Biodegradable poly (lactic acid) blends toughened with in situ formed core-shell structure by reactive processing

IF 4.5 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2025-03-28 DOI:10.1016/j.polymer.2025.128330
Wei Bao , Yunbao Gao , Jianing Zhang , Jing Jin , Na Zhang , Baijun Liu , Mingyao Zhang , Zhaohui Su , Hongwen Liang , Xiangling Ji , Wei Jiang
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Abstract

Biodegradable poly (lactic acid) (PLA) blends toughened with a core-shell structure were successfully prepared by melt-blending PLA with poly (butylene adipate-co-terephthalate) (PBAT) and poly (ether-block-amide) (PEBA). Scanning electron microscopy (SEM) and atomic force microscopy-infrared (AFM-IR) analyses confirmed the presence of core-shell structure in the PLA matrix, in which the core and the shell are PBAT and PEBA, respectively. To enhance the interfacial compatibility between PLA and PEBA, glycidyl methacrylate (GMA) was grafted onto PEBA, yielding the PEBA-GMA copolymer. The epoxy groups in PEBA-GMA reacted with the end groups (-OH, –COOH) of PBAT and PLA, which enhanced the interfacial compatibility of PLA/PEBA and PEBA/PBAT, thereby facilitating the formation of a smaller dispersed phase with core-shell structure. Consequently, a super-toughened PLA/PEBA-GMA/PBAT blend was prepared. The PLA/PEBA-GMA5/PBAT (70/15/15) blends achieved a notched Izod impact strength of 72.9 kJ/m2. Moreover, with a fixed PLA matrix content of 80 wt%, the upper limit of core PBAT content in PLA/PEBA-GMA3/PBAT blends was 18 wt%, while the minimum shell PEBA-GMA3 content was 2 wt% to ensure that the blends were ductile fracture. The composite of this blend had a lower stiffness loss, i.e., 26 %, demonstrating a well-balanced toughness and stiffness. Furthermore, the PLA/PEBA-GMA3/PBAT (70/25/5) blend exhibited excellent toughness at low temperatures, achieving a notched Izod impact strength of 47.1 kJ/m2 at −20 °C. Enzyme degradation experiments confirmed that the PLA blends retained the biodegradability of PLA, PBAT, and PEBA, ensuring that the blends were environmentally friendly.

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生物可降解聚乳酸共混物通过反应处理原位增韧形成核-壳结构
通过将聚乳酸与聚己二酸丁二醇酯(PBAT)和聚醚嵌段酰胺(PEBA)熔融混合,成功制备了具有核壳结构的可生物降解聚乳酸(PLA)增韧共混物。扫描电子显微镜(SEM)和原子力显微镜-红外(AFM-IR)分析证实,聚乳酸基质中存在核壳结构,其中核和壳分别为 PBAT 和 PEBA。为了增强聚乳酸和 PEBA 之间的界面相容性,在 PEBA 上接枝了甲基丙烯酸缩水甘油酯(GMA),从而得到 PEBA-GMA 共聚物。PEBA-GMA 中的环氧基团与 PBAT 和 PLA 的端基(-OH、-COOH)发生反应,增强了 PLA/PEBA 和 PEBA/PBAT 的界面相容性,从而促进了具有核壳结构的较小分散相的形成。因此,制备出了超增韧聚乳酸/PEBA-GMA/PBAT 共混物。聚乳酸/PEBA-GMA5/PBAT(70/15/15)混合物的缺口伊佐德冲击强度达到 72.9 kJ/m2。此外,在固定聚乳酸基体含量为 80 wt.%的情况下,聚乳酸/PEBA-GMA3/PBAT 共混物的核心 PBAT 含量上限为 18 wt.%,而外壳 PEBA-GMA3 的最低含量为 2 wt.%,以确保共混物具有韧性断裂。这种混合物的复合材料刚度损失较低,仅为 26%,表明韧性和刚度得到了很好的平衡。此外,聚乳酸/PEBA-GMA3/PBAT(70/25/5)共混物在低温条件下表现出优异的韧性,在-20 °C时的缺口伊佐德冲击强度达到47.1 kJ/m2。酶降解实验证实,聚乳酸共混物保留了聚乳酸、PBAT 和 PEBA 的生物降解性,确保了共混物的环境友好性。
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文献相关原料
公司名称
产品信息
麦克林
Glycidyl methacrylate
麦克林
N-Vinyl-2-pyrrolidinone
麦克林
Glycidyl methacrylate (GMA)
麦克林
N-Vinyl-2-pyrrolidinone (NVP)
阿拉丁
di-cumyl peroxide
阿拉丁
proteinase K
阿拉丁
proteinase K
来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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