弹性体
聚氨酯
木质素
极限抗拉强度
材料科学
延伸率
聚合物
氢键
化学工程
高分子化学
复合材料
化学
有机化学
分子
工程类
作者
Haixu Wang,Jianhua Huang,Weifeng Liu,Jinhao Huang,Dongjie Yang,Xueqing Qiu,Jiaren Zhang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2022-09-28
卷期号:55 (19): 8629-8641
被引量:29
标识
DOI:10.1021/acs.macromol.2c01401
摘要
In this work, tough and fast light-controlled healable lignin-containing polyurethane elastomers (LPUes) with a dynamic dual-crosslinking network were successfully synthesized. The network consisted of dynamic noncovalent bonds (hydrogen bonds and Zn2+-based coordination bonds) and dynamic carbamate bonds, which endowed LPUes with excellent mechanical properties (31.4 MPa, 1528%), reprocessability, and healing properties. After 4 times of reprocessing, the retention ratios of tensile strength and elongation at break for LPUes maintained above 85 and 95%, respectively. The incorporation of Zn2+-based coordination bonds significantly enhanced the photothermal conversion capability of LPUes, with the maximum surface temperature reaching above 160 °C in 2 min under the near-infrared (NIR) illumination of 1.2 W/cm2. The prepared LPUes exhibited rapid and outstanding light-controlled healing performance with 98% healing efficiency of mechanical properties under 10 min of NIR irradiation. This work demonstrated the novel application of biomass lignin in recyclable and light-driven smart polyurethane elastomers with good mechanical properties.
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