An upcycling strategy for polyamide 6: preparing thermoplastic polyamide elastomers from glycolysates produced by controlled degradation†

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2024-12-16 DOI:10.1039/D4GC03815K
Ji Lan, Cong Deng, Ze-Yong Zhao and Yu-Zhong Wang
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引用次数: 0

Abstract

Polyamides (PAs) represent a class of polymers conducive to chemical recycling, where the amide group acts as a reactive site for degradation agents. However, the inherent stability of the amide group means that chemical recycling of PAs often necessitates stringent conditions, such as high temperatures and pressures, significantly hindering advancements in PA chemical recycling. Moreover, the effectiveness of chemically recycling polyamides into monomers or oligomers—essential components for subsequent polymer synthesis—has not been conclusively verified through comprehensive research. Here, we present the first demonstration of a method for the upcycling of PA6 into high-performance PA derivatives. In the proposed method, PA6 is first degraded into oligomers with reactive end groups via glycolysis, with the reactivity of the resulting glycolysates subsequently verified. This oligomer acts as an intermediate in thermoplastic polyamide elastomer (TPAE) synthesis, facilitating direct integration with flexible polyethylene glycol oligomers into TPAE without requiring further degradation to monomers. The mechanical properties of the resultant TPAEs are commensurate with those previously reported for PA6-based TPAEs. By fine-tuning the reaction time and catalyst concentration, it is possible to control the molecular weight of the PA6 glycolysates, thus adjusting the TPAE's mechanical properties. This study presents an innovative approach that seamlessly combines the degradation process of PA6 with the synthesis pathway of TPAE, thus achieving the cost-effective upcycling of PA6 into TPAE.

Abstract Image

聚酰胺6的升级回收策略:由受控降解产生的糖酵解物制备热塑性聚酰胺弹性体
聚酰胺(PAs)代表一类有利于化学回收的聚合物,其中酰胺基团作为降解剂的反应位点。然而,酰胺基团固有的稳定性意味着PA的化学回收通常需要严格的条件,例如高温和高压,这极大地阻碍了PA化学回收的进展。此外,将聚酰胺化学回收为单体或低聚物(后续聚合物合成的必要成分)的有效性尚未得到全面研究的最终验证。在这里,我们首次展示了一种将PA6升级为高性能PA衍生物的方法。在所提出的方法中,PA6首先通过糖酵解降解为具有活性端基的低聚物,随后验证所得糖酵解物的反应性。该低聚物作为热塑性聚酰胺弹性体(TPAE)合成的中间体,促进与柔性聚乙二醇低聚物直接整合成TPAE,而无需进一步降解为单体。所得TPAEs的力学性能与先前报道的pa6基TPAEs相当。通过对反应时间和催化剂浓度的微调,可以控制PA6糖酵解物的分子量,从而调节TPAE的力学性能。本研究提出了一种创新的方法,将PA6的降解过程与TPAE的合成途径无缝结合,从而实现了PA6经济高效地升级回收为TPAE。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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