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Photochemical Decomposition of Oxalate Precipitates in Nitric Acid Medium
Korea Atomic Energy Research Institute, P.O. Box 105, Yusong, Taejon 305-600, Korea
ehkim1@nanum.kaeri.re.kr
Korean Journal of Chemical Engineering, May 1999, 16(3), 351-356(6), 10.1007/BF02707124
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Abstract
This work has been performed as a part of the partitioning of minor actinides. Minor actinides can be recovered from high-level wastes as oxalate precipitates, but they tend to be co-precipitated together with lanthanide oxalates. This requires another partitioning step for mutual separation of actinide and lanthanide groups. Accordingly, the objective of this study was to decompose and dissolve oxalate precipitates into a dilute nitric acid solution by using a photochemical reaction. In order to do this, oxalic acid and neodymium oxalate precipitate were used in this study. Neodymium oxalate was chosen as a stand-in element representing americium curium and lanthanides. As a result, decomposition characteristics of oxalic acid were first investigated and then on the basis of these results, the decomposition of neodymium oxalate precipitates was evaluated. From results using oxalic acid, the oxalate decomposition appeared to take place due to the reaction between the oxalate ion and hydroxyl radical generated from the nitric acid by photo-radiation. And the oxalate decomposition rate was measured in the experiments for various nitric acid contents when a mercury lamp (λ=254 nm) was used as a light source. The maximum decomposition rate was obtained when the nitric acid concentration was around 0.5 M, while the decomposition rate was reduced with an increase in the nitric acid concentration at more than 0.5 M. The photo-decomposition rate of neodymium oxalate precipitates was found to be 0.0034 M/h at the condition of 0.5 M HNO3.
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Sarakha M, Boule P, Lenoir D, J. Photochem. Photobiol. A-Chem., 75, 61 (1993)
