Ultrasonic-assisted synthesis of highly active catalyst Au/MnOx-CeO2 used for the preferential oxidation of CO in H2-rich stream

被引:53
作者
Tu, Yun-Bao [1 ]
Luo, Jin-Yong [1 ]
Meng, Ming [1 ]
Wang, Gang [1 ]
He, Jun-Jun [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Catalysis Sci & Technol, Tianjin Key Lab Catalysis Sci & Engn, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Ultrasonic pretreatment; Gold catalysts; Preferential CO oxidation; Manganese oxide; WATER-GAS SHIFT; LOW-TEMPERATURE OXIDATION; FUEL-CELL APPLICATIONS; GOLD-CERIA CATALYSTS; SELECTIVE OXIDATION; CARBON-MONOXIDE; HYDROGEN; H-2; DEPOSITION; PERFORMANCE;
D O I
10.1016/j.ijhydene.2009.03.015
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
A series of nano-gold catalysts supported on binary oxides MOx-CeO2 (atomic ratio W Ce = 1:1, M = Mn, Fe, Co, Ni) are prepared by deposition-precipitation (DP). An innovative and rather convenient ultrasonic pretreatment of the support is employed for AU/MnOx-CeO2 preparation. It is found that for preferential CO oxidation Au/MnOx-CeO2 is more active than Au/CeO2. Ultrasonic pretreatment of MnOk-CeO2 further promotes the performance of Au/MnOx-CeO2, with CO conversion increased by 24 % at 120 degrees C. Meanwhile, the selectivity of oxygen to CO2 is promoted in the whole temperature range, especially in 80-120 degrees C, the selectivity is increased by 15-21%. HR-TEM and XRD results indicate that ultrasonic pretreatment is favorable to the formation of much smaller gold nanoparticles (<5 nm). The characterization of XPS, UV-vis DRS, H-2-TPR and CO-TPR confirms that the strong interaction between Au and the support effectively inhibits the dissociation and oxidation of H-2 over the ultrasonically pretreated catalyst Au/MnOx-CeO2, making it highly selective to CO oxidation. (C) 2009 International Association for Hydrogen Energy. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:3743 / 3754
页数:12
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