Sie sind auf Seite 1von 9

162 Ind. Eng Chem. Process Des. Dev.

1982, 21, 162-170

Generaiized Correlation for Mass Transfer in Packed Distillation


Columns
Jose L. Bravo and James R. Fair’
Department of Chemical Engineering, The University of Texas at Austin, Austin, Texas 78712

An improved correlation of mass transfer rates for commercial-scale packed distillation columns has been de-
veloped. The correlation is based on effective area for mass transfer

a = 0.498a p($)(Ca ,Re,)0.392

,,
where a e is effective area for transfer, a is specific surface of the packing material, Z is height of packed bed
(ft), u is surface tension (dynkm), and CaLand Re, are dimensionless liquid capillary number and gas Reynolds
number, respectively. Packings represented are of the randomly arranged ring and saddle types. Basic data are
from a bank of 231 evaluated runs covering eleven distillation systems. The correlation Is shown to be more reliable
and more general than previously published models, with 96% of the calculated data falling within f20% of the
observed values. For 95% confidence in design, a 1.6 safety factor is required.

Packed columns have been used extensively for distil- from simple, naturally occurring materials, such as chunks
lation applications, especially those in which pressure drop of coke, to carefully fabricated geometric shapes such as
is critical. The columns have usually been filled with metallic or ceramic saddles, and from tiny devices for
randomly arranged packing elements of the ring or saddle laboratory use to large commercial packing elements with
type, and it is on these “random packings” that most ex- nominal sizes of 3 in. and larger.
perimental investigations of mass transfer rates have been An extensive review of earlier data pertinent to com-
made. While there is increasing interest in the so-called mercial operations was presented by Cornel1 et al.
“regular packings” (mesh, grids, etc.), their applications (1960a,b). These data are mainly from studies that used
tend to be limited by high cost and incomplete perform- either Berl saddles or Raschig rings. Also, the data were
ance documentation. These latter packings are normally obtained largely from tests with unidirectional mass
handled on a proprietary basis through the experience of transfer, gas-to-liquid or liquid-to-gas. A more recent paper
their vendors. by Charpentier (1976) presents a good general overview
In 1979 Bolles and Fair described a large data base that of additional data and of some of the approaches that
they assembled from published tests of flooding, pressure investigators have used in dealing with the prediction and
drop, and mass transfer in columns containing random description of mass transfer in packed columns.
packings. They utilized the base to evaluate existing As noted earlier, the 1979 paper by Bolles and Fair
packed column models. They did not attempt to improve included an extensive data bank for a wide range of
the existing models for flooding or pressure drop, but did packings, column sizes, and systems. Many of the data
develop a mass transfer model that was superior to those in this bank are for distillation conditions and include
previously published. Their model generalized on fluid results of work done by Fractionation Research, Incorpo-
properties and flow rates, but required two inputs: prior rated (FRI). This data bank provided all of the model
validation for a specific packing type and size, and a validation material for the present work. As is appropriate
consistent (if not completely reliable) method for pre- for differential contacting, the Bolles and Fair model
dicting the flooding condition for the system and packing utilizes the transfer unit approach, equivalent to the mass
under scrutiny. transfer coefficient approach
The present work represents an attempt to develop a
general design model for distillation applications, a model
that would not require previous validation for the packing
type or size and which hopefully could be extended to the where the effective interfacial area a, may differ from the
regular packings. Furthermore, the Bolles-Fair require- actual interfacial area.
ment of flooding knowledge was thought to be an encum- The volumetric mass transfer coefficient KOGae in eq 1
brance as well as a limitation on reliability, and it was may be divided into coefficient and area components for
hoped that such requirement would not be needed with fundamental analysis, and this approach has been used by
a new model. The model, if successful, could then be a number of workers (Shulman et al., 1955a-c; Yoshida and
applied to a variety of packing sizes and shapes while still Koyanagi, 1954; Onda et al., 1968,1972;Hughmark, 1980).
being general with respect to properties and flow condi- Most of the work was confined to Raschig ring and Berl
tions; in view of the continuing development of packing saddle packings.
types, such a model should be well received by process The work by Shulman can be considered as the basis
engineers and packing vendors alike. for the present effort, as it has been for most other mass
Previous Work transfer efficiency studies that describe the transfer
A vast amount of literature dealing with mass transfer coefficient and the effective area.
in randomly packed columns is available. Studies have The work by Onda and co-workers is based on the
covered a wide variety of packing types and sizes ranging concept of wetted packing area, as opposed to interfacial
0196-4305/82/1121-0162$01.25/0 0 1981 American Chemical Society
Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1, 1982 163

area. The work draws on the earlier efforts by Yoshida Both correlations for the individual mass transfer
and co-workers and uses the wetted area as a geometric coefficients show the same type of dependence on key
parameter in determining the Reynolds number for the variables such as diffusivity and velocity.
liquid. The equations describing kL and kG in the Shulman
The Onda and Shulman models, which form a part of model are
the basis for the present model, will be described fully in
the next section.

z]
Model Development
The two-film mass transfer model as well as the concept 0.45
of the transfer unit provide the basis for this work. Al-
ternate maw transfer models based on the penetration and kLdp/DL = 25.1[ (SC~)O.~O (9)
surface renewal theories may provide a more realistic
physical description of the mass transfer mechanisms, but In eq 8 and 9 d , is the diameter of a sphere having the
at the present stage of development they have not changed same surface area as an element of packing under con-
significantly the mass transfer relationships based on the sideration.
film model. On the other hand, the model developed by Onda is
An exception to the above may be found in the value described as follows
for the exponent affecting the diffusion coefficient in the
general flux equation. The two-film theory predicts an
exponent of unity whereas the penetration theory predicts
a value of one-half. The applicable mass transfer coeffi-
cient correlations, especially the two used in the present
work (by Shulman and by Onda), show a dependence on
the diffusivity intermediate between film and penetration
predictions: a two-thirds exponent for the gas side and
[ pL
kL( gPL )"'I = 0.0051( %PL ) 3 ( S c L ) - 1 / 2 ( a p d

(11)
a one-half exponent for the liquid side.
Using the two-film model, and allowing for significant
resistance to mass transfer in both phases, the overall
transfer unit height results from individual phase transfer
unit heights (12)
HOG = HG + AH, (2) where
where X = mGMLM, or the ratio of slopes of the equilibrium L
and operating lines. RetL = - (13)
UpPL
The integration of the general flux equation, coupled
with the definition of the number of transfer units, leads aPL2
to defining expressions for the heights of individual FrL = - (14)
transfer units gPL2
HG = G / ( ~ G ~ ~ ' M G ) (3) L2
WeL= -
H L = L/@ L ~ , P L ) (4) apWL
where a, is the effective interfacial mass transfer area. and u,, a critic& surface tension, = 61 Ljm/cm for ceramic
At this point it is important to note that the value for packings, 75 dyn/cm for steel packings, and 33 dyn/cm
a, in a given system is considered equal for the gas and for polyethylene packings.
liquid phases, since it consists of the area through which The data bank provided input variables to enable cal-
mass transfer occurs at the interface. It is also to be ob- culation of effective areas by the Shulman and Onda
served that the value of a, is composed not only by the models. These areas were compared with the known
wetted area over the packing but also by the area provided specific areas of the packings used.
by suspended and falling droplets, gas bubbles within The Onda correlation gave more moderate a, values than
liquid puddles, ripples on the liquid film surface, and any the Shulman correlation (a, values never greatly above the
contribution from film falling on the walls of the column. value for the specific area, a,, of the packing under con-
A combination of eq 2, 3, and 4 gives sideration) and also covered a wider range of packing types
and sizes as well as test systems. Therefore, it was selected
a, = ( a 3 G + XaaL)/HOG (5) as a source of kL and kG values. It was recognized that
Thus, an effective area can be calculated from available future work leading to improved methods for predicting
mass transfer coefficients kG and kL, themselves based on kL and kG could lead to improvements in the present work.
known values of G , L, MG, ML, P, and pL. Because of the nature of the hydraulics and geometry
Clearly, the selection of a specific mass transfer coef- of packed beds with gas and liquid in counterflow, a cor-
ficient correlation is critical to the present work. The respondence between liquid holdup and effective transfer
correlations by Onda and co-workers (1968,1972) and by area is to be expected; thus, the trends observed in liquid
Shulman and co-workers (1955a-c) were selected for our holdup behavior at varying loading conditions should apply
analysis because they conform to the commonly accepted for effective area. Also, an added gas kinetic energy effect
functionalities should be included for the area analysis because of its
influence on film surface rippling, liquid droplet dispersion,
k$MG/G = QReG'ScG" (6) and the occurrence of gas bubbling in puddles. It can be
and reasoned that the behavior of liquid holdup for different
flow conditions should be similar to that of the interfacial
kLC&lL/L = Q'ReLrScLs (7) area, the latter possibly showing a greater influence from
164 Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1, 1982

gas velocity and density. Accordingly, a significant gas Table I. Symbols for Figures 1-17
effect was included in the present work since it is generally
practical to operate commercial packed columns a t high A Cyclohexane/n-Heptane 5.0 p s i a
gas loadings and relatively close to flooding conditions.
In analyzing the various forces acting in such systems, X Cyclohexane/n-Heptane 24.0 p s i a
it was concluded that an improved correlation should be
able to deal with the following considerations. (a) The
effective transfer area should be proportional to the liquid
+ n -But ane/i-But ane 165.0 p s i a
rate since increased liquid velocities would provide a better
wetting of the packing, rippling of the film surface, and 0 %Pro panol/wat e r 14.7 psia
a more effective renewal of the liquid in the puddles. (b)
Systems with low surface tensions should provide increased X Sthylbenzene/Styrrne 2.0 p s i a
wettability as well as smaller droplets yielding in this sense
more interfacial area. On the other hand, a lower surface
tension would make the liquid separate more easily from
m Methanol/Ethanol 14.7 p s i a

the packing at high gas rates, thus reducing the effec- 0 Ethanol/water 1L.7 p s i a
tiveness of the packing. (c) Increased kinetic energy of the
gas should tend to increase the effective area. (d) A
packing with a high specific surface should yield a rela- 23 Ethylbenzene/Styrene 1.0 p s i a
tively high value for the net interfacial area under similar
flow conditions. (e) A correlation for liquid maldistribution X n-Heptane/Toluene 1L.7 p i a
due to column height and diameter should be expected.
With these considerations in mind, and after different Y NHg/H2Q/air 1L.7 p s i a
schemes were tried unsuccessfully, the following func-
tionality was proposed X o2/H20/air 1L.7 p s i a
a e p / a p = f(L,G,ZPc,u) (16)
The values for asp(the effective mass transfer area for the + Benzene/Dichloroethane lL.7 p s i a
packing alone) were obtained by correcting the total ef-
fective area (a,) for column wall effects .%p 1-Oct ane/Toluene 20.0 p s i a
uep = U , - CY~/D, (17) Various combinations of these dimensionless groups
were tried in searching for the best grouping of the data.
The factor a allows for wall blockage by packing elements Most combinations showed a very significant packing
and should not exceed unity. For the present work a value size/type dependence, and in most instances, the trends
of a = 1.0 was assumed, since for large columns the wall followed by the correlating coefficients were not distin-
correction essentially disappears. guishable among the different packings and were highly
Modification of the fmdings of Cornell et al. (196Oa) and random. For these cases, it was impossible to establish a
of Fair and Moczek (1964) led to a corrected effective relationship between the variation in the value of the
packing area correlating coefficients with the differences in packing size
a* = a,J04/&5 (18) and type.
To circumvent this problem, a function of the type
where a* is an adjusted effective area suitable for analysis u * / u , = A(CULX ReG)b
or design of commercial equipment. Equation 20 proved (22)
to be a good choice since all of the available data grouped was used, and ita application showed all the data for either
very nicely when the adjustment, combined with the distillation or absorption (each operation independently)
previously mentioned diameter correction, was applied. It in what appeared to be one single group, regardless of
should be noted that eq 18 is dimensional, although it packing size or type. This finding led us to the proposal
could be made dimensionless by using height and surface of one single correlation for all of the packings studied.
tension ratio to base values (e.g., 2 = 10 ft and a, = surface The form of the equation selected meets all of the re-
tension of water = 72 dyn/cm). As used in this work, 2 quirements outlined above with the added advantage of
has units of feet and u has units of dyn/cm. generality toward packing size/ type. Nevertheless, this
In order to incorporate the liquid and gas rate effects form has some limitations, particularly in distillation using
as well as the contributions from the viscous forces within low reflux ratios. These limitations are discussed in the
the liquid, the following dependence was then proposed Conclusions section and some recommendations are also
a*/ap = f ( C a ~R, e d (19) made.
Data Presentation and Correlation
In eq 19, CuL is the dimensionless capillary number The functional relationship of eq 22 is shown in Figure
CUL = NLL/(PLugc) (20) 1 through 13 (see Table I for symbols) for the packings
listed in Table 11and the systems listed in Table III. The
which provides the ratio of viscous forces to surface tension values of a*/apwere obtained from the Bolles-Fair data
forces. The dimensionless Reynolds number ReG is defined bank by using physical properties at the experimental
as conditions, the geometric parameters of the experimental
ReG = ~ G / ( ~ , , P G ) (21) column and packing, mass transfer coefficients computed
by the Onda model, and the reported equilibrium and
which in turn provides the ratio of inertial forces to viscous HETP or Hm data. The systems analyzed, as well as their
forces in the gas. Note that the length criterion is the important physical properties, are shown in Table 111.
diameter of a sphere having the same surface to volume An inspection of Figures 1-13 shows clearly that the
ratio as the packing element under consideration. functionality of eq 22 holds regardless of the system and
Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1, 1982 185
0 a
VI 1"CERRMIC 8. S. VI
1"CERRMIC R . R.
-1 -1
a

,.
N N
O

d
I I
I I
I I
al
0 I a
al
I
0 f 0- I
e
a
I a.
a
\ / \

:: Master c o r r e l a t i o n / Master c o r r e l a t i o n

0
\y/ 0-
/
m
0

6-

bO '
dI ' Ibl '
"""" ' """ 1b2 '
1b3 1b4 Yb
C F I L s R E G s l E 03
Figure 1. Area ratio for 1-in. ceramic Berl saddles. Figure 4. Area ratio for 1-in. ceramic Raschig rings.

0
VI VI
0
1/ 2 ' 'CERFIM I C R. R. 1. 5 ' ' C E R R M I C R . R .

a
N
I' I
I
I I
I I
I
0
m I
/I
e
a
\
0-

/
; Master correlation

2:
&-

m
d
Master c o r r e l a t i o n

/.
/

0
/
0- /
/

0
a
VI
3 / 4 ' ' C E R F I M I C R. R. 3"CERFiMIC R. R

1'
Ln

7 X

XX
I I
I i
I I

a.
/ d x !I
I

a
1 x//
\'
Master c o r r e l a t i o n /
/
x /
/ /
/
/

3-
/'
/ X
/
/
/ Master c o r r e l a t i o n
/,/

a
0 //'

C F I L s R E G s l E 03
Figure 3. Area ratio for 3/r-in. ceramic Raschig rings. Figure 6. Area ratio for 3-in. ceramic Raschig rings.
166 Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1, 1982

0
Lo Lo
0
1 ' ' M E T i l i 8. R. 5 / 8 ' ' M E T R L P. R.
-1

/ I
0 / I
I 0 I
I
L
a & I
\
/
/
/
/
/
/
/

In
0
1. 5 ' ' M E T F I L R . R.
-1

I . /
I I
I I
I O
m I
/ 0- I
/ Q /
a /

v
/ \

\i
M a s t e r correlation !?aster c o r r e l a t i o n
E:
0-
I /

pi
d

Figure 11. Area ratio for 1-in. metal Pall rings.


Ln
0
m
0
2 ' ' M E T i i i R. F. 1. 5 ' ' M E T R L P. R.
1'
Fi I
-1 I
I
I
I
I
I
i I

Figure 9. Area ratio for 2-in. metal Raschig rings.


Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1, 1982 167
I
n
0 MQSTER C O R R E L R T I O N FOR D I S T I L L R T I C I N
c
- 2 ''METRL P. R. m
0

a
+ X
+
-
N
rf
i
xx +
I
/ /
i
/ +
I i
I
0 P'
ai x /+

C R L r R E G s l E 03
Figure 13. Area ratio for 2-in. metal Pall rings. Figure 14. Master correlation for distillation.
Table 11. Packings Included in Data Bank and or liquid rate or both. Thus, the product Ca$eG can be
Used in the Present Work
viewed as a loading parameter, but no effort here has been
SP made to generalize it in terms of experimental observations
nominal surface, of loading and/or flooding.
size, void a ,
packing type in. material fraction ftzf)ft3 Figures 1-13 do not include flooding conditions, but they
do include experiments under high loadings. The increase
Berl saddles 1 ceramic 0.68 76 in the slope of the curve, at high values of CaL X ReG and
Raschig rings ceramic 0.64 112 a * / a is in accordance with the well known behavior of
Raschig rings 'I4 ceramic 0.72 74
Raschig rings 1 ceramic 0.74 58 HEgP at higher loadings.
Raschig rings 111, ceramic 0.73 37 Figure 14 shows all of the distillation data in one single
Raschig rings 2 ceramic 0.74 28 plot combining all of the test systems and packings used
Raschig rings 3 ceramic 0.75 19 in the correlation. The relationship that best describes
Raschig rings 1 steel 0.86 56 these data is
Raschig rings 11/, steel 0.90 39
Raschig rings 2 steel 0.92 29 a * / a p = 0.498(CaLx ReG)0.392 (23)
Pall ringsa =is steel 0.93 104
Pall rings 1 steel 0.94 63 The fit of this equation to the data is discussed in the
Pall rings 2 steel 0.96 31 following section. Equation 23 is presented in Figures 1
This packing type is marketed under the names of Pall to 14 as a dashed line for comparison. No data are shown
rings, Flexirings, and Ballast rings. for distillation in 2-in. ceramic Raschig rings because the
data bank does not include distillation runs for this
experimental conditions under consideration. The data packing. After analyzing the fit for the other packings,
also line up very nicely when values for different packings especially for 1 and 1.5-in. ceramic Raschig rings it was
are plotted together. Thus, for a given value of CaL X ReG concluded that the correlation should include 2-in. ceramic
the corresponding value for a*/apappears to be the same Raschig rings. The same reasoning was applied to Berl
for different systems and/or packing type or size. saddles in the range of 1 to 2 in.
It is well known that a packed column loading/flooding The proposed correlation fits the individual data for
condition can be approached by increasing either gas rate each packing very well except for the case of 3-in. ceramic
Table 111. Test Systems Considered in the Present Work
surface
pressure, gas density, liquid density, tension, re1
system psia lb/ft' lb/ft3 dynlcm volatility
cyclohexane/n-heptane 5.0 0.06 44 20 1.9
cyclohexaneln-heptane 24.0 0.30 42 15 1.6
n-bu t anel isobu tane 165.0 1.76 31 6 1.3
2-propanol/water 14.7 0.11 47 17 1.6
ethylbenzenelstyrene 1.0 0.016 52 27 1.4
ethylbenzene/styrene 2.0 0.03 52 26 1.3
methanol/ethanol 14.7 0.08 47 19 1.7
ethanollwater 14.7 0.09 48 22 1.4
n-heptane/toluene 14.7 0.20 41 15 1.3
benzeneldichloroethane 14.7 0.20 63 22 1.1
isooctane 1toluene 20.0 0.28 41 14 1.2
NH,/H,O/air 14.7 0.08 62 74 a
0,/H,O /air 14.7 0.07 62.3 73 a
a These are absorption systems; all others are distillations.
168 Ind. Eng. Chem. Process Des. Dev., Vol. 21, No. 1. 1982

M A S T E R P L U T FUR A B S U R P T I U N P A R I T Y PLOT D I S T I L L A T I O N
YI
0

’1 a
0

I
I
I
I
/

/
/’
/
+/
/” x
x x
/
/

..

Figure 15. Master plot for absorption. %:oo o:ro o:ao 1: 20 1:60 2: 00
b / R P IBBSVl
Raschig rings with cyclohexaneln-heptane at 24 psia as Figure 16. Parity plot for distillation.
the test system. This same system also falls somewhat out
of line for 3/rin.ceramic h c h i g rings as shown in Figure PQRITY PLUT D I S T I L L f l T I U N
3. Figure 5 indicates that at low loadings the iso-
octaneltoluene system does not correlate very well. These
deviations could not be explained when analyzing the data. m
0

Nevertheless, we do not think they seriously affect the fit


of the overall correlation due to the large number of points
(the deviated ones included) taken into consideration. -r
W
The absorption data as shown in Figure 15 also group 01
0
adequately when plotting a * / a pvs. CaL X ReG. These data
show lower values of effective area when compared to
distillation data under similar conditions. This marked
difference could not be readily explained, but may be due
to the existence of vapor condensation simultaneous with
liquid bubbling under distillation conditions. These two
phenomena occurring at the same time should provide
added mass transfer surface within the bulk of each phase.
This added surface could account for part of the difference
between absorption and distillation effective areas.
On the other hand, factors influencing the mass transfer
coefficients and the use of a characteristic value for the
slope of the equilibrium line in distillation could also in-
tervene in explaining this difference in the deduced values =: I/
for a,.
Yoshida and Koyanagi (1962) and Onda et al. (1968) also
observed the difference between distillation and absorption Figure 17. Parity plot for distillation (expanded lower region).
effective mass transfer areas. Yoshida and Koyanagi offer,
a qualitative explanation of this difference through surface Reliability and Comparison with Other
tension effects since the absorption data they used had Correlations
water as the irrigating liquid, and the distillation data they In this section reference is made to observed and cal-
analyzed were for organic liquids. In the present work, culated values for the ratio a*/u,. The observed values
even though the ethanol/water system is included in the are obtained from data bank values plus the Onda corre-
correlation, the surface tensions for the liquids in the lation for masa tranfer coefficients. The calculated values
distillation data are lower than the surface tension in the are obtained by the use of the equation
absorption systems. Thus,surface tension of the irrigating (a*/a,)CdCd = 0.498(CuL X ReG)0.392 (23)
liquid could also account for the difference between the
effective interfacial areas in distillation and absorption. The statistical analysis of the correlation can be de-
Figures 16 and 17 show a parity plot for the distillation scribed as follows. (a) The total number of data points
data using the deduced values for a * / a , and the calculated used in the correlation is 231, with 11 different systems
ones from eq 23 with Figure 17 representing an expanded included. (b) The average absolute deviation was found
section of Figure 16. The degree of scatter shown in these to be 22%
plots does not seem to vary with the value of a*/a,; thus av abs dev = Cabs [l - (a*/ap)~cd/(u*/up)o~sdllOO/n
the degree of loading or approach to flood does not appear
to influence the fit of eq 23. ( c ) The average ratio ( a * / a , ) ~ , d / ( u * / u p was
) o ~equal to
Ind. Eng. Chem. Process Des, Dev., Vol. 21, No. 1, 1982 169

Table Iv. Model Reliability Analysis and Comparison the present time, such an extension is not recommended.
Bolles and Fair this work Conclusions a n d Recommendations
0.042 -3.42 x 10-14 The independent treatment of the individual mass
OF, transfer coefficients and the effective interfacial area for
S 0.323 0.286
F s (95% confidence) 1.70 1.60 mass transfer appears to provide a logical and fundamental
approach to the description of mass transfer in counterflow
1.042. (d) For the 231 points, 96% of the calculated values gas-liquid packed column. Transfer rates within a single
of Q* were within f20% of the observed values, 71% phase should depend on the available concentration gra-
within &lo%,and 40% within f5%. dient, the degree of turbulence in that phase, and on the
Bolles and Fair (1979) used and recommended a relia- physical properties of the fluid. The bulk-to-interface
bility analysis procedure based on a logaritmic ratio ob- transfer rates (or the individual mass transfer Coefficients)
jective function, which in the case of this work is should be much more heavily dependent on the system
itself than on the geometric characteristics of the packing.
OFi = In ((a*/Qp)obsd/(Q*/Qp)calcd) (24) On the other hand, the effective interfacial area for mass
transfer at any given point in the bed should depend only
The lower bound of this objective function was selected
to be the critical one since the conservative approach is on the relative kinetic energy of the phases, the geometry
of the packing, the wettability of the packing surface, and
to assume that the actual design value for the effective area the tendency toward rippling and/or droplet formation in
will be smaller than the one obtained from the model. (For
the liquid. The extrapolation of this “point” area to a
an HOG,objective function like the one proposed by Bolles complete column should be some function of the overall
and Far, the upper bound will be the critical one since the dimensions of the bed.
height of a transfer unit is inversely proportional to the The product of the capillary number for the liquid
effective area.) (which accounts for the liquid viscous and surface tension
Following the procedure presented by Bolles and Fair, forces) and the Reynolds number for the gas (which de-
the following expression for lower bound critical is obtained scribes the inertial and viscous forces in the gas) seems to
provide an appropriate parameter for describing effective
areas.
where OF, = mean of the objective function = COFi/n, Through the course of this work it was observed that
n = number of observations, OFi = objective function for for similar flow conditions the available area for mass
the ith observation, S = standard deviation of the objective transfer was substantially higher in distillation systems
function = [C(OFi- - l)]0.5,
and t = Student’s than in absorption systems. The increased area in dis-
“t” for a certain degree of confidence. tillation could be explained by the existence of simulta-
The real measure of the reliability of the model is the neous and significant boiling in the liquid phase with
standard deviation or scatter of the objective function. condensation in the vapor phase. These two effects are
Thus the “safety factor”, Fs = ets, should provide the best thought to provide a continuous formation of interfacial
reliability measure for the model for a certain percent area within each phase, thus providing an increased net
confidence. effective area.
The analysis described above was applied to the present Most of the distillation data used in the correlation were
model for a 95% confidence (t = 1.645) and the results as reported under total reflux conditions. Thus, a separation
well as a comparison with the Bolles and Fair model are of the liquid and gas velocity effects could not be studied
presented in Table IV. from the available data. The work of Clump (1953), while
The present model appears to be slightly more reliable not conclusive, indicated little effect of liquid/vapor ratio
than the one by Bolles and Fair. These authors show in on measured Hoc values. The work of Eckert and Walter
their paper an improvement over the models of Onda and (1964) showed that for the rectifying section a decrease in
Comell et al. Based on this comparison,the present model liquid/vapor ratio (operation at fiiite reflux) the measured
appears to be the most reliable of the four. It should be HETP decreased. An analysis of the effects of varying
noted, however, that the other three models are not spe- liquid and vapor rates, according to the models presented
cifically for distillation as the present one is, so a greater here, indicates compensating effects in the rectifying and
scatter is present in those models that encompass different stripping sections of a distillation column such that the
mass transfer operations in packed columns. predicted total reflux Hoc should be satisfactory for finite
Extension to Other Packings reflux operation, being somewhat conservative.
When the correlation is applied to new designs, a
The model described here is based on randomly ar- question of limits on packed height can arise. The data
ranged packing elements that can be characterized as bank included studies of mass transfer in heights up to 33
having a nominal diameter d’,,. This diameter is used in ft. However, prudent design often limits the height of an
the calculation of phase transfer coefficients k, and k ~ . individual section of packing to about 20 ft. Thus, the
One would expect the model to apply to packings other height correction appears to be valid within the range of,
than those tested so long as the packings have similar practical application.
shapes and identifiable nominal diameters. For example, In conclusion, an improved mass transfer model has
ceramic Intalox saddles were not included in the data bank been developed for application to distillation in columns
and thus did not contribute to the general development containing random packings. The model is more funda-
of the model; however, they are similar to Berl saddles with mental than those previously published and on the basis
about 12% higher specific surface up. The model would of testing against a large data bank is more reliable than
show that ceramic Intalox saddles would have a somewhat those currently available. More work will be needed before
higher mass transfer efficiency than ceramic Berl saddles, the model can be extended to nondistillation systems and
for the same phase rates and system properties. to nonrandom packings.
Extension of the model to the nonrandom packing ma-
terials would call for assumptions of equivalent diameter Nomenclature
that could only be validated by considerable test data. At A = coefficient in eq 22
170 Ind. Eng. Chem. Process Des. Dev. 1982, 21, 170-173

a* = corrected effective area, (ft2/ft3)(fto.4/


(dyn/~m)O.~) S C=~Schmidt number for the gas
a, = effective interfacial area, ft2/ft3 ScL = Schmidt number for the liquid
aep= effective area provided by packing alone, ft2/ft3 S = standard deviation
a,, = specific surface of the packing, ft2/ft3 T = absolute temperature
a, = wetted area, ft2/ft3 t = Student’s t
b = exponent in eq 22 u, u = exponents in eq 6
CaL = capillary number for the liquid WeL = Weber number for the liquid
D, = column diameter, f t 2 = height of packing in column, f t
DG = diffusion coefficient for the gas
DL = diffusion coefficient for the liquid Greek Symbols
d, = diameter of a sphere with the same surface area as one a = factor to correct for available column wall surface
packing element t = void fraction
d 6 = nominal diameter of the packing element X = ratio of slopes (equil. line/operating line = mG,/L,)
F, = safety factor for model reliability i . ~= viscosity
FrL = Froude number for the liquid p = density
G = gas superficial mass velocity (r = surface tension, dyn/cm
G, = gas superficial molar mass velocity a, =critical surface tension, dyn/cm
g = acceleration of gravity Subscripts
g, = force/mass conversion factor
HG = height of a gas transfer unit, f t G = referred to the gas
HL = height of a liquid transfer unit, f t L = referred to the liquid
H E = height of an overall gas transfer unit, f t GM = molar property for the gas
HETP = height equivalent to a theoretical plate, f t L i t e r a t u r e Cited
kG = mass transfer coefficient for the gas phase
Bolles. W. L.; Fair. J. R. Inst. Chem. Eng. Symp. Ser. 1979. 5 6 , 3/35.
kL = mass transfer coefficient for the liquid phase Charpentier, J. C. Chem. Eng. J . 1976, I f , 161.
K O G = overall gas mass transfer coefficient, based on gas Clump. C. W. W.D. Dissertation, Carnegie Instltute of Technology, Pittsburgh,
concentration Pa.. 1953.
L = liquid superficial mass velocity Cornell, D.; Knapp, W. G., Falr, J. R. Chem. Eng. Rog. 1960a, 56(8) 68.
Cornell. D.; Knapp, W. G.; Close, H. J.; Falr, J. R. Chem. fng. Rog. 1960b,
L, = liquid superficial molar mass velocity 56(6) 46.
m = slope of the equilibrium line Eckert, J. S.; Walter, L. F. ~&ocarbonRocess. 1964, 43, 107.
M = molecular weight Fair, J. R., Moczek, J. S., Presented at Les Vegas AICM Meeting, Aug 1964.
n = number of observations Hughmark, G. A. Ind. Eng. Chem. Fundam. 1960, 79, 385.
Onda, K.; Takeuchl. H.; Okumoto, Y. J . Chem. €ng. Jpn. 1966, I , 56.
OFi = objective function for observation i Onda, K. Mem. Fac. Eng., Nagoya Unlv. 1972, 24(2) 164.
OF, = mean of the objective function Shulman, H. L.; Ullrlch. C. F.; Wells, N. AI&€ J . 1955a, 7 , 247.
P = total pressure Shulman, H. L.; Ullrlch, C. F.; Proulx, A. 2.; flmmerman. J. 0. AIChE J .
Q, Q’ = coefficients in eq 6 and 7 1955b, I , 253.
Shulman, H. L.; Ullrlch, C. F.; Wells, N.; Proulx, A. 2. A I C M J . 1 9 5 5 ~ .I .
ReG = Reynolds number for the gas (= 6 G / ( a M G ) 259.
ReL = Reynolds number for the liquid (= 6Lfia L) Yoshkla, F.; Koyanagi. T. Ind. Eng. Chem. 1954, 46, 1756.
ReG‘ = modified gas Reynolds number (= R e G / 8 Yoshkla, F.; Koyanagi. T. AI&.€ J . 1962, 8 , 309.
ReL’ = modified liquid Reynolds number (= ReL/6)
R = universal gas constant Receiued for review May 22, 1981
r, s = exponents in eq 7 Accepted September 10, 1981

Upgrading of Recycle Solvent Used in the Direct Liquefaction of


Wyodak Coal
Ronald L. Mlller and Howard F. Sliver’
Chemical Engineering Depaflment, University of Wyoming, Laramle, Wyoming 8207 1

Robert J. Hurtublse
Chemishy Depaflmnt, University of Wyoming, Laramie, Wyoming 82071

Hydrogen donor characteristics are one of the most important properties of a coalderived recycle solvent used
in the direct liquefaction of coal. This property can be modified by direct catalytic hydrogenation to increase the
solvent hydrogen content. Results of this work using 22 solvents derived from three coals indicate that recycle
solvent effectiveness goes through a maximum as the hydrogen content of the solvent increases. However, the
solvent hydrogen content at which the observed maximum occurs differs for different solvents. Weight percent
hydrogen in a solvent at observed maximum llquefaction effectiveness has been correlated as a linear function
of a Watson-type characterization factor, K,.

Introduction coal dissolver reaction conditions but also on the quality


The extent to which coal can be directly converted to of the recycle solvent used. A good recycle solvent must
gases and benzene soluble liquids depends not only on the be physicallv compatible with the coal fragments formed
0196-4305/82/1121-0170$01.25/0 0 1981 Americar, Chemical Society