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Evolution of Iron States and Formation of α-Sites upon Activation of FeZSM-5 Zeolites Full article

Journal Journal of Catalysis
ISSN: 0021-9517 , E-ISSN: 1090-2694
Output data Year: 2002, Volume: 207, Number: 2, Pages: 341-352 Pages count : 12 DOI: 10.1006/jcat.2002.3552
Tags Fe complexes, FeZSM-5, Monooxygenase, N2O decomposition, Oxidation of benzene, Phenol, α-oxygen, α-sites
Authors Dubkov K.A. 1 , Ovanesyan N.S. 2 , Shteinman A.A. 2 , Starokonʹ E.V. 1 , Panov G.I. 1
Affiliations
1 Boreskov Institute of Catalysis, Novosibirsk 630090, Russia
2 Institute of Problems of Chemical Physics, Chernogolovka, Moscow oblast 142432, Russia

Abstract: Mössbauer spectroscopy in situ was used to study the effect of high-temperature activation on the evolution of iron introduced into a ZSM-5 zeolite matrix by various methods. The activation process (calcination in air, in vacuum, or in the presence of water vapor) was shown to cause an intensive reduction of iron, yielding two types of dinuclear Fe2+ complexes, which may comprise more than 60% of the total metal content. Reduced Fe2+ ions are stable in the presence of O2 but are reversibly oxidized to Fe3+ by nitrous oxide, generating active α-oxygen species, which bring unique oxidation properties to the zeolite. After coordinative saturation by adsorbed water molecules, both iron complexes show identical Mössbauer spectra, which are close to the spectra of dinuclear iron sites in the MMO enzyme. A thorough quantitative comparison between the number of α-oxygen atoms and the number of Fe atoms involved in redox transition shows that α-sites are dinuclear complexes in which both Fe atoms are capable of α-oxygen generation.
Cite: Dubkov K.A. , Ovanesyan N.S. , Shteinman A.A. , Starokonʹ E.V. , Panov G.I.
Evolution of Iron States and Formation of α-Sites upon Activation of FeZSM-5 Zeolites
Journal of Catalysis. 2002. V.207. N2. P.341-352. DOI: 10.1006/jcat.2002.3552 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Oct 16, 2001
Accepted: Jan 29, 2002
Published print: Apr 25, 2002
Published online: May 25, 2002
Identifiers:
Web of science: WOS:000175354900020
Scopus: 2-s2.0-0037171522
Elibrary: 13416343
Chemical Abstracts: 2002:278465
Chemical Abstracts (print): 136:331131
OpenAlex: W2063896065
Citing:
DB Citing
Web of science 335
Scopus 355
Elibrary 351
OpenAlex 356
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