Journal
JOURNAL OF CLEANER PRODUCTION
Volume 330, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.129821
Keywords
Uranyl(VI); Photocatalysis; 3D g-C3N4; H2O2; Immobilization
Categories
Funding
- Fundamental Research Funds of the Central Universities [2021MS036]
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The three-dimensional g-C3N4 enhanced the photocatalytic production of H2O2 during U(VI) recycling, while the overlooked photoinduced uranyl(VI) photocatalysis process significantly contributed to the immobilization of U(VI) in the actual environment.
Uranium contamination derived from nuclear mining and nuclear waste has caused severe environmental and public health problems. Photocatalysis has been proved to be an available method for U(VI) elimination. However, photoinduced uranyl(VI) photocatalysis process tends to be overlooked. Herein, we reported that three-dimensional g-C3N4 boosted the production of photocatalytic H2O2 during recycling of U(VI). UO22+ was first excited to *UO22+ under visible light irradiation, then *UO22+ was further converted to UO2+ under organics, whereas UO2+ transferred into UO22+ and H2O2 was generated under the dissolving O-2 condition (UO22+ -> *UO22+ -> UO2+ -> UO22+). Meanwhile, massive H2O2 was produced from photogenerated electrons derived from the converting dissolving O-2 on 3D g-C3N4 under visible light irradiation. The high-efficiency U(VI) immobilization was ascribed to the reaction of U(VI) and H2O2 to form uranyl peroxides (nano-metastudtite, UO2(O-2)center dot 2H(2)O, similar to 20 nm width*40 nm length). These observations give valuable insights into the photoinduced U(VI) immobilization in actual environment.
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