Zhang Jingxian, Shi Xiaowen, Zhao Zhongtao, Wang Manya, Deng Hongbing, Du Yumin
School of Resource and Environmental Science, Hubei Engineering Center of Natural Polymers-Based Medical Materials, Hubei Biomass-Resource Chemistry and Environmental Biotechnology Key Laboratory, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Wuhan University, Wuhan, 430079, China.
Adv Sci (Weinh). 2024 Nov;11(44):e2409287. doi: 10.1002/advs.202409287. Epub 2024 Oct 7.
Various strategies are developed to engineer aligned hierarchical architectures in polymer hydrogels for enhanced mechanical performance. However, chain alignment remains impeded by the presence of hydrogen bonds between adjacent chains. Herein, a facile sacrificial micelle-assisted-alignment strategy is proposed, leading to well-aligned, strong and tough pure chitosan hydrogels. The sacrificial sodium dodecyl sulfate micelles electrostatically interact with the protonated chitosan chains, enabling chain sliding and alignment under uniaxial forces. Subsequently, sacrificial micelles can be easily removed via NaOH treatment, causing the reforming of H-bond in the chain networks. The strength of the pure chitosan hydrogels increases 140-fold, reaching 58.9 ± 3.4 MPa; the modulus increases 595-fold, reaching 226.4 ± 42.8 MPa. After drying-rehydration, the strength and modulus further rise to 70.3 ± 2.4 and 403.5 ± 76.3 MPa, marking a significant advancement in high-strength pure chitosan hydrogel films. Furthermore, the designed multiscale architectures involving enhanced crystallinity, well-aligned fibers, strong interfaces, robust multilayer Bouligand assembly contribute to the exact replica of lobster underbelly with impact resistance up to 6.8 ± 1.0 kJ m. This work presents a promising strategy for strong, tough, stiff and impact-resistant polymer hydrogels via well-aligned hierarchical design.
人们开发了各种策略来构建聚合物水凝胶中的排列有序的分级结构,以提高其机械性能。然而,相邻链之间存在的氢键阻碍了链的排列。在此,我们提出了一种简便的牺牲性胶束辅助排列策略,可制备出排列良好、强度高且坚韧的纯壳聚糖水凝胶。牺牲性的十二烷基硫酸钠胶束与质子化的壳聚糖链发生静电相互作用,使链在单轴力作用下滑动并排列。随后,通过氢氧化钠处理可轻松去除牺牲性胶束,从而使链网络中的氢键重新形成。纯壳聚糖水凝胶的强度提高了140倍,达到58.9±3.4兆帕;模量提高了595倍,达到226.4±42.8兆帕。经过干燥-再水化后,强度和模量进一步提高到70.3±2.4和403.5±76.3兆帕,这标志着高强度纯壳聚糖水凝胶薄膜取得了重大进展。此外,所设计的多尺度结构,包括增强的结晶度、排列良好的纤维、强界面、坚固的多层布利冈组装,有助于精确复制龙虾腹部,抗冲击性高达6.8±1.0千焦/平方米。这项工作通过排列有序的分级设计,为制备强韧、坚硬且抗冲击的聚合物水凝胶提供了一种有前景的策略。