Article | REF: J2612 V1

Distillation of non-ideal mixtures

Authors: Vincent GERBAUD, Ivonne RODRIGUEZ-DONIS

Publication date: September 10, 2010, Review date: March 1, 2015

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ABSTRACT

In order to separate a non-ideal A-B mixture an entrainer E must generally be added to the load (azeotropic distillation) or in continuous mode (extractive distillation). In order to increase the driving force of the separation, the selectivity of E must be the furthest from 1. This parameter is assessed by the ratio of activity coefficients or of the relative volatilities of A and B at infinite dilution in E. The process can be carried out thermodynamically if there is a composition profile between the composition of the boiler and that of the liquid in equilibrium with the overhead vapor sum of the profiles in each section of the column rectification section, stripping and/or extractive according to the configurations of the columns. For every A-B-E mixture from the same class of network residue curve, the feasibility study is the same and is based on the properties of the residue curves and, in addition on those of the relative volatility curves for extractive distillation.

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AUTHORS

  • Vincent GERBAUD: Chemical engineering engineer from ENSIGC - Doctorate in Process Engineering from INPT - CNRS Research Fellow, Chemical Engineering Laboratory, Toulouse

  • Ivonne RODRIGUEZ-DONIS: Chemical engineer from the University of Havana, Cuba - Doctorate in Process Engineering from INPT - Researcher at the Instituto Superior de Tecnologías y Ciencias Aplicadas (INSTEC), Cuba

 INTRODUCTION

In this brief, theoretical and practical elements are applied to design distillation units for separating non-ideal mixtures, including azeotropic mixtures with minimum bubble temperature (noted T min ), azeotropic mixtures with maximum bubble temperature (noted T max ) and mixtures with close relative volatility.

These concepts, presented in the previous dossier "Distillation of non-ideal mixtures. Residue curves and other design tools" [J 2 611] , are as follows:

  • residue curve, similar to the composition profile of a continuous distillation column operating at full reflux, indicating the distillate possible in batch distillation;

  • relationship between the stability of singular points, pure bodies and azeotropes, and their boiling temperature within a distillation region ;

  • properties of residue curve networks with distillation boundaries separating distillation regions ;

  • classification of residual curve networks ;

  • univolatility curve identifying the regions of order of volatility in composition diagrams and therefore the ability of a pure body to be at the top or bottom of a column;

  • unidistribution curve associated with the shape and curvature of residual curves.

While distillation with pressure change is mentioned, the dossier focuses on azeotropic or extractive distillation, which requires the addition of a third E-body/entrainer.

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Distillation of non-ideal mixtures