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Nanostructure and dynamic mechanical properties of silane-functionalized montmorillonite/epoxy nanocomposites

机译:硅烷官能化蒙脱土/环氧树脂纳米复合材料的纳米结构和动态力学性能

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摘要

In this work sodium montmorillonite (Na-MMT) was functionalized with N-(2-aminoethyl)-3-aminopropyl-trimethoxysilane and the corresponding silylated clay was used to modify epoxy matrix cured with triethyle-netetramine. The grafting/intercalation of the aminosilane inside the clay galleries were followed by infrared spectroscopy, X-ray diffraction, thermogravimetric analysis and ~29Si cross-polarization magic-angle-spinning nuclear magnetic-resonance (CP/MAS NMR) spectroscopy. Epoxy-based nanocomposites were prepared with different amounts of silylated clay or commercial organoclay, Cloisite 30B, whose intercalating agent consists of a methyl, tallow, bis-2-hydroxyethyl quaternary ammonium salt. The degree of intercalation/exfoliation was estimated by X-ray diffraction experiments and confirmed by small angle X-ray scattering. Nanocomposites prepared with silylated clay displayed no peak in both XRD and SAXS curves whereas those prepared with Cloisite 30B exhibited a clear interference peak corresponding to an interlayer spacing dooi of 4.1 nm. The former also presented a better dispersion, with a high proportion of tactoids smaller than 2 nm, as estimated by SAXS. From the results of dynamic mechanical analysis it was observed that most of the nanocomposites display higher storage modulus mainly at temperatures above the glass transition temperature. The glass transition temperature is similar or higher than the neat epoxy network for nanocomposites containing 1 wt.% of silylated clay or higher.
机译:在这项工作中,将蒙脱土钠(Na-MMT)用N-(2-氨基乙基)-3-氨基丙基-三甲氧基硅烷官能化,并将相应的甲硅烷基化粘土用于改性用三乙基-四乙胺固化的环氧基质。在红外通道,X射线衍射,热重分析和〜29Si交叉极化魔角旋转核磁共振(CP / MAS NMR)光谱之后,对氨基硅烷在粘土通道内进行接枝/插入。用不同量的甲硅烷基化粘土或市售有机粘土Cloisite 30B制备基于环氧树脂的纳米复合材料,其嵌入剂由甲基,牛脂,双-2-羟乙基季铵盐组成。通过X射线衍射实验估计插层/剥落的程度,并通过小角度X射线散射来确认。用甲硅烷基化粘土制备的纳米复合材料在XRD和SAXS曲线中均未显示峰,而使用Cloisite 30B制备的纳米复合物则显示出明显的干扰峰,对应于4.1 nm的层间间距。前者还表现出更好的分散性,如SAXS估计的那样,高比例的类触觉分子小于2 nm。从动态力学分析的结果可以看出,大多数纳米复合材料主要在高于玻璃化转变温度的温度下显示出较高的储能模量。对于包含1重量%或更高的甲硅烷基化粘土的纳米复合材料,玻璃化转变温度与纯环氧网络相似或更高。

著录项

  • 来源
    《Applied clay science》 |2011年第2期|p.151-158|共8页
  • 作者单位

    Macromolecular Institute (IMA), Federal University of Rio de Janeiro (UFRJ), 21945-970, Rio de Janeiro-R], Brazil;

    Macromolecular Institute (IMA), Federal University of Rio de Janeiro (UFRJ), 21945-970, Rio de Janeiro-R], Brazil;

    Macromolecular Institute (IMA), Federal University of Rio de Janeiro (UFRJ), 21945-970, Rio de Janeiro-R], Brazil;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    organosilane; montmorillonite; epoxy; nanocomposite; saxs;

    机译:有机硅烷蒙脱石环氧纳米复合材料萨克斯;

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