The extension of surfactant-based technologies for use in remediation of mercuric ion [Hg(ll)]-impacted soils and groundwaters was explored. In concept, a target metal ion can be selectively sequestered and mobilized from the subsurface by a ligand solubilized in surfactant solution. The selected ligand, 1-decyl-2-thiourea (DTU), was used in this study due to its extremely high selectivity for Hg2+ and its compatibility with micellar solubilization. In batch semiequilibrium dialysis studies using a mixture of 0.3 mM DTU and 30 mM cetylpyridinium nitrate (a cationic surfactant), 99.8% of applied Hg(ll) (0.1 mM) was retained, thus demonstrating the effectiveness of this ligandsurfactant system for separating the mobile contaminant from the waste stream. Isolation of the target metal ion from the complex is desirable to allow for ligand and surfactant reuse. As a function of the ligand type, this can be achieved by precipitation, pH stripping, or ligand-ligand exchange. In theory, for DTU, Hg(ll) removal can be done at an elevated pH by formation of a soluble mercury-hydroxide complex, which would pass a secondary ultrafiltration stage, allowing retention and reuse of the ligandsurfactant colloid. While only batch studies were conducted for this feasibility study, the possibility of utilizing flow-through ultrafiltration units coupled with contaminant isolation steps in pump-and-treat field applications is discussed.