Title The viscosity of argon, nitrogen and air at ...
Transcript of Title The viscosity of argon, nitrogen and air at ...
Title The viscosity of argon, nitrogen and air at pressures up to800kg/cm2
Author(s) Makita, Tadashi
Citation The Review of Physical Chemistry of Japan (1957), 27(1): 16-21
Issue Date 1957
URL http://hdl.handle.net/2433/46745
Right
Type Departmental Bulletin Paper
Textversion publisher
Kyoto University
The Review of Physical Chemistry of Japan Vol. 27 No. 1 (19
THE VISCOSITY OF ARGON, NITROGEN AND AIR
AT PRESSURES UP TO 80o KG/CMZ
BY TAD,\SHr MAXTIAi
The recent survey of available data concerning the viscosity of gases, which was carried out
by Hilsenrath and Touloukiantl, reveals that accurate data on the viscosity of gases at [he wide
region of pressure and temperature are still very scarce. The present investigation has been
undertaken to obtain some new values of thz viscosity of argon, nitrogen and air at the extended
conditions of pressure and temperature. That is, the measurement of the viscosity is made under
pressures up to 800 kg/cm= at 25, 50, 75, 100 and 150°C for argon, and at temperatures up to
200°C for nitrogen and air, by a rolling-ball method described previouslyzl.
On the viscosity of argon, Kiyama and biakitaal determined first by a rolling-ball method
under pressures up to t00kg/cm= at five different temperatures: 50, 100, 150, 200 and 300°C.
Recently, Kestin and Pilarczykt> used an oscillating-disk viscometer and measured the viscosity
of argon up to 70 atm at 20°C, and Michels, Botzen and Schuurmans>, who used a transpiration
method, covered Che range of up to about 2000 atm at 25. 50 and i5°C.
The effect of pressure on the viscosity of nitrogen was carefully determined by Michels and
Gibsons> under pressures up Co 970 atm at 25, 50 and 75C, using a transpiration method. And
H. Iwasaki73 measured it by an oscillating-disk method under pressures up to about 200 atm at
25, 100 and 150°C, and Kestin and Pilarczyk+~ also determined it a[ 1^70 atm and 21°C.
Finally, on the viscosity of air, I. F. Golubeval used a transpiration method and covered the
range of pressures up to 300 kg/cm= at four different temperatures: 0, 16, 50 and 100`C; H,
Iwasaki9> determined it at pressures up to about 200 atm and three different temperatures: 50, 100
and 150`C; and recently Kestin and Pilarczyk<> measured it under pressures up to 70 atm at
21`C.
Experim=ntals
The apparatus and its experimental procedure were described in details in the previous
paperz>. In the measurement of the viscosity of air at 150 and 200°C, the contact surfaces of the electrodes are covered by platinum in order to prevent them from oxidation.
+ Present address, Kyoao Technical University 1) J. Hilsenrath and 1'. S. Touloukian, Traru. ASAfE, 76, 967 (1914) 2) R. Kiyama and T. 1laki ta, This Joan:al, 20, 70 (1916) 3) R. Kiyama and T. )Iakita, ihid., 2v, 49 (1952) 4) J. Kestin and R. Pilarczyk, Trans. ASlf$ 76, 987 (1914) 5) A. Michels, A. Botzen and lV. Schuurman, Phytica, 20, 1141 ([954) 6) A. Michels and R. O. Gibson, Proc. Roy. Soc. London, 131 A, 288 (1931) 7) H. Iwasaki, Btdl. Chem. Research Institute of Non•aqueaus Solutions, 3, 117 (1953) 8) I. F. Golubev, d Teck. Phys. GSSR, 8, 1931 (1938) 9) H. Iwasaki, Brc![. Chem. Researh Inslilafa of Nom-aqueous SaGdions, I, 2i (1951)
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The Review of Physical Chemistry of Japan Vol. 27 No. 1 (1957)1
The Viscosity o[ Argon, Nitrogen a¢d Air at Pressures up to 800 kg/cm= 17
The argon and nitrogen used in this measurement have been obtained from commercial sources
and are not further purified. The puiities of argon and nitrogen as indicated by the manufacturers
are 99.9% and 99.8%, respectively.
The values of the density of gases which are necessary for the calculation of the viscosity
have been ohtained from the compressibility data of A. Micheh, Huh Wijker and Hk. Wijkerr¢)
for argon, and of E. H. AmagatrU for nitrogen and air.
The present
SO and 75°C xnd
600
,~ s
b V ~E
x 400 .~ .~
300
200
results of
of Kestin
iso• im'
argon
e1 al.
Resulks and Considerations
are given in Fig, I, where the values
at 20'C are also plotted. Although the
zs' so• ~s'
of Michels et al. at 25,
values of Michels et al.
100' 150"
~~ 60' zs
200 400 600 Pressure, kg/cm'
Fig. 1 Viscosity isotherms of argon -0-: Author, -----: Kestin and Pilarczyk,
~: 2>°C, ~: >0° and /: 7SC of Afichels et al.
200 kg/cm' are smaller by about 2°' than the
800
ill ,,
~s.
~i: ~~
~'~ ~~i ,;
r~
f~ ~,
I ~. `~ 1~
!i
~i ~U
h•
0
under pressures lower than 200 kg/cros are smaller by about 2°' than the present ones, the good agreement is found between both under pressures higher than 300 kg/cm= at the three temperatures.
The values of Kestin et al. are not comparable with the present ones because of the difference
in temperature , but it seems that the value at 70 kgJcm= of Kestin et al. is iarger. Finally, the
present values under 100 kg/cm"- agree with the previous ones within the experimental error, as
considered in the case of oxygenz>. There are no comparative values under pressures higher than
10) A. Jlichels, Hub. Wijker and Hk. Wijker, Physics, 15, 627 (1949) Il) E. H. Amagat, .9nn. chim. phys., 29. 6g (1g93)
I
J
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~~
The Review of Physical Chemistry of Japan Vol. 27 No. 1 (1
18
100 kg/cm° at 100 and
The present results
150°C.
of the viscosity
T. Makila
of nitrogen are plotted in Fig. 2, in which the values
~ aoo .~
b .~
a. 300 .~
Z00
ADO'
100'
so• ~s
21'
zs sv ~•
lOD' 150' 20D'
0 200 400 600 Pressure, kg/cm`
Fig. 2 Viscosity isotherms of nitrogen -0-= Author , -----: Restin and Pilartzyk, ~: 25, 50 and is'C of Nickels and Gibson, p: 25, tW and ISO'C of H. Rvasaki.
B00
of hlithels et al. at 25,
at 21`C are also plotted.
described previous1y21.
at 2S`C. but the former
50 and i5°C, Iwasaki's at 2S, 100 and ISO°C, and the data of Keslin et al,
The values of ;Nickels et a!. agree very well with the present resultr as
The agreement between Iwasaki's data and the present ones is also good
arc smaller at both 100 and 150°C. I[ Seems that the value at i0kg(cm'
.g
d C ~E
a: .~
400
300
200
200' 150' 100' ^-o-
zs
so•
~s
zi
~s, so'
zs
100' 150'
200'
0 200 400 600 Pressure. kgicm'
Fig. 3 Viscosity isotherms of air -G-: Author , -----: Resin and Pilarczyk, ~: 50' and ~: 100°C of I. F. Goluber•, ~^: SD', U: 100' and ~: 150'C of H. Io•asaki.
800
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The Review of Physical Chemistry of Japan Vol. 27 No. 1
The Viscosity of Argon, Nitrogen and Air at Pressures up to 800 kg/cm"- 19
of Kestin eE ¢l. is larger as mentioned in the case of argon. No comparative dsta on the effect
of pressure upon the viscosity of nitrogen at 200°C have been traced. The results of air are given in Fig. 3, where Golubev's values at i0 and lOD'C, Iwasaki'sat
i0, 100 and 150°C, and the data of Kestin et n1. at 21`C are also plotted. The present isotherms
of 50 and 100`C lie between Golubev's and Iwasaki's ones, Golubev's values being larger by about
2-..3^,d than the present ones, and Iwasaki's data at 150°C are also smaller. It seems that the
value of Kestin eE al. is larger at 70kgfcm=. No comparative value_ under pressures at 200°C
have been reported.
The smoothed values which have been read from these isotherms are given in Table 1, where
the values of the National Bureau of Standards, USAfzI, at [he ordinary pressure are also tabulated.
To conclude these results, i[ can be seen that the effect of pressure upon the viscosity of gases
is always positive at a certain temperature, and that the viscosity at low temperatures increases
with pressure more rapidly than at higher temperatures. Therefore, the isotherms cross each other
as seen in these figures, [hat is, the temperature coefficient of the viscosity at constant pressure,
(o"plBT)„ is positive at low pressures as is the normal case for gases and becomes smaller with
Table 1 Smoothed values of viscosity in micro-poi=_e
957J(1
Pressurc
Temperature1 atm 100 200
kg/cm~ 300 400 500 600 700 800
25'C
50
75
l00
lso
2fi
50
75
100
150
t00
25
50
73
t00
150
zoo
218 (188)
Zi3 (243)
258 (258)
273 (172)
300 (299)
158
171
282
292
312
305
3I0
3t7
313
33fi
ARGON
3fi2 422
354 406
355 398
357 394
362 389
482
458
445
433
a17
537
510
489
473
a5o
593
558
533
iti
484
64i
.608
577
556
sta
177 (178) 189 (189)
199 (199) 211 (209) 231 (129) 251 (248)
199
109
217
228
143
258
228
233
238
248
257
2fifi
NITROGEN
263 302
262 297
266 295
270 293
273 289
277 289
341
331
325
319
309
303
379
364
iii
346
330
320
41fi
398
385
372
353
339
452
430
4I3
394
376
357
t85 (184)
t97 {195) 208 (206)
219 (2 U) 238 (238) 257 (257)
207
216
22i
134
Z51
164
24I
246
251
256
265
273
281
280
279
219
28l
283
A1R
3L
3I3
30i
300
297
294
359
346
334
325
315
307
397
379
3fi5
ail
335
321
434
413
395
379
359
340
471
44fi
425
407
382
362
The pasenthesized values
12J Gates.
U.
PP•
5. Department of 69, 118, 357, Wash
are calculated from 11,e Tables
Commerce, iVational Bureau ington (1955)
o,(
of
the National
Standards,
Bureau of Standards.
Tebles of Tberm¢l Properties of
The Review of Physical Chemistry of Japan Vol. 27 No. 1 (1957
20 T. Makita
increasing pressure, and its sign is converted at the crossing point from positive to negative~as
is common for liquids. And the pressure of the inversion point of the sign of (Br~Jr3T), becomes
higher with intteasing temperature. If the viscosity is plotted against the density, the isotherms
at different temperatures do not intersect and (8n/o"T)P remains practically constant over tht whole
range of the density for the three gases, and the diagram for nitrogen is given in Fig. 4.
400
ss .$
a ~E
T .~
.'+
zoo•
~~o•
ioo•
T'
50'
26'
0 0.1 0.2 0.3 0.4 OS Density, g/a
Fig. 4 Viscosity versus density diagram of nitrogen
A Corcelation of the Viscosity under Pressures
The results of the present measuremee[ are summarized and correlated by means of the
principle of corresponding states. The viscosity coefficients are reduced by [heir limiting values
at low density. For most gases it is satisfactory to take the value of [he viscosity at 1 atm to
be the limiting value at zero pressure, since [he coefficient of viscosity is relatively independent
of pressure at low density. In this case the reduced viscosity is defined as ~"=Tjn/r/r, where >)n
and ~, are the viscosity coefficients under high pressure and 1 atm, respective]y, at a certain
temperature. According to the principle of corresponding states, this reduced viscosity is a function
of the reduced pressure P, and the reduced temperature Tr.
The present values of the viscosity of argon, nitrogen, air and ozygenzl have been plotted as
isobars of P, on r,'-T, diagram, and it is found that these isobars can reproduce all the experi-
mental points within the deviation of 5%. Comings, ~fayland and Eglytsl published a generalized
viscosity chart based on [he similar principle, and covered the region of P,=0.110 and Tr=
0.8-3.0. In the prexnt investigation the region is extended up to P,=25 and Tr=4.0. Further-
more, the reduced viscosity has been calculated and plotted by the following data: argon (1000
t3) E. ~i'. Comings, B. J. btayland and R. S. Egly, Eniv. /ffi,wis &eg. Ezpt. SNtian Dull. serier 354 (1944)
r
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The Review of Physical Chemistry of Japan Vol. 27 No. 1 (1957)
The Viscosity of Argon, Nitrogen and Air at Pressures up to 800 kg/cmz 21
2000 atm at 0, 25, 50 and 75 C)s>, hydrogen (I ~ 1000 atm at 25, 50, 75, 100 and 12SC)1t1, and
nitrogen-hydrogen mixtures (1200 atm at 50 and I00°C)~>, covering the region up to P,=40
and T>=t0. The generalized viscosity char[ obtained is given in Fig. 5, where the reduced
5 ~ ~ \\~ \
•':, \\ \ \\~ -The present work 4
\v \ \\ --- Correlation of Comings of aL"'
\\ \ ~ ~.4 '-'- Argon by MirMle et aL° `
3 \P \ •,, \ ~ -Hydrogen by Mtchels of al,°~
,; ~\ ~ --- Interpolated or extrapolated .~ :;\ rs \\ \\\ \\
.~ ! \
~ 2 !2 \ o \
~ S \ ~ ~ \ ~ ~
1S ~• ~ ~
2S . .,_!
11 15 2 3 4 5 6 7 8 9 10
Reduced temperature, T>=T/T~ Fig. 3 Generalized correlation chart (or the viscosity of gases
viscosity rl$ is shown as a function of the pressure P, and temperature T,. This chart provides a
a practical method of predicting the viscosity of gases under conditions where no data exist or no
satisfactory theoretical treatmeeu may be applied.
The author Las great pleasure is expressing his sincere thaals to Prof. Ryo Kiyama for his
valuable guidance and encouragement throughout the course of this research .
Laboratory of Physical Chemistry,
Kyoto University
14) A. Michels, A. C. J. Schipper and LS'. H. Rintoul, Physics, 19, IOll (1953)
~ \ \~~ 1
The preseot wor&
Correiatan of Conungs d a1.
Argon by MirMle et al.°
Hydrogen by Mxhels of al;°~
Interpolated or extrapolated
~~_ ~ ~
\` ~ ~ \\
'~ ~
~~~
~.4~a
~ ;~;~\~
`. ~
\\\\~. I_
F I s\ !2 \\ •\\.
~
\ ~.
~~
_ ~-~'
2s ..~
-.
~ ,
~: ~I
_~-1~.. _E=,