乙二醇
材料科学
混溶性
共聚物
差示扫描量热法
结晶
增塑剂
极限抗拉强度
可生物降解聚合物
化学工程
高分子化学
复合材料
聚乳酸
韧性
聚合物
聚酯纤维
艾氏冲击强度试验
工程类
物理
热力学
作者
Chao Chen,Ying Tian,Fenglong Li,Han Hu,Kai Wang,Zhengyang Kong,Wu Ying,Ruoyu Zhang,Jin Zhu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2020-12-23
卷期号:22 (2): 374-385
被引量:17
标识
DOI:10.1021/acs.biomac.0c01236
摘要
Polylactic acid (PLA) is a biodegradable thermoplastic polyester produced from natural resources. Because of its brittleness, many tougheners have been developed. However, traditional toughening methods cause either the loss of modulus and strength or the lack of degradability. In this work, we synthesized a biobased and potentially biodegradable poly(butylene 2,5-furandicarboxylate)-b-poly(ethylene glycol) (PBFEG50) copolymer to toughen PLA, with the purpose of both keeping mechanical strength and enhancing the toughness. The blend containing 5 wt % PBFEG50 exhibited about 28.5 times increase in elongation at break (5.5% vs 156.5%). At the same time, the tensile modulus even strikingly increased by 21.6% while the tensile strength was seldom deteriorated. Such a phenomenon could be explained by the stretch-induced crystallization of the BF segment and the interconnected morphology of PBFEG50 domains in PLA5. The Raman spectrum was used to identify the phase dispersion of PLA and PBFEG50 phases. As the PBFEG50 content increased, the interconnected PBFEG50 domains start to separate, but their size increases. Interestingly, tensile-induced cavitation could be clearly identified in scanning electron microscopy images, which meant that the miscibility between PLA and PBFEG50 was limited. The crystallization of PLA/PBFEG50 blends was examined by differential scanning calorimetry, and the plasticizer effect of the EG segment on the PLA matrix could be confirmed. The rheological experiment revealed decreased viscosity of PLA/PBFEG50 blends, implying the possible greener processing. Finally, potential biodegradability of these blends was proved.
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