Systematic investigations involving laboratory, analytical, and field trials were carried out to obtain the most efficient adsorbent for the removal of congo red (CR) dye from industrial effluent. Modification of the zeolite (Z) by the Acanthophora Spicifera algae (AS; marine algae) was evaluated in terms of adsorption capability of the zeolite to remove CR dye from aqueous solution. The zeolite/algae composite (ZAS) was fabricated using the wet impregnation technique. The AS, Z, and the synthesized ZAS composite were analyzed utilizing various characterization techniques. The newly synthesized ZAS composite has an adsorption capacity that is significantly higher than that of Z and AS, particularly at low CR concentrations. Batch experiments were carried out to explore the effects of different experimental factors, as well as the dye adsorption isotherms and kinetics. Owing to the presence of intermolecular interactions, the computational analysis showed that the adsorption of the CR molecule on zeolite surfaces is exothermic, energetically favorable, and spontaneous. Furthermore, growing the zeolite surface area has no discernible effect on the adsorption energies in all configurations. The ZAS composite may be used as a low-cost substitute adsorbent for the removal of anionic dyes from industrial wastewater at lower dye concentrations, according to the experimental results. Adsorption of CR dye onto Z, AS, and ZAS adsorbents was adequately explained by pseudo-second-order kinetics and the Langmuir isotherm. The sorption mechanism was also evaluated using Weber’s intra-particle diffusion module. Finally, field testing revealed that the newly synthesized adsorbent was 98.0% efficient at extracting dyes from industrial wastewater, proving the foundation of modern eco-friendly materials that aid in the reuse of industrial wastewater.

Water pollution remains a critical concern, one necessitated by rapidly increasing industrialization and urbanization. Among the various strategies for water purification, membrane technology stands out, with polyethersulfone (PES) often being the material of choice due to its robust mechanical properties, thermal stability, and chemical resistance. However, PES-based membranes tend to exhibit low hydrophilicity, leading to reduced flux and poor anti-fouling performance. This study addresses these limitations by incorporating titanium dioxide nanotubes (TiO₂NTs) into PES nanofiltration membranes to enhance their hydrophilic properties. The TiO₂NTs, characterized through FTIR, XRD, BET, and SEM, were embedded in PES at varying concentrations using a non-solvent induced phase inversion (NIPS) method. The fabricated mixed matrix membranes (MMMs) were subjected to testing for water permeability and solute rejection capabilities. Remarkably, membranes with a 1 wt% TiO₂NT loading displayed a significant increase in pure water flux, from 36 to 72 L m² h⁻¹ bar⁻¹, a 300-fold increase in selectivity compared to the pristine sample, and a dye rejection of 99%. Furthermore, long-term stability tests showed only a slight reduction in permeate flux over a time of 36 h, while dye removal efficiency was maintained, thus confirming the membrane’s stability. Anti-fouling tests revealed a 93% flux recovery ratio, indicating excellent resistance to fouling. These results suggest that the inclusion of TiO₂ NTs offers a promising avenue for the development of efficient and stable anti-fouling PES-based membranes for water purification.

This work developed new electrocatalysts for direct alcohol oxidation fuel cells (DAFCs) by using graphene and reduced graphene oxides (GO and rGO) as supporting nanomaterials for copper–nickel (CuNi) nanocomposites. The manufacture of CuNi, CuNi-GO, and CuNi-rGO nanocomposites was realized through the adaptation of Hummer’s method and hydrothermal techniques, with subsequent analysis using a range of analytical tools. The electrocatalytic behavior of these materials in DAFCs, with methanol and ethanol as the fuels, was scrutinized through various methods, including cyclic voltammetry, linear sweep, chronoamperometry, and electrochemical impedance spectroscopy. This investigation also assessed the stability and charge transfer dynamics. The rGO-based CuNi nanocomposite demonstrated a remarkable performance boost, showing increases of approximately 319.6% for methanol and 252.6% for ethanol oxidation compared to bare CuNi. The integration of silver nanoparticles into the Ag-CuNi-rGO electrode led to a current density surge to 679.3 mA/g, which signifies enhancements of 254.2% and 812.6% relative to the CuNi-rGO and CuNi electrodes, respectively. These enhancements are ascribed to the augmented densities of hot sites and the synergistic interactions within the nanocatalysts. The findings underscore the potential of Ag and rGO as effective supports for CuNi nanocomposites, amplifying their catalytic efficiency in DAFC applications.