TRUEX Processing of Plutonium Analytical Solutions at Argonne National Laboratory
David B. Chamberlain, C. Conner, Joseph C. Hutter, R. A. Leonard, D.G. Wygmans, George F. Vandegrift
Abstract
David B. Chamberlain, C. Conner, Joseph C. Hutter, R. A. Leonard, D.G. Wygmans, George F. Vandegrift
Abstract
The TRUEX (TRansUranic EXtraction) solvent extraction process was developed at Argonne National Laboratory (ANL) for the Department of Energy. A TRUEX demonstration completed at ANL involved the processing of analytical and experimental waste generated there and at the New Brunswick Laboratory. A 20-stage centrifugal contactor was used to recover plutonium, americium, and uranium from the waste. Approximately 84 g of plutonium, 18 g of uranium, and 0.2 g of americium were recovered from about 118 L of solution during four process runs. Alpha decontamination factors as high as 65,000 were attained, which was especially important because it allowed the disposal of the process raffinate as a lowlevel waste. The recovered plutonium and uranium were converted to oxide; the recovered americium solution was concentrated by evaporation to approximately 100 mL. The flowsheet and operational procedures were modified to overcome process difficulties. These difficulties included the presence of complexants in the feed, solvent degradation, plutonium precipitation, and inadequate decontamination factors during startup. This paper will discuss details of the experimental effort.
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The TRUEX (TRansUranic EXtraction) solvent extraction process was developed at Argonne National Laboratory (ANL) for the Department of Energy. A TRUEX demonstration completed at ANL involved the processing of analytical and experimental waste generated there and at the New Brunswick Laboratory. A 20-stage centrifugal contactor was used to recover plutonium, americium, and uranium from the waste. Approximately 84 g of plutonium, 18 g of uranium, and 0.2 g of americium were recovered from about 118 L of solution during four process runs. Alpha decontamination factors as high as 65,000 were attained, which was especially important because it allowed the disposal of the process raffinate as a lowlevel waste. The recovered plutonium and uranium were converted to oxide; the recovered americium solution was concentrated by evaporation to approximately 100 mL. The flowsheet and operational procedures were modified to overcome process difficulties. These difficulties included the presence of complexants in the feed, solvent degradation, plutonium precipitation, and inadequate decontamination factors during startup. This paper will discuss details of the experimental effort.
Key concepts: Plutonium, Americium, National laboratory, Plutonium-240, Raffinate, Uranium, Chemistry, Human decontamination