Multiphase Bioreactor Design

(avery) #1

Figure 8.7 The substrate, biocatalyst,


investment and operating,


downstream-processing, and overall


costs per kg of product ($s, $e, $io, $dp,


and $ov, respectively) as a function of


the ratio of the initial biocatalyst


concentration (Ce(0)) and the initial


substrate concentration (Cs(0)) in a


batch reaction crystallizer;


were formulated. In batch systems, conversions of 80–100% are reported for every type
of solid-to-solid bioconversion, even when hardly any liquid phase is present, and it
seems that these systems can easily be scaled-up. Kinetic studies of these solid-to-solid
bioconversions give rise to further development of two kinds of systems in the future: 1)
batch systems with very high concentrations of undissolved substrate, and 2) continuous
systems for solid-to-solid bioconversions. In continuous systems an optimum
supersaturation (∆Copt) exists. The main advantage of continuous systems over batch
systems is that they are able to maintain a constant (optimal) supersaturation, resulting in
more homogeneous product crystals, and thus lower downstream-processing costs. In this
work, two continuous systems for solid-to-solid bioconversions are proposed: a draft-tube
baffled continuous crystalliser and a fluidised-bed continuous crystalliser, both with
immobilised biocatalyst. Crystallisation in the pores of the support of the immobilised


Solid-to-solid bioconversions 257
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