Abstract

The oxidation of benzene and ethylacetate, present in trace amounts in air, over Pt supported on γ-Al 2O 3, SiO 2, TiO 2 and TiO 2 (W 6+) carriers has been studied. It was found that doping of the TiO 2 support with W 6+ cations has a positive effect on the activity of Pt catalysts for benzene and ethylacetate oxidation. A maximum in activity enhancement has been observed at a W 6+ content of 0.45 at% in the TiO 2 support. The Pt/TiO 2 (0.45 at% W 6+) catalyst is over two orders of magnitude more active than the Pt/γ-Al 2O 3 catalyst in the case of ethylacetate oxidation and an order of magnitude more active in the case of benzene oxidation. Doping of TiO 2 with W 6+ cations enhances its activity for ethylacetate degradation towards smaller organic intermediates, such as ethanol, acetic acid and ethylene, and it also affects product distribution. The enhanced activity of the Pt/TiO 2 (W 6+) catalysts is attributed to complementary bifunctional steps occuring on sites offered by Pt metal and by the support. During oxidation of benzene-ethylacetate-water mixtures, benzene oxidation is strongly suppressed in the presence of ethylacetate, while water acts as an inhibitor for both volatile organic compounds (VOC) oxidations.

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