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Mass transfer occurs in mixtures containing local concentration variation. For example, when dye is dropped into a cup of water, mass-transfer processes are responsible for the movement of dye molecules through the water until equilibrium is established and the concentration is uniform. Mass is transferred from one place to another under the influence of a concentration difference or concentration gradient in the system. Gas-liquid mass transfer is extremely important in bioprocessing because many processes are aerobic, oxygen must first be transferred from gas bulk through a series of steps onto the surfaces of cells before it can be utilized.
The solubility of oxygen within broth is very poor. Therefore, the enhancement of gas-liquid mass transfer during aerobic cultures and fermentations is always put into priority.
CA Concentration of A, a C A2
C A1
(7.1)
Solid-phase reaction In biological systems, reactions are sometimes mediated by catalysts in solid form, e.g. clumps, flocs and films of cells and immobilized-enzyme and -cell particles. When cells or enzyme molecules are clumped together into a solid particle, substrates must be transported into the solid before reaction can take place. Mass transfer within solid particles is usually unassisted by bulk fluid convection; the only mechanism for intraparticle mass transfer is molecular diffusion. As the reaction proceeds, diffusion is also responsible for removing of product molecules away from the site of reaction, this will be discussed more fully in heterogeneous bioreaction kinetics. When reaction is coupled with diffusion,
the overall reaction rate can be significantly reduced if diffusion is low. Mass transfer across a phase boundary Mass transfer between phases occurs often in bioprocesses. Oxygen transfer from gas bubbles to fermentation broth, penicillin recovery from aqueous to organic liquid, and glucose transfer from liquid medium into mould pellets are typical examples. When different phases come into contact, fluid velocity near the phase interface is significantly decreased and diffusion becomes crucial for mass transfer across the phase interface.
C A1 Phase 1
Film 2
Film 1
(7.2)
Mass transfer coupled with fluid flow is a more complicated process than diffusive mass transfer. The value of the mass-transfer coefficient reflects the contribution to mass transfer from all the processes in the system that affect the boundary layer. k depends on the combined effects of flow velocity, geometry of equipment, and fluid properties such as viscosity and diffusivity. Because the hydrodynamics of most practical systems are not easily characterized, k cannot be calculated reliably from theoretical equations. Instead, it is measured experimentally or estimated using correlations available from the literatures. In general, reducing the thickness of the boundary layer or improving the diffusion coefficient in the film will result in enhancement of k and improvement in the rate of mass transfer.
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(7.3)
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At steady state, there is no accumulation of component A at the interface or anywhere else in the system, and component A transported through liquid 1 must be transported through phase 2, that is NA1 = NA2 = NA. If CA1i and CA2i are equilibrium concentrations, they can be related using the distribution coefficient m.
m=
(7.6)
Therefore:
NA( 1 k L1a + m k L2 a ) = C A1 C A2 (7.7)
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and
NA( C 1 1 + ) = A1 C A2 mk L1a k L 2 a m (7.8)
(7.9)
and
1 1 1 = + KL 2a mk L1a k L 2 a (7.10)
Therefore:
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NA = KL1a(CA1 mCA2)
and
(7.11)
NA = KL2a(
C A1 CA2) m
(7.12)
These two Eqs indicate that the rate of mass transfer between two phases is not dependent simply on the concentration difference; the equilibrium relationship is also an important factor. The driving force for transfer component A out of liquid 1 is the difference between the bulk concentration CA1 and the concentration of component A in liquid 1 which would be in equilibrium with concentration CA2 in liquid 2.
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Liquid film
Gas film
The rate of mass transfer of component A through the gas boundary layer is:
NAG = kGa(CAG CAG i) (7.13)
and the rate of mass transfer of component A through the liquid boundary layer is:
NAL = kLa(CALi CAL) (7.14)
If we assume that equilibrium exists at the interface, CAGi and CALi can be related. For dilute concentration of most gases and for a wide range of concentration for some gases, equilibrium concentration in the gas phase is a linear function of liquid concentration. Therefore:
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CAGi = mCALi
Therefore,
(7.15)
NA(
1 kG a
m ) = C AG mC AL kLa
(7.16)
and
C AG 1 1 NA( + )= C AL mk G a k L a m
(7.17)
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1 1 m = + K G a kG a k L a
(7.18)
1 1 1 = + K L a mk G a k L a
Thus:
(7.19)
NA = KGa(CAG mCAL)
(7.20)
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and
(7.21)
NA = KGa(CAG CAG*)
and
(7.22)
NA = KLa(CAL* CAL)
(7.23)
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When solute A is very soluble in the liquid, for example, ammonia, the liquid-phase resistance is small compared with that posed by the gas interfacial film, therefore,
NA = kGa(CAG CAG*)
(7.24)
Conversely, if component A is poorly soluble in the liquid, e.g. oxygen, the liquid-phase mass-transfer resistance dominates and kGa is much larger than kLa, thus:
NA = kLa(CAL* CAL)
(7.25)
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7.2 Oxygen Uptake in Cell Culture (contd) Cells in aerobic culture take up oxygen from broth. The rate of oxygen transfer from gas to liquid is therefore of prime important, especially at high cell densities when cell growth is likely to be limited by availability of oxygen. The solubility of oxygen in aqueous solutions at ambient temperature and pressure is only about 10 ppm. This amount of oxygen is quickly consumed in aerobic cultures and must be constantly replaced by sparging. This is not an easy task because the low solubility of oxygen guarantees that the concentration difference (CAL* CAL) is always very small. Design of fermenters for aerobic operation must take these factors into account and provide optimum mass-transfer conditions.
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Typically, specific oxygen demand passes through a maximum in early exponential phase as illustrated below, even though the cell concentration is relatively low at that time
100 q o , g h g (cell dry wt) 80 60 100 40 20 0 0 20 40 60 Time, h 80 100 qo 50 0 x 200 150 Dry weight x, g l
-1
Fig 7.5 Variation in specific rate of oxygen consumption and biomass concentration during batch culture
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-1
-1
If QO is the oxygen uptake rate per volume of broth and qO is the specific oxygen uptake rate:
QO = qOx
(7.26)
The inherent demand of an organism for oxygen depends primarily on the biochemical nature of the cell and its nutritional environment. However, when the level of dissolved oxygen in the broth falls below a certain point, the specific rate of oxygen uptake is also dependent on the oxygen concentration in the broth.
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Ccrit
Fig 7.6 Relationship between specific oxygen uptake rate and dissolved-oxygen concentration
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To eliminate dissolved oxygen limitations and allow cell metabolism to function at its optimum, the dissolved oxygen concentration at every point in the fermenter must be above Ccrit. The exact value of Ccrit depends on the organism, but under average operation conditions usually falls between 5~10% of air saturation. For cells with relatively high Ccrit level, the task of transferring sufficient oxygen to maintain CLA > Ccrit is always more challenging than for cultures with low Ccrit. Choice of substrate for the fermentation can also significantly affect oxygen demand. Because glucose is generally consumed more rapidly than other sugars or carbon-containing substrates, rates of oxygen demand are higher when glucose is used.
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For example, maximum oxygen-consumption rates of 5.5, 6.1 and 12.0 mmol l1 h1 have been observed for Penicillium mould growing on lactose, sucrose and glucose, respectively.
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Stagnant region
8 5 6 7
Gas-liquid interface
Solid-liquid interface
Fig 7.7 Steps for oxygen transport from gas bubble to cell
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Transfer through the bulk gas phase in the bubble is relatively fast. The gas-liquid interface itself contributes negligible resistance. The liquid film around is a major resistance to oxygen transfer. In a well mixed fermenter, concentration gradients in the bulk liquid are minimized and mass-transfer resistance in this region are small. Because single cells are much smaller than gas bubbles, the liquid film surrounding each cell is much thinner than that around the bubbles and its effect on mass transfer can generally be neglected. On the other hand, if the cells form large clumps, liquid-film resistance can be significant.
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Resistance at the cell-liquid interface is generally neglected. When the cells are in clumps, intraparticle resistance is likely to be significant as oxygen has to diffuse through the solid pellets to reach the interior cells. The magnitude of this resistance depends on the size of the clumps. Intracellular oxygen-transfer resistance is negligibile because of the small distances involved.
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(7.27)
We can use this Eq. to predict the response of the fermenter to changes in mass-transfer operating conditions. For example, if the rate of cell metabolism remains unchanged but kLa is increased by raising the stirrer speed to reduce the thickness of the boundary layer around the bubbles, the dissolved-oxygen concentration CAL must rise in order for the left-hand side to remain equal to the righthand side. Similarly, if the rate of oxygen consumption by the cells accelerates while kLa is unaffected, CAL must decrease.
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Further, we can deduce some important relationship for fermenter operations. First, let us estimate the maximum cell concentration that can be supported by the fermenters oxygen-transfer system. For a given set of operating conditions, the maximum rate of oxygen transfer occurs when the concentration-difference driving force (CAL* CAL) is highest, i.e. when the concentration of dissolved oxygen CAL is zero. Therefore, the maximum cell concentration that can be supported by the mass-transfer function of the reactor is:
x max k L aC AL * = qO
(7.28)
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Another important parameter is the minimum kLa required to maintain CAL > Ccrit in the fermenter. This can also be determined as:
(k L a ) crit =
qO x C AL C crit
*
(7.29)
Example 7.1 Cell concentration in aerobic culture A strain of Azotobacter vinelandii is cultured in a 15 m3 stirred fermenter for alginate production. Under current operating conditions kLa is 0.17 s1. Oxygen solubility in the broth is approximately 8 103 kg m3. (a) The specific rate of oxygen uptake is 12.5 mmol g1 h1. What is the maximum possible cell concentration?
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(b) The bacteria suffer growth inhibition after copper sulphate is accidentally added to the fermentation broth. This causes a reduction in oxygen uptake rate to 3 mmol g1 h1. What maximum cell concentration can now be supported by the fermenter? Solution: (a) From Eq.(7.28):
x max
(b) Assume that addition of copper sulphate does not affect CAL* and kLa. If qO is reduced by a factor of 12.5/3 = 4.167, xmax is increased to: xmax' = 4.167 12 = 50 g l1 To achieve the calculated cell concentrations all of other conditions must be favorable, e.g. sufficient substrate and time.
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Anode
Cathode
The electrode response time can be determined by quickly transferring the probe from a beaker containing medium saturated with nitrogen to one saturated with air. The response time is defined as the time taken for the probe to indicate 63% of the total change in dissolved-oxygen level. For commercially-available steamsterilisable electrodes, response times are usually 10 ~ 100 s. Polarographic electrodes measure the partial pressure of dissolved oxygen or oxygen tension in the fermentation broth, not the true dissolved-oxygen concentration, it is necessary to know the solubility of oxygen in the broth at the temperature and pressure of measurement.
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Table 7.3 Solubility of oxygen in sugar solutions under 1 atm oxygen pressure Sugar Glucose 0 0.7 1.5 3.0 Sucrose 0 0.4 0.9 1.2 15 15 15 15 20 20 20 20 Concentration gmol per kg H2O Temperature C Oxygen solubility kg m 3 4.50 10 2 3.81 10 2 3.18 10 2 2.54 10 4.95 10 2 4.25 10 2 3.47 10 2 3.08 10
2 2
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Quicker et al have developed an empirical correlation to correct values of oxygen solubility in water for the effects of cations, anions and sugars:
*
log
C AL 0 C AL
= 0.5 H i z i CiL + K j C jL
2 i j
(7.31)
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P kLa = ( ) u G V
(7.32)
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C AL2
C AL
C AL1
C crit t0
Air on
t1 Time, t
t2
During the re-oxygenation, the system is at an unsteady state. The rate of change in dissolved-oxygen concentration is equal to the rate of oxygen transfer from gas to broth, minus the rate of oxygen uptake by the cells:
dC AL * = k L a (C AL C AL ) qO x dt
(7.33)
where qOx is the rate of oxygen consumption. We can determine an expression for qOx by considering the final steady dissolved-oxygen concentration. When dCAL/dt = 0, therefore:
qOx = kLa(CAL* C AL )
(7.34)
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thus,
dC AL = k L a (C AL C AL ) dt
Integrating:
(7.35)
ln(
kLa =
C AL C AL1 ) C AL C AL 2 t 2 t1
(7.36)
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(7.37)
or
Fg p AG Fg p AG 1 NA = [( )i ( )o ] RVL T T (7.38)
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Summary
At the end of this chapter, you should: know the two-film theory of mass transfer between phases and the Ficks law; be able to identity which steps are most likely to be major resistances to oxygen mass transfer from bubbles to cells; know the importance of the critical oxygen concentration; understand how oxygen mass-transfer kLa can limit the biomass density in fermenters; know how temperature, total pressure, oxygen partial pressure and presence of dissolved material in the broth affect oxygen solubility and rates of oxygen mass transfer in fermenters; and know the techniques of dynamic method for experimental determination of kLa for oxygen transfer.
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