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Singlet oxygen in surface waters. 3. Photochemical formation and steady-state concentrations in various types of waters
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1986
Year
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.