Telatin Tommaso, De la Flor Silvia, Montané Xavier, Serra Àngels
Department of Analytical and Organic Chemistry, Universitat Rovira i Virgili, C/Marcel·lí Domingo 1, 43007 Tarragona, Spain.
Department of Mechanical Engineering, Universitat Rovira i Virgili, Av. Països Catalans 26, 43007 Tarragona, Spain.
Polymers (Basel). 2024 Sep 29;16(19):2754. doi: 10.3390/polym16192754.
This study presents the development of a diglycidyl monomer containing two imine groups that can act as dynamic and reversible bonds. During the curing of the monomer with two different amine hardeners, we confirmed the formation of new imine groups due to the transamination reaction between the imine groups of the diepoxy monomer with the amine groups of the hardener. The effect of this structural change was observed in the stress relaxation behavior, resulting in the overlapping of two different relaxation modes. The analytical modelling was able to extract two distinct characteristic relaxation times using a double-element Maxwell model. A second characterization of the stress relaxation process by frequency sweep experiments was performed to corroborate the results obtained, confirming speedy stress relaxation. Acid-catalyzed hydrolysis was performed on the studied materials, demonstrating the complete degradation of the network. We finally confirmed that the synthesized diepoxy compound is suitable for preparing carbon-fiber-reinforced composite materials, demonstrating easy fiber impregnation, fast reshaping, and especially a total degradation of the polymer matrix that allows for the recovery of the carbon fibers in mild conditions. This epoxy-amine system is an excellent candidate for overcoming the traditional limits of thermosets in preparing fiber-reinforced composites.
本研究介绍了一种含有两个亚胺基团的二缩水甘油单体的开发,该亚胺基团可作为动态可逆键。在用两种不同的胺类固化剂固化单体的过程中,我们证实了由于二环氧单体的亚胺基团与固化剂的胺基团之间的转氨反应而形成了新的亚胺基团。在应力松弛行为中观察到了这种结构变化的影响,导致两种不同的松弛模式重叠。通过双元件麦克斯韦模型进行的分析建模能够提取两个不同的特征松弛时间。通过频率扫描实验对应力松弛过程进行了第二次表征,以证实所获得的结果,确认了快速应力松弛。对所研究的材料进行了酸催化水解,证明了网络的完全降解。我们最终证实,合成的二环氧化合物适用于制备碳纤维增强复合材料,表现出易于纤维浸渍、快速重塑,特别是聚合物基体的完全降解,使得在温和条件下能够回收碳纤维。这种环氧 - 胺体系是克服热固性材料在制备纤维增强复合材料方面传统局限性的极佳候选材料。