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   <subfield code="a">A calorimetric study of the acid dissociation of the conjugate acids of poly( N -vinylimidazole) and polyallylamine</subfield>
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   <subfield code="c">[H. Kodama, T. Miyajima, H. Tabuchi, S. Ishiguro]</subfield>
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   <subfield code="a">Thermodynamic parameters for acid dissociation of the conjugate acids of poly(N-vinylimidazole) and polyallylamine have been determined in the presence of sodium chloride and sodium nitrate. Even though the plots of ΔG 0 against the degree of dissociation, α, are highly dependent on the added salt concentration levels, the concentration effect has never been observed for the corresponding ΔH 0 versus α plots. The effect on the ΔG 0 versus α plots has been attributed to the entropy change of the counterions between a polyelectrolyte phase and a bulk solution phase. The α dependency of ΔH 0 is affected remarkably by the kinds of cationic polymers and counter-anions. Each ΔH 0 value at completely neutralized conditions is quite close to the corresponding ΔH 0 value of the monomer analog. The difference in the ΔH 0 values at fully charged conditions has been explained by the heats due to The ion-pair formation of chloride anion to the conjugate acids of poly(N-vinylimidazole) and polyallylamine has been supported by 35Cl NMR measurement. It has also been suggested that chloride anions bind the basic polymer molecules even at fully neutralized conditions.</subfield>
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