Bioreactor Design
MATA KULIAH: PENGANTAR TEKNOLOGI BIOPROSES
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Bioreactor: device, usually a vessel, used to direct the activity of a biological catalyst to achieve a desired chemical transformation.
Product Bioreactor
Recycle
Product
separation & purification Nutrients tank
Waste Input
Pre-filtration
Fermenter: type of bioreactor in which the biocatalyst is a living cell.
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What is a bioreactor?
1
Biomass concentration
Nutrient supply
Sterile conditions Effective
agitations
Heat removal
Shear conditions
Product removal Product
inhibition
Aeration
Microbial activities
Bioreactor Performance
2
1. Aerobic bioreactor: Need adequate mixing and aeration 2. Anaerobic bioreactor: no need agitation
3. Semiaerobic bioreactor: No mixing, but need aeration
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20%
70%
10%
aerobic anaerobic semiaerobic
Groups of Bioreactor
3
-1. Stirred tank
•Baffles are usually used to reduce vortex. D=3m, 4 baffles. D>3m, 6-8 baffles
• Applications: free and immobilized enzyme reactions. High shear forces may damage cells
•Require high energy
input. Cooling can be used to cover excess heat
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(+) Low cost
4
- 2. Bubble column
Application: production of baker’s
yeast, beer, vinegar, and waste water treatment
Mixing method: Gas sparging
•Simple design
•Good heat and mass transfer
•Low energy input
Gas-liquid mass transfer coefficients depend largely on bubble diameter and gas hold-up.
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1< H/D < 6
- 3. Airlift reactor
There are two liquid steams: up-flowing and down-flowing steams.
Liquid circulates in an airlift reactor as a result of density difference between riser and downcomer. Aplication: alcoholic fermentation
Steril
Large capacity
Low shear
High cost
Poor nutrient distribution
Foaming
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6
Packed-bed reactors are used with
immobilized or particulate
biocatalysts.
Medium can be fed either at the top or bottom and forms a continuous liquid phase.
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- 4. Packed-bed reactor
7
•The trickle-bed reactor is another
variation of the packed bed reactors.
•Liquid is sprayed onto the top of the packing and trickles down
through the bed in small rivulets.
• Application: aerobic wastewater treatment
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- 5. Trickle-bed reactor
8
•When the packed beds are operated in upflow
mode, the bed expands at high liquid flow rates due to upward motion of the particles.
•Channelling and clogging of the bed are avoided.
•Application: wastewater treatment and the
production of vinegar.
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- 6. Fluidized bed reactor
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FED
BATCH
PLUG
FLOW CSTR
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Bioreactor Operation Modes
BATCH
10
A batch bioreactor is normally equipped
with an agitator to mix the reactant, and the pH of the reactant is maintained by
employing either
buffer solution or a pH controller
S m
S s
C K
C r
dt r dC
max C C r t
C
K C
s ss s
m 0 max
ln
0
Change of Cs with time, t
Batch operation with stirring
•A foam breaker may be installed to disperse foam
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-1.a. Batch Operation
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-1.b. Fed Batch Operation
11
In a plug-flow
reactor, the substrate enters one end of a cylindrical tube with is packed with
immobilized enzyme and the product steam leaves at the other
end.
0
max
ln
0C C r
C
K C
s ss s
m
F, Cs0 F, Cs
t = 0
F
V
An ideal plug-flow reactor can approximate the long tube, packed-bed and hollow
fiber or multistaged reactor
Residence time Continuous operation
without stirring
V
-2. Plug-flow mode
12
A continuous stirred- tank reactor (CSTR) is an ideal reactor which is based on the
assumption that the reactants are well mixed.
Continuous operation with
stirring
F, Cs0
F, Cs V
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-3. Continuous stirred-tank
dt V dX V
r X
X
F( 0 ) x
F, Cs0
F, Cs V
Mass balance of cell:
on Accumulati G
Output -
Input eneration
the ratio of biomass rate of generation to biomass concentration, rx/X, that is the specific growth rate; μ
) (
)
( 0
X X D
r X
V X F
x
X
rx
D
0 dt dX s Steady state:
V D
F
1
0
0
No cell in inlet:
X
-3. Continuous stirred-tank – cont.
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Monod rate:
S K
S
s
max
S K
D S
s
max
D S DKs
max
At steady state, substrate utilisation is balanced with a rate equation:
S V K
S S S
F
s
max
0 )
(
K S
S S S
D
s max
0 )
(
S S
X Y X
0
0
D
S DK Y
X
X s
max 0
0
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Bioreactor Design Properties
1
• Mass Transfer
2
• Heat Transfer
3
• Dimension
4
• Power consumption
5
• Hold Up
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1
• Mass Transfer
Determine KLa
α is proportionality factor, 2x10-3
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2
• Heat Transfer
The reaction in bioreactor, especially fermentation:
generate HEAT
Need cooling (coils or jacket in vessel)
Conduction
single layer
multi layer
Convection
Natural Forced
x kA T
q
x T
q
x hANur Istianah-THP-FTP-UB-2014
3
• Dimension
1. Reactor volume 2. Reactor diameter
3. Ratio of reactor diameter to impeller diameter Dt/Di
4. Ratio of the height of the liquid level to impeller diameter, HL/Di
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4
• Power consumption
Power consumption per unit volume of liquid
Power consumption:
5 3
i c
p N D
N Pg
c i p
g
D N P N
5
3
NP is a function of Re and type of impeller Use graph
N = rpm/60
= ... rps
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Correction factors are used to define actual power
Pact = P. Fc. number of impeller
There is a further discussion for aeration power
(next subject)
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5
• Hold Up
Assume air in water
Ykcal
C V
q 1
Heat production rate:
q : heat production rate, kcal/ls
V: reactor liquid volume, l
: specific growth rate, s-1 C: biomass concentration (g/l) Ykcal: a yield coefficient given as
grams of cells formed per kcal energy released, g cells/kcal
Heat load: Heat load is determined by energy balances Practical Issues for Bioreactors
- Temperature Control (Heat Load)
Popular method
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-Temperature control (heat transfer)
Heat transfer surface area:
1. Low in (a) external jacket and (b) external coil for small reactors
2. High in (c) internal helical coil and (d) internal baffle coil for large reactors 3. Easily adjustable in (e) a separate external heat exchange unit
Difficult to clean Easily fouled by cell
growth on the surface
No cleaning problem
• Sterility requirement
• Shear forces imposed on cells
• Depletion of oxygen
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1. Biological reactions almost invariably are three-phase reactions (gas-liquid-solid). Effective mass transfer between phases is often crucial. For example, for aerobic fermentation, the supply of
oxygen is critical.
H P
CA* Ag
A Ag
l
A
K C C
J
*
The equation governing the oxygen transfer rate is:
Agitation:
•Mechanical stirring (for small reactors, and/or viscous liquids, low reaction heat)
•Air-driven agitation (for large reactors and/or high reaction heat)
-Agitation (gas transfer)
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1. Mechanical foam breaker (a supplementary
impeller)
2. Chemical antifoam agents (may reduce the rate of oxygen transfer)
- Foaming removal
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1. Aseptic operation (3-5% of fermentations in an
industrial plant are lost due to failure of sterilization.
2. Construction materials (glass for small
bioreactors, e.g., < 30 liters and corrosion-resistant stainless steel for large reactors)
3. Sparage design (three designs: porous, orifice and nozzle)
4. Evaporation control due to dry air input - Other issues
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THANKS FOR YOUR ATTENTION
The best person is one give something useful always
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