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- W2729544692 abstract "Water body contamination with radioactive species is an important issue due to significant developments in nuclear energy. Cesium (137 Cs) radioisotope is a non-actinide fission product of uranium and plutonium that is long-lived. Hence, selective removal/capture of cesium is essential for managing radioactive waste. Herein, a detailed Cs+ ion-exchange study on a potassium intercalated layered metal thiophosphate, K0.48 Mn0.76 PS3 ⋅H2 O (K-MPS-1), is reported. The sorption of Cs+ by K-MPS-1 follows the Langmuir model with a high capacity of 337.5 mg g-1 and high distribution coefficients in the order of about 104 mL g-1 . K-MPS-1 can sequester Cs+ efficiently, even from very low concentrations (ppb level). K-MPS-1 exhibits high cesium uptake over a broad pH range of 2-12 and the ion-exchange process reaches equilibrium within a short time (≈15 min), following pseudo-second-order kinetics. Moreover, K-MPS-1 demonstrates selectivity towards Cs+ capture in the presence of complex solutions containing excess Na+ , Ca2+ , and Mg2+ ions; this is due to favorable interactions between Cs (soft Lewis acid) and S (soft Lewis base). K-MPS-1 reversibly captures Cs+ and it can be regenerated by treating Cs-MPS-1 with a solution of KCl." @default.
- W2729544692 created "2017-07-14" @default.
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- W2729544692 date "2017-07-26" @default.
- W2729544692 modified "2023-09-30" @default.
- W2729544692 title "Reversible and Efficient Sequestration of Cesium from Water by the Layered Metal Thiophosphate K<sub>0.48</sub> Mn<sub>0.76</sub> PS<sub>3</sub> ⋅H<sub>2</sub> O" @default.
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- W2729544692 doi "https://doi.org/10.1002/chem.201701883" @default.
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