Electroreduction of Ni2+ and Fe2+ in a fused electrolyte
Identifieur interne : 000585 ( France/Analysis ); précédent : 000584; suivant : 000586Electroreduction of Ni2+ and Fe2+ in a fused electrolyte
Auteurs : Frédéric Lantelme [France] ; Ahmed Derja [France] ; Naoaki Kumagai [France]Source :
- Journal of Electroanalytical Chemistry [ 0022-0728 ] ; 1988.
Abstract
It is shown that the simultaneous electroreduction of Ni2+ and Fe2+ ions dissolved in a fused electrolyte (LiCl+KCl) at 503°C is controlled by ion diffusion and by metal interdiffusion. These transport properties are studied by chronopotentiometry. During the reduction step two transition times are observed; these times depend on the diffusion fluxes of Ni2+ and Fe2+ ions. At the end of this reduction pulse, oxidation of the alloy coating by Ni2+ ions gives rise to a potential jump which characterizes the metal interdiffusion. At short times a large increase of the interdiffusion rate is observed; this effect is attributed to a rapid transport process occurring in the very first atomic layers of the coating; it presents some similitude with the underpotential shift observed in metal deposition at room temperature.
Url:
DOI: 10.1016/0022-0728(88)85097-6
Affiliations:
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ISTEX:30F2C992A6DE2AB3428E41775EE1EE249ED4B223Le document en format XML
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<front><div type="abstract" xml:lang="en">It is shown that the simultaneous electroreduction of Ni2+ and Fe2+ ions dissolved in a fused electrolyte (LiCl+KCl) at 503°C is controlled by ion diffusion and by metal interdiffusion. These transport properties are studied by chronopotentiometry. During the reduction step two transition times are observed; these times depend on the diffusion fluxes of Ni2+ and Fe2+ ions. At the end of this reduction pulse, oxidation of the alloy coating by Ni2+ ions gives rise to a potential jump which characterizes the metal interdiffusion. At short times a large increase of the interdiffusion rate is observed; this effect is attributed to a rapid transport process occurring in the very first atomic layers of the coating; it presents some similitude with the underpotential shift observed in metal deposition at room temperature.</div>
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