ETH Zurich, Institute for Mechanical Systems, 8092, Zurich, Switzerland.
Empa, Swiss Federal Laboratories for Materials Science and Technology, 8600, Dubendorf, Switzerland.
Nat Commun. 2019 Feb 15;10(1):792. doi: 10.1038/s41467-019-08723-y.
Fracture toughness characterizes the ability of a material to maintain a certain level of strength despite the presence of a macroscopic crack. Understanding this tolerance for defects in soft collagenous tissues (SCT) has high relevance for assessing the risks of fracture after cutting, perforation or suturing. Here we investigate the peculiar toughening mechanisms of SCT through dedicated experiments and multi-scale simulations, showing that classical concepts of fracture mechanics are inadequate to quantify and explain the high defect tolerance of these materials. Our results demonstrate that SCT strength is only modestly reduced by defects as large as several millimeters. This defect tolerance is achieved despite a very narrow process zone at the crack tip and even for a network of brittle fibrils. The fracture mechanics concept of tearing energy fails in predicting failure at such defects, and its magnitude is shown to depend on the chemical potential of the liquid environment.
断裂韧性表征了材料在存在宏观裂纹的情况下保持一定强度的能力。了解软胶原蛋白组织 (SCT) 对缺陷的这种容忍度对于评估切割、穿孔或缝合后的骨折风险具有重要意义。在这里,我们通过专门的实验和多尺度模拟研究了 SCT 的特殊增韧机制,表明经典的断裂力学概念不足以定量和解释这些材料的高缺陷容忍度。我们的结果表明,缺陷大到几毫米时,SCT 的强度仅略有降低。尽管在裂纹尖端的过程区非常狭窄,甚至对于脆性纤维网络,也能实现这种缺陷容忍度。撕裂能的断裂力学概念在预测这种缺陷下的失效时失效,并且其大小被证明取决于液体环境的化学势。