肿胀 的
木质素
化学
自愈水凝胶
灵敏度(控制系统)
化学工程
高分子化学
材料科学
复合材料
有机化学
电子工程
工程类
作者
Xiangzhen Meng,Jing Zhou,Xin Jin,Changlei Xia,Shanyu Ma,Shu Hong,John Tosin Aladejana,Anran Dong,Yujia Luo,Jianzhang Li,Xianxu Zhan,Rui Yang
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2024-02-21
卷期号:25 (3): 1696-1708
被引量:8
标识
DOI:10.1021/acs.biomac.3c01228
摘要
Wood-derived hydrogels possess satisfactory longitudinal strength but lack excellent swelling resistance and dry shrinkage resistance when achieving high anisotropy. In this study, we displayed the preparation of highly dimensional stable wood/polyacrylamide hydrogels (wood/PAM-Al3+). The alkali-treated wood retains lignin as the skeleton of the hydrogel. Second, Al ions were added to the metal coordination with lignin. Finally, by employing free radical polymerization, we construct a conductive electronic network using polyaniline within the wood/PAM-Al3+ matrix to create the flexible sensor. This approach leverages lignin's integrated structure within the middle lamella to provide enhanced swelling resistance and stronger binding strength in the transverse direction. Furthermore, coordination between lignin and Al ions improves the mechanical strength of the wood hydrogel. Polyaniline provides stable linear pressure and temperature responses. The wood/PAM-Al3+ exhibits a transverse swelling ratio of 3.90% while achieving a longitudinal tensile strength of 20.5 MPa. This high-strength and high-stability sensor is capable of monitoring macroscale human behavior. Therefore, this study presents a simple yet innovative strategy for constructing tough hydrogels while also establishing an alternative pathway for exploring lignin networks in new functional materials development.
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