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生物系统的容错块状和表面纳米结构。

Flaw tolerant bulk and surface nanostructures of biological systems.

作者信息

Gao Huajian, Ji Baohua, Buehler Markus J, Yao Haimin

机构信息

Max Planck Institute for Metals Research, Heisenbergstrasse 3, D-70569, Stuttgart, Germany.

出版信息

Mech Chem Biosyst. 2004 Mar;1(1):37-52.

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.

摘要

类骨生物材料通过矿物质与蛋白质的分级复合结构实现了卓越的力学性能。壁虎和许多昆虫进化出了分级表面结构以获得非凡的粘附能力。我们发现纳米尺度在使这些生物系统实现其卓越性能方面起着关键作用。我们认为容错原理可能对类骨材料的整体纳米结构和壁虎类动物物种的表面纳米结构的进化产生了全面影响。我们证明纳米尺度尺寸使骨中的矿物纳米颗粒能够实现最佳断裂强度,而壁虎的纳米级刚毛状突起能够实现最佳粘附强度。在这两种系统中,通过将基本结构组件的特征尺寸限制在纳米尺度,使裂纹状缺陷不会扩展以破坏所需的结构连接,从而实现强度优化。已进行连续介质建模和原子模拟以验证纳米尺度的容错概念。已开发出一个简单的拉伸 - 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,虽然通过将晶体尺寸限制在纳米尺度缓解了矿物晶体低韧性的问题,但通过采用大纵横比的矿物薄片解决了蛋白质低模量的问题。发现生物复合材料的断裂能与蛋白质在其变形至断裂路径上的有效剪切应变和有效剪切应力成正比。生物工程化的矿物 - 蛋白质复合材料非常适合耗散断裂能,因为蛋白质结构域展开和沿蛋白质 - 矿物界面滑动的蜿蜒路径在断裂前会导致非常大的有效应变。生物聚合物通常的熵弹性可能涉及相对较小的有效应力,可能无法确保结构域同时展开和界面滑动。诸如骨中Ca++诱导的牺牲键等交联机制可以增加蛋白质以及沿蛋白质 - 矿物界面的剪切应力,有效地将熵弹性行为转变为类似于金属塑性的行为。牺牲键机制不仅在蛋白质中建立起大的有效应力,而且还允许蛋白质变形和界面滑动在相似应力水平下同时发生,从而有可能在显著应力下设计出非常长的变形范围以最大化能量吸收。发现将矿物薄片优化至接近理论强度对于通过诸如Ca++诱导的牺牲键等交联机制在蛋白质中建立大的有效应力至关重要。同样,对于壁虎的粘附,发现单个刚毛状突起的强度优化在提高更高层次的粘附能方面起着关键作用。

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