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Synthesis of Phosphazene-Containing Bisphenol A-Based Benzoxazines and Properties of Corresponding Polybenzoxazines

机译:含磷双酚A的苯并恶嗪的合成及相应的聚苯并恶嗪的性质

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摘要

With the aim of obtaining halogen-free polybenzoxazazines with reduced flammability, phosphazene-containing benzoxazines (PhBZ) were synthesized in a two-stage method. In the first stage of the reaction of hexachlorocycotriphosphazene with bisphenol A at molar ratios of 1:12, 1:16, and 1:24, respectively, mixtures of bisphenol and hydroxyaryloxycyclotriphosphazenes were obtained, which mainly contained P N [OC H C(CH ) C H OH] . In the second stage, when these mixtures interacted with aniline and an excess of paraformaldehyde in toluene at 80–90 °C, PhBZ containing 20–50% of the phosphazene component with M 1200–5800 were formed. According to H and C NMR spectroscopy, PhBZ contain a small amount of oligomeric compounds with Mannich aminomethylene bridges. With an increase of the content of the phosphazene component, the curing temperature of PhBZ decreases from 242 °C to 215 °C. Cured PhBZ samples with a phosphorus content of more than 1.5% have increased flammability resistance according to UL-94.
机译:为了获得可燃性降低的无卤素聚苯并恶嗪,以两步法合成了含磷腈的苯并恶嗪(PhBZ)。在六氯环三磷腈与双酚A的摩尔比分别为1:12、1:16和1:24的反应的第一阶段,获得了双酚和羟芳氧基环三磷腈的混合物,其主要含有PN [OC HC(CH)CH OH]。在第二阶段,当这些混合物与苯胺相互作用,并在80–90°C的甲苯中有过量的多聚甲醛时,会形成含有20–50%磷腈组分和M 1200–5800的PhBZ。根据1 H和13 C NMR光谱,PhBZ包含少量带有曼尼希氨基亚甲基桥的低聚物。随着磷腈组分含量的增加,PhBZ的固化温度从242°C降至215°C。根据UL-94,磷含量超过1.5%的硫化PhBZ样品具有更高的可燃性。

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