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dc.contributor.author
Pieck, Carlos Luis  
dc.contributor.author
Vera, Carlos Roman  
dc.contributor.author
Peirotti, Eduardo M.  
dc.contributor.author
Yori, Juan Carlos  
dc.date.available
2018-03-27T19:42:03Z  
dc.date.issued
2002-03  
dc.identifier.citation
Pieck, Carlos Luis; Vera, Carlos Roman; Peirotti, Eduardo M.; Yori, Juan Carlos; Effect of water vapor on the activity of Pt-Pd/Al2O3 catalysts for methane combustion; Elsevier Science; Applied Catalysis A: General; 226; 1-2; 3-2002; 281-291  
dc.identifier.issn
0926-860X  
dc.identifier.uri
http://hdl.handle.net/11336/40204  
dc.description.abstract
A study on the deactivation phenomena affecting the catalysts of small-scale natural gas catalytic combustors was undertaken in this work. The influence of simulated aging pretreatments on the activity of Pt-Pd catalysts supported over gamma alumina for the catalytic combustion of CH4 was assessed under atmospheric conditions and in the 50–950 °C temperature range. Accelerated deactivation tests consisted of steaming at temperatures between 500–800 °C. The results showed that the activity of the deactivated catalysts depended on two opposite phenomena. An enhancement of the activity was encountered for low aging temperatures and was addressed to chlorine (Cl) elimination (as detected by chemical analysis). Conversely, at higher temperatures the accelerated aging treatment produced a decrease in the activity, and this was allegedly linked to a decrease in the available metal surface area produced by sintering. During the catalyst lifespan and under real operation conditions, a first period is therefore expected where the catalytic activity improves due to the Cl elimination by the water (H2O) produced during combustion. Afterwards, the activity would decrease because of the sintering of the metal phase. Both processes, Cl elimination and sintering, occur simultaneously. Five different catalyst formulations with variable Pt and Pd contents were tried and 0.4%Pt-0.8%Pd was found to be the most active. The results found are discussed in terms of the activity of the monometallic catalysts, the degree of interaction of the Pt and Pd phases and the previously mentioned phenomena of sintering and Cl elimination.  
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
Catalytic Combustion  
dc.subject
Pt-Pd  
dc.subject
Methane  
dc.subject
Deactivation  
dc.subject
Sintering  
dc.subject.classification
Ingeniería Medioambiental y Geológica, Geotécnicas  
dc.subject.classification
Ingeniería del Medio Ambiente  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Effect of water vapor on the activity of Pt-Pd/Al2O3 catalysts for methane combustion  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-03-16T15:42:19Z  
dc.journal.volume
226  
dc.journal.number
1-2  
dc.journal.pagination
281-291  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdan  
dc.description.fil
Fil: Pieck, Carlos Luis. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.description.fil
Fil: Vera, Carlos Roman. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.description.fil
Fil: Peirotti, Eduardo M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.description.fil
Fil: Yori, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Investigaciones en Catálisis y Petroquímica ; Argentina  
dc.journal.title
Applied Catalysis A: General  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/S0926-860X(01)00914-0  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X01009140