THERMODYNAMICS OF PHASE-EQUILIBRIA IN AQUEOUS-ORGANIC SYSTEMS WITH SALT

被引:103
作者
ZERRES, H
PRAUSNITZ, JM
机构
[1] Chemical Engineering Dept, University of California, Berkeley, Berkeley Chemical Sciences Div, Lawrence Berkeley Laboratory, Berkeley, California
关键词
D O I
10.1002/aic.690400411
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A semiempirical thermodynamic method is developed to establish a framework for calculating vapor-liquid and liquid-liquid equilibria in ternary systems containing water, an organic solvent, and a salt. Careful attention is given to precise definition of standard states. Short-range ion-solvent forces are taken into account primarily by a chemical-equilibrium method based on stepwise ion solvation; ho wever, physical contributions also contribute. Water-cosolvent nonideality is described by an extended equation of the van Laar form. Long-range electrostatic forces between ions are taken into account by an extended Debye-Huckel equation with corrections for transferring from a McMillan-Mayer to a Lewis-Randall framework. The new method is illustrated with results for several systems including saturated aqueous mixtures of LiBr or LiCl with methanol where the salt concentration exceeds 20 molal. The method developed here is of particular interest for process calculations in extractive crystallization, a low-energy operation for producing salt from aqueous solution.
引用
收藏
页码:676 / 691
页数:16
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