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Differences in Curing Behavior of Cocured and IPN Materials

机译:共固化和IPN材料固化行为的差异

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This study addressed the blending and cocuring of resole and epoxy, using NaOH and 4,4' -diaminodiphenylmethane as curing agents. m band shifts regarding the molecular interactions were investigated with FTm. Exothermic peak shifts during cocur- ing reactions were studied with dynamic DSC. Viscosity increases were measured with a Brookfield LVT viscometer at lOO°C. The dynamic mechanical properties of the (,'OCured samples were investigated using rheometric dynamic spectroscopy (RDS). Experimental results revealed that the molecular interactions between resole and epoxy resulted in good compatibility as shown by the single damping peak in the RDS curve and the single glass transition for each cocured sample. Also apparent were accelerated curing rates, leading to shifts of the exothermic peaks to lower temperature and faster viscosity increases. Never- theless, enhanced gel fractions and increased glass-transition temperatures (T g~ of the samples were generally observed for this cocured system. The average molecular weight between crosslinked points calculated for the cocured materials also showed much less than the two components. These curing behaviors were quite different from those of the Interpenetrating Polymer Network (IPN) materials, which usually indicated lowered gel fractions, decreased T g' and higher average molecular weight between crosslinkings than -. for components.
机译:这项研究解决了使用NaOH和4,4'-二氨基二苯甲烷作为固化剂对甲阶和环氧的共混和共固化。关于分子相互作用的m带位移用FTm研究。用动态DSC研究了共固化反应过程中的放热峰位移。用Brookfield LVT粘度计在100℃下测量粘度增加。使用流变动态光谱法(RDS)研究了固化样品的动态力学性能。实验结果表明,甲阶酚醛和环氧之间的分子相互作用导致了良好的相容性,如RDS曲线中的单个阻尼峰和单个每个共固化样品的玻璃化转变温度也很明显,加速了固化速度,导致放热峰向较低温度移动,粘度增加更快,但凝胶分数增加,玻璃化转变温度升高(T g〜)。该共固化体系通常观察到的结果。计算出的共固化材料的交联点之间的平均分子量也远小于这两种组分。这些固化行为与互穿聚合物网络(IPN)材料的行为大不相同,通常表明其降低了凝胶分数,降低的T g'和较高的平均分子量之间交联比-。用于组件。

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