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Kinetic Studies of Methanol Dehydrogenation. Part III: Carbon-Supported Copper Catalysts Full article

Journal Reaction Kinetics, Mechanisms and Catalysis
ISSN: 1878-5190 , E-ISSN: 1878-5204
Output data Year: 2017, Volume: 122, Number: 1, Pages: 385-398 Pages count : 14 DOI: 10.1007/s11144-017-1214-y
Tags Carbon-supported copper catalysts, Kinetics, Methanol dehydrogenation, Methyl formate, Rate constants, Sibunit
Authors Shelepova Ekaterina V. 1 , Ilina Ludmila Yu. 1 , Vedyagin Aleksey A. 1,2
Affiliations
1 Boreskov Institute of Catalysis SB RAS, pr. Ac. Lavrentieva, 5, Novosibirsk, Russia 630090
2 National Research Tomsk Polytechnic University, Lenin av., 30, Tomsk, Russia 634050

Funding (2)

1 Federal Agency for Scientific Organizations 0303-2016-0014
2 Russian Foundation for Basic Research 16-38-00095

Abstract: Kinetics of methanol dehydrogenation reaction over carbon-supported copper catalyst was studied. The catalyst was prepared by incipient wetness impregnation of carbonaceous graphite-like material Sibunit with aqueous solution of copper nitrate. Resulting Cu/C samples were calcined and reduced in a hydrogen flow within temperature interval of 200-400 °C. Experiments were carried out in a flow-through fixed-bed tubular reactor. Observable rate constants were determined for the reactions of methanol dehydrogenation to methyl formate and methyl formate decomposition on carbon monoxide and hydrogen. The process of methanol dehydrogenation in tubular reactor was simulated by means of mathematical modeling. Estimation of kinetic parameters in accordance with experimental data obtained for the Cu/C sample reduced at 300 °C has allowed us to consider the reversibility of methanol dehydrogenation reaction.
Cite: Shelepova E.V. , Ilina L.Y. , Vedyagin A.A.
Kinetic Studies of Methanol Dehydrogenation. Part III: Carbon-Supported Copper Catalysts
Reaction Kinetics, Mechanisms and Catalysis. 2017. V.122. N1. P.385-398. DOI: 10.1007/s11144-017-1214-y WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: May 3, 2017
Accepted: Jun 9, 2017
Published online: Jun 14, 2017
Published print: Oct 1, 2017
Identifiers:
Web of science: WOS:000408706800027
Scopus: 2-s2.0-85020754367
Elibrary: 31022546
Chemical Abstracts: 2017:1002060
Chemical Abstracts (print): 168:358741
OpenAlex: W2625099921
Citing:
DB Citing
Web of science 9
Scopus 9
Elibrary 9
OpenAlex 9
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