环氧树脂
咪唑
差示扫描量热法
化学计量学
固化(化学)
放热反应
玻璃化转变
等温过程
高分子化学
活化能
化学
材料科学
有机化学
复合材料
热力学
聚合物
物理
作者
Won Ho Park,Jong Keun Lee,Kee Jeong Kwon
出处
期刊:Polymer Journal
[Springer Nature]
日期:1996-05-01
卷期号:28 (5): 407-411
被引量:48
标识
DOI:10.1295/polymj.28.407
摘要
The cure behavior of an epoxy-anhydride system with one of imidazole derivatives as an accelerator was investigated for both stoichiometric and epoxy-rich formulations. The mixtures were isothermally cured for different times at various temperatures, and the glass transition temperature (Tg) was determined by differential scanning calorimetry (DSC). There was a considerable increase in the Tg during curing, and master curves were formed by shifting and superposing the Tg vs. cure time curves. The activation energies obtained by the shift were 15.2 kcal mol−1 and 16.5 kcal mol−1 for the stoichiometric and epoxy-rich systems, respectively. For the epoxy-rich one, plateaus were observed on the Tg vs. cure time curves, and two exothermic peaks appeared on DSC curves in the early stage of cure and became one thereafter. This phenomenon is related to the competitive reactions between esterification and etherification reactions. We found that the maximum Tgs were 80°C for esterification and 125°C for etherification in the excess epoxy system.
科研通智能强力驱动
Strongly Powered by AbleSci AI