Volume 33, Issue 5 pp. 730-742
Review

Prediction of Activity Coefficients for Uni-univalent Electrolytes in Pure Aqueous Solution

J. I. Partanen

J. I. Partanen

Laboratory of Physical Chemistry, Department of Chemical Technology, Faculty of Technology, Lappeenranta University of Technology, Finland

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R. K. Salmimies

R. K. Salmimies

Laboratory of Separation Technology, Department of Chemical Technology, Faculty of Technology, Lappeenranta University of Technology, Finland

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L. J. Partanen

L. J. Partanen

Laboratory of Physical Chemistry, Department of Chemistry, University of Helsinki, Finland

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M. Louhi-Kultanen

M. Louhi-Kultanen

Laboratory of Separation Technology, Department of Chemical Technology, Faculty of Technology, Lappeenranta University of Technology, Finland

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First published: 28 April 2010
Citations: 9

Abstract

Parameter-free activity coefficient equations were tested in addition to those containing one, two, three or four electrolyte-dependent parameters with the experimental activity coefficients obtained from the literature data for aqueous solutions of the following electrolytes at 298.15 K: KCl, NaCl, RbCl, KBr, RbBr, CsBr, KI, RbI, KNO3, and KH2PO4. The experimental activity coefficients of each electrolyte considered can be reproduced within the uncertainty of the measurements up to the molality of the saturated solution by using a three-parameter equation of the extended Hückel type. The best Hückel equations are given for all electrolytes in question. The results from the present studies reveal that the parameter-free equations can be reliably used in thermodynamic studies only for very dilute electrolyte solutions. On the other hand, in most cases, a good agreement with the experimental data is obtained with the one-parameter equations of Bromley [14] and Kusik and Meissner [13], with the two-parameter equation of Bretti et al. [15], and with the three- or four-parameter equation of Hamer and Wu [19] in addition to the three-parameter Pitzer equation [23], with almost all parameter values suggested in the literature. In several cases, these equations seem to apply to much higher molalities than those used in the parameter estimations. Therefore, the best of these equations may have important applications in calculations associated with the dissolution and crystallization processes of these salts.

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