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具有可调海水生物降解性的超序列控制聚(L-丙交酯)基生物塑料。

Superior sequence-controlled poly(L-lactide)-based bioplastic with tunable seawater biodegradation.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

J Hazard Mater. 2024 Aug 5;474:134819. doi: 10.1016/j.jhazmat.2024.134819. Epub 2024 Jun 4.

Abstract

Developing superior-performance marine-biodegradable plastics remains a critical challenge in mitigating marine plastic pollution. Commercially available biodegradable polymers, such as poly(L-lactide) (PLA), undergo slow degradation in complex marine environments. This study introduces an innovative bioplastic design that employs a facile ring-opening and coupling reaction to incorporate hydrophilic polyethylene glycol (PEG) into PLA, yielding PEG-PLA copolymers with either sequence-controlled alternating or random structures. These materials exhibit exceptional toughness in both wet and dry states, with an elongation at break of 1446.8% in the wet state. Specifically, PEGPLA copolymer biodegraded rapidly in proteinase K enzymatic solutions and had a significant weight loss of 71.5% after 28 d in seawater. The degradation primarily affects the PLA segments within the PEG-PLA copolymer, as evidenced by structural changes confirmed through comprehensive characterization techniques. The seawater biodegradability, in line with the Organization for Economic Cooperation and Development 306 Marine biodegradation test guideline, reached 72.63%, verified by quantitative biochemical oxygen demand analysis, demonstrating rapid chain scission in marine environments. The capacity of PEG-PLA bioplastic to withstand DI water and rapidly biodegrade in seawater makes it a promising candidate for preventing marine plastic pollution.

摘要

开发性能优越的海洋可生物降解塑料仍然是减轻海洋塑料污染的一个关键挑战。商业上可用的可生物降解聚合物,如聚(L-丙交酯)(PLA),在复杂的海洋环境中降解缓慢。本研究介绍了一种创新的生物塑料设计,该设计采用开环和偶联反应将亲水性的聚乙二醇(PEG)引入 PLA 中,得到具有序列可控交替或无规结构的 PEG-PLA 共聚物。这些材料在干湿两种状态下均表现出优异的韧性,在湿态下的断裂伸长率达到 1446.8%。具体而言,PEG-PLA 共聚物在蛋白酶 K 酶溶液中快速生物降解,在海水中 28 天后重量损失显著,达到 71.5%。降解主要影响 PEG-PLA 共聚物中的 PLA 段,这可以通过全面的表征技术证实结构变化得到证实。根据经济合作与发展组织 306 海洋生物降解测试指南,海水生物降解率达到 72.63%,通过定量生化需氧量分析得到验证,表明在海洋环境中快速发生链断裂。PEG-PLA 生物塑料能够耐受 DI 水并在海水中快速生物降解,这使其成为防止海洋塑料污染的有前途的候选材料。

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