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Intradiffusion coefficients for perchlorate ions in zinc perchlorate and zinc chloride solutions at 25°C: Comparing transport properties of zinc chloride and zinc perchlorate systems
Authors:William E. Price  Lawrence A. Woolf
Affiliation:(1) Department of Chemistry, University of Wollongong, Northfields Avenue, 2522 Wollongong, NSW, Australia;(2) Diffusion Research Unit, Atomic and Molecular Physics Labs., Research School of Physical Sciences and Engineering, Australian National University, 2601 Canberra, ACT, Australia
Abstract:Intradiffusion coefficients for36ClO4 have been measured in solutions of zinc perchlorate of concentration 0.1 to 3 mol dm–3 at 25°C by the diaphragm cell technique. In addition, intradiffusion coefficients for perchlorate ions in zinc chloride solutions have been measured over a concentration range at 25°C. The results confirm previous work on the effect of complexation on diffusion in zinc chloride solutions above a salt concentration of 0.1M. The present data, together with literature data for diffusion coefficients of the other species present in the zinc perchlorate electrolyte system, have enabled a simple analysis of the hydration around the zinc ions to be carried out. This indicates that the water diffusion data are consistent with the zinc ions having an effective hydration sphere of 11 (±2) water molecules. This is in keeping with values obtained for other simple divalent electrolytes using the same model. The model is extended here to allow analysis of water diffusion in zinc chloride solutions taking into account the presence of complexed chloro-zinc species. The experimental data are consistent with the effective hydration of the chloro-zinc complexes being independent of the number of chloride ligands and equal to 18±3 over a concentration range of 0 tol mol-dm–3. This postulate is discussed in terms of its consequences on the water ligand dynamics for the complex equilibria.
Keywords:Intradiffusion  hydration  perchlorate ions  complexation  zinc chloride  zinc perchlorate
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