...
首页> 外文期刊>Journal of Applied Polymer Science >Fourier transform IR and differential scanning calorimetry study of curing of trifunctional amino-epoxy resin
【24h】

Fourier transform IR and differential scanning calorimetry study of curing of trifunctional amino-epoxy resin

机译:三官能氨基环氧树脂固化的傅里叶变换红外和差示扫描量热法研究

获取原文
获取原文并翻译 | 示例

摘要

The curing process was studied for a trifunctional epoxy resin, triglycidyl-p-aminophenol, using the hardener 4,4'-diaminodiphenylsulfone. Two curing cycles were carried out: one following the manufacturer's guidelines (2 h at 80 degrees C, 1 h at 100 degrees C, 4 h at 150 degrees C, and 24 h at 200 degrees C) and another proposed in this study, in which the two stages at low temperatures were excluded. Fourier transform IR spectroscopy was used to quantity the conversion of different functional groups (primary amine, secondary amine, epoxide, hydroxyl and ether functional groups), and these conversions could be used to infer the type of reactions that took place. These results allowed us to analyze the evolution of the curing process over time and the influence of the curing cycle. Furthermore, the enthalpy of the curing process was determined using differential scanning calorimetry, and from this the thermal conversion for the whole process was evaluated. By taking into account the autocatalytic kinetic model, the rate constants were evaluated. The glass-transition temperatures were also estimated by applying different curing cycles to the resin. (c) 2005 Wiley Periodicals, Inc.
机译:使用固化剂4,4'-二氨基二苯砜研究了三官能环氧树脂三缩水甘油基对氨基苯酚的固化过程。进行了两个固化周期:一个遵循制造商的指导原则(在80摄氏度下2个小时,在100摄氏度下1个小时,在150摄氏度下4个小时,在200摄氏度下24个小时),并且在本研究中提出了另一个其中排除了低温下的两个阶段。傅里叶变换红外光谱用于定量不同官能团(伯胺,仲胺,环氧化物,羟基和醚官能团)的转化率,这些转化率可用于推断发生的反应类型。这些结果使我们能够分析固化过程随时间的演变以及固化周期的影响。此外,使用差示扫描量热法确定固化过程的焓,并由此评估整个过程的热转化率。通过考虑自催化动力学模型,评估了速率常数。还通过对树脂施加不同的固化循环来估计玻璃化转变温度。 (c)2005年Wiley Periodicals,Inc.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号