掺杂氯化锂的环氧胺体系硬化动力学

V. Demchenko, L. Matkovska, О. Matkovska
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引用次数: 0

摘要

分析热固性聚合物体系固化过程的动力学方法是控制粘度形成条件的一个重要领域,这取决于复合材料的温度和化学成分。固化反应决定了体系的形态和结构,影响最终材料的性能。本文分析了环氧低聚物-聚乙二醇二甘油酯醚(DEG)、聚多胺硬化剂(PEPA)和高氯酸锂盐LiClO4为基体的聚合物复合材料的固化过程。研究了初始组分、DEG/PEPA混合组分和添加盐的DEG/PEPA/LiClO4体系。利用傅里叶变换红外光谱和动态流变分析方法,确定了体系的固化条件。结果表明,DEG/PEPA和DEG/PEPA/LiClO4体系的红外光谱振动带分布是初始组分红外光谱的叠加。高氯酸锂在盐掺杂的初始体系中处于未解离状态,并在体系固化过程中随着时间的推移在聚合物基体中解离。特别地,利用红外光谱数据分析了用积分强度比计算的DEG/PEPA体系中环氧化物基团浓度的时间依赖性。为了研究增加反应大分子的节段迁移率的固化过程,在50°C下进行了流变动力学测量。对弹性模量和黏度模量随时间变化的性质的分析使我们能够估计初始和掺杂体系的凝胶时间。分析了两种体系在三维结构形成前和凝胶点的红外光谱差异,以及固化反应后的红外光谱差异。研究了掺杂剂对DEG/PEPA/LiClO4混合/复合材料固化过程的影响性质及其状态。高氯酸锂LiClO4是氧环氨解的有效催化剂,这解释了盐存在时体系固化反应加速的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
KINETICS OF HARDENING OF EPOXY-AMINE SYSTEMS DOPED WITH LiClO4
Kinetic methods for analyzing the curing process of thermosetting polymer systems are an important area for controlling the formation conditions for viscosity, which depends on the temperature and chemical composition of the composite. The curing reactions determine the morphology and structure of the system, affecting the properties of the final material. This work analyzes the curing process of po­lymer composites based on epoxy oligomer - polyethylene glycol diglycidyl ether (DEG), polyethylene polyamine hardener (PEPA) and lithium perchlorate salt LiClO4. The initial components, the mixture of DEG/PEPA composition and the DEG/PEPA/LiClO4 system supplemented with salt were investigated. Using the methods of Fourier-transform infrared spectroscopy and rheological analysis in dynamic mode the curing conditions of the systems were established. It was shown that the nature of the distribution of vibration bands in the IR spectra of the DEG/PEPA and DEG/PEPA/LiClO4 systems is a superposition of the IR spectra of the initial components. Lithium perchlorate in the salt-doped initial system is in an undissociated state and dissociates in the polymer matrix over time during the curing of the system. In particular, the time dependences of the concentration of epoxide groups in the DEG/PEPA system calculated using the integral intensity ratios were analyzed by IR spectroscopy data. To study the curing process with increased segmental mobility of the reacting macromolecules, rheokinetic measurements were performed at 50°C. Analysis of the nature of changes in the elastic and viscosity moduli over time allowed us to estimate the gel time of the initial and doped systems. Differences in the IR spectra for both systems before the formation of the three-dimensional structure and at the gel point, as well as the IR spectra of these systems after the curing reaction, were analyzed. Attention was also paid to the nature of the influence of dopant on the curing process and its state in the mixture/composite of DEG/PEPA/LiClO4 composition. Lithium perchlorate LiClO4 is an effective catalyst for the aminolysis of the oxirane ring, which explains the acceleration of the curing reaction of the system in the presence of salt.
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