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Respiration  Calorimeters  for  Studying 

the  Respiratory  Exchange  and 

Energy  Transformations 

of  Man 


BY 
FRANCIS  G.  BENEDICT  and  THORNE  M.  CARPENTER 


WASHINGTON,  D.  C. 
Published  by  the  Carnegie  Institution  of  Washington 

1910 


CARNEGIE  INSTITUTION  OF  WASHINGTON 
Publication  No.  123 


%%l  JSor*  (g&ttimovt  (pvte* 

BALTIMORE,  MD.,  V.  8.  A. 


PREFACE. 


The  immediate  development  and  construction  of  suitable  apparatus  for 
studying  the  complicated  processes  of  metabolism  in  man  was  obviously  the 
first  task  in  equipping  the  Nutrition  Laboratory.  As  several  series  of  ex- 
periments have  already  been  made  with  these  respiration  calorimeters,  it  is 
deemed  advisable  to  publish  the  description  of  the  apparatus  as  used  at 
present.  New  features  in  the  apparatus  are,  however,  frequently  introduced 
as  opportunity  to  increase  accuracy  or  facilitate  manipulation  is  noted. 

We  wish  here  to  express  our  sense  of  obligation  to  the  following  asso- 
ciates: Mr.  W.  E.  Collins,  mechanician  of  the  Nutrition  Laboratory,  con- 
structed the  structural  steel  framework  and  contributed  many  mechanical 
features  to  the  apparatus  as  a  whole ;  Mr.  J.  A.  Eiche,  formerly  associated 
with  the  researches  in  nutrition  in  the  chemical  laboratory  of  Wesleyan 
University,  added  his  previous  experience  in  constructing  and  installing  the 
more  delicate  of  the  heating  and  cooling  devices.  Others  who  have  aided  in 
the  painstaking  construction,  testing,  and  experimenting  with  the  apparatus 
are  Messrs.  W.  H.  Leslie,  L.  E.  Emmes,  F.  L.  Dorn,  C.  F.  Clark,  F.  A. 
Kenshaw,  H.  A.  Stevens,  Jr.,  Miss  H.  Sherman,  and  Miss  A.  Johnson. 

The  numerous  drawings  were  made  by  Mr.  E.  H.  Metcalf,  of  our  staff. 

Boston,  Massachusetts, 

August  10, 1909. 

iii 


CONTENTS. 


PAGE 

Introduction  1 

Calorimeter  laboratory 3 

General  plan  of  calorimeter  laboratory 3 

Heating  and  ventilating 7 

The  calorimeter 10 

Fundamental  principles  of  the  apparatus 10 

The  calorimeter  chamber 11 

General  construction  14 

Prevention  of  radiation 17 

The  thermo-electric  elements 19 

Interior  of  the  calorimeter 20 

Heat-absorbing  circuit 22 

Thermometers   26 

Mercurial  thermometers 26 

Electric-resistance  thermometers 28 

Air-thermometers    28 

Wall  thermometers 29 

Electrical  rectal  thermometer 29 

Electric-resistance  thermometers  for  the  water-current 29 

Observer's  table 31 

Connections  to  thermal- junction  systems 33 

Rheostat  for  heating 34 

Wheatstone  bridges  34 

Galvanometer  35 

Resistance  for  heating  coils 35 

Temperature  recorder  36 

Fundamental  principle  of  the  apparatus 38 

The  galvanometer 39 

The  creeper 40 

The  clock 42 

Installation  of  the  apparatus 42 

Temperature  control  of  the  ingoing  air 43 

The  heat  of  vaporization  of  water 44 

The  bed  calorimeter 45 

Measurements  of  body-temperature 48 

Control  experiments  with  the  calorimeter 50 

Determination  of  the  hvdrothermal  equivalent  of  the  calorimeter 52 

General  description  of  the  respiration  apparatus 54 

Testing  the  chamber  for  tightness 54 

Ventilation  of  the  chamber : 54 

Openings  in  the  chamber 55 

Ventilating  air-current   57 

Blower    57 

Absorbers  for  water-vapor 58 

v 


VI  CONTENTS. 

PAGE 

General  description  of  the  respiration  apparatus — Continued. 

Potash-lime  cans . 60 

Balance  for  weighing  absorbers 61 

Purification  of  the  air-current  with  sodium  bicarbonate 63 

Valves 63 

Couplings 64 

Absorber  table 65 

Oxygen  supply 67 

Automatic  control  of  oxygen  supply 69 

Tension  equalizer  71 

Barometer  72 

Analysis  of  residual  air 73 

Gas-meter 75 

Calculation  of  results 76 

Analysis  of  oxygen 76 

Advantage  of  a  constant-temperature  room  and  temperature  control 77 

Variations  in  the  apparent  volume  of  air 77 

Changes  in  volume  due  to  the  absorption  of  water  and  carbon  dioxide  78 

Respiratory  loss 78 

Calculation  of  the  volume  of  air  residual  in  the  chamber 79 

Residual  analyses  80 

Calculation  from  residual  analyses 80 

Influence  of  fluctuations  in  temperature  and  pressure  on  the  apparent 

volume  of  air  in  the  system 83 

Influence  of  fluctuations  in  the  amounts  of  carbon  dioxide  and  water- 
vapor  upon  residual  oxygen 83 

Control  of  residual  analyses 84 

Nitrogen  admitted  with  the  oxygen 84 

Rejection  of  air 85 

Interchange  of  air  in  the  food  aperture 85 

Use  of  the  residual  blank  in  the  calculations 86 

Abbreviated  method  of  computation  of  oxygen  admitted  to  the  chamber 

for  use  during  short  experiments 88 

Criticism  of  the  method  of  calculating  the  volume  of  oxygen 89 

Calculation  of  total  output  of  carbon  dioxide  and  water-vapor  and  oxygen 

absorption   91 

Control  experiments  with  burning  alcohol * 91 

Balance  for  weighing  subject 93 

Pulse  rate  and  respiration  rate 95 

Routine  of  an  experiment  with  man 96 

Preparation  of  subject 96 

Sealing  in  the  cover. . . , 97 

Routine  at  observer's  table 97 

Manipulation  of  the  water-meter 98 

Absorber  table 99 

Supplemental  apparatus  100 


ILLUSTRATIONS, 


PAGE 

Fig.l.  General  plan  of  respiration  calorimeter  laboratory 4 

2.  General  view  of  laboratory  taken  near  main  door 4 

3.  General  view  of  laboratory  taken  near  refrigeration  room 4 

4.  General  view  of  laboratory  taken  near  temperature  recorder 4 

5.  View  of  laboratory  taken  from  entrance  of  bed  calorimeter 4 

6.  Plan  of  heating  and  ventilating  the  calorimeter  laboratory 6 

7.  Horizontal  cross-section  of  chair  calorimeter 11 

8.  Vertical  cross-section  of  chair  calorimeter 12 

9.  Vertical  cross-section  of  chair  calorimeter  from  front  to  back 13 

10.  Photograph  of  framework  of  chair  calorimeter 14 

11.  Photograph  of  portion  of  framework  and  copper  shell 14 

12.  Cross-section  in  detail  of  walls  of  calorimeter 16 

13.  Detail  of  drop-sight  feed-valve  and  arrangement  of  outside  cooling 

circuit 18 

14.  Schematic  diagram  of  water-circuit  for  the  heat-absorbers  of  the  calo- 

rimeter    22 

15.  Detail  of  air-resistance  thermometer 28 

16.  Details  of  resistance  thermometers  for  water-circuit 30 

17.  Diagram  of  wiring  of  observer's  table 32 

18.  Diagram  of  rheostat  and  resistances  in  series  with  it 36 

19.  Diagram  of  wiring  of  differential  circuit  with  shunts  used  with  resist- 

ance thermometers  for  water-circuit 38 

20.  Diagram  of  galvanometer  coil,  used  with  recording  apparatus  for  resist- 

ance thermometers  in  water-circuit 40 

21.  Diagram  of  wiring  of  circuits  actuating  plunger  and  creeper 41 

22.  Diagram  of  wiring  of  complete  110-volt  circuit 41 

23.  Temperature  recorder 42 

24.  Detailed  wiring  diagram  showing  all  parts  of  the  recording  apparatus, 

together  with  wiring  to  thermometers 42 

25.  Section  of  calorimeter  walls  and  portion  of  ventilating  air-circuit 43 

26.  Cross-section  of  bed  calorimeter 46 

27.  Diagram  of  ventilation  of  the  respiration  calorimeter 57 

28.  Cross-section  of  sulphuric  acid  absorber 59 

29.  Balance  for  weighing  absorbers 62 

30.  Diagram  of  absorber  table 66 

31.  Diagram  of  oxygen  balance  and  cylinders 68 

32.  The  oxygen  cylinder  and  connections  to  tension  equalizer 70 

vii 


RESPIRATION  CALORIMETERS  FOR  STUDYING  THE 

RESPIRATORY  EXCHANGE  AND  ENERGY 

TRANSFORMATIONS  IN  MAN. 


INTRODUCTION. 

The  establishment  in  Boston  of  an  inquiry  into  the  nutrition  of  man 
with  the  construction  of  a  special  laboratory  for  that  purpose  is  a  direct 
outcome  of  a  series  of  investigations  originally  undertaken  in  the  chemical 
laboratory  of  Wesleyan  University,  in  Middletown,  Connecticut,  by  the  late 
Prof.  W.  0.  Atwater.  Appreciating  the  remarkable  results  of  Pettenkofer 
and  Yoit  *  and  their  associates,  as  early  as  1892  he  made  plans  for  the 
construction  of  a  respiration  apparatus  accompanied  by  calorimetric  fea- 
tures. The  apparatus  was  designed  on  the  general  ventilation  plan  of  the 
above  investigators,  but  in  the  first  description  of  this  apparatus  f  it  is  seen 
that  the  method  used  for  the  determination  of  carbon  dioxide  and  water- 
vapor  was  quite  other  than  that  used  by  Voit.  Each  succeeding  year  of 
active  experimenting  brought  about  new  developments  until,  in  1902,  the 
apparatus  was  essentially  modified  by  changing  it  from  the  open-circuit 
type  to  the  closed-circuit  type  of  Eegnault  and  Eeiset.  This  apparatus, 
thus  modified,  has  been  completely  described  ■  in  a  former  publication.  J 
The  calorimetric  features  likewise  underwent  gradual  changes  and,  as 
greater  accuracy  was  desired,  it  was  found  impracticable  to  conduct  calo- 
rimetric investigations  to  the  best  advantage  in  the  basement  of  a  chemical 
laboratory.  With  four  sciences  crowded  into  one  building  it  was  practically 
impossible  to  devote  more  space  to  these  researches.  Furthermore,  the  in- 
vestigations had  proceeded  to  such  an  extent  that  it  seemed  desirable  to 
construct  a  special  laboratory  for  the  purpose  of  carrying  out  the  calori- 
metric and  allied  investigations  on  the  nutrition  of  man. 

In  designing  this  laboratory  it  was  planned  to  overcome  the  difficulties 
experienced  in  Middletown  with  regard  to  control  of  the  room-temperature 
and  humidity,  and  furthermore,  while  the  researches  had  heretofore  been 

*  Pettenkofer  and  Voit:  Ann.  der  Chem.  u.  Pharm.  (1862-3),  Supp.  Bd.  2,  p.  17. 

t  Atwater,  Woods,  and  Benedict:  Report  of  preliminary  investigations  on  the 
metabolism  of  nitrogen  and  carbon  in  the  human  organism  with  a  respiration 
calorimeter  of  special  construction,  U.  S.  Dept.  of  Agr.,  Office  of  Experiment 
Stations  Bulletin  44.     (1897.) 

JW.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42.     (1905.) 

1 


2  CALORIMETERS   FOR   STUDYING   RESPIRATORY    EXCHANGE,    ETC. 

carried  on  simultaneously  with  academic  duties,  it  appeared  absolutely 
necessary  to  adjust  the  research  so  that  the  uninterrupted  time  of  the  ex- 
perimenters could  be  given  to  work  of  this  kind.  Since  these  experiments 
frequently  continued  from  one  to  ten  days,  their  satisfactory  conduct  was 
not  compatible  with  strenuous  academic  duties. 

As  data  regarding  animal  physiology  began  to  be  accumulated,  it  was 
soon  evident  that  there  were  great  possibilities  in  studying  abnormal  rneta-. 
holism,  and  hence  the  limited  amount  of  pathological  material  available  in 
Middletown  necessitated  the  construction  of  the  laboratory  in  some  large 
center. 

A  very  careful  consideration  was  given  to  possible  sites  in  a  number  of 
cities,  with  the  result  that  the  laboratory  was  constructed  on  a  plot  of  ground 
in  Boston  in  the  vicinity  of  large  hospitals  and  medical  schools.  Advantage 
was  taken,  also,  of  the  opportunity  to  secure  connections  with  a  central 
power-plant  for  obtaining  heat,  light,  electricity,  and  refrigeration,  thus 
doing  away  with  the  necessity  for  private  installation  of  boilers  and  electrical 
and  refrigerating  machinery.  The  library  advantages  in  a  large  city  were 
also  of  importance  and  within  a  few  minutes'  walk  of  the  present  location 
are  found  most  of  the  large  libraries  of  Boston,  particularly  the  medical 
libraries  and  the  libraries  of  the  medical  schools. 

The  building,  a  general  description  of  which  appeared  in  the  Year  Book 
of  the  Carnegie  Institution  of  Washington  for  1908,  is  of  plain  brick  con- 
struction, trimmed  with  Bedford  limestone.  It  consists  of  three  stories  and 
basement  and  practically  all  the  space  can  be  used  for  scientific  work. 
Details  of  construction  may  be  had  by  reference  to  the  original  description 
of  the  building.  It  is  necessary  here  only  to  state  that  the  special  feature 
of  the  new  building  with  which  this  report  is  concerned  is  the  calorimeter 
laboratory,  which  occupies  nearly  half  of  the  first  floor  on  the  northern  end 
of  the  building. 


CALORIMETER  LABORATORY.  3 

CALORIMETER   LABORATORY. 

The  laboratory  room  is  entered  from  the  main  hall  by  a  double  door. 
The  room  is  14.2  meters  long  by  10.1  meters  wide,  and  is  lighted  on  three 
sides  by  7  windows.  Since  the  room  faces  the  north,  the  temperature  con- 
ditions are  much  more  satisfactory  than  could  be  obtained  with  any  other 
exposure.  In  constructing  the  building  the  use  of  columns  in  this  room 
was  avoided,  as  they  would  interfere  seriously  with  the  construction  of  the 
calorimeters  and  accessor}-  apparatus.  Pending  the  completion  of  the  five 
calorimeters  designed  for  this  room  a  temporary  wooden  floor  was  laid, 
thus  furnishing  the  greatest  freedom  in  placing  piping  and  electric  wiring 
beneath  the  floor.  As  fast  as  the  calorimeters  are  completed,  permanent 
flooring  with  suitably  covered  trenches  for  pipes  is  to  be  laid.  The  room 
is  amply  lighted  during  the  day,  the  windows  being  very  high,  with  glass 
transoms  above.  At  night  a  large  mercury-vapor  lamp  in  the  center  of  the 
room,  supplemented  by  a  number  of  well-placed  incandescent  electric  lights, 
gives  ample  illumination. 

GENERAL  PLAN  OF  CALORIMETER  LABORATORY. 

The  general  plan  of  the  laboratory  and  the  distribution  of  the  calorime- 
ters and  accessory  apparatus  are  shown  in  fig.  1.  The  double  doors  lead 
from  the  main  hall  into  the  room.  In  general,  it  is  planned  to  conduct  all 
the  chemical  and  physical  observations  as  near  the  center  of  the  laboratory 
as  possible,  hence  space  has  been  reserved  for  apparatus  through  the  center 
of  the  room  from  south  to  north.  The  calorimeters  are  on  either  side.  In 
this  way  there  is  the  greatest  economy  of  space  and  the  most  advantageous 
arrangement  of  apparatus. 

At  present  two  calorimeters  are  completed,  one  under  construction,  and 
two  others  are  planned.  The  proposed  calorimeters  are  to  be  placed  in  the 
spaces  inclosed  by  dotted  lines.  Of  the  calorimeters  that  are  completed, 
the  so-called  chair  calorimeter,  which  was  the  first  built,  is  in  the  middle  of 
the  west  side  of  the  room,  and  immediately  to  the  north  of  it  is  the  bed  calo- 
rimeter, already  tested  and  in  actual  use.  On  the  east  side  of  the  room  it  is 
intended  to  place  large  calorimeters,  one  for  continuous  experiments  extend- 
ing over  several  days  and  the  other  large  enough  to  take  in  several  indi- 
viduals at  once  and  to  have  installed  apparatus  and  working  machinery  re- 
quiring larger  space  than  that  furnished  by  any  of  the  other  calorimeters. 
Near  the  chair  calorimeter  a  special  calorimeter  with  treadmill  is  shortly  to 
be  built. 

The  heat  insulation  of  the  room  is  shown  by  the  double  windows  and  the 
heavy  construction  of  the  doors  other  than  the  double  doors.  On  entering 
the  room,  the  two  calorimeters  are  on  the  left,  and,  as  arranged  at  present, 
both  calorimeters  are  controlled  from  the  one  platform,  on  which  is  placed 
the  observer's  table,  with  electrical  connections  and  the  Wheatstone  bridges 


4  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

for  temperature  measurements;  above  and  behind  the  observer's  table  are 
the  galvanometer  and  its  hood.  At  the  left  of  the  observer's  platform  is  a 
platform  scale  supporting  the  water-meter,  with  plug  valve  and  handle  con- 
veniently placed  for  emptying  the  meter.    The  absorption  system  is  placed 


Fig.  1. — General   plan  of  respiration  calorimeter  laboratory. 

on  a  special  table  conveniently  situated  with  regard  to  the  balance  for  weigh- 
ing the  absorbers.  The  large  balance  used  for  weighing  the  oxygen  cylinders 
is  directly  across  the  center  aisle  and  the  analytical  balance  for  weighing  the 
U-tubes  for  residual  analysis  is  near  by. 


General  view  of  laboratory  taken  near  the  temperature  recorder.  The  bed  calorimeter  is  at  the  right, 
the  absorber  table  in  the  immediate  foreground,  back  of  it  the  chair  calorimeter  and  observer's  table,  and  at 
the  left  the  balance  for  weighing  absorbers.  Near  the  ceiling  are  shown  the  ducts  for  the  cold  air  used  for 
temperature  control. 


Fig.   5 
View  of  laboratory  taken  from  the  entrance  of  the  bed  calorimeter,  with  balance  for  weighing  oxygen 
cylinders  at  the  left.     The  structural  steel  skeleton  of  the  calorimeter  for  long  experiments  is  at  the  right  and 
sections  of  the  copper  lining  are  in  the  rear,  resting  against  the  wall. 


CALORIMETER  LABORATORY.  5 

The  barometer  is  on  the  south  wall  of  the  room,  to  avoid  temperature 
fluctuations,  and  a  special  electrical  recording  apparatus  for  recording  tem- 
perature differences  is  placed  on  the  north  wall  near  the  windows,  where  it 
may  be  conveniently  observed  either  from  the  observer's  platform  or  from 
any  subsequent  platform  that  may  be  built.  Pending  the  construction  of 
other  calorimeters,  apparatus  for  gas  analysis,  spirometers,  and  special  appa- 
ratus for  studying  the  respiratory  exchange  are  placed  in  the  east  end  of  the 
room.  On  the  inside  wall,  near  the  double  doors,  are  the  telephone  and  racks 
containing  the  extra  carbon-dioxide  absorbing  cans. 

It  is  thus  seen  that  the  room  as  arranged  permits  the  concentration  of 
all  the  physical  observations  and  chemical  work  in  the  center  of  the  room, 
the  calorimeters  lying  on  either  side.  The  bed  calorimeter  is  so  placed  that 
the  subject  can  easily  be  brought  to  its  front  end  on  a  stretcher  and  slid 
into  the  chamber  easily.  The  subject  enters  the  chair  calorimeter  from  the 
top.  The  other  calorimeters  will  have  entrances  facing  the  center  aisle,  so 
that  the  subjects  and  apparatus  can  be  placed  inside  without  difficulty.  The 
subjects  will  also  be  under  more  general  observation  by  having  the  entrance 
openings  toward  the  center  of  the  room. 

A  general  view  of  the  laboratory  taken  at  the  right  of  the  main  door  is 
shown  in  figure  2.  In  the  immediate  foreground  is  seen  the  balance  for 
weighing  the  absorber  system.  A  porcelain  sulphuric-acid  vessel  is  shown 
suspended  on  the  left-hand  arm  of  the  balance.  The  large  lead  counter- 
poises used  for  weighing  are  on  the  shelf  in  front  of  the  balance  at  the  right. 
On  the  floor  of  the  laboratory,  in  front  of  the  door,  beneath  the  balance,  is 
seen  a  second  sulphuric-acid  absorber,  while  inside  the  cupboard  beneath 
the  balance  case  at  the  extreme  right  is  a  broken  absorber  which  gives  an 
idea  of  the  internal  construction.  The  pneumatic  elevator  with  its  valve 
is  shown  in  the  middle  of  the  cupboard  beneath  the  balance. 

At  the  right  of  the  figure  is  seen  the  absorber  table  with  the  gas-meter 
used  for  the  residual  analysis  on  the  top  shelf.  The  two  rubber  pipes  con- 
necting the  absorber  table  to  the  chair  calorimeter  are  shown  connected, 
and  beneath  them  in  the  rear  is  the  bed  calorimeter.  At  the  left  are  the 
chair  calorimeter  and  the  observer's  table  with  the  chair  used  by  the 
observer.  At  the  extreme  left,  on  the  floor,  is  the  balance  for  weighing  the 
water  used  to  bring  away  the  heat  from  the  calorimeters,  and  above  the 
chair  calorimeter  is  shown  the  large  balance  for  weighing  the  subject. 

In  obtaining  the  photograph  from  which  the  figure  is  made,  care  was 
taken  to  minimize  the  reflections  from  the  glass  of  the  balance  case;  hence, 
the  apparatus  seen  through  this  glass  is  substantially  as  actually  installed 
and  is  not  distorted  by  reflections.  The  observer's  table  is  somewhat  ele- 
vated and  steps  lead  to  it.  The  galvanometer  is  but  imperfectly  shown  at 
the  right  of  the  balance  case,  immediately  above  the  bed  calorimeter  and 
suspended  from  the  ceiling. 


6  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

Another  view  of  the  laboratory,  taken  near  the  door  leading  to  the 
refrigeration  room,  is  shown  in  fig.  3.  At  the  right  is  seen  the  balance  used 
for  weighing  absorbers,  and  back  of  it,  imperfectly  shown,  is  the  case  sur- 
rounding the  balance  for  weighing  oxygen  cylinders.  On  the  wall,  in  the 
rear,  is  the  recording  apparatus  for  electric  resistance  thermometers  in  the 
water-circuit,  a  detail  of  which  is  shown  in  fig.  23.  In  the  foreground  in 
the  center  is  seen  the  observer's  table;  at  the  right  of  this  is  shown  the 


SECTION 
C-D 


BRINE    COILS 
REHEATER      BENEATH 


/V  >-"/     Pendant    thcbmostat* \«*.  Y\ 


&K 


Fig.  6. — Plan  of  heating  and  ventilating  calorimeter  laboratory,  showing 
general  plan  of  circulation  of  the  special  cooling  system  and  the  posi- 
tion of  the  thermostats  and  radiators  which  they  control.  The  two 
small  diagrams  are  cross-sections  of  brine  and  heating  coils. 

table  for  the  absorption  system,  and  at  the  left  the  chair  calorimeter  with 
the  balance  for  weighing  subjects  above  it.  The  mercury-vapor  light,  which 
is  used  to  illuminate  the  room,  is  immediately  above  the  balance  for  weighing 
absorbers. 

The  bed  calorimeter  and  the  absorbing-system  table  are  better  shown  in 
fig.  4,  a  general  view  of  the  laboratory  taken  near  the  temperature  recorder. 
In  the  immediate  foreground  is  the  table  for  the  absorption  system,  and 
back  of  it  are  the  observer's  table  and  chair  calorimeter.    At  the  right,  the 


CALORIMETER  LABORATORY.  7 

bed  calorimeter  with  the  front  removed  and  the  rubber  hose  connections  as 
carried  from  the  absorber  table  to  the  bed  calorimeter  are  shown.  At  the 
extreme  left  is  the  balance  for  weighing  the  absorbers.  Above  the  chair 
calorimeter  can  be  seen  the  balance  for  weighing  the  subject,  and  at  its 
right  the  galvanometer  suspended  from  the  ceiling. 

The  west  side  of  the  laboratory  at  the  moment  of  writing  contains  the 
larger  proportion  of  the  apparatus.  On  the  east  side  there  exist  only  the 
balance  for  weighing  oxygen  cylinders  and  an  unfinished  *  large  calorim- 
eter, which  will  be  used  for  experiments  of  long  duration.  A  view  taken 
near  the  front  end  of  the  bed  calorimeter  is  shown  in  fig.  5.  At  the  right, 
the  structural  skeleton  of  the  large  calorimeter  is  clearly  shown.  Some  of 
the  copper  sections  to  be  used  in  constructing  the  lining  of  the  calorimeter 
can  be  seen  against  the  wall  in  the  rear. 

At  the  left  the  balance  for  weighing  the  oxygen  cylinders  is  shown  with 
its  counterpoise.  A  reserve  oxygen  cylinder  is  standing  immediately  in 
front  of  it.  A  large  calorimeter  modeled  somewhat  after  the  plan  of 
Sonden  and  Tigerstedtfs  apparatus  in  Stockholm  and  Helsingfors  is  planned 
to  be  built  immediately  back  of  the  balance  for  weighing  oxygen  cylinders. 

HEATING  AND  VENTILATING. 

Of  special  interest  in  connection  with  this  calorimeter  laboratory  are  the 
plans  for  maintaining  constant  temperature  and  humidity  (fig.  6).  The 
room  is  heated  by  five  steam  radiators  (each  with  about  47  square  feet  of 
radiating  surface)  placed  about  the  outer  wall,  which  are  controlled  by  two 
pendant  thermostats.  A  certain  amount  of  indirect  ventilation  is  provided, 
as  indicated  by  the  arrows  on  the  inner  wall.  The  room  is  cooled  and  the 
humidity  regulated  by  a  system  of  refrigeration  installed  in  an  adjoining 
room.  This  apparatus  is  of  particular  interest  and  will  be  described  in 
detail. 

In  the  small  room  shown  at  the  south  side  of  the  laboratory  is  placed  a 
powerful  electric  fan  which  draws  the  air  from  above  the  floor  of  the  calo- 
rimeter laboratory,  draws  it  over  brine  coils,  and  sends  it  out  into  a  large 
duct  suspended  on  the  ceiling  of  the  laboratory.  This  duct  has  a  number 
of  openings,  each  of  which  can  be  controlled  by  a  valve,  and  an  unlimited 
supply  of  cold  air  can  be  directed  to  any  portion  of  the  calorimeter  room 
at  will.  To  provide  for  more  continuous  operation  and  for  more  exact 
temperature  control,  a  thermostat  has  been  placed  in  the  duct  and  is  so 
constructed  as  to  operate  some  reheater  coils  beneath  the  brine-coils  in  the 
refrigerating  room.  This  thermostat  is  set  at  60°  F.,  and  when  the  tem- 
perature of  the  air  in  the  duct  falls  below  this  point,  the  reheater  system 
is  automatically  opened  or  closed.    The  thermostat  can  be  set  at  any  point 

*  As  this  report  goes  to  press,  this  calorimeter  is  well  on  the  way  to  completion. 


8  CALORIMETERS    FOR    STUDYING   RESPIRATORY   EXCHANGE,  ETC. 

desired.  Up  to  the  present  time  it  has  been  unnecessary  to  utilize  this 
special  appliance,  as  the  control  by  hand  regulation  has  been  most  satis- 
factory. 

Two  vertical  sections  through  the  refrigerating  coils  are  shown  in  fig.  6. 
Section  A-B  shows  the  entrance  near  the  floor  of  the  calorimeter  room. 
The  air  is  drawn  down  over  the  coils,  passes  through  the  blower,  and  is 
forced  back  again  to  the  top  of  the  calorimeter  room  into  the  large  duct.  If 
outdoor  air  is  desired,  a  special  duct  can  be  connected  with  the  system  so  as 
to  furnish  outdoor  air  to  the  chamber.  This  has  not  as  yet  been  used. 
Section  C-D  shows  the  fan  and  gives  a  section  through  the  reheater.  The 
brine  coils,  400  meters  long,  are  in  triplicate.  If  one  set  becomes  covered 
with  moisture  and  is  somewhat  inefficient,  this  can  be  shut  off  and  the 
other  two  used.  When  the  frozen  moisture  melts  and  drops  off,  the  single 
coil  can  be  used  again.  It  has  been  found  that  the  system  so  installed  is 
most  readily  controlled. 

The  degree  of  refrigeration  is  varied  in  two  ways:  (1)  the  area  of  brine- 
coils  can  be  increased  or  decreased  by  using  one,  two,  or  all  three  of  the 
coils;  or  (2)  the  amount  of  air  passing  over  the  cooling  pipes  may  be  varied 
by  changing  the  speed  of  the  blower.  In  practice  substantially  all  of  the 
regulation  is  effected  by  varying  the  position  of  the  controlling  lever  on  the 
regulating  rheostat.  The  apparatus  functionates  perfectly  and  the  calo- 
rimeter room  can  be  held  at  20°  C.  day  in  and  day  out,  whether  the  tem- 
perature outdoors  is  40°  below  or  100°  above  0°  F. 

It  can  be  seen,  also,  that  this  system  provides  a  very  satisfactory  regu- 
lation of  the  humidity,  for  as  the  air  passes  over  the  brine  coils  the  moisture 
is  in  large  part  frozen  out.  As  yet,  no  hygrometric  study  has  been  made 
of  the  air  conditions  over  a  long  period,  but  the  apparatus  is  sufficiently 
efficient  to  insure  thorough  electrical  insulation  and  absence  of  leakage  in 
the  intricate  electrical  connections  on  the  calorimeters. 

The  calorimeters  employ  the  thermo-electric  element  with  its  low  poten- 
tial and  a  D'Arsonval  galvanometer  of  high  sensibility,  and  in  close  proximity 
it  is  necessary  to  use  the  110-volt  current  for  heating,  consequently  the 
highest  degree  of  insulation  is  necessary  to  prevent  disturbing  leakage  of 
current. 

The  respiration  calorimeter  laboratory  is  so  large,  the  number  of  assist- 
ants in  the  room  at  any  time  is  (relatively  speaking)  so  small,  seldom  ex- 
ceeding ten,  and  the  humidity  and  temperature  are  so  very  thoroughly  con- 
trolled, that  as  yet  it  has  been  entirely  unnecessary  to  utilize  even  the 
relatively  small  amount  of  indirect  ventilation  provided  in  the  original 
plans. 

During  the  greater  part  of  the  winter  it  is  necessary  to  use  only  one  of 
the  thermostats  and  the  radiators  connected  with  the  other  can  be  shut  off, 
since  each  radiator  can  be  independently  closed  by  the  valves  on  the  steam 


CALORIMETER  LABORATORY.  9 

supply  and  return  which  go  through  the  floor  to  the  basement.  The  tem- 
perature control  of  this  room  is  therefore  very  satisfactory  and  economical. 
It  is  not  necessary  here  to  go  into  the  advantages  of  temperature  control 
of  the  working  rooms  during  the  summer  months.  Every  one  seems  to  be 
thoroughly  convinced  that  it  is  necessary  to  heat  rooms  in  the  winter,  but 
our  experience  thus  far  has  shown  that  it  is  no  less  important  to  cool  the 
laboratory  and  control  the  temperature  and  moisture  during  the  summer 
months,  as  by  this  means  both  the  efficiency  and  endurance  of  the  assistants, 
to  say  nothing  of  the  accuracy  of  the  scientific  measurements,  are  very 
greatly  increased.  Arduous  scientific  observations  that  would  be  wholly 
impossible  in  a  room  without  temperature  control  can  be  carried  on  in  this 
room  during  the  warmest  weather. 


10  CALOKIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,    ETC. 

THE  CALORIMETER. 

In  describing  this  apparatus,  for  the  sake  of  clearness,  the  calorimetric 
features  will  be  considered  before  the  appliances  for  the  determination  of 
the  respiratory  products. 

FUNDAMENTAL  PRINCIPLES  OF  THE  APPARATUS. 

The  measurements  of  heat  eliminated  by  man,  as  made  by  this  apparatus, 
are  based  upon  the  fact  that  the  subject  is  inclosed  in  a  heat-proof  chamber 
through  which  a  current  of  cold  water  is  constantly  passing.  The  amount 
of  water,  the  flow  of  which,  for  the  sake  of  accuracy,  is  kept  at  a  constant 
rate,  is  carefully  weighed.  The  temperatures  of  the  water  entering  and 
leaving  the  chamber  are  accurately  recorded  at  frequent  intervals.  The 
walls  of  the  chamber  are  held  adiabatic,  thus  preventing  a  gain  or  loss  of 
heat  by  arbitrarily  heating  or  cooling  the  outer  metal  walls,  and  the  with- 
drawal of  heat  by  the  water-current  is  so  controlled,  by  varying  the  tem- 
perature of  the  ingoing  water,  that  the  heat  brought  away  from  the  calo- 
rimeter is  exactly  equal  in  amount  to  the  heat  eliminated  by  radiation  and 
conduction  by  the  subject,  thus  maintaining  a  constant  temperature  inside 
of  the  chamber.  The  latent  heat  of  the  water  vaporized  is  determined  by 
measuring  directly  the  water  vapor  in  the  ventilating  air-current. 

In  the  construction  of  the  new  calorimeters  a  further  and  fundamental 
change  in  construction  has  been  made  in  that  all  the  thermal  junctions, 
heating  wires,  and  cooling  pipes  have  been  attached  directly  to  the  zinc  wall 
of  the  calorimeter,  leaving  the  outer  insulating  panels  free  from  incum- 
brances, so  that  they  can  be  removed  readily  and  practically  all  parts  in- 
spected whenever  desired  without  necessitating  complete  dismantling  of  the 
apparatus.  This  arrangement  is  possible  except  in  those  instances  where 
connections  pass  clear  through  from  the  interior  of  the  chamber  to  the 
outside,  namely,  the  food-aperture,  air-pipes,  water-pipes,  electrical  connec- 
tions, and  tubes  for  connections  with  pneumograph  and  stethoscope;  but 
the  apparatus  is  so  arranged  as  to  have  all  of  these  openings  in  one  part  of 
the  calorimeter.  It  is  possible,  therefore,  to  remove  all  of  the  outer  sections 
of  the  calorimeter  with  the  exception  of  panels  on  the  east  side. 

This  fundamental  change  in  construction  has  proven  highly  advan- 
tageous. It  does  away  with  the  necessity  of  rolling  the  calorimeter  out  of 
its  protecting  insulating  house  and  minimizes  the  delay  and  expense  inci- 
dental to  repairs  or  modifications.  As  the  calorimeter  is  now  constructed, 
it  is  possible  to  get  at  all  parts  of  it  from  the  outside,  with  the  exception  of 
one  small  fixed  panel  through  which  the  above  connections  are  passed. 
This  panel,  however,  is  made  as  narrow  as  possible,  so  that  practically  all 
changes  can  be  made  by  taking  out  the  adjacent  panels. 


THE    CALORIMETER. 


11 


THE  CALORIMETER  CHAMBER. 

The  respiration  chamber  used  in  Middletown,  Connecticut,  was  designed 
to  permit  of  the  greatest  latitude  in  the  nature  of  the  experiments  to  be 
made  with  it.  As  a  result,  it  was  found  at  the  end  of  a  number  of  years  of 
experimenting  that  this  particular  size  of  chamber  was  somewhat  too  small 


Fig.  7. — Horizontal  cross-section  of  chair  calorimeter,  showing  cross-section  of 
copper  waU  at  A,  zinc  waU  at  B,  hair-felt  at  E,  and  asbestos  outer  waU 
at  F;  also  cross-section  of  all  upright  channels  in  the  steel  construction. 
At  the  right  is  the  location  of  the  ingoing  and  outgoing  water  and  the 
thermometers.  At  C  is  shown  the  food  aperture,  and  D  is  a  gasket  sepa- 
rating the  two  parts.  The  ingoing  and  outeoming  air-pipes  are  shown  at 
the  right  inside  the  copper  wall.  The  telephone  is  shown  at  the  left,  and 
in  the  center  of  the  drawing  is  the  chair  with  its  foot-rest,  G.  In  dotted 
line  is  shown  the  opening  where  the  man  enters. 

for  the  most  satisfactory  experiments  during  muscular  work  and,  on  the 
other  hand,  somewhat  too  large  for  the  best  results  during  so-called  rest 
experiments.  In  the  earlier  experiments,  where  no  attempt  was  made  to 
determine  the  consumption  of  oxygen,  these  disadvantages  were  not  so 
apparent,  as  carbon  dioxide  could  be  determined  with  very  great  accuracy; 


12  CALORIMETERS   FOR  STUDYING  RESPIRATORY   EXCHANGE,  ETC. 

but  with  the  attempts  to  measure  the  oxygen  it  was  found  that  the  large 
volume  of  residual  air  inside  the  chamber,  amounting  to  some  4,500  liters, 
made  possible  very  considerable  errors  in  this  determination,  for,  obviously, 
the  subject  could  draw  upon  the  oxygen  residual  in  the  air  of  the  chamber, 
nearly  1,000  liters,  as  well  as  upon  the  oxygen  furnished  from  outside 
sources.     The  result  was  that  a  very  careful  analysis  of  the  residual  air 


Fig.  8. — Vertical  cross-section  of  chair  calorimeter,  showing  part  of 
rear  of  calorimeter  and  structural-steel  frame.  N,  cross-section 
of  bottom  horizontal  channel  supporting  asbestos  floor  J;  H,  H, 
upright  channels  (at  the  right  is  a  side  upright  channel  and  to 
the  left  of  this  is  an  upright  rear  channel) ;  M,  horizontal  3-inch 
channel  supporting  calorimeter;  Zn,  zinc  wall;  Cu,  copper  wall; 
J,  insulating  asbestos. 

must  be  made  frequently  in  order  to  insure  that  the  increase  or  decrease  in 
the  amount  of  oxygen  residual  in  the  air  of  the  chamber  was  known  accu- 
rately at  the  end  of  each  period.  Analysis  of  this  large  volume  of  air  could 
be  made  with  considerable  accuracy,  but  in  order  to  calculate  the  exact 
total  of  oxygen  residual  in  the  air  it  was  necessary  to  know  the  total  volume 
of  air  inside  the  chamber  under  standard  conditions.  This  necessitated, 
therefore,  a  careful  measurement  of  temperature  and  pressure,  and  while 
the  barometric  pressure  could  be  measured  with  a  high  degree  of  accuracy, 


THE   CALORIMETER. 


13 


it  was  found  to  be  very  difficult  to  determine  exactly  the  average  tempera- 
ture of  so  large  a  mass  of  air.  The  difficulties  attending  this  measurement 
and  experiments  upon  this  point  are  discussed  in  detail  elsewhere.*  Con- 
sequently, as  a  result  of  this  experience,  in  planning  the  calorimeters  for 
the  Nutrition  Laboratory  it  was  decided  to  design  them  for  special  types 
of  experiments.     The  first  calorimeter  to  be  constructed  was  one  which 


1    Meter 


Fig.  9. — Vertical  cross-section  erf  chair  calorimeter  from  front  to  back, 
showing  structural  steel  supporting  the  calorimeter  and  the  large 
balance  above  for  weighing  the  subject  inside  the  calorimeter. 
The  chair,  method  of  suspension,  and  apparatus  for  raising  and 
lowering  are  shown.  Part  of  the  heat-absorbers  is  shown,  and 
their  general  direction.  The  ingoing  and  outgoing  air-pipes  and 
direction  of  ventilation  are  also  indicated.  The  positions  of  the 
food-aperture  and  wire  mat  and  asbestos  support  are  seen.  Sur- 
rounding the  calorimeter  are  the  asbestos  outside  and  hair-felt 
lining. 


*  W.  0.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42,  p.  91.     (1905.) 

Francis  G.  Benedict:  The  influence  of  inanition  on  metabolism.  Carnegie  In- 
stitution of  Washington  Publication  No.  77,  p.  451.     (1907.) 


14  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

would  have  general  use  in  experiments  during  rest  and,  indeed,  during 
experiments  with  the  subject  sitting  quietly  in  the  chair. 

It  may  well  be  asked  why  the  first  calorimeter  was  not  constructed  of 
such  a  type  as  to  permit  the  subject  assuming  a  position  on  a  couch  or 
sofa,  such  as  is  used  by  Zuntz  and  his  collaborators  in  their  research  on  the 
respiratory  exchange,  or  the  position  of  complete  muscular  rest  introduced 
by  Johansson  and  his  associates.  While  the  body  positions  maintained  by 
Zuntz  and  Johansson  may  be  the  best  positions  for  experiments  of  short 
duration,  it  was  found,  as  a  result  of  a  large  number  of  experiments,  that 
subjects  could  be  more  comfortable  and  quiet  for  periods  of  from  6  to  8 
hours  by  sitting,  somewhat  inclined,  in  a  comfortable  arm-chair,  provided 
with  a  foot-rest.  With  this  in  mind  the  first  calorimeter  was  constructed 
so  as  to  hold  an  arm-chair  with  a  foot-rest  so  adjusted  that  the  air-space 
between  the  body  of  the  subject  and  the  walls  of  the  chamber  could  be  cut 
down  to  the  minimum  and  thus  increase  the  accuracy  of  the  determination 
of  oxygen.  That  the  volume  has  been  very  materially  reduced  may  be  seen 
from  the  fact  that  the  total  volume  of  the  first  calorimeter  to  be  described 
is  less  than  1,400  liters,  or  about  one-third  that  of  the  Middletown  apparatus. 

GENERAL    CONSTRUCTION. 

A  horizontal  cross-section  of  the  apparatus  is  shown  in  fig.  7,  and  a 
vertical  cross-section  facing  the  front  is  given  in  fig.  8.  Other  details  of 
structural  steel  are  seen  in  fig.  9. 

In  constructing  the  new  chambers,  the  earlier  wood  construction,  with  its 
tendency  to  warp  and  its  general  non-rigidity,  was  avoided  by  the  use  of 
structural  steel,  and  hence  in  this  calorimeter  no  use  whatever  is  made  of 
wood  other  than  the  wood  of  the  chair. 

To  avoid  temperature  fluctuations  due  to  possible  local  stratification  of 
the  air  in  the  laboratory,  the  calorimeter  is  constructed  so  as  to  be  prac- 
tically suspended  in  the  air,  there  being  a  large  air-space  of  some  76  centi- 
meters between  the  lowest  point  of  the  calorimeter  and  the  floor,  and  the 
top  of  the  calorimeter  is  some  212  centimeters  below  the  ceiling  of  the  room. 
Four  upright  structural-steel  channels  (4-inch)  were  bolted  through  the 
floor,  so  as  to  secure  great  rigidity,  and  were  tied  together  at  the  top  with 
structural  steel.  As  a  solid  base  for  the  calorimeter  chamber  two  3-inch 
channels  were  placed  parallel  to  each  other  70  centimeters  from  the  floor, 
joined  to  these  uprights.  Upon  these  two  3-inch  channels  the  calorimeter 
proper  was  constructed.  The  steel  used  for  the  most  part  in  the  skeleton  of 
the  apparatus  is  standard  2|-inch  channel.  This  steel  frame  and  its  support 
are  shown  in  fig.  10,  before  any  of  the  copper  lining  was  put  into  position. 
The  main  4-inch  channels  upon  which  the  calorimeter  is  supported,  the  tie- 
rods  and  turn-buckles  anchoring  the  framework  to  the  ceiling,  the  I-beam 
construction  at  the  top  upon  which  is  subsequently  installed  the  large  balance 


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THE   CALORIMETER.  15 

for  weighing  the  man,  the  series  of  small  channels  set  on  edge  upon  which 
the  asbestos  floor  is  laid,  and  the  upright  row  of  channel  ribs  are  all  clearly 
shown. 

A  photograph  taken  subsequently,  showing  the  inner  copper  lining  in 
position,  is  given  in  fig.  11. 

The  floor  of  the  chamber  is  supported  by  7  pieces  of  2^-inch  channel 
(N,  1ST,  N,  fig.  8),  laid  on  top  and  bolted  to  the  two  3-inch  channels  (M, 
fig.  8).  On  top  of  these  is  placed  a  sheet  of  so-called  asbestos  lumber  (J', 
fig.  8)  9.5  millimeters  thick,  cut  to  fit  exactly  the  bottom  of  the  chamber. 
Upright  2^-inch  channels  (H,  fig.  8)  are  bolted  to  the  two  outside  channels 
on  the  bottom  and  to  the  ends  of  three  of  the  long  channels  between  in 
such  a  manner  as  to  form  the  skeleton  of  the  walls.  The  upper  ends  of 
these  channels  are  fastened  together  by  pieces  of  piping  (P,  P,  P,  fig.  8) 
with  lock-nuts  on  either  side,  thus  holding  the  whole  framework  in  position. 

The  I-beams  and  channels  used  to  tie  the  four  upright  channels  at  the  top 
form  a  substantial  platform  upon  which  is  mounted  a  large  balance  (fig.  9). 
This  platform  is  anchored  to  the  ceiling  at  four  points  by  tie  rods  and  turn- 
buckles,  shown  in  fig.  1.  The  whole  apparatus,  therefore,  is  extremely  rigid 
and  the  balance  swings  freely. 

The  top  of  the  chamber  is  somewhat  restricted  near  the  edges  (fig.  8) 
and  two  lengths  of  2^-inch  channel  support  the  sides  of  the  opening  through 
which  the  subject  enters  at  the  top  (fig.  7). 

Both  the  front  and  back  lower  channels  upon  which  the  bottom  rests  are 
extended  so  as  to  provide  for  supports  for  the  outer  walls  of  asbestos  wood, 
which  serve  to  insulate  the  calorimeter.  Between  the  channels  beneath  the 
calorimeter  floor  and  the  3-inch  channels  is  placed  a  sheet  of  zinc  which 
forms  the  outer  bottom  metallic  wall  of  the  chamber. 

In  order  to  prevent  conduction  of  heat  through  the  structural  steel  all 
contact  between  the  inner  copper  wall  and  the  steel  is  avoided  by  having 
strips  of  asbestos  lumber  placed  between  the  steel  and  copper.  These  are 
shown  as  J  in  fig.  8  and  fig.  12.  A  sheet  of  asbestos  lumber  beneath  the 
copper  bottom  likewise  serves  this  purpose  and  also  serves  to  give  a  solid 
foundation  for  the  floor.  The  supporting  channels  are  placed  near  enough 
together  to  reinforce  fully  the  sheet  of  asbestos  lumber  and  enable  it  to  sup- 
port solidly  the  weight  of  the  man.  The  extra  strain  on  the  floor  due  to 
tilting  back  a  chair  and  thus  throwing  all  the  weight  on  two  points  was  taken 
into  consideration  in  planning  the  asbestos  and  the  reinforcement  by  the 
steel  channels.    The  whole  forms  a  very  satisfactory  flooring. 

Wall  construction  and  insulation. — The  inner  wall  of  the  chamber  con- 
sists of  copper,  preferably  tinned  on  both  sides,  thus  aiding  in  soldering,  and 
the  tinned  inner  surface  makes  the  chamber  somewhat  lighter.  Extra  large 
sheets  are  obtained  from  the  mill,  thus  reducing  to  a  minimum  the  number  of 


16 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


seams  for  soldering,  and  seams  are  made  tight  only  with  difficulty.  The  cop- 
per is  of  standard  gage,  the  so-called  14-ounce  copper,  weighing  1.1  pounds 
per  square  foot  or  5.5  kilograms  per  square  meter.  It  has  a  thickness  of  0.5 
millimeter.  The  whole  interior  of  the  skeleton  frame  of  the  structural  steel 
is  lined  with  these  sheets ;  fig.  11  shows  the  copper  shell  in  position. 

For  the  outer  metallic  wall,  zinc,  as  the  less  expensive  metal,  is  used.  One 
sheet  of  this  material  perforated  with  holes  for  the  attachment  of  bolts  and 
other  appliances  is  shown  in  position  on  the  outside  of  the  wall  in  fig.  11. 
The  sheet  zinc  of  the  floor  is  obviously  put  in  position  before  the  channels 
upon  which  it  rests  are  laid.    The  zinc  is  obtained  in  standard  size,  and 


ZINC, 


COPPER 


■ 

^iittuttiiitiu««tt<t 


Fig.  12. — Cross-section  in  detail  of  walls  of  calorimeter,  showing  zinc  and  copper 
walls  and  asbestos  outside  (A) ;  hair-felt  lining  (B) ;  cross-section  of  channel  iron 
(H);  brass  washer  soldered  to  copper  (K);  asbestos  insulation  between  channel 
iron  and  copper  (J);  bolt  holding  the  whole  together  (I);  heating  wire  (W)  and 
insulator  holding  it  (F)  shown  in  air-space  between  zinc  and  hair-felt;  section  of 
one  of  the  cooling  pipes  (C)  and  its  brass  support  (G) ;  threaded  rod  (E)  fastened 
into  H  at  one  end  and  passing  through  asbestos  wall  with  a  nut  on  the  outside; 
and  iron  pipe  (W)  used  as  spacer  between  asbestos  and  zinc. 


is  the  so-called  9-ounce  zinc,  or  0.7  pound  to  the  square  foot,  or  3.5  kilo- 
grams to  the  square  meter.  The  sheet  has  a  thickness  of  0.5  millimeter. 
In  the  cross-section,  fig.  7,  A  represents  the  copper  wall  and  B  the  zinc 
wall.  Surrounding  this  zinc  wall  and  providing  air  insulation  is  a  series  of 
panels  constructed  of  asbestos  lumber,  very  fire-resisting,  rigid,  and  light. 
The  asbestos  lumber  used  for  these  outer  panels  is  6.4  millimeters  (0.25 
inch)  thick.  To  further  aid  in  heat  insulation  we  have  glued  to  the  inner 
face  of  the  different  panels  a  patented  material  composed  of  two  layers  of 
sheathing-paper  inclosing  a  half-inch  of  hair-felt.     This  material  is  com- 


THE   CALORIMETER.  17 

monly  used  in  the  construction  of  refrigerators.    This  is  shown  as  E  in  fig.  7, 
while  the  outer  asbestos  panels  are  shown  as  F. 

A  detail  of  the  construction  of  the  walls,  showing  in  addition  the  heating 
and  cooling  devices,  is  given  in  fig.  12,  in  which  the  copper  is  shown  held 
firmly  to  the  upright  channel  H  by  means  of  the  bolt  I,  screwing  into  a 
brass  or  copper  disk  K  soldered  to  the  copper  wall.  The  bolt  I  serves  the 
purpose  of  holding  the  copper  to  the  upright  channel  and  likewise  by  means 
of  a  washer  under  the  head  of  the  screw  holds  the  zinc  to  the  channel.  In 
order  to  hold  the  asbestos-lumber  panel  A  with  the  hair-felt  lining  B  a 
threaded  rod  E  is  screwed  into  a  tapped  hole  in  the  outer  part  of  the  upright 
channel  H.  A  small  piece  of  brass  or  iron  tubing,  cut  to  the  proper  length, 
is  slipped  over  this  rod  and  the  asbestos  lumber  held  in  position  by  a  hex- 
agonal nut  with  washer  on  the  threaded  rod  E.  In  this  manner  great  rig- 
idity of  construction  is  secured,  and  we  have  two  air-spaces  corresponding  to 
the  dead  air-spaces  indicated  in  fig.  7,  the  first  between  the  copper  and  zinc 
and  the  second  between  the  zinc  and  hair-felt. 

PREVENTION    OF    RADIATION. 

As  can  be  seen  from  these  drawings  the  whole  construction  of  the  appa- 
ratus is  more  or  less  of  the  refrigerator  type,  i.  e.,  there  is  little  opportunity 
for  radiation  or  conduction  of  heat.  Such  a  construction  could  be  multi- 
plied a  number  of  times,  giving  a  greater  number  of  insulating  walls,  and 
perhaps  reducing  radiation  to  the  minimum,  but  for  extreme  accuracy  in 
calorimetric  investigations  it  is  necessary  to  insure  the  absence  of  radiation, 
and  hence  we  have  retained  the  ingenious  device  of  Eosa,  by  which  an 
attempt  is  made  arbitrarily  to  alter  the  temperature  of  the  zinc  wall  so  that 
it  always  follows  any  fluctuations  in  the  temperature  of  the  copper  wall. 
To  this  end  it  is  necessary  to  know  first  that  there  is  a  temperature  differ- 
ence between  zinc  and  copper  and,  second,  to  have  some  method  for  con- 
trolling the  temperature  of  the  zinc.  Leaving  for  a  moment  the  question 
of  measuring  the  temperature  differences  betwen  zinc  and  copper,  we  can 
consider  here  the  methods  for  controlling  the  temperature  of  the  zinc  wall. 

If  it  is  found  necessary  to  warm  the  zinc  wall,  a  current  of  electricity  is 
passed  through  the  resistance  wire  W,  fig.  12.  This  wire  is  maintained 
approximately  in  the  middle  of  the  air-space  between  the  zinc  wall  and  hair- 
felt  by  winding  it  around  an  ordinary  porcelain  insulator  F,  held  in  posi- 
tion by  a  threaded  rod  screwed  into  a  brass  disk  soldered  to  the  zinc  wall. 
A  nut  on  the  end  of  the  threaded  rod  holds  the  insulator  in  position.  Much 
difficulty  was  had  in  securing  a  resistance  wire  that  would  at  the  same  time 
furnish  reasonably  high  resistance  and  would  not  crystallize  or  become 
brittle  and  would  not  rust.  At  present  the  best  results  have  been  obtained 
by  using  enameled  manganin  wire.  The  wire  used  is  No.  28  American  wire- 
gage  and  has  resistance  of  approximately  1.54  ohms  per  foot.     The  total 


18 


CALORIMETERS    FOR   STUDYING-   RESPIRATORY    EXCHANGE,   ETC. 


amount  of  wire  used  in  any  one  circuit  is  equal  to  a  resistance  of  approxi- 
mately 92  ohms.  This  method  of  warming  the  air-space  leaves  very  little 
to  be  desired.  It  can  be  instantaneously  applied  and  can  be  regulated  with 
the  greatest  ease  and  with  the  greatest  degree  of  refinement. 

If,  on  the  other  hand,  it  becomes  necessary  to  cool  the  air-space  next  to 
the  zinc  and  in  turn  cool  the  zinc,  we  must  resort  to  the  use  of  cold  water, 
which  is  allowed  to  flow  through  the  pipe  C  suspended  in  the  air-space 
between  the  zinc  and  hair-felt  at  approximately  the  same  distance  as  is  the 
heating  wire.  The  support  of  these  pipes  is  accomplished  by  placing  them 
in  brass  hangers  G,  soldered  to  the  zinc  and  provided  with  an  opening  in 
which  the  pipe  rests. 

In  the  early  experimenting,  it  was  found  impracticable  to  use  piping  of 
very  small  size,  as  otherwise  stoppage  as  a  result  of  sediment  could  easily 
occur.  The  pipe  found  best  adapted  to  the  purpose  was  the  so-called 
standard  one-eighth  inch  brass  pipe  with  an  actual  internal  diameter  of 

7  millimeters.  The  opening  of  a  valve 
allowed  cold  water  to  flow  through  this  pipe 
and  the  considerable  mass  of  water  passing 
through  produced  a  very  noticeable  cooling 
effect.  In  the  attempt  to  minimize  the 
cooling  effect  of  the  mass  of  water  remain- 
ing in  the  pipe,  provision  was  made  to  allow 
water  to  drain  out  of  this  pipe  a  few  mo- 
ments after  the  valve  was  closed  by  a  system 
of  check-valves.  In  building  the  new  appa- 
ratus, use  was  made  of  the  compressed-air 
service  in  the  laboratory  to  remove  the  large 
mass  of  cold  water  in  the  pipe.  As  soon  as 
the  water-valve  was  closed  and  the  air-cock 
opened,  the  compressed  air  blew  all  of  the 
water  out  of  the  tube. 
The  best  results  have  been  obtained,  however,  with  an  entirely  new  prin- 
ciple, namely,  a  few  drops  of  water  are  continually  allowed  to  pass  into  the 
pipe,  together  with  a  steady  stream  of  compressed  air.  This  cold  water  is 
forcibly  blown  through  the  pipe,  thus  cooling  to  an  amount  regulated  by 
the  amount  of  water  admitted.  Furthermore,  the  relatively  dry  air  evap- 
orates some  of  the  water,  thereby  producing  a  somewhat  greater  cooling 
effect.  By  adjusting  the  flow  of  water  through  the  pipe  a  continuous  cool- 
ing effect  of  mild  degree  may  be  obtained.  While  formerly  the  air  in  the 
space  next  the  zinc  wall  was  either  cooled  or  heated  alternately  by  opening 
the  water-valve  or  by  passing  a  current  through  the  heating  coil,  at  present 
it  is  found  much  more  advantageous  to  allow  a  slow  flow  of  air  and  water 
through  the  pipes  continuously,  thus  having  the  air-space  normally  some- 


Fig.  13. — Detail  of  drop-sight  feed-valve 
and  arrangement  of  outside  cooling 
circuit.  The  water  enters  at  A,  and 
the  flow  is  regulated  by  the  needle- 
valve  at  left-hand  side.  Rate  of  flow 
can  be  seen  at  end  of  exit  tube  just 
above  the  union.  The  water  flows 
out  at  C  and  compressed  air  is  ad- 
mitted at  B,  regulated  by  the  pet- 
cock. 


THE   CALORIMETER.  19 

what  cooler  than  is  desired.  The  effect  of  this  cooling,  therefore,  is  then 
counterbalanced  by  passing  an  electric  current  of  varying  strength  through 
the  heating  wire.  By  this  manipulation  it  is  unnecessary  that  the  observer 
manipulate  more  than  one  instrument,  namely,  the  rheostat,  while  formerly 
he  had  to  manipulate  valves,  compressed-air  cocks,  and  rheostat.  The 
arrangement  for  providing  for  the  amount  of  compressed  air  and  water  is 
shown  in  fig.  13,  in  which  it  is  seen  that  a  small  drop-sight  feed-water  valve 
is  attached  to  the  pipe  C  leading  into  the  dead  air-space  surrounding  the 
calorimeter  chamber.  Compressed  air  enters  at  B  and  the  amount  entering 
can  be  regulated  by  the  pet-cock.  The  amount  of  water  admitted  is  readily 
observed  by  the  sight  feed- valve.  When  once  adjusted  this  form  of  apparatus 
produces  a  relatively  constant  cooling  effect  and  facilitates  greatly  the 
manipulation  of  the  calorimetric  apparatus  as  a  whole. 

THE  THEKMO-ELECTBIC  ELEMENTS. 

In  order  to  detect  differences  in  temperature  between  the  copper  and 
zinc  walls,  some  system  for  measuring  temperature  differences  between  these 
walls  is  essential.  For  this  purpose  we  have  found  nothing  that  is  as  prac- 
tical as  the  system  of  iron-German-silver  thermo-electric  elements  origi- 
nally introduced  in  this  type  of  calorimeter  by  E.  B.  Rosa,  of  the  National 
Bureau  of  Standards,  formerly  professor  of  physics  at  Wesleyan  University. 
In  these  calorimeters  the  same  principle,  therefore,  has  been  applied,  and  it 
is  necessary  here  only  to  give  the  details  of  such  changes  in  the  construc- 
tion of  the  elements,  their  mounting,  and  their  insulation  as  have  been  made 
as  a  result  of  experience  in  constructing  these  calorimeters.  An  element 
consisting  of  four  pairs  of  junctions  is  shown  in  place  as  T-.T  in  fig.  25. 

One  ever-present  difficulty  with  the  older  form  of  element  was  the  ten- 
dency for  the  German-silver  wires  to  slip  out  of  the  slots  in  which  they  had 
been  vigorously  crowded  in  the  hard  maple  spool.  In  thus  slipping  out  of 
the  slots  they  came  in  contact  with  the  metal  thimble  in  the  zinc  wall  and 
thus  produced  a  ground.  In  constructing  the  new  elements  four  pairs  of 
iron-German-silver  thermal  junctions  were  made  on  essentially  the  same 
plan  as  that  previously  described,*  the  only  modification  being  made  in  the 
spool.  While  the  ends  of  the  junctions  nearest  the  copper  are  exposed  to 
the  air  so  as  to  take  up  most  rapidly  the  temperature  of  the  copper,  it  is 
somewhat  difficult  to  expose  the  ends  of  the  junctions  nearest  the  zinc  and 
at  the  same  time  avoid  short-circuiting.  The  best  procedure  is  to  extend 
the  rock  maple  spool  which  passes  clear  through  the  ferule  in  the  zinc 
wall  and  cut  a  wide  slot  in  the  spool  so  as  to  expose  the  junctions  to  the 
air  nearest  the  ferule.    By  so  doing  the  danger  to  the  unprotected  ends  of 

*W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington  Pub- 
lication No.  42,  p.  114.     (1905.) 


20  CALORIMETERS   FOR   STUDYING  RESPIRATORY  EXCHANGE,   ETC. 

the  junctions  is  much  less.  The  two  lead-wires  of  German  silver  can  be 
carried  through  the  end  of  the  spool  and  thus  allow  the  insulation  to  be 
made  much  more  satisfactorily.  In  these  calorimeters  free  use  of  these 
thermal  junctions  has  been  made.  In  the  chair  calorimeter  there  are  on 
the  top  16  elements  consisting  of  four  junctions  each,  on  the  rear  18,  on 
the  front  8,  and  on  the  bottom  13.  The  distribution  of  the  elements  is 
made  with  due  reference  to  the  direction  in  which  the  heat  is  most  directly 
radiated  and  conducted  from  the  surface  of  the  body. 

While  the  original  iron-German-silver  junctions  have  been  retained  in 
two  of  these  calorimeters  for  the  practical  reason  that  a  large  number  of 
these  elements  had  been  constructed  beforehand,  we  believe  it  will  be  more 
advantageous  to  use  the  copper-constantin  couple,  which  has  a  thermo- 
electric force  of  40  microvolts  per  degree  as  against  the  25  of  the  iron- 
German-silver  couple.  It  is  planned  to  install  the  copper-constantin  junc- 
tions in  the  calorimeters  now  building. 

INTERIOR  OF  THE  CALORIMETER. 

Since  the  experiments  to  be  made  with  this  chamber  will  rarely  exceed 
6  to  8  hours,  there  is  no  provision  made  for  installing  a  cot  bed  or  other 
conveniences  which  would  be  necessary  for  experiments  of  long  duration. 
Aside  from  the  arm-chair  with  the  foot-rest  suspended  from  the  balance, 
there  is  practically  no  furniture  inside  of  the  chamber,  and  a  shelf  or  two, 
usually  attached  to  the  chair,  to  support  bottles  for  urine  and  drinking- 
water  bottles,  completes  the  furniture  equipment.  The  construction  of  the 
calorimeter  is  such  as  to  minimize  the  volume  of  air  surrounding  the  subject 
and  yet  secure  sufficient  freedom  of  movement  to  have  him  comfortable. 
A  general  impression  of  the  arrangement  of  the  pipes,  chair,  telephone,  etc., 
inside  the  chamber  can  be  obtained  from  figs.  7  and  9.  The  heat-absorber 
system  is  attached  to  rings  soldered  to  the  ceiling  at  different  points.  The 
incoming  air-pipe  is  carried  to  the  top  of  the  central  dome,  while  the  air  is 
drawn  from  the  calorimeter  at  a  point  at  the  lower  front  near  the  position 
of  the  feet  of  the  subject.  From  this  point  it  is  carried  through  a  pipe  along 
the  floor  and  up  the  rear  wall  of  the  calorimeter  to  the  exit. 

With  the  perfect  heat  insulation  obtaining,  the  heat  production  of  the 
man  would  soon  raise  the  temperature  to  an  uncomfortable  degree  were 
there  no  provisions  for  withdrawing  it.  It  is  therefore  necessary  to  cool 
the  chamber  and,  as  has  been  pointed  out,  the  cooling  is  accomplished  by 
passing  a  current  of  cold  water  through  a  heat-absorbing  apparatus  per- 
manently installed  in  the  interior  of  the  chamber.  The  heat-absorber  con- 
sists of  a  continuous  copper  pipe  of  6  millimeters  internal  diameter  and  10 
millimeters  external  diameter.  Along  this  pipe  there  are  soldered  a  large 
number  of  copper  disks  5  centimeters  in  diameter  at  a  distance  of  5  milli- 
meters from  each  other.    This  increases  enormously  the  area  for  the  absorp- 


THE   CALORIMETER.  21 

tion  of  heat.  In  order  to  allow  the  absorber  system  to  be  removed,  added  to, 
or  repaired  at  any  time,  it  is  necessary  to  insert  couplings  at  several  points. 
This  is  usually  done  at  corners  where  the  attachment  of  disks  is  not  prac- 
ticable. The  total  length  of  heat-absorbers  is  5.6  meters  and  a  rough  calcu- 
lation shows  that  the  total  area  of  metal  for  the  absorption  of  heat  is  4.7 
square  meters.  The  total  volume  of  water  in  the  absorbers  is  254  cubic 
centimeters. 

It  has  been  found  advantageous  to  place  a  simple  apparatus  to  mix  the 
water  in  the  water-cooling  circuit  at  a  point  just  before  the  water  leaves 
the  chamber.  This  water-mixer  consists  of  a  15-centimeter  length  of  stand- 
ard 1-inch  pipe  with  a  cap  at  each  end.  Through  each  of  these  caps  there 
is  a  piece  of  one-eighth-inch  pipe  which  extends  nearly  the  whole  length  of 
the  mixer.  The  water  thus  passing  into  one  end  returns  inside  the  1-inch 
pipe  and  leaves  from  the  other.  This  simple  device  insures  a  thorough 
mixing. 

The  air-pipes  are  of  thin  brass,  1-inch  internal  diameter.  One  of  them 
conducts  the  air  from  the  ingoing  air-pipe  up  into  the  top  of  the  central 
dome  or  hood  immediately  above  the  head  of  the  subject.  The  air  thus 
enters  the  chamber  through  a  pipe  running  longitudinally  along  the  top 
of  the  dome.  On  the  upper  side  of  this  pipe  a  number  of  holes  have  been 
drilled  so  as  to  have  the  air-current  directed  upwards  rather  than  down 
against  the  head  of  the  subject.  With  this  arrangement  no  difficulties  are 
experienced  with  uncomfortable  drafts  and  although  the  air  enters  the 
chamber  through  this  pipe  absolutely  dry,  there  is  no  uncomfortable  sensa- 
tion of  extreme  dryness  in  the  air  taken  in  at  the  nostrils,  nor  is  the  absorp- 
tion of  water  from  the  skin  of  the  face,  head,  or  neck  great  enough  to  pro- 
duce an  uncomfortable  feeling  of  cold.  The  other  air-pipe,  as  suggested, 
receives  the  air  from  the  chamber  at  the  lower  front  and  passes  around  the 
rear  to  the  point  where  the  outside  air-pipe  leaves  the  chamber. 

The  chamber  is  illuminated  by  a  small  glass  door  in  the  food  aperture. 
This  is  a  so-called  "  port "  used  on  vessels.  Sufficient  light  passes  through 
this  glass  to  enable  the  subject  to  see  inside  the  calorimeter  without  diffi- 
culty and  most  of  the  subjects  can  read  with  comfort.  If  an  electric  light 
is  placed  outside  of  the  window,  the  illumination  is  very  satisfactory  and 
repeated  tests  have  shown  that  no  measurable  amount  of  heat  passes  through 
the  window  by  placing  a  32  c.  p.  electric  lamp  0.5  meter  from  the  food 
aperture  outside.  More  recently  we  have  arranged  to  produce  directly 
inside  the  chamber  illumination  by  means  of  a  small  tungsten  electric  lamp 
connected  to  the  storage  battery  outside  of  the  chamber.  This  lamp  is 
provided  with  a  powerful  mirror  and  a  glass  shade,  so  that  the  light  is  very 
bright  throughout  the  chamber  and  is  satisfactory  for  reading.  It  is  neces- 
sary, however,  to  make  a  correction  for  the  heat  developed,  amounting 
usually  to  not  far  from  3  calories  per  hour. 


22 


CALORIMETERS   FOR    STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


By  means  of  a  hand  microphone  and  receiver,  the  subject  can  communi- 
cate with  the  observers  outside  at  will.  A  push-button  and  an  electric  bell 
make  it  possible  for  him  to  call  the  observers  whenever  desired. 

HEAT-ABSORBING    CIRCUIT. 

To  bring  away  the  heat  produced  by  the  subject,  it  is  highly  desirable 
that  a  constant  flow  of  water  of  even  temperature  be  secured.  Direct  con- 
nection with  the  city  supply  is  not  practicable,  owing  to  the  variations  in 
pressure,  and  hence  in  constructing  the  laboratory  building  provision  was 
made  to  install  a  large  tank  on  the  top  floor,  fed  with  a  supply  controlled 
by  a  ball-and-cock  valve.     By  this  arrangement  the  level  in  the  tank  is 

maintained  constant  and 
the  pressure  is  therefore 
regular.  As  the  level  of 
the  water  in  the  tank  is 
approximately  9  meters 
above  the  opening  in  the 
calorimeter,  there  is  am- 
ple pressure  for  all  pur- 
poses. 

The  water  descends 
from  this  tank  in  a  large 
2-inch  pipe  to  the  ceiling 
of  the  calorimeter  labora- 
tory, where  it  is  subdi- 
vided into  three  1-inch 
pipes,  so  as  to  provide 
for  a  water-supply  for 
three  calorimeters  used 
simultaneously,  if  neces- 
sary, and  eliminate  the 
influence  of  a  variation 
in  the  rate  of  flow  in  one 
calorimeter  upon  the  rate  of  flow  in  another.  These  pipes  are  brought 
down  the  inner  wall  of  the  room  adjacent  to  the  refrigeration  room  and  part 
of  the  water  circuit  is  passed  through  a  brass  coil  immersed  in  a  cooling- 
tank  in  the  refrigeration  room.  By  means  of  a  by-pass,  water  of  any  degree 
of  temperature  from  2°  C.  to  20°  C.  may  be  obtained.  The  water  is  then 
conducted  through  a  pipe  beneath  the  floor  to  the  calorimeter  chamber, 
passed  through  the  absorbers,  and  is  finally  measured  in  the  water-meter. 
A  diagrammatic  sketch  showing  the  course  of  the  water-current  is  given 
(fig.  14),  in  which  A  is  the  tank  on  the  top  floor  controlled  by  the  ball 
cock  and  valve,  and  a  is  the  main  valve  which  controls  this  supply  to  the 


Fig.  14. — Schematic  diagram  of  water  circuit  for  heat-absorbers  of 
calorimeter.  A,  constant-level  tank  from  which  water  de- 
scends to  main  pipe  supplying  heat-absorbers;  o,  valve  for 
controlling  supply  from  tank  A;  B,  section  of  piping  passing 
into  cold  brine;  6,  valve  controlling  water  direct  from  large 
tank  A;  c,  valve  controlling  amount  of  water  from  cooling 
section  B;  C,  thermometer  at  mixer;  D,  electric  heater  for 
ingoing  water;  E,  thermometer  for  ingoing  water;  d  d  d, 
heat-absorbers  inside  calorimeter;  F,  thermometer  indicating 
temperature  of  outcoming  water;  G,  can  for  collecting  water 
from  calorimeter;  f,  valve  for  emptying  G. 


THE   CALORIMETER-  23 

cooler  B,  and  by  adjusting  the  valve  6  and  valve  c  any  desired  mixture  of 
water  can  be  obtained.  A  thermometer  C  gives  a  rough  idea  of  the  tem- 
perature of  the  water,  so  as  to  aid  in  securing  the  proper  mixture.  The 
water  then  passes  under  the  floor  of  the  calorimeter  laboratory  and  ascends 
to  the  apparatus  D,  which  is  used  for  heating  it  to  the  desired  temperature 
before  entering  the  calorimeter.  The  temperature  of  the  water  as  it  enters 
the  calorimeter  is  measured  on  an  accurately  calibrated  thermometer  E, 
and  it  then  passes  through  the  absorber  system  d  d  d  and  leaves  the  calo- 
rimeter, passing  the  thermometer  F,  upon  which  the  final  temperature  is 
read.  It  then  passes  through  a  pipe  and  falls  into  a  large  can  G,  placed 
upon  scales.  When  this  can  is  filled  the  water  is  deflected  for  a  few  minutes 
to  another  can  and  by  opening  valve  /  the  water  is  conducted  to  the  drain 
after  having  been  weighed. 

Brine-tank. — The  cooling  system  for  the  water-supply  consists  of  a  tank 
in  which  there  is  immersed  an  iron  coil  connected  by  two  valves  to  the 
supply  and  return  of  the  brine  mains  from  the  central  power-house.  These 
valves  are  situated  just  ahead  of  the  valves  controlling  the  cooling  device  in 
the  refrigeration  room  and  permit  the  passage  of  brine  through  the  coil 
without  filling  the  large  coils  for  the  cooling  of  the  air  in  the  calorimeter 
laboratory.  As  the  brine  passes  through  this  coil,  which  is  not  shown  in 
the  figure,  it  cools  the  water  in  which  it  is  immersed  and  the  water  in  turn 
cools  the  coil  through  which  the  water-supply  to  the  calorimeter  passes. 
The  brass  coil  only  is  shown  in  the  figure.  The  system  is  very  efficient  and 
we  have  no  difficulty  in  cooling  the  water  as  low  as  2°  C.  As  a  matter  of  fact 
our  chief  difficulty  is  in  regulating  the  supply  of  brine  so  as  not  to  freeze 
the  water-supply. 

Water-mixer. — If  the  valve  6  is  opened,  water  flows  through  this  short 
length  of  pipe  much  more  rapidly  than  through  the  long  coil,  owing  to  the 
greater  resistance  of  the  cooling  coil.  In  conducting  these  experiments  the 
valve  c  is  opened  wide  and  by  varying  the  amount  to  which  the  valve  &  is 
opened,  the  water  is  evenly  and  readily  mixed.  The  thermometer  C  is  in 
practice  immersed  in  the  water-mixer  constructed  somewhat  after  the  prin- 
ciple of  the  mixer  inside  the  chamber  described  on  page  21.  All  the  piping, 
including  that  under  the  floor,  and  the  reheater  D,  are  covered  with  hair-felt 
and  well  insulated. 

Rate-valves. — It  has  been  found  extremely  difficult  to  secure  any  form  of 
valve  which,  even  with  a  constant  pressure  of  water,  will  give  a  constant 
rate  of  flow.  In  this  type  of  calorimeter  it  is  highly  desirable  that  the  rate 
of  flow  be  as  nearly  constant  as  possible  hour  after  hour,  as  this  constant 
rate  of  flow  aids  materially  in  maintaining  the  calorimeter  at  an  even 
temperature.  Obviously,  fluctuations  in  the  rate  of  flow  will  produce  fluc- 
tuations in  the  temperature  of  the  ingoing  water  and  in  the  amount  of 


24  CALORIMETERS    FOR   STUDYING   RESPIRATORY    EXCHANGE,   ETC. 

heat  brought  away.  This  disturbs  greatly  the  temperature  equilibrium, 
which  is  ordinarily  maintained  fairly  constant.  Just  before  the  water 
enters  the  reheater  D  it  is  caused  to  pass  through  a  rate-valve,  which  at 
present  consists  of  an  ordinary  plug-cock.  At  present  we  are  experimenting 
with  other  types  of  valves  to  secure  even  greater  constancy,  if  possible. 

Electric  reheater. — In  order  to  control  absolutely  the  temperature  of  the 
water  entering  at  E,  it  is  planned  to  cool  the  water  leaving  the  water- 
mixer  at  C  somewhat  below  the  desired  temperature,  so  that  it  is  necessary 
to  reheat  it  to  the  desired  point.  This  is  done  by  passing  a  current  of 
electricity  through  a  coil  inserted  in  the  system  at  the  point  D.  This 
electric  reheater  consists  of  a  standard  "  Simplex "  coil,  so  placed  in  the 
copper  can  that  the  water  has  a  maximum  circulation  about  the  heater. 
The  whole  device  is  thoroughly  insulated  with  hair-felt.  By  connecting 
the  electric  reheater  with  the  rheostat  on  the  observer's  table,  control  of  the 
quantity  of  electricity  passing  through  the  coil  is  readily  obtained,  and 
hence  it  is  possible  to  regulate  the  temperature  of  the  ingoing  water  to 
within  a  few  hundredths  of  a  degree. 

The  control  of  the  amount  of  heat  brought  away  from  the  chamber  is 
made  either  by  (1)  increasing  the  rate  of  flow  or  (2)  by  varying  the  tem- 
perature of  the  ingoing  water.  Usually  only  the  second  method  is  neces- 
sary. In  the  older  form  of  apparatus  a  third  method  was  possible,  namely, 
by  varying  the  area  of  the  absorbing  surface  of  the  cooling  system  inside 
of  the  chamber.  This  last  method  of  regulation,  which  was  used  almost 
exclusively  in  earlier  experiments,  called  for  an  elaborate  system  of  shields 
which  could  be  raised  or  lowered  at  will  by  the  operator  outside,  thus 
involving  an  opening  through  the  chamber  which  was  somewhat  difficult 
to  make  air-tight  and  also  considerably  complicating  the  mechanism  inside 
the  chamber.  The  more  recent  method  of  control  by  regulating  the  tem- 
perature of  the  ingoing  water  by  the  electric  reheater  has  been  much  refined 
and  has  given  excellent  service. 

Insulation  of  water-pipes  through  the  wall. — To  insulate  the  water-pipes 
as  they  pass  through  the  metal  walls  of  the  calorimeter  and  to  prevent  any 
cooling  effect  not  measured  by  the  thermometers  presented  great  difficulties. 
The  device  employed  in  the  Middletown  chamber  was  relatively  simple,  but 
very  inaccessible  and  a  source  of  more  or  less  trouble,  namely,  a  large-sized 
glass  tube  embedded  in  a  large  round  wooden  plug  with  the  annular  space 
between  the  glass  and  wood  filled  with  wax.  An  attempt  was  made  in  the 
new  calorimeters  to  secure  air  insulation  by  using  a  large-sized  glass  tube, 
some  15  millimeters  internal  diameter,  and  passing  it  through  a  large  rub- 
ber stopper,  fitting  into  a  brass  ferule  soldered  between  the  zinc  and  copper 
walls.  (See  N,  fig.  25.)  So  far  as  insulation  was  concerned,  this  arrange- 
ment was  very  satisfactory,  but  unfortunately  the  glass  tubes  break  readily 


THE   CALORIMETER.  25 

and  difficulty  was  constantly  experienced.  An  attempt  was  next  made  to 
substitute  hard-rubber  tubing  for  the  glass  tube,  but  this  did  not  prove  to 
be  an  efficient  insulator.  More  recently  we  have  used  with  perfect  success 
a  special  form  of  vacuum-jacketed  glass  tube,  which  gives  the  most  satis- 
factory insulation.  However,  this  system  of  insulation  is  impracticable 
when  electric-resistance  thermometers  are  used  for  recording  the  water- 
temperature  differences  and  can  be  used  only  when  mercurial  thermometers 
exclusively  are  employed.  The  electric-resistance  thermometers  are  con- 
structed in  such  a  way,  however,  as  to  make  negligible  any  inequalities  in 
the  passage  of  heat  through  the  hard-rubber  casing.  This  will  be  seen  in 
the  discussion  of  these  thermometers. 

Measuring  the  water. — As  the  water  leaves  the  respiration  chamber  it 
passes  through  a  valve  which  allows  it  to  be  deflected  either  into  the  drain 
during  the  preliminary  period,  or  into  a  small  can  where  the  measure- 
ments of  the  rate  of  flow  can  readily  be  made,  or  into  a  large  tank  (G,  fig. 
14)  where  the  water  is  weighed.  The  measurement  of  the  water  is  made  by 
weight  rather  than  by  volume,  as  it  has  been  found  that  the  weighing  may 
be  carried  out  with  great  accuracy.  The  tank,  a  galvanized-iron  ash-can, 
is  provided  with  a  conical  top,  through  an  opening  in  which  a  funnel  is 
placed.  The  diagram  shows  the  water  leaving  the  calorimeter  and  entering 
the  meter  through  this  funnel,  but  in  practice  it  is  adjusted  to  enter  through 
an  opening  on  the  side  of  the  meter.  After  the  valve  f  is  tightly  closed  the 
empty  can  is  weighed. 

When  the  experiment  proper  begins  the  water-current  is  deflected  so  as 
to  run  into  this  can  and  at  the  end  of  an  hour  the  water  is  deflected  into 
a  small  can  used  for  measuring  the  rate  of  flow.  While  it  is  running  into 
this  can,  the  large  can  G  is  weighed  on  platform  scales  to  within  10  grams. 
After  weighing,  the  water  is  again  deflected  into  the  large  can  and  that 
collected  in  the  small  measuring  can  is  poured  into  G  through  the  funnel. 
The  can  holds  about  100  liters  of  water  and  consequently  from  3  to  8  one- 
hour  periods,  depending  upon  the  rate  of  flow,  can  be  continued  without 
emptying  the  meter.  When  it  is  desired  to  empty  the  meter  at  the  end  of 
the  period,  the  water  is  allowed  to  flow  into  the  small  can,  and  after  weigh- 
ing G,  the  valve  f  is  opened.  About  4  minutes  are  required  to  empty  the 
large  can.  After  this  the  valve  is  again  closed,  the  empty  can  weighed,  and 
the  water  in  the  small  measuring-can  poured  into  the  large  can  G  through 
the  funnel.  The  scales  used  are  the  so-called  silk  scales  and  are  listed  by 
the  manufacturers  to  weigh  150  kilograms.  This  form  of  scales  was  formerly 
used  in  weighing  the  man  inside  the  chamber.* 


*W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42,  p.  158.     (1905.) 


26  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,  ETC. 

THERMOMETERS. 

In  connection  with  the  calorimeter  and  the  accessories,  mercurial  and 
electric-resistance  thermometers  are  employed.  For  measuring  the  tem- 
perature of  the  water  as  it  enters  and  leaves  the  chamber  through  horizontal 
tubes,  mercurial  thermometers  are  used,  and  these  are  supplemented  by 
electric-resistance  thermometers  which  are  connected  with  a  special  form  of 
recording  instrument  for  permanently  recording  the  temperature  differ- 
ences. For  the  measurement  of  the  temperatures  inside  of  the  calorimeter, 
two  sets  of  electric-resistance  thermometers  are  used,  one  of  which  is  a 
series  of  open  coils  of  wire  suspended  in  the  air  of  the  chamber  so  as  to 
take  up  quickly  the  temperature  of  the  air.  The  other  set  consists  of  resist- 
ance coils  encased  in  copper  boxes  soldered  to  the  copper  wall  and  are 
designed  to  indicate  the  temperature  of  the  copper  wall  rather  than  that 
of  the  air. 

MERCURIAL  THERMOMETERS. 

The  mercurial  thermometers  used  for  measuring  the  temperature  differ- 
ences of  the  water-current  are  of  special  construction  and  have  been  cali- 
brated with  the  greatest  accuracy.  As  the  water  enters  the  respiration 
chamber  through  a  horizontal  tube,  the  thermometers  are  so  constructed 
and  so  placed  in  the  horizontal  tubes  through  which  the  water  passes  that 
the  bulbs  of  the  thermometers  lie  about  in  a  plane  with  the  copper  wall, 
thus  taking  the  temperature  of  the  water  immediately  as  it  enters  and  as  it 
leaves  the  chamber.  For  convenience  in  reading,  the  stem  of  the  ther- 
mometer is  bent  at  right  angles  and  the  graduations  are  placed  on  the 
upright  part. 

The  thermometers  are  graduated  from  0°  to  12°  C.  or  from  8°  to  20°  C. 
and  each  degree  is  divided  into  fiftieths.  Without  the  use  of  a  lens  it  is 
possible  to  read  accurately  to  the  hundredth  of  a  degree.  For  calibrating 
these  thermometers  a  special  arrangement  is  necessary.  The  standards  used 
consist  of  well-constructed  metastatic  thermometers  of  the  Beckmann  type, 
made  by  C.  Eichter,  of  Berlin,  and  calibrated  by  the  Physikalische  Tech- 
nische  Eeichsanstalt.  Furthermore,  a  standard  thermometer,  graduated 
from  14°  to  24°  C,  also  made  by  Eichter  and  standardized  by  the  Physi- 
kalische Technische  Eeichsanstalt,  serves  as  a  basis  for  securing  the  absolute 
temperature.  Since,  however,  on  the  mercurial  thermometers  used  in  the 
water-current,  differences  in  temperature  are  required  rather  than  absolute 
temperatures,  it  is  unnecessary,  except  in  an  approximate  way,  to  stand- 
ardize the  thermometers  on  the  basis  of  absolute  temperature.  For  cali- 
brating the  thermometers,  an  ordinary  wooden  water-pail  is  provided  with 
several  holes  in  the  side  near  the  bottom.  One-hole  rubber  stoppers  are 
inserted  in  these  holes  and  through  these  are  placed  the  bulbs  and  stems  of 
the  different  thermometers  which  are  to  be  calibrated.     The  upright  por- 


THE   CALORIMETER.  27 

tion  of  the  stem  is  held  in  a  vertical  position  by  a  clamp.  The  pail  is  filled 
with  water,  thereby  insuring  a  large  mass  of  water  and  slow  temperature 
fluctuations,  and  the  water  is  stirred  by  means  of  an  electrically  driven 
turbine  stirrer. 

The  Beckmann  thermometers,  of  which  two  are  used,  are  so  adjusted 
that  they  overlap  each  other  and  thus  allow  a  range  of  8°  to  14°  C.  without 
resetting.  For  all  temperatures  above  14°  C,  the  standard  Richter  ther- 
mometer can  be  used  directly.  For  temperatures  at  8°  C.  or  below,  a  large 
funnel  filled  with  cracked  ice  is  placed  with  the  stem  dipping  into  the  water. 
As  the  ice  melts,  the  cooling  effect  on  the  large  mass  of  water  is  sufficient 
to  maintain  the  temperature  constant  and  compensate  the  heating  effect  of 
the  surrounding  room-air.  The  thermometers  are  tapped  and  read  as  nearly 
simultaneously  as  possible.  A  number  of  readings  are  taken  at  each  point 
and  the  average  readings  used  in  the  calculations.  Making  due  allowance 
for  the  corrections  on  the  Beckmann  thermometers,  the  temperature  differ- 
ences can  be  determined  to  less  than  0.01°  C.  The  data  obtained  from  the 
calibrations  are  therefore  used  for  comparison  and  a  table  of  corrections  is 
prepared  for  each  set  of  thermometers  used.  It  is  especially  important  that 
these  thermometers  be  compared  among  themselves  with  great  accuracy, 
since  as  used  in  the  calorimeter  the  temperature  of  the  ingoing  water  is 
measured  on  one  thermometer  and  the  temperature  of  the  outgoing  water 
on  another. 

Thermometers  of  this  type  are  extremely  fragile.  The  long  angle  with 
an  arm  some  35  centimeters  in  length  makes  it  difficult  to  handle  them 
without  breakage,  but  they  are  extremely  sensitive  and  accurate  and  have 
given  great  satisfaction.  The  construction  of  the  bulb  is  such,  however, 
that  the  slightest  pressure  on  it  raises  the  column  of  mercury  very  percep- 
tibly, and  hence  it  is  important  in  practical  use  to  note  the  influence  of  the 
pressure  of  the  water  upon  the  bulbs  and  make  corrections  therefor.  The 
influence  of  such  pressure  upon  thermometers  used  in  an  apparatus  of  this 
type  was  first  pointed  out  by  Armsby,*  and  with  high  rates  of  flow,  amount- 
ing to  1  liter  or  more  per  minute,  there  may  be  a  correction  on  these  ther- 
mometers amounting  to  several  hundredths  of  a  degree.  We  have  found 
that,  as  installed  at  present,  with  a  rate  of  flow  of  less  than  400  cubic  cen- 
timeters per  minute,  there  is  no  correction  for  water  pressure. 

In  installing  a  thermometer  it  is  of  the  greatest  importance  that  there 
be  no  pressure  against  the  side  of  the  tube  through  which  the  thermometer 
is  inserted.  The  slightest  pressure  will  cause  considerable  rise  in  the  mer- 
cury column.  Special  precautions  must  also  be  taken  to  insulate  the  tube 
through  which  the  water  passes,  as  the  passage  of  the  water  along  the  tube 
does  not  insure  ordinarily  a  thorough  mixing,  and  by  moving  the  thermom- 

*  Armsby:  U.  S.  Dept.  of  Agr.,  Bureau  of  Animal  Industry  Bull.  51  p  34 
(1903.) 


28 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


eter  bulb  from  the  center  of  the  tube  to  a  point  near  the  edge,  the  water, 
which  at  the  edge  may  be  somewhat  warmer  than  at  the  center,  immediately 
affects  the  thermometer.  By  use  of  the  vacuum  jacket  mentioned  above, 
this  warming  of  the  water  has  been  avoided,  and  in  electric-resistance  ther- 
mometers special  precautions  are  taken  not  only  with  regard  to  the  relative 
position  of  the  bulb  of  the  mercury  thermometer  and  the  resistance  ther- 
mometer, but  also  with  regard  to  the  hard-rubber  insulation,  to  avoid  errors 
of  this  nature. 

ELECTRIC-RESISTANCE  THERMOMETERS. 

Electric-resistance  thermometers  are  used  in  connection  with  the  respira- 
tion calorimeter  for  several  purposes :  first,  to  determine  the  fluctuations  in 
the  temperature  of  the  air  inside  the  chamber;  second,  to  measure  the 
fluctuations  of  the  temperature  of  the  copper  wall  of  the  respiration  cham- 
ber; third,  for  determining  the  variations  in  body  tem- 
perature ;  finally,  for  recording  the  differences  in  tempera- 
ture of  the  incoming  and  outgoing  water.     While  these 
thermometers  are  all  built  on  the  same  principle,  their 
installation  is  very  different,  and  a  word  regarding  the 
method  of  using  each  is  necessary. 

AIR  THERMOMETERS. 

The  air  thermometers  are  designed  with  a  special  view 
to  taking  quickly  the  temperature  of  the  air.  Five  ther- 
mometers, each  having  a  resistance  of  not  far  from  4  ohms, 
are  connected  in  series  and  suspended  3.5  centimeters  from 
the  wall  on  hooks  inside  the  chamber.  They  are  surrounded 
for  protection,  first,  with  a  perforated  metal  cylinder,  and 
outside  this  with  a  wire  guard. 

The  details  of  construction  and  method  of  installation 
are  shown  in  fig.  15.  Four  strips  of  mica  are  inserted  into 
four  slots  in  a  hard  maple  rod  12.5  centimeters  long  and 
12  millimeters  in  diameter,  and  around  each  strip  is  wound 
5  meters  of  double  silk-covered  pure  copper  wire  (wire-gage 
No.  30).  By  means  of  heavy  connecting  wires,  five  of  these 
thermometers  are  connected  in  series,  giving  a  total  resist- 
ance of  the  system  of  not  far  from  20  ohms.  The  ther- 
mometer proper  is  suspended  between  two  hooks  by  rubber 
bands  and  these  two  hooks  are  in  turn  fastened  to  a  wire 
guard  which  is  attached  to  threaded  rods  soldered  to  the  inner  surface  of  the 
copper  wall,  thus  bringing  the  center  of  the  thermometer  3.4  centimeters 
from  the  copper  wall.  Two  of  these  thermometers  are  placed  in  the  dome 
of  the  calorimeter  immediately  over  the  shoulders  of  the  subject,  and  the 
other  three  are  distributed  around  the  sides  and  front  of  the  chamber.    This 


Fig.  15.— Detail  of 
air-resistanae 
thermometer, 
showing  method 
of  mounting  and 
wiring  the  ther- 
mometer. Parts 
of  the  wire  guard 
and  brass  guard 
are  shown,  cut 
away  so  that  in- 
terior structure 
can  be  seen. 


THE   CALORIMETER.  29 

type  of  construction  gives  maximum  sensibility  to  the  temperature  fluctua- 
tions of  the  air  itself  and  yet  insures  thorough  protection.  The  two  termi- 
nals are  carried  outside  of  the  respiration  chamber  to  the  observer's  table, 
where  the  temperature  fluctuations  are  measured  on  a  Wheatstone  bridge. 

WALL  THEBMOMETEBS. 

The  wall  thermometers  are  designed  for  the  purpose  of  taking  the  tem- 
perature of  the  copper  wall  rather  than  the  temperature  of  the  air.  When 
temperature  fluctuations  are  being  experienced  inside  of  the  respiration 
chamber,  the  air  obviously  shows  temperature  fluctuations  first,  and  the 
copper  walls  are  next  affected.  Since  in  making  corrections  for  the  hydro- 
thermal  equivalent  of  the  apparatus  and  for  changes  in  the  temperature 
of  the  apparatus  as  a  whole  it  is  desirable  to  know  the  temperature  changes 
of  the  wall  rather  than  the  air,  these  wall  thermometers  were  installed  for 
this  special  purpose.  In  construction  they  are  not  unlike  the  thermometers 
used  in  the  air,  but  instead  of  being  surrounded  by  perforated  metal  they 
are  encased  in  copper  boxes  soldered  directly  to  the  wall.  Five  such  ther- 
mometers are  used  in  series  and,  though  attached  permanently  to  the  wall, 
they  are  placed  in  relatively  the  same  position  as  the  air  thermometers.  The 
two  terminals  are  conducted  through  the  metal  walls  to  the  observer's  table, 
where  variations  in  resistance  are  measured.  The  resistance  of  the  five 
thermometers  is  not  far  from  20  ohms. 

ELECTRICAL  RECTAL  THERMOMETER. 

The  resistance  thermometer  used  for  measuring  the  temperature  of  the 
body  of  the  man  is  of  a  somewhat  different  type,  since  it  is  necessary  to 
wind  the  coil  in  a  compact  form,  inclose  it  in  a  pure  silver  tube,  and  con- 
nect it  with  suitable  rubber-covered  connections,  so  that  it  can  be  inserted 
deep  in  the  rectum.  The  apparatus  has  been  described  in  a  number  of 
publications.*  The  resistance  of  this  system  is  also  not  far  from  20  ohms, 
thus  simplifying  the  use  of  the  apparatus  already  installed  on  the  observer's 
table. 

ELECTRIC-RESISTANCE  THERMOMETERS  FOR  THE  WATER-CURRENT. 

The  measurement  of  the  temperature  differences  of  the  water-current  by 
the  electric-resistance  thermometer  was  tried  a  number  of  years  ago  by 
Rosa,f  but  the  results  were  not  invariably  satisfactory  and  in  all  the  sub- 

*  Benedict  and  Snell:  Eine  neue  Methode  um  Korpertemperaturen  zu  messen. 
Archiv  f.  d.  ges.  Physiologic  Bd.  88,  pp.  492-500.     (1901.) 

W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42,  p.  156.     (1905.) 

fRosa:     U.  S.  Dept.  of  Agric,  Office  of  Experiment  Stations  Bui.  63,  p.  25. 


30 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,    ETC. 


sequent  experimenting  the  resistance  thermometer  could  not  be  used  with 
satisfaction.  More  recently,  plans  were  made  to  incorporate  some  of  the 
results  of  the  rapidly  accumulating  experience  in  the  use  of  resistance  ther- 
mometers and  consequently  an  electric-resistance  thermometer  was  devised 
to  meet  the  conditions  of  experimentation  with  the  respiration  calorimeter 
by  Dr.  E.  F.  Northrup,  of  the  Leeds  &  Northrup  Company,  of  Philadelphia. 
The  conditions  to  be  met  were  that  the  thermometers  should  take  rapidly 
the  temperature  of  the  ingoing  and  outcoming  water  and  that  the  fluctua- 
tions in  temperature  difference  as  measured  by  the  resistance  thermometers 
should  be  controlled  for  calibration  purposes  by  the  differences  in  tempera- 
ture of  the  mercurial  thermometers. 

For  the  resistance  thermometer,  Dr.  Northrup  has  used,  instead  of  copper, 
pure  nickel  wire,  which  has  a  much  higher  resistance  and  thus  enables  a 


J"       A 


Fig.  16. — Details  of  resistance  thermometers  for  water-circuit.  Upper  part  of 
figure  shows  a  sketch  of  the  outside  of  the  hard-rubber  case.  In  lower  part 
is  a  section  showing  interior  construction.  Flattened  lead  tube  wound  about 
central  brass  tube  contains  the  resistance  wire.  A  is  enlarged  part  of  the  case 
forming  a  chamber  for  the  mercury  bulb.  Arrows  indicate  direction  of  flow 
on  resistance  thermometer  for  ingoing  water. 


much  greater  total  resistance  to  be  inclosed  in  a  given  space.  The  insu- 
lated nickel  wire  is  wound  in  a  flattened  spiral  and  then  passed  through  a 
thin  lead  tube  flattened  somewhat.  This  lead  tube  is  then  wound  around 
a  central  core  and  the  flattened  portions  attached  at  such  an  angle  that  the 
water  passing  through  the  tubes  has  a  tendency  to  be  directed  away  from 
the  center  and  against  the  outer  wall,  thus  insuring  a  mixing  of  the  water. 
Space  is  left  for  the  insertion  of  the  mercurial  thermometer.  With  the 
thermometer  for  the  ingoing  water,  it  was  found  necessary  to  extend  the 
bulb  somewhat  beyond  the  resistance  coil,  so  that  the  water  might  be 
thoroughly  mixed  before  reaching  the  bulb  and  thus  insure  a  steady  tem- 
perature. Thus  it  was  found  necessary  to  enlarge  the  chamber  A  (fig.  16) 
somewhat  and  the  tube  leading  out  of  the  thermometer,  so  that  the  bulb  of 
the  thermometer  itself  could  be  placed  almost  directly  at  the  opening  of  the 
exit  tube.  Under  these  conditions  perfect  mixing  of  water  and  constancy 
of  temperature  were  obtained. 


THE   CALORIMETER.  31 

In  the  case  of  the  thermometer  which  measured  the  outcoming  water, 
the  difficulty  was  not  so  great,  as  the  outcoming  water  is  somewhat  nearer 
the  temperature  of  the  chamber,  and  the  water  as  it  leaves  the  thermometer 
passes  first  over  the  mercurial  thermometer  and  then  over  the  resistance 
thermometer.  By  means  of  a  long  series  of  tests  it  was  found  possible  to 
adjust  these  resistance  thermometers  so  that  the  variations  in  resistance 
were  in  direct  proportion  to  the  temperature  changes  noted  on  the  mercu- 
rial thermometers.  Obviously,  these  differences  in  resistance  of  the  two 
thermometers  can  be  measured  directly  with  the  Wheatstone  bridge,  but, 
what  is  more  satisfactory,  they  are  measured  and  recorded  directly  on  a 
special  type  of  automatic  recorder  described  beyond. 

OBSERVER'S  TABLE. 

The  measurements  of  the  temperature  of  the  respiration  chamber,  of  the 
water-current,  and  of  the  body  temperature  of  the  man,  as  well  as  the  heating 
and  cooling  of  the  air-spaces  about  the  calorimeter,  are  all  under  the  control 
of  the  physical  assistant.  The  apparatus  for  these  temperature  controls 
and  measurements  is  all  collected  compactly  on  a  table,  the  so-called  "  ob- 
server's table."  At  this,  the  physical  assistant  sits  throughout  the  experi- 
ments. For  convenience  in  observing  the  mercurial  thermometers  in  the 
water-current  and  general  inspection  of  the  whole  apparatus,  this  table 
is  placed  on  an  elevated  platform,  shown  in  fig.  3.  Directly  in  front  of  the 
table  the  galvanometer  is  suspended  from  the  ceiling  and  a  black  hood 
extends  from  the  observer's  table  to  the  galvanometer  itself.  On  the  ob- 
server's table  proper  are  all  the  electrical  connections  and  at  the  left  are  the 
mercurial  thermometers  for  the  chair  calorimeter.  Formerly,  when  the 
method  of  alternately  cooling  and  heating  the  air-spaces  was  used,  the 
observer  was  able  to  open  and  close  the  water-valves  without  leaving  the 
chair. 

The  observer's  table  is  so  arranged  electrically  as  to  make  possible  tem- 
perature control  and  measurement  of  either  of  the  two  calorimeters.  It  is 
impossible,  however,  for  the  observer  to  read  the  mercurial  thermometers 
in  the  bed  calorimeter  without  leaving  his  chair,  and  likewise  he  must 
occasionally  alter  the  cooling  water  flowing  through  the  outer  air-spaces 
by  going  to  the  bed  calorimeter  itself.  The  installation  of  the  electric- 
resistance  thermometers  connected  with  the  temperature  recorder  does  away 
with  the  reading  of  the  mercurial  thermometers,  save  for  purposes  of  com- 
parison, and  hence  it  is  unnecessary  for  the  assistant  to  leave  the  chair  at 
the  observer's  table  when  the  bed  calorimeter  is  in  use.  Likewise  the  sub- 
stitution of  the  method  of  continuously  cooling  somewhat  the  air-spaces 
and  reheating  with  electricity,  mentioned  on  page  18,  does  away  with  the 
necessity  for  alternately  opening  and  closing  the  water-valves  of  the  chair 
calorimeter  placed  at  the  left  of  the  observer's  table. 


32 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,    ETC. 


Of  special  interest  are  the  electrical  connections  on  the  observer's  table 
itself.  A  diagrammatic  representation  of  the  observer's  table  with  its  con- 
nections is  shown  in  fig.  17.  The  heavy  black  outline  gives  in  a  general 
way  the  outline  of  the  table  proper  and  thus  shows  a  diagrammatic  distribu- 
tion of  the  parts.     The  first  of  the  electrical  measurements  necessary  dur- 

RESISTANCE     THERMOMETERS 
WALL  AIR  RECTAL 


y WVWV 1 


67*  s 


O    O    O    0   o 


5432) 


7S7 

tow 


www 


www 


S,o 


Fig.  17. — Diagram  of  wiring  of  observer's  table.  Wi,  W2,  Wheatstone  bridges  for  resistance  thermom- 
eters; Ki,  K2,  double  contact  keys  for  controlling  Wheatstone  circuits;  Si,  S2,  Ss,  double-pole  double- 
throw  switches  for  changing  from  chair  to  bed  calorimeter;  S4,  double-pole  double-throw  switch  for 
changing  from  wall  to  air  thermometers;  G,  galvanometer;  R2,  rheostat.  1,  2,  3,  4,  5,  wires  connect- 
ing with  resistance-coils  A  B  D  E  F  and  a  b  d  e  f;  S7,  6-point  switch  for  connecting  thermal- 
junction  circuits  of  either  bed  or  chair  calorimeter  with  galvanometer;  Si0,  10-point  double-throw 
switch  for  changing  heating  circuits  and  thermal -junction  circuits  to  either  chair  or  bed  calorimeter; 
Ri,  rheostat  for  controlling  electric  heaters  in  ingoing  water  in  calorimeters;  SB,  double-pole  single- 
throw  switch  for  connecting  110-v.  current  with  connections  on  table;  S9,  double-pole  single-throw 
switch  for  connecting  Ri  with  bed  calorimeter. 


THE   CALORIMETER.  33 

ing  experiments  is  that  of  the  thermo-electric  effect  of  the  thermal  junction 
systems  installed  on  the  calorimeters.  To  aid  in  indicating  what  parts  of 
the  zinc  wall  need  cooling  or  heating,  the  thermal  junction  systems  are,  as 
has  already  been  described,  separated  into  four  sections  on  the  chair  calo- 
rimeter and  three  sections  on  the  bed  calorimeter;  in  the  first  calorimeter, 
the  top,  front,  rear,  and  bottom;  in  the  bed  calorimeter,  the  top,  sides,  and 
bottom. 

CONNECTIONS   TO   THERMAL-JUNCTION   SYSTEMS. 

Since  heretofore  it  has  been  deemed  unwise  to  attempt  to  use  both  calo- 
rimeters at  the  same  time,  the  electrical  connections  are  so  made  that,  by 
means  of  electrical  switches,  either  calorimeter  can  be  connected  to  the 
apparatus  on  the  table. 

The  thermal-junction  measurements  are  made  by  a  semicircular  switch 
S-.  The  various  points,  I,  n,  in,  rv,  etc.,  are  connected  with  the  different 
thermal-junction  systems.  Thus,  by  following  the  wiring  diagram,  it  can 
be  seen  that  the  connections  with  I  run  to  the  different  binding-posts  of  the 
switch  S10,  which  as  a  matter  of  fact  is  placed  beneath  the  table.  This 
switch  S10  has  three  rows  of  binding-posts.  The  center  row  connects  di- 
rectly with  the  apparatus  on  the  observer's  table,  the  outer  rows  connect 
with  either  the  chair  calorimeter  or  the  bed  calorimeter.  The  points  marked 
a,  b,  d,  e,  f,  etc.,  connect  with  the  bed  calorimeter  and  A,  B.  D,  etc.,  connect 
with  the  chair  calorimeter.  Thus,  by  connecting  the  points  g  and  t  with 
the  two  binding-posts  opposite  them  on  the  switch  S10,  it  can  be  seen  that 
this  connection  leads  directly  to  the  point  I  on  the  switch  S7,  and  as  a 
matter  of  fact  this  gives  direct  connection  with  the  galvanometer  through 
the  key  on  S7,  thus  connecting  the  thermal- junction  system  on  one  section 
of  the  bed  calorimeter  between  g  and  t  directly  with  the  galvanometer. 
Similar  connections  from  the  other  points  can  readily  be  followed  from 
the  diagram.  The  points  on  the  switch  S7  indicated  as  i,  11,  m,  rv,  cor- 
respond respectively  to  the  thermal-junction  systems  on  the  top,  rear,  front, 
and  bottom  of  the  chair  calorimeter. 

By  following  the  wiring  diagram  of  the  point  v,  it  will  be  seen  that  this 
will  include  the  connections  with  the  thermal  junctions  connected  in  series 
and  thus  give  a  sum  total  of  the  electromotive  forces  in  the  thermal  junc- 
tions. The  point  vi  is  connected  with  the  thermal- junction  system  in  the 
air  system,  indicating  the  differences  in  temperature  between  the  ingoing 
and  outgoing  air.  It  will  be  noted  that  there  are  four  sections  in  the  chair 
calorimeter,  while  in  the  bed  calorimeter  there  are  but  three,  and  hence  a 
special  switch  S8  is  installed  to  insure  proper  connections  when  the  bed 
calorimeter  is  in  use. 

This  system  of  connecting  the  thermal  junctions  in  different  sections  to 
the  galvanometer  makes  possible  a  more  accurate  control  of  the  tempera- 


34  CALORIMETERS    FdR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

tures  in  the  various  parts,  and  while  the  algebraic  sum  of  the  temperature 
differences  of  the  parts  may  equal  zero,  it  is  conceivable  that  there  may  be 
a  condition  in  the  calorimeter  when  there  is  a  considerable  amount  of  heat 
passing  out  through  the  top,  for  example,  compensated  exactly  by  the  heat 
which  passes  in  at  the  bottom,  and  while  with  the  top  section  there  would  be 
a  large  plus  deflection  on  the  galvanometer,  thus  indicating  that  the  air 
around  the  zinc  wall  was  too  cold  and  that  heat  was  passing  out,  there 
would  be  a  corresponding  minus  deflection  on  the  bottom  section,  indicat- 
ing the  reverse  conditions.  The  two  may  exactly  balance  each  other,  but 
it  has  been  found  advantageous  to  consider  each  section  as  a  unit  by  itself 
and  to  attempt  delicate  temperature  control  of  each  individual  unit.  This 
has  been  made  possible  by  the  electrical  connections,  as  shown  on  the 
diagram. 

RHEOSTAT  FOR  HEATING. 

The  rheostat  for  heating  the  air-spaces  and  the  returning  air-current 
about  the  zinc  wall  is  placed  on  the  observer's  table  and  is  indicated  in  the 
diagram  as  E2.  There  are  five  different  sets  of  contact-points,  marked  1,  2, 
3,  4,  and  5.  One  end  of  the  rheostat  is  connected  directly  with  the  110- 
volt  circuit  through  the  main  switch  S5.  The  other  side  of  the  switch  S5 
connects  directly  with  the  point  on  the  middle  of  switch  S10,  and  when  this 
middle  point  is  joined  with  either  f  and  F,  direct  connection  is  insured 
between  all  the  various  heating-circuits  on  the  calorimeter  in  use.  The 
various  numbered  points  on  the  rheostat  R2  are  connected  with  the  binding 
posts  on  S10,  and  each  can  in  turn  be  connected  with  a  or  A,  &  or  B,  etc. 
The  heating  of  the  top  of  the  chair  calorimeter  is  controlled  by  the  point  5 
on  the  rheostat  E2,  the  rear  by  the  point  4,  the  front  by  the  point  3,  and 
the  bottom  by  the  point  2.  Point  1  is  used  for  heating  the  air  entering  the 
calorimeter  by  means  of  an  electric  lamp  placed  in  the  air-pipe,  as  shown 
in  fig.  25. 

The  warming  of  the  electrical  reheater  placed  in  the  water-circuit  just 
before  the  water  enters  the  calorimeter  is  done  by  an  electrical  current  con- 
trolled by  the  resistance  Rx.  This  Rx  is  connected  on  one  end  directly  with 
the  110-volt  circuit  and  the  current  leaving  it  passes  through  the  resistance 
inside  the  heater  in  the  water-current.  The  two  heaters,  one  for  each  calo- 
rimeter, are  indicated  on  the  diagram  above  and  below  the  switch  S9.  The 
disposition  of  the  switches  is  such  as  to  make  it  possible  to  use  alternately 
the  reheaters  on  either  the  bed  or  the  chair  calorimeter,  and  the  main 
resistance  Ra  suffices  for  both. 

WHEATSTONE  BRIDGES. 

For  use  in  measuring  the  temperature  of  the  air  and  of  the  copper  wall 
of  the  calorimeters,  as  well  as  the  rectal  temperature  of  the  subject,  a  series 


/ 


THE   CALORIMETER.  35 

of  resistance  thermometers  is  employed.  These  are  so  connected  on  the 
observers  table  that  they  may  be  brought  into  connection  with  two  Wheat- 
stone  bridges,  Wx  and  W2.  Bridge  W,  is  used  for  the  resistance  ther- 
mometers indicating  the  temperature  of  the  wall  and  the  air.  Bridge  W2 
is  for  the  rectal  thermometer.  Since  similar  thermometers  are  inserted  in 
both  calorimeters,  it  is  necessary  to  introduce  some  switch  to  connect  either 
set  at  will  and  hence  the  double-throw  switches  S1?  S2,  and  S3  allow  the  use 
of  either  the  wall,  air,  or  rectal  thermometer  on  either  the  bed  or  chair 
calorimeter  at  will.  Since  the  bridge  Wx  is  used  for  measuring  the  tem- 
perature of  both  the  wall  and  the  air,  a  fourth  double-pole  switch,  S4,  is 
used  to  connect  the  air  and  wall  thermometers  alternately.  The  double- 
contact  key,  K1?  is  connected  with  the  bridge  vv\  and  is  so  arranged  that  the 
battery  circuit  is  first  made  and  subsequently  the  galvanometer  circuit. 
A  similar  arrangement  in  K2  controls  the  connections  for  the  bridge  W2. 

GALVANOMETER. 

The  galvanometer  is  of  the  Deprez-d'Arsonval  type  and  is  extremely 
sensitive.  The  sensitiveness  is  so  great  that  it  is  desirable  to  introduce  a 
resistance  of  some  500  ohms  into  the  thermal-junction  circuits.  This  is 
indicated  at  the  top  of  the  diagram  near  the  galvanometer.  The  maximum 
sensitiveness  of  the  galvanometer  is  retained  when  the  connection  is  made 
with  the  Wheatstone  bridges.  The  galvanometer  is  suspended  from  the 
ceiling  of  the  calorimeter  laboratory  and  is  free  from  vibration. 

RESISTANCE  FOR  HEATING  COILS. 

To  vary  the  current  passing  through  the  manganin  heating  coils  in  the 
air-spaces  next  the  zinc  wall,  a  series  of  resistances  is  installed  connected 
directly  with  the  rheostat  E2  in  fig.  17.  The  details  of  these  resistances 
and  their  connection  with  the  rheostat  are  shown  in  fig.  18.  The  rheostat, 
which  is  in  the  right  part  of  the  figure,  has  five  sliding  contacts,  each  of 
which  can  be  connected  with  ten  different  points.  One  end  of  the  rheostat 
is  connected  directly  with  the  110-volt  circuit.  Beneath  the  observer's 
table  are  fastened  the  five  resistances,  which  consist  of  four  lamps,  each 
having  approximately  200  ohms  resistance  and  then  a  series  of  resistance- 
coils  wound  on  a  long  strip  of  asbestos  lumber,  each  section  having  approxi- 
mately 15  ohms  between  the  binding-posts.  A  fuse-wire  is  inserted  in 
each  circuit  to  protect  the  chamber  from  excessive  current.  Of  these  re- 
sistances, No.  1  is  used  to  heat  the  lamp  in  the  air-current  shown  in  fig.  25, 
and  consequently  it  has  been  found  advisable  to  place  permanently  a  second 
lamp  in  series  with  the  first,  but  outside  of  the  air-pipe,  so  as  to  avoid 
burning  out  the  lamp  inside  of  the  air-pipe.  The  other  four  resistances, 
2,  3,  4,  and  5,  are  connected  with  the  different  sections  on  the  two  calorim- 
eters.    No.  5  corresponds  to  the  top  of  both  calorimeters.     No.  4  corre- 


36 


CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


sponds  to  the  rear  section  of  the  chair  calorimeter  and  to  the  sides  of  the 
bed  calorimeter.  No.  3  corresponds  to  the  front  of  the  chair  calorimeter 
and  is  without  communication  with  the  bed  calorimeter.  No.  2  connects 
with  the  bottom  of  both  calorimeters. 

It  will  be  seen  from  the  diagrams  that  each  of  these  resistances  can  be 
connected  at  will  with  either  the  bed  or  the  chair  calorimeter  and  at  such 
points  as  are  indicated  by  the  lettering  below  the  numbers.  Thus,  section 
1  can  be  connected  with  either  the  point  A  or  point  a  on  fig.  17  and  thus 
directly  control  the  amount  of  current  passing  through  the  corresponding 
resistance  in  series  with  the  lamp  in  the  air-current.    The  sliding  contacts 


I5~    PER    SECTION 


SLIDINC     CONTACT 


Fig.  18. — Diagram  of  rheostat  and  resistances  in  series  with  it.  At  the  right  are 
shown  the  sliding  contacts,  and  in  the  center  places  for  lamps  used  as  resist- 
ances, and  to  left  the  sections  of  wire  resistances. 

at  present  in  use  are  ill  adapted  to  long-continued  usage  and  will  therefore 
shortly  be  substituted  by  a  more  substantial  instrument.  The  form  of  re- 
sistance using  small  lamps  and  the  resistance  wires  wound  on  asbestos  lumber 
has  proven  very  satisfactory  and  very  compact  in  form. 


TEMPERATURE  RECORDER. 

The  numerous  electrical,  thermometric,  and  chemical  measurements  neces- 
sary in  the  full  conduct  of  an  experiment  with  the  respiration  calorimeter 
has  often  raised  the  question  of  the  desirability  of  making  at  least  a  por- 
tion of  these  observations  more  or  less  automatic.  This  seems  particularly 
feasible  with  the  observations  ordinarily  recorded  by  the  physical  observer. 
These  observations  consist  of  the  reading  of  the  mercurial  thermometers 
indicating  the  temperatures  of  the  ingoing  and  outcoming  water,  records 


THE   CALORIMETER.  37 

with  the  electric-resistance  thermometers  for  the  temperature  of  the  air 
and  the  walls  and  the  body  temperatures,  and  the  deflections  of  the  thermo- 
electric elements. 

Numerous  plans  have  been  proposed  for  rendering  automatic  some  of 
these  observations,  as  well  as  the  control  of  the  heating  and  cooling  of  the 
air-circuits.  Obviously,  such  a  record  of  temperature  measurements  would 
have  two  distinct  advantages:  (1)  in  giving  an  accurate  graphic  record 
which  would  be  permanent  and  in  which  the  influence  of  the  personal 
equation  would  be  eliminated;  (2)  while  the  physical  observer  at  present 
has  much  less  to  do  than  with  the  earlier  form  of  apparatus,  it  would 
materially  lighten  his  labors  and  thereby  tend  to  minimize  errors  in  the 
other  observations. 

The  development  of  the  thread  recorder  and  the  photographic  registration 
apparatus  in  recent  years  led  to  the  belief  that  we  could  employ  similar 
apparatus  in  connection  with  our  investigations  in  this  laboratory.  To 
this  end  a  number  of  accurate  electrical  measuring  instruments  were  pur- 
chased, and  after  a  number  of  tests  it  was  considered  feasible  to  record 
automatically  the  temperature  differences  of  the  ingoing  and  outcoming 
water  from  the  calorimeter.  Based  upon  our  preliminary  tests,  the  Leeds  & 
Xorthrup  Company  of  Philadelphia,  whose  experience  with  such  problems 
is  very  extended,  were  commissioned  to  construct  an  apparatus  to  meet 
the  requirements  of  the  respiration  calorimeter.  The  conditions  to  be  met 
by  this  apparatus  were  such  as  to  call  for  a  registering  recorder  that  would 
indicate  the  differences  in  temperature  between  the  ingoing  and  outcoming 
water  to  within  0.5  per  cent  and  to  record  these  differences  in  a  permanent 
ink  line  on  coordinate  paper.  Furthermore,  the  apparatus  must  be  installed 
in  a  fixed  position  in  the  laboratory,  and  connections  should  be  such  as  to 
make  it  interchangeable  with  any  one  of  five  calorimeters. 

After  a  great  deal  of  preliminary  experimenting,  in  which  the  Leeds  & 
Northrup  Company  have  most  generously  interpreted  our  specifications, 
they  have  furnished  us  with  an  apparatus  which  meets  to  a  high  degree  of 
satisfaction  the  conditions  imposed.  The  thermometers  themselves  have 
already  been  discussed.  (See  page  30.)  The  recording  apparatus  consists 
of  three  parts:  (1)  the  galvanometer;  (2)  the  creeper  or  automatic  sliding- 
contact;  (3)  the  clockwork  for  the  forward  movement  of  the  roll  of  co- 
ordinate paper  and  to  control  the  periodic  movement  of  the  creeper. 

Under  ordinary  conditions  with  rest  experiments  in  the  chair  calorim- 
eter or  bed  calorimeter,  the  temperature  differences  run  not  far  from  2°  to 
4°.  Thus,  it  is  seen  that  if  the  apparatus  is  to  meet  the  conditions  of  the 
specifications  it  must  measure  differences  of  2°  C.  to  within  0.01°  C.  Pro- 
vision has  also  been  made  to  extend  the  measurement  of  temperature  differ- 
ences with  the  apparatus  so  that  a  difference  of  8°  can  be  measured  with  the 
same  percentage  accuracy. 


38 


CALORIMETERS    FOR    STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


5 


FUNDAMENTAL  PRINCIPLE  OF  THE  APPARATUS. 

The  apparatus  depends  fundamentally  upon  the  perfect  balancing  of  the 
two  sides  of  a  differential  electric  circuit.  A  conventional  diagram,  fig.  19, 
gives  a  schematic  outline  of  the  connections.  The  two  galvanometer  coils, 
fl  and  fr,  are  wound  differentially  and  both  coils  most  carefully  balanced 
so  that  the  two  windings  have  equal  temperature  coefficients.  This  is  done 
by  inserting  a  small  shunt  y,  parallel  with  the  coil  fl,  and  thus  the  tempera- 
ture coefficient  of  fl  and  fr  are  made 
absolutely  equal.  The  two  thermome- 
ters are  indicated  as  T1  and  T,  and  are 
inserted  in  the  ingoing  and  outgoing 
water  respectively.  A  slide-wire  resist- 
ance is  indicated  by  J,  and  r  is  the  re- 
sistance for  the  zero  adjustment.  Ba, 
Z,  and  Z1  are  the  battery  and  its  variable 
series  resistances.  If  Tt  and  T2  are 
exactly  of  the  same  temperature,  i.  e., 
if  the  temperature  difference  of  the  in- 
going and  outeoming  water  is  zero,  the 
sliding  contact  q  stands  at  0  on  the 
slide-wire  and  thus  the  resistance  of 
the  system  from  0  through  fl,  r,  and  Tx 
back  to  the  point  C  is  exactly  the  same 
as  the  resistance  of  the  slide-wire  J 
plus  the  coil  fr  plus  T2  back  to  the 
point  C.  A  rise  in  temperature  of  T2 
gives  an  increase  of  resistance  in  the 
circuit  and  the  sliding  contact  q  moves 
along  the  slide- wire  toward  J  maximum 
until  a  balance  is  obtained. 

Provision  is  made  for  automatically 
moving  the  contact  q  by  electrical 
means  and  thus  the  complete  balance 
of  the  two  differential  circuits  is  maintained  constant  from  second  to  second. 
As  the  contact  q  is  moved,  it  carries  with  it  a  stylographic  pen  which  travels 
in  a  straight  line  over  a  regularly  moving  roll  of  coordinate  paper,  thus  pro- 
ducing a  permanently  recorded  curve  indicating  the  temperature  differences. 
The  slide-wire  J  is  calibrated  so  that  any  inequalities  in  the  temperature 
coefficient  of  the  thermometer  wires  are  equalized  and  also  so  that  any  unit- 
length  on  the  slide-wire  taken  at  any  point  along  the  temperature  scale  rep- 
resents a  resistance  equal  to  the  resistance  change  in  the  thermometer  for 
that  particular  change  in  temperature.  With  the  varying  conditions  to  be 
met  with  in  this  apparatus,  it  is  necessary  that  varying  values  should  be 


Fig.  19. — Diagram  of  wiring  of  differential  cir- 
cuit with  its  various  shunts,  used  in  con- 
nection with  resistance  thermometers  on 
water-circuit  of  bed  calorimeter. 


THE   CALORIMETER.  39 

assigned  at  times  to  J  and  to  r.  This  necessitates  the  use  of  shunts,  and  the 
recording  range  of  the  instrument  can  be  easily  varied  by  simple  shunting, 
i.  e .,  by  changing  the  resistance  value  of  J  and  r,  providing  these  resistances 
unshunted  have  a  value  which  takes  care  of  the  highest  obtained  temperature 
variations. 

Fig.  19  shows  the  differential  circuit  complete  with  all  its  shunts.  S  is 
a  fixed  shunt  to  obtain  a  range  on  J ;  S'  is  a  variable  shunt  to  permit  very 
slight  variations  of  J  within  the  range  to  correct  errors  due  to  changing  of 
the  initial  temperatures  of  the  thermometers ;  y  is  a  permanent  shunt  across 
the  galvanometer  coil  fl,  to  make  the  temperature  coefficients  of  fl  and  fr 
absolutely  equal;  Z  is  the  variable  resistance  in  the  battery-circuit  to  keep 
the  current  constant;  r  is  a  permanent  resistance  to  fix  the  zero  on  varying 
ranges;  S"  plus  Sx  constitutes  a  variable  shunt  to  permit  slight  variations 
of  r  to  finally  adjust  0  after  S'  is  fixed  and  t  is  a  permanent  shunt  across 
the  thermometer  Tx  to  make  the  temperature  coefficient  of  T1  equal  to  that 
of  T2. 

The  apparatus  can  be  used  for  measuring  temperature  differences  from 
0°  to  4°  or  from  0°  to  8°.  When  on  the  0°  to  8°  range,  the  shunt  S  is 
open-circuited  and  the  shunt  S'  alone  used.  The  value  of  S,  then,  is  pre- 
determined so  as  to  affect  the  value  of  the  wire  J  and  thus  halve  its  influence 
in  maintaining  the  balance.  Similarly,  when  the  lower  range,  t.  e.,  from 
0°  to  4°,  is  used,  the  resistance  r  is  employed,  and  when  the  higher  range  is 
used  another  value  to  r  must  be  given  by  using  a  plug  resistance-box,  in  the 
use  of  which  the  resistance  r  is  doubled. 

The  resistance  S"  and  Sx  are  combined  in  a  slide-wire  resistance-box  and 
are  used  to  change  the  value  of  the  whole  apparatus  when  there  are  marked 
changes  in  the  position  of  the  thermometric  scale.  Thus,  if  the  ingoing 
water  is  at  2°  C.  and  the  outcoming  water  at  5°  C.  in  one  instance,  and  in 
another  instance  the  ingoing  water  is  13°  and  the  outgoing  water  is  15°,  a 
slight  alteration  in  the  value  of  Sx,  and  also  of  S',  is  necessary  in  order  to 
have  the  apparatus  draw  a  curve  to  represent  truly  the  temperature  differ- 
ences. These  slight  alterations  are  determined  beforehand  by  careful  tests 
and  the  exact  value  of  the  resistances  in"  S'  and  in  Si  are  permanently 
recorded  for  subsequent  use. 

THE  GALVANOMETER. 

The  galvanometer  is  of  the  Deprez-d'Arsonval  type  and  has  a  particularly 
powerful  magnetic  field,  in  which  a  double  coil  swings  suspended  similar 
to  the  marine  galvanometer  coils.  This  coil  is  protected  from  vibrations 
by  an  anti-vibration  tube  A,  fig.  20,  and  carries  a  pointer  P  which  acts  to 
select  the  direction  of  movement  of  the  recording  apparatus,  the  movable 
contact  point  q,  fig.  19.  In  front  of  this  galvanometer  coil  and  inclosed  in 
the  same  air-tight  metal  case  is  the  plunger  contact  PI,  fig.  21.     The  gal- 


40 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


vanometer  pointer  P  swings  freely  below  the  silver  contacts  Ss  and  S2,  just 
clearing  the  ivory  insulator  i.  The  magnet  plunger  makes  a  contact  de- 
pending upon  the  adjustment  of  a  clock  at  intervals  of  2  seconds.  So 
long  as  both  galvanometer  coils  are  influenced  by  exactly  the  same  strength 
of  current,  the  pointer  will  stand  in  line  with  and  immediately  below  i  and 
no  current  passes  through  the  recording  apparatus.  Any  disturbance  of  the 
electrical  equilibrium  causes  the  pointer  P  to  swing  either  toward  St  or  S2, 
thus  completing  the  circuit  at  either  the  right  hand  or  the  left  hand,  at 


A 


F10.  20. — Diagram  of  galvanometer  coil  used  in  connection  with  record- 
ing apparatus  for  resistance  thermometers  in  the  water-circuit  of 
bed  calorimeter.     A,  anti-vibration  tube;  P,  pointer. 

intervals  of  2  seconds.  The  movement  of  the  pointer  away  from  its  normal 
position  exactly  beneath  i  to  either  St  on  the  left  hand  or  S2  on  the  right, 
results  from  an  inequality  in  the  current  flowing  through  the  two  coils  in 
the  galvanometer.  The  difference  in  the  two  currents  passing  through  these 
coils  is  caused  by  a  change  in  temperatures  of  the  two  thermometers  in  the 
water  circuit. 

THE  CREEPER. 

The  movement  of  the  sliding-contact  q,  fig.  19,  along  the  slide- wire  J,  is 
produced  by  means  of  a  special  device  called  a  creeper,  consisting  of  a  piece 
of  brass  carefully  fitted  to  a  threaded  steel  rod  some  30  centimeters  long. 
The  movement  of  this  bar  along  this  threaded  rod  accomplishes  two  things. 


THE   CALORIMETER. 


41 


The  bar  is  in  contact  with  the  slide-wire  J  and  therefore  varies  the  position 
of  the  point  q  and  it  also  carries  with  it  a  stylographic  pen.  The  movements 
of  this  bar  to  the  right  or  the  left  are  produced  by  an  auxiliary  electric 
current,  the  contact  of  which  is  made  by  a  plunger-plate  forcing  the  pointer 
P  against  either  St  or  S2.  P  makes  the  contact  between  PI  and  either  St 
or  S,  and  sends  a  current  through,  solen- 
oids at  either  the  right  or  the  left  of  the 
creeper.  At  intervals  of  every  2  seconds 
the  plunger  rises  and  forces  the  pointer  P 
against  either  Sx,  ft,  or  S2  above.  The 
movement  of  this  plunger  is  controlled  by 
a  current  from  a  110- volt  circuit,  the  con- 
nections of  which  are  shown  in  fig.  22.  If 
the  contact  is  made  at  T,  the  current 
passes  through  2,600  ohms,  directly  across 
the  110- volt  circuit,  and  consequently 
there  is  no  effective  current  flowing 
through  the  plunger  PI.  When  the  con- 
tact T  is  open,  the  current  flows  through  the  plunger  in  series  with  2,600 
ohms  resistance.  T  is  opened  automatically  at  intervals  of  2  seconds  by  the 
clock. 

The  movement  of  the  contact  arm  along  the  threaded  rod  is  produced 
by  the  action  of  either  one  of  two  solenoids,  each  of  which  has  a  core  at- 
tached to  a  rack  and  pinion  at  either  end  of  the  rod.     If  the  current  is 

passed  through  the  contact  St, 


Fig.    21. — Diagram    of    wiring 
actuating  plunger  and  creeper. 


1 


IIO  v 


600^ 


ooo°[^vvw\/lM/wwli 

L-^V^-       350^.        350A     -WV-1 
IOQOOA 


Lwm 


a  current  passes  through  the 
left-hand  solenoid,  the  core 
moves  down,  the  rack  on  the 
core  moves  the  pinion  on  the 
rod  through  a  definite  fraction 
of  a  complete  revolution  and 
this  movement  forces  the 
creeper  in  one  direction.  Con- 
versely, the  passing  of  the  cur- 
rent through  the  solenoid  at 
the  other  end  of  the  threaded 
rod  moves  the  creeper  in  the  other  direction.  The  distance  which  the  iron 
rack  on  the  end  of  the  core  is  moved  is  determined  carefully,  so  that  the 
threaded  rod  is  turned  for  each  contact  exactly  the  same  fraction  of  a  revolu- 
tion. For  actuating  these  solenoids,  the  110-volt  circuit  is  again  used.  The 
wire  connections  are  shown  in  part  in  fig.  21,  in  which  it  is  seen  that  the 
current  passes  through  the  plunger-contact  and  through  the  pointer  P  to 
the  silver  plate  Sx  and  then  along  the  line  Gx  throusrh  350  ohms  wound 
4 


Fig.  22. — Diagram  of  wiring  of  complete  110-volt  circuit. 


42 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


GALVANOMETER 


about  the  left-hand  solenoid  back  through  a  600-ohm  resistance  to  the  main 
line.  The  use  of  the  110-volt  current  under  such  circumstances  would  nor- 
mally produce  a  notable  sparking  effect  on  the  pointer  P,  and  to  reduce  this 
to  a  minimum  there  is  a  high  resistance,  amounting  to  10,000  ohms  on  each 
side,  shunted  between  the  main  line  and  the  creeper  connections.  This 
shunt  is  shown  in  diagram  in  fig.  22.  Thus  there  is  never  a  complete  open 
circuit  and  sparking  is  prevented. 

THE  CLOCK. 

The  clock  requires  winding  every  week  and  is  so  geared  as  to  move  the 
paper  forward  at  a  rate  of  3  inches  per  hour.  The  contact-point  for  open- 
ing the  circuit  T  on  fig.  22  is  likewise  connected  with  one  of  the  smaller 
wheels  of  the  clock.  This  contact  is  made  by  tripping  a  little  lever  by 
means  of  a  toothed  wheel  of  phosphor-bronze. 

INSTALLATION  OF  THE  APPARATUS. 

The  whole  apparatus  is  permanently  and  substantially  installed  on  the 
north  wall  of  the  calorimeter  laboratory.  A  photograph  showing  the  vari- 
ous parts  and  their  installation 
is  given  in  fig.  23.  On  the  top 
shelf  is  seen  the  galvanometer 
and  on  the  lower  shelf  the  re- 
corder with  its  glass  door  in 
front  and  the  coordinate  paper 
dropping  into  the  box  below. 
The  curve  drawn  on  the  co- 
ordinate paper  is  clearly  shown. 
Above  the  recorder  are  the  re- 
sistance-boxes, three  in  num- 
ber, the  lower  one  at  the  left 
being  the  resistance  8M  the 
upper  one  at  the  left  being  the 
resistance  S',  and  the  upper 
one  at  the  right  being  the  re- 
sistance Z1#  Immediately  above 
the  resistance-box  Z1  is  shown 
the  plug  resistance-box  which 
controls  on  the  one  hand  the 
resistance  r  and  on  the  other  hand  the  resistance  S,  both  of  which  are  sub- 
stantially altered  when  changing  the  apparatus  to  register  from  the  0°  to  4 c 
scale  to  the  0°  to  8°  scale.    A  detailed  wiring  diagram  is  given  in  fig.  24. 


IIOvDC 


Fig.  24.— Detailed  wiring  diagram  showing  all  parts  of 
recording  apparatus,  together  with  wiring  to  ther- 
mometers complete,   including  all  previous  figures. 


Fig.  23 

Temperature  recorder.  The  recorder  with  the  co-ordinate  paper 
in  the  lower  box  with  a  glass  door.  A  curve  representing  the  tempera- 
ture difference  between  the  ingoing  and  outgoing  water  is  directly  drawn 
on  the  co-ordinate  paper.  Above  are  three  resistance  boxes,  and  the 
switches  for  electrical  connections  are  at  the  right.  On  the  top  shelf 
is  the  galvanometer,  and  immediately  beneath,  the  plug  resistance  box 
for  altering  the  value  of  certain  shunts. 


THE    CALORIMETER. 


43 


TEMPERATURE  CONTROL  OF  THE  INGOING  AIR. 

In  passing  the  current  of  air  through  the  calorimeter,  temperature  con- 
ditions may  easily  be  such  that  the  air  entering  is  warmer  than  the  out- 
coming  air,  in  which  case  heat  will  be  imparted  to  the  calorimeter,  or  the 
reverse  conditions  may  obtain  and  then  heat  will  be  brought  away.  To 
avoid  this  difficulty,  arrangements  are  made  for  arbitrarily  controlling  the 
temperature  of  the  air  as  it  enters  the  calorimeter.  This  temperature  con- 
trol is  based  upon  the  fact  that  the  air  leaving  the  chamber  is  caused  to 
pass  over  the  ends  of  a  series  of  thermal  junctions  shown  as  0  in  fig.  25. 


Fig.  25. — Section  of  calorimeter  walls  and  part  of  ventilating  air-circuit,  showing  part  of  pipes  for 
ingoing  air  and  outgoing  air.  On  the  ingoing  air-pipe  at  the  right  is  the  lamp  for  heating  the 
ingoing  air.  Just  above  it,  H  is  the  quick-throw  valve  for  shutting  off  the  tension  equalizer  IJ.  I 
is  the  copper  portion  of  the  tension  equalizer,  while  J  is  the  rubber  diaphragm;  K,  the  pet -cock 
for  admitting  oxygen;  F,  E,  G,  the  lead  pipe  conducting  the  cold  water  for  the  ingoing  air;  and  C, 
the  hair-felt  insulation.  N,  N  are  brass  ferules  soldered  into  the  copper  and  zinc  walls  through 
which  air-pipes  pass;  M,  a  rubber  stopper  for  insulating  the  air-pipe  from  the  calorimeter;  O,  the 
thermal  junctions  for  indicating  differences  of  temperature  of  ingoing  and  outgoing  air  and  U,  the 
connection  to  the  outside;  QQ,  exits  for  the  air-pipes  from  the  box  in  which  thermal  junctions  are 
placed;  P,  the  dividing  plate  separating  the  ingoing  and  outgoing  air;  R,  the  section  of  piping 
conducting  the  air  inside  the  calorimeter;  S,  a  section  of  piping  through  which  the  air  passes  from 
the  calorimeter;  A,  a  section  of  the  copper  wall;  Y,  a  bolt  fastening  the  copper  wall  to  the  2%-inch 
angle  W;  B,  a  portion  of  zinc  wall;  C,  hair-felt  lining  of  asbestos  wall  D;  TJ,  a  thermal  junction 
In  the  walls. 

These  thermal  junctions  have  one  terminal  in  the  outgoing  air  and  the 
other  in  the  ingoing  air,  and  consequently  any  difference  in  the  temperature 
of  the  two  air-currents  is  instantly  detected  by  connecting  the  circuit  with 
the  galvanometer.  Formerly  the  temperature  control  was  made  a  varying 
one,  by  providing  for  either  cooling  or  heating  the  ingoing  air  as  the  situa- 
tion called  for.    The  heating  was  done  by  passing  the  current  through  an 


44  CALORIMETERS    FOR    STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

electric  lamp  placed  in  the  cross  immediately  below  the  tension  equalizer  J. 
Cooling  was  effected  by  means  of  a  current  of  water  through  the  lead  pipe 
E  closely  wrapped  around  the  air-pipe,  water  entering  at  F  and  leaving 
at  G.  This  lead  pipe  is  insulated  by  hair-felt  pipe-covering,  C.  More 
recently,  we  have  adopted  the  procedure  of  passing  a  continuous  current  of 
water,  usually  at  a  very  slow  rate,  through  the  lead  pipe  E  and  always 
heating  the  air  somewhat  by  means  of  the  lamp,  the  exact  temperature  con- 
trol being  obtained  by  varying  the  heating  effect  of  the  lamp  itself.  This 
has  been  found  much  more  satisfactory  than  by  alternating  from  the  cool- 
ing system  to  the  heating  system.  In  the  case  of  the  air-current,  however, 
it  is  unnecessary  to  have  the  drop-sight  feed-valve  as  used  for  the  wall  con- 
trol, shown  in  fig.  13. 

THE  HEAT  OF  VAPORIZATION  OF  WATER. 

During  experiments  with  man  not  all  the  heat  leaves  the  body  by  radia- 
tion and  conduction,  since  a  part  is  required  to  vaporize  the  water  from 
the  skin  and  lungs.  An  accurate  measurement  of  the  heat  production  by 
man  therefore  required  a  knowledge  of  the  amount  of  heat  thus  vaporized. 
One  of  the  great  difficulties  in  the  numerous  forms  of  calorimeters  that  have 
been  used  heretofore  with  man  is  that  only  that  portion  of  heat  measured 
by  direct  radiation  or  conduction  has  been  measured  and  the  difficulties 
attending  the  determination  of  water  vaporized  have  vitiated  correspond- 
ingly the  estimates  of  the  heat  production.  Fortunately,  with  this  apparatus 
the  determinations  of  water  are  very  exact,  and  since  the  amount  of  water 
vaporized  inside  the  chamber  is  known  it  is  possible  to  compute  the  heat 
required  to  vaporize  this  water  by  knowing  the  heat  of  vaporization  of  water. 

Since  the  earlier  reports  describing  the  first  form  of  calorimeters  were 
written,  there  has  appeared  a  research  by  one  of  our  former  associates,  Dr. 
A.  W.  Smith  *  who,  recognizing  the  importance  of  knowing  exactly  the 
heat  of  vaporization  of  water  at  20°,  has  made  this  a  special  object  of  inves- 
tigation. When  connected  with  our  laboratory  a  number  of  experiments 
were  made  by  Doctors  Smith  and  Benedict  in  an  attempt  to  determine 
the  heat  of  vaporization  of  water  directly  in  a  large  calorimeter;  but  for 
lack  of  time  and  pressure  of  other  experimental  work  it  was  impossible  to 
complete  the  investigation.  Subsequently  Dr.  Smith  has  carried  out  the 
experiments  with  the  accuracy  of  exact  physical  measurements  and  has 
given  us  a  very  valuable  series  of  observations. 

Using  the  method  of  expressing  the  heat  of  vaporization  in  electrical 
units,  Smith  concludes  that  the  heat  of  vaporization  of  water  between  14° 
and  40°  is  given  by  the  formula 

L  (in  joules)  =2502.5-2.43  T 

♦Smith:  Heat  of  evaporation  of  water.  Physical  Review,  vol.  25,  p.  145. 
(1907.) 


THE   CALORIMETER.  45 

and  states  that  the  "  probable  error  "  of  values  computed  from  this  formula 
is  0.5  joule.  The  results  are  expressed  in  international  joules,  that  is,  in 
terms  of  the  international  ohm  and  1.43400  for  the  E.  M.  F.  of  the  Clark 
cell  at  15°  C,  and  assuming  that  the  mean  calorie  is  equivalent  to  4.1877 
international  joules,*  the  formula  reads 

L  (in  mean  calories)  =597.44-0.580  T 

With  this  formula  Smith  calculates  that  at  15°  the  heat  of  vaporization 
of  water  is  equal  to  588.73  calories;  at  20°,  585.84  calories;  at  25°,  582.93 
calories;  at  30°,  580.04  calories  ;f  and  at  35°,  577.12  calories.  In  all  of 
the  calculations  in  the  researches  herewith  we  have  used  the  value  found 
by  Smith  as  586  calories  at  20°.  Inasmuch  as  all  of  our  records  are  in 
kilo-calories,  we  multiply  the  weight  of  water  by  the  factor  0.586  to  obtain 
the  heat  of  vaporization. 

THE  BED  CALORIMETER. 

The  chair  calorimeter  was  designed  for  experiments  to  last  not  more 
than  6  to  8  hours,  as  a  person  can  not  remain  comfortably  seated  in  a 
chair  much  longer  than  this  time.  For  longer  experiments  (experiments 
during  the  night  and  particularly  for  bed-ridden  patients)  a  type  of  calo- 
rimeter which  permits  the  introduction  of  a  couch  or  bed  has  been  devised. 
This  calorimeter  has  been  built,  tested,  and  used  in  a  number  of  experi- 
ments with  men  and  women.  The  general  shape  of  the  chamber  is  given 
in  fig.  26.  The  principles  involved  in  the  construction  of  the  chair  calo- 
rimeter are  here  applied,  t.  e.,  the  use  of  a  structural-steel  framework,  inner 
air-tight  copper  lining,  outer  zinc  wall,  hair-felt  insulation,  and  outer 
asbestos  panels.  Inside  of  the  chamber  there  is  a  heat-absorbing  system 
suspended  from  the  ceiling,  and  air  thermometers  and  thermometers  for  the 
copper  wall  are  installed  at  several  points.  The  food-aperture  is  of  the  same 
general  type  and  the  furniture  here  consists  simply  of  a  sliding  frame  upon 
which  is  placed  an  air-mattress.  The  opening  is  at  the  front  end  of  the 
calorimeter  and  is  closed  by  two  pieces  of  plate  glass,  each  well  sealed  into 
place  by  wax  after  the  subject  has  been  placed  inside  of  the  chamber. 
Tubes  through  the  wall  opposite  the  food-aperture  are  used  for  the  intro- 
duction of  electrical  connections,  ingoing  and  outgoing  water,  the  air-pipes, 
and  connections  for  the  stethoscope,  pneumograph,  and  telephone. 

The  apparatus  rests  on  four  heavy  iron  legs.  Two  pieces  of  channel  iron 
are  attached  to  these  legs  and  the  structural  framework  of  the  calorimeter 
chamber  rests  upon  these  irons.  The  method  of  separating  the  asbestos 
outer  panels  is  shown  in  the  diagram.     In  order  to  provide  light  for  the 

♦Philosophical  Transactions,  vol.  199,  A,  p.  149.     (1902.) 
t  This  is  in  agreement  with  the  value  579.6  calories  found  by  F.  Henning,  Ann. 
d.  Physik,  vol.  21,  p.  849.    (1906.) 


46  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,  ETC. 

chamber,  the  outer  wall  in  front  of  the  glass  windows  is  made  of  glass 
rather  than  asbestos.  The  front  section  of  the  outer  casing  can  be  removed 
easily  for  the  introduction  of  a  patient. 

In  this  chamber  it  is  impossible  to  weigh  the  bed  and  clothing,  and  hence 
this  calorimeter  can  not  be  used  for  the  accurate  determination  of  the 
moisture  vaporized  from  the  lungs  and  skin  of  the  subject,  since  here  (as 
in  almost  every  form  of  respiration  chamber)  it  is  absolutely  impossible  to 
distinguish  between  the  amount  of  water  vaporized  from  bed-clothing  and 
that  vaporized  from  the  lungs  and  skin  of  the  subject.  With  the  chair 
calorimeter,  the  weighing  arrangements  make  it  possible  to  weigh  the  chair, 


Meter 


Fig.  26. — Cross-section  of  bed  calorimeter,  showing:  part  of  steel  construction,  also  copper  and  zinc  walls, 
food-aperture,  and  wall  and  air-resistance  thermometers.  Cross-section  of  opening-,  cross-section  of 
panels  of  insulating;  asbestos,  and  supports  of  calorimeter  itself  are  also  indicated. 

clothing,  etc.,  and  thus  apportion  the  total  water  vaporized  between  losses 
from  the  chair,  furniture,  and  body  of  the  man.  In  view  of  the  fact  that 
the  water  vaporized  from  the  skin  and  lungs  could  not  be  determined,  the 
whole  interior  of  the  chamber  of  the  bed  calorimeter  has  been  coated  with 
a  white  enamel  paint,  which  gives  it  a  bright  appearance  and  makes  it  much 
more  attractive  to  new  patients.  An  incandescent  light  placed  above  the 
head  at  the  front  illuminates  the  chamber  very  well,  and  as  a  matter  of 
fact  the  food-aperture  is  so  placed  that  one  can  lie  on  the  cot  and  actually 
look  outdoors  through  one  of  the  laboratory  windows. 

Special  precaution  was  taken  with  this  calorimeter  to  make  it  as  com- 
fortable and  as  attractive  as  possible  to  new  and  possibly  apprehensive 
patients.  The  painting  of  the  walls  unquestionably  results  in  a  condensa- 
tion of  more  or  less  moisture,  for  the  paint  certainly  absorbs  more  moisture 


THE   CALORIMETER.  47 

than  does  the  metallic  surface  of  the  copper.  The  chief  value  of  the  deter- 
mination of  the  water  vaporized  inside  of  the  chamber  during  an  experi- 
ment lies,  however,  not  in  a  study  of  the  vaporization  of  water  as  such,  but 
in  the  fact  that  a  certain  amount  of  heat  is  required  to  vaporize  the  water 
and  obviously  an  accurate  measure  of  the  heat  production  must  involve  a 
measure  of  the  amount  of  water  vaporized.  So  far  as  the  measurement  of 
heat  is  concerned,  it  is  immaterial  whether  the  water  is  vaporized  from  the 
lungs  or  skin  of  the  subject  or  the  clothing,  bedding,  or  walls  of  the  cham- 
ber; since  for  every  gram  of  water  vaporized  inside  of  the  chamber,  from 
whatever  source,  0.586  calorie  of  heat  must  have  been  absorbed. 

The  apparatus  as  perfected  is  very  sensitive.  The  sojourn  in  the  chamber 
is  not  uncomfortable;  as  a  matter  of  fact,  in  an  experiment  made  during 
January,  1909,  the  subject  remained  inside  of  the  chamber  for  30  hours. 
With  male  patients  no  difficulty  is  experienced  in  collecting  the  urine.  No 
provision  is  made  for  defecation,  and  hence  it  is  our  custom  in  long  experi- 
ments to  empty  the  lower  bowel  with  an  enema  and  thus  defer  as  long  as 
possible  the  necessity  for  defecation.  With  none  of  the  experiments  thus 
far  made  have  we  experienced  any  difficulty  in  having  to  remove  the  patient 
because  of  necessity  to  defecate  in  the  cramped  quarters.  It  is  highly  prob- 
able that,  with  the  majority  of  sick  patients,  experiments  will  not  extend 
for  more  than  8  or  10  hours,  and  consequently  the  apparatus  as  designed 
should  furnish  most  satisfactory  results. 

In  testing  the  apparatus  by  the  electrical-check  method,  it  has  been  found 
to  be  extremelv  accurate.  When  the  test  has  been  made  with  burning  alco- 
hoi,  as  described  beyond,  it  has  been  found  that  the  large  amount  of  mois- 
ture apparently  retained  by  the  white  enamel  paint  on  the  walls  vitiates 
the  determination  of  water  for  several  hours  after  the  experiment  begins, 
and  only  after  several  hours  of  continuous  ventilating  is  the  moisture  con- 
tent of  the  air  brought  down  to  a  low  enough  point  to  establish  equilibrium 
between  the  moisture  condensed  on  the  surface  and  the  moisture  in  the  air 
and  thus  have  the  measured  amount  of  moisture  in  the  sulphuric  acid 
vessels  equal  the  amount  of  moisture  formed  by  the  burning  of  alcohol. 
Hence  in  practically  all  of  the  alcohol-check  experiments,  especially  of 
short  duration,  with  this  calorimeter,  the  values  for  water  are  invariably 
somewhat  too  high.  A  comparison  of  the  alcohol-check  experiments  made 
with  the  bed  and  chair  calorimeters  gives  an  interesting  light  upon  the 
power  of  paint  to  absorb  moisture  and  emphasizes  again  the  necessity  of 
avoiding  the  use  of  material  of  a  hygroscopic  nature  in  the  interior  of  an 
apparatus  in  which  accurate  moisture  determinations  from  the  body  are  to 
be  made. 

The  details  of  the  bed  calorimeter  are  better  shown  in  fig.  4.  The  open- 
ing at  the  front  is  here  removed  and  the  wooden  track  upon  which  the 
frame,  supporting  the  cot,  slides  is  clearly  shown.     The  tension  equalizer 


48  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

(see  page  71)  partly  distended  is  shown  connected  to  the  ingoing  air-pipe, 
and  on  the  top  of  the  calorimeter  connected  to  the  tension  equalizer  is  a 
Sonden  manometer.  On  the  floor  at  the  right  is  seen  the  resistance  coil 
used  for  electrical  tests  (see  page  50).  A  number  of  connections  inside 
the  chamber  at  the  left  are  made  with  electric  wires  or  with  rubber  tubing. 
Of  the  five  connections  appearing  through  the  opening,  reading  from  left 
to  right,  we  have,  first,  the  rubber  connection  with  the  pneumograph,  then 
the  tubing  for  connection  with  the  stethoscope,  then  the  electric-resistance 
thermometer,  the  telephone,  and  finally  a  push  button  for  bell  call.  The 
connections  for  the  pneumograph  and  stethoscope  are  made  with  the  in- 
struments outside  on  the  table  at  the  left  of  the  bed  calorimeter. 

MEASUREMENTS  OF  BODY-TEMPERATURE. 

While  it  is  possible  to  control  arbitrarily  the  temperature  of  the  calo- 
rimeter by  increasing  or  decreasing  the  amount  of  heat  brought  away,  and 
thus  compensate  exactly  for  the  heat  eliminated  by  the  subject,  the  hydro- 
thermal  equivalent  of  the  system  itself  being  about  20  calories — on  the 
other  hand  the  body  of  the  subject  may  undergo  marked  changes  in  tem- 
perature and  thus  influence  the  measurement  of  the  heat  production  to  a 
noticeable  degree ;  for  if  heat  is  lost  from  the  body  by  a  fall  of  body-tem- 
perature or  stored  as  indicated  by  a  rise  in  temperature,  obviously  the  heat 
produced  during  the  given  period  will  not  equal  that  eliminated  and  meas- 
ured by  the  water-current  and  by  the  latent  heat  of  water  vaporized.  In 
order  to  make  accurate  measurements,  therefore,  of  the  heat-production  as 
distinguished  from  the  heat  elimination,  we  should  know  with  great  accuracy 
the  hydrothermal  equivalent  of  the  body  and  changes  in  body  temperature. 
The  most  satisfactory  method  at  present  known  of  determining  the  hydro- 
thermal  equivalent  of  the  body  is  to  assume  the  specific  heat  of  the  body 
as  0.83.*  This  factor  will  of  course  vary  considerably  with  the  weight  of 
body  material  and  the  proportion  of  fat,  water,  and  muscular  tissue  present 
therein,  but  for  general  purposes  nothing  better  can  at  present  be  employed. 
From  the  weight  of  the  subject  and  this  factor  the  hydrothermal  equivalent 
of  the  body  can  be  calculated.  It  remains  to  determine,  then,  with  great 
exactness  the  body  temperature. 

Recognizing  early  the  importance  of  securing  accurate  body-temperatures 
in  researches  of  this  kind,  a  number  of  investigations  were  made  and  pub- 
lished elsewhere  f  regarding  the  body-temperature  in  connection  with  the 

*Pembrey:    Schafer's  Text-book  of  Physiology,  vol.  1,  p.  838.     (1898.) 
f  Benedict  and  Snell:  Korpertemperatur  Schwankungen  mit  besonderer  Rtick- 
sicht  auf  den  Einfluss,  welchen  die  Umkehrung  der  taglichen  Lebensgewohnheit 
beim  Menschen  ausiibt.    Archiv  f.  d.  ges.  Physiologie,  Bd.  90.  p.  33.     (1902.) 

Benedict:  Studies  in  body-temperature:  I.  The  influence  of  the  inversion  of 
the  daily  routine:  the  temperature  of  night-workers.  American  Journal  of  Phy- 
siology, vol.  11,  p.  145.     (1904.) 


THE   CALORIMETER-  49 

experiments  with  the  respiration  calorimeter.  It  was  soon  found  that  the 
ordinary  mercurial  clinical  thermometer  was  not  best  suited  for  the  most 
accurate  observations  of  body-temperature  and  a  special  type  of  thermome- 
ter employing  the  electrical-resistance  method  was  used.  In  many  of  the 
experiments,  however,  it  is  impracticable  with  new  subjects  to  complicate 
the  experiment  by  asking  them  to  insert  the  electrical  rectal  thermometer, 
and  hence  we  have  been  obliged  to  resort  to  the  usual  clinical  thermometer 
with  temperatures  taken  in  the  mouth,  although  in  a  few  instances  they 
have  been  taken  in  the  axilla  and  the  rectum.  For  the  best  results  the 
electrical  rectal  thermometer  is  used.  This  apparatus  permits  a  continuous 
measurement  of  body  temperature,  deep  in  the  rectum,  unknown  to  the 
subject  and  for  an  indefinite  period  of  time,  it  being  necessary  to  remove 
the  thermometer  only  for  defecation. 

As  a  result  of  these  observations  it  was  soon  found  that  the  body  tem- 
perature was  not  constant  from  hour  to  hour,  but  fluctuated  considerably 
and  underwent  more  or  less  regular  rhythm  with  the  minimum  between  3 
and  5  o'clock  in  the  morning  and  the  maximum  about  5  o'clock  in  the 
afternoon.  In  a  number  of  experiments  where  the  mercurial  thermometer 
was  used  under  the  tongue  and  observations  thus  taken  compared  with 
records  with  the  resistance  thermometer,  it  was  found  that  with  careful 
manipulation  and  avoiding  muscular  activity,  mouth  breathing,  and  the 
drinking  of  hot  or  cold  liquid,  a  fairly  uniform  agreement  between  the  two 
could  be  obtained.  Such  comparisons  made  on  laboratory  assistants  can 
not  be  duplicated  with  the  ordinary  subject. 

It  is  assumed  that  fluctuations  in  temperature  measured  by  the  rectal 
thermometer  likewise  hold  true  for  the  average  temperature  of  the  whole 
body,  but  evidence  on  this  point  is  unfortunately  not  as  complete  as  is 
desirable.  In  an  earlier  report  of  investigations  of  this  nature,  a  few  experi- 
ments on  comparison  of  measurements  of  resistance  thermometer  deep  in 
the  rectum  and  in  a  well-closed  axilla  showed  a  distinct  tendency  for  the 
curves  to  continue  parallel.  A  research  is  very  much  needed  at  present  on 
a  topographical  distribution  of  body  temperature,  and  particularly  on  the 
course  of  the  fluctuations  in  different  parts  of  the  body.  A  series  of  electric- 
resistance  thermometers  placed  at  different  points  in  the  colon,  at  different 
points  in  a  stomach  tube,  in  the  well-closed  axilla,  possibly  attached  to  the 
surface  of  the  body,  and  in  women  in  the  vagina,  should  give  a  very  accurate 
picture  of  the  distribution  of  the  body-temperature  and  likewise  indicate 
the  proportionality  of  the  fluctuations  in  different  parts  of  the  body.  Until 
such  a  research  is  completed,  however,  it  is  necessary  to  assume  that 
fluctuations  in  body-temperature  as  measured  by  the  electric  rectal  ther- 
mometer are  a  true  measure  of  the  average  body-temperature  of  the  whole 
body.  Indeed  it  is  upon  this  assumption  that  it  is  necessary  for  us  to  make 
corrections  for  heat  lost  from  or  stored  in  the  body.     It  is  our  custom, 


50  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

therefore,  to  compute  the  hydrothermal  equivalent  by  multiplying  the  body- 
weight  by  the  specific  heat  of  the  body,  commonly  assumed  as  0.83,  and  then 
to  make  allowance  for  fluctuations  in  body-temperature. 

When  it  is  considered  that  with  a  subject  having  a  weight  of  70  kilos  a 
difference  in  temperature  of  1°  C.  will  make  a  difference  in  the  measure- 
ment of  heat  of  some  60  calories,  it  is  readily  seen  that  the  importance  of 
knowing  the  exact  body-temperature  can  not  be  overestimated;  indeed,  the 
whole  problem  of  the  comparison  of  the  direct  and  indirect  calorimetry 
hinges  more  or  less  upon  this  very  point,  and  it  is  strongly  to  be  hoped  that 
ere  long  the  much-needed  observations  on  body-temperature  can  be  made. 

CONTROL  EXPERIMENTS   WITH  THE   CALORIMETER. 

After  providing  a  suitable  apparatus  for  bringing  away  the  heat  gene- 
rated inside  the  chamber  and  for  preventing  the  loss  of  heat  by  maintaining 
the  walls  adiabatic,  it  is  still  necessary  to  demonstrate  the  ability  of  the 
calorimeter  to  measure  known  amounts  of  heat  accurately.  In  order  to  do 
this  we  pass  a  current  of  electricity  of  known  voltage  through  a  resistance 
coil  and  thus  develop  heat  inside  the  respiration  chamber.  While,  un- 
doubtedly, the  use  of  a  standard  resistance  and  potentiometer  is  the  most 
accurate  method  for  measuring  currents  of  this  nature,  thus  far  we  have 
based  our  experiments  upon  the  measurements  made  with  extremely  accu- 
rate Weston  portable  voltmeter  and  mil-ammeters.  Thanks  to  the  kind- 
ness of  one  of  our  former  co-workers,  Mr.  S.  C.  Dinsmore,  at  present  asso- 
ciated with  the  Weston  Electrical  Instrument  Company,  we  have  been 
able  to  obtain  two  especially  exact  instruments.  The  mil-ammeter  is  so 
adjusted  as  to  give  a  maximum  current  of  1.5  amperes  and  the  voltmeter 
reads  from  zero  to  150  volts.  The  direct  current  furnished  the  building  is 
caused  to  pass  through  a  variable  resistance  for  adjusting  minor  variations 
in  voltage  and  then  through  the  mil-ammeter  into  a  manganin  resistance- 
coil  inside  the  chamber,  having  a  resistance  of  84.2  ohms.  Two  leads  from 
the  terminals  of  the  manganin  coil  connect  with  the  voltmeter  outside  the 
chamber,  and  hence  the  drop  in  potential  can  be  measured  very  accurately 
and  as  frequently  as  is  desired.  The  current  furnished  the  building  is 
remarkably  steady,  but  for  the  more  accurate  experiments  a  small  degree  of 
hand  regulation  is  necessary. 

The  advantage  of  the  electrical  method  of  controlling  the  apparatus  is 
that  the  measurements  can  be  made  very  accurately,  rapidly,  and  in  short 
periods.  In  making  experiments  of  this  nature  it  is  our  custom  first  to 
place  the  resistance-coil  in  the  calorimeter  and  make  the  connections.  The 
current  is  then  passed  through  the  coil,  and  simultaneously  the  water 
is  started  flowing  through  the  heat-absorbing  system  and  the  whole  calo- 
rimeter is  adjusted  in  temperature  equilibrium  as  soon  as  possible.  When 
the  temperature  of  the  air  and  walls  is  constant  and  the  thermal- junction 


THE   CALORIMETER.  51 

system  in  equilibrium,  the  exact  time  is  noted  and  the  water-current 
deflected  into  the  meter.  At  the  end  of  one  hour,  the  usual  length  of  a 
period,  the  water-current  is  deflected  from  the  meter,  the  meter  is  weighed, 
and  the  average  temperature-difference  of  the  water  obtained  by  averaging 
the  results  of  all  the  temperature  differences  noted  during  the  hour.  Usu- 
ally during  an  experiment  of  this  nature,  records  of  the  water-temperatures 
are  made  every  4  minutes ;  occasionally,  when  the  fluctuations  are  somewhat 
greater  than  usual,  records  are  made  every  2  minutes. 

The  calculation  of  the  heat  developed  in  the  apparatus  is  made  by  means 
of  the  formula  CxExf  X0.2385  =  calories,  in  which  C  equals  the  current 
in  amperes,  E  the  electromotive  force,  and  t  the  time  in  seconds.  This 
gives  the  heat  expressed  in  calories  at  15°  C.  This  procedure  we  have  fol- 
lowed as  a  result  of  the  recommendation  of  Dr.  E.  B.  Eosa,  of  the  National 
Bureau  of  Standards.  In  order  to  convert  the  values  to  20°,  the  unit  com- 
monly employed  in  calorimetric  work,  it  has  been  necessary  to  multiply  by 
the  ratio  of  the  specific  heat  of  water  at  15°  to  that  of  water  at  20°.  As- 
suming the  specific  heat  of  water  at  20°  to  be  1,  the  specific  heat  at  15° 
is  1.001.* 

Of  the  many  electrical  check-tests  made  with  this  type  of  apparatus,  but 
one  need  be  given  here,  pending  a  special  treatment  of  the  method  of  con- 
trol of  the  calorimeter  in  a  forthcoming  publication.  An  electrical  check- 
experiment  with  the  chair  calorimeter  was  made  on  January  4,  1909,  and 
continued  6  hours.  The  voltmeter  and  mil-ammeter  were  read  every  few 
minutes,  the  water  collected  in  the  water-meter,  carefully  weighed,  and  the 
temperature  differences  as  measured  on  the  two  mercury  thermometers 
were  recorded  every  4  minutes. 

The  heat  developed  during  the  experiment  may  be  calculated  from  the 
data  as  follows:  Average  currents  1.293  amperes;  average  E.  M.  F. 
=  109.15  volts;  time  =  21,600  seconds;  factor  used  to  convert  watt-seconds 
to  calories =0.2385.  (1.293x109.15x21600x0.2385)  x  1.001  =  727.8  calo- 
ries produced. 

During  the  6  hours  237.63  kilograms  of  water  passed  through  the  absorb- 
ing system. 

The  average  temperature  rise  was  3.04°  C,  the  total  heat  brought  away 
was  therefore  (237.63x3.04)  x  1.0024  f  =724.1  calories. 

Thus  in  6  hours  there  were  about  3.7  calories  more  heat  developed  inside 
the  apparatus  than  were  measured  by  the  water-current,  a  discrepancy  of 
about  0.5  per  cent. 

*  W.  O.  Atwater  and  E.  B.  Rosa :  Description  of  a  new  respiration  calorimeter 
and  experiments  on  the  conservation  of  energy  in  the  human  body.  U.  S.  Dept. 
of  Agr.,  Office  of  Experiment  Stations  Bui.  63.     (1899.) 

f  Specific  heat  of  water  at  average  temperature  of  the  water  in  the  heat-absorb- 
ing system  referred  to  the  specific  heat  of  water  at  20°  C. 


52  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

Under  ideal  conditions  of  manipulation,  the  withdrawal  of  heat  from  the 
calorimeter  should  be  at  just  such  a  rate  as  to  exactly  compensate  for  the 
heat  developed  by  the  resistance-coil.  Under  these  conditions,  then,  there 
would  be  no  heat  abstracted  from  nor  stored  by  the  calorimeter  and  its 
temperature  should  remain  constant  throughout  the  whole  experiment. 
Practically  this  is  very  difficult  to  accomplish  and  there  are  minor  fluctua- 
tions in  temperature  above  and  below  the  initial  temperature  during  a  long 
experiment  and,  indeed,  during  a  short  experimental  period.  If  a  certain 
amount  of  heat  has  been  stored  up  in  the  calorimeter  chamber  or  has  been 
abstracted  from  it,  there  should  be  corrections  made  for  the  variations  in 
the  temperature  of  the  chamber.  Such  corrections  are  impossible  unless  a 
proper  determination  of  the  hydrothermal  equivalent  has  been  made.  A 
number  of  experiments  to  determine  this  hydrothermal  equivalent  have 
been  made  and  the  results  are  recorded  beyond,  together  with  a  discussion 
of  the  nature  of  the  experiments.  As  a  result  of  these  experiments  it  has 
been  possible  to  make  correction  for  the  slight  temperature  changes  in  the 
calorimeter. 

It  is  interesting  to  note  that  these  fluctuations  are  small  and  there  may 
therefore  be  a  considerable  error  in  the  determination  of  the  hydrothermal 
equivalent  without  particularly  affecting  the  corrections  applied  in  the 
ordinary  electrical  check-test.  The  greatest  difficulty  experienced  with  the 
calorimeter  as  a  means  of  measuring  heat  has  been  to  secure  the  average 
temperature  of  the  ingoing  water.  The  temperature  difference  between  the 
mass  of  water  flowing  through  the  pipes  and  the  outer  wall  of  the  pipe  is 
at  best  considerable.  The  use  of  the  vacuum- jacketed  glass  tubes  has  min- 
imized the  loss  of  heat  through  this  tube  considerably,  but  it  is  advisable 
that  the  bulb  of  the  thermometer  be  placed  exactly  in  the  center  of  the 
water-tube,  as  otherwise  too  high  a  temperature-reading  will  be  secured. 
When  the  proper  precautions  are  taken  to  secure  the  correct  temperature- 
reading,  the  results  are  most  satisfactory. 

In  testing  both  calorimeters  a  large  number  of  electrical  check  experi- 
ments have  led  to  the  conclusion  that  discrepancies  in  results  were  inva- 
riably due,  not  to  the  loss  of  heat  through  the  walls  of  the  calorimeter,  but 
to  erroneous  measurement  of  the  temperature  of  the  water-current. 

DETERMINATION  OF  THE  HYDROTHERMAL  EQUIVALENT  OF  THE 

CALORIMETER. 

While  the  temperature  control  of  the  calorimeter  is  such  that  in  general 
the  average  temperature  varies  but  a  few  hundredths  of  a  degree  between 
the  beginning  and  the  end  of  an  experimental  period,  in  extremely  accurate 
work  it  is  necessary  to  know  the  amount  of  heat  which  is  absorbed  with  any 
increase  in  temperature.  In  other  words,  the  determination  of  the  hydro- 
thermal  equivalent  is  essential. 


THE   CALORIMETER.  53 

The  large  majority  of  the  methods  for  determining  the  hydrothermal 
equivalent  of  materials  are  at  once  eliminated  when  the  nature  of  the  calo- 
rimeter here  used  is  taken  into  consideration.  Obviously,  in  warming  up 
the  chamber  there  are  two  sources  of  heat :  first,  the  heat  inside  of  the  cham- 
ber; second,  the  heat  in  the  outer  walls.  As  has  been  previously  described, 
the  zinc  wall  is  arbitrarily  heated  so  that  its  temperature  fluctuations  will 
follow  exactly  those  of  the  inner  wall,  hence  it  is  impossible  to  compute  from 
the  weight  of  the  metal  the  hydrothermal  equivalent.  By  means  of  the 
electrical  check  experiments,  however,  a  method  for  determining  the  hydro- 
thermal  equivalent  is  at  hand.    The  general  scheme  is  as  follows. 

During  an  electrical  check  experiment,  when  thermal  equilibrium  has 
been  thoroughly  established  and  the  heat  brought  away  by  the  water-current 
exactly  counterbalances  the  heat  generated  in  the  resistance-coil  inside  the 
chamber,  the  temperature  of  the  calorimeter  is  allowed  to  rise  slowly  by 
raising  the  temperature  of  the  ingoing  water  and  thus  bringing  away  less 
heat.  At  the  same  time  the  utmost  pains  are  taken  to  maintain  the  adia- 
batic  condition  of  the  metal  walls.  Since  the  temperature  is  rising  during 
this  period,  it  is  necessary  to  warm  the  air  in  the  outer  spaces  by  the 
electric  current.  By  this  method  it  is  possible  to  raise  the  temperature  of 
the  calorimeter  1  degree  or  more  in  2  hours  and  establish  thermal  equi- 
librium at  the  higher  level.  The  experiment  is  then  continued  for  2  hours 
at  this  level,  and  the  next  2  hours  the  temperature  is  gradually  allowed  to 
fall  by  lowering  the  temperature  of  the  ingoing  water  so  that  more  heat  is 
brought  away  than  is  generated,  care  being  taken  likewise  to  keep  the  walls 
adiabatic.  Under  these  conditions  the  heat  brought  away  by  the  water- 
current  during  the  period  of  rising  temperature  is  considerably  less  than 
that  actually  developed  by  the  electric  current  and  the  difference  repre- 
sents the  amount  of  heat  absorbed  by  the  calorimeter  in  the  period  of  the 
temperature  rise.  Conversely,  during  the  period  when  the  temperature  is 
falling,  there  is  a  considerable  increase  in  the  amount  of  heat  brought 
away  by  the  water-current  over  that  generated  in  the  resistance-coil  and  the 
difference  represents  exactly  the  amount  of  heat  given  up  by  the  calorim- 
eter during  the  fall  in  temperature.  It  is  thus  possible  to  measure  the 
capacity  of  the  calorimeter  for  absorbing  heat  during  a  rise  in  temperature 
and  the  amount  of  heat  lost  by  it  during  cooling.  A  number  of  such 
experiments  have  been  made  with  both  calorimeters  and  it  has  been  found 
that  the  hydrothermal  equivalent  of  the  bed  calorimeter  is  not  far  from  21 
kilograms.  For  the  chair  calorimeter  a  somewhat  lower  figure  has  been 
found,  t.  e.,  19.5  kilograms. 


54  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

GENERAL  DESCRIPTION  OF  RESPIRATION  APPARATUS. 

This  apparatus  is  designed  much  after  the  principle  of  the  Eegnault- 
Eeiset  apparatus,  in  that  there  is  a  confined  volume  of  air  in  which  the 
subject  lives  and  which  is  purified  by  its  passage  through  vessels  containing 
absorbents  for  water  and  carbon  dioxide.  Fresh  oxygen  is  added  to  this 
current  of  air  and  it  is  then  returned  to  the  chamber  to  be  respired.  This 
principle,  in  order  to  be  accurate  for  oxygen  determinations,  necessitates  an 
absolutely  air-tight  system  and  consequently  special  precautions  have  been 
taken  in  the  construction  of  the  chamber  and  accessories. 

TESTING  THE  CHAMBER  FOR  TIGHTNESS. 

As  already  suggested,  the  walls  are  constructed  of  the  largest  possible 
sheets  of  copper  with  a  minimum  number  of  seams  and  opportunities  for 
leakage.  In  testing  the  apparatus  for  leaks,  the  greatest  precaution  is 
taken.  A  small  air-pressure  is  applied  and  the  variations  in  height  of  a 
delicate  manometer  noted.  In  cases  of  apparent  leakage,  all  possible  sources 
of  leak  are  gone  over  with  soapsuds  when  there  is  a  slight  pressure  on 
the  chamber.  As  a  last  resort,  which  has  ultimately  proven  to  be  the  best 
method  of  testing,  an  assistant  goes  inside  of  the  chamber,  it  is  then  her- 
metically sealed,  and  a  slight  diminished  pressure  is  produced.  Ether  is 
then  poured  about  the  walls  of  the  chamber  and  the  odor  of  ether  soon 
becomes  apparent  inside  of  the  chamber  if  there  is  a  leakage.  Many  leaks 
that  could  not  be  found  by  soapsuds  can  be  readily  detected  by  this  method. 

VENTILATION  OF  THE  CHAMBER. 

The  special  features  of  the  respiration  chamber  are  the  ventilating-pipe 
system  and  openings  for  supplementary  apparatus  for  absorption  of  water 
and  carbon  dioxide.  The  air  entering  the  chamber  is  absolutely  dry  and  is 
directed  into  the  top  of  the  chamber  immediately  above  the  head  of  the 
subject.  The  moisture  given  off  from  the  lungs  and  skin  and  the  expired 
gases  all  tend  to  mix  readily  with  this  dry  air  as  it  descends,  and  the  final 
mixture  of  gases  is  withdrawn  through  an  opening  near  the  bottom  of  the 
chamber  at  the  front.  Under  these  conditions,  therefore,  we  believe  we  have 
a  maximum  intermingling  of  the  gases.  However,  even  with  this  system 
of  ventilation,  we  do  not  feel  that  there  is  theoretically  the  best  mixture  of 
gases,  and  an  electric  fan  is  used  inside  of  the  chamber.  In  experiments 
where  there  is  considerable  regularity  in  the  carbon-dioxide  production  and 
oxygen  consumption,  the  system  very  quickly  attains  a  state  of  equilibrium, 
and  while  the  analysis  of  the  outcoming  air  does  not  necessarily  represent 
fairly  the  actual  composition  of  the  air  inside  of  the  chamber,  it  evidently 
represents  to  the  same  degree  from  hour  to  hour  the  state  of  equilibrium 
that  is  usually  maintained  through  the  whole  of  a  6-hour  experiment. 


GENERAL   DESCRIPTION    OF   RESPIRATION   APPARATUS.  55 

The  interior  of  the  chamber  and  all  appliances  are  constructed  of  metal 
except  the  chair  in  which  the  subject  sits.  This  is  of  hard  wood,  well  shel- 
lacked, and  consequently  non-porous.  With  this  calorimeter  it  is  desired 
to  make  studies  regarding  the  moisture  elimination,  and  consequently  it  is 
necessary  to  avoid  the  use  of  all  material  of  a  hygroscopic  nature.  Although 
the  chair  can  be  weighed  from  time  to  time  with  great  accuracy  and  its 
changes  in  weight  obtained,  it  is  obviously  impossible,  in  any  type  of 
experiment  thus  far  made,  to  differentiate  between  the  water  vaporized 
from  the  lungs  and  skin  of  the  man  and  that  from  his  clothes.  Subsequent 
experiments  with  a  metal  chair,  with  minimum  clothing,  with  cloth  of 
different  textures,  without  clothing,  with  an  oiled  skin,  and  various  other 
modifications  affecting  the  vaporization  of  water  from  the  body  of  the  man 
will  doubtless  throw  more  definite  light  upon  the  question  of  the  water 
elimination  through  the  skin.  At  present,  however,  we  resort  to  the  use  of 
a  wooden  chair,  relying  upon  its  changes  in  weight  as  noted  by  the  balance 
to  aid  us  in  apportioning  the  water  vaporized  between  the  man  and  his 
clothing  and  the  chair. 

The  walls  of  the  chamber  are  semi-rigid.  Owing  to  the  calorimetric  fea- 
tures of  this  apparatus,  it  is  impracticable  to  use  heavy  boiler-plate  or  heavy 
metal  walls,  as  the  sluggishness  of  the  changes  in  temperature,  the  mass  of 
metal,  and  its  relatively  large  hydrothermal  equivalent  would  interfere 
seriously  with  the  sensitiveness  of  the  apparatus  as  a  calorimeter.  Hence 
we  use  copper  walls,  with  a  fair  degree  of  rigidity,  attached  to  a  substan- 
tial structural-steel  support;  and  for  all  practical  purposes  the  apparatus 
can  be  considered  as  of  constant  volume.  Particularly  is  this  the  case 
when  it  is  considered  that  the  pressure  inside  of  the  chamber  during  an 
experiment  never  varies  from  the  atmospheric  pressure  by  more  than  a  few 
millimeters  of  water.  It  is  possible,  therefore,  from  the  measurements  of 
this  chamber,  to  compute  with  considerable  accuracy  the  absolute  volume. 
The  apparent  volume  has  been  calculated  to  be  1,347  liters. 

OPENINGS  IN  THE  CHAMBER. 

In  order  to  communicate  with  the  interior  of  the  chamber,  maintain  a 
ventilating  air-current,  and  provide  for  the  passage  of  the  current  of  water 
for  the  heat-absorber  system  and  the  large  number  of  electrical  connections, 
a  number  of  openings  through  the  walls  of  the  chamber  were  necessary. 
The  great  importance  of  maintaining  this  chamber  absolutely  air-tight 
renders  it  necessary  to  minimize  the  number  of  these  openings,  to  reduce 
their  size  as  much  as  possible,  and  to  take  extra  precaution  in  securing 
their  closure  during  an  experiment.  The  largest  opening  is  obviously  the 
trap-door  at  the  top  through  which  the  subject  enters,  shown  in  dotted  out- 
line in  fig.  7.  While  somewhat  inconvenient  to  enter  the  chamber  in  this 
way,  the  entrance  from  above  possesses  many  advantages.     It  is  readily 


56  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

closed  and  sealed  by  hot  wax  and  rarely  is  a  leakage  experienced.  The  trap- 
door is  constructed  on  precisely  the  same  plan  as  the  rest  of  the  calorim- 
eter, having  its  double  walls  of  copper  and  zinc,  its  thermal-junction  system, 
its  heating  wires  and  connections,  and  its  cooling  pipes.  When  closed  and 
sealed,  and  the  connections  made  with  the  cooling  pipes  and  heating  wires, 
it  presents  an  appearance  not  differing  from  any  other  portion  of  the 
calorimeter. 

The  next  largest  opening  is  the  food-aperture,  which  is  a  large  sheet- 
copper  tube,  somewhat  flattened,  thus  giving  a  slightly  oval  form,  closed 
with  a  port,  such  as  is  used  on  vessels.  The  door  of  the  port  consists  of 
a  heavy  brass  frame  with  a  heavy  glass  window  and  it  can  be  closed  tightly 
by  means  of  a  rubber  gasket  and  two  thumbscrews.  On  the  outside  is  used 
a  similar  port  provided  with  a  tube  somewhat  larger  in  diameter  than  that 
connected  with  the  inner  port.  The  annular  space  between  these  tubes  is 
filled  with  a  pneumatic  gasket  which  can  be  inflated  and  thus  a  tight  closure 
may  be  maintained.  When  one  door  is  closed  and  the  other  opened,  articles 
can  be  placed  in  and  taken  out  of  the  chamber  without  the  passage  of  a 
material  amount  of  air  from  the  chamber  to  the  room  outside  or  into  the 
chamber  from  outside. 

The  air-pipes  passing  through  the  wall  of  the  calorimeter  are  of  standard 
1-inch  piping.  The  insulation  from  the  copper  wall  is  made  by  a  rubber 
stopper  through  which  this  piping  is  passed,  the  stopper  being  crowded 
into  a  brass  ferule  which  is  stoutly  soldered  to  the  copper  wall.  This  is 
shown  in  detail  in  fig.  25,  in  which  N  is  the  brass  ferule  and  M  the  rubber 
stopper  through  which  the  air-pipe  passes.  The  closure  is  absolutely  air- 
tight and  a  minimum  amount  of  heat  is  conducted  out  of  the  chamber, 
owing  to  the  insulation  of  the  rubber  stopper  M.  The  water-current  enters 
and  leaves  the  chamber  through  two  pipes  insulated  in  two  similar  brass 
ferules  soldered  to  the  copper  and  zinc  walls.  The  insulation  between  the 
water-pipe  and  the  brass  ferule  has  been  the  subject  of  much  experimenting 
and  is  discussed  on  page  24.  The  best  insulation  was  secured  by  a  vacuum- 
jacketed  glass  tube,  although  the  special  hard-rubber  tubes  surrounding  the 
electric-resistance  thermometers  have  proven  very  effective  as  insulators  in 
the  bed  calorimeter. 

A  series  of  small  brass  tubes,  from  10  to  15  millimeters  in  diameter,  are 
soldered  into  the  copper  wall  in  the  vicinity  of  the  water-pipes.  These  are 
used  for  electrical  connections  and  for  connections  with  the  manometer, 
stethoscope,  and  pneumograph.  All  of  these  openings  are  tested  carefully 
and  shown  to  be  absolutely  air-tight  before  being  put  in  use. 

In  the  dome  of  the  calorimeter,  and  directly  over  the  head  of  the  subject, 
is  the  opening  for  the  weighing  apparatus.  This  consists  of  a  hard-rubber 
tube,  threaded  at  one  end  and  screwed  into  a  brass  flange  heavily  soldered 
to  the  copper  wall  (fig.  9).    When  not  in  use,  a  solid  rubber  stopper  on  a 


GENERAL  DESCRIPTION*  OF  RESPIRATION  APPARATUS. 


57 


brass  rod  is  drawn  into  this  opening,  thus  producing  an  air-tight  closure. 
When  in  actual  use  during  the  process  of  weighing,  a  thin  rubber  diaphragm 
prevents  leakage  of  air  through  this  opening.  The  escape  of  heat  through 
the  weighing-tube  is  minimized  by  having  this  tube  of  hard  rubber. 


VENTILATING  AIR-CURRENT. 


The  ventilating  air-current  is  so  adjusted  that  the  air  which  leaves  the 
chamber  is  caused  to  pass  through  purifiers,  where  the  water-vapor  and 
the  carbon  dioxide  are  removed,  and  then,  after  being  replenished  with  fresh 
oxygen,  it  is  returned  to  the 

O  TENSION 
EQUALIZER 


T"T 


r-n- 


INTRODUCED 


0 


^ 


r 


chamber  ready  for  use.  The 
general  scheme  of  the  respi- 
ration apparatus  is  shown  in 
fig.  .27.  The  air  leaving  the 
chamber  contains  carbon  di- 
oxide and  water-vapor  and 
the  original  amount  of  nitro- 
gen and  is  somewhat  deficient 
in  oxygen.  In  order  to  pur- 
ify the  air  it  must  be  passed 
through  absorbents  for  car- 
bonic acid  and  water-vapor 
and  hence  some  pressure  is 
necessary  to  force  the  gas 
through  these  purifying  ves- 
sels. This  pressure  is  ob- 
tained by  a  small  positive 
rotary  blower,  which  has  been 
described  previously  in  de- 
tail.* The  air  is  thus  forced 
successively  through  sulphu- 
ric acid,  soda  or  potash  lime, 
and  again  sulphuric  acid.  Finally  it  is  directed  back  to  the  respiration 
chamber  free  from  carbon  dioxide  and  water  and  deficient  in  oxygen.  Pure 
oxygen  is  admitted  to  the  chamber  to  make  up  the  deficiency,  and  the  air 
thus  regenerated  is  breathed  again  by  the  subject. 


Ht0 
ABSORBED 


H2S  0, 


n 


CO, 

ABSORBED 

P  OTA  S  H 

LIMC 


HzO 

ABSORBED 


L_L 


HjSO. 


Fig.  27. — Diagram  of  ventilation  of  respiration  calorimeter. 
The  air  ia  taken  out  at  lower  right-hand  corner  and 
forced  by  the  blower  through  the  apparatus  for  absorb- 
ing water  and  carbon  dioxide.  It  returns  to  the  calo- 
rimeter at  the  top.  Oxygen  can  be  introduced  into  the 
chamber  itself  as  need  is  shown  by  the  tension  equalizer. 


The  rotary  blower  used  in  these  experiments  for  maintaining  the  venti- 
lating current  of  air  has  given  the  greatest  satisfaction.    It  is  a  so-called 

*W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.     Carnegie   Institution  of  Washington 
Publication  No.  42,  p.  18.     (1905.) 
5 


58  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

positive  blower  and  capable  of  producing  at  the  outlet  considerable  pressure 
and  at  the  inlet  a  vacuum  of  several  inches  of  mercury.  At  a  speed  of  230 
revolutions  per  minute  it  delivers  the  air  at  a  pressure  of  43  millimeters  of 
mercury,  forcing  it  through  the  purifying  vessels  at  the  rate  of  75  liters 
per  minute.  This  rate  of  ventilation  has  been  established  as  being  satis- 
factory for  all  experiments  and  is  constant.  Under  the  pressure  of  43  mil- 
limeters of  mercury  there  are  possibilities  of  leakage  of  air  from  the  blower 
connections  and  hence,  to  note  this  immediately,  the  blower  system  is 
immersed  in  a  tank  filled  with  heavy  lubricating  oil.  The  connections  are  so 
well  made,  however,  that  leakage  rarely  occurs,  and,  when  it  does,  a  slight 
tightening  of  the  stuffing-box  on  the  shaft  makes  the  apparatus  tight  again. 

ABSORBERS  FOR  WATER-VAPOR. 

To  absorb  25  to  40  grams  of  water- vapor  in  an  hour  from  a  current  of  air 
moving  at  the  rate  of  75  liters  per  minute  and  leaving  the  air  essentially 
dry  under  these  conditions  has  been  met  by  the  apparatus  herewith  described. 
The  earlier  attempts  to  secure  this  result  involved  the  use  of  enameled- 
iron  soup-stock  pots,  fitted  with  special  enameled-iron  covers  and  closed 
with  rubber  gaskets.  For  the  preliminary  experimenting  and  for  a  few 
experiments  with  man  these  proved  satisfactory,  but  in  spite  of  their 
resistance  to  the  action  of  sulphuric  acid,  it  was  found  that  they  were  not 
as  desirable  as  they  should  be  for  continued  experimenting  from  year  to 
year.  Recourse  was  then  had  to  a  special  form  of  chemical  pottery,  glazed, 
and  a  type  that  usually  gives  excellent  satisfaction  in  manufacturing  con- 
cerns was  used. 

This  special  form  of  absorbers  presented  many  difficulties  in  construc- 
tion, but  the  mechanical  difficulties  were  overcome  by  the  potter's  skill  and 
a  number  of  such  vessels  were  furnished  by  the  Charles  Graham  Chemical 
Pottery  Works.  Here  again  these  vessels  served  our  purpose  for  several 
months,  but  unfortunately  the  glaze  used  did  not  suffice  to  cover  them  com- 
pletely and  there  was  a  slight,  though  persistent,  leakage  of  sulphuric  acid 
through  the  porous  walls.  To  overcome  this  difficulty  the  interior  of  the 
vessels  was  coated  with  hot  paraffin  after  a  long-continued  washing  to  remove 
the  acid  and  after  they  had  been  allowed  to  dry  thoroughly.  The  paraffin- 
treated  absorbers  continued  to  give  satisfaction,  but  it  was  soon  seen  that 
for  permanent  use  something  more  satisfactory  must  be  had.  After  innu- 
merable trials  with  glazed  vessels  of  different  kinds  of  pottery  and  glass, 
arrangements  were  made  with  the  Eoyal  Berlin  Porcelain  Works  to  mold 
and  make  these  absorbers  out  of  their  highly  resistant  porcelain.  The  result 
thus  far  leaves  nothing  to  be  desired  as  a  vessel  for  this  purpose.  A  number 
of  such  absorbers  were  made  and  have  been  constantly  used  for  a  year  and 
are  absolutely  without  criticism. 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS. 


59 


Fig.  28  shows  the  nature  of  the  interior  of  the  apparatus.     The  air 
enters  through  one  opening  at  the  top,  passes  down  through  a  bent  pipe, 
and  enters  a  series  of  roses,  consisting  of  inverted  circular  saucers  with 
holes  in  the  rims.    The  position  of  the  holes  is  such  that  when  the  vessel  is 
one-fourth  to  one-third  full  of  sulphuric  acid  the  air  must  pass  through 
the  acid  three  times.    To  prevent  spattering,  a  small  cup-shaped  arrange- 
ment, provided  with  holes,  is  attached  to  the  opening  through  which  the  air 
passes  out  of  the  absorber,  and  for  filling  the  vessel  with  acid  a  small  open- 
ing is  made  near  one  edge.    The  speci- 
fications  required   that  the   apparatus 
should  be  made  absolutely  air-tight  to 
pressures  of  over  1  meter  of  water,  and 
that  there  is  no  porosity  in  these  vessels 
under  these  conditions  is  shown  by  the 
fact  that  such  a  pressure  is  held  indefi- 
nitely.   The  inside  and  outside  are  both 
heavily  glazed.     There  is  no  apparent 
action  of  sulphuric  acid  on  the  vessels 
and  the  slight  increase  in  temperature 
resulting  from  the  absorption  of  water- 
vapor  as  the  air  passes  through  does  not 
appear  to  have  any  deleterious  effect. 
The  vessels  without  filling  and  with- 
out rubber  elbows  weigh  11.5  kilograms; 
with  the  special  elbows  and  couplings 
attached  so  as  xo  enable  them  to  be  con- 
nected with  the  ventilating  air-system, 
the  empty  absorbers  weigh  13.4  kilo- 
grams; and  filled  with  sulphuric  acid 
they   weigh   19   kilograms.     Repeated 
tests  have  shown  that  5.5  kilograms  of  sulphuric  acid  will  remove  the  water- 
vapor  from  a  current  of  air  passing  through  the  absorbers  at  the  rate  of  75 
liters  of  air  per  minute,  without  letting  any  appreciable  amount  pass  by 
until  500  grams  of  water  have  been  absorbed.    At  this  degree  of  saturation 
a  small  persistent  amount  of  moisture  escapes  absorption  in  the  acid  and 
consequently  a  second  absorber  will  begin  to  gain  in  weight    Experiments 
demonstrate  that  the  first  vessel  can  gain  1,500  grams  of  water  before  the 
second  gains  5  grams.    As  a  matter  of  fact,  it  has  been  found  more  advan- 
tageous to  use  but  one  absorber  and  have  it  refilled  as  soon  as  it  has  gained 
400  grams,  thus  allowing  a  liberal  factor  of  safety  and  no  danger  of  loss  of 
water. 


Fig.  28. — Cross-section  of  sulphuric-acid  ab- 
sorber. The  air  enters  at  the  top  of  the 
right-hand  opening,  descends  to  the  bot- 
tom of  the  absorber,  and  then  passes 
through  three  concentric  rings,  which  are 
covered  with  acid,  and  it  finally  passes  out 
at  the  left-hand  opening.  Beneath  the  left- 
hand  opening  is  a  cup  arrangement  for  pre- 
venting the  acid  being  carried  mechanic- 
ally out  through  the  opening.  The  opening 
for  filling  and  emptying  the  absorber  is 
shown  midway  between  tie  two  large  open- 
ings. 


60  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


POTASH-LIME  CANS. 


The  problem  of  absorbing  the  water-vapor  from  so  rapid  a  current  of  air 
is  second  only  to  that  of  absorbing  the  carbon  dioxide  from  such  a  current. 
All  experiments  with  potassium  hydroxide  in  the  form  of  sticks  or  in  solu- 
tion failed  to  give  the  desired  results  and  the  use  of  soda-lime  has  supple- 
mented all  other  forms  of  carbon  dioxide  absorption.  More  recently  we 
have  been  using  potash-lime,  substituting  caustic  potash  for  caustic  soda  in 
the  formula,  and  the  results  thus  obtained  are,  if  anything,  more  satisfac- 
tory than  with  the  soda-lime. 

The  potash-lime  is  made  as  follows :  1  kilogram  of  commercial  potassium 
hydroxide,  pulverized,  is  dissolved  in  550  to  650  cubic  centimeters  of  water 
and  1  kilogram  of  pulverized  quicklime  added  slowly.  The  amount  of 
water  to  be  used  varies  with  the  moisture  content  of  the  potash.  There  is 
a  variation  in  the  moisture  content  of  different  kegs  of  potash,  so  when  a 
keg  is  opened  we  determine  experimentally  the  amount  of  water  to  be  used. 
After  a  batch  is  made  up  in  this  way  it  should  be  allowed  to  cool  before 
testing  whether  it  has  the  right  amount  of  water,  and  this  is  determined  by 
feeling  of  it  and  noting  how  it  pulverizes  in  the  hand.  It  is  not  advisable 
to  make  a  great  quantity  at  once,  because  we  have  found  that  if  a  large 
quantity  is  made  and  broken  into  small  particles  and  stored  in  a  container 
it  has  a  tendency  to  cake  and  thus  interfere  with  its  ready  subsequent  use. 

A  record  was  kept  of  the  gains  in  weight  of  a  can  filled  with  potash-lime 
during  a  series  of  experiments  where  there  were  three  silver-plated  cans 
used.  This  can  was  put  at  the  head  of  the  system  and  when  it  began  to 
lose  weight  it  was  removed.  The  records  of  gains  of  weight  when  added 
together  amount  to  400  grams.  From  experience  with  other  cans  where 
the  loss  of  moisture  was  determined,  it  is  highly  probable  that  at  least  200 
grams  of  water  were  vaporized  from  the  reagent  and  thus  the  total  amount 
of  carbon  dioxide  absorbed  must  have  been  not  far  from  600  grams.  At 
present  our  method  is  not  to  allow  the  cans  to  gain  a  certain  weight,  but 
during  4-hour  or  5-hour  experiments,  in  which  each  can  may  be  used  2  or 
3  hours,  it  is  the  practice  to  put  a  new  can  on  each  side  of  the  absorber 
system  (see  page  66)  at  the  beginning  of  every  experiment.  This  insures 
the  same  power  of  absorption  on  each  side  of  the  absorption  system,  so  that 
the  residual  amount  of  carbon  dioxide  in  the  chamber  from  period  to  period 
does  not  undergo  very  marked  changes.  This  has  been  found  the  best 
method,  because  if  one  can  is  left  on  a  day  longer  than  the  other  there  is 
apt  to  be  alternately  a  rise  and  fall  in  the  amount  of  residual  carbon  dioxide 
in  the  apparatus,  owing  to  the  unequal  efficiency  of  the  absorbers. 

These  cans  are  each  day  taken  to  the  basement,  where  the  first  section  * 

*  For  a  description  of  the  apparatus  and  the  method  of  filling  see  W.  O.  At- 
water  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances  for  the 
direct  determination  of  oxygen.  Carnegie  Institution  of  Washington  Publication 
No.  42,  p.  27.     (1905.) 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS.  61 

only  is  taken  out  and  replaced  with  new  potash-lime.  Thus,  three-quarters 
of  the  contents  of  the  can  is  used  over  and  over,  while  the  first  quarter  is 
freshly  renewed  every  day.  Potash-lime  has  not  been  found  practicable  for 
the  U-tubes  because  one  can  not,  as  in  the  case  of  soda-lime,  see  the  whiten- 
ing of  the  reagent  where  the  carbon  dioxide  is  absorbed. 

The  importance  of  having  the  soda-lime  or  potash-lime  somewhat  moist, 
to  secure  the  highest  efficiency  for  the  absorption  of  the  carbon  dioxide, 
makes  it  necessary  to  absorb  the  moisture  taken  up  by  the  dry  air  in  passing 
through  the  potash-lime  can.  Consequently  a  second  vessel  containing 
sulphuric  acid  is  placed  in  the  system  to  receive  the  air  immediately  after 
it  leaves  the  potash-lime  can.  Obviously  the  amount  of  water  absorbed 
here  is  very  much  less  than  in  the  first  acid  absorber  and  hence  the  same 
absorber  can  be  used  for  a  greater  number  of  experiments. 

BALANCE  FOB  WEIGHING   ABSOBBEBS. 

The  complete  removal  of  water-vapor  and  carbon  dioxide  from  a  current 
of  air  moving  at  the  rate  of  75  liters  per  minute  calls  for  large  and  some- 
what unwieldly  vessels  in  which  is  placed  the  absorbing  material.  This  is 
particularly  the  case  with  the  vessels  containing  the  rather  large  amounts 
of  sulphuric  acid  required  to  dry  the  air.  In  the  course  of  an  hour  there 
is  ordinarily  removed  from  the  chamber  not  far  from  25  grams  of  water- 
vapor  and  20  to  30  grams  of  carbon  dioxide.  This  necessitates  weighing 
the  absorbers  to  within  0.25  gram  if  an  accuracy  of  1  per  cent  is  desired. 
The  sulphuric-acid  absorbers  weigh  about  18  kilograms  when  filled  with 
acid.  In  order  to  weigh  this  receptacle  so  as  to  measure  accurately  the 
increase  in  weight  due  to  the  absorption  of  water  to  within  less  than  1  per 
cent,  we  use  the  balance  shown  in  fig.  29.  This  balance  has  been  employed 
in  a  number  of  other  manipulations  in  connection  with  the  respiration  calo- 
rimeter and  accessory  apparatus  and  the  general  type  of  balance  leaves 
nothing  to  be  desired  as  a  balance  capable  of  carrying  a  heavy  load  with 
remarkable  sensitiveness. 

The  balance  is  rigidly  mounted  on  a  frame  consisting  of  four  upright 
structural-steel  angle-irons,  fastened  at  the  top  to  a  substantial  wooden  bed. 
Two  heavy  wooden  pieces  run  the  length  of  the  table  and  furnish  a  sub- 
stantial base  to  which  the  standard  of  the  balance  is  bolted.  The  balance 
is  surrounded  by  a  glass  case  to  prevent  errors  due  to  air-currents  (see 
fig.  2).  The  pan  of  the  balance  is  not  large  enough  to  permit  the  weigh- 
ing of  an  absorber,  hence  provision  is  made  for  suspending  it  on  a  steel  or 
brass  rod  from  one  of  the  hanger  arms.  This  rod  passes  through  a  hole  in 
the  bottom  of  the  balance  case,  and  its  lower  end  is  provided  with  a  piece 
of  pipe  having  hooks  at  either  end.  Since  the  increase  in  weight  rather 
than  the  absolute  weight  of  the  absorber  is  used,  the  greater  part  of  the 
weight  is  taken  up  by  lead  counterpoises  suspended  above  the  pan  on  the 


62 


CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


right-hand  arm  of  the  balance.    The  remainder  of  the  weight  is  made  up 
with  brass  weights  placed  in  the  pan. 

In  order  to  suspend  this  heavy  absorber,  a  small  elevator  has  been  con- 
structed, so  that  the  vessel  may  be  raised  by  a  compressed-air  piston.    This 


Fio.  29. — Balance  for  weighing  absorbers,  showing  general  type  of  balance  and 
case  surrounding  it,  with  counterpoise  and  weights  upon  right-hand  pan.  A 
sulphuric-acid  absorber  is  suspended  in  position  ready  for  weighing.  Elevator 
with  compressed-air  system  is  shown  in  lower  part  of  case. 

piston  is  placed  in  an  upright  position  at  the  right  of  the  elevator  and  is 
connected  with  the  compressed-air  service  of  the  building.  The  pressure  is 
about  25  pounds  per  square  inch  and  the  diameter  of  the  cylinder  is  2.5 
inches,  thus  giving  ample  service  for  raising  and  lowering  the  elevator  and 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS.  63 

its  load.  By  turning  a  3-way  valve  at  the  end  of  the  compressed-air  supply- 
pipe,  so  that  the  air  rushes  into  the  cylinder  above  the  piston,  the  piston 
is  pushed  to  the  base  of  the  cylinder  and  the  elevator  thereby  raised.  The 
pressure  of  the  compressed  air  holds  the  elevator  in  this  position  while  the 
hooks  are  being  adjusted  on  the  absorber.  By  turning  the  3-way  valve  so 
as  to  open  the  exhaust  leading  to  the  upper  part  of  the  cylinder  to  the  air, 
the  weight  of  the  elevator  expels  the  air,  and  it  soon  settles  into  the  posi- 
tion shown  in  the  figure.  The  weighing  can  then  be  made  as  the  absorber 
is  swinging  freely  in  the  air.  After  the  weighing  has  been  made,  the  ele- 
vator is  again  lifted,  the  hooks  are  released,  and  by  turning  the  valve  the 
elevator  and  load  are  safely  lowered- 

The  size  of  the  openings  of  the  pipes  into  the  cylinder  is  so  adjusted  that 
the  movement  of  the  elevator  is  regular  and  moderate  whether  it  is  being 
raised  or  lowered,  thus  avoiding  any  sudden  jars  that  might  cause  an 
accident  to  the  absorbers.  With  this  system  it  is  possible  to  weigh  these 
absorbers  to  within  0.1  gram  and,  were  it  necessary,  probably  the  error 
could  be  diminished  so  that  the  weight  could  be  taken  to  0.05  gram.  On 
a  balance  of  this  type  described  elsewhere,*  weighings  could  be  obtained  to 
within  0.02  gram.  For  all  practical  purposes,  however,  we  do  not  use  the 
balance  for  weighing  the  absorbers  closer  than  to  within  0.10  gram.  In 
attempting  to  secure  accuracy  no  greater  than  this,  it  is  unnecessary  to 
lower  the  glass  door  to  the  balance  case  or,  indeed,  to  close  the  two  doors  to 
the  compartment  in  which  the  elevator  is  closed,  as  the  slight  air-currents 
do  not  affect  the  accuracy  of  the  weighing  when  only  0.1  gram  sensitiveness 
is  required. 

PURIFICATION  OF  THE  AIB-CURRENT  WITH  SODIUM   BICARBONATE. 

As  is  to  be  expected,  the  passage  of  so  large  a  volume  of  air  through  the 
sulphuric  acid  in  such  a  relatively  small  space  results  in  a  slight  acid  odor 
in  the  air-current  leaving  this  absorber.  The  amount  of  material  thus 
leaving  the  absorber  is  not  weighable,  as  has  been  shown  by  repeated  tests, 
but  nevertheless  there  is  a  sufficiently  irritating  acid  odor  to  make  the  air 
very  uncomfortable  for  subsequent  respiration.  It  has  been  found  that  this 
odor  can  be  wholly  eliminated  by  passing  the  air  through  a  can  containing 
cotton  wool  and  dry  sodium  bicarbonate.  This  can  is  not  weighed,  and 
indeed,  after  days  of  use,  there  is  no  appreciable  change  in  its  weight. 


In  order  to  subdivide  experiments  into  periods  as  short  as  1  or  2  hours, 
it  is  necessary  to  deflect  the  air-current  at  the  end  of  each  period  from  one 
set  of  purifiers  to  the  other,  in  order  to  weigh  the  set  used  and  to  measure 

*  W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42,  p.  56.     (1905.) 


64  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

the  quantity  of  carbon  dioxide  and  water-vapor  absorbed.  The  conditions 
under  which  these  changes  from  one  system  to  another  are  made,  and  which 
call  for  an  absolutely  gas-tight  closure,  have  been  discussed  in  detail  else- 
where.* It  is  sufficient  to  state  here  that  the  very  large  majority  of  me- 
chanical valves  will  not  serve  the  purpose,  since  it  is  necessary  to  have  a 
pressure  of  some  40  millimeters  of  mercury  on  one  side  of  the  valve  at 
the  entrance  to  the  absorber  system  and  on  the  other  side  atmospheric  pres- 
sure. A  valve  with  an  internal  diameter  of  not  less  than  25  millimeters 
must  be  used,  and  to  secure  a  tight  closure  of  this  large  area  and  permit 
frequent  opening  and  shutting  is  difficult.  After  experimenting  with  a 
large  number  of  valves,  a  valve  of  special  construction  employing  a  me- 
chanical seal  ultimately  bathed  in  mercury  was  used  for  the  earlier  appa- 
ratus. The  possibility  of  contamination  of  the  air-current  by  mercury 
vapor  was  duly  considered  and  pointed  out  in  a  description  of  this  appa- 
ratus. It  was  not  until  two  years  later  that  difficulties  began  to  be  experi- 
enced and  a  number  of  men  were  severely  poisoned  while  inside  the  cham- 
ber. A  discussion  of  this  point  has  been  presented  elsewhere.f  At  that 
time  mercury  valves  were  used  both  at  the  entrance  and  exit  ends  of  the 
absorber  system,  although  as  a  matter  of  fact,  when  the  air  leaves  the  last 
absorber  and  returns  to  the  respiration  chamber,  the  pressure  is  but  a 
little  above  that  of  the  atmosphere.  Consequently,  mechanical  valves  were 
substituted  for  mercurial  valves  at  the  exit  and  the  toxic  symptoms  dis- 
appeared. In  constructing  the  new  calorimeters  it  seemed  to  be  desirable 
to  avoid  all  use  of  mercury,  if  possible.  We  were  fortunate  in  finding  a 
mechanical  valve  which  suited  this  condition  perfectly.  These  valves,  which 
are  very  well  constructed,  have  never  failed  to  show  complete  tightness 
under  all  possible  tests  and  are  used  at  the  exit  and  entrance  end  of  the 
absorber  system.  Their  workmanship  is  of  the  first  order,  and  the  valve 
is  somewhat  higher  in  price  than  ordinary  mechanical  valves.  They  have 
been  in  use  on  the  apparatus  for  a  year  now  and  have  invariably  proved 
to  be  absolutely  tight.  They  are  easy  to  obtain  and  are  much  easier  to 
manipulate  and  much  less  cumbersome  than  the  mercury  valves  formerly 
used. 

COUPLINGS. 

Throughout  the  construction  of  the  respiration  apparatus  and  its  various 
parts,  it  was  constantly  borne  in  mind  that  the  slightest  leak  would  be 
very  disastrous  for  accurate  oxygen  determinations.  At  any  point  where 
there  is  a  pressure  greater  or  less  than  that  of  the  atmosphere,  special  pre- 

*  W.  O.  Atwater  and  F.  G.  Benedict:  A  respiration  calorimeter  with  appliances 
for  the  direct  determination  of  oxygen.  Carnegie  Institution  of  Washington 
Publication  No.  42,  p.  20.     (1905.) 

fThorne  M.  Carpenter  and  Francis  G.  Benedict:  Mercurial  poisoning  of  men 
in  a  respiration  chamber.  American  Journal  of  Physiology,  vol.  24,  p.  187. 
(1909.) 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS.  65 

caution  must  be  taken.  At  no  point  in  the  whole  apparatus  is  it  necessary 
to  be  more  careful  than  with  the  couplings  which  connect  the  various 
absorber  systems  with  each  other  and  with  the  valves;  for  these  couplings 
are  opened  and  closed  once  every  hour  or  two  and  hence  are  subject  to 
considerable  strain  at  the  different  points.  If  they  are  not  tight  the 
experiment  is  a  failure  so  far  as  the  determination  of  oxygen  is  concerned. 
For  the  various  parts  of  the  absorber  system  we  have  relied  upon  the  ori- 
ginal type  of  couplings  used  in  the  earlier  apparatus.  A  rubber  gasket  is 
placed  between  the  male  and  female  part  of  the  coupling  and  the  closure 
can  be  made  very  tight.  In  fact,  after  the  absorbers  are  coupled  in  place 
they  are  invariably  subjected  to  severe  tests  to  prove  tightness. 

For  connecting  the  piping  between  the  calorimeter  and  the  absorption 
system  we  use  ordinary  one-inch  hose-couplings,  firmly  set  up  by  means 
of  a  wrench  and  disturbed  only  when  necessary  to  change  from  one  calo- 
rimeter chamber  to  another. 

ABSORBER  TABLE. 

The  purifying  apparatus  for  the  air-current  is  compactly  and  conven- 
iently placed  on  a  solidly  constructed  table  which  can  be  moved  about  the 
laboratory  at  will.  The  special  form  of  caster  on  the  bottom  of  the  posts 
of  the  table  permits  its  movement  about  the  laboratory  at  will  and  by 
screwing  down  the  hand  screws  the  table  can  be  firmly  fixed  to  the  floor. 

The  details  of  the  table  are  shown  in  fig.  30.  (See  also  fig.  4,  page  4.) 
The  air  coming  from  the  calorimeter  passes  in  the  direction  of  the  down- 
ward arrow  through  a  J-inch  pipe  into  the  blower,  which  is  immersed  in 
oil  in  an  iron  box  F.  The  blower  is  driven  by  an  electric  motor  fastened 
to  a  small  shelf  at  the  left  of  the  table.  The  air  leaving  the  blower  ascends 
in  the  direction  of  the  arrow  to  the  valve  system  H,  where  it  can  be  directed 
into  one  of  the  two  parallel  sets  of  purifiers;  after  it  passes  through  these 
purifiers  (sulphuric-acid  vessel  2,  potash-lime  container  K,  and  sulphuric- 
acid  vessel  1)  it  goes  through  the  sodium-bicarbonate  can  G  to  a  duplicate 
valve  system  on  top  of  the  table.  From  there  it  passes  through  a  pipe  along 
the  top  of  the  table  and  rises  in  the  vertical  pipe  to  the  hose  connection 
which  is  coupled  with  the  calorimeter  chamber. 

The  electric  motor  is  provided  with  a  snap-switch  on  one  of  the  posts  of 
the  table  and  a  regulating  rheostat  which  permits  variations  in  the  speed 
of  the  motor  and  consequently  in  the  ventilation  produced  by  the  blower. 
The  blower  is  well  oiled,  and  as  oil  is  gradually  carried  in  with  the  air,  a 
small  pet-cock  at  the  bottom  of  the  T  following  the  blower  allows  any 
accumulated  oil  to  be  drawn  away  from  time  to  time.  The  air  entering 
the  valve  system  at  H  enters  through  a  cross,  two  arms  of  which  connect 
with  two  "  white  star "  valves.    The  upper  part  of  the  cross  is  connected 


66 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


to  a  small  rubber  tubing  and  to  the  mercury  manometer  D,  which  also 
serves  as  a  valve  for  passing  a  given  amount  of  air  through  a  series  of 
U -tubes  for  analysis  of  the  air  from  time  to  time.  It  is  assumed  that  the 
air  drawn  at  the  point  H  is  of  substantially  the  same  composition  as  that 
inside  the  chamber,  an  assumption  that  may  not  be  strictly  true,  but  doubt- 
less the  sample  thus  obtained  is  constantly  proportional  to  the  average 
composition,  which  fluctuates  but  slowly.  Ordinarily  the  piping  leading 
from  the  left-hand  arm  of  the  tube  D  is  left  open  to  the  air  and  conse- 


Fig.  30. — Diagram  of  absorber  table.  1  and  2  contain  sulphuric  acid;  K  contains 
potash-lime;  G,  sodium  bicarbonate  can;  F,  rotary  blower  for  maintaining  air- 
current;  H,  valves  for  closing  either  side;  and  D,  mercury  manometer  and 
valve  for  diverting  air  to  U  -tubes  on  table.  Air  leaves  A,  passes  through  the 
meter,  and  then  through  drying  tower  B  and  through  C  to  ingoing  air-pipe. 
At  the  left  is  the  regulating  rheostat  and  motor  and  snap-switch.  General 
direction  of  ventilation  is  indicated  by  arrows. 


quently  the  difference  in  the  level  of  the  mercury  in  the  two  arms  of  D 
indicates  the  pressure  on  the  system.  This  is  ordinarily  not  far  from  40  to 
50  millimeters  of  mercury. 

The  absorber  table,  with  the  U  -tubes  and  meter  for  residual  analyses,  is 
shown  in  the  foreground  in  fig.  2.  The  two  white  porcelain  vessels  with  a 
silver-plated  can  between  them  are  on  the  middle  shelf.  The  sodium  bicar- 
bonate can,  for  removing  traces  of  acid  fumes,  is  connected  in  an  upright 


GENERAL   DESCRIPTION    OF   RESPIRATION   APPARATUS.  67 

position,  while  the  motor,  the  controlling  rheostat,  and  the  blower  are  sup- 
ported by  the  legs  near  the  floor.  The  two  rubber  pipes  leading  from  the 
table  can  be  used  to  connect  the  apparatus  either  with  the  bed  or  chair 
calorimeter.  In  fig.  4  the  apparatus  is  shown  connected  with  the  bed  calo- 
rimeter, but  just  above  the  lowest  point  of  the  rubber  tubing  can  be  seen  in 
the  rear  the  coupling  for  one  of  the  pipes  leading  from  the  chair  calo- 
rimeter.   The  other  is  immediately  below  and  to  the  left  of  it. 

OXYGEN  SUPPLY. 

The  residual  air  inside  of  the  chamber  amounts  to  some  1,300  liters  and 
contains  about  250  liters  of  oxygen.  Consequently  it  can  be  seen  that  in 
an  8-hour  experiment  the  subject  could  easily  live  during  the  entire  time 
upon  the  amount  of  oxygen  already  present  in  the  residual  air.  It  has  been 
repeatedly  shown  that  until  the  per  cent  of  oxygen  falls  to  about  11,  or 
about  one-half  normal,  there  is  no  disturbance  in  the  respiratory  exchange 
and  therefore  about  125  liters  of  oxygen  would  be  available  for  respiration 
even  if  no  oxygen  were  admitted.  Inasmuch  as  the  subject  when  at  rest 
uses  not  far  from  11  to  15  liters  per  hour,  the  amount  originally  present 
in  the  chamber  would  easily  suffice  for  an  8-hour  experiment.  Moreover, 
the  difficulties  attending  an  accurate  gas  analysis  and  particularly  the  calcu- 
lation of  the  total  amount  of  oxygen  are  such  that  satisfactory  determina- 
tions of  oxygen  consumption  by  this  method  would  be  impossible.  Further- 
more, from  our  previous  experience  with  long-continued  experiments  of 
from  10  days  to  2  weeks,  it  has  been  found  that  oxygen  can  be  supplied  to 
the  system  readily  and  the  amount  thus  supplied  determined  accurately. 
Consequently,  even  in  these  short  experiments,  we  adhere  to  the  original 
practice  of  supplying  oxygen  to  the  air  and  noting  the  amount  thus  added. 

The  oxygen  supply  was  formerly  obtained  from  small  steel  cylinders  of 
the  highly  compressed  gas.  This  gas  was  made  by  the  calcium-manganate 
method  and  represented  a  high  degree  of  purity  for  commercial  oxygen. 
More  recently  we  have  been  using  oxygen  of  great  purity  made  from  liquid 
air.  Inasmuch  as  this  oxygen  is  very  pure  and  much  less  expensive  than 
the  chemically-prepared  oxygen,  extensive  provisions  have  been  made  for 
its  continued  use.  Instead  of  using  small  cylinders  containing  10  cubic 
feet  and  attaching  thereto  purifying  devices  in  the  shape  of  soda-lime 
U -tubes  and  a  sulphuric-acid  drying- tube,  we  now  use  large  cylinders  and 
we  have  found  that  the  oxygen  from  liquid  air  is  practically  free  from 
carbon  dioxide  and  water-vapor,  the  quantities  present  being  wholly  negli- 
gible in  experiments  such  as  these.  Consequently,  no  purifying  attachments 
are  considered  necessary  and  the  oxygen  is  delivered  directly  from  the 
cylinder.  The  cylinders,  containing  100  cubic  feet  (2,830  liters),  under 
a  pressure  of  120  atmospheres,  are  provided  with  well-closing  valves  and 
weigh  when  fully  charged  57  kilograms. 


68 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


It  is  highly  desirable  to  determine  the  oxygen  to  within  0.1  gram,  and 
we  are  fortunate  in  having  a  balance  of  the  type  used  frequently  in  this 


Fig.  31.— Diagram  of  oxygen  balance  and  cylinder.  At  the  top  is  the  balance 
arrangement,  and  at  the  center  its  support.  At  the  left  is  the  oxygen 
cylinder,  with  reducing  valve  A,  rubber  tube  D  leading  from  it,  F  the 
electro-magnet  which  opens  and  closes  D,  K  the  hanger  of  the  cylinder  and 
support  for  the  magnet,  R  the  lever  which  operates  the  supports  for  the 
cylinder  and  its  counterpoise  S,  T'  a  box  which  is  raised  and  lowered  by 
R,  and  T  its  surrounding  box. 

laboratory  which  will  enable  us  to  weigh  this  cylinder  accurately  with  a 
sensitiveness  of  less  than  0.1  gram.  Since  1  liter  of  oxygen  weighs  1.43 
grams,  it  can  be  seen  that  the  amount  of  oxygen  introduced  into  the  cham- 


GENERAL  DESCRIPTION  OF  RESPIRATION  APPARATUS.         69 

ber  can  be  measured  by  this  method  within  70  cubic  centimeters.  Even 
in  experiments  of  but  an  hour's  duration,  where  the  amount  of  oxygen 
admitted  from  the  cylinder  is  but  25  to  30  grams,  it  can  be  seen  that  the 
error  in  the  weighing  of  the  oxygen  is  much  less  than  1  per  cent. 

The  earlier  forms  of  cylinders  used  were  provided  with  valves  which 
required  some  special  control  and  a  rubber  bag  was  attached  to  provide 
for  any  sudden  rush  of  gas.  The  construction  of  the  valve  and  valve-stem 
was  unfortunately  such  that  the  well-known  reduction  valves  could  not 
be  attached  without  leakage  under  the  high  pressure  of  120  atmospheres. 
With  the  type  of  cylinder  at  present  in  use,  such  leakage  does  not  occur  and 
therefore  we  simply  attach  to  the  oxygen  cylinder  a  reduction-valve  which 
reduces  the  pressure  from  120  atmospheres  to  about  2  or  3  pounds  to  the 
square  inch.  The  cylinder,  together  with  the  reduction  valve,  is  suspended 
on  one  arm  of  the  balance.  The  equipment  of  the  arrangement  is  shown 
in  fig.  31.  (See  also  fig.  5,  page  4.)  The  cylinder  is  supported  by  a 
clamp  K  hung  from  the  balance  arm,  and  the  reduction-valve  A  is  shown 
at  the  top.  The  counterpoise  S  consists  of  a  piece  of  7-inch  pipe,  with 
caps  at  each  end.  At  a  convenient  height  a  wooden  shelf  with  slightly 
raised  rim  is  attached. 

In  spite  of  the  rigid  construction  of  this  balance,  it  would  be  detrimental 
to  allow  this  enormous  weight  to  remain  on  the  knife-edges  permanently,  so 
provision  is  made  for  raising  the  cylinders  on  a  small  elevator  arrangement 
which  consists  of  small  boxes  of  wood,  T,  into  which  telescope  other  boxes, 
T'.  A  lever  handle,  E,  when  pressed  forward,  raises  T'  by  means  of  a 
roller  bearing  U,  and  when  the  handle  is  raised  the  total  weight  of  the 
cylinders  is  supported  on  the  platforms. 

The  balance  is  attached  to  an  upright  I-beam  which  is  anchored  to  the 
floor  and  ceiling  of  the  calorimeter  laboratory.  Two  large  turnbuckle  eye- 
bolts  give  still  greater  rigidity  at  the  bottom.  The  whole  apparatus  is 
inclosed  in  a  glass  case,  shown  in  fig.  5. 

AUTOMATIC  CONTROL  OF  OXYGEN  SUPPLY. 

The  use  of  the  reduction-valve  has  made  the  automatic  control  of  the 
oxygen  supply  much  simpler  than  in  the  apparatus  formerly  used.  The 
details  of  the  connections  somewhat  schematically  outlined  are  given  in 
fig.  32,  in  which  D  is  the  oxygen  cylinder,  K  the  supporting  band,  A  the 
reduction-valve,  and  J  the  tension-equalizer  attached  to  one  of  the  calo- 
rimeters. Having  reduced  the  pressure  to  about  2  pounds  by  means  of 
the  reduction-valve,  the  supply  of  oxygen  can  be  shut  off  by  putting  a 
pinch-cock  on  a  rubber  pipe  leading  from  the  reduction-valve  to  the  calo- 
rimeters. Instead  of  using  the  ordinary  screw  pinch-cock,  this  connection 
is  closed  by  a  spring  clamp.  The  spring  E  draws  on  the  rod  which  is  con- 
nected at  L  and  pinches  the  rubber  tube  tightly.    The  tension  at  E  can  be 


70 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


released  by  an  electro-magnet  F,  which  when  magnetized  exercises  a  pull  on 
the  iron  rod,  extends  the  spring  E,  and  simultaneously  releases  the  pressure 
on  the  rubber  tube  at  L.  To  make  the  control  perfectly  automatic,  the 
apparatus  shown  on  the  top  of  the  tension-equalizer  J  is  employed.  A  wire 
ring,  with  a  wire  support,  is  caused  to  pass  up  through  a  bearing  fastened 


Fig.  32. — Part  of  the  oxygen  cylinder  and  connections  to  tension-equalizer.  At  the  left  is  shown  the 
upper  half  of  the  oxygen  cylinder  with  a  detail  of  the  electro-magnet  and  reducing-valve.  D  is  the 
cylinder;  K,  the  band  supporting  the  oxygen  cylinder  and  electro-magnet  arrangement;  F,  the 
electro-magnet;  E,  the  tension  spring;  and  L,  the  rubber  tubing  at  a  point  where  it  is  closed  by  the 
clamp.  The  tension-equalizer  and  the  method  of  closing  the  circuit  operating  it  are  shown  at  the 
right.  C  and  C  are  two  mercury  cups  into  which  the  wire  loop  dips,  thus  closing  the  circuit.  B 
is  a  lever  used  for  short-circuiting  for  filling  the  diaphragm  J.  G  is  a  sulphuric-acid  container;  H, 
the  quick- throw  valve  for  shutting  off  the  tension  equalizer  J;  M,  part  of  the  ingoing  air-pipe;  N,  a 
plug  connecting  the  electric  circuit  with  the  electro-magnet;  and  O,  a  storage  battery. 


to  the  clamp  above  J.  As  the  air  inside  of  the  whole  system  becomes 
diminished  in  volume  and  the  rubber  cap  J  sinks,  there  is  a  point  at  which  a 
metal  loop  dips  into  two  mercury  cups  C  and  C,  thus  closing  the  circuit, 
which  causes  a  current  of  electricity  to  pass  through  F.  This  releases  the 
pressure  at  L,  oxygen  rushes  in,  and  the  rubber  bag  J  becomes  distended. 
As  it  is  distended,  it  lifts  the  metal  loop  out  of  the  cups,  C  and  C,  and 
the  circuit  is  broken.  There  is,  therefore,  an  alternate  opening  and  closing 
of  this  circuit  with  a  corresponding  admission  of  oxygen.  The  exact  posi- 
tion of  the  rubber  diaphragm  can  be  read  when  desired  from  a  pointer  on  a 
graduated  scale  attached  to  a  support  holding  the  terminals  of  the  electric 
wires.    More  frequently,  however,  when  the  volume  is  required,  instead  of 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS.  71 

filling  the  bag  to  a  definite  point,  as  shown  by  the  pointer,  a  delicate  man- 
ometer is  attached  to  the  can  by  means  of  a  pet-cock  and  the  oxygen  is 
admitted  by  operating  the  switch  B  nntil  the  desired  tension  is  reached. 

In  order  to  provide  for  the  maximum  sensitiveness  for  weighing  D  and 
its  appurtenances,  the  electric  connection  is  broken  at  the  cylinder  by  means 
of  the  ping  X  and  the  rubber  tube  is  connected  by  a  glass  connector  which 
can  be  disconnected  during  the  process  of  weighing.  Obviously,  provision 
is  also  made  that  there  be  no  leakage  of  air  out  of  the  system  during  the 
weighing.  The  current  at  F  is  obtained  by  means  of  a  storage  battery  0. 
The  apparatus  has  been  in  use  for  some  time  in  the  laboratory  and  has 
proved  successful  in  the  highest  degree. 

TENSION-EQUALIZER. 

The  rigid  walls  of  the  calorimeter  and  piping  necessitate  some  provision 
for  minor  fluctuations  in  the  absolute  volume  of  air  in  the  confined  system. 
The  apparatus  was  not  constructed  to  withstand  great  fluctuations  in  pres- 
sure, and  thin  walls  were  used,  but  it  is  deemed  inadvisable  to  submit  it 
even  to  minor  pressures,  as  thus  there  would  be  danger  of  leakage  of  air 
through  any  possible  small  opening.  Furthermore,  as  the  carbon  dioxide 
and  water-vapor  are  absorbed  out  of  the  air-current,  there  is  a  constant 
decrease  in  volume,  which  is  ordinarily  compensated  by  the  admission  of 
oxygen.  It  would  be  very  difficult  to  adjust  the  admission  of  oxygen  so  as 
to  exactly  compensate  for  the  contraction  in  volume  caused  by  the  absorp- 
tion of  water-vapor  and  carbon  dioxide.  Consequently  it  is  necessary  to 
adjust  some  portion  of  the  circulating  air-current  so  that  there  may  be  a 
contraction  and  expansion  in  the  volume  without  producing  a  pressure  on 
the  system.  This  was  done  in  a  manner  similar  to  that  described  in  the 
earlier  apparatus,  but  on  a  much  simpler  plan. 

To  the  air-pipe  just  before  it  entered  the  calorimeter  was  attached  a 
copper  can  with  a  rubber  diaphragm  top.  This  diaphragm,  which  is,  as  a 
matter  of  fact,  a  ladies'  pure  rubber  bathing-cap,  allows  for  an  expansion  or 
contraction  of  air  in  the  system  of  2  to  3  liters.  The  apparatus  shown 
in  position  is  to  be  seen  in  fig.  25,  in  which  the  tin  can  I  is  covered  with  the 
rubber  diaphragm  J.  If  there  is  any  change  in  volume,  therefore,  the  rub- 
ber diaphragm  rises  or  falls  with  it  and  under  ordinary  conditions  of  an 
experiment  this  arrangement  results  in  a  pressure  in  the  chamber  approxi- 
mately that  of  the  atmosphere.  It  was  found,  however,  that  even  the  slight 
resistance  of  the  piping  from  the  tension-equalizer  to  the  chamber,  a  pipe 
some  26  millimeters  in  diameter  and  60  centimeters  long,  was  sufficient  to 
cause  a  slightly  diminished  pressure  inside  the  calorimeter,  inasmuch  as  the 
air  was  sucked  out  by  the  blower  with  a  little  greater  speed  than  it  was 
forced  in  by  the  pressure  at  the  diaphragm.  Accordingly  the  apparatus 
has  been  modified  so  that  at  present  the  tension-equalizer  is  attached  di- 
rectly to  the  wall  of  the  calorimeter  independent  of  the  air-pipe. 


72  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

In  most  of  the  experiments  made  thus  far  it  has  been  our  custom  to 
conduct  the  supply  of  fresh  oxygen  through  pet-cock  K  on  the  side  of  the 
tension-equalizer.  This  is  shown  more  in  detail  in  fig.  32,  in  which,  also,  is 
shown  the  interior  construction  of  the  can.  Owing  to  the  fact  that  the  air 
inside  of  this  can  is  much  dryer  than  the  room  air,  we  have  followed  the 
custom  with  the  earlier  apparatus  of  placing  a  vessel  containing  sulphuric 
acid  inside  the  tension-equalizer,  so  that  any  moisture  absorbed  by  the  dry 
air  inside  the  diaphragm  may  be  taken  up  by  the  acid  and  not  be  carried 
into  the  chamber.  The  air  passing  through  the  pipe  to  the  calorimeter  is,  it 
must  be  remembered,  absolutely  dry  and  hence  there  are  the  best  conditions 
for  the  passage  of  moisture  from  the  outside  air  through  the  diaphragm 
to  this  dry  air.  Attaching  the  tension-equalizer  directly  to  the  calorimeter 
obviates  the  necessity  for  this  drying  process  and  hence  the  sulphuric-acid 
vessel  has  been  discarded. 

The  valve  H  (fig.  25)  is  used  to  cut  off  the  tension-equalizer  completely 
from  the  rest  of  the  system  at  the  exact  moment  of  the  end  of  the  experi- 
mental period.  After  the  motor  has  been  stopped  and  the  slight  amount  of 
air  partly  compressed  in  the  blower  has  leaked  back  into  the  system,  and 
the  whole  system  is  momentarily  at  equal  tension,  a  process  occupying  some 
3  or  4  seconds,  the  gate-valve  H  is  closed.  Oxygen  is  then  admitted  from 
the  pet-cock  K  until  there  is  a  definite  volume  in  J  as  measured  by  the 
height  to  which  the  diaphragm  can  rise  or  a  second  pet-cock  is  connected 
to  the  can  I  and  a  delicate  petroleum  manometer  attached  in  such  a  manner 
that  the  diaphragm  can  be  filled  to  exactly  the  same  tension  each  time. 
Under  these  conditions,  therefore,  the  apparent  volume  of  air  in  the  sys- 
tem, exclusive  of  the  tension-equalizer,  is  always  the  same,  since  it  is  con- 
fined by  the  rigid  walls  of  the  calorimeter  and  the  piping.  Furthermore, 
the  apparent  volume  of  air  in  the  tension-equalizer  is  arbitrarily  adjusted 
to  be  the  same  amount  at  the  end  of  each  period  by  closing  the  valve  and 
introducing  oxygen  until  the  tension  is  the  same. 

BAROMETER. 

Eecognizing  the  importance  of  measuring  very  accurately  the  barometric 
pressure,  or  at  least  its  fluctuations,  we  have  installed  an  accurate  barome- 
ter of  the  Fortin  type,  made  by  Henry  J.  Green.  This  is  attached  to  the 
inner  wall  of  the  calorimeter  laboratory,  and  since  the  calorimeter  labora- 
tory is  held  at  a  constant  temperature,  temperature  corrections  are  unnec- 
essary, for  we  have  here  to  deal  not  so  much  with  the  accurate  measure- 
ment of  the  actual  pressure  as  with  the  accurate  measurement  of  differences 
in  pressure.  For  convenience  in  reading,  the  ivory  needle  at  the  base  of  the 
instrument  and  the  meniscus  are  well  illuminated  with  electric  lamps 
behind  a  white  screen,  and  a  small  lamp  illuminates  the  vernier.  The 
barometer  can  be  read  to  0.05  millimeter. 


GENERAL    DESCRIPTION    OF   RESPIRATION   APPARATUS.  73 

ANALYSIS  OF  RESIDUAL  AIR. 

The  carbon-dioxide  production,  water-vapor  elimination,  and  oxygen 
absorption  of  the  subject  during  1  or  2  hour  periods  are  recorded  in  a 
general  way  by  the  amounts  of  carbon  dioxide  and  water-vapor  absorbed 
by  the  purifying  vessels  and  the  loss  of  weight  of  the  oxygen  cylinder ;  but, 
as  a  matter  of  fact,  there  may  be  considerable  fluctuations  in  the  amounts 
of  carbon  dioxide  and  water-vapor  and  particularly  oxygen  in  the  large 
volume  of  residual  air  inside  the  chamber.  With  carbon  dioxide  and  water- 
vapor  this  is  not  as  noticeable  as  with  oxygen,  for  in  the  1,300  liters  of  air 
in  the  chamber  there  are  some  250  liters  of  oxygen,  and  slight  changes  in 
the  composition  of  this  air  indicate  considerable  changes  in  the  amount  of 
oxygen.  Great  changes  may  also  take  place  in  the  amounts  of  carbon 
dioxide  and  water-vapor  under  certain  conditions.  In  some  experiments, 
particularly  where  there  are  variations  in  muscular  activity  from  period  to 
period,  there  may  be  a  considerable  amount  of  carbon  dioxide  in  the  residual 
air  and  during  the  next  period,  when  the  muscular  activity  is  decreased,  for 
example,  the  percentage  composition  of  the  air  may  vary  so  much  as  to 
indicate  a  distinct  fall  in  the  amount  of  carbon  dioxide  present.  Under 
ordinary  conditions  of  ventilation  during  rest  experiments  the  quantity  of 
carbon  dioxide  present  in  the  residual  air  is  not  far  from  8  to  10  grams. 
There  are  usually  present  in  the  air  not  far  from  6  to  9  grams  of  water- 
vapor,  and  hence  this  residual  amount  can  undergo  considerable  fluctua- 
tions. When  it  is  considered  that  an  attempt  is  made  to  measure  the  total 
amount  of  carbon  dioxide  expired  in  one  hour  to  the  fraction  of  a  gram,  it 
is  obvious  that  fluctuations  in  the  composition  of  residual  air  must  be  taken 
into  consideration. 

It  is  extremely  difficult  to  get  a  fair  sample  of  air  from  the  chamber. 
The  air  entering  the  chamber  is  free  from  water-vapor  and  carbon  dioxide. 
In  the  immediate  vicinity  of  the  entering  air-tube  there  is  air  which  has  a 
much  lower  percentage  of  carbon  dioxide  and  water-vapor  than  the  average, 
and  on  the  other  hand  close  to  the  nose  and  mouth  of  the  subject  there  is  air 
of  a  much  higher  percentage  of  carbon  dioxide  and  water-vapor  than  the 
average.  It  has  been  assumed  that  the  composition  of  the  air  leaving  the 
chamber  represents  the  average  composition  of  the  air  in  the  chamber. 
This  assumption  is  only  in  part  true,  but  in  rest  experiments  (and  by  far 
the  largest  number  of  experiments  are  rest  experiments)  the  changes  in  the 
composition  of  the  residual  air  are  so  slow  and  so  small  that  this  assump- 
tion is  safe  for  all  practical  purposes. 

Another  difficulty  presents  itself  in  the  matter  of  determining  the  amount 
of  carbon  dioxide  and  water-vapor;  that  is,  to  make  a  satisfactory  analvsis 
of  air  without  withdrawing  too  great  a  volume  from  the  chamber.  The 
difficulty  in  analysis  is  almost  wholly  confined  to  the  determination  of 


74  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

water-vapor,  for  while  there  are  a  large  number  of  methods  for  determin- 
ing small  amounts  of  carbon  dioxide  with  great  accuracy,  the  method  for 
determining  water-vapor  to  be  accurate  calls  for  the  use  of  rather  large 
quantities  of  air.  From  preliminary  experiments  with  a  sling  psychrom- 
eter  it  was  found  that  its  use  was  precluded  by  the  space  required  to  suc- 
cessfully use  this  instrument,  the  addition  of  an  unknown  amount  of  water 
to  the  chamber  from  the  wet  bulb,  and  the  difficulties  of  reading  the  in- 
strument from  without  the  chamber.  Recourse  was  had  to  the  determina- 
tion of  moisture  by  the  absolute  method,  in  that  a  definite  amount  of  air 
is  caused  to  pass  over  pumice-stone  saturated  with  sulphuric  acid.  It  is  of 
interest  here  to  record  that  at  the  moment  of  writing  a  series  of  experiments 
are  in  progress  in  which  an  attempt  is  being  made  to  use  a  hair  hygrometer 
for  this  purpose. 

The  method  of  determining  the  water-vapor  and  carbon  dioxide  in  the 
residual  air  is  extremely  simple,  in  that  a  definite  volume  of  air  is  caused 
to  pass  over  sulphuric  acid  and  soda-lime  contained  in  U -tubes.  In  other 
words,  a  small  amount  of  air  is  caused  to  pass  through  a  small  absorbing- 
system  constructed  of  U-tubes  rather  than  of  porcelain  vessels  and  silver- 
plated  cans.  Formerly  a  very  elaborate  apparatus  was  employed  for  aspi- 
rating the  air  from  the  chamber  through  U-tubes  and  then  returning  the 
aspirated  air  to  the  chamber.  This  involved  the  use  of  a  suction-pump  and 
called  for  a  special  installation  for  maintaining  the  pressure  of  water  con- 
stant. More  recently  a  much  simpler  device  has  been  employed,  in  that 
we  have  taken  advantage  of  the  pressure  in  the  ventilating  air-system 
developed  by  the  passage  of  air  through  the  blower.  After  forcing  a  definite 
quantity  of  air  through  the  reagents  in  the  U-tubes,  it  is  then  conducted 
back  to  the  system  after  having  been  measured  in  a  gas-meter. 

This  procedure  is  best  noted  from  fig.  30.  The  connected  series  of  three 
U-tubes  on  the  rack  on  the  table  is  joined  on  one  end  by  well-fitting  rubber 
connections  to  the  tube  leading  from  the  mercurial  manometer  and  on  the 
other  end  to  the  rubber  tube  A  leading  to  the  gas-meter.  On  lowering  the 
mercury  reservoir  E,  the  mercury  is  drained  out  of  the  tube  D  and  air 
passes  through  both  arms  of  the  tube  and  then  through  the  three  U-tubes. 
In  the  first  of  these  it  is  deprived  of  moisture,  and  in  the  last  two  of 
carbon  dioxide.  The  air  then  enters  the  meter,  where  it  is  measured  and 
leaves  the  meter  through  the  tube  B,  saturated  with  water-vapor  at  the 
room  temperature.  To  remove  this  water-vapor  the  air  is  passed  through 
a  tower  filled  with  pumice-stone  drenched  with  sulphuric  acid.  It  leaves 
the  tower  through  the  tube  C  and  enters  the  ventilating  air-pipe  on  its 
way  to  the  calorimeter. 

The  method  of  manipulation  is  very  simple.  After  connecting  the 
U-tubes  the  pet-cock  connecting  the  tube  C  with  the  pipe  is  opened,  the 
mercury  reservoir  E  is  lowered,  and  air  is  allowed  to  pass  through  until 


GENERAL   DESCRIPTION   OF   RESPIRATION   APPARATUS.  75 

the  meter  registers  10  liters.  By  raising  the  reservoir  E  the  air  supply  is 
shut  off,  and  after  closing  the  stop-cock  at  C  the  tubes  are  disconnected,  a 
second  set  is  put  in  place,  and  the  operation  repeated.  The  U-tubes  are  of 
a  size  having  a  total  length  of  the  glass  portion  equal  to  270  millimeters 
and  an  internal  diameter  of  16  millimeters.  They  permit  the  passage  of 
3  liters  of  air  per  minute  through  them  without  a  noticeable  escape  of 
water-vapor  or  carbon  dioxide.  The  U-tubes  filled  with  pumice-stone  and 
sulphuric  acid  weigh  90  grams.  They  are  always  weighed  on  the  balance 
with  a  counterpoise,  but  no  attempt  is  made  to  weigh  them  closer  than  to 
0.5  milligram. 

GAS-METER. 

The  gas-meter  is  made  by  the  Dansk  Maalerfabrik  in  Copenhagen,  and 
is  of  the  type  used  by  Bohr  in  many  of  his  investigations.  It  has  the 
advantage  of  showing  the  water-level,  and  the  volume  may  be  read  directly. 
The  dial  is  graduated  so  as  to  be  read  within  50  cubic  centimeters. 

The  Elster  meter  formerly  used  for  this  purpose  was  much  smaller  than 
the  meter  of  the  Dansk  Maalerfabrik  we  are  now  using.  The  volume 
of  water  was  much  smaller  and  consequently  the  temperature  fluctuations 
much  more  rapid.  While  the  residual  analyses  for  which  the  meter  is  used 
are  of  value  in  interpolating  the  results  for  the  long  experiments,  and 
consequently  errors  in  the  meter  would  be  more  or  less  constant,  affecting 
all  results  alike,  we  have  nevertheless  carefully  calibrated  the  meter  by 
means  of  the  method  of  admitting  oxygen  from  a  weighed  cylinder.*  The 
test  showed  that  the  meter  measured  1.4  per  cent  too  much,  and  conse- 
quently this  correction  must  be  applied  to  all  measurements  made  with  it. 

*  Francis  G.  Benedict:  A  method  of  calibrating  gas-meters.  Physical  Review, 
vol.  22,  p.  294.     (1906.) 


76  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

CALCULATION  OF  RESULTS. 

With  an  apparatus  as  elaborate  as  is  the  respiration  calorimeter  and  its 
accessories,  the  calculation  of  results  presents  many  difficulties,  but  the 
experience  of  the  past  few  years  has  enabled  us  to  lessen  materially  the 
intricacies  of  the  calculations  formerly  thought  necessary. 

The  total  amount  of  water-vapor  leaving  the  chamber  is  determined  by 
noting  the  increase  in  weight  of  the  first  sulphuric-acid  vessel  in  the 
absorber  system.  This  vessel  is  weighed  with  a  counterpoise  and  hence 
only  the  increment  in  weight  is  recorded.  A  slight  correction  may  be 
necessary  here,  as  frequently  the  absorber  is  considerably  warmer  at  the 
end  of  the  period  than  at  the  beginning  and  if  weighed  while  warm  there 
may  be  an  error  of  0.1  to  0.2  gram.  If  the  absorbers  are  weighed  at  the 
same  temperature  at  the  beginning  and  end,  this  correction  is  avoided. 

The  amount  of  carbon  dioxide  absorbed  from  the  ventilating  air-current 
is  found  by  noting  the  changes  in  weight  of  the  potash-lime  can  and  the 
last  sulphuric-acid  vessel.  As  shown  by  the  weights  of  this  latter  vessel, 
it  is  very  rare  that  sufficient  water  is  carried  over  from  the  potash-lime  to 
the  sulphuric  acid  to  cause  a  perceptible  change  in  temperature,  and  no 
temperature  corrections  are  necessary.  It  may  occasionally  happen  that 
the  amount  of  carbon  dioxide  absorbed  is  actually  somewhat  less  than  the 
amount  of  water-vapor  abstracted  from  the  reagent  by  the  dry  air-current 
as  it  passes  through  the  can.  The  conditions  will  then  be  such  that  there 
will  be  a  loss  in  weight  of  the  potash-lime  can  and  a  large  gain  in  weight 
of  the  sulphuric-acid  vessel.  Obviously,  the  algebraic  sum  of  these  amounts 
will  give  the  true  weight  of  the  carbon  dioxide  absorbed. 

The  amount  of  oxygen  admitted  is  approximately  measured  by  noting 
the  loss  in  weight  of  the  oxygen  cylinder.  Since,  however,  in  admitting 
the  oxygen  from  the  cylinder  there  is  a  simultaneous  admission  of  a  small 
amount  of  nitrogen,  a  correction  is  necessary.  This  correction  can  be 
computed  either  by  the  elaborate  formulas  described  in  the  publication  of 
Atwater  and  Benedict  *  or  by  the  more  abbreviated  method  of  calculation 
which  has  been  used  very  successfully  in  all  short  experiments  in  this  labora- 
tory. In  either  case  it  is  necessary  to  know  the  approximate  percentage  of 
nitrogen  in  the  oxygen. 

ANALYSIS  OF  OXYGEN. 

With  the  modified  method  of  computation  discussed  in  detail  on  page  88 
it  is  seen  that  such  exceedingly  exact  analyses  of  oxygen  as  were  formerly 
made  are  unnecessary,  and  further  calculation  is  consequently  very  simple 
if  we  know  the  percentage  of  nitrogen  to  within  a  fraction  of  1  per  cent. 
We  have  used  a  Haldane  gas-analysis  apparatus  for  analyzing  the  oxygen, 
although  the  construction  of  the  apparatus  is  such  that  this  presents  some 

*  Atwater  and  Benedict:     hoc  cit.,  p.  38. 


CALCULATION   OF   RESULTS.  77 

little  difficulty.  It  is  necessary,  for  example,  to  accurately  measure  about 
16  cubic  centimeters  of  pure  nitrogen,  pass  it  into  the  potassium  pyrogal- 
late  pipette,  and  then  (having  taken  a  definite  sample  of  oxygen)  gradually 
absorb  the  oxygen  in  the  potassium  pyrogallate  and  measure  subsequently 
the  accumulated  nitrogen.  The  analysis  is  tedious  and  not  particularly 
satisfactory.  Having  checked  the  manufacturer's  analysis  of  a  number  of 
cylinders  of  oxygen  and  invariably  found  them  to  agree  with  our  results, 
we  are  at  present  using  the  manufacturer's  guaranteed  analysis.  If  there 
was  a  very  considerable  error  in  the  gas  analysis,  amounting  even  to  1  per 
cent,  the  results  during  short  experiments  would  hardly  be  affected. 

ADVANTAGE  OF  A  CONSTANT-TEMPERATURE  ROOM  AND 
TEMPERATURE  CONTROL. 
A  careful  inspection  of  the  elaborate  method  of  calculation  required  for 
use  with  the  calorimeter  formerly  at  Wesleyan  University  shows  that  a 
large  proportion  of  it  can  be  eliminated  owing  to  the  fact  that  we  are  here 
able  to  work  in  a  room  of  constant  temperature.  It  has  been  pointed  out 
that  the  fluctuations  in  the  temperature  of  the  gas-meter  affect  not  only 
the  volume  of  the  gas  passing  through  the  meter,  but  likewise  the  tension 
of  aqueous  vapor.  The  corrections  formerly  made  for  temperature  on  the 
barometer  are  now  unnecessary;  finally  (and  perhaps  still  more  important) 
it  is  no  longer  necessary  to  subdivide  the  volume  of  the  system  into  por- 
tions of  air  existing  under  different  temperatures,  depending  upon  whether 
they  were  in  the  upper  or  lower  part  of  the  laboratory.  In  other  words,  the 
temperature  of  the  whole  ventilating  circuit  and  chamber,  with  the  single 
exception  of  the  air  above  the  acid  in  the  first  sulphuric-acid  absorber,  may 
be  said  to  be  constant.  During  rest  experiments  this  assumption  can  be 
made  without  introducing  any  material  error,  but  during  work  experiments 
it  is  highly  probable  that  some  consideration  must  be  given  to  the  possi- 
bility of  the  development  of  a  considerable  temperature  rise  in  the  air  of 
the  potash-lime  absorbers,  due  to  the  reaction  between  the  carbon  dioxide 
and  the  solid  absorbent.  It  is  thus  apparent  that  the  constant-temperature 
conditions  maintained  in  the  calorimeter  laboratory  not  only  facilitate 
calorimetric  measurements,  but  also  simplify  considerably  the  elaborate 
calculations  of  the  respiratory  exchange  formerly  required. 

VARIATIONS  IN  THE  APPARENT  VOLUME  OF  ALR. 

In  the  earlier  form  of  apparatus  the  largest  variation  in  the  apparent 
volume  of  air  was  due  to  the  fluctuations  in  the  height  of  the  large  rubber 
diaphragms  used  on  the  tension  equalizer.  In  the  present  form  of  appa- 
ratus there  is  but  one  rubber  diaphragm,  and  this  is  small,  containing  not 
more  than  3  to  4  liters  as  compared  to  about  30  liters  in  the  earlier  double 
rubber  diaphragms.    As  now  arranged,  all  fluctuations  due  to  the  varying 


78  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

positions  of  the  tension-equalizer  are  eliminated  as  each  experimental  period 
is  ended  with  the  diaphragm  in  exactly  the  same  position,  i.  e.,  filled  to  a 
definite  tension. 

In  its  passage  through  the  purifiers  the  air  is  subjected  to  more  or  less 
pressure,  and  it  is  obvious  that  if  these  absorbers  were  coupled  to  the  venti- 
lating system  under  atmospheric  pressure,  and  then  air  caused  to  pass 
through  them,  there  would  be  compression  in  a  portion  of  the  purifier 
system.  Thus  there  would  be  a  contraction  in  the  volume,  and  air  thus 
compressed  would  subsequently  be  released  into  the  open  air  when  the 
absorbers  were  uncoupled.  The  method  of  testing  the  system  outlined  on 
page  100  equalizes  this  error,  however,  in  that  the  system  is  tested  under 
the  same  pressure  used  during  an  actual  experiment,  and  hence  between 
the  surface  of  the  sulphuric  acid  in  the  first  porcelain  vessel  and  the  sul- 
phuric acid  in  the  second  porcelain  vessel  there  is  a  confined  volume  of  air 
which  at  the  beginning  of  an  experimental  period  is  under  identically  the 
same  pressure  as  it  is  at  the  end.  There  is,  then,  no  correction  necessary 
for  the  rejection  of  air  with  the  changes  in  the  absorber  system. 

CHANGES   IN   VOLUME   DUE   TO   THE  ABSORPTION   OF   WATER   AND 
CARBON  DIOXIDE. 

As  the  water-vapor  is  absorbed  by  the  sulphuric  acid,  there  is  a  slight 
increase  in  volume  of  the  acid.  This  naturally  results  in  the  diminution 
of  the  apparent  volume  of  air  and  likewise  again  affects  the  amount  of 
oxygen  admitted  to  produce  constant  apparent  volume  at  the  end  of  each 
experimental  period.  The  amount  of  increase  which  thus  takes  place  for 
each  experimental  period  is  very  small.  It  has  been  found  that  an  increase 
in  weight  of  25  grams  of  water- vapor  results  in  an  increase  in  volume  of 
the  acid  of  some  15  cubic  centimeters.  Formerly  this  correction  was  made, 
but  it  is  now  deemed  unnecessary  and  unwise  to  introduce  a  refinement  that 
is  hardly  justified  in  other  parts  of  the  apparatus.  Similarly,  there  is 
theoretically  at  least  an  increase  in  volume  of  the  potash-lime  by  reason  of 
the  absorption  of  the  carbon  dioxide.  This  was  formerly  taken  into  con- 
sideration, but  the  correction  is  no  longer  applied. 

RESPIRATORY    LOSS. 

With  experiments  on  man,  there  is  a  constant  transformation  of  solid 
body  material  into  gaseous  products  which  are  carried  out  into  the  air- 
current  and  absorbed.  Particularly  where  no  food  is  taken,  this  solid 
material  becomes  smaller  in  volume  and  consequently  additional  oxygen  is 
required  to  take  the  place  of  the  decrease  in  volume  of  body  substance. 
But  this  so-called  respiratory  loss  is  more  theoretical  than  practical  in 
importance,  and  in  the  experiments  made  at  present  the  correction  is  not 
considered  necessary. 


CALCULATION   OF   RESULTS.  79 

CALCULATION  OF  THE  VOLUME  OF  AIR  RESIDUAL  IN  THE  CHAMBER. 

The  ventilating  air-circuit  may  be  said  to  consist  of  several  portions  of 
air.  The  largest  portion  is  that  in  the  respiration  chamber  itself  and  con- 
sists of  air  containing  oxygen,  nitrogen,  carbon  dioxide,  and  water-vapor. 
This  air  is  assumed  to  have  the  same  composition  up  to  the  moment  when 
it  begins  to  bubble  through  the  sulphuric  acid  in  the  first  acid-absorber. 
The  air  in  this  absorber  above  the  acid,  amounting  to  about  14  liters,  has  a 
different  composition  in  that  the  water-vapor  has  been  completely  removed. 
The  same  14  liters  of  air  may  then  be  said  to  contain  carbon  dioxide,  nitro- 
gen, and  oxygen.  This  composition  is  immediately  disturbed  the  moment 
the  air  enters  the  potash-lime  can,  when  the  carbon  dioxide  is  absorbed 
and  the  volume  of  air  in  the  last  sulphuric-acid  absorber,  in  the  sodium- 
bicarbonate  can,  and  in  the  piping  back  to  the  calorimeter  may  be  said  to 
consist  only  of  nitrogen  and  oxygen.  The  air  then  between  the  surface  of 
the  sulphuric  acid  in  the  last  porcelain  absorber  and  the  point  where  the 
ingoing  air  is  delivered  to  the  calorimeter  consists  of  air  free  from  carbon 
dioxide  and  free  from  water.  Formerly  this  section  also  included  the 
tension-equalizer,  but  very  recently  we  have  in  both  of  the  calorimeters 
attached  the  tension-equalizer  directly  to  the  respiration  chamber. 

In  the  Middletown  apparatus,  these  portions  of  air  of  varying  compo- 
sition were  likewise  subject  to  considerable  variations  in  temperature,  in 
that  the  temperature  of  the  laboratory  often  differed  materially  from  that 
of  the  calorimeter  chamber  itself,  especially  as  regards  the  apparatus  in 
the  upper  part  of  the  laboratory  room.  It  is  important,  however,  to  know 
the  total  volume  of  the  air  inclosed  in  the  whole  system.  This  is  obtained 
by  direct  measurement.  The  cubic  contents  of  the  calorimeter  has  been 
carefully  measured  and  computed ;  the  volumes  of  air  in  the  pipes,  valve 
systems,  absorbing  vessels,  and  tension-equalizer  have  been  computed  from 
dimensions,  and  it  has  been  found  that  the  total  volume  in  the  apparatus 
is,  deducting  the  volume  of  the  permanent  fixtures  in  the  calorimeter,  1,347 
liters.  The  corresponding  volume  for  the  bed  calorimeter  is  875.  These 
values  are  altered  by  the  subject  and  extra  articles  taken  into  the  chamber. 

From  a  series  of  careful  measurements  and  special  tests  the  following 
apparent  volumes  for  different  parts  of  the  system  have  been  calculated: 

Liters. 

Volume  of  the  chair  calorimeter  chamber  (without  fixtures) 1360.0 

Permanent  fixtures  (5) ;  chair  and  supports  (8) 13.0 

Apparent  volume  of  air  inside  chamber 1347.0 

Air  in  pipes,  blower,  and  valves  to  surface  of  acid  in  first  acid  vessel 4.5 

Apparent  volume  of  air  containing  water-vapor 1351.5 

Air  above  surface  of  acid  in  first  sulphuric-acid  vessel  and  potash-lime  can .  16.0 

Apparent  volume  of  air  containing  carbon  dioxide 1367.5 

Air   in   potash-lime   can,   second   sulphuric-acid   vessel    and   connections, 

sodium-bicarbonate  cans,  and  pipes  to  calorimeter  chamber 23.5 

Apparent  volume  of  air  containing  carbon  dioxide,  water,  oxygen,  _ 
and  nitrogen  1391.0 


80  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

These  volumes  represent  conditions  existing  inside  the  chamber  without 
the  subject,  i.  e.,  conditions  under  which  an  alcohol  check-test  would  be 
conducted.  In  an  experiment  with  man  it  would  be  necessary  to  deduct 
the  volume  of  the  man,  books,  urine  bottles,  and  all  supplemental  apparatus 
and  accessories.  Under  these  circumstances  the  apparent  volume  of  the 
air  in  the  chamber  may  at  times  be  diminished  by  nearly  90  to  100  liters. 
At  the  beginning  of  each  experiment  the  apparent  volume  of  air  is  calcu- 
lated. 

RESIDUAL  ANALYSES. 
CALCULATION  FROM  RESIDUAL  ANALYSES. 

The  increment  in  weight  of  the  absorbers  for  water  and  carbon  dioxide 
and  the  loss  in  weight  of  the  oxygen  cylinder  give  only  an  approximate 
idea  of  the  amounts  of  carbon  dioxide  and  water-vapor  produced  and 
oxygen  absorbed  during  the  period,  and  it  is  necessary  to  make  correction 
for  change  in  the  composition  of  the  air  as  shown  by  the  residual  analyses 
and  for  fluctuations  in  the  actual  volume.  In  order  to  compute  from  the 
analyses  the  total  carbon-dioxide  content  of  the  residual  air,  it  is  necessary 
to  know  the  relation  of  the  air  used  for  the  sample  to  the  total  volume,  and 
thus  we  must  know  accurately  the  volume  of  air  passing  through  the  gas- 
meter. 

In  the  earlier  apparatus  10-liter  samples  were  used,  and  the  volume  of 
the  respiration  chamber  was  so  large  that  it  was  necessary  to  multiply  the 
values  found  in  the  residual  sample  by  a  very  large  factor,  500.  Hence, 
the  utmost  caution  was  taken  to  procure  an  accurate  measurement  of  the 
sample,  the  exact  amounts  of  carbon  dioxide  absorbed,  and  water-vapor 
absorbed.  To  this  end  a  large  number  of  corrections  were  made,  which 
are  not  necessary  with  the  present  type  of  apparatus  with  a  volume  of  resid- 
ual air  of  but  about  1,300  liters,  and  accordingly  the  manipulation  and 
calculations  have  been  very  greatly  simplified. 

While  formerly  pains  were  taken  to  obtain  the  exact  temperature  of  the 
air  leaving  the  gas-meter,  with  this  apparatus  it  is  unnecessary.  When  the 
earlier  type  of  apparatus  was  in  use  there  were  marked  changes  in  the 
temperature  of  the  calorimeter  laboratory  and  in  the  water  in  the  meter 
which  were  naturally  prejudicial  to  the  accurate  measurement  of  the  volume 
of  samples,  but  with  the  present  control  of  temperature  in  this  laboratory 
it  has  been  found  by  repeated  tests  that  the  temperature  of  the  water  in 
the  meter  does  not  vary  a  sufficient  amount  to  justify  this  painstaking 
measurement  and  calculation.  Obviously,  this  observation  also  pertains  to 
the  corrections  for  the  tension  of  aqueous  vapor.  It  has  been  found  pos- 
sible to  assume  an  average  laboratory  temperature  and  reduce  the  volume 
as  read  on  the  meter  by  means  of  a  constant  factor. 


CALCULATION    OF   RESULTS.  81 

The  quantity  of  air  passing  through  the  meter  is  so  adjusted  that  ex- 
actly 10  liters  as  measured  on  the  dial  pass  through  it  for  one  analysis. 
The  air  as  measured  in  the  meter  is,  however,  under  markedly  different 
conditions  from  the  air  inside  the  respiration  chamber.  While  there  is  the 
same  temperature,  there  is  a  material  difference  in  the  water-vapor  present, 
and  hence  the  moisture  content  as  expressed  in  terms  of  tension  of  aqueous 
vapor  must  be  considered.  This  obviously  tends  to  diminish  the  true 
volume  of  air  in  the  meter. 

Formerly  we  made  accurate  correction  for  the  tension  of  aqueous  vapor 
based  upon  the  barometer  and  the  temperature  of  the  meter  at  the  end  of 
the  period,  but  it  has  now  been  found  that  the  reduction  of  the  meter 
readings  to  conditions  inside  of  the  chamber  can  be  made  with  a  sufficient 
degree  of  accuracy  by  multiplying  the  volume  of  air  passing  through  the 

meter  by  a  fraction,  ,  in  which  h  represents  the  barometer  and  t  the 

tension  of  aqueous  vapor  at  the  temperature  of  the  laboratory,  20°  C. 
Since  the  tension  of  aqueous  vapor  at  the  laboratory  temperature  is  not  far 
from  15  mm.,  a  simple  calculation  will  show  that  there  may  be  consider- 
able variations  in  the  value  of  h  without  affecting  the  fraction  materially, 
and  we  have  accordingly  assumed  a  value  of  h  as  normally  760  mm.,  and 

the  correction  thus  obtained  is  7o^~15  =0.98,  and  all  readings  on  the 

760 

meter  should  be  multiplied  by  this  fraction. 

On  the  one  hand,  then,  there  is  the  correction  on  the  meter  itself,  which 
correction  is  +1-4  per  cent  (see  page  75) ;  and  on  the  other  hand  the  cor- 
rection on  the  sample  for  the  tension  of  aqueous  vapor,  which  is  —2.0  per 
cent,  and  consequently  the  resultant  correction  is  —0.6  per  cent.  From 
the  conditions  under  which  the  experiments  are  made,  however,  it  is  rarely 
possible  to  read  the  meter  closer  than  ±0.05  liter,  as  the  graduations  on 
the  meter  correspond  to  50  cubic  centimeters.  It  will  be  seen,  then,  that 
this  final  correction  is  really  inside  the  limit  of  error  of  the  instrument, 
and  consequently  with  this  particular  meter  now  in  use  no  correction  what- 
ever is  necessary  for  the  reduction  of  the  volume.  The  matter  of  tem- 
perature corrections  has  been  taken  up  in  great  detail  in  an  earlier  publi- 
cation, and  where  there  are  noticeable  differences  in  temperature  between 
the  meter  and  the  calorimeter  chamber  the  calculation  is  very  much  more 
complicated. 

For  practical  purposes,  therefore,  we  may  assume  that  the  quantity  of 
air  passed  through  the  meter,  as  now  in  use,  represents  exactly  10  liters 
measured  under  the  conditions  obtaining  inside  of  the  respiration  chamber, 
and  in  order  to  find  the  total  amount  of  water-vapor  present  in  the  chamber 
it  is  necessary  only  to  multiply  the  weight  of  water  found  in  the  10-liter 
sample  by  one-tenth  of  the  total  volume  of  air  containing  water-vapor. 


82  CALOEIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

The  total  volume  of  air  which  contains  water-vapor  is  not  far  from  1,360 
liters;  consequently  multiplying  the  weight  of  water  in  the  sample  by  136 
gives  the  total  amount  of  water  in  the  chamber  and  the  piping.  The 
volume  of  air  containing  carbon  dioxide  is  that  contained  in  the  chamber 
and  piping  to  the  first  sulphuric-acid  vessel  plus  16  liters  of  air  above  the 
sulphuric  acid  and  connections  in  the  first  porcelain  vessel,  and  in  order 
to  obtain  the  amount  of  carbon  dioxide  from  the  sample  it  is  only  necessary 
to  multiply  the  weight  of  carbon  dioxide  in  the  sample  by  137.6. 

Since  in  the  calculation  of  the  total  amount  of  residual  oxygen  volumes 
rather  than  weights  of  gases  are  used,  it  is  our  custom  to  convert  the 
weights  of  carbon  dioxide  and  water-vapor  in  the  chamber  to  volumes  by 
multiplying  by  the  well-known  factors.  The  determination  of  oxygen 
depends  upon  the  knowledge  of  the  true  rather  than  the  apparent  volume 
of  air  in  the  system,  and  consequently  the  apparent  volume  must  be  reduced 
to  standard  conditions  of  temperature  and  pressure  each  time  the  calcula- 
tion is  made.  To  this  end,  the  total  volume  of  air  in  the  inclosed  circuit 
(including  that  in  the  tension-equalizer,  amounting  to  1,400  liters  in  all) 
is  reduced  to  0°  and  760  millimeters  by  the  usual  methods  of  computation. 
The  total  volume  of  air  (which  may  be  designated  as  V)  includes  the 
volumes  of  carbon  dioxide,  water-vapor,  oxygen,  and  nitrogen.  From  the 
calculations  mentioned  above,  the  volumes  of  water-vapor  and  carbon  di- 
oxide have  been  computed,  and  deducting  the  sum  of  these  from  the  reduced 
volume  of  air  gives  the  volume  of  oxygen  plus  nitrogen.  If  the  volume  of 
nitrogen  is  known,  obviously  the  volume  of  oxygen  can  be  found. 

At  the  beginning  of  the  experiment,  it  is  assumed  that  the  chamber  is 
filled  with  ordinary  air.  By  calculating  the  amount  of  nitrogen  in  the 
chamber  at  the  start  as  four-fifths  of  the  total  amount,  no  great  error  is 
introduced.  In  many  experiments  actual  analyses  of  the  air  have  been 
made  at  the  moment  of  the  beginning  of  the  experiment  The  important 
thing  to  bear  in  mind  is  that  having  once  sealed  the  chamber  and  closed 
it  tightly,  no  nitrogen  can  enter  other  than  that  admitted  with  the  oxygen, 
and  hence  the  residual  amount  of  nitrogen  remains  unaltered  save  for  this 
single  exception.  If  care  is  taken  to  keep  an  accurate  record  of  the  amount 
of  nitrogen  admitted  with  the  oxygen,  the  nitrogen  residual  in  the  chamber 
at  any  given  time  is  readily  computed.  While  from  an  absolute  mathe- 
matical standpoint  the  accuracy  of  this  computation  can  be  questioned, 
here  again  we  are  seeking  an  accurate  record  of  differences  rather  than  an 
absolute  amount,  and  whether  we  assume  the  volume  of  the  air  in  the 
chamber  to  contain  20.4  per  cent  of  oxygen  or  21.6  per  cent  is  a  matter  of 
indifference.  It  is  of  importance  only  to  note  the  increases  in  the  amount 
of  nitrogen,  since  these  increases  represent  decrease  in  the  residual  oxygen 
and  it  is  with  the  changes  in  the  residual  oxygen  that  we  particularly  have 
to  do. 


CALCULATION   OF   RESULTS.  83 

INFLUENCE  OF   FLUCTUATIONS   IN   TEMPERATURE  AND   PRESSURE   ON   THE 
APPARENT  VOLUME  OF  ATR  IN  THE  SYSTEM. 

The  air,  being  confined  in  a  space  with  semi-rigid  walls,  is  subjected 
naturally  to  variations  in  true  volume,  depending  upon  the  temperature 
and  barometric  pressure.  If  the  air  inside  of  the  chamber  becomes  con- 
siderably warmer  there  is  naturally  an  expansion,  and  were  it  not  for  the 
tension-equalizer  there  would  be  pressure  in  the  system.  Also,  if  the  ba- 
rometer falls,  there  is  an  expansion  of  air  which,  again,  in  the  absence  of 
the  tension-equalizer,  would  produce  pressure  in  the  system.  It  is  neces- 
sary, therefore,  in  calculating  the  true  volume  of  air,  to  take  into  account 
not  only  the  apparent  volume,  which,  as  is  shown  above,  is  always  a  con- 
stant amount  at  the  end  of  each  period,  but  the  changes  in  temperature  and 
barometric  pressure  must  also  be  noted.  Since  there  is  a  volume  of  about 
1,400  liters,  a  simple  calculation  will  show  that  for  each  degree  centigrade 
change  in  temperature  there  will  be  a  change  in  volume  of  approximately 
4.8  liters.  In  actual  practice,  however,  this  rarely  occurs,  as  the  tempera- 
ture control  is  usually  inside  of  0.1°  C.  and  for  the  most  part  within  a  few 
hundredths.  A  variation  in  barometric  pressure  of  1  millimeter  will  affect 
1,400  liters  by  1.8  liters. 

In  actual  practice,  therefore,  it  is  seen  that  if  the  barometer  falls  there 
will  be  an  expansion  of  air  in  the  system.  This  will  tend  to  increase  the 
volume  by  raising  the  rubber  diaphragm  on  the  tension-equalizer,  the 
ultimate  result  of  which  is  that  at  the  final  filling  with  oxygen  at  the  end 
of  the  period  less  is  used  than  would  be  the  case  had  there  been  no  change 
in  the  barometer.  In  other  words,  for  each  liter  expansion  of  air  inside 
of  the  system,  there  is  1  liter  less  oxygen  required  to  bring  the  apparent 
volume  the  same  at  the  end  of  the  period.  Similarly,  if  there  is  an  increase 
in  temperature  of  the  air,  there  is  expansion,  and  a  smaller  amount  of 
oxygen  is  required  than  would  be  the  case  had  there  been  no  change;  and 
conversely,  if  the  barometer  rises  or  the  temperature  falls,  more  oxygen 
would  be  supplied  than  is  needed  for  consumption.  It  is  thus  seen  that  the 
temperature  and  barometer  changes  affect  the  quantity  of  oxygen  admitted 
to  the  chamber. 

INFLUENCE  OF  FLUCTUATIONS  IN  THE  AMOUNTS  OF  CARBON  DIOXIDE  AND 
WATER-VAPOR  UPON  RESIDUAL  OXYGEN. 

Any  variations  in  the  residual  amount  of  carbon  dioxide  or  water-vapor 
likewise  affect  the  oxygen.  Thus,  if  there  is  an  increase  of  1  gram  in  the 
amount  of  residual  carbon  dioxide,  this  corresponds  to  0.51  liter,  and  con- 
sequently an  equal  volume  of  oxygen  is  not  admitted  to  the  chamber  during 
the  period,  since  its  place  has  been  taken  by  the  increased  volume  of  carbon 
dioxide.  A  similar  reasoning  will  show  that  increase  in  the  water-vapor 
content  will  have  a  similar  effect,  for  each  gram  of  water-vapor  corresponds 


84  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

to  1.25  liters  and  therefore  influences  markedly  the  introduction  of  oxygen. 
All  four  of  the  factors,  therefore  (barometric  pressure,  temperature,  residual 
carbon  dioxide,  and  residual  water- vapor) ,  affect  noticeably  the  oxygen 
determination. 

CONTROL   OF   RESIDUAL  ANALYSES. 

Of  the  three  factors  to  be  determined  in  the  residual  air,  the  oxygen 
(which  is  most  important  from  the  standpoint  of  the  relative  weight  to  be 
placed  upon  the  analysis)  unfortunately  can  not  be  directly  determined 
without  great  difficulty.  Furthermore,  any  errors  in  the  analysis  may  be 
very  greatly  multiplied  by  the  known  errors  involved  in  the  determination 
of  the  true  volume  of  the  air  in  the  chamber  as  a  result  of  the  difficulties 
in  obtaining  the  average  temperature  of  the  air.  Believing  that  the  method 
of  analysis  as  outlined  above  should  be  controlled  as  far  as  possible  by 
other  independent  methods,  we  were  able  to  compare  the  carbon  dioxide  as 
determined  by  the  soda-lime  method  with  that  obtained  by  the  extremely 
accurate  method  used  by  Sonden  and  Pettersson.  An  apparatus  for  the 
determination  of  carbon  dioxide  and  oxygen  on  the  Pettersson  principle 
has  been  devised  by  Sonden  and  constructed  for  us  by  Grave,  of  Stockholm. 

In  the  control  experiments,  the  air  leaving  the  mercury  valve  D  (fig.  30, 
page  66)  was  caused  to  pass  through  a  T-tube,  one  arm  of  which  connected 
directly  with  the  sampling  pipette  of  the  Sonden  gas-analysis  apparatus, 
the  other  arm  connecting  with  the  U-tubes  for  residual  analyses.  By  lower- 
ing and  raising  the  mercury  reservoir  on  the  gas-analysis  apparatus,  a 
sample  of  air  could  be  drawn  into  the  apparatus  for  analysis.  The  results 
of  the  analysis  were  expressed  on  the  basis  of  moist  air  in  volume  per 
cents  rather  than  by  weight,  as  is  done  with  the  soda-lime  method.  Hence 
in  comparison  it  was  necessary  to  convert  the  weights  to  volume,  and 
during  this  process  the  errors  due  to  not  correcting  for  temperature  and 
barometer  are  made  manifest.  However,  the  important  point  to  be  noted 
is  that  whatever  fluctuations  in  composition  of  the  residual  air  were  noted 
by  the  soda-lime  method,  similar  fluctuations  of  a  corresponding  size  were 
recorded  by  the  volumetric  analysis  with  the  Sonden  apparatus.  Under 
these  conditions,  therefore,  we  believe  that  the  gravimetric  method  out- 
lined above  is  sufficiently  satisfactory,  so  far  as  the  carbon-dioxide  content 
is  concerned,  for  ordinary  work  where  there  are  no  wide  variations  in  the 
composition  of  the  air  from  period  to  period. 

NITROGEN  ADMITTED  WITH   THE  OXYGEN. 

It  is  impossible  to  obtain  in  the  market  absolutely  chemically  pure  oxy- 
gen. All  the  oxygen  that  we  have  thus  far  been  able  to  purchase  contains 
nitrogen  and,  in  some  instances,  measurable  amounts  of  water-vapor  and 
carbon  dioxide.  The  better  grade  of  oxygen,  that  prepared  from  liquid  air, 
is  practically  free  from  carbon  dioxide  and  water-vapor,  but  it  still  contains 


CALCULATION    OF   RESULTS.  85 

nitrogen,  and  hence  with  every  liter  of  oxygen  admitted  there  is  a  slight 
amount  of  nitrogen  added.  This  amount  can  readily  be  found  from  the 
gasometric  analysis  of  the  oxygen  and  from  the  well-known  relation  between 
the  weight  and  the  volume  of  nitrogen  the  weight  can  be  accurately  found. 
This  addition  of  nitrogen  played  a  very  important  role  in  the  calculation 
of  the  oxygen  consumption  as  formerly  employed.  As  is  seen  later,  a  much 
abbreviated  form  of  calculation  is  now  in  use  in  which  the  nitrogen  admitted 
with  the  oxygen  does  not  influence  the  calculation  of  the  residual  oxygen. 

REJECTION   OF   AIR. 

In  long-continued  experiments,  where  there  is  a  possibility  of  a  notice- 
able diminution  in  the  percentage  of  oxygen  in  the  chamber — a  diminu- 
tion caused  either  by  a  marked  fall  in  barometer,  which  expands  the  air 
inside  of  the  chamber  and  permits  admission  of  less  oxygen  than  would 
otherwise  be  required,  or  by  the  use  of  oxygen  containing  a  high  percentage 
of  nitrogen,  thus  continually  increasing  the  amount  of  nitrogen  present 
in  the  system — it  is  highly  probable  that  there  may  be  such  an  accumula- 
tion of  nitrogen  as  to  render  it  advisable  to  provide  for  the  admission  of  a 
large  amount  of  oxygen  to  restore  the  air  to  approximately  normal  condi- 
tions. In  rest  experiments  of  short  duration  this  is  never  necessary. 
The  procedure  by  which  such  a  restoration  of  oxygen  percentage  is  accom- 
plished has  already  been  discussed  elsewhere.*  It  involves  the  rejection 
of  a  definite  amount  of  air  by  allowing  it  to  pass  into  the  room  through 
the  gas-meter  and  then  making  proper  corrections  for  the  composition  of 
this  air,  deducting  the  volume  of  oxygen  in  it  from  the  excess  volume  of 
oxygen  introduced  and  correcting  the  nitrogen  residual  in  order  to  deter- 
mine the  oxygen  absorption  during  the  period  in  which  the  air  has  been 
rejected. 

INTERCHANGE  OF  AIR  IN  THE  FOOD-APERTURE. 

The  volume  of  air  in  the  food-aperture  between  the  two  glass  doors  is 
approximately  5.3  liters.  When  the  door  on  the  inside  is  opened  and  the 
material  placed  in  the  food-aperture  and  the  outer  door  is  subsequently 
opened,  there  is  by  diffusion  a  passage  outward  of  air  of  the  composition  of 
the  air  inside  of  the  chamber,  and  the  food-aperture  is  now  filled  with  room 
air.  When  the  inner  door  is  again  opened  this  room  air  enters  the  chamber 
and  is  replaced  by  air  of  the  same  composition  as  that  in  the  chamber.  It 
is  seen,  then,  that  there  may  theoretically  be  an  interchange  of  air  here 
which  may  have  an  influence  on  the  results.  In  severe  work  experiments, 
where  the  amount  of  carbon  dioxide  in  the  air  is  enormously  increased, 
such  interchange  doubtless  does  take  place  in  measurable  amounts  and 
correction  should  undoubtedly  be  made.     In  ordinary  rest  experiments, 

•Atwater  and  Benedict:  Carnegie  Institution  of  Washington  Publication  No. 
42,  p.  77. 


86  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

where  the  composition  of  the  air  in  the  chamber  is  much  more  nearly  nor- 
mal, this  correction  is  without  special  significance.  Furthermore,  in  the 
two  forms  of  calorimeter  now  in  use,  the  experiments  being  of  but  short 
duration,  provision  is  made  to  render  it  unnecessary  to  open  the  food- 
aperture  during  the  experiment  proper.  Consequently  at  present  no  cor- 
rection for  interchange  of  air  in  the  food-aperture  is  made,  and  for  the 
same  reason  the  slight  alteration  in  volume  resulting  from  the  removal  or 
addition  of  material  has  also  not  been  considered  here. 

USE  OF  THE  RESIDUAL  BLANK  IN  THE  CALCULATIONS. 

To  facilitate  the  calculations  and  for  the  sake  of  uniformity  in  express- 
ing the  results,  a  special  form  of  blank  is  used  which  permits  the  recording 
of  the  principal  data  regarding  the  analyses  of  air  in  the  chamber  at  the 
end  of  each  period.  Thus  at  the  head  of  the  sheet  are  recorded  the  time, 
the  number  of  the  period,  kind  of  experiment,  the  name  or  initials  of  the 
subject,  and  the  statement  as  to  which  calorimeter  is  used.  The  barometer 
recorded  in  millimeters  is  indicated  in  the  column  at  the  left  and  imme- 
diately below  the  heading,  together  with  the  temperature  of  the  calorimeter 
as  expressed  in  degrees  centigrade.  The  temperature  of  the  calorimeter  as 
recorded  by  the  physical  observer  is  usually  expressed  in  the  arbitrary 
scale  of  the  Wheatstone  bridge  and  must  be  transposed  into  the  centigrade 
scale  by  means  of  a  calibration  table. 

The  apparent  air-volumes  in  the  subsections  of  the  ventilating  system 
are  recorded  under  the  headings  I,  which  represents  the  volume  of  air  con- 
taining water-vapor  and  therefore  is  the  air  in  the  chamber  plus  the  air  in 
the  piping  to  the  surface  of  the  acid  in  the  first  sulphuric-acid  absorber; 
I-II,  which  represents  the  air  containing  carbonic  acid  and  includes  volume 
I  plus  the  volume  of  the  air  in  the  first  sulphuric-acid  vessel  and  the 
volume  of  air  in  the  potash-lime  absorber;  I-II  I,  which  includes  the  total 
confined  volume  of  the  whole  system,  since  this  air  contains  both  oxygen 
and  nitrogen.  These  volumes  change  somewhat,  depending  upon  the  size 
of  the  body  of  the  subject,  the  volume  of  the  materials  taken  into  the 
chamber,  and  the  type  of  calorimeter. 

The  data  for  the  residual  analyses  are  recorded  in  the  lower  left-hand 
corner :  first  the  weight  of  the  water  absorbed  from  10  liters  of  air  passing 
through  the  meter ;  to  the  logarithm  of  this  is  added  the  logarithm  of  volume 
I ;  the  result  is  the  logarithm  of  the  total  weight  of  water-vapor  in  the  venti- 
lating air-current.  To  convert  this  into  liters  the  logarithmic  factor  09462* 
is  added  to  the  logarithm  of  the  weight  of  water  and  (a)  is  the  logarithm 
of  water  expressed  in  liters.  A  similar  treatment  is  accorded  the  weight 
of  carbon  dioxide  absorbed  from  the  air-sample,  (b)  being  ultimately  the 
logarithm  of  the  volume  of  carbon  dioxide. 

*  In  the  use  of  logarithms  space  is  saved  by  not  employing  characteristics. 


CALCULATION   OF   RESULTS. 


87 


In  order  to  determine  the  total  volume  of  air  in  the  chamber  under  stan- 
dard conditions  of  temperature  and  pressure,  to  the  logarithm  of  volume 
I-III  is  added,  first,  a  logarithmic  factor  for  the  temperature  recorded 
for  the  calorimeter  to  correct  the  volume  of  air  to  standard  temperature. 
As  the  temperature  fluctuations  are  all  within  1  degree,  a  table  has  been 

prepared  giving  the  standard  fluctuation  represented  by  the  formula  -  , 

in  which  t  is  the  temperature  of  the  calorimeter.  The  correction  for  pres- 
sure has  also  been  worked  out  in  a  series  of  tables  and  the  logarithmic 

factor  here  corresponds  to  the  ratio  x.'  ,  in  which  p  is  the  observed  ba- 
rometer. The  logarithm  of  the  total  volume  is  recorded  as  a  result  of  the 
addition  of  these  three  logarithms  enumerated,  and  from  this  logarithm 
is  expressed  the  total  volume  of  air  in  liters.  Deducting  the  sum  of  the 
values  (a)  and  (&)  from  the  total  volume  leaves  the  volume  of  oxygen  plus 
nitrogen. 

The  calculation  of  the  residual  volume  of  nitrogen  and  the  record  of  the 
additions  thereto  was  formerly  carried  out  with  a  refinement  that  to-day 
seems  wholly  unwarranted  when  other  factors  influencing  this  value  are 
taken  into  consideration.  For  the  majority  of  experiments  the  residual 
volume  of  nitrogen  may  be  considered  as  constant  in  spite  of  the  fact  that 
some  nitrogen  is  regularly  admitted  with  the  oxygen.  The  significance  of 
this  assumption  is  best  seen  after  a  consideration  of  the  method  of  calcu- 
lating the  amount  of  oxygen  admitted  to  the  chamber. 


RESIDUAL  SHEET 


No.  1. 


Calculation  of  residual  amounts  of  nitrogen,  oxygen,  carbon  dioxide  and  water-rapor 
remaining  in  chamber  at  8.10  A.  M.,  June  24,  1909. 

Residual  at  end  of  Prelim,  period.  Exp. :  Parturition.  No 

Subject:  Mrs.  Whelan.  Calorimeter:  Bed. 


Barometer,    766.95  mm. 
Temp,  cal.,      20.08  °C 


Apparent  Volume  of  Air 
I  containing  H,0    716.  liters 

I -II  "  CO,    731.      " 

I  -  III  "  O+N  766.      " 

Log.  wt.  H,0  in  residual 
.0816  =    91116 

Log.  I  =    86431 

76647    =    6.83  gms.  HoO 
Gms.  to  liters.  09462 

(a)  86009    =    7.26  1.  H20 
Log.  wt.  CO,  in  residual 

0423  =    62634 

Log.  I-II      =    86392 

49026    =    3.09  gms.  CO, 
Gms.  to  liters,  70680 

(b)  19706    =    1.57  1.  CO, 


Miscellaneous  Calculations 


875 
164.66 

710.45 
4.6 

48.65 

25.9 

•0. 

164.66 

716.0    I 
16 

731.0    I-II 
24 

766.0    I-III 

(a) 
(b) 

7.26  1. 
1.67  1. 

8.82      = 

1.  CO,+H,0 

Log.  I-III 
"     temp.       = 
"    pressure  = 

87795 
96912 
99826 

Total  volume       84633    = 
Volume  CO,+H,0          = 

700.37  1. 
8.82  1. 

"        O+N 

N 

- 

691.66  1. 
552.98  1. 

=    138.67  1. 


88  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

ABBREVIATED  METHOD  OF  COMPUTATION  OF  OXYGEN  ADMITTED  TO  THE 
CHAMBER  FOR  USE  DURING  SHORT  EXPERIMENTS. 

Desiring  to  make  the  apparatus  as  practicable  and  the  calculations  as 
simple  as  possible,  a  scheme  of  calculation  has  been  devised  whereby  the 
computations  may  be  very  much  abbreviated  and  at  the  same  time  there 
is  not  too  great  a  sacrifice  in  accuracy.  The  loss  in  weight  of  the  oxygen 
cylinder  has,  in  the  more  complicated  method  of  computation,  been  con- 
sidered as  due  to  oxygen  and  about  3  per  cent  of  nitrogen.  The  amount 
of  nitrogen  thus  admitted  has  been  carefully  computed  and  its  volume 
taken  into  consideration  in  calculating  the  residual  oxygen.  If  it  is  con- 
sidered for  a  moment  that  the  admission  of  gas  out  of  the  steel  cylinder  is 
made  at  just  such  a  rate  as  to  compensate  for  the  decrease  in  volume  of  the 
air  in  the  system  due  to  the  absorption  of  oxygen  by  the  subject,  it  can  be 
seen  that  if  the  exact  volume  of  the  gas  leaving  the  cylinder  were  known 
it  would  be  immaterial  whether  this  gas  were  pure  oxygen,  oxygen  with 
some  nitrogen,  or  oxygen  with  any  other  inert  gas  not  dangerous  to  respira- 
tion or  not  absorbed  by  sulphuric  acid  or  potash-lime.  If  10  liters  of 
oxygen  had  been  absorbed  by  the  man  in  the  course  of  an  hour,  to  bring  the 
system  back  to  constant  apparent  volume  it  would  be  necessary  to  admit 
10  liters  of  such  a  gas  or  mixture  of  gases,  assuming  that  during  the  hour 
there  had  been  no  change  in  the  temperature,  the  barometric  pressure,  or 
the  residual  amounts  of  carbon  dioxide  or  water-vapor. 

Under  these  assumed  conditions,  then,  it  would  only  be  necessary  to 
measure  the  amount  of  gas  admitted  in  order  to  have  a  true  measure  of 
the  amount  of  oxygen  absorbed.  The  measure  of  the  volume  of  the  gas 
admitted  may  be  used  for  a  measure  of  the  oxygen  absorbed,  even  when  it  is 
necessary  to  make  allowances  for  the  variations  in  the  amount  of  carbon 
dioxide  or  water-vapor  in  the  chamber,  the  temperature,  and  barometric 
pressure.  From  the  loss  in  weight  of  the  oxygen  cylinder,  if  the  cylinder 
contained  pure  oxygen,  it  would  be  known  that  10  liters  would  be  admitted 
for  every  14.3  grams  loss  in  weight. 

From  the  difference  in  weight  of  1  liter  of  oxygen  and  1  liter  of  nitrogen, 
a  loss  in  weight  of  a  gas  containing  a  mixture  of  oxygen  with  a  small  per 
cent  of  nitrogen  would  actually  represent  a  somewhat  larger  volume  of  gas 
than  if  pure  oxygen  were  admitted.  The  differences  in  weight  of  the  two 
gases,  however,  and  the  amount  of  nitrogen  present  are  so  small  that  one 
might  almost  wholly  neglect  the  error  thus  arising  from  this  admixture  of 
nitrogen  and  compute  the  volume  of  oxygen  directly  from  the  loss  in  weight 
of  the  cylinder. 

As  a  matter  of  fact,  it  has  been  found  that  by  increasing  the  loss  in 
weight  of  the  cylinder  of  oxygen  containing  3  per  cent  nitrogen  by  0.4  per 
cent  and  then  converting  this  weight  to  volume  by  multiplying  by  0.7,  the 
volume  of  gas  admitted  is  known  with  great  accuracy.     This  method  of 


CALCULATION   OF   RESULTS.  89 

calculation  has  been  nsed  with  success  in  connection  with  the  large  chamber 
and  particularly  for  experiments  of  short  duration.  It  has  also  been  intro- 
duced with  great  success  in  a  portable  type  of  apparatus  described  else- 
where.* Under  these  conditions,  therefore,  it  is  unnecessary  to  make  any 
correction  on  the  residual  volume  of  nitrogen  as  calculated  at  the  beginning 
of  the  experiment.  When  a  direct  comparison  of  the  calculated  residual 
amount  of  oxygen  present  is  to  be  made  upon  determinations  made  with  a 
gas-analysis  apparatus  the  earlier  and  much  more  complicated  method  of 
calculation  must  be  employed. 

CRITICISM  OF  THE  METHOD  OF  CALCULATING  THE  VOLUME  OF  OXYGEN. 

Since  the  ventilating  air-current  has  a  confined  volume,  in  which  there 
are  constantly  changing  percentages  of  carbon  dioxide,  oxygen,  and  water- 
vapor,  it  is  important  to  note  that  the  nitrogen  present  in  the  apparatus 
when  the  apparatus  is  sealed  remains  unchanged  throughout  the  whole 
experiment,  save  for  the  small  amounts  added  with  the  commercial  oxygen — 
amounts  well  known  and  for  which  definite  corrections  can  be  made.  Con- 
sequently, in  order  to  find  the  amount  of  oxygen  present  in  the  residual  air 
at  any  time  it  is  only  necessary  to  determine  the  amounts  of  carbon  dioxide 
and  water-vapor  and,  from  these  two  factors  and  from  the  known  volume  of 
nitrogen  present,  it  is  possible  to  compute  the  total  volume  of  oxygen  after 
calculating  the  total  absolute  volume  of  air  in  the  chamber  at  any  given 
time. 

While  the  apparent  volume  of  the  air  remains  constant  throughout  the 
whole  experiment,  by  the  conditions  of  the  experiment  itself  the  absolute 
amount  may  change  considerably,  owing  primarily  to  the  fluctuations  in 
barometric  pressure  and  secondarily  to  slight  fluctuations  in  the  tempera- 
ture of  the  air  inside  of  the  chamber.  Although  the  attempt  is  made  on 
the  part  of  the  observers  to  arbitrarily  control  the  temperature  of  this  air 
to  within  a  few  hundredths  of  a  degree,  at  times  the  subject  may  inadvert- 
ently move  his  body  about  in  the  chair  just  a  few  moments  before  the  end 
of  the  period  and  thus  temporarily  cause  an  increased  expansion  of  the  air. 
The  apparatus  is,  in  a  word,  a  large  air-thermometer,  inside  the  bulb  of 
which  the  subject  is  sitting.  If  the  whole  system  were  inclosed  in  rigid 
walls  there  would  be  from  time  to  time  noticeable  changes  in  pressure  on 
the  system  due  to  variations  in  the  absolute  volume,  but  by  means  of  the 
tension-equalizer  these  fluctuations  in  pressure  are  avoided. 

The  same  difficulties  pertain  here  which  were  experienced  with  the  earlier 
type  of  apparatus  in  determining  the  average  temperature  of  the  volume  of 
air  inside  of  the  chamber.  We  have  on  the  one  hand  the  warm  surface  of 
the  man's  body,  averaging  not  far  from  32°  C.    On  the  other  hand  we  have 

*  Francis  G.  Benedict :  An  apparatus  for  studying  the  respiratory  exchange. 
American  Journal  of  Physiology,  vol.  24,  p.  368.     (1909.) 


90  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

the  cold  water  in  the  heat-absorbers  at  a  temperature  not  far  from  12°  C. 
Obviously,  the  air  in  the  immediate  neighborhood  of  these  two  localities  is 
considerably  warmer  or  colder  than  the  average  temperature  of  the  air. 
The  disposition  of  the  electric-resistance  thermometers  about  the  chamber 
has,  after  a  great  deal  of  experimenting,  been  made  such  as  to  permit  the 
measurement  as  nearly  as  possible  of  the  average  temperature  in  the  cham- 
ber. But  this  is  at  best  a  rough  approximation,  and  we  must  rely  upon  the 
assumption  that  while  the  temperatures  which  are  actually  measured  may 
not  be  the  average  temperature,  the  fluctuations  of  the  average  temperature 
are  parallel  to  the  fluctuations  in  the  temperatures  measured.  Since  every 
effort  is  made  to  keep  these  fluctuations  at  a  minimum,  it  is  seen  that  the 
error  of  this  assumption  is  not  as  great  as  might  appear  at  first  sight. 
However,  the  calculation  of  the  residual  amount  of  oxygen  in  the  chamber 
is  dependent  upon  this  assumption  and  hence  any  errors  in  the  assumption 
will  affect  noticeably  the  calculation  of  the  residual  oxygen. 

Attempts  to  compare  the  determination  of  the  oxygen  by  the  exceedingly 
accurate  Sonden  apparatus  with  that  calculated  after  determining  the 
water-vapor  and  carbon  dioxide,  temperature  and  pressure  of  the  air  in  the 
chamber  have  thus  far  led  to  results  which  indicate  one  of  three  things: 
(1)  that  there  is  not  a  homogeneous  mixture;  (2)  that  during  the  time 
required  for  making  residual  analyses,  i.  e.,  some  three  or  four  minutes, 
there  may  be  a  variation  in  the  oxygen  content  in  the  air  of  the  chamber 
due  to  the  oxygen  continually  added  from  the  cylinder;  (3)  that  the  oxygen 
supplied  from  the  cylinder  is  not  thoroughly  mixed  with  the  air  in  the 
chamber  until  some  time  has  elapsed.  That  is  to  say,  with  the  method 
now  in  use  it  is  necessary  to  fill  the  tension-equalizer  to  a  definite  pres- 
sure immediately  at  the  end  of  each  experimental  period.  This  is  done  by 
admitting  oxygen  from  the  cylinder,  and  obviously  this  oxygen  was  not 
present  in  the  air  when  analyzed.  A  series  of  experiments  with  a  somewhat 
differently  arranged  system  is  being  planned  in  which  the  oxygen  will  be 
admitted  to  the  respiration  chamber  directly  and  not  into  the  tension-equal- 
izer, and  at  the  end  of  the  experiment  the  tension-equalizer  will  be  kept  at 
such  a  point  that  when  the  motor  is  stopped  the  amount  of  oxygen  to  be 
added  to  bring  the  tension  to  a  definite  point  will  be  small. 

Under  these  conditions  it  is  hoped  to  secure  a  more  satisfactory  compari- 
son of  the  analyses  as  made  by  means  of  the  Sonden  apparatus  and  as  calcu- 
lated from  the  composition  of  the  residual  air  by  the  gravimetric  analysis. 
It  remains  a  fact,  however,  that  no  matter  with  what  skill  and  care  the  gaso- 
metric  analysis  is  made,  either  gravimetrically  or  volumetrically,  the  calcu- 
lation of  the  residual  amount  of  oxygen  presents  the  same  difficulties  in 
both  cases. 


CALCULATION   OF   RESULTS.  91 

CALCULATION  OF  TOTAL  OUTPUT  OF  CARBON  DIOXIDE  AND  WATER- VAPOR 
AND  OXYGEN  ABSORPTION. 

From  the  weights  of  the  sulphuric-acid  and  potash-lime  vessels,  the 
amounts  of  water-vapor  and  carbon  dioxide  absorbed  out  of  the  air-current 
are  readily  obtained.  The  loss  in  weight  of  the  oxygen  cylinder  increased 
by  0.4  per  cent  (see  page  88)  gives  the  weight  of  oxygen  admitted  to  the 
chamber.  It  remains,  therefore,  to  make  proper  allowance  for  the  varia- 
tions in  composition  of  the  air  inside  the  chamber  at  the  beginning  and  end 
of  the  different  periods.  From  the  residual  sheets  the  amounts  of  water- 
vapor,  carbonic  acid,  and  oxygen  present  in  the  system  at  the  beginning 
and  end  of  each  period  are  definitely  known.  If  there  is  an  increase,  for 
example,  in  the  amount  of  carbon  dioxide  in  the  chamber  at  the  end  of  a 
period,  this  increase  must  be  added  to  the  amount  absorbed  out  of  the  air- 
current  in  order  to  obtain  the  true  value  for  the  amount  produced  during 
the  experimental  period. 

A  similar  calculation  holds  true  with  regard  to  the  water-vapor  and 
oxygen.  For  convenience  in  calculating,  the  amounts  of  water-vapor  and 
carbon  dioxide  residual  in  the  chamber  are  usually  expressed  in  grams, 
while  the  oxygen  is  expressed  in  liters.  Hence,  before  making  the  additions 
or  subtractions  from  the  amount  of  oxygen  admitted,  the  variations  in  the 
amount  of  oxygen  residual  in  the  system  should  be  converted  from  liters 
to  grams.    This  is  done  by  dividing  by  0.7. 

CONTROL  EXPERIMENTS  WITH  BURNING  ALCOHOL. 

After  having  brought  to  as  high  a  degree  of  perfection  as  possible  the 
apparatus  for  determining  carbon  dioxide,  water,  and  oxygen,  it  becomes 
necessary  to  submit  the  apparatus  to  a  severe  test  and  thus  demonstrate 
its  ability  to  give  satisfactory  results  under  conditions  that  can  be  accu- 
rately controlled.  The  liberation  of  a  definite  amount  of  carbon  dioxide 
from  a  carbonate  by  means  of  acid  has  frequently  been  employed  for  con- 
trolling an  apparatus  used  for  researches  in  gaseous  exchange,  but  this  only 
furnishes  a  definite  amount  of  carbon  dioxide  and  throws  no  light  what- 
ever upon  the  ability  of  the  apparatus  to  determine  the  other  two  factors, 
water-vapor  and  oxygen.  Some  of  the  earlier  experimenters  have  used  burn- 
ing candles,  but  these  we  have  found  to  be  extremely  unsatisfactory.  The 
necessity  for  an  accurate  elementary  analysis,  the  high  carbon  content  of 
the  stearin  and  paraffin,  and  the  possibility  of  a  change  in  the  chemical 
composition  of  the  material  all  render  this  method  unfit  for  the  most 
accurate  testing.  As  a  result  of  a  large  number  of  experiments  with  dif- 
ferent materials,  we  still  rely  upon  the  use  of  ethyl  alcohol  of  known  water- 
content.  The  experiments  with  absolute  alcohol  and  with  alcohol  con- 
taining varying  amounts  of  water  showed  no  differences  in  the  results,  and 


92 


CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 


hence  it  is  now  our  custom  to  obtain  the  highest  grade  commercial  alcohol, 
determine  the  specific  gravity  accurately,  and  burn  this  material.  We  use 
the  Squibb  pyknometer  *  and  thereby  can  determine  the  specific  gravity  of 
the  alcohol  to  the  fifth  or  sixth  decimal  plaee  with  a  high  degree  of  accuracy. 
Using  the  alcoholometric  tables  of  Squibb  f  or  Morley,$  the  percentage  of 
alcohol  by  weight  is  readily  found,  and  from  the  chemical  composition  of 
the  alcohol  can  be  computed  not  only  the  amount  of  carbon  dioxide  and 
water-vapor  formed  and  oxygen  absorbed  by  the  combustion  of  1  gram  of 
ethyl  hydroxide  containing  a  definite  known  amount  of  water,  but  also 
the  heat  developed  during  its  combustion. 

With  the  construction  of  this  apparatus  it  was  found  impracticable  to 
employ  the  type  of  alcohol  lamp  formerly  used  with  success  in  the  Wesleyan 
University  respiration  chamber.  Inability  to  illuminate  the  gage  on  the 
side  of  the  lamp  and  the  small  windows  on  the  side  of  the  calorimeter 
precluded  its  use.  It  was  necessary  to  resort  to  the  use  of  an  ordinary 
kerosene  lamp  with  a  large  glass  font  and  an  Argand  burner.  Of  the  many 
check-tests  made  we  quote  one  of  December  31,  1908,  made  with  the  bed 
calorimeter : 

Several  preliminary  weights  of  the  rates  of  burning  were  made  before  the  lamp 
was  introduced  into  the  chamber.  The  lamp  was  then  put  in  place  and  the  ven- 
tilation started  without  sealing  the  cover.  The  lamp  burned  for  about  one  hour 
and  a  quarter  and  was  then  weighed  again.  Then  the  window  was  sealed  in  and 
the  experiment  started  as  soon  as  possible.  At  the  end  of  the  experiment  the 
window  was  taken  out  immediately  and  the  lamp  blown  out  and  then  weighed. 
The  amount  burned  between  the  time  of  weighing  the  alcohol  and  the  beginning 
of  the  experiment  was  calculated  from  the  rate  of  burning  before  the  experiment 
and  this  amount  subtracted  from  the  total  burned  from  the  time  that  the  lamp 
was  weighed  before  being  sealed  in  until  the  end,  when  it  was  weighed  the 
second  time.  For  the  minute  which  elapsed  between  the  end  of  the  experiment 
and  the  last  weighing,  the  rate  for  the  length  of  the  experiment  itself  was  used. 

During  the  experiment  there  were  burned  142.7  grams  of  92.20  per  cent  alcohol 
of  a  specific  gravity  of  0.8163. 

A  tabular  summary  of  results  is  given  below : 


Found. 

Required. 

Carbon  dioxide  .  gms. 
Water-vapor  ...    " 

252.9 
273.5 
165.8 
829.0 

251.4 
274.3 
165.6 
834.5 

Thus  does  the  apparatus  prove  accurate  for  the  determination  of  all  four 
factors. 


♦Squibb:    Journal  of  American  Chemical  Society,  vol.  19,  p.  111.     (1897.) 

f  Squibb:    Ephemeris,  1884  to  1885,  part  2,  pp.  562-577. 

JMorley:    Journal  of  American  Chemical  Society,  vol.  26,  p.  1185.     (1904.) 


BALANCE   FOR    WEIGHING    SUBJECT.  93 

BALANCE  FOR  WEIGHING  SUBJECT. 

The  loss  or  gain  in  body-weight  has  always  been  taken  as  indicating  the 
nature  of  body  condition,  a  loss  usually  indicating  that  there  is  a  loss  of 
body  substance  and  a  gain  the  reverse.  In  experiments  in  which  a  delicate 
balance  between  the  income  and  outgo  is  maintained,  as  in  these  experi- 
ments, it  is  of  special  interest  to  compare  the  losses  in  weight  as  determined 
by  the  balance  with  the  calculated  metabolism  of  material  and  thus  obtain 
a  check  on  the  computation  of  the  whole  process  of  metabolism.  Since  the 
days  of  Sanctorius  the  loss  of  weight  of  the  body  from  period  to  period  has 
been  of  special  interest.  The  most  recent  contribution  to  these  investiga- 
tions is  that  of  the  balance  described  by  Lombard,*  in  which  the  body- 
weight  is  recorded  graphically  from  moment  to  moment  with  an  extra- 
ordinarily sensitive  balance. 

In  connection  with  the  experiments  here  described,  however,  the  weighing 
with  the  balance  has  a  special  significance,  in  that  it  is  possible  to  have  an 
indirect  determination  of  the  oxygen  consumption.  As  pointed  out  by 
Pettenkofer  and  Yoit,  if  the  weight  of  the  excretions  and  the  loss  in  body- 
weight  are  taken  into  consideration,  the  difference  between  the  weight  of  the 
excretions  and  the  loss  in  body-weight  should  be  the  weight  of  the  oxygen 
absorbed.  With  this  apparatus  we  are  able  to  determine  the  water-vapor, 
the  carbon-dioxide  excretion,  and  the  weight  of  the  urine  and  feces  when 
passed.  If  there  is  an  accurate  determination  of  the  body-weight  from 
hour  to  hour,  this  should  give  the  data  for  computing  exactly  the  oxygen 
consumption.  Moreover,  we  have  the  direct  determination  of  oxygen  with 
which  the  indirect  method  can  be  compared. 

In  the  earlier  apparatus  this  comparison  was  by  no  means  as  satisfactory 
as  was  desired.  The  balance  there  used  was  sensitive  only  to  2  grams,  the 
experiments  were  long  (24  hours  or  more),  and  it  seemed  to  be  absolutely 
impossible,  even  by  exerting  the  utmost  precaution,  to  secure  the  body- 
weight  of  the  subject  each  day  with  exactly  the  same  clothing  and  acces- 
sories. Furthermore,  where  there  is  a  constant  change  in  body-weight 
amounting  to  0.5  gram  or  more  per  minute,  it  is  obvious  that  the  weighing 
should  be  done  at  exactly  the  same  moment  from  day  to  day.  It  is  seen, 
therefore,  that  the  comparison  with  the  direct  oxygen  determination  is  in 
reality  an  investigation  by  itself,  involving  the  most  accurate  measurements 
and  the  most  painstaking  development  of  routine. 

With  the  hope  of  contributing  materially  to  our  knowledge  regarding  the 
indirect  determination  of  oxygen,  the  special  form  of  balance  shown  in 
fig.  9  was  installed  above  the  chair  calorimeter.    This  balance  is  extremely 

*  W.  P.  Lombard :  A  method  of  recording  changes  in  body- weight  which  occur 
within  short  intervals  of  time.  The  Journal  of  the  American  Medical  Associa- 
tion, vol.  47,  p.  1790.     (1906.) 


94  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

sensitive.  With  a  dead  load  of  100  kilograms  in  each  pan  it  has  shown  a 
sensitiveness  of  0.1  gram,  but  in  order  to  have  the  apparatus  absolutely  air- 
tight for  the  oxygen  and  carbon-dioxide  determination,  the  rod  on  which 
the  weighing-chair  is  suspended  must  pass  through  an  air-tight  closure. 
For  this  closure  we  have  used  a  thin  rubber  membrane,  weighing  about  1.34 
grams,  one  end  of  which  is  tied  to  a  hard-rubber  tube  ascending  from  the 
chair  to  the  top  of  the  calorimeter,  the  other  end  being  tied  to  the  suspen- 
sion rod.  In  playing  up  and  down  this  rod  takes  up  a  varying  weight  of  the 
rubber  diaphragm,  depending  upon  the  position  which  it  assumes,  and  there- 
fore the  sensitiveness  noted  by  the  balance  with  a  dead  load  and  swinging 
freely  is  greater  than  that  under  conditions  of  actual  use.  Preliminary 
tests  with  the  balance  lead  us  to  believe  that  with  a  slight  improvement  in 
the  technique  a  man  can  be  weighed  to  within  0.3  gram  by  means  of  this 
balance.  A  series  of  check-experiments  to  test  the  indirect  with  the  direct 
determination  of  oxygen  are  in  progress  at  the  moment  of  writing,  and  it 
is  hoped  that  this  problem  can  be  satisfactorily  solved  ere  long. 

During  the  process  of  weighing,  the  ventilating  air-current  is  stopped 
so  as  to  prevent  any  slight  tension  on  the  rubber  diaphragm  and  furnish 
the  best  conditions  for  sensitive  equilibrium.  After  the  weighing  has  been 
made  and  the  time  exactly  recorded,  the  load  is  thrown  off  the  knife-edges 
of  the  balance,  and  then  provision  has  been  made  to  raise  the  rod  supporting 
the  chair  and  simultaneously  force  a  rubber  stopper  tightly  into  the  hard- 
rubber  tube  at  the  top  of  the  calorimeter,  thus  making  the  closure  absolutely 
tight.  It  is  somewhat  hazardous  to  rely  during  the  entire  period  of  an 
experiment  upon  the  thin  rubber  membrane  for  the  closure  when  the  blower 
is  moving  the  air-current. 

To  raise  the  chair  and  the  man  suspended  on  it  in  such  a  way  as  to  draw 
the  cork  into  the  hard-rubber  tube,  we  formerly  used  a  large  hand-lever, 
which  was  not  particularly  satisfactory.  Thanks  to  the  suggestion  of  Mr. 
E.  H.  Metcalf,  we  have  been  able  to  attach  a  pneumatic  lift  (fig.  9)  in 
that  the  cross-bar  above  the  calorimeter  chamber,  to  which  the  suspension 
rod  is  attached,  rests  on  two  oak  uprights  and  can  be  raised  by  admitting 
air  into  an  air-cushion,  through  the  central  opening  of  which  passes  the 
chair-suspending  rod.  As  the  air  enters  the  air-cushion  it  expands  and 
lifts  a  large  wooden  disk  which,  in  turn,  lifts  the  iron  cross-bar,  raising 
the  chair  and  weight  suspended  upon  it.  At  the  proper  height  and  when 
the  stopper  has  been  thoroughly  forced  into  place,  two  movable  blocks  are 
slipped  beneath  the  ends  of  the  iron  cross-bar  and  thus  the  stopper  is  held 
firmly  in  place.  The  tension  is  then  released  from  the  air-cushion.  This 
apparatus  functionates  very  satisfactorily,  raising  the  man  or  lowering  him 
upon  the  knife-edges  of  the  balance  with  the  greatest  regularity  and  ease. 


PULSE   RATE   AND  RESPIRATION    BATE.  95 

PULSE  RATE  AND  RESPIRATION  RATE. 

The  striking  relationship  existing  betwen  pulse  rate  and  general  metab- 
olism, noted  in  the  fasting  experiments  made  with  the  earlier  apparatus, 
has  impressed  upon  us  the  desirability  of  obtaining  records  of  the  pulse 
rate  as  frequently  as  possible  during  an  experiment.  Records  of  the  res- 
piration rate  also  have  an  interest,  though  not  of  as  great  importance.  In 
order  to  obtain  the  pulse  rate,  we  attach  a  Bowles  stethoscope  over  the 
apex  beat  of  the  heart  and  hold  it  in  place  with  a  light  canvas  harness. 
Through  a  long  transmission-tube  passing  through  an  air-tight  closure  in 
the  walls  of  the  calorimeter  it  is  possible  to  count  the  beats  of  the  heart 
without  difficulty.  The  respiration  rate  is  determined  by  attaching  a  Fitz 
pneumograph  about  the  trunk,  midway  between  the  nipples  and  the  umbili- 
cus. The  excursions  of  the  tambour  pointer  as  recorded  on  the  smoked 
paper  of  the  kymograph  give  a  true  picture  of  the  respiration  rate. 

Of  still  more  importance,  however,  is  the  fact  that  the  expansion  and 
contraction  of  the  pneumograph  afford  an  excellent  means  for  noting  the 
minor  muscular  activity  of  a  subject,  otherwise  considered  at  complete  rest. 
The  slightest  movement  of  the  arm  or  the  contraction  or  relaxation  of  any 
of  the  muscles  of  the  body-trunk  results  in  a  movement  of  the  tambour 
quite  distinct  from  the  respiratory  movements  of  the  thorax  or  abdomen. 
These  movements  form  a  very  true  picture  of  the  muscular  movements  of 
the  subject,  and  these  graphic  records  have  been  of  very  great  value  in 
interpreting  the  results  of  many  of  the  experiments. 


96  CALORIMETERS   FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

ROUTINE  OF  AN  EXPERIMENT  WITH  MAN. 

In  the  numerous  previously  published  reports  which  describe  the  con- 
struction of  and  experiments  with  the  respiration  calorimeter,  but  little 
attention  has  been  devoted  to  a  statement  of  the  routine.  Since,  with  the 
increasing  interest  in  this  form  of  apparatus  and  the  possible  construction 
of  others  of  similar  form,  a  detailed  description  of  the  routine  would  be  of 
advantage,  it  is  here  included. 

PREPARATION  OF  SUBJECT. 

Prior  to  an  experiment,  the  subject  is  usually  given  either  a  stipulated 
diet  for  a  period  of  time  varying  with  the  nature  of  the  experiment  or,  as 
in  the  case  of  some  experiments,  he  is  required  to  go  without  food  for  at 
least  12  hours  preceding.  Occasionally  it  has  been  deemed  advisable  to 
administer  a  cup  of  black  coffee  without  sugar  or  cream,  and  by  this  means 
we  have  succeeded  in  studying  the  early  stages  of  starvation  without  making 
it  too  uncomfortable  for  the  subject.  The  stimulating  effect  of  the  small 
amount  of  black  coffee  on  metabolism  is  hardly  noticeable  and  for  most 
experiments  it  does  not  introduce  any  error. 

The  urine  is  collected  usually  for  24  hours  before,  in  either  6  or  12  hour 
periods.  During  the  experiment  proper  urine  is  voided  if  possible  at  the 
end  of  each  period.  This  offers  an  opportunity  for  studying  the  periodic 
elimination  of  nitrogen  and  helps  frequently  to  throw  light  upon  any  pecu- 
liarities of  metabolism. 

Even  with  the  use  of  a  long-continued  preceding  diet  of  constant  com- 
position, it  is  impossible  to  rely  upon  any  regular  time  for  defecation  or  for 
any  definite  separation  of  feces.  For  many  experiments  it  is  impracticable 
and  highly  undesirable  to  have  the  subject  attempt  to  defecate  inside  the 
chamber,  and  for  experiments  of  short  duration  the  desire  to  defecate  is 
avoided  by  emptying  the  lower  bowel  with  a  warm-water  enema  just  before 
the  subject  enters  the  chamber.  Emphasis  should  be  laid  upon  the  fact 
that  a  moderate  amount  of  water  only  should  be  used  and  only  the  lower 
bowel  emptied,  so  as  not  to  increase  the  desire  for  defecation. 

The  clothing  is  usually  that  of  a  normal  subject,  although  occasionally 
experiments  have  been  made  to  study  the  influence  of  various  amounts  of 
clothing  upon  the  person.  There  should  be  opportunity  for  a  comfortable 
adjustment  of  the  stethoscope  and  pneumograph,  etc.,  and  the  clothing 
should  be  warm  enough  to  enable  the  subject  to  remain  comfortable  and 
quiet  during  his  sojourn  inside  the  chamber. 

The  rectal  thermometer,  which  has  previously  been  carefully  calibrated, 
is  removed  from  a  vessel  of  lukewarm  water,  smeared  with  vaseline,  and 
inserted  while  warm  in  the  rectum  to  the  depth  of  10  to  12  centimeters. 
The  lead  wires  are  brought  out  through  the  clothing  in  a  convenient  position. 


ROUTINE   OF   AX    EXPERIMENT   WITH    MAN.  97 

The  stethoscope  is  attached  as  nearly  as  possible  over  the  apex  beat  of 
the  heart  by  means  of  a  light  harness  of  canvas.  In  the  use  of  the  Bowles 
stethoscope,  it  has  been  found  that  the  heart-beats  can  easily  be  counted  if 
there  is  but  one  layer  of  clothing  between  the  stethoscope  and  the  skin. 
Usually  it  is  placed  directly  upon  the  undershirt  of  the  subject. 

The  pneumograph  is  placed  about  the  body  midway  between  the  nipple 
and  the  umbilicus  and  sufficient  traction  is  put  upon  the  chain  or  strap 
which  holds  it  in  place  to  secure  a  good  and  clear  movement  of  the  tambour 
for  each  respiration. 

The  subject  is  then  ready  to  enter  the  chamber  and,  after  climbing  the 
stepladder,  he  descends  into  the  opening  of  the  chair  calorimeter,  sits  in 
the  chair,  and  is  then  ready  to  take  care  of  the  material  to  be  handed  in  to 
him  and  adjust  himself  and  his  apparatus  for  the  experiment.  Usually 
several  bottles  of  drinking-water  are  deposited  in  the  calorimeter  in  a 
convenient  position,  as  well  as  some  urine  bottles,  reading  matter,  clinical 
thermometer,  note-book,  etc.  Before  the  cover  is  finally  put  in  place,  the 
pneumograph  is  tested,  stethoscope  connections  are  tested  to  see  if  the 
pulse  can  be  heard,  the  rectal  thermometer  connections  are  tested,  and  the 
telephone,  call-bell,  and  electric  light  are  all  put  in  good  working  order. 
When  the  subject  has  been  weighed  in  the  chair,  the  balance  is  tested  to  see 
that  it  swings  freely  and  has  the  maximum  sensibility.  All  the  adjustments 
are  so  made  that  only  the  minimum  exertion  will  be  necessary  on  the  part 
of  the  subject  after  the  experiment  has  once  begun. 

SEALING  IN  THE  COVER. 

The  cover  is  put  in  place  and  wax  is  well  crowded  in  between  it  and  the 
rim  of  the  opening.  The  wax  is  preferably  prepared  in  long  rolls  about  the 
size  of  a  lead-pencil  and  25  to  30  centimeters  long.  This  is  crowded  into 
place,  a  flat  knife  being  used  if  necessary.  An  ordinary  soldering-iron, 
which  has  previously  been  moderately  heated  in  a  gas  flame,  is  then  used  to 
melt  the  wax  into  place.  This  process  must  be  carried  out  with  the  utmost 
care  and  caution,  as  the  slightest  pinhole  through  the  wax  will  vitiate  the 
results.  The  sealing  is  examined  carefully  with  an  electric  light  and 
preferably  by  two  persons  independently.  After  the  sealing  is  assured,  the 
plugs  connecting  the  thermal  junctions  and  heating  wires  of  the  cover  with 
those  of  the  remainder  of  the  chamber  are  connected,  the  water-pipe  is 
put  in  place,  and  the  unions  well  screwed  together.  After  seeing  that  the 
electrical  connections  can  not  in  any  way  become  short-circuited  on  either 
the  metal  chamber  or  metal  pipes,  the  asbestos  cover  is  put  in  place. 

ROUTINE  AT  OBSERVER'S  TABLE. 

Some  time  before  the  man  enters  the  chamber,  an  electric  lamp  of  from 
16  to  24  candle-power  (depending  upon  the  size  of  the  subject)  is  placed 
inside  of  the  chamber  as  a  substitute   for  the  man,  and  the  cooling  water- 


98  CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

current  is  started  and  the  whole  apparatus  is  adjusted  to  bring  away  the 
heat  prior  to  the  entrance  of  the  man.  The  rate  of  flow  with  the  chair 
calorimeter  is  not  far  from  350  cubic  centimeters  per  minute  with  a  resting 
man.  The  proper  mixture  of  cold  and  warm  water  is  made,  so  that  the 
electric  reheater  can  be  controlled  readily  by  the  resistance  in  series  with  it. 
Care  is  taken  not  to  allow  the  water  to  enter  the  chamber  below  the  dew- 
point  and  thus  avoid  the  condensation  of  moisture  on  the  absorbers.  The 
thermal  junctions  indicate  the  temperature  differences  in  the  walls  and  the 
different  sections  are  heated  or  cooled  as  is  necessary  until  the  whole  system 
is  brought  as  near  thermal  equilibrium  as  possible. 

After  the  man  enters,  the  lamp  is  removed  and  the  water-current  is  so 
varied,  if  necessary,  and  the  heating  and  cooling  of  the  various  parts  so 
adjusted  as  to  again  secure  temperature  equilibrium  of  all  parts.  When  the 
amount  of  heat  brought  away  by  the  water-current  exactly  compensates 
that  generated  by  the  subject,  when  the  thermal-junction  elements  in  the 
walls  indicate  a  0  or  very  small  deflection,  when  the  resistance  thermometers 
indicate  a  constant  temperature  of  the  air  inside  the  chamber  and  the  walls 
of  the  chamber,  the  experiment  proper  is  ready  to  begin. 

The  physical  observer  keeps  the  chemical  assistant  thoroughly  informed 
as  to  the  probable  time  for  the  beginning  of  the  experiment,  so  that  there 
will  be  ample  time  for  making  the  residual  analyses  of  the  air.  After  these 
analyses  have  been  made  and  the  experiment  is  about  to  begin,  the  observer 
at  the  table  calls  the  time  on  the  exact  minute,  at  which  time  the  blower  is 
stopped  and  the  purifying  system  changed.  The  physical  observer  takes 
the  temperatures  of  the  wall  and  air  by  the  electric-resistance  thermometers, 
reads  the  mercury  thermometers,  records  the  rectal  thermometer,  and  at  the 
exact  moment  of  beginning  the  experiment  the  current  of  water  which  has 
previously  been  running  into  the  drain  is  deflected  into  the  water-meter. 
At  the  end  of  the  period  this  routine  is  varied  only  in  that  the  water-cur- 
rent is  deflected  from  the  water-meter  into  a  small  can  holding  about  4 
liters,  into  which  the  water  flows  while  the  meter  is  being  weighed. 

MANIPULATION  OF  THE  WATER-METER. 

The  rate  of  flow  of  water  through  the  apparatus  is  determined  before  the 
experiment  begins.  This  is  done  by  deflecting  the  water  for  a  certain 
number  of  seconds  into  a  graduate  or  by  deflecting  it  into  the  small  can  and 
weighing  the  water  thus  collected.  The  water  is  then  directed  into  the 
drain  during  the  preliminary  period.  Meanwhile  the  main  valve  at  the 
bottom  of  the  water-meter  is  opened,  such  water  as  has  accumulated  from 
tests  in  preceding  experiments  is  allowed  to  run  out,  and  the  valve  is  closed 
after  the  can  is  empty.  The  meter  is  then  carefully  balanced  on  the  scales 
and  the  weight  is  recorded.  At  the  beginning  of  the  experiment  the  water 
is  deflected  from  the  drain  into  the  meter.     At  the  end  of  the  period, 


ROUTINE   OF  AN   EXPERIMENT    WITH    MAN.  99 

while  the  water  is  running  into  the  small  can,  the  water-meter  is  again 
carefully  weighed  and  the  weight  recorded.  Having  recorded  the  weight, 
the  water  is  again  deflected  into  the  large  meter  and  what  has  accumulated 
in  the  small  can  is  carefully  poured  into  the  large  meter  through  a  funnel. 
If  the  meter  is  nearly  full,  so  that  during  the  next  period  water  will  accu- 
mulate and  overflow  the  meter,  it  is  emptied  immediately  after  weighing 
and  while  the  small  can  is  filling  up.  About  4  minutes  is  required  to  empty 
the  can  completely. 

After  it  is  emptied,  it  is  again  weighed,  the  water-current  deflected  from 
the  small  can  to  the  meter,  and  the  water  which  has  accumulated  in  the 
small  can  carefully  poured  into  the  meter.  All  weights  on  the  water-meter, 
both  of  the  empty  can  and  the  can  at  the  end  of  each  period,  are  checked 
by  two  observers. 

ABSORBER  TABLE. 

Shortly  after  the  subject  has  entered  the  chamber  and  in  many  instances 
before  the  sealing-in  process  has  begun,  the  ventilating  air-current  is  started 
by  starting  the  blower.  The  air  passes  through  one  set  of  purifiers  during 
this  preliminary  period,  and  as  no  measurements  are  made  for  this  period 
it  is  not  necessary  that  the  weights  of  the  absorbers  be  previously  known. 

All  precautions  are  taken,  however,  so  far  as  securing  tightness  in  coup- 
ling and  installing  them  on  the  absorber  system  are  concerned.  During  this 
period  the  other  set  of  absorbers  is  carefully  weighed  and  made  ready  to 
be  put  in  place  and  tested  and  about  10  minutes  before  the  experiment 
proper  begins  the  residual  analyses  are  begun.  The  series  of  U-tubes,  which 
have  previously  been  carefully  weighed,  are  placed  on  small  inclined  racks 
and  are  connected  with  the  meter  and  also  with  the  tube  leading  to  the 
mercury  valve.  The  pet-cock  which  connects  the  return  air-pipe  with  the 
drying-tower  and  the  gas-meter  is  then  opened  and  the  mercury  reservoir 
is  lowered.  The  rate  of  flow  of  air  through  the  U-tubes  is  regulated  by  a 
screw  pinch-cock  on  the  rubber  tube  leading  to  the  first  U-tube.  This  rate 
is  so  adjusted  by  means  of  the  pinch-cock  that  about  3  liters  of  air  per 
minute  will  flow  through  the  U-tubes,  and  as  the  pointer  on  the  gas-meter 
approaches  10  liters  the  mercury  reservoir  is  raised  at  just  such  a  point, 
gained  by  experience,  as  will  shut  off  the  air-current  when  the  total  volume 
registers  10  liters  on  the  meter.  The  pet-cock  in  the  pipe  behind  the  meter 
is  then  closed,  the  U-tubes  disconnected,  and  a  new  set  put  in  place.  A 
duplicate  and  sometimes  a  triplicate  analysis  is  made. 

When  the  physical  observer  calls  the  time  for  the  end  of  the  period,  the 
switch  which  controls  the  motor  is  opened  and  the  chemical  assistant  then 
opens  the  rear  valve  of  the  new  set  of  absorbers  and  closes  the  rear  valve 
of  the  old  set,  and  likewise  opens  the  front  valve  of  the  new  set  and  closes 
the  front  valve  of  the  old  set.    As  soon  as  the  signal  is  given  that  the  oxygen 


100         CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

connections  have  been  properly  made  and  that  the  oxygen  has  been  admitted 
to  the  chamber  in  proper  amount,  the  blower  is  again  started.  It  is  then 
necessary  to  weigh  the  U -tubes  and  disconnect  the  old  set  of  absorbers  and 
weigh  them.  If  the  sulphuric-acid  absorbers  have  not  exceeded  the  limit  of 
gain  in  weight  they  are  used  again ;  if  they  have,  new  ones  are  put  in  their 
place. 

The  first  sulphuric-acid  absorber  is  connected  to  the  front  valve,  then 
the  potash-lime  can,  and  then  the  last  sulphuric-acid  absorber;  but  before 
connecting  the  last  sulphuric-acid  absorber  with  the  sodium-bicarbonate 
can,  a  test  is  made  of  the  whole  system  from  the  front  valve  to  the  end  of 
the  second  sulphuric-acid  absorber.  This  is  made  by  putting  a  solid-rubber 
stopper  in  the  exit  end  of  the  second  sulphuric-acid  absorber  and,  by  means 
of  a  bicycle  pump,  forcing  compressed  air  in  through  a  pipe  tapped  into 
the  pipe  from  the  valve  at  the  front  end  until  a  pressure  of  about  2  feet 
of  water  is  developed  in  this  part  of  the  system.  This  scheme  for  testing 
and  the  method  of  connecting  the  extra  pipe  have  been  discussed  in  detail 
in  an  earlier  publication.*  Eepeated  tests  have  shown  that  this  method  of 
testing  the  apparatus  for  tightness  is  very  successful,  as  the  minutest  leak 
is  quickly  shown. 

After  the  system  has  been  thoroughly  tested,  the  rubber  stopper  in  the 
exit  end  of  the  second  sulphuric-acid  absorber  is  first  removed,  then  the 
tube  connected  with  the  pump  and  manometer  is  disconnected  and  its  end 
placed  in  the  reservoir  of  mercury.  Occasionally,  through  oversight,  the 
pressure  is  released  at  the  testing-tube  with  the  result  that  the  air  com- 
pressed in  the  system  expands,  forcing  sulphuric  acid  into  the  valves  and 
down  into  the  blower,  thus  spoiling  completely  the  experiment.  After  the 
testing,  the  last  sulphuric-acid  absorber  is  coupled  to  the  sodium-bicarbo- 
nate can.  It  is  seen  that  this  last  connection  is  the  only  one  not  tested,  and 
it  has  been  found  that  care  must  be  taken  to  use  only  the  best  gaskets  at 
this  point,  as  frequently  leaks  occur;  in  fact,  it  is  our  custom  to  moisten 
this  connection  with  soapsuds.  If  new  rubber  gaskets  are  used  a  leak  is 
never  found. 

SUPPLEMENTAL  APPARATUS. 

To  maintain  the  apparent  volume  of  air  through  the  whole  system  con- 
stant, oxygen  is  admitted  into  the  tension-equalizer  until  the  same  tension 
is  exerted  on  this  part  of  the  system  at  the  end  as  at  the  beginning.  This 
is  done  by  closing  the  valve  connecting  the  tension-equalizer  with  the  sys- 
tem and  admitting  oxygen  to  the  tension-equalizer  until  the  petroleum 
manometer  shows  a  definite  tension.  After  the  motor  is  stopped,  at  the 
end  of  the  experimental  period,  there  is  a  small  amount  of  air  compressed 
in  the  blower  which  almost  instantly  leaks  back  through  the  blower  and  the 
whole  system  comes  under  atmospheric  pressure,  save  that  portion  which 

*  Atwater  and  Benedict:    hoc.  cit.,  p.  21. 


ROUTINE  OF  AN  EXPERIMENT  WITH  MAN.  101 

is  sealed  off  between  the  two  levels  of  the  sulphuric  acid  in  the  two  absorb- 
ing vessels.  A  few  seconds  after  the  motor  is  stopped  the  valve  cutting  off 
the  tension-equalizer  from  the  rest  of  the  system  is  closed,  the  pet-cock  con- 
necting this  with  the  petroleum  manometer  is  opened,  and  oxygen  is 
admitted  by  short-circuiting  the  electrical  connections  at  the  two  mercury 
cups.  This  is  done  by  the  hands  of  the  observer  and  must  be  performed 
very  gently  and  carefully,  as  otherwise  oxygen  will  rush  in  so  rapidly  as  to 
cause  excessive  tension.  As  the  bag  fills  with  gas,  the  index  on  the  petro- 
leum manometer  moves  along  the  arc  of  a  circle  and  gradually  reaches  the 
desired  point.  At  this  point,  the  supply  of  oxygen  is  cut  off,  the  valve  con- 
necting the  tension-equalizer  with  the  main  system  is  opened,  and  simul- 
taneously the  needle-valve  on  the  reduction-valve  of  the  oxygen  cylinder  is 
tightly  closed,  preliminary  to  weighing  the  cylinder.  At  this  point  the 
motor  can  be  started  and  the  experiment  continued. 

It  is  necessary,  then,  that  the  oxygen  cylinder  be  weighed.  This  is  done 
after  first  closing  the  pet-cock  on  the  end  of  the  pipe  conducting  the  gas 
beneath  the  floor  of  the  calorimeter  room,  slipping  the  glass  joint  in  the 
rubber  pipe  leading  from  the  reduction  valve  to  the  pet-cock,  and  breaking 
the  connections  between  the  two  rubber  pipes,  the  one  from  the  pet-cock 
and  the  other  to  the  reduction  valve,  also  breaking  the  electrical  connection 
leading  to  the  magnet  on  the  cylinder.  The  cylinder  is  then  ready  to  swing 
freely  without  any  connections  to  either  oxygen  pipe  or  electrical  wires. 
It  is  then  weighed,  the  loss  in  weight  being  noted  by  removing  the  brass 
weights  on  the  shelf  attached  to  the  counterpoise.  It  is  important  to  see 
that  there  is  a  sufficient  number  of  brass  weights  always  on  the  shelf  to 
allow  for  a  maximum  loss  of  weight  of  oxygen  from  the  cylinder  during 
a  given  period.  Since  the  cylinders  contain  not  far  from  4  to  5  kilograms 
of  oxygen,  in  balancing  the  cylinders  at  the  start  it  is  customary  to  place 
at  least  4  kilograms  of  brass  weights  on  the  shelf  and  then  adjust  the 
counterpoise  so  as  to  allow  for  the  gradual  removal  of  these  weights  as  the 
oxygen  is  withdrawn. 

As  soon  after  the  beginning  of  the  period  as  possible,  the  U- tubes  are 
weighed  on  the  analytical  balance,  and  if  they  have  not  gained  too  much 
they  are  connected  ready  for  the  next  analysis.  If  they  have  already  ab- 
sorbed too  much  water  or  carbon  dioxide,  they  are  replaced  by  freshly  filled 
tubes. 

Immediately  at  the  end  of  the  experimental  period  the  barometer  is 
carefully  set  and  read,  and  the  reading  is  verified  by  another  assistant. 
Throughout  the  whole  experiment  an  assistant  counts  the  pulse  of  the  sub- 
ject frequently,  by  means  of  the  stethoscope,  and  records  the  respiration 
rate  by  noting  the  lesser  fluctuations  of  the  tambour  pointer  on  the  smoked 
paper.  These  observations  are  recorded  every  few  minutes  in  a  book  kept 
especially  for  this  purpose. 


102         CALORIMETERS    FOR   STUDYING   RESPIRATORY   EXCHANGE,   ETC. 

A  most  excellent  preservation  of  the  record  of  the  minor  muscular  move- 
ments is  obtained  by  dipping  the  smoked  paper  on  the  kymograph  drum  in 
a  solution  of  resin  and  alcohol.  The  lesser  movements  on  the  paper  indi- 
cate the  respiration  rate,  but  every  minor  muscular  movement,  such  as 
moving  the  arm  or  shifting  the  body  in  any  way,  is  shown  by  a  large  deflec- 
tion of  the  pointer  out  of  the  regular  zone  of  vibration.  These  records  of 
the  minor  muscular  activity  are  of  great  importance  in  interpreting  the 
results  of  the  chemical  and  physical  determinations. 


(*(*- 


mmBMM^^m^mmmKBmm^^Bm^&BmmimMi^mK^mi 


QP     Benedict,  Francis  Gano 
171       Respiration  calorimeters 
B472 

Biological 
&  Medical 


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