Mechanically Robust Polyvalerolactone Thermosets with Dual Recyclability

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Hongyi Gu, , , Hao Ju, , , Kun Chen, , , Chang Sun, , , Lin Li, , , Jiayao Chen, , , Zhen Zhang*, , and , Peng-Fei Cao*, 
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Abstract

While the incorporation of dynamic covalent bonds (DCBs) in thermosets is widely employed, the materials inevitably downgrade substantially during repetitive physical recycling. Meanwhile, chemical recycling of polymers back to starting monomers often requires significant energy/resource input during the (de/re)polymerization process. To address such a dilemma, we propose a dual-recycling strategy that integrates the advantages of DCBs and chemical recycling by cross-linking chemically recyclable polyesters with DCB-containing cross-linkers. A series of poly(valerolactone) (PVL)-based covalent adaptable networks (CANs) were constructed featuring a functionalized PVL backbone and dynamic boronic-ester-containing cross-linkers to enable simultaneous physical and chemical recyclability. Through fine-tuning the balance between crystallinity and cross-linking density, the CANs exhibited outstanding mechanical properties, including a tensile strength up to 17.7 MPa and an elongation at a break of 1164%. Owing to the dynamic exchange characteristic of boronic esters, the CANs retained nearly identical performance to the original samples after five cycles of physical recycling. Furthermore, the CANs could undergo catalytically assisted chemical recycling with Sn(Oct)2, allowing the recovery of starting monomer. This work provided a valuable approach for the development of dual-recyclable high-performance polymer networks as a potential solution to the current challenges in thermosets recycling.

Abstract Image

Abstract Image

机械坚固的聚戊内酯热固性双可回收性
虽然在热固性材料中加入动态共价键(DCBs)被广泛应用,但在重复的物理回收过程中,材料不可避免地会大幅降级。同时,在(脱/重)聚合过程中,将聚合物化学回收为起始单体往往需要大量的能量/资源投入。为了解决这一困境,我们提出了一种双重回收策略,通过将化学可回收聚酯与含dcb的交联剂交联,将dcb和化学回收的优势结合起来。采用功能化聚戊内酯(PVL)骨架和动态含硼酯交联剂构建了一系列基于聚戊内酯(PVL)的共价自适应网络(can),以实现同时的物理和化学可回收性。通过对结晶度和交联密度之间的平衡进行微调,获得了优异的力学性能,抗拉强度达17.7 MPa,断裂伸长率达1164%。由于硼酯的动态交换特性,经过5次物理循环后,can的性能与原样品基本一致。此外,can可以用Sn(Oct)2进行催化辅助化学回收,从而回收起始单体。这项工作为开发双可回收的高性能聚合物网络提供了一种有价值的方法,作为解决当前热固性回收挑战的潜在解决方案。
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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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