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Lu and Wang ( 3 ) . This has the advantage that in the x = mole fraction
absence of quaternary data, the corresponding &jkl may y = activity coefficient
be set to zero to obtain a better approximation than by
setting (Eijkl - C i j k l ) to zero. LITERATURE CITED
1. Benedict, M., C. A. Johnson, E. Solomon, and L. C. Rubin,
NOTATION Trans. Am. Inst. Chem. Engrs., 41, 371-392 (1945).
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 (1)
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 V Van Heerden, et a l . ( Z Z )
the two consecutive sieve openings without introducing
serious errors ( 2 6 ) . 0 Fancher and Lewis (9)
The major differences between the two correlations are o.ol - Narsimhan's correlation I
the minimum fluidization voidage emf and the shape factor 0.001 aooz 0.004 aoi aoz 03
4%.
1. Narsimhan considered that for spherical dp (in.)
emf has the value of 0.35 and is independent of trrticles
e parti-
cle diameter, provided that the wall effect can be neg- 986 emf
Fig. 1. Correlation of voidage shape factor function .-
lected. From the literature data (16, 20, 2 4 ) , as well as (1 -emf)2
0
I I I I I / I
001
0008
V
0.006
0.004
o LIYO, e i 01 (151
S h i m (21)
van Heerden, et 0 1 (221
Io 0
Brownell and Kot2 (51
Foochar and Lewis ( 9 )
Norsrmhanr 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
TABLE1. COMPARISON
OF EQUATION
( 1) AND
NARSIMHANS
CORRELATIONS
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