Published 2014 | Version v1
Journal article

Sorption of cesium in young till soils

  • 1. Helsinki Univ. (Finland). Laboratory of Radiochemistry
  • 2. Saanio and Riekkola Oy, Consulting Engineers, Helsinki (Finland)
  • 3. Posiva Oy, Eurajoki (Finland)

Description

Soil samples from three forest soil pits were examined down to a depth of approximately three metres using 1 M ammonium acetate extraction and microwave-assisted extraction with concentrated nitric acid (HNO3), to study the binding of cesium (Cs) at Olkiluoto Island, southern Finland. Ammonium acetate was used to extract the readily exchangeable Cs fractions roughly representing the Cs fraction in soil which is available for plants. Microwave-assisted HNO3 extraction dissolves various minerals, e.g. carbonates, most sulphides, arsenides, selenides, phosphates, molybdates, sulphates, iron (Fe) and manganese (Mn) oxides and some silicates (olivine, biotite, zeolite), and reflects the total Cs concentrations. Cs was mostly found in the strongly bound fraction obtained through HNO3 extraction. The average Cs concentrations found in this fraction were 3.53 ± 0.30 mg/kg (d.w.), 3.06 ± 1.86 mg/kg (d.w.) and 1.83 ± 0.42 mg/kg (d.w.) in the three soil pits, respectively. The average exchangeable Cs found in the ammonium acetate extraction in all three sampling pits was 0.015 ± 0.008 mg/kg (d.w.). In addition, Cs concentrations in the soil solution were determined and in situ distribution coefficients (Kd) for Cs were calculated. Furthermore, the in situ Kd data was compared with the Cs Kd data obtained using the model batch experiments. The in situ Kd values were observed to fairly well follow the trend of batch sorption data with respect to soil depth, but on average the batch distribution coefficients were almost an order of magnitude higher than the in situ Kd data. In situ Cs sorption data could be satisfactory fitted with the Langmuir sorption isotherm, but the Freundlich isotherm failed to fit the data. Finally, distribution coefficients were calculated by an ion exchange approach using soil solution data, the cation exchange capacity (CEC) as well as Cs to sodium (Na) and Cs to potassium (K) ion exchange selectivity coefficients. The calculated distribution coefficients corresponded well with the in situ distribution coefficient values. (orig.)

Additional details

Publishing Information

Journal Title
Radiochimica Acta
Journal Volume
102
Journal Issue
7
Journal Page Range
p. 645-658
ISSN
0033-8230
CODEN
RAACAP