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.