The activity and characterization of CeO2-TiO2 catalysts prepared by the sol-gel method for selective catalytic reduction of NO with NH3

被引:454
作者
Gao, Xiang [1 ]
Jiang, Ye [1 ]
Zhong, Yi [1 ]
Luo, Zhongyang [1 ]
Cen, Kefa [1 ]
机构
[1] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
Selective catalytic reduction; NO; Ce-Ti mixed oxide; Sol-gel method; WET AIR OXIDATION; NITRIC-OXIDE; MIXED OXIDES; XPS; MANGANESE/TITANIA; OXYGEN; RAMAN; IRON;
D O I
10.1016/j.jhazmat.2009.09.112
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A series of Ce-Ti mixed-oxide catalysts were prepared by the sol-gel method for selective catalytic reduction (SCR) of NO with ammonia as reductant. These catalysts were characterized by XRD, BET, and XPS techniques. The experimental results show that the best Ce-Ti mixed-oxide catalyst yielded 98.6% NO conversion, and 100% N-2 selectivity at typical SCR reaction temperatures (300-400 degrees C) and the high gas hourly space velocity of 50,000 h(-1). As the Ce loading (the mass ratio of CeO2/TiO2) Was increased from 0 to 0.6, NO conversion increased markedly, but decreased at higher Ce loading. The most active catalyst was obtained with a Ce loading of 0.6. The high activity might be attributed to high Ce loading, strong interaction between Ce and Ti, high concentration of amorphous Ce on the catalyst surface, or the increase of chemisorbed oxygen or/and weakly bonded oxygen species, resulting from the presence of Ce3+ after Ce addition. The effect of the calcination temperature was also investigated, and the optimal calcination temperature was 500 degrees C. The presence of oxygen played an essential role in NO reduction, and the activity of the Ce(0.6)Ti catalyst was not depressed when oxygen concentration was higher than 1%. The effect of SO2 and H2O on the activity of the Ce(0.6)Ti catalyst was bound up with the reaction temperature. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:734 / 739
页数:6
相关论文
共 31 条
[1]  
Bosch H., 1988, Catalysis Today, V2, P369, DOI [DOI 10.1016/0920-5861(88)80002-6, 10.1016/B978-0-444-98919-2.50005-3, DOI 10.1016/B978-0-444-98919-2.50005-3]
[2]   SATELLITE STRUCTURE IN X-RAY PHOTOELECTRON-SPECTRA OF SOME BINARY AND MIXED OXIDES OF LANTHANUM AND CERIUM [J].
BURROUGHS, P ;
HAMNETT, A ;
ORCHARD, AF ;
THORNTON, G .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1976, (17) :1686-1698
[3]   INTERACTIONS IN ALUMINA-BASED IRON-OXIDE VANADIUM-OXIDE CATALYSTS UNDER HIGH-TEMPERATURE CALCINATION AND SO2 OXIDATION CONDITIONS [J].
CLARK, FT ;
SPRINGMAN, MC ;
WILLCOX, D ;
WACHS, IE .
JOURNAL OF CATALYSIS, 1993, 139 (01) :1-18
[4]   Effect of oxygen concentration on the NOx reduction with ammonia overV2O5-WO3/TiO2 catalyst [J].
Djerad, S ;
Crocoll, M ;
Kureti, S ;
Tifouti, L ;
Weisweiler, W .
CATALYSIS TODAY, 2006, 113 (3-4) :208-214
[5]   Oxidation of sulfur dioxide to sulfur trioxide over supported vanadia catalysts [J].
Dunn, JP ;
Koppula, PR ;
Stenger, HG ;
Wachs, IE .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 19 (02) :103-117
[6]   Systematic XPS studies of metal oxides, hydroxides and peroxides [J].
Dupin, JC ;
Gonbeau, D ;
Vinatier, P ;
Levasseur, A .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (06) :1319-1324
[7]   Heterogeneous mercury reaction on a selective catalytic reduction (SCR) catalyst [J].
Eom, Yujin ;
Jeon, Seok Ho ;
Ngo, Thanh An ;
Kim, Jinsoo ;
Lee, Tai Gyu .
CATALYSIS LETTERS, 2008, 121 (3-4) :219-225
[8]   Spectroscopic studies of interfacial structures of CeO2-TiO2 mixed oxides [J].
Fang, Jun ;
Bi, Xinzhen ;
Si, Dejun ;
Jiang, Zhiquan ;
Huang, Weixin .
APPLIED SURFACE SCIENCE, 2007, 253 (22) :8952-8961
[9]  
HYDE EC, 1990, IND ENG CHEM RES, V29, P1985
[10]   MECHANISM OF THE REACTION OF NO AND NH3 ON VANADIUM-OXIDE CATALYST IN THE PRESENCE OF OXYGEN UNDER THE DILUTE GAS CONDITION [J].
INOMATA, M ;
MIYAMOTO, A ;
MURAKAMI, Y .
JOURNAL OF CATALYSIS, 1980, 62 (01) :140-148