Sciact
  • EN
  • RU

In situ High Temperature MAS NMR Study of the Mechanisms of Catalysis. Ethane Aromatization on Zn-Modified Zeolite BEA Full article

Journal Solid State Nuclear Magnetic Resonance
ISSN: 0926-2040 , E-ISSN: 1527-3326
Output data Year: 2009, Volume: 35, Number: 2, Pages: 113-119 Pages count : 7 DOI: 10.1016/j.ssnmr.2008.12.005
Tags Aromatization, Ethane, High-temperature MAS NMR, In situ NMR, Kinetics, Zn/H-BEA zeolite
Authors Arzumanov Sergei S. 1 , Gabrienko Anton A. 1,2 , Freude Dieter 3 , Stepanov Alexander G. 1,2
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova Str. 2, Novosibirsk 630090, Russia
3 Abteilung Grenzfla¨chenphysik, Universita¨t Leipzig, Linne´straße 5, 04103 Leipzig, Germany

Funding (3)

1 Russian Foundation for Basic Research 07-03-00136
2 German Research Foundation FR 902/15
3 Russian Science Support Foundation

Abstract: Ethane conversion into aromatic hydrocarbons over Zn-modified zeolite BEA has been analyzed by high-temperature MAS NMR spectroscopy. Information about intermediates (Zn-ethyl species) and reaction products (mainly toluene and methane), which were formed under the conditions of a batch reactor, was obtained by 13C MAS NMR. Kinetics of the reaction, which was monitored by 1H MAS NMR in situ at the temperature of 573 K, provided information about the reaction mechanism. Simulation of the experimental kinetics within the frames of the possible kinetic schemes of the reaction demonstrates that a large amount of methane evolved under ethane aromatization arises from the stage of direct ethane hydrogenolysis.
Cite: Arzumanov S.S. , Gabrienko A.A. , Freude D. , Stepanov A.G.
In situ High Temperature MAS NMR Study of the Mechanisms of Catalysis. Ethane Aromatization on Zn-Modified Zeolite BEA
Solid State Nuclear Magnetic Resonance. 2009. V.35. N2. P.113-119. DOI: 10.1016/j.ssnmr.2008.12.005 WOS Scopus РИНЦ ANCAN PMID OpenAlex
Dates:
Submitted: Oct 27, 2008
Published online: Jan 4, 2009
Published print: Apr 1, 2009
Identifiers:
Web of science: WOS:000265325200010
Scopus: 2-s2.0-63449089921
Elibrary: 13600858
Chemical Abstracts: 2009:420772
Chemical Abstracts (print): 151:77542
PMID: 19186034
OpenAlex: W2052492127
Citing:
DB Citing
Web of science 47
Scopus 49
Elibrary 44
OpenAlex 49
Altmetrics: