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Synthesis and characterization of high performance polymeric materials: Poly(arylene ether)s, polyamides, polyesters and liquid crystalline polyarylates.

机译:高性能聚合物材料的合成和表征:聚(亚芳基醚),聚酰胺,聚酯和液晶性聚芳酯。

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摘要

Poly(arylene ether)s (PAEs) were synthesized via the silyl ether displacement route. Both AA, BB, and AB silylated monomers were prepared by partial or complete hydrolysis of the dihalide using potassium hydroxide in aqueous dimethyl sulfoxide followed by silylation with hexamethyl disilazane. Both linear and star-branched structures of PAEs were synthesized and this polymerization route allowed both random and block copolymers to be prepared. Triaryl phosphine oxide containing homo- & co-PAEs exhibited very high char yields, which suggested that these polymers were potentially flame-resistant materials. The AB type halogenophenols were also polymerized in the presence of diphenylsulfone as a diluent and potassium carbonate as a base at elevated temperatures.;Hydrolytically stable triaryl phosphine oxide containing dicarboxylic acid monomers were synthesized and were chemically incorporated into the poly(hexamethylene adipamide) backbone to produce improved flame-resistant copolymers. The content of triaryl phosphine oxide comonomer in the melt synthesized copolymers was controlled from 0-30 mole%. The copolymers were melt crystallizable only at 10 and 20 mole% incorporation of the phosphine oxide comonomer. Cone calorimetric tests were employed to investigate the fundamental flame retardancy behavior of the copolymers. The tests were conducted in a constant heat environment (40 kW/m;The triaryl phosphine oxide dicarboxylic methyl ester was also introduced into poly(ethylene terephthalate) via melt transesterification to produce copolymers which had increased char yields as the P(O) content increased. However, crystallinity was totally disrupted at 20 mole percent P(O) incorporation in compression molded specimen.;Novel star-branched liquid crystalline polyarylates (LCP) were made via melt acidolysis which were subsequently transformed to liquid crystalline foams by supersaturation of carbon dioxide followed by thermal blowing. It was found that the AB type monomers were essential to generate star shaped LCPs without crosslinking. The branching agents were necessary to control the molecular weights, disrupt crystallinity and to allow for higher gas uptake by the polymer matrix.;Poly(
机译:聚(亚芳基醚)(PAEs)通过甲硅烷基醚置换路线合成。 AA,BB和AB甲硅烷基化的单体均通过使用二甲基亚砜水溶液中的氢氧化钾对二卤化物进行部分或完全水解,然后用六甲基二硅氮烷进行甲硅烷基化来制备。合成了PAE的线性和星形分支结构,并且该聚合路线允许制备无规和嵌段共聚物。含三芳基氧化膦的均聚和共聚PAE表现出非常高的炭收率,这表明这些聚合物是潜在的阻燃材料。 AB型卤代苯酚还可以在高温下在二苯砜作为稀释剂和碳酸钾作为碱的存在下进行聚合;合成了具有水解稳定性的含三羧酸三芳基膦氧化物的二羧酸单体,并将其化学结合到聚(六亚甲基己二酰胺)骨架中生产改进的阻燃共聚物。熔融合成的共聚物中三芳基氧化膦共聚单体的含量控制在0-30摩尔%。该共聚物仅在氧化膦共聚单体的掺入量为10和20摩尔%时才可熔融结晶。锥形量热试验用于研究共聚物的基本阻燃性能。该试验在恒定热环境(40 kW / m)下进行;三芳基氧化膦二羧酸甲酯也通过熔融酯交换反应引入聚对苯二甲酸乙二酯中,制得的共聚物随着P(O)含量的增加而炭化率提高然而,在压塑样品中掺入20%(摩尔)的P(O)时,结晶度完全被破坏;通过熔融酸解法制备了新的星形支化液晶聚芳酯(LCP),随后通过二氧化碳的过饱和将其转变为液晶泡沫发现AB型单体对于生成星形LCP而不交联是必不可少的;支化剂对于控制分子量,破坏结晶度和允许聚合物基质吸收更高的气体是必需的。 (

著录项

  • 作者

    Wan, I-Yuan.;

  • 作者单位

    Virginia Polytechnic Institute and State University.;

  • 授予单位 Virginia Polytechnic Institute and State University.;
  • 学科 Chemistry Polymer.;Plastics Technology.
  • 学位 Ph.D.
  • 年度 1994
  • 页码 230 p.
  • 总页数 230
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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