弹性体
天然橡胶
酯交换
极限抗拉强度
聚合物
单体
结晶
玻璃化转变
材料科学
缩聚物
共聚物
化学工程
高分子化学
压缩成型
化学
有机化学
复合材料
催化作用
工程类
模具
作者
Hao Lin,Wen Li,Qingpeng Ou,Jie Liu,Zhaoyang Wei,Zhao Wang,Dean Shi,Weiwei Lei,Liqun Zhang
标识
DOI:10.1021/acssuschemeng.4c00423
摘要
Biomass feedstock is an accessible alternative to finite fossil chemical resources for fabricating durable and high-performance polymers. In this study, fully biobased poly(1,5-pentylene succinate-co-itaconate-co-furanoate) (PPeSIFs) copolyesters were synthesized by using transesterification and melt polycondensation methods from dimethyl furandicarboxylate, dimethyl succinate, dimethyl itaconate, and 1,5-pentanediol. Dimethyl itaconate was incorporated to provide the cross-linkable reaction sites. Four kinds of monomers were employed to regulate the glass transition temperature and suppress crystallization. Silica/PPeSIF nanocomposites exhibited good mechanical properties, such as an ultimate tensile strength of 17.2 MPa and an elongation at break of 253%. This elastomer displayed outstanding gas barrier properties comparable to those of butyl rubber, with an O2 permeability 13 times lower than that of natural rubber. Positron annihilation lifetime spectroscopy tests demonstrated that furan moieties significantly reduced the free volume of PPeSIFs. This work provides a promising route for preparing a biobased elastomer with intrinsic high gas barrier properties.
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