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(a) epoxy curing (b) characterization of epoxy/SWNT nanocomposites & (c) MNO2 nanostructures for catalysis

机译:(a)环氧固化(b)环氧/ SWNT纳米复合材料的表征和(c)用于催化的MNO2纳米结构

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摘要

The main objective of this study is to prepare a better material, i.e. stronger, lighter, heat impact and gas permeable for aerospace application. In recent years, the development of filler/epoxy composites has shown large potential for new materials with improved properties. This work was focused on two aspects of epoxy composites: A) the study of cure behavior of sample epoxy amine systems B) the characterization of thermal and mechanical properties of the epoxy nanocomposites. The cure behavior of the sample epoxy amine systems at different concentrations of curing agents and ramp rates were studied by differential scanning calorimetry (DSC). Solvent-dispersed single-walled nanotubes (SWNTs) are incorporated into epoxy matrices, followed by evaporation of the solvent before curing. The effect of solvent choice in thermal and mechanical properties of the resulting nanocomposites is evaluated using N-methyl pyrrolidone and dimethyl formamide. In this study, fluorescence is used as the tool to monitor the dispersions of SWNTs in the solvent and epoxy matrix. This study also compares the thermal and mechanical properties of these epoxy nanocomposites with a nanotube loading ranging from 0.001-0.01 wt. %. Dynamic mechanical analysis results showed increase in the storage modulus of epoxy/SWNT nanocomposites compared to plain epoxy composite. The presence of residual solvent in the epoxy composites is determined by thermogravimetric analysis (TGA). Contact angle measurements showed an increase in the hydrophobicity of the epoxy/SWNT nanocomposites compared to plain epoxy composite.;alpha-, -beta, and gamma-MnO2 were synthesized by hydrothermal methods, and were characterized using x-ray diffraction, scanning electron microscopy, Brunauer Emmett and Teller (BET) surface area, and TGA. TGA analysis showed that alpha-MnO2 has greater water content compared to the beta- and gamma- forms of MnO2. BET measurements confirmed that the surface areas are in the order of beta > alpha > gamma-MnO 2 samples. The catalytic activities of these samples against oxidation of arylmethylene compounds were studied, revealing that the primary factor controlling catalytic activity is the amount of adsorbed water. Additionally, novel structural features of the various forms of MnO2 will be reported.
机译:这项研究的主要目的是为航空航天应用准备更好的材料,即更坚固,更轻,热冲击和透气性。近年来,填料/环氧树脂复合材料的开发显示出具有改进性能的新型材料的巨大潜力。这项工作集中在环氧复合材料的两个方面:A)研究样品环氧胺体系的固化行为B)表征环氧纳米复合材料的热和机械性能。通过差示扫描量热法(DSC)研究了样品环氧胺体系在不同浓度的固化剂和升温速率下的固化行为。将分散有溶剂的单壁纳米管(SWNT)掺入环氧基质中,然后在固化前蒸发掉溶剂。使用N-甲基吡咯烷酮和二甲基甲酰胺评估溶剂选择对所得纳米复合材料的热和机械性能的影响。在这项研究中,荧光被用作监测SWNTs在溶剂和环氧基质中的分散性的工具。这项研究还比较了纳米管负载量为0.001-0.01 wt。%的环氧纳米复合材料的热和机械性能。 %。动态力学分析结果表明,与纯环氧复合材料相比,环氧/ SWNT纳米复合材料的储能模量增加。环氧复合材料中残留溶剂的存在通过热重分析(TGA)确定。接触角测量结果表明,与普通环氧复合材料相比,环氧/ SWNT纳米复合材料的疏水性有所提高。通过水热法合成了α-,β和γ-MnO2,并使用X射线衍射,扫描电子显微镜对其进行了表征,Brunauer Emmett和Teller(BET)表面积以及TGA。 TGA分析表明,与β型和γ型MnO2相比,α-MnO2的水分含量更高。 BET测量证实表面积按β>α>γ-MnO2样品的顺序排列。研究了这些样品对芳基亚甲基化合物氧化的催化活性,发现控制催化活性的主要因素是吸附的水量。另外,将报道各种形式的MnO2的新颖结构特征。

著录项

  • 作者

    Lageshetty, Sathish Kumar.;

  • 作者单位

    Oklahoma State University.;

  • 授予单位 Oklahoma State University.;
  • 学科 Chemistry.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 81 p.
  • 总页数 81
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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