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石墨烯诱导水凝胶成核的高强韧人造蛛丝
引用本文:何文倩,邸亚,姜南,刘遵峰,陈永胜.石墨烯诱导水凝胶成核的高强韧人造蛛丝[J].物理化学学报,2022,38(9):2204059.
作者姓名:何文倩  邸亚  姜南  刘遵峰  陈永胜
作者单位:1 南开大学药物化学生物学国家重点实验室, 高分子所, 化学学院, 天津 3000712 航宇救生装备有限公司武汉创新中心, 武汉 430000
基金项目:国家自然科学基金(52090034);国家自然科学基金(51973093);国家自然科学基金(51773094);国家重点研发项目(2019YFE0119600);南开大学新有机质前沿科学中心(63181206)
摘    要:天然蜘蛛丝是由β-sheet交联的蛛丝蛋白溶剂流入S-型导管后经牵引拉伸形成,它显示了高强度与高韧性的完美结合。其优异的力学性质主要源于它的多级结构:交联、线性排列的纳米组装体以及核壳结构。受此启发,我们合成了一种交联的水凝胶,通过牵引拉丝的方法,制备了交联的、含有取向排列的纳米组装体结构以及核壳结构的凝胶纤维,并通过少量引入二维纳米材料—氧化石墨烯(0.01%),进一步调控纳米组装体的取向和尺寸,实现了蜘蛛丝般优异的力学性能(断裂强度560 MPa,断裂韧性200 MJ·m–3,缓冲能94%)。这种纤维可以用于高速下落物体的能量耗散和降低冲击力。

关 键 词:功能纤维  聚合物复合物  仿生  纺丝  纳米材料  氧化石墨烯  缓冲  
收稿时间:2022-04-30

Graphene-Oxide Seeds Nucleate Strong and Tough Hydrogel-Based Artificial Spider Silk
Wenqian He,Ya Di,Nan Jiang,Zunfeng Liu,Yongsheng Chen.Graphene-Oxide Seeds Nucleate Strong and Tough Hydrogel-Based Artificial Spider Silk[J].Acta Physico-Chimica Sinica,2022,38(9):2204059.
Authors:Wenqian He  Ya Di  Nan Jiang  Zunfeng Liu  Yongsheng Chen
Institution:1. State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Functional Polymer Materials, College of Chemistry, Nankai University, Tianjin 300071, China;2. Innovation Center of Hangyu Lifesaving Equipment, Wuhan 430000, China
Abstract:Natural spider silk is composed of spun spidroin protein containing beta-sheet crosslinking sites drawn from an S-shaped spinning duct. It exhibits an excellent combination of strength (1150 ± 200 MPa) and toughness (165 ± 30 MJ·m–3) that originates from its hierarchical structure, including crosslinking sites, highly aligned nano-aggregates, and a sheath-core structure. In this work, we prepared a hydrogel fiber that contains crosslinking sites, highly aligned nano-aggregates, and a sheath-core structure, by draw-spinning a bulk hydrogel composed of polyacrylic acid crosslinked with vinyl-functionalized silica nanoparticles (SNVs). The core-sheath structure was prepared by the water-evaporation-controlled self-assembly of the polyacrylic hydrogel, while nanometer-sized aggregates were formed by the self-assembly of polyacrylic acid chains. The addition of a tiny amount of graphene oxide (GO: 0.01%), a 2D nanomaterial, enhanced the mechanical properties of the fiber (breaking strength: 560 MPa; fracture toughness: 200 MJ·m–3; damping capacity: 94%). In addition, we investigated the factors responsible for the mechanical properties of the gel fibers, including fiber diameter, drying time in air, relative air humidity, and stretching speed. A higher breaking strength and a lower fracture strain was obtained by decreasing the fiber diameter, increasing the drying time, or increasing the stretching speed, while a lower fracture strain and higher breaking strength were obtained by increasing the relative air humidity. Polarized optical and SEM images revealed that the GO-seeded material is better aligned and contains smaller nano-aggregates, with GO seeding found to play a key role in the formation of nano-aggregates and polymer-chain alignment. The prepared fiber exhibited excellent mechanical properties compared to gel fibers prepared by other methods (e.g., electro-, wet, dry, and microfluidic spinning, as well as templating, and 3D printing, etc.). Repeated mechanical testing involving stretch-release cycles to 70% strain at 20% relative humidity revealed that the fibers have an energy-damping capacity of 93.6%, which exceeds that of natural spider silk and many types of artificial fiber. The relaxed stretched fiber recovered its initial length when exposed to 80% relative humidity, while the fiber recovered its initial mechanical properties when stored for 2 h at room temperature. A yarn composed of three hundred of the prepared gel fibers was shown to lift a 3 kg object without breaking; the prepared fiber was also shown to absorb dynamic energy and lower the impact force of a falling object.
Keywords:Functional fiber  Polymer composite  Biomimetic  Spinning  Nanomaterials  Graphene oxide  Damp capacity  
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