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Toughness modification of cationic UV-cured cycloaliphatic epoxy resin by hydroxyl polymers with different structures

机译:不同结构羟基聚合物阳离子UV固化环脂族环氧树脂的韧性改性

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In this work, cationic UV-curable epoxy-expansive matrix composites based on cycloaliphatic epoxy resin (CE) were prepared using trarysulfonium hexafluorophosphate salt as photoinitiator, and hyperbranched polyester terminated with 6 hydroxy groups (H2004) or linear hydroxy-ended polytetramethylene ether glycol (PTMG) as toughness modifiers. Effects of H2004 and PTMG on the UV-curing kinetics, mechanical and thermal properties were systematically compared. An acceleration phenomenon was observed by real-time FTIR characterisation during the UV-curing of CE/H2004, which may be attributed to the hydroxy group participation of H2004 based on an activated monomer mechanism. However, the epoxy group conversion in the CE/PTMG composite decreased during UV irradiation owing to the random coil morphology of PTMG. Thermal-mechanical properties of the CE/H2004 composite were investigated by dynamic mechanical thermal analysis, which revealed that the glass transition temperature (Tg) decreased slightly as the H2004 dosage increased, in contrast to the Tg of the CE/PTMG composite, which increased as the PTMG content rose. Compared with CE, the thermal stability of CE/H2004 and CE/PTMG was less, but toughness was improved dramatically by increasing the content of H2004 or PTMG. At concentrations of H2004 and PTMG of 20% and 30%, respectively, the impact strength was improved from 1.14 J/cm(2) for CE to 4.62 J/cm(2) for CE/H2004 and 10.44 J/cm(2) for CE/PTMG. This was further elucidated by fracture surface analysis with a scanning electron microscope.
机译:在这项工作中,使用三raryliuphophate盐作为光引发剂制备基于脂环族环氧树脂(Ce)的阳离子UV可固化的环氧树脂 - 膨胀基质复合材料,用6个羟基(H2004)或线性羟基结束的聚二甲基醚乙二醇终止超支化聚酯( ptmg)作为韧性改性剂。系统地比较H2004和PTMG对UV固化动力学,机械和热性能的影响。通过在CE / H2004的UV固化期间通过实时FTIR表征观察到加速现象,这可能归因于基于活化的单体机制H2004的羟基群参与。然而,由于PTMG的随机线圈形态,在紫外线照射期间CE / PTMG复合材料中的环氧树脂转化率降低。通过动态机械热分析研究了CE / H2004复合材料的热电力学,显示玻璃化转变温度(Tg)略微降低,因为H2004剂量增加,与CE / PTMG复合材料的Tg相比随着PTMG含量上升。与Ce相比,Ce / H2004和Ce / Ptmg的热稳定性较小,但通过增加H2004或PTMG的含量显着提高韧性。在H2004和PTMG的浓度下,分别为CE / H2004和10.44J / cm(2)的CE至4.62J / cm(2)的1.14J / cm(2),改善冲击强度。对于CE / PTMG。通过用扫描电子显微镜进行裂缝表面分析进一步阐明了这一点。

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