Author/Authors :
L. TUCK?، نويسنده , , M. SAYER، نويسنده , , M. MACKENZIE، نويسنده , , J. HADERMANN، نويسنده , , D. Dunfield، نويسنده , , A. Pietak، نويسنده , , J. W. REID، نويسنده , , A. D. Stratilatov، نويسنده ,
Abstract :
Silicon stabilized tricalcium phosphate (Si-TCP) is formed, among other phases, as a result of
sintering hydroxyapatite (HA) in the presence of silica (SiO2) at >800◦C. Calcium phosphate
films sintered at 1000◦C on quartz substrates are examined with and without additional SiO2
added to the starting precipitate. Data from transmission electron microscopy (TEM) and X-ray
photoelectron spectroscopy (XPS) separate the undoped film morphology into a surface layer
with a monoclinic crystal structure P21/a characteristic of α or Si-tricalcium phosphate and grain
size in the range 100–1000 nm and a substrate layer with a crystal structure which is
predominantly apatitic P63/m and grain size in the range 30–100 nm. The silicon content is
greatest in the substrate layer. The addition of SiO2 to the film material during fabrication
induces a more uniform grain size of 10–110 nm and a higher Si content. The structural and
phase evolution of these films suggests the nucleation of α-TCP by the local formation of
Si-TCP at a SiO2-hydroxyapatite interface. The results are consistent with X-ray diffraction
studies and are explained by a model of nucleation and growth developed for bulk powders.
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