The worldwide water crisis and water pollution have put forward great challenges to the current membrane technology. Although poly(vinylidene fluoride) (PVDF) porous membranes can find diverse applications for water treatments, the inherent hydrophilicity must be tuned for an energy-/time-saving process. Herein, the surface wettability of PVDF membranes transforming from highly hydrophobicity to highly hydrophilicity was realized via one-step reaction of plant-derived phenol gallic acid and γ-aminopropyltriethoxysilane in aqueous solutions. The surface hydrophilicization can be achieved on porous PVDF membranes by virtue of integration of a mussel-inspired coating and in situ silicification via a "pyrogallol-amino covalent bridge" toward excellent antifouling performance and highly efficient infiltration ability for oily emulsion and protein wastewater treatment. The water flux of a surface-manipulated microfiltration membrane can reach ca. 9246 L m h (54-fold increment compared to that of pristine membrane), oil rejection >99.5% in a three-cycle emulsion separation; the modified ultrafiltration membrane demonstrated benign performance in bovine serum albumin protein interception (rejection as high as ca. 96.6% with water flux of ca. 278.2 L m h) and antifouling potential (increase of ca. 70.8%). Our in situ biomimetic silicification under "green" conditions exhibits the great potential of the developed strategy in fabrication of similar multifunctional membranes toward environmental remediation.

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As increasing demand for hemodialysis (HD) treatment incurs significant financial burden to healthcare systems and ecological burden as well, novel therapeutic approaches as well as innovations and technological advances are being sought that could lead to the development of purification devices such as dialyzers with improved characteristics and wearable technology. Novel knowledge such as the development of more accurate kinetic models, the development of novel HD membranes with the use of nanotechnology, novel manufacturing processes, and the latest technology in the science of materials have enabled novel solutions already marketed or on the verge of becoming commercially available. This collaborative article reviews the latest advances in HD as they were presented by the authors in a recent symposium titled “Frontiers in Haemodialysis,” held on 12th December 2019 at the Royal Society of Medicine in London.

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Inorganic-polymer hybrid, thinfilm nanocomposite nanofiltration (TFN-NF) membranes prepared by in situ interfacial polymerization of branched polyethyleneimine and trimesoyl chloride, with simultaneous impregnation of as-synthesized hexagonal wurtzite ZnO nanocrystals (nano-ZnO), either through aqueous or organic phase, have been extensively characterized. XPS analysis revealed that there was no inter-atomic charge transfer between nano-ZnO and host polyamide matrix, indicating that no formation of chemical bonding occurred between them in the skin layers of the membranes. The type of interaction present within the nanocomposite polyamide matrices of the membranes was through formation of noncovalent type secondary chemical interactions with peripheral hydroxyl groups of nano-ZnO and polyamide network as substantiated through FTIR analysis. SEM revealed the formation of distinct patterns and coils, through multiple-point interactions between the nano-ZnO and the polyamide network in the membranes' skin surfaces when introduced through aqueous amine phase.However, when introduced through the organic phase, nanomaterials remained distributed as discrete clusters within the membranes' skin layers because of lack of polar environment around the reaction zone, further emphasizing the role of the medium in which the nanomaterials are incorporated. AFM showed variation of surface roughness features with change in the precursor medium of introduced nano-ZnO. Nanofiltration performance towards different solutes, providing differential rejections in the order of MgCl 2 > NaCl $ Na 2 SO 4 , revealed that the membranes were distinctly positively charged.Solvent fluxes of the membranes were significantly higher when nanomaterials were introduced through the aqueous phase as compared to the organic phase.

The salient features of a nanostructured carbonaceous material like graphene or graphene oxide have provided innovative alternatives for the development of nanocomposite membranes with better selectivity without having a compromise in throughput, which as a result have a promising role to play in desalination and water purification. Here, nanostructured reduced graphene oxide (nRGO) is synthesized from graphite powder and characterized. Using non-solvent induced phase inversion technique, a series of nanocomposite ultrafiltration (UF) membranes are developed by in situ impregnation of the as synthesized nRGO in polysulfone (Ps) polymer matrix with variation of nRGO from 1 to 8 w/w%. The physicochemical features and transport properties offered by the membranes are evaluated. Structural characterization of the Ps-nRGO composite UF membranes is done by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. The variation in porous morphology of the membranes upon impregnation of nRGO is evaluated by scanning electron microscopy. Variation in skin surface topography is analyzed by atomic force microscopy. The change in surface hydrophilicity is evaluated by contact angle studies. The thermal and mechanical properties of the membranes are assessed by thermogravimetric analysis and tensile strength measurements, respectively. The studies reveal that an optimum loading of nRGO (2 w/w%) in the Ps matrix resulted in membranes with elimination of the trade-off between the flux and selectivity that exists with the conventional UF membranes. In addition, the optimum loading of nRGO resulted in membranes with improved thermal and mechanical stability. Thus, nRGO as an emerging potential nanofiller can lead to the development of an ideal membrane with desirable attributes.

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