Thermodynamics and kinetics of ion speciation in supercritical aqueous solutions: a molecular-based study

被引:14
作者
Chialvo, AA
Cummings, PT
Simonson, JM
Mesmer, RE
机构
[1] Univ Tennessee, Dept Chem Engn, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Chem Technol, Oak Ridge, TN 37831 USA
[3] Oak Ridge Natl Lab, Div Chem & Analyt Sci, Oak Ridge, TN 37831 USA
关键词
ion speciation; supercritical solutions; polarization effects; ion solvation; mean-force potential; water models;
D O I
10.1016/S0378-3812(98)00281-7
中图分类号
O414.1 [热力学];
学科分类号
摘要
Molecular simulation of infinitely dilute NaCl aqueous solutions are performed to study the Na+/Cl- ion pairing in a polarizable and a non-polarizable solvent at supercritical conditions. The simple point charge (SPC), the Pettitt-Rossky and the Fumi-Tosi models for the water-water the ion-water, and the ion-ion interactions are used in the determination of the degree of dissociation, its temperature and density dependence, and the kinetics of the interconversion between ion-pair configurations in a non-polarizable medium. To assess the effect of the solvent polarizability on the stability of the ion-pair configurations we replace the SPC by the polarizable point charge (PPC) water model and determine the anion-cation potential of mean force at T-r=1.20 at rho(r)=1.5. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 115
页数:9
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