Electrolytic oxidation of trichloroethylene using a ceramic anode

G. Chen, E. A. Betterton, R. G. Arnold

Research output: Contribution to journalArticlepeer-review

77 Scopus citations


Trichloroethylene (TCE) was transformed to CO2, CO, Cl- and ClO3- at the anode of a two-chambered electrolytic cell. The working electrode was constructed from Ebonex, an electrically conductive ceramic (Ti4O7). Under our experimental conditions (anode potential Ea = 2.5 to 4.3 V vs SSCE), the disappearance of TCE was first order in TCE concentration. The transformation rate was independent of pH in the range 1.6<pH<11. TCE oxidation occurred only on the anodic surface and was limited by mass transport at high potentials (Ea>4.0 V). The maximum (transport-limited), surface-area-normalized rate constant was about 0.002 43 cm s-1. Carbon-containing products included CO2 primarily with traces of CO. At neutral and alkaline pHs, the only chlorine-containing products were Cl- and ClO3-. Hydroxyl radicals were detected in the anodic compartment using a spin trap (4-POBN). A kinetic model was successfully correlated with experimental results.

Original languageEnglish (US)
Pages (from-to)961-970
Number of pages10
JournalJournal of Applied Electrochemistry
Issue number8
StatePublished - 1999

ASJC Scopus subject areas

  • Chemical Engineering(all)
  • Electrochemistry
  • Materials Chemistry


Dive into the research topics of 'Electrolytic oxidation of trichloroethylene using a ceramic anode'. Together they form a unique fingerprint.

Cite this