The Impact of Water on CO Oxidation with Au/TiO2 Catalysts: Poison or Promotor? A Study with an Au-TiO2/MCM-48 Model Catalyst

被引:3
|
作者
De Toni, Andrea [1 ]
Gies, Hermann [2 ]
Gruenert, Wolfgang [1 ]
机构
[1] Ruhr Univ Bochum, Lab Ind Chem, D-44780 Bochum, Germany
[2] Ruhr Univ Bochum, Crystallog Lab, D-44780 Bochum, Germany
关键词
Gold; Titania; MCM-48; CO oxidation; Water; Host-guest systems; Poisoning; MESOPOROUS MCM-48; DEACTIVATION;
D O I
10.1007/s10562-011-0663-6
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CO oxidation was studied with a model catalyst containing Au and TiO (x) nanoaggregates confined in a siliceous MCM-48 host. With this material, which has a particular small ratio between the TiO (x) and Au components, activities well comparable to those of unconfined Au/TiO2 catalysts were obtained in particular when a thermal activation in inert gas at temperatures between 523 and 673 K was applied. When the subsequent catalytic tests were performed in a feed containing ca. 20 ppm H2O, strong deactivation phenomena were observed which could be reverted by repeated thermal treatment and are most likely caused by carbonate deposition. This deactivation was strongly attenuated when the water content of the feed was decreased to ca. 6 ppm, which suggests that water plays an important role in the formation of the poisoning species. With unconfined Au/TiO2 catalysts, a promoting role of water on the formation of catalyst poison was observed as well, but to a much lower extent. The effect may therefore have escaped undetected so far as a contribution to the well-known catalyst deactivation by carbonate species.
引用
收藏
页码:1282 / 1287
页数:6
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