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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Structure?Property relationships in nanocomposites based on cyanate ester resins and 1-heptyl pyridinium tetrafluoroborate ionic liquid
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Structure?Property relationships in nanocomposites based on cyanate ester resins and 1-heptyl pyridinium tetrafluoroborate ionic liquid

机译:基于氰酸酯树脂的纳米复合材料和1-庚基吡啶四氟硼酸盐离子液体的结构?

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摘要

Novel thermosetting systems based on cyanate ester resins (CERs) have been created through the polycyclotrimerization reaction of dicyanate ester of bisphenol E (DCBE) in the presence of different amounts of 1-heptyl pyridinium tetrafluoroborate [HPyr][BF4] Ionic Liquid (IL). A significant accelerating effect on the curing kinetics of DCBE was found by FTIR analysis. The reaction mechanism for the [HPyr][BF4]-catalyzed polycyclotrimerization of DCBE was newly proposedviathe formation of a [CN]δ+–[HPyr]δ?complex as a key intermediate. Structure–properties relationships for the thermostable CER/IL networks were investigated by using DSC, DMTA, dielectric spectroscopy, tensile testing, quasi-dc measurements (I-Vcharacteristics), and TGA. All the nanocomposites showed excellent thermal stability up to 300?°C, indicating the formation of a densely crosslinked network even at high IL content (40?wt%), and they could be used at high temperatures above theirTgwithout significant thermal degradation. Nanoscale phase separation led to the creation of ionic channels within the CER matrix to ensure photosensitivity properties.
机译:基于氰酸酯树脂(CERs)的新型热固性系统通过双酚E(DCBE)的二氰酸酯酯的多环二聚体反应在不同量的1-庚基吡啶吡啶鎓四氟硼酸盐[HPYR] [BF4]离子液体(IL)存在下产生。通过FTIR分析发现了对DCBE的固化动力学的显着加速效果。 [HPyr] [BF4]的反应机理 - 催化DCBE的多环rimerization是新建的via [Cn]δ+ - [HPyr]δαα复合物作为关键中间体。通过使用DSC,DMTA,介电光谱,拉伸试验,准直流测量(I-VCRACERISTIS)和TGA来研究恒温CER / IL网络的结构性质关系。所有纳米复合材料显示出高达300Ω°C的优异的热稳定性,表明即使在高IL含量(40μl%)上也形成密集交联的网络,并且它们可以在高于其高于其显着的热降解的高温下使用。纳米级相分离导致CER基质内的离子通道的产生以确保光敏性。

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