Anthracene photolysis in aqueous solution and ice: photon flux dependence and comparison of kinetics in bulk ice and at the air-ice interface.

We report an investigation of the photolysis kinetics of polycyclic aromatic hydrocarbons (PAHs) in aqueous solution, frozen in ice, and at air-ice interfaces. Measurements of PAH photolysis rates in aqueous solution and at air-ice interfaces as a function of lamp power show that the kinetics depend nonlinearly on photon flux. In both media, the rates do not increase when lamp powers are above 0.1 W, which corresponds to total photon fluxes lower than 10(13) photon cm(-2) s(-1) in the actinic region. This suggests that extrapolating laboratory-measured rates to expected atmospheric photon fluxes may not yield accurate lifetimes for some species. In the plateau region of the photon flux dependence, anthracene located within the ice matrix (or in liquid pockets or veins in the ice) undergoes photolysis at a similar rate to that in room temperature aqueous solution, but the rate of anthracene photolysis at air-ice interfaces is five times greater. This indicates that in order to accurately predict the lifetimes of aromatic pollutants in snow and ice, the quasi-liquid layer (QLL) must be treated separately from bulk ice.