Three empirical rules of interfacial potential and Gibb's energy with the radius,charge number of transfer ions and dielectric constant of organic phase are obtained for the ion transfer across the liquid-liquid i...Three empirical rules of interfacial potential and Gibb's energy with the radius,charge number of transfer ions and dielectric constant of organic phase are obtained for the ion transfer across the liquid-liquid interface,which are verified by the transfer of simple anions,dye ions and metal ions facilitated by neutral ionophores across the interface between water and some organic solvents, and deduced theoretically based on the electrostatic interaction of ion and high-permittivity solvent. The rules are proved to be effective of choosing supporting electrolytes and searching for new transfer system which follows the rule that r/n of transfer ion should be larger than that of electrolytes ion in water phase and less than that in organic phase.A rule for judgement of the charge sign of transfer ion is suggested firstly based on the relationship between interfacial half-wave potential and dielectric constant of organic phase.展开更多
基金This work was supported by the National Natural Science Foundation of China.
文摘Three empirical rules of interfacial potential and Gibb's energy with the radius,charge number of transfer ions and dielectric constant of organic phase are obtained for the ion transfer across the liquid-liquid interface,which are verified by the transfer of simple anions,dye ions and metal ions facilitated by neutral ionophores across the interface between water and some organic solvents, and deduced theoretically based on the electrostatic interaction of ion and high-permittivity solvent. The rules are proved to be effective of choosing supporting electrolytes and searching for new transfer system which follows the rule that r/n of transfer ion should be larger than that of electrolytes ion in water phase and less than that in organic phase.A rule for judgement of the charge sign of transfer ion is suggested firstly based on the relationship between interfacial half-wave potential and dielectric constant of organic phase.