Abstract

Nowadays, wastewater treatment is a critical concern, particularly regarding the removal of heavy metals through adsorption methods. Extensive research has been conducted on obtaining high-yield and environmentally friendly adsorbents. Natural polymer adsorbents especially have shown promise in ion and organic molecule adsorption. To enhance the practical applicability of adsorbents, the combination of biopolymers to form biocomposites is a promising alternative. In this study, adsorbents based on a 1:1 wt./wt. of chitosan (CS) and alginate (SA) were prepared. The influence of the regeneration route and drying conditions on the copper adsorption capacity was investigated, along with reaction parameters such as contact time, adsorbent particle size, and pH. The highest adsorption capacity was observed in the composite material obtained through a one-pot regeneration process and freeze-dried. The CSAR3L sample exhibited a remarkable adsorption capacity of 288 mg Cu(II)/g after 360 min at 25 °C. The synergistic effect between the CS and SA precursors was confirmed by analyzing the individual precursors and their mechanical mixture. The initial adsorption rates at pH 6 followed the order: CSAR3-L > Bk-CSR3L > Bk-SAR3L + Bk-CSR3L > Bk-SAR3L. The physicochemical and morphological properties of the materials were studied by FTIR, XRD, DLS, XPS, optical microscopy, EDS-SEM, elemental chemical analysis, and TGA-DTG. The utilization of different drying methods resulted in the formation of calcium carbonate crystalline phases in the as-prepared materials, thus creating substantial adsorption active sites. After the adsorption process, hydroxylated copper sulfate phases and a significant decrease in calcium concentration were observed, indicating that an ion exchange adsorption mechanism occurred. The analysis of adsorption kinetics and the shape of the adsorption isotherms, in agreement with the characterization results, suggested the presence of multiple active sites and the formation of a chemisorption monolayer.

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