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Synthesis, X‐ray Structural Analysis and Spectroscopic Investigations (IR and 31 P MAS NMR) of Mixed Barium/Strontium Fluoroapatites
Author(s) -
Aissa Abdallah,
Badraoui Béchir,
Thouvenot René,
Debbabi Mongi
Publication year - 2004
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200400224
Subject(s) - chemistry , strontium , barium , rietveld refinement , crystallography , lattice constant , powder diffraction , analytical chemistry (journal) , crystal structure , inorganic chemistry , diffraction , physics , organic chemistry , chromatography , optics
Continuous solid solutions of barium/strontium fluoroapatites Ba (10− x ) Sr x (PO 4 ) 6 F 2 (Ba (10− x ) Sr x FAp; 0 ⩽ x ⩽ 10) were obtained in an aqueous medium. They were investigated by Rietveld structure‐refinement methods using powder X‐ray diffraction patterns and by chemical analysis, IR spectroscopy and 31 P MAS NMR spectroscopy. Replacement of barium by strontium induces a regular decrease of the lattice constants a and c according to Vegard’s law. The results of the powder‐fitting structure refinements indicate a clear preference of strontium for the S(1) site of the apatitic structure. A high‐wavenumber shift of the IR absorption bands characteristic of PO 4 internal modes is also observed, in agreement with the diminution of the ionic character of the M−O bonds. For increasing strontium content, a regular δ iso increase is shown in the 31 P MAS NMR spectra, from δ = 0.91 ppm for Ba 10 FAp to δ = 3.06 ppm for Sr 10 FAp. For all mixed Ba/Sr fluoroapatites, the low intensities of the spinning bands reflect the weak 31 P chemical‐shift anisotropy, in agreement with the low distortion of the PO 4 tetrahedron, as shown by Rietveld refinement. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)