The increasing presence of pollutants, including pharmaceuticals and pesticides, in water resources necessitates the development of effective remediation technologies. Zeolites are promising agents for pollutant removal due to their high surface area, ion-exchange capacity, natural abundance, and diverse tailorable porous structures. This review focuses on the efficient application of modified zeolites and mesoporous materials as photocatalysts and adsorbents for removing contaminants from water bodies. The adsorption and photodegradation of pesticides and selected non-steroidal anti-inflammatory drugs and antibiotics on various zeolites reveal optimal adsorption and degradation conditions for each pollutant. In most reported studies, higher SiO₂/Al₂O₃ ratio zeolites exhibited improved adsorption, and thus photodegradation activities, due to increased hydrophobicity and lower negative charge. For example, SBA-15 demonstrated high efficiency in removing diclofenac, ibuprofen, and ketoprofen from water in acidic conditions. Metal doped into the zeolite framework was found to be a very active catalyst for the photodegradation of organic pollutants, including pesticides, pharmaceuticals, and industrial wastes. It is shown that the photocatalytic activity depends on the zeolite-type, metal dopant, metal content, zeolite pore structure, and the energy of the irradiation source. Faujasite-type Y zeolites combined with ozone achieved up to 95% micropollutant degradation. Bentonite modified with cellulosic biopolymers effectively removed pesticides such as atrazine and chlorpyrifos, while titanium and/or silver-doped zeolites showed strong catalytic activity in degrading carbamates, highlighting their environmental application potential.

Water scarcity poses a formidable challenge around the world, especially in arid regions where limited availability of freshwater resources threatens both human well-being and ecosystem sustainability. Membrane-based desalination technologies offer a viable solution to address this issue by providing access to clean water. This work ultimately aims to develop a novel permselective polymeric membrane material to be employed in an electrochemical desalination system. This part of the study addresses the optimization, preparation, and characterization of a polyvinylidene difluoride (PVDF) polymeric membrane using the electrospinning technique. The membranes produced in this work were fabricated under specific operational, environmental, and material parameters. Five different additives and nano-additives, i.e., graphene oxide (GO), carbon nanotubes (CNTs), zinc oxide (ZnO), activated carbon (AC), and a zeolitic imidazolate metal–organic framework (ZIF-8), were used to modify the functionality and selectivity of the prepared PVDF membranes. Each membrane was synthesized at two different levels of additive composition, i.e., 0.18 wt.% and 0.45 wt.% of the entire PVDF polymeric solution. The physiochemical properties of the prepared membranes were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), zeta potential, contact angle, conductivity, porosity, and pore size distribution. Based on findings of this study, PVDF/GO membrane exhibited superior results, with an electrical conductivity of 5.611 mS/cm, an average pore size of 2.086 µm, and a surface charge of −38.33 mV.

Photocatalytic degradation of harmful dye pollutants and electrochemical hydrogen generation via water splitting show strong in addressing environmental pollution and energy scarcity. In this study, a V₂O₅ (VO) interstitially modified g-C₃N₄/MWCNT Z-scheme heterostructure (VMG) was synthesized using an ultrasonication assisted wet impregnation method. The resulting photocatalyst was utilized for the degradation of mixed dyes (Rhodamine B (RhB) & Methylene blue (MB) in aqueous solution. The VMG nanocomposite, exhibited outstanding photocatalytic performance, achieving 92.0% degradation of MB and 88.0% degradation of RhB within 100 min under visible-light irradiation. The degradation efficiency remained above 87.0% and 83.0% against MB and RhB, respectively after five consecutive cycles. The XRD and SEM analyses post-reaction showed no significant structural or microstructural changes, confirming the excellent stability of the photocatalyst. Radical trapping experiments identified superoxide radicals as the dominant active species. From XPS/UPS analysis, the work functions were estimated and the Z-scheme charge transfer pathway was proposed to explain the enhanced photocatalytic activity in alignment with the proposed antibacterial mechanism. The ternary composite showed potent light-activated antibacterial activity, with complete inhibition of gram-positive M. luteus at 50 µg/mL. In addition, the electrocatalytic properties of the VMG nanocomposite were investigated for hydrogen evolution in KOH electrolyte medium. Electrochemical measurements revealed a low overpotential (71 mV), a high electrochemically active surface area (10.87 mF/cm²), a low Tafel slope (140 mV/dec), and a reduced charge-transfer resistance compared to the pure VO sample. The robust interfacial interaction within the VMG heterostructure was found to significantly enhance catalytic activity and cycling stability. Overall, this work highlights the multi-functionality of the synthesized VMG nanocomposite in organic pollutant degradation, sustainable hydrogen generation, and antimicrobial applications.

This work provides a systematic experimental study for the electrochemical desalination of saline water using an electrospun permselective polyvinylidene difluoride (PVDF) membrane. Several nano additives were initially screened during membrane development; however, only the materials that demonstrated stable dispersion, reproducible membrane formation, and consistent electrochemical behaviour, namely graphene oxide (GO) and carbon nanotubes (CNTs) were selected for full analysis in this study. Accordingly, the study focuses on pure PVDF, PVDF/GO, and PVDF/CNTs membranes integrated with an alternating Ag/AgCl electrode system. The silver electrode is prepared by spray-coating of silver nanoparticles on high surface carbon cloth, whereas the AgCl electrode was prepared electrochemically from the Ag electrode using a three-electrode electrochemical cell. The electrochemical behaviour of various modified electrodes (bare carbon cloth, Ag/carbon cloth, Ag/nafion/carbon black/PVDF, and Ag/nafion/carbon cloth) was evaluated using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and X-Ray Diffraction (XRD). The electrode prepared using Nafion and PVDF as binders with carbon black as conductive additive exhibited the highest current response and lowest charge-transfer resistance. When coupled with this optimized electrode, the PVDF/GO membrane delivered the best desalination performance, achieving an ion removal efficiency of 68%, a salt adsorption capacity (SAC) of 775.40 mg/g, and a specific energy consumption (SEC) of 16.17 kJ/mole values superior to those reported in the literature.