Materials Science

Toughening Hydrogels Through Force-triggered Chemical Reactions that Lengthen Polymer Strands

Abstract

The utility and lifetime of materials made from polymer networks, including hydrogels, depend on their capacity to stretch and resist tearing. In gels and elastomers, those mechanical properties are often limited by the covalent chemical structure of the polymer strands between cross-links, which is typically fixed during the material synthesis. Here, we report polymer networks in which the constituent strands lengthen through force-coupled reactions that are triggered as the strands reach their nominal breaking point. Reactive strand extensions of up to 40% lead to hydrogels that stretch 40-50% further than, and exhibit tear energies twice that of, networks made from analogous control strands. The enhancements are synergistic with those provided by double network architectures, and complement other existing toughening strategies.

Content

Thumbnail image of Toughening Hydrogels Through Force-triggered Chemical Reactions that Lengthen Polymer Strands.pdf

Supplementary material

Thumbnail image of DN1-con-tensile test.mp4
DN1-con-tensile test
Thumbnail image of DN1-tensile test.mp4
DN1-tensile test
Thumbnail image of Supplementary Materials-Toughening Hydrogels Through Force-triggered Chemical Reactions that Lengthen Polymer Strands .pdf
Supplementary Materials-Toughening Hydrogels Through Force-triggered Chemical Reactions that Lengthen Polymer Strands