Anti-Ultraviolet Biobased Polyesters Synthesized by Acyclic Diene Metathesis Polymerization

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-06-11 DOI:10.1021/acs.macromol.4c00593
Qiubo Wang, Xinyu Hu, Shuyao Wang, Xiaojuan Liao, Ruyi Sun, Qiancai Liu* and Meiran Xie*, 
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Abstract

Synthesis of copolymers using 2,5-furandicarboxylic acid (FDCA) and isosorbide (IS) as renewable feedstocks remains a challenge in conventional melt polycondensation. Herein, acyclic diene metathesis (ADMET) polymerization of several kinds of α,ω-dienes containing an FDCA or IS moiety was performed under mild conditions to afford biobased polyesters with an unsaturated chain structure and tunable glass transition temperature between −40 and 34 °C. Meanwhile, FDCA-derived α,ω-diene was used as a comonomer to undergo inverse vulcanization with elemental sulfur, affording a polysulfide as the cross-linking agent suitable for modifying ADMET polyesters. The cross-linked polyesters showed improved mechanical properties and good reprocessability. Furthermore, the modified polyester composites exhibited excellent anti-ultraviolet (UV) performance with a high UV protection factor of 251 and maintained almost the original mechanical properties even after 72 h of UV light exposure. This work provided a practical approach for the high-value-added utilization of ADMET polyesters as sustainable functional materials.

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通过无环二烯偏聚合成法合成的抗紫外线生物基聚酯
使用 2,5-呋喃二甲酸(FDCA)和异山梨醇苷(IS)作为可再生原料合成共聚物仍然是传统熔融缩聚法的一项挑战。在此,我们在温和的条件下对几种含有 FDCA 或 IS 分子的 α,ω-二烯进行了无环二烯偏聚 (ADMET),从而得到了具有不饱和链结构且玻璃化转变温度在 -40 至 34 °C 之间的生物基聚酯。同时,以 FDCA 衍生的 α,ω-二烯为共聚单体,与元素硫进行反硫化反应,得到一种多硫化物作为交联剂,适用于改性 ADMET 聚酯。交联聚酯具有更好的机械性能和良好的再加工性。此外,改性后的聚酯复合材料具有优异的抗紫外线(UV)性能,紫外线防护系数高达 251,即使在紫外线照射 72 小时后仍能保持几乎原有的机械性能。这项研究为将 ADMET 聚酯作为可持续功能材料进行高附加值利用提供了一种实用方法。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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