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The dynamic precipitation characteristics of UO(4) in different solution conditions (pH, ionic strength, uranium and H(2)O(2) concentrations) were characterized by measuring changes in the absorbance of the precipitation solution and by monitoring the change of particle size in a circulating particle size analyzer. The precipitation solution conditions affected the precipitation characteristics such as the induction time, precipitation rate, overall precipitation time, and particle size in a complex manner. With increases in both pH and ionic strength, the induction time was prolonged, and the individual particle size decreased, but the individual particles tended to grow by aggregation to form larger precipitates. The uranium concentration and the ionic strength of the solution affected the induction time and precipitation rate to the greatest extent., (Copyright © 2011 Elsevier B.V. All rights reserved.)

This work studied the dissolution of uranium dioxide and precipitation characteristics of uranyl ions in alkaline and acidic solutions depending on the presence of carbonate ions and H2O2 in the solutions at different pHs controlled by adding HNO3 or NaOH in the solution. The chemical structures of the precipitates generated in different conditions were evaluated and compared by using XRD, SEM, TG-DT, and IR analyses together. The sizes and forms of the precipitates in the solutions were evaluated, as well. The uranyl ions were precipitated in the various forms, depending on the solution pH and the presences of hydrogen peroxide and carbonate ions in the solution. In a 0.5 M Na2CO3 solution with H2O2, where the uranyl ions formed mixed uranyl peroxy-carbonato complexes, the uranyl ions were precipitated as a uranium peroxide of UO4(H20)4 at pH 3-4, and precipitated as a clarkeite of Na2U2Ox(OH)y(H2O)z above pH 13. In the same carbonate solution without H2O2, where the uranyl ions formed uranyl tris-carbonato complex, the uranyl ions were observed to be precipitated as a different form of clarkeite above pH 13. The precipitate of uranyl ions in a nitrate solution without carbonate ions and H2O2 at a high pH were studied together to compare the precipitate forms in the carbonate solutions.

Abstract: This work studied a process to recover uranium from contaminated (U,Gd)O2 scraps generated from nuclear fuel fabrication processes by using the dissolution of (U,Gd)O2 scraps in a carbonate with H2O2 and the precipitation of the dissolved uranium as UO4. The dissolution characteristics of uranium, Gd, and impurity metal oxides were tested, and the behaviors of UO4 precipitation and Gd solubility were evaluated with changes of the pH of the solution. A little Gd was entrained in the UO4 precipitate to contaminate the uranium precipitate. Below a pH of 3, the uranium dissolved in the form of uranyl peroxo-carbonato complex ions in the carbonate solution was precipitated as UO4 with a high precipitation yield, and the Gd had a very high solubility. Using these characteristics, the Gd-contaminated UO4 could be purified using dissolution in a 1-M HNO3 solution with heating and re-precipitation upon addition of H2O2 to the solution. Finally, an environmentally friendly and economical process to recover pure uranium from contaminated (U,Gd)O2 scraps was suggested. [Copyright &y& Elsevier]