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  Nanostructured supported palladium catalysts—Non-oxidative methane coupling

Moya, S. F., Martins, R. L., Ota, A., Kunkes, E. L., Behrens, M., & Schmal, M. (2012). Nanostructured supported palladium catalysts—Non-oxidative methane coupling. Applied Catalysis A: General, 411-412, 105-113. doi:10.1016/j.apcata.2011.10.025.

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Pd_nano_revised_final.pdf (beliebiger Volltext), 1001KB
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2012
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 Urheber:
Moya, Silvia F.1, Autor
Martins, Ruth L.1, Autor
Ota, Antje2, Autor           
Kunkes, Edward L.2, Autor           
Behrens, Malte2, Autor           
Schmal, Martin1, Autor
Affiliations:
1Federal University of Rio de Janeiro, Programa de Engenharia Química/COPPE/NUCAT, Cidade Universitária, 68502, Rio de Janeiro, RJ, 21941-972, Brazil, ou_persistent22              
2Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Schlagwörter: Palladium; Nanostructure; Sonochemistry; Colloidal method; Methane activation; Non-oxidative process;
 Zusammenfassung: The Pd on α-Al2O3 catalysts with Pd particles in the low nanometer range have been prepared by a sonochemical reduction and a colloidal method, respectively. The two catalysts differ in their particle size, the widths of their particle size distributions and the amount of carbon incorporation in the Pd lattice. The adsorptive properties of the Pd/Al2O3 samples are different as a result of the different preparation methods. The methane adsorption capacity of that sample with smaller particles is lower than that of the catalyst with larger particles and the energy of activation is nearly doubled. DRIFTS and TPD results of CO adsorption supported by transmission electron microscopy data indicate that the PdSON catalyst with smaller and more homogeneous particles than PdCOL is highly dispersed which influences the coupling-hydrogenolysis process. The catalytic activity evidenced the formation of different adspecies during methane coupling and chemisorption on both catalysts. During the hydrogenation the carbon adspecies formed mainly methane at low adsorption temperatures. The significant amount of adsorbed methane at 773 K is governed by the highly active coordination unsaturated sites at the surface.

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Sprache(n): eng - English
 Datum: 2012-01-16
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1016/j.apcata.2011.10.025
 Art des Abschluß: -

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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: 411-412 Artikelnummer: - Start- / Endseite: 105 - 113 Identifikator: ISSN: 0926-860X
CoNE: https://pure.mpg.de/cone/journals/resource/954925567761_1