双酚A型苯并恶嗪树酯热解的ReaxFF反应动力学模拟毕业论文.pdf
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双酚A型苯并恶嗪树酯热解的ReaxFF反应动力学模拟毕业论文.pdf

双酚A型苯并恶嗪树酯热解的ReaxFF反应动力学模拟毕业论文.pdf

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双酚A型苯并噁嗪树酯热解的ReaxFF反应动力学模拟ThermalDecompositionofBisphenolATypeBenzocainefromReactiveDynamicsUsingtheReaxFFReactiveForceField目录摘要·········································································································································IAbstract······························································································································II引言···································································································································1第一章文献综述··············································································································21.1酚醛树脂的发展介绍······························································································21.1.1酚醛树脂的现状···································································································21.1.2改性酚醛树脂·······································································································21.2苯并噁嗪树脂简介··································································································31.2.1苯并噁嗪的发现···································································································31.2.2苯并噁嗪树脂特点·······························································································41.2.3苯并树脂的研究意义···························································································41.2.4苯并噁嗪树脂的应用···························································································51.2.5苯并噁嗪树脂的固化···························································································51.2.6苯并噁嗪树脂热解方法研究···············································································61.3双酚A型苯并噁嗪树脂的研究·············································································61.4ReaxFF反应动力学及反应场研究··········································································61.5本实验的目的和意义···································