Bimetallic Ru–Pd supported on CeO2 for the catalytic partial oxidation of methane into syngas

A series of monometallic Ru, Pd, and bimetallic Ru–Pd catalysts loaded on CeO2 support have been prepared via mechanochemical and conventional incipient wetness impregnation methods and used in the partial oxidation of methane (POM) to obtain synthesis gas (H2 and CO). The influence of the preparati...

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Detalhes bibliográficos
Autores: Fazlikeshteli, Shiva, Vendrell Villafruela, Xavier|||0000-0003-4705-8253, Llorca Piqué, Jordi|||0000-0002-7447-9582
Tipo de documento: artigo
Data de publicação:2023
País:España
Recursos:Universitat Politècnica de Catalunya (UPC)
Repositório:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglês
OAI Identifier:oai:upcommons.upc.edu:2117/385894
Acesso em linha:https://hdl.handle.net/2117/385894
https://dx.doi.org/10.1016/j.fuel.2022.126799
Access Level:Acceso aberto
Palavra-chave:Catalysis
Nanochemistry
Partial oxidation of methane
Syngas
Bimetallic catalysts
Noble metal catalysts
Ceria catalysts
Mechanochemistry
Catàlisi
Nanoquímica
Àrees temàtiques de la UPC::Enginyeria química
Descrição
Resumo:A series of monometallic Ru, Pd, and bimetallic Ru–Pd catalysts loaded on CeO2 support have been prepared via mechanochemical and conventional incipient wetness impregnation methods and used in the partial oxidation of methane (POM) to obtain synthesis gas (H2 and CO). The influence of the preparation method, the order of addition of the metals, the Ru:Pd metal ratio, and the milling energy and time for samples prepared by the mechanochemical method, have been evaluated between 300 and 600 °C. The results revealed that bimetallic Ru–Pd/CeO2 catalysts outperform monometallic Ru–CeO2 and Pd–CeO2 for POM, both in terms of catalytic activity and stability. Additionally, the bimetallic Ru–Pd/CeO2 catalysts prepared by ball milling produced syngas at a much lower temperature compared to the conventional catalysts prepared by incipient wetness impregnation. Raman spectroscopy, temperature programmed reduction (H2–TPR), X–ray photoelectron spectroscopy (XPS) and high–resolution transmission electron microscopy (HRTEM) have been used to characterize the catalysts before and after reaction.