School of Chemistry, South China Normal University, GDMPA Key Laboratory for Process Control and Quality Evaluation of Chiral Pharmaceuticals, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, Guangzhou, Guangdong 510006, PR China.
School of Chemistry, South China Normal University, GDMPA Key Laboratory for Process Control and Quality Evaluation of Chiral Pharmaceuticals, Guangzhou Key Laboratory of Analytical Chemistry for Biomedicine, Key Laboratory of Theoretical Chemistry of Environment, Ministry of Education, Guangzhou, Guangdong 510006, PR China; Guangdong Esquel Textiles Co., Ltd., Foshan, Guangdong 528500, PR China.
Int J Biol Macromol. 2024 Mar;262(Pt 1):129998. doi: 10.1016/j.ijbiomac.2024.129998. Epub 2024 Feb 7.
How to effectively improve the poor interfacial adhesion between polylactic acid/poly(butylene adipate-co-terephthalate) (PLA/PBAT) matrix and thermoplastic starch (TPS) is still a challenge. Therefore, this work aims to introduce a convenient method to enhance the performance of PLA/PBAT/TPS blend by melt reactive extrusion. Here, using 4,4'-methylene-bis(N,N-diglycidyl-aniline) (MBDG) containing four epoxy groups as a reactive compatibilizer, and respectively using 1-methylimidazole (MI) or triethylenediamine (TD) as a catalyzer, serial PLA/PBAT/TPS ternary bio-composites are successfully prepared via melt reactive extrusion. The results showed that, under the catalysis of organic base, especially MI, the epoxy groups of MBDG can effectively react with hydroxyl and carboxyl groups of PLA/PBAT and hydroxyl groups in TPS to form chain-expanded and cross-linked structures. The tensile strength of the composites is increased by 20.0 % from 21.1 MPa, and the elongation at break is increased by 182.4 % from 17.6 % owing to the chain extension and the forming of cross-linked structures. The molecular weight, thermal stability, crystallinity, and surface hydrophobicity of the materials are gradually improved with the increase of MBDG content. The melt fluidity of the composites is also improved due to the enhancement of compatibility. The obtained PLA/PBAT/TPS materials have the potential to be green plastic products with good properties.
如何有效提高聚乳酸/聚对苯二甲酸丁二醇酯共聚物(PLA/PBAT)基体与热塑性淀粉(TPS)之间的界面粘结性仍然是一个挑战。因此,本工作旨在通过熔融反应挤出引入一种方便的方法来提高 PLA/PBAT/TPS 共混物的性能。在这里,使用含有四个环氧基团的 4,4'-亚甲基双(N,N-二缩水甘油基苯胺)(MBDG)作为反应性增容剂,并分别使用 1-甲基咪唑(MI)或三乙烯二胺(TD)作为催化剂,通过熔融反应挤出成功制备了系列 PLA/PBAT/TPS 三元生物复合材料。结果表明,在有机碱,特别是 MI 的催化作用下,MBDG 的环氧基团可以与 PLA/PBAT 的羟基和羧基以及 TPS 中的羟基有效反应,形成链扩展和交联结构。复合材料的拉伸强度从 21.1 MPa 提高了 20.0%,断裂伸长率从 17.6%提高了 182.4%,这是由于链扩展和交联结构的形成。随着 MBDG 含量的增加,材料的分子量、热稳定性、结晶度和表面疏水性逐渐提高。复合材料的熔体流动性也由于相容性的提高而得到改善。所得 PLA/PBAT/TPS 材料具有成为性能良好的绿色塑料产品的潜力。