共 38 条
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
相关论文