Mechanism and Kinetics of the Selective NO Reduction over Co-ZSM-5 Studied by the SSITKA Technique: 2. Reactivity of NOx-Adsorbed Species with Methane
Full article
| Общее |
Language:
Английский,
Genre:
Full article,
Status:
Published,
Source type:
Original
|
| Journal |
Journal of Catalysis
ISSN: 0021-9517
, E-ISSN: 1090-2694
|
| Output data |
Year: 2004,
Volume: 225,
Number: 1,
Pages: 179-189
Pages count
: 11
DOI:
10.1016/j.jcat.2004.03.032
|
| Tags |
Active sites, CH4-SCR, Co-ZSM-5, Cobalt species, deNOx, Kinetics, Mechanism, SSITKA |
| Authors |
Sadovskaya E.M.
1
,
Suknev A.P.
1
,
Pinaeva L.G.
1
,
Goncharov V.B.
1
,
Balʹzhinimaev B.S.
1
,
Chupin C.
2
,
Pérez-Ramı́rez J.
2
,
Mirodatos C.
2
|
| Affiliations |
| 1 |
Boreskov Institute of Catalysis, pr. Lavrentieva, 5, 630090 Novosibirsk, Russia
|
| 2 |
Institut de Recherches sur la Catalyse, 2 av. A. Einstein, F-69626 Villeurbanne cedex, France
|
|
Funding (2)
|
1
|
Russian Foundation for Basic Research
|
00-03-22004
|
|
2
|
Institute of Researches on Catalysis and Environment in Lyon
|
|
Steady-state isotopic transient kinetic analysis (SSITKA) was applied to study the reactivity of adsorbed NOx species with methane over Co-ZSM-5 during CH4-SCR of NO at different partial oxygen concentrations. Numerical analysis of the isotope responses after switching from 14N16O to 15N18O, from 16O2 to 18O2, from 12CH4 to 13CH4, and from C16O2 to C18O2 in the feed gas was performed. This enables determination of (i) the concentration of different forms of NOx adspecies on Co sites, (ii) their reaction rates with methane, and (iii) the concentration of surface intermediates resulting from the interaction of NOx species with methane. The NO reduction with CH4 in the presence of oxygen was shown to proceed by two different pathways with participation of (1) NO2δ+ species (formed on nanoclusters of cobalt oxide located inside the zeolite channels) and (2) NO2− nitrite complexes (formed on larger cobalt oxide particles located outside the zeolite channels), the reaction rate by the former being appreciably higher under the SCR reaction conditions studied. Mononitrosyl species appear not to be directly involved in the overall process. Modeling results indicate that the rate of the first route is limited by the interaction of NO2δ+ species and adsorbed methane, while in the second route the formation of nitrite species is a rate-determining step. Based on the obtained results, an overall reaction mechanism of the CH4-SCR of NO in the presence of oxygen is proposed.