聚二甲基硅氧烷
弹性体
材料科学
硅氧烷
弹性(物理)
烷基
玻璃化转变
结晶
聚合
化学工程
高分子化学
复合材料
聚合物
有机化学
化学
工程类
作者
Zhen Niu,Ruiyao Wu,Lingyun Huang,Yinxin Yang,Zhu Xia,Weifeng Fan,Wu Sun,Quanquan Dai,Jianyun He,Chenxi Bai
标识
DOI:10.1016/j.eurpolymj.2022.111303
摘要
Elastomers that services under ultra-low temperature environments are of great strategic and technological importance. Among them, polysiloxanes are excellent precursors, however, the unfavorable crystallization greatly limits its ultra-low temperature application. Herein, we explore the synthesis, glass transition temperature (Tg), cross-linking behavior and long-time ultra-low temperature elasticity characterization of polydimethylsiloxane (PDMS) with flexible alkyl branches. The results demonstrated that the flexible alkyl branches play a dual role in PDMS, for it can not only unlock its ultra-low temperature elasticity by suppressing crystallization, but also provide more free radical attack sites to enhance the cross-linking activity. The resulting elastomer with a Tg lower than −120 °C exhibits excellent elasticity at such a low temperature down to −110 °C. Moreover, the facile and efficient one-step thiol-ene addition post-polymerization enables the large-scale preparation of this ultra-low temperature elastomer. The work demonstrated here reveals a general practical strategy to unlock PDMS ultra-low temperature performance, which is conducive to the development of cutting-edge scientific research.
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