Fracture of polymer networks with diverse topological defects

被引:59
作者
Lin, Shaoting [1 ]
Zhao, Xuanhe [1 ,2 ]
机构
[1] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Civil & Environm Engn, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
CHAIN; ELASTICITY; HYDROGELS; STRENGTH;
D O I
10.1103/PhysRevE.102.052503
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Polymer networks are pervasive in biological organisms and engineering materials. Topological defects such as cyclic loops and dangling chains are ubiquitous in polymer networks. While fracture is a dominant mechanism for mechanical failures of polymer networks, existing models for fracture of polymer networks neglect the presence of topological defects. Here, we report a defect-network fracture model that accounts for the impact of various types of topological defects on fracture of polymer networks. We show that the fracture energy of polymer networks should account for the energy from multiple layers of polymer chains adjacent to the crack. We further show that the presence of topological defects tends to toughen a polymer network by increasing the effective chain length, yet to weaken the polymer network by introducing inactive polymer chains. Such competing effects can either increase or decrease the overall intrinsic fracture energy of the polymer network, depending on the types and densities of topological defects. Our model provides theoretical explanations for the experimental data on the intrinsic fracture energy of polymer networks with various types and densities of topological defects.
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页数:8
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