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Studies on New Type of Phenolic Resin by Ring Opening Reaction of Benzoxazine (V) Curing reaction of phenol-novolac based benzoxazine with bisoxazoline and the properties of the cured resin

机译:苯并恶嗪的开环反应研究新型酚醛树脂(V)酚醛清漆型苯并恶嗪与双恶唑啉的固化反应及固化树脂的性能

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摘要

As a series of studies on a new type of phenolic resin by the ring opening reaction of benzoxazines, two kinds of phenol-novolac based benzoxazines having different molecular weights were prepared from the corresponding phenol-novolacs, formaline, and aniline. Curing reaction of above benzoxazines with bisoxazoline and the properties of cured resins were investigated. With triphenylphosphite as a catalyst, the ring opening reaction of benzoxazine occurred at 170 deg C at first to generate a phenolic hydoroxyl group., and then the reaction of which with oxazoline ring followed at 200 deg C. The difference in the curing reactivity by the molecular weight of benzoxazines was as follows: the lower the mol3ecular weight, the faster the curing reaction due to molecular mobility. The both cured resins showed better heat- and water-resistance and fracture toughness, compared with the conventional cured resins from phenol-novolacs and bisoxazoline. As for the properties of the cured resin from different molecular weights of benzoxazines, the resin having a lower molecular weight showed better fracture toughness, while he resin having a higher molecular weight showed better heat- and water-resistance, and electrical insulation.
机译:作为通过苯并恶嗪的开环反应对新型酚醛树脂进行的一系列研究,由相应的苯酚-新戊酸,福尔马林和苯胺制备了两种分子量不同的酚-酚醛基苯并恶嗪。研究了以上苯并恶嗪与双恶唑啉的固化反应及固化树脂的性能。以亚磷酸三苯酯为催化剂,苯并恶嗪的开环反应首先在170℃发生,生成酚醛氧基,然后在200℃与恶唑啉环反应。苯并恶嗪的分子量如下:分子量越低,由于分子移动性,固化反应越快。与酚醛清漆和双恶唑啉的传统固化树脂相比,两种固化树脂均显示出更好的耐热性和耐水性以及断裂韧性。至于来自不同分子量的苯并恶嗪的固化树脂的性能,具有较低分子量的树脂显示出更好的断裂韧性,而具有较高分子量的树脂显示出更好的耐热性和耐水性以及电绝缘性。

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