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THE MOLECULAR STRUCTURE OF IMIDAZOLE DERIVATIVES ON COPPER (EPOXY RESIN).

机译:咪唑衍生物在铜(环氧树脂)上的分子结构。

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摘要

The molecular structure of imidazoles on copper and copper oxide, thermal stability of imidazoles on copper, and the chemical reaction of epoxy resin with imidazole-treated copper are studied in order to understand molecular mechanism of anticorrosion and adhesion promotion. Fourier-transform infrared reflection-absorption spectroscopy is used to observe the structural change of imidazole films on substrates. Imidazoles show flat orientation on gold and random orientation on copper. The imidazole rings cleave and the alkyl substituents are eliminated upon heating in air on copper. Different carbonyl groups are produced followed by the appearance of the nitrile group in the final oxidation stage. The difference in morphology and orientation of 2-undecylimidazole on oxide is mainly due to the reactivity of the imidazole and the substrate surface. The degration is catalysed by two types of copper, copper in the film and from the substrate. The rate determining step of the degradation is the reactivity of the carboxylic acid produced in the intermediate step of the degradation and the surface oxide. The inner layer of the deposited film on the slightly preoxidized copper showed a semi-crystalline structure as revealed by chemical depth profile. At elevated temperatures in the range of 150-180(DEGREES)C, production of 4(5H) undecylimidazolone was postulated near the substrate/imidazole interface as initial oxidation compounds. Alkylimidazole copper (II) complexes are synthesized to model the complexes on copper. The difference in oxidation between imidazoles on copper and synthesized imidazole complexes are due to the catalytic effect of the copper ion migrating from the copper substrate and different morphological structure. An epoxy resin shows an appreciable amount of polymerization on the imidazole complex/copper at 100(DEGREES)C. The thickness of the epoxy coating is increased while the imidazole complex dissolved into the bulk resin above this temperature. However, only a small amount of epoxy resin remains on the copper at elevated temperatures.
机译:研究了咪唑在铜和氧化铜上的分子结构,咪唑在铜上的热稳定性以及环氧树脂与咪唑处理过的铜的化学反应,以了解其防腐蚀和促进粘合的分子机理。用傅里叶变换红外反射吸收光谱法观察底物上咪唑膜的结构变化。咪唑在金上显示平面取向,在铜上显示随机取向。咪唑环裂解并且在空气中在铜上加热时消除烷基取代基。产生不同的羰基,然后在最终氧化阶段出现腈基。 2-十一烷基咪唑在氧化物上的形态和取向的差异主要是由于咪唑与底物表面的反应性。脱盐由两种类型的铜催化,一种是薄膜中的铜,另一种是来自基材的铜。降解的速率确定步骤是在降解的中间步骤中产生的羧酸与表面氧化物的反应性。如化学深度分布所揭示的那样,在稍微被预氧化的铜上的沉积膜的内层显示出半结晶结构。在150-180(摄氏度)范围内的高温下,在底物/咪唑界面附近假定生成4(5H)十一烷基咪唑酮作为初始氧化化合物。合成烷基咪唑铜(II)配合物以在铜上模拟配合物。铜上的咪唑与合成的咪唑配合物之间的氧化差异是由于铜离子从铜基质迁移而来的催化作用和不同的形态结构所致。环氧树脂在100(DEGREES)C下在咪唑配合物/铜上显示出可观的聚合反应量。在该温度以上,咪唑配合物溶解到本体树脂中时,环氧涂层的厚度增加。但是,在高温下,只有少量环氧树脂残留在铜上。

著录项

  • 作者

    YOSHIDA, SHUUJI.;

  • 作者单位

    Case Western Reserve University.;

  • 授予单位 Case Western Reserve University.;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 1983
  • 页码 258 p.
  • 总页数 258
  • 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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