Low permeability zone remediation of trichloroethene via coupling electrokinetic migration with in situ electrochemical hydrodechlorination.

Abstract To address the challenge of trichloroethene (TCE) remediation in low permeability zone, an inexpensive Cu–Ni bimetallic cathode was proposed in electrokinetic (EK) remediation system to couple electrokinetic migration with in situ electrochemical hydrodechlorination. Aqueous phase TCE was originally added into the anolyte so that breakthrough curves through the low permeability porous soil compartment could be obtained to better understand TCE migration driven by electroosmosis flow using different cathodes. The Cu–Ni cathode resulted in more TCE migration of 7.64 mg compared to that of 5.99 mg with Ni and 4.22 mg with mixed metal oxide (MMO) cathode, suggesting that the Cu–Ni cathode was capable of driving more TCE flux out of the contaminated soil. With the Cu–Ni cathode, 98.4% of TCE flux that reached the cathode was electrochemically reduced on the cathode, which was much higher than that with MMO cathode (77.9%) or Ni cathode (59.6%). TCE mass that was transported by electroosmosis flow increased from 2.04 to 6.68 mg when the voltage gradient increased from 1 to 4 V cm−1, with the normalized energy consumption increasing from 0.06 to 0.16 kWh kg−1 per unit water movement, and from 0.54 to 2.55 kWh g−1 per unit TCE transport. For TCE that did reach the cathode compartment, > 98% degradation maintained at the Cu–Ni cathode with various voltage gradients. The coupled electrokinetic and electrochemical hydrodechlorination technology appears to be a promising strategy for the remediation of low permeability porous media.