dc.creatorPavesi Contreras, Camila Andrea
dc.creatorBlanco, Elodie
dc.creatorPazo Carballo, César Alexander
dc.creatorDongil, A.B.
dc.creatorEscalona Burgos, Nestor Guillermo
dc.date.accessioned2024-03-15T19:17:49Z
dc.date.accessioned2024-05-02T18:56:28Z
dc.date.available2024-03-15T19:17:49Z
dc.date.available2024-05-02T18:56:28Z
dc.date.created2024-03-15T19:17:49Z
dc.date.issued2024
dc.identifier10.1016/j.apcata.2023.119535
dc.identifier0926-860X
dc.identifierSCOPUS_ID:85180411802
dc.identifierhttps://doi.org/10.1016/j.apcata.2023.119535
dc.identifierhttps://repositorio.uc.cl/handle/11534/84564
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/9271590
dc.description.abstractMolybdenum carbide catalysts supported on monoclinic and tetragonal zirconium oxide were studied for hydrogen production through aqueous phase reforming of ethanol. Catalysts were characterized by N2 physisorption, XRD, TPR and XPS. Results showed that 10%Mo2C/m-ZrO2 was less carburized and had a lower surface area than 10%Mo2C/t-ZrO2 and 10%MoC/t-ZrO2. Mo oxide was identified on the surface as well as two types of Mo oxycarbide and Mo oxynitride. The α crystalline phase of the carbide was more active than β phase and was ascribed to its higher relative superficial distribution. However, the α phase generated less H2 probably because there was less oxycarbide presence. 10%Mo2C/m-ZrO2 produced significantly more H2 and was stable for five consecutive reactions. This catalyst showed higher carburization degree after the reaction, which greatly enhanced the generation of H2, suggesting that carbides species improved H2 production compared to oxycarbides.
dc.languageen
dc.rightsacceso restringido
dc.subjectAqueous phase reforming
dc.subjectHydrogen production
dc.subjectMolybdenum carbide
dc.titleH2 production through aqueous phase reforming of ethanol over molybdenum carbide catalysts supported on zirconium oxide
dc.typeartículo


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