Isobaric Vapor–Liquid Equilibrium for the Butyl Acetate + Ethyl Lactate Binary System at 101.3, 80.0, 60.0, and 40.0 kPa

Vapor–liquid equilibrium (VLE) is crucial for the design of waste photoresists and solvent recycling processes. Isobaric VLE data for the butyl acetate + ethyl lactate binary system were experimentally determined using a modified Othmer still at pressures of 101.3, 80.0, 60.0, and 40.0 kPa. The thermodynamic consistency of experimental VLE data was rigorously validated using Fredenslund’s test and Van Ness’s point-to-point test. The data were then correlated to the Wilson, NRTL, and UNIQUAC models. The results demonstrate that the three local composition models provide an excellent fit to the experimental data, significantly outperforming the predictive UNIFAC model. The thermodynamic consistency of the regressed binary interaction parameters was further confirmed through a graphical analysis of the Gibbs energy of mixing. These findings are essential for the accurate design and simulation of distillation processes and facilitate the development of sustainable solvent recovery technologies for the semiconductor industry.

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Publication Details

Journal
Journal of Chemical & Engineering Data
Published
2025-12-15
DOI
https://doi.org/10.1021/acs.jced.5c00562
Primary Topic
Phase Equilibria and Thermodynamics
Type
article
Field-Weighted Citation Impact
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article

Isobaric Vapor–Liquid Equilibrium for the Butyl Acetate + Ethyl Lactate Binary System at 101.3, 80.0, 60.0, and 40.0 kPa

Xuee Wu, Liming Che, Yunan Wu, Hua Zhou
Journal of Chemical & Engineering Data
Phase Equilibria and Thermodynamics
article

Isobaric Vapor–Liquid Equilibrium for the Butyl Acetate + Ethyl Lactate Binary System at 101.3, 80.0, 60.0, and 40.0 kPa

Xuee Wu, Liming Che, Yunan Wu, Hua Zhou
article en

Abstract

Vapor–liquid equilibrium (VLE) is crucial for the design of waste photoresists and solvent recycling processes. Isobaric VLE data for the butyl acetate + ethyl lactate binary system were experimentally determined using a modified Othmer still at pressures of 101.3, 80.0, 60.0, and 40.0 kPa. The thermodynamic consistency of experimental VLE data was rigorously validated using Fredenslund’s test and Van Ness’s point-to-point test. The data were then correlated to the Wilson, NRTL, and UNIQUAC models. The results demonstrate that the three local composition models provide an excellent fit to the experimental data, significantly outperforming the predictive UNIFAC model. The thermodynamic consistency of the regressed binary interaction parameters was further confirmed through a graphical analysis of the Gibbs energy of mixing. These findings are essential for the accurate design and simulation of distillation processes and facilitate the development of sustainable solvent recovery technologies for the semiconductor industry.

Journal of Chemical & Engineering DataVol. 71(1)
Xiamen University (CN)
Openalex Percentile: Top 61%
Phase Equilibria and Thermodynamics
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