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Synthesis and structure-property studies of polysiloxane polyurethane isocyanate-functional polymeric silanes.

机译:聚硅氧烷聚氨酯异氰酸酯官能聚合硅烷的合成和结构性能研究。

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摘要

A novel type of polymeric isocyanate-functional silane of polysiloxane was synthesized for the first time from an acrylate-functional silane. Also employed were acrylate-functional isocyanates, acrylate-functional polyether or polyester urethane isocyanates and polyhydrogen methyl siloxane which reacted Si-H with a vinyl group. The synthetic yields of the polymers were studied by HPLC and found to be higher than 96%. The molecular weights obtained were acceptable. The density and the intrinsic viscosity of the graft copolymers were measured by standard methods. The surface chemical structure of the graft copolymers was investigated by ATR-FTIR. Shown are the special structures for a 60% silane side chain especially for the polyether urethane polyisocyanate-functional polymers.The morphology of the graft copolymers was investigated by FTIR and DSC. Hydrogen bonding between NH and C=O groups resulted in a special arrangement of the polymeric isocyanate-functional silanes of polysiloxane. These graft copolymers had a high percentage of strong hydrogen bonding between NH and C=O groups. DSC showed the crystallization morphology of silane on the polysiloxane chain and a lot of phase separation. The SEM results supported surface morphology which had a roller-like crystallization or regular arrangement.Kinetic studies confirmed that the functional groups had a reactivity similar to that of monomeric groups. As coupling agents used in composite and adhesive systems, these polymers were superior to those formed from monomeric silanes. This strength of coupling can be explained by a three-component interpenetrating polymer network adhesion theory.
机译:首次从丙烯酸酯官能硅烷合成了新型的聚硅氧烷聚合异氰酸酯官能硅烷。还使用了使Si-H与乙烯基反应的丙烯酸酯官能的异氰酸酯,丙烯酸酯官能的聚醚或聚酯氨基甲酸酯异氰酸酯和聚氢甲基硅氧烷。通过HPLC研究了聚合物的合成产率,发现其高于96%。获得的分子量是可接受的。通过标准方法测量接枝共聚物的密度和特性粘度。通过ATR-FTIR研究了接枝共聚物的表面化学结构。显示了60%硅烷侧链的特殊结构,特别是对于聚醚氨基甲酸酯多异氰酸酯官能聚合物。接枝共聚物的形貌通过FTIR和DSC进行了研究。 NH和C = O基团之间的氢键导致聚硅氧烷的聚合异氰酸酯官能硅烷的特殊排列。这些接枝共聚物在NH和C = O基团之间具有高百分比的强氢键。 DSC显示硅烷在聚硅氧烷链上的结晶形态和许多相分离。 SEM结果支持了具有辊状结晶或规则排列的表面形态。运动学研究证实官能团具有与单体基团相似的反应性。作为用于复合材料和粘合剂系统的偶联剂,这些聚合物优于由单体硅烷形成的聚合物。这种偶联的强度可以通过三组分互穿聚合物网络的粘附理论来解释。

著录项

  • 作者

    Dai, Zhisheng.;

  • 作者单位

    University of Detroit Mercy.;

  • 授予单位 University of Detroit Mercy.;
  • 学科 Chemistry Polymer.Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 1993
  • 页码 176 p.
  • 总页数 176
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:50:06

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