The oxidation processes of cyanide and cyanate ions on a Pt electrode in aqueous and methanol solutions were studied by infrared spectroscopy. In aqueous solution, the cyanide ion was oxidized to cyanate and successively to carbon dioxide. The reaction proceeded on an oxidized platinum surface. In m
Anodic oxidation of potassium cyanide on platinum electrode
โ Scribed by H. Tamura; T. Arikado; H. Yoneyama; Y. Matsuda
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 402 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
The mechanism of anodic oxidation of cyanide on platinum electrode was studied electrochemically and chemically. Cyanide was oxidized at a first order with respect to hydroxyl ion and at zero with respect IO cyanide ion on the rate determining step. On the other hand. the potential controlled coulometry at O-45 V us N.H.E.) indicated that two moles of hydroxyl ion and two faradays electricity were consumed during anodic oxidation of one mole of cyanide.
Several consecutive reaction paths for the oxidation of cyanide were proposed on the basis of the above diagnostic criteria. Among them, the mechanism invoking metal peroxide would be available in view of the chemical properties of several intermediate species.
๐ SIMILAR VOLUMES
Cyclic voltammetry experiments performed in acid solutions of cyclohexene on platinized platinum anodes show that platinum oxide must play a role in the anodic oxidation of the hydrocarbon through a mechanisticscheme of the type proposed by Gilman[lO].
The anodic evolution of oxygen was investigated on the platinum oxide electrode, prepared by a thermal decomposition method, in alkaline solutions; the overvoltage data were reproducible on this electrode. On the basis of reliable mechanistic observations, the most probable path under Langmuir condi