Constructing multiple sites porous organic polymers for highly efficient and reversible adsorption of triiodide ion from water

三碘化物 吸附 多孔性 离子 聚合物 多孔介质 材料科学 化学工程 无机化学 化学 有机化学 物理化学 电解质 电极 色素敏化染料 工程类
作者
Zhiyong Li,Yibo Fu,Yilong Li,Ruipeng Li,Yuanchao Pei,Yunlei Shi,Huiyong Wang
出处
期刊:Green Energy & Environment [KeAi]
卷期号:10 (8): 1807-1818 被引量:31
标识
DOI:10.1016/j.gee.2025.03.005
摘要

The utilization of nuclear power will persist as a prominent energy source in the foreseeable future. However, it presents substantial challenges concerning waste disposal and the potential emission of untreated radioactive substances, such as radioactive 129 I and 131 I. The transportation of radioactive iodine poses a significant threat to both the environment and human health. Nevertheless, effectively, rapidly removing iodine ion from water using porous adsorbents remains a crucial challenge. In this work, three kinds of multiple sites porous organic polymers (POPs, POP-1, POP-2, and POP-3) have been developed using a monomer pre-modification strategy for highly efficient and fast I 3 − absorption from water. It is found that the POPs exhibited exceptional performance in terms of I 3 − adsorption, achieving a top-performing adsorption capacity of 5.25 g g −1 and the fastest average adsorption rate (K 80 % = 4.25 g g −1 h −1 ) with POP-1. Moreover, POP-1 exhibited exceptional capacity for the removal of I 3 − from flowing aqueous solutions, with 95% removal efficiency observed even at 0.0005 mol L −1 . Such results indicate that this material has the potential to be utilized for the emergency preparation of potable water in areas contaminated with radioactive iodine. The adsorption process can be effectively characterized by the Freundlich model and the pseudo-second-order model. The exceptional I 3 − absorption capacity is primarily attributed to the incorporation of a substantial number of active adsorption sites, including bromine, carbonyl, and amide groups. The porous organic polymer adsorbent demonstrated outstanding performance in I3-adsorption, achieving an exceptional adsorption capacity, the highest average adsorption rate, and notable low-concentration adsorption efficiency. • Multiple sites POPs were prepared by monomer pre-modification strategy. • POP-1 exhibit a top-performing adsorption capacity of 5.25 g g −1 • POP-1 has a fastest average adsorption rate (K 80 % = 4.25 g g −1 h −1 ). • Multiple sites cooperative interactions of I 3 − with the groups in POPs is the adsorption mechanism.
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