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Formation of apatites in the system: KCl-CaCl_2-Ca_3(PO_4)_2-K_3PO_4-H_2O at 25 deg C

机译:在系统中形成磷灰石:KCl-CaCl_2-CA_3(PO_4)_2-K_3PO_4-H_2O,25°C

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Apatites from the system, KCl-CaCl_2-Ca_3(PO_4)_2-K_3PO_4-H_2O at 25 deg C were obtained and characterized using x-ray diffraction, infrared absorption spectroscopy and chemical analysis. The crystallinity of the apatite depended on the initial solution composition and on the solution pH at equilibrium. Apatites poor in crystalinity were usually obtained from solutions with high pH. The maximum amount of chloride, Cl~- ion incorporated in the apatite crystals was about 5.0 wtpercent (1.4 M). This amount was higher than that obtained in previous preparations at 100 deg C by hydrolysis of CaHPO_4 or by precipitation method (about 3 wtpercent of 1 M); but lower than the amount for a fully substituted chlor-apatite, Ca_(10)(PO_4)_6Cl_2 which is 7.0 wtpercent (2.0 M). The incorporation of potassium in the apatite was limited to 1.2 wtpercent (0.3 M). Variations in a- and c-axis dimensions (increase and decrease, respectively) indicated a Cl-for-OH substitution: (Ca,K)_(10)(HPO_4,PO_4)_6(Cl,OH)_2. The incorporation of K~+ in these apatites appeared to very limited and not related to the incorporation of Cl~- when the pH effect is neglected.
机译:从系统中磷灰石,使用X射线衍射,红外吸收光谱和化学分析得到25℃的KCl-CaCl_2-CA_3(PO_4)_2-K_3PO_4-H_2O。磷灰石的结晶度依赖于初始溶液组合物和溶液pH平衡时。液态化差异差,通常从具有高pH的溶液中获得。在磷灰石晶体中掺入的最大量的氯化物,Cl〜离子约为5.0(1.4μm)。该量高于在100℃下通过水解CaHPO_4或通过沉淀法(约3℃的沉淀法在100℃下获得的量高;但低于完全取代的氯磷灰石的量,Ca_(10)(PO_4)_6Cl_2,其为7.0 WTPercent(2.0米)。磷灰石中的钾掺入限于1.2 WTPENCE(0.3μm)。 A-和C轴尺寸的变化(分别增加和减少)表明了CL-FOR-OH替代:(CA,K)_(10)(HPO_4,PO_4)_6(CL,OH)_2。这些磷灰石中的K〜+掺入非常有限,与Cl〜 - 忽略pH效应时不相关。

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