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Accurate characterization of pure silicon-substituted hydroxyapatite powders synthesized by a new precipitation route

机译:通过新的沉淀途径合成的纯硅取代羟基磷灰石粉末的准确表征

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This paper presents a new aqueous precipitation method to prepare silicon-substituted hydroxyapatites Ca10(PO4) 6-y(SiO4)y(OH)2- y(VOH)y (SiHAs) and details the characterization of powders with varying Si content up to y = 1.25 mol mol SiHA -1. X-ray diffraction, transmission electron microscopy, solid-state nuclear magnetic resonance and Fourier transform infrared spectroscopy were used to accurately characterize samples calcined at 400 C for 2 h and 1000 C for 15 h. This method allows the synthesis of monophasic SiHAs with controlled stoichiometry. The theoretical maximum limit of incorporation of Si into the hexagonal apatitic structure is y 1.5. This limit depends on the OH content in the channel, which is a function of the Si content, temperature and atmosphere of calcination. These results, particularly those from infrared spectroscopy, raise serious reservations about the phase purity of previously prepared and biologically evaluated SiHA powders, pellets and scaffolds in the literature.
机译:本文提出了一种新的水相沉淀法来制备硅取代的羟基磷灰石Ca10(PO4)6-y(SiO4)y(OH)2- y(VOH)y(SiHAs),并详细描述了直至Si含量变化的粉末的表征。 y = 1.25mol mol SiHA -1。使用X射线衍射,透射电子显微镜,固态核磁共振和傅立叶变换红外光谱法来准确表征400℃下煅烧2 h和1000℃下煅烧15 h的样品。该方法允许以受控的化学计量合成单相SiHA。将Si掺入六角形非晶体结构的理论最大极限是y <1.5。该极限取决于通道中的OH含量,该含量是Si含量,温度和煅烧气氛的函数。这些结果,特别是来自红外光谱的结果,对文献中先前制备和经过生物学评估的SiHA粉末,粒料和支架的相纯度提出了严重保留。

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