Diffusion coupling in multiply associating electrolyte solutions

Jean-Pierre Simonin (1) , José Miguel Ramos (2) , José Torres-Arenas (2)

1 PHENIX - PHysicochimie des Electrolytes et Nanosystèmes InterfaciauX
2 Universidad de Guanajuato

Diffusion coupling in multiply associating aqueous electrolyte solution is studied. The process is illustrated in the case of zinc(II) ion which forms a set of complexes, ZnCl 2−n n (with n = 1, .., 4), in the presence of chloride ions. The transport of zinc ion, taken in radioactive form 65 Zn 2+ , in the electric field created by a gradient of LiCl, is investigated experimentally by employing an adaptation of the closed capillary technique. The transient diffusion process is modeled by using two different treatments: finite difference (FD) simulation and normal mode (NM) analytic solution. Deviations from ideality are taken into account with the use of the mean spherical approximation (MSA), and the internal electric field is calculated using the dynamical electroneu-trality condition. The theoretical FD and NM results are compared with the experimental data about the diffusion of zinc.

Mots clés: Electrolytes; association; non-ideal; diffusion; mean-spherical approximation (MSA)

Domaines: Chimie organique

Jean-Pierre Simonin, José Miguel Ramos, José Torres-Arenas. Diffusion coupling in multiply associating electrolyte solutions. Journal of Molecular Liquids, 2016, 215, pp.69-76. ⟨10.1016/j.molliq.2015.12.020⟩. ⟨hal-01252050⟩