Au/PO43-/TiO2 and PO43-/Au/TiO2 catalysts for CO oxidation:: Effect of synthesis details on catalytic performance

被引:54
作者
Ma, Zhen [1 ]
Brown, Suree [1 ]
Overbury, Steven H. [1 ]
Dai, Sheng [1 ]
机构
[1] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
关键词
gold catalysis; CO oxidation; titania; phosphate; dopant; sintering; deactivation;
D O I
10.1016/j.apcata.2007.05.019
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
Supported gold catalysts are active for CO oxidation, but the high-temperature deactivation is a shortcoming that may constrain their applications. Herein, we attempted to address this problem by using phosphate-doped Au/TiO2 synthesized via two routes. In route I, Au/PO43-/TiO2 catalysts were prepared by treating TiO2 (Degussa P25) with diluted H3PO4, followed by loading gold via deposition-precipitation. In route II, PO43-/Au/TiO2 catalysts were prepared by treating H-2-reduced Au/TiO2 with diluted H3PO4. These catalysts were systematically pretreated at 200 or 500 degrees C before reaction testing. The overall CO conversion on 200 degrees C-pretreated Au/PO43-/TiO2 or PO43- /Au/TiO2 was always lower than that on 200 degrees C-pretreated Au/TiO2. However, the advantage of the phosphate addition became apparent after thermal treatment at a higher temperature. Both Au/PO43-/TiO2 and PO43-/Au/TiO2, pretreated at 500 degrees C retained significant activities at room temperature, whereas 500 degrees C-pretreated Au/ TiO2 lost its activity. Control experiments and catalyst characterization were performed to investigate the impact of synthesis details on catalytic performance. Published by Elsevier B.V.
引用
收藏
页码:226 / 237
页数:12
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