Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts

Autores
Gutierrez, Victoria Soledad; Alvarez, Mariana; Volpe, María Alicia
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The selective hydrogenation of cinnamaldehyde is carried out in a batch reactor, at 100 °C and 1 MPa of H 2 using isopropyl alcohol as the solvent, over a series of copper supported catalysts: Cu/Al 2O 3, Cu/SiO 2 Cu/MCM-48, Cu/CeO 2 and Cu/α-Fe 2O 3. The selectivity of the samples is compared with that corresponding to Pti/SiO 2. Reduced Cu/Al 2O 3 and Cu/SiO 2 showed lower selectivity to the cinnamyl alcohol (16-22%) than Pt/SiO 2 (35%), at 15% of conversion. Following a calcination at 300 °C both, activity and selectivity of copper catalysts were increased. The calcined surface would hydrogenate CO bond by hydrogen transfer from the solvent. TPR, XRD and FTIR of adsorbed CO showed that Cu (I) species are stabilized on the mesoporous structure of MCM-48. This particular feature renders Cu/MCM-48 a selective catalyst, reaching high selectivity values (51%, at 15% of conversion). Cu/CeO 2 and Cu/α-Fe 2O 3 showed higher selectivity than Pt based catalyst due to a promotion of the catalytic properties of copper by reduced support species.
Fil: Gutierrez, Victoria Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina
Fil: Alvarez, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Fil: Volpe, María Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina
Materia
Α,Β-UNSATURATED ALDEHYDES
CERIA
CONJUGATED CARBONYL
COPPER OXIDE
SELECTIVE HYDROGENATION
SUPPORTED COPPER
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/126803

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network_name_str CONICET Digital (CONICET)
spelling Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalystsGutierrez, Victoria SoledadAlvarez, MarianaVolpe, María AliciaΑ,Β-UNSATURATED ALDEHYDESCERIACONJUGATED CARBONYLCOPPER OXIDESELECTIVE HYDROGENATIONSUPPORTED COPPERhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The selective hydrogenation of cinnamaldehyde is carried out in a batch reactor, at 100 °C and 1 MPa of H 2 using isopropyl alcohol as the solvent, over a series of copper supported catalysts: Cu/Al 2O 3, Cu/SiO 2 Cu/MCM-48, Cu/CeO 2 and Cu/α-Fe 2O 3. The selectivity of the samples is compared with that corresponding to Pti/SiO 2. Reduced Cu/Al 2O 3 and Cu/SiO 2 showed lower selectivity to the cinnamyl alcohol (16-22%) than Pt/SiO 2 (35%), at 15% of conversion. Following a calcination at 300 °C both, activity and selectivity of copper catalysts were increased. The calcined surface would hydrogenate CO bond by hydrogen transfer from the solvent. TPR, XRD and FTIR of adsorbed CO showed that Cu (I) species are stabilized on the mesoporous structure of MCM-48. This particular feature renders Cu/MCM-48 a selective catalyst, reaching high selectivity values (51%, at 15% of conversion). Cu/CeO 2 and Cu/α-Fe 2O 3 showed higher selectivity than Pt based catalyst due to a promotion of the catalytic properties of copper by reduced support species.Fil: Gutierrez, Victoria Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; ArgentinaFil: Alvarez, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; ArgentinaFil: Volpe, María Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; ArgentinaElsevier Science2012-01-31info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/126803Gutierrez, Victoria Soledad; Alvarez, Mariana; Volpe, María Alicia; Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts; Elsevier Science; Applied Catalysis A: General; 413-414; 31-1-2012; 358-3650926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2011.11.028info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0926860X11006995?via%3Dihubinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:52:12Zoai:ri.conicet.gov.ar:11336/126803instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:52:12.714CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
title Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
spellingShingle Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
Gutierrez, Victoria Soledad
Α,Β-UNSATURATED ALDEHYDES
CERIA
CONJUGATED CARBONYL
COPPER OXIDE
SELECTIVE HYDROGENATION
SUPPORTED COPPER
title_short Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
title_full Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
title_fullStr Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
title_full_unstemmed Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
title_sort Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts
dc.creator.none.fl_str_mv Gutierrez, Victoria Soledad
Alvarez, Mariana
Volpe, María Alicia
author Gutierrez, Victoria Soledad
author_facet Gutierrez, Victoria Soledad
Alvarez, Mariana
Volpe, María Alicia
author_role author
author2 Alvarez, Mariana
Volpe, María Alicia
author2_role author
author
dc.subject.none.fl_str_mv Α,Β-UNSATURATED ALDEHYDES
CERIA
CONJUGATED CARBONYL
COPPER OXIDE
SELECTIVE HYDROGENATION
SUPPORTED COPPER
topic Α,Β-UNSATURATED ALDEHYDES
CERIA
CONJUGATED CARBONYL
COPPER OXIDE
SELECTIVE HYDROGENATION
SUPPORTED COPPER
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The selective hydrogenation of cinnamaldehyde is carried out in a batch reactor, at 100 °C and 1 MPa of H 2 using isopropyl alcohol as the solvent, over a series of copper supported catalysts: Cu/Al 2O 3, Cu/SiO 2 Cu/MCM-48, Cu/CeO 2 and Cu/α-Fe 2O 3. The selectivity of the samples is compared with that corresponding to Pti/SiO 2. Reduced Cu/Al 2O 3 and Cu/SiO 2 showed lower selectivity to the cinnamyl alcohol (16-22%) than Pt/SiO 2 (35%), at 15% of conversion. Following a calcination at 300 °C both, activity and selectivity of copper catalysts were increased. The calcined surface would hydrogenate CO bond by hydrogen transfer from the solvent. TPR, XRD and FTIR of adsorbed CO showed that Cu (I) species are stabilized on the mesoporous structure of MCM-48. This particular feature renders Cu/MCM-48 a selective catalyst, reaching high selectivity values (51%, at 15% of conversion). Cu/CeO 2 and Cu/α-Fe 2O 3 showed higher selectivity than Pt based catalyst due to a promotion of the catalytic properties of copper by reduced support species.
Fil: Gutierrez, Victoria Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina
Fil: Alvarez, Mariana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Química del Sur. Universidad Nacional del Sur. Departamento de Química. Instituto de Química del Sur; Argentina
Fil: Volpe, María Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Planta Piloto de Ingeniería Química. Universidad Nacional del Sur. Planta Piloto de Ingeniería Química; Argentina
description The selective hydrogenation of cinnamaldehyde is carried out in a batch reactor, at 100 °C and 1 MPa of H 2 using isopropyl alcohol as the solvent, over a series of copper supported catalysts: Cu/Al 2O 3, Cu/SiO 2 Cu/MCM-48, Cu/CeO 2 and Cu/α-Fe 2O 3. The selectivity of the samples is compared with that corresponding to Pti/SiO 2. Reduced Cu/Al 2O 3 and Cu/SiO 2 showed lower selectivity to the cinnamyl alcohol (16-22%) than Pt/SiO 2 (35%), at 15% of conversion. Following a calcination at 300 °C both, activity and selectivity of copper catalysts were increased. The calcined surface would hydrogenate CO bond by hydrogen transfer from the solvent. TPR, XRD and FTIR of adsorbed CO showed that Cu (I) species are stabilized on the mesoporous structure of MCM-48. This particular feature renders Cu/MCM-48 a selective catalyst, reaching high selectivity values (51%, at 15% of conversion). Cu/CeO 2 and Cu/α-Fe 2O 3 showed higher selectivity than Pt based catalyst due to a promotion of the catalytic properties of copper by reduced support species.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-31
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/126803
Gutierrez, Victoria Soledad; Alvarez, Mariana; Volpe, María Alicia; Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts; Elsevier Science; Applied Catalysis A: General; 413-414; 31-1-2012; 358-365
0926-860X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/126803
identifier_str_mv Gutierrez, Victoria Soledad; Alvarez, Mariana; Volpe, María Alicia; Liquid phase selective hydrogenation of cinnamaldehyde over copper supported catalysts; Elsevier Science; Applied Catalysis A: General; 413-414; 31-1-2012; 358-365
0926-860X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2011.11.028
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0926860X11006995?via%3Dihub
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Science
publisher.none.fl_str_mv Elsevier Science
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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