首页> 外文期刊>Journal of the mechanical behavior of biomedical materials >Development of hydroxyapatite/calcium silicate composites addressed to the design of load-bearing bone scaffolds.
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Development of hydroxyapatite/calcium silicate composites addressed to the design of load-bearing bone scaffolds.

机译:羟基磷灰石/硅酸钙复合材料的开发致力于承重骨支架的设计。

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This work deals with the preparation of bioactive ceramic composites to be employed for the development of load-bearing bone substitutes, made of hydroxyapatite (Ca(10)(PO(4))(6)(OH)(2), HA) and bioactive dicalcium silicate (Ca(2)SiO(4), C(2)S) as a reinforcing phase. The composite materials were prepared by Fast Hot-Pressing (FHP), which allowed the rapid sintering of monolithic ceramics at temperatures up to 1500 degrees C, well above the commonly adopted temperatures for the consolidation of hydroxyapatite (1200-1300 degrees C). The purpose was to achieve the grain coalescence of both HA and the strengthening phase, so that to obtain a homogeneous ceramic material characterized by controlled phase composition and improved mechanical strength; the dwell time was reduced as much as possible to prevent HA decomposition and excessive grain growth. The most remarkable result, in terms of phase composition, was the absence of any secondary phases in the final ceramics other than HA and C(2)S, even after sintering at 1500 degrees C. The flexure strength of the composite materials was found to be much higher than that of HA alone. Further mechanical characterization was also carried out on HA and composites, sintered in different conditions, to evaluate the elastic properties and fracture toughness, and properties close to those of mineral bone were found. These preliminary results confirmed that composites of HA and Ca(2)SiO(4) are promising for the development of bioactive load-bearing ceramic bone substitutes with controlled phase composition.
机译:这项工作涉及生物活性陶瓷复合材料的制备,该复合材料可用于开发由羟基磷灰石(Ca(10)(PO(4))(6)(OH)(2),HA)制成的承重骨替代物。生物活性硅酸钙(Ca(2)SiO(4),C(2)S)作为增强相。复合材料是通过快速热压(FHP)制备的,它允许在高达1500摄氏度的温度下快速烧结整体陶瓷,该温度远高于用于固结羟基磷灰石的常用温度(1200-1300摄氏度)。目的是实现HA和强化相的晶粒结合,从而获得具有可控相组成和改善的机械强度的均质陶瓷材料。尽可能减少停留时间,以防止HA分解和晶粒过度生长。就相组成而言,最显着的结果是最终陶瓷中除了HA和C(2)S之外,甚至在1500摄氏度下烧结后都没有任何第二相。发现复合材料的弯曲强度达到远远高于仅HA的水平。还对在不同条件下烧结的HA和复合材料进行了进一步的机械表征,以评估其弹性性能和断裂韧性,并且发现了与矿物骨接近的性能。这些初步结果证实,HA和Ca(2)SiO(4)的复合材料有望发展具有可控相组成的生物活性承重陶瓷骨替代品。

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