Effect of the Incorporation of ZIF-8@GO into the Thin-Film Membrane on Salt Rejection and BSA Fouling.

A series of Zeolitic imidazole framework-8 (ZIF-8) clusters supported on graphene oxide (ZIF-8@GO) nanocomposites were prepared by varying the ratios of ZIF-8 to GO. The resultant nanocomposites were characterized using various techniques, such as Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), thermogravimetric analysis (TGA), Fourier Transform Infrared (FTIR) and Raman spectroscopy. These nanocomposites were incorporated into the thin film layer during interfacial polymerisation process of m-phenylenediamine (aqueous phase which contained the dispersed nanocomposites) and trimesoyl chloride (TMC, organic phase) at room temperature onto polyethersulfone (PES) ultrafiltration (UF) support membrane. The membrane surface morphology, cross section and surface roughness were characterized using SEM and AFM, respectively. Compared to the baseline membranes, the thin film nanofiltration (TFN) membranes exhibited improved pure water flux (from 1.66 up to 7.9 L.m-2h-1), salt rejection (from 40 to 98%) and fouling resistance (33 to 88%). Optimum ZIF-8 to GO ratio was established as indicated in observed pure water flux, salt rejection and BSA fouling resistance. Therefore, a balance in hydrophilic and porous effect of the filler was observed to lead to this observed membrane behaviour suggesting that careful filler design can result in performance gain for thin film composite (TFC) membranes for water treatment application.

Mussel-inspired tannic acid/polyethyleneimine assembling positively-charged membranes with excellent cation permselectivity.

The extraction of valuable target ions through monovalent cation exchange membranes (MCEMs) has been increasingly attracting in modern energy and environmental fields. However, the separation performance of MCEMs in terms of the permselectivity and cation fluxes, is typically restricted by membrane architecture and applied materials. Recently, mussel-inspired surface modification methods have been deployed in new membrane fabrications with special surface characteristics and functions. Herein, a facile layer-by-layer assembly method was designed to construct a series of de novo positively-charged tannic acid/polyethyleneimine (TA/PEI) membranes containing a negatively-charged support membrane and a TA/PEI selective layer. Notably, the peculiar support membrane with a much dense structure and abundant cation exchange groups can enable our TA/PEI membranes to possess high total cation fluxes. The selective layer with vast positive charges ensures mussel-inspired TA/PEI assembled positively-charged membranes to have a high permselectivity. Most importantly, compared with the separation performance of the state-of-the-art MCEMs, the superior separation performance of our developed new MCEMs at 5 mA·cm-2 and 10 mA·cm-2 is beyond the current "Upper Bound" plot between Na+ flux and the permselectivity (Na+/Mg2+), which opens new avenues for the construction of MCEMs. Furthermore, high purity of Li+ (95.37%) can be obtained through deploying mussel-inspired TA/PEI assembled positively-charged membranes with high permselectivity of Li+/Mg2+ (13.72), proving its great potentials in the field of resource recovery towards sustainability.

Effect of the Zwitterion, p(MAO-DMPA), on the Internal Structure, Fouling Characteristics, and Dye Rejection Mechanism of PVDF Membranes.

The zwitterion poly-(maleic anhydride-alt-1-octadecene-3-(dimethylamino)-1-propylamine) (p(MAO-DMPA)) synthesized using a ring-opening reaction was used as a poly(vinylidene fluoride) (PVDF) membrane modifier/additive during phase inversion process. The zwitterion was characterized using proton nuclear magnetic resonance (1HNMR) and attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR). Atomic force microscopy (AFM), field emission scanning electron microscope (SEM), FTIR, and contact angle measurements were taken for the membranes. The effect of the zwitterionization content on membrane performance indicators such as pure water flux, membrane fouling, and dye rejection was investigated. The morphology of the membranes showed that the increase in the zwitterion amount led to a general decrease in pore size with a concomitant increase in the number of membrane surface pores. The surface roughness was not particularly affected by the amount of the additive; however, the internal structure was greatly influenced, leading to varying rejection mechanisms for the larger dye molecule. On the other hand, the wettability of the membranes initially decreased with increasing content to a certain point and then increased as the membrane homogeneity changed at higher zwitterion percentages. Flux and fouling properties were enhanced through the addition of zwitterion compared to the pristine PVDF membrane. The high (>90%) rejection of anionic dye, Congo red, indicated that these membranes behaved as ultrafiltration (UF). In comparison, the cationic dye, rhodamine 6G, was only rejected to <70%, with rejection being predominantly electrostatic-based. This work shows that zwitterion addition imparted good membrane performance to PVDF membranes up to an optimum content whereby membrane homogeneity was compromised, leading to poor performance at its higher loading.

The Synthesis and Characterization of Novel Bi-/Trimetallic Nanoparticles and Their Nanocomposite Membranes for Envisaged Water Treatment.

The impact of worldwide water scarcity, further exacerbated by environmental pollution, necessitates the development of effective water treatment membranes. Herein, we report the synthesis and characterization of nanocomposite membranes containing hyperbranched polyethyleneimine (HPEI) stabilized bi-and trimetallic nanoparticles. These membranes were prepared by blending a pre-grafted Polyethersulfone (PES) powder with the Pd@Fe@HPEI and Pd@FeAg@HPEI nanoparticles followed by phase inversion. The membranes, together with stabilized nanoparticles, were characterized by several analytical techniques, such as attenuated total reflectance-Fourier transform infra-red spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffractometry (XRD), optical contact angle (OCA), scanning electron microscopy (SEM), atomic force microscopy (AFM), and high-resolution transmission electron microscopy (HRTEM). These techniques revealed the elemental composition, zerovalent nature of the nanoparticles, and their small and even size distribution. Surface analysis showed chemical bonding between the polymeric functional groups and the supported nanoparticles. Furthermore, the nanocomposite membranes were found to be hydrophilic. Additionally, the membranes were investigated for swelling (water uptake), porosity, pore size, pure water permeation fluxes, and they indicated a decreased protein adhesion property. As such, the membranes fabricated in this work indicate the required properties for application in water treatment.

Zeolitic Imidazolate Framework-8-Encapsulated Nanoparticle of Ag/Cu Composites Supported on Graphene Oxide: Synthesis and Antibacterial Activity.

The rational approach motivated the design of novel antimicrobial silver and silver-copper bimetallic nanoparticles contained within zeolitic imidazolate framework-8 supported on graphene oxide (GO), Ag@ZIF-8@GO, and AgCu@ZIF8@GO. In the resultant composites, ZIF-8 was able to prevent the stacking of GO sheets and also acted as a carrier for the nanoparticles within its cavities. GO, on the other hand, acted as an anchoring support enabling uniform dispersion of the nanocomposites, thus eliminating their aggregation. The morphological and physicochemical properties of the composites were determined through a variety of characterization techniques, for example, transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectroscopy, p-X-ray diffraction (XRD), nitrogen sorption, and X-ray photoelectron spectroscopy (XPS). The energy-dispersive system and XPS supplied evidence of the presence of all expected components in the composites. The XRD provided proof of a crystalline, distorted ZIF-8 structure. Ag@ZIF8@GO and Ag-Cu@ZIF-8@GO composites were effective against both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria as determined by the disc diffusion method. The role of silver nanoparticles (AgNPs) in the antibacterial activity of both Ag@ZIF8@GO and AgCu@ZIF8@GO was highlighted as crucial in the probable pathway in the antimicrobial activity of the composites.