Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions
Abstract In this work, selenium (IV) ions were adsorbed from aqueous solutions by the strongly basic anion exchange resin Amberlite IRA-400. The morphology of the resin before and after Se(IV) sorption was investigated using different techniques such as energy dispersive X-ray spectroscopy (EDX), Fo...
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2025-01-01
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author | A. El-Tantawy E. M. Abu Elgoud S. E. A. Sharaf El-Deen |
author_facet | A. El-Tantawy E. M. Abu Elgoud S. E. A. Sharaf El-Deen |
author_sort | A. El-Tantawy |
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description | Abstract In this work, selenium (IV) ions were adsorbed from aqueous solutions by the strongly basic anion exchange resin Amberlite IRA-400. The morphology of the resin before and after Se(IV) sorption was investigated using different techniques such as energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). To determine the ideal sorption conditions, a batch approach was used to examine the variables affecting Se(IV) sorption performance, including pH, shaking time, adsorbent dosage, initial metal ion concentration, and temperature. The results showed the optimal parameters for the highest percentage of selenium (80.25%) at an initial concentration of 100.0 mg L−1, pH 3.0, the adsorbent dosage of 10.0 mg, and the shaking time of 60.0 min. According to the experimental findings, the sorption process was satisfactorily explained by the pseudo-second-order kinetic model. The maximum adsorption capacity at pH 3.0 was 18.52 mg g−1, and the adsorption rather well followed the Langmuir adsorption isotherm. Moreover, exothermic and spontaneous sorption reaction was the result of thermodynamic properties (negativity of both ΔG° and ΔH°). The adsorption phase's random distribution of the resin-solution interface is indicated by the positive value of ΔSo. Finally, the desorption study was performed using different concentrations of desorbing agents; HNO3, HCl, and sodium acetate. The results illustrated that the effective desorbing agent was 1.0 mol L-1 HNO3, with desorption efficiency reaching about 96.4%. Finally, the Amberlite IRA-400 demonstrated excellent adsorption–desorption behavior over five times, suggesting that the Amberlite IRA-400 could be an effective candidate for the sorption of Se(IV) from several metal ions that occur in fission products. |
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publishDate | 2025-01-01 |
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spelling | doaj-art-147486a100ce4d529ca07849a1258ef92025-01-12T12:06:41ZengBMCBMC Chemistry2661-801X2025-01-0119111110.1186/s13065-024-01356-3Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutionsA. El-Tantawy0E. M. Abu Elgoud1S. E. A. Sharaf El-Deen2Nuclear Fuel Technology Department, Hot Laboratories Center, Egyptian Atomic Energy AuthorityNuclear Fuel Chemistry Department, Hot Laboratories Center, Egyptian Atomic Energy AuthorityNuclear Chemistry Department, Hot Laboratories Center, Egyptian Atomic Energy AuthorityAbstract In this work, selenium (IV) ions were adsorbed from aqueous solutions by the strongly basic anion exchange resin Amberlite IRA-400. The morphology of the resin before and after Se(IV) sorption was investigated using different techniques such as energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). To determine the ideal sorption conditions, a batch approach was used to examine the variables affecting Se(IV) sorption performance, including pH, shaking time, adsorbent dosage, initial metal ion concentration, and temperature. The results showed the optimal parameters for the highest percentage of selenium (80.25%) at an initial concentration of 100.0 mg L−1, pH 3.0, the adsorbent dosage of 10.0 mg, and the shaking time of 60.0 min. According to the experimental findings, the sorption process was satisfactorily explained by the pseudo-second-order kinetic model. The maximum adsorption capacity at pH 3.0 was 18.52 mg g−1, and the adsorption rather well followed the Langmuir adsorption isotherm. Moreover, exothermic and spontaneous sorption reaction was the result of thermodynamic properties (negativity of both ΔG° and ΔH°). The adsorption phase's random distribution of the resin-solution interface is indicated by the positive value of ΔSo. Finally, the desorption study was performed using different concentrations of desorbing agents; HNO3, HCl, and sodium acetate. The results illustrated that the effective desorbing agent was 1.0 mol L-1 HNO3, with desorption efficiency reaching about 96.4%. Finally, the Amberlite IRA-400 demonstrated excellent adsorption–desorption behavior over five times, suggesting that the Amberlite IRA-400 could be an effective candidate for the sorption of Se(IV) from several metal ions that occur in fission products.https://doi.org/10.1186/s13065-024-01356-3Amberlite IRA-400 Cl−Se(IV)SorptionIsotherm and kineticsDesorption and regeneration |
spellingShingle | A. El-Tantawy E. M. Abu Elgoud S. E. A. Sharaf El-Deen Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions BMC Chemistry Amberlite IRA-400 Cl− Se(IV) Sorption Isotherm and kinetics Desorption and regeneration |
title | Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions |
title_full | Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions |
title_fullStr | Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions |
title_full_unstemmed | Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions |
title_short | Evaluation of anion exchange resin for sorption of selenium (IV) from aqueous solutions |
title_sort | evaluation of anion exchange resin for sorption of selenium iv from aqueous solutions |
topic | Amberlite IRA-400 Cl− Se(IV) Sorption Isotherm and kinetics Desorption and regeneration |
url | https://doi.org/10.1186/s13065-024-01356-3 |
work_keys_str_mv | AT aeltantawy evaluationofanionexchangeresinforsorptionofseleniumivfromaqueoussolutions AT emabuelgoud evaluationofanionexchangeresinforsorptionofseleniumivfromaqueoussolutions AT seasharafeldeen evaluationofanionexchangeresinforsorptionofseleniumivfromaqueoussolutions |