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CHEMO-RHEOLOGICAL CHARACTERIZATION OF EPOXY- AMINE THERMOSETS WITH EMBEDDED REACTIVE MATERIALS

机译:包埋反应物对环氧-氨基热敏化学流变学的表征

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Epoxy matrix materials are well utilized and studied in composites. We think it is desirable to produce epoxy-amine matrix materials that contain embedded latent reactive materials for use after cure and during utilization. A concern developed during our blending experiments was related to potential competing mechanisms between the additive material and the parent matrix epoxy and amine functional groups. For the paper presented here, blocked isocyanates synthesized by reacting isophorone diisocyanate individually with JV-methyl aniline, e-caprolactam and 4-hydroxy TEMPO were incorporated into epoxy-amine thermosetting systems as embedded agents. Near infrared (NIR) spectroscopy and dynamic rheology were used in combination to quantify the effects of conversion at 30 ℃ in the presence and absence of reactive additives. Compared to the control (no additive), variations in gel points and ultimate epoxy conversion were observed in systems containing blocked isocyanates based on JV-methyl aniline and e-caprolactam, however, no significant variation was detected with the 4-hydroxy TEMPO blocked isocyanate. The kinetic rate of the epoxy-amine reaction, measured by NIR, decreased by approximately 0.0015 mol~*kg~(-1)min~(-1) for every 5 wt% of additive within the matrix. The consistent loss of reaction rates with increasing additive concentration suggests that the effect on kinetic rate is due to decreasing concentration of reacting functional groups and was not attributed to the presence of a competing mechanism.
机译:环氧树脂基体材料得到了很好的利用,并在复合材料中进行了研究。我们认为需要生产包含嵌入的潜在反应性材料的环氧-胺基材料,以供固化后和使用期间使用。在我们的混合实验过程中,人们担心的一个问题是添加剂材料与母体基体环氧和胺官能团之间的潜在竞争机制。对于此处介绍的论文,将异佛尔酮二异氰酸酯分别与JV-甲基苯胺,ε-己内酰胺和4-羟基TEMPO反应合成的嵌段异氰酸酯作为嵌入剂掺入环氧胺热固性体系中。结合近红外(NIR)光谱和动态流变学来定量分析在有和无反应性添加剂存在下30℃时的转化效果。与对照(无添加剂)相比,在含有基于JV-甲基苯胺和ε-己内酰胺的封端异氰酸酯的系统中,观察到了凝胶点和最终环氧转化率的变化,但是,使用4-羟基TEMPO封端的异氰酸酯未检测到显着变化。对于基体中每5重量%的添加剂,通过NIR测量的环氧-胺反应的动力学速率降低约0.0015mol·kg·(-1)min·(-1)。随着添加剂浓度的增加,反应速率的持续降低表明对动力学速率的影响是由于反应性官能团浓度的降低,而不是由于存在竞争机制。

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