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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 Na 2 SO 4 (96.9 ± 0.7%) but a low rejection for NaCl (18.9 ± 2.5%), demonstrating an excellent selectivity between SO 4 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. [Display omitted] • Electrophoretic deposition (EPD) is used to assemble ZIF-8 into polyamide membrane. • Uniform and sufficient assembly of ZIF-8 is achieved by precisely controlling the ageing and EPD times. • Uniform ZIF-8 assembly into the polyamide layer creates extra nano-channels for enhanced flux. • ZIF-8 assembly by EPD tailors the surface charge of TFN membranes, yielding an enhanced selectivity between SO 4 2− and Cl−. [ABSTRACT FROM AUTHOR]

[Display omitted] • Rapid co-deposition of dopamine and APTS was used to construct superhydrophilic membranes. • Superhydrophilic membrane had an effective oil repellency with underwater oil contact angle of ∼163.5°. • Superhydrophilic membrane has a fast gravity-driven filtration for oil-in-water emulsions with a separation efficiency of >99.9 % • Incorporation of Cu NPs and polydopamine enables the membranes with complete antibacterial activity. Substantial discharge of industrial oily wastewater calls for an efficient and sustainable treatment for resource recovery. Superwetting membranes offer a feasible approach to fractionate oil species and water from oily wastewater for addressing this technical challenge. In this study, we proposed a useful strategy for constructing a superhydrophilic membrane with superior antibacterial properties through rapid co-deposition of dopamine and 3-aminopropyltriethoxysilane (APTS) initiated by ammonium persulfate on the Cu nanoparticles-loaded porous PVDF substrate. The resultant superhydrophilic membrane yielded an underwater oil contact angle of 163.5°, enabling a fast and robust gravity-driven filtration for various oil-in-water emulsions with a separation efficiency of >99.9 %. Additionally, incorporating of Cu nanoparticles and polydopamine endowed the superhydrophilic membrane with superior antibacterial activity (100 % inhibition efficiency against Escherichia coli), and thereby remarkably enhancing the anti-biofouling performance. This study provides a viable approach to design high-performance membranes for separation of oil-in-water emulsions, with promising applications in the industrial and environmental sectors. [ABSTRACT FROM AUTHOR]

• Tight UF membrane with 1700 Da MWCO was designed by rapid co-deposition of PDA/PEI triggered by APS. • Tight UF membrane had an impressive rejection of >98.2% for 6 reactive dyes with >97.0% salt permeation. • Integrated UF-diafiltration enriched reactive blue 4 from 2.04 to 50.70 g·L−1 with 0.9% dye loss. • 99.95% salt removal was obtained by integrated UF-diafiltration with 8 diavolumes. • Tight UF membrane yielded a 90.6% flux recovery by water rinsing, showing a low fouling propensity. Mussel-inspired polydopamine (PDA) coating has received increasing interest in membrane modification for versatile liquid filtration applications, due to its intrinsic adhesion nature. Nevertheless, the bio-inspired PDA deposition initiated by air-oxidation is time-consuming process and generally results in an uneven and unstable coating, which compromises the membrane filtration performance. In this study, the PDA/polyethylenimine (PEI) co-deposition triggered by ammonium persulfate (APS) was conducted to fabricate the tight ultrafiltration (t-UF) membranes with 1000–5000 Da molecular weight cut-offs (MWCOs) for sustainable treatment of highly-saline textile wastewater. APS with strong oxidation capacity can rapidly induce the co-deposition of PDA/PEI layer onto hydrolyzed polyacrylonitrile (HPAN) substrate through the Michael addition or Schiff base reactions, simultaneously minimizing the covalent polymerization of dopamine for PDA aggregation. With 1.5-h coating, a smooth, compact and defect-free PDA/PEI layer with 1700 Da MWCO was evolved on the HPAN substrate, evincing a >98.2% retention for various reactive dyes (610–1000 Da molecular weights) with >97.0% permeation of inorganic salts. In addition, an integrated UF-diafiltration procedure was applied to fractionate the reactive blue 4 (RB4)/NaCl and RB4/Na 2 SO 4 mixtures, enriching the RB4 dye from ca. 2.04 to 50.70 g·L−1 with ca. 99.95% desalination efficiency and ca. 99.2% dye recovery. These results demonstrate that the bio-inspired t-UF membrane through fast PDA/PEI co-deposition is of great promise to sufficiently fractionate the dyes and salts for dye desalination and recovery, realizing the sustainable management of highly-saline textile wastewater. [ABSTRACT FROM AUTHOR]