热固性反应共混:分子、形态和力学分析

E. Martuscelli, P. Musto, G. Ragosta, G. Scarinzi
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引用次数: 14

摘要

许多不同的方法被用来提高韧性的三和四功能环氧树脂和不饱和聚酯树脂。在环氧树脂的情况下,坚韧,热稳定,工程热塑性塑料,即双酚a聚碳酸酯和热塑性聚醚亚胺(Ultem 1000)被用作改性剂。对于不饱和聚酯,采用了不同的方法:对两种商业液体橡胶进行化学改性,以增强其对基体功能的反应性。其中,端羟基聚丁二烯和端氨基丁二烯-丙烯腈共聚物分别转化为端异氰酸酯橡胶和端马来酰亚胺橡胶。在本贡献中描述的进一步系统旨在减轻聚酯基体的另一个缺陷,即其在室温以上温度下迅速降低的刚性。在这种情况下,热固性双马来酰亚胺被掺入树脂作为共反应的第二组分。
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Reactive blending of thermosets: Molecular, morphological and mechanical analysis
A number of different approaches were used to enhance the toughness of tri- and tetrafunctional epoxies and of unsaturated polyester resins. In the case of epoxies, tough, thermally stable, engineering thermoplastics, namely a bisphenol-A polycarbonate and a thermoplastic poly(ether imide) (Ultem 1000) were employed as modifiers. For unsaturated polyesters a different approach was adopted: two commercial liquid rubbers were chemically modified to enhance their reactivity towards the matrix functionalities. In particular, a hydroxy-terminated polybutadiene and an aminoterminated butadiene-acrylonitrile copolymer were transformed into isocyanate-terminated and maleimide-terminated rubbers, respectively. A further system which is described in the present contribution is aimed at mitigating another deficiency of the polyester matrix, namely its rapidly decreasing rigidity at temperatures above room temperature. In this case, a thermosetting bismaleimide was incorporated into the resin as a co-reactive second component.
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