Abstract

The relationship between catalytic activity in the complete oxidation of benzene and the structure of supported vanadium oxide catalysts modified by palladium was studied. Chemical analysis, X-ray diffraction, ESR spectroscopy and diffuse reflectance spectroscopy indicated that the formation of a catalytically active phase occurs through partial reduction of V 5+ to V 4+. The V 4+ ions in a matrix of vanadium pentoxide form clusters in which the electrons possess high mobility. Further, a phase similar to V 4O 9 is formed. The promoting effect of palladium is related to the activation of oxygen and the transition of oxygen and the transition of the low-valent vanadium species to V 5+. A scheme of the redox mechanism is proposed.

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