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Thin film nanocomposite (TFN) polyamide (PA) membranes has drawn increasing attention due to the improved physicochemical properties of the top layer for versatile separation performance. However, the commonly used fabrication approach, lacking a controllable loading of nanofillers, leads to a random and insufficient distribution of nanofillers into the PA layer and generates interfacial defects that deteriorate the membrane performance. Herein, a rational strategy for incorporating metal-organic frameworks (i.e., ZIF-8) into the PA layer via electrophoretic deposition (EPD) was proposed. Driven by an external direct current field, the ZIF-8 nanoparticles were uniformly assembled onto a porous ultrafiltration (UF) substrate for fabrication of high-performance TFN nanofiltration membranes by vacuum-assisted interfacial polymerization (IP). The resultant TFN nanofiltration membrane yielded an enhanced water permeability of 22.4 ± 1.2 L⋅m− 2 ⋅h− 1 ⋅bar− 1, due to incorporation of ZIF-8 nanoparticles which created extra nano-channels for fast water permeation. Additionally, such an EPD process effectively tailored the membrane surface properties (e.g., zeta potential) and conferred a considerably high rejection for Na2SO4 (96.9 ± 0.7%) but a low rejection for NaCl (18.9 ± 2.5%), semonstrating an excellent selectivity between SO4 2− and Cl− ions. This study highlights the impressive efficacy of the EPD process in precisely anchoring nanomaterials to design high-performance TFN nanofiltration membranes for target separations.

Designing a stable and uniform hydrophilic material for separation of oil and water is strongly desired for sustainable management of oily wastewater. Herein, a stable and uniform bio-inspired coating onto the non-woven fabric substrate with superhydrophilicity and underwater superoleophobicity via rapid co-deposition of dopamine and polyethylenimine was demonstrated. Ammonium persulfate outperformed other oxidants (e.g., Cu2+-H2O2 and NaIO4) to rapidly trigger the co-deposition of dopamine and polyethylenimine for homogeneous superhydrophilic and underwater superoleophobic surface engineering. Furthermore, the co-deposition conditions, i.e., concentration of ammonium persulfate and exposure duration, have a positive dependence on the hydrophilicity and underwater oleophobicity of the coated fabric membranes. Specifically, the superhydrophilicity and underwater superoleophobicity (underwater oil contact angle of 165.4 ± 1.1°, sliding angle of 2.5 ± 0.5°) can be obtained for the coated fabric membranes at the optimal co-deposition condition (i.e., 28.5 mmol L- 1 persulfate and coating duration of 7 h), showing a great potential in gravitational oil-water separation (permeation flux >115,000 L m-2 h-1; oil rejection >99.2%). Integrating with a superhydrophobic copper mesh, the oil-water mixed solution can be continuously and sufficiently separated, realizing simultaneous recovery of pure oil and water from oily wastewater. In addition, the bio-inspired coating displays a strong long-term chemical robustness and stability in extreme environments (i.e., acidic/alkaline solutions and oils). The study provides a facile, cost-effective and practical strategy in constructing superhydrophilic and underwater superoleophobic interfaces for sustainable treatment of oily wastewater.