Abstract
Zdanovskii’s rule is the simplest isopiestic molality relation of mixed electrolyte aqueous solutions and the McKay–Perring equation is a differentio-integral equation particularly suitable for calculating solute activity coefficients from isopiestic measurements. However, they have two unsolved problems, which have puzzled solution chemists for several decades: (1) Zdanovskii’s rule has been verified by precise isopiestic measurements. But, several scientists suggested that the rule contradicts the Debye–Hückel limiting law for extremely dilute unsymmetrical mixtures. (2) In the McKay–Perring equation, a solute activity coefficient is multiplied by a solute composition variable. Different scientists have suggested that the composition variable may be the total ionic strength, common ion concentration, total ionic concentration, or an additive function with arbitrary proportionality constants. But, the different choices of the composition variable may lead to different activity coefficient results. Here, I derive a modified McKay–Perring equation in which the composition variable has the exclusive physical meaning of total ionic concentration for mixed electrolyte solutions (or of total solute particle concentration for the mixed solutions containing nonelectrolyte solutes). I also demonstrate that Zdanovskii’s rule is consistent with the Debye–Hückel limiting law for extremely dilute unsymmetrical mixtures. I derive two particular solutions of the modified McKay–Perring equation: one for the systems obeying Zdanovskii’s rule and another for the systems obeying a limiting linear concentration rule. These theoretical results have been verified with literature experiments and model calculations.
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Notes
One of the Reviewers has presented an alternative derivation of Eq. 10. First, without the restriction of \( \ln a_{W} \to 0, \) an equation \( \left( {{{\nu_{1} m_{1}^{0} } \mathord{\left/ {\vphantom {{\nu_{1} m_{1}^{0} } {\nu_{2} m_{2}^{0} }}} \right. \kern-0pt} {\nu_{2} m_{2}^{0} }}} \right)_{{a_{\text{W}} }} = \left( {{{\phi^{0(2)} } \mathord{\left/ {\vphantom {{\phi^{0(2)} } \phi }} \right. \kern-0pt} \phi }^{0(1)} } \right)_{{a_{\text{W}} }} \) for single aqueous solutions is derived from the definition \( \phi^{0(i)} = - {{1000\ln a_{\text{W}}^{0(i)} } \mathord{\left/ {\vphantom {{1000\ln a_{\text{W}}^{0(i)} } {M\nu_{i} m_{i}^{0} }}} \right. \kern-0pt} {M\nu_{i} m_{i}^{0} }} . \) When applied to the restricted concentration region where the Debye–Hückel limiting law is valid and when using the Debye–Hückel limiting law expression for the osmotic coefficient, it leads to \( \left( {{{\nu_{1} m_{1}^{0} } \mathord{\left/ {\vphantom {{\nu_{1} m_{1}^{0} } {\nu_{2} m_{2}^{0} }}} \right. \kern-0pt} {\nu_{2} m_{2}^{0} }}} \right)_{{a_{\text{W}} }} = \left\{ {{{\left[ {1 - \left( {{{\left| {z_{a}^{0(2)} z_{c}^{0(2)} } \right|A} \mathord{\left/ {\vphantom {{\left| {z_{a}^{0(2)} z_{c}^{0(2)} } \right|A} 3}} \right. \kern-0pt} 3}} \right)I^{{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-0pt} 2}}} } \right]} \mathord{\left/ {\vphantom {{\left[ {1 - \left( {{{\left| {z_{a}^{0(2)} z_{c}^{0(2)} } \right|A} \mathord{\left/ {\vphantom {{\left| {z_{a}^{0(2)} z_{c}^{0(2)} } \right|A} 3}} \right. \kern-0pt} 3}} \right)I^{{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-0pt} 2}}} } \right]} {\left[ {1 - \left( {{{\left| {z_{a}^{0(1)} z_{c}^{0(1)} } \right|A} \mathord{\left/ {\vphantom {{\left| {z_{a}^{0(1)} z_{c}^{0(1)} } \right|A} 3}} \right. \kern-0pt} 3}} \right)I^{{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-0pt} 2}}} } \right]}}} \right. \kern-0pt} {\left[ {1 - \left( {{{\left| {z_{a}^{0(1)} z_{c}^{0(1)} } \right|A} \mathord{\left/ {\vphantom {{\left| {z_{a}^{0(1)} z_{c}^{0(1)} } \right|A} 3}} \right. \kern-0pt} 3}} \right)I^{{{1 \mathord{\left/ {\vphantom {1 2}} \right. \kern-0pt} 2}}} } \right]}}} \right\}_{{a_{\text{W}} }} . \) A similar derivation can be used for the mixed solution. They will further lead to \( \mathop {lim}_{{\ln a_{\text{W}} \to 0}} \left( {{{\nu_{1} m_{1}^{0} } \mathord{\left/ {\vphantom {{\nu_{1} m_{1}^{0} } {\nu_{2} m_{2}^{0} }}} \right. \kern-0pt} {\nu_{2} m_{2}^{0} }}} \right)_{{a_{\text{W}} }} = 1 \) and \( \mathop {lim}_{{\ln a_{\text{W}} \to 0}} \left\{ {{{(\nu_{1} m_{1} + \nu_{2} m_{2} )} \mathord{\left/ {\vphantom {{(\nu_{1} m_{1} + \nu_{2} m_{2} )} {\nu_{i} m_{i}^{0} }}} \right. \kern-0pt} {\nu_{i} m_{i}^{0} }}} \right\}_{{a_{\text{W}} }} = 1, \) resulting in Eq. 10.
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The author thanks Dr. Joseph A. Rard for helpful comments and for supplying Ref. [15].
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Wang, ZC. Modified McKay–Perring Equation and Its Two Particular Solutions. J Solution Chem 47, 484–497 (2018). https://doi.org/10.1007/s10953-018-0723-2
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DOI: https://doi.org/10.1007/s10953-018-0723-2