Photochemical oxidation of Cr(III) to Cr(VI) in the presence of Fe(III): Influence of Fe(III) concentration and UV wavelength

被引:0
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作者
Yen, Chun-Chien [1 ,4 ]
Chen, Kai-Yue [2 ]
Ahmed, M. M. M. [1 ,3 ]
Syu, Chien-Hui [4 ]
Liu, Yu-Ting [1 ,3 ]
Hsieh, Yi-Cheng [5 ]
Jien, Shih-Hao [1 ]
Tzou, Yu-Min [1 ,3 ]
机构
[1] Natl Chung Hsing Univ, Dept Soil & Environm Sci, Taichung 40227, Taiwan
[2] Natl Chiayi Univ, Dept Agron, Chiayi 600355, Taiwan
[3] Natl Chung Hsing Univ, Innovat & Dev Ctr Sustainable Agr, Taichung 40227, Taiwan
[4] Minist Agr, Taiwan Agr Res Inst, Agr Chem Div, Taichung 413008, Taiwan
[5] Texas A&M Univ Syst, Off Texas State Chemist, Texas A&M AgriLife Res, College Stn, TX 77843 USA
关键词
Ultraviolet light; Fe(OH)2+photolysis; Hydroxyl radical; Chromium oxidation; Environmental toxicity; REDUCTION; REMOVAL; WATER; IRON; CHROMIUM; DEGRADATION; SPECIATION; COMPLEXES; ACID; ENVIRONMENT;
D O I
10.1016/j.jhazmat.2024.136852
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The reduction of Cr(VI) to Cr(III) is key to lowering environmental toxicity and mobility, but the reverse process remains less understood. We investigated Cr(III) oxidation mechanisms across various pH levels and light wavelengths (185, 254, and 358 nm) in the presence of Fe(III). At pH 3.0 under 358 nm light, Cr(VI) production peaked at 11.65 mu M, driven by photo-reactive Fe(OH)2+ producing center dot OH radicals. While Fe(III) generally promotes Cr(III) oxidation, concentrations above 0.5 mM inhibited the process. Oxidation was most intense under 185 nm light, generating up to 217 mu M of Cr(VI), due to Fe(III) and water photolysis. At 254 and 358 nm, center dot OH was solely produced by Fe(III) photolysis, where center dot OH oxidized Fe(II), which then reduced Cr(VI), slowing Cr(III) oxidation. Short-wavelength, high-energy light significantly enhances Cr(III) oxidation. Under such UV exposure in the
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页数:10
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