摘要
Employment of noncovalent bonds as reversible crosslinks have been applied in weldable and self-healing crosslinked polymer networks but result in limited mechanical properties. Herein, a robust, tunable, and fast healable poly(urethane-urea)-GMA (PG) elastomer with a combination of multiple hydrogen bonds and dynamic covalent urea bonds was designed via a photo-induced copolymerization. The resultant PG60 exhibited a tensile strength of 12.3 MPa, an elongation at break of 229%, a toughness of 16.08 MJ m 3, and a self-healing efficiency of 100.0%. By adjusting the content of dynamic crosslinkers, the mechanical strength and self-healability of the resulting elastomers can be optimized. The exceptional properties of the networks, including self-healing capability and remarkable robust mechanical behavior, are attributed to the presence of reversibly non-covalent hydrogen bonds and dynamically covalent urea bonds, which have been confirmed through stress relaxation tests. More importantly, this study not only presents a facile fabrication method for designing me-chanically robust and fast self-healing crosslinked elastomers, but also shows great potential in smart humidity sensor.
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单位茂名学院; 桂林理工大学