Mostrar el registro sencillo del ítem

dc.contributor.author
Ballarini, Adriana Daniela  
dc.contributor.author
Basile, Francesco  
dc.contributor.author
Benito, Patricia  
dc.contributor.author
Bersani, I.  
dc.contributor.author
Fornasari, G.  
dc.contributor.author
de Miguel, Sergio Ruben  
dc.contributor.author
Maina, Silvia Carolina Palmira  
dc.contributor.author
Vilella, Irene María Julieta  
dc.contributor.author
Vaccari, A.  
dc.contributor.author
Scelza, Osvaldo Antonio  
dc.date.available
2025-10-07T14:39:53Z  
dc.date.issued
2012-08  
dc.identifier.citation
Ballarini, Adriana Daniela; Basile, Francesco; Benito, Patricia; Bersani, I.; Fornasari, G.; et al.; Platinum supported on alkaline and alkaline earth metal-doped alumina as catalysts for dry reforming and partial oxidation of methane; Elsevier Science; Applied Catalysis A: General; 433-434; 8-2012; 1-11  
dc.identifier.issn
0926-860X  
dc.identifier.uri
http://hdl.handle.net/11336/273034  
dc.description.abstract
Pt catalysts with low metal loadings (0.02, 0.1 and 0.5 wt%) supported on alkaline (Na and K) or alkaline earth (Mg) metals-doped alumina were tested in the catalytic partial oxidation and dry reforming of methane. Supports were characterized by X-ray diffraction and also by determining their BET surface area, temperature-programmed desorption of CO2, and isopropanol dehydration; while catalysts were characterized by X-ray diffraction, temperature programmed reduction, tests of cyclohexane dehydrogenation, temperature-programmed oxidation, and transmission electronic microscopy. The presence of the dopants modified the thermal stability of the ?Á-Al2O3 phase by calcination at 1000 ??C and the acidity of the support. The ?Á ?¨ ?Æ transition took place for K- and Na-doped catalysts, the acidity being almost suppressed. Conversely, the Mg-doped ?Á-Al2O3 was thermally stable, and the catalysts still showed some acidic sites. The catalytic performances in both partial oxidation and dry reforming processes were dependent on the support dopants, with a more notable effect observed at low-noble-metal loadings. K- and Na-doped catalysts showed poor activities in the catalytic partial oxidation reaction, whereas the presence of Mg in the alumina promoted the catalytic activity. In the dry reforming reaction an improvement was found in the catalytic activity for the sample with the highest Pt content; moreover, the K-doped catalysts were slightly more efficient.  
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
methane  
dc.subject
H2 production  
dc.subject
catalytic partial oxidation  
dc.subject
dry reforming  
dc.subject
alkaline or alkaline earth metal-doped alumina.  
dc.subject
supported Pt  
dc.subject.classification
Ingeniería de Procesos Químicos  
dc.subject.classification
Ingeniería Química  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Platinum supported on alkaline and alkaline earth metal-doped alumina as catalysts for dry reforming and partial oxidation 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
2025-10-02T11:01:20Z  
dc.journal.volume
433-434  
dc.journal.pagination
1-11  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Amsterdam  
dc.description.fil
Fil: Ballarini, Adriana Daniela. 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: Basile, Francesco. Università di Bologna; Italia  
dc.description.fil
Fil: Benito, Patricia. Università di Bologna; Italia  
dc.description.fil
Fil: Bersani, I.. Universidad de Bologna; Italia  
dc.description.fil
Fil: Fornasari, G.. Universidad de Bologna; Italia  
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: 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: 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: Vaccari, A.. Universidad de Bologna; Italia  
dc.description.fil
Fil: Scelza, Osvaldo Antonio. 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
Applied Catalysis A: General  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2012.04.037