Abstract
During this work the determination of uranium in the range of μg·L−1 to tens of μg·L−1 was done by alpha-spectrometry after electroplating the aliquots of water sample using (NH4)2SO4 as an electrolyte. In general, the determination of uranium by alpha-spectrometry needs its separation from other transuranics specially thorium. The process described here does not involve any sample digestion and radiochemical separation of uranium from other transuranics. In this method an aliquot (1 to 3 mL) of the sample was dried and dissolve in (NH4)2SO4 and thereafter the sample was electroplated on a stainless steel (SS) planchet by using an electrochemical cell of special design. The proposed techniques have a distinct advantage over the determination of uranium by adsorptive stripping voltammetry (AdSV) in which uranium-chloranilic (2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone) acid complex was used for concentrating the uranium from the solution. Since in the case of AdSv, the determination of uranium was not possible for samples having dissolved organic carbon (DOC) more than 15 mg·L−1 and Cl− concentration is in the range of 40,000 μ·g−1. In the case of spike experiments with 232U the recovery was observed in the range of 90–95% in aqueous medium having higher concentration of Cl− and DOC as indicated above.
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Singhal, R.K., Preetha, J., Karpe, R. et al. Improvement in the determination of traces of uranium in aqueous medium having high dissolved organic carbon and chloride ion by alpha-spectrometry. J Radioanal Nucl Chem 279, 301–306 (2009). https://doi.org/10.1007/s10967-007-7294-4
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DOI: https://doi.org/10.1007/s10967-007-7294-4