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CURE KINETICS OF NANOCOMPOSITES PREPARED FROM AQUEOUS DISPERSION OF NANOCLAY

机译:用纳米粘土水分散体制备的纳米复合材料的固化动力学

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The effect of nanoclay on the cure kinetics of glass/waterborne epoxy nanocomposites is investigated. First step in sample preparation involves dispersing Cloisite Na+, a natural montmorillonite, in distilled water at 70°C with the aid of a sonicator. Then, desired amounts of dicyandiamide and 2-methyl imidazole, serving as cross-linkers, are mixed to the aqueous nanoclay solution. As the mixing continues, Epi-Rez 3522-W-60 waterborne epoxy resin is introduced to the solution and the compound is mixed for an additional 30 minutes. The nanoclay content of this batch is adjusted to be at 2wt%. An identical second batch, which does not comprise nanoclay, is also prepared to serve as the baseline data. Glass/waterborne epoxy prepregs containing 30% glass fibers are prepared from these batches and used to characterize the effects of nanoclay. The evolution of viscoelastic properties during curing are characterized by the APA2000 rheometer. Using the storage and loss moduli profiles during curing, gel time and maximum storage modulus are characterized. Effect of nanoclay on the glass transition temperature is determined by applying an additional temperature cycle following the cure cycle. In addition, mechanical performances of the samples are characterized by three point bending tests. Nanoclay is observed to yield 2-fold higher storage modulus during curing. Rate of curing is measured to be substantially slower for the samples comprising nanoclay. In addition, glass transition temperature improved by 5% to 99°C with the addition of nanoclay compared to 94.5°C for the samples without nanoclay. Flexural stiffness of the samples containing nanoclay is measured to be 20% higher than the samples without nanoclay while the strength remained virtually unaffected.
机译:研究了纳米粘土对玻璃/水性环氧纳米复合材料固化动力学的影响。样品制备的第一步涉及在70℃下借助于超声波仪在70℃下分散溶液Na +,天然蒙脱石。然后,用作交联剂的所需量的双氰胺和2-甲基咪唑与纳米碳粘土溶液混合。随着混合的继续,将EPI-REZ 3522-W-60水性环氧树脂引入溶液中,并将化合物混合另外30分钟。将该批料的纳米粘土含量调节为2wt%。还制备不包含纳米粘土的相同的第二批次以用作基线数据。含有30%玻璃纤维的玻璃/水性环氧树脂预浸料由这些批次制备,用于表征纳米粘土的作用。固化过程中粘弹性的进化的特征在于APA2000流变仪。使用固化过程中的存储和损耗模型,表征凝胶时间和最大存储模量。纳米荧光对玻璃化转变温度的影响通过在固化循环之后施加另外的温度循环来确定。此外,样品的机械性能特征在于三点弯曲试验。观察到纳米粘土在固化过程中产生2倍的储存模量。测量固化速率以基本上较慢,用于包含纳米碳的样品。另外,在没有纳米粘土的样品的情况下,玻璃化转变温度加入纳米粘土的加入量增加了5%至99℃。含有纳米粘土的样品的抗弯刚度测量比没有纳米粘土的样品高出20%,而强度几乎不受影响。

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