木质素
热固性聚合物
环氧化大豆油
极限抗拉强度
材料科学
环氧树脂
热稳定性
玻璃化转变
聚合物
动态力学分析
固化(化学)
复合材料
化学工程
化学
有机化学
原材料
工程类
作者
Xiang Zhen,Xiping Cui,Akram Ali Nasser Mansoor Al‐Haimi,Xiaobing Wang,Huijun Liang,Zhongbin Xu,Zhongming Wang
标识
DOI:10.1016/j.ijbiomac.2023.127760
摘要
The application of epoxidized soybean oil (ESO) in thermosetting polymers is impeded by its unsatisfactory thermomechanical properties. Here, in order to address the limitation, technical lignin was modified by tung oil anhydride and then used as the hardener to compensate for the inherent flexibility defects of ESO thermosets (TLs). As the lignin content increased, a notable improvement in the activation energy of TLs was observed, attributed to the restraining effect of lignin's rigid structure on segmental relaxation. Concurrently, the tensile strength of TLs increased from 2.8 MPa to 34.0 MPa, concomitant with a decrease in elongation at break from 32.9 % to 8.0 %. Comparative analysis with TL-0 (devoid of lignin) demonstrated substantial enhancements in glass transition temperature, shape fixation ratio, and shape recovery ratio for TL-50 (comprising 50 wt% of lignin), elevating from 16.9 °C, 89.1 %, and 89.5 % to 118.6 °C, 94.0 %, and 99.3 %, respectively. These results unequivocally highlight the favorable dynamic mechanical and shape memory properties conferred upon TLs by lignin addition. While the introduction of lignin adversely affected thermal stability, a notable improvement in char yield (800 °C) was observed. Collectively, these findings underscore the potential of technical lignin as a promising bio-based curing agent for ESO.
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