dc.creatorMilt, Viviana Guadalupe
dc.creatorIvanova, S.
dc.creatorSanz, O.
dc.creatorDomínguez, M. I.
dc.creatorCorrales, A.
dc.creatorOdriozola, J.A.
dc.creatorCenteno, M.A.
dc.date.accessioned2017-07-24T20:21:48Z
dc.date.accessioned2018-11-06T14:01:00Z
dc.date.available2017-07-24T20:21:48Z
dc.date.available2018-11-06T14:01:00Z
dc.date.created2017-07-24T20:21:48Z
dc.date.issued2013-01
dc.identifierMilt, Viviana Guadalupe; Ivanova, S.; Sanz, O.; Domínguez, M. I.; Corrales, A.; et al.; Au/TiO2 supported on ferritic stainless steel monoliths as CO oxidation catalysts; Elsevier; Applied Surface Science; 270; 1-2013; 169-177
dc.identifier0169-4332
dc.identifierhttp://hdl.handle.net/11336/21225
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1881793
dc.description.abstractMetallic supported structured catalysts were obtained by washcoating AluchromYHf monoliths with an Au/TiO2 catalyst. The powder catalyst was synthesized by DAE (direct anionic exchange) method. Using this catalyst, a stable slurry was prepared and used to washcoat the monoliths. TEM and SEM studies revealed that gold nanoparticles in the Au/TiO2 powder catalyst had an average diameter of 3–4 nm, but during the preparation of the structured catalyst, aggregate Au particles of the slurry reached diameters of 9 nm. Before coating, Aluchrom YHf monoliths were thermally treated to generate a homogeneous and well-adhered oxide rough surface layer, mainly composed of -Al2O3 whiskers, which favored the anchoring of the catalyst. The catalytic layer deposited was well attached and contained not only the Au/TiO2 catalyst but also metallic oxides formed from stainless steel components that diffused through the oxide scale. The structural characterization was performed by XRD, XRF, TEM, SEM, GD-OES and SBET.<br />The catalytic activity of the powder and structured catalysts was tested in the oxidation of the CO<br />reaction. Catalysts demonstrated to be active at room temperature. After a first activation run, and in spite of their larger gold particle size, the catalytic activities of the structured catalysts overcame those of the powder catalyst. This improvement is probably due to the segregation of the transition metal oxides toward the surface oxide scale.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apsusc.2012.12.159
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S016943321300007X
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectSTRUCTURED CATALYSTS
dc.subjectAU/TIO2
dc.subjectCO OXIDATION
dc.subjectMETALLIC CATALYSTS
dc.subjectAluchrom YHf
dc.titleAu/TiO2 supported on ferritic stainless steel monoliths as CO oxidation catalysts
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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