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Functional Carbon Capsules Supporting Ruthenium Nanoclusters for Efficient Electrocatalytic 99 TcO 4 - /ReO 4 - Removal from Acidic and Alkaline Nuclear Wastes.

Xiaolu LiuYinghui XieYang LiMengjie HaoZhongshan ChenHui YangGeoffrey I N WaterhouseShengqian MaXiangke Wang
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
The selective removal of the β-emitting pertechnetate ion ( 99 TcO 4 - ) from nuclear waste streams is technically challenging. Herein, a practical approach is proposed for the selective removal of 99 TcO 4 - (or its surrogate ReO 4 - ) under extreme conditions of high acidity, alkalinity, ionic strength, and radiation field. Hollow porous N-doped carbon capsules loaded with ruthenium clusters (Ru@HNCC) are first prepared, then modified with a cationic polymeric network (R) containing imidazolium-N + units (Ru@HNCC-R) for selective 99 TcO 4 - and ReO 4 - binding. The Ru@HNCC-R capsules offer high binding affinities for 99 TcO 4 - /ReO 4 - under wide-ranging conditions. An electrochemical redox process then transforms adsorbed ReO 4 - to bulk ReO 3 , delivering record-high removal capacities, fast kinetics, and excellent long-term durability for removing ReO 4 - (as a proxy for 99 TcO 4 - ) in a 3 m HNO 3 , simulated nuclear waste-Hanford melter recycle stream and an alkaline high-level waste stream (HLW) at the U.S. Savannah River Site (SRS). In situ Raman and X-ray absorption spectroscopy (XAS) analyses showed that adsorbed Re(VII) is electrocatalytically reduced on Ru sites to a Re(IV)O 2 intermediate, which can then be re-oxidized to insoluble Re(VI)O 3 for facile collection. This approach overcomes many of the challenges associated with the selective separation and removal of 99 TcO 4 - /ReO 4 - under extreme conditions, offering new vistas for nuclear waste management and environmental remediation.
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