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Ozone-Facilitated Formation of Uranyl Peroxide in Humid Conditions.

Savannah E BenjaminJay A LaVerneGinger E SigmonPeter C Burns
Published in: Inorganic chemistry (2022)
Metaschoepite, [(UO 2 ) 8 O 2 (OH) 12 ](H 2 O) 10 , maintained in a high relative humidity (RH) environment with air initially transformed into an intermediate phase that subsequently was replaced by the peroxide phase studtite, [(UO 2 )(O 2 )(H 2 O) 2 ](H 2 O) 2 , over the course of 42 days, as observed using Raman and infrared spectroscopy and powder X-ray diffraction. Addition of atmospheric ozone vastly increased the rate and extent of the transformation to studtite but only in a high-RH atmosphere. Owing to its strong affinity for peroxide, uranyl reacted with hydrogen peroxide as it formed and precipitated stable studtite. In this work, we provide a previously unidentified source of hydrogen peroxide and make a case for the re-examination of storage systems where the consequences of atmospheric ozone are not considered.
Keyphrases
  • hydrogen peroxide
  • nitric oxide
  • particulate matter
  • high resolution
  • computed tomography
  • magnetic resonance
  • carbon dioxide
  • crystal structure
  • contrast enhanced