4.7 Article Proceedings Paper

Recovery of dilute acetic acid through esterification in a reactive distillation column

Journal

CATALYSIS TODAY
Volume 60, Issue 1-2, Pages 147-157

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0920-5861(00)00326-6

Keywords

reactive distillation; esterification; acetic acid; n-butanol; iso-amyl alcohol; n-butyl acetate; iso-amyl acetate; ion-exchange resin

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The recovery of acetic acid from its dilute aqueous solutions is a major problem in both petrochemical and fine chemical industries. The conventional methods of recovery are azeotropic distillation, simple distillation and liquid-liquid extraction. Physical separations such as distillation and extraction suffer from several drawbacks. The esterification of an aqueous solution (30%) of acetic acid with n-butanol/iso-amyl alcohol is a reversible reaction. As excess of water is present in the reaction mixture, the conversion is greatly restricted by the equilibrium limitations. The esters of acetic acid, namely, n-butyl acetate and iso-amyl acetate, have a wide range of applications. In view of the appreciable value of these esters, the present work was directed towards recovery of 30% acetic acid by reaction with n-butanol and iso-amyl alcohol in a reactive distillation column (RDC) using macroporous ion-exchange resin. Indion 130, as a catalyst bed, confined in stainless steel wire cages. Experiments were conducted in order to achieve an optimum column configuration for the synthesis of n-butyl acetate/iso-amyl acetate in an RDC. The effect of various parameters, e.,g. total feed flowrate, length of catalytic section, reflux ratio, mole ratio of the reactants. location of feed points and effect of recycle of water were studied. (C) 2000 Elsevier Science B.V. All rights reserved.

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