A Generalized Method For Predicting The
A Generalized Method For Predicting The
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zyxwvuts
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( E i j k t - CijkJ presented here is equal to the E used by T = absolute temperature
zyxwvu zy
Lu and Wang ( 3 ) . This has the advantage that in the
absence of quaternary data, the corresponding &jkl may
be set to zero to obtain a better approximation than by
setting (Eijkl - C i j k l ) to zero.
NOTATION
x
y
= mole fraction
= activity coefficient
LITERATURE CITED
1. Benedict, M., C. A. Johnson, E. Solomon, and L. C. Rubin,
zyxwvutsrqpon
Trans. Am. Inst. Chem. Engrs., 41, 371-392 (1945).
zyxwvutsrqponmlkjihgfed
zyxwvut
a = interaction coefficient 2. Jordan, D., J. A. Gerster, A. P. Colburn, and K. Wohl,
A = binary two- and three-suffix coefficient Chem. Eng. Progr., 46, 601-613 (December, 1950).
C = ternary coefficient
3. Lu, C.-H., and Y.-L. Wang, Znd. Eng. Chem. Fundamentals,
3, 271-272 (August, 1964).
D = binary four-suffix coefficient 4. Marek, J., Chem. Listy, 47, 739 (1953); Collection Czech.
E = quaternary coefficient Chem. Commun., 1 9 , l ( 1954).
A G= ~ molar
~ excess Gibbs free energy 5. Redlich, O., and A. T. Kister, Znd. Eng. Chem., 40, 345-348
i, i, k, 1, m, n, p = index representing components ( 1948).
n = moles 6. Wohl, K., Trans. Am. Inst. Chem. Eng., 42, 215-249 (April,
P =pressure 1946).
R = gas constant 7. - , Chem. Eng. Progr., 49, 218-219 (April, 1953).
In a recent article Narsimhan (18) presented a gen- from the experimental data of the present investigation
eralized expression for the minimum fluidization velocity ( 2 3 ) , emf for spherical particles can be shown to vary
by extending the correlation proposed by Leva, Shirai, from 0.36 to 0.46. Different average values of emf have
and Wen (14) into intermediate and turbulent flow re-
ions. Based on a similar approach by employing the
&ed-bed pressure drop equation of Ergun ( 7 ) , an expres-
sion for the minimum fluidization velocity quite different
from that of Narsimhan has been obtained ( 2 3 ) .
It is the purpose of this communication to compare
these two correlations and to examine the validity and
applicability of each.
The generalized expression given by Narsimhan con-
sists of three equations [Equations ( 6 ) , (9), and ( 11) in
his communication (18)1.
The correlation obtained by Wen and Yu ( 2 3 ) can be
represented by
( N R ~=)d ~( 3 ~3 . 7 ) ' + 0.0408 N G -~ 33.7
For nonspherical particles, the particle diameter dp is de-
fined as the equivalent diameter of a spherical particle
with the same volume. As an approximation, the particle
diameter may be calculated from the geometric mean of
the two consecutive sieve openings without introducing
zyxwvu
(1)
V Van Heerden, et a l . ( Z Z )
zyxwvutsr 0
I I I I I / I
zyxwvutsrqponml
zyxwvutsrqp
001
0008
V
0.006
0.004
zyxwvutsrqpon Io
o LIYO, e i 01
S h i m (21)
(151
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0 Foochar and Lewis ( 9 )
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Norsrmhan’r Correlation
0001
05 06 0.7 0.8 0.9 1.0 1.1 1.2 1.3 1.4
(I - Emf)
+s
(1 --Emf)
Fig. 2. Correlation of voidage shape factor function .-
@S
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been reported, such as, 0.386 ( 2 1 ) , 0.40 ( 4 ) , or 0.42
( 2 3 ) .Therefore, the value of 0.35 used by Narsimhan for
spheres seems to be too small.
2. For nonspherical particles, Narsimhan considered
that Emf depends on the particle diameter if it is less than
0.02 in. On the other hand, if greater than 0.02 in., he
considered that Emf is independent of particle diameter.
From Figures 1 and 2, Narsimhan’s correlations for
small particles are seen to be valid only for a limited
10
Fig. 4.
Id3
n
:’-
00
I
II o2 10’
10’
I
I I
I
Ndmf
1
10
0
1
I
II ‘
0
‘
0
:
1
I
I
lo“
lo“
TABLE1. COMPARISON
OF EQUATION
( 1) AND
NARSIMHAN’S
CORRELATIONS
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This work was supported in part by the National Science 7 . Ergun, S., and A. A. Oming, lnd. Eng. C b m . , 41, 1179
Foundation Grant GP-560. (1949).
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8. Fan, L. T., and C . J. Swartz, Can. J . Chem. Eng., 37, 204
(1959).
NOTATION 8a. Fan, L. T., Kansas State Univ. BuU., 43, 4 (1959).
‘tp L 9. Fancher, G. H., and J. A. Lewis, lnd. Eng. Chem., 25,
zyxwv
= particle diameter,
1139 (1933).
f( ) = function of ( ) 10. Fetterman, C. P., M.S. thesis, Univ. Washington, Seattle,
g = acceleration due to gravity, L/02 (1958).
G,f = minimum fluidization flow rate, M/L20 11. Furukawa, J., T. Ohmae, and I. Ueki, Chem. High Poly-
Nca = Galileo number = 4 3 pf(ps - pf)g/pz mers, Tokyo, 8(2), 111 (1951).
N R e = particle Reynolds number = ( 4p f V / p ) 12. Johanson, L. N., Unclassified Rept. HW-52891, General
( N R e ) m f = particle Reynolds number at onset of fluidiza- Electric Co. (September, 1957).
tion 13. Kelly, V. P., M.S. thesis, Univ. Idaho, Moscow (1958).
N R e t = particle Reynolds number at terminal falling 14. Leva, Max, T. Shirai, and C. Y. Wen, Genie Chim., 75(2),
velocity 33 (1956).
V 15. Leva, Max, M. Weintraub, M. Grummer, M. Pollchik, and
= superficial fluid velocity, L/0
H. H. Storch, U . S . Bureau Mines Bull. 504 (1951).
pf = fluid density, M/L3 16. Lewis, W. K., E. R. Gilliland, and W. C. Bauer, Ind. Eng.
ps = particle density, M/L3 Chem., 41, 1104 (1949).
p = fluid viscosity, M/LB 17. Miller, C . O., and A. K. Logwinuk, ibid., 43, 1220 (1951)
emf = minimum fluidization voidage 18. Narsimhan, G., A.1.Ch.E. J., 11, No. 3, 550 (1965).
4s = 19. Oman, A. O., and K. M. Watson, Natl. Petrol. News, 36,
surface area of sphere having the same volume as particle R795 (1944).
20. Shannon, P. T., Ph.D. thesis, Illinois Inst. Technol., Chi-
surface area of particle cago ( 1961).
zyxwvutsrqp
’
21. Shirai, T., “Fixed Bed, Fluidized Bed, and the Fluid Re-
sistance. Heat Transfer and Mass Transfer of a Single
LITERATURE CITED Particle: Res. Rept., Tokyo Inst. Technol., Japan ( 195z).
22. Van Heerden, C., A. P. P. Nobel, and D. W. Van Krevelen.
1. Baerg, A.. 1. Klassen, and P. E. Gisher, Can. J. Res., F28, Chem. Eng. Sci., 1, No. 1, 37 ( 1951).
287 [igso j. 23. Wen, C. Y., and Y. H. Yu, Chem. Eng. Progr. Symposium
2. Berl., E., Catalog of Ditt and Frees, Wiesbaden (1930). Ser. No. 62, 62 ( 1966).
3. Blake, F. C., Trans. Am. Inst. Chem. Engrs., 14, 415
( 1922). 201 (1948).
-
24. Wilhelm, R. H., and M. Kwauk, Chem. Eng. Progr., 44.
Y
4. Bransom, S. H., and S. Pendse, lnd. Eng. Chem., 53, 575 25. Yagi, S., I. Muchi, and T. Aochi, Chem. Eng. (Japan),
(1961). 16.307 (1952).
5. Brownell, L. E., and D. L. Katz, Chem. Eng. Progr., 43, 26. Yn‘, Y. H., M.S. thesis, West Virginia Univ., Morgantown
537 (1947). ( 1965).
Residence time distributions are valuable for under- cases of practical interest, it is necessary to determine the
standing the performance of many continuous flow sys- distributions experimentally. This study investigates the
tems and for formulating mathematical models of such possibility of determining residence time distributions of
systems. The residence time distribution Y (X) referred process systems from experimental tests performed on suit-
to in this communication is defmed as: Y(X)dX is the ably scaled laboratory models.
fraction of the inflowing (outflowing) stream which will
spend (has spent) a time between X and X +dX in the CRITERIA FOR MODELS
system. For ideal cases such as plug flow, perfectly stirred
vessels, laminar flow, etc., the residence time distribu- As early as 1953 the conditions under which residence
tions may be obtained analytically. However, in many time distributions of large systems can be predicted from