Abstract

Radioactive iodine generated from nuclear waste and nuclear accidents can cause serious hazards to the environment and human body. In this study, bismuth-doped ZIF-8 composites (Bi2O3@ZIF-8) were synthesized by in situ synthesis at room temperature to study their adsorption of iodine in gaseous state and in solution. The Bi2O3@ZIF-8 composites were characterized and analyzed by means of tests. Bi2O3@ZIF-8 exhibited high specific surface area and contained abundant microporous structures. However, when the bismuth doping amount reached 10%, 10%-Bi2O3@ZIF-8 appeared mesoporous. The specific surface area of 1%-Bi2O3@ZIF-8, 5%-Bi2O3@ZIF-8 and 10%-Bi2O3@ZIF-8 could reach 1110.6 m2/g, 973.21 m2/g and 927.82 m2/g, respectively. The adsorption of gaseous iodine by 5%-Bi2O3@ZIF-8 reached equilibrium after 3.5 h with the maximum adsorption capacity of 298 wt%. And the maximum adsorption capacity of iodine in solution was 751.4 mg/g. The effects of the initial concentration of the solution, reaction temperature and contact time on the adsorption process were investigated. The adsorption of Bi2O3@ZIF-8 on iodine was consistent with the pseudo-second-order kinetics and the Langmuir model. The results of thermodynamic studies indicated that the adsorption of iodine by Bi2O3@ZIF-8 was spontaneous and exothermic. This study provides a reference for the synthesis of metal organic framework-based materials and provides theoretical guidance for the removal of practical radioactive iodine.

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