Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite

Autores
Regenhardt, Silvina Andrea; Meyer, Camilo Ignacio; Trasarti, Andres Fernando; Monzón, A.; Garetto, Teresita Francisca
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In this contribution we present the results of a kinetic study of the catalytic combustion of carbon tetrachloride over several catalysts of Y-zeolite exchanged with Cr, Co, Mn and Fe. The catalysts were prepared by ion exchange and characterized, before and after catalytic tests, by atomic absorption, N2 physisorption (BET surface measurement) and X-ray diffraction. The experimental results have been analyzed using both empirical, -power-law pseudo-homogenous-, and mechanistical -Langmuir-Hinshelwood-models. The catalytic results indicate the following order ofactivity: Y-Co > Y-Cr=Y-Fe > Y-Mn. According to the mechanism assumed to explain the kinetic results obtained, the oxygen molecule adsorbs over the surface Co++ species, and the carbon tetrachloride interacts with the H+ ion on the Brönsted acid site. It was also obtained that the presence of water in the feed is necessary to avoid the deactivation of the catalyst. This effect is probably due to the capacity of water to restore the Brönsted acid sites depleted during the reaction.
Fil: Regenhardt, Silvina Andrea. 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: Meyer, Camilo Ignacio. 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: Trasarti, Andres Fernando. 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: Monzón, A.. Universidad de Zaragoza; España
Fil: Garetto, Teresita Francisca. 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
Carbon tetrachloride combustion
Exchanged Y-zeolite
Co-zeolite
LangmuirHinshelwood mechanism
Kinetic modeling
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:11336/268166
Acceder
id CONICETDig_5316fce3c803b6ded2f6024e435ed66b
oai_identifier_str oai:ri.conicet.gov.ar:11336/268166
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeoliteRegenhardt, Silvina AndreaMeyer, Camilo IgnacioTrasarti, Andres FernandoMonzón, A.Garetto, Teresita FranciscaCarbon tetrachloride combustionExchanged Y-zeoliteCo-zeoliteLangmuirHinshelwood mechanismKinetic modelinghttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2In this contribution we present the results of a kinetic study of the catalytic combustion of carbon tetrachloride over several catalysts of Y-zeolite exchanged with Cr, Co, Mn and Fe. The catalysts were prepared by ion exchange and characterized, before and after catalytic tests, by atomic absorption, N2 physisorption (BET surface measurement) and X-ray diffraction. The experimental results have been analyzed using both empirical, -power-law pseudo-homogenous-, and mechanistical -Langmuir-Hinshelwood-models. The catalytic results indicate the following order ofactivity: Y-Co > Y-Cr=Y-Fe > Y-Mn. According to the mechanism assumed to explain the kinetic results obtained, the oxygen molecule adsorbs over the surface Co++ species, and the carbon tetrachloride interacts with the H+ ion on the Brönsted acid site. It was also obtained that the presence of water in the feed is necessary to avoid the deactivation of the catalyst. This effect is probably due to the capacity of water to restore the Brönsted acid sites depleted during the reaction.Fil: Regenhardt, Silvina Andrea. 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: Meyer, Camilo Ignacio. 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: Trasarti, Andres Fernando. 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: Monzón, A.. Universidad de Zaragoza; EspañaFil: Garetto, Teresita Francisca. 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 SA2012-08info: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/11336/268166Regenhardt, Silvina Andrea; Meyer, Camilo Ignacio; Trasarti, Andres Fernando; Monzón, A.; Garetto, Teresita Francisca; Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite; Elsevier Science SA; Chemical Engineering Journal; 198-199; 8-2012; 18-261385-8947CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.cej.2012.05.055info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:05:31Zoai:ri.conicet.gov.ar:11336/268166instacron: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 10:05:31.602CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
title Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
spellingShingle Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
Regenhardt, Silvina Andrea
Carbon tetrachloride combustion
Exchanged Y-zeolite
Co-zeolite
LangmuirHinshelwood mechanism
Kinetic modeling
title_short Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
title_full Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
title_fullStr Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
title_full_unstemmed Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
title_sort Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite
dc.creator.none.fl_str_mv Regenhardt, Silvina Andrea
Meyer, Camilo Ignacio
Trasarti, Andres Fernando
Monzón, A.
Garetto, Teresita Francisca
author Regenhardt, Silvina Andrea
author_facet Regenhardt, Silvina Andrea
Meyer, Camilo Ignacio
Trasarti, Andres Fernando
Monzón, A.
Garetto, Teresita Francisca
author_role author
author2 Meyer, Camilo Ignacio
Trasarti, Andres Fernando
Monzón, A.
Garetto, Teresita Francisca
author2_role author
author
author
author
dc.subject.none.fl_str_mv Carbon tetrachloride combustion
Exchanged Y-zeolite
Co-zeolite
LangmuirHinshelwood mechanism
Kinetic modeling
topic Carbon tetrachloride combustion
Exchanged Y-zeolite
Co-zeolite
LangmuirHinshelwood mechanism
Kinetic modeling
purl_subject.fl_str_mv https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
dc.description.none.fl_txt_mv In this contribution we present the results of a kinetic study of the catalytic combustion of carbon tetrachloride over several catalysts of Y-zeolite exchanged with Cr, Co, Mn and Fe. The catalysts were prepared by ion exchange and characterized, before and after catalytic tests, by atomic absorption, N2 physisorption (BET surface measurement) and X-ray diffraction. The experimental results have been analyzed using both empirical, -power-law pseudo-homogenous-, and mechanistical -Langmuir-Hinshelwood-models. The catalytic results indicate the following order ofactivity: Y-Co > Y-Cr=Y-Fe > Y-Mn. According to the mechanism assumed to explain the kinetic results obtained, the oxygen molecule adsorbs over the surface Co++ species, and the carbon tetrachloride interacts with the H+ ion on the Brönsted acid site. It was also obtained that the presence of water in the feed is necessary to avoid the deactivation of the catalyst. This effect is probably due to the capacity of water to restore the Brönsted acid sites depleted during the reaction.
Fil: Regenhardt, Silvina Andrea. 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: Meyer, Camilo Ignacio. 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: Trasarti, Andres Fernando. 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: Monzón, A.. Universidad de Zaragoza; España
Fil: Garetto, Teresita Francisca. 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 In this contribution we present the results of a kinetic study of the catalytic combustion of carbon tetrachloride over several catalysts of Y-zeolite exchanged with Cr, Co, Mn and Fe. The catalysts were prepared by ion exchange and characterized, before and after catalytic tests, by atomic absorption, N2 physisorption (BET surface measurement) and X-ray diffraction. The experimental results have been analyzed using both empirical, -power-law pseudo-homogenous-, and mechanistical -Langmuir-Hinshelwood-models. The catalytic results indicate the following order ofactivity: Y-Co > Y-Cr=Y-Fe > Y-Mn. According to the mechanism assumed to explain the kinetic results obtained, the oxygen molecule adsorbs over the surface Co++ species, and the carbon tetrachloride interacts with the H+ ion on the Brönsted acid site. It was also obtained that the presence of water in the feed is necessary to avoid the deactivation of the catalyst. This effect is probably due to the capacity of water to restore the Brönsted acid sites depleted during the reaction.
publishDate 2012
dc.date.none.fl_str_mv 2012-08
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/11336/268166
Regenhardt, Silvina Andrea; Meyer, Camilo Ignacio; Trasarti, Andres Fernando; Monzón, A.; Garetto, Teresita Francisca; Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite; Elsevier Science SA; Chemical Engineering Journal; 198-199; 8-2012; 18-26
1385-8947
CONICET Digital
CONICET
url http://hdl.handle.net/11336/268166
identifier_str_mv Regenhardt, Silvina Andrea; Meyer, Camilo Ignacio; Trasarti, Andres Fernando; Monzón, A.; Garetto, Teresita Francisca; Catalytic oxidation of carbon tetrachloride on metal exchanged Y-zeolite; Elsevier Science SA; Chemical Engineering Journal; 198-199; 8-2012; 18-26
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.2012.05.055
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 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
_version_ 1844613892491182080
score 13.070432

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