Design of Polyurethane Based on a Dual-Repair Mechanism of Dynamic Disulfide Bonds and Hydrogen Bonds

Chuanxiu Hu, Y. H. Qu, Wenbo Guo, Xiaodong Liu, Hao Liu, Quan Zhang, Zhiwen Xu, Chao Jiang, Lei Liu, Ruliang Zhang, Yang Yu, Jian Liu
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引用次数: 2

Abstract

Self-healing polyurethane can ensure the operational stability of flexible strain sensors. However, achieving efficient self-healing at room temperature while simultaneously maintaining a high mechanical toughness remains a significant challenge. Here, we have proposed a molecular design driven simultaneously by dynamic disulfide bonds and hydrogen bonds and introduce Penta-EG into the main chain structure of polyurethane to form a certain hierarchical hydrogen bond structure and improve biocompatibility. Based on this design, we have successfully fabricated an elastomer that is self-healing and tough at room temperature. After healing at room temperature for 24 h, the healing efficiency of this elastomer reached 74.35%, and it exhibited excellent mechanical properties (a tensile strength of 4.64 MPa, an elongation at break of 1670%, a tear energy of 15,492.9 J/m2, and a puncture energy of 125.3 mJ). Moreover, the prepared strain sensor possessed high sensitivity and could be applied to detect human movement.
基于动态二硫键和氢键双修复机制的聚氨酯设计
自修复聚氨酯可以保证柔性应变传感器的工作稳定性。然而,在室温下实现有效的自愈,同时保持高机械韧性仍然是一个重大挑战。在此,我们提出了一种由动态二硫键和氢键同时驱动的分子设计,并将Penta-EG引入聚氨酯的主链结构中,形成一定的层次化氢键结构,提高生物相容性。基于这种设计,我们成功地制造了一种在室温下具有自愈性和韧性的弹性体。在室温下修复24 h后,该弹性体的愈合效率达到74.35%,具有优异的力学性能(抗拉强度4.64 MPa,断裂伸长率1670%,撕裂能15492.9 J/m2,穿刺能125.3 mJ)。此外,所制备的应变传感器具有较高的灵敏度,可用于人体运动检测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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