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Polymer nanofilms with enhanced microporosity by interfacial polymerization

机译:通过界面聚合提高微孔性的聚合物纳米薄膜

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摘要

Highly permeable and selective membranes are desirable for energy-efficient gas and liquid separations. Microporous organic polymers have attracted significant attention in this respect owing to their high porosity, permeability and molecular selectivity. However, it remains challenging to fabricate selective polymer membranes with controlled microporosity that are stable in solvents. Here we report a new approach to designing crosslinked, rigid polymer nanofilms with enhanced microporosity by manipulating the molecular structure. Ultrathin polyarylate nanofilms with thickness down to 20 nm are formed in situ by interfacial polymerization. Enhanced microporosity and higher interconnectivity of intermolecular network voids, as rationalized by molecular simulations, are achieved by using contorted monomers for the interfacial polymerization. Composite membranes comprising polyarylate nanofilms with enhanced microporosity fabricated in situ on crosslinked polyimide ultrafiltration membranes show outstanding separation performance in organic solvents, with up to two orders of magnitude higher solvent permeance than membranes fabricated with nanofilms made from non-contorted planar monomers.
机译:对于高能效的气体和液体分离,需要高渗透性和选择性的膜。微孔有机聚合物由于其高孔隙率,渗透性和分子选择性而在这方面引起了极大的关注。然而,制造在溶剂中稳定的具有受控的微孔率的选择性聚合物膜仍然具有挑战性。在这里,我们报告了一种通过操纵分子结构来设计具有增强的微孔性的交联的刚性聚合物纳米膜的新方法。通过界面聚合原位形成厚度低至20nm的超薄聚芳酯纳米膜。通过使用扭曲的单体进行界面聚合,可以实现分子模拟网络合理化的增强的微孔性和分子间网络空隙的更高互连性。在交联的聚酰亚胺超滤膜上原位制备的包含具有增强的微孔性的聚芳酯纳米膜的复合膜在有机溶剂中表现出出色的分离性能,其溶剂渗透性比由非扭曲平面单体制备的纳米膜制备的膜高多达两个数量级。

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  • 来源
    《Nature Materials》 |2016年第7期|760-767|共8页
  • 作者单位

    Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK;

    Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK;

    Department of Chemistry, Imperial College London, London SW7 2AZ, UK;

    Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK;

    Department of Chemical Engineering, Imperial College London, London SW7 2AZ, UK;

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