Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts

Autores
Campo, Betiana Carla; Petit, Corinne; Volpe, María Alicia
Año de publicación
2008
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 °C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. © 2007 Elsevier Inc. All rights reserved.
Fil: Campo, Betiana Carla. 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: Petit, Corinne. Centre National de la Recherche Scientifique; Francia
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
Ceria
Crotonaldehyde Hydrogenation
Gold
Selective Hydrogenation
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:11336/62300

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network_name_str CONICET Digital (CONICET)
spelling Hydrogenation of crotonaldehyde on different Au/CeO2 catalystsCampo, Betiana CarlaPetit, CorinneVolpe, María AliciaCeriaCrotonaldehyde HydrogenationGoldSelective Hydrogenationhttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 °C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. © 2007 Elsevier Inc. All rights reserved.Fil: Campo, Betiana Carla. 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: Petit, Corinne. Centre National de la Recherche Scientifique; FranciaFil: 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; ArgentinaAcademic Press Inc Elsevier Science2008-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/62300Campo, Betiana Carla; Petit, Corinne; Volpe, María Alicia; Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts; Academic Press Inc Elsevier Science; Journal of Catalysis; 254; 1; 2-2008; 71-780021-9517CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.jcat.2007.11.018info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0021951707004411info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:08:43Zoai:ri.conicet.gov.ar:11336/62300instacron: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 10:08:44.374CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
title Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
spellingShingle Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
Campo, Betiana Carla
Ceria
Crotonaldehyde Hydrogenation
Gold
Selective Hydrogenation
title_short Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
title_full Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
title_fullStr Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
title_full_unstemmed Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
title_sort Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
dc.creator.none.fl_str_mv Campo, Betiana Carla
Petit, Corinne
Volpe, María Alicia
author Campo, Betiana Carla
author_facet Campo, Betiana Carla
Petit, Corinne
Volpe, María Alicia
author_role author
author2 Petit, Corinne
Volpe, María Alicia
author2_role author
author
dc.subject.none.fl_str_mv Ceria
Crotonaldehyde Hydrogenation
Gold
Selective Hydrogenation
topic Ceria
Crotonaldehyde Hydrogenation
Gold
Selective Hydrogenation
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 °C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. © 2007 Elsevier Inc. All rights reserved.
Fil: Campo, Betiana Carla. 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: Petit, Corinne. Centre National de la Recherche Scientifique; Francia
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 gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 °C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. © 2007 Elsevier Inc. All rights reserved.
publishDate 2008
dc.date.none.fl_str_mv 2008-02
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/11336/62300
Campo, Betiana Carla; Petit, Corinne; Volpe, María Alicia; Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts; Academic Press Inc Elsevier Science; Journal of Catalysis; 254; 1; 2-2008; 71-78
0021-9517
CONICET Digital
CONICET
url http://hdl.handle.net/11336/62300
identifier_str_mv Campo, Betiana Carla; Petit, Corinne; Volpe, María Alicia; Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts; Academic Press Inc Elsevier Science; Journal of Catalysis; 254; 1; 2-2008; 71-78
0021-9517
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.jcat.2007.11.018
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0021951707004411
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
dc.publisher.none.fl_str_mv Academic Press Inc Elsevier Science
publisher.none.fl_str_mv Academic Press Inc 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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