Journal
CATALYSIS LETTERS
Volume 135, Issue 3-4, Pages 182-189Publisher
SPRINGER
DOI: 10.1007/s10562-010-0270-y
Keywords
NO selective catalytic reduction; Ethylene; CoH-ZSM-5; DRIFTS; Active sites
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Funding
- National Natural Science Foundation of China [20673016]
- New Century Excellent Talents in University [NCET-07-0136]
- National High Technology and Development Program (863 program) of China [2007AA06Z311]
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The selective catalytic reduction of NO with ethylene was investigated and compared over fresh CoH-ZSM5, H-2-reduced (450 degrees C) CoH-ZSM-5 and H-ZSM-5. The dispersion of cobalt species for fresh and H-2-reduced CoH-ZSM-5 was studied by UV-vis and FTIR spectra. Combined with DRIFTS results of ad-species and reaction experiments, the active sites of CoH-ZSM-5 for the C2H4-SCR were identified and the catalytic functions of active cobalt species and support were also clarified. Notably, the formation of -CN or -NCO species was heavily dependent on the type of nitrates. Co3O4 particles contributed to the oxidation of NO to bidentate nitrates. The latter species were crucial for the formation of -NCO. Whereas exchanged Co2+ ions facilitated the oxidation of NO to monodentate and/or bridged nitrates which participated in the formation of -CN species.
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