Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes

Autores
Vicerich, Maria Ana; Benitez, Bibiana M.; Especel, Catherine; Epron, Florence; Pieck, Carlos Luis
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The influence of Ir content on the properties of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes was studied. It was found that these catalysts display a strong Pt–Ir interaction but only a weak metal–support interaction. Catalyst acidities depend on the metal loading, but opposite effects were observed on alumina (decrease) or titania (increase) as the metal loading increased. The results obtained from test reactions (cyclohexane dehydrogenation and cyclopentane hydrogenolysis) showed that titania supported catalysts were less active than their alumina supported counterparts. This behavior could be due to the partial blockage of metallic sites by migrated TiOx species and the sinterization of metallic phase during the reduction step. The methylcyclopentane ring opening reaction was found to occur through a partially selective mechanism, and an increase in activity as the Ir loading increased was observed. The selective mechanism was favored by higher total metal loadings, possibly due to an increase in the size of metallic aggregates. Alumina supported catalysts present higher ring opening selectivities. The activity for decalin ring opening increased both with metal loading and reaction temperature level.
Fil: Vicerich, Maria Ana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
Fil: Benitez, Bibiana M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
Fil: Especel, Catherine. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia
Fil: Epron, Florence. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia
Fil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
Materia
Selective Ring Opening
Pt–Ir
Decalin
Methylcyclopentane
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:11336/21224
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/21224
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network_name_str CONICET Digital (CONICET)
spelling Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenesVicerich, Maria AnaBenitez, Bibiana M.Especel, CatherineEpron, FlorencePieck, Carlos LuisSelective Ring OpeningPt–IrDecalinMethylcyclopentanehttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2The influence of Ir content on the properties of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes was studied. It was found that these catalysts display a strong Pt–Ir interaction but only a weak metal–support interaction. Catalyst acidities depend on the metal loading, but opposite effects were observed on alumina (decrease) or titania (increase) as the metal loading increased. The results obtained from test reactions (cyclohexane dehydrogenation and cyclopentane hydrogenolysis) showed that titania supported catalysts were less active than their alumina supported counterparts. This behavior could be due to the partial blockage of metallic sites by migrated TiOx species and the sinterization of metallic phase during the reduction step. The methylcyclopentane ring opening reaction was found to occur through a partially selective mechanism, and an increase in activity as the Ir loading increased was observed. The selective mechanism was favored by higher total metal loadings, possibly due to an increase in the size of metallic aggregates. Alumina supported catalysts present higher ring opening selectivities. The activity for decalin ring opening increased both with metal loading and reaction temperature level.Fil: Vicerich, Maria Ana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; ArgentinaFil: Benitez, Bibiana M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; ArgentinaFil: Especel, Catherine. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; FranciaFil: Epron, Florence. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; FranciaFil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; ArgentinaElsevier2013-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/21224Vicerich, Maria Ana; Benitez, Bibiana M.; Especel, Catherine; Epron, Florence; Pieck, Carlos Luis; Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes; Elsevier; Applied Catalysis A: General; 453; 2-2013; 167-1740926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0926860X12007740info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2012.12.015info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:43:15Zoai:ri.conicet.gov.ar:11336/21224instacron: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:34982025-10-15 14:43:16.271CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
title Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
spellingShingle Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
Vicerich, Maria Ana
Selective Ring Opening
Pt–Ir
Decalin
Methylcyclopentane
title_short Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
title_full Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
title_fullStr Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
title_full_unstemmed Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
title_sort Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes
dc.creator.none.fl_str_mv Vicerich, Maria Ana
Benitez, Bibiana M.
Especel, Catherine
Epron, Florence
Pieck, Carlos Luis
author Vicerich, Maria Ana
author_facet Vicerich, Maria Ana
Benitez, Bibiana M.
Especel, Catherine
Epron, Florence
Pieck, Carlos Luis
author_role author
author2 Benitez, Bibiana M.
Especel, Catherine
Epron, Florence
Pieck, Carlos Luis
author2_role author
author
author
author
dc.subject.none.fl_str_mv Selective Ring Opening
Pt–Ir
Decalin
Methylcyclopentane
topic Selective Ring Opening
Pt–Ir
Decalin
Methylcyclopentane
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 influence of Ir content on the properties of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes was studied. It was found that these catalysts display a strong Pt–Ir interaction but only a weak metal–support interaction. Catalyst acidities depend on the metal loading, but opposite effects were observed on alumina (decrease) or titania (increase) as the metal loading increased. The results obtained from test reactions (cyclohexane dehydrogenation and cyclopentane hydrogenolysis) showed that titania supported catalysts were less active than their alumina supported counterparts. This behavior could be due to the partial blockage of metallic sites by migrated TiOx species and the sinterization of metallic phase during the reduction step. The methylcyclopentane ring opening reaction was found to occur through a partially selective mechanism, and an increase in activity as the Ir loading increased was observed. The selective mechanism was favored by higher total metal loadings, possibly due to an increase in the size of metallic aggregates. Alumina supported catalysts present higher ring opening selectivities. The activity for decalin ring opening increased both with metal loading and reaction temperature level.
Fil: Vicerich, Maria Ana. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
Fil: Benitez, Bibiana M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
Fil: Especel, Catherine. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia
Fil: Epron, Florence. Université de Poitiers. Institut de Chimie des Milieux et Matériaux de Poitier; Francia
Fil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera". Universidad Nacional del Litoral. Instituto de Investigaciones En Catalisis y Petroquímica "ing. Jose Miguel Parera"; Argentina
description The influence of Ir content on the properties of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes was studied. It was found that these catalysts display a strong Pt–Ir interaction but only a weak metal–support interaction. Catalyst acidities depend on the metal loading, but opposite effects were observed on alumina (decrease) or titania (increase) as the metal loading increased. The results obtained from test reactions (cyclohexane dehydrogenation and cyclopentane hydrogenolysis) showed that titania supported catalysts were less active than their alumina supported counterparts. This behavior could be due to the partial blockage of metallic sites by migrated TiOx species and the sinterization of metallic phase during the reduction step. The methylcyclopentane ring opening reaction was found to occur through a partially selective mechanism, and an increase in activity as the Ir loading increased was observed. The selective mechanism was favored by higher total metal loadings, possibly due to an increase in the size of metallic aggregates. Alumina supported catalysts present higher ring opening selectivities. The activity for decalin ring opening increased both with metal loading and reaction temperature level.
publishDate 2013
dc.date.none.fl_str_mv 2013-02
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/11336/21224
Vicerich, Maria Ana; Benitez, Bibiana M.; Especel, Catherine; Epron, Florence; Pieck, Carlos Luis; Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes; Elsevier; Applied Catalysis A: General; 453; 2-2013; 167-174
0926-860X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/21224
identifier_str_mv Vicerich, Maria Ana; Benitez, Bibiana M.; Especel, Catherine; Epron, Florence; Pieck, Carlos Luis; Influence of iridium content on the behavior of Pt-Ir/Al2O3 and Pt-Ir/TiO2 catalysts for selective ring opening of naphthenes; Elsevier; Applied Catalysis A: General; 453; 2-2013; 167-174
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/http://www.sciencedirect.com/science/article/pii/S0926860X12007740
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2012.12.015
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
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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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score 13.22299

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