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Influence of cure via network structure on mechanical properties of a free-radical polymerizing thermoset.

机译:通过网络结构固化对自由基聚合热固性塑料机械性能的影响。

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The matrix of a composite material exerts influence over composite properties. The hypothesis is that control of molecular architecture of the matrix allows for the control of resin properties and therefore impacts composite properties. The objective of this research is to define the relationship between cure chemistry, network structure, and final physical properties of vinyl ester-styrene (VE/S) resin, a free-radical polymerizing thermoset polymer often used as the matrix of fiber reinforced polymers.; Tensile and fracture properties of the polymer are found to depend on both cure schedule and cure formulation. The possibilities of phase separation and microgel formation being the cause for the differences in mechanical properties are examined. This research shows that the VE/S system does not phase separate under the conditions studied. This proven, the research examines changes in network architecture under different cure conditions. It is found that though bulk properties of the resin are unaffected by the details of the cure, the microscopic morphology, in particular the type of crosslink formed (intermolecular bond or intramolecular bond), is sensitive to both cure temperature and initiation mechanism as determined by cure formulation. Thus, the molecular architecture of the network is responsible for the bulk mechanical properties of the resin.; A kinetic analysis shows that both temperature and initiation mechanism affect the apparent “reaction order” of the VE/S system as determined by the autoacceleration equation. This apparent reaction order is interpreted as being an indication of the degree of heterogeneity in the resin. By controlling cure temperature and cure formulation, it is possible to minimize the apparent reaction order and thereby optimize physical properties. Finally, a theory is adapted from other non-network polymer systems to describe qualitatively how cure temperature and initiation mechanism may alter the heterogeneity in network structure via microgel formation and how these changes in structure affect changes in the mechanical properties.
机译:复合材料的基质会影响复合材料的性能。假设是控制基质的分子结构可以控制树脂性能,从而影响复合材料性能。这项研究的目的是确定乙烯基酯-苯乙烯(VE / S)树脂(一种自由基聚合的热固性聚合物,通常用作纤维增强聚合物的基质)的固化化学,网络结构和最终物理性能之间的关系。 ;发现聚合物的拉伸和断裂性能取决于固化时间表和固化配方。研究了相分离和微凝胶形成的可能性,这是机械性能差异的原因。这项研究表明,VE / S系统在所研究的条件下不会发生相分离。事实证明,该研究检查了不同固化条件下网络体系结构的变化。发现尽管树脂的整体性能不受固化细节的影响,但微观形态,特别是形成的交联类型(分子间键或分子内键)对固化温度和引发机理均敏感,如固化配方。因此,网络的分子结构决定了树脂的整体机械性能。动力学分析表明,温度和引发机制均会影响VE / S系统的表观“反应顺序”,这由自动加速方程确定。该表观反应顺序被解释为指示树脂中的不均匀程度。通过控制固化温度和固化配方,可以使表观反应顺序最小化,从而优化物理性能。最后,从其他非网络聚合物体系改编的理论定性地描述了固化温度和引发机理如何通过微凝胶形成来改变网络结构的不均匀性,以及这些结构变化如何影响机械性能的变化。

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