Activities of supported copper oxide catalysts in the NO plus CO reaction at low temperatures

被引:97
作者
Hu, YH [1 ]
Dong, L [1 ]
Wang, J [1 ]
Ding, WP [1 ]
Chen, Y [1 ]
机构
[1] Nanjing Univ, Dept Chem, Inst Mesoscop Solid State Chem, Nanjing 210093, Peoples R China
关键词
NO reduction; supported catalysts; ceria; CuO; ESR; XRD; TPR;
D O I
10.1016/S1381-1169(00)00299-5
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
The activities of copper oxide supported on CeO2, gamma -Al2O3 and ceria-modified gamma -Al2O3 catalysts for the NO + CO reaction at low temperature (200 degreesC) have been investigated. The results show that the activities of the surface-dispersed copper species are greatly enhanced due to the presence of ceria, whether it was used as a support or as the pre-dispersed species on gamma -Al2O3. The activities decrease in the order: CuO/CeO2 > CuO/CeO2/gamma -Al2O3 > CuO/gamma -Al2O3. For the CuO/CeO2/gamma -Al2O3 catalysts, it is shown that NO conversions are not improved significantly with the increasing of CuO and/or ceria loadings, however, the him-over number for the catalysts is found to be strongly relative to ceria loadings. Ey a combination of X-ray diffraction (XRD), electron spin resonance (ESR) and temperature programmed reduction (TPR) results, the states and properties of copper oxide species, as well as the interactions among the surface-dispersed copper oxide species, ceria species and support, are also studied. All the results are tentatively discussed according to the incorporation model proposed previously. (C) 2000 Published by Elsevier Science B.V.
引用
收藏
页码:307 / 316
页数:10
相关论文
共 27 条
[11]  
JAVIER S, 1996, J CHEM FARADAY T, V92, P1619
[12]  
KLIMISH RL, 1993, ENVIRON SCI TECHNOL, V7, P127
[13]   CATALYTIC CHEMISTRY OF NITRIC-OXIDE .2. REDUCTION OF NITRIC-OXIDE OVER NOBLE-METAL CATALYSTS [J].
KOBYLINSKI, TP ;
TAYLOR, BW .
JOURNAL OF CATALYSIS, 1974, 33 (03) :376-384
[14]   Complete oxidation of CO, ethanol, and ethyl acetate over copper oxide supported on titania and ceria modified titania [J].
Larsson, PO ;
Andersson, A .
JOURNAL OF CATALYSIS, 1998, 179 (01) :72-89
[15]   Selective adsorption of NOx from hot combustion gases by Ce-doped CuO/TiO2 [J].
Li, WB ;
Yang, RT ;
Krist, K ;
Regalbuto, JR .
ENERGY & FUELS, 1997, 11 (02) :428-432
[16]   COMPLETE OXIDATION OF CARBON-MONOXIDE AND METHANE OVER METAL-PROMOTED FLUORITE OXIDE CATALYSTS [J].
LIU, W ;
SAROFIM, AF ;
FLYTZANI-STEPHANOPOULOS, M .
CHEMICAL ENGINEERING SCIENCE, 1994, 49 (24A) :4871-4888
[17]   SIMULTANEOUS INFRARED AND KINETIC STUDY OF REDUCTION OF NITRIC-OXIDE BY CARBON-MONOXIDE OVER COPPER OXIDE [J].
LONDON, JW ;
BELL, AT .
JOURNAL OF CATALYSIS, 1973, 31 (01) :96-109
[18]  
OELKER P, 1995, IFEC 95 TOK
[19]   INFLUENCE OF METAL-PARTICLE SIZE AND SUPPORT ON THE CATALYTIC PROPERTIES OF SUPPORTED RHODIUM - CO-O2 AND CO-NO REACTIONS [J].
OH, SH ;
EICKEL, CC .
JOURNAL OF CATALYSIS, 1991, 128 (02) :526-536
[20]   Catalytic removal of NO [J].
Pârvulescu, VI ;
Grange, P ;
Delmon, B .
CATALYSIS TODAY, 1998, 46 (04) :233-316