Abstract
Abstract
This study proposed a new model based on the solvation phenomena. The ionic activity coefficients of individual ions of some 1:1 and 1:2 salts were correlated successfully. Comparison was made between the results of the present model and those of Khoshkbarchi–Vera (KV), Pitzer, and Lin–Lee models. The average relative errors for cation and anion were 3.03, 3.53, 3.45 and 1.24, 1.14, 1.38, respectively, in Lin–Lee, KV, Pitzer models, whereas they are 1.81 and 0.66 in the proposed model.These results show that the proposed model improved the correlation of the individual ionic activity coefficients. Contrary to arguments found in the literature, it is also demonstrated that the short-range solvation contribution is a linear function of ionic strength.
Subject
Modelling and Simulation,General Chemical Engineering
Reference50 articles.
1. RE Extension of the Wilson model to electrolyte solutions Fluid Phase;Zhao,2000
2. and Correlation of the Individual Ionic Activity Coefficients of Aqueous Electrolyte Solutions of;Taghikhani;Measurement Can J Chem Eng,2000
3. Correlation and prediction of osmotic coefficient and water activity of aqueous electrolyte solutions by a two - ionic parameter model;Pazuki;J Chem Thermodyn,2005
4. New local composition model for electrolyte solutions Fluid Phase;Sadeghi,2005
5. Activity coefficients in electrolyte solutions nd ed;Pitzer,1991
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献