首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Amorphous phenolphthalein-based poly(arylene ether) modified cyanate ester networks: 1. Effect of molecular weight and backbone chemistry on morphology and toughenability
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Amorphous phenolphthalein-based poly(arylene ether) modified cyanate ester networks: 1. Effect of molecular weight and backbone chemistry on morphology and toughenability

机译:非晶酚酞基聚(亚芳基醚)改性的氰酸酯网络:1.分子量和主链化学对形态和韧性的影响

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Low toughness is a major drawback with most cross-linked thermosetting materials, including the cyanate ester networks. Reactive functional thermoplastic toughness modifiers not only enhance toughness but also permit highly desirable stability to solvent stress cracking without seriously affecting the moderately high modulus. Careful control of the heterophase morphological structure is necessary to achieve significant toughening. Tn the present work, hydroxyl functional phenolphthalein-based amorphous poly(arylene ether ketone)s, poly(arylene ether sulfone)s and poly(arylene ether phosphine oxide)s were investigated as potential toughness modifiers for the bisphenol-A based cyanate ester networks. In particular, the use of poly(arylene ether sulfone)s resulted in remarkable improvements in toughness. Multiphase networks were generated without compromising either T-g or the moderately high modulus of the unmodified cyanate ester networks. It was demonstrated that the toughenability of these systems is governed by microphase-separated morphologies and the sizes of the phase separated domains. The formation of these heterophase morphological structures is strongly influenced by the backbone chemistry and the molecular weight of the thermoplastic modifier, probably via control of the polymer-polymer interaction parameter. (C) 1998 Elsevier Science Ltd. All rights reserved. [References: 62]
机译:低韧性是大多数交联的热固性材料(包括氰酸酯网络)的主要缺点。反应性功能性热塑性韧性改性剂不仅增强了韧性,而且还允许对溶剂应力开裂具有非常理想的稳定性,而不会严重影响适度的高模量。要实现显着的增韧,必须小心控制异​​相形态结构​​。在本工作中,研究了羟基官能酚酞基无定形聚(亚芳基醚酮),聚(亚芳基醚砜)和聚(亚芳基醚氧化膦)作为双酚A基氰酸酯网络的潜在韧性改进剂。 。特别地,使用聚(亚芳基醚砜)导致韧性的显着改善。生成了多相网络,而不损害T-g或未改性的氰酸酯网络的中等高模量。结果表明,这些系统的可韧性由微相分离的形态和相分离域的大小决定。这些异相形态结构​​的形成受骨架化学和热塑性改性剂分子量的影响很大,可能是通过控制聚合物-聚合物相互作用参数来实现的。 (C)1998 Elsevier ScienceLtd。保留所有权利。 [参考:62]

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