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dc.contributor.author
Regenhardt, Silvina Andrea
dc.contributor.author
Meyer, Camilo Ignacio
dc.contributor.author
Garetto, Teresita Francisca
dc.contributor.author
Marchi, Alberto Julio
dc.date.available
2018-07-17T14:40:14Z
dc.date.issued
2012-10
dc.identifier.citation
Regenhardt, Silvina Andrea; Meyer, Camilo Ignacio; Garetto, Teresita Francisca; Marchi, Alberto Julio; Selective gas phase hydrogenation of maleic anhydride over Ni-supported catalysts: Effect of support on the catalytic performance; Elsevier Science; Applied Catalysis A: General; 449; 10-2012; 81-87
dc.identifier.issn
0926-860X
dc.identifier.uri
http://hdl.handle.net/11336/52373
dc.description.abstract
The gas phase hydrogenation of maleic anhydride to obtain γ-butyrolactone was studied using Ni supported on SiO2, SiO2–Al2O3 and zeolite H-BEA as catalysts. The samples were prepared by incipient wetness impregnation and characterized by N2 adsorption at −196 °C (Sg), X-ray diffraction (XRD), temperature programmed reduction (TPR), temperature programmed desorption of NH3 (TPD-NH3) and chemisorption of H2. The reaction was carried out at 170 °C and 220 °C in a fixed bed reactor operating at atmospheric pressure. From the characterization results, it was determined that the degree of Ni2+–support interaction varies according to the following pattern: Ni/HBEA > Ni/SiO2–Al2O3 > Ni/SiO2. All catalysts were very active in the hydrogenation of maleic anhydride to succinic anhydride. However, hydrogenolytic activity and stability of nickel-based catalyst varies with the degree of interaction Ni2+–support. Ni/H-BEA, in which Ni2+–support interaction is the highest, was active in the hydrogenolysis of succinic anhydride to γ-butyrolactone but it was not stable. By contrast, Ni/SiO2–Al2O3 and Ni/SiO2, with medium or low degree of Ni2+–support interaction, were more stable than Ni/H-BEA. In addition, Ni/SiO2–Al2O3, with a medium degree of Ni2+–support interaction, was the most stable and selective to γ-butyrolactone, especially when the reaction was carried out at 220 °C.
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
Hydrogenation
dc.subject
Hydrogenolysis
dc.subject
Ni-Based Catalysts
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Gamma-Butyrolactone
dc.subject.classification
Otras Ingeniería Química
dc.subject.classification
Ingeniería Química
dc.subject.classification
INGENIERÍAS Y TECNOLOGÍAS
dc.title
Selective gas phase hydrogenation of maleic anhydride over Ni-supported catalysts: Effect of support on the catalytic performance
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-07-11T14:10:27Z
dc.journal.volume
449
dc.journal.pagination
81-87
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: Regenhardt, Silvina Andrea. 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: Meyer, Camilo Ignacio. 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: Garetto, Teresita Francisca. 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: Marchi, Alberto Julio. 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/url/www.sciencedirect.com/science/article/pii/S0926860X12006163
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2012.09.023
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