极限抗拉强度
弹性体
材料科学
多元醇
相容性(地球化学)
木质素
热稳定性
聚氨酯
聚合物
复合数
化学工程
延伸率
生物高聚物
复合材料
溶剂
高分子化学
热塑性弹性体
高分子
艾氏冲击强度试验
聚合度
水溶液
抗撕裂性
湿强度
作者
Changgeng Li,Lu Wu,Zhongshan Wang,Rui Xiao,Lina Shi,Wenchao Jia,Lingzhi Huang,Haiqiang Shi
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-03-02
卷期号:27 (4): 2752-2761
标识
DOI:10.1021/acs.biomac.5c02578
摘要
The poor compatibility and low degree of substitution of lignin severely limit its application as a polyol substitute in polyurethane elastomers. Herein, by regulating the molecular weight of lignin, high-content and uniform bonding of lignin in polyurethane (PU) has been achieved. Even at a substitution degree of 15%, lignin can still be fully integrated into the macromolecular chains of PU, resulting in a 27% increase in tensile strength and a 124% increase in elongation at break of the elastomer, respectively. Furthermore, a remarkable enhancement of over 165% in the tensile strength of the elastomer has been realized through adjusting the molecular weight of lignin. And through life cycle assessment, the importance of using lignin as a substitute for polyols has been confirmed. Notably, the thermal stability and surface hydrophobicity of the elastomer have also been significantly improved, and it can be combined with MXene to fabricate composite devices with sensitive strain responsiveness. This promising advancement is expected to promote the green and sustainable development of PU and its application in multifunctional wearable devices.
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