Abstract

The separation of enantiomers is of great importance due to their possible differences in therapeutic properties. Preferential crystallization in various configurations of coupled batch crystallizers is used as an attractive means to separate the conglomerate-forming enantiomers from racemic mixtures. However, the productivity of such batch processes can be limited by the nucleation of the counter enantiomer and consumption of the supersaturation. In this work, a recently proposed process configuration, which uses coupled mixed suspension mixed product removal (MSMPR) with liquid phase exchange, is investigated by simulation studies. A detailed study on the effect of process parameters (e.g., feed flow rate, seed mass, and liquid phase exchange) on the productivity and yield of the coupled MSMPR has been presented. Moreover, a comparison of various coupled crystallizer configurations is carried out. It is shown through simulation studies that the productivity of the enantiomeric separation can be significantly improved compared to the previously proposed batch modes when the continuous configuration is used. The effect of nucleation kinetic parameters on the performances of various crystallizer configurations is studied as well. A set of coupled population balance equations (PBEs) was used to describe the evolution of the crystal phase of the both enantiomers in each vessel. These equations were solved numerically using the quadrature method of moments. The insights obtained in this study will be useful in the process design of coupled crystallizer systems.

Highlights

  • Enantiomers are the result of the chirality or handedness of molecules which are the non-superimposable mirror images of each other

  • The results obtained from coupled preferential crystallization (CPC)-mixed suspension mixed product removal (MSMPR) are compared with the conventional CPC and coupled preferential crystallization-dissolution (CPC-D)

  • First, we investigate the effect of various process parameters on the productivity and yield of the various process configurations with particular focus on the recently proposed CPC-MSMPR

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Summary

Introduction

Enantiomers are the result of the chirality or handedness of molecules which are the non-superimposable mirror images of each other. Enantiomers are widely found in organic compounds and their separation is a major concern in the modern pharmaceutical, food, and agricultural industries. Separation of the enantiomorphs is important in pharmaceutical industry, since very often one of the enantiomers exhibits the intended therapeutic activity while the other is inert. In some cases the counter enantiomer can cause toxicity or adverse effects. S(−)-fluoxetine shows remarkable therapeutic effects in preventing migraines, while the racemic (equimolar mixture of both enantiomers) drug (the antidepressant Prozac) has no effect [1].

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