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Effect of the nature of the support on the catalytic performance of noble metal catalysts for the water–gas shift reaction

Dimitris I. Kondarides, Panagiotopoulou Paraskevi

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URIhttp://purl.tuc.gr/dl/dias/9D4C31D8-7C17-406A-AB31-5278767FCD42-
Identifierhttps://doi.org/10.1016/j.cattod.2005.11.026-
Languageen-
ExtentPages 49–52en
TitleEffect of the nature of the support on the catalytic performance of noble metal catalysts for the water–gas shift reactionen
Creator Dimitris I. Kondaridesen
CreatorPanagiotopoulou Paraskevien
CreatorΠαναγιωτοπουλου Παρασκευηel
PublisherElsevieren
Content SummaryThe catalytic activity of supported noble metal catalysts (Pt, Rh, Ru, and Pd) for the WGS reaction is investigated with respect to the physichochemical properties of the metallic phase and the support. It has been found that, for all metal-support combinations investigated, Pt is much more active than Pd, while Rh and Ru exhibit intermediate activity. The turnover frequency (TOF) of CO conversion does not depend on metal loading, dispersion or crystallite size, but depends strongly on the nature of the metal oxide carrier. In particular, catalytic activity of Pt and Ru catalysts, is 1-2 orders of magnitude higher when supported on “reducible” (TiO2, CeO2, La2O3, and YSZ) rather than on “irreducible” (Al2O3, MgO, and SiO2) metal oxides. In contrast to what has been found in our previous study over Pt/TiO2 catalysts, catalytic activity of dispersed Pt does not depend on the structural and morphological characteristics of CeO2, such as specific surface area or primary crystallite size.en
Type of ItemPeer-Reviewed Journal Publicationen
Type of ItemΔημοσίευση σε Περιοδικό με Κριτέςel
Licensehttp://creativecommons.org/licenses/by/4.0/en
Date of Item2015-10-23-
Date of Publication2006-
Bibliographic CitationP. Panagiotopoulou, D.I. Kondarides,“Effect of the nature of the support on the catalytic performance of noble metal catalysts for the Water-Gas Shift Reaction”, Catalysis Today, Vol. 112, no. 1-4, pp. 49-52, Mar. 2006. doi:10.1016/j.cattod.2005.11.026. en

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