增塑剂
生物降解
玻璃化转变
差示扫描量热法
乳酸
聚乳酸
化学
韧性
聚合物
苏贝林
可生物降解聚合物
发泡剂
聚羟基丁酸酯
化学工程
材料科学
高分子化学
复合材料
有机化学
木质素
物理
遗传学
生物
细菌
工程类
热力学
聚氨酯
作者
Hyejung Yoon,Bumyong Yoon,Seung-Hyun Cho,Tae Hoon Oh,Jonghwan Suhr
标识
DOI:10.1016/j.indcrop.2023.117990
摘要
In this study, the inherent brittleness of biodegradable poly(lactic acid) (PLA) was mitigated through the utilization of a carbon-neutral biomass—depolymerized suberin derivatives (DSDs)—as a plasticizer. The DSDs were subjected to repolymerization under mild conditions, resulting in weight-average molecular weights of 2744 g/mol and 11546 g/mol. These polymerized DSDs (pDSDs) were subsequently blended with PLA, leading to a notable reduction in the glass transition temperature of the blends, confirmed through differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) characterizations. Remarkably, the tensile toughness exhibited a substantial increase up to 1148% from 0.56 MJ/m3 in the neat PLA to a range of 4.37–6.99 MJ/m3 for blends incorporating more than 3 wt% of pDSDs. Furthermore, the blends demonstrated a marked reduction in shear viscosity compared to neat PLA, corroborated by an increased melt flow index which shifted from 10.0 g/10 min to a range of 29.3–33.3 g/10 min. This alteration promises to be beneficial in enhancing the quality and producibility during the injection molding process. Importantly, the biodegradability of the pDSDs/PLA blends remained comparable to that of the neat PLA, showing a 90% degree of disintegration in 12 weeks from the biodisintegration test. This study can pave the way to valorize other bio-based materials with aliphatic compounds for the plasticizing modification of various polymers. Furthermore, understanding the interactions between different bio-based aliphatic compounds and various polymers could lead to tailor-made solutions for specific applications, ranging from biomedical devices to structural parts, further broadening the scope of biodegradable and sustainable materials in many engineering fields.
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