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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Bibliographic Details
Authors: Merlo, Andrea Beatriz, Vetere, Virginia, Ramallo Lopez, Jose Martin, Requejo, Felix Gregorio, Casella, Mónica Laura
Format: article
Status:Published version
Publication Date:2011
Country:Argentina
Institution:Consejo Nacional de Investigaciones Científicas y Técnicas
Repository:CONICET Digital (CONICET)
Language:English
OAI Identifier:oai:ri.conicet.gov.ar:11336/181530
Online Access:http://hdl.handle.net/11336/181530
Access Level:Open access
Keyword:BIMETALLIC CATALYSTS
FURFURAL HYDROGENATION
PTSN AND PTGE
SURFACE ORGANOMETALLIC CHEMISTRY
https://purl.org/becyt/ford/2.5
https://purl.org/becyt/ford/2
Description
Summary: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.