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dc.contributor.authorPena, O.-
dc.contributor.authorCailleaux, X.-
dc.contributor.authorPiriou, B.-
dc.contributor.authordel Canto, M.-
dc.contributor.authorAbarca, S.-
dc.contributor.authorRios, E.-
dc.contributor.authorOrtiz, J.-
dc.contributor.authorGautier, J. L.-
dc.contributor.authorLisboa Filho, Paulo Noronha-
dc.contributor.authorMoure, C.-
dc.date.accessioned2014-05-20T15:19:24Z-
dc.date.accessioned2016-10-25T17:52:15Z-
dc.date.available2014-05-20T15:19:24Z-
dc.date.available2016-10-25T17:52:15Z-
dc.date.issued2007-01-01-
dc.identifierhttp://dx.doi.org/10.1016/j.jeurceramsoc.2007.02.058-
dc.identifier.citationJournal of the European Ceramic Society. Oxford: Elsevier B.V., v. 27, n. 13-15, p. 3911-3914, 2007.-
dc.identifier.issn0955-2219-
dc.identifier.urihttp://hdl.handle.net/11449/30900-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/30900-
dc.description.abstractMagnetic properties of two spinel oxides solid solutions, Cul+xMn2-xO4 and Ni1+xMn2-xO4 are reported. These series are characterized by two magnetic transitions: the upper one, of ferrimagnetic type, occurs at about 85 K (for copper-based) and at 105-110 K (for nickel-based spinels), independently of the x-content: the lower transition may be related to a Neel-type collinear ordering and takes place at 30 and 45 K, respectively. Application of moderate fields (H > 250 Oe) make both transitions to merge into one broad maximum in the magnetization, which takes place at lower temperature when applying larger fields. Magnetization cycles with temperature (ZFC/FC) or field (loops) allowed us to well characterize the ordered state. The effective moment follows the expected behavior when manganese ions are being substituted by ions of lower magnetic moment (Ni(2+)andCU(2+)). (c) 2007 Elsevier Ltd. All rights reserved.en
dc.format.extent3911-3914-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectspinelspt
dc.subjectmagnetic propertiespt
dc.subjectsoft magnetspt
dc.subjectferrimagnetismpt
dc.titleMagnetic properties of Cu1+xMn2-xO4 and Ni1+xMn2-xO4 solid solutionsen
dc.typeoutro-
dc.contributor.institutionUniv Rennes 1-
dc.contributor.institutionUniv Santiago-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionCSIC-
dc.description.affiliationUniv Rennes 1, CNRS, UMR 6226, Sci Chim Rennes, F-35042 Rennes, France-
dc.description.affiliationUniv Santiago, Fac Quim & Biol, Dept Chem Mat, Santiago, Chile-
dc.description.affiliationUniv Estadual Paulista, Dept Fis, UNESP, Bauru, Brazil-
dc.description.affiliationCSIC, Electroceram Dept, Inst Ceram & Vidrio, E-28049 Madrid, Spain-
dc.description.affiliationUnespUniv Estadual Paulista, Dept Fis, UNESP, Bauru, Brazil-
dc.identifier.doi10.1016/j.jeurceramsoc.2007.02.058-
dc.identifier.wosWOS:000248822800071-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of the European Ceramic Society-
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