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Observation of Radiolytic Field Alteration of the Uranyl Cation in Bicarbonate Solution

Published online by Cambridge University Press:  26 February 2011

Lanee Snow
Affiliation:
lanee.snow@pnl.gov, Battelle, Richland, WA, 99352, United States
Bruce McNamara
Affiliation:
bruce.mcnamara@pnl.gov, Pacific Northwest Laboratory, Radiochemical Processing, Battelle, PO Box 999, MS:P7-25, Richland, Wa 99352, Richland, WA, 99352, United States, 509-376-1408
Sergei Sinkov
Affiliation:
sergei.sinkov@pnl.gov, Battelle, Richland, WA, 99352, United States
Herman Cho
Affiliation:
herman.cho@pnl.gov, Battelle, Richland, WA, 99352, United States
Judah Friese
Affiliation:
judah.friese@pnl.gov, Battelle, Richland, WA, 99352, United States
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Abstract

Auto radiolysis of uranium (VI) carbonate solutions between pH 5.9 and 7.2 is shown to alter the uranium speciation over relatively short periods of time and was followed by 13C NMR and visible spectrophotometry, using dissolved [233(UO2)3(CO3)6]6- both as the radiolysis source (DÑ= 14.9 Gy/hr) and as a trap for the newly formed hydrogen peroxide. The speciation is different than the uranyl mixed peroxy carbonate species that have been reported for higher pH carbonate solutions.

Type
Research Article
Copyright
Copyright © Materials Research Society 2007

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