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首页> 外文期刊>CERAMICS INTERNATIONAL >Improved properties of hydroxyapatite-carbon nanotube biocomposite: Mechanical, in vitro bioactivity and biological studies
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Improved properties of hydroxyapatite-carbon nanotube biocomposite: Mechanical, in vitro bioactivity and biological studies

机译:羟基磷灰石-碳纳米管生物复合材料的改进性能:机械,体外生物活性和生物学研究

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摘要

The present work describes a simple shear mixing technique for developing a hydroxyapatite (HAp)-carbon nanotube (CNT) nanocomposite and the effect of reinforcement on the physical, mechanical, in vitro bioactivity and biological properties of HAp. XRD and FTIR confirmed that the main phase of the composites is HAp. HRTEM images demonstrated the formation of a two-dimensional nanocomposite structure, whereas FESEM images indicated the formation of nanosized HAp grains featuring sporadically distributed CNT molecules. No major phase changes in HAp were observed with up to 5% added CNT. However, adding more than 1% CNTs caused an increase in internal crystal strain and increased substitution of CO_3~(2-) for OH~- and PO_4~(3-) groups in pure HAp. The average crystallite size increased from ~46 nm to ~ 100 nm with only 0.5% added CNT, remained nearly unaffected up to 2% CNTs thereafter and suddenly decreased at 5% CNTs (~61 nm). The FESEM and HRTEM images clearly showed the attachment of MWCNT chains on HAp grains, which directly affected the samples' fracture toughness and flexural strength. Of the samples, 1% showed maximum values of K_(1C), whereas 5% showed maximum values of HV and three-point bending flexural strength. The in vitro bioactivity indicated increased apatite formation on the sample surface up to 1 % CNTs after 24 weeks. However, adding 2% and 5% CNTs resulted in a manifold increase in apatite formation up to 12 weeks, after which dissolution increased up to 24 weeks, possibly due to increased substitution of CO_3~(2-) for OH~- and PO_4~(3-) groups. This result is confirmed by the FTIR studies. For all added CNT contents, all samples exhibited high haemocompatibility. However, there was a compromise between the observed mechanical properties and in vitro bioactivity studied up to 24 weeks, and care must be taken before selecting any final application of the nanocomposites.
机译:本工作描述了一种简单的剪切混合技术,用于开发羟基磷灰石(HAp)-碳纳米管(CNT)纳米复合材料以及增强剂对HAp的物理,机械,体外生物活性和生物学性质的影响。 XRD和FTIR证实复合材料的主要相为HAp。 HRTEM图像显示了二维纳米复合结构的形成,而FESEM图像显示了具有零星分布的CNT分子的纳米级HAp晶粒的形成。最多添加5%的CNT时,未观察到HAp的主要相变。然而,添加超过1%的CNT会导致内部晶体应变增加,并增加纯HAp中OH〜-和PO_4〜(3-)基团对CO_3〜(2-)的取代。平均微晶尺寸从〜46 nm增加到〜100 nm,仅添加0.5%的CNT,此后直到2%CNT几乎保持不受影响,并在5%CNTs(〜61 nm)时突然减小。 FESEM和HRTEM图像清楚地表明MWCNT链附着在HAp晶粒上,这直接影响了样品的断裂韧性和弯曲强度。在样品中,有1%显示出K_(1C)的最大值,而有5%显示了HV和三点弯曲抗弯强度的最大值。体外生物活性表明,在24周后,样品表面磷灰石的形成增加,直至CNTs达到1%。然而,添加2%和5%的CNT导致磷灰石形成最多增加12周,此后溶解增加最多24周,这可能是由于CO_3〜(2-)取代了OH〜-和PO_4〜 (3-)组。 FTIR研究证实了这一结果。对于所有添加的CNT含量,所有样品均表现出较高的血液相容性。然而,长达24周的研究机械性能和体外生物活性之间存在折衷,因此在选择最终用途的纳米复合材料之前必须小心。

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