Effective capture of radioactive iodine is of paramount importance for the safe and long-term storage of fission products in the nuclear fuel cycle. Herein, a series of functionalized Th-UiO-66 MOFs was employed as a model to investigate the effects of substituents on iodine adsorption in both solution and vapor states. Sorption studies revealed that the electro-donating amino group exhibits the most positive role on increasing the removal rate of iodine from cyclohexane and the uptake capacity of iodine vapor. Particularly, the disubstituted Th-UiO-66-(NH2 )2 can effectively remove 91.9 % of iodine (300 mg L-1 ) from cyclohexane and capture 969 mg g-1 iodine vapor, significantly higher than 59.6 % and 334 mg g-1 of untagged Th-UiO-66, respectively. In addition, the substituent effect on the radiolytic stability of MOFs was for the first time investigated, leading to the unearthing of one of the most radioresistant MOFs Th-UiO-66-NH2 reported to date.
Keywords: iodine; metal-organic frameworks; radioresistance; substituent effects; thorium.
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