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作 者:张保龙[1] 张会旗[1] 丁培元[1] 由英才[1] 杜宗杰[1] 周杏弟[1] 王涛[1] 黄吉甫[1]
机构地区:[1]南开大学化学系
出 处:《高分子学报》1996年第6期697-704,共8页Acta Polymerica Sinica
摘 要:合成了含不同分子量柔性间隔基的扩链脲(Ui),并对其与双氰双胺共同固化环氧树脂体系的反应活性、抗冲击性能、动态力学性能、形态结构及贮存性能进行了考察。结果表明:含分子量为400的聚乙二醇柔性链的扩链脲/双氰双胺/环氧树脂固化体系的抗冲击强度较单纯双氰双胺/环氧树脂固化体系提高了7倍左右,其冲击试样断面电镜照片呈韧性断裂的特征。扩链脲的反应活性基本不受分子中聚乙二醇链段分子量的影响。环氧树脂/扩链脲/双氰双胺体系在50℃下贮存期可达1~2天。A series of chain-extended ureas containing polyethylene glycol (PEG) spacers with different molecular weight were synthesized and the reactive activity,impact strength,the dynamic mechanical behavior,the morphology and the storage property of the epoxy resin/Ui/dicyandiamide system were studied.Experimental results revealed that the impact strength of the epoxy resin/chain-extended urea containing PEG flexible spacer with molecular weight 400/dicyandiamide system was seven times higher than that of the epoxy resin/dicyandiamide system,and the SEM micrographs of the impact fractured surfaces howed the tough fracture characters. Results also showed that the molecular weight of PEG flexible spacers in chain-extended ureas basically had no influence on the reactive activity of the ureas.The storage life of epoxy resin/Ui/dicyandiamide systems at50℃ was one to two days.
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