Ionic Conductivity, Diffusion Coefficients, and Degree of Dissociation in Lithium Electrolytes, Ionic Liquids, and Hydrogel Polyelectrolytes

被引:18
|
作者
Garrido, Leoncio [1 ]
Aranaz, Inmaculada [1 ,2 ]
Gallardo, Alberto [1 ]
Garcia, Carolina [1 ]
Garcia, Nuria [1 ]
Benito, Esperanza [1 ]
Guzman, Julio [1 ]
机构
[1] ICTP CSIC, Juan Cierva 3, Madrid 28006, Spain
[2] Univ Complutense Madrid, Fac Farm, Inst Estudios Biofunc, Dept Quim Ciencias Farmaceut, Plaza Ramon Y Cajal S-N, E-28040 Madrid, Spain
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2018年 / 122卷 / 34期
关键词
DOUBLE-NETWORK HYDROGELS; ELECTROPHORETIC NMR; FREEZING-POINT; TRANSPORT; THERMODYNAMICS; WATER; MEMBRANES; GRADIENT; LI+;
D O I
10.1021/acs.jpcb.8b06424
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The conductive and diffusional behavior of electrolytes in media with different dielectric and viscoelastic properties is investigated. A revised model to separate the contribution of dissociated and nondissociated species to the diffusion coefficients determined with NMR is proposed. Impedance spectroscopy is used to measure the ionic conductivity of lithium salts in aqueous medium, ionic liquids in aprotic solvents, and hydrogel polyelectrolytes. The diffusion coefficients of the species of interest in those systems are determined with multinuclear pulsed-gradient spin-echo (PGSE) NMR. The results are analyzed using the revised model. It is shown that the degree of ionization could be determined directly from measurements of ionic conductivity and diffusion coefficients in very different types of electrolytes and in a wide range of concentrations. Furthermore, these findings support the original Arrhenius hypothesis about electrolytes and show that the assumption of a complete dissociation is not required to describe their conductive behavior. The reduced conductivity observed in hydrogels, at or near swelling equilibrium, compared to that in solutions could be attributed mainly to the hindered ionic mobility caused by the network structure.
引用
收藏
页码:8301 / 8308
页数:8
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