Toughening of an epoxy resin with an isocyanate-terminated polyether

被引:16
作者
Soares, Bluma G. [1 ]
Gonçalez, Viviane [1 ]
Galimberti, Rurik [1 ]
Sirqueira, Alex S. [1 ]
Barcia, Fabio L. [1 ]
Simao, Renata A. [2 ]
机构
[1] Univ Fed Rio de Janeiro, Ctr Technol, Inst Macromol, BR-21945970 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Dept Mat Engn, Coodernacao Programas Pos Grad & Engn, Rio De Janeiro, RJ, Brazil
关键词
curing of polymers; morphology; networks; polyethers; rheology; toughness;
D O I
10.1002/app.26991
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A low-molar-mass, hydroxyl-terminated polyether [polypropylene glycol/poly(ethylene glycol) copolymer (POPE)] was functionalized with isocyanate groups and used to improve the impact resistance of a diglycidyl ether of bisphenol A based epoxy resin cured with triethylene tetramine (TETA). The effect of polyether-based modifiers (with and without NCO groups) on the curing rate of the epoxy/TETA system was investigated with rheological techniques. The NCO-functionalized polyether reduced the gel time, and this indicated an accelerating effect of the curing process. In addition, a significant improvement in the impact resistance was observed with only a slightly detrimental effect on the stiffness and mechanical strength. Scanning electron microscopy of the corresponding epoxy network revealed a homogeneous morphology with no phase separation. The miscibility of NCO-modified POPE and the epoxy resin was also confirmed with atomic force microscopy. The glass-transition temperature of the epoxy networks was also investigated with dynamic mechanical techniques. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:159 / 166
页数:8
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