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Lecture 8 (Enzyme Reactors)

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Babu Ponnusami
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0% found this document useful (0 votes)
28 views29 pages

Lecture 8 (Enzyme Reactors)

Uploaded by

Babu Ponnusami
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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CHE1009-BIOCHEMICAL ENGINEERING

MODULE-II
LECTURE – 8

Dr.A.Babu Ponnusami
Associate Professor
SCHEME
1
Enzyme reactor design
Levenspiel’s four fundamental questions
• In approaching the design of a reactor system the engineer has to
answer a number of important priliminary questions before
embarking on his detailed calculations. These questions are as follows:
1. Do I have the right reactor type in mind: should it be plug flow,
mixed flow, recycle, multistage or what?
2. What temperature progression should I aim for: constant, rising,
falling etc. and should that require heat exchange, may be
multistage?
3. For a catalytic reaction what size of particle should be used? This
tells what type of reactor should be used: packed bed, fluidized etc?
4. Does the catalyst deactivate and if so, does it deactivate rapidly or
slowly?
Platform to simulate and optimize the
enzyme reactor operation

BR – Batch reactor,
BRP – Batch reactor with intermittent addition of enzyme
SBR – Semi-batch reactor,
MACR – mechanically agitated continuous reactor,
FXBR – Fixed bed batch reactor
Mass Balance on Reactive System
• In - out + gen - cons = accumulation
FA0 FA
Rate of flow in Rate of flow out
System

GA
Rate of
generation/
consumption

• A mass balance for the system is


dN
FA0  FA  G A  A
dt

• NA is the mass of “A” inside the system.


• The reaction term can be written in more familiar
terms,
G A = rA V
• V is volume of the system.
• Note that the units for this relation are consistent:
mass mass
  volume
time volume  time

• If GA (and hence rA) varies with position in the


system volume, we can take this into account by
evaluating this term at several locations. Then DGA1
= rA1 DV1,
• Summing the reactions over the entire volume
yields:

k k
G A  G Ai  rAi Vi
i 1 i 1

k
• As (that is, as we decrease the size of these cubes and

V  0
increase their number)
• which gives
V
G A rA dV
Generalized Design Equation for Reactors

• In - out + gen - cons = accumulation

V
dN A
FA0  FA  rA dV 
dt
Types of Reactors
• Batch
– No flow of material in or out of reactor Changes with
time
• Fed- Batch
– Either an inflow or an outflow of material but not both
Changes with time
• Continuous
– Flow in and out of reactor
– Continuous Stirred Tank Reactor (CSTR)
– Plug Flow Reactor (PFR)
– Steady State Operation
Batch Reactor
• Generalized Design Equation for
Reactors V
dN
0 A
A
F
AFr
A 
dV
dt
• No flow into or out of the reactor,
then, FA = FA0 = 0
dN A V
 rA dV
dt
• Good mixing, constant volume

dN A d N A V  dC A
rAV or  rA
dt dt dt
Enzyme Batch Reactor
(constant volume, well mixed)

dS vmax S
r  
dt K M  S
• integrate from t = 0 to t = t, we obtain
Kmln (S0/S) + (S0 -S) = vmax t

• Batch reactors are often used in the early stage of


development due to their ease of operation and
analysis
Batch Enzyme Reactor Determination of
M-M kinetic
Linear form becomes parameters
(S0 – S) t
= - KM + Vmax
ln(S0/S) ln(S0/S)

(S0 – S)
ln(S0/S)

Vmax

t
- KM
ln(S0/S)
Fed Batch Reactor
• Reactor Design Equation
V dN A
FA0  FA   rA dV 
dt
• No outflow FA = 0
• Good Mixing rA dV term
out of the integral

dN A d C A V 
FA0  rA V  
dt dt
Fed Batch Continued
• Convert the mass (NA) to concentration. Applying
integration by parts yields

dV
• Since FA0
dt
• Then dC A
FA0  rAV V  C A FA0
dt

• Rearranging
dC A FA0 C A FA0
  rA 
dt V V
Fed Batch Continued
• Or
dC A FA0
 1  C A  rA
dt V

• Used when there is substrate inhibition and


for bioreactors with cells.
Assumptions for a fed batch reactor
include
1. Only a feed in
2. Either a feed in or a
removal stream
3. Steady state
4. 2 and 3
5. All of the above
Continuous Stirred Tank Reactor

• Assume rate of flow in = rate of flow out


• FA = v CA and FA0 = v CA0
• v = volumetric flow rate (volume/time)
CSTR - continued
• General Reactor Design Equation
V dN A
FA0  FA   rA dV 
dt
dN A
• Assume Steady State 0
dt

V
• Well Mixed  r dV Vr
A A

FA0  FA
• So FA0  FA  VrA 0 or V 
 rA
CSTR for Enzymes
(Enzyme remains inside)

• Input - output + generation - consump = accumulation


dS
FS0  FS  rV v
dt
• F - flow rate l/hr
• S - substrate conc.
• V- reactor volume
• r - reaction rate
• at Steady State dS/dt = 0
CSTR - enzymes
rV = F(S0 - S)
and
vmax S
r
KM  S
Introducing space-time θ ( = V/F) and r in above equation we get

VmaxS
S0 =S + θ
KM + S
Continuous Stirred Tank Enzyme Reactor at steady-state
Linear form becomes

S = - KM + Vmax
(S0 – S)

S
Determination of
M-M kinetic
parameters
Vmax


- KM
(S0-S)
Plug Flow Reactor (PFR)

• Tubular Reactor
• Pipe through which fluid flows and reacts.
• Poor mixing
• Difficult to control temperature variations.
• An advantage is the simplicity of construction.
PFR Design Equation for Product
formation
• Design Equation V dN A
FA0  FA   rA dV 
dt
• Examine a small volume element (DV) with length Dy
and the same radius as the entire pipe.
Flow of
Flow of
A out of
A into
Element
Element
• If the element is small, then spatial variations in rA
are negligible, and Assumption of “good
V mixing” applies only to

 r dV r V
A A
the small volume
element
• If volume element is very small, then assume steady
state with no changes in the concentration of A.
dN A
0
dt
• Simplify design equation to:
FA y  FA y  y  rA V 0
• rA is a function of position y, down the length of the
pipe and reactant concentration
• The volume of an element is the product of the
length and cross-sectional area,
DV = A Dy
• Design Equation becomes:
 FA y  y  FA y 
   ArA
 y 
• take the limit where the size of a volume
element becomes infinitesimally small
dFA
lim
y  0 dy
 ArA

• or since Dy A = V,
dFA
rA
dV
• This is the Design Equation for a PFR
• Bioapplications - Sometimes hollow fiber
reactor analysis is simplified to a PFR
Plug-flow Enzyme Reactor at steady-state

F F F F
S0 S S+dS Sf

dV
Mass balance for the substrate over dV:
FS = F(S + dS) + (-rS) dV

The above can be simplified to - FdS / dV = -rS

F for the steady flow rate through the reactor


S for concentration of the substrate
dV for small volume of the reacting mixture
(-rS) for substrate utilization rate in dV
Plug-flow Enzyme Reactor at steady-state

F F F F
S0 S S+dS Sf

dV
Introducing space-time θ ( = V/F), we get

- dS / dθ = -rS

F for the steady flow rate through the reactor


S for concentration of the substrate
dV for small volume of the reacting mixture
(-rS) for substrate utilization rate in dV
Plug-flow Enzyme Reactor at steady-state
Substituting (-rS) for the simple enzyme reaction in, we get

dS VmaxS
- =
dθ KM + S
Rearranging above equation we get
S θ

∫( ) ∫
KM + S
- dS =
S Vmax dθ
S0 0
Integrating above gives

()
S0
KM ln + (S0 – S) = Vmax θ
S
Plug flow enzyme reactor Determination of
M-M kinetic
Linear form becomes parameters
(S0 – S) θ
= - KM + Vmax
ln(S0/S) ln(S0/S)

(S0 – S)
ln(S0/S)

Vmax

θ
- KM
ln(S0/S)

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