化学
结晶
水溶液
高氯酸盐
溶解度
苯
齿合度
产量(工程)
核化学
放射化学
无机化学
锝
晶体结构
有机化学
冶金
材料科学
作者
Rongzhen Xie,Nan‐Nan Shen,Xijian Chen,Jie Li,Yaxing Wang,Chao Zhang,Chengliang Xiao,Zhifang Chai,Shuao Wang
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-04-15
卷期号:60 (9): 6463-6471
被引量:23
标识
DOI:10.1021/acs.inorgchem.1c00187
摘要
99Tc is one of the most abundant radiotoxic isotopes in used nuclear fuel with a high fission yield and a long half-life. Effective removal of pertechnetate (TcO4–) from an aqueous solution is important for nuclear waste separation and remediation. Herein, we report a series of facilely obtained benzene-linked guanidiniums that could precipitate TcO4– and its nonradioactive surrogate ReO4– from a high-concentration acidic solution through self-assembly crystallization. The resulting perrhenate and pertechnetate solids exhibit exceptionally low aqueous solubility. The benzene-linked guanidiniums hold one of the highest TcO4– removal capacities (1279 mg g–1) among previously reported materials and possess a removal percentage of 59% for ReO4– in the presence of Cl– over 50 times. The crystallization mechanism was clearly illustrated by the single-crystal structures and density functional theory calculations, indicating that TcO4– is captured through a charge-assisted hydrogen bonding interaction and stabilized by π–π stacking layers. In addition, the removal process is easily recycled and no toxic organic reagents are introduced. This work provides a green approach to preliminarily separate TcO4– from high-level nuclear wastes.
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