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Structural, mechanical, thermal, and thermomechanical properties of phenolic silica nanocomposites.

机译:酚醛二氧化硅纳米复合材料的结构,机械,热和热机械性能。

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摘要

In order to evaluate the structural, mechanical, thermal, and thermomechanical properties of phenolic silica nanocomposites, we developed phenolic silica nanocomposites using two different techniques. In the first case, nano silica particles were dispersed within phenolic matrix, whereas in the second case, the nano silica particles were condensed in situ with the matrix by using sol-gel technique.; Our thermal analysis of the curing reaction of the phenolic resin, when its physical dimensions are in nano scale, indicated that the curing reaction temperature and enthalpy were dependent on the physical size of the material. Furthermore, the formation of Si-O-Si bonds during the condensation of the silicon hydroxides within a phenolic matrix perturbed the curing reaction of the resin.; X-ray diffraction measurements of both the nanocomposites irrespective of their mode of fabrication showed only a broad peak at 2theta = 18.6° due to the diffraction by the adjacent polymer chains. Our scanning electron microscope images, on the other hand, indicated that the silica particles in both cases were actually formed from the networking of smaller silica particles.
机译:为了评估酚醛二氧化硅纳米复合材料的结构,机械,热和热机械性能,我们使用两种不同的技术开发了酚醛二氧化硅纳米复合材料。在第一种情况下,将纳米二氧化硅颗粒分散在酚醛基质中,而在第二种情况下,通过使用溶胶-凝胶技术将纳米二氧化硅颗粒与基质原位冷凝。我们对酚醛树脂的固化反应进行热分析,当其物理尺寸为纳米级时,表明固化反应温度和焓取决于材料的物理尺寸。此外,在酚醛基质中氢氧化硅的缩合过程中形成Si-O-Si键会干扰树脂的固化反应。两种纳米复合材料的X射线衍射测量结果(无论其制备方式如何)均由于相邻聚合物链的衍射而在2θ= 18.6°处仅显示一个宽峰。另一方面,我们的扫描电子显微镜图像表明,两种情况下的二氧化硅颗粒实际上都是由较小的二氧化硅颗粒的网络形成的。

著录项

  • 作者

    Amanuel, Samuel.;

  • 作者单位

    Southern Illinois University at Carbondale.;

  • 授予单位 Southern Illinois University at Carbondale.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2004
  • 页码 156 p.
  • 总页数 156
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

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