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A Facile and Scalable Fabrication Procedure for Thin-Film Composite Membranes: Integration of Phase Inversion and Interfacial Polymerization

机译:薄膜复合膜的一种简便,可扩展的制备程序:相转化和界面聚合的集成

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摘要

Conventional dense thin-film composite (TFC) membranes evince a universally low water permeability,the increase of which typically relies on introducing additional transport channels based on intricate steps within a membrane preparation process.In this study,we reported a novel and simplified procedure for the fabrication of high-performance TFC membranes.Specifically,the dissolution of aqueous monomers in the casting solution was utilized for the following interfacial polymerization (IP).Since the monomers diffused to the water bath during phase inversion,the control of precipitation time enabled an effective regulation of the monomer concentration in the formed polymeric substrates,where the IP reaction was initiated by the addition of the organic phase.The entire and uniform embedment of aqueous monomers inside the substrates contributed to the formation of ultrathin and smooth selective layers.An excellent separation performance (i.e.,water permeability: 34.7 L m~(-2) h~(-1) bar~(-1); Na_2SO_4 rejection: ~96%) could be attained using two types of aqueous monomers (i.e.,piperazine and β-cyclodextrin),demonstrating the effectiveness and universality of this method.Compared to the conventional immersion-based process,this novel procedure shows distinct advantages in reducing monomer usage,shortening the production cycle,and achieving a more superior membrane performance,which is highly promising for large-scale membrane manufacture.
机译:常规的致密薄膜复合(TFC)膜普遍具有较低的水渗透性,其渗透率的提高通常取决于在膜制备过程中基于复杂步骤引入额外的运输通道。在这项研究中,我们报道了一种新颖且简化的方法具体而言,利用流延单体在浇铸溶液中的溶解进行后续的界面聚合(IP)。由于单体在相转化过程中扩散到水浴中,因此沉淀时间的控制可以实现有效调节所形成的聚合物基材中的单体浓度,其中IP反应是通过添加有机相而引发的。水性单体在基材中完全均匀地包埋有助于形成超薄而光滑的选择性层。分离性能(即水渗透率:34.7 L m〜(-2)h〜(-1)bar〜( -1);使用两种类型的水性单体(哌嗪和β-环糊精)可以达到Na_2SO_4截留率(〜96%),证明了该方法的有效性和通用性。与传统的基于浸没的方法相比,该新方法显示出明显的优势在减少单体用量,缩短生产周期和获得更优异的膜性能方面,这对于大规模的膜生产具有很高的希望。

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  • 来源
    《Environmental Science & Technology》 |2020年第3期|1946-1954|共9页
  • 作者单位

    State Key Joint Laboratory of Environment Simulation and Pollution Control School of Environment Tsinghua University Beijing 100084 China Department of Chemical Engineering KU Leuven Leuven B-3001 Belgium;

    School of Chemical Engineering and Energy Zhengzhou University Zhengzhou 450001 China Department of Chemical Engineering KU Leuven Leuven B-3001 Belgium;

    Department of Chemical Engineering KU Leuven Leuven B-3001 Belgium;

    State Key Joint Laboratory of Environment Simulation and Pollution Control School of Environment Tsinghua University Beijing 100084 China;

    School of Chemical Engineering and Energy Zhengzhou University Zhengzhou 450001 China;

    State Key joint Laboratory of Environment Simulation and Pollution Control School of Environment Tsinghua University Beijing 100084 China;

    Department of Chemical Engineering KU Leuvm Leuven B-3001 Belgium Faculty of Engineering and the Built Environment Tshwane University of Technology Pretoria 0001 South Africa;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-18 05:15:08

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