Mass Notes 3
Mass Notes 3
30 Mar
Mass Transfer
↑
- The objective is to provide efficient contact between the two immiscible phases to
facilitate diffusion of one component from one phase to the other.
- Examples are devices in which liquid is dispersed into thin films or drops, such as
wetted-wall towers, sprays and spray towers and packed towers.
↑ ↑
gas ↓
- Spray towers: liquid is sprayed through nozzles into a gas stream to form fine Penetrates
through
stage
2
droplets of liquid. Low pressure drop for gas phase, but high pumping cost for liquid these
small holes
↑ ↑ a
through the nozzles. Liquid entrainment in outlet gas is possible, mist eliminator may in which mass
transfer
be needed. occurs
Trays in Tray
- Tray (plate) tower: liquid and gas are brought into contact in trays with holes as Towers
bubble caps Stage =
Tray
2
Gas-Liquid Operations Bubble Coloumn Packed Tower
Random
- Bubble coloumn (sparger): gas is dispersed as bubbles through the liquid phase
Packing
&
- Packed Towers: tower is filled with either random or structured packing with large
surface area.
- In general the ratio of packing diameter to tower diameter should be 1/15 to avoid
channeling.
- Void fraction in packing should be high enough to allow passage and reduce pressure covered
drop of gas. not
- Packing should be chemically inert and mechanically strong to permit easy handling
and installation.
* Packing is a solid material that is
- Packing Types: that enhances
designed in a
shape
and
1. Structured Packing: the contact between gases
2. Random Packing:
• Cheaper than structured
• Tower is filled with packing material Random Packing
• Packing size is typically 3 to 75 mm
• Materials are typically clay, porcelain, metal and plastics
• Provides low pressure drop
• Relatively lower surface area for gas and liquid contact
• More advanced packings provide higher separation efficiency with lower pressure drops
• As packing size increases, mass transfer efficiency and pressure drop may decrease (compromise
between the two)
• To minimize channeling of liquid, the nominal packing size should be less than 1/8th of the
coloumn diameter
increasing Liquid
If
* you increase the Liquid flow rate
flow rate Causes
increasing in the
there will be more
pressure drop that
Liquid holdup to be faced
is
going by the
gas/vapor
.
Le
-
upwards
:
going
With
--
certain amount If the velocity is Constant and going
a I gas
of Liquid being held at up
, Liquid flow rate the pressure
the
up as
you increase
Layer rises
at the top of the packing and the coloumn is flooded. This is the flooding point. as the
Velocity
which
at
velocity flooding
alld Point
- A region exists between the flooding point and the loading point, called the loading region. This region is rises
reach the
happens
- Flooding Velocity (VF): upper limit of the gas flowrate, above which liquid can no longer flow down the tower.
5
L -
Liquid Holdup – in the preloading region - before the loading region occurs
↓ ↑
- Specific liquid holdup, hL: volume of liquid in bed per unit volume of bed in the preloading region (below the loading point)
↓
/
/
/↓
= he x
↑
volume of the packed bed
↓ /
// /
↑
&
d V
&
If take any instant
1
we
will
of time then there
in this
be some Liquid
Column the volume of the
,
need to calculate.
Example: An absorption column is to be designed using an absorbent oil with a kinematic viscosity of 3.0x10-6 m2/s. The
superficial liquid velocity will be 0.01 m/s , which is safely above the minimum value for good wetting. The superficial gas
velocity will be such that operation will be in the preloading region. Two random packings are being considered: (1) 50-mm
metal Pall rings and (2) 50-mm metal Hiflow rings (resembling the Pall ring, but with wider openings). Estimate the specific
liquid holdup for each of these two packings. Answers: (1) hL = 0.0663 m3/m3 (2) hL = 0.0637 m3/m3 6
Kinematic viscosity = 30 .
x 10% mys =
Viscosity
city-
Superficial Liquid Velocity , V = 0 . 01M/s
01 M/s 01 M/s
=
0
Rec =
0
29 603 Ren 36 114
. .
=
. >5 =
> 5
= - = .
(112 .
63) L OX10t . (3 .
0x100
Fr = ) -
Fr = ) 1
2.
= =
1 1478
. x 10 = =
9 408
. x
fo fo
23 23
ChRe0 ChRe0
. .
an = 0 . 85
an = 0 . 85
25 25
603(0 1478x103) (0 (9 408x10-7 ;
- -
= 0 .
85 (0 784) 229
.
. (1 . = 0 . 789 = 0 .
85 (0 876) 236 114
. . . = 0 .
909
h =
[12ET's / h =
[12ET's /
=
[12 1703 J's 7897 0 .
=
0 .
066 =
[12 400- Js 09097 = 0 . 0636
Pressure Drop
- Packed coloumn diameter is determined such that flooding is avoided and operation is done in the preloading region, with a pressure
-
"
"! = #!
&
$ = %$
$ $%
Actual superficial gas velocity
- The flooding curve can be accurately described by the polynomial regression:
we can
T
this
find the
Flooding
velocity from
, VaF
Generalised pressure drop correlation for packed
beds
convert to volumetric flow
rate
m use gas
*
entering
->
which will give you 7the
J
Packing diameter
.
Pressure Drop
- Typically the coloumn is designed in such a way that the pressure drop is 200 to 400 Pa/m of the packed depth, atmospheric
fractionators from 400 to 600 Pa/m and vacuum still for 8 to 40 Pa/m.
- The correlations and curve can be used to find the coloumn diameter and actual pressure drop in the coloumn.
1. Find X and use it to find Yflood. Using Yflood , find Cs,flood. Using Cs,flood find vGF.
2. Find packed tower diameter D
3. Find superficial gas velocity vG = f⋅vGF
4. Use the figure with X and Y to find the pressure drop
Example: Air containing 5 mol% NH3, at a total flow rate of 20 kmol/h enters a packed column operating at 293 K and 1 atm where 90% of
the ammonia is scrubbed by a countercurrent flow of 1500 kg/h of pure liquid water. Estimate the superficial gas velocity and pressure
drop at flooding, and the column inside diameter and pressure drop for operation at 70% of flooding for packing material: 25-mm ceramic
Raschig rings (Fp = 179 ft2/ft3). Liquid viscosity = 0.001 Pa.s = 1 cp. Liquid density = 1000 kg/m3. For operation, gas phase velocity = 70% of
the flooding velocity.
Detailed Answer
From Table on Raschig ring: uploaded in Bb
8
20 Mar
Wed
Mass Transfer
CHEG 324 – Spring 2024
5 - Absorption and Stripping – Packed Towers
Faisal Abdulla AlMarzooqi
WEDNESDAY, MARCH 20, 2024
Absorption and Stripping units
- Examples of absorption and stripping processes in industry:
Tray Tower Packed Tower
- Removal of Ammonia
- Removal of Benzene and Toluene L2 V2 L2 V2
- Removal of Hydrogen Sulfide xA2 yA2 xA2 yA2
2
Packed Towers
Definitions: where mass transfer will be happening(Packing is
facilitating the transfer of mass between LandV]
X
A = Total interfacial area (m2) - Total Surface Area that is available based on the packing Packed Tower
2 3
a = Interfacial area per unit volume of packing or Specific surface area of packing (m /m )
LS VS
S = cross sectional area of packing (m2)
S
Pv2 -
III
LS /S
/ We will alway L2 V2
Z = Packing / Bed height (m) that our assume xAL2 yAG2
OM
! = $×&×' Constant
↓
Since a and S are constant with Z, (! = $ × & × ('
changing
across the
↓ tower
11//////
↑
Z
Packing isCylindrical
↓ Z
↑
Vol
A]
= 2x S
Constant
Material balance: volxa =
M2 Why?
xm3 =
* All
the A that
the gas
needs
Rate of mole change in gas phase = Rate of mole change in liquid phase leaves
Liquid
to go to the
((*+!" ) = ((-.!# )
and viceversa
.
L1 V1
xAL1 yAG1
now ?
( *+!" = /! (! = /! $&(0 NAA =A
>
-
-
Flow
>
-
YAG = NA
rate
"
&! &'" '($#( ( '($#$
/! = 1$ +!" − +!% = '($# $%&
+!" − +!% = 1) .!% − .!# = '()# $%&
.!% − .!# 1 − +! %#* = )*!#(
- +,
I )*!#$
'($#( ( '($#$
1 − +! %#* =
+,
)*!#(
)*!#$
Packed Tower
Total
Volume
&
LS VS
*=
-+
∴ ( *+!" = (
-+
+!" =
-+
(+!" =
-
(+!" L2 V2
'($#( '($#( '($#( , '($#(
xAL2 yAG2
>
- Vs = V (1-YA2)
( *+!" = /! $&(0
* 1$.
(+!" = +!" − +!% $&(0 Z
1 − +!" 1 − +! %#*
1 − +! %#* *(+!"
(0 =
1$. $& +!" − +!% 1 − +!" L1 V1
xAL1 yAG1
Replace +!" = + and +!% = +%
0 $)
* $) *
' = 5 (0 = 5 (+ = 5 ∗ (+
/ $, 1 . $& 1 − + + − +% $, 6 . $& 1 − + + − +
$ $ 4
1 − + %#* 1 − + ∗#*
Packed Towers Design
To find the general solution of Z, we can either use numerical integration or graphical method to find the area
under the curve in the integral. D
L1 V1
An analytical solution is possible with some simplifications:
xA1 yA1
For dilute gas mixtures: i.e. x, y < 10% = dilute. Some of the the terms can be taken out of the integral since
we can use their average values (from top to bottom of the coloumn): if the question
In 5
* Chapter ,
even
dilute
that it is a
5
Packed Towers Design
For dilute mixtures:
Packed Tower
I
L2 V2
J
'($ $%& $ 4$ $)($, -
= 1 and ∫$ ) = ∴ +' − +7 = 1$. $' + − +% #* = 6$. $' + − + ∗ #*
'($ 26 , $($$ $($$ %& 3 xA2 yA2
#
3
.' − .7 = 1). $' .% − . #* = 6). $' . ∗ − . #*
-)8-, #)8#, D
For V and L take the averages: *= and - =
7 7
L1 V1
For a very dilute systems, 1 − + %#* = 1 remember 1$. = 1$ xA1 yA1
6
Packed Towers Design
Steps to follow:
1. Plot the operating line as a straight line. Find V1, V2, V, L1, L2 and L.
2. Using the mass transfer coefficients, find the interfacial compositions (xi1, yi1) and
(xi2, yi2) by plotting the lines P1M1 and P2M2.
."'/ ."'/
& 2 )*' $%& )*')
Slope = − &' 2 = − ."!/
=− ."!/
(Approximation for dilute solutions) ↓
! lead to
)*! $%& )*!)
crossing
Point in the
The slope of the line P2M2 is:
&
equilibrium
."'/ ."'/
& 2 )*' $%& )*',
Slope = − &' 2 = − ."!/
=− ."!/
(Approximation for dilute solutions)
!
)*! $%& )*!)
3. If the overall mass transfer coefficients 6). 896$. are being used then +'∗ , +7∗ , .'∗
and .7∗ are determined.
4. Calculate the appropriate log mean driving force, [e.g. (y-yi)LM]
5. Get the coloumn height for packing, Z.
7
Packed Towers Design
·
Only for Absorption
- $)($,
Note: use ah instead of a
- $)($,
Last time we solved the equation to find Z: ' = &" 2 3
× $($$ %&
we can re-write this as, ' = :" × /" where :" = &" 2 3
and /" = $($$ %&
! 0 ! 0
General Equations You
start with to
In general we can write, ' = :" × /" = :# × /# = :9" × /9" = :9# × /9# : find []
We are
- - $)($, - - $)($,
:" = "
&!203
= &!20 '($ $%&3
using
/" = $($$ %&
| :9" = 5" 2 3
=5 /9" = $($∗ %&
- an and ! 0 !20 '($ ∗%&3
= =
-
-
-
not a
# # ))(), # # ))(),
:# = &" 2 3
=& /# = | :9# = 5" 2 =5 /9# = )∗() %&
' 0 '20 '() $%&3 )$ () %& ' 0 3 '20 '() ∗%&3
=
--
= - -
∗
'($#( ( '($#$ '($#( ( '($#
1−+ %#* = | 1−+ ∗#* =
)*!
+, )*!#(
#$
+,
)*!#(
)*!∗#
for stripping
You Flip the
$)($$) ( $,($$, $)($)∗ ( $,($,∗
+ − +% #* = ! *!
| + − +∗ #* = ! *! ∗ equations
+, ) $) +, ) )∗
!,*!$, !,*!,
Ex : Abs stripping
Yai Yac
∗
'()#% ( '()#$ '()#% ( '()#
1−. %#* = )*'#% | 1−. ∗#* = )*'#% Yaa-Yai - -
+, +,
)*'#$ )*'∗#
YAG-YA * -> -YAY
)$)()) ( )$,(), ))∗()) ( ),∗(), Y
,
.% − . #* = '$)*')
| .∗ −. #* = '∗)*') Y, -
%i) - Yil -
+, +,
'$,*', '∗,*',
y* Y
,
y y*
-
- -
,
8
Example
S T P
Acetone is being absorbed by pure water in a packed tower with cross sectional area = 0.186 293 K and 1 atm m2 at
pressure. The inlet gas mixture of air and acetone contains 2.6 mol% acetone, and outlet gas contains 0.5 mol%
acetone. The gas flow rate is 13.65 kmol/h, and water flow rate is 45.36 kmol/h. Given: kyah = 0.0378
kmol/s.m3.mol frac. kxah = 0.0616 kmol/s.m3.mol frac. Equilibrium line: y = 1.186 x (Dilute system: equilibrium line
will be straight line following Henry’s law)
0.03
Find:
gas outlet
1- Tower height using kyah Liquid inlet 7 %
,
5 moly. Acetone 0 005 - -
0.025
=
flow water
Knol rate D
U2 = ?
Kx9n = 0 . 0016
sm3 molfrac Le 45
Kmol
0.02
= .
36 T
Knol
Kyan = 0 .
y
y 1 186 X Pure water A 186 m
= .
= 0 .
# T = 293K 0.01
P = 1 atm
·
Dilute System Y2
0.005
P2
D
Ky' =
Ky
kx = kx
0
gas flow rate 0 0.005 0.01 0.015
V 65
- Kmol X2
x
= 13 .
,
h
Liquid outlet
F
gas inlet
7 026
2 6 mol %.
Acetone ->
= 0 .
9
· .
① For Kyan
= =e 164-0026 andend
=
Ha
noth min 2
=
13
361
.
X X
-
Knol
-
13 50595
. h 60 min 60S 13 50595
-
. -
=
h
0 .
0378kml - 0 . 186 m2
Frac
= 0 .
53360M V1 + 22 = Vz + L
, V Y.
.
+ 122 = Vale + L, X ,
Y = 1 186X
. ?
L = Vi + Le V= -
X1 + 2 VeYz
4 ,
-
Yiel
=
= , -Yi ; P = (, ) = e 26) ; = 13 05 + 45
. . 36 13 3619
- .
Li
**
(1 65 (0 026) 3619
(x2 , (2) (0 005) 245 36 (0)
Pz 213 20 005)
m
+
45 6481
.
-
0
. .
=
. .
= . =
, = .
Kmol
45 6481
.
Th
(Yc Yiz)
-any
10-3
-
-yes
~ ~
=
6 311
.
x
slope -an
-an
an
= =
slope = = -
Ky9n Ky9n
V V
Y= 1 186 Xi
026-21 .1xil)
0 =0 31 186 Xin
.003-11 .16) 06
.
0
-
=
.
-
.
10 .
026 -
1 186
.
xi) (0 .
037) =
(-0 0616) (6
.
.
311x10- -
Xi)) ↑ ic = 0 . 0017758
9 . 62x10-4 - 0 .
043882Xi1 = -3 . 887576x10" + 0 .
0616 Xi) Yi z =
1 186
.
(0 .
0017758) = 0 . 0021061
-ii)
9 62 . x 10-4 + 3 887576
. x10Y =
Xi 20 0616 .
+ 0 .
043882) (4-7 : ) = =
10 026-0015187)
. -
10 005 : -0 .
00200le
In (0 026-0 015187)
.
.
Xi1 0 01281
(Yc Yiz)
= .
-
20 005-0 0021061)
.
.
↑i = 1 186
.
(0 01281) . = 0 .
015187 = 0 . 008
Na =
(Y, -
Y2( 0.
026 -
0 .
005 35
.
=> =
( Y ; SLM
-
0 .
006
z = Hax Na = 0 53360 x 3 5
. .
= 1 8676
.
Bb
Uploaded in
Example
It is desired to reduce the ammonia content of 2.031 mol/s of an ammonia-air mixture (300 K and 1
atm) from 5.0 to 0.04 mol% by water scrubbing. A 0.3-m-diameter tower packed with 25-mm ceramic
Raschig rings to a depth of 3.5 m is available. Is the tower satisfactory, and if so, what water rate
should be used? At 300 K, ammonia-water solutions follow Henry's law up to 5 mol% ammonia in the
liquid, with m = 1.414.
0.05
0.04
0.03
y
Bb 0.02
Uploaded in
0.01
0
0 0.01 0.02 0.03 0.04
x 10
Example
In the Fertil Company in UAE, a waste gas stream from a processing plant contains 96 mol% air and 4
mol% ammonia. Pure water with a flow rate of 2×Ls,min is to be used as a solvent to reduce its
ammonia content in a packed absorption tower being operated at 293 K and 1 atm pressure. It is
desired to have the outlet gas stream with 99.5 mol% air and 0.5 mol% ammonia. The inlet gas flow
rate is 57800 mol/h. Find the height of packed tower.
GIVEN:
Water density = 1000 kg/m3. Water viscosity = 0.8 cP = 0.8 × 10-3 Pa.s.
Gas viscosity = 0.0184 cP = 1.84 × 10-5 Pa.s.
Molecular weights of water, NH3 and air are 18, 17, and 29 g/mol, respectively.
Packing material is 25-mm Raschig rings with specific surface area, a = 190 m2/m3, ah = 49.6 m2/m3,
and packing factor, Fp = 179 ft2/ft3.
Fraction of flooding = 0.6.
Equilibrium line equation: y = 1.5x.
OVERALL mass transfer coefficients,%&% = %% = 0.3 mol/s.m2, and %&' = %' = 0.2 mol/s.m2
Bb
Uploaded in
11
for information
Tray Towers considerations: * Just
-
our
- The fraction of component absorbed in a counter current operation depends on the number of stages and the absorption factor, A = Ls/mVs
- The larger the value of A the fewer the number of stages required, however very large values of A will correspond to very large flowrates of
liquid solvent, which may mean that the operation can be economically infeasible. From an economic standpoint 1.25 < A < 2 is typically
used.
- In an ideal stage/tray the gas and liquid leaving the stage/tray are in equilibrium and Vapour-Liquid Equilibrium (VLE) laws can be applied.
- To determine the ideal number of trays we can use the graphical method which is called McCabe Thiele method
- For a dilute mixture, the equilibrium relationship is linear (Henry’s law) and the total liquid and vapour flowrate are very similar to the
solvents liquid and vapour flowrates (LS ∼ L and VS ∼ V) ∴ A = Ls/mVs ≃ L/mV.
- To allow for the small variations in A from one end of the tower to the other due to the change in L/V as a result of absorption or desorption
can be roughly considered using the geometric mean of A, !26 = !:;< !=;::;>
- For these cases modified Kremser equations are used with L and V, to calculate the number of ideal stages.
12
* Important
Tray Efficiency:
- Insufficient contact time may not allow equilibrium to be achieved, in such cases the tray/stage
is not ideal and actual number of stages needs to be calculated following the overall tray
oa -
eff =
xideal
trasa
efficiency equation:
overall efficiency of all
-always between
tray, ·
Efficiency is 100%
[ I a
ifthetrayten
↑
Number of ideal trays
=9 = trays
= stages
Number of actual trays
- -
- this
in
Real reality
- Another efficiency definition is Murphee tray efficiency (varies across the tower):
!? $ ($
=* = !@ = $1∗ ($12)
1 12)
1
Number of ideal trays ln 1 + =* ! − 1
=9 = =
Number 1
ln
!
#
!= P = slope of equilibrium line, =9 is valid only when m and L/V are constant 13
>-
CHEG324 Mass Transfer
Faisal Abdulla AlMarzooqi
1
Single-Stage Operation – Flash Vaporisation
Components in a binary mixture (two component mixture) can be separated if their volatility is significantly different.
This separation can be achieved via flash vaporization / distillation, in a single-stage operation
The binary feed mixture is partially vaporized and is allowed to reach vapour-liquid
equilibrium (VLE) in the flash drum. Vapour phase composition of the most volatile
component (yD) and liquid phase composition of the most volatile component (xW) Flash Drum
leaving the unit are in equilibrium.
The pressure is reduced in the flash drum, causing vapour formation from the liquid in an adiabatic condition. The more
volatile component vaporizes more than the less volatile component.
Product D is entirely vapour and is rich in the more volatile component, product W is liquid and is lean in the more volatile
component.
To better understand this process we need to establish Equilibrium Relationships and Boiling-Point Diagrams 2
Single-Stage Operation – Flash Vaporisation
Vapour-Liquid Equilibrium (VLE): Binary mixture of components (A) and (B) and two phases Vapour and Liquid
𝐵 T = Temperature
Objective is to separate (A) and (B) Antoine’s equation log10 𝑃𝐴 = 𝐴 − A, B and C = Constants of
𝐶+𝑇
chemical
Raoult’s law: pA = PAxA pA = partial pressure of component (A) PA = Vapour pressure of component (A)
xA = composition of (A) in liquid phase
Dalton’s law: pA = yAPTotal yA = composition of (A) in vapour phase PTotal = Total pressure
From the diagram find the boiling temperature of pure (A) and pure
(B)?
Azeotropes: for certain binary mixtures (e.g. ethanol-water) the boiling point diagram
is not ideal as the one on the right hand side here. Instead it follows the trend shown
= xA1
below:
Minimum-boiling Azeotrope
Boiling Point Diagram
4
Single-Stage Operation – Flash Vaporisation
= yA1
Boiling-Point Diagrams:
T1
Azeotropes: Nitric acid and water form a maximum-boiling azeotrope. Flash Drum
Depending on where the initial starting composition of the azeotropic mixture is, it is
possible to get a pure sample of one of the components and impossible to get a pure
sample of the other.
= xA1
Maximum-boiling Azeotrope
Boiling Point Diagram
5
Single-Stage Operation – Flash Vaporisation
How to draw a boiling point diagram: = yA1
1. Plot the boiling points of the pure components using the boiling point
T1
temperatures of the two pure components (TbA and TbB) Flash Drum
2. Choose a temperature T between TbA and TbB
3. Calculate PA and PB for the chosen T using Antoine’s equation
4. Calculate xA using PAxA + PB(1-xA) = PTotal
5. Calculate yA using PAxA = yAP
6. Plot the two points using the calculated coordinates (T,xA) and (T,yA)
= xA1
7. Repeat steps 2 to 7 using a different temperature each time
Lever-rule:
M1
6
Single-Stage Operation – Flash Vaporisation
Material balance:
−𝑊 𝐹 −𝑊 𝐹
𝑦𝐷 = 𝑥𝑊 + 𝑧𝐹 or arbitrarily 𝑦= 𝑥+ 𝑧𝐹 = yA1
𝐷 𝐷 𝐷 𝐷
when 𝑥 = 𝑧𝐹 ⟶ 𝑦 = 𝑧𝐹
T1
−𝑊 𝐹 Flash Drum
∴ line 𝑦 = 𝑥+ 𝑧𝐹 is a straight line that crosses coordinates 𝑧𝐹 , 𝑧𝐹
𝐷 𝐷
−𝑊
and 𝑥𝑊 , 𝑦𝐷 and has a slope of
𝐷
equilibrium
−𝑾 𝑭
𝒚= 𝒙+ 𝒛 = xA1
𝑫 𝑫 𝑭 y=x
𝒚𝑫 𝒙 𝑾 , 𝒚𝑫
𝒛𝑭
𝒛𝑭 , 𝒛𝑭
7
𝒙𝑾 𝒛𝑭
Example 1
A stream of a heptane-octane mixture, containing 70 mol% heptane is continuously flashed in a flash distillation drum at 1 bar, such that 70% of
the feed is vaporized. Find out the compositions of the vapour and liquid streams leaving the flash distillation drum. What is the Temperature of
the streams leaving the unit?