The thermal stability of calcium hydroxyapatites (CaHAp) as prepared by traditional methods is quite low, with the preponderance of CaHAp being converted to Ca 3 (PO 4 ) 2 at temperatures as low as 973 K. In contrast, control of the pH during preparation markedly enhances the thermal stability of Ca
Preparation, Characterization, and Thermal Stability of Lead Hydroxyapatite
โ Scribed by Shigeru Sugiyama; Tomomi Nakanishi; Tomohiro Ishimura; Toshihiro Moriga; Hiromu Hayashi; Naoya Shigemoto; John B. Moffat
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 158 KB
- Volume
- 143
- Category
- Article
- ISSN
- 0022-4596
No coin nor oath required. For personal study only.
โฆ Synopsis
Lead hydroxyapatites (PbHAp) have been prepared from H3PO4 and Pb(NO3)2 โข 5PbO (1), the latter of which was obtained through dehydration of basic lead nitrates such as 2Pb(NO3)2 โข 5Pb(OH)2 (2) and Pb(NO3)2 โข 5Pb(OH)2 (3). The amount of 2 with respect to 3, as well as the quantity of an unidentified water-soluble compound (4), decreased with increasing reaction time. The dehydration of 2 and 3, but not of 4, yielded the desired compound with expected X-ray diffraction pattern and infrared spectra. When the prepared PbHAp was heated at 773, 973, and 1173 K for 3 h, the XRD patterns showed the apatite structure, respectively, but PbHAp heated at 1173 K was partly converted to an amorphous compound. At 1473 K, PbHAp completely melted. X-ray absorption fine structure analyses showed that the nearest-neighbor distance of the Pb-O bond in PbHAp was 2.18 A s , which was shorter than that of the Ca-O bond of calcium hydroxyapatite and Sr-O bond of strontium hydroxyapatite.
๐ SIMILAR VOLUMES
Carbonated barium hydroxyapatite (Ba10(PO4)6(OH)2-2x(CO3)x, X = 0.30-0.57, BaHAP) particles with different Ba/P molar ratios were prepared by a wet method. CO2-3 ions were incorporated into OH- sites of a BaHAP lattice during the preparation at high solution pH. The obtained BaHAP particles were wel
Hydroxyapatite (HA) coatings on titanium alloy substrates were prepared by an alkaline treatment of electrodeposited precursors. The structure, residual stress, and bond strength of the coatings were investigated. Test results showed that the coatings processed in this study exhibited fairly low ten