Dyes are responsible for major environmental issues globally due to their toxicity, large-scale production, and extensive use in various industrial sectors. Pollution caused by hazardous dyes is mainly due to textile waste, which is constantly discharged into the aquatic system, often causing harm to humans and affecting water quality. In recent years, the removal of dyes from industrial textile wastewater has been a major challenge. Numerous technologies and methods have been developed to remove dyes from wastewater and meet clean water requirements. In this study, the effectiveness of activated carbon prepared by chemical activation of jujube stones for textile wastewater treatment was investigated. The effects of the concentration of H₃PO₄ and the carbonization temperature on the activated carbon’s properties were studied. Several physicochemical methods, including Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction, methylene blue index, Boehm titration, iodine index and pH point of zero charge, were considered to characterize the produced adsorbents. To assess the quality of the two studied textile effluents (Mustard and Violet), the following parameters were used: biological oxygen demand (BOD), chemical oxygen demand (COD), turbidity, suspended particles and dissolved solids, before and after treatment with the produced activated carbon. Untreated wastewater analysis revealed high values for almost all parameters: pH > 9, COD of 302.72 mg/L and 230.68 mg/L for Mustard and Violet effluent, respectively. Both effluents from an industrial textile factory exhibited a COD/BOD ratio higher than three, which restricts their biodegradability. Examination of the effect of contact time and activated carbon dosage on the treatment of the two effluents showed that 4 g/L of activated carbon and 60 min of contact time were sufficient for optimal treatment, resulting in pollutant removal rates of 81.03 and 84.65% for the Violet and Mustard effluents, respectively. The results of this research highlight the efficiency of activated carbon derived from jujube stones as a cost-effective adsorbent for the treatment of real textile wastewater.

The hydrothermal production of chitosan from the carapaces of gray shrimp was carried out, and the obtained material was characterized via X-ray diffraction analysis, infrared spectroscopy, and pH zero-charge point, giving the expected results. Orange G dye adsorption onto synthetized chitosan was investigated in a batch system, the kinetic study was well-described by a nonlinearized pseudo-second-order model, and the equilibrium data indicated that the nonlinear Langmuir form was appropriate to describe the adsorption system with a maximum adsorption capacity of 34.63 mg/g compared with that found experimentally of 31.9 mg/g. The influences of most of the operating parameters, such as pH, adsorbent concentration, temperature, initial dye concentration, and contact time, were studied. These five independent variables acting on the adsorption performance of Orange G were selected for optimization and modeling processes through a central rotating composite design using response surface methodology (RSM). The percentage of removal of Orange G by chitosan prepared from shrimp shells was predicted with a second-degree polynomial equation, and the postulated model was valid and represented well the phenomenon studied in the experimental domain, with an R² = 0.98 and an R_Adj = 0.95. An initial Orange G concentration of 10 mg/L, a pH of 6.5, a chitosan amount of 0.3 g/L, a temperature of 25 °C, and an adsorption time of 450 min were found to be the optimum conditions in batch mode for the maximum uptake of Orange G (removal of 97.43%).

Chitosan was hydro-thermally extracted from grey shrimp carapaces and characterized using various techniques (degree of deacetylation (DD), viscosity, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and surface area analysis (BET)). It was then used for Cu(II) removal in a batch system, achieving a maximum capacity of 89 mg/g under standard conditions. Both pseudo-first-order and pseudo-second-order nonlinear kinetic models described the adsorption of Cu(II) ions on chitosan well, with a better fit of the pseudo-first-order model at low concentrations, while the equilibrium data suggested that the Langmuir model was suitable for describing the adsorption system, with a maximum adsorption capacity of 123 mg/g. A response surface methodology and central composite design were used to optimise and evaluate the effects of six independent parameters: initial Cu(II) concentration, pH, chitosan concentration (S/L), temperature (T), contact time (t), and NaCl concentration on the adsorption efficiency of Cu(II) by the synthesised chitosan. The proposed model was confirmed to accurately describe the phenomenon within the experimental range, achieving an R² value of 1. ANOVA indicated that the initial concentrations of Cu(II) and chitosan concentration (S/L) were the most significant factors, while the other variables had no significant effect on the process. The adsorption capacity of Cu(II) onto the prepared chitosan was also optimised and modelled using artificial neural networks (ANNs). The maximum amount, qmax = 468 mg·g⁻¹, shows that chitosan is a highly effective adsorbent, chelating and complexing for copper ions.

Ternary heterojunction photocatalysts enhance the separation and transport of photogenerated charge carriers, thereby boosting their redox activity for use in environmental and sustainable energy applications. This study focuses on the synthesis of a TiO₂/Bi₂O₃/g-C₃N₄ heterojunction composite via a ceramic method with TiO₂ loadings of 80%, 85%, and 90% (denoted 80T-BC, 85T-BC, and 90T-BC, respectively) to investigate structure–property–performance relationships in photocatalytic dye degradation. The structural, optical, and morphological properties of the synthesised materials were characterised using X-ray diffraction (XRD), scanning electron microscopy (SEM), and diffuse reflectance UV–Vis spectroscopy (DRS). The photocatalytic performance was evaluated by measuring the degradation of Rhodamine B under visible light irradiation. Under optimised conditions (pH 6, initial RhB concentration of 5 mg/L, and a reaction time of 120 min), a degradation rate of 99% was achieved. Furthermore, the semiconductor demonstrated significant antibacterial activity against both Gram-negative (Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus) bacteria. This study presents a promising strategy for modifying TiO₂-based semiconductors by incorporating different metal oxides. The formation of the resulting heterojunction significantly enhances photocatalytic efficiency, demonstrating strong potential for practical environmental remediation.