A Highly Stretchable Polymer that Can Be Thermally Healed at Mild Temperature
Xiao-Yong Jia1, Jin-Feng Mei1, Jian-Cheng Lai1
1State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Advanced Microstructures, Nanjing University, Nanjing, 210093, P. R. China.
Macromolecular Rapid Communications
|April 30, 2016
Summary
This study developed a highly elastic polymer using dynamic Fe(III)-triazole coordination bonds in polydimethylsiloxane (PDMS). The material exhibits excellent stretchability and over 90% self-healing efficiency after thermal treatment.
Area of Science:
- Materials Science
- Polymer Chemistry
Background:
- Achieving both high stretchability and self-healing in synthetic materials is difficult.
- Self-healing often requires weaker bonds that are not ideal for elastic materials.
Purpose of the Study:
- To create a highly elastic polymer with efficient self-healing capabilities.
- To investigate the role of dynamic Fe(III)-triazole coordination bonds in achieving these properties.
Main Methods:
- Incorporating dynamic Fe(III)-triazole coordination bonds into a polydimethylsiloxane (PDMS) backbone.
- Characterizing the material's stretchability and thermal self-healing performance.
Main Results:
- The resulting polymer demonstrated high elasticity, stretching up to 3400% strain.
- The material achieved over 90% healing efficiency after thermal treatment at 60 °C for 20 hours.
Conclusions:
- Dynamic Fe(III)-triazole coordination bonds enable simultaneous stretchability and thermal self-healing in PDMS.
- The unique coordination chemistry of Fe(III)-triazole complexes is key to the material's enhanced properties.
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