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Nanoporous thermosetting membranes using reactive block polyme templates.

机译:使用反应性嵌段聚合物模板的纳米孔热固性膜。

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摘要

Pressure driven membrane filtrations are a facile means of performing aqueous separations. The efficiency of these processes depends on the permeability and selectivity of a membrane, which is determined by its structure. This dissertation describes research investigating nanoporous thermosets templated by reactive block polymers as alternatives to current ultrafiltration membranes. The goal of the research was to develop materials with narrow pore size distributions and high void fractions for forming membranes with increased selectivity and permeability.The flux, filtration and fouling characteristics of membranes formed by selective removal of poly(lactide) from crosslinked films of dicyclopentadiene (DCPD) and the reactive block polymer poly(norbornenylethyl styrene- s-styrene)-b-poly(lactide) (PNS-PLA) were first explored. The results suggest that thin film composite membranes could achieve permeabilities and selectivities greater than current ultrafiltration membranes without excessive fouling characteristics. Additionally, hydrophilic and stimuli responsive membranes templated by reactive triblock terpolymers exhibited environmentally dependent fluxes demonstrating the ease of creating functionalized membranes using reactive triblock terpolymers.Further investigation into the compositional influences on the morphology of nanostructured PNS-PLA/PDCPD materials revealed that nanoporous bicontinuous structures form over a wide composition range and that different pore sizes are achievable by varying the PLA block size. Extension of reactive block polymer templating to vinyl crosslinking systems was demonstrated by crosslinking a poly(lactide)-b-poly(cyclooctene-s-norbornenylmethacrylate)- b-poly(lactide) reactive triblock copolymer with a variety of vinyl monomers. Although the soft nature of the poly(cyclooctene) prevented removal of polylactide due to collapse of the pores, nanoporous vinyl thermosets were realized by crosslinking a polylactide-b-poly(styrene- s-hydroxyethyl methacrylate-s-ethylene glycol dimetacrylate) reactive diblock copolymer with styrene and divinyl benzene.
机译:压力驱动的膜过滤是进行水分离的简便方法。这些过程的效率取决于膜的渗透性和选择性,这由膜的结构决定。本论文描述了以反应性嵌段聚合物为模板的纳米孔热固性材料作为当前超滤膜的替代品的研究。该研究的目的是开发具有窄孔径分布和高空隙率的材料,以形成具有更高选择性和渗透性的膜。通过从双环戊二烯的交联膜中选择性去除聚丙交酯形成的膜的通量,过滤和结垢特性(DCPD)和反应性嵌段聚合物聚(降冰片烯基乙基苯乙烯-s-苯乙烯)-b-丙交酯(PNS-PLA)进行了探索。结果表明,与目前的超滤膜相比,薄膜复合膜可以实现更大的渗透性和选择性,而不会产生过多的结垢特性。此外,以反应性三嵌段三元共聚物为模板的亲水性和刺激性响应膜表现出与环境有关的通量,这表明使用反应性三嵌段三元共聚物可轻松创建功能化膜。进一步研究组成对纳米结构PNS-PLA / PDCPD材料形态的影响后,发现纳米多孔双连续结构在较大的组成范围内形成PVA,并且通过改变PLA嵌段的尺寸可以获得不同的孔径。通过将聚(丙交酯)-b-聚(环辛烯-s-降冰片烯基甲基丙烯酸酯)-b-聚(丙交酯)反应性三嵌段共聚物与多种乙烯基单体交联,证明了将反应性嵌段聚合物扩展至乙烯基交联体系。尽管聚(环辛烯)的柔软性质阻止了由于孔的塌陷而除去聚丙交酯,但是通过交联聚丙交酯-b-聚(苯乙烯-甲基丙烯酸羟乙酯-s-乙二醇二甲基丙烯酸酯)反应性二嵌段,实现了纳米孔乙烯基热固性塑料与苯乙烯和二乙烯基苯的共聚物。

著录项

  • 作者

    Amendt, Mark A.;

  • 作者单位

    University of Minnesota.;

  • 授予单位 University of Minnesota.;
  • 学科 Chemistry Polymer.Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 298 p.
  • 总页数 298
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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