Trichloroacetic acid dehalogenation by reductive radicals

P. DAVID GARA; E. BUCHARSKY; M. WÖRNER,; A.M. BRAUN; D.O. MÁRTIRE; M.C. GONZALEZ

INORGANICA CHIMICA ACTA

elsevier

Año: 2007 vol. 360 p. 1209 - 1216

0020-1693

Advanced oxidation processes, using either UVC/H2O2 or UVC/K2S2O8, both in the presence of H2CO2 or CH3OH are very efficient in mineralizing aqueous solutions of trichloroacetic acid (TCAA) leaving no toxic residues. The main reaction initiating TCAA depletion is its reduction by the radicals CO2-. or .CH2OH to yield .CCl2CO2- radicals and Cl- anions. Further thermal reactions of .CCl2CO2- lead to the formation of CO2 and HCl. Molecular oxygen competes with TCAA for CO2.- and .CH2OH radicals. However, in experiments under continuous irradiation of initially air-saturated solutions in closed reactors, the dissolved molecular oxygen concentration was depleted to low enough levels to favor the reaction of the reducing radicals with TCAA. A general reaction mechanism is proposed and discussed. The reaction between superoxide radical anions and TCAA was found to be of low efficiency.