Selective and highly efficient removal of uranium from radioactive effluents by activated carbon functionalized with 2-aminobenzoic acid as a new sorbent.

The purpose of this study was modification of activated carbon (AC) to prepare a new selective sorbent for removal of uranium ion. The modification was performed by introducing carboxyl groups onto AC using ammonium persulfate (APS) in sulfuric acid solution followed by functionalization with 2-aminobenzoic acid (ABA) as a selective ligand for U (VI) ion (UO22+) adsorption. The characterization of the synthetized sorbent (AC-ABA) was carried out through several methods including potentiometry, scanning electron microscopy, energy dispersive spectroscopy, x-ray diffraction and FT-IR to confirm successful functionalization of the sorbent surface with oxygen and amine groups. The sorption of U (VI) on the unmodified AC and AC-ABA was investigated as a function of contact time, sorbent content, initial uranium concentration, solution pH, and temperature using batch sorption technique. In addition, the effect of various parameters on the U (VI) sorption capacity was optimized by the response surface methodology as a potent experimental design method. The results indicated that sorption of U (VI) under the optimal conditions was significantly improved onto AC-ABA compared to AC. Kinetic studies displayed that the sorption process reached equilibrium after 100 min and followed the pseudo-second-order rate equation. The isothermal data fitted better with the Langmuir model than the Freundlich model. The maximum sorption capacity of AC-ABA for U(VI) was obtained to be 194.2 mg g-1 by the Langmuir model under optimum conditions, which demonstrates the sorption capacity has been improved by the modification process. The thermodynamic parameters (ΔH, ΔS and ΔG) indicated that sorption of uranium onto AC-ABA was an endothermic and spontaneous process. The sorption studies on radioactive effluents of the nuclear fuel plant represented high selectivity of AC-ABA for removal of uranium in the presence of other metal ions, and the selectivity coefficients significantly improved after modification of the sorbent. Application of AC-ABA for treatment of industrial effluents containing heavy and radioactive metal ions show high potential and capability of the proposed method.

Efficient removal and recovery of uranium from industrial radioactive wastewaters using functionalized activated carbon powder derived from zirconium carbide process waste.

Development of efficient sorbents for selective removing and recovery of uranium from radioactive wastewaters is highly important in nuclear fuel industries from the standpoint of resource sustainability and environmental safety issues. In this study, carbon powder waste was modified by various chemical activating agents under atmosphere of nitrogen gas at 725 °C to prepare an efficient sorbent for removal and recovery of uranium ions from radioactive wastewaters of nuclear fuel conversion facility. Activation of the carbon powder with KOH, among different activators, provided maximum porosity and surface area. The activated samples were modified by reacting with ammonium persulfate in sulfuric acid solution to generate surface functional groups. The synthetized sorbents were characterized with FT-IR, XRD, BET, and SEM-EDS techniques. The effects of solution pH, contact time, initial uranium concentration, and temperature on the sorption capacity of the sorbent with respect to U(VI) from wastewater were investigated by batch method, followed by optimizing the effect of influential parameters by experimental design using central composite design. The sorption of UO22+ ions on the sorbents follows the Langmuir isotherm and pseudo-second-order kinetic models. Maximum sorption capacity for U(VI) was 192.31 mg g-1 of the modified sorbent at 35 °C. Thermodynamic data showed that sorption of U(VI) on the sorbent was through endothermic and spontaneous processes. The sorption studies on radioactive effluents of the nuclear industry demonstrated that the modified sorbent had a favorable selectivity for uranium removal in the presence of several other metal ions.