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Room temperature synthesis of highly hemocompatible hydroxyapatite, study of their physical properties and spectroscopic correlation of particle size

机译:室温合成高度hemocompatible羟磷灰石、学习的物理性质和光谱相关性粒子的大小

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摘要

Needle shaped nanoparticles of hydroxyapatite (HA) have been synthesized at room temperature using orthophosphoric acid as the source of (PO4)~(3-) ions, while calcium chloride, the calcium source, is suitably complexed with citric acid/tartaric acid/acetic acid. The presence of ligands inhibits the growth along [001] and [100] directions of the crystal and thus, helps in formation of needle shaped nanoparticles. The chemical compositions of the samples have been established through AAS and FTIR spectroscopy, while the crystallinity has been assessed through XRD and by the spectral changes in the v1 and v3 frequencies of the phosphate group in the respective FTIR spectra. The particle sizes of the samples have been determined from line broadening studies and correlations have been established between the curve fitted percentage area of FTIR and full width half height (FWHH) of the XRD peaks. TEM studies revealed the particle to be needle-shaped with a length and diameter in the range of 20-65 nm and 4-11 nm respectively. Changes in the surface charge of the water dispersed HA samples have been determined at different pH and the isoelectric point for the samples have been found in the range of 3.1-3.4. Finally, the morphology, surface area and hemocompatibility characteristics of the HA samples, prepared by using different complexing agents, have been compared.
机译:针形状的纳米颗粒的羟磷灰石(HA)已经合成了室温下使用正磷酸的来源(PO4) ~ (3 -)离子,而氯化钙、钙源,是适当与柠檬酸/酒石的酸/醋酸。抑制经济增长[001]和[100]晶体的方向,因此,帮助针形状的纳米颗粒的形成。化学成分的样品通过原子吸收光谱法和红外光谱,建立而结晶度被评估XRD和v1和v3的光谱变化磷酸基的频率各自的红外光谱谱。样品已经从线确定扩大研究和相关性之间建立曲线拟合比例红外光谱和全宽度高度(FWHH)的一半XRD峰。针状的长度和直径的范围分别为20 - 65 nm和4海里。水的表面电荷的改变已确定分散HA样本不同的pH值和等电点样本中发现了3.1 - -3.4的范围。最后,形态学,表面积和本文以HA的特征准备的样品,使用不同的络合代理,进行比较。

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