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Simulation studies of diblock-copolymer grafted nanoparticle assembly in solvent and polymer matrix.

机译:在溶剂和聚合物基质中二嵌段共聚物接枝纳米颗粒组装体的模拟研究。

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摘要

Macroscopic properties of polymer nanocomposites are fundamentally linked to the morphology (or assembled structure) of its constituents. In order to design composites to have specific macroscopic properties it is important to be able to control the assembly of the constituents in the composite. In this thesis we use molecular simulations to study the molecular-level interactions and assembly of one class of polymer nanocomposites, namely diblock-copolymer grafted nanoparticles in solvent and in polymer matrix.;First, we study how the molecular features of the diblock-copolymer grafts affect the assembly of grafted nanoparticles in a (implicit) small molecule solvent. Using coarse-grained molecular dynamics simulations we study the effects of graft length, particle size, solvent selectivity, and copolymer composition on the particle assembly. This knowledge informs experiments on what diblock copolymer grafted nanoparticles properties to synthesize to achieve a target assembled structure.;Second, we elucidate how the chemistry of a homopolymer matrix affects the graft and matrix polymer conformations and the interactions between diblock copolymer grafted particles in the homopolymer matrix. Using coarse-grained simulations and umbrella sampling technique we calculate the potential of mean force between two grafted particles within polymer matrix. We vary the chemistry of the homopolymer matrix and the copolymer grafts through systematic variations in the monomer interaction potentials. This gives insight into how the diblock copolymer grafted layer and the matrix environment influence the effective interactions between the particles in a polymer matrix.;Third, we investigate diblock copolymer grafted particles as compatibilizing agents in a polymer matrix consisting of an immiscible homopolymer blend. The phase separation of homopolymers within the blend leads to formation of domains and interfaces that weaken the composite materials' mechanical properties. There is a need optimal compatibilizers that stabilize these polymer interfaces in the blend, and as a result strengthen the composite material. Using simulations we compare the compatibilizing properties of diblock copolymer grafted particles to those of other compatibilizers, such as free diblock copolymers and Janus nanoparticles. Beyond their role as superior compatibilizers, we also find that diblock copolymer grafted nanoparticles provide control over the glass transition temperature of the polymer nanocomposite.
机译:聚合物纳米复合材料的宏观性能从根本上与其组成的形态(或组装结构)有关。为了将复合材料设计成具有特定的宏观性能,重要的是能够控制复合材料中成分的组装。本文通过分子模拟研究了一类聚合物纳米复合材料在溶剂和聚合物基体中的二嵌段共聚物接枝纳米颗粒的分子水平相互作用和组装。首先,研究了二嵌段共聚物的分子特征。接枝会影响(隐式)小分子溶剂中接枝纳米颗粒的组装。使用粗粒度的分子动力学模拟,我们研究了接枝长度,粒度,溶剂选择性和共聚物组成对颗粒组装的影响。该知识可指导实验合成哪些二嵌段共聚物接枝的纳米颗粒,以实现目标组装结构。其次,我们阐明均聚物基质的化学性质如何影响接枝聚合物和基质聚合物的构象,以及均聚物中二嵌段共聚物接枝颗粒之间的相互作用矩阵。使用粗粒度模拟和伞状采样技术,我们计算了聚合物基质内两个接枝颗粒之间的平均力。我们通过单体相互作用势的系统变化来改变均聚物基质和共聚物接枝的化学性质。这使我们深入了解了二嵌段共聚物接枝层和基质环境如何影响聚合物基质中颗粒之间的有效相互作用。共混物中均聚物的相分离导致形成域和界面,从而削弱了复合材料的机械性能。需要最佳的增容剂,以稳定共混物中的这些聚合物界面,从而增强复合材料。使用模拟,我们比较了二嵌段共聚物接枝颗粒与其他增容剂(如游离二嵌段共聚物和Janus纳米颗粒)的相容性。除了它们作为优异的增容剂的作用外,我们还发现二嵌段共聚物接枝的纳米颗粒可控制聚合物纳米复合材料的玻璃化转变温度。

著录项

  • 作者

    Estridge, Carla E.;

  • 作者单位

    University of Colorado at Boulder.;

  • 授予单位 University of Colorado at Boulder.;
  • 学科 Physical chemistry.;Polymer chemistry.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 195 p.
  • 总页数 195
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:52:55

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