Abstract
A three-step method has been developed for extracting trace amounts of selenium from biological samples for neutron activation analysis /NAA/. After acid digestion, the sample is first extracted with lead diethyldithiocarbamate at pH 4 to remove a number of interfering elements. Next, selenium is extracted with sodium diethyldithiocarbamate into chloroform at pH 1.5. Finally, selenium is back-extracted with concentrated nitric acid for NAA. Analysis of selenium extracted from four standard reference materials resulted in excellent agreement with the certified values of selenium concentration. A detection limit of 0.05 μg has been achieved.
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Hani, N.M., Wai, C.M. & Willmes, H. Dithiocarbamate extraction of trace amounts of selenium from biological samples for neutron activation analysis. Journal of Radioanalytical and Nuclear Chemistry Letters 104, 19–28 (1986). https://doi.org/10.1007/BF02165417
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DOI: https://doi.org/10.1007/BF02165417