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Polymer composites and porous materials prepared by thermally induced phase separation and polymer-metal hybrid methods.

机译:通过热诱导相分离和聚合物-金属杂化方法制备的聚合物复合材料和多孔材料。

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摘要

The primary objective of this research is to investigate the morphological and mechanical properties of composite materials and porous materials prepared by thermally induced phase separation. High melting crystallizable diluents were mixed with polymers so that the phase separation would be induced by the solidification of the diluents upon cooling. Theoretical phase diagrams were calculated using Flory-Huggins solution thermodynamics which show good agreement with the experimental results.;Porous materials were prepared by the extraction of the crystallized diluents after cooling the mixtures (hexamethylbenzene/polyethylene and pyrene/polyethylene). Anisotropic structures show strong dependence on the identity of the diluents and the composition of the mixtures. Anisotropic crystal growth of the diluents was studied in terms of thermodynamics and kinetics using DSC, optical microscopy and SEM. Microstructures of the porous materials were explained in terms of supercooling and dendritic solidification.;Dual functionality of the crystallizable diluents for composite materials was evaluated using isotactic polypropylene (iPP) and compatible diluents that crystallize upon cooling. The selected diluents form homogeneous mixtures with iPP at high temperature and lower the viscosity (improved processability), which undergo phase separation upon cooling to form solid particles that function as a toughening agent at room temperature. Tensile properties and morphology of the composites showed that organic crystalline particles have the similar effect as rigid particles to increase toughness; de-wetting between the particle and iPP matrix occurs at the early stage of deformation, followed by unhindered plastic flow that consumes significant amount of fracture energy. The effect of the diluents, however, strongly depends on the identity of the diluents that interact with the iPP during solidification step, which was demonstrated by comparing tetrabromobisphenol-A and phthalic anhydride. A simple method to prepare composite surfaces that can change the wettability in response to the temperature change was proposed and evaluated. Composite surfaces prepared by nanoporous alumina templates filled with polymers showed surface morphology and wettability that depend on temperature. This effect is attributed to the significant difference in thermal conductivity and the thermal expansion coefficient between the alumina and the polymers. The reversibility in thermal response depends on the properties of the polymers.
机译:这项研究的主要目的是研究通过热诱导相分离制备的复合材料和多孔材料的形态和力学性能。将高熔点的可结晶稀释剂与聚合物混合,这样冷却时稀释剂的固化将引起相分离。用Flory-Huggins溶液热力学计算理论相图,与实验结果吻合良好。冷却混合物(六甲基苯/聚乙烯和pyr /聚乙烯)后,通过萃取结晶的稀释剂制备多孔材料。各向异性结构显示出对稀释剂的身份和混合物组成的强烈依赖性。使用DSC,光学显微镜和SEM在热力学和动力学方面研究了稀释剂的各向异性晶体生长。用过冷和树枝状凝固来解释多孔材料的微观结构。使用等规聚丙烯(iPP)和在冷却时会结晶的相容性稀释剂,评估了复合材料的可结晶稀释剂的双重功能。选定的稀释剂在高温下与iPP形成均匀的混合物,并降低了粘度(提高了可加工性),冷却后发生相分离,形成了在室温下起增韧剂作用的固体颗粒。复合材料的拉伸性能和形态表明,有机晶体颗粒与刚性颗粒具有相似的作用,以增加韧性。颗粒和iPP基质之间的脱湿发生在变形的早期,随后是无阻碍的塑性流动,这消耗了大量的断裂能。但是,稀释剂的效果在很大程度上取决于在固化步骤中与iPP相互作用的稀释剂的特性,这通过比较四溴双酚A和邻苯二甲酸酐来证明。提出并评估了一种简单的制备复合材料表面的方法,该复合材料表面可响应温度变化而改变润湿性。由填充有聚合物的纳米多孔氧化铝模板制备的复合材料表面显示出取决于温度的表面形态和润湿性。该效果归因于氧化铝和聚合物之间的热导率和热膨胀系数的显着差异。热响应的可逆性取决于聚合物的性能。

著录项

  • 作者

    Yoon, Joonsung.;

  • 作者单位

    University of Massachusetts Amherst.;

  • 授予单位 University of Massachusetts Amherst.;
  • 学科 Chemistry Polymer.;Engineering Materials Science.;Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 169 p.
  • 总页数 169
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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