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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Crosslinkable hyperbranched poly(arylene ether nitrile) modifier for phthalonitrile resins: Synthesis, chain-end functionalization and properties
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Crosslinkable hyperbranched poly(arylene ether nitrile) modifier for phthalonitrile resins: Synthesis, chain-end functionalization and properties

机译:酞氯腈树脂的可交联超支化聚(亚芳基醚丁腈)改性剂:合成,链末官能化和性能

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摘要

Soluble hyperbranched poly(arylene ether nitrile)s end-capped by either hydroxyl (HBPAEN-OHs) or phthalonitrile groups (HBPAEN-PNs) were synthesized via nucleophilic substitution reactions, where activated carbon supported calcium oxide was used as the catalyst to avoid crosslinking at high conversion. In order to evaluate their potential application in phthalonitrile resins, these hyperbranched polymers were blended with 1,3-bis(3,4-dicyanophenoxy)benzene and 4-(4-aminophenoxy)phthalonitrile, then cured into polymers. Curing mechanisms of different prepolymers were proposed and compared, and processability, thermal and mechanical properties were characterized. The introduction of HBPAEN-OHs was found to postpone the curing, while thermal and mechanical properties were compromised. On the contrary, the usage of HBPAEN-PNs was beneficial to both processability and thermal properties. More importantly, the impact strength for polymers containing HBPAEN-PN could be as high as 12.92 kJ m(-2), indicating such resin could be potentially applied as high temperature structural composite matrices. In addition, the toughening mechanism was proposed and discussed.
机译:通过亲核取代反应合成通过羟基(HBPAEN-OHS)或邻苯二乙腈基团(HBPAEN-PNS)的可溶性超接收的聚(亚烷基醚丁腈)的端盖,其中活性炭负载氧化钙作为催化剂,以避免交联高转换。为了评估它们在酞氯硝基树脂中的潜在应用,将这些超支化聚合物与1,3-双(3,4-二氰基氧基)苯和4-(4-氨基苯氧基)邻苯二甲腈混合,然后固化成聚合物。提出并比较了不同预聚物的固化机制,并表征了加工性,热和机械性能。发现HBPAEN-OHS的引入推迟了固化,而热和机械性能受到损害。相反,HBPaen-PNS的使用有利于可加工性和热性能。更重要的是,含有HBPaen-Pn的聚合物的冲击强度可以高达12.92kJ m(-2),表明这种树脂可能被视为高温结构复合基质。此外,提出并讨论了增韧机制。

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