催化作用
苯胺
化学
路易斯酸
沮丧的刘易斯对
铀
溶剂
多相催化
氧气
单线态氧
组合化学
光化学
有机化学
键裂
协同催化
高分子化学
化学工程
无机化学
浓缩铀
工作(物理)
氧化还原
部分氧化
浸出(土壤学)
溶解
能源
作者
Yuhui Han,Jiaheng Qin,Xu Qiu,Tong Li,Jie Song,Linkun Dong,Feng Zhao,Weiwen Mao,Duoqiang Pan,Yu Long
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-10-16
卷期号:15 (21): 17971-17981
被引量:4
标识
DOI:10.1021/acscatal.5c05695
摘要
The accumulation of depleted uranium (DU), a byproduct of nuclear energy production, poses significant environmental concerns. Converting DU into functional catalysts represents a promising strategy for its resource valorization. Herein, we report a 238U-based catalyst, UO4·2H2O, with negligible radioactivity, synthesized from DUF6-derived α-U3O8 via a dissolution–precipitation method, enabling selective oxidation of aniline to nitrosobenzene, azobenzene, and azoxybenzene by solvent tuning. Structural and mechanistic studies reveal that surface defects form frustrated Lewis pairs (FLPs). Its Lewis acidic U6+ sites strengthen the U═O bond and shorten its length, enhancing electron-withdrawing ability and promoting aniline adsorption, while the basic oxygen-vacancy sites facilitate H2O2 activation and singlet oxygen generation, thereby promoting aniline oxidation. Notably, the catalyst is regenerable via calcination-reprecipitation for up to 60 cycles, with an E-factor well below the fine chemical benchmark. This work provides a scalable strategy for DU valorization and a practical platform for the synthesis of nitrogen-containing fine chemicals.
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