Transformation of tetrachloroethylene in a flow-through electrochemical reactor.

Electrochemical transformation of harmful tetrachloroethylene (PCE) is evaluated as a method for management of groundwater plumes to protect the drinking water resource, its consumers and the environment. In contrast to previous work that reported transformation of trichloroethylene, a byproduct of PCE, this work focuses on transformation of PCE in a saturated porous matrix and the influence of design parameters on the removal performance. Design parameters investigated were electrode configuration, catalyst load, electrode spacing, current intensity, orientation of reactor and flow through a porous matrix.

Electrochemical transformation of an aged tetrachloroethylene contamination in realistic aquifer settings.

Electrochemical removal of chlorinated ethenes in groundwater plumes may potentially overcome some of the challenges faced by current remediation technologies. So far, studies have been conducted in simplified settings of synthetic groundwater and inert porous matrices. This study is a stepwise investigation of the influence of field-extracted groundwater, sandy sediment and groundwater aquifer temperatures on the removal of an aged partially degraded contamination of tetrachloroethylene (PCE) at a typical groundwater flow rate.

Electrokinetics applied in remediation of subsurface soil contaminated with chlorinated ethenes - A review.

Electrokinetics is being applied in combination with common insituremediation technologies, e.g. permeable reactive barriers, bioremediation and in-situ chemical oxidation, to overcome experienced limitations in remediation of chlorinated ethenes in low-permeable subsurface soils.

Challenges in electrochemical remediation of chlorinated solvents in natural groundwater aquifer settings.

Establishment of electrochemical zones for remediation of dissolved chlorinated solvents in natural settings was studied. An undivided 1D-experimental column set-up was designed for the assessment of the influence of site-extracted contaminated groundwater flowing through a sandy aquifer material, on the execution of laboratory testing. A three-electrode system composed of palladium coated pure iron cathodes and a cast iron anode was operated at 12 mA under varying flow rates.