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    磺酸基共价有机框架纳米片中间层介导的聚酰胺纳滤膜

    Polyamide Nanofiltration Membranes by Sulfonated Covalent Organic Framework Nanosheet Interlayer

    • 摘要: 针对传统聚酰胺(PA)纳滤膜界面聚合(IP)过程难以精准调控,导致膜层厚度失控及“渗透-选择”权衡的问题,提出利用富含磺酸基且具有有序孔道的共价有机框架(COF)纳米片作为功能化中间层制备高性能纳滤膜。基于形貌与结构的演变推测,磺酸基COF纳米片中间层的功能基团可以均匀化富集哌嗪(PIP)单体、限域孔道可以缓解PIP的传质动力学,从而调控界面聚合过程、诱导形成具有细密结节形貌、高交联度(72.73%)且超薄(< 30 nm)的PA活性层。实验结果表明,在5 μg·cm−2的最佳沉积量下,磺酸基COF纳米片中间层调控的膜的通量达44.3 L·m−2·h−1·bar−1,较对照组PA膜提升3倍以上,同时对Na2SO4保持96.2%的高截留率。此外,该膜表现出优异的抗压实性能与长期运行稳定性。本研究为利用功能化COF介导界面聚合制备新一代高渗透纳滤膜提供了支撑。

       

      Abstract: To address uncontrollable layer thickness and "permeability-selectivity" trade-off in traditional interfacial polymerization (IP) process for polyamide (PA) nanofiltration membranes, sulfonated covalent organic framework (COF) nanosheets with ordered nanochannels were used as functionalized interlayers to prepare high-performance nanofiltration membranes. Based on the morphological and structural evolution, the functional groups within the sulfonated COF nanosheet interlayer could uniformly enrich piperazine (PIP) monomers, while its confined nanochannels could mitigate piperazine (PIP) transport kinetics. This synergy effectively regulated the IP process, inducing an ultra-thin (<30 nm) PA layer with finely nodular morphology and high cross-linking degree (72.73%). At 5 μg·cm−2 loading, the PAN-COF-PA membrane achieved 44.3 L·m−2·h−1·bar−1 water permeability (3-fold increase over PAN-PA) and 96.2% Na2SO4 rejection. The membrane showed excellent compact resistance and long-term stability. This COF-mediated interfacial polymerization provides a strategy for fabricating next-generation high-permeability nanofiltration membranes.

       

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