Oxalic acid is one of the proposed metabolites of the anodic oxidation of more complex organic molecules. In spite of its simple structure, its mineralization strongly depends on the nature of the electrode material at which the process is carried out. Sargisyan and Vasil'ev [Elektrokhimiya, 18 (1982) 845] pointed out such dependence, investigating the kinetic behavior of OA at different metal (Rh, Pd, Os, Ir, Pt and Au), at dimensionally stable anodes (Ru02-Ti02) and at glassy carbon (GC) electrodes. Their conclusions highlighted the important role played by the organic anion adsorption step, claiming that OA is oxidized with increasing difficulty at electrode materials having higher oxygen affinity. More recently, these assumptions have been supported by data on OA oxidation at high anodic potentials [Electrochimica Acta, 49 (2004) 4027]. To further enrich the picture, in the present paper, kinetic investigations were carried out at different mixed-oxides, Pt, glassy carbon and highly conductive, boron-doped diamond electrodes, with either oxygen or fluorine at their surface.

Electroxidation of oxalic acid at different electrode materials

MARTINEZ, Carlos Alberto;FERRO, Sergio;DONATONI, Martina;DE BATTISTI, Achille
2008

Abstract

Oxalic acid is one of the proposed metabolites of the anodic oxidation of more complex organic molecules. In spite of its simple structure, its mineralization strongly depends on the nature of the electrode material at which the process is carried out. Sargisyan and Vasil'ev [Elektrokhimiya, 18 (1982) 845] pointed out such dependence, investigating the kinetic behavior of OA at different metal (Rh, Pd, Os, Ir, Pt and Au), at dimensionally stable anodes (Ru02-Ti02) and at glassy carbon (GC) electrodes. Their conclusions highlighted the important role played by the organic anion adsorption step, claiming that OA is oxidized with increasing difficulty at electrode materials having higher oxygen affinity. More recently, these assumptions have been supported by data on OA oxidation at high anodic potentials [Electrochimica Acta, 49 (2004) 4027]. To further enrich the picture, in the present paper, kinetic investigations were carried out at different mixed-oxides, Pt, glassy carbon and highly conductive, boron-doped diamond electrodes, with either oxygen or fluorine at their surface.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1685231
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