A series of Sr-substituted hydroxyapatites, (Sr x Ca 1− x ) 5(PO 4) 3OH, where x = 0.00, 0.25, 0.50, 0.75 and 1.00, were made by a standard wet chemical route and investigated using X-ray diffraction (XRD), Rietveld refinement and Raman spectroscopy. We report apatites manufactured by two synthesis routes under 90 °C, and only the fully Sr-substituted sample had a small amount of an impurity phase, which is believed to be strontium pyrophosphate. Lattice parameters ( a and c), unit cell volume and density were shown to increase linearly with strontium addition and were consistent with the addition of a slightly larger and heavier ion (Sr) in place of Ca. XRD Lorentzian peak widths increased to a maximum at x = 0.50, then decreased with increasing Sr content. This indicated an increase in crystallite size when moving away from the x = 0.50 composition ( d ≈ 9.4 nm). There was a slight preference for strontium to enter the Ca(II) site in the mixed apatites (6 to 12% depending on composition). The position of the Raman band attributed to v 1 PO 4 3 - at around 963 cm −1 in hydroxyapatite decreased linearly to 949 cm −1 at full Sr-substitution. The full width at half maximum of this peak also correlated well and increased linearly with increasing crystallite size calculated from XRD.
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