Environmental Science & Technology · 1986 · 537 citations · 0 references
Natural SciencesEarth SciencesEnvironmental SciencesAtmospheric ChemistryChemical OceanographyEnvironmental ChemistryAquatic ChemistryOxygen EvolutionWater ChemistryWater PollutionWater QualityDissolved OxygenPhotochemical Formation PathwaysPhotochemical ReactivitySinglet Oxygen ChemistrySinglet Oxygen FormationSinglet Oxygen Generation
For prediction of the rate with which organic compounds are oxidized and photoproducts formed in the aquatic environment by the <sup>1</sup>O<sub>2</sub> route, the steady-state concentrations of <sup>1</sup>O<sub>2</sub> in various waters were determined by using furfuryl alcohol as a trapping agent. Under noon, summer sunlight (Switzerland) in lake, river, and wastewaters, surface concentrations were (0.3-3) x 10<sup>-14</sup> M <sup>1</sup>O<sub>2</sub> per mg of DOC/L. The more highly colored waters actually tend to produce less <sup>1</sup>O<sub>2</sub> for a given amount of adsorbed light. Separation of natural aquatic organic compounds by gel permeation chromatography resulted in fractions showing little correlation between <sup>1</sup>O<sub>2</sub> production efficiency and molecular weight, indicating that large macromolecular structures are not a prerequisite for the sensitization of <sup>1</sup>O<sub>2</sub> formation. Application of the specific <sup>1</sup>O<sub>2</sub> concentration data to the estimation of lifetimes of environmental pollutants yields half-lives as short as several hours only for a few especially reactive types of compounds but orders of magnitude longer for most of the compounds expected to be found in the aquatic environment.