Low-temperature selective catalytic reduction of N2O by CO over Fe-ZSM-5 catalysts in the presence of O2

被引:67
作者
You, Yanchen [1 ]
Chen, Siyu [1 ]
Li, Jiayin [1 ]
Zeng, Jie [1 ]
Chang, Huazhen [1 ]
Ma, Lei [2 ]
Li, Junhua [3 ]
机构
[1] Renmin Univ China, Sch Environm & Nat Resources, Beijing 100872, Peoples R China
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, SKLESPC, Beijing 100084, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Selective catalytic reduction of N2O by CO; Fe-ZSM-5; O-2; resistance; alpha-Sites; METAL OXIDE CATALYSTS; NITROUS-OXIDE; NOBLE-METAL; ALPHA-SITES; DECOMPOSITION; OXIDATION; IRON; OPTIMIZATION; PRETREATMENT; PERFORMANCE;
D O I
10.1016/j.jhazmat.2019.121117
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Nitrous oxide (N2O) is an important ozone-depletion substance and greenhouse gas. Selective catalytic reduction (SCR) of N2O by CO is considered an effective method for N2O elimination. However, O-2 exhibited a significant inhibition effect on the catalytic performance of N2O reduction by CO. A series of iron-based catalysts were prepared to investigate the effect of O-2 in SCR of N2O by CO. The Fe-Z-pH2 (Fe-ZSM-5 ion-exchanged under pH of 2) catalyst manifested superior activity at low temperature and excellent O-2 resistance in N2O reduction process. The characterization results from UV-vis DR spectra and XPS indicated that a-sites are the main active sites in Fe-Z-pH2, and they were inert to O-2 but highly active to N2O. It could be concluded that the competition effect between N2O and O-2 was very important over different catalysts. O-2 is more prevalent over alpha-Fe2O3 catalyst, while N2O dominates over Fe-Z-pH2 catalyst. Moreover, in the presence of O-2, Fe-Z-pH2 exhibited better performance for N2O removal than non-noble mixed oxide catalysts, which might broaden the application of low-temperature SCR of N2O by CO.
引用
收藏
页数:9
相关论文
共 44 条
[1]   Insights into the redox properties of ceria-based oxides and their implications in catalysis [J].
Aneggi, E ;
Boaro, M ;
de Leitenburg, C ;
Dolcetti, G ;
Trovarelli, A .
JOURNAL OF ALLOYS AND COMPOUNDS, 2006, 408 :1096-1102
[2]  
[Anonymous], [No title captured]
[3]  
[Anonymous], [No title captured]
[4]   Temperature-dependent N2O decomposition over Fe-ZSM-5:: Identification of sites with different activity [J].
Berrier, E. ;
Ovsitser, O. ;
Kondratenko, E. V. ;
Schwidder, M. ;
Gruenert, W. ;
Brueckner, A. .
JOURNAL OF CATALYSIS, 2007, 249 (01) :67-78
[5]   Catalytic decomposition of N2O over monolithic supported noble metal-transition metal oxides [J].
Boissel, Viviane ;
Tahir, Saad ;
Koh, Carolyn Ann .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 64 (3-4) :234-242
[6]  
Bouwman L., 2013, Drawing down N2O to protect climate and the ozone layer. A UNEP Synthesis Report
[7]   The State of the Art in Selective Catalytic Reduction of NOx by Ammonia Using Metal-Exchanged Zeolite Catalysts [J].
Brandenberger, Sandro ;
Kroecher, Oliver ;
Tissler, Arno ;
Althoff, Roderik .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2008, 50 (04) :492-531
[8]   Selective catalytic reduction of N2O in industrial emissions containing O2, H2O and SO2:: behavior of Fe/ZSM-5 catalysts [J].
Centi, G ;
Vazzana, F .
CATALYSIS TODAY, 1999, 53 (04) :683-693
[9]   Analysis of N2O decomposition over fixed bed mixed metal oxide catalysts made from hydrotalcite-type precursors [J].
Chang, KS ;
Song, H ;
Park, YS ;
Woo, JW .
APPLIED CATALYSIS A-GENERAL, 2004, 273 (1-2) :223-231
[10]   Evolution of iron states and formation of α-sites upon activation of FeZSM-5 zeolites [J].
Dubkov, KA ;
Ovanesyan, NS ;
Shteinman, AA ;
Starokon, EV ;
Panov, GI .
JOURNAL OF CATALYSIS, 2002, 207 (02) :341-352