ABSTRACT
The objective of this study was to assess the efficacy of fungal chitosan-polystyrene-Co-nanocomposites (FCPNC) as a material for the adsorptive removal of cadmium (Cd) ions from aqueous solutions. The synthesis and characterization of FCPNC were accomplished using various analytical techniques, including Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), Brunauer-Emmett-Teller (BET) analysis, and dynamic light scattering (DLS). The effectiveness of this adsorbent in removing Cd(ii) species from solution matrices was systematically investigated, resulting in the achievement of a maximum adsorption capacity of approximately 112.36 mg g-1. This high adsorption capacity was detected using the following operational parameters: solution pH equals 5.0, 60 min as a contact time between the adsorbent and Cd(ii) solution, Cd initial concentration of 50 ppm, adsorbent dosage of 0.5 g L-1 and room temperature. The process of cadmium adsorption by FCPNC was found to follow the Langmuir isotherm model, suggesting that a chemical reaction occurs on the biosorbent surface. Kinetic studies have demonstrated that the cadmium removal process aligns well with the pseudo-second-order model. The thermodynamic analysis revealed the following values: ΔH° = 25.89 kJ mol-1, ΔG° = -21.58 kJ mol-1, and ΔS° = 159.30 J mol-1 K-1. These values indicate that the sorption process is endothermic, spontaneous, and feasible. These findings suggest the potential of FCPNC as an exceptionally effective biosorbent for the removal of water contaminants.
ABSTRACT
A direct reaction is described to prepare hydrophobic α-aminomethylphosphonic acid as a novel chitosan-based material. It exhibits chelating properties for polyvalent metal ions such as U(VI) and Nd(III) ions. The new sorbent was fully characterized using Elemental analysis, scanning electron microscope (SEM) and FTIR spectra. Different parameters were examined in order to evaluate the optimum conditions for U(VI) and Nd(III) ions biosorption. Sorption mechanisms of metal ions were investigated using kinetic and isotherm models. In addition, the sorbent selectivity was tested for both metal ions together in a binary solution.
