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Development of high reliability and high processability thermosets for electronic packaging applications based on ternary systems of benzoxazine, epoxy and phenolic resins.

机译:基于苯并恶嗪,环氧和酚醛树脂三元体系的电子封装应用高可靠性和高加工性热固性材料的开发。

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摘要

We have developed new polymeric systems based on the ternary mixture of benzoxazine, epoxy, and phenolic novolac resins. Low melt viscosity resins render void free specimens with minimal processing steps. The material properties show a wide range of desirable reliability and processability which are highly dependent on the composition of the monomers in the mixture. Fourier transform mechanical spectroscopy techniques (FTMS) are utilized as a powerful tool to study the sol-gel transition of covalently bonded polymeric networks. The gelation of the ternary mixture shows an Arrhenius-type behavior and the gel time can be well-predicted by the Arrhenius equation.;The synergism in the glass transition temperature of these ternary systems is also reported. The molecular rigidity from benzoxazine and the improved crosslink density from epoxy contribute to the synergestic behavior. The mechanical relaxation spectra of the fully cured ternary systems in the temperature range of -140°C to 350°C show four types of relaxation transitions i.e. gamma, beta, alpha1, and alpha2-transitions. Thermal conductivity of the molding compounds based on these ternary mixtures exhibits a very high value of about 27 W/mk in aggregate-type boron nitride filler and the value of about 8.6 W/mk in flake-like crystal boron nitride filler comparing at the same filler loading of 68% by volume. The presence of epoxy resin in the ternary systems is found to provide improvement in a high temperature adhesion.;The curing kinetics based on dynamic DSC results of this ternary system show nth order kinetics with an overall reaction order of 1.5 having activation energy of 111 kJ/mol whereas that of the gelation process is 75 kJ/mol. Thermal degradation process of this resin is deceleratory type with activation energy of 185 kJ/mol. A choice of a resin used for the study can provide maximum Tg of about 220°C in its fully cured specimen. The system has a potential use as high performance electronic packaging molding compounds or highly filled systems.
机译:我们已经基于苯并恶嗪,环氧和酚醛线型酚醛树脂的三元混合物开发了新的聚合物系统。低熔融粘度树脂可通过最少的处理步骤使试样无空隙。材料性能显示出很大范围的所需可靠性和可加工性,这在很大程度上取决于混合物中单体的组成。傅里叶变换机械光谱技术(FTMS)被用作研究共价键聚合网络的溶胶-凝胶转变的有力工具。三元混合物的凝胶化表现出Arrhenius型行为,并且凝胶时间可以通过Arrhenius方程很好地预测。;还报道了这些三元体系在玻璃化转变温度中的协同作用。苯并恶嗪的分子刚性和环氧的改进交联密度有助于协同行为。在-140℃至350℃的温度范围内,完全固化的三元体系的机械弛豫谱显示出四种弛豫转变,即γ,β,α1和α2转变。基于这些三元混合物的模塑料的热导率在骨料型氮化硼填料中显示出非常高的约27 W / mk的值,而在片状晶体氮化硼填料中则显示出约8.6 W / mk的高值。填充量为68%(体积)。发现三元体系中环氧树脂的存在可改善高温粘合性。基于此三元体系的动态DSC结果,固化动力学显示n级动力学,总反应级数为1.5,活化能为111 kJ / mol,而胶凝过程的为75 kJ / mol。该树脂的热降解过程是减速型,活化能为185 kJ / mol。选择用于研究的树脂可以在其完全固化的样品中提供约220°C的最大Tg。该系统具有用作高性能电子包装模塑料或高填充系统的潜在用途。

著录项

  • 作者

    Rimdusit, Sarawut.;

  • 作者单位

    Case Western Reserve University.;

  • 授予单位 Case Western Reserve University.;
  • 学科 Engineering Chemical.;Plastics Technology.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2000
  • 页码 245 p.
  • 总页数 245
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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