Isothermal Vapor-Liquid Equilibria and Excess Gibbs Energies for Binary Mixtures of Cyclic Ethers with 1,2-Dichloroethane

被引:4
作者
Amireche, Fouzia [1 ,2 ]
Belaribi, Farid Brahim [1 ]
Mokbel, Ilham [3 ]
Jose, Jacques [3 ]
机构
[1] Univ Sci & Technol Houari Boumediene, Fac Chem, Crystallog & Thermodynam Lab, POB 32 El Alia, Algiers 16111, Algeria
[2] Higher Natl Vet Sch Algiers, POB 161 El Alia, Algiers 16111, Algeria
[3] Claude Bernard Univ Lyon I, Lab Thermodynam & Analyt Chem, 43 Blvd 11 Novembre 1918, F-9622 Villeurbanne, France
关键词
MODIFIED UNIFAC MODEL; THERMODYNAMIC PROPERTIES; 1,4-DIOXANE; OXAALKANES; PRESSURE; SYSTEMS; ENTHALPIES; DORTMUND; ACETALS; ALKANES;
D O I
10.1021/acs.jced.7b01091
中图分类号
O414.1 [热力学];
学科分类号
摘要
Isothermal vapor-liquid equilibria (VLE) are measured for three binary systems containing cyclic ethers: 1,3-dioxolane, 1,4-dioxane, or tetrahydropyran in mixture with 1,2-dichloroethane at 10 temperatures ranging from 273.15 to 353.15 K. A laboratory apparatus using the static method was employed to carry out the vapor pressures of the pure components and the mixtures. The VLE data were reduced by the Redlich-Kister equation and used to calculate activity coefficients then excess molar Gibbs free energies G(E). The non ideality of the vapor pressure was considered in terms of the second molar virial coefficient. Both the mixtures formed by tetrahydropyran or 1,3-dioxolane with 1,2-dichloroethane show a minimum boiling point azeotrope. The experimental data were compared with the results provided for the modified UNIFAC (Do) and the DISQUAC models.
引用
收藏
页码:1568 / 1577
页数:10
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