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Catalytic Properties of Massive Iron-Subgroup Metals in Dichloroethane Decomposition into Carbon Products Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2011, Volume: 52, Number: 4, Pages: 547-554 Pages count : 8 DOI: 10.1134/S002315841104001X
Tags Chlorinate Hydrocarbon; Excess Hydrogen; Massive Metal; Nichrome Wire; Nanocarbon Material
Authors Bauman Y.I. 1 , Mishakov I.V. 1 , Buyanov R.A. 1 , Vedyagin A.A. 1 , Volodin A.M. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russia

Funding (3)

1 Novosibirsk National Research University
2 The Ministry of Education and Science of the Russian Federation
3 Президиум РАН 522

Abstract: The formation of nanocarbon materials on massive nickel, nichrome, and some other alloys via the carbide cycle mechanism is reported using 1,2-dichloroethane decomposition as an example. The role of the physical stage of the carbide cycle is elucidated, and massive metal surface activation methods ensuring the realization of this stage are considered. The surface layer of massive nickel or some nickel alloys is most effectively activated by the action of chlorine resulting from the catalytic decomposition of 1,2-dichloroethane. It has been demonstrated by ferromagnetic resonance (FMR) spectroscopy that the activation of the massive metal surface in 1,2-dichloroethane decomposition to nanocarbon is due to the surface undergoing crystal chemical restructuring. The microstructuring of the surface yields fine Ni particles similar in size (0.2–0.3 μm) and shape, whose FMR spectra are anisotropic and have similar magnetic resonance parameters. Both chlorine-free and chlorinated hydrocarbons decompose over these particles via the carbide cycle mechanism. It is demonstrated that it is possible to design catalytic reactors packed with massive nickel or its alloy. The nanocarbon material obtained in such a reactor will not be contaminated by components of conventional catalyst supports (Al, Mg, etc.). The stable performance temperature of the catalyst will be increased, and this will allow the equilibrium outlet methane concentration to be reduced.
Cite: Bauman Y.I. , Mishakov I.V. , Buyanov R.A. , Vedyagin A.A. , Volodin A.M.
Catalytic Properties of Massive Iron-Subgroup Metals in Dichloroethane Decomposition into Carbon Products
Kinetics and Catalysis. 2011. V.52. N4. P.547-554. DOI: 10.1134/S002315841104001X WOS Scopus РИНЦ ANCAN OpenAlex
Original: Бауман Ю.И. , Мишаков И.В. , Буянов Р.А. , Ведягин А.А. , Володин А.М.
Каталитические свойства массивных металлов подгруппы железа в процессе разложения дихлорэтана с получением углеродных продуктов
Кинетика и катализ. 2011. Т.52. №4. С.557-564. РИНЦ
Dates:
Submitted: Jun 22, 2010
Published print: Jul 1, 2011
Published online: Aug 7, 2011
Identifiers:
Web of science: WOS:000293639300013
Scopus: 2-s2.0-80051636290
Elibrary: 18058857
Chemical Abstracts: 2011:985816
Chemical Abstracts (print): 155:254025
OpenAlex: W1987166873
Citing:
DB Citing
Web of science 30
Scopus 31
Elibrary 30
OpenAlex 33
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