Cobalt based catalysts for CO Preferential Oxidation
- Autores
- Gómez, Leticia Ester; Boix, Alicia Viviana
- Año de publicación
- 2019
- Idioma
- inglés
- Tipo de recurso
- parte de libro
- Estado
- versión publicada
- Descripción
- In this work, catalysts based oncobalt supported on ZrO2 and CeO2, and CoCeMnOx were studiedfor the CO preferential oxidation (COPrOx) in rich-hydrogen stream able to feedfuel cells. Among them, the CoCeMnOx formulation showed the highest COconversion at low temperatures, while the cobalt oxide supported on ceriapresented the best selectivity toward CO2.The Co3O4 spinel was theactive phase for the CO Preferential Oxidation detected in all catalysts.However, the CoOx-CeO2 and CoCeMnOx catalysts resulted more activethan cobalt oxide supported on zirconia. The presence of ceria close to cobaltspecies promote the redox properties and enhance the catalytic activity. In theCoCeMnOx catalyst prepared by co-precipitation, the incorporation of Mnrepresented an additional positive effect. The presence of Mn promoted there-oxidation of Co2+ to Co3+ and, consequently, theactivity increased at low temperature. By XRD of CoOx-ZrO2 and theCoOx-CeO2 catalysts, the Co3O4 spinel and ZrO2or CeO2 were identified in agreement with Laser-Raman spectra.At the same time the CoCeMnOx catalyst, prepared by co-precipitation ofprecursor salts, showed an incipient development of a new phase (Mn,Co)3O4mixed spinel, due to the intimate contact between elements.
Fil: Gómez, Leticia Ester. 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: Boix, Alicia Viviana. 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
-
COPROX
(MnCo)3O4 MIXED SPINEL
REDOX COUPLE
CoCeMnOx
CeO2 SUPPORT
XPS
LASER RAMAN SPECTROSCOPY - 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:11336/119211
Ver los metadatos del registro completo
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Cobalt based catalysts for CO Preferential OxidationGómez, Leticia EsterBoix, Alicia VivianaCOPROX(MnCo)3O4 MIXED SPINELREDOX COUPLECoCeMnOxCeO2 SUPPORTXPSLASER RAMAN SPECTROSCOPYhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1In this work, catalysts based oncobalt supported on ZrO2 and CeO2, and CoCeMnOx were studiedfor the CO preferential oxidation (COPrOx) in rich-hydrogen stream able to feedfuel cells. Among them, the CoCeMnOx formulation showed the highest COconversion at low temperatures, while the cobalt oxide supported on ceriapresented the best selectivity toward CO2.The Co3O4 spinel was theactive phase for the CO Preferential Oxidation detected in all catalysts.However, the CoOx-CeO2 and CoCeMnOx catalysts resulted more activethan cobalt oxide supported on zirconia. The presence of ceria close to cobaltspecies promote the redox properties and enhance the catalytic activity. In theCoCeMnOx catalyst prepared by co-precipitation, the incorporation of Mnrepresented an additional positive effect. The presence of Mn promoted there-oxidation of Co2+ to Co3+ and, consequently, theactivity increased at low temperature. By XRD of CoOx-ZrO2 and theCoOx-CeO2 catalysts, the Co3O4 spinel and ZrO2or CeO2 were identified in agreement with Laser-Raman spectra.At the same time the CoCeMnOx catalyst, prepared by co-precipitation ofprecursor salts, showed an incipient development of a new phase (Mn,Co)3O4mixed spinel, due to the intimate contact between elements.Fil: Gómez, Leticia Ester. 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: Boix, Alicia Viviana. 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"; ArgentinaIntechOpenYasemin Yildiz2019info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/bookParthttp://purl.org/coar/resource_type/c_3248info:ar-repo/semantics/parteDeLibroapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/119211Gómez, Leticia Ester; Boix, Alicia Viviana; Cobalt based catalysts for CO Preferential Oxidation; IntechOpen; 2019; 1-16978-1-78984-558-7CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.intechopen.com/chapters/68787info:eu-repo/semantics/altIdentifier/doi/10.5772/intechopen.88976info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:55:54Zoai:ri.conicet.gov.ar:11336/119211instacron: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 09:55:55.303CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Cobalt based catalysts for CO Preferential Oxidation |
title |
Cobalt based catalysts for CO Preferential Oxidation |
spellingShingle |
Cobalt based catalysts for CO Preferential Oxidation Gómez, Leticia Ester COPROX (MnCo)3O4 MIXED SPINEL REDOX COUPLE CoCeMnOx CeO2 SUPPORT XPS LASER RAMAN SPECTROSCOPY |
title_short |
Cobalt based catalysts for CO Preferential Oxidation |
title_full |
Cobalt based catalysts for CO Preferential Oxidation |
title_fullStr |
Cobalt based catalysts for CO Preferential Oxidation |
title_full_unstemmed |
Cobalt based catalysts for CO Preferential Oxidation |
title_sort |
Cobalt based catalysts for CO Preferential Oxidation |
dc.creator.none.fl_str_mv |
Gómez, Leticia Ester Boix, Alicia Viviana |
author |
Gómez, Leticia Ester |
author_facet |
Gómez, Leticia Ester Boix, Alicia Viviana |
author_role |
author |
author2 |
Boix, Alicia Viviana |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Yasemin Yildiz |
dc.subject.none.fl_str_mv |
COPROX (MnCo)3O4 MIXED SPINEL REDOX COUPLE CoCeMnOx CeO2 SUPPORT XPS LASER RAMAN SPECTROSCOPY |
topic |
COPROX (MnCo)3O4 MIXED SPINEL REDOX COUPLE CoCeMnOx CeO2 SUPPORT XPS LASER RAMAN SPECTROSCOPY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
In this work, catalysts based oncobalt supported on ZrO2 and CeO2, and CoCeMnOx were studiedfor the CO preferential oxidation (COPrOx) in rich-hydrogen stream able to feedfuel cells. Among them, the CoCeMnOx formulation showed the highest COconversion at low temperatures, while the cobalt oxide supported on ceriapresented the best selectivity toward CO2.The Co3O4 spinel was theactive phase for the CO Preferential Oxidation detected in all catalysts.However, the CoOx-CeO2 and CoCeMnOx catalysts resulted more activethan cobalt oxide supported on zirconia. The presence of ceria close to cobaltspecies promote the redox properties and enhance the catalytic activity. In theCoCeMnOx catalyst prepared by co-precipitation, the incorporation of Mnrepresented an additional positive effect. The presence of Mn promoted there-oxidation of Co2+ to Co3+ and, consequently, theactivity increased at low temperature. By XRD of CoOx-ZrO2 and theCoOx-CeO2 catalysts, the Co3O4 spinel and ZrO2or CeO2 were identified in agreement with Laser-Raman spectra.At the same time the CoCeMnOx catalyst, prepared by co-precipitation ofprecursor salts, showed an incipient development of a new phase (Mn,Co)3O4mixed spinel, due to the intimate contact between elements. Fil: Gómez, Leticia Ester. 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: Boix, Alicia Viviana. 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 work, catalysts based oncobalt supported on ZrO2 and CeO2, and CoCeMnOx were studiedfor the CO preferential oxidation (COPrOx) in rich-hydrogen stream able to feedfuel cells. Among them, the CoCeMnOx formulation showed the highest COconversion at low temperatures, while the cobalt oxide supported on ceriapresented the best selectivity toward CO2.The Co3O4 spinel was theactive phase for the CO Preferential Oxidation detected in all catalysts.However, the CoOx-CeO2 and CoCeMnOx catalysts resulted more activethan cobalt oxide supported on zirconia. The presence of ceria close to cobaltspecies promote the redox properties and enhance the catalytic activity. In theCoCeMnOx catalyst prepared by co-precipitation, the incorporation of Mnrepresented an additional positive effect. The presence of Mn promoted there-oxidation of Co2+ to Co3+ and, consequently, theactivity increased at low temperature. By XRD of CoOx-ZrO2 and theCoOx-CeO2 catalysts, the Co3O4 spinel and ZrO2or CeO2 were identified in agreement with Laser-Raman spectra.At the same time the CoCeMnOx catalyst, prepared by co-precipitation ofprecursor salts, showed an incipient development of a new phase (Mn,Co)3O4mixed spinel, due to the intimate contact between elements. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/bookPart http://purl.org/coar/resource_type/c_3248 info:ar-repo/semantics/parteDeLibro |
status_str |
publishedVersion |
format |
bookPart |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/119211 Gómez, Leticia Ester; Boix, Alicia Viviana; Cobalt based catalysts for CO Preferential Oxidation; IntechOpen; 2019; 1-16 978-1-78984-558-7 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/119211 |
identifier_str_mv |
Gómez, Leticia Ester; Boix, Alicia Viviana; Cobalt based catalysts for CO Preferential Oxidation; IntechOpen; 2019; 1-16 978-1-78984-558-7 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.intechopen.com/chapters/68787 info:eu-repo/semantics/altIdentifier/doi/10.5772/intechopen.88976 |
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 |
dc.publisher.none.fl_str_mv |
IntechOpen |
publisher.none.fl_str_mv |
IntechOpen |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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1842269372217819136 |
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13.13397 |