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Cyclic, tethered and nanoparticulate silicones for material modification.

机译:环状,束缚和纳米颗粒有机硅,用于材料改性。

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摘要

I have examined three different topological forms of a material modifier. The modifier is silicone and the three topological forms are cyclic, linear tethers and networked siloxane bonds in the form of a nanoparticulate. Often silicones, or siloxanes, are added to a material because of its unique properties that are related to its inorganic or inorganic-organic hybrid character. This dissertation addresses either the synthesis of silicones for material modification or the effect of the adding silicones to a variety of substrates and polymeric systems.;Chapters 2 and 3 present research focused on the first topological form, cyclic PDMS. The synthesis of cyclic polymers is very important to the synthesis and subsequent characterization of cyclic containing multi-component materials. Cyclic PDMS is formed via ring-chain depolymerization and bimolecular coupling and the unique issues associated with the formation, purification and analysis of cyclic polymer topologies. The goal of the work described in these chapters was to find a straightforward high-yield route to form large cycles of PDMS in a relatively high purity.;Chapter 4 focuses on the modification of the next topological form, linear polymers as tethers for surface modification and presents a novel concept for surface-modifying compounds; the incorporation of an ionic-reactive functionality into PDMS is presented. The idea being its ionic character will increase affinity for the surface, surface coverage and levelness, while the subsequent reactive fixation will permanently modify the surface to improve retention and fastness. The use of such chemistry has not been applied for surface modification protocols.;Chapters 5, 6 and 7 discuss the characterization of systems with the third topological form incorporated. They include differences in the viscoelastic behavior of PVAc/silica nanocomposites and the neat PVAc matrix, relating those differences to polymer dynamics and structure as determined by several solid-state NMR experiments. The latter two chapters pertain to PVAc/silica nanocomposites with PDMS surface treatments. Specifically, evaluating how polymer dynamics and structure changes particularly at the interfaceinterphase with various PDMS surface treatments having different topologies at the surface.
机译:我研究了材料修改器的三种不同的拓扑形式。改性剂是硅酮,三种拓扑形式是环状,线性束缚和纳米颗粒形式的网状硅氧烷键。通常,由于其与无机或无机-有机杂化特性相关的独特特性,会将有机硅或硅氧烷添加到材料中。本论文探讨了用于材料改性的有机硅的合成或在各种基材和聚合物体系中添加有机硅的效果。第二章和第三章目前的研究集中于第一种拓扑形式,环状PDMS。环状聚合物的合成对于含环状多组分材料的合成和随后的表征非常重要。环状PDMS是通过环链解聚和双分子偶联以及与环状聚合物拓扑结构的形成,纯化和分析相关的独特问题形成的。这些章节中描述的工作目标是找到一条简单的高产途径,以较高的纯度形成较大的PDMS循环。;第4章着重介绍下一种拓扑形式的改性,即线性聚合物作为用于表面改性的束缚剂并提出了一种表面改性化合物的新概念;提出了将离子反应性官能团结合到PDMS中的方法。其离子特性的想法将增加对表面的亲和力,表面覆盖率和水平度,而随后的反应性固着将永久性地改变表面,以改善保留率和坚牢度。尚未将这种化学方法用于表面修饰方案。第5、6和7章讨论了结合了第三种拓扑形式的系统的表征。它们包括PVAc /二氧化硅纳米复合材料和纯净的PVAc基质的粘弹性行为的差异,这些差异与通过数个固态NMR实验确定的聚合物动力学和结构有关。后两章涉及采用PDMS表面处理的PVAc /二氧化硅纳米复合材料。具体来说,评估各种表面上具有不同拓扑结构的PDMS表面处理的聚合物动力学和结构如何变化,尤其是在界面界面处。

著录项

  • 作者

    Foston, Marcus Bernard.;

  • 作者单位

    Georgia Institute of Technology.;

  • 授予单位 Georgia Institute of Technology.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 298 p.
  • 总页数 298
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 高分子化学(高聚物);
  • 关键词

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