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Pathways Contributing to the Formation and Decay of Ferrous Iron in Sunlit Natural Waters

机译:在阳光下的天然水域中有助于光线形成和腐烂的途径

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Pathways contributing to the formation and decay of Fe(Ⅱ) in sunlit natural waters are investigated in this chapter with insights drawn from both laboratory experiments and kinetic modelling. Our results support previous findings that superoxide-mediated iron reduction (SM1R) is the main pathway for photochemical reduction of Fe(III) at pH 8 while light-induced ligand to metal charge transfer (LMCT) is important in low pH environments. Furthermore, our work shows that triplet oxygen and photo-produced species are the main oxidants of Fe(Ⅱ) while hydrogen peroxide, a relatively stable end product of SRFA photolysis, is not involved in Fe(Ⅱ) oxidation. A kinetic model based on these observations is presented which provides an excellent description of the experimental results and is consistent with observations from a wide range of studies investigating the redox cycling of iron.
机译:在本章中调查了在本章中调查了阳光自然水域中的Fe(Ⅱ)的途径,并从实验室实验和动力学建模中汲取了洞察力。我们的研究结果支持以前发现超氧化物介导的铁还原(SM1R)是pH8在pH 8的Fe(III)的光化学还原的主要途径,而光诱导的配体对金属电荷转移(LMCT)在低pH环境中是重要的。此外,我们的作品表明,三重氧和光产生的物种是Fe(Ⅱ)的主要氧化剂,而过氧化氢,SRFA光解的相对稳定的最终产物,不参与Fe(Ⅱ)氧化。提出了一种基于这些观察结果的动力学模型,其提供了实验结果的优异描述,并且与来自各种研究的观察结果一致地研究铁的氧化还原循环。

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