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Magnesium Substitution in Hydroxyapatite Synthesized by Sol-Gel Method

机译:溶胶 - 凝胶法合成羟基磷灰石中的镁取代

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The ionic substitutions have been proposed as a tool to improve the biological performance of hydroxyapatite (HAp) based materials. In the present work, the systems of Ca_(10-x)Mg_x(PO_4)_6(OH)_2 (MgHAp, x = 0, 1, 2, and 3) were successfully synthesized by sol-gel method. To obtain nanocrystalline of MgHAp, the prepared precursors were calcined in air at 600°C for 2 h. The samples were characterized by X-ray diffraction (XRD) and transmission electron microscope (TEM) observation. The XRD results confirm the formation of pure phase of HAp with the lattice parameter a in the range of 0.9417-0.9479 nm and c of 0.6841-0.6919 nm. The crystallite sizes of the powder are found to be 35-46 nm as evaluated by the XRD line broadening method. The morphology of the samples are spherical shape of diameter less than 100 nm as evaluated by TEM. The corresponding selected area electron diffraction (SAED) analysis further confirms the formation of hexagonal structure of HAp.
机译:已经提出了离子取代作为提高羟基磷灰石(HAP)基材料的生物学性能的工具。在本作工作中,通过溶胶 - 凝胶法成功地合成了CA_(10-X)Mg_X(PO_4)_6(OH)_6(OH)(MGHAP,X = 0,1,2和3)的系统。为了获得MGHAP的纳米晶体,将制备的前体在空气中在600℃下在空气中煅烧2小时。通过X射线衍射(XRD)和透射电子显微镜(TEM)观察来表征样品。 XRD结果证实了HAP的纯相的形成,晶格参数A在0.9417-0.9479 nm和c的范围内为0.6841-0.6919 nm。粉末的微晶尺寸被发现为35-46nm,如XRD线宽化方法所评估的。样品的形态是直径小于100nm的球形,如通过TEM评估的。相应的选择区域电子衍射(SAED)分析进一步证实了HAP的六边形结构的形成。

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