ACS Appl Mater Interfaces. 2010 Jul;2(7):1788-93. doi: 10.1021/am100288r.
The novelty of this work is based on designing the chemistry of the electrospun nanofibers, so that the resultant composites substantially benefit from cross-linking between the nanofibers and the polymer matrix. Specifically, the solution of in-house synthesized copolymers polystyrene-co-glycidyl methacrylate P(St-co-GMA) is electrospun to produce mats of surface reactive nano-to-submicron scale fibers that are accompanied later by spraying over the ethylenediamine (EDA) as a supplementary cross-linking agent for epoxy. The P(St-co-GMA)/EDA fiber mats are then embedded into an epoxy resin. Analysis of the three-point-bending mode of the composites reveals that the storage modulus of P(St-co-GMA)/EDA nanofiber-reinforced epoxy are about 10 and 2.5 times higher than that of neat and P(St-co-GMA) nanofiber-reinforced epoxy, respectively, even though the weight fraction of the nanofibers was as low as 2 wt %. The significant increase in the mechanical response is attributed to the inherently cross-linked fiber structure and the surface modification/chemistry of the electrospun fibers, that results in cross-linked polymer matrix-nanofiber interfacial bonding.
这项工作的新颖之处在于设计了电纺纳米纤维的化学性质,使得所得复合材料从纳米纤维与聚合物基体之间的交联中获得实质性的益处。具体来说,将内部合成的共聚物聚苯乙烯-甲基丙烯酸缩水甘油酯 P(St-co-GMA)的溶液进行静电纺丝,以生产表面反应性纳米至亚微米级纤维的垫,随后再喷洒乙二胺(EDA)作为环氧的补充交联剂。然后将 P(St-co-GMA)/EDA 纤维垫嵌入到环氧树脂中。对复合材料的三点弯曲模式的分析表明,即使纳米纤维的重量分数低至 2wt%,P(St-co-GMA)/EDA 纳米纤维增强环氧树脂的储能模量分别比纯环氧树脂和 P(St-co-GMA)纳米纤维增强环氧树脂高约 10 和 2.5 倍。机械响应的显著增加归因于固有交联的纤维结构和电纺纤维的表面改性/化学性质,这导致交联聚合物基体-纳米纤维界面键合。