• DocumentCode
    309479
  • Title

    Calcium phosphate bioceramics with improved properties: chemical synthesis

  • Author

    Thorne, Kevin ; Saint-Pierre, Philippe D. ; Hepler, Brad

  • Author_Institution
    Dept. of Restorative Dentistry, Illinois Univ., Urbana, IL, USA
  • fYear
    1997
  • fDate
    4-6 Apr 1997
  • Firstpage
    260
  • Lastpage
    263
  • Abstract
    As compared to metallic skeletal restorations, calcium phosphate ceramics offer superior properties, including: strong chemical resistance to environmental and microbial corrosion, compositionally controllable in vivo biological performance (bioactivity, solubility), high wear resistances, and excellent mechanical properties. Unfortunately, these ideal properties have not been obtained because commercial calcium phosphate ceramics vary notably in purity, crystal structure, and particle size. As a novel processing solution, a two-step processing technique was developed to result in a wide compositional range of pure, stoichiometric calcium phosphates [xCaO·P2 O5; x=3.0-3.3], The first step involved the low temperature (⩽5°C) reaction between CaO and high purity phosphoric acid [H3PO4, Na-2 ppb]. After eliminating soluble reactants and impurity calcium phosphate phases, a crystalline calcium orthophosphate [CaHPO4] powder was obtained in 61.1% yields. Thermal analysis (TGA, DTA), X-ray diffraction (XRD) and optical pyncnometry indicated that this product endothermically transforms at 460°C [92.7% yield] into a highly pure, crystalline calcium pyrophosphate (2CaO·P2O5) with an average particle size of 3.8 μm (2-15 μm). In the second step, 2CaO·P2O5 was intimately blended with low alkali impurity CaCO3 (1,1,3 mole%) and calcined in pure oxygen atmospheres to result in controlled composition calcium phosphate ceramics (xCaO·P2O5). To demonstrate the potential of this technique, crystalline oxyapatite ceramics (3.33CaO·P2O5) were obtained in high yields (85.8%) at temperatures exceeding 1000°C with average crystalline particle sizes of 3.8 μm (2-20 μm). Petrographic, refractive index characterization of the ceramic precursor powders indicate that in all stages of processing, high purity, spherical powders of uniform crystallinity and particle size were obtained. In contrast to conventional calcium phosphate ceramics, this novel processing technique results in crystalline precursor powders of high purity, controlled composition, uniform crystal structure, and homogeneous particle size distribution. These ceramic precursor powders can be used with conventional ceramic processing techniques to result in products with the improved properties required for clinical success
  • Keywords
    X-ray diffraction; calcium compounds; ceramics; chemical reactions; materials preparation; particle size; phosphorus compounds; powder technology; prosthetics; refractive index; stoichiometry; thermal analysis; 1 to 14 mum; 1000 degC; 2 to 15 mum; 2 to 20 mum; 460 degC; 5 degC; CaCO3; CaHPO4; CaO-P2O5; H3PO4; X-ray diffraction; bioactivity; calcium phosphate bioceramics; ceramic processing techniques; chemical synthesis; clinical success; compositionally controllable in vivo biological performance; controlled composition; crystal structure; crystalline calcium orthophosphate powder; crystalline oxyapatite ceramics; environmental corrosion; high purity; high wear resistances; homogeneous particle size distribution; low temperature reaction; mechanical properties; microbial corrosion; optical pyncnometry; particle size; petrographic characterization; purity; refractive index characterization; skeletal restorations; solubility; strong chemical resistance; thermal analysis; two-step processing technique; uniform crystal structure; uniform crystallinity; Bioceramics; Calcium; Ceramics; Chemicals; Corrosion; Crystallization; Immune system; Impurities; Mechanical factors; Powders;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Biomedical Engineering Conference, 1997., Proceedings of the 1997 Sixteenth Southern
  • Conference_Location
    Biloxi, MS
  • ISSN
    1086-4105
  • Print_ISBN
    0-7803-3869-3
  • Type

    conf

  • DOI
    10.1109/SBEC.1997.583278
  • Filename
    583278