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Novel interphases: Synthesis, molecular orientation and grafting of liquid crystal polymers on carbon fibers.

机译:新型相:碳纤维上液晶聚合物的合成,分子取向和接枝。

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摘要

The objective of this research has been to study composite materials containing liquid crystal polymers either as matrices or in interfacial boundary zones. The fundamental point of interest here is the interfacial response that fiber surfaces can potentially induce in self ordering polymers. This investigation includes studies in three broad categories: molecular orientation of nematic melts containing dispersed carbon fibers, the chemical grafting of a liquid crystal polymer to these fibers by in-situ polymerization of monomeric melts, and the synthesis and anchoring on fibers of specially designed liquid crystal monomers and polymers containing pendant chemical functions on their mesogenic groups.;The matrix polymer used in orientation studies is a chemically disordered thermotropic copolyester synthesized from the monomers p-acetoxybenzoic acid, diacetoxyhydroquinone and pimelic acid. Broadline proton NMR studies revealed enhanced rates of magnetic orientation in the polymer melt when carbon fibers are dispersed in the medium. Polarized optical microscopy studies of these composite samples revealed that fiber surfaces influence the orientation of mesomorphic molecules in their immediate surroundings. Inspite of this orienting influence of fibers on the matrix molecules, fracture surface analysis of composite specimens by SEM revealed poor wetting of the fibers by the matrix polymer. It was possible to induce excellent wetting of this polymer on carbon fibers by in-situ polymerization of the monomers in the presence of functionalized fibers which result in covalent grafting of mesogenic chains on fiber surfaces. New hydroxy-functionalized side chain liquid crystal polymers were synthesized which could be useful in the molecular design of interfacial boundary layers in polymer-based composites. Optical observations reveal that the phenolic monomer has an exceptionally strong tendency for orthogonal anchoring on glass surfaces. However, this anchoring by glass is disturbed around carbon fibers dispersed in the monomeric melt. From studies with a compensator, it is inferred that these "boundary zones" contain arrays of molecules oriented in two different directions. In contrast to the monomer, the orienting behavior of the polymer or either glass or carbon surfaces is less defined. However, this property of the polymer could be improved significantly by replacing some phenolic groups by bulky, nonpolar silyl ether groups.
机译:这项研究的目的是研究包含液晶聚合物的复合材料,它们既可以作为基质,也可以位于界面边界区域。这里关注的基本点是纤维表面可能在自定序聚合物中诱发的界面反应。这项研究包括三大类的研究:含分散碳纤维的向列熔体的分子取向;通过单体熔体的原位聚合将液晶聚合物化学接枝到这些纤维上;以及特殊设计的液体在纤维上的合成和固定结晶单体和在其介晶基团上具有侧基化学官能团的聚合物。取向研究中使用的基质聚合物是一种化学无序的热致共聚酯,由单体对乙酰氧基苯甲酸,二乙酰氧基氢醌和庚二酸合成。粗线质子NMR研究表明,当碳纤维分散在介质中时,聚合物熔体中磁取向的速率提高。对这些复合样品的偏振光学显微镜研究表明,纤维表面会影响其周围环境中的同构分子的取向。尽管纤维对基体分子有这种定向影响,但是通过SEM对复合材料样品的断裂表面分析显示基体聚合物对纤维的润湿性较差。在功能化纤维的存在下,通过单体的原位聚合,有可能引起这种聚合物在碳纤维上的优异润湿,从而导致介晶链在纤维表面的共价接枝。合成了新的羟基官能化的侧链液晶聚合物,可用于聚合物基复合材料界面边界层的分子设计。光学观察表明,酚类单体具有在玻璃表面上正交锚固的极强趋势。然而,玻璃的这种锚固在分散在单体熔体中的碳纤维周围受到干扰。从补偿器的研究中可以推断出,这些“边界区”包含沿两个不同方向取向的分子阵列。与单体相反,聚合物或玻璃或碳表面的定向行为较少定义。然而,通过用大体积的非极性甲硅烷基醚基团代替一些酚基基团可以显着改善聚合物的这种性能。

著录项

  • 作者

    Sastri, Satya Bhama.;

  • 作者单位

    University of Illinois at Urbana-Champaign.;

  • 授予单位 University of Illinois at Urbana-Champaign.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 1990
  • 页码 239 p.
  • 总页数 239
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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