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A Comparative Study of the Activity of Oxide Catalysts in the Oxidation of Methane and 1,1-Dimethylhydrazine Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2004, Volume: 45, Number: 5, Pages: 722-729 Pages count : 8 DOI: 10.1023/B:KICA.0000044985.63655.a1
Tags FeO2; Perovskite; Fixed Nitrogen; Oxide Catalyst; Catalytic Oxidation
Authors Ismagilov I.Z. 1 , Kuznetsov V.V. 1 , Nemudryi A.P. 2 , Pod''yacheva O.Y. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090 Russia
2 Institute of Solid-State Chemistry and Mechanochemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630128 Russia

Funding (4)

1 Netherlands Organisation for Scientific Research 2000
2 International Science and Technology Center 959
3 International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union 2000-00180
4 International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union 99-1044

Abstract: The catalytic oxidation of methane and 1,1-dimethylhydrazine ((CH3)2N–NH2, unsymmetrical dimethylhydrazine (UDMH)) with air on oxide catalysts was studied. Two pairs of perovskites (Ca0.7Sr0.3FeO2.5(3.0) and La0.7Sr0.3CoO2.5(3.0), stoichiometric and superstoichiometric with respect to oxygen) and a supported spinel (20%(CuxMg1– x Cr2O4)/γ-Al2O3, IC-12-73) were used as catalysts. The experiments were performed using two laboratory flow-type systems: in a catalytic fixed-bed reactor (the oxidation of CH4) and in a gradientless vibrationally fluidized bed reactor (the oxidation of CH4 and UDMH) at 150–700°C. In the oxidation of CH4, the IC-12-73 catalyst was more active than the perovskite catalysts, although particular perovskite catalysts can exhibit higher activity in the region of low temperatures. In the oxidation of UDMH, the activity of perovskites in the test temperature region was lower than that of IC-12-73; this correlates with the higher activity of IC-12-73 in the oxidation of CH4. The Ca0.7Sr0.3FeO3.0 and La0.7Sr0.3CoO2.5(3.0) perovskites exhibited similar activities in the deep oxidation of UDMH, which were higher than the activity of Ca0.7Sr0.3FeO2.5. A comparison between the selectivities of the conversion of fixed nitrogen, which is a constituent of UDMH, into nitrogen oxides (SNNOx) demonstrated that, on all of the perovskites, SNNO was higher and SNN2O was lower than the corresponding values on IC-12-73. Additional information on the possible mechanisms of intermediate formation in the adsorption and oxidation of UDMH on IC-12-73 was obtained using Fourier transform IR spectroscopy.
Cite: Ismagilov I.Z. , Kuznetsov V.V. , Nemudryi A.P. , Pod''yacheva O.Y.
A Comparative Study of the Activity of Oxide Catalysts in the Oxidation of Methane and 1,1-Dimethylhydrazine
Kinetics and Catalysis. 2004. V.45. N5. P.722-729. DOI: 10.1023/B:KICA.0000044985.63655.a1 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Исмагилов И.З. , Кузнецов В.В. , Немудрый А.П. , Подъячева О.Ю.
Сравнительное исследование активности оксидных катализаторов в окислении метана и 1,1-диметилгидразина
Кинетика и катализ. 2004. Т.45. №5. С.763-770. РИНЦ
Dates:
Submitted: Jul 4, 2003
Published print: Sep 1, 2004
Identifiers:
Web of science: WOS:000224886200015
Scopus: 2-s2.0-6344292471
Elibrary: 14396060
Chemical Abstracts: 2004:840791
Chemical Abstracts (print): 142:113509
OpenAlex: W2080210782
Citing:
DB Citing
Web of science 11
Scopus 13
Elibrary 11
OpenAlex 12
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