Methanol steam reforming behavior of copper impregnated over CeO2-ZrO2 derived from a surfactant assisted coprecipitation route

A series of ceria-zirconia solid solutions has been prepared by a surfactant assisted coprecipitation method. After impregnation of copper, their activities have been assessed for methanol steam reforming. The results indicate that the compositions with 10 and 15 at.% loading of copper on Ce0.6Zr0.4...

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Detalles Bibliográficos
Autores: Llorca Piqué, Jordi|||0000-0002-7447-9582, Colussi, Sara, Domínguez Escalante, Montserrat|||0000-0002-2613-888X, Trovarelli, Alessandro, Gayen, Arup, Das, Dipak
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/79996
Acceso en línea:https://hdl.handle.net/2117/79996
https://dx.doi.org/10.1016/j.ijhydene.2015.06.130
Access Level:acceso abierto
Palabra clave:Steam
Copper alloys
Methanol
Zirconium alloys
Copper
Ceria-zirconia
Methanol steam reforming
Cu-sintering
Coking
Regeneration
Oxygen storage capacity
Hydrogen-production
Cuo/zno/ceo2/zro2/al2o3 catalysts
Cu/zno/al2o3 catalysts
Support material
Oxide catalysts
Zirconia
Ceria
Deactivation
Hydrocarbons
Vapor
Coure--Aliatges
Metanol
Zirconi--Aliatges
Àrees temàtiques de la UPC::Energies
Àrees temàtiques de la UPC::Enginyeria dels materials
Descripción
Sumario:A series of ceria-zirconia solid solutions has been prepared by a surfactant assisted coprecipitation method. After impregnation of copper, their activities have been assessed for methanol steam reforming. The results indicate that the compositions with 10 and 15 at.% loading of copper on Ce0.6Zr0.4O2 exhibit maximum catalytic efficiency. Detailed structural analyses reveal high degree of copper dispersion on the ceria-zirconia matrix. In situ XPS studies confirm reduction of surface CuO species with concomitant lowering of Cu-surface atomic composition and increase of carbon. These evidences point to the formation of large aggregates of copper covered with coke that is suggested to be responsible for on stream activity loss. On regeneration, these aggregates break into a mixture of oxidized (Cu2+) and reduced (Cu-o and Cu+) copper species showing similar activity to the as prepared catalysts. In general, we have attributed catalytic activity to different proportions of copper components in the various forms of these catalysts. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.