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dc.contributor.author
Carrara, Carlos Roberto
dc.contributor.author
Múnera Agudelo, John Fernando
dc.contributor.author
Lombardo, Eduardo Agustin
dc.contributor.author
Cornaglia, Laura Maria
dc.date.available
2018-11-26T16:37:44Z
dc.date.issued
2008-12
dc.identifier.citation
Carrara, Carlos Roberto; Múnera Agudelo, John Fernando; Lombardo, Eduardo Agustin; Cornaglia, Laura Maria; Kinetic and Stability Studies of Ru/La2O3 Used in the Dry Reforming of Methane; Springer/Plenum Publishers; Topics In Catalysis; 51; 1-4; 12-2008; 98-106
dc.identifier.issn
1022-5528
dc.identifier.uri
http://hdl.handle.net/11336/65163
dc.description.abstract
The catalytic activity toward hydrogen production through the dry reforming of methane was determined for Ru supported on lanthanum oxide. The catalyst remained stable for more than 80 h in the 823-903 K temperature range and reactant partial pressure ratio (PCO2/PCH 4) equal to unity. However, a significant deactivation was observed during the kinetic measurements when the catalyst was exposed to P CO2/PCH4 > 1 at 823 K. In order to establish why the catalyst deactivated, the Ru reactivity in reductive and CO2 rich atmospheres was studied by in situ LRS and XPS spectroscopies. The partial re-oxidation of metallic Ru could be one of the factors that produce the catalyst deactivation. To perform the kinetic measurements, the temperature range and the partial pressure ratios were selected within the window where the Ru catalyst was stable. The kinetic data and supporting spectroscopic evidence is consistent with a mechanism in which the metal and the oxide play key roles in decomposing the paraffin and activating the CO2, respectively.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Springer/Plenum Publishers
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
In Situ Lrs
dc.subject
Kinetics
dc.subject
Ru Species
dc.title
Kinetic and Stability Studies of Ru/La2O3 Used in the 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
2018-11-15T15:58:56Z
dc.journal.volume
51
dc.journal.number
1-4
dc.journal.pagination
98-106
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Carrara, Carlos Roberto. 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: Múnera Agudelo, John Fernando. 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: Lombardo, Eduardo Agustin. 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: Cornaglia, Laura Maria. 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.journal.title
Topics In Catalysis
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007/s11244-008-9131-y
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s11244-008-9131-y
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