Novel nano-scale Au/α-Fe2O3 catalyst for the preferential oxidation of CO in biofuel reformate gas

被引:43
作者
Shodiya, Titilayo [1 ]
Schmidt, Oliver [1 ]
Peng, Wen [1 ]
Hotz, Nico [1 ]
机构
[1] Duke Univ, Dept Mech Engn & Mat Sci, Thermodynam & Sustainable Energy Lab, Durham, NC 27708 USA
关键词
CO preferential oxidation (PROX); Inverse catalyst; H2O effects; CO2; effects; Gold; Iron oxide; Reaction mechanism; LOW-TEMPERATURE OXIDATION; SELECTIVE OXIDATION; CARBON-MONOXIDE; GOLD; HYDROGEN; KINETICS; H-2; ADSORPTION; AU/FE2O3; SUPPORT;
D O I
10.1016/j.jcat.2012.12.027
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
Au/alpha-Fe2O3 catalyst was synthesized using a modified co-precipitation method to generate an inverse catalyst model. The effects of introducing CO2 and H2O during preferential oxidation (PROX) of CO were investigated. The goal of this work was >= 99.8% CO conversion at 80 degrees C. There was an increase in the conversion at all temperatures with the introduction of CO2 and 100% of the CO was converted at the target temperature of 80 degrees C for any amount of CO2. Furthermore, there was an increase in conversion to 100% for water fractions ranging from 3% to 10%. Finally, for realistic conditions of (bio-)fuel reforming, 24% CO2 and 10% water, 99.85% conversion was achieved. A long-term test of 200 h showed no significant deactivation of the catalyst at a temperature of 80 degrees C in presence of 24% CO2 and 3% water. The mechanism for PROX is not known definitively; however, current literature believes the gold particle size is the key. In contrast, we emphasize the tremendous role of the support particle size. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:63 / 69
页数:7
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