The kinetics of bromide oxidation and Br3- reduction were studied at polycrystalline Pt electrodes in acidic media. The electrochemical behavior of equimolar Br3- and Br- solutions was investigated, in a concentration range of the electroactive species between 0.1 and 1.0 M. E–log j plots did not exhibit linear segments, most probably because of extensive adsorption of bromine radicals. Further analysis supported the hypothesis of a Volmer–Tafel mechanism, with the chemical recombination step as rate determining. Electrosorption isotherms for Br radicals were found to be of the Frumkin type. The kinetics of Br3- reduction was controlled by the surface dissociation of the Br2 molecules.

The Bromine Electrode. Part II: Reaction Kinetics at polycrystalline Pt

FERRO, Sergio;DE BATTISTI, Achille
2005

Abstract

The kinetics of bromide oxidation and Br3- reduction were studied at polycrystalline Pt electrodes in acidic media. The electrochemical behavior of equimolar Br3- and Br- solutions was investigated, in a concentration range of the electroactive species between 0.1 and 1.0 M. E–log j plots did not exhibit linear segments, most probably because of extensive adsorption of bromine radicals. Further analysis supported the hypothesis of a Volmer–Tafel mechanism, with the chemical recombination step as rate determining. Electrosorption isotherms for Br radicals were found to be of the Frumkin type. The kinetics of Br3- reduction was controlled by the surface dissociation of the Br2 molecules.
2005
Ferro, Sergio; Orsan, C.; DE BATTISTI, Achille
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1200774
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