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Effect of Copper State in Cu/H-ZSM-5 on Methane Activation by Brønsted Acid Sites, Studied by 1H MAS NMR In Situ Monitoring the H/D Hydrogen Exchange of the Alkane with Brønsted Acid Sites Full article

Journal The Journal of Physical Chemistry C
ISSN: 1932-7447 , E-ISSN: 1932-7455
Output data Year: 2021, Volume: 125, Number: 3, Pages: 2182–2193 Pages count : 12 DOI: 10.1021/acs.jpcc.0c10261
Tags Chemical activation; Hydrocarbons; Hydrogen; Methane; Paraffins; Zeolites
Authors Gabrienko Anton A. 1,2 , Kolganov Alexander A. 1 , Arzumanov Sergei S. 1,2 , Yashnik Svetlana A. 1 , Kriventsov Vladimir V. 1 , Freude Dieter 3 , Stepanov Alexander G. 1,2
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia
2 Novosibirsk State University, Faculty of Natural Sciences, Department of Physical Chemistry, Novosibirsk 630090, Russia
3 Universität Leipzig, Fakultät für Physik und Geowissenschaften, 04103 Leipzig, German

Funding (3)

1 Russian Foundation for Basic Research 18-03-00189
2 Russian Foundation for Basic Research 18-03-01251
3 Ministry of Science and Higher Education of the Russian Federation 0239-2021-0003

Abstract: With regard to possible involvement of zeolite Brønsted acid sites (BAS) in the activation of methane molecules for methane transformation to methanol, the effect of different Cu(II) species loaded in the zeolite on the kinetic parameters of the reaction of H/D hydrogen exchange of the alkane with BAS of Cu-modified ZSM-5 zeolites has been investigated with 1H MAS NMR in situ at 533–563 K. It is found that the acceleration of the H/D exchange by 1 order of magnitude occurs for zeolite containing Cu2+ cations (Z2Cu(II) sites) or [Cu3(μ-O)3]2+ oxo-clusters (Z2[Cu3(μ-O)3] sites) compared to pure H-form zeolite. It is thus inferred that both Z2Cu(II) and Z2[Cu3(μ-O)3] sites exhibit the promoting effect of copper on the activation of methane C–H bonds by BAS. Acceleration of the H/D exchange is rationalized by the change of the mechanism of the exchange accepted for the H-form zeolites for the mechanism that involves the formation of a transient molecular complex of methane with Cu(II) species, preceding the H/D exchange reaction. The formation of the complex of methane with both Z2Cu(II) and Z2[Cu3(μ-O)3] sites is confirmed by DRIFTS. BASs with a higher strength than in H-ZSM-5, generated in the zeolite at copper loading, are concluded to not be responsible for the H/D exchange reaction acceleration.
Cite: Gabrienko A.A. , Kolganov A.A. , Arzumanov S.S. , Yashnik S.A. , Kriventsov V.V. , Freude D. , Stepanov A.G.
Effect of Copper State in Cu/H-ZSM-5 on Methane Activation by Brønsted Acid Sites, Studied by 1H MAS NMR In Situ Monitoring the H/D Hydrogen Exchange of the Alkane with Brønsted Acid Sites
The Journal of Physical Chemistry C. 2021. V.125. N3. P.2182–2193. DOI: 10.1021/acs.jpcc.0c10261 WOS Scopus РИНЦ AN OpenAlex
Dates:
Submitted: Nov 13, 2020
Accepted: Jan 11, 2021
Published online: Jan 17, 2021
Published print: Jan 28, 2021
Identifiers:
Web of science: WOS:000614317500056
Scopus: 2-s2.0-85100263181
Elibrary: 44964329
Chemical Abstracts: 2021:142230
OpenAlex: W3124476134
Citing:
DB Citing
Scopus 21
Web of science 20
Elibrary 16
OpenAlex 21
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