Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions

We report the study of the catalytic hydrogen combustion over Pt-impregnated powdery silicon carbide (SiC) using H2PtCl6 as precursor. The reaction was conducted in excess of oxygen. β-SiC was selected for the study because of its thermal conductivity, mechanical properties, chemical inertness and s...

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Autores: Arzac, G. M., Montes, O., Fernández Camacho, Asunción
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2016
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/80246
Acceso en línea:https://hdl.handle.net/11441/80246
https://doi.org/10.1016/j.apcatb.2016.08.042
Access Level:acceso abierto
Palabra clave:Hydrogen
Catalytic combustion
Pt-impregnated catalysts
Powdery SiC
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spelling Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditionsArzac, G. M.Montes, O.Fernández Camacho, AsunciónHydrogenCatalytic combustionPt-impregnated catalystsPowdery SiCWe report the study of the catalytic hydrogen combustion over Pt-impregnated powdery silicon carbide (SiC) using H2PtCl6 as precursor. The reaction was conducted in excess of oxygen. β-SiC was selected for the study because of its thermal conductivity, mechanical properties, chemical inertness and surface area. The obtained Pt particles over SiC were medium size (average particle diameter of 5 nm for 0.5 wt% Pt). The activity of the Pt-impregnated catalyst over SiC was compared to those obtained in oxidized form over TiO2 and Al2O3 commercial supports (Pt particles very small in size, average particle diameter of 1 nm for 0.5 wt% Pt in both cases). The case of a SiO2 support was also discussed. Those Pt/SiC particles were the most active because of their higher contribution of surface Pt0, indicating that partially oxidized surfaces have better activity than those totally oxidized in these conditions. SiC was modified with an acid treatment and thus bigger (average particle diameter of 7 nm for 0.5 wt% Pt) and more active Pt particles were obtained. Durability of the SiC and TiO2 supported catalysts was tested upon 5 cycles and both have shown to be durable and even more active than initially. Exposure to the oxidative reaction mixture activates the catalysts and the effect is more pronounced for the completely oxidized particles. This is due to the surface oxygen chemisorption which activates catalystś surface.Junta de Andalucía PE2012-TEP862Ministerio de Economía y Competitividad CTQ2012-32519, CTQ2015-65918-RConsejo Superior de Investigaciones Científicas PIE-201460E018Elsevier2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/80246https://doi.org/10.1016/j.apcatb.2016.08.042reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésApplied Catalysis B - Environmental, 201, 391-399.PE2012-TEP862CTQ2012-32519CTQ2015-65918-RPIE-201460E018http://dx.doi.org/10.1016/j.apcatb.2016.08.042info:eu-repo/semantics/openAccessoai:idus.us.es:11441/802462026-06-17T12:51:07Z
dc.title.none.fl_str_mv Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
title Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
spellingShingle Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
Arzac, G. M.
Hydrogen
Catalytic combustion
Pt-impregnated catalysts
Powdery SiC
title_short Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
title_full Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
title_fullStr Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
title_full_unstemmed Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
title_sort Pt-impregnated catalysts on powdery SiC and other commercial supports for the combustion of hydrogen under oxidant conditions
dc.creator.none.fl_str_mv Arzac, G. M.
Montes, O.
Fernández Camacho, Asunción
author Arzac, G. M.
author_facet Arzac, G. M.
Montes, O.
Fernández Camacho, Asunción
author_role author
author2 Montes, O.
Fernández Camacho, Asunción
author2_role author
author
dc.subject.none.fl_str_mv Hydrogen
Catalytic combustion
Pt-impregnated catalysts
Powdery SiC
topic Hydrogen
Catalytic combustion
Pt-impregnated catalysts
Powdery SiC
description We report the study of the catalytic hydrogen combustion over Pt-impregnated powdery silicon carbide (SiC) using H2PtCl6 as precursor. The reaction was conducted in excess of oxygen. β-SiC was selected for the study because of its thermal conductivity, mechanical properties, chemical inertness and surface area. The obtained Pt particles over SiC were medium size (average particle diameter of 5 nm for 0.5 wt% Pt). The activity of the Pt-impregnated catalyst over SiC was compared to those obtained in oxidized form over TiO2 and Al2O3 commercial supports (Pt particles very small in size, average particle diameter of 1 nm for 0.5 wt% Pt in both cases). The case of a SiO2 support was also discussed. Those Pt/SiC particles were the most active because of their higher contribution of surface Pt0, indicating that partially oxidized surfaces have better activity than those totally oxidized in these conditions. SiC was modified with an acid treatment and thus bigger (average particle diameter of 7 nm for 0.5 wt% Pt) and more active Pt particles were obtained. Durability of the SiC and TiO2 supported catalysts was tested upon 5 cycles and both have shown to be durable and even more active than initially. Exposure to the oxidative reaction mixture activates the catalysts and the effect is more pronounced for the completely oxidized particles. This is due to the surface oxygen chemisorption which activates catalystś surface.
publishDate 2016
dc.date.none.fl_str_mv 2016
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/11441/80246
https://doi.org/10.1016/j.apcatb.2016.08.042
url https://hdl.handle.net/11441/80246
https://doi.org/10.1016/j.apcatb.2016.08.042
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Applied Catalysis B - Environmental, 201, 391-399.
PE2012-TEP862
CTQ2012-32519
CTQ2015-65918-R
PIE-201460E018
http://dx.doi.org/10.1016/j.apcatb.2016.08.042
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:idUS. Depósito de Investigación de la Universidad de Sevilla
instname:Universidad de Sevilla (US)
instname_str Universidad de Sevilla (US)
reponame_str idUS. Depósito de Investigación de la Universidad de Sevilla
collection idUS. Depósito de Investigación de la Universidad de Sevilla
repository.name.fl_str_mv
repository.mail.fl_str_mv
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