13C solid-state NMR analysis of the DGEBA/TETA epoxy system

被引:0
作者
Tavares, MIB
D'Almeida, JRM
Monteiro, SN
机构
[1] Univ Fed Rio de Janeiro, Inst Macromol, BR-21945970 Rio De Janeiro, Brazil
[2] Pontificia Univ Catolica Rio de Janeiro, Dept Mat Sci & Met, BR-22453900 Rio De Janeiro, Brazil
[3] Univ Estadual Norte Fluminense, Ctr Sci & Technol, BR-28015820 Campos, RJ, Brazil
关键词
epoxy resins; NMR; macromolecular structure;
D O I
10.1002/1097-4628(20001220)78:13<2358::AID-APP120>3.0.CO;2-T
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Mechanical properties measurements, like Charpy impact tests, provided evidence that the macromolecular network of the epoxy system formed by the hexafunctional triethylene tetramine hardener, TETA, with the diglycidyl ether of bisphenol A monomer, DGEBA, can be modified by changing the hardener content. The previously analyzed monomer-to-hardener ratios were here studied by C-13-NMR solid state techniques. The results from crosspolarization/magic angle spinning (CPMAS) C-13-NMR spectra, together with the evaluation of proton spin-lattice relaxation time in the rotating frame (T(1)(H)rho), display the behavior of these epoxy/hardener mixtures considering the mobility and interaction of molecular segments present at the macromolecular structure. The results also show that the epoxy-rich mixtures form tight, and therefore brittle, structures as previously observed by mechanical tests. The stoichiometric monomer-to-hardener ratio is a transition point where an increase in the mobility was found. For the amine-rich mixtures the obtained results suggest the presence of domains with different segmental mobilities. (C) 2000 John Wiley & Sons, Inc.
引用
收藏
页码:2358 / 2362
页数:5
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