With the prompt development in intellectualization nowadays, the smart materials with multifunctionality or multi-responsiveness are highly expected. But it is a big challenge to integrate the different actuating unit...With the prompt development in intellectualization nowadays, the smart materials with multifunctionality or multi-responsiveness are highly expected. But it is a big challenge to integrate the different actuating units into a single system in a synergy pattern. Herein, we put forward a new strategy to develop the polyurethane networks which can present shape-memory effect and self-healing effect in independent way as well as simultaneous acting mode. To realize this goal, poly(tetremethylene ether) glycol was chosen as the soft segment to ensure the polymer chains a good mobility, and disulfide bond as the dynamic covalent bond was embedded in the backbone of polyurethane to endow it with desirable self-healing capacity under mild condition. Moreover, a rational control of the architecture of the networks by adjusting the content of disulfide bond and the degree of cross-linking, a broad glass transition temperature(T_g) was achieved, which enabled the network a versatile shape-memory effect, covering from dual-, triple-so far as to quadrupleshape memory effect. More importantly, the shape recovery and healing process can be realized simultaneously because of the highly matched actuating condition in this system.展开更多
基金supported financially by the National Natural Science Foundation of China (51773131 and 51721091)the International S&T Cooperation Project of Sichuan Province (2017HH0034)
文摘With the prompt development in intellectualization nowadays, the smart materials with multifunctionality or multi-responsiveness are highly expected. But it is a big challenge to integrate the different actuating units into a single system in a synergy pattern. Herein, we put forward a new strategy to develop the polyurethane networks which can present shape-memory effect and self-healing effect in independent way as well as simultaneous acting mode. To realize this goal, poly(tetremethylene ether) glycol was chosen as the soft segment to ensure the polymer chains a good mobility, and disulfide bond as the dynamic covalent bond was embedded in the backbone of polyurethane to endow it with desirable self-healing capacity under mild condition. Moreover, a rational control of the architecture of the networks by adjusting the content of disulfide bond and the degree of cross-linking, a broad glass transition temperature(T_g) was achieved, which enabled the network a versatile shape-memory effect, covering from dual-, triple-so far as to quadrupleshape memory effect. More importantly, the shape recovery and healing process can be realized simultaneously because of the highly matched actuating condition in this system.