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Chapter 5 - Absorption (Part 1)
Chapter 5 - Absorption (Part 1)
Part (1)
Pressure Drop
Pressure in packing is an important consideration in design of a tower
Empirical correlations are available for various types of packing based on experimental
data and used to determine pressure drop in the gas flow
Pressure Drop in Random Packing Figure 10.6-5
It is important for proper design to be able to predict the flooding pressure drop in
towers and, hence, the limiting flow rates at flooding
The limiting pressure drop at flooding can be determined using the following
empirical equation:
Pflood : in in.H2O/ft height of packing
Pflood 0.115Fp0.7
Fp : packing factor, ft-1, from Table 10.6-1
Solution:
The gas and liquid flows in the bottom of the tower
are the largest, so the tower will be sized for these flows.
From Table 10.6-1: for 1 –in, Pall rings, FP = 56 ft-1 (packing factor).
Using Fig. 10.6.5, a capacity parameter is (ordinate) of 1.7 is read off the plot:
Using this value of 0.85 and the same flow parameter, 0.06853:
Ac / 4 D2 D 1.446 ft 0.441 m
- Assume that approx. all the ammonia is absorbed , the amount of ammonia in the outlet
- Liquid flow rate is 2 × gas flow rate → the total liquid flow rate is 2(1440) = 2880 lbm/h
→ The flow rate of the pure inlet water = 2880 - 25.68 = 2854.32 lbm/h
→ D = 1.241 ft
Note: the tower with structured packing uses about 25% less cross-sectional area.
Design of Plate Absorption Towers
The process flow diagram is the same as the countercurrent multiple stage process
In absorption, solute A is diffusing through a stagnant gas B and then into a
stagnant fluid C
Example: absorption of acetone (A) from air (B) by water (C)
Moles of inert air and moles of inert water maintain constant
If V’: kg mol inert air (B)/s L’: kg mol inert water (C)/s V1, y1 L0, x0
yN+1 = 0.20 (Entering Gas from the bottom 20 mol % SO2 ) N-1
y1 = 0.02, (2% leaving in the gas ) N
x0 = 0. (pure liquid ) VN+1, yN+1 LN, xN
(3)Substituting into overall material balance equation and solving for xN.
0 0.2 xN
5.18
0.02
333 5.18 333
1 0 1 0.20 1 xN 1 0.02
xN 0.00355
(4) Substituting into operating (dashed) line eq., using V' and L' as kg mol/h.m2
instead of kg mol/s.m2.
0 yn 1 x
5.18
0.02
333 5.18 333 n
1 0 1 yn 1 1 xn 1 0.02
(5)In order to plot the operating line, several intermediate points will be
calculated. Setting yn+1 =0.07 and substituting into the operating equation,
0.07 xn 0.02
0 5.18 333
5.18
1 0.07 1 xn 1 0.02
Hence, xn = 0.000855. To calculate another intermediate point, we set yn+1 = 0.13,
and xn is calculated as 0.00201.
(6)The two end points and the two intermediate points on the operating line are
plotted in Fig.10.6-8, as are the equilibrium data from Appendix A.3.
y2 (top)
y
y
y2 (top) x ' y1 ' x1 ' y
L' V L V
1 x 1 y1 1 x1 1 y
y1 (bottom)
x2 x1 x1 x2
x
y1 (tower bottom)
x
y2 (top)
y
y
y2 (top) L x V y1 L x1 V y
' ' ' '
y1 (bott)
x2 x x1 x1 x
2
Limiting and Optimum L′/V′ ratio V2, y2 L2, x2
In absorption processes:
V1, y1 are generally set y2 is set by designer
x2 is fixed by process requirements
The objective is to have minimum L′ under such conditions
Remember slope of operating line = L’/V ’
Minimum slope Gives minimum L V 1, y 1 L1, x1
This can be done by moving the operating line, so that
it touches the equilibrium line at point P
y1
At point P, liquid flow L’ is a minimum at L’min P
Substitute y1 and x1max into the op. line eq. → L’min Eqm. line
y
Op. line for minimum
Optimum L’/V’
depends on economic balance: y2 liquid flow
Too high L’/V’ large tower diameter
Small L’/V’ high tower costly
x x1 x1 max
Typical value for optimum liquid flow L' 1.5L'min x2
V2, y2 L2, x2
In stripping processes:
L2, x2 are generally set x1 is set by designer
y1 is fixed by process requirements
The objective is to have minimum V ’ under such conditions
Remember operating line (slope = L’/V ’ ) should be below eqm line
Maximum slope Gives minimum V
V1, y1 L1, x1
This can be done by moving the operating line,
so that it touches the equilibrium line at point P
y2 max
At point P, gas flow V is a minimum at V
’ ’
min
P
y2
Typical value for optimum gas flow: Op. line for
Eqm. line minimum
y
V 1.5V
' '
min
gas flow
actual
y1
op. line
Remember minimum flow corresponds to x2
x1
infinite number of trays x
Analytical Equations for Theoretical Number of Stages
These are similar to the ones for calculating the number of stages in
countercurrent stages.
3. Draw a straight line from (x2,y2) to intersect the equilibrium line at (x1 max ,y1) or a
straight line tangently to the equilibrium line to give x1 max.
x y x y
L' 2 V ' 1 L' 1 V ' 2
1 x2 1 y1 1 x1 1 y2
0 0.022 ' 0.03235 0.002244
L'min 97.8 L min 97.8
1 0 1 0.022 1 0.03235 1 0.002244
Lmin 59.24 kg.mol / h
9. L′=1.5Lmin=1.5(59.24) = 88.86 kg mol/h
10. Using L` in the overall material balance equation and solving for the outlet
concentration , x1 = 0.0218
11. The top operating line now is plotted as a straight line through the points y2,x2 and
y1,x1 .
12. An intermediate point is calculated by setting y=0.012 in operating line equation
and solving for x= 0.01078. plotting this point shows that the operating line is very
linear . This occurs because the solutions are dilute
13. The number of theoretical trays obtained by stepping them off is 4.0 trays
Analytical Solution:
A1 = L1/mV1 = 1.336
A2 = L2/mV2 = 1.333
A A1 A2 1.335
y mx2 1 1
ln 1 1
y2 mx2 A A
N 4.04
ln( A)
Design method for packed towers using mass-transfer coefficients
Because of difficulties in measuring interfacial area A m2 between phases L and V and
k’x, k’y, K’y and K’x experimental measurements in packed tower yields a volumetric
mass-transfer coefficients which combines interfacial area and mass-transfer coefficient:
yAi
'
k
x
x Ai x AL
(1 x A ) iM y*
Multiplying by dA and setting dA = aSdz xAL xAi x*
k y' a k x' a
N A dA y AG y Ai Sdz x Ai x AL Sdz
(1 y A ) iM (1 x A ) iM
where NA dA = kg mol A transferred/s in height dz, which could be d(VyAG) or d(LxAL)
k y' a
d (Vy AG ) y AG y Ai Sdz
(1 y A ) iM k x' a
and d ( Lx AL ) x Ai x AL Sdz
(1 x A ) iM
V' y ' (1 y ) dy ydy
d {Vy} d y V 'd V
1 y 1 y 1 y 2
' dy
'
V dy dy
V 2
V
1 y 1 y 1 y 1 y
Vdy k y' a Note that subscripts A, G
y yi Sdz and L are dropped
1 y (1 y ) iM
Repeating same procedure for liquid phase, where L’ = L(1 - x):
Ldx k x' a
xi x Sdz
1 x (1 x) iM
z y1
V dy
Upon integration:
dz z
0 y2
k y' aS 1 y y yi
(1 y )iM
z x1
L dx
dz z
0
x2
k x' aS 1 x xi x
(1 x)iM
In a similar manner, the final equations can be derived using overall coefficients:
y1 x1
V dy L dx
z
y2
K y' aS 1 y y y*
z K x' aS 1 x x* x
x2
(1 y )*M (1 x)*M
V (1 y )iM y1
dy L (1 x)iM
x1
dx
z '
k y aS 1 y
avg
y2
y yi
z '
x
k aS 1 x
avg
x2
xi x
V (1 y )*M y1
dy L (1 x)*M
x1
dx
z '
1 y
y y*
z '
x* x
K y aS avg y2 x
K aS 1 x avg x2
For dilute mixtures (x, y < 0.1) with straight operating and
straight equilibrium lines
Equilibrium line: y * mx c
@ 1: y1* mx1 c y2* y1*
m
@ 2: y2* mx2 c x2 x1
V
Operating line: L( x x1 ) V ( y y1 ) x ( y y1 ) x1
L
V
Equilibrium line equation then becomes: y * m ( y y 1) x 1 c
L
y2 y2
For dilute mixtures: dy
dy V
y y * y1
y1 y m (y y 1) x 1 c
L
y2
dy
mV mV
y1 y y y1 mx1 c
y2 L L
dy
mV mV
y1
1 y y1 mx1 c
L L
y2
1 mV / L y2 (mV / L) y1 mx1 c
dy 1
ln
y1 y y* 1 mV / L 1 mV / L y1 (mV / L) y1 mx1 c
1 1 mV / L y2 (mV / L) y1 mx1 c
ln
1 mV / L y1 mx1 c
Note that, y1* mx1 c
y2
y2 (mV / L)( y1 y2 ) y1*
dy 1
ln
y1 y y *
1 mV / L y1 y1*
Also: m y2 y1
* * L y2 y1
and
x2 x1 V x2 x1
mV y2* y1* mV y2 y1 y2* y1* y2 y2* y1 y1*
, and 1
L y2 y1 L y2 y1 y2 y1
Hence, y2
y2 y1 y2 y1* y2* y1*
dy
y
y
1
y* y 2 y *
2 y1 y1
*
ln
y1 y *
1
y2 y1 y2 y2*
ln
y2 y2 y1 y1
* *
y1 y1*
Since,
y y2* y1 y1* y2
( y2 y1 )
( y y * ) LM
2 dy
y2 y *
ln 2
y1
y y* ( y y * ) LM
y1 y1*
dx
where, ( x *
x ) 2 2
x* x ( x* x ) LM x2* x2
LM
x1 ln *
x1 x1
x x2 xi1 x1
x2
( x2 x1 )
dx
where, ( xi x ) LM i2
x1
xi x ( xi x ) LM x x2
ln i 2
xi1 x1
y2
( y2 y1 ) where, ( y y ) y2 yi 2 y1 yi1
i LM
dy
y yi1
y1
y yi ( y yi ) LM ln 2
y1 yi1
Substituting these integrals in the four z-expressions in slide 27 gives assuming
that: (1 – y)iM/(1 – y) = (1 – y)*M/(1 – y) = (1 – x)iM/(1 – x) = (1 – x)*M/(1 – x) 1.0
V L
y1 y2 k y' az y yi LM x1 x2 k x' az xi x LM
S S
V L
y1 y2 K y' az y y* LM x1 x2 K x' az x* x LM
S S
Left side kg mol absorbed/s.m2 by material balance
Right side kg mol absorbed/s.m2 by rate equation for mass transfer
V1 V2 L1 L2
V L
2 2
General steps for calculating z using previous equations (see page 672)
1. Plot the operating line equation. Calculate Vav, and Lav.
2. If k’xa and k’ya are available, determine the interface compositions yi1 and xi1 at point 1
and point 2 using the procedure previously discussed using line P1M1 (see Example 10.4-1)
eqm
k x' a /(1 x) iM kx a y1 P1
slope
k a /(1 y ) iM
'
y kya
yi1 M1
As previously shown, this involves trial and error
procedure. For dilute solutions, use: y*1 P
k x' a /(1 x1 ) y2 2
slope '
k y a /(1 y1 ) yi2 M2
y*2
Similarly, use line P2M2 to determine yi2 and xi2
x2 xi2 x*2 x1 xi1 x*1
3. If K’ya is used get y* 1 and y*2; if , K’xa get x*1 and x*2
4. Calculate (y – yi)M if k’ya is used. For K’ya, (y – y*)M is calculated. Similarly, if liquid
coefficients are used.
5. Calculate the column height z m by substituting into the appropriate equations (slide 31)
Example 10.6-4: Absorption of Acetone in a Packed Tower
Acetone is being absorbed by water in a packed tower having a cross sectional area of
0.186 m2 at 293 K and 101.32 (1 atm). The inlet air contains 2.6 mol % acetone and outlet
0.5%. The gas flow is 13.65 kg mol inert air/h. The pure water inlet flow is 45.36 kg mol
water/h. Film coefficients for the given flows in the tower are k’y a = 3.78 x 10-2 kg
mol/s.m3.mol frac and k’x a = 6.16 x10-2 kg mol/s.m3.mol frac. Equilibrium data are given
in Appendix A.3.
dz
L'= 45.36 kg mol/h, V' = 13.65 kg mol/h
x1 = ? y1= 0.026
L1 V1
Solution:
From Appendix A.3 for acetone-water at 293 K
At xA = 0.0333: yA = 30/760 = 0.0395
Mole fraction acetone Partial pressure of
in liquid, xA acetone in vapor, pA,
mmHg
Hence, the equilibrium line is
0 0
yA = mxA or 0.0395 = m(0.0333) 0.0333 30
0.072 62.8
Then, y = 1.186 x. (plotted in Fig. 10.6-14) 0.117 85.4
Plotting this line through (y1 ,x1) , the line intersects the equilibrium line at yi1 = 0.0154
and xi1 = 0.0130. Also, y*1 = 0.0077.
Calculate a more accurate slope, the preliminary values of yi1 and xi1 will be used in
the trial-and-error solution.
(1 yi1 ) (1 y1 ) (1 0.00648) (1 0.026)
(1 y)iM 0.979
ln[(1 yi1 ) /(1 y1 )] ln[(1 0.0154) /(1 0.020)]
yi1 0.016
0.012
Hence, the approximate slope and interface values are accurate enough.
L
x1 x2 k x' az xi x LM
S
1.260 102
(0.026 0.005) (6.16 102 ) z (0.00368)
0.186
z 1.936 m
(1 y1 ) (1 y1 )
(1 y )M
ln[(1 y1 ) /(1 y1 )]
(1 0.0077) (1 0.026)
0.983
ln[(1 0.0077) /(1 0.026)]
the slope changes little in the tower
1 1 m'
' '
K y a /(1 y )M k y a /(1 y )iM k x a /(1 x)iM
'
1 1 1.186
K y' a / 0.983 3.78 10 2 / 0.979 6.16 10 2 / 0.993
K y' a 2.183 10 2 kgmol / s.m3 .molfrac.
( y1 y1 ) ( y2 y2 )
( y y )M
ln[( y1 y1 ) /( y2 y2 )]
(0.026 0.0077) (0.005 0)
0.01025
ln[(0.026 0.0077) /(0.005 0)]
Finally
V
( y1 y2 ) K y' az ( y y ) M
S
3.852 10 3
(0.026 0.005) (2.183 102 ) z (0.01025)
0.186
z 1.944m