Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation
- Autores
- Marchesini, Fernanda Albana; Irusta, S.; Querini, Carlos Alberto; Miro, Eduardo Ernesto
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Bimetallic Pt-In and Pd-In catalysts supported on alumina or silica were studied for the reduction of nitrate to N2 in water, using H2 as reducing agent. Characterization results indicate that bimetallic particles with the surface enriched in indium, metallic crystals of Pt or Pd, and oxides of Pt or Pd and In2O3 are the main surface species present in the catalysts. Several catalysts studied in this work could fulfill the requirements usually established as limit values: 50 ppm of-NO3-, 0.1 ppm of NO2- and 0.5 ppm of NH4+. The reaction rate is strongly influenced by either the Pt:In or the Pd:In ratio, the optimum being observed at low contents of In. Of all the catalysts studied in this work, Pd(1 wt.%)In(0.25 wt.%)/Al2O3 is the most active one, but unfortunately, it presents an undesirable high selectivity towards ammonia when nitrate conversion reaches 100%. Pt(1.0%)In(0.25%)/Al2O3 presents a high initial activity but it fastly deactivates during reaction. In general, Pd-In catalysts are more active for nitrate conversion than Pt-In, and alumina is a better support than silica. The composition of the catalysts changes both after reduction and after contacting the liquid reaction media. These changes have been observed by XPS and TEM. In general, the samples used in the reaction have lower dispersion of metallic phases than the fresh-calcined ones. For most of the catalysts used in this work, the Pt:In or Pd:In surface ratio is lower than the bulk ones, this probably being the reason for the low amount of In that is sufficient to have an optimal performance for nitrate conversion.
Fil: Marchesini, Fernanda Albana. 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: Irusta, S.. Universidad de Zaragoza; España
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
-
Bimetallic Catalysts
Catalytic Reduction
Nitrates
Nitrites - 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:11336/65153
Ver los metadatos del registro completo
id |
CONICETDig_de5b080cbd692b1cd77469e3ceaf02fb |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/65153 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenationMarchesini, Fernanda AlbanaIrusta, S.Querini, Carlos AlbertoMiro, Eduardo ErnestoBimetallic CatalystsCatalytic ReductionNitratesNitriteshttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2Bimetallic Pt-In and Pd-In catalysts supported on alumina or silica were studied for the reduction of nitrate to N2 in water, using H2 as reducing agent. Characterization results indicate that bimetallic particles with the surface enriched in indium, metallic crystals of Pt or Pd, and oxides of Pt or Pd and In2O3 are the main surface species present in the catalysts. Several catalysts studied in this work could fulfill the requirements usually established as limit values: 50 ppm of-NO3-, 0.1 ppm of NO2- and 0.5 ppm of NH4+. The reaction rate is strongly influenced by either the Pt:In or the Pd:In ratio, the optimum being observed at low contents of In. Of all the catalysts studied in this work, Pd(1 wt.%)In(0.25 wt.%)/Al2O3 is the most active one, but unfortunately, it presents an undesirable high selectivity towards ammonia when nitrate conversion reaches 100%. Pt(1.0%)In(0.25%)/Al2O3 presents a high initial activity but it fastly deactivates during reaction. In general, Pd-In catalysts are more active for nitrate conversion than Pt-In, and alumina is a better support than silica. The composition of the catalysts changes both after reduction and after contacting the liquid reaction media. These changes have been observed by XPS and TEM. In general, the samples used in the reaction have lower dispersion of metallic phases than the fresh-calcined ones. For most of the catalysts used in this work, the Pt:In or Pd:In surface ratio is lower than the bulk ones, this probably being the reason for the low amount of In that is sufficient to have an optimal performance for nitrate conversion.Fil: Marchesini, Fernanda Albana. 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: Irusta, S.. Universidad de Zaragoza; EspañaFil: 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 Science2008-09info: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/11336/65153Marchesini, Fernanda Albana; Irusta, S.; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation; Elsevier Science; Applied Catalysis A: General; 348; 1; 9-2008; 60-700926-860XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.apcata.2008.06.026info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:58:02Zoai:ri.conicet.gov.ar:11336/65153instacron: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 09:58:02.43CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
title |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
spellingShingle |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation Marchesini, Fernanda Albana Bimetallic Catalysts Catalytic Reduction Nitrates Nitrites |
title_short |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
title_full |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
title_fullStr |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
title_full_unstemmed |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
title_sort |
Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation |
dc.creator.none.fl_str_mv |
Marchesini, Fernanda Albana Irusta, S. Querini, Carlos Alberto Miro, Eduardo Ernesto |
author |
Marchesini, Fernanda Albana |
author_facet |
Marchesini, Fernanda Albana Irusta, S. Querini, Carlos Alberto Miro, Eduardo Ernesto |
author_role |
author |
author2 |
Irusta, S. Querini, Carlos Alberto Miro, Eduardo Ernesto |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Bimetallic Catalysts Catalytic Reduction Nitrates Nitrites |
topic |
Bimetallic Catalysts Catalytic Reduction Nitrates Nitrites |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.4 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Bimetallic Pt-In and Pd-In catalysts supported on alumina or silica were studied for the reduction of nitrate to N2 in water, using H2 as reducing agent. Characterization results indicate that bimetallic particles with the surface enriched in indium, metallic crystals of Pt or Pd, and oxides of Pt or Pd and In2O3 are the main surface species present in the catalysts. Several catalysts studied in this work could fulfill the requirements usually established as limit values: 50 ppm of-NO3-, 0.1 ppm of NO2- and 0.5 ppm of NH4+. The reaction rate is strongly influenced by either the Pt:In or the Pd:In ratio, the optimum being observed at low contents of In. Of all the catalysts studied in this work, Pd(1 wt.%)In(0.25 wt.%)/Al2O3 is the most active one, but unfortunately, it presents an undesirable high selectivity towards ammonia when nitrate conversion reaches 100%. Pt(1.0%)In(0.25%)/Al2O3 presents a high initial activity but it fastly deactivates during reaction. In general, Pd-In catalysts are more active for nitrate conversion than Pt-In, and alumina is a better support than silica. The composition of the catalysts changes both after reduction and after contacting the liquid reaction media. These changes have been observed by XPS and TEM. In general, the samples used in the reaction have lower dispersion of metallic phases than the fresh-calcined ones. For most of the catalysts used in this work, the Pt:In or Pd:In surface ratio is lower than the bulk ones, this probably being the reason for the low amount of In that is sufficient to have an optimal performance for nitrate conversion. Fil: Marchesini, Fernanda Albana. 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: Irusta, S.. Universidad de Zaragoza; España 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 |
Bimetallic Pt-In and Pd-In catalysts supported on alumina or silica were studied for the reduction of nitrate to N2 in water, using H2 as reducing agent. Characterization results indicate that bimetallic particles with the surface enriched in indium, metallic crystals of Pt or Pd, and oxides of Pt or Pd and In2O3 are the main surface species present in the catalysts. Several catalysts studied in this work could fulfill the requirements usually established as limit values: 50 ppm of-NO3-, 0.1 ppm of NO2- and 0.5 ppm of NH4+. The reaction rate is strongly influenced by either the Pt:In or the Pd:In ratio, the optimum being observed at low contents of In. Of all the catalysts studied in this work, Pd(1 wt.%)In(0.25 wt.%)/Al2O3 is the most active one, but unfortunately, it presents an undesirable high selectivity towards ammonia when nitrate conversion reaches 100%. Pt(1.0%)In(0.25%)/Al2O3 presents a high initial activity but it fastly deactivates during reaction. In general, Pd-In catalysts are more active for nitrate conversion than Pt-In, and alumina is a better support than silica. The composition of the catalysts changes both after reduction and after contacting the liquid reaction media. These changes have been observed by XPS and TEM. In general, the samples used in the reaction have lower dispersion of metallic phases than the fresh-calcined ones. For most of the catalysts used in this work, the Pt:In or Pd:In surface ratio is lower than the bulk ones, this probably being the reason for the low amount of In that is sufficient to have an optimal performance for nitrate conversion. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008-09 |
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/11336/65153 Marchesini, Fernanda Albana; Irusta, S.; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation; Elsevier Science; Applied Catalysis A: General; 348; 1; 9-2008; 60-70 0926-860X CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/65153 |
identifier_str_mv |
Marchesini, Fernanda Albana; Irusta, S.; Querini, Carlos Alberto; Miro, Eduardo Ernesto; Spectroscopic and catalytic characterization of Pd-In and Pt-In supported on Al2O3 and SiO2, active catalysts for nitrate hydrogenation; Elsevier Science; Applied Catalysis A: General; 348; 1; 9-2008; 60-70 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.2008.06.026 |
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 |
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 |
_version_ |
1842269497239535616 |
score |
13.13397 |