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Chitosan, a biopolymer known for its biocompatibility, biodegradability, and chemical adaptability, has attracted significant attention in scientific research. Chitosan-metal nanocomposites represent an emerging area of exploration. Among these, Chitosan-Fe nanocomposite has gained prominence due to its various applications, including photoremediation, bioimaging, and drug delivery systems. In this study, we delved into the synthesis and physicochemical properties of Chitosan-Fe nanocomposites. These nanocomposites exhibited a spherical structure with active binding sites that allowed for the functionalization of Fe3+ ions on their surface. Density functional theory simulations corroborated this alteration, demonstrating changes in surface charge properties resulting in increased mechanical strength. A key finding of this study is the enhanced antibacterial activity exhibited by the Cs-Fe nanocomposites against both Escherichia coli (62.5 µg/mL) and Staphylococcus aureus (125.25 µg/mL), surpassing that of bare Chitosan nanoparticles. Furthermore, our investigation confirms the therapeutic safety of the Chitosan-Fe nanocomposite. The cell viability calculated by MTT assay and accepted therapeutic dose concentration for CS-Fe NC was 125 ug/mL whereas for CSNP < 15.62 µg/mL. This underscores the nanocomposite’s potential in biomedical applications. In addition to its biomedical promise, the Chitosan-Fe nanocomposite also demonstrates remarkable potential in environmental remediation, particularly in the removal of hexavalent chromium.

The public health and environment are currently facing significant risks due to the discharge of industrial wastewater, which contains harmful heavy metals and other contaminants. Therefore, there is a pressing need for sustainable and innovative technologies to treat wastewater. The main objective of this research was to develop novel composites known as chitosan,  Padina pavonica,  Fe(III), and nano MgO incorporated onto pomegranate peel with the specific purpose of removing Cd (II) and Cu (II) ions from aqueous solutions. The characterization of these nanocomposites involved the utilization of several analytical methods, including Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, thermal gravimetric analysis, and X-ray photoelectron spectroscopy. The efficiency of these nanocomposites was evaluated through batch mode experiments, investigating the impact of factors such as pH, initial concentration, contact time, and adsorbent dose on the adsorption of Cu(II) ions. The optimum conditions for the removal of ions were pH = 5 for Cu (II) and 6 for Cd (II), contact time: 120 min, adsorbent dosage: 0.2 g, initial metal ion concentration: 50 mg/L for each metal ion for the present study. The MgO@Pp demonstrated the highest removal efficiencies for Cu(II) and Cd(II) at 98.2% and 96.4%, respectively. In contrast, the CS@Fe-PA achieved removal efficiencies of 97.2% for Cu(II) and 89.2% for Cd(II). The modified MgO@Pp exhibited significantly higher total adsorption capacities for Cu(II) and Cd(II) at 333.3 and 200 mg/g, respectively, compared to CS@Fe-PA, which had capacities of 250 and 142 mg/g, respectively. The adsorption of Cd (II) and Cu (II) ions by MgO@Pp was found to be a spontaneous process. The R 2 values obtained using the Freundlich and Redlich-Peterson models were the highest for the MgO@Pp composite, with values of 0.99, 0.988, 0.987, and 0.994, respectively, for Cu (II) and Cd (II). The pseudo-second-order equation was determined to be the best-fit kinetic model for this process. Reusability experiments confirmed that the adsorbents can be utilized for up to four regeneration cycles. Based on the findings of this study, MgO @ Pp is the most promising alternative and could be instrumental in developing strategies to address existing environmental pollution through adsorption.