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Phase formation and microstructure in ultra-thin epoxy films on metals

机译:金属上超薄环氧膜的相形成和微观结构

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The curing reaction and the resulting network structure in 2-part epoxy adhesives strongly depend on the curing temperature and on the mixing ratio. Besides these obvious influences further factors affect the kinetics and the structure of network formation. Especially in ultra-thin films (100 nm range) the curing process differs from the behaviour in the bulk state and the final microstructure in the adhesive is depending on film thickness. Many factors are responsible for these structural variations in the interphase region of adhesive joints. The most important reasons must be seen in the influence of the adjacent substrate surface which besides its chemical influence and besides its potentially catalytic effects can induce phase separations or may lead to an immobilisation of one adhesive component by preferential adsorption. Furthermore, it is well-known that because of the dimensional constraints the molecular dynamics in ultra-thin polymer films is significantly altered as compared to the bulk behaviour. For a reacting system this change in mobility has an additional effect on the developing molecular structure of the network during adhesive cure. Together, all these effects lead to laterally inhomogeneous topologies and contribute to structure gradients in the thin films. Since exactly the interphase region predominantly determines the overall performance and the bond strength for adhesive systems which show near-interface failure, e.g. like many aluminium-epoxy bonds, it is necessary to study how the curing process and the resulting adhesive microstructure vary for ultra-thin adhesive films (100 ― 200 nm) and how they are changed compared to the bulk adhesive.
机译:两部分环氧胶粘剂的固化反应和所得的网状结构在很大程度上取决于固化温度和混合比。除了这些明显的影响,其他因素也会影响动力学和网络形成的结构。尤其是在超薄薄膜(100 nm范围)中,固化过程不同于本体状态下的行为,并且粘合剂中的最终微观结构取决于薄膜厚度。胶粘剂相间区域中的这些结构变化是由许多因素引起的。必须在相邻基材表面的影响中看到最重要的原因,除了其化学影响和潜在的催化作用外,它还可能引起相分离或通过优先吸附而导致一种粘合剂组分的固定化。此外,众所周知,由于尺寸限制,与整体性能相比,超薄聚合物膜中的分子动力学显着改变。对于反应体系,迁移率的这种变化对粘合剂固化过程中网络中不断发展的分子结构具有额外的影响。所有这些效应共同导致横向不均匀的拓扑结构,并导致薄膜中的结构梯度。由于恰好相间区域主要决定了粘合剂体系的整体性能和粘结强度,而粘合剂体系表现出接近界面的破坏,例如像许多铝-环氧键一样,有必要研究超薄粘合剂膜(100-200 nm)的固化过程和所得的粘合剂微观结构如何变化,以及与本体粘合剂相比它们如何变化。

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