摘要
Emerging contaminants (ECs) such as pharmaceuticals pose increasing threats to aquatic environments and human health. Therefore, it is urgent to develop high-performance nanofiltration (NF) membranes for the efficient removal of ECs. In this work, we present a scalable and energy-efficient strategy for fabricating a novel covalent organic framework (COF)-based NF membrane under mild conditions. The membrane was prepared via electrospinning and subsequent electrostatic assembly, consisting of a porous PAN@TpPa support layer and a precisely deposited TpPa-SO 3 H selective layer. We employed a key interfacial engineering approach, in which protonated TpPa interlayer enhanced electrostatic interactions between layers, thereby forming a dense and negatively charged interface with outstanding long-term stability. The optimized membrane with 72 h TpPa growth time and 30 mg TpPa-SO 3 H loading, achieved a high rejection of 98.89 % for diclofenac sodium (DS) and an excellent permeance of 16.79 L m −2 h −1 ·bar −1 , outperforming commercial NF membranes. Moreover, the PAN@TpPa/TpPa-SO 3 H composite membrane exhibited remarkable long-term stability and superior antifouling performance. Molecular dynamics simulations revealed that the superior separation performance results from the synergistic effects of size sieving and Donnan exclusion. This work provides a mild and scalable interfacial engineering strategy for developing COF-based NF membranes, demonstrating great potential for the effective removal of ECs from wastewater.
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