The effects of H2O and SO2 on the behaviour of CuSO4-CeO2/TS for low temperature catalytic reduction of NO with NH3

被引:14
作者
Tong, Hua [1 ]
Dai, Junhong [1 ]
He, Yong [2 ]
Tong, Zhiquan [2 ]
机构
[1] Beijing Univ Chem Technol, Dept Environm Engn, Beijing 100029, Peoples R China
[2] Xiangtan Univ, Dept Environm Engn, Xiangtan 411105, Peoples R China
关键词
cupric sulphate; cerium dioxide; TiO2-SiO2; NH3-SCR; nitric oxide; water; sulphur dioxide; CARBON-COATED MONOLITHS; OXIDE CATALYSTS; NITRIC-OXIDE; SCR; PROMOTION; MECHANISM; AMMONIA;
D O I
10.1080/09593330.2010.517219
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The catalyst CuSO4-CeO2/TiO2-SiO2 (CuSO4-CeO2/TS), for low temperature catalytic reduction (LT-SCR) of NO with NH, was prepared by the impregnation method. The impacts of H2O and SO2 on the catalyst were investigated. Experiments showed that H2O brought down the catalyst's activity at low reaction temperature. However, this negative effect of H2O could be mostly eliminated with a raised temperature of above 220 degrees C. In a 10-hour experiment on the catalyst's resistibility to SO2 poisoning, NO conversion increased slightly by the promoting effect of SO2. The same catalyst underwent continuous examination with both SO2 and H2O in the feed gas; NO conversion of around 90.2% was maintained for 37 hours, showing better performance than CuSO4-CeO2/TiO2. This suggested that SiO2 in the TiO2-SiO2 catalyst supported the supression of the oxidization of SO2 to SO3. Therefore, the formation of ammonium sulphate over the catalyst and the sulphation of CeO2 in the catalyst were greatly alleviated, leading to a better resistibility of the catalyst to SO2 poisioning. After the 37 hours, the catalyst activity began to fall, and an irrecoverable deactivation of the catalyst was observed.
引用
收藏
页码:891 / 900
页数:10
相关论文
共 26 条
[1]   Present status and perspectives in de-NOx SCR catalysis [J].
Forzatti, P .
APPLIED CATALYSIS A-GENERAL, 2001, 222 (1-2) :221-236
[2]   NH3-SCR of NO at low temperatures over sulphated vanadia on carbon-coated monoliths:: Effect of H2O and SO2 traces in the gas feed [J].
García-Bordejé, E. ;
Pinilla, J. L. ;
Lázaro, M. J. ;
Moliner, R. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 66 (3-4) :281-287
[3]   Promotion by a second metal or SO2 over vanadium supported on mesoporous carbon-coated monoliths for the SCR of NO at low temperature [J].
García-Bordejé, E ;
Monzón, A ;
Lázaro, MJ ;
Moliner, R .
CATALYSIS TODAY, 2005, 102 :177-182
[4]  
[何勇 HE Yong], 2009, [过程工程学报, The Chinese Journal of Process Engineering], V9, P360
[5]   Catalytic abatement of nitrogen oxides-stationary applications [J].
Heck, RM .
CATALYSIS TODAY, 1999, 53 (04) :519-523
[6]   Low temperature SCR of NO with NH3 over carbon nanotubes supported vanadium oxides [J].
Huang, Bichun ;
Huang, Rong ;
Jin, Dongjie ;
Ye, Daiqi .
CATALYSIS TODAY, 2007, 126 (3-4) :279-283
[7]   Selective catalytic reduction of NO with NH3 at low temperatures over iron and manganese oxides supported on mesoporous silica [J].
Huang, Jihui ;
Tong, Zhiquan ;
Huang, Yan ;
Zhang, Junfeng .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 78 (3-4) :309-314
[8]  
Huang ZG, 2001, CHINESE J CATAL, V22, P532
[9]   Manganese oxide catalysts for NOx reduction with NH3 at low temperatures [J].
Kang, Min ;
Park, Eun Duck ;
Kim, Ji Man ;
Yie, Jae Eui .
APPLIED CATALYSIS A-GENERAL, 2007, 327 (02) :261-269
[10]   FT-IR spectroscopic investigation of the reactivity of NOx species adsorbed on Cu2+/ZrO2 and CuSO4/ZrO2 catalysts toward decane [J].
Kantcheva, M .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 42 (01) :89-109