Abstract
The growing reliance on nuclear energy and uncharacteristic accidents, such as those in Chornobyl and Fukushima, have emphasized the need for effective radiocesium (r-Cs: 137Cs) removal from environmental wastewater. This study presents the development of DFDB18C6@SBA-NH2, a novel solid-phase sorbent designed to remove r-Cs from aqueous environments selectively. The sorbent was synthesized by tethering a macrocyclic ligand, DFDB18C6 (di-formyl dibenzo-18-crown-6-ether), to amino-functionalized mesoporous SBA-15 (Santa Barbara Amorphous-15). The sorbent’s structure, thermal properties, and surface morphology were comprehensively characterized. Batch sorption experiments were performed to evaluate the influence of different operating factors on r-Cs sorption, including solution pH, contact duration, initial ion concentration, ambient temperature, and matrix ions contents. The sorption behavior was better explained with the pseudo-second-order kinetic and Langmuir isotherm models, which suggest a probable monolayer chemisorption process. The thermodynamic evaluation indicated the exothermic nature of the sorption process. The DFDB18C6@SBA-NH2 sorbent demonstrated significant 137Cs removal (approximately 85 %) from Fukushima-originated wastewater, with competing matrix ions such as Ca2+, Mg2+, Na+, and K+. These results highlight the potential of DFDB18C6@SBA-NH2 as a potential solid-phase sorbent for efficient and selective r-Cs decontamination in waste aqueous matrices.
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