Vapor-liquid equilibria and density measurement for binary mixtures of o-xylene plus NMF, m-xylene plus NMF and p-xylene + NMF at 333.15 K, 343.15 K and 353.15 K from 0 kPa to 101.3 kPa

被引:7
|
作者
Chen, Wei-Kuan [1 ]
Lee, Kun-Jung [1 ]
Chang, Chieh-Ming J. [1 ]
Ko, Jing-Wei [2 ]
Lee, Liang-Sun [3 ]
机构
[1] Natl Chung Hsing Univ, Dept Chem Engn, Taichung 402, Taiwan
[2] Refining & Mfg Res Inst, Proc Res Dept, Chiayi 600, Taiwan
[3] Natl Cent Univ, Dept Chem & Mat Engn, Chungli 32001, Taiwan
关键词
Isothermal vapor-liquid equilibrium; Xylenes; NMF; Density; Excess Gibbs energy; N-METHYLFORMAMIDE; BENZENE; SYSTEMS; WATER; EXPRESSION; TOLUENE; ENERGY;
D O I
10.1016/j.fluid.2009.12.002
中图分类号
O414.1 [热力学];
学科分类号
摘要
Isothermal vapor-liquid equilibria at 333.15 K, 343.15 K and 353.15 K for three binary mixtures of o-xylene, m-xylene and p-xylene individually mixed with N-methylformamide (NMF), have been obtained at pressures ranged from 0 kPa to 101.3 kPa over the whole composition range. The Wilson, NRTL and UNIQUAC activity coefficient models have been employed to correlate experimental pressures and liquid mole fractions. The non-ideal behavior of the vapor phase has been considered by using the Peng-Robinson equation of state in calculating the vapor mole fraction. Liquid and vapor densities were measured by using two vibrating tube densitometers. The excess molar volumes of the liquid phase were also determined. Three systems of o-xylene + NMF. m-xylene + NMF and p-xylene + NMF mixtures present large positive deviations from the ideal solution and belong to endothermic mixings because their excess Gibbs energies are positive. Temperature dependent intermolecular parameters in the NRTL model correlation were finally obtained in this study. (C) 2009 Elsevier B.V. All rights reserved.
引用
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页码:40 / 47
页数:8
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