TiO2-photocatalyzed oxidative degradation of CH3CN, CH3OH, C2HCl3, and CH2Cl2 supplied as vapors and in aqueous solution under similar conditions

Acetonitrile (CH3CN), methanol (CH3OH), trichloroethylene (C2HCl3 TCE), and methylene chloride (CH2Cl2) were degraded in stirred batch reactors in the presence of O-2 at room temperature over films of pristine P-25 TiO2 under irradiation centered at 360 nm. Molarities of organics, activities of O-2, irradiation flux, deployment of catalyst, and reactor configuration were matched for vaporized and aqueous organics. The dependence of initial rates and the photoefficiencies of removal on concentrations of rea cta nts and photon flux were measured. ldentities and rates of formation and decay of some intermediates were determined. Langmuir coefficients were determined for dark adsorption of the organic vapors on films of P-25 in the presence of dry and water-saturated air. Surface concentrations in equilibrium with aqueous solutions in the dark were calculated with the aid of Henry's law constants from the Langmuir coefficients of the water-saturated vapors. Initial rates of removal of all four compounds from the vapor phase were much higher than from aqueous solution. Initial photoefficiencies of greater than or equal to 1 molecule removed per incident photon were observed with vaporized CH3OH and TCE in dry air. Water vapor strongly inhibited the conversion of CH3OH and CH2Cl2. CH3CN, TCE, and CH2Cl2 vapors appeared to react with both electrons and holes, and homolytic dissociation of the C-C and C-CI bonds of CH3CN and CH2Cl2 appeared to occur.