Tailoring pore size of positively-charged nanofiltration membrane via a facile self-assembly method

Positively-charged nanofiltration (NF) membranes have attracted more attention compared with traditional negative NF membranes. In this work, one-step self-assembly strategy was designed to prepare positively-charged NF separation layer by the close packing of poly(styrene- r -quaternized 2-(dimethylamino)ethyl methacrylate) (P(St- r -QDMA)) nanoparticles (NPs) with intramolecular crosslinking structure. Meanwhile, the pore size of NF membrane was tailored by regulating the aggregation of the NPs using different ions and annealing conditions. Herein, water was used as a dispersant to obtain P(St- r -QDMA) NPs dispersion, which is non-toxic and green. The pore size cut-off (PSCO) of the separation layer is well controlled in the range of 0.98–4.04 nm. The optimal membrane showed molecular weight cut-off (MWCO) of 380 Da (i.e., PSCO, 0.98 nm) with the isoelectric point of 9.4, which effectively improved the separation performance for divalent cations (97.2 % for MgCl 2 and 96.0 % for CaCl 2 ) and neutral small molecules (97.7 % for VB 12 and 92.5 % for PEG400). This work gives a novel and convenient method to construct positively-charged NF membrane with controlled pore sizes, which will be a promising candidate for water softening and molecular separation.