蠕动
弹性体
聚二甲基硅氧烷
热稳定性
硅醚
乙醚
材料科学
硅烷化
高分子化学
复合材料
化学工程
化学
有机化学
工程类
催化作用
作者
Siyuan Chen,Jie Cao,Junping Zheng
标识
DOI:10.1021/acsapm.4c00291
摘要
Introducing covalent adaptable networks (CANs) into polydimethylsiloxane (PDMS) elastomers is an effective approach to solving the recycling issue of thermoset PDMS materials. However, CANs generally exhibit favorable dynamic properties to achieve efficient recycling, which leads to poor thermal stability and creep resistance. Herein, we successfully constructed dynamic silyl ether-based networks within the PDMS system by incorporating thermally stable silyl ether linkages, resulting in reprocessable PDMS elastomers with excellent mechanical properties, remarkable thermal stability, and desirable creep resistance. Compared with the samples without silyl ether-based networks, the prepared PDMS elastomer presented a 70 °C increase in T50 (the temperature at 50% weight loss), reaching as high as 635 °C. Meanwhile, after 10 reprocessing cycles, the mechanical properties of the prepared elastomer can still be almost completely restored, demonstrating superior reprocessability. More importantly, owing to the thermal stability of silyl ether-based networks, the prepared PDMS elastomer exhibited a desirable creep resistance at 120 °C. Therefore, the rational construction of dynamic silyl ether-based networks within the PDMS system can achieve an effective balance between thermal stability and recyclability.
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