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影响 pH 值对含有天然有机物的模拟淡水中铁的氧化还原转化。

Impact of pH on Iron Redox Transformations in Simulated Freshwaters Containing Natural Organic Matter.

机构信息

School of Civil and Environmental Engineering , The University of New South Wales , Sydney , New South Wales 2052 , Australia.

出版信息

Environ Sci Technol. 2018 Nov 20;52(22):13184-13194. doi: 10.1021/acs.est.8b03855. Epub 2018 Nov 7.

Abstract

The impact of the pH of natural waters on the various pathways contributing to the formation and decay of Fe(II) in the presence of Suwannee River Fulvic Acid (SRFA) is investigated in this study. Our results show that thermal Fe(III) reduction occurs as a result of the presence of hydroquinone-like moieties in SRFA with the rate of Fe(III) reduction by these entities relatively invariant with change in pH in the range 6.8-8.7. The Fe(II) oxidation rate in the dark is controlled by its interaction with O and increases with increase in pH with the overall outcome that the steady-state Fe(II) concentration in the dark is strongly affected by solution pH. On irradiation, a portion of the hydroquinone-like moieties present are oxidized to form semiquinones that are capable of reducing Fe(III) and/or oxidizing Fe(II) under circumneutral pH conditions. The extent of photogeneration of semiquinones on irradiation of SRFA and the persistence of these radicals increases significantly with decrease in pH. Due to the higher concentration and longevity of these organic moieties under low pH conditions, the impact of pH on steady-state Fe(II) concentration is less pronounced in previously irradiated SRFA solution compared to that observed in dark SRFA solution. Under irradiated conditions, the rates of Fe transformation (including both Fe(II) oxidation and Fe(III) reduction) are nearly independent of pH. While ligand-to-metal charge transfer (LMCT) is the dominant pathway for photochemical Fe(III) reduction, Fe(II) oxidation under irradiated conditions mainly occurs as a result of interaction with O, semiquinones and other short-lived oxidants. Overall, our data supports the conclusion that, as a result of the contribution from photogenerated organic moieties to Fe redox transformations, the steady-state Fe(II) concentration in irradiated surface waters containing natural organic matter may not be impacted significantly by changes in pH.

摘要

本研究考察了天然水中 pH 值对苏万尼河腐殖酸(SRFA)存在时 Fe(II) 形成和衰减各种途径的影响。研究结果表明,热 Fe(III) 还原是由于 SRFA 中存在对苯二酚样结构单元所致,这些结构单元还原 Fe(III) 的速率在 pH6.8-8.7 范围内相对不变。黑暗中 Fe(II) 的氧化速率受其与 O 的相互作用控制,并随 pH 值的增加而增加,其结果是黑暗中 Fe(II) 的稳态浓度强烈受溶液 pH 值的影响。在光照下,部分对苯二酚样结构单元被氧化形成半醌,在近中性 pH 条件下能够还原 Fe(III) 和/或氧化 Fe(II)。在光照下 SRFA 中半醌的光生成程度以及这些自由基的持久性随 pH 值的降低而显著增加。由于在低 pH 条件下这些有机结构单元的浓度更高且寿命更长,因此与黑暗 SRFA 溶液相比,先前辐照的 SRFA 溶液中 pH 值对稳态 Fe(II)浓度的影响不太明显。在辐照条件下,Fe 转化(包括 Fe(II)氧化和 Fe(III)还原)的速率几乎与 pH 值无关。虽然配体到金属电荷转移(LMCT)是光化学 Fe(III)还原的主要途径,但在辐照条件下 Fe(II)氧化主要是由于与 O、半醌和其他短寿命氧化剂的相互作用所致。总的来说,我们的数据支持这样的结论,即由于光生有机物质对 Fe 氧化还原转化的贡献,含有天然有机物的辐照地表水的稳态 Fe(II)浓度可能不会受到 pH 值变化的显著影响。

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