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Autor(en) / Beteiligte
Titel
Functionalized Iron–Nitrogen–Carbon Electrocatalyst Provides a Reversible Electron Transfer Platform for Efficient Uranium Extraction from Seawater
Ist Teil von
  • Advanced materials (Weinheim), 2021-12, Vol.33 (51), p.e2106621-n/a
Ort / Verlag
Germany: Wiley Subscription Services, Inc
Erscheinungsjahr
2021
Quelle
Wiley Online Library
Beschreibungen/Notizen
  • Uranium extraction from seawater provides an opportunity for sustainable fuel supply to nuclear power plants. Herein, an adsorption–electrocatalysis strategy is demonstrated for efficient uranium extraction from seawater using a functionalized iron–nitrogen–carbon (Fe–Nx–C–R) catalyst, comprising N‐doped carbon capsules supporting FeNx single‐atom sites and surface chelating amidoxime groups (R). The amidoxime groups bring hydrophilicity to the adsorbent and offer surface‐specific binding sites for UO22+ capture. The site‐isolated FeNx centres reduce adsorbed UO22+ to UO2+. Subsequently, through electrochemical reduction of the FeNx sites, unstable U(V) ions are reoxidized to U(VI) in the presence of Na+ resulting in the generation of solid Na2O(UO3·H2O)x, which can easily be collected. Fe–Nx–C–R reduced the uranium concentration in seawater from ≈3.5 ppb to below 0.5 ppb with a calculated capacity of ≈1.2 mg g‐1 within 24 h. To the best of the knowledge, the developed system is the first to use the adsorption of uranyl ions and electrodeposition of solid Na2O(UO3.H2O)x for the extraction of uranium from seawater. The important discoveries guide technology development for the efficient extraction of uranium from seawater. A novel adsorption–electrocatalysis system is developed for efficiently extracting uranium from seawater. Amidoxime groups impart Fe–Nx–C–R with hydrophilicity and a high binding affinity for uranyl ions, whilst the iron sites provides a reversible electron‐transfer platform for the eventual production of Na2O(UO3·H2O)x in the presence of Na+, thus allowing facile uranium recovery and Fe–Nx–C–R reuse.
Sprache
Englisch
Identifikatoren
ISSN: 0935-9648
eISSN: 1521-4095
DOI: 10.1002/adma.202106621
Titel-ID: cdi_proquest_journals_2612295610

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