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Toughening of tetrafunctional (TGDDM) epoxy resins with telechelic extended perfluoroligomers

机译:用遥螯剂扩展的全氟聚合物对四官能(TGDDM)环氧树脂进行增韧

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摘要

Telechelic extended perfluoroether oligomers containing carboxylic acid terminal groups were found to be miscible in mixtures of a tetrafunctional epoxy resin (TGDDM) and methyl nadic anhydride. After curing the resin system remained transparent. SAXS examination revealed the presence of a two-phase morphology with domains of the order of 16-17 nm. The glass transition of the cured resin system showed a maximum at perfluoroether concentrations in the region of 5% and remained at about the same level as the unmodified system at concentrations as high as 20 wt%. The critical strain energy release rate (Gc) for these systems was found to increase very rapidly in the region of 5 to 15 wt% fluoroligomer to reach values about 8 times higher than those obtained for the control resin system. This was accompanied by a small reduction in modulus and yield strength. The main reason for the enhanced toughness, however, is attributed to the increased size of the yield zone at the crack tip. The fluoroligomer modified cured resin systems exhibited an unusual change in water diffusion characteristics. At about 15 wt% concentration of fluoroligomer modifier the diffusion coefficient increased by a factor of 70, while the equilibrium water absorption was reduced by more than 10 wt%.
机译:发现含有羧酸端基的远螯长链全氟醚低聚物可与四官能环氧树脂(TGDDM)和甲基纳迪克酸酐的混合物混溶。固化后,树脂体系保持透明。 SAXS检查显示存在两相形态,其畴域为16-17 nm。固化树脂体系的玻璃化转变在全氟醚浓度为5%时显示出最大值,并以高达20 wt%的浓度保持与未改性体系大约相同的水平。发现这些系统的临界应变能释放速率(Gc)在含氟聚合物的5至15%(重量)范围内非常迅速地增加,达到的值比对照树脂系统获得的值高约8倍。这伴随着模量和屈服强度的少量降低。但是,韧性提高的主要原因是裂纹尖端屈服区的尺寸增加。含氟聚合物改性的固化树脂体系在水扩散特性方面表现出不寻常的变化。在约15wt%浓度的含氟聚合物改性剂时,扩散系数增加了70倍,而平衡吸水率降低了超过10wt%。

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