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dc.creatorBaronetti, Graciela Teresita-
dc.creatorThomas, Horacio Jorge-
dc.creatorQuerini, Carlos Alberto-
dc.date2018-05-08T15:07:36Z-
dc.date2018-05-08T15:07:36Z-
dc.date2001-09-
dc.date2018-03-19T17:27:35Z-
dc.date.accessioned2019-04-29T15:45:36Z-
dc.date.available2019-04-29T15:45:36Z-
dc.date.issued2001-09-
dc.identifierBaronetti, Graciela Teresita; Thomas, Horacio Jorge; Querini, Carlos Alberto; Wells–Dawson heteropolyacid supported on silica: isobutane alkylation with C4 olefins; Elsevier Science; Applied Catalysis A: General; 217; 1-2; 9-2001; 131-141-
dc.identifier0926-860X-
dc.identifierhttp://hdl.handle.net/11336/44417-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/301328-
dc.descriptionThe alkylation of isobutane with C4 olefins is studied, using heteropolyacids (HPA) with Wells–Dawson (WD) structure supported on silica (WD/SiO2). The catalytic performance of these catalysts is compared with a lanthanum-exchanged Y-zeolite catalyst. The loading of the HPA on silica was varied between 9 and 28 wt.%. These catalysts have activity for trimethylpentanes (TMP) production. The selectivity towards these products is not as high as in the case of the lanthanum containing Y-zeolite. The acidity of WD/SiO2 catalysts increases as the loading increases, as seen by MAS-NMR. Correspondingly, a better TMP production is observed. The increase both in acidity and in the TMP production as a function of the WD content is more noticeable at low loading. The coke formed during the reaction requires high temperatures, 550°C approximately, in order to be fully removed with an oxygen containing carrier gas. The temperature-programmed oxidation (TPO) profile of this coke displays two peaks, the first one between 80 and 300°C associated with hydrocarbons that are released upon heating, and the second between 300 and 550°C, associated with coke that changed its structure during the heating. A regeneration at intermediate temperatures, e.g. 300°C, removes the coke that corresponds to the first peak, but does not restore the initial activity. If the regeneration is carried out at higher temperatures, e.g. 500°C, most of the coke is removed, but this treatment leads to changes in the structure of the HPA, as indicated by FTIR and MAS-NMR analysis. Regeneration with O3 at low temperature (125°C) is effective both for coke removal and to recover the catalytic activity.-
dc.descriptionFil: Baronetti, Graciela Teresita. 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.descriptionFil: Thomas, Horacio Jorge. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Centro de Investigación y Desarrollo en Ciencias Aplicadas "Dr. Jorge J. Ronco". Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Centro de Investigación y Desarrollo en Ciencias Aplicadas; Argentina-
dc.descriptionFil: Querini, Carlos Alberto. 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.formatapplication/pdf-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherElsevier Science-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/S0926-860X(01)00576-2-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X01005762-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/18804-
dc.subjectIsobutane alkylation-
dc.subjectHeteropolyacids-
dc.subjectWells-Dawson-
dc.subjectRegeneration-
dc.subjectOtras Ingeniería Química-
dc.subjectIngeniería Química-
dc.subjectINGENIERÍAS Y TECNOLOGÍAS-
dc.titleWells–Dawson heteropolyacid supported on silica: isobutane alkylation with C4 olefins-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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