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Synthesis and characterization of thermoplastic polyphenoxyquinoxalines.

机译:热塑性聚苯氧基喹喔啉的合成与表征。

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摘要

This research was divided into two main parts. In the first part, a new facile route to relatively inexpensive thermoplastic polyphenoxyquinoxalines was developed. The synthetic route involves the aromatic nucleophilic substitution reaction of bisphenols with 2,3-dichloroquinoxaline. The dichloro monomer was prepared in two steps. In the first step, oxalic acid was condensed with o-phenylenediamine to give 2,3-dihydroxyquinoxaline. In the second step, 2,3-dihydroxyquinoxaline was treated with thionyl chloride to give 2,3-dichloroquinoxaline. This monomer was successfully polymerized with bisphenol-A, bisphenol-S, hexafluorobisphenol-A and 9,9-bis(4-hydroxyphenyl)fluorenone. Hydroquinone and biphenol, however, can not be polymerized to high molecular weight polymers because of the premature precipitation of crystalline oligomers. The glass transition temperatures of the high molecular weight polymers prepared from a series of bisphenols range from 191°C to 279°C, and their thermal decomposition temperatures are around 500°C. The polymers are soluble in a wide range of solvents and can be solution-cast into thin films that are colorless and transparent. The polymers have tensile strengths ranging from 61 to 107 MPa, and tensile moduli ranging from 3.5 to 2.3 GPa. The synthesis of polymer obtained from 2,3-dichloroquinoxaline and bisphenol-A was scaled up to afford 500 g of material. This polymer is a thermoplastic with a melt-viscosity less than 1000 Pa.s. at 300°C. The notched Izod impact strength of injection-molded samples of this polymer is 40.7 J/m.;In the second part of this research, the synthetic method has been modified to allow the preparation of quinoxaline containing polyimides. Thus, 2,3-dichloroquinoxaline was treated either with p-nitrophenol followed by reduction of nitro groups, or with p-aminophenols to directly obtain the desired 2,3-(4-aminophenoxy)quinoxaline. This diamine was polymerized with 3,3',4,4'-biphenyldianhydride, 4,4'-oxydiphthalic anhydride and 2,2'-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride. The polymerizations were carried out by the two step method. The poly(amic acid) intermediates were thermally imidized. Although they have high molecular weights judged by their inherent viscosities ranging from 0.51 to 1.01, thin films of all these polyimides were brittle. The glass transition temperatures of the polyimides range from 259°C to 282°C with thermal decomposition temperatures around 550°C. The polyimide obtained from 2,3-(4-aminophenoxy)quinoxaline and 3,3',4,4'-biphenyldianhydride was found to be semi-crystalline.
机译:这项研究分为两个主要部分。在第一部分中,开发了一条相对便宜的热塑性聚苯氧基喹喔啉的简便生产路线。合成途径涉及双酚与2,3-二氯喹喔啉的芳香亲核取代反应。分两步制备二氯单体。在第一步中,草酸与邻苯二胺缩合得到2,3-二羟基喹喔啉。第二步,用亚硫酰氯处理2,3-二羟基喹喔啉,得到2,3-二氯喹喔啉。该单体已成功与双酚A,双酚S,六氟双酚A和9,9-双(4-羟苯基)芴酮聚合。然而,由于结晶低聚物的过早沉淀,对苯二酚和双酚不能聚合成高分子量聚合物。由一系列双酚制备的高分子量聚合物的玻璃化转变温度为191°C至279°C,并且它们的热分解温度约为500°C。该聚合物可溶于多种溶剂,并可溶液浇铸成无色透明的薄膜。聚合物的拉伸强度为61至107 MPa,拉伸模量为3.5至2.3 GPa。由2,3-二氯喹喔啉和双酚-A获得的聚合物的合成按比例放大以提供500g的材料。该聚合物是熔体粘度小于1000 Pa.s的热塑性塑料。在300°C下。该聚合物注塑样品的缺口悬臂梁式冲击强度为40.7 J / m .;在本研究的第二部分中,对合成方法进行了改进,以制备含喹喔啉的聚酰亚胺。因此,用对硝基苯酚,然后还原硝基,或用对氨基苯酚处理2,3-二氯喹喔啉,以直接获得所需的2,3-(4-氨基苯氧基)喹喔啉。该二胺与3,3′,4,4′-联苯二酐,4,4′-氧二邻苯二甲酸酐和2,2′-双(3,4-二羧苯基)六氟丙烷二酐聚合。通过两步法进行聚合。将聚(酰胺酸)中间体热酰亚胺化。尽管通过其固有粘度在0.51至1.01的范围内判断它们具有高分子量,但是所有这些聚酰亚胺的薄膜都是脆性的。聚酰亚胺的玻璃化转变温度为259°C至282°C,热分解温度约为550°C。由2,3-(4-氨基苯氧基)喹喔啉和3,3′,4,4′-联苯二酐获得的聚酰亚胺是半结晶的。

著录项

  • 作者

    Erdem, Haci Bayram.;

  • 作者单位

    The University of Akron.;

  • 授予单位 The University of Akron.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 137 p.
  • 总页数 137
  • 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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