材料科学
共聚物
聚酰胺
高分子化学
丙交酯
缩聚物
韧性
二胺
化学工程
产量(工程)
聚合
形态学(生物学)
聚合物
复合材料
工程类
生物
遗传学
作者
Seung-Ju Hong,Gyu Ri Kim,Nam Kyun Kim,Jihoon Shin,Young‐Wun Kim
出处
期刊:ACS applied polymer materials
[American Chemical Society]
日期:2024-01-04
卷期号:6 (2): 1224-1235
标识
DOI:10.1021/acsapm.3c02147
摘要
We added a block copolymer compatibilizer to a thermodynamically immiscible blend of poly(lactide) (PLA) and poly(amide11) (PA11) and achieved a maximum strain at break (εb) and toughness (γ) of 467% and 157 MJ m–3, respectively, which were about 30 times higher than those of the neat PLA/PA11 blend system, while maintaining a yield stress (σyield) of 87% that of the neat PLA homopolymer. The PLA and PA11 based di-, tri-, and multiblock copolymer compatibilizers were synthesized via bulk polycondensation reactions of 11-aminoundecanoic acid (11-AUDA) and hexamethylene diamine (HMDA) or decylamine without the use of solvents. This was followed by a mechanochemical ball milling reaction between the resulting polyamide 11 containing di- or mono terminated amine end-groups and d,l-lactide through ring-opening polymerization (ROP) and urethane linkage reaction. The morphology of the prepared PLA/PA11/compatibilizer blend was investigated by O-PTIR and AFM analyses. As the content of the multiblock compatibilizer increased from 0 to 0.2, 0.5, and 1 wt %, the size of the domain droplets dramatically decreased, from 2.4 to 1.4 μm, and the interfacial thickness increased from 17.0 to 25.5, 55.2, and 76.9 Å, thereby supporting increased adhesion at the PLA/PA11 interface. Mechanical property analyses demonstrated that the mechanical properties improved as the amount of compatibilizer was increased from 0 to 0.2, 0.5, and 1 wt %, as the molecular weight (MW) of the blocks increased beyond the critical molecular weight (Mc) and the MW for cocrystallization, and as the number of blocks increased. The findings of this study demonstrate the potential of enhancing the mechanical properties of biobased polymer blends by incorporating block copolymer compatibilizers. This could help expand the broad range of applications for biobased polymers suitable for various fields.
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