A square-well equation of state for aqueous strong electrolyte solutions

被引:36
|
作者
Haghtalab, Ali [1 ]
Mazloumi, Seyed Hossein [1 ]
机构
[1] Tarbiat Modares Univ, Dept Chem Engn, Tehran, Iran
关键词
Equation of state; Electrolyte; Mean activity coefficient; Osmotic coefficient; Square-well; MEAN SPHERICAL APPROXIMATION; ASSOCIATING FLUID THEORY; EXCESS GIBBS ENERGY; THERMODYNAMIC PROPERTIES; PRIMITIVE MODEL; SYSTEMS; SUBSTANCES; IONS;
D O I
10.1016/j.fluid.2009.07.018
中图分类号
O414.1 [热力学];
学科分类号
摘要
A simple and accurate electrolyte-equation of state is introduced for correlation of the mean activity coefficients of strong aqueous electrolyte solutions. The nonelectrolyte contribution of the new electrolyte-equation of state is based on the cubic square-well equation of state, SWEOS, that is composed of the van der Waals repulsive part of EOS and the attractive term is based on the square-well potential. The explicit version of the mean spherical approximation (MSA) is adopted for electrostatic contribution of electrolyte solution. The new electrolyte-equation of state, eEOS, has three adjustable parameters per each salt that are optimized by correlation of the mean activity coefficients of more than 130 binary aqueous electrolyte solutions at 25 degrees C and I bar. Furthermore, the parameters are used for prediction of the osmotic coefficients and densities of several aqueous binary electrolyte solutions at 25 degrees C. Also the mean activity and osmotic coefficient of a number of electrolytes have been correlated in temperature range of 0-100 degrees C. Moreover, the ionic specific parameters are obtained for five binary aqueous electrolyte solutions by simultaneous fitting of mean activity, osmotic coefficient and apparent molal volume. The results demonstrate that the new eEOS can be applied for accurate representation of the activity and osmotic coefficients of the aqueous electrolyte solutions at wide range of the electrolyte concentration and temperature of binaries. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 104
页数:9
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