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Properties of carbon-supported precious metals catalysts under reductive treatment and their influence in the hydrodechlorination of dichloromethane
dc.contributor.author | Arevalo-Bastante, Alejandra | |
dc.contributor.author | Martin-Martinez, Maria | |
dc.contributor.author | Álvarez Montero, Ariadna | |
dc.contributor.author | Rodriguez, Juan J. | |
dc.contributor.author | Gómez Sainero, Luisa María | |
dc.contributor.other | UAM. Departamento de Ingeniería Química | es_ES |
dc.date.accessioned | 2019-05-20T14:31:59Z | |
dc.date.available | 2019-05-20T14:31:59Z | |
dc.date.issued | 2018-12-18 | |
dc.identifier.citation | Catalysts 8.12 (2018): 664 | es_ES |
dc.identifier.issn | 2073-4344 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10486/687568 | |
dc.description.abstract | This study analyzes the effect of the reduction temperature on the properties of Rh, Pt and Pd catalysts supported on activated carbon and their performance in the hydrodechlorination (HDC) of dichloromethane (DCM). The reduction temperature plays an important role in the oxidation state, size and dispersion of the metallic phase. Pd is more prone to sintering, followed by Pt, while Rh is more resistant. The ratio of zero-valent to electro-deficient metal increases with the reduction temperature, with that effect being more remarkable for Pd and Pt. The higher resistance to sintering of Rh and the higher stability of electro-deficient species under thermal reductive treatment can be attributed to a stronger interaction with surface oxygen functionalities. Dechlorination activity and a TOF increase with reduction temperature (250–450 ◦ C) occurred in the case of Pt/C catalyst, while a great decrease of both was observed for Pd/C, and no significant effect was found for Rh/C. Pt 0 represents the main active species for HDC reaction in Pt/C. Therefore, increasing the relative amount of these species increased the TOF value, compensating for the loss of dispersion. In contrast, Pd n+ appears as the main active species in Pd/C and their relatively decreasing occurrence together with the significant decrease of metallic area reduces the HDC activity. Rh/C catalyst suffered only small changes in dispersion and metal oxidation state with the reduction temperature and thus this variable barely affected its HDC activity | en_US |
dc.description.sponsorship | The authors gratefully acknowledge financial support from the Spanish Ministerio de Economía y Competitividad (MINECO) through the projects CTM 2014-53008 and CTM2017-85498-R. A. Arevalo Bastante acknowledges MINECO for her research grant. M. Martín Martínez acknowledges the postdoc grant 2017-T2/AMB-5668 from Comunidad de Madrid, Programme “Atracción de talento investigador” | en_US |
dc.format.extent | 14 pag. | en |
dc.format.mimetype | application/pdf | en |
dc.language.iso | eng | en |
dc.publisher | MDPI AG | en_US |
dc.relation.ispartof | Catalysts | en_US |
dc.rights | © 2018 by the authors. Licensee MDPI, Basel, Switzerland. | en_US |
dc.subject.other | Dispersion | es_ES |
dc.subject.other | Hydrodechlorination | en_US |
dc.subject.other | Precious metals | en_US |
dc.subject.other | Reduction temperature | en_US |
dc.subject.other | Turnover frequency | en_US |
dc.subject.other | XPS | en_US |
dc.title | Properties of carbon-supported precious metals catalysts under reductive treatment and their influence in the hydrodechlorination of dichloromethane | en_US |
dc.type | article | en |
dc.subject.eciencia | Química | es_ES |
dc.relation.publisherversion | https://doi.org/10.3390/catal8120664 | es_ES |
dc.identifier.doi | 10.3390/catal8120664 | es_ES |
dc.identifier.publicationfirstpage | 664-1 | es_ES |
dc.identifier.publicationissue | 12 | es_ES |
dc.identifier.publicationlastpage | 664-14 | es_ES |
dc.identifier.publicationvolume | 8 | es_ES |
dc.relation.projectID | Gobierno de España. CTM 2014-53008 | es_ES |
dc.relation.projectID | Gobierno de España. CTM2017-85498-R | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | en |
dc.rights.cc | Reconocimiento | es_ES |
dc.rights.accessRights | openAccess | en |
dc.facultadUAM | Facultad de Ciencias |