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dc.contributor.author
de Miguel, Sergio Ruben
dc.contributor.author
Vilella, Irene María Julieta
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Maina, Silvia Carolina Palmira
dc.contributor.author
San José-Alonso, D.
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Román-Martínez, M.C.
dc.contributor.author
Illán-Gómez, M.J.
dc.date.available
2019-06-21T00:23:46Z
dc.date.issued
2012-09
dc.identifier.citation
de Miguel, Sergio Ruben; Vilella, Irene María Julieta; Maina, Silvia Carolina Palmira; San José-Alonso, D.; Román-Martínez, M.C.; et al.; Influence of Pt addition to Ni catalysts on the catalytic performance for long term dry reforming of methane; Elsevier Science; Applied Catalysis A: General; 435-436; 9-2012; 10-18
dc.identifier.issn
0926-860X
dc.identifier.uri
http://hdl.handle.net/11336/78592
dc.description.abstract
The influence of Pt addition (in very low concentrations) to a Ni/(10%)/Al 2O 3 catalyst in its catalytic performance during long-term experiments of dry reforming of methane was studied. The monometallic Pt(0.5%)/Al 2O 3 catalyst displayed a pronounced deactivation during 6500 min reaction time, mainly due to a significant sintering of the metallic phase, whereas the monometallic Ni(10%)/Al 2O 3 catalyst showed a high and stable activity along the reaction time. Compared with the Ni(10%)/Al 2O 3 catalyst, the bimetallic Ni(10%)Pt(0.5%)/Al 2O 3 sample showed a higher, and stable catalytic activity during the 6500 min reaction time and a markedly lower carbon deposition. TEM images reveal much less carbon formation and filament grow and this leads to expect a higher stability in long term processes. Characterization techniques indicate that nickel and platinum are in close contact during the simultaneous reduction of the two oxide precursors and that geometric effects (dilution and blocking) are mainly responsible for the excellent catalytic behaviour of the bimetallic NiPt catalyst.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier Science
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Alumina-Based Catalysts
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Catalyst Deactivation
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Methane Dry Reforming
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Ptni Catalysts
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Otras Ingeniería Química
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Ingeniería Química
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INGENIERÍAS Y TECNOLOGÍAS
dc.title
Influence of Pt addition to Ni catalysts on the catalytic performance for long term dry reforming of methane
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-06-19T12:19:31Z
dc.journal.volume
435-436
dc.journal.pagination
10-18
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: de Miguel, Sergio Ruben. 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
dc.description.fil
Fil: Vilella, Irene María Julieta. 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
dc.description.fil
Fil: Maina, Silvia Carolina Palmira. 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
dc.description.fil
Fil: San José-Alonso, D.. Universidad de Alicante; España
dc.description.fil
Fil: Román-Martínez, M.C.. Universidad de Alicante; España
dc.description.fil
Fil: Illán-Gómez, M.J.. Universidad de Alicante; España
dc.journal.title
Applied Catalysis A: General
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2012.05.030
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