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Crystallization study of sol-gel derived 13-93 bioactive glass powder

机译:溶胶 - 凝胶衍生13-93生物活性玻璃粉的结晶研究

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摘要

Multicomponent silicate bioactive glass (BG) (53SiO(2)-20CaO-6Na(2)O-4P(2)O(5)-12K(2)O(5)MgO in wt. %) (13-93 composition) was prepared via the sol-gel process. The influence of thermal treatment on the crystallization was evaluated using differential scanning calorimetry (DSC), X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray nano-computed tomography (nano-CT). The temperature and time of the thermal treatment strongly influenced the formation of the crystalline phases. The preliminary outcomes demonstrate the possibility of tailoring the crystallinity of 13-93 BG powder in the range 5-43 wt. % by controlling the temperature and time of the heat treatment. The microstructure of powders sintered at two different temperatures (650 degrees C and 700 degrees C from 30 min to 4 h) was evaluated by TEM. X-ray nano-computed tomography (nano-CT) was used to visualize the 3D morphology and distribution of crystallization areas in the samples in powder form. A large range between the glass transformation and the crystallization temperatures is observed, which provides the prospect of a suitable material to manufacture directly 3D structures (e.g. porous scaffolds) without an intermediate processing step.
机译:采用溶胶-凝胶法制备了重量百分比为53SiO(2)-20CaO-6Na(2)O-4P(2)O(5)-12K(2)O(5)MgO(13-93组分)的多组分硅酸盐生物活性玻璃(BG)。采用差示扫描量热法(DSC)、X射线衍射(XRD)、透射电子显微镜(TEM)和X射线纳米计算机断层扫描(nano-CT)评估了热处理对结晶的影响。热处理温度和时间对晶相的形成有很大影响。初步结果表明,通过控制热处理的温度和时间,可以将13-93 BG粉末的结晶度调整为5-43 wt.%。通过TEM评估了在两种不同温度(650摄氏度和700摄氏度,30分钟至4小时)下烧结的粉末的微观结构。X射线纳米计算机断层扫描(nano-CT)用于可视化粉末状样品中结晶区域的三维形态和分布。观察到玻璃转变和结晶温度之间的大范围变化,这提供了一种无需中间处理步骤即可直接制造3D结构(例如多孔支架)的合适材料的前景。

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