2018Journal of Chemical & Engineering DataRequires access

Isobaric Vapor–Liquid Equilibrium Measurements for Separation of Azeotrope (Methanol + Methyl Acetate)

Shiliang Jiang, Jun Gao, Rui Li, Dongmei Xu, Lianzheng Zhang, Yinglong Wang

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Abstract

For separation of the azeotrope (methanol + methyl acetate), extractive distillation is applied and isobutyl acetate, isopentyl acetate, and p -xylene are chosen as the entrainers. To obtain the binary interaction parameters of thermodynamic models for design of the extractive distillation process, the isobaric vapor–liquid equilibrium (VLE) data for the three binary systems of (methyl acetate + isobutyl acetate), (methyl acetate + isopentyl acetate), and (methyl acetate + p -xylene) were determined at the pressure of 101.3 kPa. The thermodynamic consistency for the VLE experimental data of the three mixtures were tested by the Herington and van Ness methods. The NRTL, UNIQUAC, and Wilson thermodynamic models were adopted to correlate the VLE experimental data, and the binary interaction parameters of the three models were regressed.

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What this paper is about

For separation of the azeotrope (methanol + methyl acetate), extractive distillation is applied and isobutyl acetate, isopentyl acetate, and p -xylene are chosen as the entrainers. To obtain the binary interaction parameters of thermodynamic models for design of the extractive distillation process, the isobaric vapor–liquid equilibrium (VLE) data for the three binary systems of (methyl acetate + isobutyl acetate), (methyl acetate + isopentyl acetate), and (methyl acetate + p -xylene) were determined at the pressure of 101.3 kPa. The thermodynamic consistency for the VLE experimental data of the three mixtures were tested by the Herington and van Ness methods. The NRTL, UNIQUAC, and Wilson thermodynamic models were adopted to correlate the VLE experimental data, and the binary interaction parameters of the three models were regressed.

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Available abstract

For separation of the azeotrope (methanol + methyl acetate), extractive distillation is applied and isobutyl acetate, isopentyl acetate, and p -xylene are chosen as the entrainers. To obtain the binary interaction parameters of thermodynamic models for design of the extractive distillation process, the isobaric vapor–liquid equilibrium (VLE) data for the three binary systems of (methyl acetate + isobutyl acetate), (methyl acetate + isopentyl acetate), and (methyl acetate + p -xylene) were determined at the pressure of 101.3 kPa. The thermodynamic consistency for the VLE experimental data of the three mixtures were tested by the Herington and van Ness methods. The NRTL, UNIQUAC, and Wilson thermodynamic models were adopted to correlate the VLE experimental data, and the binary interaction parameters of the three models were regressed.

Key concepts: Azeotrope, UNIQUAC, Isobaric process, Methyl acetate, Extractive distillation, Thermodynamics, Chemistry, Non-random two-liquid model

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