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Environmental Fate Article

Robust Prediction of Kd from Soil Properties for Environmental Assessment

Pages 263-279 | Received 02 Dec 2009, Published online: 13 Feb 2011
 

ABSTRACT

Soil solid/liquid partition coefficients (Kd) are commonly used in quantitative environmental assessments as a means to predict retention of contaminant metals and radionuclides in soils. There are Kd data for most elements in the literature, and they can be measured for specific sites. However, there is also a need for robust, defensible relationships to predict the variation in Kd as a function of soil characteristics. This article reports relationships for As, Cd, Ce, Cl, Co, Cr, Cs, Cu, Fe, Ho, I, La, Mn, Mo, Nb, Nd, Ni, Np, Pa, Pb, Pu, Ra, Sb, Se, Sm, Sn, Sr, Tc, Th, Tl, Tm, U, W, and Yb, most based on a wide range of soil properties. Soil pH, clay content, and organic carbon content were the independent variables considered in all cases, and methodology variables were invoked for Cs, Mn, and Ni. The underlying Kd data were considered representative of steady state conditions: most were measured by desorption of the indigenous element at realistic field moisture contents. The equations, developed by forward or backward stepwise regression, were all statistically highly significant. Estimates from the equations were compared to data for seven site-specific soils and generally were within 95th percentile bounds.

ACKNOWLEDGMENTS

The author is grateful for financial and technical support from the Swedish Nuclear Fuel and Waste Management Co. (Svensk Kärnbränslehantering AB), Stockholm. B. Sanipelli of ECOMatters Inc. assisted with the literature review. G. Sohlenius of Sveriges geologiska undersökning, Uppsala conducted the field sampling and characterization of Swedish soils used in this study.

Notes

aFor desorption of indigenous Cs the Kd values will be 4.2-fold higher than predicted by the equation, and for sorption of new 137Cs, they will be 4.2-fold lower.

bFor desorption of indigenous Mn the Kd values will be 4.0-fold higher than predicted by the equation, and for sorption of new 54Mn, they will be 4.0-fold lower.

cFor desorption of indigenous Ni the Kd values will be 6.2-fold higher than predicted by the equation, and for sorption of new Ni, they will be 6.2-fold lower.

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