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Kinetic Studies of Chemical Shrinkage and Residual Stress Formation in Thermoset Epoxy Adhesives under Confined Curing Conditions

机译:密闭固化条件下热固性环氧粘合剂中化学收缩和残余应力形成的动力学研究

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Faultless processing of thermoset polymers in demanding applications requires a profound mastering of the curing kinetics considering both the physico-chemical changes in the transition from the liquid to the solid state and the consolidation of the polymers network in the diffusion controlled curing regime past the gel point. Especially in adhesive joints shrinkage stress occurring at an early state of the curing process under confined conditions is likely to cause defects due to local debonding and thus reduce their strength and durability. Rheometry is considered the method of choice to investigate the change of elastic and viscous properties in the progress of curing. Drawbacks however relate to experimental challenges in accessing the full range of kinetic parameters of thermoset resins with low initial viscosity from the very beginning of the curing reaction to the post-cure consolidation of the polymer due to the formation of secondary chemical bonds. Therefore the scope of this study was to interrelate rheological data with results from in-situ measurements of the shrinkage stress formation in adhesive joints and with the change of refractive index in the progress of curing. This combination of different methods has shown to be valuable in gaining advanced insight into the kinetics of the curing reaction. The experimental results are based on a multi component thermoset epoxy-amine adhesive.
机译:考虑到从液体过渡到固态的过渡到固态的物理化学变化以及聚合物网络在扩散控制固化方案中的巩固中,考虑到固化动力学的缺陷,需要深入掌握固化动力学以及在凝胶点的扩散控制固化方案中的聚合物网络的整合。特别是在粘合接缝中,在狭窄条件下在固化过程的早期状态发生的收缩应力可能导致由于当地剥离而导致缺陷,从而降低它们的强度和耐用性。流变测量被认为是研究固化过程中弹性和粘性特性变化的选择方法。然而,缺点涉及在通过形成二次化学键的形成,从固化反应的初始粘度获得低初始粘度的实验挑战,其具有低初始粘度,从而从固化反应的后期固化。因此,本研究的范围是将流变数据与原位测量的结果与粘合剂接头中的收缩应力形成的结果相互联系,并随着折射率的变化在固化过程中。这种不同方法的组合表明,在获得高级了解固化反应的动力学方面具有有价值的。实验结果基于多组分热固性环氧 - 胺粘合剂。

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