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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/21224
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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 Técnicas2025-09-29T09:49:11Zoai: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:34982025-09-29 09:49:12.23CONICET 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) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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1844613524917059584 |
score |
13.070432 |