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Effects of Glass Fibers and Polypropylene/Glass Fiber Hybrid Fibers on the Kinetics and Mechanical Properties of Epoxy Composites

机译:玻璃纤维和聚丙烯/玻璃纤维杂化纤维对环氧复合材料动力学和力学性能的影响

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摘要

Curing reactions of diglycidyl ether of bisphenol F (DGEBP-F) and pre-catalyzed methyltetrahydrophthalic anhydride (MrnPA) with benzyl triethyl ammonium chlo- ride (BTEAC) were studied and effects of glass fibers evaluated. The influence on the kinetics of glass fibers and a hybrid blend of maleated polypropylene + glass fibers is studied. Isafuermal and dynamic kinetic parameters are detemlined by differential scanning calorimetry (DSC). Applicability of the autocatalytic model is investi- gated. The model serves well in the range of degrees of conversion between 25 and 800/0. At high conversion rates the diffusion control becomes apparent. Glass fibers accelerate the curing. shortening the time needed to reach the maximum reaction rate; this is reflected in lower activation energies for curing in comparison to the neat resin. The effects observed can be explained by a reaction between the amine group present on the fiber surfaces and the epoxy glycidyl groups. The result of both isothermal and non-isothermal curing of resin + glass fibers commingled with polypropylene are close to those for the neat resin. The reinforcement itlcreases the elastic modulus 12 times. the tensile strength 2 times. and the impact strength 285 times. The glass fibers + commingled polypropylene reinforcement provides comparable mechanical properties as glass fibers alone when normalized with respected to the density fraction of the fibers.
机译:研究了双酚F的二缩水甘油醚(DGEBP-F)和预催化的甲基四氢邻苯二甲酸酐(MrnPA)与苄基三乙基氯化铵(BTEAC)的固化反应,并评估了玻璃纤维的效果。研究了玻璃纤维和马来酸化聚丙烯+玻璃纤维混合共混物对动力学的影响。通过差示扫描量热法(DSC)确定了等黄和动态动力学参数。研究了自动催化模型的适用性。该模型在25和800/0之间的转换度范围内效果很好。在高转化率下,扩散控制变得明显。玻璃纤维加快了固化速度。缩短达到最大反应速率所需的时间;与纯树脂相比,这反映在较低的固化活化能上。观察到的效果可以通过纤维表面上存在的胺基与环氧缩水甘油基之间的反应来解释。树脂+与聚丙烯混合的玻璃纤维的等温和非等温固化的结果都接近纯树脂的结果。增强材料将弹性模量提高了12倍。抗拉强度的2倍。冲击强度285倍。当相对于纤维的密度分数归一化时,玻璃纤维+混合的聚丙烯增强物提供与单独的玻璃纤维相当的机械性能。

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