CH351 Mass Transfer 21Sep07 - Clarkson Universitypeople.clarkson.edu/~skrishna/CH351 Mass Transfer...
Transcript of CH351 Mass Transfer 21Sep07 - Clarkson Universitypeople.clarkson.edu/~skrishna/CH351 Mass Transfer...
1
CH351 Mass TransferCH351 Mass Transfer
Sitaraman Krishnan9/26/07
2FickFick’’ss First Law: Steady State First Law: Steady State
Molecular DiffusionMolecular Diffusion
axis- along gradient ionconcentrat
/scm t,coefficien diffusion
s)mol/(cm axis,- along A component offlux
A
2AB
2A,z
AABA,z
zz
cD
zJz
cDJ
=∂∂
=
⋅=∂∂
−=
3
( ) ( ) ( )2
31
B3
1A
21
AB
75.1
AB00143.0
:equation Giddings and Schetler Fuller,
⎥⎦⎤
⎢⎣⎡ Σ+Σ
=
vvMP
TD
molecule a of mass molecules )(spherical of diameter
tcoefficien diffusion self 3
2
:GasesDensity Low orTheory Kinetic From
*AA
21
33
223*AA
==
=
⎟⎟⎠
⎞⎜⎜⎝
⎛ κ
π=
mdD
mT
PdD
4
( )
B solvent in diffusing is A Species
104.7
:Liquids in Diffusion for Equation Chang-Wilke
6.0AB
21BB
8
VTMDAB
η
Φ×=
−
5
• pi = partial pressure of component i
• ci = molar conc. of component i
• P = total pressure (atm, bar, N/m2, mmHg, Torr)
• c = total molar concentration of gas (mol/cm3, mol/m3, …)
( ) ( )
cRTP
RTccpp
RTcpRTcp
RTVnpRTnVp
=
+=+
=
=
=⇒=
BABA
BB
AA
AAAA
Partial Pressures, Molar Partial Pressures, Molar ConcetrationsConcetrations, Total Pressure, Total Pressure
6 Concentrations, Partial Concentrations, Partial Pressures, and Mole FractionsPressures, and Mole Fractions
Pp
ccy
Pp
ccy
BBB
AAA
B of fraction Mole
A of fraction Mole
===
===
• At constant total pressure, P, and constant temperature, T, total molar concentration, c, is constant.
• For each species, mole fraction ∝concentration ∝ partial pressure
cRTPRTcpRTcp
==
=
BB
AA
7FickFick’’ss First Law in terms of Mole First Law in terms of Mole
FractionsFractions
zy
RTPD
zycD
zcDJ
∂∂
−=
∂∂
−=
∂∂
−=
AAB
AAB
AABA,z
zy
RTPD
zycD
zcDJ
∂∂
−=
∂∂
−=
∂∂
−=
BBA
BBA
BBAB,z
8
What is the net molar flux of A that a stationary observer would measure?
fluid element
direction of bulk flowdirection of bulk flow
direction of direction of diffusionaldiffusional
flowflowcA
position
observer stationary to relative A ofvelocity A,z =
=
vvcN A,zAA,z
9What is the net molar flux of A that an observer who moves with the fluid element would measure?
Moving observer will measure only flux due to diffusion.
( )
zcD
vvcJ A,zAA,z
∂∂
−=
−=
AAB
z *
10
Total Flux, Total Flux, NNA,zA,z = = JJA,zA,z + + ccAAvvzz**
( )
scmmol
scm
cmmol
**
23
A,zAA,z
B,zBA,zAz
zA,zAA,z
⋅=×
=
+=
−=
vcN
vyvyvvvcJ • vA,,z = velocity of A
measured by a stationary observer
• vB,z = velocity of B measured by a stationary observer
• vz* = molar average velocity
11
General Form of General Form of FickFick’’ss First LawFirst Law
( )
( )B,zA,zAA
ABA,z
BAAA,zA,z
zAA,zA,z
motion bulk to dueflux flux diffusive*
NNyz
ycDN
NNyJN
vcJN
++∂∂
−=
++=
+=
+=
12 EquimolarEquimolar Counter Diffusion Counter Diffusion (EMCD)(EMCD)
• A simplifying assumption that– allows easier
solution of the general form of Fick’s first law
– makes analytical solution possible
( )
zcDJN
NNyJN
NN
∂∂
−==
++=∴
−=
AABA,zA,z
B,zA,zAA,zA,z
B,zA,z
0
13
Problem 1 (EMCD assumption)Problem 1 (EMCD assumption)
⎟⎟⎠
⎞⎜⎜⎝
⎛−−
=
∂∂
−==
12
A,2A,1ABA,z
AABA,zA,z
zzyy
RTPDN
zy
RTPDJN
Mixture of two gases, A and B, in a tube with conc. gradient
z-axis
z = z1 = 0
yA,1
pA,1P = constant, T = constant
yA,2
pA,2
z = z2
( )112
A,2A,1A,1A zz
zzyy
yy −⎟⎟⎠
⎞⎜⎜⎝
⎛−−
−=
CONCENTRATION PROFILEFLUX
14 Problem 2 (EMCD assumption)Problem 2 (EMCD assumption)
sA
vpA
vpA
cRTpc
pp
RrA
RrA
==
=∴
=
=
0 bAA ≈=
∞→cc
r
Evaporation from surface of naphthalene ball
Air near surface is saturated with naphthalene
r
r+Δr
R
( )
( )
( ) ⎟⎠⎞
⎜⎝⎛−π=
−×π=
⎟⎠⎞
⎜⎝⎛−
=
=−
−⇒=⎟
⎠⎞
⎜⎝⎛
∂∂
∂∂
∂∂
−=
=
smol4
4 rate nEvaporatio
s cmmol
0
state,steady At
bA
sAAB
bA
sA
AB2
2
bA
sA
ABA
bA
sA
bAAA2
AABA
ccDR
RccDR
RccDN
rR
cccc
rcr
r
rcDN
Rr
rr
15
UnimolecularUnimolecular DiffusionDiffusion( )
zy
yRTPD
yJ
N
NyJN
N
NNyJN
∂∂
⎟⎟⎠
⎞⎜⎜⎝
⎛−
⎟⎠⎞
⎜⎝⎛−=
−=
+=∴
=
++=
A
A
AB
A
A,zA,z
A,zAA,zA,z
B,z
B,zA,zAA,zA,z
11
1
0
16
Solvent Evaporation (UMD)Solvent Evaporation (UMD)
Liquid, A
z = z1 = 0 pA1, yA1
pA2, yA2
z
z = z2
• At z = z1, air is saturated with liquid: pA1 = vap. pressure
• At z = z2, all A carried away by air: pA2 ~ 0
17
Solvent EvaporationSolvent Evaporation
⎟⎟⎠
⎞⎜⎜⎝
⎛
−=
⎟⎟⎠
⎞⎜⎜⎝
⎛−−
⎟⎟⎠
⎞⎜⎜⎝
⎛⎟⎠⎞
⎜⎝⎛=
∂∂
⎟⎟⎠
⎞⎜⎜⎝
⎛⎟⎠⎞
⎜⎝⎛−=
B,1
B,2
B,1B,2lmB,
12
A,2A,1
lmB,
ABA
A
B
ABA,z
ln
1
1
yy
yyy
zzyy
yRTPDN
zy
yRTPDN
⎟⎟⎠
⎞⎜⎜⎝
⎛−−
⎟⎟⎠
⎞⎜⎜⎝
⎛
−−
=⎟⎟⎠
⎞⎜⎜⎝
⎛
−− 12
1
A,1
A,2
A,1
A
11
11 zz
zz
yy
yy
FLUX
CONC. PROFILE
18 Evaporation of Benzene Evaporation of Benzene ((bpbp 80 80 °°C) at 25 C) at 25 °°C and 70 C and 70 °°CC
25 25 °°CC 70 70 °°CC
19
Flux Profiles (UMD)Flux Profiles (UMD)
20 Evaporation of Dichloromethane Evaporation of Dichloromethane ((bpbp 40 40 °°C) at 25 C) at 25 °°CC
21Diffusion Into a Falling Liquid FilmDiffusion Into a Falling Liquid Film
( )⎥⎥⎦
⎤
⎢⎢⎣
⎡⎟⎠⎞
⎜⎝⎛δ
−μδρ
=22
y 12
zgzv
z
yLiquid
Gasvy(z)
cA(z)cA,i
W
x
OBJECTIVE:• To determine molar flux
(mol cm−1 s−1) at the gas−liquid interface.
• The overall rate of mass transfer (mol/s).
( )entrance top the from position at
)0( interface atflux molar local0zA
y
zyN ===
22
Liquid Element
y
y+Δy
zz+Δz
( ) ( )
( ) ( )
0
0
0
A,zyA,
zA,zzzA,zyyA,yyyA,
zzA,zzA,z
yyyA,yyA,
=∂
∂+
∂
∂
=Δ
−+
Δ
−
=Δ⋅−Δ⋅+
Δ⋅−Δ⋅
Δ+Δ+
Δ+
Δ+
zN
yN
z
NN
y
NN
yWNyWN
zWNzWN
*
*
zAA
ABA,z
yAA
AByA,
vcz
cDN
vcycDN
+∂∂
−=
+∂∂
−=
2A
2
ABA
y zcD
ycv
∂∂
=∂∂
yyA,N
zA,zN
ΔyyyA, +N
ΔzzA,z +N Δz Δy
W
23
z
yLiquid
Gasvy(z)
cA(z)cA,i
W
x
2A
2
ABA
y zcD
ycv
∂∂
=∂∂
( )
yvD
cz
cDN
vyD
zcy,zc
zz π
=∂∂
−=
⎟⎟⎟⎟⎟
⎠
⎞
⎜⎜⎜⎜⎜
⎝
⎛
=
==
maxy,ABiA,
0
AAB0A,z
maxy,AB
iA,A
4erfc
:solution eApproximat
24
( ) ( )
( ) ( )
( )yWy
vDc
yWN
y
yvD
cz
cDN
z
zz
d
d
area flux position at second per dtransferre A of Moles
maxy,ABiA,
0A,z
maxy,ABiA,
0
AAB0A,z
⋅×⎟⎟
⎠
⎞
⎜⎜
⎝
⎛
π=
⋅×=
×=
π=
∂∂
−=
=
==
25
( )
gas and element liquid between contact of time where
12
2
2
d1
d
tower the of length over second per dtransferre A of moles total
ABiA,
maxy,ABiA,
maxy,ABiA,
0
maxy,ABiA,
0
maxy,ABiA,
=τ
⎟⎠⎞
⎜⎝⎛τ
⎟⎠⎞
⎜⎝⎛
π×=
π×=
π=
π=
⋅×⎟⎟
⎠
⎞
⎜⎜
⎝
⎛
π=
∴
∫
∫
DcWL
LvD
cWL
LvDWc
yy
vDWc
yWy
vDc
L
L
L
26
Mass Transfer CoefficientMass Transfer Coefficient
• Fick’s law: flux ∝ conc. gradient– const. of proportionality = diffusion coefficient
• Another approach to quantify flux:– Flux ∝ conc. driving force, ΔcA
– const. of proportionality = mass transfer coefficient, k
– Similar to Newton’s “law” of cooling
27
⎟⎠⎞
⎜⎝⎛Δ⋅⎟
⎠⎞
⎜⎝⎛=⎟
⎠⎞
⎜⎝⎛
⋅
=
Δ⋅=
ΔΔ
=
3A2A
AA
AABA
cmmol
scm
scmmol
scm of units has
tcoefficien transfer mass :approach gEngineerin
:law sFick'
ckN
k
kckN
zcDN
28 Evaporation from surface of Evaporation from surface of naphthalene ballnaphthalene ball
bA
sA
vpA
cc
cRTpc
rA
RrA
=
==
∞→
=
( )
cNk
ccc
Δ=
−=Δ=
A
bA
sA
t,coefficien transfer Mass
transfer mass for force driving Conc.
R
( )
( )( ) R
DccR
ccD
cNk
RccDN
Rr
ABb
As
A
bA
sA
AB
A
A
bA
sA
ABA
:us given hadlaw sFick' of Solution
=−
−
=Δ
=∴
−=
=
29
Sherwood NumberSherwood Number• For evaporation from surface of a sphere, we obtained:
• kD/DAB is a dimensionless quantity that often appears in mass transfer calculations.
• It is called the Sherwood number and is denoted by Sh.
• For diffusion from surface of a sphere into a stagnant fluid, Sh = 2
2
diameter) sphere (2
AB
ABAB
=⋅
∴
===
DDk
DD
DR
Dk
30
Convective Mass TransferConvective Mass Transfer• Material is transported between
– a solid surface and a moving fluid (gas or liquid)
– two relatively immiscible moving fluids (gas and liquid, or liquid and liquid)
• Examples– Mass-transfer of gas into a falling liquid film– Mass-transfer of naphthalene into a flowing
gas stream– Mixing in a stirred vessel
31
Turbulent FlowTurbulent Flow
• Laminar flow is characterized by streamlines
• Turbulent flow is characterized by chaotic flow of packets of fluid called “eddies”
• Rate of mass transfer in laminar flow is determined by molecular diffusivity, DAB
• Rate of mass transfer in turbulent flow is determined by both molecular diffusivity, DAB
and turbulent diffusivity, Dt
32 Mass Transfer Correlations for Mass Transfer Correlations for Convective FlowsConvective Flows
•• Dimensional AnalysisDimensional Analysis• Example
– The inner wall of a circular tube is coated with species A (e.g., naphthalene)
– Mass transfer occurs to a fluid flowing through the tube (e.g., air)
cAs cA
b D (cm)ρ (g cm−3)μ cm−1 s−1)DAB (cm2 s−1)
v (cm s−1)kc (cm s−1)
33
edcba
−1−1−100−1s21−1−311cm001100gm
DABvμρDkc
equations 3 variables, 51
1230
−=−−−=++−−
=+
edcedcba
cb
cedcaedb
cb
+−=−−+−=++−
−=
1123
( )
[ ]( ) ( ) ( ) ( ) ( )eABdcba
c
c
bA
sAcA
constant
tcoefficien transfer mass convective
DvDk
kcckN
μρ=
=
−⋅=
34
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
−−+−
=⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
==⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
+−+−
−
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡−−−=
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
=⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
+−+−
−=
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
−−−
−−
caa
c
edb
cca
c
edb
cca
c
edb
1
11
113213
001
11
110213001
BAxAxA
BAx
11
35 [ ]( ) ( ) ( ) ( ) ( )[ ]( ) ( ) ( ) ( ) ( )
[ ] ( ) ( ) ( )
[ ]
[ ]
( )ydiffusivit mass
ydiffusivit momentumnumber Schmidt
constant
constant
1constant
constant
constant
AB
1ca
AB
1a
AB
c
caAB
1ca11a
caAB
1acca
eAB
dcbac
=ρμ
==
=
⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=⎟⎟⎠
⎞⎜⎜⎝
⎛
μρ⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=
μρ=
μρ=
βα
+++
−−++−−−+
−−+−
DSc
ScReSh
DDv
DDk
DDDv
DvD
DvDk
ca
36 [ ]( ) ( ) ( ) ( ) ( )
[ ] ( ) ( ) ( )
[ ]
[ ]
[ ] ( )
factor-J Colburn and Chilton
constant
constant
constant
constant
constant
D3/2c
323/2c
c
1ca
AB
ac
caAB
caa
caAB
1accac
==
=
=
⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=⎟⎠
⎞⎜⎝
⎛
μρ⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=
μρ=
+δγ
δγ
++
−−+−−
−−+−
JScvk
ScReScvk
ScRevk
DDv
vk
vDDv
DvDk
ca
37
Turbulent Flow Inside PipesTurbulent Flow Inside Pipes
33.083.0
ABAB
c
Re023.0
:300060 and 2100 When
ScSh
Sc . Re
DScDvRe
DDkSh
=
<<>
ρμ
=μρ
==
In general, Sc for gases is in the range 0.5−3, and for liquids, Sc > 100.
38
Flow Past Single SpheresFlow Past Single Spheres
3/162.0
3/15.0
3/153.0
ABAB
c
Re347.0 :70001Re2000 liquids, For
Re95.02 :2000Re2 whenliquids, For
552.02
2.70.6 and 48000,1 whengases, For
ScSh
ScSh
ScReSh
ScRe
DScDvRe
DDkSh
=<<
+=<<
+=
<<<<
ρμ
=μρ
==
39
Naphthalene EvaporationNaphthalene Evaporation
• A sphere of naphthalene having a diameter of 1 cm is suspended in air at 1 atm, and flowing at a velocity of 0.3 m/s. The diffusion coefficient of naphthalene in air at this temperature is 6.92×10−6 m2/s. The molar density of naphthalene solid is 8.86×10−3 mol/cm3. Calculate the initial rate of evaporation of naphthalene from the surface. Estimate the time required to reduce the diameter from 1 to 0.5 cm.
40 Mass Transfer in Packed BedsMass Transfer in Packed Beds
tube of area sectional-crossrateflow volumetric
packing withouttubeempty the invelocity average gas of '
spheres the of diameter0.5. and 0.3 betweenusually is of value The
solid plus space void of volume totalspace void of volumebed the in fraction void
''
4548.0,0000110 whenspheres, of bed packed a in gases For
p
AB
p32cD
4069.0D
=
==
=ε
==ε
ρμ
=μ
ρ==
ε=
<<
−
velocity lsuperficiav
D
DSc
vDReSc
vkJ
ReJ
Re
41
Mass Transfer in Packed BedsMass Transfer in Packed Beds
( )
particles. spherical-non the of area surface the use flux, calculate Toparticle solid given the as area surface same the withsphere a of dia.
particles, spherical-non For
Re250.006901165 and ,150055 whenliquids, For
Geankoplis and WilsonRe09.170000165 and ,550.0016 whenliquids, For
p
31.0D
32D
=
ε=
<<<<ε
=
<<<<
−
−
D
J
ScRe
J
ScRe
42 Packed Bed of Benzoic Acid Packed Bed of Benzoic Acid SpheresSpheres
• Water at 26.1 °C flows at a rate of 5.514×10−7
m3/s through a packed bed of benzoic acid spheres having a diameter of 6.375 mm. The void fraction of the bed is 0.436. The tower diameter is 0.0667 m and the tower height is 0.1 m. The solubility of benzoic acid in water is 2.948 ×10−2 kg mol/m3. Predict the mass transfer coefficient kc and the outlet concentration of benzoic acid in water.
43
ε = 0.436Dp = 6.375×10−3 m, Ap = 0.01198 m2
DAB = 1.25×10−9 m2/s (Wilke-Chang)
( )
( )
( )( )( ) 150.1108718.0
7.99610578.110375.6'
sm10578.1
0667.04
10514.5
4
'
6.70210245.17.996
108718.0
3
43p
4
2
7
2
9
3
AB
=×××
=μ
ρ=
×=π
×=
π=
=×
×=
ρμ
=
−
−−
−−
−
−
vDRe
T
Qv
DSc
Water flow rate, Q = 5.514×10−7 m3/sμ = 0.8718×10−3 Pa·s, ρ = 996.7 kg/m3
cA,2 = ?
Tower dia. T = 0.0667 m; Height H = 1 m
cA,1 = 0
44
( )
( )( )( )
( ) ( )
( )
( )
( )( ) ( )( ) 2
3
3
p
b
2pp
b3
pp
p
b
3322b
63/243/2Dc
3/23/2D
4
m 1855.010375.6
436.0110494.3616
spheres of area surface Total
16
bed the in spheres of number Let1 bed the in spheres of volume
fraction Void
m 10494.31.00667.044
bed of volume Total
m/s 10447.46.70210578.1277.2'
277.2150.10436.009.109.1
m/s 10578.1'150.16.702
=×
−×=
ε−⋅=
π⋅==
ε−⋅=⎟⎠⎞
⎜⎝⎛ π⋅∴
=
ε−⋅=∴ε=
×=π
=π
==
×=×=⋅⋅=
==ε
=
×===
−
−
−
−−−−
−−
−
DV
DNA
VDN
NV
HTV
ScvJk
ReJ
vReSc
45
( ) ( )
( ) ( ) ( )( )( )
( )( ) A,22
bA
3A,11
bA
32sA
2b
As
A
1b
As
A
2b
As
A1b
As
Alm
bA
sA
3
3
32
A,1A,2lmb
As
Ac
c outlet at acidbenzoic of conc.
mol/m kg 0c inlet at acidbenzoic of conc.
mol/m kg 10948.2
ln
mmol kg
sm
mmol kgm
sm
:balance Mole
==
===
×=
⎪⎭
⎪⎬⎫
⎪⎩
⎪⎨⎧
−
−
−−−=−
⋅⋅⋅
−⋅=−⋅⋅
−
c
c
c
cccc
cccccc
ccQccAk
46
( ) ( )
( )
( )32
7
622
cA,1
sA
sAA,2
A,1A,2
A,2s
A
A,1s
A
A,1A,2c
mol/m kg 10287.2
10514.51855.010447.4exp*010948.210948.2
exp
ln
−
−
−−−
×=
⎟⎟⎠
⎞⎜⎜⎝
⎛
×××
−−×−×=
⎟⎠
⎞⎜⎝
⎛−−−=∴
−⋅=
⎟⎟⎠
⎞⎜⎜⎝
⎛
−
−
−⋅⋅
QAkcccc
ccQ
cccc
ccAk
47 Mass Transfer to Bubbles and Mass Transfer to Bubbles and ParticlesParticles
• Small particles in suspension– Mass transfer from small gas bubbles to liquid
phase– Mass transfer from liquid phase to the surface
of catalyst particles, microorganisms, liquid drops, etc.
– Mass transfer coefficient depends on free fall or rise of particles due to gravitational forces
48• Mass transfer coefficient, kc, in mass transfer to small particles is
affected by natural convection. Natural convection occurs when there is significant density difference between the particles of the dispersed phase (gas bubbles or liquid drops) and the fluid (continuous phase). In such cases, kc is expected to depend on: – diameter Dp of the particles of dispersed phase (e.g., O2 bubble)
– density ρc of the continuous phase (e.g., water)
– viscosity μc of the continuous phase (e.g., water)
– the buoyant force gΔρ where Δρ is the density difference between the dispersed and continuous phases, and g is the acceleration due to gravity (9.81 m/s2)
– the diffusion coefficient of the molecules of dispersed phase (oxygen) in the continuous phase (water).
• Using dimensional analysis, derive an expression for the mass transfer coefficient in terms of the dimensionless numbers Sh and Sc. The dimensionless group with the buoyant force variable, gΔρ, is called the Grashof number, Gr. Derive an expression for Gr.
49
( )
positive) (always phases continuous and dispersed the between differencedensity the of magnitude
m/s 9.81
solution the ofviscosity
particle solid or bubble gas the of diameter solution in A solute the ofy diffusivit
tcoefficien transfer mass side'-liquid'
31.02
2c
p
AB
L
3/1
2c
c3/2
p
ABL
=ρΔ=
=μ
ρμ=
==
=
⎟⎟⎠
⎞⎜⎜⎝
⎛
ρ
ρμΔ+= −
g
DSc
DDk
gScDDk
ABcc
Mass Transfer to Small Particles Mass Transfer to Small Particles (< 0.6 mm)(< 0.6 mm)
LOW DENSITY SOLIDS OR SMALL GAS BUBBLES IN AGITATED SYSTEMS
50 Mass Transfer to Large Gas Mass Transfer to Large Gas Bubbles or Liquid Drops (> 2.5 mm)Bubbles or Liquid Drops (> 2.5 mm)
positive) (always phases continuous and dispersed the between differencedensity the of magnitude
m/s 9.81
solution the ofviscosity
tcoefficien transfer mass side'-liquid'
42.0
2c
ABc
c
L
3/1
2c
c5.0L
=ρΔ=
=μ
ρμ
=
=
⎟⎟⎠
⎞⎜⎜⎝
⎛
ρ
ρμΔ= −
g
DSc
k
gSckAERATION OF PURE LIQUIDS IN MIXING VESSELS; SIEVE-PLATE COLUMNS
51 Mass Transfer to Particles in Mass Transfer to Particles in Highly Turbulent MixersHighly Turbulent Mixers
• Turbulent forces become larger than gravitational forces. Mass transfer coefficient is determined primarily by agitation power-input and not by buoyant forces (natural convection).
( )
solution the ofdenstity solution the ofviscosity
tcoefficien transfer mass side'-liquid'
/13.0
c
c
ABc
c
L
3/1
2c
c3/2L
=ρ
=μ
ρμ
=
=
⎟⎟⎠
⎞⎜⎜⎝
⎛
ρ
μ= −
DSc
k
VPSck
52 InterInter--phase Mass Transferphase Mass Transfer• Mass transfer at gas−liquid or liquid−liquid
interfaces• Consider mass transfer from naphthalene to air,
or from benzoic acid to water– Mass transfer rate is determined by concentration
gradients in air or water
• In mass transfer at interface of two immiscible liquids A and B (or gas A and liquid B)
• Mass transfer rate is determined by concentration gradients on both sides of the interface (in phase A and phase B)
53
Concentration Profile at InterfaceConcentration Profile at Interface
• Consider evaporation of napthalene from surface of a sphere (1 cm dia.) at 45 °C and 1 atm total pressure.
bAA
sAA
A2 0
cc
cc
rcr
r
r
Rr
=
=
=⎟⎠⎞
⎜⎝⎛
∂∂
∂∂
∞→
=
rR
cccc
=−
−∴ b
As
A
bAA
cm 5.0mol/cm 0
mol/cm 10798.23b
A
38sA
=
≈
×= −
Rc
c
54
55 ‘‘TwoTwo--FilmFilm’’ Theory & Overall Theory & Overall Mass Transfer CoefficientMass Transfer Coefficient
gas−liquid interface
Gas phase Liquid phase
Mass transfer from gas to liquid
pAb
pAi
cAi
cAb
56 ( )
( )
( ) ( )bA
iAl
iA
bAgA
l
2b
Ai
Al
2g
2i
Ab
Ag
equal. are interface the across fluxes two Thes
cmtcoefficien transfer mass side-liquid
scmmol side'-liquid' onFlux
scmatmmoltcoefficien transfer mass side-gas
scmmol side'-gas' onFlux
cckppkN
k
cck
k
ppk
−=−=⇒
⎟⎠⎞
⎜⎝⎛=
⎟⎠⎞
⎜⎝⎛
⋅−=
⎟⎠⎞
⎜⎝⎛
⋅⋅=
⎟⎠⎞
⎜⎝⎛
⋅−=
57
⎟⎠⎞
⎜⎝⎛
⋅
⋅=∴
3
A
iAA
iA
cmatmmol Aspecies for
constant) sHenry' (e.g., constant mequilibriu the is
solution liquid the and mixture gas the between mequilibriu is there interface, the at that, Assume
H
pHc
58
. is phase gas the in A of pressure partial
the whenliquid the in A of conc. saturation ** ionconcentrat Define
1: for Solving
and Now,
bA
A
bAAA
lg
A
bA
bAA
AA
l
AbA
g
AbAA
g
AbA
iA
l
AbA
iA
p
cpHc
kkH
cpHNN
kNc
kNpH
kNpp
kNcc
=
=
+
−=
⎟⎟⎠
⎞⎜⎜⎝
⎛+=⎟
⎟⎠
⎞⎜⎜⎝
⎛−∴
⎟⎟⎠
⎞⎜⎜⎝
⎛−=⎟⎟
⎠
⎞⎜⎜⎝
⎛+=
59
additive. are interface an across sresistance transfer mass Thus,
'resistance transfer mass'tcoefficien transfer mass
1
11
11
* t,coefficien transfer mass all'-Over'
1*
lg
A
L
lg
Ab
AA
AL
lg
A
bAA
A
=
+=∴
⎟⎟⎠
⎞⎜⎜⎝
⎛+
=−
=
+
−=∴
kkH
K
kkHcc
NK
kkH
ccN
60 Laminar Boundary Layer on a Laminar Boundary Layer on a Flat Plate (Flat Plate (ReRexx < 5< 5××101055))
x
y
x = 0
v0
Flat plate
0.99v0
δxvx
0.99v0
Velocity Velocity boundary boundary
layerlayer
3
xx0
x5.0
x
x0x 5.05.196.4
⎟⎟⎠
⎞⎜⎜⎝
⎛δ
−⎟⎟⎠
⎞⎜⎜⎝
⎛δ
==δ
μρ
=yy
vv
RexxvRe
61 Laminar Boundary Layer on a Laminar Boundary Layer on a Flat PlateFlat Plate
( )μρ
=⎟⎠⎞
⎜⎝⎛−=
∂∂
=
0x
3/12/1x
sA
bA
0
A where332.0 xvReScRex
ccyc
y
Conc. Conc. boundary boundary
layerlayer
x
y
x = 0
v0
Flat plate
δc
cA
cAs
cAb
62
( ) ( )
3/12/13/1
AB
2/10
AB
c
0xc,c
3/12/1xx
3/1
AB
2/10
AB
xc,
bA
sA
0
AAB
bA
sA
xyA,xc,
664.0664.0
d1 : length and widthof plate flat a
overflow laminar for tcoefficien transfer-mass Mean
332.0332.0
n)(definitio
:by given is tcoefficien transfer mass convection Local
ScReShD
LvD
Lk
xkL
kLW
ScReShD
xvD
xk
cc
ycD
cc
Nk
LL
L
y
=⇒⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=⎟⎟⎠
⎞⎜⎜⎝
⎛
=
=⇔⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
⎟⎟⎠
⎞⎜⎜⎝
⎛μρ
=
−
⎟⎟⎠
⎞⎜⎜⎝
⎛∂∂
−
=−
≡
∫
=
63
edcba
−1−2−100−1s2−2−1−311cm011100gm
DABgΔρμρDkc
equations 3 variables, 512
12230
−=−−−=+−−−
=++
edcedcba
dcb
dcedceba
dcb
212123
−−=++=+−
−−=
[ ]( ) ( ) ( ) ( ) ( )eABdcba
c constant DgDk ρΔμρ=
PROBLEM 18
64
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
−−−−−
=⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
==⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
−−++−−
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡ −=
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
=⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
−−++−−
=⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡
⎥⎥⎥
⎦
⎤
⎢⎢⎢
⎣
⎡−
−−
dcdc
d
eba
dcdc
dc
eba
dcdc
dc
eba
21
13
2121
100001213
2121
100231010
BAxAxA
BAx
11
65
[ ]( ) ( ) ( ) ( ) ( )[ ]( ) ( ) ( ) ( ) ( )
[ ]( ) ( ) ( ) ( ) ( )
[ ] ( ) ( ) ( )
( ) ( ) 2dc2dcAB
d
2dcc2dcdc3d2dc
AB
2dcAB
dcdc3d
AB
c
2dc1AB
dcdc13d
eAB
dcbac
constant
constant
constant
constant
++−−
−−++−−+
−−−−
−−−−−
ρΔ
μρ⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
=
ρΔμρ=∴
ρΔμρ=
ρΔμρ=
Dg
DD
DgDD
DkDgD
DgDk
66
[ ] ( ) ( ) ( ) ( ) ( )
[ ]
[ ]
2
3
2
32dc
ABAB
c
0AB
d2dd3d2dc
ABAB
c
number Grashof
constant
constant
constant
μρΔρ
==
=
⎟⎟⎠
⎞⎜⎜⎝
⎛
μρΔρ
⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
=⎟⎟⎠
⎞⎜⎜⎝
⎛
ρΔμρ⎟⎟⎠
⎞⎜⎜⎝
⎛ρμ
=⎟⎟⎠
⎞⎜⎜⎝
⎛
βα
+
−+
gDGr
GrScSh
gDDD
Dk
DgDDD
Dk
d
67 PROBLEM 17
( ) ( )
( )
38
3s
A
sAc
sAc
bA
sAc
cmmol 10797.2
K 4515.273molK
atm cm 06.82
1atm760555.0
0 surface atFlux
−×=
+××⎟
⎠⎞
⎜⎝⎛=
=−≈−=
c
ckckcck
68
503.13552.02
2.70.6 and 48000,1 whengases, For:SPHERE SINGLE A PAST FLOW
514.2
scm 0692.0
scm 0.174
41.172
scm 0.174
scm 30 cm 1
cm 1 Initially,
3/153.0
2
2
ABAB
2
=+=
<<<<
==ν
=ρμ
=
=×
=ν
=μρ
=
=
ScReSh
ScRe
DDSc
DvDvRe
D
69
( ) ( )
smol 10211.8
cm 0.1cmmol 10797.2
scm934.0
s
mol nevaporatio of rate Initial
scm 934.0
cm 1
cm 0692.0503.13
503.13
8
223
8
2sAc
2
ABc
AB
c
−
−
×=
×π×××=
π×=⎟⎠⎞
⎜⎝⎛
=×
=⋅
=∴
==
Dck
sDDShk
DDkSh
70
scm 10267.9
cmmol 1086.8
smol 10211.8
s
cm nevaporatio of rate Initial
36
33
8
m
2sAc
3
−
−
−
×=
×
×=
ρπ×
=
⎟⎟⎠
⎞⎜⎜⎝
⎛
Dck
71
m
sAc
m
2sAc2
m
2sAc
m
2sAc
2
3
dd
4dd4
4dd
dd4
dd
34
ρ−=⇒
ρπ×
−=π∴
ρπ×
−=ρ
π×−=−=
π=
π=
cktR
RcktRR
RckDckQtV
tRR
tV
RV
72
R
DRv
RcD
t
DRv
RcD
tR
DRv
RDSh
RD
DDShk
cktR
d2552.02
2d
2552.0221
dd
2552.0222
dd
33.0
AB
53.0sAAB
m
33.0
AB
53.0
m
sAAB
33.0
AB
53.0ABABAB
c
m
sAc
⎪⎭
⎪⎬⎫
⎪⎩
⎪⎨⎧
⎟⎟⎠
⎞⎜⎜⎝
⎛ ν⎟⎠⎞
⎜⎝⎛
ν+
⎟⎟⎠
⎞⎜⎜⎝
⎛ ρ−=∴
⎪⎭
⎪⎬⎫
⎪⎩
⎪⎨⎧
⎟⎟⎠
⎞⎜⎜⎝
⎛ ν⎟⎠⎞
⎜⎝⎛
ν+⋅⎟
⎠⎞
⎜⎝⎛⋅⎟
⎟⎠
⎞⎜⎜⎝
⎛
ρ−=∴
⎪⎭
⎪⎬⎫
⎪⎩
⎪⎨⎧
⎟⎟⎠
⎞⎜⎜⎝
⎛ ν⎟⎠⎞
⎜⎝⎛
ν+==
⋅=
ρ−=
73
cm 0.5 and cm 1
d2
d2552.02
2d
21
sAAB
m
33.0
AB
53.0sAAB
m
0
1
2
2
1
==
⋅⎟⎟⎠
⎞⎜⎜⎝
⎛ ρ=
⎪⎭
⎪⎬⎫
⎪⎩
⎪⎨⎧
⎟⎟⎠
⎞⎜⎜⎝
⎛ ν⎟⎠⎞
⎜⎝⎛
ν+
⋅⎟⎟⎠
⎞⎜⎜⎝
⎛ ρ−=
∫
∫∫
RR
RShR
cDt
R
DRv
RcD
t
R
R
R
R
t
74 D R Re Sc Sh 2R/Shcm cm cm1.00 0.50 172.414 2.514 13.503 0.07410.98 0.49 168.966 2.514 13.380 0.07320.96 0.48 165.517 2.514 13.257 0.07240.94 0.47 162.069 2.514 13.132 0.07160.92 0.46 158.621 2.514 13.006 0.07070.90 0.45 155.172 2.514 12.878 0.06990.88 0.44 151.724 2.514 12.749 0.06900.86 0.43 148.276 2.514 12.619 0.06820.84 0.42 144.828 2.514 12.487 0.06730.82 0.41 141.379 2.514 12.354 0.06640.80 0.40 137.931 2.514 12.220 0.06550.78 0.39 134.483 2.514 12.084 0.06460.76 0.38 131.034 2.514 11.946 0.06360.74 0.37 127.586 2.514 11.806 0.06270.72 0.36 124.138 2.514 11.665 0.06170.70 0.35 120.690 2.514 11.521 0.06080.68 0.34 117.241 2.514 11.376 0.05980.66 0.33 113.793 2.514 11.229 0.05880.64 0.32 110.345 2.514 11.080 0.05780.62 0.31 106.897 2.514 10.928 0.05670.60 0.30 103.448 2.514 10.775 0.05570.58 0.29 100.000 2.514 10.618 0.05460.56 0.28 96.552 2.514 10.459 0.05350.54 0.27 93.103 2.514 10.298 0.05240.52 0.26 89.655 2.514 10.134 0.05130.50 0.25 86.207 2.514 9.966 0.0502
Integral 0.0157 cm
t 71875.03 s1197.92 min19.97 h
( ) ( ) ( )xyyyyyxy n
x
x
n
Δ⋅⎭⎬⎫
⎩⎨⎧ +++++= −∫ 132n12
1d1
L
75
Evaporation in Stagnant AirEvaporation in Stagnant Air
m
sAAB
m
sAAB2
m
sAAB
2
3
dd
4dd4
4dd
dd4
dd
34
ρ−=⇒
ρπ
−=π∴
=ρ
π−=−=
π=
π=
cDtRR
RcDtRR
RcDQtV
tRR
tV
RV
76
( )
( )
( )( )
days 97.4s 35.429147
cm25.05.0
cmmol10797.2
scm0692.02
cmmol1086.8
2
02
222
38
2
33
22
21s
AAB
m
m
sAAB
2 2
1
==
−
⎟⎠⎞
⎜⎝⎛××⎟⎟
⎠
⎞⎜⎜⎝
⎛×
⎟⎠⎞
⎜⎝⎛×
=
−ρ
=∴
−ρ
−=⎥⎦
⎤⎢⎣
⎡
−
−
RRcD
t
tcDRR
R
77
9/28/079/28/07
• Dimensional analysis– Application in developing correlations
• Correlations for convective mass transfer coefficients
• Mass transfer calculations for packed beds
78
10/3/0710/3/07
• Inter-phase mass transfer– Two-Film theory– Gas-side and liquid-side mass transfer
coefficients– Overall mass transfer coefficient
• Review– Dimensional analysis (HW Problem 18)– Mass transfer coefficient (HW Problem 17)
• Use of correlation
79
HW ProblemsHW Problems
• Mass transfer in packed beds (benzoic acid): Problem 19, HW # 5
• Kinematic viscosity (slide 35): – ν = μ / ρ (cm2/s)– Re = D v ρ/μ = D v / ν– Sc = μ / (ρ DAB) = ν / DAB
• Problem 14: “Write 3 sentences explaining the answers to part 3 of problems 11 and 13.”
80
10/5/0710/5/07
• Inter-phase mass transfer• Review of topics covered• Simple quiz on fundamental concepts?
– Definitions, units, < 5-min problems, etc.
81
ReviewReview
• Slides 42 to 46• Correlations
[ ]
33.083.0023.0:pipes throughflow Turbulent
constant
ScReSh
ScReSh
=
= βα
82
• Quiz–16 questions, < 40 min
–Questions at the beginning require less time than those at the end
• Course evaluation–CH351: Mass Transfer and
Stagewise Operations
–Instructor: Sitaraman Krishnan
83 Benzoic acid spheres in a Benzoic acid spheres in a packed bedpacked bed
cA,2
cA,1Saturation solubility of benzoic acid in water = cA
s
Mass transfer driving force at inlet = cA
s – cA,1
= (2.948×10−5 − 0) mol/cm3
Mass transfer driving force at outlet = cA
s – cA,2
= (2.948×10−5 − cA,2) mol/cm3