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首页> 外文期刊>Journal of inorganic and organometallic polymers and materials >Synthesis of Mesoporous Hydroxyapatite with Controlled Pore Size Using the Chitosan as an Organic Modifier: Investigating the Effect of the Weight Ratio and pH Value of Chitosan on the Structural and Morphological Properties
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Synthesis of Mesoporous Hydroxyapatite with Controlled Pore Size Using the Chitosan as an Organic Modifier: Investigating the Effect of the Weight Ratio and pH Value of Chitosan on the Structural and Morphological Properties

机译:使用壳聚糖作为有机改性剂合成具有控制孔径的中孔羟基磷灰石:研究壳聚糖对壳聚糖的重量比和pH值对结构和形态特性的影响

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摘要

In the present research, the mesoporous hydroxyapatite nanoparticles were synthesized by the chemical precipitation method in the absence and presence of different weight ratios (0, 0.1, and 0.3 g) of chitosan as an organic modifier. The effects of different weight ratios and pH values (8, 9, and 10) of chitosan on the structural characteristics of the mesoporous hydroxyapatite nanoparticles were also investigated. Then, all the prepared samples were calcined at 650 degrees C for 3 h and their structure, morphology, surface area, and pore size distribution were characterized by X-ray Diffraction (XRD) technique, Field Emission Scanning Electron and Transmission Electron Microscopy (FE-SEM & TEM), Fourier Transform Infrared spectroscopy (FT-IR), Energy Dispersive X-ray spectrometer (EDX), and finally Brunauer-Emmett-Teller (BET) technique. The XRD analysis showed that the crystalline size of the synthesized HA decreased from 38 to 24 nm at pH 8, 40 to 30 nm at pH 9 as well as from 48 to 32 nm at pH 10. The same trend of decrease in the crystalline size was observed when the chitosan concentration increased from 0.0 to 0.3 g. The results revealed that the crystalline size, pore size, and surface area of the synthesized HA can be controlled by adjusting the chitosan weight ratio in the initially prepared samples. Mesopores in HA were observed for the samples synthesized at different pH values, by removing the organic template. Furthermore, the pore size of the prepared chitosanHA samples was found to be 13-38 nm, which seems to be suitable for cell attachment and slow-release drug delivery, especially in treatment of osteoporosis.
机译:在本研究中,通过化学沉淀方法在不存在和存在的不同重量比(0,0.1和0.3g)的壳聚糖作为有机改性剂中,通过化学沉淀方法合成了介孔羟基磷灰石纳米颗粒。还研究了壳聚糖对壳聚糖对介孔羟基磷灰石纳米粒子的结构特征的不同重量比和pH值(8,9和10)的影响。然后,通过X射线衍射(XRD)技术,现场发射扫描电子和透射电子显微镜(Fe)以650℃以650℃煅烧所有制备的样品,其结构,形态,表面积和孔径分布。(FE -SEM&TEM),傅里叶变换红外光谱(FT-IR),能量分散X射线光谱仪(EDX),最后Brunauer-Emmett-Teller(Bet)技术。 XRD分析表明,合成的HA的结晶尺寸在pH 8,40至30nm下在pH 9下减少38至24nm,以及在pH10的48至32nm下。结晶尺寸的降低趋势当壳聚糖浓度从0.0至0.3g增加时,观察到。结果表明,通过调节最初制备的样品中的壳聚糖重量比来控制合成的HA的结晶尺寸,孔径和表面积。通过除去有机模板,观察到在不同pH值以不同pH值合成的样品中的eSopors。此外,发现制备的壳聚糖/ NHA样品的孔径为13-38nm,似乎适用于细胞附着和缓释药物递送,特别是在治疗骨质疏松症。

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