Modeling and visualizing the transport and retention of cationic and oxyanionic metals (Cd and Cr) in saturated soil under various hydrochemical and hydrodynamic conditions.

Abstract Cationic and oxyanionic metals are widely existed in the aquatic and soil environment with the process of industrialization and they may behave different transport properties in aquifer systems due to the opposite charges. In this study, the comparative transport behaviors of Cd2+ and CrO42− in water-saturated soil columns were investigated under a variety of hydrochemical and hydraulic conditions such as pH, ionic strength (IS), and flow rate. The transport mechanisms of Cd(II) and Cr(VI) were explored by fitting the breakthrough curves with a two-site non-equilibrium transport model. Results indicated that high solution pH inhibited the transport of Cd(II) due to the enhanced electrostatic interaction. In contrast, the migration of Cr(VI) was promoted with the least amount of Cr(VI) (1.23 mg) being retained in soil at high pH, ascribing to the stronger electrostatic repulsion between anions and soil surface. Meanwhile, high pH conditions were not favorable for the participation of reduced iron in the reduction process of Cr(VI), resulting in the least amount of Cr(III) detected (22%). The increase in ionic strength decreased the negativity of the potential at the adsorption plane, which enhanced the transport of cationic Cd(II) and the retardation of anionic Cr(VI). In addition, the increase in flow rate facilitated the transport of Cd(II) and Cr(VI), mainly due to the decreasing contacting with porous media and enhanced dispersion effect. These findings demonstrated that the fate and environmental behavior of metal cations and anions differed with the change of hydrochemical and hydrodynamic properties, which should be considered for the risk assessment and remediation of metal contaminated sites.