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Kinetics and mechanism of water catalytic oxidation by a Ru3+(bpy)3 complex in the presence of colloidal cobalt hydroxide

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Abstract

Kinetics of the catalytic oxidation of water to molecular oxygen by a tris(bipyridyl) Ru(III) complex is studied in the presence of colloidal cobalt hydroxide stabilized by starch. Oxidant consumption follows the first-order rate law with respect to the oxidant concentration. The dependence of the apparent rate constant of this process on the catalyst concentration, initial oxidant concentration, and initial concentration of its reduced form was determined. The dependence of the oxygen yield on H+ at pH 7–11 and a catalyst concentration of 10-7-10-3 mol1 is studied. An intermediate product of the reaction was found, which is probably a bridged peroxo complex of cobalt. The kinetic scheme and mechanism of the reaction is proposed, which agree with experimental observations.

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Authors and Affiliations

  1. Boreskov Institute of Catalysis, Siberian Division, Russian Academy of Sciences, 630090, Novosibirsk, Russia

    O. P. Pestunova, G. L. Elizarova & V. N. Parmon

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  1. O. P. Pestunova
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  2. G. L. Elizarova
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  3. V. N. Parmon
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Pestunova, O.P., Elizarova, G.L. & Parmon, V.N. Kinetics and mechanism of water catalytic oxidation by a Ru3+(bpy)3 complex in the presence of colloidal cobalt hydroxide. Kinet Catal 41, 340–348 (2000). https://doi.org/10.1007/BF02755370

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  • DOI: https://doi.org/10.1007/BF02755370

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