Probing the Catalytic Activity of Sulfate-Derived Pristine and Post-Teatred Porous TiO2(101) Anatase Mesocrystals by the Oxidative Desulfurization of Dibenzothiophenes.

dc.creatorRivoira , Lorena Paola
dc.creatorMartínez , María Laura
dc.creatorFalcón , Horacio
dc.creatorBeltramone , Andrea Raquel
dc.creatorCampos , Martín
dc.creatorFierro, José
dc.creatorTartaj, Pedro
dc.creatorMartínez , María Laura
dc.date.accessioned2025-04-30T19:39:39Z
dc.date.issued2017
dc.description.abstractMesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimiza- (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur com pounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain (pores around 3−4 nm and surface areas around 200 m2 /g). Ultimately, this stability has allowed us to compare the catalytic activity of anatasesthat expose a high number of aligned single crystal-like surfaces while differing in controllable surface essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil− the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative establish that (101) anatase mesocrystals with excellent textural propertiesshow adequate stability to withstand several post treatments without losing their initial mesocrystalline character and therefore could serve as modelsfor catalytic processes different from the one studied here.
dc.description.affiliationFil: Rivoira, Lorena Paola. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
dc.description.affiliationFil: Martínez, María Laura. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
dc.description.affiliationFil: Falcón, Horacio. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
dc.description.affiliationFil: Beltramone, Andrea Raquel. Universidad Tecnológica Nacional. Facultad Regional Córdoba. Centro de Investigación Nanociencia y Nanotecnología; Argentina.
dc.description.affiliationFil: Campos, Martín. Universidad Cantoblanco. Instituto de Catálisis y Petroleoquímica. Energy and Sustainable Chemistry Group; España.
dc.description.affiliationFil: Fierro, José. Universidad Cantoblanco. Instituto de Catálisis y Petroleoquímica. Energy and Sustainable Chemistry Group; España.
dc.description.affiliationFil: Tartaj, Pedro. Universidad Cantoblanco. Instituto de Ciencia de Materiales; España.
dc.formatpdf
dc.identifier.citationAmerican Chemical Society,2017.
dc.identifier.urihttps://hdl.handle.net/20.500.12272/12838
dc.language.isoen
dc.publisherUnivesidsad Tecnológica Nacional.
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.holderRivoiraq, Lorena Paola; Martínez, María Laura; Falcón, Horacio; Beltramone, Andrea Raquel; Campos, Martín; Fierrro, José; Tartaj, Pedro.
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.usehttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCatalitic activity
dc.subjectPorous TiO2(101)
dc.subjectAnatase
dc.titleProbing the Catalytic Activity of Sulfate-Derived Pristine and Post-Teatred Porous TiO2(101) Anatase Mesocrystals by the Oxidative Desulfurization of Dibenzothiophenes.
dc.typeinfo:eu-repo/semantics/article
dc.type.versionacceptedVersion

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