Thermodynamics of binary mixtures containing organic carbonates Part XI.: SLE measurements for systems of diethyl carbonate with long n-alkanes:: comparison with DISQUAC and modified UNIFAC predictions

被引:11
作者
Domanska, U [1 ]
Szurgocinska, M
González, JA
机构
[1] Warsaw Univ Technol, Fac Chem, Div Phys Chem, PL-00664 Warsaw, Poland
[2] Univ Valladolid, Fac Ciencias, Dept Termodinam & Fis Aplicada 2, Valladolid 47071, Spain
关键词
experimental; solid-liquid equilibria; diethyl carbonate; long-chain n-alkanes; correlations; Wilson; UNIQUAC; NRTL; group contributions; DISQUAC; UNIFAC;
D O I
10.1016/S0378-3812(01)00564-7
中图分类号
O414.1 [热力学];
学科分类号
摘要
Using the available interaction parameters for organic carbonate + alkane mixtures the ability of the DISQUAC and modified UNIFAC group contribution model to predict solid-liquid equilibria (SLE) is investigated. Six sets of the SLE temperatures for diethyl carbonate + n-alkane (octadecane, eicosane, docosane, tetracosane, hexacosane, octacosane) systems have been measured by a dynamic method from 278.65 K to the melting point of the long chain n-alkane. The data have been correlated by three equations: Wilson, UNIQUAC and NRTL. The existence of a solid-solid first-order phase transition in n-alkanes has been taken into consideration in the solubility calculations. The relative standard deviations of the solubility temperature correlation for all measured data vary from 0.31 to 0.34 K and depend on the particular equation used. The SLE curves are usually well predicted by DISQUAC and modified UNIFAC models with average standard deviation of < 1.35 K. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:15 / 31
页数:17
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