Ultrahigh Water Permeance of Reduced Graphene Oxide Membrane for Radioactive Liquid Waste Treatment

Membrane methods exhibit great potential for application in radioactive liquid waste treatment. In this work, we prepared a reduced graphene oxide using the amino-hydrothermal method (AH-rGO) that exhibited effective rejection rates of 99.9% for CoCl2, ZnCl2, NiCl2, and radionuclide 60Co solutions with an ultrahigh water permeance of >71.9 L m−2 h−1 bar−1. The thickness of the AH-rGO membranes affects the water permeance, as the membrane with a thickness of ≈250 nm has the highest water permeance of up to 125.1 L m−2 h−1 bar−1 with the corresponding rejection rate of 86.8%. Importantly, this is the most permeable membrane with a satisfactory level of the rejection rate for typical radioactive ions of Co2+, Zn2+, and Ni2+. Moreover, the AH-rGO membranes presented excellent stability. These findings demonstrate the potential of reduced graphene oxide (rGO) membranes for radioactive liquid waste treatment.

MoS2-Cysteine Nanofiltration Membrane for Lead Removal

To overcome the limitations of polymers, such as the trade-off relationship between water permeance and solute rejection, as well as the difficulty of functionalization, research on nanomaterials is being actively conducted. One of the representative nanomaterials is graphene, which has a two-dimensional shape and chemical tunability. Graphene is usually used in the form of graphene oxide in the water treatment field because it has advantages such as high water permeance and functionality on its surface. However, there is a problem in that it lacks physical stability under water-contacted conditions due to the high hydrophilicity. To overcome this problem, MoS2, which has a similar shape to graphene and hydrophobicity, can be a new option. In this study, bulk MoS2 was dispersed in a mixed solvent of acetone/isopropyl alcohol, and MoS2 nanosheet was obtained by applying sonic energy to exfoliate. In addition, Cysteine was functionalized in MoS2 with a mild reaction. When the nanofiltration (NF) performance of the membrane was compared under various conditions, the composite membrane incorporated by Cysteine 10 wt % (vs. MoS2) showed the best NF performances.

Alginate Hydrogel Assisted Controllable Interfacial Polymerization for High-Performance Nanofiltration Membranes

The deepening crisis of freshwater resources has been driving the further development of new types of membrane-based desalination technologies represented by nanofiltration membranes. Solving the existing trade-off limitation on enhancing the water permeance and the rejection of salts is currently one of the most concerned research interests. Here, a facile and scalable approach is proposed to tune the interfacial polymerization by constructing a calcium alginate hydrogel layer on the porous substrates. The evenly coated thin hydrogel layer can not only store amine monomers like the aqueous phase but also suppress the diffusion of amine monomers inside, as well as provide a flat and stable interface to implement the interfacial polymerization. The resultant polyamide nanofilms have a relatively smooth morphology, negatively charged surface, and reduced thickness which facilitate a fast water permeation while maintaining rejection efficiency. As a result, the as-prepared composite membranes show improved water permeance (~30 Lm−2h−1bar−1) and comparable rejection of Na2SO4 (>97%) in practical applications. It is proved to be a feasible approach to manufacturing high-performance nanofiltration membranes with the assist of alginate hydrogel regulating interfacial polymerization.