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Preparation of hydroxyapatite/zirconia bioceramic nanocomposites for orthopaedic and dental prosthesis applications

机译:用于骨科和牙齿修复的羟基磷灰石/氧化锆生物陶瓷纳米复合材料的制备

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摘要

Homogeneous mixtures of hydroxyapatite (HAp) and yttria-stabilized zirconia (YSZ) nanoparticles were successfully synthesized using chemical co-precipitation and subsequent calcination. For the synthesis of HAp/YSZ nanopowder, the Ca/P atomic ratio was 1.73 to obtain high-content stoichiometric hydroxyapatite phase and to suppress beta-tricalcium phosphate (beta-TCP) formation. The agglomerated crystalline powders were milled using YSZ ball media to obtain well-separated nanoparticles. The final particle size of the HAp and YSZ was approx 50-70 and approx 15-30 nm, respectively. The crystallinity and morphological feature of the nanopowder was analysed using x-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) analyses. The ball-milled nanopowder mixture was hot pressed at 1100 deg C for 1 h under 20 MPa in vacuum atmosphere. The sintered HAp/YSZ nanocomposites exhibited approximately 99 percent of the theoretical density, due not only to the fine nanoscale of the particles, but also to the homogeneous distribution of the nanoparticle mixture. They also showed fine grain structures of the HAp phase due to the suppressed grain growth by YSZ particles. The nanocomposites showed improved mechanical properties, flexural strength of approx 155 MPa and fracture toughness of approx 2.1 MP m~(1/2), due to the YSZ contribution to the HAp matrix.
机译:使用化学共沉淀和随后的煅烧成功地合成了羟基磷灰石(HAp)和氧化钇稳定的氧化锆(YSZ)纳米粒子的均质混合物。对于HAp / YSZ纳米粉的合成,Ca / P原子比为1.73,以获得高含量的化学计量羟基磷灰石相并抑制β-磷酸三钙(β-TCP)的形成。使用YSZ球状介质将团聚的结晶粉末进行研磨,以获得分离良好的纳米颗粒。 HAp和YSZ的最终粒径分别约为50-70和15-30 nm。使用X射线衍射(XRD)和高分辨率透射电子显微镜(HRTEM)分析了纳米粉末的结晶度和形态特征。将球磨的纳米粉末混合物在真空气氛中,在20 MPa下于1100℃热压1小时。烧结的HAp / YSZ纳米复合材料的理论密度约为99%,这不仅是由于颗粒的细纳米级,而且由于纳米颗粒混合物的均匀分布。由于YSZ颗粒抑制了晶粒的生长,它们还显示了HAp相的细晶粒结构。由于YSZ对HAp基体的贡献,纳米复合材料具有改善的机械性能,约155 MPa的抗弯强度和约2.1 MP m〜(1/2)的断裂韧性。

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