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https://hdl.handle.net/20.500.14279/2240
Τίτλος: | The water-gas shift reaction on pt/γ-ai2O3 catalyst: operando ssitka-drifts-mass spectroscopy studies | Συγγραφείς: | Efstathiou, Angelos M. Kalamaras, Christos M. Olympiou, Georgios |
Major Field of Science: | Natural Sciences | Field Category: | Biological Sciences | Λέξεις-κλειδιά: | Water-gas;Mass spectrometry;Water--Analysis | Ημερομηνία Έκδοσης: | 2008 | Πηγή: | Catalysis Today, 2008, vol. 138, iss. 3-4, pp. 228-234 | Volume: | 138 | Issue: | 3-4 | Start page: | 228 | End page: | 234 | Περιοδικό: | Catalysis Today | Περίληψη: | Steady-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. | URI: | https://hdl.handle.net/20.500.14279/2240 | ISSN: | 9205861 | DOI: | 10.1016/j.cattod.2008.06.010 | Rights: | © Elsevier | Type: | Article | Affiliation: | Cyprus University of Technology | Affiliation: | University of Cyprus | Publication Type: | Peer Reviewed |
Εμφανίζεται στις συλλογές: | Άρθρα/Articles |
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