Degradation of 15 halogenated hydrocarbons by 5 unactivated <i>in-situ</i> chemical oxidation oxidants

Oxidants used in the ISCO technology usually require activation by activators to degrade contaminants. However, this study investigated degradation of 15 typical halogenated hydrocarbons by five common ISCO oxidants (PS, PMS, H₂O₂, KMnO₄, SPC) without activation in both pure water and real groundwater. Unactivated PS could degrade 14 halogenated hydrocarbons, excluding tetrachloromethane. Unactivated KMnO₄ could degrade chlorinated alkenes. Unactivated SPC could degrade 1,1,2,2-tetrachloroethane by a base-promoted second-order elimination reaction. PMS, H₂O₂, and SPC could be activated by the natural matrix constituents in groundwater, enabling them to degrade some halogenated hydrocarbons. Among the 15 halogenated hydrocarbons studied, only tetrachloromethane cannot be degraded by any oxidant due to its carbon being in its highest oxidation state. The experimental data in the pure water indicate that the overall degradation rate of unactivated PS for chlorinated alkanes increased with increases in the number of chlorine substituents. The degradation rate of unactivated PS for halogenated hydrocarbons decreased with increases in the carbon chain length. Chlorinated alkenes are more easily degraded than chlorinated alkanes while chlorinated alkanes are more readily degraded than brominated alkanes. The degradation rate of unactivated KMnO₄ for chlorinated alkenes decreased with increases in the number of chlorine substituents and decreased with increases in the carbon chain length. Overal, results of this study show that unactivated ISCO is a promising and environmentally friendly <i>in-situ</i> remediation technology that may be a good candidate for the remediation of contaminated sites by halogenated hydrocarbons.