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Higher oxidation states of americium have long been known; however, options for their preparation in acidic solution are limited. The conventional choice, silver-catalyzed peroxydisulfate, is not useful at nitric acid concentrations above about 0.3 M. We investigated the use of sodium bismuthate as an oxidant for Am (3+) in acidic solution. Room-temperature oxidation produced AmO 2 (2+) quantitatively, whereas oxidation at 80 degrees C produced AmO 2 (+) quantitatively. The efficacy of the method for the production of oxidized americium was verified by fluoride precipitation and by spectroscopic absorbance measurements. We performed absorbance measurements using a conventional 1 cm cell for high americium concentrations and a 100 cm liquid waveguide capillary cell for low americium concentrations. Extinction coefficients for the absorbance of Am (3+) at 503 nm, AmO 2 (+) at 514 nm, and AmO 2 (2+) at 666 nm in 0.1 M nitric acid are reported. We also performed solvent extraction experiments with the hexavalent americium using the common actinide extraction ligand tributyl phosphate (TBP) for comparison to the other hexavalent actinides. Contact with 30% tributyl phosphate in dodecane reduced americium; it was nevertheless extracted using short contact times. The TBP extraction of AmO 2 (2+) over a range of nitric acid concentrations is shown for the first time and was found to be analogous to that of uranyl, neptunyl, and plutonyl ions.

5729 4. Redox Potentials and Thermodynamic Properties 5730 4.1. Am(IV)/(III) 5730 4.2. Am(V)/Am(III) 5731 4.3. Am(VI)/Am(III) 5731 4.4. Am(VI)/(V) 5731 4.5. Am(VII)/(VI) 5731 4.6. Thermodynamic data for Am(IV), Am(V), and

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Radiolysis / Linear energy transfer / Redox reactions / Ligand degradation / Free radicals / Solvent extractionSummary. Radiochemistry deals with the chemistry of the radioactive elements. In the nuclear industry successful fuel reprocessing, high-level waste treatment, and long-term storage of spent fuel depend on an understanding of the radiochemistry of actinides and fission products in these settings. Radiation chemistry is concerned with the chemical effects of ionizing radiation, with the most common types of radiation encountered by the radiochemist being low linear energy transfer (LET) β − and γ radiation, and higher LET α radiation. These radiations can have profound and important effects on radiochemistry, including changes in metal oxidation states and degradation of the organic ligands designed to complex radioelements. This may occur by direct action of the incident radiation on compounds present with high abundance or by reaction with radiolytically produced reactive species for trace components, such as the complexing agents. This review examines the role of reactive species created in irradiated aqueous and organic solution and their effects on radiochemistry. The sources and nature of these reactive species are discussed. Examples of radiation chemical effects are provided related to solvent extraction of the actinides from acidic solution, metal complexation and technetium redox chemistry in alkaline tank waste, and the corrosion of spent fuel stored in repository brine.

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Selective oxidation of trivalent americium (Am) could facilitate its separation from lanthanides in nuclear waste streams. Here, we report the application of a high-surface-area, tin-doped indium oxide electrode surface-derivatized with a terpyridine ligand to the oxidation of Am(III) to Am(V) and Am(VI) in nitric acid. Potentials as low as 1.8 volts (V) versus the saturated calomel electrode were applied, 0.7 V lower than the 2.6 V potential for one-electron oxidation of Am(III) to Am(IV) in 1 molar acid. This simple electrochemical procedure provides a method to access the higher oxidation states of Am in noncomplexing media for the study of the associated coordination chemistry and, more important, for more efficient separation protocols.