Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts
- Autores
- Sanchez, Barbara Sabrina; Querini, Carlos Alberto; Miro, Eduardo Ernesto
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- In this paper we analyzed the effect of potassium on the thermal stability of NOx species adsorbed on lanthanum supported catalysts. Catalysts containing only noble metals (Pt and/or Rh) or noble metals and potassium were prepared. The soot combustion process in the presence of NOx species previously adsorbed on the catalysts has also been studied in order to evaluate the possibility of using these materials for the simultaneous abatement of soot and nitrogen oxides. It was shown that lanthanum supported catalysts containing Pt and/or Rh exhibited great capacity to decompose previously adsorbed nitrate species in an inert atmosphere. When potassium was added to the formulation this capacity was modified, which proves the existence of a strong interaction between the potassium and noble metals. Such interaction was much stronger in the case of platinum and, therefore, the Pt-K catalyst was able to decompose only a small fraction of the adsorbed compounds in helium stream. However, when decomposition took place in reducing atmosphere (H2), the NO x species were reduced at a lower temperature in the presence of platinum. For all the lanthanum supported catalysts under study, the activity for soot combustion increased in the presence of previously adsorbed nitrate species, even though some of the samples were not very effective for NO x decomposition. This indicates that NOx species are capable of reacting with soot in oxidant atmosphere without the need for their previous decomposition, as previously observed in an inert stream.
Fil: Sanchez, Barbara Sabrina. 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: Querini, Carlos Alberto. 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: Miro, Eduardo Ernesto. 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
-
Nox Reduction
Potassium
Pt
Rh - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/54015
Ver los metadatos del registro completo
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Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalystsSanchez, Barbara SabrinaQuerini, Carlos AlbertoMiro, Eduardo ErnestoNox ReductionPotassiumPtRhhttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2In this paper we analyzed the effect of potassium on the thermal stability of NOx species adsorbed on lanthanum supported catalysts. Catalysts containing only noble metals (Pt and/or Rh) or noble metals and potassium were prepared. The soot combustion process in the presence of NOx species previously adsorbed on the catalysts has also been studied in order to evaluate the possibility of using these materials for the simultaneous abatement of soot and nitrogen oxides. It was shown that lanthanum supported catalysts containing Pt and/or Rh exhibited great capacity to decompose previously adsorbed nitrate species in an inert atmosphere. When potassium was added to the formulation this capacity was modified, which proves the existence of a strong interaction between the potassium and noble metals. Such interaction was much stronger in the case of platinum and, therefore, the Pt-K catalyst was able to decompose only a small fraction of the adsorbed compounds in helium stream. However, when decomposition took place in reducing atmosphere (H2), the NO x species were reduced at a lower temperature in the presence of platinum. For all the lanthanum supported catalysts under study, the activity for soot combustion increased in the presence of previously adsorbed nitrate species, even though some of the samples were not very effective for NO x decomposition. This indicates that NOx species are capable of reacting with soot in oxidant atmosphere without the need for their previous decomposition, as previously observed in an inert stream.Fil: Sanchez, Barbara Sabrina. 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: Querini, Carlos Alberto. 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: Miro, Eduardo Ernesto. 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 Science2011-01info: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/11336/54015Sanchez, Barbara Sabrina; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts; Elsevier Science; Applied Catalysis A: General; 392; 1-2; 1-2011; 158-1650926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2010.11.003info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X10007568info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:34:08Zoai:ri.conicet.gov.ar:11336/54015instacron: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:34982025-10-22 11:34:09.133CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| title |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| spellingShingle |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts Sanchez, Barbara Sabrina Nox Reduction Potassium Pt Rh |
| title_short |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| title_full |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| title_fullStr |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| title_full_unstemmed |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| title_sort |
Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts |
| dc.creator.none.fl_str_mv |
Sanchez, Barbara Sabrina Querini, Carlos Alberto Miro, Eduardo Ernesto |
| author |
Sanchez, Barbara Sabrina |
| author_facet |
Sanchez, Barbara Sabrina Querini, Carlos Alberto Miro, Eduardo Ernesto |
| author_role |
author |
| author2 |
Querini, Carlos Alberto Miro, Eduardo Ernesto |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Nox Reduction Potassium Pt Rh |
| topic |
Nox Reduction Potassium Pt Rh |
| 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 paper we analyzed the effect of potassium on the thermal stability of NOx species adsorbed on lanthanum supported catalysts. Catalysts containing only noble metals (Pt and/or Rh) or noble metals and potassium were prepared. The soot combustion process in the presence of NOx species previously adsorbed on the catalysts has also been studied in order to evaluate the possibility of using these materials for the simultaneous abatement of soot and nitrogen oxides. It was shown that lanthanum supported catalysts containing Pt and/or Rh exhibited great capacity to decompose previously adsorbed nitrate species in an inert atmosphere. When potassium was added to the formulation this capacity was modified, which proves the existence of a strong interaction between the potassium and noble metals. Such interaction was much stronger in the case of platinum and, therefore, the Pt-K catalyst was able to decompose only a small fraction of the adsorbed compounds in helium stream. However, when decomposition took place in reducing atmosphere (H2), the NO x species were reduced at a lower temperature in the presence of platinum. For all the lanthanum supported catalysts under study, the activity for soot combustion increased in the presence of previously adsorbed nitrate species, even though some of the samples were not very effective for NO x decomposition. This indicates that NOx species are capable of reacting with soot in oxidant atmosphere without the need for their previous decomposition, as previously observed in an inert stream. Fil: Sanchez, Barbara Sabrina. 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: Querini, Carlos Alberto. 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: Miro, Eduardo Ernesto. 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 paper we analyzed the effect of potassium on the thermal stability of NOx species adsorbed on lanthanum supported catalysts. Catalysts containing only noble metals (Pt and/or Rh) or noble metals and potassium were prepared. The soot combustion process in the presence of NOx species previously adsorbed on the catalysts has also been studied in order to evaluate the possibility of using these materials for the simultaneous abatement of soot and nitrogen oxides. It was shown that lanthanum supported catalysts containing Pt and/or Rh exhibited great capacity to decompose previously adsorbed nitrate species in an inert atmosphere. When potassium was added to the formulation this capacity was modified, which proves the existence of a strong interaction between the potassium and noble metals. Such interaction was much stronger in the case of platinum and, therefore, the Pt-K catalyst was able to decompose only a small fraction of the adsorbed compounds in helium stream. However, when decomposition took place in reducing atmosphere (H2), the NO x species were reduced at a lower temperature in the presence of platinum. For all the lanthanum supported catalysts under study, the activity for soot combustion increased in the presence of previously adsorbed nitrate species, even though some of the samples were not very effective for NO x decomposition. This indicates that NOx species are capable of reacting with soot in oxidant atmosphere without the need for their previous decomposition, as previously observed in an inert stream. |
| publishDate |
2011 |
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2011-01 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
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publishedVersion |
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http://hdl.handle.net/11336/54015 Sanchez, Barbara Sabrina; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts; Elsevier Science; Applied Catalysis A: General; 392; 1-2; 1-2011; 158-165 0926-860X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/54015 |
| identifier_str_mv |
Sanchez, Barbara Sabrina; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Potassium effect on the thermal stability and reactivity of NOx species adsorbed on Pt,Rh/La2O3 catalysts; Elsevier Science; Applied Catalysis A: General; 392; 1-2; 1-2011; 158-165 0926-860X CONICET Digital CONICET |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2010.11.003 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X10007568 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
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application/pdf application/pdf application/pdf |
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Elsevier Science |
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Elsevier Science |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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