Multi-surface modeling of Ni(II) and Cd(II) partitioning in soils: Effects of salts and solid/liquid ratios

Abstract

Metal partitioning in soils is a key process controlling metal bioavailability and mobility and is greatly influenced by the solid/liquid ratio. However, metal partitioning is difficult to describe either by a simple partition coefficient or by isotherm adsorption equations. This study investigated the solubility of Ni(II) and Cd(II) in 19 soils as a function of three extraction reagents (water, 0.01 M NaNO₃, and 0.01 M CaCl₂), five solid/liquid ratios (5-400 g/L) and field condition extracted by Rhizon samplers. Thermodynamically based multi-surface models (MSMs) that included generic parameters were used to describe metal partitioning under the studied conditions. The results showed that Ni/Cd solubility depended on the soil type, extraction reagent, and solid/liquid ratio. Soil major background cations (especially Ca²⁺, Mg²⁺, Fe³⁺ and Al³⁺) had a significant effect on the model's prediction ability. The MSM was able to predict the extractable metal in 0.01 M CaCl₂ in various soils at different solid/liquid ratios when soil background cations were included in the calculation; without the background cations, the model was able to predict metal partitioning only at solid/liquid ratios of <100 g/L. In addition, the model failed to predict water-extracted and 0.01 M-NaNO₃-extracted Ni/Cd if background cations were not included, but could reasonably do so if they were included. More importantly, after the background cations were included, MSMs relatively well predicted the Ni/Cd content in soil pore water under 80% field capacity conditions with water as the solution matrix.

Keywords: Field condition; Multi-surface model; Pore water; Suspension density.