Abstract

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%), demonstrating an excellent selectivity between SO42− 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.

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