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Title: Investigation of molybdate melts as an alternative method of reprocessing used nuclear fuel

Journal Article · · Journal of Nuclear Materials
 [1]; ORCiD logo [2];  [3];  [2];  [2]
  1. Oregon State Univ., Corvallis, OR (United States); Argonne National Lab. (ANL), Argonne, IL (United States)
  2. Argonne National Lab. (ANL), Argonne, IL (United States)
  3. Oregon State Univ., Corvallis, OR (United States)

Here, an investigation of molybdate melts containing sodium molybdate (Na2MoO4) and molybdenum trioxide (MoO3) to achieve the separation of uranium from fission products by crystallization has been performed. The separation is based on the difference in solubility of the fission product metal oxides compared to the uranium oxide or molybdate in the molybdate melt. The molybdate melt dissolves uranium dioxide at high temperatures, and upon cooling, uranium precipitates as uranium dioxide or molybdate, whereas the fission product metals remain soluble in the melt. Small-scale experiments using gram quantities of uranium dioxide have been performed to investigate the feasibility of UO2 purification from the fission products. The composition of the uranium precipitate as well as data for partitioning of several fission product surrogates between the uranium precipitate and molybdate melt for various melt compositions are presented and discussed. The fission products Cs, Sr, Ru and Rh all displayed very large distribution ratios. The fission products Zr, Pd, and the lanthanides also displayed good distribution ratios (D > 10). A melt consisting of 20 wt% MoO3-50 wt% Na2MoO4-30 wt% UO2 heated to 1313 K and cooled to 1123 K for the physical separation of the UO2 product from the melt, and washed once with Na2MoO4 displays optimum conditions for separation of the UO2 from the fission products.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Nuclear Energy (NE); USDOE Office of Nuclear Energy (NE), Reactor Fleet and Advanced Reactor Development. Office of Nuclear Energy Technologies
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1363800
Alternate ID(s):
OSTI ID: 1419390
Journal Information:
Journal of Nuclear Materials, Vol. 486, Issue C; ISSN 0022-3115
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 2 works
Citation information provided by
Web of Science