There is an urgent need for the development of sustainable transformation of today's membrane distillation approaches into a greener way.

Membrane distillation (MD) is a promising technology for seawater desalination due to the ability to process high-salinity waters and the ability to be driven by low-grade or waste heat. However, practical applications of MD membranes are limited by the low vapor flux and fouling problem. Recently, there is a growing interest in developing novel MD membrane materials with enhanced hydrophobicity to improve the efficiency of desalination performance. Interestingly, the incorporation of nanomaterials for tailoring superhydrophobic properties of MD membranes has attracted enormous attention in MD. Herein, according to the new insights of the available literature data, the current trend for achieving superhydrophobic MD membranes by embedding inorganic nanomaterials is provided. The influence of the inorganic additives on membrane fouling, stability, separation performance, is also discussed. Finally, theoretical principles of MD, the milestones of the evolution of developing superhydrophobic membrane surfaces, and future trends are also given for the new readers in the field. Graphical Abstract

Seawater desalination is a worldwide concern for the sustainable production of drinking water. In this regard, membrane distillation (MD) has shown the potential for effective brine treatment. However, the lack of appropriate MD membranes limits its industrial expansion since they experience fouling and wetting issues. Therefore, hydrophobic membranes are promising candidates to successfully deal with such phenomena that are typical for commercially available membranes. Here, several graphene/polyvinylidene (PVDF_G) membranes with different graphene loading (0–10 wt%) were prepared through a phase inversion method. After full characterization of the resulting membranes, the surface revealed that the well-dispersed graphene in the polymer matrix (0.33 and 0.5 wt% graphene loading) led to excellent water repellence together with a rough structure, and a large effective surface area. Importantly, antifungal activity tests of films indicated an increase in the inhibition percentage for PVDF_G membranes against the Curvularia sp. fungal strain. However, the antifungal surface properties were found to be the synergistic result of graphene toxicity and surface topography.

The prevalence of the antibiotic resistant bacteria remains a global issue. Cheap, sustainable and multifunctional antibacterial membranes are at the forefront of filtrating materials capable of treating multiple flow streams, such as water cleansing treatments. Carbon nanomaterials are particularly interesting objects shown to enhance antibacterial properties of composite materials. In this article, amino-functionalized, photoluminescent carbon nanodots (CNDs) were synthesized from chitosan by bottom-up approach via simple and green hydrothermal carbonization. A chemical model for the CNDs formation during hydrothermal treatment of chitosan is proposed. The use of urea as an additional nitrogen source leads to the consumption of hydroxyl groups of chitosan and higher nitrogen doping level as pyridinic and pyrrolic N-bonding configurations in the final carbonaceous composition. These functionalized carbon nanodots that consist of carbon core and various surface functional groups were used to modify the commercially available membranes in order to enhance their anti-biofouling properties and add possible functionalities, including fluorescent labelling. Incorporation of CNDs to membranes increased their hydrophilicity, surface charge without compromising membranes integrity, thereby increasing the factors affecting bacterial wall disruption. Membranes modified with CNDs effectively stopped the growth of two Gram-negative bacterial colonies: Klebsiella oxytoca (K. oxytoca) and Pseudomonas aeruginosa (P. aeruginosa).

Graphene-coated membranes for membrane distillation have been fabricated by using a wet-filtration approach. Graphene nanoplatelets have been deposited onto PVDF membrane surfaces. Morphology and physicochemical properties have been explored to evaluate the changes in the surface topography and related effects on the membrane performance in water desalination. The membranes have been tested in membrane distillation plants by using mixtures of sodium chloride and humic acid. The multi-scale rough structure of the surface has been envisaged to amplify the wetting and fouling resistance of the graphene-coated membranes so that a better flux and full salt rejection have been achieved in comparison with pristine PVDF. Total salt rejection and an increase of 77% in flux have been observed for coated membrane with optimized graphene content when worked with NaCl 0.6 M (DCMD, ΔT ≈ 24 °C) over a test period of 6 h. The experimental findings suggest these novel graphene-coated membranes as promising materials to develop functional membranes for high-performing water desalination.