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hal.structure.identifierU.R. Matériaux Inorganiques, Département de Chimie
dc.contributor.authorBOUGHZALA, Khaled
hal.structure.identifierU.R. Matériaux Inorganiques, Département de Chimie
dc.contributor.authorBEN SALEM, Ezzedine
hal.structure.identifierDepartment of Chemistry
dc.contributor.authorKOOLI, Fethi
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorGRAVEREAU, Pierre
hal.structure.identifierU.R. Matériaux Inorganiques, Département de Chimie
dc.contributor.authorBOUZOUITA, Khaled
dc.date.issued2008
dc.identifier.issn1002-0721
dc.description.abstractEnStrontium-britholites whose chemical formula was Sr10−xLax(PO4)6−x(SiO4)xF2, where x=0, 1, 2, and 4 were prepared by solid state reaction. The structural refinement carried out using the Rietveld method indicated that La3+ ions were located into the two sites with a strong preference for metal (2) sites especially for low contents. A progressive shift of the F− position along the c-axis outside the centre of the triangle formed by metal (2)-atoms was observed with the increase of x. The infrared and Raman spectra exhibited the characteristic vibration modes of PO4 and SiO4 groups confirming the incorporation of this last group into the apatite structure. The 29Si MAS-NMR spectra exhibited one resonance peak confirming the data obtained by X-ray diffraction, indicating that P and Si were located in the same crystallographic site.
dc.language.isoen
dc.publisherElsevier
dc.subject.enStrontium
dc.subject.enBritholites
dc.subject.enRietveld refinement
dc.subject.enInfrared spectroscopy
dc.subject.enNuclear magnetic resonance (NMR)
dc.subject.enRaman spectroscopy
dc.subject.enRare earths
dc.title.enSpectroscopic studies and Rietveld refinement of strontium-britholites
dc.typeArticle de revue
dc.identifier.doi10.1016/S1002-0721(08)60123-4
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Rare Earths
bordeaux.page483-489
bordeaux.volume26
bordeaux.issue4
bordeaux.peerReviewedoui
hal.identifierhal-00322323
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00322323v1
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