聚乳酸
有机溶剂
甲基丙烯酸缩水甘油酯
材料科学
结晶度
热重分析
极限抗拉强度
嫁接
傅里叶变换红外光谱
差示扫描量热法
结晶
化学工程
反应挤出
复合材料
纤维素
增容
热变形温度
高分子化学
扫描电子显微镜
热稳定性
接触角
过氧化苯甲酰
混溶性
自由基引发剂
表面改性
核化学
作者
Shallal Alshammari,Amir Ameli
出处
期刊:ACS omega
[American Chemical Society]
日期:2024-08-06
卷期号:9 (33): 35937-35949
被引量:1
标识
DOI:10.1021/acsomega.4c05212
摘要
Glycidyl methacrylate (GMA) was grafted onto a melt-flowable organosolv lignin, called bioleum (BL), using a melt mixing process. Then, up to 40 wt % of BL-g-GMA was blended with polylactic acid (PLA) in the presence of dicumyl peroxide as a free radical initiator utilizing a melt extrusion method. Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis, differential scanning calorimetry, scanning electron microscopy, and tensile testing were performed to characterize the biocomposites' performance. The FTIR results revealed a successful grafting of GMA onto BL. Overall, BL and PLA compatibility increased significantly with the grafting and resulted in decreased domain size of BL-g-GMA and thus enhanced all the tensile properties (strength, modulus, and elongation at break) at BL loadings as high as 40 wt %. For instance, in the biocomposites containing 30 wt % BL, the GMA grafting increased the tensile strength by 23%. The presence of BL and BL-g-GMA hindered PLA's crystallization even when it was cooled at a rate of 1 °C/min. However, the composites with BL-g-GMA showed a crystallinity value comparable to that of PLA during isothermal crystallization, but with a slower crystallization rate. This work reveals a facile and scalable method that can be adopted to enhance the performance of lignin-based biocomposites.
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