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It is challenging to effectively purge wastewater containing heavy metal ions at low concentration. In order to remove trace Cr (VI) from wastewater efficiently, a positively charged microporous membrane was prepared by firstly non-solvent induced phase separation (NIPS) of amphiphilic polymer and secondly surface quaternization modification. The morphologies, surface roughness, surface charge, hydrophilicity, and pore size of membranes were characterized. Based on the dual action of micellar adsorption and charge repulsion, when surfactant is 4 mM and Cr (VI) is 60 ppm, the surface quaternization membrane (Q-MPVD) achieves 99.8 % Cr (VI) rejection simultaneously accompanied by a permeability of 100 LMH/bar. Meanwhile, the effects of STAC concentration, Cr (VI) concentration, pH as well as inorganic salt concentration on the composite micellar size, and Cr (VI) rejection performance were investigated, respectively. Moreover, the Q-MPVD membrane shows an excellent separation stability over a wide pH range, indicating its application perspective in engineering process. In summary, this work provided a positively charged membrane with high-efficiency performance for treating practical trace Cr (VI)-containing industrial wastewater.

Separating low/high-valent ions with sub-nanometer sizes is a crucial yet challenging task in various areas (e.g., within environmental, healthcare, chemical, and energy engineering). Satisfying high separation precision requires membranes with exceptionally high selectivity. One way to realize this is constructing well-designed ion-selective nanochannels in pressure-driven membranes where the separation mechanism relies on combined steric, dielectric exclusion, and Donnan effects. To this aim, charged nanochannels in polyamide (PA) membranes are created by incorporating ionic polyamidoamine (PAMAM) dendrimers viainterfacial polymerization. Both sub-10 nm sizes of the ionic PAMAM dendrimer molecules and their gradient distributions in the PA nanofilms contribute to the successful formation of defect-free PA nanofilms, containing both internal (intramolecular voids) and external (interfacial voids between the ionic PAMAM dendrimers and the PA matrix) nanochannels for fast transport of water molecules. The external nanochannels with tunable ionizable groups endow the PA membranes with both high low/high-valent co-ion selectivity and chemical cleaning tolerance, while the ion sieving/transport mechanism was analyzed by employing the Donnan steric pore model with dielectric exclusion.

High-efficiency dye desalination is crucial in the textile industry, considering its importance for human health, safe aquatic ecological systems, and resource recovery. In order to solve the problem of effective separation of univalent salt and ionic dye under the condition of high salt, ionic hyperbranched poly(amido-amine) (HBPs) were synthesized based on a simple and scalable one-step polycondensation method and then incorporated into the polyamide (PA) selective layers to construct charged nanochannels through interfacial polymerization (IP) on the surface of a polyvinyl chloride ultrafiltration (PVC-UF) hollow fiber membrane. Both the internal nanopores of HBPs (internal nanochannels) and the interfacial voids between HBPs and the PA matrix (external nanochannels) can be regarded as a fast water molecule transport pathway, while the terminal ionic groups of ionic HBPs endow the nanochannels with charge characteristics for improving ionic dye/salt selectivities. The permeate fluxes and dye/salt selectivities of HBP-TAC/PIP (57.3 L m–2h–1and rhodamine B (RB)/NaCl selectivity of 224.0) and HBP-PS/PIP (63.7 L m–2h–1and lemon yellow (LY)/NaCl selectivity of 664.0) membranes under 0.4 MPa operation pressure are much higher than PIP-only and HBP-NH2/PIP membranes. At the same time, this project also studied the membrane desalination process in a simulated high-salinity dye/salt mixture system to provide a theoretical basis and technical support for the actual dye desalination process.