Analysis of Mg2+/Li+ separation mechanism by charged nanofiltration membranes: visual simulation.

The mechanism of the nanofiltration (NF) membrane separation of Mg2+ and Li+ needs to be further investigated, but some commonly used model theories are abstract, which makes them difficult to understand. More importantly, the relationship between the membrane charge and separation performance of Mg2+ and Li+ cannot be quantitatively analyzed. It is worth studying these challenges and providing a performance boost for Mg2+/Li+ filtration applications of NF membranes. Here, various NF membranes, with the membrane volumetric charge density increasing from -4.69 to 7.02 mol · m-3, were fabricated via interfacial polymerization. For these membranes, the separation factor S Mg,Li was decreased from 0.41 to 0.20. Importantly, the visual simulation results were consistent with the experimental results as a whole. The separation factor S Mg,Li decreased with the increase of volumetric charge density, and the minimum separation factor S Mg,Li of the NF membranes was 0.20 (experiment) and 0.17 (simulation), respectively. This meant that the performance of the positively charged NF membrane was not fully developed. Furthermore, we analyzed the relationship between the membrane charge and separation performance, and visualized the simulation of the NF membrane filtration and separation.

Constructing dense and hydrophilic forward osmosis membrane by cross-linking reaction of graphene quantum dots with monomers for enhanced selectivity and stability.

This paper reports a novel thin-film nanocomposite (TFN) membrane with a dense, flat, and hydrophilic polyamide (PA) layer. The atypical PA structure was obtained by the cross-linking reaction of graphene oxide quantum dots containing amino groups (NH2-GOQDs) with triacyl chloride and polyamide oligomers. And the resulting TFN membrane showed a flat (small-scale ridge structure) and smooth surface. Meanwhile, the introduction of oxygen-containing and amino functional groups increased surface hydrophilicity. The reaction of amino groups on the NH2-GOQDs with acid chloride groups and the carboxyl groups (in the linear part of the polyamide) enhanced the degree of cross-linking of the PA layer, forming a compact surface. Owning to the dense surface structure, excellent hydrophilicity, and small water transmission distance, the optimized TFN membrane exhibited an enhanced water flux of 26.57 L⋅m-2⋅h-1 with a low reverse salt flux of 6.0 g⋅m-2⋅h-1. Furthermore, nano-indentation/scratch results showed the interface adhesion between substrate and PA layer was improved due to the physical anchoring of NH2-GOQDs in the substrate. And in the long-term FO test, the TFN membrane showed stable selectivity. This work proves that the targeted structural design of the PA layer at the nanoscale will have a positive impact on desalination field.

In Situ Synthesis of Au Nanoparticles on Viscose Cellulose Sponges for Antibacterial Activities.

Antibacterial viscose cellulose sponges (VCSs) were fabricated by heating cellulose xanthogenate (viscose) containing HAuCl4·nH2O. Viscose was used as the reducing agent and stabilizer for the in situ synthesis of Au nanoparticles (AuNPs) onto the VCSs. The morphology, structures, thermal properties, mechanical performance, and antibacterial activities of the sponges were investigated. Results indicate that AuNPs were uniformly immobilized in the VCSs, and the resulting complexes (AuNPs@VCSs) showed enhanced thermal stability and mechanical properties. Additionally, the AuNPs@VCSs exhibited remarkable antibacterial activities, with zone of inhibition diameter of 35.7 and 37.1 mm for Staphylococcus aureus and Escherichia coli, respectively. The process is simple and applicable at the industrial level and can be applied to the fields of cleaning and sanitation.

Decreased cross-linking in interfacial polymerization and heteromorphic support between nanoparticles: Towards high-water and low-solute flux of hybrid forward osmosis membrane.

Realizing that one main factor affecting development of forward osmosis (FO) membrane was internal concentration polarization (ICP), graphene oxide (GO) with two-dimensional structure and oxidized carbon nanotubes (OCNTs) with one-dimensional structure were linked by oxygen-containing groups to form water channels in the polyamide layer. OCNTs and GO were used for producing reactions among oxygen-containing groups of nanoparticles and polymer chains, and oxygen-containing groups were fully exposed because GO and OCNTs restrained aggregation. Decrease of cross-linking degree for interfacial polymerization layer was confirmed due to reaction from GO/OCNTs/m-phenylene diamine/1,3,5-benzenetricarbonyl trichloride. Moreover, OCNTs formed an appropriate supporting effect for GO to improve hydrophilic properties, which was confirmed by transmission electron microscopy, scanning electron microscope and contact angle. Resulting membrane PA-GO-OCNTs showed high water flux (114 LMH and 84.6 LMH in the PRO (active layer facing draw solution) and FO (active layer facing feed solution) mode, respectively) and low solute flux (5.17 gMH and 3.4 gMH in the PRO and FO mode, respectively) under this condition that 0.5 M NaCl and deionized water were used as draw solution and feed solution respectively. It was worth mentioning that water flux of FO membrane was far higher than that in reported literatures while its structural parameter S was only 203 µm, which led to decrease of ICP.

Manipulating Migration Behavior of Magnetic Graphene Oxide via Magnetic Field Induced Casting and Phase Separation toward High-Performance Hybrid Ultrafiltration Membranes.

Hybrid membranes blended with nanomaterials such as graphene oxide (GO) have great opportunities in water applications due to their multiple functionalities, but they suffer from low modification efficiency of nanomaterials due to the fact that plenty of the nanomaterials are embedded within the polymer matrix during the blending process. Herein, a novel Fe3O4/GO-poly(vinylidene fluoride) (Fe3O4/GO-PVDF) hybrid ultrafiltration membrane was developed via the combination of magnetic field induced casting and a phase inversion technique, during which the Fe3O4/GO nanocomposites could migrate toward the membrane top surface due to magnetic attraction and thereby render the surface highly hydrophilic with robust resistance to fouling. The blended Fe3O4/GO nanocomposites migrated to the membrane surface with the magnetic field induced casting, as verified by X-ray photoelectron spectroscopy, elemental analysis, and energy dispersive X-ray spectroscopy. As a result, the novel membranes exhibited significantly improved hydrophilicity (with a contact angle of 55.0°) and water flux (up to 595.39 L m(-2) h(-1)), which were improved by 26% and 206%, 12% and 49%, 25% and 154%, and 11% and 33% compared with those of pristine PVDF membranes and PVDF hybrid membranes blended with GO, Fe3O4, and Fe3O4/GO without the assistance of magnetic field during membrane casting, respectively. Besides, the novel membranes showed high rejection of bovine serum albumin (>92%) and high flux recovery ratio (up to 86.4%). Therefore, this study presents a novel strategy for developing high-performance hybrid membranes via manipulating the migration of nanomaterials to the membrane surface rather than embedding them in the membrane matrix.