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Título: | Monitoring the Reaction Mechanism in Model Biogas Reforming by In Situ Transient and Steady-State DRIFTS Measurements |
Autor: | Bobadilla, Luis F.; Garcilaso, Victoria; Centeno, Miguel Ángel CSIC ORCID; Odriozola, José Antonio CSIC ORCID | Fecha de publicación: | 2017 | Editor: | Wiley-VCH | Citación: | ChemSusChem 10: 1193- 1201 (2017) | Resumen: | In this work, the reforming of model biogas was investigated on a Rh/MgAlO catalyst. In situ transient and steady-state diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) measurements were used to gain insight into the reaction mechanism involved in the activation of CH and CO. It was found that the reaction proceeds through of an initial pathway in which methane and CO are both dissociated on Rh metallic sites and additionally a bifunctional mechanism in which methane is activated on Rh sites and CO is activated on the basic sites of the support surface via a formate intermediate by H-assisted CO decomposition. Moreover, this plausible mechanism is able to explain why the observed apparent activation energy of CO is much lower than that of CH. Our results suggest that CO dissociation facilitates CH activation, because the oxygen-adsorbed species formed in the decomposition of CO are capable of reacting with the CH species derived from methane decomposition. | URI: | http://hdl.handle.net/10261/149737 | DOI: | 10.1002/cssc.201601379 | Identificadores: | doi: 10.1002/cssc.201601379 issn: 1864-564X |
Aparece en las colecciones: | (ICMS) Artículos |
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Accepted Article ChemSusChem.pdf | 1,06 MB | Adobe PDF | Visualizar/Abrir |
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