The present study reports the engineering of functionalized chitosan (CH)-based biosorbent material. Herein, a two-step reaction was performed to chemically modify the CH using 1,4-bis(3-aminopropyl) piperazine to incorporate nitrogen basic centers for cations sorption from the aqueous environment. The resultant functionalized chitosan-based sorbent material was designated as CH-ANP and characterized using various analytical techniques, including elemental analysis, Fourier-transform infrared spectroscopy (FTIR), ¹³C NMR (in solid-state), X-ray diffraction, and thermal analysis. Then, the newly engineered CH-ANP was employed for the removal of copper, lead, and cadmium in the aqueous medium. Langmuir sorption isotherm analysis revealed that the highest sorption abilities achieved were 2.82, 1.96, and 1.60 mmol g⁻¹ for copper, cadmium, and lead, respectively. Linear and nonlinear regression methods were deployed on the sorption data to study the behavior of the Langmuir, the Freundlich, and the Temkin sorption isotherms. Among the four different forms, the Langmuir isotherm type 1 fit well to the experimental data as compared to the other models. It also showed the lowest values of error, and a higher correlation coefficient than the Freundlich and Temkin models; thus it was the best fit with the experimental data compared to the latter two models. In conclusion, the findings suggest that chemically modified novel materials with enhanced Lewis basic centers are useful and promising candidates for the sorption of various toxic cations in aqueous solution.

Herein, we report the development of chitosan (CH)-based bio-composite modified with acrylonitrile (AN) in the presence of carbon disulfide. The current work aimed to increase the Lewis basic centers on the polymeric backbone using single-step three-components (chitosan, carbon disulfide, and acrylonitrile) reaction. For a said purpose, the thiocarbamate moiety was attached to the pendant functional amine (NH₂) of chitosan. Both the pristine CH and modified CH-AN bio-composites were first characterized using numerous analytical and imaging techniques, including ¹³C-NMR (solid-form), Fourier-transform infrared spectroscopy (FTIR), elemental investigation, thermogravimetric analysis, and scanning electron microscopy (SEM). Finally, the modified bio-composite (CH-AN) was deployed for the decontamination of cations from the aqueous media. The sorption ability of the CH-AN bio-composite was evaluated by applying it to lead and copper-containing aqueous solution. The chitosan-based CH-AN bio-composite exhibited greater sorption capacity for lead (2.54 mmol g⁻¹) and copper (2.02 mmol g⁻¹) than precursor chitosan from aqueous solution based on Langmuir sorption isotherm. The experimental findings fitted better to Langmuir model than Temkin and Freundlich isotherms using linear regression method. Different linearization of Langmuir model showed different error functions and isothermal parameters. The nonlinear regression analysis showed lower values of error functions as compared with linear regression analysis. The chitosan with thiocarbamate group is an outstanding material for the decontamination of toxic elements from the aqueous environment.

Wastewater containing dyes is considered as the top-priority pollutant when discharged into the environment. Herein, we report for the applicability of 254 nm ultraviolet light and electrochemical process using a titanium ruthenium oxide anode for the degradation of Allura red and erythrosine dyes. During the photolytic process, 95% of Allura red dye (50 ppm) was removed after 1 h at pH 12 and 35 °C, whereas 90% color removal of erythrosine dye (50 ppm) was achieved after 6 h of treatment at pH 6.0 and 30 °C. On the other hand, 99.60% of Allura red dye (200 ppm) was removed within 5 min by the electrochemical process applying a current density (5 mA cm−2) at pH 5.0 and 0.1 mol L−1 sodium chloride (NaCl) electrolytic medium. Similarly, 99.61% of erythrosine dye (50 ppm) degradation was achieved after 10 min at a current density of 8 mA cm−2, pH 6.0, and 0.1 mol L−1 of NaCl electrolyte. The minimum energy consumption value for Allura red and erythrosine dyes (0.196 and 0.941 kWh m–3, respectively) was calculated at optimum current densities of 5 and 8 mA cm−2. The results demonstrated that the electrochemical process is more efficient at removing dyes in a shorter time than the photolytic process since it generates powerful oxidants like the chlorine molecule, hypochlorous acid, and hypochlorite on the surface of the anode and initiates a chain reaction to oxidize the dyes molecules.