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dc.creatorGardey Merino, María
dc.date.accessioned2023-12-15T14:48:59Z
dc.date.available2023-12-15T14:48:59Z
dc.date.issued2015-01-01
dc.identifier.citationProcedia Materials Sciencees_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12272/9227
dc.description.abstractCo3O4 powders are used as pigment in solar selective paints. In this work, two new gel-combustion processes for the synthesis of Co3O4 nanopowders with lysine (Lys) or ethylenediaminetetraacetic acid (Edta) as fuel are presented. The first route is a conventional, stoichiometric process, while the second one is a non-stoichiometric, pH-controlled process. The samples were calcined in air at 500 ºC. They were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectrum (FTIR), Thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) and the optical properties of the pigments were assessed with a spectrophotometer. In all cases, powders exhibited the Co3O4 crystalline structure. A minimum crystallite average size of 19 nm for powders obtained by the “stoichiometric/Lys” combustion route was observed, meanwhile, a maximum value of 47 nm was stated for powders obtained by the “non-stoichiometric/Edta” combustion process. The average particle size ranged between 50 and 100 nm. The powders obtained by the stoichiometric nitrate–lysine route were selected to study its optical properties, their solar absorption was 88%, compared with the references, evidencing their aptitude to be used in solar absorbent paintses_ES
dc.formatpdfes_ES
dc.language.isoenges_ES
dc.rightsopenAccesses_ES
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.rights.uriCC0 1.0 Universal*
dc.sourceProcedia Materials Science 8 , 526 – 534. ( 2015 )es_ES
dc.subjectCombustion synthesis, Co3O4, Selective painting, Pigmentses_ES
dc.titleCombustion Syntheses of Co3O4 Powders Using Different Fuelses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderUniversidad Tecnológica Nacional. Facultad Regional Mendozaes_ES
dc.description.affiliationUniversidad Tecnológica Nacional. Facultad Regional Mendoza; Argentinaes_ES
dc.description.peerreviewedPeer Reviewedes_ES
dc.type.versionacceptedVersiones_ES
dc.rights.useAtribuciónes_ES
dc.identifier.doidoi: 10.1016/j.mspro.2015.04.105


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