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Kinetic and mechanical analysis of anhydride-cured linear and non-linear epoxies.

机译:酸酐固化的线性和非线性环氧树脂的动力学和力学分析。

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The anhydride cure of epoxy resins was studied experimentally. First, an amorphous, thermoplastic resin formulated with phenyl glycidyl ether (PGE), nadic methyl anhydride (NMA) and the catalyst benzyldimethylamine (BDMA) was investigated. Oligomeric species were synthesized and fractionated by reversed phase high performance liquid chromatography (HPLC). Molecular dynamics was traced by the measurement of population density distribution (PDD) as a function of the conversion of oxirane moieties. Kinetic data interpretation yielded distinct rate constants for initiation and propagation reactions, which caused a PDD narrower than the Poisson molar distribution. Fourier transform infrared (FTIR) spectroscopy proved that the ester forming propagation reactions were dominant. Polymeric kinetics of the thermoplastic resin was also attacked using multiple angle laser light scattering with gel permeation chromatography (GPC-MALLS). Experimental-theoretical comparison of the molecular size distributions and moment analysis revealed the presence of secondary reactions when the concentration of alcoholic initiator is low.; Based on molecular insight gained from the experimental investigation on the linear analog, attention was then directed to a diglycidyl ether of bisphenol A (DGEBA) based thermoset DGEBA/NMA/BDMA. Molecular characterization of the sol fraction was performed using GPC-MALLS. Observed kinetic reaction information provided a basis for rigorous examination of the kinetic reaction model and was also used in a molecular feedback sense along with the sol/gel partition measurements for the description of chain topology within the insoluble gel fraction (crosslinking density and concentration of permanent entanglements etc.) as a function of extent of cure. This ultimately enabled the prediction of the equilibrium modulus at elevated temperatures. Results in this regard when evaluated with the viscoelastic properties measured with the aide of dynamic mechanical thermal analysis (DMTA) offered an examination of the applicability of the rubber elasticity theory to this anhydride cured thermosetting epoxy.
机译:实验研究了环氧树脂的酸酐固化。首先,研究了由苯基缩水甘油醚(PGE),纳迪克酸酐(NMA)和催化剂苄二甲基胺(BDMA)配制的无定形热塑性树脂。合成了寡聚物种,并通过反相高效液相色谱(HPLC)进行了分馏。通过测量人口密度分布(PDD)作为环氧乙烷部分转化的函数来追踪分子动力学。动力学数据解释为引发和扩散反应产生了不同的速率常数,这导致PDD比Poisson摩尔分布窄。傅立叶变换红外光谱(FTIR)证明了酯形成的传播反应是主要的。热塑性树脂的聚合物动力学也受到凝胶渗透色谱法(GPC-MALLS)的多角度激光散射的影响。分子大小分布和矩量分析的实验理论比较表明,当酒精引发剂的浓度较低时,存在副反应。基于从线性类似物的实验研究中获得的分子见解,然后将注意力转向了基于双酚A(DGEBA)的热固性DGEBA / NMA / BDMA的二缩水甘油醚。溶胶级分的分子表征使用GPC-MALLS进行。观察到的动力学反应信息为严格检验动力学反应模型提供了基础,并且还用于分子反馈意义上的溶胶/凝胶分配测量,用于描述不溶性凝胶级分中的链拓扑(交联密度和永久性浓度)缠结等)作为固化程度的函数。这最终使人们能够预测高温下的平衡模量。当用动态力学热分析(DMTA)辅助测量的粘弹性质进行评估时,这方面的结果可检验橡胶弹性理论对这种酸酐固化的热固性环氧树脂的适用性。

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