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Mass Transfer in Semifluidized Beds

For Solid-Liquid System LIANG-TSENG FAN and YUNG-CHIA YANG


Kans.ar State University, Manhattan, Kansas

CH IN-Y UNG WEN


West Virginia University, Morgantown, W e s t Virginia

A new fluid-solid contacting technique known as Semifluidization has been studied. Mass
transfer data were obtained for a benzoic acid-water system, and correlations in terms of mass
transfer factors and over-all void fractions (for both packed and fluidized sections) are pre- depth and prevent the complete expansion
of the solid bed.
sented. Previous mass transfer correlations for fixed and fluidized beds are critically evaluated
with respect to the limitation and applicability and are discussed in relation to semifluidized-bedFor the second series of experiments the
mass transfer correlations. apparatus was modified.
In the first series only the inlet and out-
Semifluidization is a type of fluid- correlation of over-all mass transfer co- let concentrations were measured, whereas
solid contact operation in which the efficients and the comparison of the in the second series the axial concentration
expansion of a fluidized bed is partially correlations obtained with those of the gradient of the fluid was measured. Since
restricted. Under such conditions the fluidized and packed beds. the samples were obtained from inlet and
porosity of a semifluidized bed is inter- The relationships among the over-all outlet pipes in the first series of experiments,
mediate between the rigidly packed mass transfer coefficients, the mass they could be considered as the average
bed and the completely fluidized bed. transfer coefficients in each individual samples across the cross section of the
Some of the characteristics of a semi- bed, and the internal structure of the column. The sampling lines having l j 4 - h .
I.D. were employed in the second series of
fluidized bed, such as the simultaneous bed (that is, the relative size of the experiments. They were sufficiently large
formation of a packed section and a packed and fluidized sections in the to assume withdrawal of uniform average
fluidized section in the bed, were re- bed) were carefully considered. samples across the cross section of the
ported in a previous communication column, as evidenced by the fact that the
(9). The purpose of this paper is to EXPERIMENTAL concentration of outlet samples obtained
report the results of experimental work from the sampling line just above the top
The experimental apparatus consisted of of the screen was almost identical with
on the mass transfer aspect in a semi-
a main test column in which granular those obtained from the outlet of the
fluidized bed of a solid-liquid system. benzoic acid particles were dissolved by a column. The apparatus used in the latter
Aside from its practical significance measured stream of upward flowing water. series was the same as for the former
in mass transfer operations, the study A container was provided for retention of series, except the test section. This new
of rate of mass transfer is of general samples of each run for analysis. Figure 1 test section was made from a 2-in. I.D.
significance because it often leads to shows the diagram of the apparatus. standard iron pipe with cocks attached for
better understanding of other aspects Water was supplied from a 50-gal. con- sampling, at 2-in. spacings. A sheet of filter
of chemical engineering operations and stant-head tank ( A ) and was forced cloth was cemented to the inside wall over
heat transfer. through the system by a centrifugal pump the outlet of each cock to prevent the
Since the mechanism of interphase ( B ) . The water was initially directed plugging of the solid benzoic acid particles
through the globe valve and a flowmeter from the sampling lines. The sizes of
mass transfer in a fluidized bed is al- ( C ) as a means of controlling and measur- particles used (8 24 mesh) were much
N
ready complicated ( 4 , 2 4 ) , no particu- ing the rate of flow. The test column con- larger than the opening of the filter cloths,
lar attempts were made to analyze the sisted of two parts, a calming section ( D ) and the particles were freed from the dust
data in the light of the rigorous theo- and a test section ( F ) . The test section by a washing process suggested by Evans
ries of interphase mass transfer. Rather, was a vertical Pyrex tube 2 in. I.D. and and Gerald ( 8 ) . No escaping of the parti-
emphasis was placed on the empirical 24 in. high. Two brass plates clamping a cles from the sampling cocks was observed.
filter cloth ( E ) were placed between the Although the solubility of the benzoic
A WATLR TANK
calming and the test sections to establish acid in water is low, in order to minimize
(I?W? an even distribution of the upward flow. A the change of geometric shape of the par-
C ILOIYLTER
D C U Y l N D SCCTIOII
rigid close-fitting sieve plate ( G ) was at- ticles during the experimental runs the in-
E m . T U CLOTH tached to a long rod which could be moved dividual runs were not permitted to exceed
F TEST SECTION
B TO? SIEVE ?LATE
up or down to a fixed position. This was an 80-sec. duration. A decrease of less
M SAWLIMO OUTLET installed in the test column to adjust bed than 3% of the initial weight of the solid
I RCTLWTlON TbNK
particles for a single run was experienced.
Intermittent analysis of effluent liquid con-
centration during the run indicates that
steady state operation has been achieved.
....
...
-- ...
O

S I
I I

-.....
c
5
5 ...
:k ....
0..

...
I 11
e ..I 0.1

I
..I
11.
e.. ..I ...
Fig. 1. Diagram of experimental apparatus. Fig. 2. Axial concentration profile. Fig. 3. Axial concentration gradient.

A.1.Ch.E. Journal September, 1960


TABLE1. CALCULATION OF FmsT SERIES OF employed in the present investigation were
SEMIFLUIDIZED
DATA( REPRESENTATIVE RUNS) prepared in three screen ranges of 8 to 10
mesh, 12 to 14 mesh, and 20 to 24 mesh
Run by the method of Evans and Gerald (8).
no. T, "C. W, Ib. h., ft. h, ft. hi, ft. Several tests indicated that the reproduci-
bility of the particle characteristics by the
A- 1 22.3 0.4916 0.5888 0.8091 0.4008 Evans and Gerald method was excellent
B- 1 21.00 0.2533 0.2999 0.5008 0.3342 with deviation of less than A l % error.
c-1 22.60 0.2645 0.3093 0.4675 0.2550 Significant characteristics of the particles
are summarized in the Evans and Gerald
Run hP-7 X R over-all) DP, A, paper ( 8 ) .
no. ft. - -
E(
- ft. sq. ft. Solution saturated with the benzoic acid
used in the present investigation was found
A- 1 0.4083 0.6935 1.3732 0.6548 0.00690 10.40 by titration to be in agreement with the
B-1 0.1666 0.5555 1.6700 0.7129 0.004531 7.62 literature value ( 22 ) . Also this solubility
c-1 0.2125 0.6873 1.5114 0.6787 0.002610 12.50 can be represented by an equation reported
by Ishine ( 1 6 ) as a function of tempera-
Run G, lb./(hr.) G', C., CZ, kim, lb./(h.) Ns. ture:
no. ( sq. ft. 1 lb./hr. Ib./lb. lb./lb. (sq. ft. ) ( AC) -
A- 1 16,067 350.52 0.003140 0.001640 24.90 1,120
C, = 0.17 + 0.00197t + 0.00020t"
B-1 10,610 231.47 0.003005 0.001563 22.30 1,220 (t: 0" to 30°C.) (1)
c-1 4,500 98.17 0.003177 0.003051 25.38 1,110
This value was eventually used in this
Run Nsr investigation.
no. - -
r d
The dihsivity and Schmidt number of
the benzoic acid-water system were taken
A-1 64.48 48.33 140.0 0.1670 3.87 0.1245
B- 1
c-1
39.74
24.63
20.25
5.138
70.53
15.99
0.2400
0.6045
2.46
1.61
0.1745
0.4255
directY from the data of Chang ( 2 ) ,
quote by Linton and Shenvood ( 1 9 ) .
Values of the Schmidt number at four
temperature levels were also reported by
them (2, 1 9 ) .
TABLE2. CALCULATION
OF SECOND
SERIESOF Since the concentrations of benzoic acid
SEMIFLUIDIZED
DATA(REPRESENTATIVE
RUN) solution obtained in this work were very
low, viscosity and density of water were
Run employed to calculate the Reynolds num-
no. W, lb. ho, ft. h, ft. hr, ft. bers (50).

D- 1 0.3307 0.3613 0.5717 0'3484 RANGE OF EXPERIMENT


Run hm, X DP, A, € s, I n the first series of experiments
no. ft. - ft. sq. ft. - sq. ft. measurements included the following
D-1 o.023916 variables: exit concentration, water
0.2233 0.6182 0.006890 6.97 0.7004
temperature, water flow rate, and bed
d e p h Computed variables derived
Run Height of sampling outlet, ft. C, lb./lb. at C, CZ, from these measurements included k,
no. a b C a b C lb./lb. lb./lb.
J d , N R e , N,,, Ns,, and Yd. The ranges
D-1 0.2033 0.3700 0.5717 0.000215 0.000359 0.000943 0.00030 0.000943 of major variables were as follows:
Particle diameter: 8 to 10 mesh, 12
(AC) zm (AC)tm
Run C,, Packed Fluidized Packed Fluidized to 14 mesh, and 20 to 24 mesh.
no. Ib./lb. bed bed Over-all bed bed Over-all Water temperature: 16.8" to 24°C.
Over-all bed depth: 3 to 6 in.
D-1 0.002902 0.002271 0.002752 0.002405 0.002380 0.002752 0.002460 Voidage: 0.65 to 0.90.
Modified Reynolds number ( N R e ):
G, kim ktm 5 to 130.
Run lb./( hr.) G', Packed Fluidized Packed Fluidized Over- Shenvood number ( N S h ) :21 to 116.
no. (sq. ft.) Ib./hr. bed bed Over-all bed bed all Schmidt number ( N s , ) : 1,020 to
D-1 21,524 51,477 30.83 21.08 28.97 28.68 21.08 28.32 1,540.
The data and calculated results of
Run " ~ a "Re/( 1-e) NBD Jd some representative runs from the first
no. - ACim ACtm AC im ACtm series of experiments are tabulated in
D- 1 60.88 203.30 81.00 79.3 0.1588 0.1552 Table 1.*
Table 2' contains the measured and
Run Ns. (Nab €-2)/N 1/3 se Id calculated data of representative runs
no. - ACim ACtm C h Ctm for the second series of experiments in
which the axial concentration profile of
D- 1 1,290 5.03 4.91 0.1192 0.1167
fluid was studied in addition to those
variables mentioned above. A typical
All the experiments were carried out at sodium hydroxide with phenolphthalein in- axial concentration profile and concen-
room temperature, and the fluid temper- dicator. No difficulty was encountered in
ature was measured at the inlet and outlet securing reproducible end points. The acid *Tabular material has been deposited as
document 6347 with the American Documentation
of the column. The determination of the concentration varied from 0.0004 g. acid/ Institute Photoduplication Service Libraly of
concentration of the water sample was g. water to 0.0030 g. acid/g. water. Congress' Washington 25 D. C. 'and ma be
made by direct titration with 0.04 N. Granular particles of benzoic acid obtained'for $2.50 for p6otoprin& or 51.7% for
35-mm. microfilm.

Vol. 6, No. 3 A.1.Ch.E. Journal Page 483


Correlation line of author', data
-------------- Shirai'r carrdotion line
-_--- Carrelation line of Evans 6 Gerald8 data

mesh, first series

.) 20
-x
z
\
;
;10
1 0
0

-
z
f a
4

0.06 '' ' I " I I I I I ( I l l I


I
1 I 1
I 1 I l l 7
1 1
od
2 4 6 8 10 20 40 60 00100 200

NRe

Fig. 5. (Nsn e-Z)/Ns, 1/3 vs. Nine correlation of the experi-


mental data.

tration gradient curves obtained in the dC or


second series of experiments are illus- G-=~u(C,-C) (4)
trated in Figures 2 and 3 . The break dZ k i m = (l-X)(k,)xm +X(kpa)im

point at 0.52 ft. of bed height corre- Since there exists a finite discontinu- Equation ( 7 ) may be transformed into
sponds to the boundary of fluidized ity in the axial concentration gradient
bed section and fixed bed section at
which a distinct discontinuity of con-
at the interphase of the fluidized and c, - c,
Gln -= k,, A
packed beds, (9)
centration gradient exists. c, - c,
dC '2 dC or
ANALYSIS AND CORRELATION
G f c c +Gl1= = G' (C, - C,)
OF RESULTS klm
(10)
To derive the rate equation for the A(AC),,
mass transfer between the solid parti- = (k,)Im a, r d z
In order to account for the effect of
cles and fluid in the semifluidized bed axial mixing, which was neglected, k,,
the following assumptions were made:
1. The concentration of the fluid in
+ (kps) In, up. JrdZ (5) must include a correction factor F sug-
gested by Epstein (7, 1 3 ) .
contact with the particle surface is In case the axial concentration data
or are available, as in the second series
equal to the saturated concentration.
2. The velocity distribution and
Gln - Gln-
c, - c, + c, - c, of experiments, the value of k in each
concentration of fluid are uniform at bed can be directly calculated by use
any cross section of the test section.
c,- c, c, - c, of the integrated mean driving force
as
3. The surface area of the particles
per unit volume in each bed is uni-
= (k,)Im ath, + ( h e ) l m a p a h p a
form. G' (C1- CO)
(6)
4. Axial turbulent diffusion coeffi-
cient, E,, in each bed remains constant But Equation can be further
under definite flow conditions. simplified: and
5. The process is isothermal.
The following material balance could Gln-
c.. - c, = (k,),,,,A, +
be obtained for any bed height: c. - cz
(kpa)imApe (7) The over-all mass transfer coefficient
based on integrated mean driving force
If the weighted mean value of over- may be evaluated as
all mass transfer coefficient is defined
as
When one assumes that longitudinal or
axial mixing in the bed can be negligi-
ble

Then Equation ( 2 ) can be expressed


as (1, 5 )

Page 484 A.1.Ch.E. Journal September, 1960


Equation (13) implies that The data obtained in the second ( 1 - c ) . It clearly indicates that Evans
series of experiments are also similarly and Gerald's (8) data also deviate con-
correlated, and the results are plotted sistently from the original correlation of
on Figures 4 to 6 again for comparison Chu et al. ( 3 ) with approximately the
with the results of the first series of same magnitudes as those of the semi-
experiments. fluidized bed data. Their packed bed
data are correlated as
DISCUSSION AND CONCLUSION
First, the mass transfer data were
correlated in terms of the Id factor and In order to evaluate the effect of the Id= 2.132 (+)-a'K12 (20)
1-
modified Reynolds number as is illus- packed-bed formation on the mass
trated in Figure 4 ( 3 , 1 4 ) . The mass transfer in the fluidized bed, the mech- and the fluidized bed data are corre-
transfer coefficients were calculated on anism of the packed-bed formation lated as
the basis of the over-all logarithmic should be understood. The size of the
mean driving force, as was done by packed-bed section formed must be N R s

other investi ators ( 3 , 8) for the estimated by an equation including the J d = 1.340 1- (7)
(21)
%
packed- and uidized-bed mass trans- independent variables of the experi-
fer. The effect of natural convection on ment and the characteristics of ordi- The over-all correlation of Evans and
the rate of mass transfer which would nary fluidization under similar flow Gerald's (8) data may be expressed as
become appreciable for the large parti- conditions. Such an equation was al-
cles ( D , > '/4 in.) at the very low
(7)
-8.480
ready reported by the authors in the N'Re
Jd = 1.680 1 - (22)
Reynolds numbers as indicated by previous communication (9).
Gaffney ( 1 2 ) was neglected, and no It was also reported in the commu-
attempt was made to introduce Grashof nication that the over-all mass transfer Comparison of Equations (22) with
number in the correlation of data. coefficients based on the over-all loga- (15) reveals that within the range of
The broken line in Figure 4 represents rithmic drivin forces can be correlated the variables of the present investiga-
the generalized correlation used by P
by use of J d actor suggested by Chu tion and the errors of experimentation
Chu et al. ( 4 ) to correlate the mass and his co-workers ( 3 ) within the the semifluidization data may be cor-
transfer data for both packed and range of maximum probable deviation. related as well as the data for ordinary
fluidized beds. The solid line correlated Referring to Figure 4, one can see that fluidized and packed beds by use of
all the semifluidization data with the Chu's original Jd factor correlation the Id factor VS. W R e / ( l- E ) plot
magnitude of the deviations compara- yields J d values consistently higher based on the over-all logarithmic mean
ble to the correlation used by Chu than the present experimental data. mass transfer coefficient, k,,.
et al. ( 4 ) . The equation for the solid Chu's correlation pertains only to the The data for the benzoic acid-water
line was found to be ordinary fluidized and packed beds. system were not included in Shirai's
The maximum deviation of the present ( 2 3 ) generalized correlation covering
d] z= 1.865
N)&#
l--E
(-) (15) data based on his correlation appears the data of the fluidized bed, fixed
to be 22% in the range of Reynolds bed, and a sin le particle. Evans and
numbers used. Evans and Gerald's (8) Gerald's (8) ata were again recor-
Shirai ( 2 3 ) presented the following data for the benzoic acid-water system related by the method suggested by
f
correlation of the mass transfer data in were not included in the original cor- Shirai ( 2 3 ) as illustrated in Figure 5 ,
the particle beds as suggested by the relation by Chu et al. ( 3 ) . They were which indicates that the experimental
boundary-layer theory (10, 16): recalculated in terms of J d VS. W R e / data were consistently lower than the
N ~ , -= +
E 2.0 0.75 Nge1" Nsdl'
(16)
Figure 5 shows the similar correlation
for the present data and a comparison
Correlation linr of aulhorb data
with Shirai's equation ( 2 3 ) . The re-
gression line through the data is ex-
__-__ Wnlation line of Evom8 CornIda data

pressed as
Nshc = 2.0 + 0.46 N',,O.MNs,"."
(17) mesh, second srrir
To take the effect of molecular dif-
fusion and natural convection into ac-
count the Id factor can be modified as
(23)

The s d factors are also correlated as a


function of " R e / ( 1 - -E) in Figure 6,
which yield the relationship

or
Nke, (I - 8 ,
Nsh = 2.0 + l.51[ ( 1 - -E)N'R~]''*
Fig. 6. I'd factor vs. Nm/(l-e) correlation of the experimental
( N s c ) 'I8 (19) data.

Vol. 6, No. 3 A.1.Ch.E. Journal Page 485


calculated values by approximately
38%. This is, however, within the
range of accurac expected from the
K
generalized corre ation of Shirai ( 2 3 )
for any specific system. Evans and
Gerald’s data are expressed as follows:
For packed bed:
N s h ~= 2.0 + 0.424 N’R,o’” Ns;l8

(23) 0
For fluidized bed:
Nshe = 2.0 + 0.230 NR80.868 NS:ls

Fig. 7. Comparison of experimental value of mass transfer


(24)
factor with those of hypothetical models.
For over-all correlation:
Nsae = 2.0 + 0.312 N’R.0.808 Ne.1”
as described above in correlations of
combination of Equations (14) and
In spite of the similarity and analogy
(30). Equation (30) enables one to
(25) the mass transfer data in the fluidized,estimate the over-all mass transfer co-
semifluidized, and packed beds, a efficients from the knowledge of ordi-
The over-all correlation expressed by semifluidized bed may be considered nary packed and fluidized beds oper-
Equation (25) is again very similar to neither a uniformly compressed fluid- ated under the same conditions. By
that for the semifluidized-bed data ex- ized bed nor a uniformly expanded varying X, which in turn depends on
pressed by Equation (16) and Figure packed bed as illustrated in Figure 7. the over-all porosity of the bed and
5. These similarities of the correlation The lines in Figure 7 correspond to the can be arbitrarily fixed for the semi-
between the ordinary packed beds and ratios of Equation (15) with Equa- fluidized bed, one should be able to
semifluidized beds by use of the meth- tions (20) and (21) respectively. The obtain any value of k between k f and
ods suggested by Chu et al. ( 3 ) and over-all mass transfer coefficients in kpa, Since 1 - c = ( 1 - c,) / R , Equa-
Shirai ( 2 3 ) would indicate that it is the semifluidized bed appear greater tion (15) or (19) indicates that ap-
possible, at least for the purpose of than those of the hypothetical uni- proximately such a change of over-all
correlation, to consider the semifluid- formly compressed fluidized bed with k can be controlled as inversely pro-
ized bed to possess uniform solid-dens-
ity distribution. When correlations are
the same over-all bed porosity and
smaller than those of the hypothetical
portional to dx.
This could be illus-
trated by use of the data from the ex-
not available for any specific system uniformly expanded packed bed. As perimental runs at G = 28,000 lb./
for semifluidization, the generalized can be seen from the formation of the (hr.) (sq.ft.) with the mean deviation
mass transfer correlation of the ordi- distinct sections of the fluidized and of 7%. It may be desirable to point
nary packed and fluidized beds may packed beds, which are aligned in out again that under definite 00w con-
be employed to estimate the mean series, the over-all mass transfer coeffi-
ditions the values of k, for fluidized
mass transfer coefficients. cients in the semifluidized beds would and k,, for packed beds, unlike the
Equation (19), which was derived be expected to be a weighted average corresponding k in the semifluidized
by modification of the J d factor correla- between k, and k,, obtained under the bed, are fixed for any particular system.
tion to the present data, yields a mean same flow conditions. This fact is ex- In the first series of experiments the
deviation of 11.7%; Equations (15) pressed as Equations ( 8 ) and (14). axial concentration profile was not de-
and (17) give a deviation of 9.87% Mass transfer coefficients calculated termined, and the logarithmic driving
and 11.73% respectively. This implies from these equations gave the mean force was made use of in the correla-
that the use of the modified correlation deviations from the experimental val- tion of the data. It has already been
as expressed by Equation (19) does ues of -0.78 and -4.3% respectively. pointed out that the k,,,, must contain
not improve the correlation; however, Since (9) in itself the F factor of Epstein ( 7 ) .
the form of this equation would agree The importance of the axial mixing in
with the expression predicted by the the solid-liquid contact process has
boundary-layer theory ( 16). been emphasized by various investi-
Evans and Gerald’s (8) data were gators recently (7, 26). However it
recorrelated in the form of Equation appears that so for there is no way to
( 1 9 ) . The packed-bed data are corre- predict exactly the axial mixing coeffi-
lated as cient of a particular system under cer-
Equation ( 8 ) can be written as
Nsa = 2.0 + 1.483[ ( 1 - C) N’xe]112
tain operating conditions with sufficient

(Nsc)’18 (26)
[
kl, = 1-
p,S(l--EPY)(h,.-h)
W
accuracy for mass transfer calculations.
But there is good indication that axial
mixing in the liquid-solid systems is
and the fluidized-bed data are corre- much less extensive than in the gas-
lated as solid systems (21, 2 6 ) . In Figures 4, 5,
and 6 the mass transfer coefficients cal-
Nsa = 2.0 + 1.031[ ( 1 - e)N’Re]’’’
p a S,(1- ep.) (h,,? -h) culated by use of the integrated mean
( N s c )‘Is(27)
+ W
driving force are compared with the
correlation obtained in the first series
An. over-all correlation equation may (1 - .,) of experiments. They indicate that the
be expressed as (kpa) Im (30) deviation of the second series experi-
(6, - CPB)
mental data from the correlation are
Ns, = 2.0 + 1.202[ ( 1 - e)wRe]112
An equation similar to Equation (30) within the range of the first series of
( Nsc)Iia (28) to estimate k,, can be derived by a experiments. This implies that the

Page 486 A.1.Ch.E. Journal September, 1960


F factor included in the correlation of University, for his advice and encourage- Subscript
the data in the first series of ttte experi- ment and also to the Kansas State Uni- f. = completely fluidized bed or
ments were close to unity; in other versity Engineering Experiment Station for ordinary fluidized bed
words the effect of axial concentration financial support. f = fluidized bed
gradient change and fluid mixing were p = particle
small. Since an over-all mass transfer NOTATION pa = packed bed
based on integrated mean concentra- = total particle surface area, 0 = at bed inlet
tion difEerence is employed, the radial sq. ft. 1 = at interface between packed
mixing effect is not considered here. and fluidized beds
= concentration of benzoic
The maximum deviation of the values 2 = at bed outlet
acid in water stream, lb./lb.
of F from unity for the second series m = mean value
= concentration of benzoic acid
of experiments was 7.65%. lm = logarithmic mean value
As indicated in the introduction, in saturated solution, lb./lb.
tm = integrated mean value
probably no theories of interphase mass = differential bed height, ft.
transfer based on the simple models = equivalent spherical particle
diameter, ft. LITERATURE CITED
can be adopted in the correlation of
mass transfer data in the packed or = diffusivity of benzoic acid in 1. Bennett, J. A. R., and J. B. Lewis,
fluidized bed. Danckwerts ( 4 ) in his water, (sq. ft.) /hr. A.Z.Ch.E. Journal, 4, 419 (1958).
review paper suggested the necessity = longitudinal mixing coeffi- 2. Chang, S., M. S. thesis, Mass. Inst.
Technol., Cambridge ( 1948).
of the theory difEerent from either the
boundary-layer theory or the surface-
renewal theory to explain the behavior
of gas absorption by liquid in the
cient, (sq. ft.) /hr.
= correction factor, dimension-
less
x
3. Chu, J. C., ames Kalil, and W. A.
Wettereth, C em. Eng. Progr., 49, 141
(1953).
= function of 4. Danckwerts, P. V., A.Z.Ch.E. Journal,
packed bed. The results of mass trans- = superficial mass velocity, lb./ 1, 456 ( 1955).
fer investigation by Johnson and (hr.) (sq. ft.) 5. - , and A. M. Kennedy, Trans.
Huang (17) using a series of organic = mass velocity, lb./hr. Inst. Chem. Engrs., 32, S 49 (1954).
acids including benzoic acid suggested 6. Eckert, E. R. G., “Introduction to
= height of the top sieve plate
the applicability of the surface-renewal Heat and Mass Transfer,” McGraw-
or over-all depth of bed, ft. Hill, New York (1950).
theory to the interphase mass transfer
= depth of height of initial 7. Epstein, N., Can. I. Chem. Eng., 36,
between solid and liquid. They too
bed, ft. 210 (1958).
however indicated the difficulty of ap- 8. Evans, G. C., and C. F. Gerald, Chem.
= height of fluidized bed sec-
plying the surface-renewal theory di- Eng. Progr., 49, 135 (1953).
rectly to the mass transfer in packed tion, ft.
9. Fan, L. T., Y. C. Yang, and C. Y. Wen,
beds because of the variation of the = height of packed bed sec-
A.1.Ch.E. Journal, 5, 407 (1959).
local conditions in the packed tower. tion, ft. 10. Frossling, N., Gerlands Beit. Geophys.,
A recent study by Bennett and Lewis = mass transfer factor, dimen- 52,170 ( 1938 ) .
( 1 ) indicated that the direct applica- sionless, [ ( k / G ) N82Ia] 11. Fuchs, N., 1. Phys. (U.S.S.R.), 6, 224
bility of the surface-renewal theory to = modified mass transfer fac- (1934).
the interphase mass transfer between tor, dimensionless 12. Gaffney, B. J., and T . B. Drew, Znd.
the benzoic acid and water is doubtful = mass transfer coefficient, lb./ Eng. Chem., 42, 1120 (1950).
hr. (sq. ft.) (unit C) 13. Galloway, L. R., W. Komarnicky, and
even in the rotating-cylinder apparatus N. Epstein, Can. I. Chem. Eng., 35,
with very simple geometry. Thus fur- = mass transfer coefficient, ft./
139 (1957).
ther complication in application of hr . 14. Gamer, F. H., and R. D. Suckling,
theories to the mass transfer in semi- = distance in axial direction of A.1.Ch.E. Journal, 4, 115 (1958).
fluidized bed can be easily expected bed, ft. 15. “International Critical Table,” Mc-
because of its complex structure. As = modified Reynolds number, Graw-Hill, New York ( 1926).
Equation (19) indicates, 1/3 power of dimensionless, ( D p G / p ) 16. Ishine, T., T. Otake, and T. Okaka,
Schmidt numbers has been used in the = Schmdit number, dimension- Chem. Eng. ( J a p a n ) ,15, 255 ( 1951).
present study (with a mean deviation less 17. Johnson, A. I., and C. J. Huang,
of 11.7%), which is, as described pre- = Sherwood number, dimen- A.1.Ch.E. Journal, 2,412 (1956).
sionless 18. Lemlich, Robert, and Isidoro Caldes,
viously, based on the boundary-layer Jr., ibid., 4, 376 (1958).
theory (11, 1 6 ) . Recent theory pro- = bed expansion rate, dimen-
19. Linton, W. H., Jr., and T. K. Sher-
posed by Toor and Marchello ( 2 4 ) sionless wood, Chem. Eng. Progr., 46, 259
would predict that the power for N n c = cross-section area of the col- (1950).
should vary depending on the system umn, sq. ft. 20. Perry, J. H., “Chemical Engineers’
and local flow conditions. It should be = temperature, “ C . Handbook,” 3 ed., McGraw-Hill, New
pointed out that in view of the rela- = over-all volume of the bed, York ( 1950).
tively small range of Schmidt numbers cu. ft. 21. Richardson, J. F., and A. E. Mitson,
covered in the experiments, extensive = weight of the particle bed, Trans. Inst. Chem. Eng., 36, 270
extrapolation of the empirical correla- lb. (1958).
= weight fraction of particles 22. Seidell, A., “Solubility of Organic
tions presented in this paper must be Compounds,” 3 ed., Van Nostrand,
approached with caution. in the packed bed section, New York ( 1941).
The possibility of the practical ap- dimensionless 23. Shirai, T., Ph.D. thesis, Tokyo Inst.
plication of semifluidization has been Tech., Tokyo ( 1955).
Greek Letters
described in the previous communica- 24. Toor, H. L., and J. M. Marchello,
tion (9). E = void fraction or porosity in A.Z.Ch.E. Journal, 4,97 (1958).
the bed, dimensionless 25. Wakao, N., T. Oshima, and S. Yagi,
P = fluid density, lb./cu. ft. Chem. Eng. ( J a p a n ) , 22, 780 (1958).
ACKNOWLEDGMENT PB = bulk density of the solid, 26. - , ibid., p. 786.
The authors express their appreciation lb./cu. ft. Manuscript received August 13 1959. revbwn
to Henry T. Ward, Head of the Chemical P. = solid density, lb./cu. ft. received December 7 1959. )pa er ’accepted
December 16, 1959. Palper preientecfat A.1.Ch.E.
Engineering Department, Kansas State P = viscosity, lb./(hr.) (ft.) Atlonta meeting.

Vol. 6. No.
~-3 A.1.Ch.E. Journal Page 487

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