Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation

Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model. •Distillation of isooctane fr...

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Veröffentlicht in:Chemical engineering research & design 2014-06, Vol.92 (6), p.995-1004
Hauptverfasser: Ooms, Tom, Vreysen, Steven, Van Baelen, Guy, Gerbaud, Vincent, Rodriguez-Donis, Ivonne
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container_end_page 1004
container_issue 6
container_start_page 995
container_title Chemical engineering research & design
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creator Ooms, Tom
Vreysen, Steven
Van Baelen, Guy
Gerbaud, Vincent
Rodriguez-Donis, Ivonne
description Heteroazeotropic batch distillation process to recover isooctane as product from ethyl acetate–isooctane mixture with using acetonitrile. 3.0-2 class ternary diagram and liquid–liquid and liquid–liquid–vapour equilibrium envelopes estimated by the original UNIFAC model. •Distillation of isooctane from an ethyl acetate–isooctane mixture.•Heterogeneous azeotropic distillation in a batch rectification column.•Methanol and acetonitrile heterogeneous entrainers selected among 60 candidates.•Experiments carried out in a laboratory scale column with decanter at the top.•Isooctane is the distillate product while acetonitrile achieves the best separation. This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. Pure ethyl acetate remained into the boiler at the end of each process.
doi_str_mv 10.1016/j.cherd.2013.10.010
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This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. For both methanol and acetonitrile, the main fraction was defined by the condensed vapor providing a liquid–liquid split of the isooctane/entrainer heteroazeotrope into the decanter. Ethyl acetate impurity was detected in both decanted phases, but in much lower amount when using acetonitrile as entrainer. The process with acetonitrile also resulted in a shorter operating time and higher purity and recovery yield of isooctane as the main distillate product. 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This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. 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This paper studies the separation of an ethyl acetate–isooctane mixture by heterogeneous azeotropic distillation in a batch rectifying column. An initial list of 60 candidates was studied but only methanol and acetonitrile were obtained as potential heterogeneous entrainers. These entrainers form a low boiling heterogeneous azeotrope with isooctane. Experimental verification of the miscibility gap with isooctane was performed at 25°C for each entrainer giving a smaller region for methanol than for acetonitrile. Feasibility of the heterogeneous azeotropic batch distillation was carried out experimentally in a laboratory batch distillation column having 44 theoretical equilibrium stages and using a high reflux ratio. Several distillate fractions were taken as a function of the temperature at the top of the column. 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source Elsevier ScienceDirect Journals
subjects Acetonitrile
Batch distillation
Chemical and Process Engineering
Chemical engineering
Chemical Sciences
Decantation
Distillation
Engineering Sciences
Entrainer selection
Entrainment
Ethyl acetate
Ethyl acetate–isooctane mixture
Heteroazeotropic distillation
Isooctane
Methanol
Methyl alcohol
Separation
Solvent recovery
title Separation of ethyl acetate–isooctane mixture by heteroazeotropic batch distillation
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