Please use this identifier to cite or link to this item: http://ktisis.cut.ac.cy/handle/10488/6661
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dc.contributor.authorEfstathiou, Angelos M.en,el
dc.contributor.authorKalamaras, Christos M.en,el
dc.contributor.authorOlympiou, Georgios-
dc.contributor.otherΟλυμπίου, Γεώργιος-
dc.date.accessioned2013-01-22T16:57:51Zen,el
dc.date.accessioned2013-05-16T06:25:29Z-
dc.date.accessioned2015-12-02T09:16:43Z-
dc.date.available2013-01-22T16:57:51Zen,el
dc.date.available2013-05-16T06:25:29Z-
dc.date.available2015-12-02T09:16:43Z-
dc.date.issued2008en,el
dc.identifier.citationCatalysis Today, 2008, Volume 138, Issue 3-4, Pages 228-234en,el
dc.identifier.issn09205861en,el
dc.identifier.urihttp://ktisis.cut.ac.cy/handle/10488/6661en,el
dc.description.abstractSteady-state isotopic transient kinetic analysis (SSITKA) experiments coupled with in situ DRIFTS and mass spectrometry (operando) were performed for the first time to study essential mechanistic aspects of the water-gas shift reaction (WGSR) over a 0.5 wt.% Pt/γ-Al2O3 catalyst. The chemical structure of active and inactive reaction intermediate species present in the carbon-path ("C-path") from CO to the CO2 product gas (use of 13CO) and in the hydrogen-path ("H-path") from H2O to the H2 product gas (use of D2O) of the reaction mechanism were determined. In addition, the concentrations (μmol/g) of active species in both the "C-path" and "H-path" of the WGSR at 350 °C were measured. Based on the large concentration of active species present in the "H-path" (OH/H located on the alumina support), the latter being larger than 28 equivalent monolayers of the exposed Pt metal surface, the small concentration of OH groups along the periphery of metal-support interface, and the significantly smaller concentration (μmol/g) of active species present in the "C-path" (adsorbed CO on Pt and COOH species on the alumina support and/or the metal-support interface), it might be suggested that diffusion of OH/H species on the alumina support surface towards Pt catalytic sites present in the "H-path" of reaction (back-spillover process) might be considered as a slow reaction step. The latter process was evidenced after conducting the WGS reaction (CO/H2O) in a partially deuterated alumina surface (Pt/γ-Al2O3). At least two kinds of formate (-COOH) species residing on the alumina surface have been identified, one of which was active and leads to the formation of CO2(g) and H2(g), whereas the other kind(s) is/are considered as inactive (spectator) adsorbed reaction intermediate species.en,el
dc.formatpdfen,el
dc.language.isoenen,el
dc.publisherElsevieren,el
dc.rights© 2008 Elsevier B.V. All rights reserved.en,el
dc.subjectWater-gasen,el
dc.subjectMass spectrometryen,el
dc.subjectWater--Analysisen,el
dc.titleThe water-gas shift reaction on pt/γ-ai2O3 catalyst: operando ssitka-drifts-mass spectroscopy studiesen,el
dc.typeArticleen,el
dc.affiliationCyprus University of Technologyen,el
dc.identifier.doihttp://dx.doi.org/10.1016/j.cattod.2008.06.010en,el
dc.dept.handle123456789/54en
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