首页> 外文期刊>Iranian polymer journal >Preparation and Curing Kinetics Investigation of Diglycidyl Ether of Bisphenol A/Liquid Crystalline Epoxy Resin Blends
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Preparation and Curing Kinetics Investigation of Diglycidyl Ether of Bisphenol A/Liquid Crystalline Epoxy Resin Blends

机译:双酚A /液态结晶环氧树脂共混物二缩水甘油醚的制备及固化动力学研究

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摘要

A novel liquid crystalline epoxy resin (PHQEP) was synthesized by phase transfer catalytic method and characterized as a nematic liquid crystalline by polarized optical microscope (POM). The cure kinetics of diglycidyl ether of bisphenol A (E-51 )/PHQEP blends using 4,4'-diaminodiphenylsulphone (DDS) as the curing agent was studied by non-isothermal differential scanning calorimetry (DSC) at four linearly programmed heating rates of 5, 10, 15, and 20 K/min. The apparent activation energy (E_a) was determined by Friedman method, and kinetic model was predicted by Malek method. In the curing process of PHQEP/DDS, the E_a values decreased slowly with the conversion in the region of 0.2~0.5 for the formation of liquid crystalline phase. The E_a value of PHQEP/DDS system is generally higher than those of PHQEP/E-51/DDS and E-51/DDS systems and the E_a of PHQEP/E-51/DDS system is generally higher than that of E-51/DDS. This may imply that PHQEP is less reactive than E-51 in the curing process, since the molecular movement was limited because of the aromatic ester structure and the hydrogen bonds which were formed between the carbonyl groups of PHQEP and hydroxyl groups produced in the curing process. Furthermore, autocatalyt-ic model was predicted to be the kinetic model of the above mentioned three systems. The predicted curves fit well with the experimentally obtained curves.
机译:通过相转移催化法合成了新型液晶环氧树脂(PHQEP),并通过偏振光学显微镜(POM)表征为向列型液晶。通过非等温差示扫描量热法(DSC)在4个线性程序升温速率下,通过非等温差示扫描量热法(DSC)研究了以4,4'-二氨基二苯砜(DDS)为固化剂的双酚A(E-51)/ PHQEP共混物二缩水甘油醚的固化动力学。 5、10、15和20 K / min。用弗里德曼方法确定了表观活化能(E_a),并用Malek方法预测了动力学模型。在PHQEP / DDS的固化过程中,液晶相的E_a值随着转化率在0.2〜0.5范围内缓慢下降。 PHQEP / DDS系统的E_a值通常高于PHQEP / E-51 / DDS和E-51 / DDS系统的E_a值,而PHQEP / E-51 / DDS系统的E_a值通常高于E-51 / DDS。这可能意味着PHQEP在固化过程中的反应性不如E-51,因为分子的运动受到限制,因为芳族酯结构和PHQEP羰基与固化过程中产生的羟基之间形成的氢键。此外,自催化模型被预测为上述三个系统的动力学模型。预测曲线与实验获得的曲线非常吻合。

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