Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts

Autores
Maccarrone, María Juliana; Lederhos, Cecilia Rosa; Torres, Gerardo Carlos; Betti, Carolina Paola; Coloma Pascual, Fernando; Quiroga, Monica Esther; Yori, Juan Carlos
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Partial hydrogenation of alkynes has industrial and academic relevance on a large scale, especially those with high selectivities. To increase the activity, selectivity and lifetime of low-loaded Pd monometallic catalyst, the development of bimetallic systems has been investigated. In this work Pd mono (Pd/A) and bimetallic catalysts (PdNi/A and WPd/A) supported on γ-alumina with low metal content are prepared and evaluated during the partial hydrogenation of 3-hexyne at mild conditions. XPS, XRD, TPR and hydrogen chemisorption techniques are used for the characterization, suggesting different kind of Pd species on the mono and bimetallic catalysts. Furthermore, XPS results indicate the presence of electron rich and electron-deficient palladium species (Pd δ- and Pd n+, with δ close to 0 and 0 < n < 2, respectively), electron-deficient species of nickel (Ni n+, with n close to 2) and of W ρ+ (with ρ < 6) on the surface of the bimetallic systems. The Lindlar commercial catalyst, commonly used in these types of reactions is used for comparative purposes. Bimetallic catalysts showed higher activities and very similar selectivities (>93%) than the monometallic system and further than the Lindlar catalyst. The rank of activity order is: WPd/A > PdNi/A > Pd/A Lindlar.
Fil: Maccarrone, María Juliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Lederhos, Cecilia Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Torres, Gerardo Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
Fil: Betti, Carolina Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Coloma Pascual, Fernando. Universidad de Alicante. Facultad de Ciencias; España
Fil: Quiroga, Monica Esther. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
Fil: Yori, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
Materia
ALKYNE
BIMETALLIC CATALYSTS
LINDLAR
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:11336/212097

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network_name_str CONICET Digital (CONICET)
spelling Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalystsMaccarrone, María JulianaLederhos, Cecilia RosaTorres, Gerardo CarlosBetti, Carolina PaolaColoma Pascual, FernandoQuiroga, Monica EstherYori, Juan CarlosALKYNEBIMETALLIC CATALYSTSLINDLARSELECTIVE HYDROGENATIONhttps://purl.org/becyt/ford/2.9https://purl.org/becyt/ford/2Partial hydrogenation of alkynes has industrial and academic relevance on a large scale, especially those with high selectivities. To increase the activity, selectivity and lifetime of low-loaded Pd monometallic catalyst, the development of bimetallic systems has been investigated. In this work Pd mono (Pd/A) and bimetallic catalysts (PdNi/A and WPd/A) supported on γ-alumina with low metal content are prepared and evaluated during the partial hydrogenation of 3-hexyne at mild conditions. XPS, XRD, TPR and hydrogen chemisorption techniques are used for the characterization, suggesting different kind of Pd species on the mono and bimetallic catalysts. Furthermore, XPS results indicate the presence of electron rich and electron-deficient palladium species (Pd δ- and Pd n+, with δ close to 0 and 0 < n < 2, respectively), electron-deficient species of nickel (Ni n+, with n close to 2) and of W ρ+ (with ρ < 6) on the surface of the bimetallic systems. The Lindlar commercial catalyst, commonly used in these types of reactions is used for comparative purposes. Bimetallic catalysts showed higher activities and very similar selectivities (>93%) than the monometallic system and further than the Lindlar catalyst. The rank of activity order is: WPd/A > PdNi/A > Pd/A Lindlar.Fil: Maccarrone, María Juliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Lederhos, Cecilia Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Torres, Gerardo Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; ArgentinaFil: Betti, Carolina Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; ArgentinaFil: Coloma Pascual, Fernando. Universidad de Alicante. Facultad de Ciencias; EspañaFil: Quiroga, Monica Esther. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; ArgentinaFil: Yori, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; ArgentinaElsevier Science2012-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/212097Maccarrone, María Juliana; Lederhos, Cecilia Rosa; Torres, Gerardo Carlos; Betti, Carolina Paola; Coloma Pascual, Fernando; et al.; Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts; Elsevier Science; Applied Catalysis A: General; 441-442; 10-2012; 90-980926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X12004668info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2012.07.016info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:42:33Zoai:ri.conicet.gov.ar:11336/212097instacron: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:34982025-09-29 10:42:33.651CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
title Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
spellingShingle Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
Maccarrone, María Juliana
ALKYNE
BIMETALLIC CATALYSTS
LINDLAR
SELECTIVE HYDROGENATION
title_short Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
title_full Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
title_fullStr Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
title_full_unstemmed Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
title_sort Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts
dc.creator.none.fl_str_mv Maccarrone, María Juliana
Lederhos, Cecilia Rosa
Torres, Gerardo Carlos
Betti, Carolina Paola
Coloma Pascual, Fernando
Quiroga, Monica Esther
Yori, Juan Carlos
author Maccarrone, María Juliana
author_facet Maccarrone, María Juliana
Lederhos, Cecilia Rosa
Torres, Gerardo Carlos
Betti, Carolina Paola
Coloma Pascual, Fernando
Quiroga, Monica Esther
Yori, Juan Carlos
author_role author
author2 Lederhos, Cecilia Rosa
Torres, Gerardo Carlos
Betti, Carolina Paola
Coloma Pascual, Fernando
Quiroga, Monica Esther
Yori, Juan Carlos
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv ALKYNE
BIMETALLIC CATALYSTS
LINDLAR
SELECTIVE HYDROGENATION
topic ALKYNE
BIMETALLIC CATALYSTS
LINDLAR
SELECTIVE HYDROGENATION
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.9
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv Partial hydrogenation of alkynes has industrial and academic relevance on a large scale, especially those with high selectivities. To increase the activity, selectivity and lifetime of low-loaded Pd monometallic catalyst, the development of bimetallic systems has been investigated. In this work Pd mono (Pd/A) and bimetallic catalysts (PdNi/A and WPd/A) supported on γ-alumina with low metal content are prepared and evaluated during the partial hydrogenation of 3-hexyne at mild conditions. XPS, XRD, TPR and hydrogen chemisorption techniques are used for the characterization, suggesting different kind of Pd species on the mono and bimetallic catalysts. Furthermore, XPS results indicate the presence of electron rich and electron-deficient palladium species (Pd δ- and Pd n+, with δ close to 0 and 0 < n < 2, respectively), electron-deficient species of nickel (Ni n+, with n close to 2) and of W ρ+ (with ρ < 6) on the surface of the bimetallic systems. The Lindlar commercial catalyst, commonly used in these types of reactions is used for comparative purposes. Bimetallic catalysts showed higher activities and very similar selectivities (>93%) than the monometallic system and further than the Lindlar catalyst. The rank of activity order is: WPd/A > PdNi/A > Pd/A Lindlar.
Fil: Maccarrone, María Juliana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Lederhos, Cecilia Rosa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Torres, Gerardo Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
Fil: Betti, Carolina Paola. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina
Fil: Coloma Pascual, Fernando. Universidad de Alicante. Facultad de Ciencias; España
Fil: Quiroga, Monica Esther. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
Fil: Yori, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones en Catálisis y Petroquímica "Ing. José Miguel Parera"; Argentina. Universidad Nacional del Litoral. Facultad de Ingeniería Química; Argentina
description Partial hydrogenation of alkynes has industrial and academic relevance on a large scale, especially those with high selectivities. To increase the activity, selectivity and lifetime of low-loaded Pd monometallic catalyst, the development of bimetallic systems has been investigated. In this work Pd mono (Pd/A) and bimetallic catalysts (PdNi/A and WPd/A) supported on γ-alumina with low metal content are prepared and evaluated during the partial hydrogenation of 3-hexyne at mild conditions. XPS, XRD, TPR and hydrogen chemisorption techniques are used for the characterization, suggesting different kind of Pd species on the mono and bimetallic catalysts. Furthermore, XPS results indicate the presence of electron rich and electron-deficient palladium species (Pd δ- and Pd n+, with δ close to 0 and 0 < n < 2, respectively), electron-deficient species of nickel (Ni n+, with n close to 2) and of W ρ+ (with ρ < 6) on the surface of the bimetallic systems. The Lindlar commercial catalyst, commonly used in these types of reactions is used for comparative purposes. Bimetallic catalysts showed higher activities and very similar selectivities (>93%) than the monometallic system and further than the Lindlar catalyst. The rank of activity order is: WPd/A > PdNi/A > Pd/A Lindlar.
publishDate 2012
dc.date.none.fl_str_mv 2012-10
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/11336/212097
Maccarrone, María Juliana; Lederhos, Cecilia Rosa; Torres, Gerardo Carlos; Betti, Carolina Paola; Coloma Pascual, Fernando; et al.; Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts; Elsevier Science; Applied Catalysis A: General; 441-442; 10-2012; 90-98
0926-860X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/212097
identifier_str_mv Maccarrone, María Juliana; Lederhos, Cecilia Rosa; Torres, Gerardo Carlos; Betti, Carolina Paola; Coloma Pascual, Fernando; et al.; Partial hydrogenation of 3-hexyne over low-loaded palladium mono and bimetallic catalysts; Elsevier Science; Applied Catalysis A: General; 441-442; 10-2012; 90-98
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/url/https://www.sciencedirect.com/science/article/pii/S0926860X12004668
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2012.07.016
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
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)
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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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