Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite
- Autores
- Gutierrez, Laura Beatriz; Miro, Eduardo Ernesto; Ulla, Maria Alicia del H.
- Año de publicación
- 2007
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A thorough characterization of Co-mordenite was carried out using NO-TPD, H2-TPR, Raman, DRX and FTIR with NO as probe molecule. Different cobalt-loading catalysts (8.85, 5.70, 2.91, 2.45 and 1.15 wt.%) were prepared by ion exchange over NH4-mordenite and treated with different procedures (heated on He, O2 and H2). The effect of adding water to the reaction stream at 500 °C on the location of the cobalt species was also analyzed. All catalysts were evaluated for the SCR of NOx with methane as a test reaction both under dry and wet conditions. The NO adsorption capacity depended not only on the Co/Al ratio and pretreatments but also on the presence of Co oxides. In fact, for similar Co/Al ratios, Co2.91MOR showed a lower NO/Co ratio than Co2.45MOR due to the higher Co3O4 concentration in the former. These species probably blocked the main mordenite channels and/or produced the formation of some Co island on the zeolite surface, lowering the amount of surface Co. The main NO surface species detected were dinitrosyl and mononitrosyl. Their stability and relative amount depended on the cobalt species and the pretreatments. Heating in He or H2 induced the stabilization of part of the exchanged Co in less gas-accessible sites, whereas the calcination with O2 involved the mobilization of Co to more external sites. However, those effects were less significant for samples containing Co oxides suggesting that the spinel hinders the Co migration. During the wet reaction treatment, the cobalt mobilization to hidden positions occurred along with the formation of Co-oxides, which negatively affected both the catalytic activity and the NO adsorption capacity.
Fil: Gutierrez, Laura Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Miro, Eduardo Ernesto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Ulla, Maria Alicia del H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina - Materia
-
Co Species On the Scr
Co-Mordenite
Co-No Interaction
No-Tpd - 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:11336/66120
Ver los metadatos del registro completo
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Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordeniteGutierrez, Laura BeatrizMiro, Eduardo ErnestoUlla, Maria Alicia del H.Co Species On the ScrCo-MordeniteCo-No InteractionNo-Tpdhttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2A thorough characterization of Co-mordenite was carried out using NO-TPD, H2-TPR, Raman, DRX and FTIR with NO as probe molecule. Different cobalt-loading catalysts (8.85, 5.70, 2.91, 2.45 and 1.15 wt.%) were prepared by ion exchange over NH4-mordenite and treated with different procedures (heated on He, O2 and H2). The effect of adding water to the reaction stream at 500 °C on the location of the cobalt species was also analyzed. All catalysts were evaluated for the SCR of NOx with methane as a test reaction both under dry and wet conditions. The NO adsorption capacity depended not only on the Co/Al ratio and pretreatments but also on the presence of Co oxides. In fact, for similar Co/Al ratios, Co2.91MOR showed a lower NO/Co ratio than Co2.45MOR due to the higher Co3O4 concentration in the former. These species probably blocked the main mordenite channels and/or produced the formation of some Co island on the zeolite surface, lowering the amount of surface Co. The main NO surface species detected were dinitrosyl and mononitrosyl. Their stability and relative amount depended on the cobalt species and the pretreatments. Heating in He or H2 induced the stabilization of part of the exchanged Co in less gas-accessible sites, whereas the calcination with O2 involved the mobilization of Co to more external sites. However, those effects were less significant for samples containing Co oxides suggesting that the spinel hinders the Co migration. During the wet reaction treatment, the cobalt mobilization to hidden positions occurred along with the formation of Co-oxides, which negatively affected both the catalytic activity and the NO adsorption capacity.Fil: Gutierrez, Laura Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaFil: Miro, Eduardo Ernesto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaFil: Ulla, Maria Alicia del H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaElsevier Science2007-03info: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/11336/66120Gutierrez, Laura Beatriz; Miro, Eduardo Ernesto; Ulla, Maria Alicia del H.; Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite; Elsevier Science; Applied Catalysis A: General; 321; 1; 3-2007; 7-160926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2006.12.022info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:46:57Zoai:ri.conicet.gov.ar:11336/66120instacron: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 09:46:58.188CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
title |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
spellingShingle |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite Gutierrez, Laura Beatriz Co Species On the Scr Co-Mordenite Co-No Interaction No-Tpd |
title_short |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
title_full |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
title_fullStr |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
title_full_unstemmed |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
title_sort |
Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite |
dc.creator.none.fl_str_mv |
Gutierrez, Laura Beatriz Miro, Eduardo Ernesto Ulla, Maria Alicia del H. |
author |
Gutierrez, Laura Beatriz |
author_facet |
Gutierrez, Laura Beatriz Miro, Eduardo Ernesto Ulla, Maria Alicia del H. |
author_role |
author |
author2 |
Miro, Eduardo Ernesto Ulla, Maria Alicia del H. |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Co Species On the Scr Co-Mordenite Co-No Interaction No-Tpd |
topic |
Co Species On the Scr Co-Mordenite Co-No Interaction No-Tpd |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.4 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
A thorough characterization of Co-mordenite was carried out using NO-TPD, H2-TPR, Raman, DRX and FTIR with NO as probe molecule. Different cobalt-loading catalysts (8.85, 5.70, 2.91, 2.45 and 1.15 wt.%) were prepared by ion exchange over NH4-mordenite and treated with different procedures (heated on He, O2 and H2). The effect of adding water to the reaction stream at 500 °C on the location of the cobalt species was also analyzed. All catalysts were evaluated for the SCR of NOx with methane as a test reaction both under dry and wet conditions. The NO adsorption capacity depended not only on the Co/Al ratio and pretreatments but also on the presence of Co oxides. In fact, for similar Co/Al ratios, Co2.91MOR showed a lower NO/Co ratio than Co2.45MOR due to the higher Co3O4 concentration in the former. These species probably blocked the main mordenite channels and/or produced the formation of some Co island on the zeolite surface, lowering the amount of surface Co. The main NO surface species detected were dinitrosyl and mononitrosyl. Their stability and relative amount depended on the cobalt species and the pretreatments. Heating in He or H2 induced the stabilization of part of the exchanged Co in less gas-accessible sites, whereas the calcination with O2 involved the mobilization of Co to more external sites. However, those effects were less significant for samples containing Co oxides suggesting that the spinel hinders the Co migration. During the wet reaction treatment, the cobalt mobilization to hidden positions occurred along with the formation of Co-oxides, which negatively affected both the catalytic activity and the NO adsorption capacity. Fil: Gutierrez, Laura Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina Fil: Miro, Eduardo Ernesto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina Fil: Ulla, Maria Alicia del H.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina |
description |
A thorough characterization of Co-mordenite was carried out using NO-TPD, H2-TPR, Raman, DRX and FTIR with NO as probe molecule. Different cobalt-loading catalysts (8.85, 5.70, 2.91, 2.45 and 1.15 wt.%) were prepared by ion exchange over NH4-mordenite and treated with different procedures (heated on He, O2 and H2). The effect of adding water to the reaction stream at 500 °C on the location of the cobalt species was also analyzed. All catalysts were evaluated for the SCR of NOx with methane as a test reaction both under dry and wet conditions. The NO adsorption capacity depended not only on the Co/Al ratio and pretreatments but also on the presence of Co oxides. In fact, for similar Co/Al ratios, Co2.91MOR showed a lower NO/Co ratio than Co2.45MOR due to the higher Co3O4 concentration in the former. These species probably blocked the main mordenite channels and/or produced the formation of some Co island on the zeolite surface, lowering the amount of surface Co. The main NO surface species detected were dinitrosyl and mononitrosyl. Their stability and relative amount depended on the cobalt species and the pretreatments. Heating in He or H2 induced the stabilization of part of the exchanged Co in less gas-accessible sites, whereas the calcination with O2 involved the mobilization of Co to more external sites. However, those effects were less significant for samples containing Co oxides suggesting that the spinel hinders the Co migration. During the wet reaction treatment, the cobalt mobilization to hidden positions occurred along with the formation of Co-oxides, which negatively affected both the catalytic activity and the NO adsorption capacity. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-03 |
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/11336/66120 Gutierrez, Laura Beatriz; Miro, Eduardo Ernesto; Ulla, Maria Alicia del H.; Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite; Elsevier Science; Applied Catalysis A: General; 321; 1; 3-2007; 7-16 0926-860X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/66120 |
identifier_str_mv |
Gutierrez, Laura Beatriz; Miro, Eduardo Ernesto; Ulla, Maria Alicia del H.; Effect of the location of cobalt species on NO adsorption and NOx-SCR over Co-mordenite; Elsevier Science; Applied Catalysis A: General; 321; 1; 3-2007; 7-16 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/doi/10.1016/j.apcata.2006.12.022 |
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 |
publisher.none.fl_str_mv |
Elsevier Science |
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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1842268827883143168 |
score |
13.13397 |