RRoom
 GB-ANALYSTS REPORTS
 
Integrated Knowledge-Based Analyses of Socio-Economic Issues
 

Report Catalogue Data

  Report Class   General Public Report
  Analysis Type   Situation Analysis
  Issue Category   Technology Analysis
  Release Date   06_22_2008
  Last Update   06_09_2009
  Reference Code   GPR-SA.TA.FT-20080622-MIK

Fermentation Technologies
Fermentation Microbes Immobilization - Kinetics Analysis

More Update Post 09_03_2008

Immobilized fermentation-reactions  microbes, however, were known to change their stability and characteristics; and though the reaction equations used in the design of fermentation bioreactors with immobilized microbes usually account for the immobilization effect, hence enabling the use of heterogeneous reactor as opposed to homogeneous reactor, these equations must be further adjusted for changes still due to immobilization, but not necessarily due to reaction kinetic changes. Primarily the modification results from the mass transport limitations that obtain due to the immobilization, and reflects that limitation through the degree of solute penetrability into the matrix of immobilized microbes.

The modification is captured through the mathematical description of the reactions within the matrix of the microbes:

     ∂C/∂t = V.(DeVC) + r(C)                            (1)

where the letter "V" designates the gradient derivative, and the initial condition is:

     at t = 0,   C = Co everywhere                    (1.1)

and the boundary conditions are as follows:

     at x = 0,   C = Co                                     (1.2)
     at x = ξ,   ∂C/∂x = 0                               (1.3)

There are a few aspects of this equation that are worthy of note. The model assumes of the reaction spaces as a thin rectangular slab, with the slab formed from a slab-packing of microbes. Given that the analysis subsumes the immobilization method of attachment, the assumption of a slab is clearly not limiting as the analysis could very well apply to a thin-wall hollow cylinder or a thin-wall hollow sphere. In any event, the slab having interstices between the microbes therefore somewhat permeable or porous to substrates.

The partial differential equation (1) is stated as an unsteady state equation and rightly so; the second aspect is the initial condition that when t = 0, the Substrate concentration everywhere inside the microbe matrix is the feed concentration. Previous analysis addressed ignition method and is therefore subsumed here. Then at the interface between the immobilized microbes and the bulk mash fluid set as x = 0, the substrate concentration is also always feed concentration Co. Finally, at the end of the thickness [x = ξ] of the reaction space there is no substrate transport, however, the concentration of the substrate has the form, at x = ξ, C ≥ 0. The condition at this boundary may be


different for the immobilization method of entrapment. However, for now that form of immobilization is not considered. The specifics of the prevailing boundary condition clearly will vary with each form of immobilization of microbes.

The mathematical presentation with an unsteady state model stems from the fact that in real-time when the reaction is ignited, the reaction will proceed with the microbes, farther from the bulk broth solution, consuming most of the substrate in the immediate vicinity and with future availability being dependent on the rate of diffusion of the substrate into the vicinity. The diffusivity through these interstices therefore is represented by De, of course, this value will vary for each of the substances of the reaction mixture or broth or Mash.

The solution of this problem together with the initial and boundary conditions, however, is fairly tasking because of the level of interactivity intrinsic between the microbes and the substrates; and though the equation may be expected to attain steady state after a while, this expectation would never come about: Clearly, there will be variation of the sizes and number of interstices with use, given that individual microbe will grow and therefore cause changes of the interstices. That asserts  in effect a coupling between the De and the r(C) leading to some accommodation of the form De(r(C)) resulting in a very complex descriptive equation.

In view of this coupling, the analysis of the kinetic properties of the immobilized microbes must simultaneously solve both equation (1) and the Monod Equation appropriately formulated for the applicable reaction space. Rigorous analysis, of course, requires that the rate equation r(C) be derived from the reaction mechanism of the catabolic reaction mechanism of the microbial metabolic reaction and then appropriately adjusted with the immobilization factor. Further, the Monod equation as used here must be such that the rate constants have been properly adjusted for the reaction dynamics allowing for cellular mass growth by cell division only if such situation prevails,  or not. 

However, for such solution to be efficacious in correctly determining the kinetics characteristic of the microbes, the results of the Monod Equation must somehow be related yet to another mathematical description of the variation of the cell fraction, Φ, for the full-range of the cell fraction: { 0 ≤ Φ ≤ 1.0 }. Moreover, the microbes growth-value evaluated from the combined


solution of the Monod equation and the Reaction Model (1) must be such as to be partitioned into cell-division growth-value and individual-cell growth-value, as only the latter growth directly impacts the interstices of the immobilized microbes - except if the microbes are bacteria and the new grown cells aggregate into biofilms.

Then, of course, the actual form of the rate equations as used in the reaction model (1) is of empirical derivation and the actual relationship between the cell-growth factors and the substrate oxidation must derive from the biochemical pathways description of the relationship.

Evidently then, there is now this new requirement for deriving an equation that relates the changes of the interstices to cell fractions and in turn the cell fractions to the Monod equations variable of cell growth. Of course, the interactivity with the mineral additives such as Potassium and Magnesium, to the broth necessary for cell-growth functionality must also be represented by each of the related reaction model of form (1). All these may have to be solved simultaneously in any analysis of the kinetic data of immobilized fermentation-microbes.

The use of the kinetic data of immobilized microbes for the design of heterogeneous reactors whether Batch fermentation reactors or otherwise will result in efficacious design only if based on reasoned analysis that will have accounted for the impacting factors as discussed.

 


Directory of Services:  Advertise with Us | Analysis Request | Focus Group
Privacy Policy  |  Site Navigation  |  Terms of Use

 Webloogle Blog Directory
Things are not always as they seem! Scratch beyond the surface and the truth is  always different.   

  Company 

 © 1999 - 2009 Nkassens Trust. All rights reserved