Corresponding states theories and liquid models

D. Patterson, G. Delmas
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引用次数: 333

Abstract

The general corresponding states theory of Prigogine and collaborators, applicable to the thermodynamics of mixtures of quasi-spherical molecules and polymer solutions, is compared to the theory of Flory, Abe, Orwoll and Vrij. The mixing functions are divided into two contributions: an interaction term due essentially to the weakness of (1-2) interactions, and a term due to the dissimilarity of the free volumes of the two components. The latter term is small or negligible in mixtures of quasi-spherical molecules but dominant for polymer solutions. These terms are contrasted with the contact interaction term and the equation of state term of the Flory theory. The mixing functions are calculated by a new approximate procedure, using several liquid models based on the cell partition function (including the model used by Flory and collaborators). The results are similar and the models make certain errors in common.
相应的状态理论和液体模型
将Prigogine和合作者提出的适用于准球形分子和聚合物溶液混合物热力学的一般对应态理论与Flory、Abe、Orwoll和Vrij的理论进行了比较。混合函数分为两个贡献:一个相互作用项,主要是由于(1-2)相互作用的弱点,另一个是由于两个组分的自由体积的不同。后一项在准球形分子混合物中很小或可以忽略不计,但在聚合物溶液中占主导地位。这些项与Flory理论中的接触相互作用项和状态方程项进行了对比。混合函数通过一种新的近似程序计算,使用几种基于细胞配分函数的液体模型(包括Flory和合作者使用的模型)。结果相似,各模型均存在一定的误差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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