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dc.contributor.author
Cornaglia, Carolina Andrea  
dc.contributor.author
Tosti, Silvano  
dc.contributor.author
Múnera Agudelo, John Fernando  
dc.contributor.author
Lombardo, Eduardo Agustin  
dc.date.available
2017-12-18T19:05:30Z  
dc.date.issued
2014-08  
dc.identifier.citation
Lombardo, Eduardo Agustin; Múnera Agudelo, John Fernando; Tosti, Silvano; Cornaglia, Carolina Andrea; Optimal Pt load of a Pt/La2O3·SiO2 highly selective WGS catalyst used in a Pd-membrane reactor; Elsevier; Applied Catalysis A: General; 486; 8-2014; 85-93  
dc.identifier.issn
0926-860X  
dc.identifier.uri
http://hdl.handle.net/11336/30921  
dc.description.abstract
Pt(wt%)/La2O3(27)·SiO2 catalysts with wt% = 0.02 up to 1.2 were synthesized and tested in a conventional fixed-bed reactor. In differential mode, the Pt(0.1)/La2O3(27)·SiO2 catalyst showed higher activity per gram of Pt than the other solids. XPS showed the presence of only surface metallic platinum, in both the fresh and used Pt(0.1 wt%) formulation, which could be responsible for the high catalytic activity. At higher Pt loads both Ptδ+ and Pt° species were present at the surface. The presence of La2Si2O7 in all solids was detected by XRD. Graphitic carbon in the used catalysts was not detected through laser Raman spectroscopy. Different catalytic tests were carried out in a tubular Pd-membrane reactor feeding a reformer outlet type stream with a molar composition of 40% H2, 40% H2O, 12% CO2 and 8% CO. They were performed between 673 and 723 K and at pressures ranging from 100 kPa to 800 kPa. At 723 K and 800 kPa, the CO conversion and H2 recovery values were 96% and 88%, respectively. A stability test including several start-up and shut-down cycles showed high stability of the Pt(0.1) catalyst.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Elsevier  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/  
dc.subject
Membrane Reactors  
dc.subject
Palladium  
dc.subject
Wgs  
dc.subject
H2 Purification  
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Methane Formation  
dc.subject
Binary Support  
dc.subject.classification
Otras Ingeniería Química  
dc.subject.classification
Ingeniería Química  
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS  
dc.title
Optimal Pt load of a Pt/La2O3·SiO2 highly selective WGS catalyst used in a Pd-membrane reactor  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2017-12-18T15:08:43Z  
dc.journal.volume
486  
dc.journal.pagination
85-93  
dc.journal.pais
Países Bajos  
dc.journal.ciudad
Ámsterdam  
dc.description.fil
Fil: Cornaglia, Carolina Andrea. 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: Tosti, Silvano. ENEA. Unità Tecnica Fusione; Italia  
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.journal.title
Applied Catalysis A: General  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X14005031  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2014.08.018