Gold Catalysts Supported on Crystalline Fe2O3 and CeO2/Fe2O3 for Low-temperature CO Oxidation

被引:0
作者
Liu Rui-hui [1 ,3 ]
Zhang Cun-man [1 ,2 ]
Ma Jian-xin [1 ,2 ]
机构
[1] Tongji Univ, Clean Energy Automot Engn Ctr, Shanghai 201804, Peoples R China
[2] Tongji Univ, Sch Automot Studies, Shanghai 201804, Peoples R China
[3] Tongji Univ, Sch Environm Sci & Engn, Shanghai 200092, Peoples R China
关键词
Gold catalyst; Low-temperature CO oxidation; Iron oxide; Nanoparticle; Additive; CARBON-MONOXIDE; PRETREATMENT CONDITIONS; DEPOSITION-PRECIPITATION; AU/FE2O3; CATALYSTS; IRON-OXIDE; MECHANISM; AU/AL2O3; COPRECIPITATION; AU/ALPHA-FE2O3; DEACTIVATION;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High active and stable gold catalysts supported on crystalline Fe2O3 and CeO2/Fe2O3 were prepared via the deposition-precipitation method. The catalyst with a Au load of 1.0% calcined at 180 C showed a CO conversion of 100% at -8.9 degrees C, while Au/CeO2/Fe2O3 converted CO completely at -16.1 degrees C. Even having been calcined at 500 degrees C, Au/Fe2O3 still exhibited significant catalytic activity, achieving full conversion of CO at 61.6 degrees C. The catalyst with a low Au load of 0.5% could convert CO completely at room temperature and kept the activity unchanged for at least 150 h. N-2 adsorption-desorption measurements show that the crystalline supports possessed a high specific surface area of about 200 m(2)/g. Characterizations of X-ray diffraction and transmission electron microscopy indicate that gold species were highly dispersed as nano or sub-nano particles on the supports. Even after the catalyst was calcined at 500 degrees C, the Au particles remained in a nano-size of about 6-10 nm. X-ray photoelectron spectra reveal that the supported Au existed in metallic state Au-0. The modification of Au/Fe2O3 by CeO2 proved to be beneficial to the inhibition of crystallization of Fe2O3 and the stabilization of gold particles in dispersed state, consequently promoting catalytic activity.
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页码:98 / 104
页数:7
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