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首页> 外文期刊>Biomaterials >Preparation of magnesium-substituted hydroxyapatite powders by the mechanochemical-hydrothermal method.
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Preparation of magnesium-substituted hydroxyapatite powders by the mechanochemical-hydrothermal method.

机译:机械化学-水热法制备镁取代的羟基磷灰石粉。

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摘要

Magnesium-substituted hydroxyapatite (Mg-HAp) powders with different crystallinity levels were prepared at room temperature via a heterogeneous reaction between Mg(OH)(2)/Ca(OH)(2) powders and an (NH(4))(2)HPO(4) solution using the mechanochemical-hydrothermal route. The as-prepared products contained unreacted Mg(OH)(2) and therefore had to undergo purification in ammonium citrate aqueous solutions at room temperature. X-ray diffraction, infrared spectroscopy, thermogravimetric and chemical analyses were performed and it was determined that the purified powders were phase-pure Mg-HAp containing 0.24-28.4wt% of Mg. The concentration of Mg was slightly lower near the surface than in the bulk of the HAp crystals as indicated by X-ray photoelectron spectroscopy. Dynamic light scattering revealed that the median particle size of the room temperature Mg-HAp powders was in the range of 102nm-1.2microm with a specific surface area between 91 and 269m(2)/g. Scanning electron microscopy confirmed that the Mg-HAp powders consisted of submicron agglomerates of nanosized crystals, less than approximately 20nm.
机译:通过在室温下通过Mg(OH)(2)/ Ca(OH)(2)粉末与(NH(4))(2)之间的异质反应制备具有不同结晶度的镁取代羟基磷灰石(Mg-HAp)粉末)HPO(4)解决方案使用机械化学-水热途径。所制备的产物包含未反应的Mg(OH)(2),因此必须在室温下于柠檬酸铵水溶液中进行纯化。进行了X射线衍射,红外光谱,热重和化学分析,并且确定纯化的粉末是相纯的Mg-HAp,其含有0.24-28.4wt%的Mg。 X射线光电子能谱表明,表面附近的Mg浓度略低于大部分HAp晶体。动态光散射显示室温Mg-HAp粉末的中值粒径在102nm-1.2microm范围内,比表面积在91和269m(2)/ g之间。扫描电子显微镜证实,Mg-HAp粉末由小于约20nm的纳米级晶体的亚微米团聚物组成。

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