A study of the binary cation-exchange equilibria between H + -form Amberlite IR-120 resin and aqueous solutions of lead, nickel, and chromium nitrates at pH < 3 has been made. Experiments were carried out at (283, 303, and 323) K with solutions having total cation concentrations of 0.1 eq·L −1 . The experimental equilibrium data have been satisfactorily correlated using the homogeneous mass action law model (LAM). This model assumes nonideal behavior for both the solution and the solid phase. Wilson and Pitzer equations have been used to calculate activity coefficients in the solid and liquid phases, respectively. The standard enthalpy Δ H ° AB and the standard entropy Δ S ° AB were determined. The values of both the thermodynamic constant and standard Gibbs free energy Δ G ° AB demonstrate temperature dependence. The rise in temperature caused a slight increase in the value of the equilibrium constant ( K AB ) for the ion exchange of all heavy metal ions tested in this study. According to equilibrium constants obtained, the Amberlite IR-120 exhibits the following order of selectivity, Cr 3+ > Pb 2+ > Ni 2+, in all the ranges of the temperatures studied in agreement with the rule of higher selectivity at higher counterion charge.
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Carmona et al. (2008) studied this question.
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