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Determination of lead-210 in standard samples of soil, ores, and mill tailings

Journal Article · · Anal. Chem.; (United States)
DOI:https://doi.org/10.1021/ac00155a009· OSTI ID:5572941
Up to 5-G samples were dissolved in hyrofluoric acid and pyrosulfate fusion in the presence of bismuth tracer. The cake was dissolved in hydrochloric acid and bismuth-210 was extracted into diethyldithiocarbamate, separating it from most interferences including its lead-210 parent. Bismuth was then coprecipitated with barium sulfate and counted in a low-background ..beta.. counter through a 6 mg/cm/sup 2/ aluminum absorber to remove ..cap alpha.. particles from polonium-210. After the sample was counted, the barium sulfate was dissolved in alkaline ehtylenediaminetetraacetic acid, excess potassium iodide was added, and the solution was acidified. The yellow bismuth-iodide complex was measured in a spectrophotometer and the absorbance was compared with that from an identical aliquot of the bismuth solution to determine the chemical yield. Some results obtained in the analysis of soil, uranium ores, and mill tailings that were prepared for use as standards are given. When sufficient activity was present, the relative experimental standard deviations of 10 individual measurements about their own mean was less than 2%. On standards, the results obtained were within 3% of the known values at the 95% confidence level. Chemical yields were generally higher than 98% overall and were determined to better than 0.5%. Detection limits are about 0.1 pCi/g for 5-g samples and 6-h counts.
Research Organization:
EG and G Idaho, Idaho Falls
DOE Contract Number:
AC07-76ID01570
OSTI ID:
5572941
Journal Information:
Anal. Chem.; (United States), Journal Name: Anal. Chem.; (United States) Vol. 60:4; ISSN ANCHA
Country of Publication:
United States
Language:
English