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Report Catalogue Data

  Report Class   General Public Report
  Analysis Type   Situation Analysis
  Issue Category   Technology Analysis
  Release Date   07_08_2008
  Last Update  
  Reference Code   GPR-SA.TA.FT-20080708-EIR

Fermentation Technologies
Microbes Entrapment-Immobilization Reactor


The role of the Microbes Immobilization Reactor in a bioprocess driven by any form of heterogeneous bioreactor: Packed Bed Bioreactor or in-fluid suspended-beads Heterogeneous Bioreactor is that of a mission-critical support. Hence, rational analysis of the development or engineering of such bioreactors based on the methods of pure sciences for undertaking the immobilization need to undertaken. Although the immobilization addressing colony-biofilm formation is very interesting and is being extensively studied, the entrapment immobilization method is the object of analysis here, given that the use of entrapment immobilization has been incorporated in the analyses of heterogeneous bioreactor and multi-packed bed bioreactor, the analysis of which therefore is expanded by the analysis of the entrapment method of microbes immobilization.

Noteworthy in the analyses, noted above, adopting the entrapment immobilization of microbes, the method of the pure sciences by which the entrapment is accomplished is as detailed in Immobilized Cells Reactor, ICR, in the study of S. Cerevisiae. Specifically, the method entails the squirting of a solution-mixture of Sodium Alginate and S Cerevisiae from a pipette into a solution of Calcium Chloride. The droplets falling into the Calcium Chloride solution then undergoes an interfacial reaction with the host solution. The droplet surface Sodium ion of the Sodium Alginate droplet then undergoes ion-exchange reaction with the Calcium ions of the Calcium Chloride host solution. The reaction is fast but yet of perceptible time span, and so worthy of reaction kinetic analysis, though one is not conducted in the experimental studies. The Sodium Alginate solution is of higher density and so falls down the host solution, and continues to fall even after the surface sodium ions have been exchanged with host solution calcium ions. Incorporating this science into the process engineering of a Bioprocess clearly requires a bioreactor, the Microbes Immobilization Bioreactor, within which the Calcium ions  Sodium ions exchange reaction can optimally occur.

The engineering of the Immobilization Bioreactor of course, requires detailed information about the entire science, such as the rate of reaction of the ion exchange reaction, the physicochemical properties of the Sodium Alginate solution impacting the size of the beads at squirting into the Calcium Chloride solution, the impact of the squirting device on the size of the beads as industrial operation will not use pipettes for that purpose, the impact of the size of squirts on the sphericity of the beads. These considerations over the size of and shape of the beads has as the object, the formation of beads of


virtually the same size and sphericity  as to support the uniform application of the analysis of the reaction dynamics of beads and of the related single body problem. The reaction rate is required to allow the determination of the reaction time for the formation and hardening of the container-wall of the beads; the reaction time is often generalized as the bead-particle minimum required residence time in the bioreactor for the preferred state of the beads to obtain.

Generally, the size of a droplet from an opening to a reservoir is impacted by the physiochemical properties of the solution forming the droplet and the physiochemical properties of the environment into which the droplet was being formed. A significant property in this regards is the surface tension property of the two fluids. The perspective taken here is one of direct formation of the droplet in the host fluid though the experimental studies was imprecise about whether or not the droplets were formed in the air and then fell into the Calcium Chloride host solution. This is not the assumed approach of forming the droplet rather the approach is the direct immersed "injection" or "squirting" or "sparging" into the host solution. An experimental determination of the surface tension changes with solution concentration mix changes, and the changes in bead size must be made. A theoretical computational evaluation of this relation should made and incorporated into the reactor design equations.

The determination of the reaction mechanism and kinetics for constructing the reaction rate equations as a task requires specially designed experiment. The studies should aim to determine the mechanism of exchange and the depth of penetration into the Sodium Alginate solution into which the Calcium ions diffuse and reacts with the Sodium. The interactions, if any, between the alginate components in evolving the mechanism should also be determined. The dependence of depth of penetration, or reaction band, on the concentration changes of the two alginate solutions is also of viable consideration as such should impact the toughness of the spherical shell of the beads.

With the availability of the requisite data for the design of the bioreactor, then the design can begin in earnest. Of primary considerations in the design of the reactor is the type of reactor to adopt from the several basic of types; in this context, there does not seem to be any preferred type except that the vessel must be such as to allow the droplet to suffer the least amount of rotation as that should cause a distortion of the shape of the beads and so deform the  beads from the preferred sphere shape.  Then


comes the consideration of the specialization required to embody the squirting dynamics of the bead formation method. The specifics of the design of course simply depends on whether the host solution is stagnant or flowing. In the former case the design consideration is confined to the shape of the tip from which the microbe solution is squirted. However, in the latter case, the consideration extends to include the impact of the velocity of flow of the host solution during the squirting and then interaction between the size of the squirt-orifice and the fluid dynamics and the sphericity of the beads.

Evidently, the design of the fermentation bioreactor is intimately dependent on the performance of the immobilization bioreactor, and as such the design of the latter should and ought be paid just as much attention as the former.


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