Steam-methane reforming at low temperature on nickel-based catalysts

Autores
Nieva, Maria Alejandra; Villaverde, María Magdalena; Monzón Bescós, Antonio; Garetto, Teresita Francisca; Marchi, Alberto Julio
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
In this work, we report the activity results obtained in steam-methane reforming (SMR) at 500 and 600 °C using four nickel-based catalysts: (a) Ni/Al2O3 and Ni/SiO2, prepared by incipient wetness impregnation method and (b) Ni-Zn-Al and Ni-Mg-Al, prepared by coprecipitation method. In all of the samples, the nickel load ranged between 7% and 9%. The catalytic activity in SMR at steady state followed the pattern: Ni-Mg-Al = Ni-Zn-Al > Ni/Al2O3 > Ni/SiO2. According to characterization results, the interaction between Ni2+ species and support in precursor oxides was stronger in Ni-Mg-Al and Ni-Zn-Al than in Ni/Al2O3 and Ni/SiO2. After activation in H2 flow, large metal nickel particles with low or none interaction with the support were obtained in the case of Ni/Al2O3 and Ni/SiO2. On the contrary, small metal particles, between 3 and 6 nm, in high interaction with support were obtained in Ni-Zn-Al and Ni-Mg-Al catalysts. The metal phase formed in Ni-Mg-Al and Ni-Zn-Al was the most active and resistant to sintering under reaction conditions at T < 600 °C. It was also found that carbon nanofibers were formed on Ni/Al2O3, Ni/SiO2 and Ni-Mg-Al catalysts during SMR at 600 °C. The amount and diameter of nanofibers formed on Ni-Mg-Al were lower than on catalysts prepared by impregnation method, which is in agreement with the relative sizes of metal nickel particles in each case. Amazingly, no filamentary carbon was detected on the used Ni-Zn-Al sample: only amorphous coke in low amounts was formed. This was attributed to the proper interaction of small metal nickel particles with the non-stoichiometric zinc aluminate-like phase formed after thermal treatments of catalyst precursor.
Fil: Nieva, Maria Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Villaverde, María Magdalena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Monzón Bescós, Antonio. 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: Garetto, Teresita Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Marchi, Alberto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Materia
Steam-Methane Reforming
Nickel Catalysts
Metal-Support Interaction
Synthesis Gas
Hydrogen
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:11336/31733

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Steam-methane reforming at low temperature on nickel-based catalystsNieva, Maria AlejandraVillaverde, María MagdalenaMonzón Bescós, AntonioGaretto, Teresita FranciscaMarchi, Alberto JulioSteam-Methane ReformingNickel CatalystsMetal-Support InteractionSynthesis GasHydrogenhttps://purl.org/becyt/ford/2.4https://purl.org/becyt/ford/2In this work, we report the activity results obtained in steam-methane reforming (SMR) at 500 and 600 °C using four nickel-based catalysts: (a) Ni/Al2O3 and Ni/SiO2, prepared by incipient wetness impregnation method and (b) Ni-Zn-Al and Ni-Mg-Al, prepared by coprecipitation method. In all of the samples, the nickel load ranged between 7% and 9%. The catalytic activity in SMR at steady state followed the pattern: Ni-Mg-Al = Ni-Zn-Al > Ni/Al2O3 > Ni/SiO2. According to characterization results, the interaction between Ni2+ species and support in precursor oxides was stronger in Ni-Mg-Al and Ni-Zn-Al than in Ni/Al2O3 and Ni/SiO2. After activation in H2 flow, large metal nickel particles with low or none interaction with the support were obtained in the case of Ni/Al2O3 and Ni/SiO2. On the contrary, small metal particles, between 3 and 6 nm, in high interaction with support were obtained in Ni-Zn-Al and Ni-Mg-Al catalysts. The metal phase formed in Ni-Mg-Al and Ni-Zn-Al was the most active and resistant to sintering under reaction conditions at T < 600 °C. It was also found that carbon nanofibers were formed on Ni/Al2O3, Ni/SiO2 and Ni-Mg-Al catalysts during SMR at 600 °C. The amount and diameter of nanofibers formed on Ni-Mg-Al were lower than on catalysts prepared by impregnation method, which is in agreement with the relative sizes of metal nickel particles in each case. Amazingly, no filamentary carbon was detected on the used Ni-Zn-Al sample: only amorphous coke in low amounts was formed. This was attributed to the proper interaction of small metal nickel particles with the non-stoichiometric zinc aluminate-like phase formed after thermal treatments of catalyst precursor.Fil: Nieva, Maria Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaFil: Villaverde, María Magdalena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaFil: Monzón Bescós, Antonio. 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: Garetto, Teresita Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaFil: Marchi, Alberto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; ArgentinaElsevier2013-09info: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/11336/31733Marchi, Alberto Julio; Garetto, Teresita Francisca; Monzón Bescós, Antonio; Villaverde, María Magdalena; Nieva, Maria Alejandra; Steam-methane reforming at low temperature on nickel-based catalysts; Elsevier; Chemical Engineering Journal; 235; 9-2013; 158-1661385-8947CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1385894713012011info:eu-repo/semantics/altIdentifier/doi/10.1016/j.cej.2013.09.030info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:59:51Zoai:ri.conicet.gov.ar:11336/31733instacron: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 09:59:52.032CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Steam-methane reforming at low temperature on nickel-based catalysts
title Steam-methane reforming at low temperature on nickel-based catalysts
spellingShingle Steam-methane reforming at low temperature on nickel-based catalysts
Nieva, Maria Alejandra
Steam-Methane Reforming
Nickel Catalysts
Metal-Support Interaction
Synthesis Gas
Hydrogen
title_short Steam-methane reforming at low temperature on nickel-based catalysts
title_full Steam-methane reforming at low temperature on nickel-based catalysts
title_fullStr Steam-methane reforming at low temperature on nickel-based catalysts
title_full_unstemmed Steam-methane reforming at low temperature on nickel-based catalysts
title_sort Steam-methane reforming at low temperature on nickel-based catalysts
dc.creator.none.fl_str_mv Nieva, Maria Alejandra
Villaverde, María Magdalena
Monzón Bescós, Antonio
Garetto, Teresita Francisca
Marchi, Alberto Julio
author Nieva, Maria Alejandra
author_facet Nieva, Maria Alejandra
Villaverde, María Magdalena
Monzón Bescós, Antonio
Garetto, Teresita Francisca
Marchi, Alberto Julio
author_role author
author2 Villaverde, María Magdalena
Monzón Bescós, Antonio
Garetto, Teresita Francisca
Marchi, Alberto Julio
author2_role author
author
author
author
dc.subject.none.fl_str_mv Steam-Methane Reforming
Nickel Catalysts
Metal-Support Interaction
Synthesis Gas
Hydrogen
topic Steam-Methane Reforming
Nickel Catalysts
Metal-Support Interaction
Synthesis Gas
Hydrogen
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 work, we report the activity results obtained in steam-methane reforming (SMR) at 500 and 600 °C using four nickel-based catalysts: (a) Ni/Al2O3 and Ni/SiO2, prepared by incipient wetness impregnation method and (b) Ni-Zn-Al and Ni-Mg-Al, prepared by coprecipitation method. In all of the samples, the nickel load ranged between 7% and 9%. The catalytic activity in SMR at steady state followed the pattern: Ni-Mg-Al = Ni-Zn-Al > Ni/Al2O3 > Ni/SiO2. According to characterization results, the interaction between Ni2+ species and support in precursor oxides was stronger in Ni-Mg-Al and Ni-Zn-Al than in Ni/Al2O3 and Ni/SiO2. After activation in H2 flow, large metal nickel particles with low or none interaction with the support were obtained in the case of Ni/Al2O3 and Ni/SiO2. On the contrary, small metal particles, between 3 and 6 nm, in high interaction with support were obtained in Ni-Zn-Al and Ni-Mg-Al catalysts. The metal phase formed in Ni-Mg-Al and Ni-Zn-Al was the most active and resistant to sintering under reaction conditions at T < 600 °C. It was also found that carbon nanofibers were formed on Ni/Al2O3, Ni/SiO2 and Ni-Mg-Al catalysts during SMR at 600 °C. The amount and diameter of nanofibers formed on Ni-Mg-Al were lower than on catalysts prepared by impregnation method, which is in agreement with the relative sizes of metal nickel particles in each case. Amazingly, no filamentary carbon was detected on the used Ni-Zn-Al sample: only amorphous coke in low amounts was formed. This was attributed to the proper interaction of small metal nickel particles with the non-stoichiometric zinc aluminate-like phase formed after thermal treatments of catalyst precursor.
Fil: Nieva, Maria Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Villaverde, María Magdalena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Monzón Bescós, Antonio. 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: Garetto, Teresita Francisca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
Fil: Marchi, Alberto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina
description In this work, we report the activity results obtained in steam-methane reforming (SMR) at 500 and 600 °C using four nickel-based catalysts: (a) Ni/Al2O3 and Ni/SiO2, prepared by incipient wetness impregnation method and (b) Ni-Zn-Al and Ni-Mg-Al, prepared by coprecipitation method. In all of the samples, the nickel load ranged between 7% and 9%. The catalytic activity in SMR at steady state followed the pattern: Ni-Mg-Al = Ni-Zn-Al > Ni/Al2O3 > Ni/SiO2. According to characterization results, the interaction between Ni2+ species and support in precursor oxides was stronger in Ni-Mg-Al and Ni-Zn-Al than in Ni/Al2O3 and Ni/SiO2. After activation in H2 flow, large metal nickel particles with low or none interaction with the support were obtained in the case of Ni/Al2O3 and Ni/SiO2. On the contrary, small metal particles, between 3 and 6 nm, in high interaction with support were obtained in Ni-Zn-Al and Ni-Mg-Al catalysts. The metal phase formed in Ni-Mg-Al and Ni-Zn-Al was the most active and resistant to sintering under reaction conditions at T < 600 °C. It was also found that carbon nanofibers were formed on Ni/Al2O3, Ni/SiO2 and Ni-Mg-Al catalysts during SMR at 600 °C. The amount and diameter of nanofibers formed on Ni-Mg-Al were lower than on catalysts prepared by impregnation method, which is in agreement with the relative sizes of metal nickel particles in each case. Amazingly, no filamentary carbon was detected on the used Ni-Zn-Al sample: only amorphous coke in low amounts was formed. This was attributed to the proper interaction of small metal nickel particles with the non-stoichiometric zinc aluminate-like phase formed after thermal treatments of catalyst precursor.
publishDate 2013
dc.date.none.fl_str_mv 2013-09
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/11336/31733
Marchi, Alberto Julio; Garetto, Teresita Francisca; Monzón Bescós, Antonio; Villaverde, María Magdalena; Nieva, Maria Alejandra; Steam-methane reforming at low temperature on nickel-based catalysts; Elsevier; Chemical Engineering Journal; 235; 9-2013; 158-166
1385-8947
CONICET Digital
CONICET
url http://hdl.handle.net/11336/31733
identifier_str_mv Marchi, Alberto Julio; Garetto, Teresita Francisca; Monzón Bescós, Antonio; Villaverde, María Magdalena; Nieva, Maria Alejandra; Steam-methane reforming at low temperature on nickel-based catalysts; Elsevier; Chemical Engineering Journal; 235; 9-2013; 158-166
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/url/http://www.sciencedirect.com/science/article/pii/S1385894713012011
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.cej.2013.09.030
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
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
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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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