Fracture, fatigue, and friction of polymers in which entanglements greatly outnumber cross-links

Author:

Kim Junsoo1ORCID,Zhang Guogao12ORCID,Shi Meixuanzi13ORCID,Suo Zhigang1ORCID

Affiliation:

1. John A. Paulson School of Engineering and Applied Science, Kavli Institute for Nanobio Science and Technology, Harvard University, Cambridge, MA 02138, USA.

2. State Key Laboratory of Chemical Engineering, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310027, China.

3. State Key Laboratory for Strength and Vibration of Mechanical Structures, School of Aerospace Engineering, Xi’an Jiaotong University, Xi’an 710049, China.

Abstract

Longer and stronger; stiff but not brittle Hydrogels are highly water-swollen, cross-linked polymers. Although they can be highly deformed, they tend to be weak, and methods to strengthen or toughen them tend to reduce stretchability. Two papers now report strategies to create tough but deformable hydrogels (see the Perspective by Bosnjak and Silberstein). Wang et al . introduced a toughening mechanism by storing releasable extra chain length in the stiff part of a double-network hydrogel. A high applied force triggered the opening of cycling strands that were only activated at high chain extension. Kim et al . synthesized acrylamide gels in which dense entanglements could be achieved by using unusually low amounts of water, cross-linker, and initiator during the synthesis. This approach improves the mechanical strength in solid form while also improving the wear resistance once swollen as a hydrogel. —MSL

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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