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Tough and fatigue resistant biomimetic hydrogels of interlaced self-assembled conjugated polymer belts with a polyelectrolyte network

机译:具有聚电解质网络的交错自组装共轭聚合物带的坚韧耐疲劳仿生水凝胶

摘要

Supertough biomimetic hydrogels have been fabricated through in situ synthesis and guided assembling of positively charged conjugated polymer belts by using a parent poly(2-acrylamido-2-methylpropanesulfonic acid)/poly(acrylamide) double network (PAMPS/PAAm DN) gel template. The interpenetrating structures of the poly(3,4-ethylenedioxythiophene) (PEDOT) belt mesh and PAMPS/PAAm host network have been confirmed by SEM, CLSM, and Raman spectroscopy. The presence of PEDOT belts improves the Young’s modulus, compressive strength, and toughness of the biomimetic (BM) hydrogels, in comparison to the parent DN gels. Cyclic tensile (300% strain) and compressive (even 90% strain) loadings demonstrate extraordinary fatigue resistance of these BM gels. Upon ten cycles, the compressive toughness remained about 1000 J m–2, which is comparable to that of articular cartilage. The internal fracture behavior and fatigue resistance of these biomimetic interpenetrating hydrogels are further investigated. These extremely tough and fatigue resistant BM hydrogels may find applications as promising substitutes for load-bearing tissues.
机译:通过使用母体聚(2-丙烯酰胺基-2-甲基丙烷磺酸)/聚(丙烯酰胺)双网络(PAMPS / PAAm DN)凝胶模板,通过原位合成和带正电荷的共轭聚合物带的引导组装,制备了超韧的仿生水凝胶。聚(3,4-乙撑二氧噻吩)(PEDOT)带网和PAMPS / PAAm宿主网络的互穿结构已通过SEM,CLSM和拉曼光谱法确认。与母体DN凝胶相比,PEDOT带的存在改善了仿生(BM)水凝胶的杨氏模量,抗压强度和韧性。循环拉伸(300%应变)和压缩(甚至90%应变)载荷证明了这些BM凝胶具有非凡的抗疲劳性。经过十个周期,其抗压强度保持在约1000 J m–2,与关节软骨相当。进一步研究了这些仿生互穿水凝胶的内部断裂行为和抗疲劳性。这些极其坚韧和耐疲劳的BM水凝胶可以找到有希望的替代承重组织的应用。

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