The purpose of this study was to synthesize calcium phosphates doped with titanium and fluoride ions in different combinations. Pure and doped calcium phosphates were synthesized by a precipitation method. The synthesized materials were sintered at 1100&ordm / C and 1300&ordm / C for 1h. The ceramics were characterized by density measurements to determine the effect of sintering temperature. Presence of phases and bonds were characterized by XRD diffraction and FTIR spectroscopy. Grain sizes of the samples were obtained by SEM. Microhardness test was applied on the samples to determine the mechanical properties of the samples. It was observed that Ti4+ addition decreased the density of samples significantly at 1100&deg / C, whereas increasing the sintering temperature to 1300&deg / C caused an increase. Increasing the F- ion amount increased the densification at 1100&deg / C when molar ratios were 1.0, 1.25, 1.50 and decreased the density at 1300&deg / C when Ca /P molar ratios were 1.0, 1.25, 1.67 and 2.0. Ti4+ and F- co-doped samples showed variety in their density behaviour after the sintering at 1100&ordm / C and 1300&ordm / C. The XRD analyses demonstrated that for Ca to P ratio 1 at 1100&deg / C, &beta / -CPP phase, when sintering temperature was raised to 1300&deg / C, as a second phase of &beta / -CPP and &alpha / -TCP observed. Increasing the molar ratio to 1.25 and 1.50 demonstrated &beta / -TCP and/or &beta / -CPP and &beta / -TCP/ HA at 1100&deg / C and &beta / -TCP and/or &beta / -CPP, &alpha / -TCP, TiO2 and HA, &alpha / -TCP, TiO2 phases at 1300&deg / C, respectively. In higher Ca/P molar ratios of 1.67 and 2.0, HA, &beta / -TCP, &alpha / -TCP, CaO, TiO2, CaTiO3 and HA, CaO, &alpha / -TCP, CaTiO3 phases were determined. Increasing the sintering temperature to 1300&deg / C resulted in transformation to &alpha / -TCP. In FTIR spectroscopy analysis, when the samples with molar ratio of 1, 1.25, 1.50, 1.67 and 2.0, sintered at 1100&deg / C, the characteristic bands of &beta / -CPP, OCP/&beta / -TCP, &beta / -TCP/HA, HA and HA were observed, respectively. With increasing the sintering temperature to 1300&deg / C, samples with molar ratio of 1.0 and 1.25 revealed additional secondary characteristic peaks of HA and &beta / -TCP. SEM images revealed that sintering temperature and ion amounts of dopants had significant effect on grain sizes of the samples. The grain sizes were generally increased when sintering temperature rose from 1100&deg / C to 1300&deg / C. The &mu / -hardness test demonstrated that Ti4+ and F- ions in large amounts had positive effect on the mechanical properties at the sintering temperatures of 1100&deg / C and 1300&deg / C

Reproduction de : Thèse de doctorat : Science et génie des matériaux : Toulouse, INPT : 2006. / Titre provenant de l'écran-titre. Bibliogr. 128 réf.

Hydroxyapatite (HA, Ca₁₀(PO₄)₆(OH)₂) is one of the most abundant materials in mammal bone. It crystallizes in an aqueous environment within spaces between tropocollagen protein chains. However, despite its abundance and possible usefulness in the medical field this complex physical system remains poorly understood to date. We present a theoretical study of the energetics of hydroxyapatite, its electronic, mechanical and thermodynamic properties. Our mechanical and thermodynamic properties from first principles are in excellent agreement with the rare available experimental data. The monoclinic and hexagonal phases are lowest in energy. A comparison of the phonon dispersions of these two phases reveals that a phase transition occurs due to a difference in vibrational free energy. The transition is of order-disorder type. Our calculated phase transition temperature is 680 K, in decent agreement with the experimentally determined 470 K. An alternative theoretical model yields 882 K. The phase transition is mediated by OH libration modes. We also report for the first time on a peculiarity in the phonon spectrum of hexagonal and monoclinic HA. When studying the Lyddane-Sachs-Teller shifts in the spectrum close to the [Gamma]-point we identify two vibration modes showing a systematically increasing Lyddane-Sachs-Teller shift in frequency with decreasing dielectric constant. In experiment, the dielectric constant varies between 5 and 20 depending on the Ca/P ratio in the sample. The frequency shifts in the affected modes are as large as 20 cm⁻¹ as one spans the range of the dielectric constant. Thus, a simple spectroscopic analysis of a sample of bone may determine the quality of the sample in a physiological sense. We also identify the chemically stable low energy surface configurations as function of the OH, PO₄ and Ca concentration. In the experimentally relevant OH-rich regime we find only two surfaces competing for lowest energy. The surface most stable over almost the entire OH-rich regime is OH-terminated, and is currently being investigated in the presence of water and atomic substitutions on the HA surface. / text

No description available.

Thesis (M.S.)--University of Alabama at Birmingham, 2008. / Description based on contents viewed Feb. 5, 2008; title from title screen. Includes bibliographical references (p. 65-68).

Thesis (Ph. D.)--University of Hong Kong, 2007. / Also available in print.

Thesis (Master)--İzmir Institute Of Technology, İzmir, 2006. / Keywords: Hydroxiapatites, alumina ceramic, zirconium oxide, urea, precipitations. Includes bibliographical references (leaves. 73-75).

Thesis (Ph. D.)--Medical College of Georgia, 1997. / eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Thesis (Ph. D.)--Medical College of Georgia, 1997. / eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Thesis (Ph.D.)--University of Delaware, 2009. / Principal faculty advisor: Thomas P. Beebe, Jr., Dept. of Chemistry & Biochemistry. Includes bibliographical references.