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Preparation and characterization of fast-curing powder epoxy adhesive at middle temperature

机译:中温快干粉末环氧胶粘剂的制备与表征

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摘要

At present, the disadvantage of powder epoxy adhesive is the limited application area. In order to widen the application range of powder epoxy adhesive from heat-resistant substrates (such as metals) to heat-sensitive substrates (such as plastic products, cardboard and wood), it is necessary to decrease the curing temperature. In this article, a series of fast-curing powder epoxy adhesives were prepared by the melt blending method with bisphenol A epoxy resin (E-20), hexamethylenetetramine (HMTA) as a curing agent and 2-methylimidazole (2-MI) as an accelerant. The structure and properties of the E-20/HMTA/2-MI systems were characterized by Fourier transform infrared, thermogravimetric analysis, dynamic mechanical analyser and differential scanning calorimetry (DSC). 2-MI added into the E-20/HMTA systems can simultaneously enhance toughness, tensile strength, glass transition temperature (Tg) and thermal stability in comparison with the E-20/HMTA systems. The best mechanical properties were obtained at 100/8/0.6 weight ratio of the E-20/HMTA/2-MI systems. DSC experiments revealed that the exothermic peak of the E-20/HMTA/2-MI system was about 55°C lower than that of the E-20/HMTA system. The activation energy of the cure reaction was determined by both Kissinger's and Ozawa's methods at any heating rates. The activation energy and pre-exponential factor were about 100.3 kJ mol−1 and 3.57 × 1011 s−1, respectively. According to the KAS method, the curing time of the E-20/HMTA/2-MI systems was predicted by evaluating the relationship between temperature and curing time.
机译:目前,粉末环氧粘合剂的缺点是有限的应用领域。为了拓宽粉末状环氧粘合剂的应用范围,从耐热性基材(例如金属)到热敏性基材(例如塑料制品,纸板和木材),必须降低固化温度。本文采用熔融共混法,以双酚A环氧树脂(E-20),六亚甲基四胺(HMTA)作为固化剂和2-甲基咪唑(2-MI)作为熔融混合物,制备了一系列快速固化的粉末环氧粘合剂。促进剂。 E-20 / HMTA / 2-MI系统的结构和性能通过傅立叶红外光谱,热重分析,动态力学分析仪和差示扫描量热法(DSC)进行了表征。与E-20 / HMTA系统相比,添加到E-20 / HMTA系统中的2-MI可以同时提高韧性,拉伸强度,玻璃化转变温度(Tg)和热稳定性。在E-20 / HMTA / 2-MI系统的重量比为100/8 / 0.6时,可获得最佳的机械性能。 DSC实验表明,E-20 / HMTA / 2-MI系统的放热峰比E-20 / HMTA系统的放热峰低约55°C。固化反应的活化能通过基辛格(Kissinger)方法和小泽(Ozawa)方法在任何加热速率下确定。活化能和指数前因子分别约为100.3 kJ mol -1 和3.57×10 11 s -1 。根据KAS方法,通过评估温度与固化时间之间的关系来预测E-20 / HMTA / 2-MI系统的固化时间。

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