A transient in situ FTIR and XANES study of CO oxidation over Pt/Al2O3 catalysts
2004 (English)In: Journal of Catalysis, ISSN 0021-9517, E-ISSN 1090-2694, Vol. 226, no 2, 422-434 p.Article in journal (Refereed) Published
We report experimental results for the oxidation of CO over supported Pt/Al2O3 catalysts operating in oxygen excess at atmospheric pressure. To study the reaction kinetics under transient conditions we have employed step changes of the O-2 concentration by intermittently switching off the O-2 supply at various temperatures ranging from 523 to 623 K. Detailed in situ FTIR and XANES data for CO coverage and the chemical state of Pt, respectively, are presented together with the CO conversion, which in both cases was monitored by mass spectrometry. A red-shift of the vibrational frequency of linearly bonded CO which correlates with a blue-shift of the Pt L-III binding energy indicates that the Pt catalyst initially is partially oxidised and gradually reduced when the O-2 supply is switched off. Control experiments with a NO2 oxidised Pt/Al2O3 catalyst support these findings. A hysteresis in the catalytic activity due to the different rates whereby Pt is oxidised and reduced as a function of gas-phase composition is observed. The activation energy for the Pt oxide reduction (decomposition) process is estimated to be about 50 kJ/mol. The results further emphasise that the conventional three-step Langmuir-Hinshelwood (LH) scheme used to interpret CO oxidation on Pt surfaces must be complemented by a Pt oxidation and reduction mechanism during transient conditions. Moreover, FTIR data suggest that during the extinction, the partially oxidised platinum surface is reduced by chemisorbed CO which should be explicitly accounted for in the modeling of the reaction mechanism. (C) 2004 Elsevier Inc. All rights reserved.
Place, publisher, year, edition, pages
2004. Vol. 226, no 2, 422-434 p.
catalysis, ignition, extinction, CO oxidation, platinum, platinum oxide, Pt/Al2O3, step-response experiments, FTIR, XANES
Chemical Process Engineering Materials Chemistry Physical Chemistry
IdentifiersURN: urn:nbn:se:uu:diva-235921DOI: 10.1016/j.jcat.2004.06.009ISI: 000223278100018OAI: oai:DiVA.org:uu-235921DiVA: diva2:762455