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dc.contributor.authorSchiesser, Emilio C.
dc.contributor.authorBlanco, Élodie
dc.contributor.authorDongil, Ana Belén
dc.contributor.authorZárate, Ximena P.
dc.contributor.authorSaavedra-Torres, Mario
dc.contributor.authorSchott V, Eduardo
dc.contributor.authorCanales, Roberto I.
dc.contributor.authorEscalona, Néstor
dc.date.accessioned2021-05-13T05:51:13Z
dc.date.available2021-05-13T05:51:13Z
dc.date.issued2021
dc.identifier10.1021/acs.jpcc.0c11415
dc.identifier.issn19327447
dc.identifier.urihttps://hdl.handle.net/20.500.12728/8849
dc.description.abstractCatalytic hydrodeoxygenations of furfural, guaiacol, and their mixture at different concentrations were carried out over a Ni/SiO2 catalyst to study the kinetic and competitive effects. Anisole was also studied to compare with the effects of guaiacol. Additionally, kinetic parameters were adjusted through mathematical modeling to explain the mixture behavior, and density functional theory (DFT) simulations were carried out to study the effect observed in the present work. The use of guaiacol and anisole in the mixture produces an increase in the reaction rate of furfural. Furthermore, guaiacol slightly generates a change in the selectivity of furfural products, attributed to its hydroxyl group, as such a change was not observed with anisole. DFT studies showed that the hydrogen atom of the hydroxyl group of guaiacol migrated to furfural. Both effects would be enhanced by increasing the guaiacol concentration, which could act as a stabilizing agent inhibiting the coke formation in the furfural reaction.es_ES
dc.language.isoenes_ES
dc.publisherAmerican Chemical Societyes_ES
dc.subjectAldehydeses_ES
dc.subjectAtomses_ES
dc.subjectDensity functional theoryes_ES
dc.subjectFurfurales_ES
dc.subjectMixtureses_ES
dc.titleInsights into Hydrodeoxygenation of Furfural and Guaiacol Mixture: Experimental and Theoretical Studieses_ES
dc.typeArticlees_ES


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