Hydroxyl Radical Formation upon Oxidation of Reduced Humic Acids by Oxygen in the Dark

被引:205
作者
Page, Sarah E. [2 ]
Sander, Michael [1 ]
Arnold, William A. [3 ]
McNeill, Kristopher [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Biogeochem & Pollutant Dynam, Zurich, Switzerland
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Civil Engn, Minneapolis, MN 55455 USA
关键词
DISSOLVED ORGANIC-MATTER; PHOTO-FENTON REACTION; HYDROGEN-PEROXIDE; PHOTOSENSITIZED DEGRADATION; ELECTRON-ACCEPTORS; FULVIC-ACID; BISPHENOL-A; REDUCTION; SUBSTANCES; GENERATION;
D O I
10.1021/es203836f
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Humic acids (HAs) accept and donate electrons in many biogeochemical redox reactions at oxic/anoxic interfaces. The products of oxidation of reduced HAs by O-2 are unknown but are expected to yield reactive oxygen species, potentially including hydroxyl radical (center dot OH). To quantify the formation of center dot OH upon oxidation of reduced HAs by O-2, three HAs were reduced electrochemically to well-defined redox states and were subsequently oxidized by O-2 in the presence of the center dot OH probe terephthalate. The formation of center dot OH upon oxidation increased with increasing extent of HA reduction. The yield of center dot OH ranged from 42 to 160 mmol per mole of electrons donated by the reduced HA. The intermediacy of hydrogen peroxide (H2O2) in the formation of center dot OH was supported by enhancement of center dot OH formation upon addition of exogenous H2O2 sources and by the suppression of center dot OH formation upon addition of catalase as a quencher of endogenous H2O2. The formation of center dot OH in the dark during oxidation of reduced HA represents a previously unknown source of center dot OH formation at oxic/anoxic interfaces and may affect the biogeochemical and pollutant redox dynamics at these interfaces.
引用
收藏
页码:1590 / 1597
页数:8
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