the idea that an extinct animal can always
be reconstructed from a single tooth or a single bone.
** On the Paleozoic Fossils brought by Mr. D. Forbes from Bo-
livia.” By J. W. Salter, Esq., F.G.S.
The Fossils of Carboniferous age brought home by Mr. Forbes
are the well-known species described by D’Orbigny. Several are
identical with Kuropean forms (as Productus Martini, &c.), and are
cosmopolitan ; others are peculiar to the district (as Spirifer Condor,
Orthis Andii, &c.).
Intelligence and Miscellaneous Articles. 157
Mr. Forbes has brought a “Devonian” trilobite (Phacops latifrons
or Ph, Bufo), in a rolled pebble, from Oruro: it is a widely-spread
species. Another allied form was found by Mr. Pentland, many
years back, at Aygatchi. In other respects the “ Devonian” evidence
is scanty.
In Mr. Forbes’s fine collection of Silurian fossils none of D’Or-
bigny’s ten Silurian species occur ; nearly all are such as are met
with in Lower Devonian and in Upper Silurian rocks—Homalonotus,
Tentaculites, Orthis, Ctenodonta, Pileopsis (2), Strophomena, Bellero-
phon. South Africa and the Falkland Isles yield a similar fossil
fauna.
The Bilobites in this collection differ, some of them probably ge-
nerically, from D’Orbigny’s figured species. A little Beyrichia from
the upper part of the Silurian series in Bolivia appears to be like a
North American form figured by Emmons as Silurian.
XXIV. Intelligence and Miscellaneous Articles.
ON THE POLARIZATION OF LIGHT BY DIFFUSION. BY G. GOVI,
oe polarization of atmospheric light has long since proved that
gases, as well as solid and liquid bodies, have the property of
_ polarizing light; but I am not aware that any direct experiments
have been made to prove the presence of polarizing power in the
case of gases.
I was led to the consideration of this question by the polariscopic
study of the hght of comets; and the idea occurred to me to inves-
tigate how a pencil of light would be affected by being transmitted
through a certain thickness of a gaseous medium in which it was re-
flected or diffused.
The experiment was made in the following manner:—A thick
pencil of the sun’s rays, reflected from a heliostat, was allowed to
pass into a dark room, through a hole in the window-shutter. ‘This
light was principally reflected from metal, and showed very feeble
traces of polarization. A large quantity of smoke was then pro-
duced by burning incense ; and the pencil immediately expanded and
formed a large cylinder, which diffused white light in all directions.
This light, when investigated by a polariscope, was found to be po-
larized even when the cylinder was viewed at right angles to its
axis; but the intensity of the polarization was truly extraordinary
when the direction of the visual ray, on the side of the source of light,
formed a somewhat small angle with the axis of the cylinder: one
would have said that the phenomenon was caused by the action of
a solid or liquid body on the molecules of the ether. Viewing the
cylinder in this direction, the polarization perceptibly decreased on
approaching the source of light or removing from it. The light pro-
ceeding from the column of smoke seen by reflexion upon the
aperture was only feebly polarized.
Iixcepting in its intensity, the above phenomenon presents nothing
extraordinary; but for a physicist the circumstance appears to me
important, that the light polarized by diffusion does not seem to arise
from a simple reflexion from gas moiecules, for its plane of polar-
158 Intelligence and Miscellaneous Articles.
ization is at right angles to the plane in which the reflexion ought
to occur. For on examining the cylinder of light round its axis in
the direction of the maxima of polarization, it was found that the
light proceeding from it was polarized tangential to that point of the
surface of the cylinder towards which the polariscope was directed.
Whether the plane of polarization becomes removed by its repeated
reflexions from the gas molecules, or whether the action of gases
under certain circumstances is analogous to that of refracting bodies,
are questions which hitherto I have not been able to decide by ex-
periment.
I endeavoured to depolarize the light completely on its entry into
the dark room, by allowing it to pass through a thin sheet of white
paper; but the phenomena, with the exception of the intensity of
the light, were quite the same.
Light polarized by reflexion from a black glass experienced no
perceptible change by the action of the smoke, and its plane of
polarization always retained its original direction.
It is possible, by suitably regulating the incident quantity of po-
larized light, to succeed in finding a limit to the action of the gas
molecules, beyond which the original polarization of the pencil pre-
ponderates over the molecular forces of the medium which the light
has to penetrate.
The relations which these facts may possibly bear to the pheno-
mena of atmospheric polarization, and perhaps also to fluorescence
and the peculiar colour of bodies, have induced me to publish these
observations, spite of their incompleteness.
Some days after the preceding experiments had been laid before
the Academy, I repeated them with more sensitive polariscopes, and I
found exactly the same facts; I can further state that the plane of
polarization of diffused light suddenly rotated 90°, on passing the
direction in which I had seen all trace of polarization disappear in my
previous experiments.
Thus on receiving in the polariscope the rays emanating from the
luminous track produced by the passage of the sun’s light, or of the
electric light, through the smoke of incense, it is found that under a
small inclination (the angles being measured from the luminous
source) the polarization of diffused light is already very perceptible ;
that it increases up to a certain angle, which is the maximum; it then
decreases, and at the normal it is almost nil. Up to this point the
plane of polarization is perpendicular to the plane which passes
through the source of light, the place observed, and the eye or the
polariscope. Above 90°, the polarization, although very feeble, reap-
pears, but its plane is then perpendicular to the first plane. Still
further it diminishes very rapidly, and the diffused light soon shows
no sensible traces of polarized rays.
I have investigated the smoke of tobacco in the same way; and
the results were the same, though the angle at which I found the
neutral point and the reversal of the plane of polarization was perhaps
a little less than with the smoke of incense.
It is possible that the nature of the diffused particles has an ap-
preciable influence on these phenomena, and that different gases (if
gases do diffuse light), vapours, and powders may in this manner be
‘ Intelligence wnd Miscellaneous ‘Articles. 159
distinguished. I propose to undertake a series of experiments
froni this point of view, the results of which I shall lay before the
Academy.:—Comptes Rendus, Sept. 3, and Oct. 29, 1860.
ON BLECTRIC ENDOSMOSE. BY M. C. MATTEUCCI.
Having recently had occasion to examine into the construction
and operation of the galvanic batteries used in our telegraph offices,
I have been led to make certain original experiments on the subject
of electric endosmose, a short description of which, as they seem to
throw some light on the true nature of the phenomenon in question,
I beg to lay before the Academy. MM. Porret and Becquerel were
the first who called attention to the fact that a liquid mass, sepa-
rated into two compartments by a porous diaphragm, and traversed
by an electric current, appears to be transported in the direction of
that current; that is to say, the level of the liquid is lowered in the
compartment that contains the positive pole, and raised in that which
contains the negative pole. ‘The determination of the law of this
phenomenon is due to M. Wiedemann, who proved that the quantity
of water transported is directly proportional to the intensity of the
current and the electric resistance of the liquid. M. Wiedemann
seems to have regarded this mechanical effect of the current as a
different phenomenon from its electrolytic action; while other phy-
Sicists have considered that the transportation of the liquid was only
‘a secondary effect of electrolysis. I should mention also that
MM. Van Breda and Logemann have in vain endeavoured to as-
certain whether, in the absence of a diaphragm, there is any displace-
ment of the electrolysed liquid, or whether a very light moveable
diaphragm is itself displaced in the direction of the current. Theo-
retical considerations, which easily suggest themselves to the mind,
and which I need not here specify, founded on the equality of the
electrolytic effects, whether endosmose be produced or not, give
probability to the conclusion that these phenomena are caused by
some secondary action of electrolysis. The following experiments
seem to show that this supposition is correct.
I divided a rectangular vessel of varnished wood into six com-
partments, by means of diaphragms of porous porcelain. All these
compartments were filled to the same height with well-water, the
level of which was indicated by a line of white varnish. A platinum
plate of the same size as the diaphragms was placed in each of the
end compartments, Through this apparatus I caused a current to
pass, produced sometimes by 10, sometimes by 15, and sometimes by
20 cells of a Grove’s battery. ‘The endosmose became apparent after
the current had lasted for some hours, and in every case the first
effect produced was as follows :—The level of the liquid was raised
in the compartment that contained the negative electrode, and was
lowered in the compartment next to it, while it was lowered in the
compartment that contained the positive electrode (though to a less
degree than it was elevated in the compartment at the opposite ex-
tremity), and raised in the adjoining compartment. These effects
were invariably produced, notwithstanding the change of the dia-
phragm and the reversal of the position of the vessel with respect ta
160 Intelligence and Miscellaneous Articles.
the electrodes. Floats may be put in all the compartments, except
_those containing the platinum plates, in which the liquid is too much
agitated by gaseous bubbles due to electrolysation; and on viewing
these floats with a glass, the displacements I have described become
sensible much earlier. In the intermediate compartments the liquid
remains stationary,for several hours; but after a certain time the
liquid begins to rise in the compartments towards the positive pole,
and to fall in those towards the negative pole. I shall mention but
one precaution which must not be neglected in these experiments,
namely, that the diaphragms must be as equal as possible.
In a second series of experiments I closed one end of each of two
glass tubes with a porcelain diaphragm fixed with mastic. Each
of these tubes was then placed in a glass vessel, and both vessels
and tubes were filled to the same height with well-water. The same
current passed through both tubes, in each case passing from the water
in the vessel to that in the tube, the only difference being in the
position of the platinum electrodes, which in the one case were very
near the diaphragm, while in the other they were placed at the
greatest possible distance from it. Under these circumstances I in-
variably found that the electric endosmose made its appearance much
sooner, and with much greater intensity in the first case than in the
second.
I shall not stop to discuss the consequences of these experiments,
since they appear to me to be obvious, and to prove that the phenome-
non in question is no other than that mentioned above, that is to say, a
case of endosmose produced by changes in the composition of the liquid
in contact with the two electrodes. I should mention here that the
liquid round the positive electrode always acquires an acid reaction,
while that round the negative electrode becomes alkaline, and that
these effects are produced even when distilled water is employed. I
did not content mysclf with the ancient experiments of Dutrochet,
which prove that there isa current of endosmose from an acid liquid
to water, from water to an alkaline liquid, and from an acid to an
alkaline liquid. I repeated the experiment with the two liquids
which had been in contact with the electrodes as described above,
sometimes making use of both of the liquids, sometimes testing each
of them separately with pure water. I invariably found that there
was endosmose from the liquid that had been in contact with the
positive electrode to pure water, and from pure water to the liquid
that had been in contact with the negative electrode. It appears
therefore that the conditions for the production of ordinary endosmose
are undoubtedly present in the phenomenon called electric endos-
mose. I should, however, observe that the amount of displacement
by endosmose is much less when the liquids which have been in
contact with the electrodes are experimented on simply without
any electric current, and that it is hardly perceptible in the case of
electrolysed distilled water. Without attempting to explain all the
phenomena of electric endosmose, it seems natural to suppose that
the presence of electricity, and the peculiar state in which the ele-
ments of electrolysation are produced, give to these products pro-
perties which influence the effect of endosmose, and which cease
with the cessation of the current.—Comptes Rendus, Dec. 1860,
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THE
LONDON, EDINBURGH ann DUBLIN
PHILOSOPHICAL MAGAZINE
AND
JOURNAL OF SCIENGE.
[FOURTH SERIES.]
MARCH 1861.
XXV. On Physical Lines of Force. By J. C. Maxweut, Pro-
fessor of Natural Philosophy in King’s College, London*.
- Part 1—The Theory of Molecular Vortices applied to Magnetic
Phenomena.
i all phenomena involving attractions or repulsions, or any
forces depending on the relative position of bodies, we have
to determine the magnitude and direction of the force which
would act on a given body, if placed in a given position.
In the case of a body acted on by the gravitation of a sphere,
this force is inversely as the square of the distance, and in a
straight lme to the centre of the sphere. In the case of two
attracting spheres, or of a body not spherical, the magnitude
and direction of the force vary according to more complicated
laws. In electric and magnetic phenomena, the magnitude and
direction of the resultant force at any point is the main subject
of investigation. Suppose that the direction of the force at any
point is known, then, if we draw a line so that in every part of
its course it coincides in direction with the force at that point,
this line may be called a line of force, since it imdicates the
direction of the force in every part of its course.
By drawing a sufficient number of lines of force, we may
indicate the direction of the force in every part of the space in
which it acts.
Thus if we strew iron filmgs on paper near a magnet, each
filmg will be magnetized by induction, and the consecutive
filings will unite by their opposite poles, so as to form fibres,
and these fibres will indicate the direction of the lines of force.
The beautiful illustration of the presence of magnetic force
afforded by this experiment, naturally tends to make us think of
* Communicated by the Author.
Phil. Mag. 8. 4. Vol. 21. No. 189. March 1861. M
162 Prof. Maxwell on the Theory of Molecular Vortices
the lines of force as something real, and as indicating something
more than the mere resultant of two forces, whose seat of action
is at a distance, and which do not exist there at all until a mag-
_net is placed in that part of the field. We are dissatisfied with
/ the explanation founded on the hypothesis of attractive and
repellent forces directed towards the magnetic poles, even though
we may have satisfied ourselves that the phenomenon is in strict
accordance with that hypothesis, and we cannot help thinking
_ that in every place where we find these lines of force, some phy-
sical state or action must exist in sufficient energy to produce the
actual phenomena.
My object in this paper is to clear the way for speculation in
this direction, by investigating the mechanical results of certain
states of tension and motion in a medium, and comparing these
with the observed phenomena of magnetism and electricity. By —
pointing out the mechanical consequences of such hypotheses, 1
hope to be of some use to those who consider the phenomena as
due to the action of a medium, but are in doubt as to the relation
of this hypothesis to the experimental laws already established,
which have generally been expressed in the language of other
hypotheses.
I have in a former paper* endeavoured to lay before the mind
of the geometer a clear conception of the relation of the lines of
force to the space in which they are traced. By making use of
the conception of currents in a fluid, I showed how to draw lines
of force, which should indicate by their number the amount of
force, so that each line may be called a unit-line of force (see
Faraday’s ‘ Researches,’ 3122) ; and I have investigated the path
of the lines where they pass from one medium to another.
In the same paper I have found the geometrical significance
of the “ Electrotonic State,” and have shown how to deduce the
mathematical relations between the electrotonic state, magnetism,
electric currents, and the electromotive force, using mechanical
illustrations to assist the imagination, but not to account for the
phenomena.
I propose now to examine magnetic phenomena from a mecha-
nical point of view, and to determine what tensions in, or motions
of, a medium are capable of producing the mechanical pheno-
mena observed. If, by the same hypothesis, we can connect the
phenomena of magnetic attraction with electromagnetic phe-
nomena and with those of induced currents, we shall have found a
theory which, if not true, can only be proved to be erroneous by
experiments which will greatly enlarge our knowledge of this
part of physics.
* See a paper “ On Faraday’s Lines of Force,’’ Cambridge Philosophical
Transactions, vol. x. part 1.
applied to Magnetic Phenomena. _ 163
The mechanical conditions of a medium under magnetic in-
fluence have been variously conceived of, as currents, undula-
tions, or states of displacement or strain, or of pressure or stress.
Currents, issuing from the north pole and entering the south
pole of a magnet, or circulating round an electric current, have
the advantage of representing correctly the geometrical arrange-
ment of the lines of force, if we could account on mechanical
principles for the phenomena of attraction, or for the currents
themselves, or explain their continued existence.
_ Undulations issuing from a centre would, according to the cal-
culations of Professor Challis, produce an effect similar to attrac-
tion in the direction of the centre; but admitting this to be true,
we know that two series of undulations traversing the same space
do not combine into one resultant as two attractions do, but pro-
duce an effect depending on relations of phase as well as intensity,
and if allowed to proceed, they diverge from each other without
any mutual action. In fact the mathematica! laws of attractions
are not analogous in any respect to those of undulations, while
they have remarkable analogies with those of currents, of the
conduction of heat and electricity, and of elastic bodies.
In the Cambridge and Dublin Mathematical Journal for
January 1847, Professor William Thomson has given a “ Mecha-
nical Representation of Electric, Magnetic, and Galvanic Forces,”
by means of the displacements of the particles of an elastic solid
in a state of stram. In this representation we must make the
angular displacement at every point of the solid proportional to
the magnetic force at the corresponding point of the magnetic
field, the direction of the axis of rotation of the displacement
corresponding to the direction of the magnetic force. The abso-
lute displacement of any particle will then correspond in magni-
tude and direction to that which I have identified with the elec-
trotonic state; and the relative displacement of any particle,
considered with reference to the particle in its immediate neigh-
bourhood, will correspond in magnitude and direction to the
quantity of electric current passing through the corresponding
point of the magneto-electric field. The author of this method
of representation does not attempt to explain the origin of the
observed forces by the effects due to these strains in the elastic
solid, but makes use of the mathematical analogies of the twe
problems to assist the imagination in the study of both.
We come now to consider the magnetic influence as existing
in the form of some kind of pressure or tension, or, more gene-
rally, of stress in the medium.
Stress is action and reaction between the consecutive parts of
a body, and consists in general of pressures or tensions different
in different directions at the same point of the medium.
M2
164 Prof. Maxwell on the Theory of Molecular Vortices
The necessary relations among these forces have been in-
vestigated by mathematicians; and it has been shown that the
most general type of a stress consists of a combination of three
principal pressures or tensions, in directions at right angles to
each other.
When two of the principal pressures are equal, the third be-
comes an axis of symmetry, either of greatest or least pressure,
the pressures at right angles to this axis being all equal.
When the three principal pressures are equal, the pressure is
equal in every direction, and there results a stress having no
determinate axis of direction, of which we have an example in
simple hydrostatic pressure.
The general type of a stress is not suitable as a representation
of a magnetic force, because a line of magnetic force has direc-
tion and intensity, but has no third quality indicating any dif-
ference between the sides of the line, which would be analogous
to that observed in the case of polarized light*.
We must therefore represent the magnetic force at a point by
a stress having a single axis of greatest or least pressure, and all
the pressures at right angles to this axis equal. It may be
objected that it is inconsistent to represent a line of force, which
is essentially dipolar, by an axis of stress, which is necessarily
isotropic ; but we know that every phenomenon of action and re-
action is isotropic in its results, because the effects of the force
on the bodies between which it acts are equal and opposite,
while the nature and origin of the force may be dipolar, as in
the attraction between a north and a south pole.
Let us next consider the mechanical effect of a state of stress
symmetrical about an axis. We may resolve it, in all cases, into
a simple hydrostatic pressure, combined with a simple pressure
or tension along the axis. When the axis js that of greatest
pressure, the force along the axis will be a pressure. When the
axis is that of least pressure, the force along the axis will be a
tension.
If we observe the lines of force between two magnets, as in-
dicated by iron filings, we shall see that whenever the lines of
force pass from one pole to another, there is attraction between
those poles; and where the lines of force from the poles avoid
each other and are dispersed into space, the poles repel each
other, so that in both cases they are drawn in the direction of
the resultant of the lines of force.
It appears therefore that the stress in the axis of a line of
magnetic force 1s a ¢ension, like that of a rope.
If we calculate the lines of force in the neighbourhood of two
gravitating bodies, we shall find them the same in direction as
* See Faraday’s ‘ Researches,’ 3252.
applied to Magnetic Phenomena. 165
those near two magnetic poles of the same name; but we know
that the mechanical effect is that of attraction instead of re-
pulsion. The lines of force in this case do not run between the
bodies, but avoid each other, and are dispersed over space. In
order to produce the effect of attraction, the stress along the
lines of gravitating force must be a pressure.
Let us now suppose that the phenomena of magnetism depend
on the existence of a tension in the direction of the lines of force,
combined with a hydrostatic pressure; or in other words, a pres-
sure greater in the equatorial than in the axial direction: the
next question is, what mechanical explanation can we give of
this inequality of pressures in a fluid or mobile medium? The
explanation which most readily occurs to the mind is that the
excess of pressure in the equatorial direction arises from the
centrifugal force of vortices or eddies in the medium having their
axes in directions parallel to the lines of force.
This explanation of the cause of the inequality of pressures
at once suggests the means of representing the dipolar character
of the line of force. Hvery vortex is essentially dipolar, the two
extremities of its axis being distinguished by the direction of its
revolution as observed from those points.
We alsc know that when electricity circulates in a conductor,
it produces lines of magnetic force passing through the circuit,
the direction of the lines depending on the direction of the cir-
culation. Let us suppose that the direction of revolution of our
vortices is that in which vitreous electricity must revolve in order
to produce lines of force whose direction within the circuit is the
same as that of the given lines of force.
We shall suppose at present that all the vortices in any one
part of the field are revolving in the same direction about axes
nearly parallel, but that in passing from one part of the field to
another, the direction of the axes, the velocity of rotation, and
the density of the substance of the vortices are subject to change.
We ‘shall investigate the resultant mechanical effect upon an
element of the medium, and from the mathematical expression
of this resultant we shall deduce the physical character of its
different component parts.
Prop. I.—If in two fluid systems geometrically similar the
velocities and densities at corresponding points are proportional,
then the differences of pressure at corresponding points due to
the motion will vary in the duplicate ratio of the velocities and
the simple ratio of the densities.
Let / be the ratio of the linear dimensions, m that of the velo-
cities, n that of the densities, and p that of the pressures due to
the motion. Then the ratio of the masses of corresponding por-
tions will be /°n, and the ratio of the velocities acquired in
166 ~~ Prof. Maxwell on the Theory of Molecular Vortices
traversing similar parts of the systems will be m; so that /®mn
is the ratio of the momenta acquired by similar portions in
traversing similar parts of their paths.
The ratio of the surfaces is /?, that of the forces acting on
them is /*p, and that of the times during which they act is
l : me
3 80 that the ratio of the impulse of the forces is —, and we-.
have now eck ot
m
or
mn=p ;
that is, the ratio of the pressures due to the motion (p) is com-
pounded of the ratio of the densities (n) and the duplicate ratio
of the velocities (m*), and does not depend on the linear dimen-
sions of the moving systems.
In a circular vortex, revolving with uniform angular velocity,
if the pressure at the axis is po, that at the circumference will be
Pi=Po+4pv’, where p is the density and v the velocity at the
circumference. The mean pressure parallel to the axis will be
Pot gp" =Po-
If a number of such vortices were placed together side by side
with their axes parallel, they would form a medium in which
there would be a pressure p, parallel to the axes, and a pressure
p; in any perpendicular direction. If the vortices are circular,
and have uniform angular velocity and density throughout, then
Pi —Po= apr"
If the vortices are not circular, and if the angular velocity and
the density are not uniform, but vary according to the same law
for all the vortices,
P1—Po= Cpr’,
where p is the mean density, and C is a numerical quantity de-
pending on the distribution of angular velocity and density in
the vortex. In future we shall write = instead of Cp, so that
1
Pi—Pa= Gp, RE)
where w is a quantity bearing a constant ratio to the density, and
v is the linear velocity at the circumference of each vortex.
A medium of this kind, filled with molecular vortices having
their axes parallel, differs from an ordinary fluid in having dif-
ferent pressures in different directions. If not prevented by
properly arranged pressures, it would tend to expand laterally.
In so doing, it would allow the diameter of each vortex to expand
applied to Magnetic Phenomena. 167
and its velocity to diminish in the same proportion. In order
that a medium having these inequalities of pressure in different
directions should be in equilibrium, certain conditions must be
fulfilled, which we must investigate. |
Prop. I1.—If the direction-cosines of the axes of the vortices
with respect to the axes of x, y, and z be-/, m, and n, to find the
normal and tangential stresses on the coordinate planes.
The actual stress may be resolved into a simple hydrostatic
pressure p, acting in all directions, and a simple tension p, —po,
or rae acting along the axis of stress.
Hence if py», Pyy, and pzz be the normal stresses parallel to
the three axes, considered positive when they tend to increase
those axes; and if p,,, Pex, and p,, be the tangential stresses in
the three coordinate planes, considered positive when they tend
to increase simultaneously the symbols subscribed, then by the
resolution of stresses*,
1
Psa= Ty hh Pr
1 Qin
Pyy= nee 1 ay
i 2,2
pe ge UE
Pyz= ipeemn
1 2
Pz 7 nl
1
Pay = Fe poorlm.
If we write
| a=vl, B=vm, and y=v,
then
! ]
Pes= go MO — Py Pyz= G BBY |
oe Cie
Py = rate —Pi Paa= Ge we} (2)
ae. a Sate
Pas eehY TP Pay= go Mob. j
Prop. I11.-—To find the resultant force on an element of the
medium, arising from the variation of internal stress.
* Rankine’s ‘ Applied Mechanics,’ art. 106.
168 — Prof. Maxwell on the Theory of Molecular Vortices
We have in general, for the force in the direction of 2 per unit
of volume by the law of equilibrium of stresses*,
d d d
X= 7 Peat dyP* ae zee . . . . . . . (3)
In this case the expression may be written
d (poe) de dp,
X= 7 da iki aga
d(wy) eS .
d(u)
ani nee aa
ne
4-
zs dz ie
d
Remembering that aes ee Was de ata +6? +97), this
becomes
sa aa Ag? 43 d d Dae ;
K=ai(£ (mex) + dy HP) + aS (uy) +3 he Lg + 6? + 7°)
pS dB du 1 i= dy\ _ dp,
we (5. a) +HY Ga \de 7 da). deen
The expressions for the forces parallel to the axes of y and z may
be written down from analogy.
We have now to interpret the meaning of each term of this
expression.
We suppose «, 8, y to be the components of the force which
would act upon that end of a unit magnetic bar which poits to
the north.
/ represents the magnetic inductive capacity of the medium
at any point referred to air as a standard. pa, wB, wy represent
the quantity of magnetic induction through unit of area perpen-
dicular to the three axes of a, y, 2 respectively.
The total amount of magnetic induction through a closed sur-
face surrounding the pole of a magnet, depends entirely on the
strength of that pole; so that if dw dy dz be an element, then
which represents the total amount of magnetic induction out-
wards through the surface of the element dx dy dz, represents
the amount of “imaginary magnetic matter” within the element,
of the kind which points north.
The first term of the value of X, therefore,
LP ad d )
ape(S.net oS om pth
may be written
ame bk) ita elt.niqe i
* Rankine’s ‘ Applied Mechanies,’ art. 116.
applied to Magnetic Phenomena. 169
where « is the intensity of the magnetic force, and m is the
amount of magnetic matter pointing north in unit of volume.
The physical interpretation of this term is, that the force
urging a north pole in the positive direction of # is the product
of the intensity of the magnetic force resolved in that direction,
and the strength of the north pole of the magnet.
Let the parallel limes from left to right in fig. 1 represent a
field of magnetic force such as that of the earth, sv being the
direction from south to north. The vortices, according to our
hypothesis, will be in the direction shown by the arrows in fig. 3,
that is, in a plane perpendicular to the lines of force, and revolv-
ing in the direction of the hands of a watch when observed from
s looking towards n. The parts of the vortices above the plane
of the paper will be moving towards e, and the parts below that
plane towards w. .
We shall always mark by an arrow-head the direction in which
we must look in order to see the vortices rotating in the direc-
tion of the hands of a watch. The arrow-head will then indicate
the northward direction in the magnetic field, that is, the direc-
tion in which that end of a magnet which points to the north
would set itself in the field.
Now let A be the end
of a magnet which points Big)
north. Since it repels the i a
north ends of other mag- —————_+_|__7 >
nets, the lines of force will pemCN IY 4 Su
be directed from A out- § CS ee m
wards in all directions. | Bt
On the north side the line ‘ ) a ca
AD will be in the same e a
direction with the lines of
the magnetic field, and the Fig. 2.
velocity of the vortices will a
be increased. On the south Ne ee ag
side the line A C will be in 2 MG WS ee
the opposite direction, and MS ie Oe Vee
the velocity of the vortices Oss h es
will be diminished, so that
the lines of force are more
powerful on the north side
of Athan on the southside.
We have seen that the
mechanical effect of the
vortices is to produce a
tension along their axes,
so that the resultant effect
VEY
170 ~~ Prof. Maxwell on the Theory of Molecular Vortices
on A will be to pull it more powerfully towards D than towards
C; that is, A will tend to move to the north.
Let B in fig. 2 represent a south pole. The lines of force
belonging to B will tend towards B, and we shall find that the
lines of force are rendered stronger towards E than towards F,
so that the effect in this case is to urge B towards the south.
It appears therefore that, on the hypothesis of molecular vor-
tices, our first term gives a mechanical explanation of the force
acting on a north or south pole in the magnetic field.
We now proceed to examine the second term,
| aeti
Sg sp (a? + 8? + 97).
Here «?+ 87+? is the square of the intensity at any part of
the field, and w is the magnetic inductive capacity at the same
place. Any body therefore placed in the field will be urged
towards places of stronger magnetic intensity with a force depend-
ing partly on its own capacity for magnetic induction, and partly
on the rate at which the square of the intensity increases.
If the body be placed in a fluid medium, then the medium, as
well as the body, will be urged towards places of greater intensity,
so that its hydrostatic pressure will be increased in that direc-
tion. The resultant effect on a body placed in the medium will
be the difference of the actions on the body and on the portion
of the medium which it displaces, so that the body will tend to
or from places of greatest magnetic intensity, according as it has
a greater or less capacity for magnetic induction than the sur-
rounding medium.
In fig. 4 the lines of force are represented as converging and
becoming more powerful towards the right, so that the magnetic
tension at B is stronger than at A, and the body AB will be
urged to the nght. If the capacity for magnetic induction is
greater in the body than in the surrounding medium , it will move
to the right, but if less it will move to the left.
Fig. 4, Fig. 5.
D
A B
Cc
We may suppose in this case that the lines of force are con-
verging to a magnetic pole, either north or south, on the right
hand.
In fig. 5 the lines of force are represented as vertical, and be-
applied to Magnetic Phenomena. 171
coming more numerous towards the right. It may be shown
that if the force increases towards the right, the lines of force
will be curved towards the right. The effect of the magnetic
tensions will then be to draw any body towards the right with a
force depending on the excess of its inductive capacity over that
of the surrounding medium.
We may suppose that in this figure the lines of fores are
those surrounding an electric current perpendicular to the plane
of the paper and on the right hand of the figure.
These two illustrations will show the mechanical effect on a
paramagnetic or diamagnetic body placed in a field of varying
magnetic force, whether the increase of force takes place along
the lines or trausverse to them. The form of the second term
of our equation indicates the general law, which is quite inde-
pendent of the direction of the lines of force, and depends solely
on the manner in which the force varies from one part of the
field to another.
We come now to the vee term of the value of X,
Jot
OY Tanda dy)"
Here uf is, as before, the quantity of magnetic induction through
unit of area perpendicular to the axis of y, and Ene Is a
quantity which would disappear if adx-+ @dy+ydz were a com-
plete differential, that is, if the force acting on a unit north pole
were subject to the condition that no work can be done upon
the pole in passing round any closed curve. The quantity repre-
sents the work done on a north pole im travelling round unit of
area in the direction from +z to +y parallel to the plane of zy.
Now if an electric current whose strength is 7 is traversing the
axis of z, which, we may suppose, points vertically upwards, then,
if the axis of w is east and that of y north, a unit north pole will
be urged round the axis of z in the direction from 2 to y, so
that in one revolution the work done will be = 47rr. Hence
7 = — a) represents the strength of an electric current
parallel to z through unit of area; and if we write
1 (dy =*)= eet —\-- 1) = ~(% - a) an
ale - dz) ~ aa\dz~ da) ~? Ga\de dy ae)
then p, g, r will be the quantity of electric current per unit of
area perpendicular to the axes of x, y, and z respectively.
The physical interpretation of the third term of X, —r, is
that if w8 is the quantity of magnetic induction parallel to y, and
r the quantity of electricity flowing in the direction of z, the
172 Prof. Maxwell on the Theory of Molecular Vortices
element will be urged in the direction of —z, transversely to the
direction of the current and of the lines of force; that is, an
ascending current in a field of force magnetized towards the north
would tend to move west.
To illustrate the action of the molecular vor- Fig. 6.
tices, let sm be the direction of magnetic force ~ n
in the field, and let C be the section of an
ascending magnetic current perpendicular to
the paper. The lines of force due to this current ,,
will be circles drawn in the opposite direction
from that of the hands of a watch ; that is, in the
direction nwse. At e the lines of force will be
the sum of those of the field and of the current, 8
and at w they will be the difference of the two
sets of lines; so that the vortices on the east side of the current
will be more powerful than those on the west side. Both sets
of vortices have their equatorial parts turned towards C, so that
they tend to expand towards C, but those on the east side have
the greatest effect, so that the resultant effect on the current is to
urge it towards the west.
The fourth term,
1 (de
+m {Fe oat or +uyg, . . + (10)
may be interpreted in the same way, and indicates that a current
g in the direction of y, that is, to the north, placed in a magnetic
field in which the lines are vertically upwards in the direction of
z, will be urged towards the east.
The fifth term,
dp,
Fa tue ho athe a
merely implies that the element will be urged in the direction in
which the hydrostatic pressure p, diminishes.
We may now write down the expressions for the components
of the resultant force on an element of the medium per unit of
volume, thus:
ie 4 d, .
X=am+ ws (%)—wOrt+pyg—S3, . . (12)
Losi d
Y=@m+ Sa ay Hw + mar — 7 : % hae
gpg d,
Z=ym+ 3- wo (v*)— pag +mBp — 2. wore (lp
The first term of each expression refers to the force acting on
magnetic poles.
applied to Magnetic Phenomena. 173
The second term to the action on bodies capable of magnetism
by induction. 7
The third and fourth terms to the force acting on electric
currents.
And the fifth to the effect of simple pressure.
Before going further in the general investigation, we shall
consider equations (12, 13, 14,) in particular cases, corresponding
to those simplified cases of the actual phenomena which we seek
to obtain in order to determine their laws by experiment.
We have found that the quantities p, g, and r represent the
resolved parts of an electric current in the three coordinate
directions. Let us suppose in the first instance that there is no
electric current, or that p, g, and rvanish. We have then by (9),
dy dB da dy dB da _ s
perce > ge ae ae ap ne
whence we learn that
eer eyed. 6 el suits Met we) eh e@lO)
is an exact differential of ¢, so that
tO oy hea beashesen eV
oe he’ ay dee
p is proportional to the density of the vortices, and represents the
“ capacity for magnetic induction” in the medium. It is equal
to 1 in air, or in whatever medium the experiments were made
which determined the powers of the magnets, the strengths of
the electric currents, &c.
Let us suppose constant, then
1/d d iy, )
m= 5 (7, (ue) + 5 (HB) + oe (on)
_ 1 (ad , a , dd
= (Ss + dy? + dz? ° ° ° ° e (18)
represents the amount of imaginary magnetic matter in unit of
volume. That there may be no resultant force on that unit of
volume arising from the action represented by the first term of
equations (12, 13, 14), we must have m=0, or
FD IEE 2.6) 3 nn ag EE
da® * ay? * dz?
Now it may be shown that equation (19), if true within a given
space, implies that the forces acting within that space are such
as would result from a distribution of centres of force beyond
that space, attracting or repelling inversely as the square of the
distance.
174 ~—Prof. Maxwell on the Theory of Molecular Vortices
Hence the lines of force in a part of space where is uniform,
and where there are no electric currents, must be such as would
result from the theory of “imaginary matter” acting at a di-
stance. The assumptions of that theory are unlike those of ours,
but the results are identical.
Let us first take the case of a single magnetic pole, that is,
one end of a long magnet, so long that its other end is too far
off to have a per ceptible influence on the part of the field we are
considering. The conditions then are, that equation (18) must
be fulfilled at the magnetic pole, and (19) everywhere else. The
only solution under these conditions is
m I
ae ee (20)
where 7 is the distance from the pole, and m the strength of the
pole.
The repulsion at any point on a unit pole of the same kind is
dp m1
—=— =. ; : re
oe (21)
In the standard medium w~=1 ; so that the repulsion is simply
= -> in that medium, as has been shown by Coulomb.
In a medium having a greater value of w (such as oxygen,
solutions of salts of iron, &c.) the attraction, on our theory, ought
to be ess than in air, and in diamagnetic media (such as water,
melted bismuth, &c.) the attraction between the same magnetic
poles ought to be greater than im air.
The experiments necessary to demonstrate the difference of
attraction of two magnets according to the magnetic or dia-
magnetic character of the medium in which they are placed,
would require great precision, on account of the limited range
of magnetic capacity in the fluid media known to us, and the
small amount of the difference sought for as compared with the
whole attraction.
Let us next take the case of an electric current whose quan-
tity is C, flowing through a cylindrical conductor whose radius
is R, and whose length is infinite as compared with the size of
the field of force considered.
Let the axis of the cylinder be that of z, and the direction of
the current positive, then within the conductor the quantity of
current per unit of area is
iy al dB wi), ;
nae we dy ae
L*
applied to Magnetic Phenomena. 175
so that within the conductor
C C
a= —2 py; B=2p02, cee RE yh 0 een 5)
Beyond the conductor, in the space round it,
$=2Ctan-1%, . cele ae eR green ae et
eae y __o¢__# OP 5
If p=/x? + y? is the perpendicular distance of any point from
the axis of the conductor, a unit north pole will experience a
2C :
force = ——, tending to move it round the conductor in the
direction of the hands of a watch, if the observer view it in the
direction of the current.
Let us now consider a current running parallel to the axis of
z in the plane of xz at a distance p. Let the quantity of the
current be c’, and let the length of the part considered be /, and
its section s, so that = is its strength per unit of section. Put-
ting this quantity for p in equations (12, 18, 14), we find
F
X= —pp F
per unit of volume; and multiplying by Js, the volume of the
conductor considered, we find
X= —pBell
— —2u—, Whee ial h gy ate as ° > (26)
showing that the second conductor will be attracted towards the
first with a force inversely as the distance.
We find in this case also that the amount of attraction depends
on the value of w, but that it varies directly instead of inversely
as 2; so that the attraction between two conducting wires will be
greater in oxygen than in air, and greater in air than in water.
We shall next consider the nature of electric currents and
electromotive forces in connexion with the theory of molecular
vortices.
ae.
XXVI. On the Benzole Series.
By Artuur H. Caurcu, B.A. Oxon., F.C.S.*
Part III. Note on the Oxidation of Nitrobenzole and its
Homologues.
| experiments by Hofmann, Berthelot, and others
have shown, with reference to many important organic
substances, how incorrect is any theory which does not permit
them to be viewed in more than one aspect. Is nitrobenzole
simply a hydrocarbon in which one equivalent of hydrogen is
replaced by the group NO*? or is it the hydride of nitro-
phenyle, Ob (sos) H? or, again, is it the nitrite of phenyle,
C!2H®, NO*? Some of the metamorphoses to which this inter-
esting body is subject suggest one of these views, and some
another. The ready production from nitrobenzole of phenyl-
amine, in which the group phenyle may be reasonably supposed
to exist, might induce us to regard nitrobenzole as a compound
of phenyle, possibly the nitrite ; while a reaction which I pointed
out some time agoy, in which, by the action of sulphuric acid
upon nitrobenzole, a compound acid was formed to which the
empirical name of nitrosulphobenzolic acid was assigned, and
which can hardly be regarded in any other Way. except as the
GR H, 280°,
almost obliges us to view nitrobenzole as containing nitrophenyle.
I propose in the present note to cite a few experiments which
present some of the nitro-derivatives of the benzole series in a
new light. I feel, however, that though an apology is due for
the imperfections of the present account, yet a preliminary
notice of my results (results which will require much time and
labour to bring to a satisfactory conclusion) might not be unac-
ceptable. But I should have deferred publishing any account of
my inquiries for some time longer, tad not an acid been lately
discovered homologous with benzoic acid, and isomeric, but not,
I think, identical with an acid mentioned in this paper: I refer
to collinic acid, C!? H* 04, obtained by the oxidation of gelatine.
Then, too, several of the speculations and anticipations of Ber-
thelot in his work on Organic Synthesis, trench somewhat closely
upon one of the inquiries in which I have been lately engaged.
I intend, when my inquiries are more advanced, to make the
two new acids (phenoie and nitrophenoic) mentioned in the pre-
sent notice the subject of another communication.
The oxidation of toluole, xylole, and cumole by means of bi-
sulphite of nztrophenyle and hydrogen, CO”
* Communicated by the Author.
t+ Phil. Mag. April and June 1855.
On the Oxidation of Nitrobenzole and its Homologues. 177
chromate of potassium and sulphuric acid, has been found in
each case to yield benzoic acid. Cymole, on the other hand, the
last member of the series, when treated in the same way, yields
the insolinic acid discovered by Dr. Hofmann, and not the toluic
acid which Mr. Noad obtained by acting upon this hydrocarbon
with dilute nitric acid. Benzole remains wholly unacted upon
when boiled for a very long period with bichromate of potassium
and sulphuric acid. Not so, however, with nitrobenzole, which
is slowly converted by this powerful oxidizing mixture into a
soft, white, crystalline mass of intensely acid reaction. In the
first experiment, I made use of a very excellent sample of com-
mercial nitrobenzole, a portion of which seemed to be acted on
with greater facility than the rest. An analysis of the acid
thus formed gave numbers which indicated a mixture of nitro-
benzoic and nitrophenoic acids: I propose the latter name for
the new acid, which I believe to be the next lower homologue
of the benzoic. The view that the acid burnt was a mixture, is
confirmed by another experiment, to be related further on. In
order to secure the absence of nitrotoluole from the nitrobenzole
operated upon, I converted some benzole from benzoic acid into
nitrobenzole, and repeated my experiments with this. The action
of a most concentrated oxidizing solution was now found to be
very much slower than in the former case; but after long diges-
tion the nitrobenzole solidified in great measure on cooling the
mixture, while from the solution itself numerous white crystalline
~spangles separated. The liquid and solid parts were together
poured into a funnel plugged with asbestos. To separate the
unchanged nitrobenzole, the solid stopped by the filter was
exhausted with boiling water, and the solution filtered twice
through paper. When cold, the filtrate was full of large nacreous
plates of a very pale straw colour, which by recrystallization
became perfectly white. Having had but a few grains of this
substance at my disposal, I have not yet made an accurate ex-
amination of its physical properties. I found, however, that its
reaction is strongly acid, that it is fusible without decomposi-
tion, tolerably soluble in boiling water, and that it yields cry-
stallizable salts. Not only does its origin and the method of
its formation preclude the existence of more than twelve atoms
of carbon in the new acid, but the following determination of
silver in a carefully prepared specimen of its silver-salt points
to the formula C!? H? Ag (NO*)O# for this compound, and to
C!? H3 (NO‘) O# for the acid itself :—
‘971 germ. of silver-salt gave ‘537 grm. of chloride of silver =
"4041 grm. of silver,
Phil. Mag. 8. 4. Vol. 21. No. 139. March 1861. = N
178 Mr. H. Church on the Oxidation of
corresponding to a per-centage of—
Theory,
Experiment. CH? Ag (NO*) O4,
Silvers) .4 0d SOG] A154:
So far as they have been yet examined, the properties of nitro-
phenoie acid confirm the idea that it is a true homologue of
nitrobenzoic acid.
I have made an attempt to prepare the original acid, the
phenoic, of which I have supposed the above-noticed acid to be
the nitro-derivative. Although a mixture of bichromate of po-
tassium and sulphuric acid is without action on benzole, it acts
most energetically on sulphobenzolic acid formed by dissolving
benzole in Nordhausen sulphuric acid. If to a slightly diluted
solution of sulphobenzolic acid at about 70° C. minute frag-
ments of bichromate of potassium be added, one at a time, and
the action which ensues at each addition be moderated by cooling
the apparatus, an acid distillate will be obtained, on the surface
of which small brilliant crystals, gencrally accompanied by a few
oily globules, will be found floating. It would seem that the
oily and solid portions of the distillate are alike in composition,
since the analysis of the silver-salts of the two bodies, separated
mechanically as far as possible, gave almost the same numbers.
Of the annexed determinations, I. was made with a silver-salt
prepared from the oily part, and II. with one prepared from the
crystalline part of the distillate.
I. -739 grm. gave ‘37 grm. of silver,
II. +3822 grm. gave ‘163 grm. of silver ;
corresponding to the following per-centages of silver :—
Experiment. Theory,
: II. CH Ae D4
50:06 50:06 50°23
Sulphotoluolic and sulphocumolic acids, when oxidized as de-
scribed above, yield benzoic acid inabundance. I have identified
the product by all the usual tests. I have not yet experimented
with the xylole series. Sulphocymolic acid yields a white powder,
apparently identical with insolinic acid.
Nitrotoluole, when oxidized, yielded nitrobenzoie acid, which
agreed in every respect with a pure specimen in my possession
prepared from benzoic acid. I have before mentioned the diffi-
culty with which nitrobenzole is acted on by the oxidizing mix-
ture; and if this latter be somewhat diluted, it affords a means
of separating the nitro-derivatives of toluole, &c. from nitro-
benzole, which, when the action is complete, is siphoned off and
Nitrobenzole and its Homologues. 179
washed with en alkaline solution to remove the nitrobenzoic acid
formed.
Since sulphobenzolate of ammonium, when submitted to dry
distillation, yields some quantity of benzole*, I imagined that
the nitrosulphobenzolate would yield nitrobenzole: experiment,
however, has not corroborated this view.
In 1859 I showed+ that nascent chlorine acts powerfully on
toluole, xylole, and other homologues of benzole, yielding the
chlorides of toluenyle, xylenyle, &c., from which the cyanides,
and subsequently the acids (toluic and xyloic), are producible.
I am pursuing some inquiries in this direction with benzole,
upon which unfortunately nascent chlorine acts with more diffi-
culty, and at the same time does not appear to yield such definite
results.
There is a point of view from which some of the experiments
which I have made acquire a fresh interest. If 1 vol. of light
coal-naphtha containing, say 50 per cent. of benzole, be sub-
mitted to the action of 6 vols. of oil of vitriol previously diluted
with 1 vol. of water, and the mixture heated for some time in
a suitable condensing apparatus, the benzole will remain nearly,
if not quite, unacted upon, while the other hydrocarbons will be
dissolved by the sulphuric acid. If the acid be absorbed by
small fragments of pumice and thus used, it exerts a much more
rapid and effectual action on the naphtha. The benzole, after
having been washed with water, is nearly pure. The other hy-
drocarbons which have been dissolved are now contained as sul-
photoluolic and similar acids in the liquid, which is to be collected,
diluted with half its bulk of water, and poured into a retort pro-
vided with a Liebig’s condenser. Buichromate of potassium,
about one-sixth part in weight of the acid present, is added gra-
dually to the solution, and the mixture cautiously distilled. In
this way a considerable proportion of benzoic acid may be ob-
tained.
Postscript, February 8, 1861.
Since writing the above remarks, my attention has been
directed to a short notice of some experiments by MM. Cloetz
and Guignet, who also seem to have obtained a new acid by the
oxidation of nitrobenzole. I think it mght to say that I sue-
ceeded in producing the acid which I have termed nitrophenoic
in June 1860.
* Phil. Mag. December 1859.
+ Chemical News, December 10, 1859.
N2
[ 180 ]
XXVIII. Note on the Theory of Determinants.
By A. Cayiny, Esq.* ’
f dasa following mode of arrangement of the developed expres-
sion of a determinant had presented itself to me as a con-
venient one for the calculation of a rather complicated determi-
nant of the fifth order; but I have since found that it is in
effect given, although in a much less compendious form, in a
paper by J. N. Stockwell, “On the Resolution of a System of
Symmetrical Equations with Indeterminate Coefficients,” Gould’s
‘Ast. Journal, No. 189 (Cambridge, U. 8., Sept. 10, 1860).
Suppose tnat the determinant
1t tae. ie
21. 80 438
S12 e824 BS
is represented by {123}, and so for a determinant of any order
4123 .-.n}.
Let 11], ]2], [12], [123], &c. denote as follows: viz.
fl] = 11, [2] = 22, &c.
Pie 12 ek,
} 123] = 12.23.31,
&e.,
where it is to be noticed that, with the same two symbols, e. g.
1 and 2, there is but one distinct expression |12] (an fact
}21 | = 21.12 ={12]); with the same three symbols 1, 2, 3,
there are two distinct expressions, |123]}(=12.23.381) and
, 182 | (=13.32.21); and generally with the same m symbols
1, 2, 3...m, there are 1.2.3...m—1 distinct expressions
}123...mj, which are obtained by permuting in every possible
manner all but one of the m symbols.
This beg so, and writing for greater simplicity }1}2] to
denote the product |1 | x { 2], and so in general, the values of
the determinants {12}, {123}, {1234}, {12345}, &e. are as
follows: viz.
* Communicated by the Author.
Mr. A. Cayley on the Theory of Determinanis, 181
No. of terms.
spe
eps ya eli. .e kD
=e ge! 2 | | E |
. 1+1=2
{123}=+4+ ]1[2]3] . at 1
—|l ae ee 3
tt & Bh so sin 2
o+3=6
{1234,=4+ ]1)2]3}41.- | 1
—J1l 2|3]4|. . 6
eb ss, ot4 | a
+[1L 2]3.4]}.. .
—|i 2 3-4}. 6
124+12= 24
Oo
(12345}=+ ]112]314]5]. | 1
cg SASL A | ot 10
Sly 2.31 4 [oP sty 20
eb Sd Pere ee
Bb l 2 3 4 Salis 30
aid 2 814-5) % 20
el 23.4. 5. | 04
-60+60= 120
where, as regards the signs, it is to be observed that there is a
sign — for each compartment] | contaming an even number
of symbols; thus in the expression for {1234}, the terms
J 12] 34] have thesign — — = +, and the terms| 123 4}
the sign —. Or, what comes to the same thing; when 7 is even,
the sign is + or — according as the number of compartments
is even or odd; and contrariwise when 7 is odd. As regards
the remaining part of the expression, this merely exhibits the
partitions of a set of n things; and the formule for the several
determinants up to the determinant of a given order are all of
them obtained by means of the form
182 Mr. A. Cayley on the Theory of Determinants.
which is carried up to the order 7, but which can be further ex-
tended without any difficulty whatever.
It is perhaps hardly necessary; but I give at full length the
expressions of the determinant of the third order: this is
{128} = 11/213]
—|[1 213]
—|}2 3{1| I
—|8 142]
+]1 2 3]
+]1 3 2]5°
And by writing down in like manner the expression for the
twenty-four terms of the determinant of the fourth order, the
notation will become perfectly clear.
The formula hardly requires a demonstration. The terms of a
determinant {123...n}, for example the determinant {1234} |
are obtained by permuting in every possible manner the symbols
in either column, say the second column, of the arrangement
hI
22
3.3
A 4
Mr, A. Cayley on the Theory of Determinants. 183
and prefixing the sign (+ or —) of the arrangement; and the
resulting arrangements, for instance
ol hy seks, .. eh s,
2 2 al 23
33 3.3 3 4
4. 4, 44 4]
are interpreted either into +11.22.83.44, —12.21.33.44,
—12.23.34.41, or in the notation of the formula, into
Pii2isi4i, —|12(814b -— t12341.
And so in general.
Suppose that any partition of n contains « compartments each
of a symbols, 6 compartments each of 6 symbols... (a, b,...
being all of them different and greater than unity), and p com-
partments each of a single symbol, we have
n=aa+PBb+ ...+ .
And writing, as usual, [Ia=1.2.3...a, &c., the number of
ways in which the symbols 1, 2,.8,...n, can be so arranged in
compartments is
IIn
(IIa)*(I1d)*...TeII8...1p’
but each such arrangeraent gives (II (a—1) )* ; (1I(6—1) )é
terms of the determinant, and the corresponding number of terms
therefore is
IIn
ob, Alas ..idip:
The whole number of terms of the determinant is IIn, and we
have thus the theorem
1
Wreriesitis clin Weesekl a
in which the summation corresponds to all the different partitions
n=aa+8b...+p, where a, b,... are all of them different and
ereater than unity ; a theorem given in Cauchy’s Mémoire sur les
Arrangements, &c., 1844. But it is to be noticed also that, the
number of the positive and negative terms being equal, we have
besides
ye soe hic
Wea | aipales SO EOL EE Berea 5 Oe, Sree
Mem ta lde te
184 Mr, A. Cayley on the Theory of Determinants.
or, what is the same thing,
eee amie
a*b? .. ged G: . Tp
eat ale
and thence also ~
j
t=
a* bP... ilall@... 1p’
where, as before, n=aa+ Pb...+p (a, b,... bemg all different
and greater than unity); but the summation is restricted either
to the partitions for which n—a—6...—p is even, or else to
those for which n—a—f6...—p is odd.
The formula affords a proof of the fundamental property of
skew symmetrical determmants. In such a determimant we
have not only 12=—21, &c., but also 11=0, &c. Suppose
that n, the order of the determinant, is odd; then in each line of
the expression
{123...nk=|1]2]...12]
+ &e,
of the determinant, there is at least one compartment | 1 ] or
| 123] &c. containing an odd number of symbols: let | 128 |
be such a compartment, then the determinant contains the terms
| 123] P and {182|P (where P represents the remaining
compartments), that is, 12.238.31.Pand18.82.21.P. But
in virtue of the relations 12=—21, &c., we have
19 O83 a Wao ae as
and so in all similar cases, that is, the terms destroy each other,
or the skew symmetrical determimant of an odd order is equal
to zero.
The like considerations show that a skew symmetrical deter-
minant of an even order is a perfect square. In fact, consider-
ing for greater simplicity the case n=4, any line in the foregoing
expression of 11234! for which a compartment contains an
odd number of symbols, gives rise to terms which destroy each
other, and may be omitted. The expression thus reduces itself to
{1234} = +112] 384] 3 terms
—| 12 34] 6 terms,
which is in fact the square of
12.84413.424 14.28.
For the square of aterm, say 12.54, is 12”. 342 or 12.21 .34.43,
that is, ] 12 ]34], and the double of the product of two terms,
say 12.34 and 13, 42, is 2.12.34.18.42, or —12.24.43.31
On the Chemical Analysis of the Solar Atmosphere. 185
—13.34.42.21, that is —| 1243 | —]1342 |, and so for the
other similar terms, and we have
41234) = (12 .34413.42-4+14.23)?,)
And so in general, n being any even number, the skew symme-
trical determinant $123... is equal to the square of the
Pfaffian 12..., where the law of these Pfaffian functions is
12384 =12.84 418.42 414.28
123456 = 12.3456 + 13.4562 + 14,5623 + 15.6284 + 16.2345
where, in the second equation, 3456, &c. are Pfaflians, viz.
3456 =34.564385.644+86.45; and so on.
2 Stone Buildings, W.C.,
December 28, 1860.
XXVIII. Letter from Prof. Kirncunorr on the Chemical Analysis
of the Solar Atmosphere.
To the Editors of the Philosophical Magazine and Journal.
GENTLEMEN, Owens College, Manchester,
February 1, 1860.
{ RECEIVED a short time ago from Heidelberg the enclosed
portion of a letter from Prof. Kirchhoff to Prof. Erdmann.
As it gives a later account of Kirchhoff and Bunsen’s most im-
portant researches than has yet appeared in the Nnglish journals,
I think it may be of interest to your readers.
I am, yours sincerely,
Henry HE. Roscoz.
“Since I sent in my last report to the Berlin Academy, I
have been almost uninterruptedly engaged in following out the
investigation in the direction I there indicated. I will not now
speak either of the theoretical proof I have given* of the facts I
there announced, or of the experiments by help of which Bunsen
and I+ have shown that the bright bands in the spectrum of a
flame serve as the surest indications of the metals present therein ;
I will take the liberty, in this communication, of informing you
of the progress I have made in the chemical analysis of the solar
atmosphere.
“The sun possesses an incandescent, gaseous atmosphere,
which surrounds a solid nucleus having a still higher tempera-
ture. If we could see the spectrum of the solar atmosphere, we
should see in it the bright bands characteristic of the metals
* Phil, Mag. July 1860. t+ Ibid. August 1860.
186 Prof. Kirchhoff on the Chemical Analysis
contained in the atmosphere, and from the presence of these
lines should infer that of these various metals. The more intense
luminosity of the sun’s solid body, however, does not permit the
spectrum of its atmosphere to appear; it reverses it, according
to the proposition I have announced; so that instead of the
bright lines which the spectrum of the atmosphere by itself
would show, dark lines are produced. Thus we do not see the
spectrum of the solar atmosphere, but we see a negative image
of it. This, however, serves equally well to determine with cer-
tainty the presence of those metals which occur in the sun’s
atmosphere. For this purpose we only require to possess an
accurate knowledge of the solar spectrum, and of the spectra of
the various metals.
“T have been fortunate enough to obtain possession of an appa-
ratus from the optical and astronomical manufactory of Steinheil
in Munich, which enables me to examine these spectra with a
degree of accuracy and purity which has certainly never before
been reached. The main part of the instrument consists of four
large flint-glass prisms, and two telescopes of the most consum-
mate workmanship. Jy their aid the solar spectrum is seen to
contain thousands of lines; but they differ so remarkably in
breadth and tone, and the variety of their grouping is so great,
that no difficulty is experienced in recognizing and remembering
the various details. I intend to make a map of the sun’s spec-
trum as I see it in my instrument, and I have already accom-
plished this for the brightest portion of the spectrum—that por-
tion, namely, included between Fraunhofer’s limes Fand D. By
painting the lines of various degrees of shade and of breadth, I
have succeeded in producing a drawing which represents the
solar spectrum so closely, that, on comparison, one glance suffices
to show the corresponding lines.
“The apparatus shows the spectrum of an artificial source of
light, provided it possess sufficient intensity, with as great a
degree of accuracy as the solar spectrum. A common colourless
gas-flame in which a metallic salt volatilizes, is m general not
sufficiently luminous; but the electric spark gives with great
splendour the spectrum of the metal of which the electrodes are
composed.
Of these results the first five or six are less trustworthy than
the rest,—and this for several reasons, amongst which the follow-
ing may be cited :—The rapidity of the rotation renders the de-
termination of the position of the cusp more difficult ; the proxi-
mity of the immersed axis interferes with the clear definition of
the cusp ; and lastly, the consequences of a small error in esti-
mating the distance of this cusp from the axis increase as this
distance diminishes, since the cusp approaches the axis asympto-
tically (art. 21). On the other hand, the rapid diminution of X
shown in the Table, can in some measure be accounted for by
the fact that, in order to avoid disturbing too much the surface
of the water in the bath, it was found necessary, with rapid rota-
tions, to use only one jet, and it of course issued at a small angle
towards the horizon, so that the impact between the jet and the
water in the bath was necessarily a very oblique one. But, as
already mentioned in art. 20, the tendency of this obliquity is to
diminish the velocity }. There can be no doubt that the rapid
diminution of » in the Table is to be ascribed chiefly to these
causes ; though it is also worth mentioning that the property of
the wave insisted upon by Weber, 2. e. that its velocity diminishes
as its radius increases (see art. 2), would also tend to produce
the effect observed.
In the last twelve observations recorded in the Table, two jets
(or a jet and a cylinder) were used, and the ripple of the vertical
one was chiefly examined. As a consequence, the values of A
vary far less, and 7°5 inches per second may be taken as a mean
value of the velocity with which waves thus produced are pro-
pagated.
and their relation to the Velocities of Currents. 195
30. As an interesting coincidence, it may be mentioned that
Poisson, in his memoir before referred to*, gives the results of
four experiments on the velocity of waves made by Biot. In
this case the waves were produced by suddenly withdrawing from
the water a partially immersed solid of revolution. The velocity
of the wave was found to vary with the form of the body, and
with the radius of its section at the water’s level. In one case, the
body being an ellipsoid, and the radius in question equal to 2 of
an inch, the velocity was about 54 inches per second ; in another
case, where the body was a sphere and the radius of the section
1+ inch, the velocity was 7:87 inches per second. The waves
experimented upon by Weber had a far greater velocity: they
were produced by allowing a column of liquid suspended in a
tube to descend suddenly into the general mass ; and their velo-
cities varied from 17 to 34: inches per second.
31. In the foregoing experiments, the velocity > was deter-
mined by causing an immersed cylinder to move with a given
velocity in still water. A few experiments were next made with
a view of ascertaining the value of X when a cylinder is simply
immersed in a current of known velocity. According to art. 10,
the sine of half the angle 20 between the branches of the ripple
caused by immersing a cylinder in a current is inversely propor-
tional to the velocity v of the current, and directly proportional
to the velocity >) in question. In fact it was there shown that
tan 6
\/ ete ge ree (48)
To determine the velocity v at any point of the surface of a
current, a Wollaston’s current-meter was used. As is known,
this instrument consists of a screw which is made to rotate by
the force of the current. The mstrument must be immersed to
the depth of two inches at least, in order that the screw may be
completely covered by the water; and when so immersed, the
rotation of the screw can be communicated at any instant to a
divided wheel, and the communication as suddenly broken. The
space described by the current during the interval between
making and breaking this communication—an interval which
can be measured by means of an ordinary watch with a seconds’
hand—is at once read off on the wheel, the instrument having
been. previously carefully graduated.
The angle 0 was determined by means of a simple instrument,
to which we may Sive the name of ripple-meter. It consisted of a
glass plate (BCD E, PI. IV. fig. 3) 5 inches square, through which,
at a point A, a hole ;4,th of an inch in diameter was drilled in
* Mémoires de l’Acad. Roy. des Sciences de VInstitut. Année 1816,
vol, i, p. 173, a
A=v sin 0=v
196 T. A. Hirst on Ripoles,
order to insert a solid cylinder of ivory about 1 inch long. Pass-
ing through the centre of A and parallel to the sides of the glass,
a fine line Aa, an inch long, was scratched on its surface with a
diamond point ; and through the extremity a of this lme another,
mn, was drawn perpendicular to the former, and graduated on
each side from a into tenths of an inch. In using this ripple-
meter, the plate of glass was held close and parallel to the sur-
face of the current, so that the ivory pin, by becoming partially
immersed, might cause a well-defined ripple, Ac, visible through
the glass; the plate was then turned until A a bisected the angle
between the branches of this ripple, when of course the ratio ~
gave at once the tangent of the required angle @. In this case,
as in that of the rotating jet, a number of secondary ripples are
also visible: after a little practice, however, and when the cur-
rent was not too slow (the angle b A c too obtuse), it was not dif-
ficult to estimate, approximately, the value of tan @ corresponding
to the principal ripple.
The following Table contains a few of the best results of many
experiments made on streams. In it the first column gives the
values of tan @ as read off on the ripple-meter ; the second column
shows the corresponding values of the velocity v as indicated in
feet per minute by the current-meter; and the third column
contains the respective values of A, calculated according to the
formula (43), in inches per second.
tan @. Ve r.
"993 44 6:2
774 554 6:8
705 59 6°8
577 67 67
*545 71 6-8
*392 96 70
388 105 76
The observations, of which the above are some of the most
trustworthy results, were made at different periods on streams
in Hampshire and Gloucestershire. When we take into consi-
deration the fact that a stream could rarely be found where the
velocity at any one point remained constant, that in all @ases
this velocity was determined with the curreng-meter at a point
2 or 3 inches below the surface, and lastly, that the method of
estimating the angle formed by the branches of the ripple can
only lead to approximate results, the general agreement of the
values of X with those obtained from the rotatory experiments is
as close as could be expected. The results appear to indicate
and their relation to the Velocities of Currents. 197
that, with one and the same immersed body, the value of X varies
somewhat with the veloclty of the current; but there can be
little doubt that, under more favourable circumstances, this
variation would be found to be far less than that indicated by
the Table.
In many cases no ripple whatever was produced by the immer-
sion of the cylinder of ivory attached to the ripple-meter; and in
all such cases the current-meter indicated a velocity less than 7
inches per second; the quickest of such currents in fact had
only a velocity of 25 feet per minute, or 5 inches per second.
This corroborates the explanation given in art. 11, where it was
foreseen that a body immersed in a current whose velocity was
less than that of the wave, would allow the water to flow past
it without visibly rippling its surface.
The phenomenon represented by the second figure of art. 10,
where the branches of the ripple turn their concavities towards
each other, and which was shown to be a necessary consequence
of Weber’s statement, that the velocity of the wave diminishes as
its radius increases, was never observed. A slight concavity,
however, might easily have escaped detection.
32. The velocity \ being once determined for any ripple-meter,
we can of course by its means determine, conversely, the velocity
of a current, provided the latter exceeds the limit A. For this
purpose I made use of a more convenient, though perhaps less
accurate ripple-meter, with a description of which I will conclude
the present paper. AB and A Cn fig. 4 represent two strips of
brass, each 3 inches long, and made toturn round A. Theends
B and C of these strips also turn on axes at the extremities of
two brass stirrups B F and C G, through which passes a wooden
scale D EK divided into twentieths of an inch. The cylinder, of
the same dimensions as before, by whose immersion in the cur-
rent ripples are produced, is pushed through an aperture in the
joint A. The stirrup BF being fixed at the zero of the scale, is
held there by a clamping screw F, and the stirrup C G is made
to slide along the scale until the strips AB, AC are parallel
to the branches of the ripple. This adjustment once made, the
distance BC, as read off from the scale, being directly. propor-
tional to 2 sin @, is clearly inversely proportional to the velocity
of the current (arts. 10 and 31).
The decrease in velocity from the centre to the banks of a
stream is clearly indicated by this little instrument. As an illus-
tration, I give the results of a few observations made on a mill
stream at Brimscombe near Stroud. A wocden plank was thrown
across the stream, which was about 7 feet 6 inches wide, and
upon it, commencing at one bank, marks were made 9 inches
apart. By kneeling on the plank, the ripple-meter was im-
198 M.G. R. Dahlander on the Equilibrium of a Fluid Mass
mersed in the current exactly under each mark. In explanation
of the following Table, it is only necessary to add that the first
column N shows the number of the mark on the plank; the
second column D the distance, in inches, of that mark from the
bank; the third column d the depth, in inches, of the stream
at each mark; the fourth column the values proportional to
2 sin 6 as read off on the ripple-meter ; and the last column v the
velocities in feet per minute, of the current as calculated, on the
hypothesis of \=7°5 inches per second, by formula (43) :
2 sin 0.
A
0
1
2
3
a
5
6
7
8
9
0
ft
In conclusion it may be added that, if desired, more accurate
ripple-meters might easily be devised, and by means of such the
velocities of currents might be determined from the forms of their
ripples with a degree of precision little, if at all, inferior to that
possessed by the methods now in use. It is from a theoretical
point of view, however, that the relation between waves and rip-
ples, which we have endeavoured to establish, promises the great-
est interest. For there can be little doubt that a skilful experi-
menter, pursuing the subject in this direction, would greatly
extend our present knowledge with respect to the changes in the
velocity of a current at different points of its surface, and espe-
cially with respect to the velocities with which different kinds of
waves are propagated on the surface of still water, and to the
variation of this velocity during the propagation of one and the
same wave.
January 15, 1861.
XXX. On the Equilibrium of a Flud Mass revolving freely
within a Hollow Spheroid about an Axis which is not its Axis
of symmetry. By G. R. DAHLANDER*,
+ we suppose a fluid ellipsoid to revolve alone about an axis
which is not an axis of symmetry, we easily perceive that
it cannot assume a position of equilibrium. It is, however, dif-
* Communicated by the Author.
revolving freely within a Hollow Spheroid. 199
ferent if we suppose the fluid mass surrounded by a hollow sphe-
roid, the two bounding surfaces of which are not concentric.
The “fluid mass can then, under certain circumstances, actually
assume a position of equilibrium, even when its axis of rotation
is entirely external to the mass itself, and when it thus plays the
part of an inner satellite to the hollow spheroid, with which it
has a common motion of rotation. The existence of such sin-
gular states of equilibrium we will now demonstrate.
Suppose the hollow spheroid, together with the internal fluid
mass, to revolve about the axis of the outer bounding surface of
the spheroid, the axis of the inner bounding surface being parallel
to the axis ofrotation. The fluid mass can then assume a position
of equilibrium in which its figure is that of an ellipsoid of rota-
tion, whose axis is parallel to the above-mentioned axes.
Let the centre of the outer bounding surface be the origin of
a system of rectangular coordinates, the axis of z comeiding with
the axis of rotation. Let m, n, and p be the coordinates of the
centre of the inner bounding surface, and a, 8, y those of the
centre of the fluid mass. The equation of the surface of the fluid
will then be |
poe ae Sa A\2 z— 2
al al mY
If the component parts of the attraction parallel to the axes be
denoted by X, Y, Z, we have
= —Mz-+ M'(e¢—m)—M"(z—2),
Y=—My+M'(y—n) —M"y—8),
Z=—Nz+N!(z—p)—N"(¢—4).
If therefore the angular velocity be denoted by w, we get for the
differential equation of the surfaces de niveau,
(—Mz+M'(2—m)— —M"(¢@—«) ) dae + (— My +M/(y—n)
—M"(y—f) )dy+ (—Nz+N'(z a on )dze
peoecda yey 0, . wes si apc sc atuarerge ea Recs)
where M, M’, M”, N, N’, and N” are pee Ue Me or Bae
Consequently by integration we get
(—M+ M'—M"+w?)(a? + y?) +(—N+ N’—N")z?
+ 2(—M'm + M"a)a + 2(—M'n+ M"B)y
eI yee O.. ies ye oy te ep ee)
As equations (1) and (3) are to be identical, we have the fol-
lowing equations of condition :—
200 M.G. BR. Dahlander on the Equilibrium of a Fluid Mass
—Mm+M"a 7
—2= ME Mp |
—Mn+M"6
cer —M+M!—M! 4 w?’ | (4)
—Np+N'y 2? f
= ae M! + yw? am |
a —N+N!—N! |
2 —M+M RM yur |
From which we obtain
—M'm 7
*=M—M—u? |
—M!n 5
cow Te
1 EN och |
Y= N—N! J
From the first two of equations (5) it follows that
2.2 Batti
The geometrical signification of this proportion is, that the
centre of the fluid mass be in the plane which passes through
the axis of rotation and the centre of the imner bounding surface
of the spheroid. We find, moreover, that the position of this
centre in a state of equilibrium with a fixed angular velocity is
independent of the density of the fluid, supposing the form and
density of the outer spheroid to be the same. Further, we find
that if a fluid ellipsoid satisfy the conditions of equilibrium, all
other similar ellipsoids of the same density will also satisfy these
conditions. Generally, from equations (5), real finite positive or
negative values of a, 6, y can be obtained if M, M’, N, N!, m, n,
p, and ware given. But one or more of these values may become
infinite under certain circumstances. This is the case when the
two bounding surfaces of the solid spheroid are similar. Then
M=WM! and fp N’, whence the value fcr y would be infinite,
unless at the same time p=O0, m which case y can have any
value whatever.
The last of equations (4) constitutes the real equation of con-
dition, which determines the relation which must subsist between
the density, form, and angular velocity of the fluid mass, in order
that equilibrium may be possible for the given values of M, M’,
N, and N’. We shall separately consider the particular case when
es
revolving freely within a Hollow Spheroid. 201
both the bounding surfaces of the surrounding spheroid are
similar.
From what has before been stated, itisevident that pbecomes=0.
We can take for the axis of y a line which lies in the plane
passing through the centre of the fluid mass and the centres of
the bounding surfaces. In this case n=O and 6=0, and also
M=M! and N=N!. We shall now examine if an oblate ellip-
soid of rotation can satisfy the conditions of equilibrium. Sup-
2
posing zal +A?, and the density of the fluid = p, then the
last of equations (4) will become
“es
~ $n wpt (~— arc tan dQ)
2
Say ae
— 3 pf 13 (are tan rA— sa + wy?
2
If Soap b° taken =H, the equation of condition becomes
arc tan X
B= BOG? 43)—5 wee ramets)
But this equation is just the same as that we obtained in de-
termining the conditions of equilibrium of a freely revolving fluid
mass whose particles attract each other. Thus we find that pre-
cisely the same conditions of equilibrium are involved when the
fluid is revolving in a hollow ellipsoid with similar but eccentric
bounding surfaces, and when it is perfectly free. Toa given
value for > there is therefore always a corresponding angular
velocity; and to a given angular velocity there corresponds
either no ellipsoid, or one ellipsoid, or two different ellipsoids,
according as E is = 0:2246.
Between the rotation of a fluid mass confined in a hollow sphe-
roid and a mass which revolves freely, there is, however, this
important difference, that in the former case the rotation does
not take place about the axis of symmetry of the fluid unless
both the bounding surfaces of the spheroid are concentric, but
about a parallel axis which is the axis of symmetry of the outer
bounding surface of the spheroid,—the distance between the
two axes being
CC ve ° . ° ° ° e ° (7)
whence
202 Dr. Woods’s Remarks on
But M’m is the attraction which the hollow spheroid exerts on
any point within it, and aw? is the centrifugal force at the axis of
symmetry of the fluid mass. Whence we find that at the centre of
the fluid mass the acting forces counterbalance each other, which
might have been anticipated from a known theorem in mechanics.
Gothenburgh, January 7, 1861.
XXXI. Remarks on Sainte-Claire Deville’s Theory of Dissocia-
tion. By Tuomas Woops, M.D.
To the Editors of the Philosophical Magazine and Journal.
GENTLEMEN, Parsonstown, February 1861.
N an interesting paper by Sainte-Claire Deville published in
this Magazine last December, that author gives his views on
the decomposition of bodies by heat. His idea of the relation
and behaviour of the constituents forming a compound, towards
each other, is, physically considered, the same as that which I
published in this Journal so long ago as January 1852; that is,
that they act merely as the molecules of a simple body, differing
in nothing from the latter, except that, beimg diverse, they
are capable of attaining a greater proximity among themselves,
and so of causing a greater opposite movement in the particles
of other bodies. A reference to my paper will show a diagram
I gave in order to explain this similarity of constitution. The
paper was therefore the more interesting to me as it brings for-
ward fresh ideas on a thought-of subject. As Ido not, how-
ever, yet agree with what is new in it, I beg to offer a few
remarks on some of its contents; and first with respect to his
theory of dissociation.
Sainte-Claire Deville thinks that compound gases and vapours,
when heated to a certain temperature, as steam at 1000°, undergo
some such change as a solid body does when it liquefies; that
the constituent particles being removed from each other, as well
as the compound particles, the gas loses stability, and that heat
is rendered latent thereby. This condition he calls the disso-
ciated state. I do not find he offers any demonstration of this
state, but that he only ascribes to its influence the production
of some phenomena previously otherwise explained. For instance,
to account for the heat of chemical combination, he takes for
granted, as an example, that the molecules of chlorine and
hydrogen are double, and, even at low temperatures, in the disso-
ciated state; and then ascribes the heat produced by their union
to the latent heat of this particular condition, which he imagines
is given out when the gases by their combination get ito a state
of stability.
Now, if the heat produced in this instance is due to the change
Sainte-Claire Deville’s Theory of Dissociation. 203
of state of the chlorine, how does it happen that the same amount
is produced when the chlorine combines, not being in the gaseous
state at all ? If hydrochloric acid and zinc are placed together, the
chlorine unites with the zinc, and the same quantity of heat is
evolved as when the zinc burns in the gas ; and the same amount is
absorbed by the decomposition as if both the constituents again
attained the gaseous state; or if (to take an instance where no
gas is present, either in combination or decomposition) zine
causes a deposition of copper from chloride of copper, exactly the
same heat is produced by the combination of the chlorine and
copper, and exactly the same quantity is absorbed by the decom-
position, as if the chlorine and copper acted as gases, changing
their state as they combined or decomposed. Unless, therefore,
it is imagined that when the chlorine leaves the copper or hy-
drogen it becomes for a time a gas and enters into the disso-
ciated state, absorbing heat, and again becomes solid, giving it
up, I cannot see how the temperature is raised. But even
granting that it does so the phenomenon could not be accounted
for, because when zinc decomposes chloride of hydrogen or
chloride of copper, more heat is produced by the combination
than is lost by the decomposition: and such could not occur if it
were due to the latent heat of dissociation ; for the heat would be
taken in the first instance from the materials afterwards heated,
and so an exchange only, and not an increase, would be effected.
It might be said that the zinc influences the result ; that is, that
metals have a certain amount of heat connected with them which
is given out in combining, and that this being greater in some
instances than in others, might account for the increase of tem-
perature when the zinc displaces the hydrogen. But if all bodies
have definite quantities of heat, as Sainte-Claire Deville seems to
think, the same order ought to be observed in the amounts evolved
by their combination with the gases. For instance, if an equi-
valent of chlorine, by uniting with zine, copper, silver, &c., pro-
duces heat, the quantity of which varies in the order in which
the metals are named, oxygen ought to do the same, if the
heat evolved in combination was previously connected with the
combining bodies: but it is known that such is not the case.
Chlorine produces more heat with silver than it does with copper,
and oxygen the reverse. Instances of this kind might, of course,
be multiplied ; and they prove, I think, that no fixed amount of
heat, resulting either from change of condition, or from latent
heat becoming evolved as it does in the condensation of vapour,
can be connected with matter as part of its constitution, inde-
pendent of alteration of the relation of particles.
Deville, in fine, thinks that every body possesses a certain
amount of heat, or condition in itself whereby heat can be pro-
204 Dr. Woods’s Remarks on
duced; and therefore one of the combining bodies might evolve
from itself the heat of combination ; whereas the theory I pub-
lished in 1852 divests particles of any influence except that of les-
sening the distance between themselves, or of destroying volume,
as they come together, and so that at least two particles of matter
are essential to its production. In his theory each body en-
gaged in chemical action is said to give out heat by change of
condition; in mine the volume only, or distance between the
constituent particles, is supposed to bealtered. I still think the
latter theory is the more reasonable, and more in accordance with
our present scientific knowledge.
M. Deville seems to reject this latter theory, because the
contraction arising in chemical combination is not equivalent to
the expansion or heat produced; and he calculates the contrac-
tion when oxygen and hydrogen unite, to show that it is not of
the same value or extent as the increase of volume given to other
bodies as the accompanying or opposite movement. He also
shows how chlorine and hydrogen unite without contraction at all;
yet that expansion in other bodies or rise of temperature is the
result. This apparent argument against the theory, however, dis-
appears when it is considered that the particles whose combination
evolves the heat are not the same as those which determine the
volume. When oxygen and hydrogen unite, these elemental
gases themselves, by coming together, cause other bodies to
expand, and so are said to give rise to heat; but the volume
attained by the compound they produce is determined by the
distance between, not the oxygen and hydrogen, but between
the particles of the water that results. In order, therefore, to
calculate the contraction which causes the heat, we should know
what takes place between the constituents of the compound:
the bulk or volume of the compound itself tells nothing.
An argument, therefore, for some necessary change of state
in combining bodies as the cause of heat, drawn from the appa-
rent want of coincidence between the contraction on the one
hand and the heat or expansion on the other, is valueless.
Besides, I have shown (Phil. Mag., January 1852) that the co-
efficient of expansion increasing with the dilatation, the nearer
particles are to each other, the greater 1s the effect they produce
by a given contraction in causing expansion in other bodies; so
that it is not only necessary to know the amount of contraction
amongst the constituents of a compound at the time they com-
bine, but also the distance they ultimately arrive at with respect
to each other, before we can calculate the amount of heat they
ought to produce *.
* In the last edition of Grove’s ‘Correlation of the Physical Forces,’
when speaking of the theory I brought forward in 1852, to account for the
Sainte-Claire Deville’s Theory of Dissociation. 205
But this state of dissociation is altogether founded on gra-
tuitous assumptions. The ground from which it springs is this :
that as compound bodies when heated expand, the constituents
must recede from each other as well as the compound particles.
But this proposition has yet to be proved. I believe many facts
favour an opposite conclusion: for instance, not to speak of the
manner in which solids and fluids, when szmple bodies, expand,
being somewhat similar to the same process in compounds, Gay-
Lussac’s law with respect to the equal expansion of all gases and
vapours for equal increments of heat, would surely show that
the constituents of a compound do not recede from each other
in expanding. Hydrogen, or any other simple gas, and vapour
of ether, or other compound gas, expand exactly according to
the same law. Could this occur with the simple particles of
hydrogen to the same extent precisely as with compound mole-
cules of ether, where, instead of two, we have ten elementary
atoms to divide the distance and moving force between them?
The resistance to expansion of a gas by heat seems to be the
weight of the atmosphere; and consequently in all gases, the
same resistance being present, the same expansion is attained by
a certain increase of temperature. Now in a simple gas the
weight is the only resistance ; whereas, if Deville’s theory is cor-
rect, there is in compound gases not only the weight, but the
affinity of the constituents to be partly overcome; and yet the
same expansion is noticed for the same increase of temperature
in both. But this would be impossible, except we imagine that
the separation of these constituents does not absorb heat, which
we know it does.
It seems to me that this fact alone, of the similar and equal
expansion of simple and compound gases by heat, shows that
no motion takes place in one which does not occur in the other ;
therefore that no expansion of the particles themselves, that is,
that no separation of the simple constituents of the compound
molecule is produced by raising its temperature, and con-
sequently that this state of dissociation does not exist.
A consideration of other portions of the paper would lead me
too far for the present, but I may recur to it if you think the
subject sufficiently teresting for your Magazine.
Your obedient Servant,
THOMAS Woops, M. D.
heat of chemical combination, he seems to think it an objection (page 177)
that the whole expansion which would bean equivalent to the contraction
of the combining particles is not seen in the compound produced; but
surely, as this volume would be the temperature evolved by the combina-
tion, it cannot remain longer than a moment in the compound; it must
be dispersed to surrounding bodies.
[ 206 ]
XXXII. On the Temperature Correction of Siphon Barometers. By
Wixi1am Swan, Professor of Natural Philosophy in the United
College of St. Salvator and St. Leonard, St. Andrews*.
‘a the ‘ Atheneum?’ of the 5th of January, Admiral FitzRoy,
writing on the subject of the temperature correction of
siphon barometers, invites attention to an experiment recently
made by Mr. Negretti. A siphon barometer was heated to
about 110° from some lower temperature, when it was found
that, although the mercury rose in the long or vacuum leg of the
siphon, it did not rise, but seemed to be depressed, in the short,
or open leg. The late Mr. Robert Bryson of Edinburgh invented
a self-registering barometer, which is described in the Transac-
tions of the Royal Society of Edinburgh for 1844+. In that
instrument, variations in the pressure of the atmosphere were
indicated by means of a float resting on the surface of the mer-
cury in the open leg of a siphon tube, precisely as in the ordi-
nary wheel barometer. Mr. Bryson was anxious to ascertain
whether his instrument required any notable correction for tem-
perature; and to settle that point experimentally, a Bunten’s
barometer was heated to a high temperature. In Bunten’s baro-
meter the effective height of the mercurial column is ascertained
by reading two verniers; one indicating the level of the upper,
and the other that of the lower surface of the mercury in a siphon
tube. Mr. Alexander Bryson, who made the experiment, found
that the reading of the upper vernier rapidly changed with increase
of temperature, while the reading of the lower vernier remained ~
sensibly constant,—proving that the level of the mercury in the
open leg of the siphon was very little affected by change of tem-
perature. Mr. Bryson having communicated to me the result
of his experiment, I immediately gave him an investigation of
the temperature corrections of the two surfaces of the mercury
in the siphon barometer, of which the following is substantially
a reproduction. As Admiral FitzRoy has expressed some doubts
regarding the results of observations of siphon barometers “as
hitherto obtained,” I have deemed it desirable to make the fol-
lowing investigation perfectly general, so as to include every form
of tube; and in the first instance I have avoided employing any
formula which is only approximately true.
Let h,, ho be the vertical distances of the upper and lower sur-
faces of the mercury in a siphon barometer, reckoned from any
* Communicated by the Author; the results of the investigation having
been communicated, on the 2nd of February, to the Literary and Philo-
sophical Society of St. Andrews.
T Vol. xv. p. 503.
On the Temperature Correction of Siphon Barometers. 207
horizontal plane below the instrument, and / the barometric
pressure, all at a temperature of ¢ degrees Centigrade. When
the temperature rises to ¢+ A¢ degrees, let the above quantities
become
h,+Ah,, hotAh,, h+Ah;
then, if m=cubic expansion of mercury for one degree Centigrade,
Ah=mhAt.
And since
h=h,—h,
and
h+ Miz (fy + Ady) — (hp + Als),
we have
Ah, —Ah,=Ah=mhAt.
Now if
e = volume of mercury in the barometer;
a = area of the bore of the tube at upper surface of mercury;
6 = area of the bore of the tube at lower surface; all at ¢
degrees ;
9,= the superficial, and g, = the cubic dilatation of glass ;
it will be easily seen that, at the temperature ¢+ A? degrees, the
capacity of that part of the tube which was occupied by the
mercury at ¢ degrees will become c(1-+9,At); while the capacities
*of the portions of the tube at the ends of the former mercurial
column, which are now filled by the expanded mercury, and
whose lengths are Ah,, Ah,, will be
a(l+g,Az)Ah,, 65(1+9,Az)Ah,.
The whole volume of the mercury will therefore be
(aAh, + bAA,)(1+9, At) +¢e(1+9,Az).
But the volume of the expanded mercury must also be
e(1+mAz) ;sx
whence
(aAh, + bAA,) (1 +9,At) =c(m—g_) At.
This equation, along with
Ah, —Ah,=mhAt,
Ane 4e(m—go) +bmh(1 +9,Az)t =
(a+ 6)(1 + 9,42)
Difige {e(m—g.) —amh(1 +9,A?) pAt
(a+6)(1-+ 9,42)
gives
208 Prof. Swan on the Temperature Correction
Now since m is greater than g,, the coefficient of c in the above
values of Ah,, Ah, is positive; and the coefficient of h is also
positive for all possible values of At—g, being a very small quan-
tity. It is therefore obvious that Af, can never vanish, but
that Ah, may be positive, negative, or zero, according to the
values which may be assigned to a, c,andh. The depression,
by heat, of the mercury in the open leg of the siphon, or in
other words, the negative value of AA,, observed by Mr. Negretti,
and the value zero of the same quantity, observed by Mr. Alex-
ander Bryson, are therefore both perfectly accounted for.
It also appears, and this seems to be of practical importance,
that we can altogether get rid of the temperature correction for
the lower surface of the mercury, for any one given atmospheric
pressure, by properly adjusting the value of c, and that thus we
shall be able to make the temperature corrections for all other
pressures exceedingly small.
For this purpose it will be convenient to simplify the expres-
sions for Ah,, Ah, by rejecting small terms. We then obtain
c(m—go) +bmh
Ah,= oat
At,
Ai nga) One od 5
and Ah, will yanish when
__ amh
Jo
A particular case will best illustrate this. Suppose that the
siphon consists of two tubes of a uniform bore a, connected at
the bottom by a narrow channel whose capacity may be neglected.
We have then
e=a(h+2l) ;
Ah, = }(m—go)l + (m— 59o)h} At;
Ahy= }(m—go)l—FGqh} At ;
and when Ah,=0,
[ifs Sens
2(m—Jo)
We must now select some particular value of h for which the
temperature correction is to vanish; and we shall have, upon the
whole, the smallest temperature corrections for extreme values of
h if we make the temperature correction disappear for its mean
value. Assuming then A=29°5 inches as sufliciently near the
of Siphon Barometers. 209
mean atmospheric pressure, and adopting for the coefficients of
cubic expansion of mercury and glass for one degree Centigrade
the values
m='0001803, g,='0000258,
we obtain
[= 2°463 inches.
This indicates a perfectly practicable arrangement. To ren-
der the temperature correction insensible at mean atmospheric
pressures when the siphon tube has a uniform bore, we must
put so much mercury into the tube, that, when the pressure is
29°5 inches, there shall be a column of about 2°5 inches of mer-
cury in the open leg. The temperature corrections throughout
all ordinary fluctuations of atmospheric pressure for the lower
surface of the mercury will then be extremely small, as will be
seen by the following Table :—
Column of mercury Displacement of | Displacement of
Atmospheric in open leg of ~ | Upper surface for a| lower surface of
pressure siphon difference of tempe-| mercury for differ-
(h). rature Az in Centi-| enceof temp. Aé
grade degrees. in Cent. degrees.
31 inches. 1-713 inch. -+'00545 Az —°00014Aé
295 ,, 2-463 ,, +-00531 At -00000A¢
Per ser, 3-213 ,, -L-00518A¢ +-00014A¢
It may be well to observe that the numbers in the last column
of the Table show that if the barometer to which they refer
were heated, as in the experiments already described, and if the
atmospheric pressure were much greater than 29°5 inches, we
should have the result obtained by M. Negretti—a depression
of the mercury in the short leg of the siphon; while if the pres-
sure were nearly 29:5, there would be no sensible change of
level, as observed by Mr. Bryson.
I need scarcely remind the reader, in conclusion, that the for-
mule I have investigated are intended to be employed when only
the upper or only the lower surface of the mercury is observed.
When Joth surfaces are observed, as in the Bunten barometer,
we have simply to apply the ordinary and well-understood cor-
rection, due to the expansion of mercury by heat.
United College, St. Andrews,
February 16, 1861.
Phil. Mag, S. 4. Vol. 21, No, 189. March 1861 P
[A2TO.:3
XXXIII. Note on Mr. Jerrard’s Researches on the Equation of
the Fifth Order. By A. Cayuny, Esq.*
» | elena of the same set of quantities which are, by
any substitution whatever, simultaneously altered or si-
multaneously unaltered, may be called homotypical. Thus all
symmetric functions of the same set of quantities are homo-
typical: (v7+y—z—w)? and wy+zw are homotypical, &e.
It is one of the most beautiful of Lagrange’s discoveries
the theory of equations, that, given the value of any function of
the roots, the value of any homotypical function may be rationally
determined +; in other words, that any homotypical function what-
ever is a rational function of the coefficients of the equation and
of the given function of the roots.
The researches of Mr. Jerrard are contained in his work, ‘‘ An
Essay on the Resolution of Equations,’ London, Taylor and
Francis, 1859. The solution of an equation of the fifth order is
made to depend on an equation of the sixth orderin W; and he
conceives that he has shown that one of the roots of this equa-
tion is a rational function of another root: “The equation for
W will therefore belong to a class of equations of the sixth
degree, the resolution of which can, as Abel has shown, be
effected by means of equations of the second and third degrees ;
whence I infer the possibility of solving any proposed equation
of the fifth degree by a finite combination of radicals and rational
functions.”
The above property of rational expressibility, if true for W,
will be true for any function homotypicalwith W ; and conversely.
I proceed. to inquire into the form of the function W.
The function W is derived from the function P, which denotes
any one of the quantities p,, po, p3. And if x, Xo, Ly, L4, Lz are
the roots of the given equation of the fifth order, andif a, 8, y, 6, €
represent in an undetermined or arbitrary order of succession
the five indices 1, 2, 3, 4, 5, and if e denote an imaginary fifth
root of unity (I conform myself to Mr. Jerrard’s notation), then
Pv Pa Ps; and the other auxiliary quantities ¢, u, are obtained from
the system of equations—
* Communicated by the Author.
t+ The @ priori demonstration shows the eases of failure. Suppose that
the roots of a biquadratic equation are 1, 3, 5,9; then, givena+6=8, we
know that either a=3, b=5, or else a=5, b=3, and in either case ad=15;
hence in the present case (which represents the general case), a+b being
known, the homotypical function ad is rationally determined. But if the roots
are 1, 3, 5, 7 (where 1+7=3+5), then, given a+)=8, this is satisfied by
3 aes
G =). or by G = i and the conclusion is ad=15 or 7; so that here
ab is determined, not as before, rationally, but by a quadratic equation.
On the Equation of the Fifth Order. 211
Vet P\LatPo@atps= t+ uy,
apt peat pote t+ps= b+eu,
@y + Pt, + poly + py=Ct+ Pu,
25 + py X5 + po%s+pz= 3¢+ vu,
Het p Let pote tpg t+ w.
If from these equations we seek for the values of p,, Po Ps t, Uy
we have
By: Jo? 75:—t:—u=ll,: 4:1: T,: Wy: ly
where IJ,, II,,.. denote the determinants formed out of the
matrix
cc mec ame Aiea ee
v Bp x ee LBs Des Dy
ae a Bo hr akgco ees 3
& 3 ? U5, cS Wea Re uP
& 2 Cpe Bagi bcd Gea
2.e., denoting the columns of this matrix by 1, 2, 3, 4, 5, 6, we
have 11,=23456, T,= —34561, H,=45612, &e. In par-
ticular, the value of II, is
— eer @udae bs 2, Loge
aT tine OE a
PISA NG
x 33 a; 1, e 2
Ue Ras ie AA
And developing, and putting for shortness {a8} =x,49(%.—4p);
&c., we have
Tl, =( {a8} + {By} + fyot + {det + feat )\(—26+-—8 +204)
+ (faryh + {yet + feBt + 180} + {Sat )(+e4+22—23—204),
And this is also the form of the other determinants, the only
difference being as to the meaning of the symbol {a6}, which,
however, in each case denotes a function suchthat {apt =— ; Ba} :
Writing for greater shortness,
{oBryde} = faB} + {Bry} + {y8} + {oe} + feat,
and in like manner :
ee dens ca taeies Wict mune is mat lane Bas cs
I], is an unsymmetric linear function (without constant term) of
| P2
212 Mr. A.Cayley’s Note on Mr. Jerrard’s Researches
{aPryde}, Sauye8o' ; or, what is all that is material, it is an un-
symmetric function, containing only odd powers, of {aByéde},
fayeBo',
If for aByde
we substitute any one of the five arrangements
aBy de,
Bydea,
y dea,
o ea 6 y,
ea By 6,
then {aByde} and {aye8o} will in each case remain unaltered.
But if we substitute any one of the five arrangements
aedy B,
E4098 we,
oy fae,
yBae o,
Baedy,
then in each case {aPrydet and {ayeB8o} will be changed into
— SaBydel and — }ayeBo} respectively. Hence I, remains un-
altered by any one of the first five substitutions ; and it is changed
into —II, by any one of the second five substitutions. And the
like being the case as regards II,, &c., 1t follows that the quotient
a or say P, remains unaltered by any one of the ten substitu-
tions. Now the 120 permutations of «, 8, y, 6, « can be ob-
tained as follows, viz. by forming the 12 different pentagons
which can be formed with @, 8, y, 6, € (treated as five points),
and reading each of them off in either direction from any angle.
To each of the 12 pentagons there corresponds a distinct value
of P, but such value is not altered by the different modes of
reading off the pentagon ; P is consequently a 12-valued function.
But there is a more simple form of the analytical expression
of such a 12-valued function ; in fact, if [a@@yde] be any func-
tion which is not altered by any one of the above ten substitu-
tions—if, for instance, [#8] is a symmetrical function of x, @g,
and
[«Byde] = [a8] + [By] + [8] + [Se] + [ex],
[eye8d] = [ay] + [ye] + [8] + [80] + [de],
then any unsymmetrical function of [aSyde] and [ayeBd] will
be a 12-valued function homotypical with P.
an
on the Equation of the Fifth Order. 213
Mr. Jerrard’s function W is the sum of two values of his
function P ; the substitution by which the second is derived from
the first can only be that which interchanges the two functions
[«Byde] and [aye8o] ; and hence any symmetrical function of
[«Pyde] and [wyeGd] is afunction homotypical with Mr. Jerrard’s
W; such symmetric function is in fact a 6-valued function only.
Indeed it is easy to see that the twelve pentagons correspond
together in pairs, either pentagon of a pair being derived from
the other one by séed/ation, and the six values of the function in
question corresponding to the six pairs of pentagons respectively.
Writing with Mr. Cockle and Mr. Harley,
T = LyXgt Lply + XX3 t+ XjX,+L Ag
= 2,@y + LyTe+ LM gt Lets tUploy
then (r+7' is a symmetrical function of all the roots, and it
must be excluded ; but) (tT—7')? or 77’ are each of them 6-valued
functions of the form in question, and either of these functions
is linearly connected with the Resolvent Product. In Lagrange’s
general theory of the solution of equations, if
ft=2, +l, 4+ Cr+ Px, + 25,
then the ee of the equation the roots whereof are
( ft), (fe?)®, (fe*)?, (fr), and in particular the last coefficient
(fifi? Joan )5, are peta by an equation of the sixth degree ;
and this last coefficient is a perfect fifth power, and its fifth root,
or fi fi*fi* fr’, is the function just referred to as the Resolvent
Product.
The conclusion from the foregoing remarks is that 2f the equa-
tion for W has the above property of the rational expressibility of
its roots, the equation of the sixth order resulting from Lagrange’s
general theory has the same property.
T
I take the opportunity of adding a simple remark on cubic equa-
tions. The principle which fur nishes what in a foregoing foot-
note is called the @ priort demonstration of Lagrange’s theorem is
that an equation need never contain extrancous roots ; a quantity
which has only one value will, if the investigation is properly
conducted, be determined in the first instance “by a linear equa-
tion ; one ‘which has two values by a quadratic equation, and so
on ; Pie is always enough, and not more than enough, to
determine what is required.
Take Cardan’s solution of the cubic equation #?+qgxe—r=0,
we have az=a+0, and thence 3ab=—gq, a?+0°=r; and to
obtain the solution we write
. a= — 5, a+b=r,
214 Prof. Davy on some further applications of
But these two equations are not enough to precisely determine a,
they lead to the 9-valued function
Py 2 3 A os.
? 7 g 7 af eo a
2 — 4.4.4 his hating §
VJ; +a/ 4. OF ate ae 4 * 97
in order to precisely determine x, it is (as everybody knows)
necessary to use the original equation ad= — * But seek for
the solution as follows; viz. write e=ab(a+5), which gives
8a°b?=—g, a®b?(a?+b*) =r,
or what is the same thing,
As ae ~3, Plat | ee hs sual
these equations give v=ab(a+b), where
3 a hoe ere
a= ene Orie d = pan) — n/a son ee or f
ay‘ ate ? 4g? * 3’
which is a 3-valued function only, ad in this case a not given.
2 Stone Buildings, W.C.,
January 28, 186].
XXXIV. Onsome further applications of the Ferrocyande of Po-
tassium in Chemical Analysis. By KymMunpd W. Davy, A.B.,
M.B., M.RILA., Professor of Agriculture and Agricultural
Chemistry to the Royal Dublin Society*.
| HAVE recently been engaged in making some experiments
on the ferrocyanide of potassium or yellow prussiate of
potash, with a view to extend its applications in chemical ana-
lysis ; for though this important salt has already been applied to
a number of useful purposes in analytical research, still my ex-
periments have shown me that its use might be advantageously
extended, particularly as a reagent in volumetric analysis, a form
of analysis which has of late come into very general adoption,
especially for technical purposes, on account of the great quick-
ness and at the same time accuracy with which different sub-
stances may by its means be determined. The principles upon
which volumetric analysis depend are so well known, that I
need not refer to them; and though it possesses so many ad-
vantages over the older gravimetrical method, in which the dif-
ferent substances are determined by weight instead of by volume,
it yet has this drawback, that the preparation of the necessary
standard solutions often takes considerable time, first, in order
* Part of a paper read before the Royal Dublin Society, December 17,
1860 ; and communicated by the Author,
the Ferrocyanide of Potassium in Chemical Analysis. 215°
to obtain the substance to be used for this purpose in a suf-
ficiently pure and dry state, and secondly, to form a solution
of it the exact strength of which may be known: for though
it may appear avery simple operation to dissolve a known weight
of a certain substance in a given bulk of water or other solvent,
yet, when this has to be done with such great precision as is
necessary in these cases, it is a tedious and troublesome opera-
tion, and any inaccuracy in the graduation ofthe standard solu-
tion will render all determinations made with it more or less
inaccurate. It is obvious, therefore, that it would be most de-
sirable that the substances which are intended to be used as re-
agents in volumetric analysis should be easily obtained in a pure
state, and that where considerable time and trouble have been
expended in graduating solutions of those substances, they should
not be liable to undergo changes whereby their strength would
be more or less altered, but that when standard solutions have
once been made, they might be kept and used for a great num-
ber of determinations.
The ferrocyanide of potassium fulfils both those conditions ;
for it is in general met with in commerce almost chemically
pure, and in a state in which it can at once be employed asa
volumetric reagent ; andif at any time it should happen to occur
not quite so pure, it can readily be purified by recrystallization ;
and in addition to these important considerations, its solution is
not prone to change, especially if it be not left exposed to the
action of the light. In this latter respect it has a decided
advantage over several of our most useful volumetric reagents,
viz. the permanganate of potash, the protosalts of iron, sul-
phurous acid, &c., which, from their bemg so prone to undergo
spontaneous decomposition, must be either freshly prepared,
or the strength of their solutions accurately ascertained every
time they are used, if a day or so has elapsed between each de-
termination.
The employment of the ferrocyanide of potassium as a volu-
metric reagent depends on the following circumstances : viz., that
it is readily converted into the ferrideyanide of potassium (red
prussiate of potash) under different circumstances, and that the
point where the whole of the former salt has been changed into
the latter may easily be known, either by the use of a diluted
solution of a persalt of iron (which gives with a drop of the mix-
ture a blue or green coloration as long as any of the ferrocyanide
remains unchanged) or by some other simple indication. Thus,
for example, when chlorine is brought in contact with the ferro-
cyanide of potassium, this change, as is well known, takes place,
which is expressed by the following symbols :—
2 (K2, Fe Cy’) + Cl=(K? Fe? Cy®) +K Cl.
216 _ Prof. Davy on some further applications of
The same occurs, as far as the conversion of the ferrocyanide
into ferrideyanide, when an acidified solution of the former salt
is brought in contact with a solution of the permanganate of
potash, which is instantly decolorized by the reducing action of
the ferrocyanide of potassium, which is thereby converted into
the ferridcyanide, and this decoloration of the permanganate
continues as long as any of the ferrocyanide remains in the mix-
ture.
Again, if a solution of the ferrocyanide of potassium, acidified
strongly with either hydrochloric or suiphuric acid, be brought
in contact with a solution of the bichromate of potash, the same
change of the ferrocyanide into the ferridcyanide immediately
takes place.
The first reaction has been long known, and 1s the means em-
ployed at present for obtaining the ferridcyanide or red prussiate
of potash for manufacturing and other purposes; the second re-
action has been more recently discovered; but I am not aware
that the third, in the case of the bichromate, is generally known,
or that the changes which occur in the reaction have been pre-
viously studied.
From experiments which I made, it would appear that when a
solution of ferrocyanide of potassium, acidified with hydrochloric
acid, was mixed with one of the bichromate of potash, the follow-
ing reaction was produced, viz. 6(K? Fe Cy?) + KO, 2 Cr O®
+7HC]=3(K? Fe? Cy®) + 4 KC1+ Cr? C+ 7HO; for, amongst
other facts, I may observe that when I mixed together solutions
of the two salts in the proportions corresponding to 6 equiva-
lents of the ferrocyanide of potassium to 1 of the bichromate
of potash (as indicated in the above formula), acidifying the
mixture with hydrochloric acid, I found that the whole of the
ferrocyanide was converted into the ferrideyanide, and that any
quantity less than that proportion of the bichromate of potash
left more or less of the ferrocyanide unchanged. The same
results followed the use of sulphuric acid; and it appears that a
similar reaction occurs with this acid as with hydrochloric acid,
with the exception that in this case the 4 equivalents of chloride
of potassium and the 1 equivalent of sesquichloride of chromium
are replaced by 4 equivalents of sulphate of potash and 1 of the
sesquisulphate of chromium.
The proportion of either acid used, provided there is enough
to strongly acidify the mixture, does not appear to affect the re-
action; for I obtaimed precisely the same results where a very
large amount of acid was employed as where the quantity neces-
sary Only to strongly acidify the mixture had been added.
On these three reactions which I have noticed, may be based
the means of employing the ferrocyanide of potassium in several
the Ferrocyanide of Potassium in Chemical Analysis. 217
useful determinations, the first, and one of the most important,
of which is the ascertaining the amount of available chlorine in the
chloride of lime or bleaching powder, which is a matter of much
importance in many of the chemical arts, but particularly in
bleaching ; for not only does the commercial value of this sub-
stance depend on the quantity of available chlorine that it con-
tains, which is subject to great variation from exposure to the
air and other causes, but likewise it is of the greatest importance
that the bleacher should readily be able to determine from time
to time the strength of the bleaching liquor which he employs:
for if it be too strong, he knows that the fabric which he bleaches
will be injured; and if too weak, it will not be sufficiently bleached,
and the process must be repeated, which mcurs much additional
expenditure of time.
Various methods have from time to time been proposed for the
determination of the value of chloride of lime; but the greater
number of them, from the trouble required to make the test-so-
lutions, and their not keeping when made, as well as the skill re-
quired in their use, render them inapplicable for general purposes.
I shall therefore merely refer to the two methods which are
chiefly used at present to determine the value of this important
substance. The first is Gay-Lussac’s, in which the amount of
chlorine is ascertained by seeing how much chloride of lime is
necessary to convert a given quantity of arsenious into arsenic
acid ; the second is Otto’s, in which protosulphate of iron is sub-
stituted for arsenious acid, and the determination of chlorine is
made by seeing how much of the bleaching powder is required
to change a given weight of the protosulphate of iron into a per-
salt of that metal: these processes are so well known that I need
not describe them.
In both these methods I find that more or less chlorine is
always lost, which, however, may be reduced toa minute quantity
by very carefully adding the solution of chloride of lime either
to that of arsenious acid, or of protosalt of iron ; but in ordinary
hands they (especially the latter process) will yield results in
which too small a proportion of chlorine will be indicated, from
the loss of that substance which will invariably take place.
The ferrocyanide of potassium answers admirably for the
estimation of available chlorine in the chloride of lime, when used
in the manner I shall presently explain, and according to my
experiments will give in ordinary hands far more accurate results
than either Gay-Lussac’s or Otto’s method. I am aware, in-
deed, that this salt was proposed by Mr. Mercer some years ago
for this purpose; but the way which he recommended it to be
used (which consisted in dissolving a certain weight of the ferro-
cyanide in water, acidifying it, and then adding the solution of
218 Prof. Davy on some further applications of
bleaching powder from a burette till all the ferrocyanide was con-
verted into ferridcyanide) 1s, I find, not a good manner of employ-
ing the ferrocyanide in this estimation, and, like the other
methods, will lead to aloss of chlorine; for when the solution of
chloride of lime is added to the acidified ferrocyanide, a portion
of the chlorine is. separated, especially if the bleaching liquor be
added too quickly, or is not greatly diluted. But the way I pro-
pose of using the ferrocyanide of potassium in this important
valuation, is to mix together a certain quantity of a standard solu-
tion of ferrocyanide with a given amount of a graduated solution
of the chloride of lime, using more of the former salt than the
latter can convert into ferridcyanide ; then adding hydrochloric
acid to dissolve the precipitate formed and render the mixture
strongly acid, and finally ascertain, by means of a standard solu-
tion of bichromate of potash, how much of the ferrocyanide_re-
mained unconverted into the ferridcyanide by the action of the
chlorine of the chloride of lime,—which is effected by adding
slowly from a graduated burette the standard solution of bichro-
mate till a minute drop taken from the well-stirred mixture by
means of a glass rod, ceases to give, with a small drop of a very
dilute solution of perchloride of iron placed on a white plate, a
blue or greenish colour, but produces instead a yellowish brown*.
When this latter effect is observed, it indicates that all the ferro-
cyanide has been converted into ferridcyanide; and as 147-59
(one equivalent) of bichromate of potash is capable of converting
1267°32 (six equivalents) of crystallized ferrocyanide of potassium
into ferridcyanide, and as 422°44 (two equivalents) of the ferro-
cyanide are converted into the same substance by 35°5 (one
equivalent) of chlorine, as is seen by the formule already given,
knowing the amount of chloride of lime employed, we have all
the data necessary to calculate the per-centage of chlorine.
Having made two standard solutions, the first contaiming
21:122 grammes of ferrocyanide of potassium in a litre of the
solution, and the second 14°759 grammes of bichromate of pot-
ash in the same quantity of solution (weights which are to each
other as their atomic equivalents), | made several estimations of
chloride of lime with them, adopting the method I have just
described, and found that it gave the most consistent results, and
which agreed very closely with those obtained by Gay-Lussac’s
and Otto’s methods when the latter were performed with the great-
est care,—the only difference being that the results obtained by
* The yellowish-brown coloration which is at first produced when
enough of the bichromate has been added, quickly changes to a greenish
colour by some secondary reactions which take place when the persalt of
iron is left in contact with the mixture. but this does not interfere with
the test ; for it is the first effect which is produced which indicates the com-
pletion of the reaction, and not the after changes which may result.
the Ferrocyanide of Potassium in Chemical Analysis. 219
my method indicated a few hundredths of a part more of chlorine
than either of those methods did, which may be accounted for
by the unavoidable loss of a minute quantity of chlorine which
takes place in those processes.
In order to simplify the process, and render the calculation
as short as possible, | would recommend for commercial valua-
tions the following way of carrying out this principle :—
Haying obtained a flat-bottom flask or bottle which will con-
tain 10,000 grains of distilled water when filled up to a certain
mark in the neck, make two standard solutions, the first by
placing in the flask or bottle 1190 (or exactly 1189°97*) grains
of the purest crystallized ferrocyanide of potassium (yellow
prussiate of potash) reduced to powder, adding distilled water
to dissolve the salt, and when this is effected, fillmg up with
water to the mark; and having mixed the solution thoroughly,
place it in a well-stoppered bottle. The second standard solution
is made in the same manner, substituting for the ferrocyanide
138°6 (or exactly 138°58) grains of bichromate of potash which
has been purified by recrystallization and fused in a crucible at
as low a heat as possible. Both these solutions will keep un-
changed, and will answer for a number of determinations if they
are preserved in well-stoppered bottles, and the ferrocyanide
solution be kept, when not in use, excluded from. the light.
Get a burette or alkalimeter capable of holding or delivermg
1000 grains of distilled water, and divided into 100 equal
divisions ; also two small bottles, one capable of delivering 1000
grains, and the other 500 grains of distilled water when filled
up to a certain mark on the neck of eacht, which may both be
readily made by fillmg them with water, emptying them, and
after they have drained for a minute or two, weighing into each
the above weights of distilled water ; or, what will be sufficiently
accurate for most purposes, pour from the burette into one 100
divisions of distilled water, and into the other 50, and mark
with a file where the fluid stands im the neck of each bottle.
Having these all ready, take an average specimen of chloride of
lime, and weigh out 100 grains of it, and make in the usual
way a solution of it by trituration in a mortar with some
* The above numbers are obtained as follows :—35'5 parts of chlorine
are capable, as before stated, of converting 422°44 parts of the crystallized
ferrocyanide of potassium into ferridcyanide; therefore 100 parts of the
former will convert 1189°97 parts of the latter into the same compound.
Again, as before observed, 1267°32 parts of the crystallized ferrocyanide
require 147°59 parts of the bichromate of potash to convert them into the
ferridcyanide; 1189-97 parts, therefore, will take 138°58 parts of that salt
to produce the same cifect.
+ Two small pipettes capable of delivering the above quantities would
be found still more convenient,
220 Prof. Davy on some further Applications of
water; pour it into the flask which was used in preparing the
two standard solutions, and having filled up with water to the
mark in the neck, mix the solution thoroughly; and before each
time that any of the chloride of lime is taken out, shake well
the contents of the flask.
Measure out into a beaker-glass, by means of the two little
bottles, 100 divisions of the chloride of lime solution, and 50 of
the standard solution of ferrocyanide; and having mixed them
well together, add some hydrochloric acid to dissolve the preci-
pitate formed and acidify the mixture strongly ; and having
mixed the whole well, pour from the burette slowly the standard
solution of bichromate (stirring well all the while) till a drop
taken from the mixture and brought in contact with a drop of a
very weak solution of perchloride of iron produces a yellowish-
brown colour, as already noticed. Then read off the number of
divisions of the standard solution of bichromate which was
necessary to produce this effect; and this being deducted from
50, gives the per-centage by weight of chlorine.
For the standard solution of ferrocyanide having been made
so that the 10000-grain measures should be equivalent to 100
grains of chlorine, and as every division of the burette equals 10
grains, each of these divisions of the ferrocyanide solution con-
verted into ferrideyanide will indicate O°1 grain of chlorine.
Again, the 100 divisions of the solution of chloride of lime
represent lO grains of that substance, and we want to know
how many divisions of the ferrocyanide solution its chlorine has
converted into ferridcyanide. This is readily ascertained by
the bichromate solution, which has been so graduated that
each division represents a division of the ferrocyanide solution.
So that to determine the per-centage of chlorine we have only
to deduct, as before stated, the number of divisions of the
bichromate solution employed from the 50 of the ferrocyanide
solution, and the difference gives us the per-centage of chlorine
by weight in the sample; thus in four experiments 50 divisions
of the ferrocyanide solution, mixed with 100 divisions of the
solution of chloride of lime, required 18:5 divisions of the bi-
chromate solution to convert the whole of the ferrocyanide em-
ployed into ferrideyanide; this number, taken from 50, leaves
31°5 divisions of ferrocyanide, which were-converted into ferrid-
cyanide by the chlorine of the chloride of lime; and as each
division represents 0-1 grain of chlorme, 31°5 will be equivalent
to 3°15 grains of chlorine, which is the amount contaimed in 10
grains of the sample ; consequently 100 grains will contain
31°5 grains of chlorine, which is the same amount as is obtained
by simply deducting the number of divisions of bichromate solu-
tion employed from 50 of ferrocyanide used in the estimation.
the Ferrocyanide of Potassium in Chemical Analysis. 221
Though this process appears a long one, from the details which
are necessary to explain its principle, yet in practice it is very ex-
peditious, and requires only a very few minutes for its performance,
and is much quicker than either Gay-Lussac’s or Otto’s method.
Though I have as yet chiefly confined my attention to the
use of the ferrocyanide of potassium in the estimation of
chlorme in bleaching powder, I have no doubt that it may
be advantageously employed in many other useful determinations
by carrying out the principles already explained: thus, for
example, it may be used as a means of determining the amount
of bichromate of potash present in a sample of that salt, or
the quantity of chromic acid that exists under different circum-
stances. Again, the same salt may be used in different deter-
minations where a certain amount of chlerine is liberated, which
represents a proportional quantity of some other substance: thus,
for example, in the estimation of manganese ores for commercial
purposes, where they are heated with hydrochloric acid, the
quantity of chlorine disengaged will indicate a certain amount
of peroxide of manganese in the ore, on the presence of which
its commercial value almost entirely depends ; and the chlorine
evolved may be estimated by absorbing the gas in a dilute
solution of caustic potash, and then determining the amount of
chlorine in it by precisely the same process as that I have re-
commended in the valuation of chloride of lime. To test the
accuracy of this method, I heated in a small flask a given
quantity of pure bichromate of potash with an excess of strong
hydrochloric acid, and collected the evolved chlorine by means
of a dilute solution of caustic potash, employing the bulbed
retort and curved dropping tube as recommended by Bunsen in
the “‘Analysis of the Chromates” (see the last editionof Fresenius’s
‘Quantitative Analysis,’ page 234), and ascertained afterwards, by
the use of the ferrocyanide of potassium, the amount of chlozine
evolved, which corresponded almost exactly with the calculated
amount of that substance which should have been obtained by
the action of the quantity of bichromate used on the hydrochloric
acid. Again, a standard solution of ferrocyanide of potassium
may be used, as i. de Haen has shown, to determine the strength
of the permanganate of potash in the analyses of the ferrocyanide
and ferrideyanide of potassium, as an acidified solution of the
ferrocyanide, as before stated, rapidly decolorizes a solution of
permanganate of potash, whereas the ferrideyanide has no
action on that salt; and this reaction might be taken advantage
of, in the valuation of chloride of lime, to determine the excess
of ferrocyanide used in my process: but from my experiments
I found that more precise and accurate results were obtained by
the use of the bichromate of potash.
222 Prof. Davy on some further applications of
The reaction of the bichromate of potash on the ferrocyanide
might be employed in the valuation of the ferrocyanide of
potassium and other ferrocyanides—having previously,in the case
of those which were insoluble, converted them into the ferro-
cyanide of potassium by boiling them with caustic potash, and
separating the insoluble oxides by filtration.
It might also be employed for the valuation of the commercial
red prussiate of potash, which is now to some extent employed
as a bleaching agent in calico-printing, and which consists of
varying quantities of ferro- and ferrid-cyanide of potassium
together with chloride of potassium. By ascertaining first how
much a given quantity of the sample requires of a standard solu-
tion of bichromate of potash to convert the ferrocyanide present
into ferridcyanide, the per-centage of that substance would be
known ; and then by taking another portion of the sample and
converting the ferridcyanide it contained, by reducing agents,
such as the sulphites of soda and potash, &c., into the ferrocyanide,
and finally determining the amount of bichromate necessary to
bring the whole of the ferrocyanide then present into the state
of ferridcyanide, the difference in the two results would indicate
the proportion of ferridcyanide originally present in the sample.
The last application of ferrocyanide of potassium which I shall
notice in the present communication, is its employment as a
reducing agent. It has long been known that the cyanide of
potassium possesses most powerful reducing properties, and has
been very usefully employed for that purpose in the reduction of
different metallic salts under various circumstances; but I am
not aware that the ferrocyanide of potassium has been proposed
or used for similar purposes: at least, I have referred to a great
number of analytical and general chemical works, and in none
of them is this salt recommended as a reducing agent, though
the cyanide is so much extolled for that purpose. According
to my experiments, the ferrocyanide is a far more convenient
reducing agent than the cyanide, and may be substituted for it
in many cases of reduction with the best results, as it possesses
many unquestionable advantages over that salt for this purpose.
Thus the ferrocyanide does not deliquesce and decompose when
exposed to the air, whereas the cyanide rapidly absorbs moisture,
and, unless kept in very well-stoppered bottles, becomes quite wet,
and in this state quickly decomposes; and this deliquescence on the
part of the cyanide is often a source of much inconvenience in its
use as a reducing agent, owing to the almost unavoidable absorp-
tion of more or less moisture which takes place in mixing it with
the substance to be reduced, and during the introduction of the
mixture into the reducing tube. The ferrocyanide, on the other
hand, in a thoroughly dried and finely powdered state, can be
the Ferrocyanide of Potasstum in Chemical Analysis. 223
intimately mixed with the substance without any appreciable
absorption of moisture. I made the following comparative ex-
periment to ascertain the relative absorptive properties for mois-
ture of the two salts under the same circumstances. Having
thoroughly dried in a water oven, till it ceased to vary in weight,
some finely powdered ferrocyanide, I placed 50 grains of it in a
counterpoised watch-glass, and powdering in a warm mortar
some fresh cyanide of potassium, I placed the same quantity of
itn a similar counterpoised watch-glass, and left them both
exposed to the air. On examining them after four hours’ expo-
sure, I found that the former had only gained ;8>th parts of a
grain of moisture, whereas the latter had taken up 3°6 grains,
or sixty times as much moisture under the same circumstances.
After two days’ exposure I found that nearly all the cyanide had
passed into the liquid condition, having taken up 46 grains of
water ; whereas the ferrocyanide appeared perfectly dry, and
had only absorbed 1°4 grain.
The great fusibility of the cyanide is sometimes rather a dis-
advantage, which has to be lessened by mixing it with a certain
proportion of dried carbonate of soda; but the ferrocyanide not
fusing at so low a temperature, does not require in most cases
this admixture to lessen its fusibility. Again, the ferrocyanide is
not a poisonous salt, whereas the cyanide is highly so, and must
be used with great caution; and lastly, the former salt is little
more than half the price of the latter. Combined with the above
advantages, I find that the ferrocyanide is equally effective in re-
ducing metallic oxides and sulphurets, and is especially con-
venient for the reduction of different combinations of arsenic and
mercury, which are reduced by it with the greatest ease.
I made several comparative experiments with the dried ferro-
cyanide and with the cyanide as reducing agents for the sulphuret
of arsenic and arsenious acid, employing the same quantity of
arsenical compound with each salt under similar circumstances ;
and in almost every case, particularly where the quantities
operated on were minute, I obtained more satisfactory results
with the dried ferrocyanide than with the cyanide.
The followmg were amongst my experinents :—I mixed the
zath of a grain of sulphuret of arsenic with 3 grains of the dried
ferrocyanide, and made a similar experiment, substituting the
same quantity of cyanide; and on heating the mixtures in similar
glass tubes, obtained almost identically fine and characteristic
rings of metallic arsenic.
I then intimately mixed the same quantity of sulphuret of
arsenic with 49-9 grains of very finely powdered glass, and taking
5 grains of this mixture, containmg the ygoth part of a grain
of the sulphuret, mixed it with 5 grains of the dried ferrocyanide,
and made a comparative experiment with another 5 grains of the
224 Royal Society :—
mixture, substituting the same quantity of cyanide; on heating
both these mixtures in small reduction tubes, I got the charac-
teristic metallic rigs in both, but better defined in the case of
the ferrocyanide. |
I finally took 2°5 grains of the mixture of sulphuret and glass,
containing about z;%oth parts ofa grain of sulphuret of arsenic,
and treated them in the same manner, using in one case 2°5 grains
of ferrocyanide, and in the other 2°5 grains of cyanide, and
obtained in each case a minute metallic ring, which, however,
was much more distinct and satisfactory where the ferrocyanide
had been used as the reducing agent.
The same comparative experiments were made with arsenious
acid, when results similar to those in the case of the sulphuret of
arsenic were obtained.
The ferrocyanide, therefore, is a most delicate reducing agent
in the case of arsenical compounds, and where very minute quan-
tities have to be detected, appears from my experiments to give
more satisfactory results than the cyanide.
Whether the addition of dried carbonate of soda would improve
the ferrocyanide for some cases of reduction, I am not at present
able to say; but in one experiment which I made with the sul-
phuret of arsenic, I obtained as good results, using the fer-
rocyanide alone, as where it was mixed previously with its own
weight of dried carbonate of soda. In many cases the ferro-
cyanide may be used as a reducing agent in a state of powder
without separating its water of crystallization ; but, in most cases,
it will be rendered a far better reducing agent by being previously
dried at 212° in a water-bath or oven; and in this dried condition
it may be kept for any length of time in a good-stoppered or
well-corked bottle.
Though as yet my experiments have been chiefly confined to
the reduction of different compounds of arsenic and mercury, I
entertain no doubt that the ferrocyanide of potassium will be
found an equally effective reducing agent im the case of the
combinations of other metals, and that it may with great advan-
tage be substituted for the cyanide of potassium in many cases
where the latter salt is used as a reducing agent.
XXXV. Proceedings of Learned Societies.
ROYAL SOCIETY.
(Continued from p. 153.]
April 26, 1860.—Sir Benjamin C. Brodie, Bart., Pres., in the Chair.
NHE following communication was read :—
“On the Effect of the Presence of Metals and Metalloids upon
the Electric Conductivity of Pure Copper.’ By A. Matthiessen, Esq.,
and M. Holzmann, Esq.
After studying the effect of suboxide of copper, phosphorus,
Dr. Chowne on the Elastic Force of Aqueous Vapour. 225
arsenic, sulphur, carbon, tin, zine, iron, lead, silver, gold, &c., on
the conducting power of pure copper, we have come to the conclusion
that there is no alloy of copper which conducts electricity better than
the pure metal.
May 3.—Sir Benjamin C. Brodie, Bart., President, in the Chair.
The following communications were read :—
**On the relations between the Elastic Force of Aqueous Vapour,
at ordinary temperatures, and its Motive Force in producing Currents
of Air in Vertical Tubes.” By W. D. Chowne, M.D., F.R.C.P.
In 1853 the author of this communication made a considerable
number of experiments which demonstrated that when a tube, open
at both ends, was placed vertically in the undisturbed atmosphere of
a closed room, there was an upward movement of the air within the
tube of sutticient foree to keep an anemometer of light weight in a
state of constant revolution, though with a variable velocity. An
abstract of the results of these experiments was printed in the Phi-
losophical Magazine, vol. xi. p. 227.
In order to further investigate the immediate cause or nature of
the force which set the machine in motion, the author instituted a
series of fresh experiments.
These experiments were made in the room described in the former
communication, guarded in the same manner against disturbing
causes, and with such extra precautions as will be hereafter explained.
The apparatus used was a tube 96 inches long and 6°75 inches
uniform diameter, the material zinc. The upper extremity was open
to its full extent; at the lower, the aperture was a lateral one
only, into which a piece of zine tube 3 inches in diameter, and bent
once at right angles, was accurately fitted with the outer orifice
upward, Within this orifice, which was about 5 inches above the
level of the floor, an anemometer, described in the former paper, and
weighing 7 grains, was placed in the horizontal position. About
midway between the upper and, the lower extremity of the tube, a
very delicate differential thermometer was firmly and permanently
fixed, with one bulb outside and the other inside, and the aperture
through which the latter was inserted completely closed. The scale
was on the stem of the outer bulb.
The results of a long series of observations were recorded. The
state of the dry and the wet bulb of the hygrometer, as well as the
indications of the differential thermometer, was noted, in connexion
with the number of revolutions performed per minute by the ane-
mometer. While the differential thermometer indicated the same
relative differences between the heat of the atmosphere within and
without the tube, the velocity of the revolutions was found to vary
considerably. This variation was discovered to be chiefly, if not
wholly, dependent on the elasticity of vapour, due to the hygro-
- metrical state of the atmosphere, as estimated from the dry- and the
wet-bulb thermometers, and calculated from the tables of Regnault.
240 observations were recorded and afterwards separated into
groups, each group comprising those in which the differential ther-
mometer gave the same indication.
Phil. Mag. 8. 4, Vol. 21, No. 139, March 1861. Q
226 Royal Society :—
If in either of these groups we separate into two classes the cases
in which the elasticity was highest, from the cases in which it was
lowest, and multiply the mean of each with the corresponding mean
of the number of the revolutions of the anemometer, their product
is nearly a constant, thus showing that the velocity of ascent of the
atmospheric vapour is inversely as its elasticity ; and hence it follows
that the velocity of the ascending current in the tube varies inversely
as the density or elastic force of the vapour suspended in the atmo-
sphere. ‘This was rendered evident by the aid of Tables appended
to the paper.
When the mean elastic force of vapour calculated from the dry
and the wet bulbs is multiplied by the constant, 13°83, the result
gives the whole amount of water in a vertical column of the atmo-
sphere in inches; it follows therefore that when the difference of
temperature between the external air and that in the tube, as shown
by the differential thermometer, is constant, the velocity of the
current in the tube varies inversely as the weight of the vapour
suspended in the atmosphere.
In an Appendix the author describes some additional experiments,
made with the view of ascertaining whether the readings of the
differential thermometer were mainly due to actual changes of tem-
perature within the tube, or to extraneous causes acting on the
external bulb. He found that when the external bulb was covered.
with woollen cloth or protected by a zine tube of about 4 inches
diameter and 6 inches long, the temperature of the bulb was
increased about 2° on the scale of the instrument, and that when
they were removed the prior reading was restored, while the number
of revolutions of the anemometer per minute was not appreciably
affected by the change. This explains why the readings of the dif-
ferential thermometer varied from 33°:0 to 33°°5 as described in the
paper, without producing a corresponding change in the velocity of
the anemometer.
For the purpose of obtaining a. more correct estimate of the
influence of a given increase of heat within the tube, the author
introduced into the tube at its lowest extremity, a phial containing
eight ounces of water at the temperature of 100° Fahr., corked so
that no vapour could escape. The result showed that in thirteen
observations a quantity of heat equal to an increase of one-tenth of
a degree on the scale of the differential thermometer, was equivalent
to a mean velocity of the anemometer of 3°6 revolutions per minute,
the greatest number being 3°8, the least 3°3 per minute.
These observations render it still more evident, that if a higher
temperature within the tube had been the main cause of the revolu-
tions of the anemometer, the variations in their velocity would not
have been in such exact relation to the elastic force of the atmo-
spheric vapour, as has been shown to be the case. They also lead
to the inference, that the apparent excess of heat within the tube
alluded to by the author in his Paper read before the Society in
1855 did not really exist, and to the conclusion that, if such excess
had been present, the anemometer would not have been brought to a
state of rest by depriving the air of the room of a portion of the
moisture ordinarily suspended in it.
On the. Relation between Boiling-point and Composition, 227
“On the Relation between Boiling-point and Composition in
Organic Compounds.” By Hermann Kopp. — .
The author was the first to observe(in 1841) that, on comparing pairs
of analogous organic compounds, the same difference in boiling-point
corresponds frequently to the same difference in composition. This
relation between boiling-point and composition, when first pointed
out, was repeatedly denied, but is now generally admitted. The con-
tinued experiments of the author, as well as of numerous other
inquirers, have since fixed many boiling-points which had hitherto
remained undetermined, and corrected such as had been inaccu-
rately observed. In the present paper the author has collected his
experimental determinations, and has given a survey of all the facts
satisfactorily established up to the present moment regarding the
relations between boiling-point and composition.
The several propositions previously announced by the author
were :-—
1. An alcohol, Cx H,,+20., differmg in composition from ethylic
alcohol (C,H,O,, boiling at 78° C.) by « C,H,, more or less, boils
2X 19° higher or lower than ethylic alcohol.
2. The boiling-point of an acid, C,H,0O,, is 40° higher than that
of the corresponding alcohol, C,,H,+20s.
3. The boiling-point of a compound ether is 82° higher than th
boiling-point of the isomeric acid, C,H,Ou..
These propositions supply the means of calculating the boiling-
points of all alcohols, C, Hn+20z ; of all acids, C,H,,O.4; of all com-
pound ethers, C,H,Ox. The author contrasts the values thus cal-
culated for these substances with the available results of direct obser-
vation. The Table embraces eight alcohols, Cx Hn+2Q., nine acids,-
C,H, O04, and twenty-three compound ethers, C,,H,O.; the calculated
boiling-points agree, as a general rule, with those obtained by experi-
ment, as well as two boiling-points of one and the same substance
determined by different observers. We are thus justified in assuming
that the calculated boiling-point of other alcohols, acids, and ethers
belonging to this series will also be found to coincide with the results
of observation.
The boiling-points of other monatomic alcohols, Cp H»O2, other
monatomic acids, C,,H,,O,, and other compound ethers, Cp HmOus
are closely allied with the series previously discussed. A substance
containing xC more or less than the analogous term of the previous
class, in which the same number of oxygen and of hydrogen equiva-
lents is present, boils x x 14°°5 higher or lower ; or, what amounts to
the same thing, a difference of #H more or less of hydrogen lowers
or raises the boiling-pointt by «x5°. Thus benzoic acid, C,,H,O,;
boils 8 x 14°-5 higher than propionic acid, C,H,O,, or 8 x 5° higher
than cenanthylic acid, C,,H,,O,; cinnamate of ethyl, C,,H,,O,, boils
10 x 14°5 higher than butyrate of ethyl, C,,H,,O,, or 10 x 5° higher
than pelargonate of ethyl, C,,H,,O,.
The author compares the boiling-points thus calculated for five
alcohols, C,, HO; for six acids, C, H»O.; and for sixteen compound
ethers, C,, H,,.O4, with the results of observation. In almost all cases
the concordance is sufficient.
Qe
228 Royal Society :—
The author demonstrates in the next place that in many series of
compounds other than those hitherto considered, the elementary
difference, eC, H,, likewise involves a difference of x x 19° in the boil-
ing-point. He further shows that on comparing the boiling-points
of the corresponding terms in the several series of homologous sub-
stances hitherto considered, many other constant differences in boiling-
point are found to correspond to certain differences in composition.
Thus a monobasic acid is found to boil 44° higher than its ethyl
compound, and 63° higher than its methyl compound ; and this con-
stant relation holds eood even for acids other than those previously
examined, e. g. for the substitution-products of acetic acid. Also in
eabitanecs sat are not acids, the substitution of C,H, or C,H,
for H, occasionally involves a depression of the boiling-points re-
spectively of 44° and 63°; the relation, however, is by no means
generally observed.
The author, in addition to the examples previously quoted, shows
that compounds containing benzoyl (C,,H,O,) and benzyl (C,, H.)
boil 78° (=4 x 14°°5+4 x “50) higher than the corresponding terms
containing valeryl (C,,H,O,) and amyl (C,,H,,), a relation, however,
which is ieee ise not generally met with. He discusses, moreover,
other coincidences and differences of boiling-points of compounds
differing in a like manner in composition. Not in all homologous
series does the elementary difference «C,H, involve a difference of
2xX19° in boiling-point. The author shows that this difference is
greater for the hydrocarbons, C, H»-6 and CxHn+2; for the acetones
and aldehydes, C,H, Oz; for the so-called simple and mixed ethers,
C,H»+202; for the chlorides, bromides, and iodides of the alcohol
radicals, Cy, H»+1, and for several other groups; that it is, on the con-
trary, smaller for the anhydrides of monobasic acids, Cp Hn—20¢; for
the ethers, C, H»-2Og (which may be formed either by the action of
one molecule of a dibasic acid, C, H,-20s, upon two molecules of a
monatomic alcohol, C,,H,+4202, or by the action of two molecules of
a monobasic acid, C,,H,,0,, upon one molecule of a diatomic alcohol,
C,,Hn+204), and several other series.
The author thinks that the unequal differences in boiling-points
corresponding in different homplogaug series to the elementary differ-
ence wC, H,, are probably regulated by a more general law, which will
be found when the boiling-points of many substances shall have been
determined under pressures differing from those of the atmosphere.
“From the observations at present at our disposal it may be
affirmed as a general rule, that in homologous compounds belonging
to the same series, the differences in boiling-points are proportional
to the differences in the formule. Exceptions obtain only in cases
when terms of a particular group are rather difficult to prepare, or
when the substances boil at a very high temperature, at which the
observations now at our command are for the most part uncertain.
Again, it may be affirmed that the difference in boiling-points,
corresponding to the elementary difference C,H,, is in a great many
series =19° ; in some series greater, in some series less.”
The author proceeds to discuss the boiling-points of isomeric com-
pounds. Ie shows that in a great many cases isomeric compounds
On the Relation between Boiling-point andComposition. 229
belonging to the same type, and exhibiting the same chemical cha-
racter, boil at the same temperature, and that there is no reason why,
for the class of bodies mentioned, this coincidence should not obtain
generally. On the other hand, different boiling-points are observed
in isomeric compounds possessing a different chemical character,
although belonging to the same type (e. g. acids and compound ethers,
C,,H,O,; alcohols and ethers, C,,H,,,:02), and im isomeric com-
pounds belonging to different types (e. g. allylic alcohol and acetone).
The author shows that the determination of the boiling-point of a
substance, together with an inquiry into the compounds serially
allied with it by their boiling-points, constitutes a valuable means of
fixmg the character of the substance, the type to which it belongs,
and the series of homologous bodies of which it is a term. He
quotes as an illustration eugenic acid. The boiling-point of this
acid, C,,H,,0,,is 150°; and on comparing this boiling-point with the
boiling-points of benzoic acid, C,,H,O, (boiling-point 253°), and of
hydride of salicyl, C,,H,O, (boilmg-point 196°), it is obvious that
eugenic acid cannot be homologous to benzoic acid, whilst, on the
other hand, it becomes extremely probable that it is homologous to
hydride of salicyl, and consequently that it belongs rather to the
aldehydes than to the acids proper.
The author, in conclusion, calls attention to the importance of
considering the chemical character in comparing the boiling-points
of the volatile organic bases, and shows the necessity of distinguish-
ing between the primary, secondary, and tertiary monamines in order
to exhibit constant differences of boiling-point for this class of sub-
stances. He discusses the boiling-points of the several bases,
C,Hn»_sN and CrHn+3N, and points out how in many cases the
particular class to which a base belongs may be ascertained by the
determination of the boiling-point.
The comprehensive recognition of definite relations between com-
position and boiling-point is for the present chiefly limited to organic
compounds. But for the majority of these compounds, and indeed
for the most important ones, this relation assumes the form of a
simple law, which, more especially for the monatomic alcohols,
C,,H,,O2, for the monobasic acids, C,,H,,O4, and for the compound
ethers generated by the union of the two previous classes, is proved
in the most general manner ; so much so, indeed, that in many cases
the determination of the boiling-poiat furnishes most material assist-
ance in fixing the true position and character of a compound.
The author points out more especially that the simplest and most
comprehensive relations have been recognized for those classes of
organic compounds which have been longest known and most accu-
rately investigated, and that even for those classes the generality and
simplicity of the relation, on account of numerous boiling-poits in-
correctly observed at an earlier date, appeared in the commencement
doubtful, and could be more fully acknowledged only after a consi-
derable number of new determinations. Thus he considers himself
justified in hoping that also in other classes of compounds, in which
simple and comprehensive relations have not hitherto been traced,
these relations will become perceptible as soon as the verification of
230 Royal Society :—
the boiling-points of terms already known, and the examination of
new terms, shall have laid a broader foundation for our conclusions.
May 10.—Sir Benjamin C. Brodie, Bart., President, in the Chair.
The Bakerian Lecture was delivered by Mr. Fairbairn, F.R.S.
The Lecturer gave a condensed exposition of the experiments and
results detailed in the following Paper. He also exhibited the appa-
ratus employed, and explained the methods followed.
«Experimental Researches to determine the Density of Steam at
all Temperatures, and to determine the Law of Expansion of Super-
heated Steam.” By William Fairbairn, Esq., F.R.S., and Thomas
Tate, Esq.
The object of these researches is to determine by direct experiment
the law of the density and expansion of steam at all temperatures.
Dumas determined the density of steam at 212° Fahr., but at this ~
temperature only. Gay-Lussac and other physicists have deduced
the density at other temperatures by a theoretical formula true for a
perfect gas:
VP _459+T (1.)
VP. 45040... 1.
On the expansion of superheated steam, the only experiments are
those of Mr. Siemens, which give a rate of expansion extremely high,
and physicists have in this case also generally assumed the rate of
expansion of a perfect gas. Experimentalists have for some time
questioned the truth of these gaseous formule in the case of conden-
sable vapours, and have proposed new formulee derived from the
dynamic theory of heat ; but up to the present time no reliable direct
experiments have been made to determine either of the pomts at
issue. The authors have sought to supply the want of data on these
questions by researches on the density of steam upon a new and ori-
ginal method.
The general features of this method consist in vaporizing a known
weight of water in a globe of about 70 cubic inches capacity, and
devoid of air, and observing by means of a ‘‘ saturation gauge’”’ the
exact temperature at which the whole of the water is converted into
steam. ‘The saturation gauge, in which the novelty of the experi-
ment consists, is essentially a double mercury column balanced upon
one side by the pressure of the steam produced from the weighed
portion of water, and on the other by constantly saturated steam of
the same temperature. Hence when heat is applied the mercury
columns remain at the same level up to the point at which the
weighed portion of water is wholly vaporized; from this point the
columns indicate, by a difference of level, that the steam in the globe
is superheating ; for superheated steam increases in pressure at a far
lower rate than saturated steam for equal increments of temperature.
By continuing the process, and carefully measuring the difference of
level of the columns, data are obtained for estimating the rate of
expansion of superheated steam.
The apparatus for experiments at pressures of from 15 to 70 lbs.
per square inch, consisted chiefly of a glass globe for the reception of
the weighed portion of water, drawn out into a tube about 32 inches
On the Density of Steam at all Temperatures. 201
long. The globe was enclosed in a copper boiler, forming a steam-
bath by which it could be uniformly heated. The copper steam-
bath was prolonged downwards by a glass tube enclosing the globe
stem. To heat this tube uniformly with the steam-bath, an outer
oil-bath of blown glass was employed, heated like the copper bath by
gas jets. ‘The temperatures were observed by thermometers exposed
naked in the steam, but corrected for pressure. The two mercury
columns forming the saturation gauge were formed in the globe stem,
and between this and the outer glass tube; so long as the steam in
the glass globe continued in a state of saturation, the inner column
in the globe stem remained stationary, at nearly the same level as
that in the outer tube. But when, in raising the temperature, the
whole of the water in the globe had been evaporated and the steam
had become superheated, the pressure no longer balanced that in
the outer steam-bath, and, in consequence, the column in the globe
stem rose, and that in the outer tube fell, the difference of level
forming a measure of the expansion of the steam. Observations of
the levels of the columns were made by means of a cathetometer at
different temperatures, up to 10° or 20° above the saturation point ;
and the maximum temperature of saturation was, for reasons deve-
loped by the experiments, deduced from a point at which the steam
was decidedly superheated.
The results of the experiments, which in the paper are given in
detail, show that the density of saturated steam at all temperatures,
above as well as below 212°, is invariably greater than that derived
from the gaseous laws.
The apparatus for the experiments at pressures below that of the
atmosphere was considerably modified ; and the condition of the steam
was determined by comparing the column which it supported with
that of a barometer. The results of these experiments, reduced in
the same way, are extremely consistent. 7
As the authors propose to extend their experiments to steam of a
very high pressure, and to institute a distinct series on the law of
expansion of superheated steam, they have not at present given any
elaborate generalizations of their results. The following formule,
however, represent the relations of specific volume and pressure of
saturated steam, as determined in their experiments, with much
exactness.
Let V be the specific volume of saturated steam, at the pressure P,
measured by a column of mercury in inches ; then
49513
V=25°62 eRe ead e e e e e 2.
wu ee p- me
49513 :
— el 4 e. 8 ° e e e e Se
wn at SUN ses
In regard to the rate of expansion of superheated steam, the ex-
periments distinctly show that, for temperatures within about ten
degrees of the saturation point, the rate of expansion greatly exceeds
that of air, whereas at higher temperatures the rate of expansion
approaches very near that of air. Thus in experiment 6, in which
the maximum temperature of saturation is 174°°92, the coefficient of
2o2 Royal Society.
expansion between 174°'92 and 180° is ;4,, or three times that of
air; whereas between 180° and 200° the coefficient is very nearly the
same as that of air (steam= 4, air=;4,), and so on in other cases.
The mean coefficient of expansion at zero of temperature from seven
experiments below the pressure of the atmosphere, and calculated
from a point several degrees above that of saturation, is -}_, whereas
for air it is ;15. Hence it would appear that for some degrees
above the saturation point the steam is not decidedly in an aériform
state, or, in other words, that it is watery, containing floating vesicles
of unvaporized water.
Table of Results, showing the relation of density, pressure, and
temperature of saturated steam.
Pressure ~ Specific Volume. Pronarienc
ee if in Ibs.per,in inches of of saturation From enor >
; sq. in. | mercury. Fahr. experiment, Hy formula @)) ona
(e}
1 2°6 5°35 | 136-77 8266 8183 Sing
2 4°3 8°62 1ao°3a 5326 5326 0
3 4°7 945 | 159:36 4914 4900 ae
4 6°2 12°47 170°92 3717 3766 + 7k
5 6°3 12°61 171°48 3710 3740 es
6 6'8 13°62 174°92 3433 3478 + 7s
7 8-0 16°01 182:30 3046 2985 — sy
8 i 18°36 188°30 2620 2620 0
9 13 22°88 198°78 2146 2124 — 37
EY 26°5 53°61 242-90 941 937 —saE
ae 27°4 55°52 244°82 906 906 0
3’ | 276 | 55°89 | 245-22 891 900 rete
4' 30° 1 66°84 255°50 758 798 0
5' | 87:8 | 76°20 | 263-14 648 669 ote
6' 40°3 81°53 267°21 634 628 —st0
e 41°7 84°20 269°20 604 608 ++t5
8' 45°7 92°23 274°76 583 562 — sy
9' 49-4 99°60 279°42 514 519 +343
11’ 51°7 104°54 282°58 496 496 0
12’ 55°9 112°78 287°25 457 461 ++
13' | 60°6 | 122°25 | 292-53 432 428 uke
14' 56°7 114°25 288°25 448 456 + sg
Adopting the notation previously employed, and putting 7 for the
rate or coefficient of expansion of an elastic fluid at ¢, temperature,
we find Vv
- as pals
ee Se HY 9 . ° e . . (4.)
Fe obey see
1 ,
where — = the rate of expansion at zero of temperature. In the case
2)
1
of air e,= 459.
The following Table gives the value of the coefficient of expansion
of superheated steam taken at different intervals of temperature from
the maximum temperature of saturation.
Geological Society. 233
Coefficient of
Bee | mahon, | mmORBSputoniS han, | Semel | of emt
1 136°77 140 170 — ett
2 155-33 160 190 ii ere
S| soso) sie | |
5 was { been’ 180 a ay
6 17492 | ed pe = te
8 188-30 191 211 Sig ae
ees 8) aug? gag (op eae
v | 2602 1] 353 b79 es ue
9" 279-42 | a aes — =
13" Roeee boson? RG op a TE
Hence it appears, that as the steam becomes more and more super-
heated, the coefficient of expansion approaches that of a perfect gas.
The authors hope that these experiments may be continued, and that
the results obtained at greatly increased pressures will prove as
important as those already arrived at.
GEOLOGICAL SOCIETY.
[Continued from p. 157.]
December 5, 1860.—L. Horner, Esq., President, in the Chair.
The following communication was read :—
‘‘On the Structure of the North-west Highlands, and the Rela-
tions of the Gneiss, Red Sandstone, and Quartzite of Sutherland and
Ross-shire.”’ By Professor James Nicol, F.R.S.E., F.G.S.
The author first referred to his paper in the Quart. Journ. Geol.
Soc., vol. xii. pp. 17, &c., in which the order of the red sandstone
on gneiss, and of quartzite and limestone on the sandstone, was
established, and in which the relation of the eastern gneiss or mica-
schist to the quartzite was stated to be somewhat obscure on account
of the presence of intrusive rocks and other marks of disturbance.
Having examined the country four times, with the view of settling
some of the doubtful points in the sections, the author now offered
the matured result of his observations. He agrees with Sir R.
Murchison as far as the succession of the western gneiss, red sand-
stone, quartzites (quartzite and fucoid-bed), and limestone is con-
234 Geological Soctety.:—
cerned; but differs from him in maintaining that there is no upper
series of quartzite and limestone, and that there is no evidence of an
‘* upward conformable succession’’ from the quartzite and limestone
into the eastern mica-slate or gneiss—the o-called “ upper gneiss.”’
The ‘‘ upper quartzite” and “ upper limestone ” the author believes -
to be portions of the quartzite of the country, in some cases separated
by anticlines and faults and cropping out in the higher ground, and
in other instances inverted beds with the gneiss brought up by a
contiguous fault and overhanging them. ‘his latter condition of
the strata, as well as other cases where the eastern gneiss is brought
up against the quartzite series, have, according to the author, given
rise to the supposed ‘‘ upward conformable succession” above referred
to. Im some cases where “‘ gneiss ”’ is said to have been observed
overlying the quartzite, Professor Nicol has determined that the
overlying rock is granulite or other eruptive rock, not gneiss.
The sections described by the author in support of his views of
the eastern gneiss not overlying the quartzite and limestone, but
being the same as the gneiss of the west coast, and brought up by a
powerful fault along a nearly north and south line passing from
Whiten Head (Loch Erriboll) to Loch Carron and the Sound of Sleat,
are chiefly those which had been brought forward as affording the
proofs on which the opposite hypothesis is founded; and in all, the
author finds irruptions of igneous rocks, and other indications of
faults and disturbance, depriving them, in his opinion, of all weight
as evidence of a regular order of ‘ upward conformable succession.”
Prof. Nicol further argues that the mode of the distribution of the
rocks shows that there is through Sutherland and Ross-shire a real
fault, and no overlap of eastern gneiss of more than a few feet or
yards at most, and that the fact of different strata of the quartzite
series being brought against the gneiss at different places supports
this view, and points toa great denudation having taken place along
the line of fault. ‘Though the quartzite is here and there altered by
the igneous rocks, yet it is truly a sedimentary rock, and so is the
limestone ; but the eastern gneiss or mica-schist is a crystalline rock
throughout: this fact, according to the author, is inimical to the
hypothesis of the eastern gneiss overlying the limestone and quartzite.
It has been insisted upon, that the strike of the western gneiss is dif-
ferent from that of the east; but the author remarks that the strike
is not persistent in either area, and that great movements subse-
quent to the deposition of the quartzite series have irregularly affected
the whole region. With regard to mineralogical characters, Prof.
Nicol insists that both the eastern and the western gneiss are essen-
tially the same. Both are locally modified with granitic and horn-
blendic matter near igneous foci ; but no proof of a difference of age
in the two can be obtained therefrom. The alteration in bulk of the
gneiss in the western area, by the intrusion of the vast quantities of
granite now observable in it, may perhaps have caused the great
amount of crumpling and faulting along the N. and S. line of fault,
dividing the western from the eastern gneiss,—a fault comparable
with and parallel to that running from the Moray Firth to the Linnhe
Loch, and to the one passing along the south side of the Grampians.
Geological Structure of the South-west Highlands of Scotland. 235
December 19, 1860.—L. Horner, Esq., President, in the Chair.
The following communications were read :—
1. “ On the Geological Structure of the South-west Highlands of
Scotland.” By T. F. Jamieson, Esq. Communicated by Sir R. I.
Murchison, V.P.G.S.
In this paper the author attempts to throw light on the relations
of those rocks which figure in geological maps as the mica-schist,
clay-slate, the chlorite-slates, and the quartz-rock of the South-west-
ern Highlands, which range N.E. through the middle of Scotland,
forming an important feature in the geology of that country. An
examination of these rocks, as displayed in Bute and Argyleshire,
has led Mr. Jamieson to believe that, from the quartz-rock of Jura
to the border of the Old Red Sandstone, there is a conformable series
of strata, which, although closely linked together, may be classed
into three distinct groups, namely, Ist, a set of lower grits (or
quartz-rock), many thousand feet thick; 2ndly, a great mass of
thin-bedded slates, 2000 feet or more thick; and 3rdly, a set of
upper grits, with intercalated seams of slate of equal thickness.
Beds of limestone occur here and there sparingly in all the three
divisions ; the thickest being deep down in the lower grits. All the
limestones are thiclfest towards the west. The siliceous grits also
appear to be freer from an admixture of green materials towards the
west. All the members of the series (namely, the upper grits, slates,
and lower grits) have a persistent S.W.—N.E. strike, sometimes in
Bute approaching to due N. and 8. They are conformable, and
graduate one into another in such a way as to show that they belong
to one continuous succession of deposits. The materials of which they
have been formed seem to have been derived from very similar sources.
The upper and the lower grits are very similar in composition, being
made up of water-worn grains of quartz, many of which are of a
peculiar semitransparent bluish tint.
The rocks of the district have been thrown into a great undula-
tion, with an anticlinal axis extending from the north of Cantyre
through Cowal by the head of Loch Ridun on to Loch Eck (and:
probably by the head of Loch Lomond on to the valley of the Tay,
at Aberfeldy), and with a synclinal trough lying near the parallel
of Loch Swen. The anticlinal fold is well seen in the hill called
Ben-y-happel, near the Tighnabruich quay in the Kyles of Bute.
Southward of this ridge, which is composed of the lower grits or
quartzite, the thin-bedded greenish slates and the upper grits suc-
ceed conformably ; and the latter are separated by a trap-dyke from
the Old Red Sandstone of Rothsay. ‘This section the author de-
scribed in detail; also the corresponding section to the north of the
anticlinal axis, towards Loch Fyne, and along the west shore of Loch
Fyne. ‘The lower grits extend as far as Loch Gilp, and are then
succeeded by the green slates and the upper grits, which falling in the
synclinal trough are repeated through Knapdale towards Jura Sound,
where the green slates again form the surface along the eastern coast
of Jura, lying on the quartzite or grits of that island. Throughout
the synclinal trough and the neighbouring district (that is, from
236 Geological Society :—
Loch Fyne to Jura Sound) the grits and slates are intimately mixed,
with numerous intercalated beds of greenstone, some being of great
thickness. Mr. Jamieson pointed out that this feature of the di-
strict has hitherto in great part been misunderstood, and that Mac-
culloch was in error when he denominated these rocks ‘ chlorite-
schist.”
The probable relationship of the rocks of the Islands of Shuna,
Luing, and Scarba to those of Jura and Bute were then dwelt upon;
the greenstones of Knapdale, &c., and their relation to the sedi-
mentary rocks, were described in detail; and the limestones of
the district briefly noticed. As no fossils have hitherto been found,
paleontological evidence of the age of these rocks is wanting; but
the author, regarding their general resemblance to the quartz-rocks,
limestones, and mica-schists of Sutherlandshire, thinks them to be of
the same date as those rocks of the North-west Highlands.
2. “On the position of the beds of the Old Red Sandstone in
the Counties of Forfar and Kincardine, Scotland.” By the Rev.
Hugh Mitchell. Communicated by the Secretary. ;
In Forfar- and Kincardine-shire, south of the Grampians, the Old
Red Sandstone is developed in the following series, with local modi-
fications :—I1st (at top), Conglomerate; 2nd, grey flagstone with
intercalated sandstone (about 40 feet thick at Cauterland Den,
120 feet at Carmylie) ; 3rd, gritty ferruginous sandstone, with
occasional thin layers of purplish flagstone. Of the last, 120 feet
are seen at Cauterland Den; it occurs also at Ferry Den, &c. The
flagstone of this third or lowest member of the group yields Ripple-
marks, Rain-prints, Worm-markings, and Crustacean tracks (of
several kinds, large and small). Parka decipiens has been found in
the lowest grits; and Cephalaspis in the sandstone at Brechin, im-
mediately under the grey flagstones.
In the second member, namely the grey flags, Fish-remains have
of late been found more or less abundantly throughout the district,
together with Crustacean fossils. Cephalaspis Lyellit, Ichthyodoru-
lites, Acanthodian fishes, Pterygotus, Eurypterus, Kampecaris For-
fariensis, Stylonurus Powriensis, Parka decipiens, and vegetable re-
mains are the most characteristic fossils.
The author pointed out that some few genera of Fish and Crus-
taceans were present both in this zone and in the Upper Silurian
formation, and that still fewer links existed to connect the fauna of
the Forfarshire flags with the Old Red Sandstone north of the Gram-
pians, with which it appears to have, in this respect, almost as little
relation as with the Carboniferous system. With the Old Red of |
Herefordshire these flags appear to have some few fossils in common ;
but of about twenty species found in Forfarshire, only about four
could be quoted from Herefordshire.
In conclusion, the author noticed the vast vertical development of
the whole series, and its great geographical extent ; and particularly
dwelt upon the distinctness of the fauna of the flagstones of Forfar-
shire, as giving good grounds for the treatment of the Old Red
Fauna as peculiar to a separate geological period, both as distinct
P. B. Brodie on the Distribution of the Corals in the Lias. 237
from the Silurian System, and in some degree as divisible into two
or more members of one group :—three members, if the upper or
Holoptychius-beds of Moray, Perth, and Fife, the middle or Fish-
beds of Cromarty and Caithness, and the lowest or Forfarshire
beds be counted separately ; but two, if we regard some of the Old
Red beds north of the Grampians as equivalent in time to those on
the south.
January 9, 1861.—L. Horner, Esq., President, in the Chair.
The following communications were read :—
1. “On the Distribution of the Corals in the Lias.” By the Rev,
P. B. Brodie, M.A., F.G.S.
From observations made by himself and others, the author was
enabled to give the following notes. In the Upper Lias some Corals
of the genera Thecocyathus and Trochocyathus occur. The Middle
Lias of Northamptonshire and Somersetshire has yielded a few Corals.
The uppermost band of the Lower Lias, namely the zone with Am-
monites raricostatus and Hippopodium ponderosum, contains an unde-
scribed Coral at Cheltenham and Honeybourn in Gloucestershire ;
and a Montlivaltia in considerable abundance at Down Hatherly in
Gloucestershire, at Fenny Compton and Aston Magna in Worcester-
shire, and at Kilsby Tunnelin Northamptonshire. The middle mem-
bers of the Lower Lias appear to be destitute of Corals. In the zone
with Ammonites Bucklandi, called also the Lima-beds, Jsastrea occurs
in Warwickshire and Somersetshire. Dr. Wright states that Isastrea
Murchisoni occurs in the next lowest bed of the Lower Lias, namely
- the White Lias with Ammonites Planorbis, at Street in Somerset ;
and another Coral has been found in the same zone in Warwick-
shire. Lastly, in the ‘‘ Guinea-bed” at Binton in Warwickshire
another Coral has been met with.
The Montlivaltie of the Hippopodium-bed and the Jsastrea of the
Lima-beds appear to have grown over much larger areas in the
Liassic Sea than the other Corals here referred to.
2. ‘On the Sections of the Malvern and Ledbury Tunnels, on the
Worcester and Hereford Railway, and the intervening Line of Rail-
road.” Bythe Rev. W.S. Symonds, A.M., F.G.S., and A. Lambert,
Esq.
In this paper the authors gave an account of the different strata
exposed by the cuttings of the Worcester and Hereford Railway
(illustrated by a carefully constructed section), including the dif-
ferent members of the New Red Sandstone (on the east of the Mal-
vern Hills), the syenite and greenstone (forming the nucleus of the
Malverns), and the Upper Llandovery beds, the Woolhope shales,
the Woolhope limestone, Wenlock shales, Wenlock limestone, and
Lower Ludlow rock on the west side of the syenite, followed by some
beds of the Old Red series, violently faulted against the Ludlow rock
at the west end of the Malvern Tunnel. ‘Then the open railway
passes over Upper Ludlow rocks and some lower beds of the Old Red
series, here and there covered by drift, until the Lower Ludlow rock
is again traversed at the east end of the Ledbury Tunnel, and is
238 Intelligence and Miscellaneous Articles.
shown to be much faulted and brought up against Upper Ludlow
shales and Aymestry rocks. The Wenlock shales and the Wenlock
limestone are then traversed; these are much faulted, the Lower
Ludlow beds again coming in, followed by Aymestry rock, Upper
Ludlow shales, Downton sandstone, and, at the east end of the
tunnel, by red and mottled marls, grey shales and grits, purple
shales and sandstones, with the Auchenaspis-beds, forming the pas-
sage-beds into the Old Red Sandstone, as described in a former
paper (Quart. Journ. Geol. Soc. vol. xvi. p. 193).
In a note, Mr. J. W. Salter, F.G.S., described the great abun-
dance of Upper Silurian fossils found in these cuttings, and now
chiefly in the collection of Dr. Grindrod and other geologists at
Malvern and the neighbourhood.
XXXVI. Intelligence and Miscellaneous Articles.
ON THE FIBROUS ARRANGEMENT OF IRON AND GLASS TUBES,
[Extract from a Letter from Dr. Debus to Professor Tyndall. ]
Queenwood College, Feb. 17, 1861.
FEW weeksago Mr. E. brought me a piece of iron tube which
had been exposed for several years to the action of moist air.
Nearly the whole of the tube was converted into oxide ofiron. This
suggested certain thoughts, the results of which were new and in-
teresting to me.
You know, when a piece of glass tube, sealed and filled with water,
is heated, the tube is cracked, and cracked in a longitudinal direc-
tion. Why is this? Glass tubes are made by taking a piece of hol-
low glass in a viscous state and pulling it at both ends. Now, the
particles of the glass do not adhere to each other on all sides
with a force of the same strength, but in some directions this force
is stronger, in others weaker. Under the strain produced by the
pulling, they arrange themselves so as to offer to the pulling force
the greatest resistance. Therefore the greatest cohesion of the par-
ticles is found, in the formed tube, parallel to the length of the tube,
and the weakest cohesion in a direction perpendicular to this. This
explains the cracking of the tube as mentioned above.
Mr. E. could not give me exact information as to how iron tubes
are made, but he said they were passed through rollers. Now, if
this is correct, the particles of iron ought to arrange themselves in
a similar way to the particles in a glass tube. If such a tube oxi-
dizes, the oxygen naturally would overcome the cohesion of the iron
first in those places where this cohesion is weakest, that is, in lines
parallel with the tube. Such is actually the case. The tube men-
tioned had deep furrows, so to say, hollowed out by the oxygen along
its length, just in the same way as u glass tube would crack under
pressure.
I need not mention to you other examples; but one case more,
and then I have done. You gave some years ago an explanation of
Intelligence and Miscellaneous Articles. 239
cleavage*. The paper wherein this explanation was given never came
to my hands; and I do not remember that you explained the thing
to me when we had personal intercourse, The principle alluded to
appears to me to be the true cause of the phenomenon. ,
If a plastic mass is exposed to pressure, the particles turn until
they are in such a position as to offer the greatest resistance to the
pressure brought to bear upon them. But that direction wherein
they offer the greatest resistance to pressure is also that where the
cohesion is least. Consequently cleavage ought to take place ina
direction perpendicular to the pressure exerted.
Am I right or wrong? Of course I could say more; but why
should I carry water to the well?
H. Desvus.
ON THE CALCIUM SPECTRUM.
To the Editors of the Philosophical Magazine and Journal.
GENTLEMEN,
In acommunication published in the last Number of the Philoso-
phical Magazine, we pointed out the appearance of a well-defined blue
line in the spectrum produced by igniting the evaporated residue of
a deep-well water. From the circumstance of this line, which is situ-
ated somewhat more towards the violet end of the spectrum than the
line Sr 6, not being referred to in the paper of Profs. Kirchhoff and
Bunsen, nor indicated in their beautiful representations of the spectra
of the alkaligenous metals, we were induced to attribute its pro-
duction to the probable existence of a previously unrecognized mem-
ber of the calctum group of metals. Further experiments, however,
have satisfied us that the blue line in question really belongs to the
calcium spectrum. On finding this to be the case, we communicated
with Professor Bunsen, who in return informed us that Professor
Kirchhoff and himself had observed this line, but, not thinking it
sufficiently bright to be suitable for the recognition of calcium, had
not made reference to it in their paper. It can, however, be seen
with a degree of brilliancy at least equal to that of many of the lines
represented, when perfectly pure chloride of calcium is ignited in a
somewhat darkened room.
We remain, Gentlemen,
Your obedient Servants,
F, W. and A. Dupr&.
ON THE LUNAR TABLES AND THE INEQUALITIES OF LONG PERIOD
DUE TO THE ACTION OF VENUS. BY M. DE PONTECOULANT.
In the Number of the Comptes Rendus of the labours of the Aca-
demy of the 12th of November last, M. Delaunay has inserted a
memoir in which he gives an account of the researches in which he
has been engaged, concerning the two lunar disturbances of long
* Fibrous iron was one of my illustrations.—J, T.
240 Intelligence and Miscellaneous Articles.
period depending on the action of the planet Venus, which Professor
Hansen has proposed to introduce into the expressions for the
moon’s motions. According to M. Delaunay’s calculations (the accu- -
racy of which I have at present no intention of disputing) the value of
the coefficient of the first of these disturbances—that, namely, whose
period is about 273 years—is nearly the same as that attributed to it
by the astronomer of Gotha; but the coefficient of the second, whose
period is about 240 years (and which is the most important of the
two, since its coefficient, calculated at first by Professor Hansen at
23''-2, is according to his account at least 21'47), ought to be con-
sidered, according to the researches of M. Delaunay, as altogether
insensible, if not absolutely nothing.
This conclusion, which is moreover perfectly in accordance with
the announcement of the illustrious geometrician Poisson, published
more than twenty-seven years ago in his memoir of 1833, gives rise
to several questions of extreme importance, not only, as it seems to
me, with respect to the perfection of the lunar tables, but also on the
subject of scientific priority, and even of national honour. In order
that the members of the Academy may be able to judge of this for
themselves, it will be sufficient to mention that the principal cor-
rections which the astronomers of the Greenwich Observatory have
thought it necessary to make in the precious tables of our fellow-
countryman Damoiseau—iables which are so remarkable from the
fact that they are the first that were constructed from theory alone,
without recourse to observation,—and the preference which they have
accorded to the new lunar tables of Professor Hansen, are principally
founded on the existence (considered by them to he conclusively
demonstrated) of the two inequalities arising from the action of
Venus, which M. Delaunay has just calculated. To this it will be
sufficient to add that it was on these grounds that the extraordinary
prize of £1000 was allotted to the same Professor by the Lords of
the Admiralty, at the suggestion of the learned director of the Green-
wich Observatory, for the really marvellous addition, as Mr. Airy
calls it, which he has made to the lunar theory. This assertion, if
suffered to pass without refutation, might lead us to undervalue the
labours of those astronomers, French and foreign, who have
brought about the rapid progress of this difficult theory, and have
advanced it to its present state of perfection.
I shall not now dwell further on these observations, which from their
length would extend beyond the limits prescribed by the Academy
to its own members, and still more to strangers whose claims it admits
to the honour of an insertion in the Comptes Rendus ; but I thought
it advisable to lose no time in announcing that Iam busily occupied
in drawing up a memoir, in which all the observations called for by
a question of gravity so great that the history of science has rarely
furnished one similar to it will be detailed at length, so that it may
not be supposed, either in France or abroad, that a memoir so im-
portant as that of M: Delaunay has escaped unnoticed or remained
unanswered.—Comptes Rendus, December 1860.
ad
PRiL Mag. Ser. 4. Vol. 21.PL. 1V-
LFBASIPC, SEs
THE
LONDON, EDINBURGH ayn DUBLIN
PHILOSOPHICAL MAGAZINE
AND
JOURNAL OF SCIENGE.
[FOURTH SERIES.]
APRIL 1861.
XXXVII. On a New Proposition in the Theory of Heat.
By Professor KirncuHore*.
— few months ago I communicated to the Society cer-
tain observations, which appeared of interest because they
give some information respecting the chemical composition of the
solar atmosphere, and point the way to further knowledge on
this subject. These observations led to the conclusion that a
flame whose spectrum consists of bright lines is partially opake
for rays of light of the colour of these lines, whilst it 1s perfectly
transparent for all other light. Iu this statement we find the
explanation of Fraunhofer’s dark lines in the solar spectrum, and
the justification of the conclusions regarding the composition of
‘the sun’s atmosphere; for we find that a substance which, when
brought into a flame, produces bright limes coincident with. the
dark lines of the solar spectrum, must be present in the sun’s
atmosphere. ‘The fact that a flame is partially opake solely for
those rays which it emits, was, as I stated at the time, a matter
of some surprise to me. Since that time I have arrived, by very
simple theoretical considerations, at a proposition from which
the above conclusion is immediately derived. As this proposition
appears to me to be of considerable importance on other accounts,
I beg to lay it before the Society. A hot body emits rays of heat.
We feel this very perceptibly near a heated stove. The intensity of
the rays of heat which a hot body emits, depends on the nature
and on the temperature of the body, but is quite independent of
the nature of the bodies on which the rays fall. We feel the
rays of heat only in the case of very hot bodies; but they are
* Abstract of a Lecture delivered before the Natural History Society of
Heidelberg. Communicated by Professor Roscoe.
Phil, Mag. 8. 4, Vol. 21. No. 140, April 1861. R
242 Prof. Kirchhoff on a New Proposition
emitted from a body, whatever be its temperature, although the
amount diminishes with the temperature. In proportion as a
body radiates, it loses heat, and its temperature must sink unless
this loss is made up. A body surrounded by substances of the
same temperature undergoes no change of temperature. In this
case the loss of heat caused by its own radiation is exactly com-
pensated by the rays which surrounding substances give out, a
part of which the body absorbs. The quantity of heat which
this body absorbs in a given time must be equal to that which in
the same time it emits. This holds good whatever the nature
of the body may be; the more rays a body emits, the more of
the incident rays must it absorb. The intensity of the rays which
a body emits has been called its power of radiation or emission ;
and the nuniber denoting the fraction of the incident rays which
is absorbed has been called the power of absorption. The larger
the power of emission a body possesses, the larger must its power
of absorption be.
A somewhat closer consideration shows that the relation be-
tween the powers of emission and absorption for one temperature
is the same fer all bodies. This conclusion has been verified in
many special cases, both in the last ten years and in former
times. The foregoing proposition requires, however, that all the
rays of heat under consideration are of one and the same kind; so
that these rays are not qualitatively so far different that one part
of them are absorbed by the bodies more than another part ; for,
were this the case, we could not speak of the power of absorption
of a body, simply because it would be different for different rays.
Now we have long known that there really are different kinds of
heating rays, and that in general they are unequally absorbed by
bodies. There are both dark- and luminous-heating rays; the
former are almost all absorbed by white bodies, whilst the latter
rays are thus scarcely absorbed at all. Indeed the variety of the
rays of heat is even greater than the variety of the coloured rays
of light. The rays of heat, the dark as well as the lumimous,
are influenced in the same manner as the rays of light, by trans-
mission, reflexion, refraction, double refraction, polarization, in-
terference, and diffraction. In the case of the lummous rays of
heat, it is not possible to separate the light from the heat; when
one is diminished in a given relation, the other is diminished in
the same ratio. This has led to the conclusion that rays of light
and heat are essentially of the same nature ; that rays of light are
simply a particular class of the heat-giving rays. The dark rays of
heat are distinguished from the rays of light , Just as the differently
coloured rays are distinguished from each other, by their period
of vibration, wave- length, and refractive index. They are not
visible because the media of our eyes are not transparent to them.
in the Theory of Heat. 243
A difference of quality is noticed amongst the rays of light, not
only in respect to the colour, but also in respect to the state of
polarization. Hence not only have we to distinguish the heating
rays according to the wave-lengths, but we have also to divide
rays of one wave-length into those variously polarized. If we
take into consideration these various kinds of rays of heat, the
conclusions which we had drawn concernimg the relation between
the powers of absorption and emission cease to be binding.
Whether this relation is still found to exist when these variations
are taken into consideration, is a question which has, as yet, not
been decided either by theoretical considerations or by an appeal
to experiment. I have succeeded in fillmg up this gap; and I
have found that the proposition concerning the ratio between the
power of emission and the power of absorption remains true,
however different the rays which the bodies emit may be, as long
as the notions of emissive and absorptive powers be confined to
one kind of ray.
_ The proposition which I have discovered may be thus more
precisely defined :—Let a body C be placed behind two screens
S, and S,, in which two small openings are made. Through these
openings a pencil of rays proceeds from the body C. Of these
rays we consider that portion which corresponds to a given wave-
length A, and we divide this into two polarized components,
whose planes of polarization are two planes a and 0 at right
angles to each other, passing through the axis of the pencil of
rays. Let the intensity of the polarized component a be HE
(emissive power). Now suppose that a pencil of rays, having a
wave-length =), and polarized in the plane a, falls through the
openings 2 and J upon the body C. ‘The fraction of this pencil
which is absorbed by the body C is called A (absorptive power).
Then the relation 5
nature of the body C, and is alone determined by the size of the
openings 1 and 2, by the wave-length >, and by the tempera-
ture. I will point out the way in which I have proved this pro-
position. I began by considering that bodies are conceivable
which, although very thin, absorb all the rays which fall upon
them, or which have the capacity of absorption =1. I call such
bodies perfectly black, or simply black. I first mvestigated the
radiation of such black bodies. Let C be a black body. The
body C is supposed to be enclosed in a black envelope, of which
the screens 8, and S, are a part, and the two screens are sup-
posed to be connected by a black surface surrounding all.
Lastly, let the opening 2 be closed by a black surface, which I
will call “surface 2.” The whole system is to be considered to
possess the same temperature, and to be protected against loss
R2
is independent of the position, size, and
244. Prof. Kirchhoff on a New Proposition
of heat from without by an absolutely non-conducting medium.
Under these circumstances the temperature of the body C cannot
alter; the sum of the intensities of the rays which it emits must
therefore be equal to the sum of the intensities of the rays which
it absorbs ; and because it absorbs all those that fall upon it, the
sum of the intensities of the rays it emits must be equal to the
sum of the intensities of the rays which fall upon it. If, now,
we suppose the followmg change: The “ surface 2” is removed
and replaced by a circular mirror which reflects all the rays fall-
ing upon it, and whose centre is in the middle of opening 1.
The equilibrium of the heat must still be kept up; the sum of
the rays which fall on the body C must still remain equal to the
sum of the rays which it emits. But, as it emits just as much
as before, the quantity of rays which the mirror reflects upon
the body C must be equal to that which the surface 2 emitted.
The mirror produces an image of opening 1, which is coincident
with opening 1. For this reason, just those rays come back to
the body C, after one reflexion from the mirror, as the body C
would have emitted through the openings | and 2 if this last one
had been open; and the intensity of these rays is equal to the
intensity of the rays which the surface 2 sent back through the
opening 1. This last intensity however, is, evidently indepen-
dent of the nature of the body C; and hence it follows that the
intensity of the pencil of rays which the body C radiates through
the openings 1 and 2, is independent of the form, position, and
constitution of the body C; supposing of course that this body
is black, and that its temperature is a given one. According to
this, however, the qualitative composition of the pencil of rays
might become different if the body C were replaced by another
black body of the same temperature. This is, however, not the
ease. If I call e the power of emission of this black body com-
pared with a certain wave-length and a given plane of polariza-
tion—that, therefore, which I have called E under the suppo-
sition that C is a body of any kind—then e is independent of
the nature of the body C, if it only be black. In order to render
this evident, a further arrangement is necessary. Into the pencil
of rays which passes from the opening 1 towards the surface 2,
Jet us suppose a sinall plate placed, which is of so: slight a thick-
ness that it shows in the visible rays the colours of thin plates ;
let it be so placed that the pencil of rays is incident at the polar-
izing angle; let the material of the plate be so chosen that it
neither absorbs nor emits a sensible amount of rays; let the
envelope joining the screens 8, and S, be so shaped that the
image which the plate reflects of the surface 2 lies in the envelope.
At the position, and of the size of this image, let an opening in the
cuvelope be made; tuis I will call “opening 3.” Let a screen
in the Theory of Heat. | 245
be so placed that no straight line can be drawn from any point
of opening 1 to any point of opening 8 without passing through
the screen. Let the opening 3 be now closed with a black sur-
face, which I will call “surface 3.” The whole system is then
supposed to possess the same temperature; there is therefore im
this case equilibrium as regards the heat. This equilibrium is
supported by rays which, proceeding from surface 3, suffer
reflexion on the plate, pass through opening 1, and fall on the
body C. ‘These rays are polarized in the plane of incidence of
the plate, and contain, according to the thickness of the plate,
sometimes more of one, sometimes more of another kind of ray.
Let the surface 3 be removed and replaced by a circular mirror
whose centre is situated at the spot where the plate reflects an
image of the centre of the opening 1; then the rays emitted by
surface 3 will no longer fall on body C, but instead of them
those reflected from the mirror will fall upon it, and the equili-
brium of the temperature remains unchanged. If we reflect that
it does not matter what thickness the plate possesses, or in what
position we turn it round the axis of the pencil determined by
passing through openings | and 2, we arrive, by means of similar
considerations, at the conclusion that the power of emission of the
black body C, considered with respect to a given wave-length
and a given plane of polarization, is quite independent of the
constitution of this body. A conclusion which naturally arises
from this proposition is, that a// rays which a black body emits
are completely unpolarized. |
If we imagine that in the foregoing arrangement the body
C is not black, but of any other colour, the following equation is
found by similar reasoning :—
senate OA nua ae a
This equation indicates that the relation between emission and
absorption remains constant for all bodies. The equation may
obviously be written
B= App Pet Get Oo Say ae)
or
I will now notice some remarkable conclusions derived from
my proposition. If we heat any body, a platinum wire for ex-
ample, gradually more and more, it first emits only dark rays ;
at the temperature at which it begs to glow, red rays begin to
appear; at a certain higher temperature yellow rays are seen ;
then green rays, until at last it becomes white-hot, 2, e. emits all
246 On a New Proposition in the Theory of Heat.
the rays present in solar ight. The power of emission (E) of the
platinum wire is therefore equal to 0 for the red rays at all tem-
peratures lower than that at which the wire begins to glow; for
yellow rays it ceases to be equal to O at a rather higher tempera-
ture; for green at a still higher temperature, and soon. Accord-
ing to equation (1), the emission-power (e) of a completely black
body must cease to be equal to 0 for red, yellow, green, &c. rays at
the same temperatures at which the platinum wire began to emit
red, yellow, green, &c. rays. Let us now consider the case of
any other body which is gradually heated. According to equa-
tion (2), this body must begin to give off red, yellow, and green
rays at the same temperatures as the platinum wire. All bodies
must therefore begin to glow at the same temperature, or at the
same tempcrature begin to give off red, and at the same tempera-
ture yellow rays, &c. This is the theoretical explanation of an ex-
perimental conclusion obtained by Draper thirteen years ago. The
intensity of the rays of given colour which a body radiates at a
given temperature may, however, be very different,—according
to equation (2) it is proportional to the power of absorption (A).
The more transparent a body is, the less luminous it appears.
This is the reason why gases, in order to glow visibly, need a tem-
perature so much higher than solid or liquid bodies.
A second deduction which I will mention brings me back to
my special subject. The spectra of all opake glowing bodies are
continuous; they contain neither bright nor dark lines. Hence
we can conclude that the spectrum of a glowing black body (the
term being used in the sense already defined) must also be a con-
tinuous one. ‘The spectrum of an incandescent gas consists, at
any rate most frequently, of a series of bright lmes separated
from each other by perfectly dark spaces. If the power of emis-
: > Sa
sion of such a gas be represented by H, the relation = has an
appreciable value for those rays which correspond to the bright
lines of the spectrum of the gas, but it has an inappreciable value
for all other rays. According to equation (3), however, this
relation is equal to the absorptive power of the incandescent gas..
Hence it follows that the spectrum of an incandescent gas will be
the converse of this, as I express it, when it is placed before a
source of light of sufficient intensity, which gives a continuous
spectrum ; 2. e. the lines of the gas-spectrum, which before were
bright, will be seen as dark lines on a bright ground. A remark-
able deduction from my proposition which I will nfention is,
that, if the more remote source of light is an incandescent solid
body, the temperature of this body must be higher than that of
the mcandescent gas in order that such a conversion of the spec-
trum may occur.
On the Repulsion of an Electrical Current on ttself. 247
The sun consists of a luminous nucleus, which would by itself
produce a continuous spectrum, and of an incandescent gaseous
atmosphere, which by itself would produce a spectrum consisting
of an immense number of bright lines characteristic of the nu-
merous substances which it contains. The actual solar spectrum
is the converse of this. Were it possible to observe the spectrum
belonging to the solar atmosphere with all its attendant bright
- lines, vo one would be surprised to hear that, from the existence
of the characteristic bright lines of sodium, potassium, and iron
in the solar spectrum, the presence of these bodies in the sun’s
atmosphere has been ascertained. According to the proposition
which I have just laid down, there can, however, be just as little
doubt concerning the truth of this assertion, as if we saw the
real spectrum of the solar atmosphere.
I will, Jastly, mention a phenomenon which, although appa-
rently trivial, was of peculiar interest to me, because I foresaw it
theoretically, and afterwards verified it by experiment. Accord-
ing to theory, a body which absorbs more rays polarized in one
direction than in another, must also emit those rays in the same
proportion. A plate of tourmaline cut parailel to the optical
axis absorbs, at common temperatures, more of those rays falling
perpendicularly, whose plane of polarization is parallel to the axis
of the crystal, than of those whose plane is at mght angles to the
axis. At temperatures above a red heat, tourmaline also pos-
sesses this same property, although in a less marked degree.
Hence the rays of light which the plate of tourmaline emits per-
pendicular to its surface must be partially polarized ; and, more-
over, they must be polarized in a plane perpendicular to the plane
of polarization of the rays which have been transmitted by the
tourmalme. This theoretical conclusion is borne out by ex-
periment.
XXXVITI. Remarks on Ampére’s Experiment on the Repulsion
of a Rectilinear Electrical Current on itself. By Mr. Jamus
CroLu, Glasgow*.
q* reference to Dr. Forbes’s “ Notes on Ampére’s Experiment
on the Repulsion of a Rectilinear Electrical Current on
itself,’ which appeared in the Philosophical Magazine for Fe-
bruary, the followmg remarks may perhaps be acceptable.
I have long been under the impression that Ampére’s experi-
ment, although successful, does not prove the thing intended,
namely, that the different parts of a rectilinear electrical current
are mutually repulsive; for the motion of the wire is evidently
* Communicated by the Author.
248 Mr. J. Croll’s Remarks on Ampére’s Eaperiment on
due to the action of angular currents, and not to a repulsion ex-
isting between the current in the mercury and the current in the
branch of the wire in the same straight line.
Let abcd be the wire floating
on the mercury, P the point where
the current enters the mercury, and
N the point where it leaves it, after
passing through the wire in the di-
rection indicated by the arrows.
The common explanation is, that
the movement of the wire is due to
there being in each of the branches
ab and ed, separately, a repulsion between the current which tra-
verses them, and the current that is transmitted into the mercury
before penetrating into the wire or after going out from it; and
as the current of the mercury and that of the wire are only the
prolongation of cach other im a right Ime, this 1s considered
sufficient proof that the one part of the rectilinear current repels
the other part.
The following is, however, I think, the true explanation. The
current Pa in the mercury ts at right angics to the current bc
in the cross part of the wire. The former current is directed
towards, and the latter current from the summit of the angle
abe formed by them. Now, according to Ampére’s well-known
law of angular currents, the two currents will repel each other.
In this case the current bc being the moveable one, it will of
course recede, maintaining a position parallel to itself. This
eross current be is also at right angles to the current Nd
on the other side of the glass partition; the former moving
towards, and the latter from the summit of the angle dcd
formed by them. These two currents for the same reason will
repel cach other. The combined influence of the currents P a
and N d in the mercury will be to cause the cross section of the
wire which is at right angles to them to recede, maintaining a
position parallel to itself. It follows, therefore, according to the
law of angular currents, that Ampére’s experiment must be suc-
cessful; but then its success does not prove that the parts of a
rectilinear electrical current are repulsive of each other, but
simply that a moveable current at right angles to a fixed one is
repelled when the one current is directed towards, and the other
from the summit of the angle formed by these two currents.
It would appear from Dr. Forbes’s experiments, that the dif-
ferent sections of a rectilinear current are mutually attractive ;
not repulsive, as is generally supposed. To remoye as much as
possible all resistance to the motion of the wire, and also to sim-
plify the conditions of the experiment, imstead of floating the
the Repulsion of a Reetilinear Electrical Current on itself. 249
moveable wire upon mercury, he placed it upon one of the arms of
a delicate torsion balance. ‘The ends of the moveable wire were
made to bear slightly against the extremes of the two wires in
connexion with the poles of the pile. When the current was
established, the moveable wire placed upon the balance was
attracted by the wires proceeding from the pile, and not repelled
as in the case of Ampére’s experiment; and the stronger the
current, and the more complete the contact of the ends of the
wires, the greater the attraction was found to be.
There is one objection which may be urged against the con-
clusiveness of the experiment. It is well known that the ends
of two wires connecting the poles of a voltaic pile before they
are brought into contact, are statically charged, the one with
positive, and the other with negative electricity, the intensity of
the charge depending upon the force of the pile. Now it is evi-
dent that these two wires being charged with different electri-
cities, must attract each other. It is evident also that, however
close the two ends of the wires may be brought together, unless
they are in absolute contact in every part, a thing impossible
without soldering the ends together, the current will not pass
from the extremity of the one wire to that of the other through the
intermediate space, which is almost non-conducting, unless there
is an excess of positive electricity on the one wire and of negative
on the other; and the more.so, considering the low tension of
voltaic electricity. This being the case, the ends of the conduct-
ing wire and those of the moveable branch will always be charged
with different quantities of electricity, and hence attraction will
be the consequence; yet one would suppose that, unless the
current is in reality self-attractive, the attraction arising from
this cause would not be able to overcome the repulsion which
must ensue from the action of angular currents just considered.
There is one objection to the common notion that the parts of
a rectilinear current are mutually repulsive, that I have never
seen adduced, which isasfoliows: It results from a law of Ohm,
which has been confirmed experimentally by Kohlrausch, that in
the conductor connecting the poles of a voltaic pile, while the
current is circulating, different sections of the conductor are dif-
ferently charged. In any part of the conductor whatever, a
section taken towards the positive pole is always positive in rela-
tion to a section taken towards the negative pole; and vice
versa, a section towards the negative pole is negative in relation
to any section taken towards the positive pole. It follows from
this that the different sections of the current must attract each
other.
The difference of the tension of any two sections depends upon
the resistance to conduction ; that is to say, the force by which
250 Prof. Challis on Theories of Magnetism
any two sections of the current attract each other when the current
is passing, is always as the amount of the resistance which opposes
this attraction. The attraction must always exceed the resist-
ance, or else there can be no current. What does all this mean
if we do not admit that the sections of the current mutually
attract each other ?
The same difference of electric state exists in the various see-
tions of the pile itself; for we know that there is always an ex-
cess of positive electricity at the one pole, and of negative at the
other, and these electricities must tend to unite through the pile
itself. But there is opposed to the attractive force of the elec-
tricities for uniting, not only the resistance in the pile itself, but
also the electromotive force which decomposes the electricity.
This electromotive force must always exceed the attraction of the
electricities: this must be admitted; for unless the foree which
separates the electricities is greater than the attraetive force
which tends to unite them, there could be no decomposition of
the electricity, aud of course no current.
In the pile itself there are two forces—one tending to unite
the various sections of the current, and the other tending to
separate them; the latter force being the strongest, the sections
of the current in the pile will mutually repeleach other. In the
external conductor which unites the poles of the pile, the latter
force has no existence; hence the various sections of the current
in the conductor are mutually attractive. By virtue of the
repulsion in the pile and the attraction in the conductor, the
electricity decomposes in the former and unites in the latter; and
this constitutes what we call an electric current.
XXXIX. On Theories of Magnetism and other Forces, in reply to
Remarks by Professor Maxwell. By J. Cuarus, F.R.S.,
F.R.A.S., Plumian Professor of Astronomy and Experimental
Philosophy in the University of Cambridge *.
N an article on “ Molecular Vortices applied to Magnetic
Phenomena,” contained in the March Number of the Phi-
losophical Magazine, Professor Maxwell has made, respecting
certain points of the general physical theory which I have lately
proposed, some remarks which call fora reply. I refer chiefly
to two paragraphs in p. 163, the first of which is as follows :—
“ Currents, issuing from the north pole and entering the south
pole of a magnet, or circulating round an electric current, have
the advantage of representing correctly the geometrical arrange-
ment of the lines of force, if we could account for the pheno-
* Communicated by the Author.
and other Forces. 251
mena of attraction, or for the currents themselves, or explain
their continued existence.” The generation of such currents I
have explained on hydrodynamical principles in my theories of
galvanism and magnetism, as also in that of electricity. They
are shown to be secondary currents, which are always produced
when a uniform primary current traverses a medium, in which
there is a gradation of density, such as that which must exist
from the top to the bottom of a heavy mass resting on a hori-
zontal plane, in order that the force of gravity on the individual
particles may be counteracted. The primary currents are ascribed
exclusively to motions of the ether caused by the rotations of
the earth and of the other bodies of the solar system about their
axes. As this is a constant cause, the streams are constant.
The retention of an induced state of gradation of density from
end to end, is considered to be the distinctive property of a
magnetized bar. The observed attractions and repulsions are
satisfactorily accounted for by the variation of the fluid pressure
from point to point of space in the secondary currents considered
as instances of steady motion, such variation, together with the
dynamical effect of the currents, producing differences of pres-
sure at different points of the surfaces of the atoms of which
the substances attracted or repelled are supposed to consist.
Thus the three explanations which Professor Maxwell considers
to be requisite respecting currents to which the phenomena of
galvanism and magnetism are attributed, are in fact given by
my general theory quite consistently with its original hypotheses.
The other paragraph commences thus :—‘ Undulations issuing
from a centre would, according to the calculations of Professor
Challis, produce an effect similar to attraction in the direction
of a centre.” I consider that both central attraction and central
repulsion are accounted for by my calculations. Professor Max-
well then adduces the following objection :—“ Admitting this to
be true, we know that two series of undulations traversing the
same space do not combine into one resultant as two attractions
do, but produce an effect depending on relations of phase as
well as intensity.” This point I have considered in articles 2
and 5 of the Theory of Gravity contained in the Philosophical
Magazine for December 1859. There is no limitation as to
the function W, which expresses the velocity or condensation of
the ztherial waves, excepting that it must either be a single
circular function, or consist of the sum of several such functions.
Let it in general be represented by }.msin (b¢+c). Then, ac-
cording to the theoretical calculation, the motion of translation
given to an atom in the direction of the propagation of the
waves, that is, the repulsive action, depends on the non-periodic
part of the square of this function, the quantity which I have
252 Prof. Challis on Theories of Magnetism
called g being in this case insignificant. Now, whatever be the
phases of the several component functions, the non-periodie part
of the square of their sum is equal to the sum of the non-periodic
parts of the squares of the separate functions. In the case of
attractive action, according to the investigation given in the
Mathematical Theory of Attractive Forces contained in the Phi-
losophical Magazine for November 1859, the motion of trans-
lation depends on the value of g, and on the product of W and
d?W
dt? *
assigned, the non-periodic part of the product for the sum of
the terms is the sum of the non-periodic parts of the products
for the component terms taken separately, independently of
their phases. In short, as we are only concerned with squares
of circular functions, the mutual interferences by difference of
phase do not come under consideration. On this account the
dynamical effects of two series of undulations from separate
sources, take place independently of each other, and combine
according to the laws of the composition of accclerative forces.
To the additional objection, that, ‘‘if the series of undulations be
allowed to proceed, they diverge from each other without any
mutual action,” I can make no reply, because I do not under-
stand it. I can only conclude that it was written under some
misapprehension.
Professor Maxwell goes on to assert that “the mathematical
laws of attractions are not analogous in any respect to those of
undulations.” In making this assertion he must surely have
overlooked the very remarkable analogies exhibited by the facts,
that undulations, like central forces, diverge from a centre, and
diminish in intensity according to some law of the distance.
Each body in the universe on which a series of undulations is
incident, becomes a centre of minor undulations, just as when
waves on the surface of water encounter an insulated obstacle,
the obstacle becomes a centre of subordinate waves. The con-
tinuous generation of subordmate undulations corresponds to
- the maintenance of the gravitating power of the body.
Perhaps, however, the assertion, although it is not limited,
was intended to apply only to such attractions as are observed
in a magnetic field. If so, it is in accordance with my general
theory, which makes a distinction between attractions and repul-
sions by means of undulations, and attractions and repulsions due
to currents. Electric, galvanic, and magnetic forces are of the
latter kind. But, while it is admitted that the laws of these
forces “have remarkable analogies with those of currents,” I
should not say that they are analogous “to the laws of the con-
duction of heat and electricity, and of elastic bodies,” because,
But it is easily seen that if W have the form above
and other Forces. 2538
according to the views which I maintain, these are phenomena
which ultimately may receive explanations by means of ztherial
undulations and currents, and therefore ought not to be put in
the same category.
As the article I have been referring to contains a theory of
magnetic phenomena wholly different from that which I have
advanced, it may be worth while to point out a difference in
principle between the fundamental hypotheses of the two theories.
Professor Maxwell assumes the existence of a magnetic medium,
which is not fluid, but “ mobile,” and which acts along lines of
magnetic force by stress combined with hydrostatic pressure ; in
other words, there is greater pressure in the equatorial, than in
the axial, direction of the magnetic field. To account for this
difference of pressure, it is assumed that “ molecular vortices”
circulate about axes parallel to the lines of magnetic force. Why
they are called ‘‘ molecular” is not expressly stated im this arti-
cle; but it may be gathered from other of the author’s writings,
that he conceives the matter of the vortices to consist of mole-
ecules which by their motions may come into collision, the result-
ing dynamic effect depending on the number and frequency of
such collisions. It is not my intention to criticise these hypo-
theses, which have been adduced merely for the sake of remarking
that, as they are of a particular character, and have been framed
apparently with special reference to observed laws of magnetic
phenomena, the results of a mathematical investigation founded
on them can hardly amount to more than an empirical expression
of those laws. After all that can be done by this kind of re-
search, an independent and @ priori theory of the same kind as
that which I have proposed, if not the very one, is still needed.
The hypotheses on which my investigations have been founded
are these only. The physical forces are modes of action of the
pzessure of the ether, which is a continuous fluid medium, having
the property of pressing in proportion to its density, and filling
all space not occupied by the discrete atoms of sensible bodies,
which atoms are inert, spherical, and of different, but constant,
magnitudes. It may be remarked that these hypotheses include
no ideas that are not intelligible by sensation and experience,
and therefore conform to the rule of philosophy according to
which cur knowledge of natural operations must ultimately rest
on such ideas. Also they are strictly related to antecedent and
existing physical science. The prominent terms, ether and atom,
which had their origin in ancient speculations, have obtained. re-
markable significance in modern science,—the first, by explana-
tions of the phenomena of light, and the other, by aiding us to
conceive of chemical analyses. The hypotheses under the above
form are mainly due to Newton, who gave a definition of atoms,
254 Mr. T. Tate on certain peculiar Forms
and suggested the dynamic action of the ether; but the state of
mathematics in his day did not allow of investigating the conse-
quences of the latter idea. In attempting to do this in the pre-
sent advanced state of mathematics, I have only added, for that
purpose, to the Newtonian hypotheses, an exact definition of the
wether, and the supposition that the atoms are spherical. In the
first instance I appled the hypotheses as a foundation for a
theory of light, having long since seen that the theory which
proposes to account for the phenomena of light by the oscillations
of the diserete atoms of a medium having axes of elasticity, is
contradicted by facts, and must therefore be abandoned. This
charge [ have brought against it in an article on elliptically
polarized light in the Philosophical Magazine for April 1859
(p. 288); and it has found no defender. When this first appli-
cation was made, I had no conception of any modes of applying
the same hypotheses to explain the phenomena of gravity, elee-
tricity, galvanism, and magnetism. If they are found to admit
of applications so varied and extensive, the explanations are no
longer personal, the hypotheses themselves explain, because they:
ave true. The only advantage I pretend to possess in these re-
searches is, the discovery of the true principles of the application
of partial differential equations to determine the motion and
pressure of an elastic fluid. But this kind of reasoning, though
it is indispensable for the establishment of the truth of the
general physical theory, may be tried on its own merits, quite
independently of its applic: ition in that theory. For this reason
I expressed the intention of carefully revising the proofs of the
propositions in hydrodynamics which have been alre: ady enun-
ciated in this Journal, and the results of which have been applied
in the physical theory. But my occupations do not allow of
entering on this task ant present.
Cambridge Observatory,
March 16, 1861,
XL. On certain peculiar Forms of Capillary Action.
By Tuomas Tarn, Lsg.*
IQUIDS rise in small tubes by what is called capillary
action, that is, by the cohesion of the particles of the
liquid for one another, as well as by their adhesion to the sides
of the tube. It has been ascertained ihat the height to which a
liquid is-raised by capillary action varies inversely as the dia-
meter of the tube. The chief object of this paper is to deter-
mine, by direct experiment, the law of capillary resistance exerted
* Communicated by the Author.
of Capillary Action. 255
by a liquid filling small orifices or perforations made in rigid
plates of different thicknesses.
Let AC represent a wide glass tube, closed at Fig. 1.
the top, and having a perforated plate He, capable
of being wetted, cemented to its lower extremity ;
1B a glass tube, about half an inch in diameter,
cemented to this plate, open at its lower extremity,
and communicating with the tube AC; e asmall
perforation made in the plate; DB a glass vessel
containing water or any other liquid to be ex-
amined. ‘The tube EB is graduated from the
exterior surface of the plate into inches and
decimal parts of an inch. ‘The tubes being filled
with water, and the extremity B inserted in the
water contained in the vessel DB, it will be
found that the orifice e may be raised for some
inches above the level FD of the water in the
vessel before the atmospheric air will enter the
orifice. The height C D, at which the external
air enters the orifice, obviously gives us the measure of the ca-
pillary resistance of the liquid in the orifice. The followmg
results of experiments show that, the temperature being constant,
the height of the column C D, measuring the capillary resistance
of the liquid, varies inversely as the diameter of the orifice.
The experiments recorded in the following Table of results,
were made with the apparatus represented in fig. 1. The orifices
were made in plates of gutta percha by means of fine steel wires,
whose diameters had been previously determined, Slight oscil-
lations and other extraneous causes having been found to affect
the results of the experiments, each result here given is the mean
of five experiments.
Table of results of experiments giving the columns of capillary
resistance corresponding to different diameters of the orifices.
The liquid was water at the temperature of 56° F., and the
thickness of the plate was 05 of an inch.
Diameter of the |Corresp. column Value of h
orifice in parts | C D of capillary} by formula
of an inch, resist. in inches, ee
dD. h. ‘=39 D
es 3°35 3:32
en 1:80 1-82
ee 1-40 1:36
ds 112 l-ld
256 On certain peculiar Forms of Capillary Action.
The near coincidence of the results of the second and third
columns shows that, other things being the same, the height of the
column CD, measuring the capillary resistance, varies inversely as
the diameter of the orifice.
The column of resistance, CD, is slightly affected by the thick-
ness of the plate: thus with a half thickness of plate, and with
an orifice of th of an inch, the height of this column was found
to be 3 inches nearly.
The number of perforations made in the plate does not affect
the results.
An increase of temperature sensibly reduces the height of the
column CD: thus at the temperature of 84°, with an orifice of
7th of an inch, this column was found to be about ;45th of an
inch less than it was at the temperature of 56°.
The column of capillary resistance, C D, for viscous liquids,
such as diluted solutions of gum and sugar, was found to be
considerably greater than the corresponding column for water.
Let the tube EB (fig. 2), closed at the top by the perforated
plate Ee, be depressed in the liquid, the orifice e beg wet; it
will be found that the liquid will not rise in the tube to the same
level as the liquid im the vessel: the column of depression C D,
in this case measuring the capillary resistance under the same
Fig. 2. Fig. 3; Fig. 4.
ililitit
HANI
Vhs
ili!
ili
reat
circumstances, is nearly equal to the elevation of the column C D
of fig. 1. Here the resistance is simply due to the film of liquid
filling the orifice e. It is scarcely necessary to state that, when
the orifice e is dry, or nearly dry, the liquid will rise in the tube
to the same level as the liquid in the vessel EB.
In like manner, if the tube, partially filled with liquid, be
raised as represented in fig. 3, it will be found that the liquid
will stand in the tube some distance higher than the level of the
liquid in the vessel. The column of elevation, C D, in this case
measures the capillary resistance to the pressure of the external
air.
On a Theorem relating to Equations of the Fifth Order. 257
If the tube, completely filled with liquid, be raised as repre-
sented in fig. 4, it will be found that the liquid will stand in the
tube some distance higher than the level of the liquid in the
vessel. The column of elevation C D, measuring the capillary
action, was found, under the same circumstances, to be nearly the
same as in the preceding cases. Here the capillary action is
restricted to the orifice of the thin plate, the diameter of the
tube EB with which the experiment was performed being about
oneinch. This experiment strikingly shows that the height of
the column measuring capillary action for any given liquid at a
constant temperature depends (chiefly, if not entirely) upon the dia-
meter of that portion of the tube immediately in contact with the
upper surface of the liquid.
March 18, 1861.
XLI. On a Theorem of Abel’s relating to Equations of the
Fifth Order. By A. Cayiuny, Esq.*
P / SHE following is given (Abel, Giwvres, vol. x1. p. 253) as an -
extract of a letter to M. Crelle :—
“Si une équation du cinquiéme degré, dont les coefficients
sont des nombres rationnels, est résoluble algébriquement, on peut
donner aux racines la forme suivante,
a=c-+ Aata,? do5ag> + A,a,3 dy3 458 a5 + Agaos ag
ou
as
ay? + Asay a? 5 a3 ag ;
a=m+n/1+2 4VAl te +e? 4 -V1 +e),
a,=m—n/1+e Perv h(l +e —V1+¢ +e),
dg=m+n/1Fe—V Al +e+ V1 +e),
az=m—n/1LEE—V h(l+e— V1+e +),
A =K+4+Kla +K"a.+K"aa,, A,=K+K!a,+K"a,+ Kaya,
A,=K+K'a,+K"a + K"aa,, Az=K+Kla,+ K"a,+ K"aja,.
Ties quantités c,h, e, m,n, K, K!, K", K'" sont des nombres
rationnels.
“Mais de cette maniére léquation z°+axr+b=0 n’est pas
résoluble tant que a et 6 sont des quantités quelconques. J’ai
trouvé de pareils théorémes pour les équations du 7*™¢, 11*™,
13°m°, &c. degré. Fribourg, le 14 Mars, 1826.”
The theorem is referred to by M. Kronecker (Berl. Monatsb.
June 20, 1853), but nowhere else that I am aware of.
It is to be noticed that in the expressions for a, a, dq, a3, the
| * Communicated by the Author.
Phil. Mag, 8. 4, Vol. 21. No. 140, April 1861. S
258 Mr. A. Cayley on a Theorem of Abel’s relating
radicals are such that
SI FeV 1 t+e+ Vite) VA +e—V1+e)she(1 +e),
a rational number.
The theorem is given as belonging to numerical equations ;
but considering it as belonging to literal equations, it will be
convenient to change the notation; and in this point of view,
and to avoid suffixes and accents, I write
e=O+ Aa Bi y8 85 + BBS 258 as + Cys d5 a5 Be 4 Ddtak Biys,
where
a=m+mn/O+Vp+qV0,
B=m—n/O+V p—qV@,
y=m+n/O—Vn+qV@,
S=m—m/O—-V p—qvO;
the radicals being connected by
SOV p+yVOV p—qvO=s,
and where
A=K+lLa+My+Ney, B=K+L6+M6-+ N68,
C=K+Iy+Ma+Nay, D=K+L6+M6+ N68,
in which equations 0, m, n, p, g, ©, s, K, L, M, N are rational
functions of the elements of the given quintic equation.
The basis of the theorem is, that the expression for 2 has only
the five values which it acquires by giving to the quintic radicals
contained in it their five several values, and does not acquire any
new value by substituting for the quadratic radicals their several
values. For, this being so, # will be the root of a rational quintic ;
and conversely.
Now attending to the equation
JOVp+qVOV p—IVO=s,
the different admissible values of the radicals are
JO, Vpt+qv®, Vp—gv®,
—/6, Vp—qv0, —Vp+qVv®,
JO, —Vp+qv@, —Vp—qv®,
-J®, —Vp=4q¥6, VptqV®
corresponding to the systems
to Equations of the Fifth Order. 259
a, B ‘? oD )
ends 8, @
Y> 6, a, B
a, B ihe 6
of the roots a, 8, y, 5; 7. e. the effect of the alteration of the
values of the quadratic radicals is merely to cyclically permute
the roots a, 8, y, 6; and observing that any such cyclical per-
mutation gives rise to a like cyclical permutation of A, B, C, D,
the alteration of the quadratic radicals produces no alteration in
the expression for z.
The quantities a, 8, y, 5 are the roots of a rational quartic.
If, solving the quartic by Huler’s method, we write
a=m+/F+/G+ /H, /FGH=y, a rational function,
B=m—/F+/G—V/H,
y=m+/F—/G—VH,
S=m—/F —/G6+/H,
then the expressions for F, G, H in terms of the roots are
| (a+y—B—6)?, (a+B—y—8)*, («+6—B—y)’,
which are the roots of a cubic equation
u?—)u? + pu—v?=0,
where A, “4, v are given rational functions of the coefficients of
the quartic. We have
JG4+V/H=V(VE+ caer erat om
a OER Ree ~ VF.
So that, takmg O=F, the last-mentioned expressions for «, 8,,6
will be of the assumed form
a=m+/O0+Vn+qV0, &e.
The equation |
/ OV p+qV OV p—qV O=s
thus becomes
Re /G Hi se or F(G—H)?=s?;
that is,
—F° + F(R’ + G?+ H*) —2EGH Ss? ;
S2
260 Mr. A. Cayley on a Theorem of Abel’s relating
or, what is the same thing, and putting O for F,
—X0?+ (A?— p)O—3/?=s?.
Hence in order that the roots of the quartic may be of the
assumed form,
a=m+t+/O4Vn+9V0, &e.,
where m, p, g, © are rational, and where also
/O Jp +qVO /n—qY V@=s, a rational function,
the necessary and sufficient conditions are that the quartic should
be such that the reducing cubic
u>?—)u? + pu—v? =0
(whoseroots are (2+ 8 —y—86)?, (« +y—B—5S)?, (« +8—B—y)?)
“may have one rational root @, and moreover that the function
—r0?+ (A?— pp)O—3y?
shall be the square of a rational function s. This being so, the
roots of the quartic will be of the assumed form,
a=m+/O+Vn+qV0, &e.
And from what precedes, it is clear that any function of the roots
of the quartic which remains unaltered by the cyclical substitu-
tion «Syd, or what is the same thing, any function of the form
h(a, B, Y 6) + (8, Y> 6, c) +(y; 5, a, B) oh f(S, a, B, Y)
will be a rational function of m, ©, p, g, s, and consequently of
the coefficients of the quartic. The above are the conditions in
order that a quartic equation may be of the Abelian form.
It may be as well to remark that, assuming only the system
of equations
a=m+/O+/T,
B=m—/O4VT,
y=m+/0-VT,
S=m—/O—1/ 1’,
then any rational function of a, 8, y, 5 which remains unaltered
by the cyclical substitution «Sy5 will be a rational function of
6, T+, TY, /TT(T—-T), /O(T—-T), /O/TT.. In
fact, suppose such a function contains the term
(SOS T/T)"
then it will contain the four terms
(/6)*{0 + (— PY T/T)" + (—)"U(—
to Equations of the Fifth Order. 261
( /o)( VT) V0),
(-V6)"( VP)"(-VT)’,
( Ye)(-V/T)*(-V TY,
(—/6)"(-/T)"( 1)”,
which together are
an expression which vanishes unless (—)*, (—)” are both posi-
tive or both negative. The forms to be considered are therefore
a A Wa aed eae So
+ + +
~ + +
a — —
The first form is
(V/O)* (STP T+ (TPT),
which, «, 8, y bemg each of them even, is a rational function
of ©, T+T', TY’.
The second form is
(VOUT TY WS TPS TY»
which, « being odd and £ and y each of them even, is the pro-
duct of such a function into \/O(T—T’).
The third form is
(VOUS TPS TY —(S TS T)*5,
which, « being even and @ and y each of them odd, is the pro-
duct of such a function into »/ TT’ (T—T’).
And the fourth form is
(VO) US TPS TY + / TS T)*S,
which, a, 8, y being each of them odd, is the product of such a
function into »/@(T— 1’).
Hence if T=p+ q/ 0, T’=p—q/9, and
/OrV/ptqV/@ /p—q/ O=s,
®, T+T'(=2p), TY (=p?—¢?20), /TY(T—T' )(= =
/O(T—T’)(=2¢8), and /O/TT(=s)
are respectively rational functions. Thisis the @ posteriori veri-
PL +(-PI (VT) TY} >
262. Ona Theorem relating to Equations of the Fifth Order.
fication, that with the system of equations
a=m+/O + Vp+qv@, &e., /OV p+qV OV p—qVvO=s,
any function ,
f(a, B, ¥, 6) + (8, y, 9; a)+ oly, 6, a, B) + (6, a, B, Y)
is a rational function. }
The coefficients of the quintic equation for # must of course
be of the form just mentioned; that is, they must be functions
of a, B, y, 6, which remain unaltered by the cyclic substitution
a8yd. To form the quintic equation, I write
0—x=a,
Aa? BF y5 8? = b, DS*a? BFy?= C, BR*y28? a? =d, Cry? 83 a5 8? =e;
then we have
O=a+b+c+d-+e,
and the quintic equation is
fl fo fo? fo® fo*=0,
where is an imaginary fifth root of unity, and
fo=a-+ bo + cw? + dw? + ew*.
We have
fo fot= 0? + (o +.04)>!ab + (@? + o°) Zac,
fo? fo® = Ya? + (w* + w*)2ab + (w? + w*)2/a0,
where &! is Mr. Harley’s cyclical symbol, viz.
Dlab=ab+be+cd+de+ea;
and so in other cases, the order of the cycle being always abcde.
This gives 7
fo fo*fo* fot = Lat + Ya?b? — Lab + 2Za*bhe— Labed
—52z/a?(be+ cd) ;
and multiplying by f1, = =a, and equating to zero, the result is
found to be wh
+a°— 5abede—5>'a3(be + cd) + 5>/a(b7e? + c7d*) =0.
Or arranging in powers of a, this is
od ee 7
+a?. —5(be+cd) |
+a’. 5 (bc? + ce? + ed? -+ db*)
Ce ere 3
ry : 5 (bc + c8e + e8d+d°b) 20:
+5 (be? + c?d*?—becd)
6+c+e+4d°
ae { —5(b%de + c®bd + e?ch + dec)
+5 bd2e? + cbh2d? + ec? b? + de*ec?
On the Stability of Satellites in small Orbits. 263
the several coefficients bemg, it will be observed, cyclical func-
tions to the cycle 4, c, e, d.
Putting for a its value —(x—6), and for 4, c, d, e their values,
the quintic equation in z is
| (x—0)° 7
+ (z—9)°. —5(AC+BD)28y6 |
+(z—@)?. —5(A*Byd+ B*Cde2+C*D28 + D*ASy)a8ys
74 5(A®D 0776 + BeAyé*2 + C#Bda28 + D5C28*y)a8yd =
+5(A?C?+ B*D?—ABCD)2*6*°e . ae.
J
(A588? + Beyé8x2 + 058238? + Dea S52) 288
—5(ASBCyS + B°CDaz + C3D Az + DSABBy)a262y°S2
4.5(AB°C228 + BC*D2@2 + CD2A2y8-+ DE2A%S2) e262
where, as before,
A=K-+La+My+Nay,
B=K+L8+Mé6+N86,
C=K+ly+Ma+Nye,
D=K+L6+MS8+N68;
and the coefficients of the quintic equation are, as they should
be, cyclical functions to the cycle z8y6.
2 Stone Buildings, W.C..,
February 10, 186].
XLII. On the Stability of Satellites in small Orbits, and the
Theory of Saturn’s Rings. By Dantet VauGHAn *.
is dee mysterious revolutions of planets and comets were not
rendered intelligible to astronomers until mathematical
investigations revealed the peculiar curves which moving bodies
must describe when left to the exclusive control of solar gravity.
The process of deductive inquiry, which proved so beneficial in this
and other departments of celestial mechanics, may be successfully
applied to another problem which the results of telescopic obser-
vation have forced on the attention of mathematicians. The
physical constitution of Saturn’s rings, the circumstances on
which their stability depends, and the causes which prevent their
conversion into satellites, have already been made the subject of
many able essays; but, though regarding these productions as
valuable contributions to science, I think it advisable to select a
* Communicated by the Author.
264 Mr. 1). Vaughan on the Stability of Satellites in small Orbits,
less difficult road to the solution of the curious problem, and to
seek a clue to the stability of the annular appendage of Saturn
by investigating the form which matter must necessarily assume
in very great proximity to a central body.
In my communication published in the Philosophical Maga-
zine for last December (1860), I treated on the equilibrium of
satellites revolving extremely near to their primaries; and I
endeavoured to give an estimate of the smallest orbits which they
could describe in safety. In the cases I considered, the satellite
was supposed to have its movements adjusted for keeping the
same point of its surface always directed towards the primary,
not merely because the hypothesis facilitated the investigation,
but because observation lends it every support, and the principles
of natural philosophy furnish most cogent reasons for its adop-
tion. In describing a very small orbit without such an adjust-
ment, a satellite must experience, not only excessive tides in its
seas, but even incessant commotions in its solid matter; and the
destruction of power by friction necessarily involves a continual
change in the rotatory movement of the subordinate world, after
a manner analogous to that which I described in a paper pre-
sented to the British Association for the Advancement of Science
in 1857. This must have the ultimate effect of establishing a
synchronism of the orbital and diurnal movements, together with
a coincidence of the planes in which they are performed ; so that
the disturbimg force may give the secondary planet a permanent
elongation, without rendering it a prey to the effects of violent
dynamic action. From late researches, however, | am convinced
that a want of these peculiar conditions would not seriously
affect the fate of a large satellite when brought into dangerous
proximity to its primary; and would not change, to any great
extent, the magnitude of the orbit in which its dismemberment
must be inevitable. ;
A homogeneous fluid satellite, having its motions adapted for
keeping one part of its surface in perpetual conjunction with the
primary, must find repose in a form differing little from an ellip-
soid. This proposition, which in my last article was assumed as
true, may be proved by showing that the relation between the
forces exerted on every part of the fluid mass is almost precisely
such as is necessary for equilibrium when the figure is an ellip-
soid, the dimensions being small compared with the diameter of
its orbit. For this purpose put A, B, and C for the major, mean,
and minor semiaxes of the ellipsoid, while P, Q, and R express
the forces of attraction at their extremities in the absence of all
disturbances. Now at any point in the surface, the coordinates
of which referred to the centre are represented by a, ), and ¢,
the components of the attraction in the direction of each axis
and the Theory of Saturn’s Rings. 265
will be expressed by
aP bQ) cR e 1
“A? B? "0% e e . e e oy e ( )
If N denote the centrifugal force at the extremities of the major
axis, the intensity at the proposed pomt will be nies , and
the components in the direction of the three semiaxes will be
aN bN
eas,
To find the components of the disturbing force of the primary
when the major axis ranges with its centre, we may use methods
analogous to those pursued in the lunar theory for estimating the
amount of solar disturbance. Thus, putting # for the radius of
the circular orbit which the satellite describes, and M for the
attractive force of the primary at the distance z, the attraction
which it exerts on the satellite at the point under consideration
will be
Oe rc ce
Mz?
Pad gt ee ee (3)
This is equivalent to two forces—one acting in the direction of
the major axis and expressed by
M23
(a®—2aw +02 +b? +42)?
the other directed to the centre of the satellite and expressed by
Ma? Va? +02 + c? ; (5)
(x? —2ax +a? +b? +02)? a eee
From the first, (4), arises a disturbance operating exclusively
in the direction of the major axis, and represented by
pea es gn 8 pn
(a? —2ax + a? + b?+c?)2 &
eet
the squares and higher powers of “» °, and - being rejected as
too small to affect the result to any appreciable degree. Under
the same conditions, the radial force (5) resolved with reference
to the three axes gives the components
Ma Md Me .
Ae 3 aaa . e e 4 ) e (7)
x & 2
Accordingly, if X represent the sum of the components acting in
* A demonstration of this theorem may be found in the article on
“ Attraction ” in the eighth edition of the Encyclopedia Britannica.
266 Mr. D. Vaughan on the Stability of Satellites in small Orbits,
the direction of A, Y the sum of those in the direction of B,
and Z the sum of those in the direction of C, it appears from
(1), (2), (6), and (7) that
aP aN 2aM
le
bQ bN 6M
15 = ay B = + epi? a eh 6. cs ee (9)
Tres oh eg
Now it is well known that, to satisfy the conditions of equili-
brium, or to make gravity perpendicular to the surface in all
parts of the satellite, it is necessary that
Xda+Vdbt7de=0.. ws oe te pe
Substituting their values for X, Y, and Z, there results
P—N 2M Ree M R.M
(Sa - S )aaat (AR M54 (B 4% o \cde re
Q
But the equation of an ellipsoid is a3 -- ap + = 1, and its
differential, multiplied by the constant quantity 8S, becomes
Sada _ Shdb , Sede
=r tape + ce =0. 0"
A comparison of the corresponding terms of equations (12) and
(13) will enable us to fix the necessary relations of the constants
for satisfying the former. It thus appears that
See at ME oe
rye + oy — BY ay tat Ieee (15)
R ti bade,
These relations being independent of the values of the coordi-
nates a, b, and c, they will be the same for every part of the sur-
face of the body; and it follows that an equilibrium established
at any one locality must extend to every part of the entire mass.
Accordingly the relative magnitudes which the axes A, B, and C »
must possess, to make gravity perpendicular to the sur face at any
intermediate pot, must give gravity a like vertical direction in
all places, and secure the same stability to every portion of the
satellite which has an ellipsoidal form. This, however, would
not appear to be rigorously correct if, in the expressions for the
_and the Theory of Saturn’s Rings. 267
disturbances by the primary, the squares and higher powers of
= and - were retained; and accordingly the very close ap-
proximation to a true ellipsoid can be exhibited only when the
size of the satellite is very small compared with that of its orbit.
If the disproportion between both were not very great, the form
of the satellite would resemble that of an egg slightly flattened
by lateral pressure; yet even in such extreme cases the hypo-
thesis in regard to the ellipsoidal form can lead to no material
error in estimating the intensity of gravity on its surface, and
the dimensions of the smallest orbit in which its parts can be
held together by their mutual attraction.
From equations (8) and (14), (9) and (15), and (10) and (16),
the following are readily deduced :—
P—N 2M aS
X=a( A, Tora » or =e e - ° (17)
2—N M bS
R M cS
Z=o( G +=), or = G2 ee (19)
But calling the force of gravity at the given locality F, it is evi-
dent that F is equal to “X?+ Y?+Z?. On substituting for X,
Y, and Z their values given by the last equation, there results
as? 6282 22 Cre RS
pe — or =* Ta + abt + (20)
The quantity under the radical in the last expression is the value
of the normal of the ellipsoid; and hence the force of gravity
everywhere on the surface is proportional to the length of the
normal corresponding to the locality. At the extremity of each
axis this gravitative power, like the normal, is inversely propor-
tional to the lengths of the axes themselves—a result which might
be more readily deduced from equations (17), (18), and (19). In
the first, for instance, if the point be situated at the end of the
major axis, a becomes equal to A and X, which then expresses
that the entire gravity at the point is equal to B. ; while the two
other equations, (18) and (19), treated in a similar manner, would
give © and C for the values of the intensity of gravity at the
terminations of the mean and minor axes.
The cases in which equilibrium is impossible will be indicated
by the occurrence of imaginary radicals, when we determine the
relation between the constant quantities in formule (14), (15),
268 Mr. D. Vaughan on the Stability of Satellites in small Orbits,
and (16); and as this may be found by simple equations for all
except the semiaxes A, B, and C, it is to their values alone that
we must look for imaginary expressions. The formule referred
to give
ee ee
in (P—N)+ oar V «?(P—N)?—8SMa, }
x 1 )
Re , 1
~ 2M 2M
Now it is evident that none of the above radicals can become
imaginary except the first ; and the stability of the body ceases
to be possible when a?(P—N)?—8MSz, in passing from a posi-
tive to a negative value, becomes equal tonothing. In this case
x
A= AM (P—N). e ° ° ® ry (22)
But by comparing the expressions given in my last article for
centrifugal force and the disturbance of the primary at the extre-
mity of the major axis of the satellite, it appears that the latter
C= V/ AMSz + R22?.
is double the former, or that N equals aa We may deduce
the same result by considering that the orbital velocity of the
satellite’s centre is equal to “Mz; and from this the rotatory
velocity of the extremity of the greater axis 1s equal to 7 Ma,
or Ay/ M Calling this »,
x
v MA
N= RX? or N= Sie ; : 2 Y : (28)
This value being substituted for N in the last equation, gives
A= ea li whence Pela » 2 (24)
z w
The diminished force of gravity which, at the extremity of A,
is represented by P—N— a thus becomes
a . ap thease
the satellite were a homogeneous fluid, the stability must become
impossible when more than three-fifths of the attraction along
the major axis is neutralized by centrifugal force and the disturb-
ing influence of the central sphere.
The cause of the unstable equilibrium in such cases will be
rendered more intelligible by a further examination of equa-
and the Theory of Saturn’s Rings. 269
tion (14), which, on multiplying its members by A, becomes
2MA §
P—N as Tee — A’ e e ° ° .
The terms of the first member constitute the expression for the
force of gravity at the extremity of A; and the impossible root
merely shows that gravity at this point, after having lost over
three-fifths of its intensity by the disturbances, cannot amount
(25)
S brits :
to —, and consequently can no longer maintain the inverse ratio
A
to the length of the axis. This peculiar relation between the
length of each axis and the gravity at its extremity has already
been deduced from formula (20), and is indispensable to the
equilibrium of similar columns of fluid extending from these
points, either to the centre of the body, or through shells of
matter equally dense, and bounded by the surfaces of concentric
ellipsoids similar in position and dimensions. ‘This leads to the
conclusion maintained on different grounds in my last commu-
nication, in which I regarded the rupture of the satellite as n-
evitable, when an increase of elongation would fail to give any
preponderance to the pressure along the greater axis, or when
the ellipticity required to be increased to an infinite extent to
counteract a very slight augmentation of the disturbing forces.
My former estimates, indeed, do not agree very closely with the
present investigation in determining the amount of disturbance
necessary to bring stabiiity to an end; but in these estimates
the eccentricity of the elliptical section containing the mean and.
minor axes of the satellite was neglected ; and from more exact
calculations, which are not yet in a condition to be published, it
appears that some reduction must be made in the value I first
assigned to the smallest orbit in which a homogeneous satellite
could be preserved.
To furnish another proof that the central and the superficial
conditions of equilibrium necessarily lead to the same results in
every respect, let us suppose a portion of the fluid to be enclosed
in three tubes; two of which are connected at the centre and
extend to the nearest and most distant part of the surface, while
the third stretches along the surface to mect their extremities,
while it coincides with the plane in which they are situated.
Now the force of gravity being (PN oe at the extre-
mity of the major axis, it must be reduced to — _ oe a
along this line at a distance from the centre denoted by a, and
the element of the pressure in the tube (taking the transverse
270 Mr. D. Vaughan on the Stability of Satellites in small Orbits,
section and density of the fluid as unity) will be
Se ie
The integral of this expression, taken within the limits of a=0
and a=A, gives for the central pressure of the fluid in the
longer tube
4(p-n—=4). 4 Ly ii
A similar process applied to the fluid in the tube coinciding with
the minor axis, will give for the differential of pressure,
R M
G+) ede rae meee
and a similar integration will give for its pressure at the centre,
C MC
B (BSS). obey - oe )ada+ (e+ =) ele=0. sucked
Integrating within the limits of a=A, c=0, and a=0, c=C,
this becomes
(p-n—2*)_S(R+%2)=0. . (82)
The identity of equations (80) and (82), and the relation
between (26), (28), and (31), show that the equilibrium of the
internal and external parts of the mass depend on precisely the
‘same conditions, and that the fluid should rush to the most pro-
‘minent parts of the satellite from the surface, as well as from its
internal regions, whenever gravity along the major axis was dimi-
nished more than 60 per cent. by the disturbing forces. Brevity
compels me to omit the more lengthy investigation which would
be required to show that such consequences are not peculiar to
special localities, but are the same on all parts of the surface of
the body.
and the Theory of Saturn’s Rings. a
These results might lead us to infer that a satellite which had
been introduced into the region of instability by the action of a
resisting medium, must undergo a sudden and not a gradual
dismemberment. Before embracing this opinion, however, a few
modifying circumstances should be considered. The change in
the figure of the body must increase the time of rotation, while
the diminished size of the orbit calls for a shorter period of re-
volution ; and the synchronism of the diurnal and progressive
movements will be destroyed. But we may safely assert that
the effects of the resisting medium in producing this change are
exceedingly small compared with the influence of tidal action in
keeping the same side of the satellite always turned to its pri-
mary, especially when the distance from the latter became very
small. The result in such cases must be a little different for a
solid satellite, which accommodates its form to the new conditions
of equilibrium by a limited number of paroxysmal changes sepa-
rated by intervals of many millions of years. On such occur-
rences, the reduction of the velocity of rotation, together with
the tendency of the major axis to range with the primary*,
would lead to a series of librations, which, in a dangerous proxi-
mity to the latter body, would tend more to promote than to
prevent the final dismemberment.
It must be also recollected that our formule have been deduced
on the supposition that all parts of the satellite are equally dense ;
and some modifications are therefore required in applying them
to the cases likely to occur in the realms of Nature. If the den-
sity increased very rapidly from the surface to the centre, gravity
might be entirely suppressed at the ends of the greater axis
before it became incapable of maintaining the stability of the
internal matter; and it would seem that im such a case the
satellite might part successively with many layers of the fluid of
which it is composed, before the increased disturbance called for
a general disunion of the internal mass. If, however, the in-
creasing density towards the centre merely results from the great
pressure in these localities, the separation of matter from the
surface must weaken the tie which holds the remainder of the
satellite together; and the dismembering action, when once
begun, will proceed without interruption until a dissolution of
the entire mass is completed. Butit is in cases where the satel-
lite is solid that the mighty change im its condition assumes the
most awful character, as the cohesion of its parts must prevent
the gradual loss of matter from its surface, and keep the dis-
turbing forces under restraint until they become capable of
* There is some inaccuracy.in my last article in the incidental statement
respecting the intensity of this directive force at different distances,
272 Mr. D. Vaughan on the Stability of Satellites in small Orbits,
effecting a simultaneous dilapidation of the entire planetary
structure.
I have regarded it as important to trace the precise manner in
which these sublime catastrophes must take place; not so much
on account of their connexion with the existence of planetary
rings, as for the light which they throw on the nature of
temporary stars. In an article published in the Supplemental
Number of the Philosophical Magazine for December 1858, I
maintained that these singular displays of stellar brilliancy were
great meteoric displays in the atmospheres, or rather the dormant
photospheres, of dark central bodies of space, as they were tra-
versed by the wrecks of dilapidated worlds. The same theory
has been set forth in my paper presented to the British Associa-
tion in 1857; and I have endeavoured in other publications to
support it with satisfactory proof. But the most conclusive evi-
dence on which it depends, is to be derived from the instanta-
neous manner in which the attendant of a dark central body
must undergo a total dismemberment, as it explains the sudden
manner in which these celestial curiosities are ushered into exist-
ence with all the splendour of distant suns. Humboldt, in the
third volume of his ‘Cosmos,’ calls special attention to the fact
of the extreme brilliancy of the temporary stars in their incipient
stages, regarding it as a remarkable peculiarity, and one well
deserving of consideration.
Without adducing any further evidence on this subject, I shall
now proceed to trace the condition which matter must assume in
the region where such disturbing forces render it imcapable of
forming a single mass, held together by the power of gravity.
On the dismemberment of a satellite on this dangerous ground,
the resulting host of fragments would scatter into numberless
orbits; and the wide range over which they must extend may
be estimated from the greatest and least size of the elliptical
paths which their velocities and positions should assign to them.
For these, however, we can only give at present approximate
values, taking no cognizance of the mutual disturbances of the
fragmentary host. And in this case the matter from the most
distant part of the satellite would describe an ellipse, the dia-
meter of which is equal to
23 (a + A)
2u°—(v+A)*
The fragments from the nearest point of the dismembering mass
would describe an elliptical orbit the diameter of which is
2a°(u—A) |
22° —(e2—A)§
and the Theory of Saturn’s Rings. 273
But the size of the smallest orbits might fall considerably below
this limit, in consequence of the rupture of many of the frag-
ments at their least distances from the primary, either by the
attraction of that body, or by the heat evolved when they are
transformed into blazing meteoric masses.
The condition which matter must ultimately assume in the
central zone, where it can no longer exist as one great satellite
or in a limited number of smaller ones, must depend in some
degree on the form of the primary planet. If this body be an
oblate spheroid, considerably flattened by rapid rotation, as is
the case with Saturn, the orbits of the several fragments must
be subject to apsidal motion, to an extent depending on their
transverse axes and excentricities. Accordingly those fragments
describing the same track will be equally affected by it, and will
form a line which remains unbroken during many revolutions.
As one ring of fragments is thus made to roll within another, it
is evident that both must ultimately become circular; and the
fragmentary host will at length exhibit the nearest approxima-
tion to a state of repose, by moving in exact circles around the
central planet.
There are even more cogent provisions for equalizing the dis-
tribution of the great ocean of disconnected matter over the vast
zone in which it circulates. The attraction of the central body
which led to the great dismemberment, must be adequate not
only to forbid the reconstruction of a satellite, but even to pre-
vent the parts of the mighty wreck from congregating to any
point in an undue proportion. Whenever a preponderance of
matter occurred at any locality, the impediments of friction
would tend to equalize the angular velocity of the nearest and
most distant fragments in the group ; and the new relations be-
tween gravity and centrifugal force would immediately lead to
their dispersion by the disturbing action of the primary. If the
latter body were a very flattened spheroid, it would serve to con-
fine the great annular ocean of fragments to the same plane, in
opposition to small effects arising from the disturbances of di-
stant spheres; and Laplace has shown that, supposing Saturn’s
ring to consist of numerous independent satellites, they will be
prevented from departing from a common plane, in consequence
of the action of his equatorial matter.
In addition to the foregoing agencies for securing the peculiar
characters of the annular appendage, I must notice another which
is inseparable from the movements of such collections of fluid or
solid matter circulating in independent orbits. A vast amount
of heat must be developed by their friction and their mutual
collisions; while the calorific influence of such a mechanical
action will be augmented by the slight excentricity impressed on.
Phil. Mag. 8. 4, Vol, 21, No. 140. April 1861. T
274, Mr. J. S. Stuart Glennie on the
their orbits by the disturbances of the external satellites. The
increased temperature originating from this cause, must not only
permit the existence of fluids im the extensive fields of floating
matter, but also maintain an atmospheric covering of vapour, to
give more continuity and symmetry to the annular appendage.
If the physical characters of Saturn’s rmgs be such as matter,
not having an improbably great density, must necessarily assume
in the region which they occupy, the independent movements of
its parts may be regarded as a continual source of heat, which
may perhaps in some degree mitigate the sway of intolerable
cold in the frigid zone of the solar system.
Cincinnati, Feb. 19, 1861.
XLIII. On the Principles of Energetics.—Part I. Ordinary Me-
chanics. By J. 8. Stuart Guenniz, M.A., F.R.AS*
his | fee the introductory paper, “On the Principles of the
Science of Motion,” I suggested that this name might
be given to a new general science, rankmg with the similar
science of Growth, and not be used merely as a general name for
the sciences of Ordinary + Mechanics (Stereatics and Hydraties)
and Molecular Mechanics (Physics and Chemics{). The science
of Motion would, as a distinct science, or as a philosophy of the
Mechanical Sciences, consider, first, the relations of motions, as
motion, and without reference to their originating or determi-
ning causes or forces; and secondly, the conditions, and corre-
lations of the conditions, of Pressure, bodily, or molecular, to
which modern experiment and analysis give us the hope of being
able to refer all the forces of motion. ‘To the former section of
General Mechanics I would give the name, coined or made cur-
rent by Ampére, Kinematics§; for the latter section I would
adopt the term Energetics ||,already introduced by Rankine witha
similar meaning to that given by the above statement of its object.
2. It is proposed in the following papers partially to develope
the conceptions of the introductory paper, by stating the funda-
mental principles of the proposed Science of Energetics, with
their applications to the mechanical interpretation of phenomena.
The justification and development of these principles is the work
of the sciences of Mechanics, Physics, and Chemics respectively.
3. The science of Energetics may be defined as the theory of
* Communicated by the Author.
+ Would there not be a more definite distinction between the two
branches of Mechanics by means of the adjectives Corporal and Molecular?
{ Phil. Mag. January 1861, p. 54.
§ Essai sur la Philosophie des Sciences.
|| “A science whose subjects are material bodies, and physical pheno-
mena in general,” Edinb. Phil. Journ. N. S. ii, 1855, p. 125.
Principles of Energetics. 275
Mechanical, as distinguished from Biological Forces. And
without such a theory it is evident that no general and concur-
rent laws or relations can be established between phenomena of
Motion, as distinguished from phenomena of Growth. Attrac-
tions (gravic, electric, and magnetic) and Waves (acoustic, optic,
and thermotic) are the motions offered by Physics for explana-
tion by mechanical forces, or conditions of pressure. The con-
stitution and combination of bodies are the phenomena of which
Chemics require a similar mechanical interpretation. These
sciences may be distinguished from Mechanics, with its ordinary
limitation of meaning, as forming together the science of Mole-
cular Mechanics. But in Ordinary Mechanies also there are
phenomena, the causal relations of which have been hitherto as
little established as those of the phenomena of Attraction or of
Affinity. Such unexplained mechanical phenomena are the uni-
form motion of the planets, and their velocities of rotation, as yet
unconnected even by an empirical law.
The principles of Energetics more particularly belonging to
Ordinary Mechanics will therefore be in this paper applied to
the explanation of these mechanical facts.
4, (I.) A Force is the condition of difference between two pres-
sures in relation to a third.
5. To establish the principles of Energetics applicable to the
first part of Mechanics, it seems unnecessary to use the term pres-
surewith other than its usual limited meaning as Statical pressure.
Such a meaning would at least be wide enough for this first prin-
ciple. For it might be otherwise expressed :—the general cause of
the movement of a body is a difference between two (previously)
equilibratmg pressures upon it. But in order that it may be
seen, at least generally, how I propose to bring the idea of Pres-
sure into Physics and Chemies, and hence to make this principle
the foundation of Molecular as well as of Ordinary Mechanics,
it may be well to state at once that “ under the term Pressure I
shall include every kind of force which acts between elastic
- bodies, or the parts of an elastic body, as the cause (condition)
or effect of a state of strain, whether that force is tensile, com-
pressive, or distorting* ;” and that I consider elasticity to be
“une des propriétés générales de la matiére. lle est en effet
Porigine réelle, ou ’intermédiaire indispensable des phénoménes
physiques les plus importans de l’univers..... La gravitation et
Pelasticité doivent étre considérées comme les effets d’une méme
cause qui rend dépendantes ou solidaires toutes les parties maté-
rielles de l’univers +.”
* Rankine, Camb. and Dub. Math. Journ. 1851, vol. 11. p. 49.
+ Lamé, Théorie Mathématique de ?’ Elasticité des Corps Solides, pp. 1
2
and 2,
T2
276 Mr. J. S. Sttiart Glennie on the
6. The special application of this principle is less to pheno-
mena than to physical hypotheses. For as Force is thus
conceived, not as an absolute entity acting upon matter, but
as a condition of the parts of matter itself, “and as a condition
determined by the relative masses and distances of these parts,
any valid hypothesis of a force or of a motion to account
for any set of phenomena is thus seen to imply an assertion
as to relative masses and distances which can be more or less
readily submitted to experiment or observation and analysis.
And hypotheses of Forces which, like electric and magnetic
fluids, or “‘ uniform elastic ethers, the sole source of physical
power*,” exist absolutely, and are not merely expressions of facts
of mass- and distance-difference, are by this principle rejected as
unscientific. ‘ Lorsq’une branche de la Physique mathématique
est ainsi parvenue a écarter tout principe douteux, toute hypo-
thése restrictive, elle entre réellement dans une phase nouvelle.
Kt cette phase parait définitive, car la série historique, et en
méme temps rationnelle, des progrés accomplis, signale une ten-
dance constante vers l’indépendance de toute loi préconguet.”
How the mutually pressing or repelling parts of matter are to
be conceived in order that from facts of difference in relative
masses and distances alone, the forces of Molecular may be
referred to similar conditions with those of Ordinary Mechanics,
has been in the introductory paper indicated, and will in the
second part of this paper be more fully developed.
7. (II.) Motion, the effect of Force, whether mechanical, phy-
sical, or chemical, may be distinguished as beginning or conti-
nuous; and continuous motion as uniform or accelerated. The
condition of the beginning of motion is a difference of pressure
on the body that begins to move; the condition of a uniform
continuous motion is a neutralization of the resisting pressure ;
the condition of an accelerated continuous motion is a uniform
or varying resisting pressure.
8. This principle evidently embodies those of the Inertia of
Matter, of the Composition of Motions, and of Accelerating
Force.
The principle of Inertia is the fundamental scientific principle
of Non-spontaneity, or the impossibility of a motion undetermined
by a change in the previously existing relations of the body.
The inertia of a body or molecule is simply the relation between
its pressure and that of the bodies acting upon it. All the
meaning of this principle is in the relativity of the conception it
gives of the phenomena of matter; it appears, therefore, to betray
* Challis, “Ona Theory of Magnetic Force,” Phil. Mag. February 1861,
p. 107.
t Lamé, Théorie Analytique de la Chaleur, Discours préliminaire, p. Vi.
Principles of Energetics. 277
some obscurity of thought to speak of “intrinsic or absolute
inertia,”
The law of the Composition of Motions is but an extension of
that of Inertia*. For the compounding of a motion is but the
beginning of another motion; and the change in velocity and
line of motion of the particle due to each force (difference of
pressure) is the same as if the others did not act.
There seems to be a clearer conception afforded of uniform
and accelerated motion by referring these phenomena, as by this
principle, to their actual physical conditions.
9. The application of this principle leads to the following
theorem suggestive of an explanation of the apparent effect and
non-effect of the resisting medium on the comets and planets
respectively.
According as the resultant of a resisting medium passes or
not through the centre of gravity of a revolving body is it an
accelerating force of revolution, or a partially neutralized accele-
rating force of rotation.
If the medium is uniform, or if—though it varies in density,
according to some such law as that with so great probability
assumed for the solar medium, viz. inversely as the square of the
distance from the central body t—the face of the revolving body
is so small that the resultant of the resisting pressures thereon
passes infinitesimally near the centre of gravity of the whole
body, it may be easily proved that such a resultant of resistance
will act as an accelerating force, which, did the body move on a
solid surface, would retard its revolution, but which, as it moves
through'a fluid medium, will, by the progressive decrease of its
major axis and excentricicy, cause its orbit to approach more and
more to the circular form ; and there will hence result, as in the
case of Encke’s comet, a secular inequality in the expression of
the mean longitude, and consequently in the period.
But if, with the above law of decreasing density, the re-
sultant of resistance to revolution falls at a finite distance below
the centre of gravity of the body, it is clear that an unbalanced
pressure thus applied will affect, not the revolution, but the rota-
tion of the body ; and that the tendency either to cause or acce-
lerate rotation will be partly at least neutralized by the resistance
of the medium to this new motion.
For let a be the direction of revolution, @’ the resultant of the
resistance thereto of a medium varying in density. It is evi-
* Price, ‘ Treatise on Infinitesimal Calculus,’ vol. ii. p. 370.
Tt See Encke, Ueber die Existenz eines widerstehenden Mittels im
Weltraume; and Pontécoulant, Théorie Analytique du Systeme du Monde,
vol. tii. book 4, chap. 5,
278 Mr. J. S. Stuart Glennie on the
dent that «! will act as an
accelerating force of rota-
tion in the direction £;
and that this rotation will
be retarded, and e’ partly
neutralized by the resist~
ance in the direction #9’.
10. In the actual case
of theplanets, their masses
and velocities of rotation
are such that the solar medium can be of course conceived, not
as causing, but only as tending slightly to accelerate their
rotations. And a problem is by this theorem suggested of ex-
treme interest, but also, in the present state of hydrodynamics,
of extreme difficulty, as to how far this accelerating force of rota-
tion is neutralized. The earth’s rotation has been hitherto
considered and proved to be invariable, only in respect of the
action of the sun and moon; and it is to be remembered that
doubts have been thrown on its actual invariability even during
the short period of 4000 years; that one-tenth of a second in
10,000 years would be a large astronomical quantity; and that
their actual times are all that, at best, we know of the rotations
of the other planets. I shall not at present offer any further
remarks on this problem, considered either as a purely hydro-
dynamical one, or with the data afforded by the planetary system,
except to note that nothing seems as yet to have been done towards
determining the relative effect of a resisting medium on (what
may at any moment be called) the back of a revolving and rota-
ting body. And it should seem that little further* can be done
towards the solution of this problem without experimental data on
this point especially. The determination of the secular inequality,
the result of the variously directed and most improbably equili-
brating forces of the medium, becomes still more complicated
when such a triple motion as that of a satellite is considered.
Such, then, is the theorem I would venture to offer as, if not
giving as yet the demonstrable explanation of the effect of the
resisting medium on the bodies of the solar systemy, at least sug-
gesting new and very interesting experimental and analytical
problems m hydrodynamics.
11. (III.) The condition of Translation is a difference of
polar pressures on a point; the condition of Rotation is equal
* Stokes, ‘On Fluid Friction.’
+ I may refer to, though I cannot here discuss, the remarks on this sub-
ject of Sir John Herschel, ‘ Outlines of Astronomy,’ 5th edit. p. 389 note ;
and of Prof. Challis in his paper “ On the Resistance of the Luminiferous
Medium,” Phil. Mag. May 1859. ;
Principles of Energetics. 279
and opposite differences of polar pressures on two rigidly con-
nected points; the condition of compound Translation and Ro-
tation is unequal and opposite differences of polar pressures on
two rigidly connected points; and the relation between the
former and the latter depends on the distance between the centre
of gravity of the body and the point of application of the result-
ant of such unequal opposite forces.
12. In explanation of this principle, it will be sufficient to
remark that it is merely an expression of the ideas of a single
force at the centre of gravity, a couple, and a single force not at
the centre of gravity, in terms of the above general physical con-
ception of a Force.
13. The latter paragraph suggests the following general pro-
blem :—Given a force which, acting instantaneously at the centre
of gravity of a body of a given mass in a vacuum, gives it a cer-
tain velocity: what are the different relations between the velo-
city of revolution and that of rotation when the same body is
struck at certain different distances from the centre of gravity,
and on any axis, by the same force ?
The interest of this abstract problem is in the generality of
its application to bodies which, while trans-
lated along 2, rotate about y from a resultant z
of unequal pressures and resistances, having
its point of application in or parallel to z (a oe
wheel) ; and to bodies which, while trans- f
tive impulse” applied at some point in y (a
planet). For “le double mouvement de y,
translation et de rotation des planétes, qui
parait au premier abord si compliqué, a pu résulter d’une seule
impulsion primitive qui ne passait pas par leur centre de
gravité*.” From what previously existing conditions such a
primitive impulse originated, whether from the rotation of a
genetic ring, as in the Nebular Theory of Laplace, or other-
wise, we have not here to inquire. But towards a mechanical
explanation of the planetary elements, or a hydrodynamical
theory of the formation of the solar system, the experimental +
and analytical investigation of the above general problem seems
to open the way.
14. In reference to the application of general or particular
solutions of such a problem to the planets, it may be remarked
that, as we are not of course here given the primitive impulse,
lated along 2, rotate about z from “a primi- at
* Pontécoulant, Théorie Analytique du Systéme du Monde, vol. i. p. 144.
f~ Extend Plicker’s experiments, for stance. See Taylor’s ‘ Scientific
Memoirs,’ vol. iv. p. 16, and vol. v. pp. 584 and 621. :
280 On the Principles of Energetics.
the first step towards a rational is the discovery of an empirical
law of the rotations, in which such an element as the inclination
of the rotation axis to the plane of revolution (easily calculable
except for the two innermost and two outermost planets) would
evidently be involved.
Such a law seems pointed to by the regularity of the decrease
of the rotations, when the angular, ins stead of the linear velocities
or times are considered, The respeetive angular velocities of
rotation of the inner family are "29811, 26902, 26181, and
25879; and of Jupiter and Saturn, 63313 and ‘59907 re-
spectively.
15, The attempts I have made to discover the law of the pla-
netary rotations have had as yet no complete result*, But the
following incidental observation with regard to the angular velo-
cities of revolution and the distances may perhaps be worth noting
towards such a theory of the formation of the system as above
alluded to.
By Kepler’s third law,
r
y
P=cD*; whence = or w=cl —:
D Dp:
But under this law there might, in comparing successive velo-
cities and distances, be found relations of inequality ad infinitum.
The actual relations may, however, be thus expressed :—The
angular velocities of revolution and the distances are in inverse
gcometrical progressions with inverse differenees, except the in-
nermost planet of each family.
To say that the distances are in geometrical progression, each
nearer planet being half the distance of the next more remote,
or that the angular velocities of revolution are in geometrical
progression, cach nearer planet revolving with twice the velocity
of the next more remote, would be very far from accurate ; but
it seems interesting to ‘observe, as by this law, that when the
distance of a planet is more than twice that of the next inner,
its angular velocity of rotation is /ess than half that of the next
inner, and vice versd, And that the only exceptions to this rule
should be the innermost planet of each family, viz. Mereury and
Jupiter, appears significant,
* The results of an approximative formula were given in a paper “On a
general Law of Rotation applied to the Planets,” read by me at the Oxford
Meeting of the British Association, June 1860,
t See Tumboldt’s remarks on the Law of Bode, or rather of Titius.
Cosmos, vol, 1. pp. 319, 820,
Theory of Molecular Vortices applied to Electric Currents. 281
Mercury and Venus.
= 36,298051 =} x 68,631843 + 1,982129,
= (00029760 =2 x 0:0011651 + 0-:0006468.
ei< 5
Venus and Earth.
D=68,631843 =+4 x 94,885000 + 21,189343,
=0:00116510=2 x 0:00071676 — 0:00026842.
Earth and Mars.
D=94,885000 = x 144,575333 + 22,587334,
‘ = 0:00071676=2 x 0:00038108 — 0:00004540.
cl<
Jupiter and Saturn.
D=493,654546 = x 905,087708 +41,110692,
n=0 000060411 = 2 x 0:000024332 + 0:0000117470,
Saturn and Uranus.
D=905,087708 =4 x 1820,020075 —4,922829,
is = 0°000024382 = 2 x 0:0000085318 + 0:0000072598.
Uranus and Neptune.
D=1820,020075 =4 x 2849,991384 +395,024383,
r=0 0000085313 =2 x 0:0000043542 — 0:0000001871*.
6 Stone Buildings, Lincoln’s Inn,
March 1861.
XIV. On Phy silt vac of F Foree ce. By y ule C. Meera Pro-
fessor of Natural Philosophy in King’s College, Londont.
[With a Plate. ]
Part I1.—The Theory of Molecular Vortices applied to Electric
Currents.
WE have already shown that all the forces acting between
magnets, substances capable of magnetic induction, and
electric currents, may be mechanically accounted for on the sup-
* This fifteenth paragraph may be taken as an abstract of my paper
“On the Revolutional Velocities and Distances of the Planets,” read before
the Royal Astronomical Society,glan. 11, 1861.
+ Communicated by the Author.
282 Prof. Maxwell on the Theory of Molecular Vortices
position that the surrounding medium is put into such a state
that at every point the pressures are different in different direc-
tions, the direction of least pressure being that of the observed
lines of force, and the difference of greatest and least pressures
being proportional to the square of the intensity of the force at
that point.
Such a state of stress, if assumed to exist in the medium, and
to be arranged according to the known laws regulating lines of
force, will act upon the magnets, currents, &c. im the field with
precisely the same resultant forces as those calculated on the
ordinary hypothesis of direct action at a distance. This is true
independently of any particular theory as to the cause of this
state of stress, or the mode in which it can be sustained in the
medium. We have therefore a satisfactory answer to the ques-
tion, “Is there any mechanical hypothesis as to the condition of
the medium indicated by lines of force, by which the observed
resultant forces may be accounted for?” The answer is, the
lines of force indicate the direction of minimum pressure at every
point of the medium.
The second question must be, ‘“ What is the mechanical cause
of this difference of pressure in different directions?” We have
supposed, in the first part of this paper, that this difference of
pressures is caused by molecular vortices, having their axes
parallel to the lines of force.
We also assumed, perfectly arbitrarily, that the direction of
these vortices is such that, on looking along a line of force from
south to north, we should see the vortices revolving in the direc-
tion of the hands of a watch.
We found that the velocity of the circumference of each vortex
must be proportional to the intensity of the magnetic force, and
that the density of the substance of the vortex must be propor-
tional to the capacity of the medium for magnetic induction.
We have as yet given no answers to the questions, ‘‘ How are
these vortices set in rotation?” and “ Why are they arranged
according to the known laws of lines of force about magnets and
currents?” These questions are certainly of a higher order of
difficulty than either of the former; and I wish to separate the
suggestions I may offer by way of provisional answer to them,
from the mechanical deductions which resolved the first question,
and the hypothesis of vortices which gave a probable answer to
the second.
We have, in fact, now come to inquire into the physical con-
nexion of these vortices with electric currents, while we are still
in doubt as to the nature of electricity, whether it is one sub-
stance, two substances, or not a substance at all, or in what way
it differs from matter, and how it is connected with it,
applied to Electric Currents. 283
We know that the lines of force are affected by electric cur-
rents, and we know the distribution of those lines about a cur-
rent; so that from the force we can determine the amount of the
current. Assuming that our explanation of the lines of force
by molecular vortices is correct, why does a particular distribu-
tion of vortices indicate an electric current? A satisfactory
answer to this question would lead us a long way towards that
of a very important one, ‘‘ What is an electric current ?”
I have found great difficulty in conceiving of the existence of
vortices in a medium, side by side, revolving in the same direc-
tion about parallel axes. The contiguous portions of consecu-
tive vortices must be moving in opposite directions; and it is
difficult to understand how the motion of one part of the medium
can coexist with, and even produce, an opposite motion of a part
in contact with it.
The only conception which has at all aided me in conceiving
of this kind of motion is that of the vortices being separated by
a layer of particles, revolving each on its own axis in the oppo-
site direction to that of the vortices, so that the contiguous sur-
faces of the particles and of the vortices have the same motion.
In mechanism, when two wheels are intended to revolve in
the same direction, a wheel is placed between them so as to be
in gear with both, and this wheel is called an “idle wheel.”
The hypothesis about the vortices which I have to suggest is
that a layer of particles, acting as idle wheels, is interposed be-
tween each vortex and the next, so that each vortex has a ten-
dency to make the neighbouring vortices revolve in the same
direction with itself.
In mechanism, the idle wheel is generally made to rotate
about a fixed axle; but in epicyclic trains and other contrivances,
as, for instance, in Siemens’s governor for steam-engines*, we
find idle wheels whose centres are capable of motion. In all
these cases the motion of the centre is the half sum of the motions
of the circumferences of the wheels between which it is placed.
Let us examine the relations which must subsist between the
motions of our vortices and those of the layer of particles inter-
posed as idle wheels between them.
Prop. 1V.—To determine the motion of a layer of particles
separating two vortices.
Let the circumferential velocity of a vortex, multiplied by the
three direction-cosines of its axis respectively, be a, 6, y, as in
Prop. II. Let J, m, n be the direction-cosines of the normal to
any part of the surface of this vortex, the outside of the surface
being regarded positive. Then the components of the velocity
of the particles of the vortex at this part of its surface will be
* See Goodeve’s ‘ Elements of Mechanism,’ p. 118.
284 Prof. Maxwell on the Theory of Molecular Vortices
nB—my parallel to 2,
ly—na_ parallel to y,
ma—lB parallel to z.
If this portion of the surface be in contact with another vortex
whose velocities are «', 6’, y', then a layer of very small particles
placed between them will have a velocity which will be the mean
of the superficial velocities of the vortices which they separate, so
that if w is the velocity of the particles in the direction of a,
u= tm(y!—y)—4n(8'-8), «ss (27)
since the normal to the second vortex is in the opposite direction
to that of the first.
Prop. V.—To determine the whole amount of particles
transferred across unit of area in the direction of 2 in unit of
time.
Let 2), yj, 2; be the coordinates of the centre of the first vor-
teX, Xo) Yo) Zo those of the second, and so on. Let V,, Vo, &e.
be the volumes of the first, second, &c. vortices, and V the sum
of their volumes. Let dS be an element of the surface separa-
ting the first and second vortices, and z, y, z its coordinates.
Let p be the quantity of particles on every unit of surface.
Then if p be the whole quantity of particles transferred across
unit of area in unit of time in the direction of a, the whole mo-
mentum parallel to « of the particles within the space whose
volume is V will be Vp, and we shall have
Vor Spd S ei nude - wake een
the summation being extended to every surface separating any
two vortices within the volume V.
Let us consider the surface separating the first and second
vortices. Let an element of this surface be dS, and let its
direction-cosines be /,,m,,n, with respect to the first vortex, and
1,, Mg, 2. With respect to the second; then we know that
1+1,=0, m+m,=0, m+7,=0. . . (29)
The values of a, 8, y vary with the position of the centre of
the vortex; so that we may write
da da de
Oy = ty F dé (%—2) + dy (%a—41) + de (2g—%,), + (80)
with similar equations for 8 and y.
The value of wu may be written :—
applied to Electric Currents. 285
ld
7 3 ou (m,(e—2) re ms(2—2,) )
ld ld i
+592 (miymm) +melv—v) +592 (mlemai) mle 29)
ar i eta) t na(a—2) ) ic = (n,(y—y,) +ns(y—ys) )
—3 oF (m(e—2,) +m (2—2,)). = oie gg Md es dice s+
In effecting the summation of SupdS, we must remember that
round any closed surface =/dS and all similar terms vanish ; also
that terms of the form S/ydS, where / and y are measured in
different directions, also vanish; but that terms of the form
SledS8, where / and z refer to the same axis of coordinates, do
not vanish, but are equal to the volume enclosed by the surface.
The result is
—- 1 (/{dy
eee a,
d
=) (V,+V,+&.); » . (82)
or dividing by V=V,+ V.+ &c.,
1 (dy d8
P =e Pp (3 — re Py . . . ° e . e e (33)
If we make
1
p= a7’ ° : e > ° e e e ) e * (34)
then equation (33) will be identical with the first of equations (9),
which give the relation between the quantity of an electric cur-
rent and the intensity of the lines of force surrounding it.
It appears therefore that, according to our hypothesis, an
electric current is represented by the transference of the move-
able particles interposed between the neighbouring vortices. We
may conceive that these particles are very small compared with
the size of a vortex, and that the mass of all the particles
together is inappreciable compared with that of the vortices, and
that a great many vortices, with their surrounding particles, are
contained in a single complete molecule of the medium. The
particles must be conceived to roll without sliding between the
vortices which they separate, and not to touch each other, so
that, as long as they remain within the same complete molecule,
there is no loss of energy by resistance. When, however, there
is a general transference of>particles in one direction, they must
pass from one molecule to another, and in doimg so, may ex-
286 Prof. Maxwell on the Theory of Molecular Vortices
perience resistance, so as to waste electrical energy and generate
heat.
Now let us suppose the vortices arranged in a medium in any
arbitrary manner. The quantities i 4 , &e. will then in
general have values, so that there will at first be electrical cur-
rents in the medium. These will be opposed by the electrical
resistance of the medium ; so that, unless they are kept up by a
continuous supply of force, they will quickly disappear, and we
shall then have — = =0, &e.; that is, adx+ Bdy+rydz will
be a complete differential (see equations (15) and (16)) ; so that
our hypothesis accounts for the distribution of the lines of force.
In Plate V. fig. 1, let the vertical circle E E represent an elec-
tric current flowing from copper C to zinc Z through the con-
ductor E EH’, as shown by the arrows.
Let the horizontal circle M M' represent a line of magnetic
force embracing the electric circuit, the north and south direc-
tions bemg indicated by the ines 8 N and NS.
Let the vertical circles V and V’ represent the molecular vor-
tices of which the lme of magnetic force is the axis. V revolves
as the hands of a watch, and V’ the opposite way.
It will appear from this diagram, that if V and V! were conti-
guous vortices, particles placed between them would move down-
wards; and that if the particles were forced downwards by any
cause, they would make the vortices revolve as in the figure.
We have thus obtained a point of view from which we may regard
the relation of an electric current to its lines of force as analogous
to the relation of a toothed wheel or rack to wheels which it
drives.
In the first part of the paper we investigated the relations of
the statical forces of the system. We have now considered the
connexion of the motions of the parts considered as a system of
mechanism. It remains that we should investigate the dynamics
of the system, and determine the forces necessary to produce
viven changes in the motions of the different parts.
Prop. V1.—To determine the actual energy of a portion of a
medium due to the motion of the vortices within it.
Let «, 8, y be the components of the circumferential velocity,
as in Prop. II., then the actual energy of the vortices in unit of
volume will be proportional to the density and to the square of
the velocity. As we do not know the distribution of density and
velocity in each vortex, we cannot determine the numerical value
of the energy directly; but since y also bears a constant though
unknown ratio to the mean density, let us assume that the energy
applied to Electric Currents. 287
in unit of volume is
E=Cy(a?+ 6?+ 97),
where C is a constant to be determined.
Let us take the case in which
ae pee ae
“Tle? B= dy’ Y= ‘ge’ e ° . (35)
Let
b=, + do, sign aM hoy ie
and let
—
“all d*h, d*, oS) =m, and —— ‘iad + (oo d*ho =i) = Mp} ; 37)
dem \ dx? * “dy? du? * “dy? * de?
then ¢, is the potential at any point due to A magnetic system
m,, and ¢, that due to the distribution of magnetism represented
by m,. The actual energy of all the vortices is
B=SCy(e2+62+7%)dV, . . . . (88)
the integration being performed over all space.
This may be shown by integration by parts (see Green’s
‘Essay on Electricity,’ p. 10) to be equal to
= —4arCX (p,m, + Poma+ Pymat+ghym)dV. . (89)
Or since it has been proved (Green’s ‘ Essay,’ p. 10) that
d,m dV =Xidh.m,dV,
E= —4rC(gym, + dgmgt+2hym,)dV. . . . (40)
Now let the magnetic system m, remain at rest, and let m, be
moved parallel to itself in the direction of # through a space dz ;
then, since ¢, depends on m, only, it will remain as before, so
that $m, will be constant; and since ¢, depends on m, only,
the distribution of ¢, about m, will remain the same, so that
go mz Will be the same as before the change. The only part of
E that will be altered is that depending on 2¢,m,, because ¢,
becomes ¢, + = dz on account of the displacement. The varia-
tion of actual energy due to the displacement is therefore
sE= —4rC> (2 ma) GV 02..." Nae)
But by equation (12), the work done by the mechanical forces
on m, during the motion is
sw= = (Pima V)8e 5 ee ae
and since our hypothesis is a purely mechanical one, we must
288 Prof. Maxwell on the Theory of Molecular Vortices
have by the conservation of force,
sE+6W=0; . 4 2 3. 6 et
that is, the loss of energy of the vortices must be made up by
work done in moving magnets, so that
— 403 (2! mdV Jb +3 (“P myaV )8x=0,
or
Cg cm ko yale
~ Sar?
so that the energy of the vortices in unit of volume is
i
gp Mla + B+") 5 » Mr te
and that of a vortex whose volume is V is
a Wet B+ yV. 0
In order to produce or destroy this energy, work must be ex-
pended on, or received from, the vortex, either by the tangential
action of the layer of particles in contact with it, or by change
of form in the vortex. We shall first investigate the tangential
action between the vortices and the layer of particles in contact
with them.
Prop. VII.—To find the energy spent upon a vortex in unit of
time by the layer of particles which surrounds it.
Let P, Q, R be the forces acting on unity of the particles in
the three coordinate directions, these quantities being functions
of z, y, and z. Since each particle touches two vortices at the
extremities of a diameter, the reaction of the particle on the vor-
tices will be equally divided, and will be
‘Ie ] ]
2 ts 2 Q, 2 ;
on each vortex for unity of the particles ; but since the superficial
density of the particles is Bh (see equation (34)), the forces on
Qe
unit of surface of a vortex wili be
eee ] ]
nt gens mae — an
Now let dS be an element of the surface of a vortex. Let the
direction-cosines of the normal be /, m, x. Let the coordinates
of the element be z, y, z. Let the component velocities of the
applied to Electric Currents. 289
surface be u, v, w. Then the work expended on that element
_ of surface will be
Te =—X (Put Qt Rw)d8. . plank Sa
Let us begin with the first term, PudS. P may be written
ahr ge . BP
Pot 7 # Ty as =a dz ay . . e ° ° e (48)
and
u=nB—my.
Remembering that the surface of the vortex is a closed one, so
that
LaxdS ==Xmed8 = nydS = XmzdS=0,
and
LmydS = Znzd8S =V,
we find
dP dP
SPudS = (—s- aa ME ieeareasarge so
and the whole work done on the vortex in unit of time will be
- =— = —=(Pu-+ Qu + Rw)dS
3 = dR ees ui ak 2)
=e = de dz)* Ve?)
Prop. Be oy. find the relations Sais ee ee of
motion of the vortices, and the forces P, Q, R which they exert
on the layer of particles between them.
Let V be the volume of a vortex, then by (46) its energy is
i
K= gn Met B+ 7*)V, UP aa eS FE
and
oe ied. oe 72).
WE. age! Ns = tO tT ney
Comparing this value with that given in equation (50), we find
dQ dR _ pi) Pee ee dg
“\de dy at) tO Nae ae ee
dBi dQ dy\ _ P
+7 ae cae: ==) She ee We eee (53)
This equation being true for all values of a, 8, and y, first let
8 and y vanish, and divide by «. We find
Phil. Mag. 8. 4. Vol. 21. No. 140. April 1861. U
290 =Prof. Maxwell on the Theory of Molecular Vortices
dQ dR_ da
Eee |
Similarly,
sales dR dP_ 4B sit» ene
dz dz" dé?
and
From these equations we may determine the relation between
the alterations of motion = &c. and the forces exerted on the
layers of particles between the vortices, or, in the language of
our hypothesis, the relation between changes in the state of the
magnetic field and the electromotive forces thereby brought into
play.
In a memoir “On the Dynamical Theory of Diffraction”
(Cambridge Philosophical Transactions, vol. ix. part 1, section 6),
Professor Stokes has given a method by which we may solve
equations (54), and find P, Q, and R in terms of the quantities
on the right-hand of those equations. I have pointed out* the
application of this method to questions in electricity and mag-
netism.
Let us then find three quantities F, G, H from the equations
dG dil | ‘)
de dy rare |
dH: dF
pe das iz 55
dx dz HB; ie
dF dG |
dy nant ar = MY; J
with the conditions
i a d
and
dF dG dH
dx dy + —_ “dz =0, e e *-e@ e e e (57)
Differentiating (55) with respect to ¢, and comparing with (54),
we find
dF dG dH
P= ae? Q= — Wi? R= Fon e . © (58)
* Cambridge Philosophical Transactions, yol. x. part 1. art. 3, “On
Faraday’s Lines of Force.”
applied to Electric Currents. 291
We have thus determined three quantities, F, G, H, from which
we can find P, Q, and R by considering these latter quantities
as the rates at which the former ones vary. In the paper already
referred to, I have given reasons for considering the quantities
F, G, H as the resolved parts of that which Faraday has conjec-
tured to exist, and has called the electrotonic state. In that
paper I have stated the mathematical relations between this elec-
trotonic state and the lines of magnetic force as expressed in
equations (55), and also between the electrotonic state and elec-
tromotive force as expressed in equations (58). We must now
endeavour to interpret them from a mechanical point of view
in connexion with our hypothesis.
We shall in the first place exaraine the process by which the
lines of force are produced by an electric current.
Let AB, Pl. V. fig. 2, represent a current of electricity in the
direction from A to B. Let the large spaces above and below
AB represent the vortices, and let the small circles separating
the vortices represent the layers of particles placed between them,
which in our hypothesis represent electricity.
Now let an electric current from left to right commence in
AB. The row of vortices gh above AB will be set in motion
in the opposite direction to that of a watch. (We shall call this
direction +, and that of a watch —.) We shall suppose the
row of vortices k/ stillat rest, then the layer of particles between
these rows will be acted on by the row g/ on their lower sides,
and will be at rest above. If they are free to move, they will
rotate in the negative direction, and will at the same time move
from right to left, or in the opposite direction from the current,
and so form an imduced electric current.
If this current is checked by the electrical resistance of the
medium, the rotating particles will act upon the row of vortices
Kl, and make them revolve in the positive direction till they
arrive at such a velocity that the motion of the particles is reduced
to that of rotation, and the induced current disappears. If, now,
the primary current A B be stopped, the vortices in the row gh
will be checked, while those of the row k / still continue in rapid
motion. The momentum of the vortices beyond the layer of
particles p g will tend to move them from left to right, that is,
in the direction of the primary current; but if this motion is
resisted by the medium, the motion of the vortices beyond pq
will be gradually destroyed.
It appears therefore that the phenomena of induced currents
are part of the process of communicating the rotatory velocity of
the vortices from one part of the field to another.
[To be continued. ]
U2
[ 202 ]
XLV. Chemical Notices from Foreign Journals.
By I. Atxrnson, PA.D., F.C.S.
(Continued from p. 126.]
ERNOULLLI has published the result of an investigation of
tungsten and some of its compounds*. With a view to a
scientific investigation of the alloys of this metal, his first endea-
vour was to obtain the metal in a melted state; the result of
his researches proves, however, that all previous statements as to
the fusibility of pure tungsten are inaccurate. In his experi-
ments pure tungstic acid was used; the experiments were made
with the furnaces of the Royal Iron Foundry in Berlin, where
he was able to command temperatures higher than any previously
used in such experiments.
In one experiment a Hessian crucible was used lined with
charcoal, in which there was a cavity to receive the tungstic acid,
and over which there was a layer of charcoal powder. The eru-
cible, provided with a cover, was kept at a white heat for nearly
an hour. In this way a metallic mass was obtained free from
carbon, but without any traces of fusion. In a subsequent ex-
periment the Hessian crucible was completely fused, and accord-
ingly they were replaced by the best American graphite ern-
cibles. Even these did not resist the continuous heat of the
furnace for 24 hours. A metallic mass was obtained, which was
caked together and had some metallic lustre. This was heated
again with charcoal in a crucible protected in the most complete
manner; and the heat was greater than that ever observed in
any puddling furnace, so much so that the slag from the coke
dropped in a thin stream through the grates.
Notwithstanding this great heat the tungsten had not melted,
although it had sintered to a tolerably compact mass. The
metal thus obtained was heated for eighteen hours in a por-
eelain furnace without any change resulting.
Hence the author concludes that, with our present means,
metallic tungsten is infusible.
Bernoulli also investigated the alloys of tungsten with metals,
especially iron. Cast-iron turnings were intimately mixed with
1, 2, 3, 4, 5, 10, 15, and 20 per cent. of pure tungstic acid, in
the idea that the carbon of the iron would reduce the acid to the
state of metal. Some experiments were also made in which a
larger per-centage of acid was taken; but in this case some
powdered charcoal was added. The mixtures were heated in a
eraphite crucible to an intense white heat. With an addition of
10 per cent. of acid, the alloy had the properties of steel; it was
very sonorous, had a clear grey colour, a pure fracture, and was
* Poggendorft’s Annalen, December 1860,
Chemical Notices :—M. Bernoulli on Tungsten. 293
malleable. The addition of 15 per cent. of acid yielded an alloy
which might be considered as steel. It was very hard, but was
not sufficiently malleable. With 20 per cent. the hardness was
still greater, but the malleability much less.
The iron in these experiments was grey iron, and contained a
considerable quantity of graphite, and it was found that with
white iron a different result was obtained. The experiments
were made in the same way as the previous ones; it was found
that an alloy was only formed when charcoal dust was added ;
otherwise the tungstic acid sintered together, and very little tung-
sten combined with the iron, The alloy obtained with the addi
tion of charcoal had none of the appearance of steel; it was
white on fracture, had the structure of the iron used, and was
imperfectly malleable.
With an addition of tungstic acid in the proportion of 75 per
cent. no regulus was obtained. Analogous experiments were
made with the minerals Wolfram and Scheelite, and similar
results were obtained. The manganese present in Wolfram exerted
a considerable influence on the result ; and with Scheelite the
lime combines with the silica to form a slag, so that the alloy is
purer.
It follows from these experiments, that it is not the carbon
present in the iron in a state of chemical combination which
reduces the tungstic acid, but that which is mechanically inter-
mingled. From white east iron no carbon is withdrawn by the
tungstic acid, and accordingly no steel is obtained if charcoal be
not added.
The waste cast-iron turnings of the workshop may hence be
used for preparing directly a cast steel, to which the tungsten
imparts great hardness; or if the iron does not contain too
much sulphur, phosphorus, or silica, a very useful rough cast
steel may be obtained by fusing it directly with a quantity of
powdered Wolfram proportionate to the per-centage of carbon
which it contains.
The author determined the carbon in these alloys by three
methods. In the first, a piece of the alloy was laid upon a fused
cake of chloride of silver, and was left for several days, covered
with distilled water. In this way the iron gradually dissolved ;
and when the decomposition was complete, the charcoal and
tungsten were collected on an asbestos filter, dried and weighed,
and then the carbon determined in the usual way by combustion
with oxide of copper. In another case the alloy was decomposed
by chloride of copper, and in a third case it was digested with
iodine until the iron was dissolved. In these cases the carbon
contained in the alloy amounted to about 1 per cent.
Kxperiments to alloy tungsten with other metals were also
294 M. Bernoulli on Tungsten and its Alloys.
made. With copper, reguli were obtained, which, however, were
not homogeneous; the individual particles could be distinctly
seen. In general it was also found that copper, lead, zine,
antimony, bismuth, cobalt, and nickel only became alloyed with
tungsten when the reduction of the two metals took place simul-
taneously. The alloys are so infusible, that, with more than 10
per cent. of tungsten, no reguli are obtained, and at a higher
temperature the more volatile metals escape and metallic tungsten
is left behind. Iron differs in this respect from other metals.
It alloys in all proportions with tungsten; with above 80 per
cent., however, the alloys are infusible.
In order to prepare the tungstic acid used in these experi-
ments, powdered Wolfram was fused with excess of carbonate of
soda in an iron crucible, the fused mass dissolved, and boiled to
reduce manganic acid, and filtered. The solution, which con-
sisted of tungstate and carbonate of soda, was neutralized with
nitric acid, and the tungstate of soda crystallized out. This was
dissolved and treated with nitric acid, and the precipitate of hy-
drated tungstic acid was well washed. It was then dissolved in
ammonia, which left a residue of niobic and silicic acids; the
evaporated liquor deposited a fine crop of crystals of tungstate of
ammonia. This was well washed with water, and then repeatedly
treated with fresh quantities of nitric acid for some days to
remove nitrate of ammonia. The acid was ultimately washed
out and gently heated, by which it was obtained of a fine pure
sulphur-yellow colour.
The author found, in all these experiments, that it was not
possible to obtain pure yellow acid by directly heating the tung-
state of ammonia, even when this was done under access of air.
It invariably became of a green colour. This has been observed
before, and has been differently interpreted, some ascribing it to
the formation of a suboxide, and some to an admixture of yellow
acid and the blue oxide W? O°.
Bernoulli has found that it is a true compound. When the
yellow acid was heated to the highest temperature of a gas blow-
pipe, it gradually changed to a green colour, and from being
amorphous became crystalline. Similar results were obtained
by using the high temperature of a stoneware furnace, which
has an oxidizing flame. The tungstic acid was placed in suit-
ably protected platinum crucibles, and heated for periods varying
from eighteen to seventy-two hours. A green crystalline mass
was obtained, while on the upper part of the crucible there were
smaller crystals of the same colour. When the caked mass was
divided and subjected to a further heat for eighteen hours, the
result was confirmed; part had sublimed in fine crystalline lamin.
Bernoulli analysed these two modifications by reduction with
MM. Deville and Debray on the Preparation of Oxygen. 296
hydrogen, and found that they had the same per-centage com-
position, WO’, They must therefore be regarded as two iso-
meric modifications of the same acid, of which the yed/ow is
formed both in the moist and in the dry way, but in the latter
case only at a Jow temperature ; while the green variety is only
formed in the dry way and at a high temperature. The latter
he proposes to call pyrotungstic acid, in antithesis to Scheibler’s
acid*, which is metatungstic acid. Including the ordinary acid,
there are therefore three varieties.
Bernoulli has made a new determination of the equivalent. of
tungsten, both by oxidizing tungsten, and by reducing tungstic
acid. He obtained results varying within very narrow limits,
which lead to the number 93:4 as that of the equivalent.
Dumas had obtained the number 92+.
Bernoulli finally discusses the formula of the natural tung-
states, and attempts to show that the two modifications of
tungstic acid also occur in nature. Le adduces a great many
analyses of Wolfram. Most of them contain a certain quantity
of lime and magnesia, which he considers accidental constituents.
But in most cases a niobic acid is present—in the tungsten from
Zinnwald 1:1 per cent. ; this is to be regarded as replacing part
of the tungstic acid, with which it is therefore isomorphous.
The author finally describes the mode of analysing the tung-
sten minerals.
Engaged in investigating the methods of working up the pla-
tinum residues for the Russian Government, Deville and Debray
had occasion to examine the different methods of preparing
oxygen on a large scale. They find} that sulphate of zine,
which, as a waste product, is now so plentiful, furnishes an eco-
nomical source of this gas. When calcined in an earthen vessel,
it is converted into light white oxide, which, when the sulphate
is pure, may be used for painting. The temperature required
for its decomposition does not exceed that necessary for binoxide
of manganese. The other products of the decomposition are
sulphurous acid and oxygen, which may be separated by means
of the solubility of the former in alkalies; or the following
method may be used, which is employed by the authors for pre-
paring oxygen by the decomposition of sulphuric acid.
This body at a red heat may be decomposed into sulphurous
acid, water, and oxygen, by means of a very simple apparatus,
consisting of a retort, of about 5 litres, filled with thin platinum
foil, or, better, a serpentine tube filled with platinum sponge and
heated to redness. A thin stream of sulphuric acid passes into
* Phil. Mag. vol, xx. p. 374. t Ibid, vol. xvi. p. 211.
{ Comptes Rendus, November 26, 1860,
296 M. Carré on the Production of Low Temperatures.
this apparatus through an S tube; the products pass first through
a cooler which condenses the water, and then through a washer
of a special form. In this way pure and inodorous gas is ob-
tained, and a solution of sulphurous acid, which may be changed
either into sulphite or hyposulphite of soda, or may be used in
the sulphuric acid chambers. The expense ‘of oxygen prepared
by this plan is very small; for the method consists essentially i in
abstracting oxygen from the atmosphere. Hvenif the sulphurous
acid were not utilized, sulphuric acid would still be the cheapest
source of oxygen, cheaper even than binoxide of manganese.
M. Carré has applied* the great cold produced by the evapo-
ration of condensed ammoniacal gas to the production of low
degrees of temperature.
The apparatus he uses consists of two ordinary cylindrical
metal receivers connected by a tube. One of these is four times
the size of the other, and is filled to three-quarters its capacity
with the strongest solution of ammonia. At the time of closing
the vessel, care is taken to expel all air. The largest vessel is
placed over the fire, the smaller being immersed in cold water.
The solution is heated to 130° or 140°, the temperature being
indicated by a thermometer fitted in the larger vessel. At this
point nearly all the ammonia is expelled from the solution, and
liquefies in the second retort. When the separation is complete,
the larger vessel is cooled down: the reabsorption of the liquefied
gas commences immediately, and its volatilization produces a
degree of cold which readily freezes the water surrounding it.
The temperature sinks to —40°; and M. Balard, who tried the
experiment at the Collége de France, was able to solidify mercury.
Besides this apparatus, M. Carré has devised another form of
it, which is continuous in its action, but otherwise depends on
the same principle.
M. Leroux, of the Ecole Polytechnique, has made some deter-
minations of the refractive indices of vapours at high tempera-
tures, by means of an apparatus constructed for that purpose, on
which M. Babinet+ has reported to the Academy.
M. Dulong had found that the refractive index of oxygen
was 1:000278 ; of hydrogen, 1:000188; of nitrogen, 1-000300 ;
and of chlorine, 1:000772, that of air being 1:000294. M.
Leroux has found that the refractive indices of the vapours of
the following substances, saturated at the ordimary pressure, are
respectively—
* Comptes Rendus, December 24, 1860,
+ Ibid. November 26, 1860.
M. Leroux on Refractive Indices of Vapours. 297
Sulphur: 6: ow, L00L629
Phosphorus . . . 1:001864
PASORITCH 02 ¥5, he eet tal DOT
Merenty .)) 6 0 sie 1000896
The apparatus by which these results were obtained consists
of a very large furnace mounted on an axis, and provided at its
lower part with a divided circle, by which it can be inclined at
any angle. In the centre of the furnace there is a prism analo-
gous to that of Borda, employed by Dulong. This prism is made
of solid iron, and the rays enter and emerge through glass plates
cemented by a method peculiar to M. Leroux. The exact mea-
surement of the angle of the prism presents some ingenious
points. As in Babinet’s goniometer, the light is concentrated
on the prism, while filled with the vapour, by a telescope, and the
light on its emergence is received on another telescope provided
at its focus with a micrometric wire. With the first telescope,
its distance from the furnace, the size of the furnace, the distance
of the second telescope and its focal distance, which is above 2
yards, the extent of this gigantic goniometer is about 23 feet.
The means of verifying the results leave nothing to be desired.
Rose*, in a paper on the separation of tin from other metals,
and on its quantitative estimation, describes the following method
of effecting these objects.
The separation of tin from other metals is usually effected by
oxidation with nitric acid, so as to convert the tin into stannic
acid: in certain cases, however, this method gives inaccurate
results, and can only be said to be quite successful in the case
of the strongly basic oxides.
Another method consists in dissolving the binoxide of tin in
hydrochloric acid, and precipitating by sulphuric acid. Both
modifications of binoxide are precipitated im this manner, in the
presence of a large excess of water. The precipitates require a
long time in order to settle completely, more especially when
there is a large quantity of free hydrochloric acid. The precipi-
tate must be carefully washed free from hydrochloric acid other-
wise when it 1s ignited some tin cscapes in the form of chloride.
The ignition is best effected with the addition of some carbonate
of ammonia.
In the presence of certain substances, phosphoric acid for
example, even this method gives inaccurate results. The pre-
sence of a large excess of hydrochloric acid does not hinder the
precipitation of some phosphoric acid along with the binoxide
of tin.
When tin is to be separated from other metals, it must be
* Poggendorfi’s Annalen, January 1861,
298 Prof. H. Rose on the separation of Tin from other Metals.
oxidized with nitric acid in the usual manner, and the residue
digested with moderately strong hydrochloric acid. On the
addition of a large quantity of water, all is dissolved, and the tin
is then precipitated with sulphuric acid.
In the separation of copper and tin by the ordinary method,
the binoxide always contains a trace of copper; but by the above
process the separation of the two metals is complete, the binoxide
is quite free from copper.
Tin and lead are best separated by fusing the alloy with
sulphur and carbonate of potash. On treating the mass with
water, the sulphide of tin dissolves. This is the best method of
analysing the fusible alloy of tin, bismuth, and lead. Tin and
silver are also best separated in this way.
In an acid solution, tin and bismuth are best separated by
sulphide of ammonium.
The separation of iron from tin can only be completely effected
by oxidizing the alloy with nitric acid, dissolving in hydrochloric
acid, and saturating the hydrochloric solution with sulphuretted
hydrogen.
Tin is best separated from titanium by means of sulphide of
ammonium.
The separation of the oxides of tin from magnesia and the
alkaline earths is best effected by igniting them with sal-
ammoniac, by which the tin escapes as chloride. In general all
the tin is expelled by one ignition; but two are always amply
sufficient to remove the last traces of tin.
In the analysis of minerals, the separation and estimation of
tin is best effected by converting it ito the oxide. The volu-
metric analysis, however, is very convenient for the determina-
tion of the tin in tin-salts. The ordinary method is to convert
the protochloride of tin in hydrochloric acid solution into the
bichloride by means of oxidizing agents, such as permanganate
or bichromate of potash. But protochloride of tin absorbs atmo-
spheric oxygen, even during the determination, to such an extent
as materially to vitiate the results of analyses.
Stromeyer* has observed that good results are obtained by
the addition of sesquichloride of iron im excess to the freshly
prepared solution of tinin hydrochloric acid. The reaction is as
follows :—
Sn Cl-+ Fe? Cl? =Sn Cl? +2 Fe Cl.
The protochloride of iron formed is determined by permanga-
nate; and as it is not nearly so susceptible to atmospheric
oxygen as protochloride of tin, much more accurate results are
obtained.
* Liebig’s Annalen, February 1861.
M. Reboul on Derivatives of Glycerine. 299
_ Tin may also be directly dissolved in sesquichloride of iron to
which hydrochloric acid has been added,
Sn-+ 2 Fe? Cl?= Sn Cl?+ 4 Fe Cl.
But this method is only available with tolerably pure tin; for
-tmany other metals reduce perchloride of iron, and consume
solution of permanganate.
There are several compounds which have the formula C+ H*Cl?.
One of these is obtained by the action of pentachloride of phos-
phorus on aldehyde, and another by the action of chlorine on
chlorinated ethyle. Beilstein observed some time ago that these
two bodies were identical, and he has recently proved* that the
same is the case with two corresponding isomeric compounds of
the .benzoic acid series: the one, chlorobenzole, C!* H® Cl?, is
obtained by the action of pentachloride of phosphorus on oil of
bitter almonds; and the other is the chlorinated chloride of ben-
zyle, C'4 (H® Cl) Cl.
The latter body is formed, as Cannizaro showed, by the action
of chlorine on toluole; and Beilstein used this method of pre-
paring it. He finds that it has all the physical properties of
chlorobenzole. A careful comparison also of the chemical
actions of the two substances, both by his own direct experi-
ments and by those of other experimenters, leave no doubt as to
the complete identity of the two substances.
Reboul has published} the results of a lengthened and im-
portant investigation on some derivatives of glycerine. The
compounds which the author describes may be derived from an
oxygenized body, glycide, C® H® 04, which has not been isolated,
and which might be considered as the anhydride of glycerine, to
which it would bear the same relation as lactide does to lactic
acid. It would play the part of a diatomic alcohol, and would
yield a series of ethers, the general formation of which may be
thus expressed :—
C® H6 044 A— H? 0?=C® 4A O02,
C° Hé 04+ A A’—2H?0?=Co BH? A A’,
A and A! representing the formule of monobasic acids.
The starting-point for his research 1s hydrochloric glycide, ob-
tained by the action of potash on bihydrochloric glycerine,
C® H® Cl? 02, which simply removes hydrochloric acid,
C® A Cl? O? —HCl=C® H? C10.
Bihydrochloric glycerine itself is formed by saturating a mix-
* Liebig’s Annalen, December 1860.
+ Annales de Chimie, September 1860. Répertoire de Chimie, November
1860.
300 M. Reboul on Derivatives of Glycerine.
ture of glycerine and acetic acid with gaseous hydrochloric acid.
The chief product of the action is bihydrochloric glycerine,
which may be separated by fractional distillation; or, by heat-
ing the crude product with caustic potash, hydrochloric glycide
is directly obtained. It isa colourless liquid, heavier than water,
and smelling like chloroform. It boils at 118°—119°: it is
metameric with Geuther’s hydrochlorate of acroleine, with
Riche’s monochlorinated acetone, and with chloride of pro-
pionyle.
Monohydrochlorie glycide combines directly with fuming hy-
drochloric acid to form dihydrochloric glycide, C° H4 Cl? : this body
may also be formed by acting on hydrochloric glycide with pen-
tachloride of phosphorus, an action which gives rise to the forma-
tion of trihydrochloric glycerine,
C® H® ClO?+ PCI’ = C® H® Cl + PCI 0?;
Hydrochloric Trihydrochloric
glycide. glycerine.
and this, decomposed by potash, loses hydrochloric acid, and the
new body is formed,
C° H® C8—HCl=Cé H4 Cl?,
This body is identical with what Berthelot has called epibrom-
hydrine. It is metameric with bichlorinated propylene, and
with Geuther’s chloride of acroleine. Similar compounds con-
taining bromine and iodine were also obtained.
By the action of ammonia on bihydrochloric glycide a base is
formed, which the author considers identical with that obtained
by the action of amznonia on terbromide of allyle.
Hydrochloric glycide unites directly with the oxyacids to form
a glyceric ether, contaiming an equivalent of oxyacid and of hy-
dracid. Thus,—
C® H® C10?+ C4 H4 O*=C® H® (C4 H? O?) C104.
Hydrochloric Acetic Acetohydrochloric
glycide. acid. glycerine.
By the action of water, hydrochloric glycide fixes two equi-
valents, and monohydrochloric glycerine is formed :—
C° H® ClO? + H? O?=C® H7 C104, .
Hydrochloric Monohydrochloric
glycide. glycerine,
By the action of aleohol the hydrochloric compounds of glycide
are transformed into mixed glyceric ethers, contaimmg an equi-
valent of acid and an equivalent of alcohol,
C® H® ClO?-+ C+ H® O?= C® H® Cl (C4 H®) 04,
Hydrochloric Alcohol. Hydrochloric
glycide. ethylglycerine.
On anew Element, probably of the Sulphur Group. 301
When these bodies are treated with potash, hydrochloric acid is
removed, and the resultant compound, ethylglycide, is a glycide
containing the alcohol radical in the place of an equivalent of
hydrogen :—
C® Hé (C4 H5) Cl0*— HC1=C® Hi (C* H9) 04.
Hydrochloric Ethylglycide.
ethylglycerine.
Ethylelycide is a mobile liquid boiling at 128°. When treated
with hydrochloric acid, it yields the compound C® H® (C* H®) Cl0*,
If the compound hydrochloric amylglycerine be treated with
ethylate of soda, ethylamylglycerine is formed. Thus,—
C® H¢ (C'° H") ClO4+ C4 H® NaO?= C H$ (C!° H") (C4 H®) O° + NaCl.
Hydrochloric Ethylate Ethylamylglycerine.
amylglycerine. of soda.
The glyceric ethers containing two equivalents of the same acid
are Only a particular case of this reaction.
When hydrochloric glycide is acted upon by hydrosulphate of
sulphide of potassium, a compound is obtained analogous to
mercaptan,
C* H® ClO?+ KS HS=KCl1+ C® H® S? 0?,
Hydrochloric New body.
glycide.
A second mercaptan in this series is doubtless formed by the
action of dihydrochloric glycide on hydrosulphate of sulphide of
potassium, and which would have the formula C® H® $+.
XLVI. On the existence of a new Element, probably of the
Sulphur Group. By Witi1smM Crooxss, F.C.8S*, »
ie the year 1850 Professor Hofmann placed at my disposal
upwards of 10 lbs. of the seleniferous deposit from the
sulphuric acid manufactory at Tilkerode in the Hartz Mountains,
for the purpose of extracting from it the selenium, which was
afterwards employed in an investigation upon the selenocyanidest.
Some residues which were left in the purification of the crude
selenium, and which from their reactions appeared to contain
tellurium, were collected together and placed aside for examina-
tion at a more convenient opportunity. They remained unnoticed
until the beginning of the present year, when, requiring some
tellurium for experimental purposes, I attempted its extraction
from these residues. Knowing that the spectra of the incandescent
vapours of both selenium and tellurium were free from any
* Communicated by the Author.
+ Chem. Soc. Quart. Journ. vol. iv. p. 12, and Gmelin’s Handbook
(Cavendish Soc, Translation), vol. viii. p. 122,
802 Mr. W. Crookes on the existence of a new Element,
strongly-marked line which might lead to the identification of
either of these elements, it was not until I had in vain tried
numerous chemical methods for isolating the tellurium which I
supposed to be present, that the method of spectrum-analysis was
used. A portion of the residue, introduced into a blue gas-flame,
gave abundant evidence of selenium ; but as the alternate light
and dark bands due to this element became fainter, and I was
expecting the appearance of the somewhat similar, but closer,
bands of tellurium, suddenly a bright green line flashed into view
and as quickly disappeared. An isolated green line in this por-
tion of the spectrum was new to me. I had become intimately
acquainted with the appearances of most of the artificial spectra
during many years’ investigation, and had never before met with
a similar line to this; and as from the chemical processes through
which this residue had passed the elements which could possibly
be present were limited to a few, it became of interest to discover
which of them occasioned this green line.
After numerous experiments, I have been led to the conclu-
sion that it is caused by the presence of a new element belong-
ing to the sulphur group; but, unfortunately, the quantity of
material upon which I have been able to experiment has been
so small, that I hesitate to assert this very positively. I am, how-
ever, at work upon some of the seleniferous deposit itself, and
hope shortly to be able to speak more confidently upon this
point, as well as to give some account of its properties.
In the purest state that I have as yet succeeded in obtaining
this substance, it communicates as definite a reaction to the
flame as soda,—the smallest trace introduced into the burner
of the spectrum apparatus giving rise to a brilliant green Ime,
perfectly sharp and well-defined upon a black ground, and
almost rivalling the Na line in brilliancy. It is not, however, —
very lasting: owing to its volatility, which is almost as great as
selenium, a portion introduced at once into a flame merely shows
the line as a brilliant flash, remaining only a fraction of a
second; but if it be imtroduced into the flame gradually, the
line continues present for a much longer time.
The properties of the substance, both in solution and in the
dry state, as nearly as I can make out from the small quantity
at my disposal, are as follows :—
1. It is completely volatile below a red heat, both in the
elementary state and in combination (except when united with
a heavy fixed metal). 2. From its hydrochloric solution it is
readily precipitated by metallic zinc in the form of a heavy black
powder, insoluble in the acid liquid. 38. Ammonia added very
gradually until in slight excess to its acid solution, gives no pre-
cipitate or coloration whatever, neither does the addition of car-
probably of the Sulphur Group. 303
bonate or oxalate of ammonia to this alkaline solution. 4. Dry
chlorine passed over it at a dull red heat unites with it, forming
a readily volatile chloride soluble in water. 5. Sulphuretted
hydrogen passed through its hydrochloric solution precipitates
it incompletely, unless only a trace of free acid is present ; but
in an alkaline solution an immediate precipitation of a heavy
black powder takes place. 6. Fused with carbonate of soda and
nitre, it becomes soluble in water,—hydrochloric acid added in
excess to this liquid producing a solution which answers to the
above tests 2, 3, and 5.
An examination of these reactions shows that there are very
few elements which could by the remotest possibility be mis-
taken for it. |
The accompanying list includes every element, with the ex-
ception of the gases, bromine, iodine, and carbon. Opposite the
name of each I have placed the number of the reaction which
eliminates it from the list of possible substances, taking great
care, in every case, to give the benefit of any doubt which might
arise, on account of an imperfectly known or doubtful reaction,
in favour of the opposite opinion to that which I desire to prove,
and, in cases where several reactions would prove the same thing,
only making use of the most trustworthy.
1, 5. Aluminium. 1. Iron. Selenium.
Antimony. 1, 5. Lanthanium. 1, 5. Silicium.
Arsenic. 1. Lead. 1. Silver.
2, 3, 5. Barium. 2, 5. Lithium. 2, 5. Sodium.
2, 3, 5. Beryllium. 2, 5. Magnesium. 2, 3, 5. Strontium.
1, Bismuth. 1. Manganese. 5. Sulphur.
1, 2, 5. Boron. 3, 6. Mercury. 1. Tantalum.
6. Cadmium. 1. Molybdenum. Tellurium,
2, 5. Cesium. 1. Nickel. 1, 5. Terbium.
2, 3, 5. Calcium. 1. Niobium. 1, 5. Thorium.
1, 5. Ceriwn. 1, Norium. A pb rei
1, Chromium, Osmium. 1. Titanium.
1. Cobalt. 1. Palladium. 1. Tungsten.
1. Copper. 5. Phosphorus. 1. Uranium.
1, 5. Didymium. 1. Platinum. 1. Vanadium,
1, 5. Erbium. 2, 5. Potassium. 1, 5. Yttrium.
1. Gold. 1, Rhodium. 2. Zine.
1. Umenium. 1, Ruthenium. 1, 5. Zirconium.
1. Indium.
There are therefore left the following, amongst which, if already
known, it must occur :—antimony, arsenic, osmium, selenium,
and tellurium ; and although, to my own mind, many of the re-
actions detailed above are sufficient proof that it cannot be one
of the first three elements, yet I have thought it better to let
them pass.
Kach of the above five bodies, both in the elementary state
and in combination, has been rigidly scrutinized in the spectrum
304 Existence of a new Element, probably of the Sulphur Group.
apparatus by myself and many friends. Not a trace of such a line
is shown by either of them in the green part of the spectrum,—
Antimony, arsenic, and osmium, in fact, giving continuous spectra,
in which every colour is visible. The remaining elements, sele-
nium and tellurium, might almost be dismissed unchallenged,
inasmuch as I was first led to the examination by finding that it
was not either of these. Nevertheless I have, as stated at the
commencement of this paper, repeatedly examined their spectra,
and find no trace of such a line, the alternate light and dark
bands in the almost continuous spectra of selenium and tellurium
forming in fact so strong a contrast to the one single green ray
of the new substance, that the latter may readily be detected in
the presence of an enormous excess of either of the former.
In order to remove any remaining doubt which there might
be as to the green line being due to any of the elements men-
tioned in the above list, I have, moreover, specially examined the
spectra produced by each of these bodies in detail, either in their
elementary state, or in their most important compounds. Many
of them give rise to spectra of great and characteristic beauty,
but none give anything like the green line; nor, in fact, is there
any artificial spectrum, except that of sodium, which equals it in
simplicity.
There still may be urged the possibility of its being a compound
of two or more known elements, or an allotropic condition of one
of them ; a moment’s thought, however, will show that neither of
these hypotheses is tenable. They would in reality prove what
they are raised to oppose; for nothing less could follow than a
veritable transmutation of one body into another, and a conse-
quent annilulation of all the groundwork upon which modern
science is based. If an element can be sochanged as to have
totally different chemical reactions, and to have the spectrum of
its incandescent vapour (which is, par excellence, an elementary
property) altered to an appearance totally unlike that given by
its former self, it must have been changed into something which
it originally was not. ‘This, in the present position of science, is
an absurdity.
The method of exhaustion which I have adopted to prove
the elementary character of the body which communicates this
green line to the spectrum of the blue gas-flame*, may seem
unnecessary as well as unchemical in the present state of the
science ; I was obliged, however, to rely upon what I may call
circumstantial evidence of its not being a known element,
owing to the very small quantity of substance at my command
* TI need scarcely add that the line is quite distinct from either of the
green or blue lines seen in a gas-flame which is undergoing complete com-
bustion. It is moreover far more brilliant than these.
Geological Soctety. 305
(I believe I overestimate the amount which I have as yet ob-
tained, at two grains), which precluded me from trying many
reactions. The method of spectrum-analysis adopted to prove
the same fact, although perfectly conclusive to my own mind,
might not have been so to others, unsupported by chemical
evidence.
The following diagram will serve to show the position in the
spectrum which the new green line occupies with respect to the
two lithium and the sodium lines.
Lia Li8 Naa
j= ae
New
Green Line.
For confirmatory experiments on many of the observations
mentioned in this paper, I am indebted to my friend Mr. C.
Greville Williams. The detailed examination of the various
spectra are at present being joimtly pursued by us, and will be
published as soon as completed.
XLVII. Proceedings of Learned Societies.
GEOLOGICAL SOCIETY.
[Contined from p. 238. ]
January 23, 1861.—L. Horner, Esq., President, in the Chair.
othe following communications were read :—
1. “On the Gravel and Boulders of the Punjab.” By J.
D. Smithe, Esq., F.G.S.
In the Phimgota Valley (a continuation of the great Kangra or
Palum Valley) the drift consists of sand and shingle with boulders of
gneiss, schist, porphyry, and trap, from 6 inches to 5 feet in diameter.
Some of the boulders, having a red vitreous glaze, occur in irregular
beds. This moraine-like drift lies on the tertiary beds, which, here
dipping gently towards the plains, gradually become vertical, and
are succeeded by variegated compact sandstones, gradually inclining
away from the plains ; next come various slates, at a high angle ; and
gneissic rocks lie immediately over them.
2. “On Pteraspis Dunensis (Archeoteuthis Dunensis, Roemer).”
By Prof. T. H. Huxley, F.R.S., Sec. G.S.
The fossil referred to in this communication is from Daun in the
Eifel, and was described by Dr. Ferd. Roemer (in the ‘ Palzonto-
Phil. Mag. S. 4. Vol. 21. No. 140. April 1861. X
306 Geological Society :—
graphica,’ vol. iv. p. 72, pl. 13) as belonging to the naked Cepha-
lopods, under the name of Paleoteuthis Dunensis (changed to Archeo-
teuthis in the ‘ Leth. Geogn.’); and in the Jahrb. 1858, p. 55, Dr.
IF’. Roemer described a second specimen from Wassennach on the
Laacher See. Prof. Huxley reproduced, with remarks, Dr. Roemer’s
description of the specimens; and, after observing that Mr. S. P.
Woodward had already suggested (Manual of Mollusca, p. 417)
that Roemer’s fossil was a fish, he stated his conviction that it was
really a Pteraspis, agreeing in all essential particulars with the
British Pteraspides, though possibly of a different species.
3. ‘On the ‘ Chalk-rock ’ lying between the Lower and the Upper
Chalk in Wilts, Berks, Oxon, Bucks, and Herts.” By W. Whitaker,
Esq., B.A., F.G.S.
The author has more particularly examined the band which he
terms ‘“ Chalk-rock’’ on the northern side of the western part of the
London Basin. Here it has its greatest thickness (12 feet) to the
west, gradually thinning eastward. It is a hard chalk, dividing into
blocks, by joints perpendicular to the bedding; and it contains hard
calcareo-phosphatic nodules. It contains no flints; and in the di-
strict referred to none occur below it; but there is often a band
of them resting on its upper surface. It seems to form an exact
boundary between the Upper and the Lower Chalk, being probably
the topmost bed of the latter. In this case it will often serve as an
index of the relative thickness of these divisions, or as a datum for
the measurement of the extent of denudation that the Upper Chalk
has suffered. North of Marlborough, where it is thick, the Chalk-
rock appears to have given rise to two escarpments (an upper and a
lower) to the western portion of the Chalk Range.
Fossils are usually rare in this bed; but Mr. J. Evans, F.G.S.,
collected several from it near Boxmoor; and amongst them the
genera Belosepia (hitherto known only as Tertiary), Baculites, Nau-
tilus, Turrilites, Solarium, Inoceramus, Parasmilia, and Ventriculites
are represented; and the following species have been identified—
Litorina monilifera and a new species, Pleurotomaria sp., Myacites
Mandibula, Spondylus latus, Sp. spinosus, Rhynchonella Mantelliana,
Terebratula biplicata, and T. semiglobosa.
February 6, 1861.—L. Horner, Esq., President, in the Chair.
The followmg communication was read :—
“On the Altered Rocks of the Western and Central Highlands.”
By Sir R. I. Murchison, F.R.S., V.P.G.S., and A. Geikie, Esq.,
F.G.S.
In the introduction it was shown that the object of this paper was :
to prove that the classification which had been previously established —
by one of the authors in the county of Sutherland was applicable,
as he had inferred, to the whole of the Scottish Highlands.. The
structure of the country from the borders of Sutherland down the |
western part of Ross-shire was detailed, and illustrated by alarge map —
oe eee eee ee ee oe
On the Altered Rocks of the Western and Central Highlands. 307
of Scotland coloured according to the new classification, and by
numerous sections. Everywhere throughout this tract it could be
proved that an older gneiss, which the authors called ‘‘ Laurentian,”
was overlain unconformably by red Cambrian sandstones ; these again
unconformably by quartz-rocks, limestones, and a gneissose and
schistose series of strata, as previously shown in the typical district of
Assynt. From the base of these quartz-rocks a perfect conformable
sequence was shown to exist upward into the gneissose rocks, which
is not obliterated by granite or any similar rock.
The tract between the Atlantic and the Great Glen consists,
according to the authors, of a series of convoluted folds of the upper
gneissose rocks, until, along the line of the Great Glen, the under-
lying quartzose series is brought up on an anticlinal axis. A pro-
longation of this axis probably exists along part of the west coast of
Islay and Jura, two islands which exhibit a grand development of
the lower or quartzose portion of the altered Silurian rocks of the
Highlands.
From the line of the Great Glen north-eastward to the Highland
border, the country was explained as consisting of a great series of
anticlinal and synclinal curves, whereby the same series of altered
rocks which occurs on the north-west is repeated upon itself. One
synclinal runs in a N.E. and S.W. direction across Loch Leven.
The anticlinal of quartzose rocks that rises from under it to the S.E.
spreads over the Breadalbane Forest to the Glen Lyon Mountains,
where it sinks below the upper gneissose strata with their associated
limestones. Ben Lawers occupies the synclinal formed by these
upper strata; and the limestones and quartz-rock come up again in
another anticlinal axis corresponding with the direction of Loch
Tay. The continuity of these lines of axis was traced both to the
N.E. and $.W.
It thus appeared that the crystalline rocks of the Highlands are
capable of reduction to order; that the same curves and folds could
be traced in them asin their less altered equivalents of the South of
Scotland; and that in what had hitherto appeared as little else than
a hopeless chaos, there yet reigned a regular and beautiful simplicity.
In conclusion, Sir Roderick Murchison vindicated the accuracy
of his published sections in the N.W. of Sutherland, which had
been approved after personal inspection by Professors Ramsay and
Harkness ; and he gave detailed reasons for disbelieving the accu-
racy of the sections recently put forth by Prof. Nicol, which were
intended as corrections of his own. He concluded by affirming
that, through the aid of Mr. Geikie, the proofs of the truthful-
ness of his own sections, showing a conformable ascending order
from the quartz-rocks and limestones into crystalline and micaceous
rocks, had now been extended over such large areas that there could
no longer be any misgivings on the subject.
F ebruary 20, 1861.—L. Horner, Esq., President, in the Chair,
The following communications were read :—
1. ‘* On the Coincidence between Stratification and Foliation in
X 2
308 Geological Soctety :-—
the Crystalline Rocks of the Highlands.”” By Sir R. I. Murchison,
V.P.G.S., and A. Geikie, Esq., F.G.S.
Allusion was, in the first place, made to the early opinions of
Hutton and Macculloch, who regarded the gneissic and schistose
rocks of the Highlands as stratified. Mr. Darwin’s views of the na-
ture of the ‘‘ foliation”’ of gneiss and schist were then referred to ;
and it was insisted that this condition was not to be found in the
rocks of the Highlands,—the so-called ‘ foliation’”’ which the late
Mr. D. Sharpe had described in 1846 as characterizing the crystal-
line rocks of that country being, according to the authors, really
mineralized stratification. It was then pointed out that, as Prof.
Sedgwick had previously insisted on the wide difference between
‘‘ foliated” or ‘‘ schistose’’ and ‘‘ cleaved” or ‘‘ slaty ” rocks, and as
Prof. Ramsay had in 1840 recognized interlaminated quartz as being
parallel to stratification in the Isle of Arran, ‘‘ foliation’’ should be
regarded as coincident with stratification, and not with cleavage, in
the Scottish Highlands.
After some observations on the occurrence of cleavage in slates
at Dunkeld, Easdale, Ballahulish, and near the Spittal of Glenshee,
the authors stated their belief that all the ‘‘ foliation” of the ery-
stalline rocks of the Highlands is nothing more than lamination due
to the sedimentary origin of deposits, in which the sand, clay, lime,
mica, &c. have subsequently been more or less altered, and that the
‘arches of foliation” described by Mr. D. Sharpe (Phil. Trans.
1852) correspond in a general way with the parallel anticlinal axes
shown by the authors in a former paper to exist in the Highlands.
They remarked that the synclinal troughs, however, are not expressed
in Mr. Sharpe’s figures, and that he has omitted the bands of lime-
stone which they refer to as an important evidence of the stratifica-
tion of the district. They also pointed to the acknowledged difficulty
which the quartzites presented to Mr. Sharpe, but which readily fall
into the system of undulated strata that they have described. One
of the quartzites having yielded an Orthoceratite, and pebbles being
present in one of the schists of Ben Lomond, these facts were ad-
duced as further evidences of the real stratal condition of the schists
and quartzites of the Highlands.
2. ‘On the Rocks of portions of the Highlands of Scotland South
of the Caledonian Canal, and on their equivalents in the North of
Ireland.”” By Professor R. Harkness, F.R.S., F.G.S.
The author, having had an opportunity of examining the geology
of the North-west of Scotland in the year 1859, and more especially
the arrangement of rocks described by Sir R. Murchison as “ fun-
damental gneiss, Cambrian grits, lower quartz-rock, limestones,
upper quartz-rock, and overlying gneissose flags,” applied the results
of his observations during last summer to portions of the Highlands
lying south of the Caledonian Canal, and to the North of Ireland.
Developed over a large portion of these districts are masses of
gneissose rock, of varying mineral nature, and sometimes putting on
the aspect of a simple flaggy rock. Where these gneissose masses
Mr. Drew on the Succession of Beds in the Hastings Sand. 809
come in contact with plutonic masses, they exhibit that highly
erystalline aspect which induced Macculloch and others of the Scotch
geologists to regard them as occupying an extremely low position
among the sedimentary series, and to apply to them the Wernerian
term “primitive.’”’ Many of Macculloch’s descriptions, however,
show that this assumed low position is not the true place of this
gneiss among the sedimentary rocks which make up the Highlands
of Scotland.
In a section from the southern flank of the Grampians to Loch
Earn (and in other sections, from Loch Earn to Loch Tay, from
Dunkeld to Blair Athol, in the Ben y Gloe Mountains, in Glen
Shee, &c.), there is seen a sequence which indicates that this gneiss
is the highest portion of the series of rocks, with underlying quartz-
rock and limestone.
In the county of Donegal, Ireland, a like sequence is seen. A
section from Inishowen Head to Malin Head, along the east side of
Loch Foyle, presents us with gneissose rocks above limestone and
quartz-rocks, exactly as in Scotland. In no portion of Scotland
south of the Caledonian Canal, nor in the North of Ireland, did the
author recognize any trace of the ‘‘ fundamental gneiss.”
March 6, 1861.—Leonard Horner, Esq., President, in the Chair.
The following communications were read :—
1. “On the Succession of Beds in the Hastings Sand in the
Northern portion of the Wealden Area.” By F. Drew, Esq., F.G.S.,
of the Geological Survey of Great Britain.
Having first referred to the division of the Wealden beds by former
authors into the ‘‘ Weald Clay,” the ‘‘ Hastings Sand,” and the
“Ashburnham Beds,” and the subdivision of the ‘‘ Hastings Sand” by
Dr. Mantell into ‘‘ Horsted Sands,” ‘ Tilgate Beds,” and ‘* Worth
Sands,” and having defined the district under notice as lying be-
tween and in the neighbourhood of the towns of ‘Tenterden, Cran-
brook, ‘Tunbridge, Tunbridge Wells, East Grinstead, and Horsham,
Mr. Drew proceeded to describe, first, the several beds in the meri-
dian and vicinity of Tunbridge Wells. ‘The Weald Clay is at least
600 feet thick in this district, and is underlain by sands and sand-
stones, termed by the author the ‘‘ Tunbridge Wells Sand,” on ac-
count of its being well exposed there. ‘This subdivision is about
180 feet thick, and was described in detail,—an important feature
being the ‘ rock-sand,” or massive sandstone forming the picturesque
natural rocks of the neighbourhood. ‘The shales and clays under-
lying these sands form the ‘‘ Wadhurst Clay” of the author, and are
at places 160 feet thick. ‘This subdivision has yielded much iron-
stone in former times. It is underlain by other sand and sand-
stones, more than 250 feet thick, also yielding ironstone. ‘These
are termed ‘‘Ashdown Sand” by Mr. Drew on account of their
forming the heights of Ashdown Forest.
Eastward of the meridian of Tunbridge Wells Mr. Drew has found
310 Geological Society.
the same sequence of beds, and he believes a similar succession to
occur around Battle and Hastings. Westward of Tunbridge Wells
as far as East Grinstead, the same beds occur, but beyond that
the Weald Clay and Tunbridge Wells Sand alone are exposed; and
the latter is here divided into upper and lower beds by shale and clay
(termed ‘“ Grinstead Clay ” by the author), which thicken westward
to 50 feet and more. It is the ‘‘ Lower Tunbridge Wells Sand”
that forms natural rocks near Grinstead. Near Horsham the Weald
Clay contains, at about 120 feet from its base, bands of stone known
as the ‘‘ Horsham Stone,’’ used for roofing and paving. .
The author then explained at large the grounds on which he
proposed to replace Dr. Mantell’s term ‘‘ Horsted Sands” by “ Upper
Tunbridge Wells Sand,”’ that of ‘‘ Worth Sands” by “ Lower Tun-
bridge Wells Sand,” and that of ‘“ Tilgate Beds” by ‘‘ Wadhurst
Clay,”’ and his reason for proposing the name of “ Ashdown ” for
the next lowest bed of the “‘ Hastings Sand.”
The paper concluded with a description of some of the chief litho-
logical characters of the clays and sandstones of the Wealden area
under notice.
2. “On the Permian Rocks of the South of Yorkshire; and on
their Paleontological Relations.’ By J. W. Kirkby, Esq. Com-
municated by T. Davidson, Esq., F.G.S.
The author, after defining the area to be treated of, first noticed
the results of the labours of former observers in this district; and
then succinctly described the several strata, referring to Professor
Sedgwick’s Memoir on the Magnesian Limestone for descriptions of.
the physical geography and very much of the lithological characters
of the country under notice. The strata treated of Mr. Kirkby re-
cognizes (in descending order) as, 1. the Bunter Schiefer, about 50 feet
thick; 2. the Brotherton Beds, 150 feet; 3. the small-grained
Dolomite, 250 feet; 4. the Lower Limestone, 150 feet; 5. the
Rothliegendes or Lower Red Sandstone, 100 feet. These were then
compared and coordinated with the Permian strata of Durham, where
the three limestone members are thus represented :—1. The Upper
Limestone by the Yellow, Concretionary, and Crystaline Limestone
(250 feet) ; 2. The Middle Limestone by the Shell- and Cellular
Limestone (200 feet); and 3. The Lower Limestone by the Com-
pact Limestone (200 feet) and the Marl-slate (10 feet),—the over-
and under-lying sandstones being much alike as to thickness in the
two areas.
After some remarks on the probable geographical conditions
existing in the Permian epoch, the author proceeded to treat of the
Permian fossils of South Yorkshire in detail. These belong to about
thirty species, and are nearly all from the Lower Limestone,—three
species only occurring in the Brotherton beds. With three excep-
tions they occur also in the several limestones of Durham; five of
them are found in the lower part of the red marls of Lancashire ;
and six of them are found at Cultra and ullyconnel in Ireland.
The distribution of the species in the several beds at different loca-
Intelligence and Miscellaneous Articles. 311
lities having been fully treated of, the Permian fossils of South York-
shire were compared, first, with those of Durham; next, with those
of Lancashire; and thirdly, with those of Ireland. Remarks on the
distribution of the Permian Fauna in time concluded the paper.
XLVIII. Intelligence and Miscellaneous Articles.
SOME RESULTS IN ELECTRO-MAGNETISM OBTAINED WITH THE.
BALANCE GALVANOMETER. BY GEORGE BLAIR, M.A.
GINCE bringing the balance galvanometer, along with some other
apparatus, before the Society in the course of last session, the
writer had made some experiments with this new galvanometer, which
led to results that he did not anticipate, and which he considered to
be of sufficient importance to justify him in presenting them to the
Society. The object originally aimed at in its construction was to
obtain an exact measure, by weight, of the actual amount of deflective
force which the current exerts upon the magnetic needle. The in-
strument constructed for this purpose is represented in fig. 1. The
312 Intelligence and Miscellaneous Articles.
coil consists of a total length of 1660 feet of No. 22 copper wire,
weighing rather more than 6 lbs., and divided into four parts, the
ends of which are brought out and connected with their respective
terminals G G, so that they can be used separately or as one coil.
The needle with which the first experiments were made consisted of
a small rectangular steel bar, 14 inch in length, rather less than jth
of an inch in breadth, and about half the thickness of a shilling. It
weighed exactly 18 grains, and, when magnetized, its lifting power
was 44 grains, or nearly 24 times its own weight. The index M,
which is 9 inches in length, weighs only 2 grains. A small brass
pulley, 4th of an inch in diameter, is fixed upon the axis between the
index and the supporting screw L. ‘The balanced lever E H consists
of a thin shp of hard spring-brass, placed edgewise for strength, and
tapered, for lightness, towards the end of the long arm AH. The
short arm A E is loaded to act as a counterpoise; and to this arma
scale-pan C is suspended, at a distance from the fulcrum equal to
exactly 5th of the length of the other arm. It carries also at its
extremity a thin horizontal projection, which vibrates between two
screw-points D, D’, and by which, with the aid of the wooden foot-
screws of the instrument, the lever can be always Fig. 2.
exactly levelled when balanced. ‘The fulcrum
B is supported on a stout brass bar F, which is
firmly held in its place by means of the screw I,
and can be removed at pleasure. When it is
desired that the needle shall have hberty to
move in both directions, the extremity H of the
long arm of the lever is connected with the
needle by a slender wire suspended from a very
fine thread, fixed to the upper part of the pulley
and carried down on both sides of it, as shown
in fig. 2. The arm AH is divided into ten
equal parts, each of which is subdivided into
tenths ; and, estimating the poles of the needle
to be at a distance of about 4th of its total length
from the extremities, the diameter of the pulley
is so adjusted that a weight of 100 grains, sus-
pended at the distance of one of the large divi-
sions from the fulcrum, acts with a force of 1
grain at the poles of the needle; suspended at
division 2, it acts with a force of 2 grains; at
2°5, with a force of 21 grains, and so on.
‘The following Table exhibits the results of the first series of expe-
riments made with a small Grove’s battery, the platinum plates of
which expose only two inches of surface, and having the zine plates
immersed in a saturated solution of chloride of sodium. It is a
striking characteristic of Grove’s battery that it slightly increases in
force after being some time in action; and it would have been pre-
ferable, therefore, to use a Daniell’s, on account of its remarkable
constancy ; but the writer had not a sufficient number in series. The
fourth column indicates the weight required to bring the index of
Intelligence and Miscellaneous Articles. 313
the balance galvanometer back to zero; the fifth column expresses
the same weight reduced to the force which it exerts at the poles of
the needle, but increased in each case by half a grain, to compensate
for the small preponderance given to the long arm of the lever
in order to keep the needle vertical when not deflected by the
current ;—
Table I.
1 . 2. a 4 . 5 . 6 .
Angles on Angles on Weights Force at “at
No. of tangent balance Fi ieee to bring poles of Raped
pairs. galvya- galvanometer, the needle to needle, in nadiieedl
nometer, without weight. zero. grains, 5
Le] ! ° /
1 4 30 66 100 grs. at 2°5 3°00 3°12
2 8 30 77 30 ” ” 5°5 6:00 5°96
6 29 30 87 1000 grs. at 2°2 22°50 22°64
12 44 45 89 ” 5 4°9 49°50 39°64
It will be seen that, up to six pairs, the numbers in the fifth column,
expressing the force of the current in grains at the poles of the needle,
vary very nearly in the same ratio as the tangents of the angles of
deflection on the tangent galvanometer reduced to a comparable form
in the sixth column. With twelve pairs, however, the weight re-
quired to balance the current is 49°5, or very nearly 50 grains;
whereas, according to the tangent galvanometer, it should not have
exceeded 40 grains. Reflecting on this anomaly, the writer could
only arrive at the conclusion that the needle, surrounded by a very
powerful current in such a large coil, ceased to act as a permanent
magnet, and was temporarily charged with a higher magnetism in-
duced by the current itself. Subsequent experiments completely
confirmed this conclusion; and he was led to examine the subject
more minutely by observing that the needle, after being several times
subjected to the action of the current from twelve pairs, appeared to
have lost its permanent magnetism; for he afterwards found re-
peatedly that when the index was brought back by successive
increments of weight to 40°, the smallest possible additional weight
sent it back to zero. Before taking out the needle to ascertain
this, he submitted it a second time to the action of six and twelve
pairs, with the following results :—
Number of pairs. Current force by tang. galvan. Weights supported.
6 22°64 7'5 grains,
12 39°64 24°5 i,
whereas it will be seen, by referring to the preceding Table, that
originally it supported 22°50 and 49°50 grains respectively. The
needle was then taken out, and was found to have almost entirely
314 Intelligence and Miscellaneous Articles.
lost its magnetism. It had originally lifted 44 grains; it was
now only with the greatest precaution that it lifted 2 grains. But
7°5 > 24°5
and (22°64) : (39°64)?
A ef
bs, 3:06.
The writer had therefore little doubt that, if not merely demagnetized,
but formed of soft iron, the needle, when placed in a favourable
position, would turn with a force proportional to the square of the
current ; whereas it plainly appears from Table I., that so long as its
permanent magnetism is sufficient to resist the inducing action of
the current, the needle is deflected with a force simply proportional
to the current.
To determine this interesting question, two new needles were con-
structed, similar in shape and size to the former, but somewhat
lighter, each weighing only 17°25 grains. ‘The one was of steel,
tempered to the hardness of glass; and was magnetized till it lifted
with some difficulty 43 grains; the other was of soft hoop-iron,
well annealed. With these needles the following results were
obtained from experiments conducted very carefully, and using, for
greater accuracy, a single-thread suspension :—
Table II.
a 2. 3. 4. 5. 6.
Angles on a Deflective a "a .
| No, of tangent Tangents to force at poles | Ratioof Ratio pt
pairs. galvano- rad. 1. of needle, in | tangents. pee eee ss *
meter. grains. craps? Bo
With |( 3 | 17 40 0-318 115 115 | 114
magnetized, 6 31 20 0-609 22°0 22°0 42°1
steel 9 41 0 0°869 32°5 315 85°8
needle. | 12 | 47 0 1-072 43°5 38°8 130°6
| 3| 1740 | 0-318 60 | 60 | 60
With needle | OE asi 0 0-601 20°5 Le eee 21°5
of soft iron |) 9 40 20 0-849 400 | 161 42-9
12 47 0 1°072 57:0 20°4 68°4
A glance at the above Table will show that, with the permanently
magnetized needle, the numbers in column 4, expressing the de-
flective force of the current in grains, are very nearly proportional
to the numbers in column 5, expressing the simple ratio of the tangents
or quantities of current; whereas with the soft iron needle they are
nearly proportional to the sguares of the same quantities, reduced to
a comparable form in column 6. In both cases the only marked de-
viation coincides with the powerful current from twelve elements of
the battery, in which cuse the steel needle, evidently acting under
the superadded influence of induced temporary magnetism, is deflected
Intelligence and Miscellaneous Articles. 315
with a force which exceeds the estimated amount by 4°7 grains,
whereas the soft iron needle, under the same current force, falls
short of the calculated amount by 11°4 grains. The last effect is
probably attributable to the fact that, as the needle approaches satu-
ration, the law of the squares gradually merges into the law of
simple proportion. ‘The writer regrets that he had not at com-
mand sufficient battery power to put this point to the test of decisive
experiments, but hopes to do so shortly with a Daniell battery of 50
or 100 elements. In the meantime the results above given, having
been arrived at with great care, and amply confirmed by experiments
several times repeated, appear to establish very conclusively the
following principles :—
1. A permanently magnetized steel needle, suspended in the
middle of a galvanometer coil, is deflected with a force simply pro-
portional to the quantity of current transmitted, so long as the
current force which acts upon it is not sufficient to impart tempo-
rarily a higher magnetism than that which it permanently possesses.
Beyond this point, the deflective force exerted on the magnetized
steel needle increases in a somewhat higher ratio than the current,
and therefore the accuracy of any form of galvanometer can be
trusted only within certain limits of current force and of length and
proximity of coil.
2. A pure soft iron needle, suspended at an angle of about 40° to
the direction of the current (the angle varying according to the
shape of the needle), is deflected with a force which, within certain
limits of current power, is very exactly proportional to the squares
of the quantities of current. Beyond these limits the deflective force
exerted on the needle increases in some constantly diminishing ratio
lower than that of the squares of the current.
3. The action of the current in deflecting a magnetic needle is
precisely the same action, and follows the same law, as that which
it exerts in magnetizing a bar of soft iron. The amount of magnetism
actually imparted to a bar or needle of soft iron is directly propor-
tional to the quantity of current; for the force with which a soft iron
needle is deflected under different currents is not proportional to its
temporary magnetism in each case, but to the product of its mag-
netism multiplied by the force of the current. By increasing the
force of the current, two effects are produced ; in the first place, the
magnetism of the needle is increased in the same proportion; and
secondly, the increased current acting upon this increased magnetism
deflects the needle with a force proportional to the product of the
two, or in other words, proportional to the square of the actual
quantity of current.
1t only remains to add the results of two series of experiments,
showing the very striking difference between the defiective forces
exerted upon the two needles at different angles of inclination.
Table III. shows the increasing weights required to balance the
needles at angles successively diminished by 10°; Table LV. exhibits
the effect produced by successive additions of weights, equivalent to
a force of ten grains acting at the poles of the needles. In both
316 Intelligence and Miscellaneous Articles.
cases the battery power employed was twelve small Grove’s, but the
current declined, in the course of the experiments, from 47° to 45°
on the tangent galvanometer, which accounts for the fact that the
maximum weights supported are less than in the earlier experiments
recorded in Table II. In working out Table III., the weight em-
ployed (1000 grains) was simply advanced along the lever, and its
reduced amount at the poles of the needle noted when the index, in
gradually retreating, pointed to the successive angles specified. The
results in Table IV. were obtained by moving the weight from one
to another of the successive divisions, marked 1, 2, 3, &c. on the
lever; and the differences of the angles vary, as might be expected,
in nearly the reverse order of the differences of weights in Table
II. :—
Table III.
Angles on Weights reduced Differences of
balance to force at successive
galvanometer. |needle, in grains. | weights.
90 6'0 Se
80 6-5 oF
70 15:5 75
With magnetized steel 60 23-0 7-0
needle. 4 50 30:0 5-0
40 35:0 bs
30 39-4 af
20 41°5 0°5
see 10 42-0
gt 90 0-0 i
I § 80 155 nh
29°35
With soft iron needle. “ he 11-0
50 50:0 vs
40 53°0
Table IV.
Weights reduced} Angles on Differences of
to force at balance successive
needle, ingrains.| galvanometer. angles.
0-0 90 0 e
10-0 75 30 rete
With magnetized steel 20:0 63 0
needle. 30-0 48 30 a -
40°0 26 0
\ 4165
PU rh he aa Wi pea DEEL
10-0 84 0 see
20°0 76 30 8 10
With soft iron needle. |< 30-0 68 20
8 10
40°0 59 10 12 0
50-0 47 10
52°0 0 0
Intelligence and Miscellaneous Articles. 317
It will be observed from Table III. that a very small weight was
sufficient to throw back the steel needle to 80°, and that, on the
contrary, it is from 90° to 70° that the soft iron needle sustains
itself with comparatively the greatest power, requiring very nearly
double the weight which suffices for the steel needle to balance it at
the latter angle. When reduced to 40°, however, the smallest pos-
sible additional weight throws back the iron needle to zero, and in
every case it was necessary to moveit aside with the finger to nearly
that angle, before it would exhibit the slightest action under the
influence of the current, or, in other words, any perceptible trace of
longitudinal magnetization. In fact, being laterally magnetized
when hanging in a vertical position, it necessarily offered a certain
resistance to deflection.
On taking out the steel needle after these experiments, it was
found to have retained its original magnetism unimpaired.
The tangent galvanometer by which the force of the current was
Fig. 3.
318 Intelligence and Miscellaneous Articles.
determined in the preceding experiments, and which the writer had
also the honour of submitting to the Society last session, is repre-
sented in fig. 3. It is a very convenient modification of Gaugain’s
instrument, described in the Annales de Chimie, vol. xli. 1854. The
circular frame A, containing a variety of coils of different lengths
and sizes of covered wire, is 9°6 inches in external diameter ; so that
when the instrument is in use, the divided circle must be drawn out
till its centre is 2°4 inches in front of the coil or coils through
which the current is to be sent. To facilitate this operation, the
horizontal bar D, upon which the disk slides, has the proper distances
for each coil marked upon it, and these are successively exposed to
view at the back of the instrument, in proportion as the disk is drawn
smoothly forward by means of the handle C. The needle is only
one inch in length, but carries parallel to itself a fine filament of
glass for an index*; it is suspended by a silk fibre, and is raised so
as to hang freely within its glass shade by turning the pin E. The
ends of the coils are carried down through the hollow pillar B, and
by connecting the electrodes of the battery with the proper terminals,
the current can be sent through one or more of the coils. It canbe
sent through one convolution of No. 16, through 203 convolutions
of No. 34, or any other of the intermediate lengths and sizes of wire;
and in this way the resistance and the force exerted by the current
upon the needle can be very exactly adapted to the character of the
battery, or other rheomotor employed.—From the Proceedings of the
Glasgow Philosophical Society for January 16, 1861.
ON THE PRESENCE OF ARSENIC AND ANTIMONY IN THE SOURCES
AND BEDS OF STREAMS AND RIVERS. BY DUGALD CAMPBELL,
ANALYTICAL CHEMIST TO THE HOSPITAL FOR CONSUMPTION,
BROMPTON.
To the Editors of the Philosophical Magazine and Journal.
GENTLEMEN,
Since my communication upon the above subject, published in
the Philosophical Magazine of October last, I have repeated my
experiments upon several of the sands I then reported upon, and
with the like results which I then gave. I have also made experi-
ments upon other specimens since obtained, and in all I have hitherto
examined I have found arsenic, and generally, if not always, accom-
panied with antimony. The process followed was the same as I
formerly described, only I invariably used hydrochloric acid without
the slightest trace of arsenic in it, as some doubts had been cast
upon my former results, in a notice of my paper in the ‘ Chemical
* The thickness of the index is grossly exaggerated in the figure; it
ought to be as fine as a hair, and short in one arm.
Intelligence and Miscellaneous Articles. 319
News’ of the 20th of October last, because in my anxiety to admit
of any one testing the accuracy of my results, I had described how
the process might be conducted with what is generally sold as pure
acid, but which, if properly tested, is rarely free from arsenic.
During these last experiments, it occurred to me to distil the sands
with a second and a third dose of acid, and in most cases I have
found the yield of arsenic and antimony to be much greater, say from
two to five times, in the second distillate than in the first; and in
some I have found the third distillate to give more than the first,
but in others less.
These results induce me to say that, before a sand could be pro-
nounced not to contain any arsenic or antimony, it should be distilled
to dryness with at least three distinct doses of acid, each distillate
being tested carefully in the manner described in my former com-
munication.
I am, Gentlemen,
Your obedient Servant,
Ducatp CAMPBELL.
7 Quality Court, Chancery Lane,
March 25th, 1861.
NOTE ON A MODIFICATION OF THE APPARATUS EMPLOYED FOR
ONE OF AMPERE’S FUNDAMENTAL EXPERIMENTS IN ELECTRO-
DYNAMICS. BY PROFESSOR TAIT.
My attention was recalled by Principal Forbes’s note* (read to the
Royal Society of Edinburgh on January 7), to his request that I should
at leisure try to repeat Ampére’s experiment for the mutual repulsion
of two parts of the same straight conductor, by means of an apparatus
which he had procured for the Natural Philosophy Collection in the
University. Some days later I tried the experiment, but found that,
on account of the narrowness of the troughs of mercury, it was im-
possible to prevent the capillary forces from driving the floating wire
to the sides of the vessel. I therefore constructed an apparatus in
which the troughs were two inches wide, the arms of the float being
also at that distance apart. Making the experiment according to
Ampére’s method with this arrangement, I found one small Grove’s
cell sufficient to produce a steady motion of the float from the poles
of the pile; in fact, the only difficulty in repeating the experiment
lies in obtaining a perfectly clean mercurial surface.
Two objections have been raised against Ampére’s interpretation
of this experiment, one of which is intimately connected with the
subject of Principal Forbes’s note. This is, the difficulty of ascer-
taining exactly what takes place where a voltaic current passes from
one conducting body to another of different material. It is known
* Phil. Mag. for February 1861.
320 Intelligence and Miscellaneous Articles.
that thermal and thermo-electric effects generally accompany such a
passage. To get rid of this source of uncertainty, I have repeated
Ampére’s experiment in a form which excludes it entirely. In this
form of the experiment the polar conductors and the float form one
continuous metallic mass with the mercury in the troughs,—the float
being formed of glass tube filled with mercury, with its extremities
slightly curved downwards so as nearly to dip under the surface of
the fluid, and the wires from the battery being plunged into the
upturned outward extremities of two glass tubes, which are pushed
through the ends of the troughs so as to project an inch or two in-
wards under the surface of the mercury. A little practice is requisite
to success in filling the float and immersing it in the troughs with-
out admitting a bubble of air. This float, being heavier than the
ordinary copper wire, plunges deeper in the fluid, and encounters
more resistance to its motion; but with two small Grove’s cells only,
Ampére’s result was easily reproduced, even when the extremities
of the float rested in contact with those of the polar tubes before the
circuit was completed. It is obvious that here no thermo-electric
effects can be produced in the mercury; and I have satisfied myself
that the motion commences before the passage of the current can
have sensibly heated the fluid in the tubes.
The other class of objections to Ampére’s conclusion from this
experiment, depending on the spreading of the current in the mer-
cury of the troughs, is of course not met by this modification. I
have made several experiments with a view to obviate this also; but
my time has been so much occupied that I have not been able as yet
to put them in a form suitable for communication to this Society.—
From the Proceedings of the Royal Society of Edinburgh, vol. iv.
NOTE RESPECTING OZONE.
In the Philosophical Magazine, May 1860, page 403, is a short
account of ‘‘ the production of Ozone by means of a Platinum Wire
made incandescent by an Electric Current,” by M. Le Roux, which
has just recalled to my memory the following fact.
I have frequently observed that a coil of platinum wire heated to
whiteness in a strong jet of purified hydrogen, and then removed from
the jet, imparted a feeble ozone-like odour to the ascending stream
of hot air above the wire as long as the wire remained nearly white-
hot, and ceased to impart this odour at a somewhat lower tempe-
rature.
G. Gorr.
Birmingham.
Phil. Mag. Ser.4.Vol.21.PLV.
j Fig: 8.
J. Basire se.
Phil.Mag. Sev. 4.Vol.21. Pl.
j
i
: :
THE
LONDON, EDINBURGH anno DUBLIN
PHILOSOPHICAL MAGAZINE
AND
JOURNAL OF SCIENCE.
[FOURTH SERIES.}
MAY 1861.
XLIX. On the Determination of the Direction of the Vibrations
of Polarized Light by means of Diffraction. By L. Lorenz*.
1 ae question whether the vibrations of polarized light are
perpendicular to the plane of polarization, or in that plane,
notwithstanding its great theoretical importance, is still unde-
cided. On comparing the different arguments that may be ad-
vanced in favour of either hypothesis, only two will be found
that have an essential bearing on the subject,—the experiments,
namely, of Jamin on the reflexion of light by transparent media,
and the polarization of light caused by diffraction.
The experiments of Jamin have hitherto been explained on
the supposition that the vibrations of polarized light are perpen-
dicular to the plane of polarization. ‘This, however, is not deci-
sive of the question, since it has hitherto been assumed that
there is an instantaneous change of refractive power at the
boundary of two transparent media; whereas I shall prove, in a
subsequent essayt ‘On the Reflexion of Light,” that Jamin’s
experiments can only be brought into complete accordance with
Fresnel’s formule for the reflexion and refraction of light, on the
hypothesis that these formule hold good for infinitely small
changes of the refractive index, that is to say, on the hypothesis
that there is a gradual passage from one medium to the other.
It may be asked whether Fresnel’s formule really hold good
for an infinitely small change of refractive power, and whether
these formule may be deduced on either hypothesis as to the
direction of the vibrations of polarized light; two questions
which I shall answer in a third essay.
alee by F. Guthrie, from Poggendorff’s Anzalen, vol. exi. p. 315,
'-> See Poggendorff’s Annalen, vol. cxi. p. 460: a translation of -this
paper will be given in a future Number of this Magazine,
Phil, Mag. 8. 4, Vol. 21, No. 141. May 1861, Y
322 M. L. Lorenz on the Determination of the Direction
The change of the plane of polarization by diffraction conducts
us by another road to the determination of the same question.
Several years ago Mr. Stokes furnished a mathematical proof
that the plane of polarization must be changed by diffraction.
Doubts have, however, justly been entertained as to the accuracy
of his conclusions, because he only succeeded in solving the
problem of diffraction imperfectly ; and I have therefore sought
the complete solution of the problem by other methods, which I
have found particularly applicable in the theory of elasticity.
When an undulation passes through an opening in a solid
plane, waves proceed from the opening on both sides of the
plane. The motion in the plane is not known, except inso-
far as it is determined by the fact that the sum of the compo-
nents of the incident and reflected waves are equal to the com-
ponents of those transmitted, and that the normal and tangen-
tial pressures on both sides of the plane of the opening are the
same at every point. Let the components of the incident rays
be denoted by w, v, and w; those of the transmitted rays by w,, 24,
and w,; of the reflected by w,, vo, and w.; and let the plane. of
‘coordinates 2, y, 2 coincide with the plane of the opening.
The first condition gives, for x=0,
U+Ug—Uy;=0, V+V,~—1,=0, wt+wo—w,=0; « (1)
and by the help of these equations it may easily be deduced from
the second condition for =O, that
dictate th) 324) d(v+,—2) aU; d(w+We—W)) _ ¢, (2)
dx dx dx :
If the incident waves are waves of light, then
du dv dw
de a dy Ai a =0;
and equations (1) and (2) may be satisfied by the supposition
that
RO Ds i Pal
dx ° dy ' dz ” (3)
du, . dv, . dwe ian dhe
de dy a s2.Q);
from which it is evident that no waves of condensation can be
formed.
The law of the motion is expressed by the differential equation
a + & + a = i a (4)
te ay ew ae eo
which must satisfy all the components, where w expresses the
of the Vibrations of Polarized Light by Diffraction. 3828
rate of propagation, and¢thetime. This equation will obviously
be satistied by the expression
valea’ obi! §
Y
where r=,/x* + (y—6)?-+ (z—y)?, and therefore also by
A Se Ls p(wi—r, B,y) ‘
D= on a3 ay rere
which function ®, when the limits of integration are determined
by the boundaries of the opening, also possesses the property
that its differential coefficient with respect to z becomes equal to
d (w, t, y, z) when « decreases to nothing, and the point yz is
within the opening. If 2 increases to nothing, the value of the.
differential coefficient is —d(wt, y, 2); and if the point yz is
without the opening, it becomes nothing when x=0; for by
differentiating the integral with respect to 2, w=O enters asa
factor, thus causing every element of the integral to disappear,
except those in which r=0, that is to say, y=, z=y. Whence,
if 2 is positive, and the point (yz) is within the limits of the
integral, :
ST = feelers] Ho rmters9
and if x is negative,
di *=0
| =a Hels ys 2)
_ Introduce now other functions VY, X, ©,, V,, X,, which are
related to the respective functions yp, x, $,, Wy; X, m the same
way as ® is to @, and put
| d®, d(F+F
ee ee
Ps dv, d(F+F)) is
y= V+ a F
V+V, —¥, =V— 2p, (wt, y, z)=0, ~ + (8)
W+ WoW, = W—2yx, (wt, y, z)=0;
and by means of (2) for =O,
avg ehh _ Oe oda yaaa
dz dz
d(v+vu,—v d
eS. = 5 — yp (ut, y, 2a U, » (9)
d(w+wo—w dw
Aut aw) _ 9 vot,y, 2)=0. |
All the conditions are hereby fulfilled, and the functions ¢, ¢,,
a, &e. determined. The truth of equations (7) may now also
be easily demonstrated.
The problem of diffraction is therefore completely solved by
equations (5), (6), (8), and (9). If-we now pass to the parti-
cular case in which the incident waves lie in a plane, the compo-
nents are determined by the following equations,
u= £6, v=o, w=,
where
6= cos k(wi—ax —by — cz),
a&+bn+cf=0, a?+?+c?=1.
Since, moreover, we only require to determine the motion at
a point at a considerable distance behind, the opening in the
screen must be very great; and putting p for the distance of the
of the Vibrations of Polarized Light by Diffraction. 325
observed point from the origin of coordinates, we have
p= Vx? + (y—B)?+ (z—y)?=p—mB—ny,
where
p= Varty+2, m=
and /, m, and v being the cosines of the angles made by the
diffracted ray with the coordinate axes, /?+m?+n?=1. Now
from (9) we get
(wt, y, 2) =4ak& sin k (wi—by—cz),
O=akéS,
whence
where
nt Sa f dB {dy sin k[wt—p + (m—B)8 + (n—e)y].
And the values of the functions that enter into (5) being found
in a similar manner, we get
uy ga 1 (1E +mn +n8)]S,
v,=$k(a+l) [n—m(lE+ mn +n8)]8,
=ghk(a+l)[(€—n(lE+ mn +né) |S.
These te a hold good also for the waves reflected from
the opening, only that in this case / is negative. For a point in
the direction opposite to that of the meident ray a+/=0, and
therefore all the components of the motion are equal to nothing.
Mr. Stokes has arrived at the same result, although he did
not regard the reflected wave, and has not completely solved the
problem. Ifa plane be supposed to pass through the refracted
and the incident ray, and if « denote the angle which the vibra-
tions of the incident ray make with the normal to this plane, «,
the angle made by the vibrations of the diffracted ray with the
same normal, and 8 the angle of diffraction, then we easily find,
as Stokes has done, that
tan a, = cos P tan a,
which is independent of the form and position of the opening.
The vibrations therefore become more nearly vertical after pass-
ing through a vertical slit or grating. Accordingly, therefore,
as experiment shows that the plane of polarization is rendered
more vertical or more horizontal by diffraction, so must the vibra-
tions of polarized light be parallel or perpendicular to the plane
of polarization. It must, however, be renembered that, mathe-
matically speaking, the screen is supposed to be a plane which
does not itself vibrate, and which reflects no light from its edges. |
326 M. L. Lorenz on the Determination of the Direction
The experiments that have hitherto been tried leave this
question still undecided; for while Stokes, from experiments
made with glass gratings, found that the plane of polarization is
rendered more horizontal, Holtzmann, from experiments made
with a smoke-grating, came to the opposite conclusion. In order
finally to settle this question, I have imstituted a course of expe-
riments with gratings of various kinds.
By means of a heliostat and collecting lens, I introduce a por-
tion of the sun’s rays into a chamber. At some distance from
the focus of the first lens a smaller lens receives the rays, and
transmits them, almost parallel, through a polarizing Nicol’s
prism, which is fastened in a tube to a vertical circular are. An
index with a vernier gives the angle which the plane of polariza-
tion of the transmitted light makes with the vertical lime. At
the distance of about 7 metres the light falls on a vertical gra-
ting, which is fastened to a small plate in the middle of a hori-
zontal circular arc, which is provided with a moveable horizontal
telescope. Before the object-glass is placed a doubly-refracting
prism of rock-crystal, which divides the polarized pencil into
two, polarized perpendicularly to each other, This prism can
be turned about the axis of the telescope. In general, therefore,
two horizontal bands of light of unequal brightness will be seen
in the telescope ;, but by turning the Nicol’s prism or the doubly-
refracting crystal about its axis, the intensity of these two
images can be rendered equal.
The experiments were generally conducted as follows :—The
Nicol’s prism was turned in such a direction that the plane of
polarization made an angle of 45° with the vertical line, and the
telescope was so placed that its vertical thread passed through
the two illuminating points, while the horizontal thread lay be-
tween the two horizontal bands of diffracted hight. When the
telescope was turned through the angle 8, both bands, owing to
the position of the rock-crystal, were of equal intensity. The
telescope was then put back into its original position, and the
Nicol’s prism was turned into such a position that one of the
images entirely disappeared.
If the Nicol’s prism required to be turned through the angle
5 (or 5+ 90° or 6+180°), the plane of polarization must have
been turned through the same angle, provided that the light has
not been elliptically polarized by diffraction ; and if 6 be positive,
the plane of polarization has been rendered more horizontal.
Sometimes I first determined 6, and then the angle of diffrac-
tion 8, for which the two bands are equally bright.
There is, however, a source of error in these experiments, of
which I only became aware after some time. If, for example,
the upper half of the grating produce a more brilliant diffracted
of the Vibrations of Polarized Light by Diffraction. 327
image than the lower, then if the grating entirely cover the
object-glass, as was always the case in the above experiments,
the upper diffracted image will be too bright. And if this image
be polarized horizontally, 6 will be found too great ; if vertically,
too small. To render the experiment perfect, it is therefere neces-
sary to turn the rock-crystal through an angle of 180°, and take
the mean of the two values of 6 so obtaimed. If this precaution ™
be neglected, very considerable errors may be introduced, espe-
cially when smoke-gratings are employed, and I imagine it is
this that has misled Holtzmann. He observed, in the case of a
smoke-grating, that for a diffraction of 20° there was a very con-
siderable difference in the brightness of the horizontal and verti-
cally-polarized images. This is nearly always so with gratings
of this description: the upper or the lower image appears the
brightest, without reference to the position of the plane of polari-.
zation. With a perfectly accurate grating, M. Holtzmann would
not have been able to distinguish the slight difference that really
does exist.
_ My first experiments were made with a gold grating (1000
bars to the Paris inch). Light polarized at an angle of 45°
with the vertical, when diffracted with this grating, gave two
images, of which neither could be made entirely to disappear for
any position of the rock-crystal ; and this was still more evident
when the grating was placed obliquely. The diffracted light must.
therefore either have been elliptically polarized,or have been partly
converted into ordinary light. That the former was the case,
I inferred from the fact that elliptically-polarized light could be
converted by diffraction into circularly and plane-polarized. If,
for example, I passed light polarized at the angle « through a
Fresnel’s parallelopiped, whose reflecting surfaces made the angle
45° with the vertical, the angle a could be so chosen that one
image in the telescope could be made entirely to disappear, or,
on the other hand, so that the two images, on turning the rock-
crystal, always retained the same intensity. : fire
By- measurements made in this manner, I convinced myself.
that the phenomenon is essentially the same as that which
accompanies the ordinary reflexion of light from polished metal.
surfaces, and that the effect of the diffracted light is imper-
ceptible in comparison with that reflected from the edges.
I now provided myself with various smoke-gratings. Polished
glass surfaces were smoked with burning camphor, and then
treated with a few drops of oil of turpentine to fix the smoke to
the glass. These were then divided by means of a machine into
bars only an inch long (2, 5, 10, and 16 to the millim.).
With these gratings I no longer observed any elliptic polari-
zation. I found no observable differences in the results for the
328 MM. L. Lorenz on the Determination of the Direction
different gratings, and content myself therefore with giving the
mean results for them all.
When the grating was perpendicular to the incident ray, and
on the side of the glass towards the telescope, as was the case in
Holtzmann’s experiments, I found the angle 6, through which
the plane of polarization was turned, extraordinarily small, and ~
therefore only determined it accurately for a single angle of dif-
fraction (65°). The plane of polarization of the incident light
was in all the following experiments inclined at an angle of 45°
with the vertical.
The mean result for 8=65° was
Sead; O2's
The plane of polarization therefore had become very slightly
more horizontal. For greater values of 8 I found 6 still smaller,
which at first greatly perplexed me.
When the grating was turned round so as to be on the side
towards the incident ray and perpendicular to it, the plane of
polarization was turned through a greater angle in the same
direction, and for 8=65° I found
6=12° 30'.
These results agree neither with Holtzmann’s experiments, nor
with the conclusions that seem to follow from theory. I think,
however, they can be explained as follows. |
When the light first passes through the glass and then through
the grating, the circumstances are almost the same as when it
encounters the grating in the substance of the glass, as may be
concluded from the fact that there is no reflexion at the boundary
between the smoke and the glass. The diffraction therefore
takes place within the substance of the glass, and the diffracted
light 1s afterwards refracted in passing out of the plate. If ,
be the diffraction in the glass (8 being the observed diffraction),
and n the index of refraction of glass, then sin@=nsinf,. In
consequence of the refraction, the plane of polarization is again
altered and becomes more veréical. Supposing now that the
vibrations are perpendicular to the plane of polarization, the
change of the plane of polarization 6,, caused by the diffraction
§,, is determined by the equation
tan (45°—6,)=cos@.
If therefore 6 be the angular change of the plane of polarization
after eflexion at the first surface of the glass, we have by Fres-
nel’s formule,
__ tan (45—6,) _—cos8
tan (15° 8) = cos (B= Ai) ~ eos (B— A)
of the Vibrations of Polarized Light by Diffraction. 329
The mean index of refraction n was determined by experiment
as to the angle of polarization, and I found
log n= 0°18886.
For 8=65° we should therefore have 5=2° 11’, which agrees
pretty well with experiment, which gave 6=1° 52’, That 6
should decrease as 3 increased, as appeared from experiment,
follows also from this calculation.
If, on the contrary, the smoked side of the glass is turned
towards the incident ray, the light is diffracted before it reaches
the surface of the glass, and is afterwards twice refracted. We
have therefore
tan (45°—8) = eee ;
from which it follows that if B=65°, 5=16° 2! 30",
In this case experiment gave a decidedly less value for 6, which
shows that the actual circumstances are only approximately those
assumed, and that the diffraction of the light only takes place
partially within the substance of the glass. This is still more
evident when the grating is placed obliquely to the incident rays,
so as to make equal angles with them and the axis of the tele-
scope; since in that case for 8=90° I found 6=20° instead of
45°, which is given by calculation.
It is obvious, therefore, that the circumstances, though very
complicated, are naturally accounted for in all essential particu-
lars, on the supposition that the vibration of polarized light is
perpendicular to the plane of polarization, whereas the other hy-
pothesis is altogether irreconcileable with experiment.
In order to render these results less complicated and more
susceptible of calculation, I contrived a different arrangement ot
the smoke-gratings. Canada balsam was melted over the sur-
face of the glass, and a smooth glass plate was pressed down on
it, which it was found could easily be done without injuring the
grating. As Canada balsam has almost the same index of refrac-
tion as glass, all the circumstances could then easily be calculated.
The grating was so placed that it made equal angles with the
incident rays and the axis of the telescope. In this position of
the apparatus the vertically polarized portion of the incident
light was found to be weakened more than that polarized hori-
zontally ; and therefore the change of the plane of polarization
was positive, although reflexion at the two glass surfaces tended
to turn the plane of polarization in the opposite direction. As
the mean of many experiments with several gratings (2, 5, 10
bars to the millim.), I found—
330 Onthe Direction of the Vibrations of Polarized Light.
| 40° | 50° | 60° | 70° | so° | 90° | 100°
3 observed ......, 2:24| 30 | 4:54] @36| 742/96 | 123
Calculated... 230 | 354] 537] 7-37 | 9:53 119-22 | 15-0
where 6 is given by the equations
COS :
tan(45°—68) are Sey or sin +2, = sin 4 B,
48 being the angle which the incident ray makes with the nor-
mal to the erating, 3A, that made by the refracted ray with the
same line, while Q, is the diffraction within the substance of the
glass itself.
It will be seen that experiment agrees very well with calcd
tion, only that it gives results in all cases a little too small.
Whatever, therefore, may be the cause of this difference, experi-
ment most decidedly favours the hypothesis that the vibrations
of polarized light are perpendicular to the plane of polarization,
since in the opposite case 6 would be negative and of much
greater magnitude.
T next investigated the effect of diffraction by smoked metal
gratings. When, however, these were of a perfect dull black,
the diffraction images produced by them were far too feeble;
they were therefore rendered smoother by passing a drop of oil
of turpentine over them. Gratings of this description must,
moreover, be rather fine and very accurately made. Some expe-
riments made with a grating of 400 bars to the Paris imch (the
thickness of the wire bars was 549th of a millim.), the grating
being equally inclined to the incident light and the axis of the
telescope, gave approximately the following results :—
— |) ee ee eee eee eee eee
The change of direction is positive, but much greater than it
should be according to calculation. The polarization of the
diffracted light was moreover slightly elliptical, from which it
was evident that the reflexion from the metal surfaces of the
wires was not entirely prevented by the smoke. On endeavour-
ing to smoke the grating more perfectly, I partly destroyed its
accuracy, and rendered it unfit for further experiments of this
description. I have not succeeded in obtaining reliable results
with other gratings of this description: there are peculiar diffi-
culties in the way of checking the reflexion from the metal edges,
and at the same time cana obte the diffraction image suffi.
ciently large and distinct.
_ On the Boiling-points of different Liquids. - $831
The results obtained are, however, not unimportant, since the
excessive values of 6 can easily be accounted for on the ground
of eliptie polarization.
If it be supposed, for example, that the difference of phase of
the vertical and horizontal components is A, and that 6, is the
change of direction when there is no elliptic polarization, an easy
calculation gives
tan 26,
cos A?
whence 6 must always be greater than 6,, their signs, however,
being always the same.
As experiment gave 6 positive, it confirms the result already
obtained, that the vibration of polarized light is perpendicular to
the plane of polarization. sid td.
Copenhagen, June 28, 1860.
tan 26=
L. On certain Laws relating to the Botling-points of different
Liquids at the ordinary Pressure of the Atmosphere. By
Tuomas Tate, Hsq.* 3
T is well known that the boiling-point of water is raised by.
the addition of a soluble salt, or by the addition of a strong
acid, and that this augmentation of the boiling-temperature de-
pends upon the relative amount of salt or acid added, as the case
may be; but, as far as I know, no general formule have hitherto
been given to express the relation between the augmentation of
boiling-temperature and the relative weight of the substance
added to the water.
Different weights of anhydrous salt being dissolved in 100
parts of pure water, and the augmentation of boiling-temperature
being observed, we obtain data for expressing the relation of the
per-centage of the salt to the corresponding augmentation of
the boiling-temperature of the solution. The salts which I have
examined in this manner are as follows :—the chlorides of sodium,
potassium, barium, calcium, and strontium ; the nitrates of soda,
potassa, lime, and ammonia; and the carbonates of soda and
potassa. I have found for all these salts, that the augmentation
of boiling-temperature may be approximately expressed in a certain
power of the per-centage of the salt dissolved: thus, if k be put for —
the weight of dry salt in 100 parts of water, and T the corre-
sponding temperature of ebullition above that of boiling water
under the same atmospheric pressure, then
Pht A sh: ai dliw (EX aoe ee
* Communicated by the Author.
332 Mr. T. Tate on the Boiling-points of different Liquids
where ais constant for each salt only, and the exponent a is con-
stant for all the salts contained in certain special groups. The
salts enumerated may be divided into four distinct groups, the
salts in each possessing certain remarkable points of relationship
with respect to their boiling-temperatures ; viz., the augmentations
of boiling-temperature of the solutions in each group of salts have
a constant ratio to one another for all equal weights of salt dis-
solved. Thus if 'T and T’ be put for the augmentations of boil-
ing-temperature corresponding to any equal portions of two salts
dissolved, belonging to the same group, then
= = a constant quantity.
The constant quantity here expressed is, in some cases, nearly
equal to the inverse ratio of the combining equivalents of the
bases of the salts.
Moreover, if the weights of two portions of one kind of salt,
separately dissolved in 100 parts of water, be proportional to the
two portions of another salt belonging to the same group and
similarly dissolved, then the ratio of the augmented temperatures
of ebullition of the former will be equal (approximately) to the
ratio of the augmented temperatures of ebullition of the latter.
I
Thus if Z = o then . oe ie and conversely ;
where x, and k, are the respective weights of one kind of salt
separately dissolved in 100 parts of pure water, T, and T, the
respective augmented temperatures of ebullition; and X’,, #,,
T',, and T’, are the corresponding symbols for the other salt.
For the sake of conciseness of expression, I shall sometimes
speak of this augmentation of temperature simply as the tempe-
rature of ebullition, which, in fact, it would be if the tempera-
ture of boiling water were taken as zero.
The first group of salts comprises the chlorides of sodium, po-
tassium, and barium, together with carbonate of soda.
The second group comprises the chlorides of calcium and
strontium, and probably other salts.
The third group comprises the nitrates of soda, potassa, and
ammonia.
The fourth group comprises the carbonates of potassa, and ni-
trate of lime.
If T=af(k) represent the relation between T and & of a salt in
any group, a being constant, and f(4) a known function of f,
then T=
7 1°85, for all equal weights of the salts ;
but Equiv. of strontium — 43°75 —9.18
Equiv. of calcium ~~ 20 ° ~~
In this case the approximation is not so close.
For the nitrates of soda and potassa we have
7 = "60, for all equal weights of the salts ;
but Equiv. of soda 31°31 _
Equiv. of potassa 47:26 — o
at the ordinary Pressure of the Atmosphere. 337
Hence it appears that the same law holds (approximately) true
for these two salts.
For the nitrate of lime and the carbonate of potassa included
in the fourth group, we have
a = - =°87, for all equal weights of the salts ;
but
Equiy. carb. of potassa _ 69
Equiv. nitrate of lime ~ 82 —
In this case, for all equal weights of the salts, the boiling-tem-
peratures, T and 'T’, are (approximately) zn the inverse ratio of the
equivalents of the entire salts.
How far these laws may be extended to other substances
future researches will determine; at the same time it must be
observed that it is quite consistent with analogy to suppose that
the chemical composition of a substance should affect the boil-
ing-temperature of its solution. Although the law here indi-
cated is not strictly true, yet it is sufficiently exact to warrant
further inquiry, and the cases to which it is found to apply are
too numerous to be referred to accidental coincidence.
— ‘84,
On the boiling-point of diluted sulphuric acid.
With the exception of the sixth, seventh, and ninth experi-
ments, the following experimental results were given by Dalton.
The per-centages of concentrated acid in the liquids were calcu-
lated from the observed specific gravities of the liquids by means
of Ure’s Table, given at p. 801, fourth edition, of his work on
the Arts and Manufactures.
Augmentations of the boiling-temperatures, in degrees Fahrenheit, of
diluted sulphuric acid at mean atmospheric pressure, containing
different proportions of concentrated acid in 100 parts, the
specific gravity of the concentrated acid being 1:846.
Weight of con- | Corresponding Value of k |
a ee
the liquid, above 212°, k=14:15 TS,
k. T.
100 353 100-30
96:21 Bits) $8.08
93°66 289 93°59
90°53 261 90-43
| 86°82 223 85°81
76°88 190 73:18
48-00 40 48-39
: 41-00 28 42°S6
34:00 16 35°66
0 0 0
Phil, Mag. S. 4. Vol. 21. No. 141. May 1861. Z
8388 Prof. Maxwell on the Theory of Molecular Vortices
Here the near coincidence of the results in the first and third
columns shows that the relation between & and T may be ap-
proximately expressed by the formula
’ le 1 1B) . . . e y )
LI. On Physical Lines of Force. By J.C. Maxwetu, Professor
of Natural Philosophy in King’s College, London.
[With a Plate. ]
Part Il.—The Theory of Molecular Vertices applied to Electric
Currents.
[Concluded from p. 291.]
Ae an example of the action of the vortices in producing in-
duced currents, let us take the following case:—Let B,
Pl. V. fig. 3, be a circular rg, of uniform section, lapped uni-
formly with covered wire. It may be shown that if an electric
current is passed through this wire, a magnet placed within the
coil of wire will be strongly affected, but no magnetic effect will
be produced on any external point. The effect will be that of
a magnet bent round till its two poles are in contact.
If the coil is properly made, no effect on a magnet placed out-
side it can be discovered, whether the current is kept constant or
made to vary in strength; but if a conducting wire C be made
to embrace the rmg any number of times, an electromotive force
will act on that wire whenever the current in the coil is made to
vary; and if the circuit be closed, there will be an actual current
in the wire C.
This experiment shows that, in order to produce the electro-
motive force, it is not necessary that the conducting wire should
be placed in a field of magnetic force, or that lines of magnetic
force should pass through the substance of the wire or near it.
All that is required is that lines of force should pass through the
circuit of the conductor, and that these lines of force should vary
in quantity during the experiment.
In this case the vortices, of which we suppose the lines of
magnetic force to consist, are all within the hollow of the rig,
and outside the ring all is at rest. If there is no conducting
circuit embracing the ring, then, when the primary current is
made or broken, there is no action outside the ring, except an in-
stantaneous pressure between the particles and the vortices which
they separate. If there is a continuous conducting circuit em-
bracing the ring, then, when the primary current is made, there
will be a current*in the opposite direction through C; and when
applied to Hlectric Currents. 339
it is broken, there will be a current through C in the same direc-
tion as the primary current.
We may now perceive that induced currents are produced
when the electricity yields to the electromotive force,—this force,
however, still existing when the formation of a sensible current
is prevented by the resistance of the circuit.
The electromotive force, of which the components are P, Q, R,
arises from the action between the vortices and the interposed
particles, when the velocity of rotation is altered in any part of
the field. It corresponds to the pressure on the axle of a
wheel in a machine when the velocity of the driving wheel 1s in-
creased or diminished.
The electrotonic state, whose components are F, G, H, is
what the electromotive force would be if the currents, &c. to
which the lines of force are due, instead of arriving at their actual
state by degrees, had started instantaneously from rest with their
actual values. It corresponds to the impulse which would act on
the axle of a wheel in a machine if the actual velocity were sud-
denly given to the driving wheel, the machine being previously
at rest.
If the machine were suddenly stopped by stopping the driving
wheel, each wheel would receive an impulse equal and opposite
to that which it received when the machine was set in motion.
This impulse. may be calculated for any part of a system of
mechanism, and may be called the reduced momentum of the
machine for that point. In the varied motion of the machine,
the actual force on any part arising from the variation of motion
may be found by differentiating the reduced momentum with
respect to the time, just as we have found that the electromotive
force may be deduced from the electrotonic state by the same
process.
Having found the relation between the velocities of the vor-
tices and the electromotive forces when the centres of the vortices
are at rest, we must extend our theory to the case of a fluid
medium containing vortices, and subject to all the varieties of
fluid motion. If we fix our attention on any one elementary
portion of a fluid, we shall find that it not only travels from one
place to another, but also changes its form and position, so as to
be elongated in certain directions and compressed in others, and
at the same time (in the most general case) turned round by a
displacement of rotation.
These changes of form and position produce changes in the
velocity of the molecular vortices, which we must now examine.
The alteration of form and position may always be reduced to
three simple extensions or compressions in the direction of three
rectangular axes, together with three angular rotations about
Z 2
3840 Prof. Maxwell on the Theory of Molecular Vortices
any set of three axes. We shall first consider the effect of three
simple extensions or compressions. .
Prop. 1X.—To find the variations of «, 8, y in the parallelo-
piped z, y, z when w becomes v+ 6x; y, y+6y; and z, 2+6z;
the volume of the figure remaining the same.
By Prop. II. we find for the work done by the vortices against
pressure,
SW =p,o(ayz) — — — (atyzda + B?zxdy+y*%axydz); (59)
and by Prop. VI. we find td the variation of energy,
oh = —— fo («Bat BoB+ydy)ayz. . « . « « (60)
The sum a4 BE must be zero by the conservation of energy,
and o(vyz) =0, since xyz 1s constant ; so that
a(3a—a~)+-8(88-8 4) +(8y—-7=)=0. (61)
In order that this should be true independently of any relations
between a, 8, and y, we must have
daa, SB= =p, Sy = ay. pie ae
Pie op. X.—To find the aan of a, 8, y due toa rotation 0,
about the axis of # from y to z, a rotation 6, about the axis of y
from z to 2, and a rotation @, about the axis of z from 2 to y.
The axis of 8 will move away from the axis of « by an angle
6,; so that 8 resolved in the direction of x changes from 0 to
The axis of y approaches that of 2 by an angle @, ; so that the
resolved part of y in direction z changes from 0 to y@.
The resolved part of « in the direction of « changes by a quan-
tity depending on the second power of the rotations, ¥ which may
be neglected. The variations of a, 8, y from this cause are
therefore
du=y0,—PBO,, SB=a0,—y0,, Sy=R0,—aO,. (63)
The most general expressions for the distortion of an element
produced by the displacement of its different parts depend on the
nine quantities
Ae Ch ee d qd. dy.
ip Oe? hs 783 Fp By, dy sag = y3 £ 82, Pa 3
and these may always be pane rand in terms of nine other quan-
tities, namely, three simple extensions or compressions,
da! dy! ba!
gee OT 3
«
a “
applied to Electric Currents. 341
along three axes properly chosen, a, 7’, 2', the nine direction-
cosines of these axes with their six connecting equations, which
are equivalent to three independent quantities, and the three
rotations @,, 0, @, about the axes of 2, y, 2.
Let the direction-cosines of 2! with respect to 2; y, 2 be
J}, m,,,, those of y’, 7,, m,n, and those of 2’, U5, mg, ng 3 then
we find )
aS Phd ar the + ie
dx
# seam ston sim tte: (64)
d Sx! Sy! Sx!
Gq, ot =i =r 3; Pie y! + dstts yp — + gy |
with similar equ uations for quantities involving dy and dz.
, Let a', B', y' be the values of a, 6, y referred to the axes of
2’, y'; a; aa
a’ =latmB+ny,
falatmetnn | eRe ee OO
y! =lsa + ms8 + ngy.
We shall then have
da=/ da! + / 08! + [359 + 78, — 88s, ie on (66)
= hel +18 + hy +10,—80. (67)
By substituting the values of a’, 6’, y', and comparing with equa.
tions (64), we find
d
d
ba= a Be BT Baty 7 Be a PL ee (68)
as the variation of « due to the change of form and position of
the element. The variations of 8 andy have similar expressions,
Prop. XI.—To find the electromotive forces ina moving body,
The variation of the velocity of the vortices in a moving ele-
ment is due to two causes—the action of the electromotive forces,
and the change of form and position of theelement. The whole
variation of @ is therefore
dQ dR d d
See (2-5 7, Jt a oe WHOS B04 9-7 8e. « (69)
But since @ is a function of a, y, 2 and ¢, the variation of # may
be also written
Sax Ada 4 o = by 4 moult oat.
dx
dz dk be 6 . . e (70)
342 Prof. Maxwell on the Theory of Molecular Vortices
Equating the two values of 6a and dividing by d¢, and remem-
bering that in the motion of an incompressible medium
ddxe daddy. dd
da dt Gy dk de Be =); e e ° e e e (71)
and that in the absence of free magnetism
de dB. dy
a dy een eT ne ae
we find
1/dQ dR d dx d dz YY d dx
a a, ee re ee + B—
b\ds dy dz dt dz dt “dy dt dy dt
dydx dadz dady dBdx da
Putting
an (SF di (74)
and
de). Mf erG = la ee
ha ro et .
where F', G, and H are the values of theelectrotonic components
for a fixed point of space, our equation becomes
dx dz dG d dy ao) =
(Oto G — 1a EG) ~ lB eg HOG ay.
The expressions for the variations of @ and y give us two other
equations which may be written down from symmetry. The
complete solution of i three equations is
dz = dv |
P=pyt He, they rs
Qk : dx ‘ ay
sal iid: eid oe oe3 dt dy? f
da Fiat di dV
Mott ge Oe dsct ager anit
The first and second terms of each equation indicate the effect
of the motion of any body in the magnetic field, the third term
refers to changes in the electrotonic state produced by alterations
of position or intensity of magnets or currents in the field, and
Y is a function of 2, y, z, and ¢, which is indeterminate as far
as regards the solution of the original equations, but which may
always be determined in any given case from the circumstances
of the problem. The physical interpretation of V is, that it is
the electric tension at each point of space.
applied to Electric Currents. 343
The physical meaning of the terms in the expression for the
electromotive force depending on the motion of the body, may
be made simpler by supposing the field of magnetic force uni-
formly magnetized with intensity « in the direction of the axis
of z. Then if /, m, n be the direction-cosines of any portion of
a linear hidaathe, and § its length, the electromotive force
resolved in the direction of the conductor will be
=S(P/+Qm+Rn), 5 2... (78)
dz _ nit),
e=Sya(m Foti) bs ales Vicars @
that is, the product of we, the quantity of magnetic induction
or
== ; nl ; ), the area swept
out by the conductor 8 in unit of time, resolved perpendicular
to the direction of the magnetic force.
The electromotive force in any part of a conductor due to its
motion is therefore measured by the number of lines of magnetic
force which it crosses in unit of time; and the total electromo-
tive force in a closed conductor is measured by the change of the
number of lines of force which pass through it ; and this is true
whether the change be produced by the motion of the conductor
or by any external cause.
In order to understand the mechanism by which the motion
of a conductor across lines of magnetic force generates an elec-
tromotive force in that conductor, we must remember that in
Prop. X. we have proved that the change of form of a portion of
the medium containing vortices produces a change of the velocity
of those vortices; and in particular that an extension of the
medium in the direction of the axes of the vortices, combined
with a contraction in all directions perpendicular to this, pro-
duces an increase of velocity of the vortices ; while a shortening
of the axis and bulging of the sides produces a diminution of the
velocity of the vortices.
This change of the velocity of the vortices arises from the in-
ternal effects of change of form, and is independent of that pro-
duced by external electromotive forces. If, therefore, the change
of velocity be prevented or checked, electromotive forces will
arise, because each vortex will press on the surrounding particles
in the direction in which it tends to alter its motion.
Let A, fig. 4, represent the section of a vertical wire moving
in the direction of the arrow from west to east, across a system
of lines of magnetic force running north and south, The curved
lines in fig. 4: represent the lines of fluid motion about the wire,
the wire being regarded as stationary, and the fluid as having a
over unit of area multiplied by (m
344 Prof. Maxwell on the Theory of Molecular Vortices
motion relative toit. It is evident that, from this figure, we can
trace the variations of form of an element of the fluid, as the
form of the element depends, not on the absolute motion of the
whole system, but on the relative motion of its parts.
In front of the wire, that is, on its east side, it will be seen that
as the wire approaches each portion of the medium, that portion
is more and more compressed in the direction from east to west,
and extended in the direction from north to south; and since
the axes of the vortices lie in the north and south direction, their
velocity will continually tend to increase by Prop. X., unless
prevented. or checked by electromotive forces acting on the cir-
cumference of each vortex.
We shall consider an electromotive force as positive when the
vortices tend to move the interjacent particles upwards perpendi-
eularly to the plane of the paper.
The vortices appear to revolve as the hands of a watch when
we look at them from south to north; so that each vortex moves
upwards on its west side, and downwards on its east side. In
front of the wire, therefore, where each vortex is striving to in-
crease its velocity, the electromotive force upwards must be
greater on its west than on its east side. There will therefore
be a continual increase of upward electromotive force from the
remote east, where it is zero, to the front of the moving wire,
where the upward force will be strongest.
Behind the wire a different action takes place. As the wire
moves away from each successive portion of the medium, that
portion is extended from east to west, and compressed from north
to south, so as to tend to diminish the velocity of the vortices,
and therefore to make the upward electromotive force greater
on the east than on the west side of each vortex. The upward
electromotive force will therefore increase continually from the
remote west, where it is zero, to the back of the moving wire,
where it will be strongest.
It appears, therefore, that a vertical wire moving eastwards
will experience an electromotive force tending to produce in it
an upward current. If there. is.no conducting cireuit m_ con-
nexion with the ends of the wire,:no.current will be formed, and
the magnetic forces will not be altered; but if such a circuit
exists, there will be a current, and the lines of magnetic force
and the velocity of the vortices will be altered from their state
previous to the motion of the wire. The change in the lines of
force is shown in fig. 5. The vortices in front of the wire, instead
of merely producing pressures, actually increase in velocity, while
those behind have their velocity diminished, and those at the sices
of the wire have the direction of their axes altered ; so that the
final effect is to produce a force acting on the wire as a resist-
applied to Electric Currents. 345
ance to its motion. We may now recapitulate the assumptions
we have made, and the results we have obtained.
(1) Magneto-electric phenomena are due to the existence of
matter under certain conditions of motion or of pressure in every
part of the magnetic field, and not to direct action at a distance
between the magnets or currents. The substance producing
these effects may be a certain part of ordinary matter, or it may
be an ether associated with matter. Its density is greatest in
iron, and least in diamagnetic substances; but it must be in all
cases, except that of iron, very rare, since no other substance has
a large ratio of magnetic capacity to what we call a vacuum.
(2): The condition of any part of the field, through which limes
of magnetic force pass, is one of unequal pressure in different
directions, the direction of the lines of force being that of least
pressure, so that the lines of force may be considered lines of
tension.
(3) This inequality of pressure is produced by the existence
in the medium of vortices or eddies, having thei axes in the
direction of the lines of force, and having their direction of rota-
tion determined by that of the lines of force.
We have supposed that the direction was that of a watch to a
spectator looking from south to north. We might with equal
_ propriety have chosen the reverse direction, as far as known facts
are concerned, by supposing resinous electricityinstead of vitreous
to be positive. The effect of these vortices depends on their
density, and on their velocity at the circumference, and is inde-
pendent of their diameter. The density must be proportional to
the capacity of the substance for magnetic induction, that of the
vortices in air beg 1. The velocity must be very great, in
order to produce so powerful effects in so rare a medium.
The size of the vortices 1s indeterminate, but is probably very
small as compared with that of a complete molecule of ordinary
matter*. ’
(4) The vortices are separated: from each other by a single
layer of round particles, so that a system of cells 1s formed, the
partitions being these layers of particles, and the substance of
each cell being capable of rotating as a vortex.
(5) The particles forming the layer are in rolling contact with
both the vortices which they separate, but do not rub against
each other. They are perfectly free to roll between the vortices
* The angular momentum of the system, of vortices depends on their
average diameter; so that if the diameter were sensible, we might expect
that a magnet would behave as if it contamed a revolving body within it,
and that the existence of this rotation might be detected by experiments on
the free rotation of a magnet. I have made experiments to investigate this
question, but have not yet fully tried the apparatus.
846 Prof. Maxwell on the Theory of Molecular Vortices
and so to change their place, provided they keep within one
complete molecule of the substance ; but in passing from one
molecule to another they experience resistance, and generate
irregular motions, which constitute heat. These particles, 3 in our
theory, play the part of electricity. Their motion of translation
constitutes an electric current, their rotation serves to transmit
the motion of the vortices from one part of the field to another,
and the tangential pressures thus called into play constitute elec-
tromotive force. ‘The conception of a particle having its motion
connected with that of a vortex by perfect rolling contact may
appear somewhat awkward, I do not bring it forward as a mode
of connexion existing in nature, or even as that which IT would
willingly assent to as an electrical hypothesis, It is, however, a
mode of connexion which is mechanically conce ivable, and easily
investigated, and it serves to bring out the actual mechanical
connexions between the known electro-magnetic phenomena; so
that I venture to say that any one who understands the provisional
and temporary character of this hypothesis, will find himself
rather helped than hindered by it im his search after the true
interpretation of the phenomena.
The action between the vortices and the layers of particles is
in part tangential; so that if there were any slipping or differen-
tial motion between the parts in contact, there would be a loss of
the energy belonging to the lines of force, and a gradual trans-
formation of that energy into heat. Now we know that the
lines of foree about a magnet are maintained for an indefinite
time without any expenditure of energy ; so that we must con-
clude that wherever there is tangential action between different
parts of the medium, there is no motion of shpping between
those parts. We must therefore conceive that the vortices and
particles roll together without shpping; and that the interior
strata of each vortex receive their proper velocities from the ex-
terior stratum without slipping, that is, the angular velocity
must be the same throughout e ach vortex
The only process in whic th electro-mi enetic energy is lost and
transformed into heat, is in the passage of electricity from one
moleeule to another, In all other cases the energy of the vor-
tices ean only be diminished when an equivalent quantity of me-
chanical work is done by magnetic action.
(6) The effect of an electric current upon the surrounding
medium is to make the vortices in contact with the current
revolve so that the parts next to the current move in the same
direction as the current. The parts furthest from the current
will move in the opposite direction ; and if the medium is a con-
ductor of electricity, so that the particles are free to move in an
direction, the particles touching the outside of these vorticeswil
applied to Electric Currents. 347
be moved in a direction contrary to that of the current, so that
there will be an induced current in the opposite direction to the
primary one.
If there were no resistance to the motion of the particles, the
induced current would be equal and opposite to the primary one,
and would continue as long as the primary current lasted, so that
it would prevent all action “of the primary current at a distance.
If there is a resistance to the induced current, its particles act
upon the vortices beyond them, and transmit the motion of rota-
tion to them, till at last all the vortices in the medium are set in
motion with such velocities of rotation that the particles between
them have no motion except that of rotation, and do not produce
currents.
In the transmission of the motion from one vortex to another,
there arises a force between the particles and the vortices, by
which the particles are pressed in one direction and the vortices
in the opposite direction, We call the force acting on the par-
ticles the electromotive force. The reaction on the vortices is
equal and opposite, so that the electromotive force cannot move
any part of the medium as a whole, it can only produce currents.
When the primary current is stopped, the electromotive forces
all act in the opposite direction,
(7) When an electric current or a magnet is moved in pre-
sence of a conductor, the velocity of rotation of the vortices in
any part of the field is altered by that motion. ‘The force by
which the proper amount of rotation is transmitted to each vor-
tex, constitutes in this case also an electromotive force, and, if
permitted, will produce currents.
(8) When a conductor is moved in a field of magnetic force,
the vortices in it and in its neighbourhood are moved out of
their places, and are changed in form, The force arising from
these changes constitutes the electromotive force on a moving
conductor, and is found by calculation to correspond with that
determined by experiment.
We have now shown in what way electro-magnetic phenomena
may be imitated by an imaginary system of molecular vortices,
Those who have been already inclined to adopt an hypothesis of
this kind, will find here the conditions which must be fulfilled in
order to give it mathematical coherence, and a comparison, so
far satisfactory, between its necessary results and known facts,
Those who look in a different direction for the explanation of the
facts, may be able to compare this theory with that of the exist-
ence of currents flowing freely through bodies, and with that
which supposes electricity to act at a distance with a foree de-
pending on its velocity, and therefore not subject to the law of
conservation of energy.
348 Mr. G. B. Jerrard’s Remarks on Mr, Cayley’s Note.
The facts of electro-magnctism are so complicated and various,
that the explanation of any number of them by several different
hypotheses must be interesting, not only to physicists, but to ali
who desire to understand how much evidence the explanation of
phenomena lends to the credibility of a theory, or how far we
ought to regard a comeidence in the mathematical expression of
two sets of phenomena as an indication that these phenomena
are of the same kind. We know that partial coincidences of this
kind have been discovered; and the fact that they are only
partial is proved by the divergence of the laws of the two sets of
phenomena in other respects. We may chance to find, in the
higher parts of physics, instances of more complete coincidence,
which may require much investigation to detect their ultimate
divergence.
Note.—Since the first part of this paper was written, I have
~ seen in Crelle’s Journal for 1859, a paper by Prof. Helmholtz on
Fluid Motion, in which he has pointed out that the lines of fluid
motion are arranged according to the same laws as the lines of
magnetic force, the path of an electric current corresponding to
a line of axes of those particles of the fluid which are in a state
of rotation. This is an additional instance of a physical analogy,
the investigation of which may illustrate both electro-magnetism
and hydrodynamics.
LII. Remarks on My. Cayley’s Note. By G. B. Jerranp*.
Lye by wu, v two rational x-valued homogeneous
functions of the roots of the equation
a + Ava™—14 Aga? ,.-+-A,=0,
we find by Lagrange’s theory that
V=Mn—1 t+ Mn—2U+ fra U +e. ss :
U= Van FV V+ Va_s¥?e +. ty, otf? (e)
in which fyi, Mn—2) ++ Mor Vn—1) Yn—2)++Vq are symmetrical fune-
tions of the roots of the original equation in z; and u, v depend
separately on two equations of the nth degree
UP a, UP ont At. eee O, ln) Se
v+B, y®—14. Bo yn-2 4 Ae +B,=0, oar (V)
Gh}, tg) + «Any By, Bos,»+ Bn being, as well as y»_1,..¥g, symmetrical
functions of the roots of the equation in 2.
I ought to observe that any coefficient, u,_,, in the equation
* Communicated by the Author.
Mr. G. B. Jerrard on the Equations of the Fifth Order. 349
(e,) may take the form
Mn_s
D >]
M,_., D being expressive of whole functions, and D, which re-
mains constant while M,,_, successively becomes M,_1, M,_»,..Mo,
being such as not to vanish except when (U) has equal roots.
We find in fact from the researches of Lagrange that
HD Ply) E(u,).s Kah ‘
where F(u) =nu"-! + (n—1)a, u®-2 + (n— —2)agu"3+ aie 4c
U), Uo)». Up denoting the n roots of the equation (U).
Of the meaning of the analogous expression
Naas
Dp!
which obtains in (e,) for v,_,, 1t is needless to speak. Indeed,
having found one of the two equations (e), say (e), we may in
general deduce the other, (e,), from it by the method of the
highest common divisor.
“Let us now examine the following extract from Mr. Cayley’s
paper in the last Number (that for March) of the Philosophical
Magazine.
& Writing,” he says, “ with Mr. Cockle and Mr. Harley,
TH Uylgt Uyly + Lyle + Lsle TL Ly,
T= y2y +2, L Ag+ UUs t Leas
then (7+7' is a symmetrical function of all the roots, and it :
must be excluded; but) (r—7')? or r7' are each of them 6-valued
functions of the form in question, and either of these functions
is linearly connected with the Resolvent Product. In Lagrange’s
general theory of the solution of equations, if
fr=2,+tt,+ F034 82,4445,
then ‘the coefficients of the equation the roots whereof are ( ft)®,
(fu?)°?, (fe®)?, (fe*)®, and in particular the last coefficient
(ft fe fe fe), are determimed by an equation of the sixth
degree ; and this last coefficient is a perfect fifth power, and its
fifth root, or fu fi? fr? fu*, is the function just referred to as the
Resolvent Product.
“The conclusion from the foregoing remarks 1s, that if the
equation for W has the above property of the rational expresst-
bility of its roots, the equation of the sixth order resulting from
Lagrange’s general theory has the same property.”
Here the question arises, Is it certain that fi fi? fi? fi4 can, by
850 Mr. J. S. Stuart Glennie on the
means of Lagrange’s theory, be expressed generally in rational
terms of (ft fi? fv3 fv4)° ?*
Denoting those functions by u, v respectively, we have in this
case vu"),
A=30, w=,
Now on substituting w”—! or w° for v in the equation (e,), we
see that (e,) will merge into
. Ms Mg Ut Mgt? + 66+ (Mo—])w?=0, . « (e)
wherein, since (U) is in general irreducible+, we must have
Hs=0, f4=0,..Ho—1=0.
Accordingly, on combining the equations (e,), (U), that is to
say, (e,), (U), we find
—— 0 .
u= 953
the equation (e,) being, as we see, illusory.
We are therefore not permitted to assume that the resolvent
product can in general—that is, when (U) has no equal roots—
be expressed rationally in terms of its fifth power.
Again, it is generally possible to establish a rational commu- -
nication between that fifth power and the function W, as is
evidenced in this latter case from the non-existence of any illusory
equation corresponding to (e,).
We are thus furnished, as will be seen, with a new confirmation
of the validity of my method of solving equations of the fifth
degree.
April 1861.
[To be continued. |
Mechanics. By J. 8. Stuart Gurnniz, M.A., F.R.AS.T
Srcrion I. Physics.
16. | PROCEED to consider the Principles of Energetics, or
the science of Mechanical Forces, which seem to afford
the bases of an explanation of physical motions. There is at
present no attempt at a systematic elaboration of these principles,
or mathematical application of them to the expression and expla-
* Tt will be understood that owr present inquiry relates to the possibility
of expressing either of the two quantities w, » as a rational function of the
other and of the elements, Aj, Ag,..Am. Thus R(v,..) is supposed to mean
the same thing as R(v, Aj, Ag,..Am); R indicating a rational function.
+ As defined by Abel.
t+ Communicated by the Author. In reference to the first part of this
paper, note that the word “rotation” in the fourth line from the bottom
of p. 280 of the last Number for “ revolution.”
Principles of Energetics. 351
nation of phenomena. Previous to such an attempt, it is thought
advisable to enunciate these principles in their most general form,
and give them merely experimental illustration.
The principles to be set forth in this paper will lead me to
remark on the physical theories recently published in this Journal
by Prof. Challis and Prof. Maxwell. It will be found that as my
theory refers attractions to differential conditions of stress and
strain, of pressure and tension, among elastic bodies, it agrees
rather with the molecular theory of the latter, than with the hy-
drodynamical theory of the former; that the point of funda-
mental difference from both is in the conception offered of
Matter; and that on this point my theory is a development of
the views to which experiment has led Mr, Faraday.
17. (I.) Atoms are mutually determining centres of pressure.
18. If this idea of an atom, as a body of any size, acting and
reacting on another similar body by the pressure of the con-
tinued, infinitesimal, but similar particles of which each centre
is an aggregate, be clearly conceived, it may be expressed in
many different forms. I have, for instance, in the introductory
paper spoken of a body thus conceived as a Centre of Lines of
Pressure, or an Elastic System with a centre of resistance. But
here, more clearly to express the idea in contrast with the fun-
damental hypotheses of Prof. Challis, an atom may be defined
as a centre of an emanating elastic ether, the pressure of which
is directly as the mass of its centre, and the form of which de-
pends on the relative pressures of surrounding atoms. Thus, if
you will, matter may be said to be made up of particles in an
elastic ether. But that ether is not a uniform circumambient
fluid, but made up of the mutually determining ethers (if you
wish to give the outer part of the atom a special name) emana-
ting from the central particles. And these central particles are
nothing but what (endeavouring to make my theory clear by
expressing it in the language of the theories it opposes) I may
call zetherial nuclei.
“ Hence,” according to the conception of Faraday, “ matter
will be continuous throughout, and in considering a mass of it
we have not to suppose a distinction between its atoms and any
intervening space....... The atoms may be conceived of as
highly elastic, instead of being supposed excessively hard and
unalterable in form..... With regard also to the shape of the
SLOMS . 6. ee That which is ordinarily referred to under the
term shape would now be referred to the disposition and relative
intensity of the forces *.”
* Phil. Mag. 1844. vol. xxiv. p. 142; or Experimental Researches,
vol. ii. p. 284, See also Phil. Mag. 1846, vol. xxviii. No, 188; or Expe-
rimental Researches, vol. iii. p. 447.
852 Mr. J. S. Stuart Glennie on the
19. I venture to offer this conception of atoms, not as a mere
hypothesis, but as a fundamental scientific principle. For there
is this involved in it—that as a phenomenon is scientifically ex-
plained only when, and so far as, it is shown to be determined
by other phenomena, the conception of Matter itself must be
relative, and its parts be conceived as mutually determined.
Now Pressure is not only an ultimate idea, including all those
qualities of Matter classed by the metaphysicians as the Seeundo-
primary, but is, unlike those, for instance, of Trinal extension,
Ultimate ineompressibility, Mobility, and Situation (the primary
qualities), not an absolute, but a relative conception, and, as
such, that on which alone. can be founded a strictly scientific
theory of material phenomena. For in the foundation of a
theory based on the conception of the parts of matter as centres
of pressure, there is nothing, properly speaking, hypothetical,
as no absolute, intrinsic, or independent qualities of form, hard-
ness, motion, &c. are postulated for atoms; and in their defini-
tion nothing more is done than an expression given to our ulti-
mate and necessarily relative conception of matter.
In defining Atoms as Centres of Pressure, they are thus no less
disting uished on the one hand from Centres of Force, than from
the little hard bodies of the ordinary theories ; for such Centres
of Force are just as absolute and self-existent in the ordinary
conception of them as are those little bodies. And in a scientific
theory there can, except as temporary conveniences, be no abso-
lute existences,—entities. Ilence (Mechanical) Force, or the
cause of motion, is conceived, not as an entity, but as a condi-
tion—the condition, namely, of a difference of Pressure*; and
the figure, size, and hardness of all bodies are conceived as rela-
tive, dependent, and therefore changeable. There are thus no
absolutely ultimate bodies.
20. But the full justification of advancing this conception of
Atoms as a fundamental scientific principle, is found in the prin-
ciples of the modern critical school of philosophy—in that espe-
cially of the relativity of knowledge. From such a point of view
this principle cannot here be considered. I must limit myself,
therefore, to a criticism of the opposed conception of atoms in a
uniform ether, as developed by Prof. Challis, and to the attempt
to show that, with the conception of atoms here offered, Prof.
Maxwell’s somewhat arbitrary hypothesis of vortices becomes un-
necessary. For I agree with the former in thinking that, “after
all that can be done by this kind of research, an independent
and @ priort theory ..... 1s stillneeded t ;” and I observe that
* See the first part of this paper, Phil. Mag. April, p. 275.
+ “On Theories of Magnetism and other ‘Forees, 1 in reply to Remarks
by Professor Maxwell,” Phil. Mag. April, p. 253,
Principles of Energetics. 353
the object of the latter “is to clear the way for speculation *,”
rather than to advance a complete general theory.
In examining Professor Challis’s ‘ fundamental hypothetical
facts,” I hope to show that they are opposed (1) by Newton’s
Rules of Philosophizing; (2) by the principles of Metaphysics,
as the modern Science of the Conditions of Thought; and (3) by
the conceptions of matter, of the interaction of its different parts,
and of motion and force, to which modern experimental researches
have led.
21. “The fundamental hypothetical facts on which the [Prof.
Challis’s| theory rests are, that all substances consist of minute
spherical atoms, of different, but constant, magnitudes, and of the
same intrinsic inertia, and that the dynamical relations and
movements of different substances are determined by the mo-
tions and pressures of a uniform elastic medium pervading: all
space not occupied by atoms, and varying in pressure in propor-
tion to variations of its density+.” Prof. Challis further says
that he has “been guided by Newton’s views on the ultimate
properties of matter, especially as embodied in the Regula Tertia
Philosophandi in the Third Book of the ‘ Principia’; ” and that
he has merely “‘ added to the Newtonian hypotheses two others,
viz. that the ultimate atoms of bodies are spherical, and that they
are acted upon by the pressure of a highly elastic medium ft.”
But on reference to the cited rule, no “ Newtonian hypotheses”
will be found, only a statement of the.actual general qualities of
matter. And, setting aside the “additional hypothesis” of
sphericity, so far are the hypotheses of ultimate indivisible
atoms, and these of an indeterminate number of different sizes,
though of the same intrinsic inertia, Newtonian, that Newton
says, ‘At si vel unico constaret experimento quod particula
aliqua indivisa, frangendo corpus durum et solidum, divisionem
pateretur; concluderemus vi hujus regule, quod non solum
partes divisee separabiles essent, sed etiam quod indivise in infi-
nitum dividi possent.”” And Le Seur and Jacquier add in their
note: “Hine patet differentia Newtonianismi et hypotheseos
Atomorum; Atomiste necessario et metaphysicé atomos esse
indivisibiles volunt, ut sint corporum unitates ; Metaphysicam
hane queestionem missam facit Newtonus . . . . omnem hace de re
Theoriam Metaphysicam experimentis facile postponens.” So
that not only are Professor Challis’s hypotheses as to “ ulti-
mate” bodies unwarranted by the rule he vouches, but he
appears as of that very metaphysical school of Atomists, New-
* «The Theory of Molecular Vortices applied to Magnetic Phenomena,”
Phil. Mag. March, p. 162.
+ Phil. Mag. Feb. 1861, p. 106. t Ibid. Dec. 1859, pp, 443 and 444,
Phil. Mag, 8. 4. Vol. 21. No. 141, May 1861. 2A
854. Mr. J. S. Stuart Glennie on tne
ton’s opposition to which is implied in his Regula Tertia Philo-
sophands.
No less clear is it that the postulate of two different kinds of
matter, one with the qualities of inertia and elasticity, the other
without the second of these qualities, is opposed by the very
terms, not only of the third rule, “ Qualitates corporum que
intendi et remitti nequeunt, queeque corporibus omnibus compe-
tunt in quibus experimenta instituere licet, pro qualitatibus cor-
porum universorum habendz sunt,” but by the terms of the
first rule also, “causas rerum naturalium non plures admitti
debere, quam que et vere sint et earum phenomenis expli-
candis sufficiant.”
22. Consider, secondly, how such hypotheses are judged by
the modern principles of Metaphysics. For it is evident that
the theories of every science must ultimately be judged by the
results of a science, Téyvn Texvov Kal eTLoTHUN ETLOTNLOV,
which, defining the conditions of knowledge, gives canons for
the criticism of hypotheses. As this is no place for a metaphy-
sical discussion, let it suffice to say that the theory of the rela-
tivity of cognition seems to justify the enouncement of this canon
as a test of theories put forward as scientific. A scientific (phy-
sical) theory is founded on postulates of Relations, not on postu-
lates of absolutely existing Entities. According to this rule it is
evident that if, for instance, a theory requires an atom of a cer-
tain size or hardness, it can only be granted where it will stand
as an expression of the relation between the forces distinguished
at that point as internal and external; so if a certain elasticity,
rotatory, or other motion of a body is required, the theory must
take that elasticity or rotatory motion, not as an absolute pro-
perty, but along with those relative conditions of other bodies
which determine such elasticity or motion.
23. Without advancing any other defence, this canon may be
justified by the consequence of its neglect. For a theory founded
on postulates of absolute qualities—entities—must necessarily
reason in a circle, accounting for phenomena by the same phe-
nomena already assumed as ultimate.
Thus, though Professor Challis says that it would be contrary
to principle “to ascribe to an atom the property of elasticity,
because, from what we know of this property by experience, it is
quantitative, and being most probably dependent on an aggrega-
tion of atoms, may admit of explanation by a complete theory of
molecular forces*,” he has no hesitation in ascribing elasticity
to the particles of the ether, which, if anything, are as much
atoms of matter as the “hard” atoms. But further, as to hard-
ness, 1s it not the case that, “from what we know of this pro-
* Phil, Mag, February 1860, p. 89.
Principles of Energetics. 355
perty by experience,” it also “may admit of explanation by a
complete theory of molecular forces?” Is it not therefore self-
contradictory to attribute elasticity to one sort of matter, and
justify its denial to another, on grounds which would equally
apply to the quality by which this other sort of matter is distin-
guished from the former? And is not a theory fallacious which,
if it attempts to explain relative elasticity or relative hardness,
must do so by means of hypothetical and inconceivable, abso-
lutely elastic, and absolutely hard entities ?
24. But further, examining these fundamental facts by the
results of the analysis of the qualities of matter, it will be seen
that it is attempted to found a physical theory on the hypothesis
of a physical matter acting on a mathematical matter. An elastic
matter may be physically conceivable ; but the interaction of such
a matter and bodies without any physical quality, but mere
abstractions of the metaphysical qualities deduceable from the
respective conditions of occupying and being contained in space,
cannot but be experimentally inconceivable.
25. Consider therefore, thirdly, the experimental conceptions
to which these “hypothetical facts” are opposed; and (1) the
conception of matter.
The conception of an absolute, or uniform, and universal elastic
sether is opposed to the conception now formed of such similar
entities as the old electric fluids, &c.; namely, that electricity is
not an entity, but the expression of a certain physical relation
between bodies, the electric state being kept up by, and entirely
dependent upon, the bodies among which the electric body at
any time is, or may be brought. Hence it should seem that if a
theory requires an elastic ether, its elasticity must be conceived
as relative or determined by the masses and distances of bodies,
and hence evidently elasticity be conceived as “une des propriétés
générales de la matiére* ”’
And the notion of absolutely existing spherical atoms of dif-
ferent magnitudes not only begs as many separate creations of
atoms as our fancy may suggest differences in their size, but is
opposed to the conception of the transmutation of matter, general-
ized from the fact that we have in physics at least no creations,
but perpetual changes dependent upon the ever-varying relations
of bodies.
_ 26. But (2) the idea of motions arising from the action of an
elastic fluid on an inelastic absolutely hard and smooth body is
opposed to all experimental conceptions of the interaction of the
parts of matter. For not only do we seem to be led by experi-
ment to a conception of the continuity of every part of matter by
the cohesion of other bodies, so that it should seem to be impos-
* Lamé, quoted in Part I. of a ams Phil. Mag. April, p. 275.
2
»
356 Mr. J. S. Stuart Glennié on the
sible for a fluid to act on a solid except through a mediate or
immediate cohesion, but we are led by the Mechanical Theory of
Heat to conceive every impulse communicated to a body to be
productive of internal as well as external motion. It is of course
necessary to make abstraction, out of the infinite number of
effects, of the particular effect we may desire to consider. But
an hypothesis of infinitely hard atoms not merely requires, in the
consideration of the motion of such an atom, abstraction to be
made of the interior relative motions also consequent on that
difference of pressures which causes its external relative motion,
but explicitly denies any internal motion.
It may be here noted that the Mechanical Theory of Heat
would lead us to consider as “ ultimate’? no special class of
bodies or molecules, except simply those, of the internal motions
of which we do not in any particular theoretical, or cannot in an
experimental, investigation take account. So any hardness may
be called “infinite ”’ if we do not consider the internal motions,
or change of form, consequent on the application of a force which
causes the translation of the body. But Professor Challis re-
quires us to concede as physical facts what are properly but con-
venient mathematical abstractions.
27. Again (3), the conception of the origination of motion
under such conditions as a uniform ether and discrete atoms
therein, all of the same mass, is opposed to the experimental con-
ception ‘of motion as or iginating in difference in the mutual pres-
sures of bodies. For these hypotheses give us the conditions of
an eternal equilibrium. In the theory I propose, it is evident
that anything short of an absolute equality in the masses and
distances of the parts of matter implies infinite mutually deter-
mining motions.
And Professor Challis speaks of “the existence of the wether
as the sole source of physical power*.” But in a mechanical
theory, as 1 have in the introductory, and in the first part of
this, paper shown, nothing can be accurately spoken of as, of
itself, ‘a source of power.” ‘A source of power,” a cause of
motion, or a force, is simply the difference in relation to a third
body of two resultant pressures upon it. And there can thus be
no conceivable mechanical power in a fluid of which the elasticity
is uniform, and on whick the reaction of different solids withm
it should seem, by this theory, to be either nothing or the same.
28. Professor Challis further conceives the physical forces to
be correlated as ‘ modes of action of a single elastic medium.”
But I shall endeavour in the sequel to distinguish these cor-
relations, and to show that they are either coexisting, mutually
* Phil. Mag. February 1861, p. 106; and December 1859, p. 444.
Principles of Energetics. 357
causative, or sequential molecular motions. For the true applica-
tion of Hydrodynamics would seem to be rather to actual solids
and fluids, than to such “ hypothetical facts” as form the bases
of Professor Challis’s Theory of Physics. How much work re-
mains to be done in that true direction is well known; and the
greatness of the results in the knowledge that might thereby be
given of the formation of the solar and other sidereal systems,
makes every contribution to Hydrodynamics, whatever the
immediate particular application of the theorems, of peculiar |
value.
29. If, therefore, the true application of Hydrodynamics has
been mistaken, and if a Hydrodynamical Theory of Physics must
be founded on entities, hypothetical solids and fluids, to which
such objections as the foregoing can be urged, there remains for
us only a Molecular Theory of Physics. It is because to such a
Theory all the most important modern physical researches seem
to poimt, that I have thought it necessary to examine at such
length the “fundamental facts” of Professor Challis. For the
great result of modern science may be said to be the relative con-
ception it gives of every phenomenon, and hence the demand
that the fundamental facts of any theory be conceived, not as
absolute and independent existences, but as expressions of rela-
tions. Now a Molecular is distinguished from a Hydrodyna-
mical Theory of Physics in this,—that while in the latter the
states and motions of bodies are explained by the action on them
of some hypothetical, uniform, absolute, and all-pervading entity,
in the former theory, physical states and motions are referred to
differential conditions of stress and strain among the actual con-
stituent molecules of bodies. Hence the evident experimental
advantage of a Molecular Theory is, that its hypotheses being
as to relative conditions of Molecular pressure and tension, trans-
mission of motion, &c., they are more or less capable of experi-
mental proof or disproof; and such a theory will be at least pro-
lific in the suggestion of experiment. But where one deals with
the waves or currents of an absolute ether acting on absolute
atoms, a plausible theory may indeed be made out, but it is
because its conceptions are fundamentally opposed to, so that
its minor hypotheses cannot be checked by, experiment.
30. It is as the new fundamental principle of a Molecular
Theory of Physics that I venture to suggest the above conception
of Atoms. It is because, however convinced of the soundness of
this principle, I am very diffident of my own powers of applying
it, that I have gone at such length into its illustration, and the
criticism of the opposed conception, as developed by Professor
Challis. For should the mechanical explanation which, by
358 Chemical Notices :—M. Sawitsch on Acetylene.
means of this principle, I propose to give of physical and che-
mical phenomena be found liable to serious objection, I hope
the above remarks will have made this conception of Atoms
sufficiently clear to be applied with greater success by others.
6 Stone Buildings, Lincoln’s Inn,
April 11, 1861.
[To be continued. |
LIV. Chemical Notices from Foreign Journals.
By H. Atxinson, PA.D., F.CS.
[Continued from p. 301.]
AWITSCH* found that, under certain circumstances, mono-
brominated ethylene, €? H® Br (bromide of vinyle), parted with
hydrobromic acid and became converted into acetylene, €* H?, the
gas discovered by Edmund Davy and investigated by Berthelot.
He was led to investigate this deportment more minutely, and
having tried the action of monobrominated ethylene on amylate
of sodium, has found in it a mode of preparing this gas.
About 45 grammes of brominated ethylene were heated in a
closed vessel with amylate of sodium. An abundant precipitate
of bromide of sodium was formed, and the mass became liquid
from the regenerated amylic alcohol. The vessel was then care-
fully cooled down in a freezing mixture and opened, when
about 4 litres of a gas escaped, which, agitated with an ammo-
niacal solution of chloride of copper, gave an abundant red pre-
cipitate. When this precipitate was treated with dilute hydro-
chloric acid, it gave off about a litre of a colourless gas with a
peculiar odour, and which burned with a very fuliginous flaine.
The analysis of this gas, and its combination with copper, left no
doubt that it was acetylene.
Its formation may be thus expressed :-—
o FJ ll
‘ i 04+C?H?Br= C?H?+NaBr+@ HO.
pe ae F Monobrominated Acety- Amylic
Ba tia ethylene. lene. alcohol.
This reaction is important, as it will probably lead to the for-
mation of a new series of hydrocarbons of the general formula
©; He»-2, of which acetylene, €* H?, is the first member, from
the hydrocarbons of the general formula C, H.,. In fact
Sawitsch has subsequently { examined the action of monobromi-
* Bulletin de la Société Chimique, p. 7.
+ Phil. Mag. vol. xx. p. 196.
{ Comptes Rendus, March 4, 1861.
M. Miasnikoff on Acetylene. 359
nated propylene on ethylate of sodium, and has obtained a second
member of the series, al/ylene, C7 H*. The action is quite ana-
logous to that in the former case: the gas is passed into an am-
moniacal solution of copper, with which it forms a voluminous
flocculent precipitate. This is decomposed, when heated, with
the formation of a reddish flame; with concentrated acids it dis-
engages a gas even in the cold.
Allylene is best obtained from this precipitate by the action
of dilute aqueous hydrochloric acid, from which, when heat is
applied, there is given off a colourless gas of a strong and dis-
agreeable odour, but less so than that of acetylene. It burns
with a fuliginous flame, and precipitates silver and mercury salts,
the former grey and the latter white. These compounds are
analogous to the copper compound, and, like it, are very unstable.
The property of combining with an ammoniacal oxide of copper
appears to be characteristic of this group, and will probably lead
to the discovery of the higher members.
The formation of allylene may be thus expressed :—
C? H° NaQO+ C? H® Br= Na Br+ €? H*+€? H°O,
Ethylate of Brominated Allylene. Alcohol.
sodium. propylene.
Miasnikoff*, in some experiments with monobrominated ethyl-
ene, has also noticed a mode of the formation of acetylene, which
gives a simple and elegant method of preparing this gas.
When the vapours of crude monobrominated ethylene, prepared
in the ordinary way, are passed into an ammoniacal solution of
nitrate of silver, a precipitate forms, which is at first yellow, but
which quickly becomes converted into grey; at the same time
an oil collects at the bottom of the vessel, which is brominated
ethylene, and which can easily be separ ated by heating to 20°.
When this bromide further acts upon a fresh portion of ammo-
niacal solution, it produces no change; but after being passed
through a boiling concentrated solution of potash, it again
acquires the property of forming this grey pulverulent deposit.
By arranging the apparatus so that the vapours of brominated
ethylene pass more than once through solution of potash, a con-
siderable quantity of the pulverulent deposit can be formed.
This powder detonates strongly on the application of heat,
percussion, or friction, and also by the action of chlorine or of
gaseous hydrochloric acid. Treated with dilute hydrochloric
acid, it gives a gas which burns with a fuliginous flame, and
which reproduces the pulverulent precipitate. The analysis and
the properties of this gas show that it is acetylene; and the
analysis of the silver compound gives for it the formula
C* H? Ag’.
* Bulletin de la Société Chimique, p. 12.
360 M. Heinz on Glycolic Acid.
From the mode of its preparation, monobrominated ethylene,
in passing through strong potash, is simply resolved into acetyl-
ene and hydrobromic acid,
€? H® Br—H Br=€? H?.
Monobrominated Acetylene.
ethylene.
By a similar series of actions, M. Morkownikoff has prepared
what appears to be the gas allylene, described by Sawitsch.
According to Heinz*, the best method of preparing glycolic
acid is from monochloracetic acid, which, under the influence of
alkalies, decomposes into an alkaline glycolate and into an alka-
line chloridet. |
The hydrate of glycolic acid may readily be obtained by the
following method :—To the solution of the mixture of glycolate
of soda and chloride of sodium obtained in the above reaction, a
sufficient quantity of solution of sulphate of copper is added.
The glycolate of copper, C+ H? Cu O®, which forms, is a diffi-
cultly soluble salt; it precipitates as a crystallme mass, and
is readily obtained pure by washing. This salt is then dif-
fused in a large quantity of water, the mixture raised to boiling,
and saturated with sulphuretted hydrogen. When all the cop-
per is precipitated it is filtered; and as the filtrate is brownish,
from the solution of a small quantity of sulphide of copper, it is
evaporated to a small volume, while a slow stream of sulphuretted
hydrogen is passed through, and when now filtered, is obtained
quite colourless.
By a series of operations analogous to those by which an
alcohol of the ethyle series may be transformed into the next
higher acid, Cannizarot has obtained from anisic alcohol an acid
homologous with anisic acid.
Anisic alcohol, €® H'®Q?§, appears to contain the group
€° H® 0, which plays the part of a monoatomic radical. When
the chloride of this group, C® H9 O, Cl, was treated with cyanide
of potassium, chloride of potassium was formed, and an oil which
was the cyanide, C7 H9O EN. This oil was obtained in the im-
pure state, and was treated directly with potash at the tempera-
ture of ebullition, by which a large quantity of ammonia was
disengaged ; and on the subsequent addition of hydrochloric acid
in excess, an oil deposited which solidified to a crystalline mass.
This consisted of the new acid which Cannizaro names homoanisic
* Poggendorff’s Annalen, January 1861.
tT Plul. Mag. vol. xvi. p. 138.
{ Comptes Rendus, vol. li. p. 606,
§ Phil. Mag. vol. xx. p. 294.
M. Rossi on Homocuminic Acid. 361
acid. It crystallizes im nacreous lamine. Its formation may be
thus expressed :—
CSHIOEN+K HO+ H?O=C9 H® KO8+ NH.
Cyanide of Homoanisate
anisyle. of potash.
Rossi* has applied to cuminic alcohol the same series of trans-
formations, and has obtained a new acid homologous with cuminic
acid. He prepared the chloride of cumyle, G!° H'’ Cl, by the
action of hydrochloric acid on cuminic alcohol, and treated it
with cyanide of potassium, by which means he obtained the cor-
responding cyanide. This crude cyanide of cumyle was boiled
with strong caustic potash until its decomposition was complete ;
and to the mixture was then added hydrochloric acid in excess,
by which the new acid was precipitated. On recrystallization it
was obtained in small needles. Its formation is thus expressed :
Gl HEN + KHO+ H? O= 6"! H KO?4 NH,
Cyanide of Homocuminate
cumyle. of potash.
Homocuminic acid, G!! H!? 02, can be distilled without decom-
position. It is difficultly soluble in cold water ; but its solution
reddens litmus, and decomposes the carbonates. Its salts are
obtained by double decomposition: most of them crystallize
well. ,
As the result of a lengthened investigation on filtration of the
air in reference to fermentation, putrefaction, and crystallization,
Schroder f is led to the following conclusions :—
1. A vegetable or animal can only be formed from living vege-
table or animal organisms. Ommne vivum ex vivo.
2, There is a series of phenomena of fermentation and putre-
faction which arise solely from microscopic germs furnished by
the atmosphere. These are more especially the formation of
mould, of wine-yeast, of the lactic acid ferment, of the ferment
which produces the decomposition of urine.
3. Vegetable or animal substances, boiled and closed while
hot by means of cotton, remain im that condition quite protected
against every kind of fermentation, putrefaction, or formation of
mould, if all the germs in them capable of development are de-
stroyed by boiling; for the germs which might reach them from
the air are filtered out by the cotton.
4, The germs of most vegetable or animal substances are com-
pletely destroyed by simple boiling. A boiling for a short time
at 100° C. isalso sufficient to kill all germs furnished by the air.
* Comptes Rendus, March 4, 1861.
t+ Liebig’s Annalen, March 1861.
362 M. Schréder on Fermentation, Putrefaction, &c.
5: But milk, the yellow of egg, and meat contain germs which
are not completely destroyed by a short boiling at 100°. But
boiling at a higher temperature under a pressure of two atmo-
spheres in the digestor, or long-continued boiling at 100°, is
sufficient to kill even these germs.
6. The germs of milk, yellow of egg, and of meat, even when
they have been submitted to a boiling at 100°, not continued,
however, too long, are capable of developing themselves as a
specific putrefaction ferment, and not unfrequently, at least in
the yelk of egg, in the form of long but inert fibrils.
7. This specific putrefying ferment is of animal nature. It
developes and increases at the expense of all albuminous sub-
stances. It is, however, incapable of increase under conditions
which are all that are necessary to vegetable formations.
8. The crystallization of supersaturated solutions is com-
menced or induced by the action of the surface of solid bodies.
9. The induction necessary to set up the crystallization of the
soluble hydrates from a supersaturated solution, is less than that
necessary for the crystallization of the more difficultly soluble
hydrates.
10. The surface of a crystal of the same nature exercises the
strongest inducing action. Next to that comes the layer of air
which forms on the surface of solid bodies. These coatings are
destroyed by heating, continued wetting, or by cleaning, and are
only formed slowly again in filtered air.
1]. The crystallization of the more soluble hydrates from
supersaturated solutions, which is set up even by a feeble induc-
tion, only experiences a feeble induction on the surface of the
crystal of the same kind, and hence only progresses very slowly.
12. Supersaturated solutions closed with cotton keep for a
long time unchanged, because the cotton filters all the solid
particles from the air which gains access. Agitation has no
action on the crystallization ; it only induces it if supersaturated
solutions are in contact with such places of the surface as are
fitted to induce the crystallization.
By oxidizing cymole, €!°H", with dilute nitric acid, Noad
found that it was converted into toluylic acid, C® H® 0%, and
oxalic acid; from cumole, €? H'!*, Abel similarly obtained ben-
zoic acid, G67 H® 8%. Hence it might have been expected that
toluole, G7 H®, by analogous treatment would yield a new acid,
€ H? 62, homologous with these.
This is, however, not the case, as experiments by Fittig * have
shown. When toluole is oxidized by means of nitric acid, the
process is different. There is no formation either of oxalic or of
carbonic acid. as
, ists
it should be, the total number of triads being 8.f and 3 of them going
to a syntheme.
unsymmetrical Six-valued Function of six Letters. 375
as is number and space of the other two. Syntax and Groups
are each of them only special branches of Tactic. I shall on an-
other occasion give reasons to show that the doctrine of groups
may be treated as the arithmetic of ordinal numbers. With
respect to the twelve varieties of the A or B aggregates, they
may be obtained from the one given by combining the substitu-
tions corresponding to the six permutations of the three consti-
tuents of one nome, as 7, 8, 9, with the permutation of any two
constituents of another, as 5,6. But I have said enough for
my present purpose, which is to point out the boundless un-
trodden regions of thought in the sphere of order, and especially
in the department of syntax, which remain to be expressed,mapped
out, and brought under cultivation. The difficulty indeed is not
to find material, of which there is a superabundance, but to dis-
cover the proper and principal centres of speculation that may
serve to reduce the theory into a manageable compass.
I put on record (as a Christmas offering on the altar of science)
for the benefit of those studying the theory of groups, or com-
pound permutations (to which the prize shortly to be adjudicated
by the Institute of France for the most important addition to the
subject may tend to give a new impulse), and with an eye to the
geometrical and algebraical verities with which, as a constant of
reason, we may confidently anticipate it is pregnant, an exhaust-
ive table of the monosynthematic aggregates of the trinomial
triads that are contained in a system of three triliteral nomes.
Let these latter be called respectively 123; 456; 789; then
we have the annexed :—
Table of Synthemes of Trinomial Triads to Base 3.3.
(1.) (2.) (3.) (4.)
147 258 369 147 258 369 147 258 369 147 258 369
148 259 367 148 259 367 148 259 367 148 259 367
149 257 368 149 257 368 149 257 368 149 267 358
157 268 349 157 268 349 157 269 348 157 268 349
158 269 347 158 269 347 158 267 349 158 269 347
159 267 348 159 267 348 159 268 347 159 247 368
167 248 359 167 249 358 167 248 359 167 248 359
168 249 357 168 247 359 168 249 357 168 249 357
169 247 358 169 248 357 169 247 358 169 257 348
(9.) (6.) 7.) (8.)
147 258 369 147 258 369 147 258 369 147 258 369
148 267 359 148 267 359 148 269 357 148 269 357
149 268 357 149 257 368 149 257 368 149 267 358
157 249 368 157 268 349 157 268 349 157 268 349
158 269 347 158 269 347 158 249 367 158 249 367
159 248 367 159 248 367 159 267 348 159 247 368
167 259 348 167 259 348 167 248 359 167 248 359
168 257 349 168 249 357 168 259 347 168 259 347
169 247 358 169 247 358 169 247 358 169 257 348
A
376 On the unsymmetrical Siz-valued Function of six Letters.
The discussion of the properties of this Table, and the classi-
fication of the eight aggregates into natural families, must be
reserved for a future occasion.
Note.—A triad is called tripartite if its three elements are
culled out of three different parts or sets between which the
total number of elements is supposed to be divided; bipartite
if the elements are taken out of two distinct sets ; unipartite if
they all lie in the same set. The more ordinary method for
the reduction of synthematic arrangements from a given base
to a linear one which I employ, consists in the separate synthe-
matization inter se of all the combinations of the same kind as
regards the number of parts from which they are respectively
9
drawn. ‘Thus, ex. gr., if the distribution of the oo dae 2 —
triads to the base 30 into 20609 synthemes be required, this
2
may be effected by dividing the 30 elements in an arbitrary
manner into 15 parts, each part containing 2 elements. These
15 parts being now themselves treated as elements, are first to be
conjugated as in the old 15-school-girl problem, and each of these
7 -conjugations can be made to furnish 6 synthemes containing
exclusively bipartite triads. The same 15 parts are then to he
conjugated as in the new school-girl problem, and the 91 conju-
gations thus obtained will each furnish 4 synthemes, containing
exclusively the tripartite triads. These bipartite and tripartite
synthemes will exhaust the entire number of triads of both
kinds, and accordingly we shall find
7x6491 x 4=406
_ 29 x 28
OnE
A syntheme, I need scarcely add, is an aggregate of combina-
tions containing between them all the monadic elements of a
given system, each appearing once only. In the more general
theory of aggregation, such an aggregate would be distinguished
by the name of a monosyntheme. A disyntheme would then
signify an aggregate of combinations containing between them
the duadic elemienits; each appearing once only, and so forth.
Thus the old 15-school-girl question in my nomenclature would
be enunciated under the form of a problem “to construct a triadic
disyntheme, separable into monosynthemes to the base 15 ; ” the
new school question, as a problem “ to divide the whole of the
triads to base 15 into monosynthemes ;”’ the question which
connects the two, as a problem “to exhibit the whole of the triads
to base 15 under the form of 13 disynthemes, each separated
into 7 monosynthemes.
On. the Galvanic Polarization of buried Metal Plates. 377
_ A question of a more general kind, and embracing this last, °
would be the problem of dividing the whole of the same system
of triads into 13 disynthemes, without annexing the further con-
dition of monosynthematic divisibility. So there is the simpler
question of constructing a single disyntheme to the base 15
without any condition annexed as to its decomposability to 7
synthemes.
K, Woolwich Common,
December 1860.
LVII. On the Galvanic Polarization of buried Metal Plates.
By Dr. Pu. Caru*.
AST year, in consequence of the disturbances which were
observed in the telegraphic wires during the appearance
of the northern lights, Professor Lamont was induced to contrive
an apparatus at the observatory of Munich in order to examine
more closely into the occasional motion of the earth’s electricity,
and to determine its magnitude and direction. For this purpose
large zinc plates were buried on the north, south, east, and west
sides of the observatory garden ; the north plate being connected
with the south, and the east with the west, by means of copper
wires, which were brought into the observatory and connected
with galvanometers. As Professor Lamont, in testing this appa-
ratus, remarked certain phenomena which he attributed to gal-
vanic polarization, it appeared to me advisable to subject the
matter to a more careful examination, and to obtain more accu-
rate measurements.
_ Through the wire that connects two of the above-mentioned
zinc plates, a current, which I shall call the terrestrial current,
is perpetually circulating, the intensity of which is indicated by
a fixed deviation of the galvanometer. If a galvanic element be
inserted in these conducting wires and again removed, then, pro-
vided it has caused no modification in the conductor, the needle
of the galvanometer will return to its former position. But if,
on the other hand, a state of galvanic polarization has been pro-
duced in the zinc plates, then the deviation of the needle of the
galvanometer, after the removal of the element, will be greater
or less than that exhibited by it originally, accordingly as the
direction of the galvanic current has been opposite to, or the
same as that of the terrestrial current.
On trial, the latter result exhibited itself so unmistakeably that
no further doubt could be entertained of the occurrence of galvanic
polarization. In order to measure the magnitude of the effect
produced, I made use of a weak Daniell’s cell, which I inserted
* Translated by F, Guthrie from Poggendorft’s Annalen, No. 10, 1860,
378 On the Galvanic Polarization of buried Metal Plates.
for five minutes in the wire conductor, and I thereby obtained
the numbers exhibited in the following Table ; in which G indi-
cates the effect of the galvanic current, E that of the terrestrial
current, and P that of the polarization expressed in divisions of
the galvanometer. The effect of the polarization was observed
1 minute 30 seconds after the removal of the cell.
I. When the two currents passed in the same direction.
P
E. are a
ES G-+E
129-8 34 0-026
129:3 3-4 0-026
123-0 20 0-021
108-2 24 0-022
II. When the current passed in opposite directions.
P
ak:
: es Gan
1245 54 0-043
122-7 51 0-041
107-4 3:8 0-035
109-2 3:5 0-031
From these experiments, it follows that the mean value of
ee Spas
Gan * 0:0237, that of GE 0:0375 ; so that when the gal-
vanic and terrestrial currents pass in opposite directions, the
polarization of the buried metal plates is greater than when they
pass in the same direction. 7
Immediately on the removal of the cell, the effect of the gal-
vanic polarization was greater by two or three divisions of the
galvanometer scale than it was after the lapse of 1 minute 30
seconds ; and after that period the effect still continued gra-
dually to diminish. In order to exhibit the law of this diminu-
tion I subjoin the following Table :—
Time after the removal, Deviation of the gal-
of the cell. vanometer needle.
1 minute. 23:0 divisions.
” 21°38 ”
” 211,
” 20°7 ”
” 20:3 39
20:0 a
” 19-9 ”
”? 19:7 bP
” 19°5 ”
” 19°4 ”?
SUMMONS Str CS bo
—
On Transcendental and Algebraic Solution. 379
At the commencement of the experiment, the deviation of the
galvanometer caused by the terrestrial current was read off at
19-2 divisions.
The above experiments disclose nothing at variance with the
known laws of galvanism; but it nevertheless appeared to me
advisable to make them known, as they afford a simple expla-
nation of certain phenomena which Professor Thomson has de-
scribed*, and which he seems to attribute to entirely different
causes.
LVIII. On Transcendental and Algebraic Solution. By JamMEs
Cocks, M.A., F.R.A.S., F.C.P.S., Barrister-at-Law, of the
Middle Temple.
Saga fe=0 be an algebraic equation of the nth degree, all
the coefficients of which are functions of one parameter a.
By differentiation we obtain a result of the form
oe =Fr = +fe=0.
But, since F and f are rational functions,
de fe
da ‘Fe
Ue ee Oe ee
~ Fa.Fu,.Fa,..Fa,
where R is a rational and integral function of z And
Ra=A,a"-!+A,a"-?+..+A,,
where A is a function of a. Moreover
2
= Poa’. espace a
Hence, repeating this process, we are conducted to the system _
= Raz,
@ —Re= Aya +A,2™-?4+..+A,,
d?
eg le 14 Boa"-?+ .. +B,,
Biot
eT oe G,2"-1 + G,a"-2+ ..4+G, ;
and if we assign n—2 indeterminates A, u,..v so as to satisfy
* Report of the Twenty-ninth Meeting of the British Association for the
Advancement of Science (Transactions of the Sections), p. 26.
+ Communicated by the Author.
380 Mr. J. Cockle on Transcendental and
the n—2 conditions
AA, +B, +..+v0,4+G,=0,
AA, +uHB,+..+vC,+G6,=0,
NAn—2 + MBy_2+ ++ +VOn2+ Gn-2=0,
we shall arrive at a linear differential equation,
d”®— a d™—24 d?ax
da"- de gees B+ ae
5 ad oe
da
For, when the above conditions are satisfied, 2"-!, 2*-?,.. x?,
all the powers of x in short, save a itself, disappear; and
v,..#, A, L, M are each of them known functions of a, inasmuch
as A, B,..C, G are known functions of a.
Thus the roots of any equation whereof the coefficients are
functions of only one parameter may be expressed in terms of
algebraic, circular, or logarithmic functions, and of integrals of
algebraic functions. These integrals depend upon the quantity M.
To a form involying only one parameter, Mr. Jerrard has shown
that the general quintic may be reduced. Its resolvent sextic
may also be reduced to the same form.
Mr. Jerrard’s memorable discoveries also show that the general
sextic may be regarded as involving two parameters only. The
general sextic leads us to the consideration of the equation
dfe=Fr.da+fr.db=0,
where a and b are the independent parameters, of which the co-
efficients may be considered as functions, and 6 is the character-
istic of the Calculus of Variations.
If, in art. 62 of my “ Observations,” &c. (vol. xvii. p. 342), we
take the suffixes of @ to the modulus 6, the equations become
0,04 + 0.09 + O:05=Ys=P(x5)s
8109+ 9205+ O;0,=Y1="(2)),
0,03 + 0284+ 0;09=Ya=7 (22);
6,4, + 0,03+ 0,05=¥3=7(2#3);
@, 19 + 6365+ 8,0;=y4=7(2,).
And this system has a certain relation to the formula
6,2 Oar a 6424200245 a 424300244)
which, taking the suffixes to the modulus 6, is, for all mtegral
values of a, equal either to y, or to yy. But all the values of y
are not thence evolved ; and in order to obtain a convenient repre-
sentation of the system, I avail myself of certain cyclical forms
Algebraic Solution. 38]
which may be given to it when one of the roots is supposed to
become fixed.
The form here used will admit of an exceedingly simple repre-
sentation if, throughout my “ Observations,’”’ we replace 0, by
@,, and vice versd. This requires that in art. ‘48 (vol. xviil. p. 52)
we write
Oras =O's, Ofas) =O,
a change of definition which I shall accordingly suppose to be
made.
Further, I shall suppose that we replace 0, by 0;, where i is
an imaginary suffix defined by the congruence
t+ a=z1 (mod. 5),
a being an integer. Or, if we agree to regard the infinite suffix
oo as satisfying the congruence
o-+a=o (mod. 5),
we may replace 6, by 9,,. Lastly, I shall suppose the suffixes,
after these changes, to be taken to the modulus 5.
The changes being made, it will be found that all the fune-
tions y are deducible from the expression
0; 82+ Oa41 9044+ 80429043
by writing, successively, 0, 1, 2, 3,4 for a. In fact we have
9;09+ 994+ 9,0;=y2=1(xo),
9,0, + 9,9) + 8,0,=9,=7(2));
0; 05+ O30; + O,99=Yo=7 (Xo)
9,0; + 0495+ 697, =Y3=r(#s),
0,0, +0,03+ 9,0,=Y4=" (2,4) 5
and if, in these equations, we change
“
‘ 0, 9, 93 8% Yo %
into
Oe 95, Oy 5, 5 2s
respectively, we shall be reconducted to the system of art. 62 of
my “Observations.” More extensive changes in our funda-
mental formule and definitions would enable us to express the
system with a greater concinnity between the suffixes of 0 and
those of a, and provided that, on the right of the last system,
we interchange 2, and 2, the system may be deduced from the
equation
0:0.+ 60419044 + 904200+3=YVy=T (aa).
If, in the expression
2 0. 6, =f 644104 +3 =e 64420044)
we make a equal to 0, 1, 2, 3, 4: successively, we find the follow-
3882 Mr. J. Cockle on Transcendental and
ing relations between it and the « and 8 functions of art. 70 of
my “ Observations” (vol. xvii. p. 508), viz. :—
6;0,+ 0,0; +0,0,= a,
0,0, + 0,0,+ 6,9,=P;,
0;0,+60)+ 6,0,=8.;
003+ 040, + 0,94 = ea,
0;0,+ 005+ 9,0,;= Bo;
and in like manner from*
0.0,+ 6410 a4+2+ 00430044
we deduce
0,49 + 010+ 0;0,= e4,
0:0, + 005+ 6,0,=e,,
G,0q+t 0304+ 99, =Bs,
0;03,+0,0,+ 0,0,=R4,
0; 0+ 0.0; + 9,03= a3.
A contemplation of these systems of equations seems to lead
to the conclusion that a certain equation of the fifteenth degree,
which Mr. Jerrard supposes to be capable of decomposition into
five cubics, is not irreducible, but composed of a quintic and a
10-ic factor.
I cannot think that Abel’s conclusion is at all shaken by the
researches of Mr. Jerrard. Of his cardinal proposition, the
en
Py tiFnagt=9
of art. 106 of his ‘ Essay,’ Mr. Jerrard gives no proof. Direc-
tions to compare (ab) and (ac) are insufficient instructions for
attaiing a result fraught with difficulties so serious. For rea-
sons already assigned, I believe the proposition to be erroneous,
and incapable of proof. And with it the whole argument of Mr.
Jerrard falls.
I need not the warning from my own oversight to restrain me
from dwelling unduly upon what I believe to be an error of Mr.
Jerrard’s. But, with every recognition of his great claims to
* Mr. Harley has completely determined these « and 8 functions; and I
regret that he has not as yet published the whole of his investigations on
quintics. The proposition of Mr. Jerrard, which Mr. Jerrard supposes that
Mr. Harley has ignored, is, when considered in reference to processes which
do not involve transformation to a soluble form, rather an axiom than a
theorem. It may be stated thus: If © be equal to ©’, it is not in general
equal to 6”.
I would here add the expression of a hope that Mr. Harley, to whom I
have communicated the above results on the theory of transcendental roots, ~
may soon publish some developments of them to which he has been led.
Algebraic Solution. ; 383
the gratitude of mathematicians, it is scarcely possible to ignore
the fact that Mr. Jerrard’s hope (expressed at the conclusion of
his paper of 1845), to discuss the resolution of the trinomial
equation z°+ A,v#+A,=0, has not been realized, and that little
or no approach has yet been made towards its realization. Mr.
Jerrard’s subsequent researches on quintics seem to me, for rea-
sons already adduced, to enhance rather than dispel any diffi-
culties which arise upon the paper in question. It is perhaps
to be desired that the mathematical world should be made ac-
quainted with the whole of Mr. Jerrard’s views on this import-
ant subject.
Does an absolutely impossible, or rootless, equation, exist ?
MM. Terquem and Gilain have discussed this question in the
Nouvelles Annales de Mathématiques*, with reference ‘to the
equation
+V1+2e4+ V1—2=1.
But this equation does not in reality raise the question under
consideration. Jor (as I had occasion to write to Mr. Harley
durmg last autumn) every one of the congeneric equations
is soluble. And some one of the four values of a given by
e= +(+1)?3./3
will satisfy any one of the above four congeners. I shall there-
fore again (S. 3. vol. xxxvii. p. 281) have recourse, for illustra-
tion, to the equations
1+ Vz—44+ Vz—1=0,
1— Vx—4— Wx—1=0,
each of which must, I think, be deemed impossible or rootless.
The only gleam of a solution of the last is, so far as I can see,
one which springs from the assumptions
v=4(+1)?4+(—1)?,
A= 4( tg De; l= Ss.
while, for the first, we have the system
#=4(—1)? +(+))?,
4=4(—1)?, T=(+1)*
But how can that be called a solution which depends upon a mo-
dification of the constants of a problem (compare 8. 4. vol. ii.
p. 439)? The safer conclusion seems to be that the two equa-
tions are rootless.
Midland Circuit, at Lincoln,
March 15, 1861.
* See Mr. Wilkinson’s Note Mathematice, Mechanics’ Magazine,
vol, lxii. p. 582.
[ 384 ]
LIX. Proceedings of Learned Societies,
ROYAL SOCIETY.
(Continued from p. 233.]
May 24, 1860.—Sir Benjamin C. Brodie, Bart., Pres., in the Chair.
> me following communications were read :—
“Qn a new Method of Approximation applicable to Elliptic
and Ultra-elliptic Functions.’ By C. W. Merrifield, Esq.
On the Lunar-diurnal Variation of Magnetic Declination at the
Magnetic Equator.’’ By John Allan Broun, F.R.S., Director of the
Trevandrum Observatory.
This variation, first obtained by M. Kreil, next by myself, and
afterwards by General Sabine, presents several anomalies which re-
quire careful consideration, and especially a careful examination of
the methods employed to obtain the results. The law obtained seems
to vary from place to place even in the same hemisphere and in the
same latitude, and this to such an extent, that, for example, when the
moon is on the inferior meridian at Toronto it produces a minimum
of westerly declination, while for the moon on the inferior meridian
of Prague and Makerstoun in Scotland it produces a maximum of
westerly declination. No two places have as yet given exactly the
same result ; though the result for each place has been confirmed by
the discussion of different periods.
In order to obtain the lunar diurnal action, it has been usual to
consider the magnetic declination at any time as depending on the
sun’s and moon’s hour-angles and on irregular causes. Thus, if
at conjunction, H, be the variation due to the sun on the meridian,
and h, be that due to the moon on the meridian, H, the variation
for the sun at 1, 4, for the moon on the meridian of 1", and so on;
it is supposed that we may represent the variations for a series of
days by the following expressions, where the nearest values of / to
the whole hour-angles are given :—
Ist day. H’, +A’, +2), H+’, +2, ... H’,, +2, +2’.
2nd day. H",+h",, +2" H" +h", +2", ics HA", "5
nth day. H) +4, +e, Hy +h) +a. ... H+A +,
where 2 is qos to imaeatalit causes, and n is 7” aed of days ina
lunation nearly,
Summing these quantities we have nae
2H, +3) ji+3e, 3H, +2, Atde, , ++. SH, +23, Ate, (A)
saa the means are,
H+ ¢ +=", H+ ¢+=,... ul eee
Here the aa means are affected by the spine due to the total
action of the moon on all the meridians, and by variables depending
on disturbing causes. If, on the other hand, we arrange the series as
On the Magnetic Declination at the Magnetic Equator. 385
follows,
H’, +h’, A HW’ +A) +0’, ... HY", +h", 42",
H+", 42" en Pr eee
n—1 n—-l A-1 : n n n 34 n n
Ht” +h, +v,, Ho +h +a,... Hi +h),+z,,-
Bhisisintng these quantities we have,
eh) 0 (td) ,0 i O (24)
2) f+ 2h, + Ew ? H+ 2h +4, 1% H+ dh +%,,% (C)
and for the A
O+Ah, $=
In this case © is the mean di it observations, of which 24 give
the true means for the total solar influence, and the remaining n—25
being equally distributed through the hour-angles also give the mean
approximately.
Instead, however, of combining the observations in this way, the
following method has been preferr ed. Let, in the quantities (B),
(H,) = 1,4 ¢ +=
a ae opis ee ape.
Gs Untig
Then H’,+ 2’, e a’, — aj h', +. (@',. ye;
a + i" ot a” i- CH, fen Es + wn = d",
ol ae ig nu— nt )= a (ae 1) = ee
Summing the fi two shinies we have
awe
2d, ab fag 2 (#’)
nm—\1 } n—1
Similarly we obtain
xd, 2. a
af eis and so on.
n—1|
Loh +
It will be observed that in these summations there are two assump-
tions ; one, that the lunar diurnal law is constant throughout the
lunation, or series of lunations, for which the means are obtained ; or
that the quantity € in the expressions (B) is constant. If this be
not exact, thea the quantity — will contain the variation due to this
n
cause, and depend in part on the lunar hour-angle ; so that the mean
(H.) which is employ ed in taking the differences will eliminate part
of the lunar action and partially distort the law. The other assump-
tion is that the mean solar diurnal variation, represented by (H,),(H,)
»..., 18 nearly constant throughout the period ; for, if not, the dit-
Phil. Mag. S. 4. Vol. 21. No. 141. May 186}. 2C
386 Royal Society :—
ferences due to such changes might be sufficient to mask any lunar
law, the latter having a small range compared with the former.
Also it should be remarked that the means /,, 4,, &c. are combined
0
with the irregular effect 25(%), This effect, as far as it is due to
n—1
disturbance, we know obeys a solar diurnal law ; and if independent
of lunar action, a sufficiently large series of observations might suffice
to eliminate it, as combining with and forming part of the regular
solar diurnal variation. If, however, the series is not very large and
the irregular disturbance considerable compared with the variation
sought, it may be desirable to omit or modify the marked irregu-
larities.
As regards the first assumption referred to above, the results
obtained hitherto seem to show the error to be small, and the only
way to determine its amount will be to consider it zero in the first
instance, and thereafter a more accurate calculus may be employed.
For the second assumption, it is certain that the solar diurnal law
varies considerably in some cases within a lunation. At the mag-
netic equator, for example, the law of magnetic declination is inverted
within a few weeks near the equinoxes. The attempt to correct the
error due to considerable change in the solar diurnal variation by
taking the means, as has been done, from shorter periods than a
lunation, is liable to the serious objection that the resulting hourly
means are affected unequally by the lunar action, so that the sums
(A) take the form,
2H) + 2,A+ 2%, BH, + WA+Be,......2Hy3+ Bh 4 Baro,
where the second term in each expression is a variable. In the
discussion to which I am about to allude, the following pian has been
followed. ‘The hourly means for the following series of weeks were
taken, namely—
m, from Ist, 2nd, 3rd, and 4th weeks of the year.
m, ,, 2nd, 3rd, 4th, and 5th te is
yo. org, 4th, Sth; and. Ott Bs ~
The means of m, and m, were then taken as normals for the 3rd
or middle week, of m, and m, as normals for the 4th week, and so
on: these means were then employ red for the differences from the
corresponding hourly: observations of the weeks to which they
belonged.
With reference to the irregular effect, it is evidently desirable that
we should know in the first instance whether it may not be a function
of the lunar, as well as of the solar, hour-angle ; for this end it is
essential in the first instance to obtain the result including all the
supposed irregular actions, and afterwards to eliminate these in the
best manner possible.
In the discussion of the Makerstoun Observations I had substi-
tuted for certain observations, which gave differences from the mean
beyond a fixed limit, values derived by interpolation from pre-.
On the Magnetic Declination at the Magnetic Equator. 3887
ceding and succeeding observations. General Sabine in his discussions
has rejected wholly the observations which exceeded the limit chosen
by him. The omission of observations accidentally or intentionally,
and the taking of means without any attempt to supply the omitted
observations by approximate values, require consideration.
Let m be the true hourly mean for an hour /, derived from the
complete series of x observations; let m' be the mean derived from.
n—1 observations, one observation o being accidentally lost ; then
,__2m—o
m= >
n—1
es m! —o , m—o
m=m'— =m — .
n n— 1
If, however, we supply the omitted observation by an interpolation
between the preceding and succeeding observations, and if the inter-.
polated value be 0+, we have
“i nm+ x
. nu
lene
>
m—m
. The comparative errors of m! and m" are therefore
aS aT sa
. n—1 n
We may for any given class of observation determine the mean values
of these errors.
Example :—At Hobarton, in July 1846, the mean barometer
for 3° (Hobarton mean time) was 29°848 in., and the mean differ-
ence of an observation at that hour from the mean for the hour was
0-403 in. ; if an observation had been omitted with such a difference,
or for which o—m=0°403 in., we should have an error in the resulting:
mean of o408 = 0-016 in., and the error might have been twice as»
great had the observation with the greatest difference been rejected. .
If we now seek the error of m!', where the observation is interpolated,
we shall find for the same month that the mean value of x=0-005 in.
‘ 2 0°005 i vi
nearly ; whence the error > =—5--=0:0002 in. only, and the error
would never exceed 0°001 in. A similar though less advantageous.
result will be found in all classes of hourly observations.
In the case where observations are rejected which differ from the
mean for the corresponding hour more than a given quantity, let
us suppose, to simplify the question, that the sums of n—1 out of
m observations for each of two successive hours are each equal M,
and that the observations for the same hours of the nth day are
h : “ite
respectively m'+/ and m'+/+.2, where m= uthe, Zis the limit
beyond which observations are ‘rejected, and # is the excess of the’
observation to be omitted. The means retaining all the observations:
2C2
388 Royal Society :—
are,
M+ m'+1 l
ne a
n n,
M+ m'+l+e« Ite
IE Tae a eT ‘
a iL n
but if we reject the observation m!'+/+., we have
It is assumed that m,!—m,'=0 (any other hypothesis of variation
would give the same final result), and therefore the error of the
change from the first hour to the second, when all the observations
° e x . . e .
are retained, is —; but if the observation be rejected, the change is
nN F
ay ES eal:
m +——m =—
n n
This error, therefore, will be greater than the other if / > ; so that
the error in the resulting change from one hour to the Mext will be
less by retaining an observation than by rejecting it, if the difference
from the preceding observation be not greater than the difference
from the hourly mean; that this will most frequently be the case
will be obvious from the following fact :—At Makerstoun, in 1844,
at 1 a.m. the number of observations which exceeded the monthly
means by 3! and less than double that, or 6', was 99, while the whole
number which exceeded by more than 6! was only 16.
It will be evident also that the difference / of an observation from
the corresponding hourly mean may not be due to irregular causes,
or to causes which affect the changes from one hour to the next in a
perceptible manner, but to gradual and regular daily change. If we
examine the daily means most free from irregular or intermittent
disturbance, we shall find that they vary plus or minus of the monthly
mean; if the difference amounts to / in any case, then the whole
observations of the day may be rejected though they follow the nor-
mal law. By taking a proper value of J this case may not happen fre-
quently, but cases like the followmg will. At Hobarton the daily means
of magnetic declination differ in some months from the monthly means
by 2'0 nearly ; as the limit chosen by General Sabine is 2'4, any
observation in such days differing by 04 from the normal mean
would be rejected. The 25th ‘and 26th days of March 1844 had
been chosen by me as days free from magnetic disturbance, and fol-
lowing the normal law at Makerstoun (Mak. Obs. 1844, p. 339),
yet the means of horizontal force for these days differed 0°00064 and
0:00075 from the monthiy means; had the former quantity been
the linit, all the observations on these days might have been rejected.
Altogether it appears to me that the method of rejecting observa-
tions beyond certain limits .should. not be employed at all, or if
employed, only when interpolated observations are substituted ; and °
On the Magnetic Declination at the Magnetic Equator. 889
that this interpolation should constitute a second part of the discus-
sion, the first including all the observations*.
These considerations may appear somewhat elementary, but it is
essential that results which present such anomalies as the lunar
diurnal variation of magnetic declination should be obtained in a
manner the most free from objection, even though the objections
should touch on quantities of a second order compared with those
obtained.:
The discussion of which I now proceed to note the results,
includes all the hourly observations without exception, made in the
Trevandrum Observatory (within a degree and a half of the magnetic
equator) during the five years 1854 to 1858; the second part of the
discussion, in which days of great magnetic irregularity have been
wholly rejected, not being completed, I ‘shall reserve the details for a
more formal communication to the Royal Society. The results
obtained are as follows :—
Ist. At the magnetic equator the lunar diurnal law of magnetic
declination varies with the moon’s declination and — the sun’s
declination.
2nd. This variation is so considerable that the attempt to combine
all the observations to form the mean law for the year gives results
that are not true for any period. Hence evidently the impossibility
of relating the laws at different places. The so-called mean law for
the year at Trevandrum obtained for the moon furthest north, on the
equator going south, furthest south, and on the equator going north,
consists of ¢hree maxima and three minima,—a result wholly false,
excepting as an arithmetical operation due to combination of very
different laws.
3rd. The lunar diurnal lawvaries chiefly with the position of the sun,
the variation being comparatively small with the position of the moon.
4th. At the magnetic equator the range of the variations is mark-
edly greatest in the months of January, February, November and
December, or about perihelion.
The following results are derived after grouping the means for differ-
ent positions of the moon in periods of six months, October to March,
and April to September ; they are therefore, for the reason given in
the 2nd conclusion, not quite accurate ; but the change of the law from
month to month will be followed when the details are presented to the
Society. The following will give a general idea of the changes :—
Sth. When the moon is fur thest north.
a. About perihelion. The lunar diurnal law of magnetic declina-
tion consists of two maxzimat when the moon is near the upper and
lower meridians, the maximum for the latter being much the great-
* T should note here my belief that a peculiarity noticed by General Sabine in
his discussions as requiring explanation, namely, that the excursions of the decli-
nation needle east and west in the lunar diurnal variation have very different
magnitudes, is due to the rejection of observations, while the means by which the
differences were obtained included the rejected quantities.
+ The declination is easterly at Trevandrum, and the maxima indicate greater
easterly declination.
a
390 Royal Society :—
est; of the two minima at intermediate epochs, that for the setting
moon is the most marked.
6. About aphelion. The law consists of two nearly equal minima
near the upper and lower transits: of the two intermediate maxima,
that near the moonset is the most marked.
e. Thus the law about the winter solstice is inverted about the
summer solstice, and the one law passes into the other at the epochs
of the equinoxes, exactly as for the solar diurnal variation.
6th. For the moon on the equator going south.
a. About perihelion. The lunar diurnal law consists of two
nearly equal maxima near the superior and inferior transits: of the
two intermediate minima, the moonset minimum is by far the most
marked.
6. About aphelion. The law consists of two nearly equal minima
near the superior and inferior transits: of the two intermediate
maxima, that near moonrise is by far the most marked.
e. In this case also the laws for the solstices are the opposite of
each other, and the one law passes into the other near the epochs of
the equinoxes. :
7th. For the moon furthest south.
a. About perihelion. The lunar diurnal law consists-of maxima
near the upper and lower transits, that at the upper transit being by
far the most marked: of the intermediate minima, that near moon-
set is the greater. :
6, About aphelion. The law consists of two minima, the most
marked at the inferior transit, the other about three hours before the
superior transit; and of two equal maxima, one near moonrise, the
other near the superior transit, but varying little till 3 hours before
the inferior passage.
_ ¢. In this instance the inversion is not so complete as in the other
cases ; this, it is believed, will be found to be due to the fact that the
change from one law to the other takes place after the vernal and
before the autumnal equinox ; so that in the means for six months,
from which the above conclusions are drawn, the lunations following
the law a are combined with those belonging to 0.
8th. The moon on the equator going north.
a, About perihelion. The lunar diurnal law consists of two nearly
equal maxima when the moon is near the superior and inferior meri-.
dians ; of the two intermediate minima, that near moonrise is by far
the most marked.
b. About aphelion. The law consists of two minima at the infe-
rior and superior transits ; and of two maxima, the greatest at moon-
set, the other between the meridians of 16" and 21"; between these
points there is an inflexion constituting a slight minimum. .
c. In this case also the opposition of the laws is sufficiently well
marked ; the only divergence from opposition being that due to the
minor miininreed about the meridian of 19", due, it is believed, as
noted 7th c, to the partial combination of opposite laws in the
aphelion half-year.
9th. It will be observed that the variations of the law with refer-
On the Nature of the Light emitted by heated Tourmaline. 891
ence to the moon’s declination for any given period of the year, con-
sists chiefly in the difference of the relative values of the maxima and
minima, the differences of epochs being small. Thus for perihelion,
the moon furthest north, the principal maximum occurs at the infe-
rior passage ; the moon on the equator going south, the two maxima
are nearly equal; the moon furthest south, the maximum at the
superior passage is by far the greatest: on the equator going north,
the two maxima are again nearly equal; and so on for other epochs.
10th. The moon’s action is chiefly, if not wholly, dependent on
the position of the sun, or (which is the same thing) on the position
of the earth relatively to the sun; and the law of the lunar action at
the magnetic equator resembles in some points that for the solar
action at the same epochs. ‘Thus about aphelion there is a minimum.
of easterly (maximum of westerly) declination produced by the Junar
action, as well as by the solar action, for these two bodies near the
superior meridian; whereas about perihelion both actions for the
sun and moon near the superior meridian produce maxima of easterly
declination. A like analogy holds for near the epochs of sun-
rise and moonrise.
June 14.—General Sabine, R.A., Treasurer and Vice-President, in’
the Chair. :
The following communication was read :—
“On the Nature of the Light emitted by heated Tourmaline.” By
Balfour Stewart, Esq., M.A. :
Some months ago I had the honour of submitting to the Royal,
Society a paper on the light radiated by heated bodies, in which it
was endeavoured to explain the facts recorded by an extension of
the theory of exchanges.
Having mentioned the difficulty which I had in maintaining the
various transparent substances at a nearly steady red heat for a
sufficient length of time in experiments demanding a. dark back-
ground, Professor Stokes suggested an apparatus by means of which
this difficulty might be overcome; and it is owing to his kindness in
doing so that I have been enabled to lay these results before the
Society.
The apparatus consists of a thick, spherical, cast-iron bomb, about
5 inches in external and 3 inches in internal diameter—the thickness
of the shell being therefore 1 inch. It has a cover removeable at
pleasure. There is a small stand in the inside, upon which the sub-
stance under examination is placed, and when so placed it is pre-
cisely at the centre of the bomb. Two small round holes, opposite
to one another, viz. at the two extremities of a diameter, are bored in
the substance of the shell. If, therefore, the substance placed upon
the stand be transparent, and have parallel surfaces, by placing these
surfaces so as to front the holes, we are enabled to see through the
substance, and consequently through the bomb. Let the bomb with
the substance on the stand be heated to a good red heat, and then
withdrawn from the fire and allowed to cool. It is evident that the
eooling of the substance on the stand will proceed very slowly, as it
392 Royal Society.
is almost completely surrounded with a red-hot enclosure. It is also
evident that, by placing the bomb in a dark room, we may view the
transparent substance against a dark background. By this method
of experimenting, therefore, the difficulty above alluded to is over-
come.
Before describing the experiment performed on tourmaline, it may
be well to state what result the theory of exchanges would lead us to
expect when this mineral is heated, and we shall perceive at the same
time the importance of the experiment with tourmaline as a test of
the theory. When a suitable piece of tourmaline, with its faces cut
parallel to the axis, is used to transmit ordinary light, the hight which
it transmits is nearly completely polarized, the plane of polarization
depending on the position of the axis. The reason of this is, that if
we resolve the incident light into two portions, one of which consists
of light polarized in a plane perpendicular to the axis of the crystal,
and the other of light polarized in a plane parallel to the same axis,
nearly all the latter is absorbed, while a notable proportion of the
former is allowed to pass.
Suppose now that such a piece of tourmaline is placed in a red-hot
enclosure; the theory of exchanges, when fully carried out, demands
that the light transmitted by the tourmaline, say in a direction per-
pendicular to its surface, plus the light radiated by the tourmaline
in that direction, plus the small quantity of light reflected by the
surface of the tourmaline in that direction, shall together equal in
quantity and quality that which would have proceeded in the same
direction from the wall of the enclosure alone, supposing the tour-
maline to have been removed. Let us neglect the small quantity of
light which is reflected from the surface of the tourmaline, and,
standing in front of it, analyse with our polariscope the light which
proceeds from it. This light consists of two portions, the trans-
mitted and the radiated, both of which together ought to be equal
in quality and intensity to that which would reach our polariscope
from the enclosure alone were the tourmaline taken away. But the
light which would fall on our polariscope from the enclosure alone
would not be polarized; hence the whole body of light which falls
upon it from the tourmaline, and which is similar in quality to the
former, ought not to be polarized. Now part of this light, or that
which is transmitted by the tourmaline, is polarized; hence it fel-
lows, in order that the whole be without polarization, that the light
which is radiated should be partially polarized in a direction at right
angles to that which is transmitted.
Another way of stating this conclusion is this. The light which
the tourmaline radiates is equal to that which it absorbs, and this
equality holds separately for light polarized in a plane parallel to the
axis of the crystal, and for light polarized in a plane perpendicular
to the same. ,
The experiment was made. with a piece of brown tourmaline
having a few opake streaks, procured from Mr. Darker of Lambeth.
It was placed in a graphite frame between two circular holes made
as above described in opposite sides of the bomb, the diameter of the
Intelligence and Miscellaneous Articles. 393
holes being about ;*,ths of an inch. On Icoking in at one of these
holes you could thus sce through the tourmaline and the opposite
hole, or, in other words, see quite through the bomb. An arrange-
ment was also made by which part of the tourmaline might be viewed
with the graphite behind it.
The apparatus thus prepared was heated to a red or yellow heat
in the fire, placed on a-brick in a dark room, and the tourmaline
viewed by a polariscope which Mr. Gassiot kindly lent me. The
following was the appearance of the experiment :—
Without the polariscope the transparent parts of the tourmaline
were slightly less radiant than the field around them. When the
polariscope was used, the light from the transparent portions of the
tourmaline was found to vary in intensity as the instrument was
turned round. No change of intensity could be observed in the
light radiated by the opake streaks of the tourmaline, or by the
graphite.
The light from the transparent portions was therefore partially
polarized. The polariscope was then brought to its darkest position,
and a light from behind allowed to pass through the tourmaline.
The light was distinctly visible in this position, but by turning round
the polariscope about 90° it became eclipsed. The mean of four
sets of experiments made the difference between the position of dark-
ness for the two cases 883°. It appears, therefore, that the light
radiated by the tourmaline was partially polarized in a plane at nght
angles to that which was transmitted by it. It was also ascertained
that the light from the tourmaline which had the graphite behind it
gave no trace of polarization. |
LX. Intelligence and Miscellaneous Articles.
ON THE MOTION OF THE STRINGS OF A VIOLIN.
BY PROFESSOR H,. HELMHOLTZ,
if HAVE been studying for some time the causes of the different
qualities of sound ; and as I found that those differences depended
principally upon the number and intensity of the harmonic sounds
accompanying the fundamental one, I was obliged to investigate the
forms of elastic vibrations performed by different sounding bodies.
Among such vibrations, the form of which is not yet exactly known,
the vibrations of strings excited by the bow of a violin are peculiarly
interesting. ‘Th. Young describes them as very irregular ; but I sup-
pose that his assertion relates only to the motions which remain after
the impulse of the bow has ceased. At least, I myself found the
motion very regular as long as the bow is applied near one end of the
string, in the regular way commonly followed by players of the
violin. I used a method of observing very similar to that of
Lissajoux. Already, without the assistance of any instruments, one
can see easily that a stiing moved by the bow vibrates in one plane
only—the same plane in which the string itself and the hairs of
394 Intelligence and Miscellaneous Articles.
the bow are situated. This plane was horizontal in my experi-
ments. The string was powdered with starch, and strongly illumi-
nated. . One of the little grains of starch, looking like a bright point,
was observed by a vertical microscope, the object lens of which was
fixed to one of the branches of a tuning-fork. ‘The fork, making 120
vibrations in the second, was placed between the branches of a horse-
shoe electro-magnet, which was magnetized by an interrupted electric
current, the number of interruptions being itself_120 in the second.
In that way the fork was kept vibrating for as long a time as I de-
sired. The lens of the microscope vibrated in a direction parallel to
the string, and therefore perpendicular to its vibrations. ‘The string
I used was the second string of a violin, answering to the note A,
tuned a little higher than common, to 480 vibrations, and therefore
it performed four vibrations for every one of the tuning-fork. Look-
ing through the microscope, I observed the grain of starch describing
an illuminated curved line, the horizontal abscissze of which corre-
sponded to thedeviations of the tuning-fork, and the vertical ordinates
to the deviations of the string. I found it a matter of importance to
use a violin of most perfect construction, and I was fortunate in get-
ting a very fine instrument of Guadanini for these experiments. On
the common instruments of inferior quality I could not keep the curve
constante nough for numbering the little indentures which I shall
describe afterwards, although the general character of the curve was
the same on all the instruments I tried: the curve used to move by.
jerks along the line of abscissze ; and every jerk was accompanied by-
a scratching noise of the bow. On the contrary, with the Italian
instrument, and after some practice, I got a curve completely qui-
escent as long as the bow moved in one direction, the sound bere
very pure and free from scratching.
We may consider the motion of the string as being compen
of two different sets of vibrations, the first of which is the principal
motion as to magnitude. Its period is equal to the period of the
fundamental sound of the string, and it is independent of the situation
of the point where the bow is applied. The second motion produces
only very smali indentures of the curve. Its period of vibration
answers to one of the higher harmonics of the string. It is known
that a string, when producing only one of its higher harmonics, is
divided into several vibrating divisions of equal length, being sepa-
rated by. quiescent points, which are called nodes. In all the nodes
of the second motion of the string in the compound result at pre-
sent considered, the principal motion appears alone; and also in the
other points of the string the indentures corresponding to the second
motion are easily obliterated, if the line of light is too broad.
The principal motion of the string is such that every point of it
goes to one side with a constant velocity, and returns to the other
side with another constant velocity.
PlateV. fig. 7 represents four such vibrations, corresponding to one _
vibration of the fork. The horizontal abscisse are proportional to the
time, the vertical ordinates to the deviation of the vibrating point.
Every vibration is formed on the curve by two straight lines. The
Intelligence and Miscellaneous Articles. 395
curve is not seen quite in the same way through the microscope,
because there the horizontal abscisse are not proportional tu the time
but to the sine of the time, It must be imagined that the curve
(fig. 7) is wound up round a cylinder, so that the two ends of
it meet together, and that the whole is seen in perspective froma
great distance ; thus it had the real appearance of the curve, as repre-
sented in two different positions in fig. 8. If the number of vibra-
tions of the string is accurately equal t to four times the number of the
_tuning-fork, the curve appears quietly keeping the same position. If
there is, on the contrary, a little difference of tuning, it looks as if the
cylinder rotated slowly about its axis, and by the motion of the curve *
the observer gets as lively an impression of a cylindrical surface, on
which it seems to be drawn, as if looking at a stereoscopic picture.
The same impression may be produced by combining, stereoscopically,
the two diagrams of fig. 8.
_ We learn, therefore, by these experiments, —
1. That the strings of a violin, when sleick by the bow, heats
in one plane.
_ 2. That every point of the string moves to and fro with two con-
stant velocities.
_ These two data are sufficient for finding the complete equation of
the motion of the whole string. It is the following ; —
y= Ad 1a ; = )sin(= = ‘) } ah ocainy ste as
y is the deviation of the point whose distance from one end of the
string is 7; /, the length of the string; ¢, the time; T’, the duration
of one vibration ; A, an arbitrary constant; andz, any whole number;
and all values of the expression under the sign %, got in that way;
are to be summed. r
A comprehensive idea of the motion represented by this equation
may be given in the following way :—Let a 4, fig. 9, be the equili-
brium position of the string. During the vibration its forms will be
similar to a ¢ b, compounded of two straight lines, ac and c 6, inter-
secting in the point c. Let this point of intersection move with a
constant velocity along two flat circular arcs, lying symmetrically on
the two sides of the string, and passing through its ends, as repre~
sented in fig. 9. A motion the same as the actual motion of the
whole string is thus given.
- As for the motion of every single point, it may be deduced froth
equation (1), that the two parts ad and bc (fig. 7) of the time of
every vibration are proportional to the two parts of the string which
are separated by the observed point. The two velocities of course
are inversely proportional to the times a6 and 6c. In that half of
the string which is touched by the bow, the smaller velocity has the
same direction as the bow; in the other half of the string it has the
contrary direction. By comparing the velocity of the bow with the
velocity of the point touched by it, I found that this point of the
string adheres fast to the bow and partakes in its motion during the
396 Intelligence and Miscellaneous Articles.
time ab, then is torn off and jumps back to its first position during
the time &c, till the bow again gets hold of it.
With these principal vibrations smaller vibrations are compounded,
the nature of which I can define accurately only in the case where
the bow touches a point whose distance from the nearer end of the
string is > - 7 &c. of its whole length, or generally — if mis a
whole number. Because the point where the bow is applied is not
moved by any vibration belonging to the mth, 2mth, &c. harmonic,
_ it is quite indifferent for the motion of that point, and for the impulses
exerted by the bow upon the string, whether vibrations corresponding
to the mth harmonic exist or not. Th. Young has proved that if
we excite the vibrations of a string by bending it with the finger, as
in the harp, or hit it with a single stroke, as in the piano, in the
ensuing motion all those harmonics are wanting which have a node
in the touched point. I therefore concluded also that the bow
cannot excite those harmonics which have a node at the point where
it is applied; and I found, indeed, that if this point is distant 4 from
m
the end, the ear does not hear the mth harmonic sound, although it
distinguishes very well all the other harmonics. Therefore, in the
equation (1), all those members of the sum will be wanting in which
n is equal to m, or 2m, or 3m, &c.. ‘These members, taken together,
constitute a vibration of the string with m vibrating divisions. Every
such division performs the same form of vibration we have described
as the principal vibration of the whole string. ‘These small vibra-
tions must be subtracted from the principal vibration of the whole
string for getting its actual vibration. Curves constructed according
to this thecretical view represent very well the really observed curves.
If m=6 and the observed point is distant, | from the other end of the
string, the motion is represented in fig. 10. Near the end of the
string, where the bow is commonly applied by players, the nodes of
different harmonics are very near to each other, so that the bow is
nearly always at, or at least very near to, the place of a node.
Striking in the middle between two nodes, I could not get a curve
sufficiently constant for my observations. If I strike very near the
end, the sound changes often between the fundamental and the
second or third harmonic, which is indicated by gradual corresponding
alterations of the curve.—From the Proceedings of the Glasgow Philo-
sophical Society for Dec. 19, 1860.
ON CLAIRAUT’S THEOREM. BY PROF, HENNESSY, F.R.S.
Laplace has shown that this theorem follows, whatever may be the
density of the interior parts of the earth, provided it consists of similar
concentric strata, and that the form of the outer stratum is ellipsoidal.
In the ‘ Philosophical Transactions’ for 1826, Mr. Airy (the present
Intelligence and Miscellaneous Articles. 397
Astronomer Royal of England) has presented an equivalent result ;
more recently, Professor Stokes has shown that we can deduce the
law of variation of terrestrial gravity without any hypothesis what-
soever as to the earth’s interior structure. He assumes merely that
its surface is spheroidal, and that the equation of fluid equilibrium
holds good at that surface. In vol. vi. of the ‘ Cambridge Mathe-
matical Journal,’ Professor Haughton presented a demonstration,
founded upon the same assumptions as those of Professor Stokes,
and in which he uses certain propositions relative to attractions
which had been enunciated by Gauss and Maccullagh. While
studying the labours of those mathematicians, it appeared to me
that the question could be entirely divested of the hydrostatical
character, and that Clairaut’s theorem may be directly deduced from
the equations to the normal of any closed surface, without any con-
siderations as to the physical condition of the matter forming that
surface. ‘Thus every surface concentric with the earth, and per-
pendicular to gravity, will possess the property of exhibiting this
relation in the intensity of gravity at its various points.
Let X, Y, Z represent the components parallel to the rectangular
axes of the forces by which a point is retained at rest on a given
surface whose equation is L=Q. ‘Then from the equations of the
normal we have :
y te xo =0, 7 il yah
dx dy da dz
when the resultant of these forces is perpendicular to the given sur-
face. If we represent by V the potential of the earth on the-par-
ticle in question, by w the angular sa of rotation, we have
dV dV
X= — wy “he ’ scape Ale
and the above equations become
Ee a Ce
dy dx dx dy dy “dx}’
dV dl_dVdb_, al
dzdx dx dz "ie
If, in conformity with General Schubert’s* recent determinations,
we assume the earth’s surface to be that of an ellipsoid, with three
unequal axes, we should substitute for L
Pe y 2 ies
et ae
or
dL _ 20 di_y dl pind’
de @' dy @ dz @
* Memoires de ’ Académie Impégriale des Sciences de St. Hee, sér. 7,
tom. i.
398. Intelligence and Miscellaneous Articles.
whence we have’
ba 7 _ ay SN =w'ay (a . b°), tae —a°z = ware.
Each of these partial differential equations can be easily integrated ;
and the value of V, finally obtained, is equivalent to the equation
of fluid equilibrium, or
VtS@+y)=c.
Let 6 represent the complement of the latitude, and ¢ the longitude,
, counted from the meridian of the greatest axis, then
z=r cos 0, =r sin 6 cos ¢, y=r sin 6 sin g,
and
- rw" .
V+ = sin? @6=C.
In the case of an ellipsoid having the ellipticity e, we have, neglect-
ing small terms,
r=a (1—e cos’).
From these equations, and from the properties of Laplace’s functions
into which V can be expanded, an expression can be obtained of the
same kind as that deduced by Professor Stokes from his own and
Gauss’s theorems relative to attractions.—Proceedings of the Royal.
Irish Academy, Feb, 25, 1861.
ON A METHOD OF TAKING VAPOUR-DENSITIES AT LOW TEMPERA-
TURES. BY DR. LYON PLAYFAIR,:C.B., F.R.S.. AND J. A. WANK- =
LYN, F.R.S.E.
The authors refer to Regnault’s experiments, which have shown
that aqueous vapour in the atmosphere has the same vapour-density
at ordinary temperatures as aqueous vapour above 100° C.; and
they bring forward fresh experiments upon alcohol and ether to show
that when mixed with hydrogen these vapours preserve their normal
density at 20° or 30°C. below the boiling-points of the liquids, and
infer generally that vapours, when partially saturating a permanent
gas, retain their normal densities at low temperatures.
From their researches the authors deduce the consequence—re-
markable, but quite in harmony with theory—that permanent gases
have the property of rendering vapour truly gasecus. Stated in
more precise terms, the proposition maintained by the authors is,
«The presence of a permanent gas affects a vapour, so that its ex-
pansion-coefiicient at temperatures near its point of liquefaction
tends to approximate to its expansion-coefficient at the highest tem-
peratures.”
Intelligence and Miscellaneous Articles. 399
--The authors anticipate that admixture with a permanent gas may
serve as akind of reagent to distinguish between cases of unusually
high expansion-coefficient in a vapour, and cases where chemical
alteration takes place. It will also be possible, by the employment
of a permanent gas, to obtain vapour-densities of compounds which
will not bear boiling without undergoing decomposition.
In experimenting upon substances which may be heated above the
boiling-point, the authors employ Gay-Lussac’s process for taking
the specific gravity of vapours. A slight modification, however, is
necessary. Previous to the introduction of the bulb containing the
weighed substance, dry hydrogen is introduced into the graduated
tube and measured with all the precautions belonging to a gas ana-
lysis. It will be obvious that in the subsequent calculation the
volume of hydrogen corrected at standard temperature and pressure
must be subtracted from the volume of mixed gas and vapour, also
corrected at standard temperature and pressure.
_ When the substance will not bear heating to its boiling-point, the
authors employ a process resembling that of Dumas in principle, but
differing very widely from it in detail. Dumas’s flask with drawn-
out neck is replaced by two bulbs, together of about 300 cub. cent.
capacity, joined by a neck, and terminating on either side in a nar-
row tube. Oneof the narrow tubes has some very small dilatations
blown upon it (0), the other is merely bent (D). (See Plate V. fig. 6.)
The apparatus, whose weight should not exceed 70 grms., is weighed
in dry air, then placed in a bath, being secured by a retort-holder
grasping the neck joining the large bulbs Cand C. The end A,
projecting over the one side of the bath, is made to communicate
with a hydrogen apparatus; the end D passes through a hole -in
the opposite side of the bath, which is plugged up water-tight by
means of putty. Dry hydrogen is transmitted through the whole
arrangement, and escapes at D through a long narrow tube joined
to it by a caoutchouc connecter.
The bath is next filled with warm water until the bends a and a
are covered. The connexion with the hydrogen apparatus is then for
a moment interrupted, to allow of the introduction of a small quantity
of the substance at A. The substance, which should not more than
half-fill the small bulb 4, is partially vaporized in the stream of hydro-
gen, and in that state passes into the part CC. All the while the
temperature of the bath is kept uniform throughout by constant
stirring, and .made to rise very slowly. When within a few degrees
of the temperature at which ‘the determination is to be made, the
current of hydrogen is almost. stopped, so that the bulbs C and C
may contain less vapour than will fully saturate the gas at the tem-
perature of sealing. The water of the bath is then made to subside,
by opening a large tap placed near the bottom. The bends a and a
are thus exposed, the bulbs CC remaining covered. Immediately
the current of hydrogen has been stopped, the flame is applied at.
aa, so as to seal the apparatus hermetically. The temperature of the
bath, as well as the height of the barometer, must now be observed.
400 Intelligence and Miscellaneous Articles,
After being cleaned, the apparatus (which now consists of three
portions, viz, the portion CC hermetically sealed and the two ends
6 and D) must be weighed,
‘The capacity of the apparatus is found by filling it completely with
water and weighing; but previously to this operation the volume of
hydrogen enclosed at the time of sealing must be found. On break-
ing one extremity under water, the water will rise in the bulbs, and,
after a while, will have absorbed all the vapour, but will leave
the hydrogen, ‘The bulbs must then be lifted out of the water,
without altering their temperature, and, with the water that has
entered, weighed. ‘The difference between the latter weighing and
the weight of the bulbs quite full of water gives the weight in
grammes, which expresses in cubic centimeters the volume of hy-
drogen enclosed; the pressure is the height of the barometer minus
the column of water which had entered the bulbs; the temperature
is that of the water,
An example of a determination of the vapour-density of alcohol
at 30° C. below its boiling point is subjoined ;—
Height of the barometer (at O° C.) ...... 763°09 millims,
Temperature of the balance case ......., 75 C,
Weight of apparatus in dry air,......... 69°959 grms,
‘Temperature at time of sealing. ......... 48°C,
Weight of apparatus + hydrogen+vapour,, 69°5275 grms,
Weight of apparatus+ water (at 3°2C.)., 191°76 grms,
Weight of apparatus filled with water.... 545°36 grms.
Height of water column .. ..00. 6 ce eens 122 millims,
From which is deduced—~
Volumes corrected
at 0 C. and 760 millims. pressure,
eubie centimeters. Grn,
Hydrogen+ vapour ...... 40643 weighing 0°1695
Hydrogen, , .. weap oe Ue 341°27 ”» O0306
65°16 Or 1389
Therefore, 65°16 cub. cent. of alcohol-vapour weigh +1389
but 65°16 cub. cent. of air weigh... ...... ‘0843
"1389
Vapour-density of alcohol = = 1648,
‘OS43
The authors have extended their experiments to acetic acid and
other substances. At low temperatures the vapour-density of acetic
acid approximates to 400, no matter how much hydrogen be em-
ployed. At higher temperatures an approximation to 2°00 is ob-
tained, but without heating so high as Cahours found necessary,
The authorsare continuing these researches. — From the Proceedings
of the Royal Society of Adindurg’, January 21,1386).
THE
LONDON, EDINBURGH ann DUBLIN
PHILOSOPHICAL MAGAZINE
AND
JOURNAL OF SCIENCE.
[FOURTH SERIES, ]
JUNE 1861,
eee
LXI. On a Law of Liquid Kxpansion that connects the Volume of
a@ Liquid with its Temperature and with the Density of its satu-
rated Vapour. By Joun Jamns Warenstron*, sq.
| With a Plate. |
$1. 1 tee the archives of the Royal Society for 1852, there is
an account of observations on the density of hquids
and their superjacent vapours at high temperatures, made in sealed
graduated tubes filled with the same liquid in different propor-
tions of their volumes. The general law of density in saturated
vapours deduced from these observations, and from the various
observations of vapour-tension already published by other phy-
sicists, is therein set forth, with the assistance of a chart (No. 2
chart) in which the observations are all projected, and lines
drawn, that enables the eye to judge of the accordance between
theory and observation. (See Note A.)
An account of this general law is also given in the Philoso-
eel Magazine for Mareh 1858, in a paper entitled “On the
§vidence of a Graduated Difference between the ‘Thermometers
of Air and Mereury between 0° and 100° C.”
By the same mode of observing in sealed graduated tubes, |
afterwards extended the observations up to the transition-point
of three of the liquids, viz. aleohol, ether, and sulphate of carbon,
and found that the law of vapour-density was maintained in them
Without deviation to their extreme limiting temperatures, As
these extensive series of observations supplied the curves of ex-
pansion of the three liquids, I have occasionally tried by means
of them to discover a general law of liquid expansion, T submit
the following account of the last attempt of this kind, as it ap-
pears to be successful.
* Communicated by the Author.
Phil, Mag. 8. 4, Vol. 21, No, 142, June 1861, 2D
402 Mr. J.J. Waterston on a Law of Liquid Expansion
§ 2. The curves of expansion, drawn to a large and distinct
scale, were examined by the following graphical process :—At
four or five points nearly equidistant, tangents were drawn
(carefully judging of the direction to be given to the straight
edge by the sweep of the curve to the right and left of the point
of contact). Thus were obtained several values of the quotient
of the differential of volume by the volume or proportionate dif-
d
ferentials for constant element of temperature EA . These
were set off as ordinates to the temperatures, and the curve
drawn through the points appeared to be the common equilateral
hyperbola, havin g one asymptote coinciding with the axis of tem-
perature and the other perpendicular to it, and intersecting it at
a temperature [y] that evidently was above the transition- -point.
If this were the case, the product of the coordinates to each point
of the curve, reckoning from the point y as origin, ought to be
constant [=p]; and accordingly it was found that when the
inverse of the quotients were projected as ordinates to the tem-
peratures, the points ranged in a straight line, which being pro-
duced, cut the axis in the pomt y. The differential equation is
thus
dv y—t
He Uo ag
the integration of which is
+ k
v=4 ——
y—
in which k=(y—z) when v=1. (See Note B.)
§ 3. There is a relation between this expression and that for
saturated vapour-density which ‘seems to prove that it is not em-
pirical, but the true exponent of the physical condition of the
molecules of a body in the liquid state. The following is a state-
ment of it.
In the papers above referred to, there will be found an account —
of the law of saturated vapour-density, and the proofs on which
it rests. It is expressed by the equation
so soma
If we put A= 2 the law of liquid density is
Bata" L
(ayaa
On comparing the constants for different liquids, I find as a
general rule that the quotient is a constant quantity [KE].
that connects the Volume of a Liquid with its Temperature. 403
Thus for Alcohol my observations give E=1717
» Sther pS 5 K=1739
» Sulphate of carbon _,, H=1725
M. Muncke’s observations on sulphuric acid from 50° to 230° C,
E=1600 to 1800. (See Note C.) MM. Dulong and Petit’s
observations on the expansion of mercury between 0° and 300° C.
give p= ie The line passing through M. Avogadro’s ob-
servations on the vapour of mercury from 230° to 300° C. gives
h=1160. These combined give H=1727. I have adopted
1717 as the nearest probable value at present, because the most
labour was bestowed on the alcohol series of observations.
These values of E are derived from English measures of pres-
sure and temperature, viz. inches of mercury and degrees of
Fahrenheit scale. The value of this constant derived from French
measures is F=504°44, which corresponds with H=1717. The
ah ats Df 3x 29°922 1% bas
ratio of reduction is a= a4 eee , so that Ka=F,
a F=2-70282
rine =0°53195
ue a
§ 4. M. Regnault’s observations on the tension of the vapour
of mercury from low temperatures up to 200° C., respond to the
same value of / as those at the higher temperatures by M. Avo-
gadro, but with g augmented 12 degrees, showing a boiling-point
12 degrees higher. It is remarkable that M. Regnault’s obser-
vations on the expansion of liquid mercury differs so far from
those of MM. Dulong and Petit as to be represented with p=4
and HE=870. At 300° C. this difference amounts to about the
equivalent of 84° C. The acceleration of the rate of expansion
is in M. Regnault’s observations only one-half what is shown by
those of MM. Dulong and Petit. (See Note D.) This 1s a re-
_markable discrepancy, both being so eminent in this class of ob-
servations. r
§ 5. In all cases I have worked with temperatures reduced to
the air-thermometer by scales of correction computed from the
formula given in Appendix III. to the paper in the Philosophical
Magazine for March 1858 above referred to.
The formula is founded on MM. Dulong and Petit’s observa-
tions. I annex exact tracings of these scales (Plate VI.). In
two cases (petroleum and sulphuric acid) the temperatures were
taken uncorrected and compared with the results when corrected.
In both, the differences between theory and observation were
less when the temperatures were corrected.
2D2
404 Mr. J.J. Waterston on a Law of Liquid Expansion
It is not absolutely necessary to correct the temperatures in
order to recognize these laws of density, and for practical pur-
poses may not be required; but it seems best to accustom our-
selves to do so, in order to be prepared for the recognition of
any other relations of harmony that may exist in the thermo-
molecular physics of different bodies.
§ 6. Water is, as might be expected, an exception to the law
of liquid density, as itis to the law of capillarity and compressi-
bility (see papers by M. Grassi and M. Simon in the Annales
de Chimie). Ihave traced its curve of expansion by observations
in sealed tubes up to 210° C. air-thermometer (see Note E), and
projected the densities to the value of p required by its vapour-
gradient ; also those of M. Despretz from 0° to 100° C.; but
they do not conform to the line required at any point of its
range even at the highest temperature. These abnormal features
in this first of liquids have had a prejudicial effect on the pro-
gress of science in this department. There is no other liqmidas
yet found with such point of maximum density that remains a
liquid under its maximum ; yet such a point seems invariably to
be sought for. M. Muncke and M. Pierre have bestowed much
unavailing labour on this question. (See Note F.)
§ 7. To determine the constants of these two equations for
the density of the liquid and of its vapour, not more than four
exact observations are strictly required; two of the vapour, and
two of the liquid.
If the series of observations on the dilatation of a liquid extend
over a considerable range of temperature, and have had their
inequalities equalized by graphical processes equivalent to weigh-
ing by the method of least squares, the three constants of the
equation may be directly determined.
Thus let fo, 4, ¢ be the three temperatures, and v9, 0), vg the
corresponding volumes observed, to find p and & we have
=;
———}__9___ = ___#__0___
y-@y @y-Qy
which may be solved by trial and error. But few observations
as yet published will stand this test, the range of temperature
being too small, and the irregularities proportionably too great.
§ 8. A simple and satisfactory way to test both of these laws
of density by published observ ations, is to take two of the vapour-
tensions not far from the boiling-point and compute the value
of A. Ex. gr., let eo, e, be the two observations of the pressure
of vapour in contact with its generating liquid; To, T, the cor-
responding temperatures by air-thermometer reckoned from the
that connects the Volume of a Liquid with its Temperature. 405
zero of gaseous tension [ —461° F.,or —273°-89C.]; then we have
T,—Ty
| Fe — SENT
2@)-G
and since p= : , we obtain the index of the power of the density
of the liquid, which being set off as ordinates to the temperature,
ought to range in a straight line; and this line produced, cuts
the axis of temperature at y. If, when these points are con-
nected by distinct lines, a general convexity in the range can
be discovered, viewing it foreshortened with the eye close to the
plane of projection, then we may infer that p requires to de di-
minished if the convexity 1 is directed upwards from the axis of
temperature, and vice versd.
§ 9. Having found p and k and y, the next step is to compute
the values of ¢ from the volumes by the equation, and tabulate
the differences between the computed and observed temperatures.
This will be found attended with but little additional labour. If
we now project these differences as ordinates on an exaggerated
scale to the temperatures, we obtain a distinct impression of how
far theory and observation accord.
§ 10. Mercury and alcohol being the most important liquids
for thermometric purposes, may serve as examples of the mode
of computation.
I. Mercury.
M. Avogadro’s observations on the tension of the vapour of
mercury :—At 260° C. the observed tension was 13362 millims.,
at 290° it was 252°51 millims. The correction to reduce the
temperatures to the air-thermometer from the scale is 5°:60 at
260°, and 6°91 at 290°. Hence—
260— 5°60 + 273'89=528:29=T,, 133-62 millims. =e,
290—6'91 +273'89=556'98=T,, 252°51 millims. =e, ;
and we arrive by computation at log h=2°54796 and g=247°-45,
[I have computed the temperatures for M. Avogadro’s other
six observations. The computed, minus the observed, is, at
300= + 0°15
290= -0
280= + 0°42
270= —0°26
260= 0O
250= —0°26
240= — 1:90
230 = —4'56
= difference in tension amounting to one-third inch mercury. ]
406 Mr. J. J. Waterston on a Law of Liquid Expansion
This value of A being derived from French measures, is to be
applied to F to find us which thus comes out 1:4284.
The following are MM. Dulong and Petit’s volumes of mer-
cury computed with this index :—
Temp. Inverse of volumes
Cent. Volumes. raisedtothe power _ First Second
Air. 1 1.4984. differences. _ differences.
0 1:000000 —'1-000000 aie
100 1:0180180 "974815 025213 ‘000028
200 1:0368664 "94.9602 025236 "000023
300 = 1:0566037 "924366
The second differences indicate a slight convexity in the line
upwards. This shows that : requires augmentation. The fol-
lowing is the result of computing the same observations with
t = 1-489 :— |
' First diff. Second diff.
CE MMEH LS 0 opie a
100 973760 | 000001
200 947521 aoeen 000005
300 —--921287
To find y, we have 1—0:947521 : 200°: : 1: 3811°05=y,
8811:05—¢ 1 a, 1 fees in
and | ae 3811-05 =A=-,or(3811 05 —#)v'4°9 = 3811-05.
This expresses MM. Dulong and Petit’s observations with a
difference at 100° amounting to +,4,5th of a degree, and at 300°
the difference is =,th of a degree.
$11. To bring the D of the vapour formula to the same
standard as the A of the liquid formula, it is requisite to change
the value of / in the one and & in the other, so that the weight
in grains of a cubic inch of either may be indicated. |
Let n='0216216 = weight in grains of a cubic inch of hy-
drogen at the ‘temperature 0° C. and pressure 760
millims.
5= vapour-density of the body on the hydrogen scale.
T= temperature (reckoned from the zero of gaseous ten-
sion) at which the pressure of the saturated vapour
is 760 millims.
f= required factor
TGA BBO i, 2
ion hae
that connects the Volume of a Liquid with its Temperature, 407
By the formula,
r= 24745,
g=611°28,
also 5=101; hence ph= "=", and log wh=2'56247. Thus
we obtain
T—247-45 1 5 _
[256247] f
the general expression for the weight in grains of a cubic inch
of the saturated vapour of mercury at T° (C. A. G.), temperature
reckoned by Centigrade Air-thermometer from the zero of
Gaseous tension.
§ 12, The weight of a cubic inch of mercury at 0° is 87544
grains, hence
|
37544 _ § 3811-05 — (T—273:89) | 480 ;
v tL Mx8811:05 —?
1°489
and M= (aera) ; hence
Ree cit ate
[8:25857 | a el
the weight of a cubic inch of mercury in grains at T°
(C. A. G. temperature).
We may thus find the temperature at which a=W, or that at
which liquid and vapour would be of equal density if the laws
were maintained.
With alcohol, ether, and sulphate of carbon, transition occurs
a few degrees below the theoretical temperature of equal density.
II. Alcohol.
— § 18. M. Regnault’s observed tensions of saturated vapour :—
At 40° C. the tension is 134°1 millims.; at 70°, 589°2 millims.
40 +. 0°48 + 27389 =314'37 C.A.G.=T, | logh= 2°15392
70+ 0:41 + 27389 = 34430 =T,f g=190-70
ao = 3:5892
This gives 78°83 C. A. as boiling-point at pressure 760 millims.
M. Pierre’s observations on the expansion of aleohol were made
on a specimen that boiled at 78°°63 C. A. under pressure 758
millims., and its specific gravity at O° was 0°8151.
The following are his second series of observations computed
with the above index, 3°5392 :—
408 Mr.J. J. Waterston on a Law of Liquid Expansion
Computed
temp. minus
(=) 35392 observed
V temp.
(1) 33-46 + 0:47 = 33-93 108714 87890 = +0°21°
(2) 47:524+0°51=48-:03 1:05356 —-83140 0
(3) 50°33+0°5]=50°84 1:05676 82248 —0:19
(4) 56:26+0:50=56:76 1064.16 980245 —O0°25
(5) 60:41 +0°48=60°89 1:06989 "78736 +0°03
(6) 73°70+0°38=74:'08 1:08780 74238 0
(7) 76°73+0°35=77:08 1:09168 ‘73310 = —0°27
The computed densities (87890, &c.) set off as ordinates to
the temperatures, show atrend without any appearance of curva-
ture. The straight line seems to pass exactly through the points
of the second and fifth and sixth. Assuming it to pass through
the second and sixth, we have
83140 —°74238 = -08902 : 74°08 — 48°'03 = 26°05 : : *74238 : 217°24,
and 74°08 + 217:24=291°32=y. This line gives unity volume
at —1°-30, hence k=292°62=y—t when volume equal unity,
and the equation is (291°°32 — t)v99 = 29262. The differences
between the observed temperatures and those computed from the
observed volumes by this equation are given in the last column.
§ 14, This equation answers well to the observations of M.
Pierre above 10°; also to those of M. Muncke (St. Peters-
burgh Memoirs) above the same temperature; but in both the
trend of the points below this lies in a line inclined to that of
the equation. The divergence is the greatest in M. Pierre’s. In
neither is it a general convexity, but distinctly the contour shows
two lines diverging from about 15° to 20° C. This is most
distinct in M. Muncke’s observations. I have computed them
by the above equation, and tabulated the differences between the
observed and computed temperatures, which are set off in Pl. VI.
fig.3asordinatesto the temperatures on ten times the natural scale.
Above these, in fig. 2, M. Pierre’s differences are set off to the
same scale, and in fig. 4 the differences in my series of observa-
tions on alcohol, described in the paper above referred to as being
in the archives of the Royal Society. This alcohol was not
absolute ; it had 19 per cent. water, and the index of its power
derived from its line of vapour-density was 3°60; also y=290°89,
k=209°81, and its equation (the volume being reckoned as unity
at the boiling point) }
(2909-89 —#) v3=209°81 C. A. G.
§ 15. The deflection in M. Pierre and M. Muncke’s observa-
. sions, it will be remarked, occurs in those below atmospheric tem-
C. C. A. Ne
that connects the Volume of a Liquid with its Temperature. 409
peratures, where the reduction of temperature had to be artifici-
ally produced by mixtures of broken ice and muriate of lime, and
it represents the temperature of the mercury to be higher than
that of the alcohol. This is precisely what took place in some
observations I made on the contraction of ether about 20° below
the atmospheric temperature. A similar deflection, but in a
greater degree, appears in the ether observations of the same
authors. They are projected in figs. 5 and 6 to the same scale
as the others. (See Note G.)
The application of cold to maintain a constant temperature is
by no means under the same command as the application of
heat ; and, besides, conductibility is very much reduced at low
temperatures. There is an evident dislocation, the law of con-
tinuity is broken, but it is at the part of the scale where the mode
of obervation underwent a change. I submit, therefore, that
the verdict should be against the observations at the lower tem-
peratures, not against the law of expansion, which, if in fault,
would cause the trend of the points to have a general curvature
throughout the range.
In judging of the evidence afforded by these graphical projec-
tions, it should be kept in view that the vertical scale magnifies
the amount of the differences tenfold. The accordance of theor
with observation is in some casesremarkable. Thus, for 40° C.,
Muncke’s alcohol and Pierre’s ether do not show a difference
greater than one-sixth of a degree. We have also to keep in
mind that the power . that reduces the densities to a straight
trend, is not arbitrarily assumed to suit a particular series of ob-
servations, but that it is determined @ priori from the vapour,
If we take any other value of that that which is thus deter-
mined, the graphical projection of the computed densities shows
a general bend. If — is too great, the bow is turned downwards ;
if too small, the bow is turned upwards. The string of the bow
only makes its appearance when the value of 4 is that deduced
from the gradient of vapour-density above described.
§ 16. The time has not perhaps yet arrived for deducing these
laws of density from the dynamical theory of heat; but if we are
ever to arrive at a conception of the true ultimate nature of mo-
lecular force, it seems clear that the inductive path of least difficult
approach (if not the only one) is that which sets out from the study
of the gaseous state, and proceeds by way of that of the equili-
brated condition of saturated vapours in communication with their
410 Mr. J.J. Waterston on a Law of Liquid Expansion
generating liquids, to the molecular condition of the liquids, where
the dynamic condition of the chemical element is constrained by
the cohesive force; and the struggle in which this dynamic force
is gradually subdued by the increase of temperature is, as now
ascertained, represented by one quantitative relation throughout,
that seems to indicate a certain simplicity in the ultimate recon-
dite principle on which molecular force is based.
We know that the physics of gases conform to the physics of
media that consist of perfectly free elastic projectiles*. Their
free concourse and perfectly elastic recoil determines the resolu-
tion of their vis viva into the six rectangular directions of space ;
and it is this number that probably fixes the ratio of the propor-
tionate increment of density in a saturated vapour to the corre-
sponding proportionate increment of temperature reckoned from
the fixed limit g. But the absolute increment of density corre-
sponding to constant increment of temperature differs in different
vapours, being ruled by a gradient, the sixth root of which has a
constant ratio to the index of density of the generating liquid
expressed as a function of the temperature.
The next step that seems within reach, if we had a few more
observations to work from, is the discovery of the relation which
no doubt exists between the increase of volume and decrease of
latent heat or capillarity regarded as the integral of cohesion.
The density and the capillarity both diminish as the temperature
rises. (See Note H.) If there is a simple law of quantitative rela-
tion between them, its discovery would supply all that is now
wanting to bring the dynamical theory of heat to bear upon the
molecular physics of liquids.
Notes.
Note A. § 1.—The title of the paper is ‘‘On a General Law of
Density in Saturated Vapours,”’ illustrated by Chart No. 2. Inthe
Philosophical Transactions for 1852 there is a paper with the same
title, illustrated by a Chart No.1. (This paper was originally sent to
the British Association.) In Chart No. 1 the sixth root of density
is laid off as ordinate to the square root of the temperature reckoned
from the zero of gaseous tension. In Chart No. 2 the sixth root of
density is laid off as ordinate to the temperatures simply. In Chart
No. ] the lines appear straight at the upper part of their course, but
with an increasing flexure at the lower part of the range convex to
axis of temperature. Also there is no relation of harmony apparent
betweenthem. In No. 2 Chart (of which a tracing is to be found in
the archives of the Royal Society for 1852-53) the lines are straight
* See paper “On the Physics of Media that consist of perfectly elastic
ery in a state of Motion,” in the archives of the Royal Society,
that connects the Volume of a Liquid with its Temperature. 411
throughout, and relations of paralellism appear ; also several radiate
from the same point in the axis of temperature, showing that, as a
general law, vapours in contact with their generating liquids have, at
the same temperature, or at the same constant difference of temperature,
densities that have a constant ratio.
Note B. § 2.—This mode of graphical analysis seems a natural
mode of operating when a law of nature has to be unmasked. If the
proportionate differentials of volume had been laid off as ordinates,
not to the temperature, but to the volume, the result would be the
logarithmic curve, which might not be so easy to recognize with only
a few points to lead from. We must be guided in the selection of
the coordinate axis by the causal relation of dependent phenomena.
Heat being, as it were, the instrument of action in molecular physics,
claims the preference as a standard by which to measure the propor-
tionate differentials, and to which other variables may be referred to
as coordinate axis. As an example, the’following is the analysis of
the law of saturated vapours by this process.
The vapour-tensions being divided respectively by the correspond-
ing temperatures reckoned from the zero of gaseous tension, the quo-
tients represent densities of saturated vapour. Setting off these quo-
tients as ordinates to the temperatures, we next draw the curve, and
equalize the irregularities as far as possible; then take off the ordi-
nates of the finished curve at equal intervals of temperature, say 10°
or 5°; next take the differences of adjacent ordinates and divide each
by the intermediate ordinate. These quotients, 7 are to be laid
off as ordinates to the temperatures. The points appear to range in
a conic hyperbola, having the axis of temperature as an asymptote.
This conjecture is to be tested by laying off the inverse of these
quotients as ordinates to the temperatures. The conjecture is con-
firmed by the points ranging in a straight line which cuts the axis
at a certain temperature g. Hence (t—g)f= Gr) tod eee Gis
FO D hidit wey
1 1
The integration of this gives D=(t—g)f x = in which H=(t—g)f
when D= unity; or let A4/=H, then Df= (2) Comparing the
value of f in different vapours, it is found to be constant for all and
equal to 4.
As another example, but unconnected with heat, we may inquire
as to the possibility of ascertaining the law of gravitation from the
changes in the moon’s apparent size and motion, its actual distance
_ and the earth’s radius being supposed unknown, but assuming that
the difficulty caused by an unknown parallax and augmentation of
diameter might be evaded by taking lunar distances at equal altitudes
on both sides of the meridian.
By observations on consecutive nights, while the diameter is in-
creasing or diminishing at the maximum rate, we might obtain two
412 Mr.J. J. Waterston on a Law of Liquid Expansion
angular velocities and two measurements of diameter; hence the pro-
portionate differential of the diameter and the correction to be applied
to the angular velocities to reduce them to the same radius. We
might thus obtain the velocity, the increment of velocity, and incre-
ment of distance expressed in terms of r, the radial distance of the
moon from the earth at the middle epoch. Now since ar 2Qvdy, if
x
we had these same quantities for different values of p or 7, and pro-
jected the, different values of a as ordinates tothe correspon-
vdv
ding values of r, the points would converge in a straight line to the
zero of r; and if an approximate parallax was obtained, the point
corresponding to the value of 2vdv at the earth’s surface would fit in
and confirm the propricty of the projection. If it is a question what
should direct us to this particular projection, it might be answered
the increment of square velocity is a square quantity, and the inverse
form of function is applicable to a power depending on distance.
Note C. § 3.—The longest series of observations on the expansion
ofa liquid that I have met with is that of M. Muncke, on sulphuric
acid from —30° to +230°C. Ihave been enabled to put them to the
test by the following equation for the tension of its vapour, viz.
Sa) = p (English measures). In this the value of g=354°7
is assumed to be the same as that for steam, and for the vapours of
several hydrates of sulphuric acid observed by M. Regnault, and
referred to in § 1. of paper in the Philosophical Magazine for March
1858. ‘The value of 4(=1288) is derived from the boiling-point.
seal aeunh ea = is thus 1°33. The inverse volumes being com-
p hk
puted to this power, and laid off as ordinates to the temperatures,
were found to range well in a straight line above 30°. The line
drawn through 45° and 220° is expressed by the equation
(1433°-2—2)v5= 14361 C. A.
The differences between the temperatures computed from the volumes
by this equation and those observed are laid off in fig.1 (PI. VI.) as
ordinates to the temperatures, the scale vertical to horizontal being
10 to l.
The law of continuity is evidently broken at about 40°, the de-
flection being similar to the other cases referred to in §§ 14, 15, and
probably due to the same cause.
Fig. 7 (Plate VI.) represents the differences of Muncke’s observa-
tions on petroleum projected in the same way. ‘The equation is
(489°°5 —2) v*14=4895 C.,
in which Liia.ge has been deduced from Ure’s observations on the
Pp
that connects the Volume of a Liquid with its Temperature. 413
vapour of petroleum. It is unlikely that the liquids were exactly the
same. A slight convexity directed upwards is apparent in the trend of
the points, which a small augmentation in — would correct.
Note D. § 4.—M. Regnault stands so high as an authority, that an
error in his observations that can be clearly demonstrated from in-
ternal evidence is of importance to science. Erroneous observations
from eminent observers are serious obstacles to progress, as are un-
sound deductions from eminent men of science. ‘They are weeds
difficult to root up, and the attempt to do so is a task so ungracious
and so irreverent as to incur every discouragement.
The projection of M. Regnault’s observations on the tension of
steam above and below 100° C. is given in fig. 8. The dotted line
represents the empirical formula which had to be altered at 100°,
the point at which the method employed in making the observations
was changed. They are projected with temperatures uncorrected, in
. the manner described in § 1 of paper in the Philosophical Magazine
for March 1858, and they are orthographically foreshortened as de-
- scribed in the latter part of § 4. See also § 6, and Appendix I. of
the same paper.
The question to ask ourselves when looking at the figure 8 is, Do
the points conform to the law of continuity? Is their trend not clearly
broken at 100°? To put a series of observations to the test of this
law can always be done, but it is attended with considerable labour,
and seems to require a speciality different from that which charac-
terizes the eminent observer and experimentalist.
Note E. § 6.—The following are those observations in series along
with those of M. Despretz, both equalized graphically by elaborate
processes, and the temperatures corrected and reduced to the air-
thermometer. My observations from 100° up’to 212° F. agree so
well with M. Despretz’s, that those at the higher temperatures will, I
think, be found nearly correct, although there was some uncertainty
in consequence of absorption by corrosion of glass.
C. A. Volume. C.A. | Volume. C. A. Volume. C, A. Volume.
—10 | 1-00184 || 55 | 1-:01413 |] 100 | 1-04333 || 153 | 1-09847
— 5] 1-00068 || 6O| 1-01668 || 105 | 1-04743 || 160 | 1-10456
0} 1:00013 || 65! 1-01940 || 110] 1-05172 || 165 | 1-11083
51 100001 || 70) 1-02230 || 115 | 1-05620 || 170 | 1-11731
10 | 1-00025 || 75 | 1-02538 || 120] 1-06086 || 175 | 1-12400
15 | 1-00083 || 80! 1-02863 || 125 | 1-06570 || 180 | 1-13093
20 | 100168 || 85 | 1-03205 || 130 | 107073 || 185 | 1-13811
25 | 1-00280 || 90] 1-03563 || 135 | 1-07593 || 190 | 1-14553
30 | 1:00416 || 95 | 1-03939 || 140] 1-08130 || 195 | 1-15323
35 | 1:00575 || 100) 1-04333 || 145 | 108684 || 200 | 1-16124
40 | 1-00755 150 | 109257 || 205 | 1-16958
45 | 1-00955 | 210 | 1:17829
50.| 101175
rr rer a SS NN
414 Mr. J.J. Waterston on a Law of Liquid Expansion.
The following is an extract from note-book of the experiments :—
“The observations on pure distilled water could only be made up
to 305° F., in consequence of the glass being corroded and becoming
opake above that temperature. At the higher temperatures, five
tubes were employed with water having 3, of carbonate of soda in
solution. ‘Two only of these five were sufficiently transparent up
to 413°. But on examining them next day, ;1,th of the volume of
liquid was absorbed. This allowed for.
«« The expansion of the solution rather less than pure water. The
corrosion of the glass began immediately above the surface of the
liquid. ‘The vapour was computed from formula, assuming the law
of vapour-density maintained.”
Note F. § 6.—M. Muncke and M. Pierre have employed the general
formula 1+ A,=1-+ax+ba’?+ ca’, &c. to represent their observa-
tions, and have computed the constants for eachseries. They have
also sought, by means of the roots of this equation, to find points of
maximum density of each liquid beyond the range of their observa-
tions. Thus M. Pierre, at p. 358, vol. xv. Ann. de Chim., expresses
himself as follows :— ‘‘ ... . puisque l’équation ee. =0, dont
2
les racines doivent donner la température de ce maximum, a ses deux
racines imaginaires.”
I have traced graphically the curve of the equation and of the ob-
servations, and find that its course through them is similar to fig. 8,
interlacing at the fixed points, and departing altogether from the line
of observation beyond the extreme points to which it is bound down.
The positive and negative differences at the loops sometimes amount
to 4 degree. A conic section may be drawn to represent almost per-
fectly a series of observations if the range is not great. The hyperbola
answers well, and can be simply applied as the increasing rate of ex-
pansion adapts itself to the curve, referred to an asymptote parallel
to the axis of temperature.
Note G. § 15.—The value } 3-98 is taken from Regnault’s ob-
Pp
servations on the tension of its vapour at 0° and 20°C. The obser-
vations at 0° and 30° represent =3°25. Dalton’s observation on
Pp
the vapour give it equal to 3:2108, which is probably the most cor-
rect, as / is thus represented to be the same for sulphuric ether and
water, their lines of vapour-density being parallel.
Note H. § 16.—Ina paper on Capillarity in the Philosophical Ma-
gazine for January 1858, the proofs are given in detail of a law that
connects molecular volume with capillarity and latent heat. It is ex-
pressed by the equation mF, in which m is the cube root of the mo-
lecular volume of aliquid, p the height of the same in a capillary tube
of constant bore, and L the latent heat of the vapour of the same, all
Prof. F. von Kobell on Dianic Acid. 415
taken at the same temperature ¢. According to Wolf and Brunner
(Ann. de Chim. vol. xlix.), p= A—Odt is the empirical equation for the
capillary height in terms of the temperature. According to the law
, ‘ k \p)
of expansion, m= ) . Hence
Pein / (GE)
is the equation which, at present partly empirical, it is so desirable
to convert into one wholly expressive of a general natural law of
quantitative relation between L and V.
Edinburgh, May 6, 1861.
LXII. On a peculiar Acid (Dianic Acid) met with in the Group
of Tantalum and Niobium compounds. By Professor F. von
KoBELu*.
— G engaged in preparing a new edition of my ‘ Minera--
logical Tables,’ I was anxious, among other matters, to
arrive at as distinct chemical characters as possible for the tan-
talates and niobates with which we are familiar ; and after various
experiments, [ came to the conviction that in several of these
compounds there exists an acid different from the true tantalic
acid which occurs in the tantalite from Kimito, and also from
the niobic acid met with in the niobite from Bodenmais.
As from the previous labours of MM. Rose, Hermann,
Wohler, and others we are aware that in testing for these acids
the one is very liable to be mistaken for the other, inasmuch as
the tests give more or less various indications according to the
manner of treating the substances and the quality of the reagents
themselves, I have endeavoured in the first place to avert any
possible error arising from those causes by conducting the whole
of the assays in precisely the same manner, which I now proceed
to describe in detail.
1:5 grm. of each assay was fused in a silver crucible with 12
grms. of hydrate of potash, and the mass, which melted quietly,
was maintained for seven minutes longer in a state of fusion ; hot
water was then added till the fluid amounted to 20 cubic inches,
and when cold it was filtered. The filtrate was acidulated with
hydrochloric acid, then neutralized with ammonia, the precipitate
allowed to subside, and the liquor poured off; after this, the
precipitate, which was frequently coloured by manganese, was
shaken with caustic ammonia and filtered. I had taken somewhat
more ammonia than would have been required to remove from
the precipitate an amount of 10 per cent. of tungstic acid. By
* From the Bulletin of the Academy of Sciences of Munich, Meeting of
March 10, 1860. Communicated by W.G. Lettsom, Esq.
416 Prof. F. von Kobell on Dianie Acid.
this treatment any tungstic or molybdic acids which might have
caused the reaction described below was got rid of.
In order to employ in my experiments as equal quantities as
possible of the precipitates, which must be used when just
thrown down, I made funnels of tinfoil, which I cut into the
form of a filter one inch long in the side, and gave them the
requisite shape in a small por celain funnel. One of these funnels
was filled with the freshly filtered pasty precipitate by means of
a spatula, and then laid in a porcelain dish; the tinfoil having
been opened out, one cubic inch of concentrated hydrochloric
acid, of the specific gravity of 1:14, was added and heated to
boiling, that temperature being maintained for three minutes,
and the foil kept continually well stirred about in the fluid.
Under this treatment the appearances observed were as follows.
1. The acid of the tantalite from Kimito, and of the niobite
from Bodenmais, coloured the liquor bluish (smalt-blue); on
adding half a cubic inch of water thereto, when poured into a
glass the colour disappeared rapidly, the precipitate settled
without being dissolved; on being filtered the liquor gave a
colourless filtrate, and the precipitate, which at first was of a
bluish tint, became speedily white on a further addition of water.
2. The acids of a so-called tantalite from Tammela, the powder
of which was blackish grey, those of euxenite, zeschynite, and
samarskite, on being boiled with hydrochloric acid and tinfoil
as above described, were dissolved to a dark blue cloudy fluid,
which, when diluted with half a cubic inch of water or rather
more, became perfectly clear with a deep sapphire-blue colour, and
gave a transparent deep-blue filtrate. On being further diluted
by the addition of a twofold or threefold quantity of water, the
colour becomes indigo-blue and bluish green; and in open
vessels, after some time, olive-green, maintaining that tint for
several hours, but becoming paler. The fluid preserves its per-
fect transparency all the while, and in a closed vessel the colour
remains unchanged for weeks.
Both with the assays under (1), and also with those under
(2), I kept up the boiling for a longer time, indeed till the
liquors were tolerably concentrated ; I then added half the
volume of water and poured the whole into a glass. The
appearances observed were the same as before; the acids of (1)
remained undissolved and gave a colourless filtrate, while those
of (2) were dissolved and gave a transparent blue solution, the
colour of the filtrate being also blue. When treating euxenite
on one occasion, and conceutrating the liquor by boiling, obtained
an olive-green fluid, which was, however, transparent; on the
addition of concentrated hydrochloric acid, and boiling a second
time with tinfoil, the blue colour was restored. If, on obtaining
Prof. F. von Kobell on Dianie Acid. 417
a green fluid of this nature, it is diluted with three times its
volume of water and then slowly evaporated tillit becomes tur-
bid, on the addition of a suitable quantity of concentrated hydro-
chlorie acid and boiling for a few minutes with tinfoil, the blue
colour of the solution always appears on adding a little water.
It seems superfluous to say that a transparent blue fluid
also gives a filtrate of the same colour; and yet the case occurs
of such a fluid being coloured only from some substance being
held suspended therein in a state of extreme subdivision, the
filtrate being colourless. Such, for instance, is the behaviour of
tungstic acid when it is precipitated from tungstate of potash
with hydrochloric acid, and the precipitate boiled with con-
eentrated hydrochloric acid and tinfoil. I obtained thus a dark-
blue fluid, which, when considerably diluted, was quite trans-
parent and of a bright sapphire-blue; but both the dark-blue
and the light-blue diluted fluid gave a colourless filtrate; and
when left to themselves, both these fluids also became colourless
when the blue oxide of tungsten suspended therein, and which
in that condition retains its blue colour, had settled to the
bottom.
The tin contained in the blue solution of the acid in question
is easily got rid of by a stream of sulphuretted hydrogen, and
the acid is obtained again from the filtrate. by precipitation with
ammonia. ‘The precipitate, on being boiled with hydrochloric
acid and tinfoil, again produces the blue fluid. On evaporating
slowly the liquor filtered from the sulphide of tin (which from
its diluted state is colourless), it becomes turbid when consider-
ably concentrated. On adding a little water the cloudiness dis-
appears, and on the further addition of concentrated hydrochloric
acid a white precipitate is produced. If the hydrochloric acid
has been added in suitable quantity, and if the fluid is boiled with
a slip of tinfoil placed in it, the appearance spoken of above is
produced. The fluid becomes of a deep blue, and when poured
into a glass appears turbid; but on the addition of half its
volume of water it becomes transparent, and presents itself in the
glass like a clear sapphire. The original precipitate from the
potash solution may be freed from any manganese it may contain
by boiling it with a certain-quantity of hydrochloric acid; this
precipitate can further be boiled with tolerably strong sulphuric
acid without being deprived of the property of being soluble in
hydrochloric acid in the presence of tinfoil. The acid thus puri-
fied is white; on being heated, it assumes a very pale yellow
colour, which it loses again on cooling, taking somewhat the
appearance of porcelain.
Before the blowpipe it is dissolved in borax and salt of phos-
phorus to a colourless glass, both in the oxidating and the redu-
Phil, Mag. 8. 4. Vol. 21. No. 142, June 1861, 25
418 Prof. F. von Kobell on Dianic Acid.
cing flame. When the borax glass is saturated, it remains trans-
parent on cooling after exposure to a good heat ; on being warmed
again it becomes cloudy, and assumes the appearance of enamel.
When the acid in question is boiled with zinc instead of tin,
the blue solution is not obtained; the precipitate of the acid is
blue, it is true, but the filtrate is colourless, and the acid loses its
colour on the addition of water without being perceptibly dis-
solved. It was only with a very large quantity of hydrochloric
acid and zinc that I could obtain a dirty greenish solution, which,
however, when diluted with half its amount of water, became
speedily reduced in its colour, assuming a pale green hue with
opalescence.
If equal quantities of the acid spoken of, of tantalic acid, and
of hyponiobic acid, all three bemg measured in a platinum fun- ~
nel, are boiled for three minutes with concentrated hydrochloric
acid without tin in the manner above described, and are then
poured out into a glass, they all three give yellow milky fluids.
On the addition of a very moderate quantity of water the acid
in question becomes perfectly transparent, whereas the tantalic
acid, and also the hyponiobic acid, even on the addition of four —
or five times their volume of water, remain undissolved,
If the metallic acid im question, when freshly precipitated, is
heated to boiling in diluted sulphuric acid (1 volume of concen-
trated acid to 5 of water), it forms a cloudy fluid ; and on this being
poured into a glass with a few grains of distilled zinc, im the course
of a few minutes the acid, which was previously white, becomes
of a decided smalt-blue, even deep blue, and retains this colour for
some time on the addition of water; the filtrate, however, is
colourless. In this behaviour it resembles hyponiobic acid, whereas
tantalic acid treated in the same manner is only coloured pale
blue, which colour immediately disappears on the addition of
water. The difference in the behaviour of tantalic and hyponiobie
acids has been already mentioned by HeinrichRose as character-
istic ; as I modified the experiment, by having recourse to a boil-
ing temperature, the effect is not only produced more rapidly,
but also in a more marked manner. I look on this reaction for
distinguishing tantalic acid from other kindred acids as the most
certain, that is to say, if one does not wish to investigate the be-
haviour of the chlorides. For a qualitative testing of an acid of
this class, the first step of the inquiry would be to precipitate
it in the manner described from the solution of potash, and then
to examine the solubility of the freshly obtained precipitate with
hydrochlorie acid and tinfoil, with due attention to the condi-
tions above laid down. Should the acid not be dissolved to a blue
fluid when, after three minutes’ boiling, half a cubic inch or a
cubic inch of water is added, it is tantalic or hyponiobic acid, and
Prof. F. von Kobell on Dianic Acid, 419.
recourse must be had to an assay with sulphuric acid and zinc to
determine between these two acids. I am at least inclined to think
that our determinations, as far as correctness is concerned, will
have as great a probability in their favour as with the other
methods hitherto employed, which, as is shown by the constantly
varying indications of the acids of euxenite, yttrotantalite,
samarskite, &c., have not given any thoroughly reliable results.
With respect to the acid discovered by me, and which forms a
blue solution with hydrochloric acid and tin with such remark-
able facility, it is with certainty and ease distinguishable both
from tantalic and from hyponiobic acid, and that evidently in
a more marked manner than those acids mutually are; the me-
thod of its preparation, moreover, as above set forth, as well
also as a comparison with kindred acids under closely similar
circumstances, appear to me to exclude the idea of its being an
allotropic state, or a not hitherto observed stage of oxidation of
tantalum or niobium, and to claim for it an existence as a distinct
acid. Hermann, as is well known, several years since assumed
the occurrence in samarskite, formerly termed uranotantalite,
of a peculiar acid which he termed ilmenic acid; he was, how-.
ever, not enabled to characterize that acid with sufficient pre-
cision; and Heinrich Rose could at that time establish point by
point for his own niobic acid, now termed hyponiobic, everything
that Hermann sought to establish for ilmenic acid, so that at last
Hermann ranged his acid under niobium, and has pronounced
it to be a niobous-niobic combination*. That the acid discovered
by me is an oxide of niobium is, as far as present experience
-goes, not to be assumed ; for if it were a lower grade of oxidation
than the hyponiobic acid we are acquainted with, it must, on
being fused with potash in an open crucible, be converted to
this hyponiobic acid, inasmuch as, according to Heimrich Rose,
niobium itself is dissolved into hyponiobate of potash by boiling
potash ; and if it were a higher oxide than hyponiobic acid, it
must, on being reduced with tin, be also converted into that
acid, and consequently neither soluble in hydrochloric acid
‘under the conditions spoken of, nor impart a blue colour to the
solution, as is, however, the case.
The same argument holds good if it be regarded as an oxide
of tantalum: under the treatment referred to, it must be con-
verted into the tantalic acid with which we are familiar, and
must agree with it in its reactions, which it does not. Hein-
rich Rose has duly established that the metallic acid of the
tantalite of Bodenmais is distinct from that of certain Finland
tantalites; and to mark the difference, he called the former
* According to Hermann, it colours salt of phosphorus dark brown
before the blowpipe. 5
2K2
420 Prof. F. von Kobell on Dianic Acid.
niobie acid, now termed hyponiobic acid, and has called the.
mineral formerly designated as tantalite by the name of nio-
bite. According to my experiments, the same case occurs with
the acids of the tantalite from Kimito, and of that from Tammela
which I have examined. I will therefore name the latter, in
which I first remarked the difference, after Diana, and term it
Dianie acid; the element I shall name Dianium (D1), and the
mineral from Tammela which contains this acid, Dianite.
Besides occurring in the mineral here mentioned, this acid,
though in a less pure state, appears to occur in the Greenland
tantalite, im the pyrochlore-from the IlImen Mountains, and in
the brown Wohlerite (I have not examined the yellow). I could
only employ small quantities, however, of these minerals, and it
was not in my power to carry out the requisite investigations in
sufficient detail. A small fragment of yttrotantalite, professedly
from Ytterby, gave the reaction of dianic acid; in another assay
of a specimen, the specific gravity of which I ascertamed to be
5°5, from the collection of the late Duke of Leuchtenberg, the
acid proved to be tantalic acid. ‘The former assay refers there-
fore to a different species, the specific gravity of which I could
not determine.
When combinations of this nature contain at the same time
titanic acid, the latter is found in the residue of the potash-lye,
in which it can be easily detected even when this residue con-
tains also a small portion of dianic acid. The residue is boiled
with concentrated hydrochloric acid and filtered, the filtrate,
with a strip of tin laid in it, bemg then boiled longer. If no
dianic acid, but tantalic acid is present, the liquor on becoming
concentrated assumes a violet-blue colour, which on diluting
with water is changed very characteristically to pnk. The fluid
retains this latter colour for several days or longer. When the
solution, in addition to titanic acid, contains a portion of dianic
acid as well, the blue colour of the latter predominates ; on di-
luting it in an open glass, the pink colour due to titanic acid
makes its appearance in the course of a few hours, owing to the
colouring of the dianic acid disappearing gradually. In this
way I recognized the presence of titanic acid (as it had been esta- .
blished previously by other methods) in sschynite, pyrochlore, |
and euxenite.
I cannot of course say whether my dianic acid is contained in
all varieties, and from all the localities, of the above-named
species; with respect to the tantalites from Tammela, it is indeed
established that perhaps the majority of them contain tantalic
acid. ‘The specific gravity should probably be particularly at-
tended to. ‘The mineral from Tammela examined by me (dia-
nite) has a specific gravity of 5°5, while the tantalites from that
Prof. F. von Kobell on Dianie Acid. 42]
locality analysed by H. Rose, Weber, Jacobson, Brooke, Wornum,
and Nordenskiold, had a specific gravity of from 7°38 to 7:5 and
more. The tantalite from Kimito, moreover, from which I pro-
cured the tantalic acid employed for my investigation, has a spe-
cific gravity of 7:06. The colour of the streak of dianite is, as
before remarked, black-grey, while that of the Tammela tanta-
lites analysed by Jacobson is stated to be dark brownish red, as
is also the case with the Kimito tantalite.
In appearance dianite very closely resembles Finland tanta-
lites. The assay analysed was taken from a large tabular broken
crystal about 2 inches in size, on which, however, only two
planes occur. Their angle of inclination, as measured by the
hand-goniometer, amounts to about 151°; whether those planes
are T and R of Naumann’s tantalite, or T and G, or other ones,
cannot of course be determined. Lefore the blowpipe, dianite
affords no marked difference when compared with the Kimito
tantalite.
The samarskite which I examined is from the IImen Moun-
tains; I employed quite fresh, pure fragments, with a conchoidal
fracture and strong, somewhat metallic, vitreous lustre. The
euxenite is from Alva near Arendal (procured from Dr. Krantz) ;
the eschynite, from the IImen Mountains, was from the Leuch-
tenberg collection.
While preparing the above, I forwarded a portion of the
dianic acid in question to Professor Heinrich Rose, and communi-
cated to him the leading points of the paper, requesting his
opinion on the matter. Professor Rose was so good as to pre-
pare the chloride of this acid, and wrote to me that, in doing so,
he had met with a trace of tungstic acid, adding that the re-
action described by me might be brought about from that cireum-
stance; and he advised me, as a first step, to purify the acid by
the method suggested by him, namely, by fusing it with car-
bonate of soda and sulphur. The case might be similar to the
one which had misled Hermann.
Now I had, it is true, established, by the very ready solubility
of dianic acid in hydrochloric acid when compared with true
tantalic and hyponiobic acids under similar conditions, a
characteristic distinction for the first of these three acids;
but it was none the less essential to prove that the property
of becoming blue with hydrochloric acid and tin belonged
to the acid in question, and is not attributable to tungstic acid.
After the treatment with ammonia, to which reference has been
made, but little tungstic acid could, it is true, contaminate the
dianic acid; nevertheless the turning blue might be ascribed to
that. A plan to clear this pomt up was soon formed. [I first
422 Prof. F. von Kobell on Dianice Acid.
sought to impart to the non-colouring tantalic and hyponiobic
acids the quality of becoming coloured by an addition of tungstic
acid, and then endeavoured to ascertain how far an acid. thus
mixed was to be purified by ammonia, the process which I fol-
lowed in my original experiments. I prepared tungstate of pot-
ash of a determined strength, and mixed it with a lye of tantalic
acid in such proportions that 84 parts of tantalic acid were united
to 16 parts of tungstic acid, corresponding, as it were, to a pot-
ash solution of a tantalite that consisted of tantalic and tungstic
acids only. The mixture was divided into two portions. (by
means of a graduated glass), and precipitated with hydrochloric
acid. The precipitate of one portion was decanted and filtered,
and a tinfoil filter, one inch long in the side, being filled there-
with, it was boiled for three minutes in | cubic inch of hydro-
chloric acid as described above; 14 cubic inch of water was
added, and it was filtered. ‘The filtrate was greenish yellow;
on adding 1 cubic inch more water the fluid was yellowish, the
precipitate was not dissolved, and after the lapse of twenty-
four hours the fluid which was poured off deposited a dark blue
precipitate. The same experiment, performed in the like manner
with a similar quantity of the hyponiobic acid, gave an olive-green
filtrate, which did not materially change im twenty-four hours.
When boiled again it became of a blue colour, which was also
the hue of the filtrate. The hyponiobic acid was a little dissolved
in this experiment, as the tantalic acid was in the corresponding
one. When, however, I agitated the precipitates of the mixed
acids with ammonia (the approximate quantity required to dis-
solve the amount of tungstic acid contaied therein having been
ascertained by experiment), and then allowed them to subside,
decanted and filtered them, the precipitates thus treated,
on being boiled for three minutes, as above described, with hy-
drochloric acid and tinfoil, and diluted with half a cubic inch of
water, behaved almost entirely like the acids prepared directly
from the minerals themselves; the fluid of the tantalic acid
passed through the filter colourless, that of the niobic acid had
a slight greenish tint. These experiments prove that tantalic
and hyponiobic acids, even when containing a great amount of
tungstic acid, may be at least so far purified by ammonia as not
to produce the deep blue colour given by dianic acid; and fur-
ther, that the presence of tungstic acid in those acids, under the
conditions spoken of, does not increase their solubility in hy-
drochloric acid. The latter circumstance, although to be antici-
pated, was of more importance to me than the absence of the
blue colour; for similar experiments to these had already fully
convinced me that the removal of tungstic acid by means of am-
monia is not a perfect one. To remove, however, the last doubts
Prof. F. von Kobell on Dianic Acid. 423
as to the possible cooperation of the tungstic acid in the produc-
tion of the blue colour alluded to, the acid of the dianite from
Tammela was purified with the utmost care by the process sug-
gested by H. Rose. The filtered acid was dried down till it was
capable of being readily reduced to powder. I took 0:5 grm,
of it, which was triturated with 1:5 grm of carbonate of pot-
ash and then with 0°5 grm. sulphur. I fused the mixture in a
covered porcelain crucible over a gas-lamp, dissolved the mass
in water, and after decantation transferred the acid remaining
into a close glass vessel with sulphuretted hydrogen, which I
agitated well, leaving it thus for twenty-four hours. The liquor
was then decanted twice, and the residue boiled with diluted
hydrochloric acid and well washed ; and lastly, the metallic acid
was attacked a second time with hydrate of potash in a silver
crucible, precipitated with hydrochloric acid and filtered.
Uy Ny
that is, the discharge being constant, the dynamic effects are in the
ratio of the squares of the number of revolutions of the machine.
If n=20, and n,;=10, as in Exp. III., then i that is, in
this case the dynamic effects will be as 1 to 4, or a double num-
ber of revolutions produces a quadruple effect.
Let x be put for the number of revolutions of the machine (its
state being constant) performed in 60 seconds, or 1 minute, to
produce the same discharge as 7 revolutions in ¢ seconds; then
nt
x x 60=nt, or <= 60"
Similarly, we have for the relation of equal discharge corre-
sponding to any other state of the machine,
ately
re GOR
Now it may be presumed that the efficiency of the machine is
inversely proportional to the number of revolutions per minute
requisite to produce a given discharge; but we find
pc WALL
x nt ”
that is, the efficiency of a machine varies inversely as the product
of the number of revolutions by the corresponding time requisite to
produce a gwen discharge.
ff 7775, then TERR
that is, im this case the efficiency of a machine varies inversely as
the number of revolutions (the time being constant) requisite to
produce a given discharge.
Thus, if a machine discharges half of a cubic inch of water in
twenty revolutions in a certam time, and another machine dis-
charges the same amount of water in ten revolutions in the same
time, then the latter machine will have double the power of the
former.
Royal Society. 457
On the Dispersion of different Liquids by Electrical Action.
The siphon-electrometer enables us to determine the rate at
which electrical charges will disperse different liquids. The
liquid to be examined being placed in the jar A B, and the siphon
being brought to act in the usual manner, the discharge pro-
duced by a given number of revolutions of the machine in a
given time is determined; and having previously found the
amount of pure water discharged by the same number of revolu-
tions performed in the same time, we are enabled to estimate the
dispersiveness of the particular liquid, as compared with that of
pure water, under the same electrical action. In this manner,
saturated solutions of chloride of sodium, carbonate of soda, and
other salts were examined ; and it was found that, under the same
electrical action, the volumes of the liquid discharged were in the
inverse ratio of their specific gravities. It will be observed that
these liquids are all good conductors of electricity. But the case
is very different with respect to liquids which are imperfect con-
ductors of electricity, such as turpentine, fixed oils, and alcohol.
In twenty revolutions per minute the discharge of pure water
was about three-fourths of a cubic inch; whereas with the same
electrical action only about one-fourth of a eubic inch of turpen-
tine was discharged, and not more than one-tenth of a cubic inch
of fixed oil. Under the same electrical action, the volume of
alcohol discharged did not exceed one-fifth of a cubicinch. Now
although the specific gravities of these-liquids are less than that
of water, yet their dispersiveness, under the same electrical action,
is considerably less than that of water.
Hastings, May 18.
LXIX. Proceedings of Learned Societies.
ROYAL SOCIETY.
[Continued from p. 393. ]
June 14, 1860.—General Sabine, R.A., Treasurer and Vice-President,
in the Chair.
ee following communications were read :—
“Notes of Researches on the Poly-Ammonias.’”’—No. VIII.
Action of Nitrous Acid upon Nitrophenylenediamine. By A. W.
Hofmann, LL.D., F.R.S.
The experiments of Gottlieb have shown that dinitrophenylamine,
when boiled with sulphide of ammonium, is converted into a remark-
able base, crystallizing in crimson needles, generally known as nitra-
zophenylamine, and for which, in accordance with the views I enter-
tain regarding its constitution, I now propose the name Nitrophe-
nylenediamine. I owe to the kindness of Dr. Vincent Hall a con-
458 Royal Society :—
siderable quantity of this substance, which is not quite easily pro-
cured.
I have made a few experiments with this compound in the hope of
obtaining some insight into its molecular constitution. If, bearing
in mind the numerous analogies between the radicals ethyle and
phenyle, we assume that the latter, by the loss of hydrogen, may be
converted into a diatomic molecule, phenylene C, H,, corresponding
to ethylene, the existence of a group of bases corresponding to the
ethylene-bases cannot be doubted.
C,H, (C, Hy)”
Ethylamine H }N*. Ethylenediamine UH, N,.
H H,
C,H, (, H,)"
Phenylamine H fx. Phenylenediamine H, Ly,
H H,
With the last-named body agrees in composition the compound
known as semibenzidam, or azophenylamine, which Zinin obtained
by exhausting the action of sulphide of ammonium on dinitro-
benzole.
Those chemists, however, who have had an opportunity of be-
coming acquainted with the well-defined properties of ethylenedia-
mine, will not be easily persuaded to consider the uncouth dinitro-
benzol-product—sometimes appearing in brown flakes, sometimes as a
yellow resin, rapidly turning green in contact with the air—as stand-
ing to smooth phenylamine in a relation similar to that which obtains
between ethylenediamine and ethylamine; we much more readily
admit a relation of this description between phenylamine and Gott-
lieb’s crimson-coloured base, in which the clearly pronounced cha-
racter of the former is still distinctly visible, although of necessity
modified by the further substitution which has taken place in the
radical.
C, H, i
Phenylamine Tae Ns
H
(C, Hy)"
Phenylenediamine H, pe
(C,[H, (NO.)})"
Nitrophenylenediamine H, } N,.
H
Does the latter formula really represent the molecular constitution
of the crimson needles? The degree of substitution of this body
might have been determined by the frequently adopted process of
ethylation. But even a simpler and a shorter method appeared to
present itself in the beautiful mode of substituting nitrogen in the
place of hydrogen, lately discovered by P. Griess. ‘The red crystals
* H=1; 0=16; C=12, &.
On the Action of Nitrous Acid upon Nitrophenylenediamine. 459
undergo, indeed, the transformation, which he has already proved for
so many derivatives of ammonia, with the greatest facility.
On passing a current of nitrous acid into a moderately concen-
trated solution of the nitrate of the base, the liquid becomes slightly
warm, and deposits on cooling a considerable quantity of brilliant
white needles, the purification of which presents no difficulty: spa-
ringly soluble in cold, readily soluble in boiling water, the new com-
pound requires only to be once or twice recrystallized. Thus puri-
fied, this substance forms long prismatic crystals, frequently inter-
laced, white as long as they are in thé solution, but assuming a
shghtly yellowish tint when dried, and especially when exposed to
100°: they are readily soluble both in alcohol and in ether. The
new body exhibits a distinctly acid reaction ; it dissolves on applica-
tion of a gentle heat in potassa and in ammonia, without, however,
neutralizing the alkaline character of these liquids; it also dissolves
in the alkaline carbonates, but without expelling their carbonic acid.
The new acid fuses at 211° C., and sublimes at a somewhat higher
temperature, with partial decomposition. The sublimate consists of
small prismatic crystals.
Analysis proves this substance to contain
C, H, N, 0,,
a formula which is confirmed by the analysis of a silver-compound,
| C, (H, Ag) N,O,,
and of a potassium-salt,
C, (H, K) N, O,.
The analysis of the new compound shows that, under the influence
of nitrous acid, nitrophenylenediamine exchanges three molecules of
hydrogen for one molecule of nitrogen, three molecules of water
being eliminated.
C, H, N, 0,+H NO,=2H,0+C, H, N’’N, O,.
—_.+=,-——_—’ —————---—-—_——
Nitrophenylene- New acid.
diamine.
I do not propose a name for the new compound, which can claim
but a passing interest, as throwing, by its formation, some light on
the constitution of nitrophenylenediamine.
The composition of the new acid, and of its salts, shows that in the
crimson-red base four hydrogen molecules are still capable of re-
placement ; in other words, that this body contains four extra-radical
molecules of hydrogen. The result of these experiments appears to
confirm the view which, in the commencement of this Note, I have
taken of the constitution of this body; at all events, the mutual
relation of the several bodies is satisfactorily illustrated by the
formulze— :
4.60 Royal Society :—
(C.[H, (NO,)])" }
N..
Nitrophenylenediamine Ss
C.CH, (NO.)])"
(C.{H, (N0,)}) \y,
New acid
H
(C,[H, (NO,)])"
Silver-salt NI!" Ng.
Ag
If the admissibility of this: interpretation be confirmed by further
experiments, the reaction discovered by Griess furnishes a new and
valuable method of recognizing the degree of substitution in the
derivatives of ammonia.
The new acid differs in many respects from the substances pro-
duced from other nitrogenous compounds. As a class, these sub-
stances are remarkable for the facility with which they are changed
under the influence of acids, and more especially of bases. The new
acid exhibits remarkable stability; it may be boiled with either
potassa or hydrochloric acid without undergoing the slightest change.
Even a current of nitrous acid passed into the aqueous or alcoholic
solution is without the least effect. The latter experiment appeared
of some interest ; for if the action of nitrous acid, im a second phase
of the process, had assumed the form so frequently observed by Piria
and others, it might have led to the formation of the diatomic nitro-
phenylene-alcohol, according to the equation
(C, [H, (NO,)])”
H,
H
It deserves to be noticed that nitrophenylenediamine, although
derived from two molecules of ammonia, is nevertheless a decidedly
monacid base. Gottlieb’s analyses of the chloride, nitrate, and sul-
phate left scarcely a doubt on this pomt. However, as some of the
natural bases, quinine for instance, are capable of combining with
either one or two molecules of acid, I thought it of sufficient interest
to confirm Gottlieb’s observations by some additional experiments.
The crystals deposited on cooling from a solution of nitrophenylene-
diamine in concentrated hydrochloric acid, were washed with the
same liquid and dried zn vacuo over lime.
Analysis led to the formula
L (C,[H,(NO,)])" |
H H N, |
(C, [H, (NO,)] x O
N,+2H NO,=2H, 0+N,+ H, 2
2
2
H,
The dilute solution of this chloride is not precipitated by dichlo-
ride of platinum, nor can the double salt of the two chlorides be
obtained by evaporating the mixed solutions, which, just as Gott-
lieb observed it, is readily decomposed with separation of metallic
platinum. I had, however, no difficulty in preparing a platinum salt,
On the Action of Nitrous Acid upon Nitrophenylenediamine. 461
crystallizing in splendid long brown-red prisms, by adding the dichlo-
ride of platinum to the concentrated solution of the hydrochlorate.
The platinum determination led to the formula
fe #(@2(H, (NO,)})")° 7
A Be NIC Pele
H, val
These experiments prove that, even under the most favourable cir-
cumstances, nitrophenylenediamine combines only with 1 equiv. of
acid, while the ethylene-derivatives are decidedly diacid. The dimi-
nution of saturating power in nitrophenylenediamine, at the first
glance, seems somewhat anomalous, but the anomaly disappears if
the constitution of the body be more accurately examined. It can-
not be doubted that the diminution of the saturating power is due to
the substitution which has taken place in the radical of the diamine.
I have pointed out at an earlier period*, that the basic character of
phenylamine is considerably modified by successive changes intro-
duced into the phenyl-radical by substitution. Chlorphenylamine,
though less basic than the normal compound, still forms well-defined
salts with the acids; the salts of dichlorphenylamine, on the other
hand, are so feeble, that, under the influence of boiling water, they
are split into their constituents; in trichlorphenylamine, lastly, all
basic characters have entirely disappeared. Again, on examining the
nitro-substitutes of phenylamine, we find that even nitrophenylamine
is an exceedingly weak base, whilst dinitrophenylamine is perfectly
indifferent. What wonder, then, that a molecular system, to which
in the normal condition we attribute a diacid character, should, by
the insertion of special radicals, be reduced to monoacidity? The
normal phenylenediamine, which remains to be discovered, will doubt-
less be found to be diacid, like the diamines derived from ethylene.
Even now the group of diacid diamines is represented in the naphtyl-
series :
: C,, H,
Naphtylamine H +N monoacid.
H
(C,, H.)"
Naphtylenediamine 4H, N diacid.
3 HH
The body which I designate by the term Naphtylenediamine, is the
base which Zinin obtained by the final action of sulphide of ammo-
nium upon dinitronaphtaline. This substance, originally designated
seminaphtalidam, and subsequently described as naphtalidine, com-
bines, according to Zinin’s experiments, with 2 equivalents of hydro-
chloric acid +. .
“Qn the Formula investigated by Dr. Brinkley for the general
Term in the Development of Lagrange’s Expression for the Summa-
tion of Series and for Successive Integration.” By Sir J. F. W.
Herschel, Bart., F.R.S. &c.
* Mem. of Chem. Soc. vol. ii. p. 298.
+ Liebig’s Annalen, vol. lxxxv. p. 328.
4.62 Royal Society :—
June 21.—Sir Benjamin C. Brodie, Bart., President, in the Chair.
The following communications were read :—
*‘ Experimental Researches on various questions concerning Sen-
sibility.” By E. Brown-Séequard, M.D.
“On the Construction of a new Calorimeter for determining the
Radiating Powers of Surfaces, and its application to the Surfaces of
various Mineral Substances.”?’ By W. Hopkins, Esq., M.A., F.R.S.
When the author's Memoir on the Conductivity of various sub-
stances was presented to the Society, it was intimated to him on the
part of the Council of the Society, that it might be advisable to de-
termine absolute instead of relative conductivities, the latter only
having been attempted in his previous experiments. It is partly
in consequence of this intimation, and partly from the desire to make
his former -investigations more complete, that the author has given
his attention to the construction of a calorimeter which might serve
for this purpose. His present memoir contains a description of this
instrument, with the results obtained from its application to the
surfaces of various substances.
The apparatus used by Messrs. Dulong and Petit was more deli-
cate and complete than the simpler instrument devised by the author
of this paper, but it was calculated only to determine the radiatimg
powers of substances of which the bulb of a thermometer could be
constructed, or with which it could be delicately coated. The only
substances to which, in fact, it was applied, were glass and silver,
the radiation taking place, in the first case, from the naked bulb of
the thermometer, and, in the second, from the same bulb coated
with silver paper. In these cases, too, it was the whole heat radi-
ating In a given time from the instrument, and not that which radiated
from a given area, that was determined. For this latter purpose the
apparatus was not well calculated, on account of the difficulty of ob-
taining with accuracy the area of the surface from which radiation
took place. The instrument here described can be easily applied to
any plane radiating surface, while the area of that surface can be easily
determined to any required degree of accuracy. The quantity of
heat radiating under given conditions, froma unit of surface ina unit
of time, can thus be easily ascertained. The paper contains a detailed
description of the instrument, and of the experiments made with it.
The following are experimental results thus obtained,—the unit
of heat being that quantity of heat which would raise 1000 grs. of
distilled water 1° Centigrade. ‘The formula is that of Dulong and
Petit, where
0= temperature of the surrounding medium (the air in these ex-
periments), expressed in Centigrade degrees ;
¢= the excess of the temperature of the radiating surface above
that of the surrounding medium, in Centigrade degrees ;
p= pressure of the surrounding medium (the atmosphere in these
experiments), expressed by the height of the barometer in metres ;
a= 1:0077, a numerical quantity which is always the same for all
radiating surfaces and surrounding media.
On the Construction of a new Calorimeter. 463
Then if Q denote the quantity of heat, expressed numerically,
which radiates from a unit of surface (a square foot) in a unit of
time (one minute), we have the following results for the substances
specified :—
Glass.
9-566 a%(at'—1)+°03720 (5)
Dry Chalk.
Q= 8:613 a%(a'—1)+-03720 (5) °
Dry New Red Sandstone.
= 8:377 a%(a'—1)+-03720 (4) prs
Q
Sandstone (building stone)
Q= 8-882 a%(at—1)++03720 (4)
45
fe
Polished Limestone.
45
Q= 9:106 a%(aé'—1)+°03720 (4) gi298
Unpolished Limestone (same block as the last).
"45
@=—12:808 a9(at—1)+-03720 (4) 2233
‘On Isoprene and Caoutchine.” By C. Greville Williams, Esq.
This paper contains the results of the investigation of the two prin-
cipal hydrocarbons produced by destructive distillation of caout-
chouc and gutta percha.
Isoprene.
This substance is an exceedingly volatile hydrocarbon, boiling
between 37° and 38° C.; after repeated cohobations over sodium, it
was distilled and analysed. The numbers obtained as the mean of
five analyses were as follows :—
Experiment. Calculation.
oe a
Carbon % 1)..; «8870 Ces 160 88-2
Hydrogen. . 12°1 eats 11°8
68 100:0
Three of the specimens were from caoutchouc and two from gutta
percha. + The vapour-density was found to be at 58° C. 2°40. Theory
requires, for C** H®=4 volumes, 2°35. The density of the liquid
was 0°6823 at 20°C.
Action of Atmospheric Oxygen upon Isoprene.
Isoprene, exposed to the air for some months, thickens and acquires
powerful bleaching properties owing to the absorption of ozone. On
464 Royal Society :—
distilling the ozonized liquid, a violent reaction takes place between —
the ozone and the hydrocarbon. All the unaltered hydrocarbon distils
away, and the contents of the retort suddenly solidify to a pure,
white, amorphous mass, yielding the annexed result on combustion :—
Experiment. Calculation.
—__-_s*—————--_ Eres Ce
Carbon. °.ay73'5 C260 78°95
Piydroseny 077 Bp 8 10°52
Oxysen i. 10" O 8 10°53
76 100°00
This directly-formed oxide of a hydrocarbon is unique, as regards
both its formula and mode of production.
Caoutchine.
Himly’s analysis was correct. The mean results of three analyses
are compared in the following Table with those of M. Himly :—
Mean. Himly. Calculation.
—— at
Carbon’) >> S381 88°44 Ce 120 88°2
Hydrogen . 11:9 11°56 He! AS 11°8
136 100°0
Two of the determinations, the results of which are incorporated
in the above mean, were made on a substance from gutta percha.
The vapour-density was :—
Experiment. Himly. Calculation = 4 vols.
4°65 4°46 4°6986
We now for the first time see the relation between the two hydro-
carbons. Itis the same as between amylene and paramylene. The
author discusses the boiling-point of these bodies, and shows that
they form most decided exceptions to Kopp’s empirical law.
Action of Bromine on Caoutchine and its isomer Turpentine.
Caoutchine and turpentine act on bromine in precisely the same
manner. One equivalent of the hydrocarbon decolorizes four equi-
valents of bromine. To determine this point quantitatively, eight
experiments were made, four with turpentine and four with caout-
chine. The quantity of bromine-water employed was 20 cub. cents.
=0'2527 gramme bromine.
Mean of four turpentine experiments. Mean of four caoutchine experiments.
0°1074 grm. 0°1091 grm.
Conversion of Turpentine and Caoutchine into Cymole.
By the alternate action of bromine and sodium on caoutchine or
turpentine, two equivalents of hydrogen are removed, the final result
being cymole, having exactly the odour hitherto considered charac-
teristic of the hydrocarbon obtained from oil of cumin, and quite
distinct from that of camphogene. The liquid was identified by the,
Mr. C, G. Williams on Isoprene and Caoutchine. 465
annexed analyses. No. I. was from turpentine, II. and III. from
caoutchine.
Experiment. Calculation.
ca — a
i II. IIT. Mean.
Carbon . . 89'2 89:5 89°5 89°4 OE 120.,.1,89:6
Hydrogen . . 10°5 10°4 10°4 10°4 H“ 14 10:4
134 100°0
Agreeing perfectly with the formula C”? H™*,
Paracymole.
At the same time that cymole is formed, there is a production of
an oil having the same composition, but boiling about 300°C. The
author has provisionally named it paracymole.
Action of Sulphuric Acid on Caoutchine.
Sulphuric acid acts on caoutchine, converting it almost entirely into
a viscid fluid like hévééne, at the same time a very small quantity of a
conjugate acid is formed, having the formula
ex H’ S? O°: ;
the composition was determined from that of the lime salt, which on
ignition, &c., gave a quantity of sulphate of lime equal to 8:3 per
cent. of calcium; C* H” CaS? O° requires 8°5.
The author considers the action of heat on caoutchouc to be merely
the disruption of a polymeric body into substances having a simple
relation to the parent hydrocarbon. He deduces this view from the
similarity in composition between pure caoutchouc, isoprene, and
caoutchine.
The following Table contains the principal physical properties of
isoprene and caoutchine :—
Table of the Physical Properties of Isoprene and Caoutchine.
Vapour-density.
Name. Formula. | Boiling-point. a gee ee
; Ghanieye Expt. Calculated.
Tsoprene C10 HS Sf 0°6823 at 20° 2°44 2°349
Caoutchine| C?? H16 UALS 0°8420 4°65 4-699
In the calculations rendered necessary by the numerous vapour-
density determinations contained in this paper, and more especiall
in those ‘‘On some of the products of the Destructive Distillation of
Boghead Coal,’ the author has so repeatedly had to ascertain the
: 1 :
value of the expression ——_—______, that he was induced to calcu-
: P 1+0-00367 1"
* (Note received July 27.) Both the cymole from turpentine and that from
caoutchine were converted into insolinic acid by bichromate of potash and sul-
phuric acid. The quantitative determinations made on the silver salt of the acid
were almost theoretically exact.
Phil, Mag. 8. 4, Vol. 21, No. 142. June 1861, 2H
466 Royal Society :—
late it once for all for each degree of the Centigrade thermometer from
1° to 150°. As it is always easy so to manipulate as to prevent the
value of T falling between the whole numbers, the Table proved a
most valuable means of saving time ; the author has therefore appended
it to his paper in the hope of its proving equally useful to other work-
ing chemists.
*‘On the Thermal Effects of Fluids in Motion—Temperature of
Bodies moving in Air.” By J. P. Joule, LL.D., F.R.S., and Pro-
fessor W. Thomson, LL.D., F.R.S.
An abstract of a great part of the present paper has appeared in
the Phil. Mag. vol. xv. p. 477. To the experiments then adduced
a large number have since been added, which have been made by
whirling thermometers and thermo-electric junctions in the air. The
result shows that at high velocities the thermal effect is proportional
to the square of the velocity, the rise of temperature of the whirled
body being evidently that due to the communication of the velocity
to a constantly renewed film of air. With very small velocities of
bodies of large surface, the thermal effect was very greatly imcreased
by that kind of fluid friction the effect of which on the motion of
pendulums has been investigated by Professor Stokes.
On the Distribution of Nerves to the Elementary Fibres of
Striped Muscle.” By Lional 8. Beale, M.B., F.R.S.
On the Effects produced by Freezing on the Physiological Pro-
perties of Muscles.” By Michael Foster, B.A., M.D. Lond.
* On the alleged Sugar-forming Function of the Liver.” By
Frederick W. Pavy, M.D.
«A new. Ozone-box and Test-slips.” By E. J. Lowe, Esq.,
F.R.A.S., F.L.S. &c.
The ordinary form of Ozone-box being very cumbersome, the pre-
sent one has been contrived to supersede it*. The box is simple in
construction, small in size, and cylindrical in form; the chamber in
which the ¢est-slips are hung is perfectly dark, and at the same time
there is a constant current of air circulating through it, no matter
from what quarter of the compass the wind is blowing. The air
either passes in at the lower portion of the box and travels round a
circular chamber twice, until it reaches the centre (where the test-
slips are hung) and then out again at the upper portion of the box
in the same circular manner, or in at the top and out again at the
bottom of the box.
Fig. 1 represents a section of the upper portion of the box, showing
the manner in which the air enters and moves along to the centre
chamber (where the test-slip is hung at A), and figure 2 represents
a section of the lower half of the box where the air circulates in the
opposite direction, leaving the box on the side opposite to that on
which it had entered.
* A specimen of the instrument was forwarded with the paper.
Mr. E. J. Lowe on a new Ozone-box and Test-slips. 467
Fig. 1. Fig. 2.
The box has been tested and found to work well.
On three different dates, when there was much ozone, test-slips were
hung in one box, whilst others were hung in another which had the
two entrances sealed up in order that no current of air should pass
through ; the result was satisfactory, viz. :—
Example. New ozone-box. New ozone-box sealed up.
] 10
2 9 0
eee gi 0
Then again, in five examples of test-slips being exposed without
any box, in comparison with those placed in this new box, the result
was :—
Example. In new ozone-box. Exposed to north without
a box.
1 10 Ss
2 9 9
3 7 7
4 10 9)
4) 2 0
The ozone-box is capable of being suspended at an elevation above
the ground ; and this appears to be a great advantage, because eleva-
tion seems necessary in order to get a proper current of air to pass
across the test-slips ; indeed as an instance it may be mentioned, that
at an elevation of 20 feet there is almost always more indication of
ozone than at 5 feet.
The plan adopted here is to suspend the box to a T support, it
being drawn up to its proper place by means of a thin rope passing
over a pulley ; and there is less trouble in examining and changing
the test-slips in this manner than there was in the old method.
The box, as described, is made by Messrs. Negretti and Zambra
of Hatton Garden.
It has been urged that a box was scarcely necessary for ozone
test-slips; but as the papers fade on exposure to light, it must be
evident that in order to register the maximum amount of ozone a
dark box is required.
Test-slips.— Paper-slips being so fragile, I have substituted others
made of calico. The calico is to all intents and purposes chemically
pure, containing only a few granules of starch, used in the first pro-
cess of its manufacture, which it is very difficult to remove, being
enveloped in the cotton fibre ; it is, however, thought to be purer than
2H2
468 Royal Society.
the paper that is used for these test-slips, every precaution having
been taken to make it so.
Results of observations.—The following Tables have been con-
structed from observations made between the lst of May, 1859, and
the 3lst of March, 1860.
TABLE I,
Mean amount of Ozone observed from Test-slips hung for twelve
hours, both at night and in the daytime, in comparison with others
hung for twenty-four hours.
Papers exposed for | Papers exposed for Difference
twelve hours. twenty-four hours, ayes oa
During the month of i oe CS RE SSre cwentecoue
Day. | Night. Pate Day. | Night. oo hours.
1859. May.........{ O°4 13 0-9 Je 1:9 0:8 0-7 0-6
Sune, ..dint 03 | 09 | O1 3) 1-5, se 05 | 06
Tully... .éseck 09 | 10] O1 | 1:2 | 13 | O1 || 08g 08
August...... 07 14 | 07 1:2 18 0-6 0-5 0-4
September .| 1:9 2°6 0:7 2°5 30 0:5 0-6 O-4
October ...| 095 0-7 0:2 0:7 0-9 0-2 0-2 0-2
November..| 1:5 LZ, 0:2 1:8 2-1 0:3 0-3 0:4
December...| 1°7 2:0 0:3 2-1 25 0-4 0-4 0:5
1860. January ...} 2°38 | 2:8 | 0-0 So {oo o, | ees 0-4 | 07
February ...| 273 2°8 0:5 2°6 3°0 0-4 0-3 0-2
Marchicvens. 49 5:2 0:3 5-2 5°6 0-4 0:3 0-4
Mean scsi: 17 2-0 0:3 2-1 2°5 0-4 0:4 0-5
The ozone being always in excess in the night, and the tests exposed
for twenty-four hours showing always an excess over those only ex-
posed for twelve hours.
Mareh ..:... 0
ed
e
=)
oa
@
a]
fo)
rh
fo
~
<<
6
—
—
Go
for]
oO
TaBxe II.
Number of observations without any visible ozone.
During the night. During the day.
Month.
Twelve hours’ | Twenty-four || Twelve hours’ | Twenty-four
exposure. hours’ exposure. exposure. hours’ exposure.
1859. May......... a 4 19 12
VONE sexiness 18 10 15 9
SLY chino ab 18 12 | 18 13
August...... 10 4 15 9
September.. 2 0 0 0
October ... 16 12 18 14
November.. 10 7 10 10
December... 10 sf) 7 5
1860. January ... 8 6 “, 5
February ... 12 6 9 9
0 0 0
Cambridge Philosophical Society. 469
Mean amount of ozone with the box suspended at the height of
25 feet.
1859. December 24 hours’ exposure =3°0 48 hours’ exposure =5:0
1860. January... 24 hours’ exposure =3°9 48 hours’ exposure =4'5
February 24 hours’ exposure =3°7 48 hours’ exposure =5°4
? b]
March ... 24 hours’ exposure =5°9 48 hours’ exposure =6°4
Mean amount of ozone with the box suspended at the height of
40 feet, March 1860, with twenty-four hours’ exposure =7'l.
CAMBRIDGE PHILOSOPHICAL SOCIETY.
[ Continued from‘vel. xvii. p. 316.]
October 31, 1859.—A communication was made by Mr. Hopkins
«“‘On the construction of a new Calorimeter for determining the
Radiating Power of the Surfaces of Heated Bodies.”
November 14.—A communication was made by the Master of
Trinity College ‘‘On the Mathematical part of Plato’s Meno.”
November 28.—The Rev. Dr. Donaldson read a paper “On the
Origin and proper value of the word ‘ Argument.’ ”’
The author first investigated the etymology and meaning of the
Latin verb arguo, and its participle argutus. He showed that arguo
was a corruption of argruo = ad gruo; that gruo (in argruo, ingruo,
congruo) ought to be compared with xpotw, which means ‘to dash
one thing against another,”’ especially for the purpose of making a
shrill, ringing noise; that arguo means ‘‘ to knock something for the
purpose of making it ring, or testing its soundness,” hence “to test,
examine, and prove anything;”’ and that argutus signifies ‘“‘ made to
ring,” hence ‘making a distinct, shrill noise,” or “tested and put
to the proof.” Accordingly argumentum means id quod arguit, ‘ that
which makes a substance ring, which sounds, examines, tests, and
proves it.”
It was then shown that these meanings were not only borne out
by the classical usage of the word, but also by the technical appli-
cation of ‘‘argument” as a logical term. For it is not equivalent
to ‘argumentation,’ or the process of reasoning; it does not even
denote a complete syllogism; though Dr. Whately and some other
writers on logic have fallen into this vague use of the word, and
though it was so understood in the disputations of ;the Cambridge
schools. The proper use of the word ‘‘argument”’ in logic is to
denote ‘‘ the middle term,” 7. e. ‘‘the term used for proof.” Ina
sense similar to this the word is employed by mathematicians; and
there can be no doubt that the oldest and best logicians confine the.
word to this, which is still its most common signification.
_ The author@entered at some length into the Aristotelian definition
of the enthymeme, which may be rendered approximately by the word
“argument.” He also explained how the words ‘topic’ and
‘‘argument”’ came to denote the subject of a discourse or even of a
470 Cambridge Philosophical Society :—
‘picture. He showed, by a collection of examples from the best
English poets, that the established meanings of the word ‘“argu-
ment’”’ are reducible to three: (1) a proof or means of proving;
(2) a process of reasoning or controversy made up of such proofs;
(3) the subject matter of any discourse, writing, or picture. And he
maintained that the second of these meanings ought to be excluded
from scientific language.
December 12.—The following paper from the Astronomer Royal
was read, ‘‘Supplement to the proof of the Theorem that ‘ Every
Algebraic Equation has a Root.’ ”
‘he author expressed his want of confidence in every result ob-
tained by the use of imaginary symbols, and in this supplement
demonstrated that the left-hand member of every algebraic equation
of the form ¢(#)=0 admitted of resolution, either into real linear
factors, or into real quadratic factors.
Professor Miller also made a communication ‘‘ On a new portable
form of Heliotrope, and on the employment of Camera Lucida prisms
and right-angled prisms in surveying.”
February 13, 1860.—The Rev. H. A. J. Munro read a paper .
“On the Metre of an Inscription copied by Mr. Blakesley, and
printed by him in his ‘ Four Months in Algeria,’ p. 285.”
February 27.—The Rev. Professor Sedgwick made the following
communications :—
1. ‘* Anaccount of Mr. Barrett’s progress in the Survey of Jamaica,
with some remarks on the Distribution of Gold Veins.”
2. ‘“Some account of the Geological Discoveries in the Arctic
Regions.”
March 12.—The Rev. Professor Challis made a communication
‘On the Planet within the orbit of Mercury, discovered by M.
Lescarbault.”
By a recent comparison of the theory of Mercury’s orbit with
observation, M. Leverrier found that the calculated secular motion
of the perihelion of that planet requires to be increased by 38", and
that this difference between observation and theory cannot be ac-
counted for by the attractions of known bodies of the solar system.
In a letter addressed to M. Faye, and published in the Paris Meteo-
rological Bulletins of October 4, 5, and 6, 1859, he suggested that
the difference might be due to the attraction of a group of small
planets circulating between Mercury and the Sun. On December 22
of the same year, M. Lescarbault, a physician and amateur astro-
nomer, residing at Orgéres, about sixty miles south-west of Paris,
announced in a letter to M. Leverrier that he had seen on March 26,
1859, a small round spot traversing the sun’s disc, which he con-
sidered to be a planet inferior to Mercury. Naturally much inter-
ested by this information, M. Leverrier went to Orgéres on Decem-
ber 31, and after closely interrogating M. Lescarbault respecting the
particulars. of the observation, and the instrumental means by which
Prof. Challis on the Planet within the Orbit of Mercury. 471
it was made, he returned with the conviction that the observation
was trustworthy, and that a new planet had been discovered
(Comptes Rendus, January 2, 1860, p. 40).
M. Lescarbault had long conceived the idea of detecting inferior
planets by watching the sun’s disk for transits, and in 1858 he put
his project into execution. He was in possession of a good telescope
of 33 inches aperture and 5 feet focal length, mounted with an alti-
tude and azimuth movement, and provided with a finder magnifying
6 times. The power of the eyepiece employed in the observations
of March 26 was 150. Not being furnished with a position-circle,
he adopted the following means of obtaining angular measurements.
The eyepiece of the telescope and the eyeviece of the finder each
had at its focus two wires crossing at right angles, and the wires of
the latter were so adjusted that a star seen at their intersection was
seen at the same time at the intersection of the wires of the telescope.
There were also in the eyepiece of the finder two wires parallel to,
and on opposite sides of, each cross-wire, and distant by about 16’.
A circular card about 6 inches in diameter, and graduated to half
degrees, was placed concentric with the tube of the eyepiece of the
finder, and apparently could be moved both about the tube and, with
the tube, about the axis of the finder. A cross-wire of the telescope
and a cross-wire of the finder were adjusted vertically by looking at
a distant plumb-line, and the diameter of the card containing the
zero of its graduation was placed vertically by means of a small plumb-
line and eye-hole approximately arranged for that purpose. ‘The
mode of using this apparatus for anguiar measurements will be seen
by the following account of the observations. The observer had
also a small transit-instrument by which he obtained true time, using
for timepiece his watch, which, as it only indicated minutes, required
the supplement of a temporary seconds’ pendulum.
In the account which M. Lescarbault gives of his observations, he
says that it had been his practice to examine with the telescope the
contour of the sun for a considerable interval on each day in which
he had leisure, and that at length, on March 26, 1859, he saw a small
round spot near the limb, which he immediately brought to the inter-
section of the wires of the telescope. ‘Then, according to his state-
ment, he quickly turned the graduated card till two of the wires of
the finder were tangents to the sun’s limbs, or equidistant from them.
But it is evident that to effect an angular measurement in this way,
one of the middle wires of the finder must have been placed tangen-
tially to the sun’s limb at the point of their intersection, to which
point the spot had just been brought. Assuming that this operation
was performed, the angular distance of the point from the vertical
diameter of the sun might be read off, as the account states that it
was, by applying the plumb-line apparatus to the graduated card.
This method could only give a rough measure of the angular position
of a point very near the sun’s limb; and in fact M. Lescarbault does
not appear to have attempted to determine the position of the spot
during the interval between the beginning and the end of the
transit. He states that the spot had entered a little way on the sun
4.72 Cambridge Philosophical Society :—
when he first saw it, and that the time and place of entrance were
inferred by estimation.
The following are the immediate results of the observations :—
The spot entered at 45 5™ 36° mean time of Orgéres at the angular
distance of 57° 22' from the north point towards the west, and de-
parted at 55 22™ 44s, at 85° 45! from the south point towards the
west, occupying consequently in its transit 1" 17™ 88. The length
of the chord it described was 9! 14", and its least distance from the
sun’s centre 15! 22, M. Lescarbault also states that he judged the
apparent diameter of the spot to be at most one-fourth of that of
Mercury, when seen by him with the same telescope and magnifying
power during its transit across the sun on May 8, 1845. ‘The lati-
tude of Orgéres is 48° 8' 55", and longitude west of Paris, 2™ 355.
From these data M. Leverrier ascertained, by calculating on the
hypothesis of a circular orbit, that the longitude of the ascending
node is 12° 59!, the inclination 12° 10’, the mean distance 0°1427,
that of the earth being unity, and the periodic time 19°7 days. Also
he found that the greatest elongation of the body from the sun is 8°,
the inclination of its orbit to that of Mercury 7°, the real ratio of
its diameter to Mercury’s 1 to 2°58, and that its volume is one-
seventeenth the volume of Mercury on the supposition of equal den-
sities. This mass is much too small to account for the perturbation
of Mercury’s perihelion. According to these results, the periods at
which transits may be expected are eight days before and after
April 2 and October 5, the body being between the earth and sun
near its descending node at the former period, and near its ascend-
ing node at the latter.
After the announcement of this singular discovery, it was found
that other observations of a like kind had been previously made.
Several instances are collected by Professor Wolf in the tenth num-
ber of his Mittheilungen tiber die Sonnenflecken, eight of which are
quoted in vol. xx. (p. 100) of the Monthly Netices of the Royal
Astronomical Society. ‘I‘wo of these, the observation of Stark on
October 9, 1819, and that of Jenitsch on October 10, 1802, agree
sufficiently well with the calculated position of the node of the object
seen by Lescarbault. But the spot seen by Stark is stated to have
been about the size of Mercury.
Capel Lofft saw at Ipswich, on January 6, 1818, at 11 a.m.,a
spot of a ‘sub-elliptic form,’ which advanced rapidly on the sun’s
disc, and was not visible in the evening of the same day (Monthly
Magazine, 1818, part 1, p. 102).
Mr. Benjamin Scott, Chamberlain of London, saw about mid-
summer of 1847 a large and well-defined round spot, comparable in
apparent size with Venus, which had departed at sunrise of the next
day (Evening Mail, January 11, 1860).
Pastorff of Buchholz records that he saw on October 28 and
November 1, 1836, and on February 17, 1837, two round black,
spots of unequal size, moving across the sun at the respective hourly
rates of 14’, 7", and 28’. Also he announced, January 9, 1835, to
the Editor of the Astronomische Nachrichten, that ‘‘ six times in the
Prof. De Morgan on the Syllogism No. IV. 473
previous year he had seen two new bodies pass before the sun in dif-
ferent directions and with different velocities. ‘The larger was about
3" in diameter, and the smaller from 1” to 1°25. Both appeared
perfectly round. Sometimes the smaller preceded, and at other
times the larger. The greatest observed interval between them was
1’ 16": at times they were very near each other. Their passage
occupied a few hours. Both appeared as black as Mercury on the
sun, and had a sharp round form, which, however, especially in the
smaller, was difficult to distinguish.” Schumacher considered it his
duty as editor to insert the communication, but evidently did not
give credit to it (Astron. Nachr. No, 273).
In vol. ii. of the Correspondence between Olbers and Bessel,
mention is made in p. 162 of an observation at Vienna by Steinhtibel,
of a dark and well-defined spot of circular form which passed over
the sun’s diameter in five hours. Olbers, from these data, estimates
the distance from the sun to be 0°19, and the periodic time thirty
days. It is remarkable that Stark saw about noon of the same day
a singular and well-defined circular spot, which was not visible in
the evening. ‘This is one of the instances in vol. xx. of the Monthly
Notices of the Astronomical Society.
These accounts appear to prove that transits of dark round objects
across the sun are real phenomena; but it would perhaps be prema-
ture to conclude that they are planetary bodies. If the object ob-
served by Lescarbault be a planet, it is certainly very surprising that
it has not been often seen. Schwabe, after observations of the sun’s
face continued through thirty-three years, has recorded no instance
of such atransit. It is probable that now attention has been espe-
cially drawn to the subject, future observations, accompanied by
measures (of which Lescarbault’s are the first instance), may throw
light on the nature of these phenomena.
April 23.—Professor De Morgan read a paper ‘‘ On the Syllogism,
No. IV., and on the Logic of Relations.”
In the third paper were presented the elements of a system in
which only onymatic relations were considered; that is, relations
which arise out of the mere notion of nomenclature—relations of
name to name, as names.. The present paper considers relation in
general. It would hardly be possible to abstract the part of it
which relates to relation itself, or to the author’s controversy with
the logicians, who declare all relations material except those which
are onymatic, to which alone they give the name of formal. Mr.
De Morgan denies that there is any purely formal proposition except
“there is the probability a that X is in the relation L to Y;” and
he maintains that the notion ‘ material’ non suscipit magis et minus ;
so that the relating copula is as much materialized when for L we
read identical as when for L we read grandfather.
Let X..LY signify that X stands in the relation L to Y; and
X.LY that it does not. Let LM signify the relation compounded
of L and M, so that X..LMY signifies that X isan L of an M of Y.
In the doctrine of syllogism, it is necessary to take account of
474, Cambridge Philosophical Society :—
combinations involving a sign of inherent quantity, as follows :—
By X..LM’Y is signified that X is an L of every M of Y.
By X..L,MY it is signified that X is an L of none but Ms of Y.
The contrary relation of L, not -L, is signified by 7. Thus X. LY is
identical with X..7Y. ‘The converse of L is signified by L~*: thus
X..LY is identical with Y..L7'X. ‘This is denominated the
L-verse of X, and may be written LX by those who prefer to avoid
the mathematical symbol.
The attachment of the sign of inherent quantity to the symbols of
relation is the removal of a difficulty which, so long as it lasted, pre-
vented any satisfactory treatment of the syllogism. There is nothing
more in X..LM/Y than in every M of Y is an L~’ of X, or
MY))L~'X, X and Y being individuals; and nothing more in
X..L,MY than in L~'X))MY, except only the attachment of the
idea of quantity to the combination of the relation.
When X is related to Y and Y to Z, a relation of X to Z follows:
and the relation of X to Z is compounded of the relations of X to Y
and Y to Z. And this is syllogism. Accordingly every syllogism
has its inference really formed in the frst figure, with both premises
affirmative. For example, Y.LX and Y..MZ are premises stated
in the third figure: they amount to X..L7'Y and Y..MZ,
giving X../~*MZ for conclusion. This affirmative form of conclu-
sion may be replaced by either of the negative forms X .L~’M’Z or
Re WL
The arrangement of all the forms of syllogism, the discussion of
points connected with the forms of conclusion, the extension from
individual terms in relation to quantified propositions, the treatment
of the particular cases in which relations are convertible, or transi-
tive, or both—form the bulk of the paper, so far as it is not contro-
versially directed against those who contend for the confinement of
the syllogism to what Mr. De Morgan calls the onymatic form.
An appendix follows the paper, on syllogism of transposed quan-
tity, in which the number of instances included in one premise is
equal to the whole number of existing instances of the concluding
term in the other premise.
Mr. J. H. Rohrs also read a paper ‘“‘ On the Motion of Bows, and
thin Elastic Rods.”
May 7.—The Rev. Professor Sedgwick made a communication
“On the Succession of Organic Forms during long geological
periods; and on certain Theories which profess to account for the
origin of new species.”
May 21.—The Public Orator read a paper ‘‘ On the Pronunciation
of the Ancient and Modern Greek Languages.”
He gave a rapid sketch of the ‘‘ Reuchlin and Erasmus” contro-
versy in the sixteenth century, especially the part taken in it at
Cambridge by Cheke, Smith, Ascham, and Bishop Gardiner; and
then proceeded to show how the proper sounds of the Greek letters
may be determined from the following sources ;—~
Pronunciation of the Ancient and Modern Greek Languages. 475
1. Distinct statements of grammarians.
2. Incidental notices in other ancient authors.
3. Variations in writing of inscriptions and MSS.
4. Phonetic spelling of cries of animals.
5. Puns and riddles.
6. The value of the respective letters in other languages employ-
ing the same alphabet, especially Latin.
7. The way in which Latin proper names are spelt in Greek, and
vice versd.
8. The traditions of pronunciation preserved in modern Greek.
He concluded that, on the whole, the method of Erasmus ap-
proached more nearly to the ancient pronunciation than that of
Reuchlin.
‘«« But,” he proceeded, ‘“‘ when we consider the untrustworthiness
of each of these sources of evidence taken singly, and when moreover
we find them often in conflict with one another, it cannot be ex-
pected that the result should be very certain or very satisfactory.
There are also other considerations which enhance the difficulty of
the inquiry. As there were very marked dialectic varieties in Greece,
so there may have been local variations even in Attica itself.
“The pronunciation, too, changed from time to time. Plato gives
us proof of this in the ‘ Cratylus.’ ”
After quoting several instances, and showing that great changes
both in pronunciation and spelling had taken place in modern lan-
guages, French, Spanish, and English, ‘it would,” he said, ‘be
hopeless to attempt to determine the pronunciation of any language
by a reference to its orthography at a time when both were perpe-
tually changing. But in the history of every nation there arrives a
time when the creative energy of its literature seems to have spent
itself; when, instead of developing new forms, men begin to look
back and not forward, to comment and to criticise. ‘Then it is that
a language begins to assume, even in minor and merely outward
points, such as pronunciation and spelling, a fixity and rigidity
which it retains with scarcely any change so long as the nation
holds together. Such a period in Greek history was that which
began with the grammarian sophists in the fifth century B.c., and
culminated in Aristarchus and Aristophanes of Byzantium. In the
spelling and pronunciation of Greek there was probably very little
change from that time to the end of the third century a.p.”
October 19.—Dr. Paget made a communication ‘“‘ On some Points
in the Physiclogy of Laughter.”’
November 12.—The Public Orator read a paper (a sequel to that
on May 21) ‘‘On the Accentuation of Ancient Greek.”
The question of accents was not discussed in the Reuchlin and
Erasmus dispute. At that time all pronounced according to the
system of accents introduced by the Greeks of Constantinople, who
first taught the ancient language to the Italians.
It was probably in Elizabeth’s reign that we began to disuse the
old pronunciation of vowels both in Greek and Latin; and concur-
rently with this change we, as well as the other nations of Europe,
476 Cambridge Philosophical Society.
began to pronounce Greek, not with the modern Greek, but with
the Latin accent. Jhe reasons were :—
1. Teachers speaking the modern Greek were no longer required,
so the tradition was not kept up.
2. It saved much trouble to pronounce both languages with the
same accentuation.
3. The Greek accent perpetually clashes with quantity; the
Latin much more rarely; never, indeed, in that syllable of which
the quantity is most marked—the penultima.
Isaac Vossius (1650-60) advocated the disuse of accentual marks
altogether, as the invention of a barbarous age to perpetuate a bar-
barous pronunciation.
After showing the meaning of the word ‘accent’ as applied to
modern languages, and discussing the accentuation of the German,
English, French, &c., he proceeded to say:
‘There are three methods of emphasizing a syllable:—
1. By raising the note;
2. By prolonging the sound ;
3. By increasing its volume.
‘«Scaliger, De Causis Lingue Latine, lib. ii. cap. 52, recognizes
this division when he says that a syllable may be considered of three
dimensions in sound, having height, length, and breadth.
«‘ Now in our own language, when we accent a syllable, which
of these dimensions do we increase? Generally all three, but not
necessarily ; for when the prayers, for example, are intoned, 2. e.
read upon one note, the accent is marked by increasing the volume
of sound (the third method), which involves also a longer time in
utterance, 7. e. a lengthening of quantity. In speaking, all three
methods are employed, but one more prominently than the other,
according to individual peculiarities of the speakers. What we
blend, the Greeks kept distinct.
‘«* We cannot understand the Greek system unless we bear this in
mind. ‘They never confounded accent with quantity. Ineradicable
habit prevents us from reverting in practice to their method, just as
they would have been unable to comprehend ours.
«Tt is clear from Dionysius, De Comp. Verb. lib. xi. cap. 75, that
the dialogue in tragedy preserved the ordinary accentuation, which
was disregarded only in choral passages set to music.”
The practical conclusion was this: that while it would be desirable,
if possible, to return to the Erasmian system of pronunciation, it
would be extremely absurd to adopt the barbarous accentuation of
modern Greek, which has quite lost the old essential distinction
between accent and quantity. In this respect, as we cannot recover
practically the ancient method, it is better to keep to our own system
of the Latin accent, which does not confuse the learner’s notion of
quantity in verse as the modern Greek does.
An Athenian boy has the greatest difficulty in comprehending the
rhythm of Homer or Sophocles. Hence it is not blind prejudice
(as Professor Blackie asserts) which makes us keep to our old usage,
but a well-grounded conyiction that we should lose more by changing
than we should gain. ‘rae
Intelligence and Miscellaneous Articles. 477
November 26.—Professor Challis made a communication “‘ On the
Solar Eclipse of July 18, 1860.”
December 10.—Mr. Seeley read a “‘ Notice of Opinions on the
Red Limestone at Hunstanton.”
Professor Miller also described “ An Instrument for measuring the
radii of arcs of Rainbows.”
February 11, 1861.—Mr. H. D. Macleod read a paper ‘‘ On the
present State of the Science of Political Economy.” ,
The writer took a general survey of the science as it at present
exists, testing several generally received doctrines by the principles
of inductive logic, and earnestly enforcing the necessity of a thorough
reform of the whole science, which must be constructed on prin-
ciples analogous to those of the other inductive sciences.
February 25.—Dr. Humphry made a communication ‘On the
Growth of Bones.” }
March 11.—The Master of Trinity made a communication ‘‘ On
the Timzeus of Plato.”
LXX. Intelligence and Miscellaneous Articles.
ON THE OPTICAL PROPERTIES OF THE PICRATE OF MANGANESE.
BY M. CAREY LEA.
So and Haidinger have described a remarkable property
possessed by certain crystalline surfaces, of reflecting, besides
the ray normally polarized in the plane of incidence and reflexion,
another ray, polarized perpendicularly to that plane, and differing
from the former in being coloured—a property rendered more con-
spicuous by the fact that the colour of the ray so polarized abnormally
is either complementary to, or at least quite distinct from the colour of
the crystal itself.
I find that this property is possessed to a remarkable degree by the
picrate of manganese. ‘This salt crystallizes in large and beautiful
_ transparent right-rhombic prisms, sometimes amber-yellow, some-
times aurora-red, exhibiting generally the combination of principal
. prism, and macrodiagonal, brachydiagonal and principal end planes.
In describing this substance in a paper on picric acid and the picrates*,
I mentioned that in a great number of specimens examined, no planes
except those parallel with or perpendicular to the principal axis had
been met with. Since then I have obtained in several crystalliza-
tions specimens exhibiting a brachydiagonal doma; but this appears
to be rather unusual.
The optical properties of this salt are very interesting. It exhihits
a beautiful dichroism. If the crystal be viewed by light transmitted
in the direction of its principal axis, it appears of a pale straw-colour,
in any other direction, rich aurora-red in some specimens, in others
salmon-colour. A doubly refracting achromatized prism gives images
of these two colours, unless the light be transmitted along the principal
axis of the crystal of picrate, in which case both are pale straw-colour. -
* Silliman’s American Journal, Noy. 1858.
478 Intelligence and Miscellaneous Articles.
But it also possesses in a high degree the property of reflecting
two oppositely polarized beams ; and the great size of the crystals in
which it may readily be obtained renders it peculiarly fitted for
optical examination. If one of these crystals be viewed by reflected
light while it is held with its principal axis lying in the plane of in-
cidence and reflexion, the reflected light is found to be not pure
white, but to have a purpleshade. Examined witha rhombohedron
or an achromatized prism of Iceland spar, having its principal axis
in the plane of incidence and reflexion, the ordinary image is white
as usual, while the extraordinary is of a fine purple colour, the phe-
nomenon having the greatest distinctness when the light is incident
at the angle of maximum polarization.
The experiment may be varied and the purple light beautifully
seen without the use of a doubly reflecting prism, by allowing only
light polarized perpendicularly to the plane of incidence to fall on
the crystal; in this case the surface of the crystal appears rich deep
purple, no white light reaching the eye.
This property is not possessed by all the planes of the crystal, but
is limited to the principal prism and brachy- and macrodiagonal end
planes, in other words, to the planes parallel with the principal axis
of the crystal. The brachydiagonal doma and OP planes do not
possess it. Nor is it exhibited by the first-mentioned planes when
the crystal is turned with its prismatic axis at right angles to the
plane of incidence.
All specimens of picrate of manganese do not possess this pro-
perty to an equal extent. The crystals vary considerably in colour,
and those which are full red exhibit it more strongly than the amber-
coloured. Picric acid boiled with aqueous solution of cyanhydro-
ferric acid and saturated with carbonate of manganese, gives crystals
of a rich deep colour, which exhibit the purple polarized beam par-
ticularly well.
These properties are not possessed by the manganese salt alone,
but also by the picrates of potash and ammonia ~ (especially when
crystallized by very slow spontaneous evaporation in prisms of suffi-
cient size), and the picrates of cadmium and peroxide of iron—with
this difference, however, that while the prismatic axis of the crystal
in the case of the cadmium and manganese salts must be in the plane
of incidence, in the alkaline salts it must be perpendicular to that
plane. As they all crystallize in the right-rhombic system, it is pro-
bable that either the alkaline salts on the one hand, or the manganese
and cadmium on the other, are prismatically elongated in the direction
of a secondary axis.
It is convenient that distinct phenomena should have distinct
names; and none appears to have been assigned to this. Brewster
speaks of it as a ‘‘ property of light,” and Haidinger uses the word
“Schiller” for it. The terms dichroism, trichroism, and pleiochroism
are limited to properties of transmitted light. I therefore suggest
for the phenomenon here in question the name catachroism, using the
preposition cara in the same sense as in the word xarorzpigw, to
reflect (as a polished surface), applying it to express the property of
Intelligence and Miscellaneous Articles. 479
reflecting two beams—one normally polarized in the plane of in-
cidence, and the other polarized in a plane perpendicular to it,
The chromatic properties exhibited by the picrates of ammonia
and potash are very remarkable in their variety. Their crystals
possess :—
Ist. The well-known play of red and green light. If a little very
dilute solution of pure picrate of potash be spontaneously evaporated
in a hemispherical porcelain basin, so as to form a network of ex-
tremely slender needles, and these be viewed by gas-light, the play
of colours is singularly brilliant.
2nd. Dichroism. When by spontaneous evaporation of large quan-
_ titres of solution of potash, or, better, of ammonia salt, transparent
prisms of =); to ;4 inch diameter are obtained; these, viewed witha
doubly refracting prism by transmitted light, give two images—one
pale straw-colour, and the other deep brownish red.
3rd. The above-described property of catachroism, or reflexion in
the plane of incidence of oppositely polarized beams.—Silliman’s
American Journal, November 1860.
EXPERIMENTS ON THE POSSIBILITY OF A CAPILLARY INFILTRA-
TION THROUGH POROUS SUBSTANCES, NOTWITHSTANDING A
STRONG COUNTERPRESSURE OF VAPOUR. POSSIBLE APPLICA-
TION TO GEOLOGICAL PHENOMENA. BY M. DAUBREE.
In the grand phenomena which are to us the principal manifesta-
tions of the activity of the interior of the globe, we see every day
enormous quantities of water disengaged as steam from great depths.
It may be asked if these incessant losses are not partially at least
made up by a supply from this surface; and if so, in what way are
these infiltrations effected ?
It would be difficult to imagine that this supply was produced by a
free circulation; for the way open for a descent would at the same
time form an outlet also for the escape of vapour; and this objection
would apply more especially to the volcanic regions, where the in-
ternal vapour has sufficient tension to send columns of lava with a
density two or three times that of water, to great heights above the
level of thesea. In trying to reconcile these apparent contradictions,
I have been led to inquire if water could not reach the deep and
heated reservoirs, which yield it in a variety of ways, not by means
of extended fissures, as has hitherto been supposed, but also by the
porosity and capillarity of rocks.
M. Jamin’s ingenious experiments* have shown how considerable
is the influence which capillarity exerts in changing the conditions
of equilibrium, established through the intervention of a liquid
column, between two opposite pressures.
But in previous experiments the temperature was the same in all
parts of the capillary tube. It appeared important, more especially
in reference to the geological problemewhich I have indicated, to see
what would happen if the temperature was much higher at one part of
* Phil. Mag. vol. xix. p. 204,
480 Intelligence and Miscellaneous Articles.
the capillary passage, so as to convert the liquid into vapour, and
thus change it into a state in which it would probably not be subject
to the laws which at first had caused its infiltration.
I have constructed an apparatus, the principal object of which was
to connect, by a porous plate of fine close-grained sandstone, on the
one end a closed space in which the tension of vapour measured by
a manometer was 14 atmosphere, and on the other a space in direct
communication with the air, half-filled with water, which soon
reached the boiling-point, but where the pressure could not exceed
that of the atmosphere.
Although the thickness of the interposed plate was only 2 centi-
metres, the apparatus showed that the water is not driven back by
the counterpressure of vapour; the difference of pressure on the two
sides of the plate does not prevent the liquid from passing from the
relatively cold region towards the relatively hot one, by a sort of
capillary process, favoured by the rapid evaporation and drying of the
latter.
The effects of this apparatus, which I cannot explain in detail,
will manifestly be materially augmented by increasing the thickness
of the porous plate, and working with vapour at a higher temperature.
But even these results prove that capillarity, acting in conjunction
with gravity, can, in spite of very powerful internal counterpressures,
force water from the superficial and cold regions of the globe to the
deep and heated parts, where, in consequence of the temperature and
pressure which it acquires, the vapour becomes susceptible of pro-
ducing great mechanical and chemical effects*. Do not the prece-
ding experiments thus touch the fundamental points of the mecha-
nism of volcanos, and of the other phenomena generally attributed
to the development of vapours in the interior of the globe, espe-
cially earthquakes, the formation of certain thermal springs, the fill-
ing metalliferous veins, as well as to various cases of the metamorphism
of rocks? Without excluding the primitive water generally supposed
to be incorporated in the internal melted masses, do not the same
experiments show that infiltrations from the surface may also be
operative, so that the deeper parts of the globe would be in a daily
State of giving and taking, and that by a most simple process,
although very different from the mechanism of the siphon and of
ordinary springs? A slow, continuous, and regular phenomenon
would thus become the cause of sudden and violent manifestations,
like explosions and ruptures of equilibrium. —Comptes Rendus, Janu-
ary 28, 1861.
* It is known that water penetrates into the pores of most rocks, espe-
cially those belonging to the stratified formations, as is shown by the water
which they generally contain in nature. Bischoff has long called the atten-
tion of geologists to this fact. Although the granite on which the sedi-
mentary rocks rest is usually very impermeable, it has been traversed in
many places by injections of eruptive rocks. Among the latter there are
some, like the trachytes, so porous that they might well be particularly sus-
pected of establishing a permanent capillary communication between the
water of the surface and the heated masses which form the base of this
kind of column.
ere, A any |
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THE
LONDON, EDINBURGH ann DUBLIN
PHILOSOPHICAL MAGAZINE
AND
JOURNAL OF SCIENCE,
SUPPLEMENT to VOL. XXI. FOURTH-SERIES.
LXXI. On the Reflexion of Light at the Boundary of two Isotropic
Transparent Media. By L. Lorenz*.
AMIN, as is well known, discovered that Fresnel’s formule
for the intensity of the rays reflected and refracted at the
boundary of two isotropic transparent media do not perfectly
agree with experiment, the difference bemg very considerable
when the angle of incidence approaches to the angle of polariza-
tion. Cauchy had already proved that, under these circum-
stances, waves must be produced with longitudinal vibrations ;
and having assumed that these waves were absorbed very rapidly
(though not instantaneously, since in that case he would have
returned to the formule of Fresnel), he now introduced a cor-
rection into the formule which caused them to agree with ex-
periment.
All calculations, however, which have hitherto been made
concerning the reflexion and refraction of light, have proceeded
on the hypothesis of an instantaneous passage from one medium
to the other, and a consequent instantaneous change of the
index of refraction. Such a passage is, however, a mere meta-
physical abstraction, which cannot possibly exist in nature; and
the calculation would be more exact and more satisfactory if a
gradual passage were admitted between the two media through
a space which might afterwards be assumed to be as small as we
please. It is, moreover, a fact that bodies are really surrounded
by an atmosphere which must produce such a gradual change of
refraction.
The object of this paper is to show that Jamin’s experiments
can only be reconciled with Fresnel’s formule when the calcula-
tion is made on the above hypothesis. —
In what follows, the case of total reflexion will not be con-
sidered.
If the incident light be polarized in the plane of incidence,
* Translated by F. Guthrie, from Poggendorff’s Annalen, vol. cxi. p. 460. -
Phil, Mag. 8, 4. No. 148, Suppl, Vol. 21. 21
482 M. L. Lorenz on the Reflexion of Light at
the angle of incidence being called x, and that of refraction z,,
the ratio of the amplitudes of the incident, refracted, and reflected
light, according to Fresnel, is
2cosasinz, sin (#—z2z,)
"sin (w+ 2) ‘sin (w@+a,) (2)
1 1
For the light polarized perpendicularly to the plane of incidence,
the ratio of the same three amplitudes is
2cosx sin 2, _ _ tan (e@—2,) (2)
"sin (@+2,)cos(w—az,) © tan (w@+ 2)
Assume now that these formule are correct when the difference
between x and 2, is infinitely small, so that 2, =x+dz. - Sub-
stituting this value of x, the above expressions become -
dz dx
sin 22 ) sin 2a"
de dz
sin 2a ° tan 2a”
L:1+
1+ (4)
We suppose that the incident ray approaches the bounding sur-
face of the media at an angle a, and that its direction is there
gradually changed by having to traverse successive parallel refrac-
tive layers, until it emerges completely into the other medium
at the constant angle £.
In order to simplify the calculation, we will in the first in-
stance neglect the retardation of the ray.
Let A be the amplitude of the incident ray, and let this
become y and y+dy for the refracted ray, when the angle of
incidence, a, becomes xz and x+dz. Then, whatever may be
the polarization, we have, according to (3) and (4 (4),
dy 22 dx
y sin Qa?
from which, by integrating and determining the constants,
we get
tan @
a tan a
The ray reflected from this layer, if it be polarized in the plane
of incidence, has, according to (3), the amplitude a
and if polarized perpendicularly, it has, according to (4), the
amplitude OY These two values we indicate by xdu,
‘x
tan 22
where, in the first case,
scies doe tara). 2s: sy elena
the Boundary of two Isotropic Transparent Media. 483
and in the second,
uo led sin Dye eee eee 2 6}
The amplitude of the reflected ray is therefore
tan @
xXdu= A A/a a
and when this ray encounters a layer whose angle of refraction
is @,, its amplitude becomes
qf 2 ay / 22 ay
bane
At the boundary between this layer and the following, where
the angle of refraction is z,—dvz,, a portion of the light is again
reflected ; and uw, being the same function of z, that w is of iz
the amplitude of the twice reflected ray 1S
—A oa du du, 3
and when this ray ae traversed all the layers until its angle of
refraction has become constant and equal to @, its amplitude is ©
—A 2s B du dup.
tan e
_The angle x, may now have all values between « and x, and
a all values between « and 8. The sum, therefore, of the am-_
plitudes of all the twice reflected rays will be represented by:
the definite double integral
VE:
DEVE eng di a Fr :
where wu, and ug indicate the me a of u mt x equal to a, and a.
equal to £.
In this manner the sum of the amplitudes of the rays reflected
4, 6,.... times can easily be calculated; and as the sum of the
different rays that have been 0, 2, 4, 6... times reflected make
up the whole of the refracted ray, the amplitude of the latter is
Ee aw i au" du +f ae" anf" "a4 ditg—
tan @
which we shall indicate by
A tana)
tan a
jp @
48 4, M. L. Lorenz on the Reflexion of Light at
where
Ji) = -{" du (Jan sea)
U Uy
From the last equation we get by differentiation
f(uy= (“au fea)
Uy
and
flu =f(u) 2
flu) = cel + eye,
where the constants ¢ and e¢, are to be determined by the equa-
tions
which gives
Wh f(ua) =1, and f"(u,)=0.
ence
U—U ue —U
4 —_ € a +e€ a 2
fe) Or eae
€ tea 8B
and the value of (7) or the amplitude of the refracted ray is
oA tan 8
ee
ee Vee a
If now we wish to find the amplitude of the refracted ray
polarized in the plane of incidence, which we will call B, we
must in the above expression substitute
eae PR
u=—tlogtanz,
and we shall find
2) cos aisinye
Ba2A— eae: aa (9)
If, on the other hand, in (8) we substitute
u= + log sin 2a,
we find for B’, the amplitude of the portion of the refracted ray
polarized perpendicularly to the plane of incidence,
eis cosasin 8
Rae sin («+ 8) cos («—£)’
We return, therefore, exactly to Fresnel’s formule, which is a
remarkable property of those expressions. The calculation only
assumes the relations indicated by (3) and (4); and these expres-
sions might have been deduced from many other formule than
Fresnel’s.
The amplitude of the reflected ray, which is the sum of the
(10)
the Boundary of two Isotropic Transparent Media. 485
amplitudes of the rays reflected 1, 3,5... times, may be simi-
larly found, and may be expressed as follows:
» ? ? u
u u u u u u u Ve B
7, ( P du ( du, ( Plus+ | P du du, "dua ing | duUy—...
c e Uy e Un e Uy e uy et e uy e Vy Ug
for which we will put
A { *8 ul fu)
Ua
and
asi - ("i aes)
o uy
From the last equation we get
flu)= aes
et Uae
whence (11) or the amplitude of the reflected ray is
Ug—Ug__ Ug—Uq
oT ie ea
Pia va 2s euig—Ua
And substituting w= —4}logtanz, we get for the amplitude of
the portion polarized in the plane of incidence, which we will
call R,
_, sin (a—£)
Beran (2+)
If KR! is the amplitude of the ray polarized perpendicularly to
the plane of incidence, and if in (12) we substitute u= 4 log sin2z,
we get
(18)
1, tan (a—8)
Se oe (2+)
In this case also, therefore, we return to Fresnel’s formule.
The result is, that even if there be a gradual change of the
index of refraction between the two media, and consequently an
infinite number of reflexions at the boundary, Fresnel’s formule
nevertheless remain true so long as the thickness of the inter-
mediate layers is infinitely small as compared with the length of
a wave. If this be not the case, then the retardations of the dif-
ferent rays must be taken into consideration.
For the refracted light this correction is very small, and could
hardly be confirmed by experiment. We shall therefere proceed
to calculate it in the case of the reflected hght.
|)
heal
- 486 M. L. Lorenz on the Reflexion of Light at
A wave which is reflected by the layer whose angle of refrac-
tion is 2, Or 2), Y,-.., and afterwards interferes with the wave
reflected by the first layer, will be retarded relatively to the latter ;
and we may indicate the successive retardations of phase by the
letters 6, 5,, 6,,.... These quantities are functions of a, 2,
X_q.-.3 but may also be regarded as functions of wu, wu, Ug)... -
We ‘may therefore represent the amplitude of the ray reflected
once at the layer whose angle of refraction is 2, by ;
A cos (At—96) du,
where ¢ is the time, and £ a constant.
For reasons analogous to those stated above, it is easy to see.
that the amplitude of all the reflected rays may be expressed by |
“8 “B
A \ du cos (kt—8) — ( inf du,
Uy ”~ Uy
This series is the real part of
* (kt—8) V1
af du «€ Tu);
Uy
Pi, inthe 5 28 — 92) +.. J. 08)
“where
FL =f ay dug €6:-5:)¥=1 f(g).
Uy Uy
From this last equation we may deduce the differential equation
d | -wai |= aS ea a 8; |
then
an _ alee ie 2(u— 2(Upg— do 7
aT oc Seemmmer B ‘G (u—ug) __ 2(ug )) = du.
If in this expression we substitute the value of wu, it is obvious
a" dn.
that for all angles of incidence aa 8 small so long as 7 1S 80,
which is the only hypothesis.
If now we substitute for /(w) its values as found in (15), then
series (15) becomes the real part of
— Pp la Ug Mga as
3 eae oe ar bet de
ela— Up 4 lp Me du .
and its sum is therefore
Ug—Ug __ Ug—U, Ug 2(u—Ug) __ 2(ug—u) d,
: [ cos e+ inf Se SSeS Te eee oF :
2s > au
elas 4 Mp Ya Uy e2(u,—Ug)_ _2(U,— Mn) des
And substituting again in this expression for u its value
—tlogtanz, we get for R the amplitude of the reflected ray
polarized in the plane of incidence,
epee -/) [cos kt+ sin kt tan A]
sin (2+) ! ‘ey
_ sindcosa BD ee ee: dé
tan A= Se (cos? 6 tan 2— sin? cot A sn dz.
If, on the other hand, for u we substitute $ log sin 2z, we get
for the amplitude of the reflected ray polarized perpendicularly
to the plane of incidence,
1 _ , tan (a—P) : -
R/=—A tan (2 +8) [cos A¢-+sin kt tan A’)
sin2asin28 (8 ie 2¢ sin ad db
SS —— - = — dk.
sin? 2a—sin?26} Lsm28 sin 2z
. dz
From these equations it may be seen that tan A, for all angles
(17)
tan A! =
of incidence, is small provided Ta is so also; while, on the con-
trary, tan A’ may be infinite, as when sin 2¢=sin 28; that is,
when the angle of incidence is equal to the angle of polarization,
in which case # and 6 are complementary. m:
488 M. L. Lorenz on the Reflewion of Light at
If A’, for a given angle of incidence, is a small positive quan-
tity, it gradually approaches = as the angle of incidence ap-
proximates to the angle of polarization, and afterwards approaches
givclf, on:-the contrary, A’ is a small negative quantity, on
changing the angle of incidence A! approaches -3 and —7r.
The retardation of the phase of the reflected ray R!, compared
with the other polarized in the plane of mcidence R, may be ex-
pressed by A’—A if the coefficients of cos kt have the same sign
for both rays, that is to say, when the angle of incidence is
greater than the angle of polarization. If, however, A’ and A
be always taken in the first positive or negative quadrant, we can
introduce any multiple we please of 27, and therefore express the
retardation by A!—A + 2pzr, where p is a whole number.
If now A is positive for this angle of incidence, it will increase
as the angle of incidence diminishes ; and when the angle of in-
cidence becomes less than the angle of polarization, and A! is
taken in the first quadrant, the retardation of phase will be ex-
pressed by
A'—A+(2p+41)7r
If, on the other hand, A! is negative for an angle of incidence
greater than the angle of polarization, the retardation of phase
will become A!—A + (2p—1)z7, if the angle of incidence is made
less than that of polarization. These results agree with those of
Jamin. In the first case Jamin puts y=—1, whereby the re-
tardation of phase becomes
A'—A—27 for a+B> =,
A'—A—wa for atp ZF;
Al—A-+ @ for atB). But
we have, however, seen above that this case answers to that of
bodies with a positive reflexion.
Calculation therefore, like experiment, proves that positive
reflexion occurs in the case of bodies with a greater index of
refraction, negative reflexion in the case of bodies with a smaller
index, while the difference of phase in the case of bodies which
lie between these passes suddenly from 0 to +7.
The intensity of the reflected light polarized perpendicularly
to the plane of incidence is, according to (17),
tan? (2—£)
2 2 Al).
tan? ere is.
the intensity of the reflected light polarized in that plane is,
according to (16),
“ULL ow (1-+ tan? A),
sin? (@ + B)
If the ratio of these two intensities be expressed by k*, we get
p= 0% (2+) cosA (20)
~ cos (a—Z£) cos Al”
These results agree with those of Cauchy.
As Jamin has in his experiments determined these magnitudes
directly, it is possible from his experiments, that is, from the
Mr. A. Cayley ona Surface of the Fourth Order. 491
principal angle of incidence, and the index of refraction, to de-
cae the value of A, and consequently by (18) the value of
e dv. If now it be supposed that p can be approximately de-
I —
termined by a , the thickness of the intermediate layers
=
can be deduced from the experiments.
In this way we have a new means of testing the theory, since
this requires that the thickness in question should be small and
positive. The calculation from Jamin’s experiments shows that
this is actually the case, though, as might be expected, no great
degree of exactness can be thus attained in the determination
of these quantities. Ihave found that the thickness of the layers
a the case of the bodies experimented on lies between 55 and .
rho of the length of a wave.
It appears, therefore, that the result of Jamin’s experiments.
can be completely explained on the simple supposition of an ex-.
ceedingly thin stratum of intermediate layers in which there is
a gradual change of refractive power, a supposition which we.
have obyiously- more right to make than to omit.
- Copenhagen, June 28, 1860.
LXXII. On a Surface of the Fourth Order.
By A. Cavity, Esq.*
iP! A, B, C be fixed points; it is required to investigate
the nature of the surface, the locus of a point P such that
AAP + ~BP+rvCP=0,
where A, p, v are given coefficients; the equation depends, it is
clear, on the ratios only of these quantities.
_ The surface is easily seen to be of the fourth order; it is ob-
viously symmetrical in regard to the plane ABC; and the section
by this plane, or say the principal section, is a curve of the fourth
2 hee the locus of a point M such that
AM + pBM +7CM=0.
The curve is considered incidentally by Mr. Salmon, p. 125
of his ‘ Higher Plane Curves ;’ and he has remarked that the two
circular points at infinity are double points on the curve, which
is therefore of the eighth class. Moreover, that there are two
double foci, since at. each of these circular points there are two
tangents, each tangent of the one pair intersecting a tangent of
the other pair in a double focus; hence, further, that there are
* Communicated by the Author.
492 Mr. A. Cayley on a Surface of the Fourth Order.
four other foci, the points A, B, C, and a fourth point D lying
in a circle with A, B, C, and which are such that, selecting any
three at pleasure of the points A, B, C, D, the equation of the
curve is in respect to such three points of the same form as it is
in regard to the points A, B, C.
Consider a given point M, on the principal section, then the
equations
gain Se! gel) eee meh FN
BM CM’ CM AM’ AM’ BM
belong respectively to three spheres: each of the spheres passes
through the point M. The first of the spheres is such that,
with respect to it, B and © are the images each of the other;
that is, the centre of the sphere hes on the line BC, and the pro-
duct of its distances from B and C is equal to the square of the
radius; in like manner the second sphere is such that, with
regard to it, C and A are the images each of the other; and the
third sphere is such that, with regard to it, A and B are the
images each of the other. The three spheres intersect in a
circle through M at right angles to the principal plane (that is,
the three spheres have a common circular section), and the equa-
tions of this circle may be taken to be
Oe ee
AM” BM” CM’
It is clear that the circle of intersection lies wholly on the surface.
The spheres meet the principal plane in three circles, which
are the diametral circles of the spheres ; these circles are related
to each other and to the points A, B, C, in hke manner as the
spheres are to each other and to the same points. The circles
have thus a common chord; that is, they meet in the point M
and in another point M’. And MM! is the diameter of the circle,
the intersection of the three spheres.
It may be shown that M, M! are the images each of the other
in respect to the circle through A, B, C. In fact, consider in
the first place the two points A, B, and a circle such that, with
respect to it, A, B are the images each of the other; take Ma
point on this circle, and let Q be any point on the line at right
angles to AB through its middle point, and join OM cutting the
circle in M’; then it is easy to see that M, M’ are the images
each of the other, in regard to the circle, centre O and radius
OA (=OB). Hence starting with the pomts A, B, C and the ~
point M, let O be the centre of the circle through A, B, C, and
take M! the image of M in respect to this circle ; then considering
the circle which passes through M, and in respect to which B, C
are images each of the other, this circle passes through M’; and
Mr. A. Cayley on a Surface of ihe Fourth Order. 493
so the circle through M, in respect to which C, A are images
each of the other, and the circle through M, in respect to which
A, B are images each of the other, pass each of them through M’ ;
that is, the three circles intersect in M!.
It is to be noticed that M’, being on the surface, must be on
the principal section; that is, the principal section is such that,
taking upon it any point M, and taking M! the image of M in
regard to the circle through A, B, C, then M! is also on the
principal section. It is very easily shown that the curve of the
fourth order possesses this property ; for M, M’ being images.
each of the other in respect to the circle through A, B, C, then
A, B, C are points of this circle, or we have
MA MB MC”
WA MB MC?
that is, the equation :
AM +»BM+rvCM=0
being satisfied, the equation
VAM! + wBM!'+vCM'=0
is also satisfied.
The points M, M! of the curve, which are images each of the
other in respect to the circle through A, B, C, may be called
conjugate points of the curve. The above-mentioned circle, the
intersection of the three spheres, is the circle having MM! for
its diameter; hence the required surface is the locus of a circle at
right angles to the principal plane, and having for its diameter
MM’, where M and M! are conjugate points of the curve.
In the particular case where the equation of the surface is
BC.AP+CA.BP+AB.CP=0,
the principal section is the circle through A, B, C, twice repeated.
Any point on the circle is its own conjugate, and the radius of
the generating circle of the surface is zero; that is, the surface
is the annulus, the envelope of a sphere radius 0, having its
centre on the circle through A, B,C. Or attending to real
points only, the surface reduces itself to the circle through
A, B, C. But this last statement of the solution is an incom-
plete one. ‘The equation of an annulus, the envelope of a sphere
radius c, haying its centre ona circle radius unity, is
Vxrty=l+ V¥e—2?;
and hence putting c=0, the equation of the surface is,
Va? +y2=ltzi
494 Mr, A. Cayley on a Surface of the Fourth Order.
(if, as usual, i= “—1), or, what is the same thing, it is
af + y* + (2+1)?=0;
that is, the surface is made up of the two spheres, passing through
the points A, B, C, and having seach of them the radius zero ;
or say the two cone- spheres through the pots A, B,C. In
other words, the equation
BC,.AP+CA.BP+AB.CP=
is the condition in order that the four points A, B, C, P may lie
on a sphere radius zero, or cone-sphere. Using 1, 2, 8, din
the place of A, B, C, P to denote the four points, the last-men-
tioned equation becomes
12,34+18.42414.23=0;
and considering 12, &c. as quadratic radicals, the rational form
of this equation 1s
— 9 ee &
Oo= 0, 19, 18, ie pein oi
2] . ) 0 > 93, 24
Shin Haier oQepiaide
—ew) | ———en DB ——9
47, 42, 48, 0
In my paper “On a Theorem in the Geometry of Position,”
Camb. Math. Journ. vol. uu. pp. 267-271 (1841), I obtained
this equation, the four points being there considered as lying in
a plane, as the relation between the distances of four points in a.
circle, in addition to the relation
a AO node
Sn Ge aam o RROnramene
iy ssT
]
which exists between the distances of any four points in a plane,
The present investigation shows the signification of the equation
O = 0 between the distances of four points in space; viz. it
expresses that the four points he in a sphere radius zero, or
cone-sphere. But the formula in question is im reality eluded
in that given in the paper for the distances of five pomts in.
space. Por calling the points 0, 1, 2, 3, 4, the relation between
the distances of these five points is
Chemical Notices :—Preparation of solid Carbonic Acid, 495
peste) aciqe phe wig | ‘eal
Bie tlh geo Dk ». OR gh DBrytrer OH
er. Ye ie te
ed Ba tO eae
eee a 2, ORR
Hence if 1, 2, 3, 4 are the centres of spheres radii a, B, y, 8,
and if O is the centre of a tangent sphere radius 7, we have
Ol=r+a, O2=r+P, O8=rty, 04=r4+6;
so that, for any given combination of signs, it would at first
sight appear that r is determined by a quartic equation; but by
means of a simple transformation (indicated to me by Prof. Syl-
vester) it may be shown that the equation for 7 is really a qua-
dratic one ; morcover, the equation remains unaltered if the signs
of a, B, y, 6 and of r, are all reversed; and 7? has thus in the
whole sixteen values. In particular, if «, 8, y, 6 are each equal
0, then r? is determined by a simple equation (r the radius of
the sphere through the four points) ; and if, moreover, r=O,
then we have for the relation between the distances of the four
points, the foregoing equation 0=0.,
2 Stone Buildings, W.C.,
March 25, 1861.
cn A a = pescmmasitainnntnmmntiieniiil
-
ana a = —— = = TT
LXXIII. Chemical Notices from Foreign Journals.
By i. Arxinson, Ph.D., FCS.
[Continued from p. 365. |
M. LOIN and Drion* describe the following method of ob-
taining solid carbonic acid, merely requiring for its prepa-
ration apparatus within the ordinary reach of the laboratory. It
depends on the great cold produced by the evaporation of liquid
sulphurous acid. Liquid ammonia is placed in a glass vessel,
and connected with the receiver of an air-pump by a vessel con-
taining pumice impregnated with sulphuric acid. On exhausting,
the temperature of the liquid ammonia rapidly sinks, and it com-
mences to solidify at —81° C.; when the pressure is reduced to
1 millim., the temperature of the liquid ammonia is —89%5,
This is sufficient for the liquefaction of carbonic acid under the
ordinary atmospheric pressure ; for when a current of dry carbonie
* Comptes Rendus, April 15, 1861.
496 M. Deville on the Formation.of Staurotide and Zircon.
acid is passed through a U-tube dipping in the’ammonia, a small
portion of it liquefies.
By increasing the pressure to some extent, considerable quan-
tities of carbonic acid may be readily solidified. About 150
cubic centims. of liquid ammonia are introduced into an inverted
bell-jar provided with a collar, on which a plate perforated with
two apertures is hermetically fitted. In the central aperture there
is a tube closed at one end and reaching to the bottom of the
jar; the other aperture serves to connect the apparatus with the
air-pump. ‘The carbonic acid is produced -by heating dried bi-
carbonate of soda to reduess in a copper flask. This flask is con-
nected with the tube dipping in the liquid ammonia, and also
with a small air-manometer. All the air having been expelled
from the apparatus, and the temperature of the liquid ammonia
reduced to near solidification, the flask is heated until the mano-
meter indicates a pressure of 3 to 4 atmospheres. Crystals of
carbonic acid soon begin to form on the inside of the tube,
and in half an hour about 25 grammes of solid carbonic acid
are obtained, forming a thick layer on the inside of the tube
which dips in the liquid ammonia.
This solid carbonic acid is a colourless mass, as transparent as
glass ; it may be detached from the tube by touching it with a
glass rod, and is seen to consist of small cubical crystals. Iix-
posed to the air, these crystals slowly evaporate without leaving
any residue; they may be placed on the hand without producing
any sensation either of heat or of cold: they can be scarcely
seized between the fingers. Mixed with ether and exposed to
the air, they form a freezing mixture, the temperature of which
is —81° C.
The temperatures were observed by MM. Loir and Drion, by
means of an alcohol thermometer on which two fixed points
had been marked; that is, 0° the temperature of melting ice,
and —40° the temperature of melting mercury. The liquid
ammonia was prepared by Bussy’s method*, of passing gaseous
ammonia into a flask surrounded by liquid sulphurous acid, the
evaporation of which was promoted by the air-pump. In this
way 6 to 7 fluid ounces may be obtained without difficulty in
the course of two hours.
The following experiments by Deville} throw considerable
light on the formation of some native minerals.
When fluoride of silicon was passed over calcined alumina
heated to whiteness in a porcelain tube, fluoride of aluminium
was disengaged, and staurotide formed analogous in all its pro-
* Phil. Mag. vol. xx. p. 202.
+ Comptes Rendus, April 22, 1861.
M. Schiitzenberger on some New Salts. 497
perties to the natural mineral. This experiment was repeated in
a modified manner.
In a porcelain tube placed vertically, a series of alternate layers
of alumina and quartz were arranged, the alumina being at the
bottom, and the quartz at the top; fluoride of silicon was then,
passed through the tube at a white heat. In this way the fluo-
ride of silicon meeting alumina was decomposed, and staurotide
formed; but the fluoride of aluminium which was formed at the
same time was decomposed on coming in contact with the layer
of quartz, with the formation also of staurotide and regeneration
of fluoride of silicon. The same process followed with all the
successive layers ; so that the quartz and alumina were both con-
verted into staurotide, and, as the last layer was quartz, as much
fluoride of silicon left the apparatus as entered it. None of the
fluorine was fixed, and it served no other purpose than to cause
the combination of two of the most stable bodies in nature.
From the formula of topaz, which is a silicate of alumina and
fluoride of silicon, it was probable that it might be formed in a
similar way. But direct experiments showed that this is not the
ease; and Deville is inclined to think that it is formed in the
moist way.
In the expectation of obtaining phenakite, Deville heated glucina
in fluoride of silicon. He obtained a mineral which crystallizes
well, and consists of silica and glucina, but could not be iden-
tified with any known mineral species.
When fluoride of silicon was passed over zirconia, beautiful
octahedral crystals were obtained which had all the characters of
the native zircon. An experiment of Deville’s seems to show
that a very small quantity of fluorine can produce an indefinite
quantity of this mineral.
Alternate layers of zirconia and quartz were placed in a por-
celain tube, commencing with the former and ending with the
latter, anda current of fluoride of silicon was passed through the
tube at a white heat. The zirconia in contact with fluoride of
silicon was changed into zircon and volatile fluoride of zircon ;
the latter meeting quartz, gave zircon also and fluoride of silicon ;
and so on with the whole of the layers. The contents of the
tube were entirely mineralized, and the quantity of fluoride of
silicon which left the tube was equal to that which entered it.
No fluorine had been fixed.
In a subsequent communication Deville will describe a method
for obtaining metallic sulphurets by the dry way.
Schiitzenberger* has described a new class of salts, in which
the electro-negative elements chlorine, bromine, iodine, &c.
* Comptes Rendus, January 238, 1861.
Phil. Mag, 8. 4. No, 143, Suppl. Vol, 21. 2K
498 M. Schiitzenberger on some New Salts.
are substituted’ for the basic hydrogen, the metals, &. He
has effected this by acting on salts with such compounds as
chloride of iodine and iodide of cyanogen. The formation of
acetate of iodine will illustrate this class of actions, which is sus-
ceptible of great extension.
C4 H8 NaO4 + IC] = NaCl+C* H3I 04.
Acetate of | Chloride Acetate of
soda. of iodine. iodine.
These bodies, as may be expected, are endowed with special
properties, and especially are very unstable.
Anhydrous hypochlorous and acetic acids mixed in equivalents
form a red mixture, which soon becomes decolorized. A slight
excess of hypochlorous acid imparts to it a red tint, which is
removed by heating the mixture to a temperature not exceeding
30°. This body is the acetate of chlorme, C+ H? ClO*; its com-
position is that of chloracetic acid, but it differs greatly in pro-
perties. It dissolves immediately in water, producing hypo-
chlorous and acetic acids, and explodes at 100°, with formation
of chlorine, oxygen, and anhydrous acetic acid. Singularl
enough it is attacked by mercury even in the cold, with libera-
tion of chlorine, and formation of acetate of mercury and a little
calomel—
C* H® ClO*+ Hg =Cl+ C* H? Hg O*4,—
Acetate of Acetate of
chlorine. mercury.
a curious instance of the replacement of chlorine by a metal. _
It dissolves iodine instantaneously without becoming coloured,
and disengages chlorine; acetate of iodine is formed, a white
crystalline solid isomeric with iodacetic acid.
C* H® ClO* + T= C* H31I 04+.
Acetate of Acetate of
chlorine. iodine.
Another mode of forming this body has been given above. It
is decomposed at 100° into iodine, oxygen, and acetate of
methyle.
2(C* H 104) = I? + C? O44 C4 H8 (C? H3) Of.
Acetate of Acetate of
iodine, methyle.
It is decomposed by water into iodic acid, iodine, and acetic acid.
Butyrate of iodine is formed by the action of chloride of iodine
on butyrate of soda. Acetate of bromine is obtained by the
action of bromine on acetate of chlorine.
Sulphur dissolves in acetate of chlorine with disengagement
of chlorine; but the acetate of sulphur which forms is very un-
stable, for it soon decomposes into anhydrous acetic acid, sul-
M. Lourengo on Polyglyceric Alcohols. 499
phurous acid, sulphur, and chlorine. The action of iodide of
cyanogen on acetate of silver forms iodide of silver, and appa-
rently iodide of cyanogen.
These interesting facts are capable, as Wurtz suggests*, of
another interpretation, by assuming that the bodies are mixed
anhydrous acids. Thus the acetate of chlorine is hypochlor .
acetic anhydride, and Wurtz expresses its formation in the fol-
lowing manner :—
ayo + GeH96 $= 9 Ineghengieel Xe)
Cl C* H°0
Anhydrous Anhydrous Lt hypo-
hypochlorous acetic acid. - chioracetic acid.
acid,
Lourengo has described} a series of new compounds, the
polyglyceric alcohols. They bear the same relation to glycerine
that the polyethylenic alcohols { do to glycol. These latter bodies
were obtained by the action of hydrochloric glycol on glycol in
excess: the formation of the new bodies is quite analogous; it
ensues when hydrochlorate of glycerme acts on glycerine im
excess. Lourengo saturated a portion of glycerine with hydro-
chloric acid gas, and having added to it an equal quantity of
elycerine, he heated the whole to 180° C. for several hours in a
flask connected with a condenser so that the distillate fell again
into the flask. The result of this action was a very thick brown
liquid, which was distilled under a pressure of 10 millims. A
body was obtained boiling at 220°—230° under this pressure.
It had the composition €° H™ 0°, and its formation may be thus
expressed :—
3 yI5 3 FS 3H
a ida ee }O-+ HCL
moet New Me
RErOOhS a
glycerine.
This body, which Lourengo names pyroglycerine, or diglyceric
alcohol, is formed by the condensation of two molecules of gly-
cerine and elimination of one molecule of water. It is analogous
in its chemical eet ae to Graham’s pyrophosphoric acid.
eons" PO,
ce He" Los PO, 40%,
H+ H
Pyroglycerine. Pyrophosphoric acid.
* Répertoire de Chimie, April 1861.
t+ Comptes Rendus, February 25, 1861.
t Phil. Mag. vol. xix. p. 124.
2K2
500 M. Lourengo on Polyglyceric Alcohols.
Besides this there was formed at the same time another body
of analogous properties, but possessing a greater viscosity. It
boils at 275° to 285° under the pressure of 10 millims. ; it has
the composition €9 H®°@7, and is derived from three molecules
of glycerine with elimination of two molecules of water. It is
analogous to triethylenic alcohol in the series of condensed
glycols.
In the crude product from which these bodies were obtained,
there were several chlorine compounds which distilled at the
ordinary atmospheric pressure, and were separated by fractional
distillation. A portion of this, boiling between 230° and 270°,
which chiefly consisted of hydrochlorate and dihydrochlorate of
pyroglycerine, was treated with potash, by which chloride of
potassium was formed, and a body obtained which, on purifica-
tion and analysis, was found to have the composition
C3 H°
(6 F1294— C3 Hs}
H2
It is metameric with glycide, the existence of which has been
placed out of doubt by Reboul’s researches*. Lourenco names
it pyroglycide ; it stands in the same relation to pyroglycerine
that glycide does to glycerine, being formed from it by the eli-
mination of water.
€° H® ¢? H°
13 pO" —H?O= : how
Glycide.
2(€3 He 2(C8 HP;
(E Ht }O°—H?O= (G He +
Pyroglycide.
There is another way of obtaining these polyglyceric alcohols,
which throws some light on their formation. When glycerine
was heated, and the part collected which distilled between 130°
and 266°, and this portion treated with ether, an insoluble residue
was left. This body gave distillates up to 300°, under a pres-
sure of 10 millims., consisting of pyroglyceric alcohols. It is
highly probable that in this decomposition, glycerine losing
one molecule of water forms glycide, and this combining with
one, two, or three equivalents of glycerine, forms polyglyceric
compounds ; just as oxide of ethylene, in acting upon one, two,
or three equivalents of glycol, forms polyethylenic alcohols.
Lourenco points out that the formation of these polyethylenic
alcohols suggests a plausible explanation of the formation of the
different modifications of metaphosphorie acid, which are ob-
* Phil, Mag. April 1861.
M. Freund on Butyryle. 501
tained by heating microcosmic salt, or acid phosphate of soda.
i Graham’s metaphosphate of soda acts lke glycide or oxide of
ethylene, and by successive condensations gives rise to the differ-
ent modifications of the acid.
PO CH? 1:
20h 2
Ht 0?—H? O= Nat O?, corresponding to ~ yy to ‘
Acid phosphate Metaphosphate Glycide.
of soda. of soda.
3 ys
fo + - Nat po asg-* © Nae f Q*, corresponding to ac me ro
[?
Maddrell’s meta- ee) renee
phosphate of soda.
Freund* has made a series of experiments on the preparation
of the oxygen radicals of the formic acid series by the action of
metals on the chloride of these acids, a method analogous to that
of the preparation of the ether radicals.
When chloride of acetyle was treated with sodium-amalgam
no action ensued in the cold, and the action set up at a higher
temperature produced a complete decomposition with forma-
tion of empyreumatic substances. The action of chloride of
butyryle, €¢*H’ OCI, on sodium-amalgam gave better results.
When slightly warmed together, an action was induced which
disengaged heat sufficient to continue it ; the flask was connected
with a Liebig’s condenser, so that the distillate flowed back.
After a short time the mixture was distilled; the unaltered
chloride passed off; the residue, consisting of mercury, chloride
of sodium, and butyryle, was digested with water, and the buty-
ryle which rose to the surface removed. The chloride of buty-
ryle which had distilled off was treated again with sodium-
amalgam, and the process repeated until a large quantity of
butyryle had been accumulated. This was digested with car-
bonate of potash, washed, dried over chloride of calcium, and
rectified. No product of constant boiling-point was obtained ;
but a portion distilling between 260° and 280° gave on analysis
numbers agreeing with the formula of butyryle, or rather dibu-
tyryle, €? H'™# on Sl oo Its formation may be thus ex-
pressed :—
ieee +2Na= Gaya f 4+ 2NaCl.
Chloride of Sodium. Butyryle.
butyryle.
* Liebig’s Annale, April 1861.
502 | M. Martius on the Platinum Metals.
' The action of strong potash on butyryle is very energetic ;
butyrate of potash is formed as well as a substance of a pleasant
odour, which has the composition of the ketone of butyric acid,
but in properties appears to be quite different.
Martius* has published an investigation on the cyanides of the
metals associated with platinum. In their preparation he used
the residues obtained from the manufacture of Russian platinum.
The method of separating the metals which he adopted is a com-
bination of several methods, and presents some interesting points.
The residues were finely powdered, and the larger grains of
osmium-iridium separated by decantation. The residue having
been dried and heated, was fused with a mixture of lead and oxide
of lead, by which all the silicates and other similar impurities
passed into the slag, and a lead regulus was obtained containing ©
all the platinum metals. When this was treated with diluted
nitric acid, a residue was left consisting principally of iridium and
osmium-iridium. The latter was separated by decantation. To
bring it into a state of fine powder, which could not be effected
in the ordinary way on account of its hardness, it was melted
with zinc in a carbon crucible, by which it was dissolved ; when
this mass was afterwards heated! in a wind furnace, the zinc was
expelled and the mineral left in a state of fine powder.
The osmium-iridium was then heated in a current of oxygen ;
some osmic acid was formed, which volatilized, and was collected
in a well-cooled receiver. The residue and the iridium were
then mixed with an equal weight of common salt, and heated in
a current of chlorine; the mass was dissolved in water, and the
solution which contained the double chlorides was boiled with
aqua regia, by which osmium was removed as osmic acid, and
was received in a solution of ammonia. The residual solution
was then mixed with sal-ammoniac, which precipitated everything,
excepting a little rhodium, as ammonium double salt. The pre-
cipitate consisting principally of iridium, but containing also some
platinum and ruthenium, was fused with cyanide of potassium
to convert it into eyanides; this was boiled with hydrochloric
acid to decompose excess of cyanide of potassium, and then sul-
phate of copper added, which gave a red precipitate of the cop-
per salt.
By digesting this precipitate with baryta water, oxide of copper
was formed and the barium double cyanides. They were easily
separated by crystallization, the platimocyanide of barium being
more insoluble than the iridiocyanide of barium. The small
quantity of ruthenium was contained in the mother-liquor of this
latter salt.
* Liebig’s Annalen, March 1861.
M. Martius on the Platinum Metals. 5038
- Osmiocyanide of Potassium, Os Cy, 2 KCy -+-3HO.—This salt
was prepared byadding cyanideof potassium to a solution of osmie
‘acid, evaporating to dryness, and heating to redness in a covered
crucible. On dissolving out the mass in a small quantity of
water and crystallizing, the salt was obtained in fine yellow
laminz, which belong to the dimetric system, like the ferrocya-
nide of potassium: the osmiocyanide of potassium, besides being
analogous in composition and crystalline form to this salt, has
the still closer resemblance that it exhibits (as a special investi-
gation by Kobell showed) the same abnormities in its optical
relations which have lately been found characteristic of ferro-
cyanide of potassium.
_ By the action of nitric acid on osmiocyanide of potassium a
nitro-compound appeared to be formed. Experiments made to pre-
pare a series of compounds analogous to the ferricyanides were
unsuccessful. Chlorine passed into a solution of osmiocyanide
of potassium, produced a red colour, but on evaporation only
erystals of the double salt of chloride of osmium and chloride of
potassium were obtained.
Osmiocyanide of Hydrogen: Osmiocyanic Acid, Os Cy, 2HCy.—
This substance was obtained in a way analogous to the ferrocyanic
acid: by treating a cold saturated solution of osmiocyanide of
potassium with fuming hydrochloric acid,
_ Os Cy, 2KCy+2HCl = Os Cy, 2HCy + 2KCl,
—a reaction which distinguishes osmium and ruthenium from
other platinum metals—a precipitate was obtamed, which was
filered, washed with strong hydrochloric acid, dissolved in alcohol,
and ether added. In this way the body was obtained in trans-
parent columnar crystals of strongly acid properties.
Perfectly stable in the dry state, osmiocyanic acid decomposes,
when exposed to the air in a moist state, ito cyanide of osmium
and hydrocyanie acid.
When any osmiocyanide is boiled with strong hydrochloric
acid, hydrocyanic acid is disengaged, and a dark-violet precipitate
is formed, which is cyanide of osmium, Os Cy.
When osmiocyanide of potassium is mixed with a persalt of
iron, a splendid violet precipitate is formed, which is as delicate
a test for iron as the ferrocyanide. This precipitate could not be
analysed, on account of its retaining a quantity of water, which
eould not be expelled without decomposition ; but it 1s doubtless
formed according to the equation
2¥e? CB + 30s Cy, 6(KCy = 30s Cy, 2 Fe? Cy? + 6KCL.
When this precipitate was treated with baryta water, sesqui-
oxide of iron was formed, and osmiocyanide of barium passed into
solution and was afterwards obtained in reddish-brown crystals
504 Prof. Challis on Theoretical Physics.
of the trimetric system. Its composition is Os Cy, 2Ba Cy +6HO,
and it is isomorphous with ferrocyanide of barium.
Tridiocyanide of Barium, Ix? Cy*, 3Ba Cy + 18HO.—This salt
was obtained in the process of separating the platinum metals.
It forms well-defined crystals of the trimetric system. When
treated with a proper quantity of sulphuric acid and the mass
exhausted with ether, the iridiocyanide of hydrogen or zridto-
cyanic acid, Ir? Cy?, 3KCy, is obtained in crystalline crusts on
evaporating the etherial solution. It is strongly acid, and its
solution decomposes carbonates. Crystallized from ether it is
anhydrous. he iridiocyanide of potassium, Ir? Cy®, 3KCy, has
been already described by Wohler and by Booth. According to
Martius, the iridiocyanide of barium, which is easily obtained pure,
affords a convenient means of preparing it.
— Rhodiocyanide of Potassium, Rh? Cy?, 3 K Cy.—This salt is ana-
logous in composition and mode of preparation to the preceding
salt, but is acted upon by acetic acid, which is not the case with
the iridium salt. When treated with acetic acid, hydrocyanic
acid is disengaged and a red powder is precipitated, which is the
eyanide of rhodium, Rh? Cy®. This deportment furnishes a means
of separating the two metals.
Martius further remarks upon the preparation of the platino-
cyanides of potassium, and describes some new double cyanides.
LXXIII. On Theoretical Physics.
By Professor CHaruis, /.R.S., F.R.A.S.*
| HAVE been induced to make the following remarks chiefly
because I am unwilling to appear inattentive to the repeated
notices which Mr. Glennie has taken of my mathematical theory
of the physical forces. But I have occasion to do little more
than give my reasons for concluding that nothing which Mr.
Glennie has urged calls for a reply. Of course I do not object
to my hypotheses being tested and scrutinized in all possible ways
that are legitimate: at the same time I must maintain the New-
tonian doctrine, that no arguments can be adduced either for or
against a hypothesis which are not drawn from experience, or
from a comparison of the mathematical results of the hypothesis
with experience. Also it is a necessary condition of a hypo-
thesis that it be expressed in terms which experience makes in-
telligible. Myr, Glennie has not said that the statement of my
hypotheses does not fulfil this condition ; neither has he adduced
any facts contradictory to results mathematically deduced from
* Communicated by the Author.
Prof. Challis on Theoretical Physics. - 505
them. He has not even alluded to my mathematics. I say,
therefore, that there is no argument which I have to meet.
In prosecuting physical inquiry, it appears to be necessary to
proceed by way of hypotheses. But hypotheses of themselves
teach nothing: we /earn by mathematics, as the very name im-
plies, because by mathematics the truth of a hypothesis may be
tested or established. The existence of gravity as a force, and
the law of gravity, are truths which could not be ascertained
by observation alone; but being taken to be true hypothe-
tically, they are proved to be actually true, by the aid of mathe-
matics.
Hence hypotheses respecting the physical forces are deserving
of consideration only so far as they afford a basis for mathemati-
cal reasoning. In fact this quality of a hypothesis is a criterion
of its truth, because all quantitative laws are deducible mathe-
matically from ¢rwe hypotheses. In selecting hypotheses for the
foundation of a general theory of the physical forces, [ had
regard, in the first place, to their conformity with the antecedents
of physical science, and then to the possibility of arguing from
. them mathematically. I have not met-with any which in the
latter respect are preferable to those I have selected, which, con-
sequently, I have good reason to adhere to.
To assume that an atom is of constant form and magnitude,
is, | admit, virtually to call it an indivisible particle, and not, as
Newton does, an undivided particle, “ particula indivisa.” But
as the hypothesis is expressed in perfectly intelligible terms, it
is open to no objection, provided we admit with Newton, that if
by a single experiment it can be shown that the supposed indi-
visibie. particle is divided when a solid mass is broken, the theory
of atoms is untenable. When a physical hypothesis satisfies the
condition of being expressed in terms which common experience
renders intelligible, special observation and experiment, or com-
parisons of its mathematical consequences with facts, alone deter-
mine whether or not it be true. I do not admit that any meta-
physical argument can be adduced either in support of, or against,
a physical hypothesis. Meta-physics come after physics. Ifa
general physical theory should be established on verified hypo-
theses, we should have a secure basis for metaphysical reasoning;
and possibly it might then appear that some of the speculative
metaphysics which have prevailed during the last century are
without foundation.
By the same mode of reasoning, the hypothesis of a universal
fluid ether, the pressure of which varies proportionally to its
density,.1s unobjectionable as a hypothesis, simply because it is
expressed im terms which experience has made intelligible.
Whether it be a true hypothesis, that is, whether such an ether
506 Prof. Challis on Theoretical Physics.
be a reality, is another question. It does not admit of @ priori
proof or disproof, but may be disproved by a single contradictory
fact, or may receive accumulative evidence by the agreement of
its mathematical results with many facts. Now I venture to
assert respecting this particular hypothesis, that the mathema-
tical evidence of its truth and of the reality of a fluid ether
is so varied and comprehensive, that it may be pronounced to
be all but conclusive. My reasons for this assertion are the fol-
lowing :—When a mathematical inquiry is made into the laws of
the motion and pressure of a fluid constituted as above supposed,
certain results are obtained by the formation and solution of par-
tial differential equations which correspond to various pheno-
mena of light. The difference of the intensities of different rays,
the variation of intensity with the distance from a centre, and
the law of the variation, the coexistence at the same instant of
different portions of light in the same portions of space, the
interference and non-interference of different rays, the composite
character of light, its colour, results of compounding colours,
and lastly the polarization of light, are all phenomena which
have their exact analogues in the motions, as mathematically
deduced, of a fluid medium whose pressure varies as its density.
When the number, variety, and speciality of these analogies are
considered, it seems difficult to resist the conclusion that proper-
ties of the fluid ether explain phenomena of light, and that the
phenomena reciprocally give evidence of the reality of the ether.
Some of the properties—for instance, that of transverse vibration,
which accounts for polarization—have been deduced by mathema-
tical reasoning for which I am responsible. I have, however,
given to mathematicians the fullest opportunity of discussing
these parts of the general argument ; and when, as I hope to be
able to do, I go through a revision of the propositions, further
opportunity will be given. ‘The proof of the reality of the
eetherial medium, drawn from the explanations which the hypo-
thesis of such a medium gives of phenomena of light, is an essen-
tial preliminary of my general theory of physical force, and I am
well aware that on this ground the truth of the theory must be
contested. If this point be carried, the rest, I think, must
follow. |
There is already evidence from experiment that the action of
physical force may be explained hydrodynamically. In the Phi-
losophical Magazine for May (p. 348), Professor Maxwell has
referred to a paper by M. Helmholtz on Fluid Motion, in which
the author points out that lines of fluid motion are arranged
according to the same laws as the lines of magnetic force. This,
which Prof. Maxwell chooses to call a “ physical analogy,” I of
course take to be confirmatory of the hydrodynamical theory of
~ On the Presence of a Medium pervading all Space. 507
magnetic force. In the same light I regard the experiments of
Professor Wiedemann, mentioned in vol. xi. No. 42 of the ‘ Pro-
ceedings of the Royal Society,’ the results of which point to the
same conclusion.
Cambridge Observatory,
May 22, 186].
ney
LXXIV. On Phenomena which may be traced to the Presence of
a Medium pervading all Space. By Daniex VauGHAN.
i the permanent change which seems to have been detected
in the revolution of Encke’s comet be not sufficient to
establish the doctrine of a space-pervading ether, it may afford
reasonable motives for examining other indications of the im-
pediments of such a fluid to celestial motion. The direct in-
formation which can be obtained on this subject is at present very
limited and uncertain. The approximate investigations hitherto
given by mathematicians of the cause of the perturbation of the
planets, necessarily overlook many slight effects of their mutual
attraction ; and we are thus prevented from discovering the un-
periodical changes which a small resistance to their movements
might occasion. In addition to this, we are ncommoded by the
want of observations made during very long periods of time; for
these are as necessary in tracing the course of remote physical
events, as an extensive base-line is in determining the distances
of the fixed stars. But by investigating the necessary conse-
quence of a resisting medium, and testing the result by a com-
parison with observed facts, we may be enabled to base our con-
clusions respecting this important question on evidence no less
satisfactory than that which has already served to establish many
of the received doctrines of physical science.
As there has prevailed among some astronomers an impression,
not unwholly unfounded, in regard to a modification which the
sun’s attractive power 1s supposed to experience from the emis-
sion of his light, it seems advisable to give special attention to
cases in which the central body is not luminous; and certain
phenomena, observed in the secondary systems and in the dark
systems of space, afford evidence not vitiated by any effects which »
light might be expected to produce. In my communication in
the Philosophical Magazine for last April, 1 showed that a
satellite impeded by the resistance of a medium would, by an im-
perceptibly slow diminution of its orbit, be finally introduced
into the region of instability, where its dismemberment must be
inevitable, and where it must be transformed into a ring, similar
* Communicated by the Author.
508 Mr. D. Vaughan on Phenomena which may be traced
in all respects to those of Saturn. Butit might be premature to
suppose that the annular appendage of Saturn has originated in
this manner, or that it is to be regarded as an index of mutability
in the heavens, if the conclusion were not supported by investi-
gations of a different character. Were the rings two integral
solid masses, the imner one, even with the most favourable
velocity of rotation, would require to be composed of materials
having over two hundred times the tenacity of wrought iron to
escape being ruptured, in consequence of the enormous strain
arising from a preponderance of centrifugal force on one part, and
of gravity on the other. Even if this danger were removed, solid
rings could not be prevented from striking the planet, unless
each were loadedwith some inequality; and, according to the inves-
tigations of Professor Maxwell, the load must contain about four
anda half times as much matter as the remainder of the ring.
A slight excess or deficiency in the amount of this load would be
fatal to stability ; and the tendency of any fluid or loose solid
matter to the locality where it occurs must add much to the
serious perils and the infirmities of the annular structure.
Regarding the hypothesis of two solid rings as untenable,
Professor Maxwell considers the case of their fluidity, and he
arrives at the conclusion that the fluid composing them would
break up into satellites, unless its density were less than {',
of that of the primary. But, from the result deduced in my
articles in the Philosophical Magazine for December 1860
and April 1861, it is evident that, in so great a proximity to the
central body, any liquid matter would require a far greater
density to exist in the form of independent satellites. In inyes-
tigating the case of a rig of numerous solid satellites, or frag-
ments, he finds a combination of very extraordinary conditions
necessary to prevent the derangements and permanent changes
which collisions and friction are expected to occasion. The bodies
are to be all equal in mass, and placed in regular array around
Saturn; but the intervals between them must be very great
compared with the linear dimensions; and the ratio between
the planet and the ring must, according to his formule, be
greater than 4352 multiplied by the square of the number of
satellites composing the latter. When we consider the vast
number of such bodies required to maintain the continuity of
the ring, and the great improbability that all the immense group
should have the peculiar conditions for preventing one from
striking another, we may regard the essay of the eminent mathe-
matician as a proof that the disconnected matter composing the
annular appendage, whether it be fluid or solid, cannot be main-
tained in its present condition without the occurrence of friction —
and collisions between its parts.
to the Presence of a Medium pervading all Space.. 509
Besides the valid objections which Professor Maxwell urges
against the common idea which regards the rings as two flat
solids, others of a somewhat different character have been
suggested by Mr. Bond, who has embraced the opinion that the
ring is fluid. But whatever be its composition, or whatever
proportions of fluid and solid matter it may consist of, all its
parts must have independent movements around Saturn, and
velocities depending on their distance from his centre. The
attraction of the planet will be an insurmountable obstacle to
their conversion into satellites, and will even prevent them from
concentrating in excessive numbers in any locality; but their
incessant action must be attended with a constant development
of heat and a gradual destruction of motion. In consequence
of the necessary alteration in the orbit of its parts from this
cause, the dimensions of the ring cannot always remain the
same ; and though it is not likely that the nearest edge is ap-
proaching the planet so rapidly as the researches of Struve
and Hansen would indicate, yet, as some change of this nature
is unavoidable, we cannot resist the conclusion that the rings
have been introduced into the zone which they now occupy,
from one in which their matter could only exist im the form of
two satellites. Accordingly there appears to be no ground
for any other inference than that I have adopted, in regard
to the imperceptible diminution of the orbits of secondary
planets by the action of a resisting medium.
In tracing the ultimate effects of a similar impediment to
motion in the dark systems of remote space, we deduce so satis-
factory an explanation of the temporary stars, that we may regard
these celestial apparitions as indicating the existence of the
same ethereal fluid, and manifesting the great revolutions to
which it leads in the condition of the heavenly bodies. In my
last article, I have shown that the instantaneous manner in
which a secondary or a primary planet must undergo a total
dismemberment on coming into fatal proximity with the central
sphere harmonizes in a very decided manner with the astonish-
ing rapidity with which temporary stars attain their greatest
brillancy. This peculiarity, taken in connexion with the com-
paratively slow and gradual decline, is sufficient to set aside the
theory which ascribes such ephemeral exhibitions of light to the
rotation of great orbs, self-luminous on one side and dark on
the other. But this theory, though adopted by Arago and
other eminent astronomers, is liable to a more fatal objection.
This will be apparent when we investigate the circumstances
necessary to make a partially luminous sphere or spheroid display
its brilliancy to the inhabitants of the earth for only seven-
teen months, while its period of rotation has been estimated ‘at
510 Mr. D. Vaughan on Phenomena which may be traced
309 or 318 years. Under the most favourable circumstances
for manifesting such an extraordinary inequality between its
periods of light and darkness, the surface of the supposed
distant sphere must be nearly 200,000,000 times as great as
the part of it sending light to our planet during the period of
maximum brightness. The light, moreover, must have pro-
ceeded from the verge of the invisible disk; and this circum-
stance, taken in connexion with the surprising brilliance of
the star of 1572, together with the invariability of its position,
will compel us to ascribe to the spectral orb in question a dia-
meter far exceeding that of Neptune’s orbit. We must also
regard these vast bodies as solid; for, if composed of liquid or
gaseous matter, they could not have the luminosity confined to
particular localities. Even if stellar movements could permit
us to suppose the existence of such stupendous spheres, the
explanation would be applicable to one or two cases only; and
we must therefore reject a hypothesis whose claims rests solely
on the greater imperfections of others proposed to account for
the same phenomena.
But investigations respecting the necessary course of physical
events in the dark systems afford still more important evidence
in regard to the ethereal contents of space. Were the central
body composed of solid matter, or surrounded with an atmo-
sphere of oxygen, nitrogen, or carbonic acid, a development of
heat and light might be expected to attend the dilapidation of
one of the satellites, or the ultimate incorporation of its matter
with the great orb; but the appearance would not correspond
to that exhibited by the temporary stars. Admutting that a
solid globe, almost as large as the sun, may be rendered so
highly meandescent as to shine like the star of 1572 in its
greatest brilliancy, it would be impossible for it to cool so
rapidly as to become invisible in the course of seventeen months.
Besides this, it may be easily shown that, if our earth had a
diameter of 80,000 miles, with its present density and superfi-
cial temperature, our atmosphere would have its density reduced
a millionfold with an elevation of six or seven miles. Thus,
the greater mass we assign to the central body, the more nar-
row must we regard the atmospheric region where light can be
developed by aérial compression ; and the less display of lustre
could we expect from this cause when a satellite fell from its
stage of planetary existence. But this difficulty will disappear
when we suppose that the ether of space forms for the several
great celestial bodies extensive atmospheres, which are rendered
luminous by adequate compression, or rather by the chemical
action it induces—a theory which becomes necessary to account
for the luminosity of meteors and the perpetual brilliancy of suns,
to the Presence of a Medium pervading all Space. 511
The theory which ascribes the sun’s light to the incessant
fall of meteors to his surface, and which I have controverted in
my article in the Philosophical Magazine for December 1858,
appears to have been suggested by the recently discovered rela-
tion between heat and mechanical energy. From this it may be
estimated that a pound of solid matter, falling to the sun from
a distance of 35,000,000 miles, is capable of generating at
his surface an amount of heat about 4000 times as great as
could be developed by the combustion of a pound of coal in
oxygen gas. But the large amount of heat arising from the
combustion of hydrogen, and other facts and principles con-
nected with thermal agencies, give support to the opinion that
the development of heat must be proportional to the intensity
of the chemical forces by which it is produced; and these must
be commensurate with the degree of elasticity between the
elements concerned in the calorific or the illuminating action. We
have therefore no grounds for supposing that the accession of
temperature imparted to the solar orb by the fall of a body,
even from an infinite distance, is necessarily greater than that
originating from the chemical action of an equal amount of
matter, the elements of which were so elastic as to diffuse them-
selves into space, in opposition to the attractive power of suns
and planets. If the undulatory theory of light be admitted,
the medium which conveys it with nearly a million times the
rapidity of sound, must have a modulus of elasticity almost
1,000,000,000,000 times as great as that of common air. But
though not regarding the ether which gives birth to solar light as
sO Inconceivably elastic, we may safely presume that no matter is
better adapted for sustaining the great fountain of brilliancy by
energetic chemical action, than that whose particles are asso-
ciated with forces sufficiently powerful to cause its diffusion
through universal space.
That the fall of meteors is far more frequent and more con-
spicuous on the sun than on the earth cannot be questioned. If
these small bodies are to be regarded as independent occupants
of space, two large spheres, moving with the same velocity through
the region in which they are located, would each be likely to
receive a number of them proportional to its mass multiplied by
its diameter. The circumstances in which the earth and sun
are placed will change, to some extent, their relative capabilities
of receiving these foreign bodies; but the facts which Mr. Car-
rington’s observations have made known in regard to meteoric
phenomena on the solar disk are not inconsistent with what
might be reasonably expected, and do not indicate any special
provision for feeding our central luminary with regular supplies
of meteorites.
512 Mr. D. Vaughan on Phenomena which may be traced
The definite information which Arago was enabled to furnish
respecting the sun by means of his polariscope, has recently
received an important accession from the labours of Bunsen and
Kirchhoff. A comparison of the spectrum of the sun with that
of various metallic vapours in a state of incandescence, enabled
these chemists to show that potassium, sodium, calcium, and
other elements widely diffused on our globe, enter into the com-
position of the solar atmosphere. Their observations proved,
however, that these substances, while abundant in the sun’s en-
velope, instead of being concerned in producing his light, only
exerted a negative influence—absorbing certain rays, and causing
dark lines to replace the bright ones peculiar to their luminous
vapours. It is therefore evident that the light from the vapours
of the elements alluded to must be overpowered by the rays
emanating from some other source. Professor Kirchhoff has
embraced the opinion that the solid globe of the sun must have
a far higher temperature and a greater illuminating power than
his atmosphere; but the observations with Arago’s polariscope
have afforded positive evidence that solar light does not emanate
from an incandescent solid or liquid body. It appears more
philosophical to conclude that the hght of our great luminary
originates, not from the vapours discoverable in its atmosphere,
but from a more subtle ethereal medium combined with them,
and possessed of far greater illuminating power.
The periodical changes recently discovered in the sun’s spots
seem to furnish a fatal objection to the idea that the self-luminous
condition results from the high temperature of his solid nucleus,
or from the heat developed by its compression. It can scarcely be
doubted that the periodicity of the spots is dependent on the
movements of the planets; and the position of Jupiter seem to
exert the greatest influence on their cecurrence; as recent ob-
servations show, the period of his revolution agrees very closely
with the interval between the times at which the spots are most
numerous. Although it may be premature to express a decided
opinion on so obscure a subject, there seem to be legitimate
motives to justify an examination of the more obvious ways in
which it would be possible for a planet to affect the luminous
condition of the solar disk. If, as Helmholtz contends, the
ocean of heat and light be maintained by the compression of the
sun, the planets can only exert their influence on his spots by
diminishing the weight and pressure of his materials, in the same
manner in which the moon acts to raise tides on our oceans.
But the alteration in the weight of terrestrial matter from lunar
attraction, though extremely small, is about 80,000 times as great
as that which the component parts of the sun experience from the
attractive force of Jupiter. ‘This planet holds the highest place
to the Presence of a Medium pervading all Space., 513,
in its capability of affecting the pressure of the solar matter: it
is almost equalled by Venus, but it. is far superior to the other
members of our system. If, however, the planets moved in circles,
the peculiar action alluded to could only increase the tendency,
of the spots to appear on certain sides of the sun, without mate-
rially increasing the numbers visible during the year. When we
take into consideration the changes occasioned by the eccentri-
city of their orbits, the greatest effect must be ascribed to
Mercury; Jupiter holds the next place; after which we must
rank Saturn and the earth. But even admitting the compressi-
bility of the sun’s materials, his mean diameter could not be
altered more than the ;oth of an inch by the attraction of any of
his planetary attendants; and the variation of temperature from
this peculiar action cannot exceed giath part of a degree (F.).
That so small a variation could be manifested in the appears
ance of the sun’s disk, seems wholly improbable, especially if we
adopt the estimate of Mr. Waterston, which assigns to the great
orb a mean temperature of one thousand million degrees.
Any effect which the planets may be supposed to occasion by
their electric or magnetic forces must be also rendered extremely
feeble in consequence of their great distance. If the great ocean
of solar light is sensitive to the electricity or magnetism of Ju-
piter, the nearest satellite of this planet must feel the power of
his mysterious influence to an extent several million times as
great ; yet no indications of such a fact have been observed.
But supposing the sun’s motion through space to be concerned
in maintaining his effulgence, the planets would derive a far
more considerable influence from the general movement around
the centre of gravity of our system. The position of Jupiter
would change the progressive motion of the great luminary about
twenty-four miles an hour; and the other planets will be at-
tended with results proportional to their masses multiplied by
the square roots of their distances. Now the amount of ether
which the sun collects from space, and the density it attains on
his surface, will depend on the rapidity of his translatory motion;
but I have shown in the Philosophical Magazine for May 1858
another way in which the position of the planets would increase
or diminish the supply of ethereal fuel which sustains the great
solar conflagration.
The idea that the space-pervading medium is condensed by
the attraction of the celestial orbs, is not to be considered a new
hypothesis, but rather a necessary inference from that of Pro-
fessor Encke. Were the density of the subtle fluid uniform,
small and large planets would be so unequally affected by its re-
sistance, that their orbits could not retain the relation necessary
for their stability, and they must be destroyed by collisions long
Phil, Mag. 8. 4, No. 143, Suppl, Vol. 21, 2 1L
514 On the Presence of a Medium pervading all Space.
before the natural term of their existence. This difficulty will,
however, disappear when the effects of planetary attraction in
condensing the medium are taken into consideration. How far
observation of primary or secondary worlds give evidence of un-
periodical changes in our system has not been yet determined
with positive certainty. The constant acceleration of the moon’s
orbital velocity, during the past 2000 years, has been traced by
Laplace to a periodical change in the eccentricity of the earth’s
orbits. But an error in his investigations being lately pointed
out by Mr. Adams, there appears to be some definite ground for
regarding the lunar orbit as subject to a very slow permanent
diminution, which, after some allowance for the effects of tidal
action, we may consider as depending, to some extent, on the
resistance of a medium. The great oblateness which Arago and
Sir William Herschel assign to Mars would indicate that the
time of its rotation has been considerably lengthened, since the
remote period at which it was moulded into its present form ;
and this may be looked upon as circumstantial evidence of the
effects of an ethereal resistance in changing the diurnal motion
of planets. It is only to smaller worlds that we could look for
such results, for in larger orbs the strength of their solid matter
can have little influence in preventing alterations of form to cor-
respond with the relations of gravity and centrifugal force.
As doubts are entertained by some eminent astronomers as to
the sensible ellipticity of Mars, it may be well to refer to certain
appearances which show a slight deviation, at least, in his form
from a figure of equilibrium. The marked indications of atmo-
spheric phenomena around his poles, while they are either wholly
absent or only faintly exhibited in the vicinity of his equator, is so
much opposed to everything we might expect from the condition
of our own globe and the belted appearance of Jupiter, that we
cannot avoid concluding that the aérial ocean of Mars is much
deeper in his polar than in his equatorial regions. Perhaps this
may account for the very discordant results of observations in
determining the extent of the atmosphere of this planet by oc-
cultations of the fixed stars.
It is to the revolutions of comets that astronomical curiosity
has chiefly turned for evidence of the contents of interplanetary
space ; but the advantages of low density in these bodies have
been counterbalanced by the great elongation of their orbits,
which exposes them to very great disturbances from the planets.
During the past eighteen centuries Halley’s comet has occupied
in its revolution a period varying from 74°88 to 79°34 years, ac-
cording to the Table in Mr. Hind’s work on Comets (page 57):
Of the twenty-four consecutive revolutions here recorded, the
first eight average 77°59 years, the next eight 76°84, and the last
On a Four-valued Function of three sets of three-letters each. 515-
76°54 years. This would seem to favour the idea of a perma-
nent diminution of the orbit ; and I understand that: De Vico
regards the movements of his own comet as indicative of a similar
‘result from the widely diffused ether. But the information on
this subject hitherto deemed worthy of the most confidence, has
been derived from the successive returns of Encke’s comet. The
advantages which this body affords for such inquiries depend.
chiefly on the moderate eccentricity of its orbit and the position
of the transverse axis, which is. nearly perpendicular to the line-
of the. sun’s progressive motion. This arrangement must give
a more decided preponderance to the perihelion resistance, which
has the greatest. influence in diminishing the size of the orbit.
As shooting stars are now regarded as small bodies describing
very elongated ellipses around the sun, they seem calculated to
furnish perhaps the most satisfactory means of testing the per-
fection of the celestial vacuum. Supposing these bodies to be
more sensitive to the resistance of the medium than to planetary
disturbances, the transverse axes of their orbits will have a ten-
dency to assume a uniform direction in consequence of the sun’s
progressive motion. From the same cause the planes in which
they move will have their intersections confined for the most
part to a very limited range, and will also exhibit, though im a
less degree, a tendency to coincidence. This peculiar arrange-
ment of their orbits must cause vast swarms of these minute
cosmical bodies to congregate from the most distant parts of the
solar domain to a comparatively narrow region at their perihelion
passage. For the appearance of the zodiacal light and the perio-
dical fall of meteors, I have endeavoured to account in this man-
- ner in a paper sent to the meeting of the British Association
and. published in the Sections (1854, p. 26). My late researches
on the subject exhibit a closer accordance with observed facts
than I could then obtain, and they give much support to the
ideas very prevalent in scientific circles, with regard to the agency
of meteors in reflecting the zodiacal light.
Cincinnati, May 11th, 1861.
LXXVI. Ona Problem in Tactic which serves to disclose the ex-
istence of a Four-valued Function of three sets of three letters
each. By J.J. Syuvester, M.A., F.R.S., Professor of Mathe-
matics at the Royal Mihtary Academy, Woolwich*.
x page 375 of the May Number of the Magazine (in that
paragraph commencing at the middle of the page) I gave
a Table of Synthemes, correct as far as it went, but left in a very
* Communicated by the Author.
212
516 Prof. Sylvester on a Four-valued Function
imperfect state. It was intended to be supplemented with a
material addition which escaped my recollection when, after a
long delay, the proofs of the paper passed through my hands.
The question to which this Table refers is the following :—
Three nomes, each containing three elements, are given; the
number of ¢rinomial triads (1. e. ternary combinations, composed.
by taking one element out of each nome) will be 27, and these
27 may be grouped together into 9 synthemes (each syntheme
consisting of 3 of the triads in question, which together include
between them all the 9 elements). It is desirable to know :—
lst. How many distinct groupings of this kind can be formed.
2nd. Whether there is more than one, and, if so, how many
distinct types of groupings. ‘The criterion of one grouping
being cotypal or allotypal to another is its capability or incapa-
bility of being transformed into that other by means of an inter-
change of elements. Be it once for all stated that the question
in hand is throughout one of combinations, and not of permuta-
tions; the order of the elements in a triad, of a triad in a syn-
theme, of a syntheme in a grouping is treated as immaterial.
As we are only concerned with the elements as distributed into
nomes, the number of interchanges of elements with which we
are concerned is 6x 6? or 1296; the factor 6° arises from the
permutability of the elements of each nome inter se, the remain-
ing factor 6 from the permutability of any nome with any other.
I find, by a method which carries its own demonstration with
it on its face, that the number of distinct groupings is 40, of
which 4 belong to one type or family, and 36 to a second type
or family.
Let the nomes be 1.2.3, 4.5.6, 7.8.9, and let
ce, denote 1.4, 2.5, 3.6 C; denote 1.4, 2,6, 3.5
eno! fired SRY 6y iB o4h) hep gle) Phe,
Gog. 168, 204, B65) ey lah) de
FG 9 7, 9, 8
y denote 8, 9, 7 y' denote 9, 8, 7
apts 8, 7,9
b, denote 1.7, 2.8,3.9 6, dencte 1.7, 2.9, 3.8
bg 5p 41 26080 eee >) A
By ii ar en OF BAT PBB By, A ee
“
1 OD
ee OOD
QO KC
“
“
4, 5, 6
B denote 5, 6, 4 B' denote
6 5
“
of three sets of three letters each. 517
a, denote 4.7, 5.8, €.9 a, denote 4.7, 5.9, 6.8
Rie ets 5.9, 6. 7:..° hag. 5 apednBy, 3.76 Ga8
RIS 7628 gen gh) MeO, 5-8, 6x7
1, 2, 3 ENE
a denote 2, 3, 1 «#' denote 2, 3, 1
3, 1,2 5. Le
I
I take first the larger family of 36 groupings ; these may be
represented as follows :
! !
| aye aye aya aya aya! ay!
Ri I ty
Ae |A\a A,% |A\% Aye a
I
~
! I ! !
dae | get! |agee | age! |dgn ae! | aoe | dou Age aoa Aga | a%
I ! n| ee AAP. !
Azh |Azt |Ag% |Axe |Agh Aza || Age | Axe set (get age! Age
b,8\b,8 |b,6'|b,8 |b,8'|b,8')b,8 \b,8 |b,8'|6,8 | 6,8'\5,8"
BB | ba! by | by!) By8 |b.8' by8 | ba8'|by8 |by8!| bo |b,8'
DB bof | by | By! |ba(3!|048 | by(3' b48 |b58 |b,6"| 848" b48
ay | ay ey levy | evry! iat ci ov ey! Cy ey! ey!
Cay | Coty! | C27 | Cay CoY Cary CY the cary’ eof cory! Col co!
est | Cay | cay \esty!) esty oy est! C3 cosy ext! egy! cst
An example of the development of any one of the above sym-
bolisms into its correspondent grouping will serve to render
perfectly intelligible the whole Table.
Let it be required to develope
6,8
b, (3!
bs oy :
Since
Pi 7 2.9. 3.8 Aus eG 4» thee
mot. 2.7, 3.9. Soh 64 B= 6, d44
pebie.94) 2.8, 8.7 6) 4,5 a ag)
the development required is the following :—
om Samed fh fee fed famed fame fore famed
e e ° ° e. ° . . e
DD QD Sr Or Or
CD OWOONOON
518 Prof. Sylvester on a Four-valued Function
1.7.4 2.97235 5.5.6
127.25 92.9.) 3.8.4
1.7 .6_-2.9 435 48..p
1.8.4" 27 uate), D
128.6282 .7 0: 73.9.4:
1.8.0 2a ok ps aD
1 ls eee: eee
1.9.06 -2.8.50.3.%.4
19.09. 2.6. Od 20
The whole of this family of 36 may be represented under
the following condensed form, according to the notation usual
in the theory of substitutions.
123 123 .1238 . oct! ax aa bB °”)
123 281 312 cn! oly aa aa ae
It remains to describe the principal and most symmetrical
family. This contains only 4 groupings, and may be repre-
sented indifferently under any of the three following forms:
ay
a
a\x
As &
as
aa aa aa aa 1,8 b,f' 6,8 5, ay ey ey ey
Aint Age! det doe! or 6,8 5,6! 5,8 6/3! or Coy Cay! Coty Cony!
age dget! age age 058 0,8! 6,8 6,8! — egy egy! Cay Cty’
In developing, it will be found that each of these three represen-
tations gives rise to the same family of groupings, which from
its importance it is proper to set out in full as follows :—
2.5.8 3.6.9|/1.4.7 2.5.9 3.6.8/1.4.7 2.6.8 3.5.9|1.4.7 2.6.9 3.5%
2.5.9 3.6.7/1.4.9 2.5.8 3.6.7|1.4.8 2.6.9 3.5.7|1.4.9 2.6.8-8.5
2.9.7 3.6.8/1.4.8 2.5.7.3.6.911.4.9 2.6.7 3.5.8/1.4.8 2.627 S.b5
2.6:8 3.4.9/1.5.7 2.6.9 3.4.8/1:5.7 2.4/8 3.6.9|1.5.7 2.4.59 3.6
2.6.9 3.4.7/1.5.9 2.6.8 3.4.7/1.5.8 2.4.9 3.6.7|1.5.9 2.4.8 3.6.
2.6.7 3.4.8/1.5.8 2.6.7 3.4.9)1.5.9 2.4.7 3.6.8)/1.5.8 2.4.7 3.6
2.4.8 3.5.911.6.7 2.4.9 3.5.8|1.6.7 2.5.8 3.4.9|1.6.7 2.5,.950.45
2.4.9 3.5.7/1.6.9 2.4.8 3.5.7/1.6.8 2.5.9 3.4.7/1.659 Jane
2.4.7 3.5.8/1.6.8 2.4.7 3.5.9/1.6.9 2.5.7 3.4.8|1.6.8 2.5.7 3.4
OHO WNI OD CONT
It bios at once from the above Table, that if 3 cubic equa-
tions be given, we may form a function of the 9 roots, which,
when any of the roots of any of the equations are interchanged
inter se, or all the roots of one with all those of any other, will
receive only four distinct values. .
It also follows that we may form with 9 letters an intransitive
group (of Cauchy) containing ™°, i. e. 54, or a transitive group
of three sets of three letters each. 519
containing = ® or 324 substitutions, So the family of 36
groupings lead to the formation of an intransitive substitution
==
- Or 16
group of i. e. 18, and of a transitive group ie
substitutions.
Since 9 letters may be thrown, in at x a : i. e. 280 differ-
an ways, into nomes of 3 letters each, it further follows that by
repeating each of the above two families 280 times we shall
obtain new families remaining unaltered by any substitution of
any of the nine elements inter se, and consequently indicating
the existence of substitution-groups containing
1.°2.3894.5.6.7.38.9 Fl bs 2h Bin Fe Guy 1:8; 9
280 x 36 ia 280 x 4
1. e. 86 and 324 substitutions respectively.
~ In the above solution a little consideration will show that the
method is essentially based on the solution of a previous question,
viz. of grouping together the synthemes of binomial duads of two
nomes of three letters each, which can be done in two distinct
modes, which (if, ex. gr., we take 1.2.8, 4.5.6 as the two
nomes in question) are represented j in the notation used above by
Cy
C5 4a | és Rowe TEly, So, more generally, the groupings of the
Cg Cs
g-nomial g-ads of 7 nomes of s oars may be made to depend
on the groupings of the (g—l)-nomial (g—1)-ads of (r—1)
nomes of selements each. The more general question is to dis-
cover the groupings and their families of the synthemes composed.
of p-nomial g-ads of r nomes of s elements, of which the simplest
éxample next that which has-been considered and solved is to dis-
cover the groupings of the synthemes composed of 54 binomial
triads of 3 nomes of 3 elements each *.
The chief difficulty of calculating @ priort the number of such
groupings is of a similar nature to that which lies at the bottom
of the ordinary theory of the partition of numbers, namely, the
hability of the same groupings to make their appearance under
distinct symbolical representations. Of this we have seen an
éxample in the threefold representation of the principal family
ef 4 groupings just treated of. But for the existence of this
‘* T have ascertained, by a direct analytical method, since the above was.
el that the number of different groupings of the ‘synthemes composed.
of these binomial triads is 144. The number of distinct types or families
is three, one containing 12, another 24, and the third 108 groupings.
520 Notices respecting New Books.
multiform representation of the same grouping we could. have
affirmed: @ priori the number of groupings to be 2 x 3 x 2° or 48,
whereas the true number is only 40. I believe that the above
is the first instance of the doctrine of types making its appear-
arice explicitly, and illustrated by example in the theory of taetie.
It were much to be desired that some one would endeavour to
collect and collate the various solutions that have been given of the
noted'15-school-girl problem by Messrs. Kirkman (in the Ladies’
Diary), Moses Ansted (in the Cambridge and Dubtin Mathematical
Journal), by Messrs. Cayley and Spottiswoode (in the Philosophi-
cal Magazine and elsewhere), and Professor Pierce, the latest and
probably the best (in the American Astronomical Journal), besides
various others originating and still floating about in the fashion-
able world (one, if not two, of which I remember having been com-
municated to me many years ago by Mr. Archibald Smith, F.R.S.),
with a view to ascertain whether they belong to the same or to
distinct types of aggregation.
———
LXXVII. Notices respecting New Books.
A History of the Progress of the Calculus of Variations during the
Nineteenth Century. By 1. Topuunter, M.A., Fellow and Prin-
cipal Mathematical Lecturer of St. John's College, Cambridge.
Cambridge: Macmillan and Co. 1861.
R. ‘TODHUNTER, whose name is already so familiar to the
mathematical student, has at length produced a work of much
greater originality and research than any of his former and more ele-
mentary treatises.
The ‘Calculus of Variations,” one of the most difficult branches
of pure mathematics, has been the subject of the labours of several
eminent mathematicians, Euler, Lagrange, Gauss, Poisson, &c.,
whose successive researches and improvements form an exceedingly
interesting department of scientific history, which, however, has
hitherto been specially treated by only one writer in our own lan-
guage, viz. Woodhouse, whose ‘Treatise on Isoperimetrical Problems
and the Calculus of Variations’ was published in 1810, and is now
an extremely scarce book.
Woodhouse’s work has always received very high praise by such
competent judges as Messrs. Peacock, Herschel, and Babbage, in their
‘Examples ;’ Professor De Morgan, in his ‘ Differential and Inte-
gral Calculus ;’ and Professor Jellett, in his ‘Calculus of Variations.’
But since its publication the calculus has been greatly advanced and
improved ; and it is to record this progress that Mr. ‘l’odhunter has
written the volume before us, which commences where Woodhouse
left off. It is evidently the work of one who thoroughly understands
the science itself, and who has most conscientiously and labo-
riously consulted and studied all the available materials and sources
of information. He unites the qualifications of a sound mathe-
Roval Society. 521
matician and a good linguist—a rare combination. The Memoirs
and ‘l'reatises in the German and Italian languages, as well as those
in the French and Latin, have been completely mastered and ana-
lysed: and some account is given even of a dissertation in the Rus-
sian language. Of those works which are difficult of access to the
English student, a more copious account is given; and throughout
the whole history, ‘‘numerous remarks, criticisms, and corrections
are suggested relative to the various treatises and memoirs which are
analysed. The writer trusts that it will not be supposed that he
undervalues the labours of the eminent mathematicians in whose
works he ventures occasionally to indicate inaccuracies or imperfec-
tions, but that his aim has been to remove difficulties which might
perplex a student’”’ (Preface). We would specially point out the
last chapter in the book (pp. 505-530) as deserving attention in
this respect.
Fully agreeing with Mr. Todhunter as to the “ value of a history
of any department of science, when that history is presented with
accuracy and completeness,” we congratulate him on having pro-
duced a History which so well merits this character of ‘‘ accuracy
and completeness ;” and we sincerely hope that the success of his
present contribution to scientific history may induce him to carry out
the intention expressed in the conclusion of his Preface, viz. ‘‘ to
undertake a similar survey of some other department of science.”
ee - ee
—ee
LXXVIII. Proceedings of Learned Societies.
ROYAL SOCIETY.
(Continued from p. 469.]
June 21, 1860.—Sir Benjamin C. Brodie, Bart., Pres., in the Chair, -
tae following communications were read :—
“Qn the Sources of the Nitrogen of Vegetation ; with special
reference to the Question whether Plants assimilate free or uncom-
bined Nitrogen.” By J. B. Lawes, Esq., F.R.S.; J. H. Gilbert,
Ph.D., F.R.S. ; and Evan Pugh, Ph.D., F.C.S.
After referring to the earlier history of the subject, and especially
to the conclusion of De Saussure, that plants derive their nitrogen
from the nitrogenous compounds of the soil and the small amount of
ammonia which he found to exist in the atmosphere, the Authors
preface the discussion of their own experiments on the sources of the
nitrogen of plants, by a consideration of the most prominent facts
established by their own investigations concerning the amount of
nitrogen yielded by different crops over a given area of land, and of
the relation of these to certain measured, or known sources of it.
On growing the same crop year after year on the same land, with-
out any supply of nitrogen by manure, it was found that wheat, over
a period of 14 years, had given rather more than 30 lbs.—barley,
over a period of 6 years, somewhat less—meadow-hay, over a period
of 3 years, nearly 40 lbs.—and beans, over 11 years, rather more than
50 lbs. of nitrogen, per acre, perannum. Clover, another Leguiminous
———.
522 Royal Society :—
crop, grown in 3 out of 4 consecutive years, had giver an-average of
120 lbs. Turnips, over 8 consecutive years, had yielded about 45 lbs:
~ The Graminaceous crops had not, during the periods referred to,
shown signs of diminution of produce. The yield of the Legumi-
nous crops had fallen considerably. Turnips, again, appeared greatly
to have exhausted the immediately available nitrogen in the soil. The
amount of nitrogen harvested in the Leguminous and Root-crops was
considerably increased by the use of “‘ mineral manures,” whilst that
im the Graminaceous crops was so in a very limited degree.
' Direct experiments further showed that pretty nearly the same
amount of nitrogen was taken from a given area of land in wheat
in 8 years, whether 8 crops were grown consecutively, 4 in alterna-
tion with fallow, or 4 in alternation with beans.
Taking the results of 6 separate courses of rotation, Boussingault
obtained an average of between one-third and one-half more nitrogen
in the produce than had been supplied in manure. His largest
yields of nitrogen were in the Leguminous crops; and the cereal
crops were larger when they next succeeded the removal of the
highly nitrogenous Leguminous crops. In their own experiments
ttpon an actual course of rotation, without manure, the Authors
had obtained, over 8 years, an average annual yield of 57°7 lbs. of
nitrogen per acre; about twice as much as was obtained in either
wheat or barley, when these crops were, respectively, grown year after
year on thesameland. The greatest yield of nitrogen had been in a.
clover crop, grown once during the 8 years; and the wheat crops
grown after this clover in the first course of 4 years, and after beans
in the second course, were about double those obtained when wheat
succeeded wheat.
Thus, Cereal crops, grown year after vear on the same land, had
given an average of about 30 lbs. of nitrogen, per acre, per annum ;
and Leguminous crops much more. Nevertheless the Cereal crop
was nearly doubled when preceded by a Leguminous one. It was
also about doubled when preceded by fallow. Lastly, an entirely
unmanured rotation had yielded nearly twice as much nitrogen as
the continuously grown Cereals.
Leguminous crops were, however, little benefited, indeed fre-
quently injured, by the use of the ordinary direct nitrogenous ma-
nures. Cereal crops, on the other hand, though their yield of ni-
trogen was comparatively small, were very much increased by direct
nitrogenous manures, as well as when they succeeded a highly nitro-
i Leguminous crop, or fallow. But when nitrogenous manures
ad been “employed for the increased growth of the Cereals, the
nitrogen in the immediate increase of produce had amounted to-little
more than 40 per cent. of that supplied, and that in the increase of
the second year after the application, to little more than one-tenth
of the remainder. Estimated in the same way, there had been in
the case of the meadow grasses scarcely any larger proportion of
the supplied nitrogen recovered. In the Leguminous crops the pro-
portion so recovered appeared to be even less; whilst in the root-
erops it was probably somewhat greater. Several possible explana-
On the Sources-of the Nitrogen of Vegetation. 523
tions of this-real- or- apparent loss of the nitrogen supplied by
manure are enumerated.
The question arises—what are the sources of all the nitrogen of
our crops beyond that which is directly supplied to the soil by arti-
ficial means? The following actual or possible sonrces may be
enumerated :—the nitrogen in certain constituent minerals of the
soil; the combined nitrogen annually coming down in the direct
aqueous depositions from the atmosphere; the accumulation of
combined nitrogen from the atmosphere by the soil in other ways ;
the formation of ammonia in the soil from free nitrogen and nascent
hydrogen; the formation of nitric acid from free nitrogen; the
direct absorption of combined nitrogen from the atmosphere by
plants themselves ; the assimilation of free nitrogen by plants.
A consideration of these several sources of the nitrogen of the
vegetation which covers the earth’s surface showed that those of
them which have as yet been quantitatively estimated are inadequate
to account for the amount of nitrogen obtained in the annual pro-
duce of a given area of land beyond that which may be attributed
to supplies by previous manurmg. Those, on the other hand, which
have not yet been even approximately estimated as to quantity
—if indeed fully established qualitatively—offer many practical
difficulties in the way of such an investigation as would afford results
applicable in any such estimates as are here supposed. It appeared
important, therefore, to endeavour to settle the question whether or
not that vast storehouse of nitrogen, the atmosphere, affords to grow-
ing plants any measurable amount of its free nitrogen. Moreover,
this question had of late years been submitted to very extended and
laborious experimental researches by M. Boussingault, and M. Ville,
and also to more limited investigation by MM. Mine, Roy, Cloez,
De Luca, Harting, Petzholdt and others, from the results of which
diametrically opposite conclusions had been arrived at. Before enter-
ing on the discussion of their own experimental evidence, the Authors
give a review of these results and inferences; more especially those
of M. Boussingault who questions, and those of M. Georges Ville
who affirms the assimilation of free nitrogen in the process of vege-
tation.
The general method of experiment instituted by Boussingault,
which has been followed, with more or less modification, in most
subsequent researches, and by the Authors in the present inquiry,
was—to set seeds or young plants, the amount of nitrogen in
which was estimated by the analysis of carefully chosen similar
specimens ; to employ soils and water containing either no combined
nitrogen, or only known quantities of it; to allow the access
either of free air (the plants being protected from rain and dust)—
of a current of air freed by washing from all combined nitrogen—or
of a limited quantity of air, too small to be of any avail so far as any
compounds of nitrogen contained in it were concerned ; and finally, to
determine the amount of combined nitrogen in the plants produced
and in the soil, pot, &c., and so to provide the means of estimating
the gain or loss of nitrogen during the course of the experiment.
524 iieN ~ Royal Society :—
The plan adopted by the Authors in discussing their own experi-
mental results, was—
To consider the conditions to be fulfilled in order to effect the
solution of the main question, and to endeavour to eliminate all
sources of error in the investigation.
To examine a number of collateral questions bearing upon the
points at issue, and to endeavour so far to solve them, as to reduce
the general solution to that of a single question to be answered by
the results of a final set of experiments.
To give the results of the final experiments, and to discuss their
bearings upon the question which it is proposed to solve by them.
Accordingly, the following points are considered :—
1. The preparation of the soil, or matrix, for the reception of the
plants and of the nutriment to be supplied to them.
2. The preparation of the nutriment, embracing that of mineral
constituents, of certain solutions, and of water.
3. The conditions of atmosphere to be supplied to the plants,
and the means of securing them; the apparatus to be employed, &c.
4, The changes undergone by nitrogenous organic matter during
‘decomposition, affecting the quantity of combined nitrogen present,
in circumstances more or less analogous to those in which the expe-
rimental plants are grown.
5. The action of agents, as ozone; and the influence of other
circumstances which may affect the quantity of combined nitrogen
present im connexion with the plants, independently of the direct
action of the growing process.
In most of the experiments a rather clayey soil, ignited with free
access of air, well-washed with distilled water, and re-ignited, was used
as the matrix or soil. In a few cases washed and ignited pumice-
stone was used.
The mineral constituents were supplied in the form of the ash of
plants, of the description to be grown if practicable, and if not, of
some closely allied kind.
The distilled water used for the final rinsing of all the important
parts of the apparatus, and for the supply of water to the plants, was
prepared by boiling off one-third from ordinary water, collecting the
second third as distillate, and redistilling this, previously acidulated
with phosphoric acid.
Most of the pots used were specially made, of poreus ware, with a
great many holes at the bottom and round the sides near to the
bottom. ‘These were placed in glazed stone-ware pans with inward-
turned rims to lessen evaporation.
Before use, the red-hot matrix and the freshly ignited ash were
mixed in the red-hot pot, and the whole allowed to cool over sul-
phuric acid. The soil was then moistened with distilled water, and
after the lapse of a day or so the seeds or plants were put in.
Very carefully picked bulks of seed were chosen ; specimens of the
average weight were taken for the experiment, and in similar speci-
mens the nitrogen was determined.
The atmosphere supplied to the plants was washed free from
On the Sources of the Nitrogen of Vegetation. 525
ammonia by passing through sulphuric acid, and then over pumice-
stone saturated with sulphuric acid. It then passed through a solu-
tion of carbonate of soda before entering the apparatus enclosing the
plant, and it passed out again through sulphuric acid.
Carbonic acid, evolved from marble by measured quantities of
hydrochloric acid, was passed daily into the apparatus, after passing,
with the air, through the sulphuric acid and the carbonate of soda
solution.
The enclosing apparatus consisted of a large glass shade, resting in
a groove filled with mercury, in a slate or glazed earthenware stand,
upon which the pan, with the pot of soil, &c., was placed. Tubes
passed under the shade, for the ingress and the egress of air, for the
supply of water to the plants, and, in some cases, for the withdrawal
of the water which condensed within the shade. In other cases, the
condensed water was removed by means of a special arrangement.
One advantage of the apparatus adopted was, that the washed air
was forced, instead of being aspirated, through the enclosing vessel.
The pressure upon it was thus not only very small, and the danger
from breakage, therefore, also small, but it was exerted upon the
inside instead of the outside of the shade; hence, any leakage would
be from the inside outwards, so that there was no danger of unwashe
air gaining access to the plants.
The conditions of atmosphere were proved to be adapted for
healthy growth, by growing plants under exactly the same circum-
stances, but in a garden soil. The conditions of the artificial soil
were shown to be suitable for the purpose, by the fact that plants
grown in such soil, and in the artificial conditions of atmosphere,
developed luxuriantly, if only manured with substances supplying
combined nitrogen.
Passing to the subjects of collateral inquiry, the first question con-
sidered was, whether plants growing under the conditions stated
would be likely to acquire nitrogen from the air through the medium
of ozone, either within or around the plant, or in the soil; that bod
oxidating free nitrogen, and thus rendering it assimilable by the plants.
Several series of experiments were made upon the gases contained
in plants or evolved from them, under different circumstances’ of
light, shade, supply of carbonic acid, &e. When sought for, ozone
was in no case detected. The results of the inquiry in other re-
spects, bearing upon the points at issue, may be briefly summed up
as follows :—
1. Carbonic acid within growing vegetable cells and intercellular
passages suffers decomposition very rapidly on the penetration of
the sun’s rays, oxygen being evolved.
2. Living vegetable cells, in the dark, or not penetrated by the
direct rays of the sun, consume oxygen very rapidly, carbonic acid
being formed. 7
3. Hence, the proportion of oxygen must vary greatly according
to the position of the cell, and to the external conditions of light, and
it will oscillate under the influence of the reducing force of carbon-
matter (forming carbonic acid) on the one hand, and of that of the
526 at Royal Society :—
sun’s rays (liberating oxygen) on the other. Both actions may:
go on simultaneously according to the depth of the cell; and the
once outer cells may gradually pass from the state in which the.
sunlight is the greater reducing agent to that in which the carbon-
matter becomes the greater.
4. The great reducing power operating in those parts of the plant.
where ozone is most likely, if at all, to be evolved, seems unfavour-:
able to the oxidation of nitrogen; that is under circumstances in
which carbon-matter is not oxidized, but on the contrary, carbonic
acid reduced. And where beyond the influence of the direct rays of.
the sun, the cells seem to supply an abundance of more easily oxi-
dized carbon-matter, available for oxidation should free oxygen or
ozone be present. On the assumption that nitrates are available as
a direct source of nitrogen to plants, if it were admitted that nitrogen
is oxidated within the plant, it must be supposed (as in the case of
carbon) that there are conditions under which the oxygen compound
of nitrogen may be reduced within the organism, and that there are
others in which the reverse action, namely, the oxidation of nitrogen,
can take place.
5. So great is the reducing power of certain carbon-compounds of
vegetable matter, that when the growing process has ceased, and all
the free oxygen in the cells has been consumed, water is for a time
decomposed, carbonic acid formed, and hydrogen evolved.
_ The suggestion arises, whether ozone may not be formed under
the influence of the powerful reducing action of the carbon-com-
pounds of the cell on the oxygen eliminated from carbonic acid by
sunlight, rather than under the direct action of the sunlight itself
—in a manner analogous to that in which it is ordinarily obtained
under the influence of the active reducing agency of phosphorus?
But, even if it were so, it may be questioned whether the ozone
would not be at once destroyed when in contact with the carbon-
compounds present. It is more probable, however, that the ozone
said to be observed in the vicinity of vegetation, is due to the action
of the oxygen of the air upon minute quantities of volatile carbo-
hydrogens emitted by plants.
Supposing ozone to be present, it might, however, be supposed to
act in a more indirect manner as a source of combined and assimilable
nitrogen in the Authors’ experiments, namely,—by oxidating the
nitrogen dissolved in the condensed water of the apparatus—by
forming nitrates in contact with the moist, porous, and alkaline
soil—or by oxidating the free nitrogen in the cells of the older
roots, or that evolved in their decomposition.
Experiments were accordingly made to ascertain the influence of
ozone upon organic matter, and on certain porous and alkaline
bodies, under various circumstances.