Preparation and characterization of Nickel-and cobalt-doped magnetites

dc.date.accessioned2011-02-07T20:04:29Z
dc.date.available2011-02-07T20:04:29Z
dc.descriptionTrabalho apresentado no I Simpósio Mineiro de Ciências dos Materiais, Ouro Preto, Novembro de 2001.por
dc.identifier.citationLELIS, Maria de Fátima Fontes et al. Preparation and characterization of Nickel-and cobalt-doped magnetites. Mat. Res., São Carlos, v. 6, n. 2, p. 145-150, abr./jun. 2003. Disponível em: <http://www.scielo.br/pdf/mr/v6n2/16015.pdf>. Acesso em: 28 jan. 2011.por
dc.identifier.doi10.1590/S1516-14392003000200006
dc.identifier.issn1516-1439
dc.identifier.urihttp://repositorio.ufes.br/handle/10/541
dc.rightsopen accessen
dc.titlePreparation and characterization of Nickel-and cobalt-doped magnetitespor
dc.typearticleen
dcterms.abstractNickel- and cobalt-doped magnetites were prepared by a co-precipitation method and studied in some detail, in an effort to identify some effects of the doping cations on the magnetic, crystallographic and morphological properties of the resulting spinel. The synthetic samples were characterized by conventional chemical analysis, powder X-ray diffractometry, Mössbauer spectroscopy, saturation magnetization and scanning electron microscopy. From chemical analysis, the continuous increase of Ni2+ or Co2+ is accompanied by a simultaneous decrease of the Fe2+ contents, in the spinel structure. The magnetization values also decrease continuously with increasing doping cation contents. Mössbauer parameters are characteristic of substituted magnetites and indicate the presence of a single phase only. Based on the inverted intensities of the lines 1 (leftmost, on the negative Doppler velocity scale) and 2 of Mössbauer spectra of doped samples, relatively to the pure magnetite, it was assumed that the isomorphical substitution occurs preferentially on octahedral coordination sites of the spinel structure. The coercive field of these ferrites decrease steadily with Ni2+ but increases with Co2+ contents, reaching a maximum at x = 0.38, in the general formula CoxFe3-xO4.eng
dcterms.creatorLelis, Maria de Fátima Fontes
dcterms.creatorFabris, José Domingos
dcterms.creatorMussel, Wagner da Nova
dcterms.creatorTakeuchi, Armando Yoshihaki
dcterms.issued2003-04
dcterms.languageengen
dcterms.subjectMössbauer, Espectroscopia depor
dcterms.subjectFerritapor
dcterms.subjectMagnetizaçãopor
dcterms.subjectFerriteeng
dcterms.subjectMagnetizationeng
dcterms.subjectSpectroscopy, Mossbauereng
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