纳米羟基磷灰石/β-磷酸三钙复合粉体的致密化和硬度行为

B. Mehdikhani, B. Mirhadi
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引用次数: 2

摘要

本研究采用烧结法设计了致密、细粒的双相磷酸钙生物陶瓷。采用湿化学沉淀法,以硝酸钙和磷酸氢二铵分别为钙和磷前驱体,制备了平均粒径为80 nm的羟基磷灰石/β-三钙(HA/β-TCP)磷酸盐纳米粉体。所采用的沉淀工艺也适合于原位生产亚微米级HA/β-TCP粉末。对制备的HA/β-TCP生物陶瓷的微观结构和力学强度进行了研究。通过粉末x射线衍射(XRD)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)和密度测量等方法对生物陶瓷样品进行了表征。粉末在800、900、1000和1100℃压实和烧结后,相对密度从57%增加到93%。结果表明,在1100℃烧结时,HA/β-TCP的最大硬度为229 HV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Densification and Hardness Behaviour of Nanocrystalline Hydroxyapatite/β-Tricalcium Phosphate Composite Powders
In this study, dense, fine-grained biphasic calcium phosphate bioceramics were designed via sintering method. nanosize hydroxyapatite / β-tricalcium (HA/β-TCP) phosphate powders with average grain size of 80 nm were prepared by the wet chemical precipitation method with calcium nitrate and di-ammonium hydrogen phosphate as calcium and phosphorus precursors, respectively. The precipitation process employed was also found to be suitable for the production of sub-micrometre HA/β-TCP powder in situ. The sinterability of the nanosize powders, and the microstructure, mechanical strength of the prepared HA/β-TCP bioceramics were investigated. Bioceramic sample characterization was achieved by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), and density measurements. Powders compacted and sintered at 800, 900, 1000 and 1100°C showed an increase in relative density from 57% to 93%. The results revealed that the maximum hardness of 229 HV was obtained for HA/β-TCP sintered at 1100°C.
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