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Functional aligned porous materials via directional freezing and frozen UV initiated polymerization

机译:通过定向冻结和冻结紫外线引发的聚合功能排列多孔材料

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摘要

The work in this thesis is split into three experimental chapters: The first section involves the development of the directional freezing and frozen polymerization method to prepare crosslinked aligned porous polymers with improved mechanical stability. Monomer solutions were directionally frozen in liquid nitrogen to orientate the growth of solvent crystals and the frozen samples are polymerized by UV irradiation. The solvent is removed under vacuum at room temperature to produce aligned porous structure. The mechanical stability is improved by two orders of magnitude compared to the usually freeze-dried porous materials. The materials are modified with graphene and a conducting polymer to make conducting monoliths, whilst maintaining the aligned porous structure. The aligned porous monolith is also assessed by high performance liquid chromatography (HPLC), showing fast separation of hydrocarbon compounds with low back-pressure. The second section uses directional freezing and frozen UV initiated polymerization to prepare aligned porous stimuli-responsive hydrogels. Oligo-ethylene glycol methacrylates and dimethylamino ethyl methacrylate monomers were used to produce temperature and pH-responsive hydrogels respectively. Aligned porous morphologies are observed in both dry and hydrated states. The hydrogels exhibit stimuli-responsive behaviour in aqueous conditions and anisotropic compressive strength and diffusion behaviour with respect to freezing direction. Section three uses directional freezing and frozen UV polymerization method to prepare aligned porous monoliths containing silica. The surface of the materials was post-functionalized to make two different types of aligned porous composites. Hydrothermal synthesis using Teflon lined autoclaves was used to functionalize monoliths separately with silver and metal organic frameworks (MOFs). The MOF composite materials were used as a stationary phase to try and separate a mixture of organic compounds.
机译:本文的工作分为三个实验部分:第一部分涉及定向冷冻和冷冻聚合方法的发展,以制备具有改善的机械稳定性的交联排列的多孔聚合物。将单体溶液在液氮中定向冷冻,以定向溶剂晶体的生长,并通过紫外线照射使冷冻的样品聚合。在室温下真空除去溶剂以产生排列的多孔结构。与通常的冻干多孔材料相比,机械稳定性提高了两个数量级。用石墨烯和导电聚合物对材料进行改性,以制成导电单块,同时保持对齐的多孔结构。对齐的多孔整料还通过高效液相色谱(HPLC)进行了评估,显示出烃类化合物的快速分离和低背压。第二部分使用定向冷冻和冷冻紫外线引发的聚合反应制备取向的多孔刺激响应水凝胶。甲基丙烯酸低聚乙二醇酯和甲基丙烯酸二甲基氨基乙基酯单体分别用于生产温度和pH响应水凝胶。在干燥和水合状态下均观察到排列的多孔形态。水凝胶在水性条件下表现出刺激响应行为,并且相对于冰冻方向表现出各向异性的抗压强度和扩散行为。第三部分使用定向冷冻和冷冻UV聚合方法制备了对齐的,含有二氧化硅的多孔整料。将材料表面进行后功能处理,以制造两种不同类型的对齐多孔复合材料。使用衬有特氟隆的高压釜进行水热合成,分别利用银和金属有机骨架(MOF)对整体结构进行功能化。 MOF复合材料用作固定相,以尝试分离有机化合物的混合物。

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    Barrow M;

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  • 年度 2000
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