Predicting Reactive Intermediate Quantum Yields from Dissolved Organic Matter Photolysis Using Optical Properties and Antioxidant Capacity

• Published in: Environmental science & technology 2017-05, Vol.51 (10), p.5404-5413
• Main Authors: Mckay, Garrett, Huang, Wenxi, Romera-Castillo, Cristina, Crouch, Jenna E, Rosario-Ortiz, Fernando L, Jaffé, Rudolf
• Format: Article
• Language: English
• Subjects: Antioxidants; Chemical reactions; Dissolved organic matter; Dry season; Estuaries; Florida; Hydroxyl Radical; Hydroxyl radicals; Intermediates; Mathematical models; Optical properties; Organic Chemicals; Oxidation; Oxidation-Reduction; Oxygen; Photolysis; Predictions; Quantum physics; Regression; Regression analysis; Singlet Oxygen; Water analysis; Water sampling; Wetlands
• ISSN: 0013-936X; 1520-5851
• DOI: 10.1021/acs.est.6b06372

The antioxidant capacity and formation of photochemically produced reactive intermediates (RI) was studied for water samples collected from the Florida Everglades with different spatial (marsh versus estuarine) and temporal (wet versus dry season) characteristics. Measured RI included triplet excited states of dissolved organic matter (3DOM*), singlet oxygen (1O2), and the hydroxyl radical (•OH). Single and multiple linear regression modeling were performed using a broad range of extrinsic (to predict RI formation rates, R RI) and intrinsic (to predict RI quantum yields, ΦRI) parameters. Multiple linear regression models consistently led to better predictions of R RI and ΦRI for our data set but poor prediction of ΦRI for a previously published data set, probably because the predictors are intercorrelated (Pearson’s r > 0.5). Single linear regression models were built with data compiled from previously published studies (n ≈ 120) in which E2:E3, S, and ΦRI values were measured, which revealed a high degree of similarity between RI-optical property relationships across DOM samples of diverse sources. This study reveals that •OH formation is, in general, decoupled from 3DOM* and 1O2 formation, providing supporting evidence that 3DOM* is not a •OH precursor. Finally, ΦRI for 1O2 and 3DOM* correlated negatively with antioxidant activity (a surrogate for electron donating capacity) for the collected samples, which is consistent with intramolecular oxidation of DOM moieties by 3DOM*.