Kinetic and spectroscopic investigations to elucidate the mechanisms of CO oxidation over Ru and Au catalysts

  • The oxidation of CO over polycrystalline \(RuO_{2}\) powder was studied at ambient pressure in the temperature range from 363 to 453 K. Reaction orders with respect to CO and oxygen were determined. Using temperature-programmed reduction (TPR) and desorption (TPD) techniques subsequent to steady state CO oxidation, the most active and stable state of the unsupported Ru catalysts was identified as an ultra-thin \(RuO_{2}\) layer covering a metallic Ru core. Furthermore, employing \(\textit {in situ}\) diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) measurements, the structural changes of Ru/MgO and \(Ru/SiO_{2}\) catalysts during the oxidation of CO were probed. Thus, by comparing the present results with single crystal data, it was possible to bridge both the pressure and the materials gap. The oxidation of CO over \(Au/TiO_{2}\) and \(Au/Fe_{2}O_{3}\) catalysts was also investigated. Based on DRIFTS results an active state of the gold catalysts under reaction conditions was identified as metallic gold species.

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Metadaten
Author:Vijay Sopan NarkhedeGND
URN:urn:nbn:de:hbz:294-16301
Referee:Martin MuhlerORCiDGND, Wolfgang GrünertGND
Document Type:Doctoral Thesis
Language:English
Date of Publication (online):2006/06/22
Date of first Publication:2006/06/22
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Granting Institution:Ruhr-Universität Bochum, Fakultät für Chemie und Biochemie
Date of final exam:2006/05/19
Creating Corporation:Fakultät für Chemie und Biochemie
GND-Keyword:Ruthenium; Kohlenmonoxid; Oxidation; Desorption / Temperaturprogrammierung; Drift
Institutes/Facilities:Lehrstuhl für Technische Chemie
Dewey Decimal Classification:Naturwissenschaften und Mathematik / Chemie, Kristallographie, Mineralogie
faculties:Fakultät für Chemie und Biochemie
Licence (German):License LogoKeine Creative Commons Lizenz - es gelten der Veröffentlichungsvertrag und das deutsche Urheberrecht