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Influence of Network Structure on Dynamic Mechanical Properties of Cross-linked Polystyrene / Glass Fiber Composites

机译:网络结构对交联聚苯乙烯/玻璃纤维复合材料动态力学性能的影响

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The cross-linked polystyrene prepolymer was synthesized with divinylbenzene (DVB) as crosslinker via free-radical crosslinking copolymerization (FCC) and used as the matrix materials for E-glass fiber reinforced composites. The surface modification was performed by treatment of E-glass fiber with γ-methacryloylpropyl trimethoxysilane (MPS) solution. Fourier transform infrared spectroscopy (FTIR) was used to identify the functional groups on the surface modified glass fibers. Dynamic mechanical thermal analysis (DMTA) of these composites revealed that the dynamic storage modulus (E′) was gradually enhanced with the increasing content of DVB (0~3.0 wt %) whereas the damping parameter (tanδ) peaks are lower and broader, indicating better load bearing capacity. Moreover, the Tg was shifted to higher temperature corresponding to the increasing of crosslinking density. Morphology of fracture surfaces for these composites showed different fiber-matrix interfacial adhesion which was mainly attributed to the variation of crosslinking network structure in the interface.
机译:以二乙烯基苯(DVB)为交联剂,通过自由基交联共聚(FCC)合成了交联的聚苯乙烯预聚物,并用作电子玻璃纤维增​​强复合材料的基体材料。通过用γ-甲基丙烯酰基丙基三甲氧基硅烷(MPS)溶液处理E玻璃纤维进行表面改性。傅里叶变换红外光谱(FTIR)用于鉴定表面改性玻璃纤维上的官能团。这些复合材料的动态机械热分析(DMTA)表明,随着DVB含量的增加(0〜3.0 wt%),动态储能模量(E')逐渐增大,而阻尼参数(tanδ)峰则越来越低,表明更好的承载能力。而且,Tg转变为更高的温度,这对应于交联密度的增加。这些复合材料的断裂表面形态显示出不同的纤维-基质界面粘合性,这主要归因于界面中交联网络结构的变化。

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