Efficient
management of radionuclides that are released from various
processes in the nuclear fuel cycle is of significant importance.
Among these nuclides, radioactive iodine (mainly 129I and 131I) is a major concern due to the risk it poses to the environment
and to human health; thus, the development of materials that can capture
and safely store radioactive iodine is crucial. Herein, a novel silver–thione-functionalized
zeolitic imidazole framework (ZIF) was synthesized via postsynthetic
modification and assessed for its iodine uptake capabilities alongside
the parent ZIF-8 and intermediate materials. A solvent-assisted ligand
exchange procedure was used to replace the 2-methylimidazole linkers
in ZIF-8 with 2-mercaptoimidazole, forming intermediate compound ZIF-8
= S, which was reacted with AgNO3 to yield the ZIF-8 =
S–Ag+ composite for iodine uptake. Despite possessing
the lowest BET surface area of the derivatives, the Ag-functionalized
material demonstrated superior I2 adsorption in terms of
both maximum capacity (550 g I2/mol) and rapid kinetics
(50% loading achieved in 5 h, saturation in 50 h) compared to that
of our pristine ZIF-8, which reached 450 g I2/mol after
150 h and 50% loading in 25 h. This improvement is attributed to the
presence of the Ag+ ions, which provide a strong chemical
driving force to form a stable Ag–I species. The results of
this study contribute to a broader understanding of the strategies
that can be employed to engineer adsorbents with robust iodine uptake
behavior.