Uranyl Peroxide Nanocluster (U60) Persistence and Sorption in the Presence of Hematite

Luke R. Sadergaski, Wynn Stoxen, Amy E. Hixon

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

The presence of uranium-based nanomaterials in environmental systems may significantly impact our current understanding of the fate and transport of U(VI). Sorption of the uranyl peroxide nanocluster [(UO2)(O2)(OH)]6060- (U60) to hematite (α-Fe2O3) was studied using batch sorption experiments with varying U60, hematite, and alkali electrolyte (i.e., NaCl, KCl, and CsCl) concentrations. Data from electrospray ionization mass spectrometry and centrifugal microfiltration revealed that U60 persisted in the presence of hematite and the background electrolyte for at least 120 days. K+ ions were removed from solution with uranium whereas Li+ ions remained in solution, indicating that the U60 cluster behaved like an anion and that the Li+ ions did not play a significant role in the sorption mechanism. Analysis of the reacted mineral surface using X-ray photoelectron and Raman spectroscopies confirmed the presence of U(VI) and uranyl species with bridged peroxo groups associated with the mineral surface. These results indicate that uranyl peroxide nanoclusters may persist in the aqueous phase under environmentally relevant conditions for reasonably long periods of time, as compared to that of the uranyl cation.

Original languageEnglish
Pages (from-to)3304-3311
Number of pages8
JournalEnvironmental Science and Technology
Volume52
Issue number5
DOIs
StatePublished - Mar 6 2018
Externally publishedYes

Funding

*Phone: 574-631-1872; fax: 574-631-9236; e-mail: ahixon@nd. edu. ORCID Amy E. Hixon: 0000-0003-4513-4574 Author Contributions The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript. Funding This material is based on work supported as part of Materials Science of Actinides, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under award number DESC0001089. Notes The authors declare no competing financial interest.

FundersFunder number
Energy Frontier Research Center
U.S. Department of Energy
Office of Science
Basic Energy SciencesDESC0001089

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