The determination of the activities of different iron species in Fe-ZSM-5 for SCR of NO by NH sub(3)
The activities of different iron species in Fe-ZSM-5 for the selective catalytic reduction (SCR) of NO by NH sub(3) were determined in terms of their turnover frequencies (TOF values). The relative concentrations of different species were correlated with their measured NO sub()xreduction efficiencie...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2010-04, Vol.95 (3-4), p.348-357 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The activities of different iron species in Fe-ZSM-5 for the selective catalytic reduction (SCR) of NO by NH sub(3) were determined in terms of their turnover frequencies (TOF values). The relative concentrations of different species were correlated with their measured NO sub()xreduction efficiencies and NH sub(3) oxidation activities. Our results suggest that the SCR of NO by NH sub(3) is catalyzed by different active sites with different activation energies. At temperatures below 300 degree C, the SCR activity was observed to be primarily caused by monomeric iron sites; however, at T > 300 degree C, T >= 400 degree C and T >= 500 degree C, the contribution of dimeric iron species, oligomeric species (e.g., trimeric and tetrameric iron species) and partially uncoordinated iron sites in the outmost layer of iron oxide particles, respectively, become important. The activation energies for monomeric and dimeric sites were evaluated to be about 36 kJ/mol and 77 kJ/mol, respectively. Due to their high activation energies, dimeric sites contributed more to the overall SCR activity at higher temperatures than did monomeric sites. The clustered sites not only contributed to the SCR activity but also caused nonselective oxidation of NH sub(3) at T >= 350 degree C, whereas the dimeric species governed the NH sub(3) oxidation activity up to T = 500 degree C. The TOF values for dimeric species were estimated to be 70 +/- 13 s super(-1) at 500 degree C. Monomeric sites were found to be completely inactive for NH sub(3) oxidation up to 500 degree C. |
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ISSN: | 0926-3373 |
DOI: | 10.1016/j.apcatb.2010.01.013 |