Flaw tolerant bulk and surface nanostructures of biological systems.

Huajian Gao, B. Ji, M. Buehler, H. Yao
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引用次数: 75

Abstract

Bone-like biological materials have achieved superior mechanical properties through hierarchical composite structures of mineral and protein. Gecko and many insects have evolved hierarchical surface structures to achieve extraordinary adhesion capabilities. We show that the nanometer scale plays a key role in allowing these biological systems to achieve their superior properties. We suggest that the principle of flaw tolerance may have had an overarching influence on the evolution of the bulk nanostructure of bone-like materials and the surface nanostructure of gecko-like animal species. We demonstrate that the nanoscale sizes allow the mineral nanoparticles in bone to achieve optimum fracture strength and the spatula nanoprotrusions in Gecko to achieve optimum adhesion strength. In both systems, strength optimization is achieved by restricting the characteristic dimension of the basic structure components to nanometer scale so that crack-like flaws do not propagate to break the desired structural link. Continuum modeling and atomistic simulations have been conducted to verify the concept of flaw tolerance at nanoscale. A simple tension-shear chain model has been developed to model the stiffness and fracture energy of biocomposites. It is found that, while the problem of low toughness of mineral crystals is alleviated by restricting the crystal size to nanoscale, the problem of low modulus of protein has been solved by adopting a large aspect ratio for the mineral platelets. The fracture energy of biocomposites is found to be proportional to the effective shear strain and the effective shear stress in protein along its path of deformation to fracture. The bioengineered mineral-protein composites are ideally suited for fracture energy dissipation as the winding paths of protein domain unfolding and slipping along protein-mineral interfaces lead to very large effective strain before fracture. The usual entropic elasticity of biopolymers may involve relatively small effective stress and may not be able to ensure simultaneous domain unfolding and interface slipping. Cross-linking mechanisms such as Ca++ induced sacrificial bonds in bone can increase the shear stress in protein and along the protein-mineral interface, effectively converting the behavior of entropic elasticity to one that resembles metal plasticity. The sacrificial bond mechanism not only builds up a large effective stress in protein but also allows protein deformation and interface slipping to occur simultaneously under similar stress levels, making it possible to engineer a very long range of deformation under significant stress in order to maximize energy absorption. Optimization of mineral platelets near theoretical strength is found to be crucial for allowing a large effective stress to be built up in protein via cross-linking mechanisms such as Ca++ induced sacrificial bonds. Similarly, for gecko adhesion, the strength optimization of individual spatulas is found to play a critical role in enhancing adhesion energy at the higher hierarchical level.
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生物系统的容错体和表面纳米结构。
类骨生物材料通过矿物质和蛋白质的层次化复合结构获得了优异的力学性能。壁虎和许多昆虫进化出了分层的表面结构,以获得非凡的粘附能力。我们表明,纳米尺度在允许这些生物系统实现其优越性能方面起着关键作用。我们认为,缺陷容忍原理可能对类骨材料的体纳米结构和类壁虎动物物种的表面纳米结构的演变产生了总体影响。我们证明了纳米尺度的尺寸可以使骨中的矿物纳米颗粒达到最佳的断裂强度,而壁虎中的刮刀纳米突出物可以达到最佳的粘附强度。在这两种体系中,强度优化都是通过将基本结构部件的特征尺寸限制在纳米尺度来实现的,从而使类裂纹缺陷不会传播而破坏所需的结构环节。通过连续体模型和原子模拟验证了纳米尺度上的缺陷容限概念。建立了一个简单的拉伸-剪切链模型来模拟生物复合材料的刚度和断裂能。研究发现,通过将晶体尺寸限制在纳米尺度,可以缓解矿物晶体韧性低的问题,而采用大长宽比的矿物血小板则可以解决蛋白质模量低的问题。研究发现,生物复合材料的断裂能与蛋白质在变形至断裂过程中的有效剪切应变和有效剪切应力成正比。生物工程的矿物-蛋白质复合材料非常适合断裂能量耗散,因为蛋白质结构域沿蛋白质-矿物界面展开和滑动的缠绕路径导致断裂前的有效应变非常大。生物聚合物通常的熵弹性可能涉及相对较小的有效应力,并且可能无法同时保证域展开和界面滑动。骨中的Ca++诱导的牺牲键等交联机制可以增加蛋白质和蛋白质-矿物界面的剪切应力,有效地将熵弹性行为转化为类似金属塑性的行为。牺牲键机制不仅在蛋白质中建立了一个大的有效应力,而且允许蛋白质变形和界面滑动在相似的应力水平下同时发生,使得在显著应力下设计一个很长的变形范围成为可能,以最大限度地吸收能量。矿物血小板接近理论强度的优化被发现是允许通过交联机制(如Ca++诱导的牺牲键)在蛋白质中建立一个大的有效应力的关键。同样,对于壁虎的粘附,单个刮刀的强度优化在更高层次的粘附能量提升中起着至关重要的作用。
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