4.8 Article

Freezing-Enhanced Photoreduction of Iodate by Fulvic Acid

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 57, Issue 48, Pages 20272-20281

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.3c07278

Keywords

chemical reactions in ice; iodate reduction; reactive iodine; photosensitization; organoiodinecompounds

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This study found that the photosensitized reduction of iodate by fulvic acid is enhanced in frozen solution. The process involves the production of iodide, reactive iodine, and organoiodine compounds. The reduction increases with decreasing pH and increasing fulvic acid concentration, and is enhanced by coexisting iodide or chloride ions.
Iodate is a stable form of iodine species in the natural environment. This work found that the abiotic photosensitized reduction of iodate by fulvic acid (FA) is highly enhanced in frozen solution compared to that in aqueous solution. The freezing-induced removal of iodate by FA at an initial pH of 3.0 in 24 h was lower than 10% in the dark but enhanced under UV (77.7%) or visible light (31.6%) irradiation. This process was accompanied by the production of iodide, reactive iodine (RI), and organoiodine compounds (OICs). The photoreduction of iodate in ice increased with lowering pH (pH 3-7 range) or increasing FA concentration (1-10 mg/L range). It was also observed that coexisting iodide or chloride ions enhanced the photoreduction of iodate in ice. Fourier transform ion cyclotron resonance mass spectrometric analysis showed that 129 and 403 species of OICs (mainly highly unsaturated and phenolic compounds) were newly produced in frozen UV/iodate/FA and UV/iodate/FA/Cl- solution, respectively. In the frozen UV/iodate/FA/Cl- solution, approximately 97% of generated organochlorine compounds (98 species) were identified as typical chlorinated disinfection byproducts. These results call for further studies of the fate of iodate, especially in the presence of chloride, which may be overlooked in frozen environments.

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