Electrorecovery of actinides at room temperature

Conference · Tue Jan 01 00:00:00 EST 2008

DOI:https://doi.org/10.1149/1.3114011· OSTI ID:956652

Stoll, Michael E ^[1]; Oldham, Warren J ^[1]; Costa, David A ^[1]

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1. Los Alamos National Laboratory

There are a large number of purification and processing operations involving actinide species that rely on high-temperature molten salts as the solvent medium. One such application is the electrorefining of impure actinide metals to provide high purity material for subsequent applications. There are some drawbacks to the electrodeposition of actinides in molten salts including relatively low yields, lack of accurate potential control, maintaining efficiency in a highly corrosive environment, and failed runs. With these issues in mind we have been investigating the electrodeposition of actinide metals, mainly uranium, from room temperature ionic liquids (RTILs) and relatively high-boiling organic solvents. The RTILs we have focused on are comprised of 1,3-dialkylimidazolium or quaternary ammonium cations and mainly the {sup -}N(SO{sub 2}CF{sub 3}){sub 2} anion [bis(trif1uoromethylsulfonyl)imide {equivalent_to} {sup -}NTf{sub 2}]. These materials represent a class of solvents that possess great potential for use in applications employing electrochemical procedures. In order to ascertain the feasibility of using RTILs for bulk electrodeposition of actinide metals our research team has been exploring the electron transfer behavior of simple coordination complexes of uranium dissolved in the RTIL solutions. More recently we have begun some fundamental electrochemical studies on the behavior of uranium and plutonium complexes in the organic solvents N-methylpyrrolidone (NMP) and dimethylsulfoxide (DMSO). Our most recent results concerning electrodeposition will be presented in this account. The electrochemical behavior of U(IV) and U(III) species in RTILs and the relatively low vapor pressure solvents NMP and DMSO is described. These studies have been ongoing in our laboratory to uncover conditions that will lead to the successful bulk electrodeposition of actinide metals at a working electrode surface at room temperature or slightly elevated temperatures. The RTILs we have focused on thus far are based on 1,3-dialkylimidazolium or quaternary ammonium cations and {sup -}N(SO{sub 2}CF{sub 3}){sub 2} anions. Our results from XPS studies of e1ectrooxidized uranium metal surfaces indicate that uranium metal reacts with the anion from the RTIL, most likely through an initial f1uoride abstraction, forming decomposition products that inhibit the bulk electrodeposition of uranium metal. Similar results were found when the organic solvents were used with TBA[B(C{sub 6}F{sub 5}){sub 4}] as the supporting electrolyte, although the voltammetric data of uranium ions in these solutions is more encouraging in relation to electrodeposition of uranium metal. Preliminary results on the voltammetric behavior and bulk electrodeposition of plutonium species are also presented.

• Research Organization: Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC52-06NA25396
• OSTI ID: 956652
• Report Number(s): LA-UR-08-07929; LA-UR-08-7929; TRN: US1006244
• Resource Relation: Journal Volume: 16; Journal Issue: 36; Conference: 214th Meeting of the Electrochemical Society ; October 12, 2009 ; Honolulu, HI, USA
• Country of Publication: United States
• Language: English

Related Subjects

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
ACTINIDES
AMBIENT TEMPERATURE
ANIONS
BEHAVIOR
CATIONS
COMPLEXES
CONTROL
DECOMPOSITION
DMSO
EFFICIENCY
ELECTRODEPOSITION
ELECTRODES
ELECTRON TRANSFER
ELECTROREFINING
IMPURITIES
LIQUIDS
MEETINGS
METALS
MOLTEN SALTS
ORGANIC SOLVENTS
PLUTONIUM
PLUTONIUM COMPLEXES
SOLUTIONS
SOLVENTS
SURFACES
TEMPERATURE RANGE 0400-1000 K
URANIUM
URANIUM IONS
VAPOR PRESSURE
X-RAY PHOTOELECTRON SPECTROSCOPY