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首页> 外文期刊>Materials science & engineering. C, Biomimetic and supramolecular systems >Role of microstructure in the aging-related deterioration of the toughness of human cortical bone
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Role of microstructure in the aging-related deterioration of the toughness of human cortical bone

机译:微观结构在与老化相关的人类皮质骨韧性恶化中的作用

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摘要

The aging-related deterioration of the fracture properties of bone, coupled with higher life expectancy, is responsible for increasing incidence of bone fracture in the elderly; consequently, an understanding of how these fracture properties degrade with age is essential. In this study, ex vivo fracture experiments have been performed to quantitatively assess the effect of age on human cortical bone in the proximal-distal orientation, i.e., longitudinally along the osteons. Because cortical bone exhibits rising crack-growth resistance with crack extension, the toughness is evaluated in terms of resistance-curve (R-curve) behavior, measured for bone taken from wide range of age groups (34-99 years). Using this approach, both the crack-initiation and crack-growth toughness are determined and are found to deteriorate with age; the initiation toughness decreases some 40% over six decades from 40 to 100 years, while the growth toughness is effectively eliminated over the same age range. The reduction in crack-growth toughness is considered to be associated primarily with a degradation in the degree of extrinsic toughening, in particular, involving crack bridging in the wake of the crack. An examination of the micro-ano-structural changes accompanying the process of aging, using optical microscopy, X-ray tomography, nanoindentation and Raman spectroscopy, is shown to support such observations.
机译:与衰老相关的骨骼骨折特性的恶化,加上预期寿命的延长,导致老年人骨折的发生率增加;因此,了解这些断裂特性如何随着年龄而退化是至关重要的。在这项研究中,已经进行了离体骨折实验,以定量评估年龄对近端至远端方向(即沿骨骼的纵向)对人皮质骨的影响。由于皮质骨显示出随着裂纹扩展而增加的裂纹扩展抗性,因此根据从广泛年龄段(34-99岁)采集的骨的电阻曲线(R曲线)行为来评估韧性。使用这种方法,既确定了裂纹的始发性,又确定了裂纹扩展的韧度,并发现它们会随时间而变差。从40到100年的六十年中,初始韧性降低了约40%,而在相同的年龄范围内,增长韧性被有效地消除了。裂纹扩展韧性的降低被认为主要与外在增韧程度的降低有关,特别是涉及裂纹后的裂纹桥接。证明了使用光学显微镜,X射线断层扫描,纳米压痕和拉曼光谱对伴随老化过程的微观/纳米结构变化的检查支持了这种观察。

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