摘要
Enrichment of radioiodine accompanied by nuclear fission threatens the health of humans, and efficient capture of iodine has attracted wide public attention in recent years. Here we report a crystalline mesoporous nitrogen-containing covalent organic framework (TAPB-BPDA COF) as a highly efficient iodine adsorbent, which is synthesized by imine condensation reaction between 1,3,5-tris(4-aminophenyl)benzene and 4,4′-biphenyldicarboxaldehyde. The TAPB-BPDA COF possesses permanent porous structure, high BET surface area of 1082 m 2 /g, excellent chemical and thermal stability and plenty of nitrogen in the skeleton as effective sorption sites. It displays remarkable adsorption of iodine in aqueous solution up to 988.17 mg/g at room temperature . The adsorption kinetics of iodine onto TAPB-BPDA COF is followed the pseudo-second-order kinetic model , and the adsorption isotherm fits well with the Langmuir model. The TAPB-BPDA COF adsorbs iodine through the weak interaction between the benzene ring on its backbone and iodine, and the electron transfer between nitrogen atoms and iodine promotes the adsorption process . Moreover, TAPB-BPDA COF still maintains efficient adsorption performance after five cycles. These results suggest the great potential of TAPB-BPDA COF as a designable porous to address the problem of nuclear fission waste contamination that threatens human health.
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