钯
吸附
材料科学
共价键
聚合物
选择性
共价有机骨架
化学工程
氮气
选择性吸附
支柱
纳米技术
有机化学
催化作用
化学
复合材料
结构工程
工程类
作者
Li Wang,Yijie Wu,Jihong Li,Qing Li,Pinghua Yang,Steven D. Conradson,Yimin Cai,Wen Feng,Lihua Yuan
标识
DOI:10.1002/adfm.202304051
摘要
Abstract The capture of palladium from spent nuclear fuel is crucial for the sustainable development of nuclear energy and resource recovery. One of the most challenging issues in this direction is the survival of adsorbents under extreme reprocessing conditions such as strongly acidic media and high radiation fields while still maintaining high extraction ability and selectivity. Herein, an approach to addressing this issue is reported by incorporating macrocycle into nitrogen‐rich covalent organic polymers (COPs). Dramatically outperforming current adsorbing materials, pillar[5]arene‐based COPs with pyridyl and triazolyl functionalities display record adsorption capacity for Pd(II) at 3 M HNO 3 (403 mg g −1 ), extraordinary stability under 500 kGy gamma irradiation, and ultra‐high selectivity toward Pd(II) over both 17 coexisting cations and six anions. In particular, the material P5COP‐ m ‐BPT with the best performance also shows remarkable dynamic adsorption efficiency for Pd(II). This study not only provides a strategy to enhance all‐sided adsorption performance in palladium separation with nitrogen‐rich COPs materials but also demonstrates the superiority of customizing advanced materials with macrocycles.
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