Abstract

The electrode processes of the Ni2+ |Ni(Hg) system in aqueous azide solution at mercury electrodes have been investigated. It was found that NiN3+ reacts directly with the electrode. Consequently at low azide concentrations the electrode reaction is preceded by the process of formation of that complex from aquonickel (II) ion. At higher concentrations ([N3−]>2 m) the complex [Ni(N3)4]2− is in equilibrium with NiN3+ which is irreversibly reduced. The very high value of the apparent cathodic transfer coefficient suggests a two-step electrode reaction with a slow transfer of the second electron.

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