Excess Gibbs energies and volumes of the ternary system chloroform plus tetrahydrofuran plus cyclohexane at 298.15 K

被引:5
作者
Gianni, P. [1 ,2 ]
Lepori, L. [1 ]
Matteoli, E. [1 ]
机构
[1] CNR, Ist & Proc Chim Fis, Area Ric, I-56124 Pisa, Italy
[2] Dipartimento Chim & Chim Ind, I-56126 Pisa, Italy
关键词
Vapour-liquid equilibrium; Excess Gibbs energy; Excess volume; Activity coefficient; Apparent molar volume; Ternary mixture; Chloroform; Tetrahydrofuran; Cyclohexane; VAPOR-LIQUID-EQUILIBRIUM; MOLAR HEAT-CAPACITIES; ENTHALPIES; MIXTURES; TETRACHLOROMETHANE;
D O I
10.1016/j.fluid.2010.06.007
中图分类号
O414.1 [热力学];
学科分类号
摘要
Vapour-liquid equilibria and densities for the ternary system chloroform + tetrahydrofuran + cyclohexane and for the binary mixtures containing chloroform have been determined at 298.15 K. Vapour-liquid equilibrium data have been collected by head-space gas-chromatographic analysis of the vapour phase directly withdrawn from an equilibration apparatus. Density measurements have been carried out by means of a vibrating tube densimeter. Molar excess Gibbs energies G(E) and volumes V-E, as well as activity coefficients and apparent molar volumes of the components, have been obtained from the measured quantities and discussed. The binary chloroform + tetrahydrofuran displays negative deviations from ideality, while chloroform + cyclohexane positive deviations, for both volume and Gibbs energy. The G(E)'s and V-E's for the ternary system are positive in the region rich in cyclohexane while negative in the region rich in chloroform + tetrahydrofuran. This indicates that hydrogen bonding between chloroform and tetrahydrofuran molecules produces negative values of G(E) and V-E and strongly influences the behaviour of the ternary system. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
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