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Phenomenological characterization of sequential dual-curing of off-stoichiometric 'thiol-epoxy' systems: Towards applicability

机译:非化学计量“硫醇-环氧树脂”系统的顺序双重固化的现象学表征:趋于适用

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An extensive characterization of a sequential dual-curing system based on off-stoichiometric "thiol-epoxy" mixtures was carried out using thiol compounds of different functionality. The intermediate and final materials obtained after each curing stages at different thiol-epoxy ratios were studied by means of thermomechanical and rheological experiments. The storage and loss modulus and the loss factor tan delta were monitored during the curing process to analyse gelation and network structure build-up. The critical ratio for gelation was determined making use of the ideal Flory-Stockmayer theory and compared with experimental results. Intermediate materials obtained in the vicinity of the theoretical critical ratio did not have the mechanical consistency expected for partially crosslinkedmaterials, did not retain their shape and even experienced undesired flow upon heating to activate the second curing reaction. The rheological results showed that the critical ratio is higher than the predicted value and that a softening during the second curing stage affects the shape-retention at this ratio. From the thermomechanical results, a wide range of intermediate and final materials with different properties and applicability can be obtained by properly choosing the thiol-epoxy ratio: from liquid-like to highly deformable intermediate materials and from moderately crosslinked (deformable) to highly crosslinked (brittle) final materials. (C) 2016 Elsevier Ltd. All rights reserved.
机译:使用具有不同官能度的硫醇化合物对基于化学计量失配的“硫醇-环氧”混合物的顺序双固化系统进行了广泛的表征。通过热力学和流变实验研究了在每个固化阶段之后以不同的硫醇-环氧比率获得的中间和最终材料。在固化过程中监测储能模量和损耗模量以及损耗因子正切增量,以分析凝胶化和网络结构的建立。利用理想的Flory-Stockmayer理论确定了凝胶化的临界比率,并与实验结果进行了比较。在理论临界比附近获得的中间材料不具有部分交联材料所期望的机械稠度,不能保持其形状,甚至在加热以活化第二固化反应时经历不希望的流动。流变结果表明,临界比率高于预测值,并且在第二固化阶段的软化会影响该比率下的形状保持率。根据热力学结果,可以通过适当选择硫醇-环氧比来获得各种性质和适用性不同的中间体和最终材料:从液体状到高度可变形的中间材料,从中等交联(可变形)到高度交联(脆性)的最终材料。 (C)2016 Elsevier Ltd.保留所有权利。

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