In situ DRIFTS study during C2H4-SCR of NO over Co-ZSM-5

被引:20
作者
Chen, Xiaomei [1 ]
Yang, Xuefeng [1 ]
Zhu, Aimin [1 ]
Au, C. T. [3 ]
Shi, Chuan [1 ,2 ]
机构
[1] Dalian Univ Technol, Lab Plasma Phys Chem, Dalian 116024, Peoples R China
[2] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116012, Peoples R China
[3] Hong Kong Baptist Univ, Dept Chem, Kowloon Tong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Co-ZSM-5; Ethylene-SCR; Surface intermediates; In situ DRIFTS; Mechanism; SELECTIVE CATALYTIC-REDUCTION; CO-H-MFI; NO+O-2 COADSORPTION; FT-IR; ZEOLITE CATALYSTS; EMISSION CONTROL; NITROGEN-OXIDES; METHANE; HYDROCARBONS; REACTIVITY;
D O I
10.1016/j.molcata.2009.07.010
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
The formation of surface intermediates and their reactivities with so me reactant gases during the selective catalytic reduction of NO with ethylene (C2H4-SCR) over Co-ZSM-5 was investigated systematically by in situ diffused reflectance infrared Fourier transformed spectroscopy. Some new IR bands relevant to the surface intermediates formed in the title reaction were identified. The results show that formate species, formed during the partial oxidation of ethylene over Co-ZSM-5, is reactive towards nitrates to yield formyl nitro compound, an intermediate critical for the formation of cyanide and isocyanate species by further reacting with nitrates. Kinetics analysis suggests that the cyanide and isocyanate at different sites vary in reactivity towards nitrates. The Co2+-CN and Al3+-NCO species subsequently react with nitrates for final production of N-2, CO2 and H2O, however, the -CN bound to Bronsted and Lewis acid sites show poor reactivity towards a flow of NO + O-2/He. On the basis of these investigations, a proposed reaction mechanism explains the formation and roles of all intermediates detected by IR spectroscopy in this study. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:31 / 39
页数:9
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