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黄铁矿活化过硫酸盐氧化降解甲基橙:机制、途径及水基质的影响。

Degradation of methyl orange by pyrite activated persulfate oxidation: mechanism, pathway and influences of water substrates.

机构信息

College of Resources and Environment, Shanxi Agricultural University, Taigu 030801, PR China E-mail:

出版信息

Water Sci Technol. 2022 May;85(10):2912-2927. doi: 10.2166/wst.2022.134.

DOI:10.2166/wst.2022.134
PMID:35638796
Abstract

Degradation mechanism of methyl orange (MO), a typical azo dye, with pyrite (FeS) activated persulfate (PS) was explored. The results showed that when the initial concentration of MO was 0.1 mM, FeS was 1.6 g/L and PS was 1.0 mM, the removal rate of MO could reach 92.9% in 150 min, and the removal rate of total organic carbon could reach 14.1%. In addition, both pH ≤ 2 and pH ≥ 10 could have an inhibitory effect in the FeS/PS system. Furthermore, Cl and low concentrations of HCO had little effect on the degradation of MO with FeS/PS. However, HPO and high concentrations of HCO could inhibit the degradation of MO in the system. Besides, MO in river water and tap water were not degraded in FeS/PS system, but acidification (pH = 4) would greatly promote the degradation. In addition, the removal rate of MO with FeS/PS could still reach about 90% after five cycles of FeS. Furthermore, the intermediates and possible degradation pathways were speculated by LC-MS, and the degradation mechanism of MO by FeS/PS was that the cycle of Fe(III)/Fe(II) could continuously activate persulfate to produce SO. The results could provide technical support for azo dye degradation in the FeS/PS system.

摘要

利用黄铁矿(FeS)活化过硫酸盐(PS)降解典型偶氮染料甲基橙(MO)的降解机制。结果表明,当 MO 的初始浓度为 0.1mM,FeS 为 1.6g/L,PS 为 1.0mM 时,150min 内 MO 的去除率可达 92.9%,总有机碳去除率可达 14.1%。此外,在 FeS/PS 体系中,pH≤2 和 pH≥10 均具有抑制作用。此外,Cl 和低浓度 HCO对 FeS/PS 体系中 MO 的降解影响较小,而 HPO和高浓度 HCO会抑制体系中 MO 的降解。此外,河水和自来水中的 MO 无法在 FeS/PS 体系中降解,但酸化(pH=4)会大大促进 MO 的降解。此外,FeS 经过五次循环后,FeS/PS 对 MO 的去除率仍可达到 90%左右。此外,通过 LC-MS 推测了中间产物和可能的降解途径,并提出了 FeS/PS 降解 MO 的机制是 Fe(III)/Fe(II)循环可不断活化过硫酸盐生成 SO。该结果可为 FeS/PS 体系中偶氮染料的降解提供技术支持。

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