Mañana, JUEVES, 24 DE ABRIL, el sistema se apagará debido a tareas habituales de mantenimiento a partir de las 9 de la mañana. Lamentamos las molestias.

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dc.contributor.authorBaeza Herrera, José Alberto 
dc.contributor.authorCalvo, Luisa
dc.contributor.authorAlonso Morales, Noelia 
dc.contributor.authorHeras Muñoz, Francisco 
dc.contributor.authorEser, Semih
dc.contributor.authorRodríguez, Juan J.
dc.contributor.authorGilarranz Redondo, Miguel Ángel 
dc.contributor.otherUAM. Departamento de Ingeniería QuímicaES
dc.date.accessioned2018-08-22T14:10:35Z
dc.date.available2018-08-22T14:10:35Z
dc.date.issued2017-11-10
dc.identifier.citationChemical Engineering Science 176 (2018): 400-408en_US
dc.identifier.issn0009-2509 (print)es_ES
dc.identifier.issn1873-4405 (online)es_ES
dc.identifier.urihttp://hdl.handle.net/10486/684668
dc.description.abstractCatalysts consisting of Pd supported on virgin and heat-treated carbon blacks (homemade and commercial), graphites (natural and synthetic) and commercial carbon nanofibers were prepared and tested in the aqueous phase hydrodechlorinaton (HDC) of 4-chlorophenol (4-CP) under near ambient conditions (30 °C, 1 atm) in order to explore the effect of the support on the catalytic behavior. The homemade graphitized supports were prepared from commercial carbon black (CB) and from a carbon black-like material (CBPE) obtained from pyrolysis of low-density polyethylene. All the catalysts prepared yielded complete 4-CP conversion, although a wide range of activity was observed (10.7–173.5 mmol gPd−1 min−1). The graphitized carbon black provided the most active catalysts, showing Pd nanoparticles around 3 nm in size and a well-balanced contribution of Pd species (Pdn+/Pd0 = 0.9). Substantial differences of activity were found between the graphitized and not graphitized supports, even for catalysts with similar Pd nanoparticle size. The higher activity of the catalysts with graphitized supports can be partly associated to a more balanced initial Pdn+ to Pd0 ratio. Moreover, higher selectivity to hydrogenation products (cyclohexanone) was also achieved with those catalysts due to a higher contribution of the Pd0 speciesen_US
dc.description.sponsorshipThe authors greatly appreciate financial support from the Spanish MINECO (CTQ2012-32821)en_US
dc.format.extent29 pag.es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherElsevier Ltden_US
dc.relation.ispartofChemical Engineering Scienceen_US
dc.rights© 2017 Elsevier Ltden_US
dc.subject.otherGraphitized supporten_US
dc.subject.otherCarbon blacken_US
dc.subject.otherHydrodechlorinationen_US
dc.subject.other4-chlorophenolen_US
dc.titleEffect of structural ordering of the carbon support on the behavior of Pd catalysts in aqueous-phase hydrodechlorinationen_US
dc.typearticleen
dc.subject.ecienciaFísicaes_ES
dc.subject.ecienciaQuímicaes_ES
dc.date.embargoend2019-11-10
dc.relation.publisherversionhttps://doi.org/10.1016/j.ces.2017.11.015es_ES
dc.identifier.doi10.1016/j.ces.2017.11.015es_ES
dc.identifier.publicationfirstpage400es_ES
dc.identifier.publicationlastpage408es_ES
dc.identifier.publicationvolume176es_ES
dc.relation.projectIDGobierno de España. CTQ2012-32821es_ES
dc.type.versioninfo:eu-repo/semantics/acceptedVersionen
dc.rights.ccReconocimiento – NoComercial – SinObraDerivadaes_ES
dc.rights.accessRightsopenAccessen
dc.facultadUAMFacultad de Ciencias


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