The origin of N2O formation in the selective catalytic reduction of NOx byNH3 in O-2 rich atmosphere on Cu-faujasite catalysts

Citation
G. Delahay et al., The origin of N2O formation in the selective catalytic reduction of NOx byNH3 in O-2 rich atmosphere on Cu-faujasite catalysts, CATAL TODAY, 54(4), 1999, pp. 431-438
Citations number
27
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
CATALYSIS TODAY
ISSN journal
09205861 → ACNP
Volume
54
Issue
4
Year of publication
1999
Pages
431 - 438
Database
ISI
SICI code
0920-5861(199912)54:4<431:TOONFI>2.0.ZU;2-U
Abstract
The selective catalytic reduction (SCR) of NOx (NO+NO2) by NH3 in O-2 rich atmosphere has been studied on Cu-FAU catalysts with Cu nominal exchange de gree from 25 to 195%. NO2 promotes the NO conversion at NO/NO2=1 and low Cu content. This is in agreement with next-nearest-neighbor (NNN) Cu ions as the most active sites and with NxOy adsorbed species formed between NO and NO2 as a key intermediate. Special attention was paid to the origin of N2O formation. CuO aggregates form 40-50% of N2O at ca. 550 K and become inacti ve for the SCR above 650 K. NNN Cu ions located within the sodalite cages a re active for N2O formation above 600 K. This formation is greatly enhanced when NO2 is present in the feed, and originated from the interaction betwe en NO (or NO2) and NH3. The introduction of selected co-cations, e.g. Ba, r educes very significantly this N2O formation. (C)1999 Elsevier Science B.V. All rights reserved.