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Styrene-maleic anhydride and styrene-maleimide based copolymers as building blocks in microencapsulation procedures.

机译:苯乙烯-马来酸酐和苯乙烯-马来酰亚胺基共聚物是微囊化程序的基础。

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摘要

This thesis addresses the formation and properties of capsule walls formed from new types of wall-former materials such as styrene-maleic anhydride and styrene-maleimide based preformed hydrophobic polymers. During the course of this study two new methods of encapsulation were developed: interfacial encapsulation based on the cross-linking reaction between oil-soluble styrene-maleic anhydride (SMA) copolymer and a water-soluble polyamine, or alternatively the hydrolysis reaction of tert-butylstyrene-maleic anhydride copolymers to produce non-cross-linked microcapsules, and photoinduced phase-separation encapsulation.; The internal morphologies of the produced SMA microcapsules were found to depend primarily upon polymer/core-solvent interactions and rate of amine addition. Thus, the transition from matrix structures to hollow particles was observed with increasing volume fraction of hydrophobic non-solvent, dodecyl acetate, or alternatively by slowing the rate of polyamine addition. The effect of polymer loading, type of polymer and polyamine, and molecular weight of the preformed polymer on the observed morphologies was also investigated. The interfacial reaction between styrene-maleic anhydride type of copolymers and polyamines was shown to be fast in order of minutes. Hydrolysis, as the side reaction, was not found to play a significant role in the interfacial encapsulation reaction between SMA copolymers and amines.; Styrene-maleimide based capsules were prepared by photostimulated precipitation of azobenzene-functionalized copolymers dissolved in an oil phase and dispersed in a continuous phase. This microencapsulation process was found to be irreversible, and the resulting microcapsule walls were permanent even during storage in the dark, or irradiation with visible light.
机译:本论文研究了由新型壁形成剂材料(例如苯乙烯-马来酸酐和苯乙烯-马来酰亚胺基预制疏水聚合物)形成的胶囊壁的形成和性能。在此研究过程中,开发了两种新的封装方法:基于油溶性苯乙烯-马来酸酐(SMA)共聚物与水溶性多胺之间的交联反应的界面封装,或叔-叔丁基的水解反应。丁基苯乙烯-马来酸酐共聚物以产生非交联的微胶囊,并进行光致相分离包封。发现所产生的SMA微胶囊的内部形态主要取决于聚合物/核-溶剂相互作用和胺添加速率。因此,随着疏水性非溶剂乙酸十二烷基酯的体积分数增加或通过减慢多胺的添加速度,观察到了从基质结构到中空颗粒的过渡。还研究了聚合物负载量,聚合物和多胺的类型以及预成型聚合物的分子量对观察到的形态的影响。苯乙烯-马来酸酐类型的共聚物和多胺之间的界面反应显示出几分钟即可达到快速反应。未发现水解作为副反应在SMA共聚物和胺之间的界面封装反应中起重要作用。苯乙烯-马来酰亚胺基胶囊是通过光刺激沉淀溶解在油相中并分散在连续相中的偶氮苯官能化共聚物制得的。发现该微囊化过程是不可逆的,并且即使在黑暗中储存或在可见光照射下,所得微囊壁也是永久的。

著录项

  • 作者

    Shulkin, Anna.;

  • 作者单位

    McMaster University (Canada).;

  • 授予单位 McMaster University (Canada).;
  • 学科 Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2002
  • 页码 197 p.
  • 总页数 197
  • 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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