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  Comparison of oxidizing agents for the oxidative coupling of methane over state-of-the-art catalysts

Langfeld, K., Frank, B., Strempel, V. A., Berger-Karin, C., Weinberg, G., Kondratenko, E. V., et al. (2012). Comparison of oxidizing agents for the oxidative coupling of methane over state-of-the-art catalysts. Applied Catalysis A: General, 417-418, 145-152. doi:10.1016/j.apcata.2011.12.035.

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2011
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 Urheber:
Langfeld, Kirsten1, Autor
Frank, Benjamin2, Autor           
Strempel, Verena A.1, Autor
Berger-Karin, Claudia3, Autor
Weinberg, Gisela2, Autor           
Kondratenko, Evgenii V.3, Autor
Schomäcker, Reinhard1, Autor
Affiliations:
1Institute of Chemistry, Technical University Berlin, Straße des 17. Juni 124, 10623 Berlin, Germany, ou_persistent22              
2Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              
3Leibniz Institute for Catalysis at the University of Rostock, Albert-Einstein-Straße 29a, 18059 Rostock, Germany, ou_persistent22              

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Schlagwörter: C–H activation; Oxygen; Nitrous oxide; Cellulose templating; Deactivation
 Zusammenfassung: The synthesis of selected state-of-the-art catalysts providing high performances in the oxidative coupling of methane (OCM) with O2 was reproduced according to the respective recipes reported in literature. A reference material with identical stoichiometric composition was further synthesized by applying the cellulose templating method. This method increases the surface area and affects the phase composition and crystallite size of the catalysts as determined by N2-physisoprtion, X-ray diffraction and scanning electron microscopy. This, however, is in most cases detrimental to the catalytic OCM performance due to enhanced global activity resulting in hot spots in the catalyst bed. Catalysts were tested in the OCM under variation of temperature (973–1073 K), GHSV (3600–100,000 h−1) and oxidizing agent (O2 and N2O). In general, conversions of CH4 when using N2O are lower than in the presence of O2, however, the selectivities to C2 products ethane and ethylene are higher even at a similar level of CH4 conversion. This confirms the presence of different oxygen species formed by activation of these oxidizing agents.

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Sprache(n): eng - English
 Datum: 2011-12-312012-02-29
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1016/j.apcata.2011.12.035
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Titel: Applied Catalysis A: General
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Amsterdam : Elsevier
Seiten: - Band / Heft: 417-418 Artikelnummer: - Start- / Endseite: 145 - 152 Identifikator: ISSN: 0926-860X
CoNE: https://pure.mpg.de/cone/journals/resource/954925567761_1