Leaching of depleted uranium in soil as determined by column experiments

被引:0
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作者
W. Schimmack
U. Gerstmann
U. Oeh
W. Schultz
P. Schramel
机构
[1] Institute of Radiation Protection,GSF
[2] Institute of Ecological Chemistry,National Research Center for Environment and Health
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Uranium; Inductively Couple Plasma Mass Spectrometry; Corrosion Product; Unat; Uranium Mineral;
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摘要
The basic features of the leachability of depleted uranium (DU) projectiles in soil was investigated by using 12 projectiles (145–294 g DU) and 16 columns installed in an air-conditioned laboratory. Two soils widely distributed in Europe, a sandy-loamy cambisol and a silty-loamy luvisol, were filled into the columns (3.3 kg dry soil each). The effluents of all columns were collected weekly during the observation period of 1 year. In 648 samples, 235U and 238U were determined by inductively coupled plasma mass spectrometry. The leaching rates of 238U from natural uranium were in general about 0.01 μg week-1 or smaller, while those of 238U from the DU munitions varied considerably and reached values of up to 100 μg week-1, for the different columns. In total, about 0.3 μg natural uranium corresponding to 20 ppm of its inventory in the soil was leached during the observation period. From the projectiles, an average of about 50 μg DU were leached corresponding to 18 ppm of the corroded DU mass (about 1.6% of the mean initial DU mass of the projectiles). Assuming that corrosion and leaching continue as observed, the mobilisation of 238U from DU munitions will last, on an average, for thousands of years in the soils investigated, while the munitions themselves will have been corroded after a much shorter time. It is proposed to use, for the investigated soil types, the mean leaching rates of the six columns with projectiles for transport calculations of 238U to the groundwater and, thus, for a better risk assessment of the water-dependent uptake pathways of DU.
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页码:183 / 191
页数:8
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