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Synthesis and surface characterization of copolymers containing low-molecular weight amino-propyl-terminated siloxanes.

机译:含有低分子量氨基丙基末端硅氧烷的共聚物的合成和表面表征。

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摘要

Poly(dimethylsiloxane)s(PDMS) are often incorporated into copolymers and polymer blends due to their unique properties including, low surface energy, high gas permeability, excellent oxidative stability, low dielectric constant, low glass transition temperature (Tg), low moisture absorption and high flexibility. Due to the low surface energy of the PDMS with respect to most other materials, there is usually preferential segregation of the siloxane component to the surface in copolymer systems and blends, resulting in a surface that is comprised primarily of PDMS. This means that while the surface properties are dominated by the PDMS component of the copolymer, the overall bulk properties will be representative of both components (depending on the composition).; The extent of this preferential siloxane segregation is dependent upon many factors including casting solvent, block length, and bulk composition. In this dissertation, the effects of varying the siloxane segment length composition on the surface properties of two different copolymer systems is described. Chapter 2 focusses on the synthesis and bulk characterization of two very important siloxane containing copolymers, poly(imidesiloxane) and poly(ureaurethane)-PDMS copolymers, which were developed as adhesive materials and anti-fouling coatings respectively.; Chapters 3–5 focus on the surface characterization of these two copolymer systems utilizing both X-ray Photoelectron Spectroscopy (XPS) and Time of Flight-Secondary Ion Mass Spectrometry (TOF-SIMS). Angle Dependent XPS has been successfully used to obtain deconvoluted depth profile information from these copolymer surfaces. This process however is very controversial, and not enough is known about the accuracy of such a method. This process is therefore described in detail in chapter 3, where the accuracy of the surface overlayer thickness of PDMS is determined through comparison to a model system used to describe chain dimensions. The accuracy is further investigated utilizing a reference material containing poly(methylmethacrylate) (PMMA) on Si.; Chapters 4 and 5 are detailed surface investigations of poly(imidesiloxane) and poly(ureaurethane)-PDMS systems respectively, where both XPS and TOF-SIMS are utilized to determine the surface characteristics of copolymers containing varying siloxane segment length compositions and how they relate to their respective applications. Chapter 5 describes the first comprehensive TOF-SIMS study on the preferential segregation of PDMS segment lengths in complex copolymer systems. All of the results were consistent with a model of the surface, which has longer siloxane chain lengths preferentially segregating to the surface and dominating the surface properties.
机译:聚(二甲基硅氧烷)s(PDMS)由于其独特的特性而经常掺入共聚物和聚合物共混物中,包括低表面能,高透气性,出色的氧化稳定性,低介电常数,低玻璃化转变温度(T ),低吸湿性和高柔韧性。由于相对于大多数其他材料而言,PDMS的表面能低,通常在共聚物体系和共混物中,硅氧烷组分优先偏析在表面上,从而导致表面主要由PDMS组成。这意味着尽管表面性能由共聚物的PDMS组分决定,但整体的整体性能将代表两种组分(取决于组成)。这种优先硅氧烷偏析的程度取决于许多因素,包括浇铸溶剂,嵌段长度和本体组成。在本文中,描述了改变硅氧烷链段长度组成对两种不同共聚物体系表面性能的影响。第2章着重讨论了两种非常重要的含硅氧烷共聚物,聚(酰亚胺硅氧烷)和聚(脲氨酯)-PDMS共聚物的合成和本体表征,它们分别被开发为粘合剂材料和防污涂料。第3章至第5章着重介绍了利用X射线光电子能谱(XPS)和飞行时间二次离子质谱(TOF-SIMS)两种共聚物体系的表面表征。角度相关XPS已成功用于从这些共聚物表面获得去卷积的深度轮廓信息。然而,该过程是很有争议的,并且对于这种方法的准确性还知之甚少。因此,此过程将在第3章中进行详细描述,其中PDMS表面覆盖层厚度的精度是通过与用于描述链尺寸的模型系统进行比较来确定的。使用在硅上包含聚(甲基丙烯酸甲酯)(PMMA)的参考材料进一步研究了精度。第4章和第5章分别详细介绍了聚(酰亚胺硅氧烷)和聚(脲氨酯)-PDMS系统的表面研究,其中XPS和TOF-SIMS均用于确定包含变化的硅氧烷链段长度组成的共聚物的表面特性以及它们之间的关系他们各自的应用。第5章介绍了有关复杂共聚物系统中PDMS段长度优先偏析的首次全面TOF-SIMS研究。所有结果均与表面模型一致,该模型具有较长的硅氧烷链长度,优先偏析至表面并支配了表面性质。

著录项

  • 作者

    Mahoney, Christine Marie.;

  • 作者单位

    State University of New York at Buffalo.;

  • 授予单位 State University of New York at Buffalo.;
  • 学科 Chemistry Analytical.; Chemistry Polymer.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 340 p.
  • 总页数 340
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;高分子化学(高聚物);
  • 关键词

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