摘要
Membrane fouling, particularly that induced by microbial and organic contaminants, severely limits the efficiency and lifespan of reverse osmosis (RO) membranes in surface water treatment. Herein, a sequential covalent post-modification strategy is developed by exploiting the native carboxyl groups of a commercial RO membrane to fabricate a novel dual-defense RO membrane. Specifically, sulfaguanidine (SG) and poly(glycidyl methacrylate- co -sulfobetaine methacrylate) (PGS) are sequentially immobilized on the polyamide layer via amidation and epoxy ring-opening reactions, with SG and PGS serving as the bactericidal and antifouling components, respectively. Benefiting from this interfacial structure, the resulting membrane (ROSP) achieves a 2.4-fold higher water flux of 34.04 L·m −2 ·h −1 than that of the pristine membrane while maintaining a high NaCl rejection of 98.47%. Furthermore, the ROSP membrane exhibits low irreversible fouling ratios (< 8.27%) during 11 h cyclic fouling filtration tests, displays over 99% bactericidal efficiency against both E. coli and S. aureus , and enhances the tolerated chlorine exposure by 42.9% to 10,000 ppm·h. More importantly, during 144 h of continuous filtration using real surface water, the ROSP membrane maintains stable separation performance and a bactericidal efficiency of 92.63% against native microorganisms. This work offers an effective covalent surface-modification strategy for developing durable RO membranes for surface water treatment.
危险品化学品经营许可证(带存储)