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Thermomechanical properties of polyimide-epoxy nanocomposites from cubic silsesquioxane epoxides

机译:立方倍半硅氧烷环氧化合物制成的聚酰亚胺-环氧纳米复合材料的热力学性质

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摘要

Novel polyimide-epoxy organic - inorganic nanocomposites are prepared by in situ curing of polyamic acid macromolecules with two POSS epoxides, octa[(epoxycyclohexylethyl) dimethylsilyloxy] silsesquioxane (OC) and octa[(epoxyhexyl) dimethylsilyloxy] silsesquioxane ( OH). Comparison between two series of nanocomposites from OC and OH provides a typical example of controlling the macro-scale properties by adjusting the nano-tether structure of the POSS molecules. DMA studies conclude that the crosslink densities of the polyimide-epoxy nanocomposites increase significantly; the nanocomposite networks are predominantly formed by the linkage between the terminal amine groups of the polyimide molecules and the epoxide groups of the POSS molecules. Furthermore, it is interesting to observe that although the crosslink densities of nanocomposites increase significantly, the compressive moduli, hardness and coefficients of thermal expansion change only slightly.
机译:新型聚酰亚胺-环氧有机-无机纳米复合材料是通过用两种POSS环氧化物原位固化聚酰胺酸大分子而制备的,这些环氧化物是八[[(环氧环己基乙基)二甲基甲硅烷氧基]硅倍半氧烷(OC)和八[[(环氧己基)二甲基甲硅烷氧基]硅倍半氧烷(OH)。来自OC和OH的两个纳米复合材料系列的比较提供了一个通过调节POSS分子的纳米链结构来控制宏观性质的典型示例。 DMA研究得出的结论是,聚酰亚胺-环氧树脂纳米复合材料的交联密度显着增加。纳米复合网络主要是由聚酰亚胺分子的末端胺基与POSS分子的环氧基之间的键合形成的。此外,有趣的是,尽管纳米复合材料的交联密度显着增加,但压缩模量,硬度和热膨胀系数仅略有变化。

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