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Synthesis of cyclotriphosphazene-containing imidazole as a thermally latent hardener for epoxy resins and its application in carbon fiber reinforced composites

机译:含环三磷腈咪唑作为环氧树脂热潜伏硬化剂的合成及其在碳纤维增强复合材料中的应用

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摘要

In this study, a latent imidazole hardener (CPI) for epoxy resins was synthesized through the nucleophilic substitution reaction between 2-methyl imidazolium (2MI) and hexachlorocyclotriphosphazene (HCCP). The chemical structure of CPI was characterized by Fourier transform infrared, H-1 NMR, and P-31 NMR. Curing kinetic studies (Kissinger and Ozawa methods) manifest that epoxy systems cured by CPI show higher apparent activation energy and curing temperatures than those cured by 2MI. Compared with 2MI, CPI shows distinctly improved thermal latency toward epoxy groups at both room temperature and 80 degrees C, owing to the steric hindrance and electron-withdrawing effects of the introduced cyclotriphosphazene group. The results of dynamic mechanical analysis (DMA) and three-point bending tests indicate that the epoxy resins cured by CPI exhibit higher glass transition temperatures and comparable flexural properties in comparison to the corresponding epoxy resins cured by 2MI. As expected, the epoxy resins cured by CPI also show improved flame retardancy ascribed to the introduction of phosphorus and nitrogen elements. Finally, the optimized CPI/epoxy system was used as the polymer matrix to fabricate carbon fiber reinforced composites (CFRCs), and the resulting CFRCs show superior mechanical performance compared with the CFRCs based on the 2MI/epoxy system.
机译:本研究通过2-甲基咪唑(2MI)与六氯环三磷腈(HCCP)的亲核取代反应合成了一种环氧树脂用潜伏咪唑固化剂(CPI)。采用傅里叶变换红外、H-1 NMR和P-31 NMR对CPI的化学结构进行了表征。固化动力学研究(Kissinger 和 Ozawa 方法)表明,用 CPI 固化的环氧体系比用 2MI 固化的环氧体系表现出更高的表观活化能和固化温度。与2MI相比,由于引入的环三磷腈基团的空间位阻和吸电子效应,CPI在室温和80°C下对环氧基团的热潜伏期都有明显改善。动态力学分析(DMA)和三点弯曲试验的结果表明,与2MI固化的相应环氧树脂相比,CPI固化的环氧树脂表现出更高的玻璃化转变温度和相当的弯曲性能。正如预期的那样,通过CPI固化的环氧树脂也显示出由于引入磷和氮元素而改善的阻燃性。最后,以优化后的CPI/环氧树脂体系为聚合物基体,制备了碳纤维增强复合材料(CFRCs),与基于2MI/环氧树脂体系的CFRCs相比,所得CFRCs表现出优异的力学性能。

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