The mechanism of the effect of H2O on the low temperature selective catalytic reduction of NO with NH3 over Mn-Fe spinel

被引:100
作者
Xiong, Shangchao [1 ]
Liao, Yong [1 ]
Xiao, Xin [1 ]
Dang, Hao [1 ]
Yang, Shijian [1 ]
机构
[1] Nanjing Univ Sci & technol, Sch Environm & Biol Engn, Jiangsu Key Lab Chem Pollut Control & Resources R, Nanjing 210094, Jiangsu, Peoples R China
关键词
OXIDE CATALYSTS; MIXED OXIDES; MNOX-CEO2; SCR; MNOX/TIO2; OXIDATION; NITROGEN; AMMONIA; DRIFT; PERFORMANCE;
D O I
10.1039/c4cy01599a
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
H2O showed a notable inhibition on the low temperature selective catalytic reduction (SCR) reaction over Mn based catalysts. However, the mechanism of H2O effect was not clear. In this work, the mechanism of H2O effect on the low temperature SCR reaction over Mn-Fe spinel was studied using the transient reaction study and the steady-state kinetic analysis. According to the steady-state kinetic analysis, the reaction kinetic rate constants of NO reduction over Mn-Fe spinel (including the rate constants of N-2 formation through the Eley-Rideal mechanism and the Langmuir-Hinshelwood mechanism, and the rate constants of N2O formation) in the presence of H2O and in the absence of H2O were compared. According to the transient reaction study, the effect of H2O on the elementary reactions of NO reduction over Mn-Fe spinel through both the Eley-Rideal mechanism and the Langmuir-Hinshelwood mechanism was investigated. The results indicated that the effect of H2O on the low temperature SCR reaction over Mn-Fe spinel was not only attributed to the competition adsorption of H2O with NH3 and NOx, but also related to the decrease in the oxidation ability and the inhibition of the interface reaction.
引用
收藏
页码:2132 / 2140
页数:9
相关论文
共 29 条
[1]   Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts:: A review [J].
Busca, G ;
Lietti, L ;
Ramis, G ;
Berti, F .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (1-2) :1-36
[2]   DRIFT Study on Cerium-Tungsten/Titiania Catalyst for Selective Catalytic Reduction of NOx with NH3 [J].
Chen, Liang ;
Li, Junhua ;
Ge, Maofa .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2010, 44 (24) :9590-9596
[3]   Selective oxidation of ammonia to nitrogen on transition metal containing mixed metal oxides [J].
Chmielarz, L ;
Kustrowski, P ;
Rafalska-Lasocha, A ;
Dziembaj, R .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 58 (3-4) :235-244
[4]   Selective reduction of NO by NH3 over manganese-cerium mixed oxides:: Relation between adsorption, redox and catalytic behavior [J].
Eigenmann, F ;
Maciejewski, M ;
Baiker, A .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 62 (3-4) :311-318
[5]   Low temperature selective oxidation of ammonia to nitrogen on silver-based catalysts [J].
Gang, L ;
Anderson, BG ;
van Grondelle, J ;
van Santen, RA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 40 (02) :101-110
[6]   Low-temperature selective catalytic reduction of NO on MnOx/TiO2 prepared by different methods [J].
Jiang, Boqiong ;
Liu, Yue ;
Wu, Zhongbiao .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 162 (2-3) :1249-1254
[7]   Identification, stability, and reactivity of NOx species adsorbed on titania-supported manganese catalysts [J].
Kantcheva, M .
JOURNAL OF CATALYSIS, 2001, 204 (02) :479-494
[8]   High deNOx performance of Mn/TiO2 catalyst by NH3 [J].
Kim, Young Jin ;
Kwon, Hyuk Jae ;
Nam, In-Sik ;
Choung, Jin Woo ;
Kil, Jeong Ki ;
Kim, Hong-Jip ;
Cha, Moon-Soon ;
Yeo, Gwon Koo .
CATALYSIS TODAY, 2010, 151 (3-4) :244-250
[9]   Effect of the Mn oxidation state and lattice oxygen in Mn-based TiO2 catalysts on the low-temperature selective catalytic reduction of NO by NH3 [J].
Lee, Sang Moon ;
Park, Kwang Hee ;
Kim, Sung Su ;
Kwon, DongWook ;
Hong, Sung Chang .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2012, 62 (09) :1085-1092
[10]   Influence of H2O on the low-temperature NH3-SCR of NO over V2O5/AC catalyst: An experimental and modeling study [J].
Lei, Zhigang ;
Han, Bin ;
Yang, Kun ;
Chen, Biaohua .
CHEMICAL ENGINEERING JOURNAL, 2013, 215 :651-657