Direct synthesis of hydrogen peroxide from H2 and O2 using TiO2-supported Au-Pd catalysts

被引:472
作者
Edwards, JK
Solsona, BE
Landon, P
Carley, AF
Herzing, A
Kiely, CJ
Hutchings, GJ
机构
[1] Cardiff Univ, Sch Chem, Cardiff CF10 3AT, S Glam, Wales
[2] Lehigh Univ, Ctr Adv Mat & Nanotechnol, Bethlehem, PA 18015 USA
基金
美国国家科学基金会;
关键词
hydrogen peroxide; selective oxidation; CO oxidation; bimetallic catalysts; gold; palladium; titania; XPS; TEM; core-shell particles;
D O I
10.1016/j.jcat.2005.09.015
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
The direct synthesis of H2O2 at low temperature (2 degrees C) from H-2 and O-2 using TiO2-supported Au, Pd, and Au-Pd catalysts is discussed. The Au-Pd catalysts performed significantly better than the pure Pd/TiO2 and Au/TiO2 materials. Au-Pd particles were found with a core-shell structure. with Pd concentrated on the surface. The highest yields of H2O2 were observed with uncalcined catalysts, but these were particularly unstable. losing both metals during use. In contrast, samples calcined at 400 degrees C were stable and Could be reused several times without loss of performance. These catalysts exhibited low activity for CO oxidation at 25 degrees C; conversely, catalysts effective for low-temperature CO oxidation were inactive for H-2 oxidation to H2O2. This anticorrelation is explored in terms of the mechanism by which the catalysts function and the design of catalysts for the selective oxidation of one of these Substrates in the presence of the other. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 79
页数:11
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