Low-temperature catalytic combustion of trichloroethylene over cerium oxide and catalyst deactivation

被引:199
作者
Dai, Qiguang [1 ]
Wang, Xingyi [1 ]
Lu, Guanzhong [1 ]
机构
[1] E China Univ Sci & Technol, Res Inst Ind Catalysis, Adv Mat Lab, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
catalytic combustion; chlorinated VOCs; cerium oxide; catalyst deactivation;
D O I
10.1016/j.apcatb.2007.12.013
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
Cerium oxide catalysts prepared by a thermal decomposition method using the salt nitrate as precursor were tested for the catalytic combustion of trichloroethlyene (TCE), as a model of chlorinated volatile organic compounds (CVOCs). CeO2 catalysts calcined at different temperature were found to possess high catalytic activity for catalytic combustion of TCE, and CeO2 calcined at 550 degrees C was the most active catalyst and the complete combustion temperature (T-90%) of TCE was 205 degrees C. Effects of systematic variation of reaction conditions, including space velocity, inlet TCE concentration and water concentration on TCE catalytic combustion were investigated. Additionally, the stability and deactivation of CeO2 catalysts were studied by various characterization methods (such as TG/DTA, EDS, XRD, Raman and XPS) and other assistant experiments. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:192 / 202
页数:11
相关论文
共 54 条
[1]   CATALYST DEACTIVATION DURING DEEP OXIDATION OF CHLOROHYDROCARBONS [J].
AGARWAL, SK ;
SPIVEY, JJ ;
BUTT, JB .
APPLIED CATALYSIS A-GENERAL, 1992, 82 (02) :259-275
[2]   Catalytic hydrodechlorination over Pd supported on amorphous and structured carbon [J].
Amorim, C ;
Yuan, G ;
Patterson, PM ;
Keane, MA .
JOURNAL OF CATALYSIS, 2005, 234 (02) :268-281
[3]   Understanding the activation mechanism induced by NOx on the performances of VOx/TiO2 based catalysts in the total oxidation of chlorinated VOCs [J].
Bertinchamps, F. ;
Treinen, M. ;
Eloy, P. ;
Dos Santos, A. -M. ;
Mestdagh, M. M. ;
Gaigneaux, E. M. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2007, 70 (1-4) :360-369
[4]   Systematic investigation of supported transition metal oxide based formulations for the catalytic oxidative elimination of (chloro)-aromatics -: Part I:: Identification of the optimal main active phases and supports [J].
Bertinchamps, F. ;
Grégoire, C. ;
Gaigneaux, E. M. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 66 (1-2) :1-9
[5]   OXYGEN IN CATALYSIS ON TRANSITION-METAL OXIDES [J].
BIELANSKI, A ;
HABER, J .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1979, 19 (01) :1-41
[6]  
BOND GC, 1975, J APPL CHEM BIOTECHN, V25, P241
[7]   COMPARISON OF MODIFIED TRANSITION METAL-EXCHANGED ZEOLITE CATALYSTS FOR OXIDATION OF CHLORINATED HYDROCARBONS [J].
CHATTERJEE, S ;
GREENE, HL ;
PARK, YJ .
JOURNAL OF CATALYSIS, 1992, 138 (01) :179-194
[8]   On the selection of the catalyst among the commercial platinum-based ones for total oxidation of some chlorinated hydrocarbons [J].
Corella, J ;
Toledo, JM ;
Padilla, AM .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2000, 27 (04) :243-256
[9]   Catalytic steam reforming of chlorocarbons: trichloroethane, trichloroethylene and perchloroethylene [J].
Coute, N ;
Ortego, JD ;
Richardson, JT ;
Twigg, MV .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 19 (3-4) :175-187
[10]   On the mechanism of the catalytic destruction of 1,2-dichloroethane over Ce/Zr mixed oxide catalysts [J].
de Rivas, Beatriz ;
Lopez-Fonseca, Ruben ;
Gonzalez-Velasco, Juan R. ;
Gutierrez-Ortiz, Jose I. .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2007, 278 (1-2) :181-188