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dc.contributor.author
Gonçalves, Renato V.
dc.contributor.author
Wojcieszak, Robert
dc.contributor.author
Uberman, Paula Marina
dc.contributor.author
Teixeira, Sergio R.
dc.contributor.author
Rossi, Liane M.
dc.date.available
2017-12-26T14:39:19Z
dc.date.issued
2014-01
dc.identifier.citation
Gonçalves, Renato V.; Wojcieszak, Robert; Uberman, Paula Marina; Teixeira, Sergio R.; Rossi, Liane M.; Insights into the active surface species formed onTa2O5nanotubes in the catalytic oxidation of CO; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 16; 12; 1-2014; 5755-5762
dc.identifier.issn
1463-9076
dc.identifier.uri
http://hdl.handle.net/11336/31497
dc.description.abstract
Freestanding Ta2O5nanotubes were prepared by an anodizing method. As-anodized amorphousnanotubes were calcined at high temperature to obtain a crystalline phase. All materials were studied bymeans of BET analysis, XRD, TEM, SEM, XPS, and FTIR and were evaluated in the catalytic oxidation ofCO. An XPS study confirmed the formation of different tantalum surface species after high temperaturetreatment of amorphous Ta2O5nanotubes. Calcination at 8001C generated Ta4+while highertemperature (10001C) treatment led to the formation of Ta3+species. These materials also showedsignificant differences in catalytic activity. Higher activity was observed for samples calcined at 8001Cthan at 10001C, suggesting that Ta4+species are active sites for CO oxidation.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Royal Society of Chemistry
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Co Oxidation
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Active Surface Species
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Ta2o5 Nanotube
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Xps Studies
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Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Insights into the active surface species formed onTa2O5nanotubes in the catalytic oxidation of CO
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2017-12-21T16:30:46Z
dc.journal.volume
16
dc.journal.number
12
dc.journal.pagination
5755-5762
dc.journal.pais
Reino Unido
dc.journal.ciudad
Cambridge
dc.description.fil
Fil: Gonçalves, Renato V.. Universidade de Sao Paulo; Brasil
dc.description.fil
Fil: Wojcieszak, Robert. Universidade de Sao Paulo; Brasil
dc.description.fil
Fil: Uberman, Paula Marina. Universidade de Sao Paulo; Brasil. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Teixeira, Sergio R.. Universidade Federal do Rio Grande do Sul; Brasil
dc.description.fil
Fil: Rossi, Liane M.. Universidade de Sao Paulo; Brasil
dc.journal.title
Physical Chemistry Chemical Physics
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/c3cp54887b
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2014/CP/c3cp54887b
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