Durucan C, Brown P W
Materials Research Laboratory, The Pennsylvania State University, University Park, PA 16802, USA.
J Mater Sci Mater Med. 2000 Jun;11(6):365-71. doi: 10.1023/a:1008934024440.
The kinetics of hydroxyapatite (HAp) formation by direct hydrolysis of alpha-tricalcium phosphate (alpha-TCP) [alpha-Ca(3)(PO(4))(2)] have been investigated. Transformation kinetics were examined for reactions at 37 degrees C, 45 degrees C and 56 degrees C by isothermal calorimetric analysis. Setting times and morphologies of the resultant HAp were found to be strongly dependent on reaction temperature. XRD analysis accompanied by FTIR confirmed that phase pure calcium-deficient hydroxyapatite (CDHAp) [Ca(10-x)(HPO(4))(x)(PO(4))(6-x)(OH)(2-x)] was formed. Complete reaction occurs within 18, 11, 6.5 h at 37, 45 and 56 degrees C, respectively. The extent of HAp formation differs for particulate slurries and pre-shaped forms of reactant alpha-TCP. Formation of hydroxyapatite in pre-formed pellets was hindered due to limited water penetration, but enhanced with the presence of NaCl as a pore generator. Regardless of the precursor characteristics and temperature, HAp formation is characterized by an initial period of wetting of the alpha-TCP precursor, an induction period and a growth period during which the bulk transformation to HAp occurs. The microstructures of the resultant HAp at all temperatures were generally similar and are characterized by the formation porous flake-like morphology. Microstructural coarsening was observed for the CDHAp formed above the physiological temperature. The hardening generated by the hydrolysis reaction was demonstrated using diametrical compression tests. The original tensile strength of 56% dense alpha-TCP increased from 0.70+/-0.1 MPa to 9.36+/-0.4 MPa after hydrolysis to CDHAp at 37 degrees C, corresponding to a density of 70%.
通过直接水解α-磷酸三钙(α-TCP)[α-Ca₃(PO₄)₂]来研究羟基磷灰石(HAp)的形成动力学。通过等温量热分析研究了在37℃、45℃和56℃下反应的转变动力学。发现所得HAp的凝固时间和形态强烈依赖于反应温度。XRD分析结合FTIR证实形成了相纯的缺钙羟基磷灰石(CDHAp)[Ca₁₀₋ₓ(HPO₄)ₓ(PO₄)₆₋ₓ(OH)₂₋ₓ]。在37℃、45℃和56℃下分别在18小时、11小时和6.5小时内发生完全反应。对于颗粒浆料和反应物α-TCP的预成型形式,HAp的形成程度有所不同。由于水渗透有限,预成型颗粒中羟基磷灰石的形成受到阻碍,但在作为孔隙生成剂的NaCl存在下会增强。无论前驱体特性和温度如何,HAp的形成都具有α-TCP前驱体的初始润湿期、诱导期和生长阶段,在此期间发生向HAp的整体转变。在所有温度下所得HAp的微观结构通常相似,其特征是形成多孔片状形态。在生理温度以上形成的CDHAp观察到微观结构粗化。使用径向压缩试验证明了水解反应产生的硬化。在37℃水解为CDHAp后,56%致密α-TCP的原始拉伸强度从0.70±0.1MPa增加到9.36±0.4MPa,对应密度为70%。