Liquid-phase furfural hydrogenation employing silica-supported PtSn and PtGe catalysts prepared using surface organometallic chemistry on metals techniques

Platinum-germanium and platinum-tin catalysts supported on silica, containing different amounts of Sn and Ge, were synthesized using the surface organometallic chemistry on metals technique. The catalysts were characterized using transmission electron microscopy, X-ray photoelectron spectra and X-ra...

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Detalles Bibliográficos
Autores: Merlo, Andrea Beatriz, Vetere, Virginia, Ramallo Lopez, Jose Martin, Requejo, Felix Gregorio, Casella, Mónica Laura
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/181530
Acceso en línea:http://hdl.handle.net/11336/181530
Access Level:acceso abierto
Palabra clave:BIMETALLIC CATALYSTS
FURFURAL HYDROGENATION
PTSN AND PTGE
SURFACE ORGANOMETALLIC CHEMISTRY
https://purl.org/becyt/ford/2.5
https://purl.org/becyt/ford/2
Descripción
Sumario:Platinum-germanium and platinum-tin catalysts supported on silica, containing different amounts of Sn and Ge, were synthesized using the surface organometallic chemistry on metals technique. The catalysts were characterized using transmission electron microscopy, X-ray photoelectron spectra and X-ray absorption near edge structure and extended X-ray absorption fine structure; and were tested in the liquid-phase selective hydrogenation of furfural. The atomic ratio between the two metals resulted the key factor towards the optimization of the activity and selectivity of the bimetallic catalysts. The bimetallic catalysts were more active than the parent Pt/SiO2 catalyst in the hydrogenation of furfural. These results can be accounted for by considering a new type of active site having an architecture which would favor the hydrogenation of the C=O group is created, allowing an increased activity towards obtaining furfuryl alcohol. All the studied systems allowed to obtain furfuryl alcohol with high selectivity.