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LAYERED SILICATE-EPOXY NANOCOMPOSITES.

机译:层状硅酸盐-环氧树脂纳米复合材料。

摘要

An epoxy-silicate nanocomposite is prepared by dispersing an organically modified smectite-type clay in an epoxy resin together with diglycidyl ether of bisphenol-A (DGEBA), and curing in the presence of either nadic methyl anhydride (NMA), and/or benzyldimethyl amine (BDMA), and/or boron trifluoride monoethylamine (BTFA) at 100-200 degree C. Molecular dispersion of the layered silicate within the crosslinked epoxy matrix is obtained, with smectite layer spacings of 100Å or more and good wetting of the silicate surface by the epoxy matrix. The curing reaction involves the functional groups of the alkylammonium ions located in the galleries of the organically modified clay, which participate in the crosslinking reaction and result in direct attachment of the polymer network to the molecularly dispersed silicate layers. The nanocomposite exhibits a broadened Tg at slightly higher temperature than the unmodified epoxy. The dynamic storage modulus of the nanocomposite was considerably higher in the glassy region and very much higher in the rubbery plateau region when compared to such modulus in the unmodified epoxy.
机译:通过将有机改性的蒙脱石型粘土与双酚A的二缩水甘油醚(DGEBA)一起分散在环氧树脂中,然后在纳迪克酸酐(NMA)和/或苄基二甲基存在下进行固化,制得环氧硅酸盐纳米复合材料胺(BDMA)和/或三氟化硼单乙胺(BTFA)在100-200摄氏度下进行。获得层状硅酸盐在交联环氧基质中的分子分散体,蒙脱石层间距为100Å或更高,并且硅酸盐表面润湿良好通过环氧基质。固化反应涉及位于有机改性粘土画廊中的烷基铵离子的官能团,该官能团参与交联反应并导致聚合物网络直接附着于分子分散的硅酸盐层。该纳米复合材料在比未改性的环氧树脂稍高的温度下显示出增宽的Tg。与未改性的环氧树脂中的这种弹性模量相比,纳米复合材料的动态储能模量在玻璃态区域显着更高,而在橡胶态的高原区域则更高。

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