解聚
聚酯纤维
玻璃化转变
极限抗拉强度
材料科学
透明度(行为)
延伸率
热稳定性
化学工程
热的
溶剂
机械强度
工作(物理)
纳米技术
灵活性(工程)
聚合物
拉伸试验
二醇
化学
工艺工程
有机溶剂
铋
复合材料
转变温度
制作
作者
Xiaodong Cai,Di Wu,Jiebin Tan,Danhua Jiao,Daohai Zhang
标识
DOI:10.1021/acs.biomac.6c02202
摘要
Abstract Chemical recovery at the end-of-life while meeting stringent performance specifications remains a prominent challenge in the development of bio-based polyesters. Here, fully bio-based poly(butylene-co-trimethylcyclopentane-1,3-dimethylene furandicarboxylate) (PBTCF) copolyesters were synthesized from dimethyl 2,5-furandicarboxylate, 1,4-butanediol, and a rigid camphoric acid-derived cyclic diol (TCDM) via two-step melt transesterification-polycondensation. TCDM incorporation restricted segmental mobility, increasing the glass transition temperature from 38.4 to 64.3 °C while improving optical transparency and solvent resistance. PBTCF3 (3 mol % TCDM) combined a tensile strength of 55 MPa with 500% elongation at break. Furthermore, rapid depolymerization in THF/BDO/NaOH under mild conditions yielded FDCA (85.7% recovery; 99.1% purity) and BDO (97.8% purity). Recovered FDCA was converted to DMFD, which was then repolymerized with recovered BDO and fresh TCDM to produce a polyester comparable to the original in molecular weight, thermal properties, and mechanical properties. This work presents a viable approach to harmonizing high performance with sustainability in bio-based polymers.
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