Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation

Autores
Vilella, Irene María Julieta; de Miguel, Sergio Ruben; Scelza, Osvaldo Antonio
Año de publicación
2005
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The catalytic behavior of the Pt (1 wt%) catalysts supported on purified activated carbon felt (ACF) and powder carbon (C) has been studied in the nitrobenzene (NBZ) hydrogenation reaction in liquid phase after activation under a H2 atmosphere between 298 and 623 K. Hydrogen chemisorption measurements, temperature-programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS) were used to characterize the metallic phase of the catalysts. For Pt/ACF catalysts, the catalytic activity in nitrobenzene hydrogenation after reduction at 298 K was very high and it decreased as the reduction temperature increased up to 373 K. On the other hand, the Pt/C catalyst after reduction at 298 K was inactive. The activity of the Pt/C catalysts increased in a moderate way when the reduction temperature increases up to 373 K. Between 373 and 623 K of reduction temperature, the hydrogenation rate was modified in a minor proportion for both catalysts. The Pt/ACF catalyst previously reduced at 298 K showed a lag step before the reaction ignition. This effect could be attributed to the tendency the metallic centers have to conform the proper arrangement to hydrogenate the nitrobenzene molecule.
Fil: Vilella, Irene María Julieta. 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: de Miguel, Sergio Ruben. 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: Scelza, Osvaldo Antonio. 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
Materia
ACTIVATED CARBON FELT
ACTIVATED CARBON POWDER
NITROBENZENE HYDROGENATION
PT-SUPPORTED CATALYSTS
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:11336/78027

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oai_identifier_str oai:ri.conicet.gov.ar:11336/78027
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenationVilella, Irene María Julietade Miguel, Sergio RubenScelza, Osvaldo AntonioACTIVATED CARBON FELTACTIVATED CARBON POWDERNITROBENZENE HYDROGENATIONPT-SUPPORTED CATALYSTShttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2The catalytic behavior of the Pt (1 wt%) catalysts supported on purified activated carbon felt (ACF) and powder carbon (C) has been studied in the nitrobenzene (NBZ) hydrogenation reaction in liquid phase after activation under a H2 atmosphere between 298 and 623 K. Hydrogen chemisorption measurements, temperature-programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS) were used to characterize the metallic phase of the catalysts. For Pt/ACF catalysts, the catalytic activity in nitrobenzene hydrogenation after reduction at 298 K was very high and it decreased as the reduction temperature increased up to 373 K. On the other hand, the Pt/C catalyst after reduction at 298 K was inactive. The activity of the Pt/C catalysts increased in a moderate way when the reduction temperature increases up to 373 K. Between 373 and 623 K of reduction temperature, the hydrogenation rate was modified in a minor proportion for both catalysts. The Pt/ACF catalyst previously reduced at 298 K showed a lag step before the reaction ignition. This effect could be attributed to the tendency the metallic centers have to conform the proper arrangement to hydrogenate the nitrobenzene molecule.Fil: Vilella, Irene María Julieta. 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: de Miguel, Sergio Ruben. 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: Scelza, Osvaldo Antonio. 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"; ArgentinaElsevier Science SA2005-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/78027Vilella, Irene María Julieta; de Miguel, Sergio Ruben; Scelza, Osvaldo Antonio; Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation; Elsevier Science SA; Chemical Engineering Journal; 114; 1-3; 11-2005; 33-381385-8947CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.cej.2005.08.011info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:49:43Zoai:ri.conicet.gov.ar:11336/78027instacron: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 09:49:43.434CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
title Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
spellingShingle Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
Vilella, Irene María Julieta
ACTIVATED CARBON FELT
ACTIVATED CARBON POWDER
NITROBENZENE HYDROGENATION
PT-SUPPORTED CATALYSTS
title_short Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
title_full Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
title_fullStr Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
title_full_unstemmed Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
title_sort Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation
dc.creator.none.fl_str_mv Vilella, Irene María Julieta
de Miguel, Sergio Ruben
Scelza, Osvaldo Antonio
author Vilella, Irene María Julieta
author_facet Vilella, Irene María Julieta
de Miguel, Sergio Ruben
Scelza, Osvaldo Antonio
author_role author
author2 de Miguel, Sergio Ruben
Scelza, Osvaldo Antonio
author2_role author
author
dc.subject.none.fl_str_mv ACTIVATED CARBON FELT
ACTIVATED CARBON POWDER
NITROBENZENE HYDROGENATION
PT-SUPPORTED CATALYSTS
topic ACTIVATED CARBON FELT
ACTIVATED CARBON POWDER
NITROBENZENE HYDROGENATION
PT-SUPPORTED CATALYSTS
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 catalytic behavior of the Pt (1 wt%) catalysts supported on purified activated carbon felt (ACF) and powder carbon (C) has been studied in the nitrobenzene (NBZ) hydrogenation reaction in liquid phase after activation under a H2 atmosphere between 298 and 623 K. Hydrogen chemisorption measurements, temperature-programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS) were used to characterize the metallic phase of the catalysts. For Pt/ACF catalysts, the catalytic activity in nitrobenzene hydrogenation after reduction at 298 K was very high and it decreased as the reduction temperature increased up to 373 K. On the other hand, the Pt/C catalyst after reduction at 298 K was inactive. The activity of the Pt/C catalysts increased in a moderate way when the reduction temperature increases up to 373 K. Between 373 and 623 K of reduction temperature, the hydrogenation rate was modified in a minor proportion for both catalysts. The Pt/ACF catalyst previously reduced at 298 K showed a lag step before the reaction ignition. This effect could be attributed to the tendency the metallic centers have to conform the proper arrangement to hydrogenate the nitrobenzene molecule.
Fil: Vilella, Irene María Julieta. 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: de Miguel, Sergio Ruben. 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: Scelza, Osvaldo Antonio. 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
description The catalytic behavior of the Pt (1 wt%) catalysts supported on purified activated carbon felt (ACF) and powder carbon (C) has been studied in the nitrobenzene (NBZ) hydrogenation reaction in liquid phase after activation under a H2 atmosphere between 298 and 623 K. Hydrogen chemisorption measurements, temperature-programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS) were used to characterize the metallic phase of the catalysts. For Pt/ACF catalysts, the catalytic activity in nitrobenzene hydrogenation after reduction at 298 K was very high and it decreased as the reduction temperature increased up to 373 K. On the other hand, the Pt/C catalyst after reduction at 298 K was inactive. The activity of the Pt/C catalysts increased in a moderate way when the reduction temperature increases up to 373 K. Between 373 and 623 K of reduction temperature, the hydrogenation rate was modified in a minor proportion for both catalysts. The Pt/ACF catalyst previously reduced at 298 K showed a lag step before the reaction ignition. This effect could be attributed to the tendency the metallic centers have to conform the proper arrangement to hydrogenate the nitrobenzene molecule.
publishDate 2005
dc.date.none.fl_str_mv 2005-11
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/11336/78027
Vilella, Irene María Julieta; de Miguel, Sergio Ruben; Scelza, Osvaldo Antonio; Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation; Elsevier Science SA; Chemical Engineering Journal; 114; 1-3; 11-2005; 33-38
1385-8947
CONICET Digital
CONICET
url http://hdl.handle.net/11336/78027
identifier_str_mv Vilella, Irene María Julieta; de Miguel, Sergio Ruben; Scelza, Osvaldo Antonio; Study of the performance of Pt catalysts supported on activated carbon felt and granular carbon for nitrobenzene hydrogenation; Elsevier Science SA; Chemical Engineering Journal; 114; 1-3; 11-2005; 33-38
1385-8947
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.cej.2005.08.011
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
dc.publisher.none.fl_str_mv Elsevier Science SA
publisher.none.fl_str_mv Elsevier Science SA
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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