CeO2/CuO catalysts prepared by surfactant-template method for preferential CO oxidation in H2-rich stream
被引:0
作者:
Fan, Qi-Yuan
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机构:
School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, ChinaSchool of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, China
Fan, Qi-Yuan
[1
]
Bai, Xue
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机构:
School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, ChinaSchool of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, China
Bai, Xue
[1
]
Zeng, Shang-Hong
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机构:
School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, ChinaSchool of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, China
Zeng, Shang-Hong
[2
]
机构:
[1] School of Chemical Engineering, Inner Mongolia University of Technology, Hohhot 010051, China
[2] School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, China
来源:
Ranliao Huaxue Xuebao/Journal of Fuel Chemistry and Technology
|
2014年
/
42卷
/
05期
关键词:
Catalyst activity - Catalytic oxidation - Copper oxides - Fluorspar - Oxygen vacancies - Particle size - Particle size analysis - Surface active agents - X ray diffraction;
D O I:
暂无
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摘要:
A series of CeO2/CuO catalysts were prepared by surfactant-template method and characterized by high resolution transmission electron microscope (HRTEM), X-ray diffraction (XRD), temperature-programmed reduction (H2-TPR) and N2 sorption; their catalytic performance for preferential oxidation of CO (CO-PROX) in H2-rich stream was investigated. The results show that the 4 nm CeO2 particles with cubic fluorite structure are agglomerated into small clusters and dispersed on the bulk CuO; CeO2/CuO may belong to a type of reverse supported catalyst on the basis of particle size distribution. There are two kinds of active sites in the CeO2/CuO system, i.e. the CuO sites for CO chemisorption and the CeO2 sites supplying oxygen vacancies; the coexistence of two-kind surface sites on the contact interface is capable of promoting the preferential oxidation of CO.