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Countercurrent multistage fluidized bed reactor for immobilized biocatalysts: III. Hydrodynamic aspects
Author(s) -
Vos Henk J.,
van Houwelingen Cees,
Zomerdijk Max,
Luyben Karel Ch. A. M.
Publication year - 1990
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260360409
Subject(s) - fluidized bed , mixing (physics) , particle (ecology) , countercurrent exchange , chemical engineering , biocatalysis , materials science , mass transfer , particle size , microreactor , chemistry , chromatography , catalysis , thermodynamics , organic chemistry , physics , oceanography , quantum mechanics , engineering , geology , ionic liquid
Abstract In Parts I and II of this series we described the modelling, design, and operation of a multistage fluidized bed reactor (MFBR) for immobilized biocatalysts. This article deals with those aspects of the MFBR which are different from single‐stage fluidized beds which are operated in batch mode with respect to the solids. The semicontinuous transport of the particles requires perfect mixing of the particles in the reactor compartments, because particles are mainly transported from the bottom of these compartments. A large spread in the physical properties of the biocatalyst particles, especially of both size and density, may cause the particles to segregate into layers with different diameter and/or density. This affects the efficient use of the biocatalyst. The properties of the particles are dependent on the immobilization method. The suitability of different methods for possible future application in the MFBR is therefore compared. Because of segregation, successful use of a biofilm catalyst with a nonuniform thickness of the biofilm is doubtful. Experiments in a small scale reactor (± 0.1 m diameter) demonstrated that perfect particle mixing is possible using commercially available biocatalyst particles of uniform density. Co‐immobilization of the biocatalyst with glass powder in a gel is a simple and effective method of increasing gel density. High density particles allow high liquid flow rates, and thus an improved external mass transfer can be achieved. The distributor plates, which separate the reactor compartments, must allow unhindered transport of particles. Therefore, the holes in these plates must have a diameter of at least 4.5 times that of the largest particles which are present in the particle mixture used. Furthermore, the plates must be designed such that, when scaling‐up the reactor, a uniform liquid distribution over the cross‐sectional area of the reactor occurs. Large‐scale experiments were not carried out, but published correlations, indicate that particle mixing and a uniform liquid distribution can be accomplished in a large‐scale reactor under similar flow conditions.