• Title of article

    Composition and crystal structure of resorbable calcium phosphate thin films

  • 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 ,

  • Issue Information
    دوهفته نامه با شماره پیاپی سال 2006
  • Pages
    12
  • From page
    4273
  • To page
    4284
  • 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. C 2006 Springer Science + Business Media, Inc.
  • Journal title
    Journal of Materials Science
  • Serial Year
    2006
  • Journal title
    Journal of Materials Science
  • Record number

    831028