Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde

Detalhes bibliográficos
Autor(a) principal: Vetere,Virginia
Data de Publicação: 2010
Outros Autores: Merlo,Andrea B., Ruggera,José F., Casella,Mónica L.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000500021
Resumo: In this work, the liquid-phase chemoselective hydrogenation of furfural was studied, employing Pt, Rh and Ni-based catalysts. Bimetallic systems, containing different amounts of tin, were obtained by means of controlled surface reactions between a monometallic catalyst and Sn(C4H9)4. The results obtained when monometallic catalysts were employed suggest a relationship between metal properties and the activity and selectivity obtained. All systems allowed obtaining furfuryl alcohol with high selectivity (99, 97 and 76% were achieved with Pt, Rh and Ni catalysts, respectively). The addition of tin has different effects on the three systems, both in terms of conversion and selectivity. An interesting result was obtained for the Ni-based catalysts, for which the addition of tin led to a significant increase in furfuryl alcohol selectivity and, depending on the Sn/Ni ratio, also to an increase in the catalytic activity of the system.
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spelling Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehydefurfuralfurfuryl alcoholhydrogenationbimetallic catalystsPtSnIn this work, the liquid-phase chemoselective hydrogenation of furfural was studied, employing Pt, Rh and Ni-based catalysts. Bimetallic systems, containing different amounts of tin, were obtained by means of controlled surface reactions between a monometallic catalyst and Sn(C4H9)4. The results obtained when monometallic catalysts were employed suggest a relationship between metal properties and the activity and selectivity obtained. All systems allowed obtaining furfuryl alcohol with high selectivity (99, 97 and 76% were achieved with Pt, Rh and Ni catalysts, respectively). The addition of tin has different effects on the three systems, both in terms of conversion and selectivity. An interesting result was obtained for the Ni-based catalysts, for which the addition of tin led to a significant increase in furfuryl alcohol selectivity and, depending on the Sn/Ni ratio, also to an increase in the catalytic activity of the system.Sociedade Brasileira de Química2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000500021Journal of the Brazilian Chemical Society v.21 n.5 2010reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532010000500021info:eu-repo/semantics/openAccessVetere,VirginiaMerlo,Andrea B.Ruggera,José F.Casella,Mónica L.eng2010-07-13T00:00:00Zoai:scielo:S0103-50532010000500021Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2010-07-13T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
title Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
spellingShingle Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
Vetere,Virginia
furfural
furfuryl alcohol
hydrogenation
bimetallic catalysts
PtSn
title_short Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
title_full Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
title_fullStr Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
title_full_unstemmed Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
title_sort Transition metal-based bimetallic catalysts for the chemoselective hydrogenation of furfuraldehyde
author Vetere,Virginia
author_facet Vetere,Virginia
Merlo,Andrea B.
Ruggera,José F.
Casella,Mónica L.
author_role author
author2 Merlo,Andrea B.
Ruggera,José F.
Casella,Mónica L.
author2_role author
author
author
dc.contributor.author.fl_str_mv Vetere,Virginia
Merlo,Andrea B.
Ruggera,José F.
Casella,Mónica L.
dc.subject.por.fl_str_mv furfural
furfuryl alcohol
hydrogenation
bimetallic catalysts
PtSn
topic furfural
furfuryl alcohol
hydrogenation
bimetallic catalysts
PtSn
description In this work, the liquid-phase chemoselective hydrogenation of furfural was studied, employing Pt, Rh and Ni-based catalysts. Bimetallic systems, containing different amounts of tin, were obtained by means of controlled surface reactions between a monometallic catalyst and Sn(C4H9)4. The results obtained when monometallic catalysts were employed suggest a relationship between metal properties and the activity and selectivity obtained. All systems allowed obtaining furfuryl alcohol with high selectivity (99, 97 and 76% were achieved with Pt, Rh and Ni catalysts, respectively). The addition of tin has different effects on the three systems, both in terms of conversion and selectivity. An interesting result was obtained for the Ni-based catalysts, for which the addition of tin led to a significant increase in furfuryl alcohol selectivity and, depending on the Sn/Ni ratio, also to an increase in the catalytic activity of the system.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532010000500021
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532010000500021
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.21 n.5 2010
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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