Effect of peroxymonosulfate pre-oxidation coupled with subsequent Fe-based coagulation on the mitigation of organic matter and the formation of disinfection by-products†

IF 3.1 4区 环境科学与生态学 Q3 ENGINEERING, ENVIRONMENTAL Environmental Science: Water Research & Technology Pub Date : 2025-02-27 DOI:10.1039/D4EW01021C
Xuan Li, Keyan Liu, Zhe Ren, Zhenqi Du, Rong Xiao, Ruixue Jiang, Xiaochen Li and Tiantian Chen
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Abstract

The generative ability of abundant reactive species ensures peroxymonosulfate (PMS) pre-oxidation coupled with subsequent Fe-based coagulation (PPFeC) a promising drinking water treatment process, whereas these abundant reactive species can also oxidize chloride in water matrices to form reactive chlorine species (RCS). These RCS can further oxidize organic compounds, resulting in the unexpected cytotoxic and genotoxic disinfection by-product (DBP) formation. Thus, this study investigated the effect of PMS pre-oxidation coupled with subsequent Fe-based coagulation on the mitigation of organic matter and DBP. Here, results showed that the PPFeC process presented better dissolved organic carbon (DOC) removal performance than PMS pre-oxidation and Fe-based coagulation. Compared to Fe3+-based coagulation, Fe2+-based coagulation resulted in higher DOC removal performance (increased by 63.5% in natural water), higher DBP concentration and water toxicity (increased by 31.3% for the cytotoxicity index and 18.5% for the genotoxicity index in natural water) during the PPFeC process. DBP concentration and toxicity decreased with the increase of the pre-oxidation time, and increased with the increase of PMS concentration. Furthermore, concentration of DBP and toxicity of water initially increased and then decreased with the increase of sedimentation time and coagulant concentration. In addition, compared to SO4˙ and PMS, HO· played a more significant role in the DBP formation and toxicity during the PPFeC process. Therefore, Fe3+-based coagulants were reliable to ensure drinking water safety as PMS was applied as the pre-oxidant.

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过氧单硫酸盐预氧化与后续铁基混凝对有机物减少和消毒副产物形成的影响
丰富的活性物质的生成能力使过氧单硫酸盐(PMS)预氧化和随后的铁基混凝(PPFeC)成为一种有前途的饮用水处理工艺,而这些丰富的活性物质也可以氧化水基质中的氯形成活性氯(RCS)。这些RCS可以进一步氧化有机化合物,导致意想不到的细胞毒性和基因毒性消毒副产物(DBP)的形成。因此,本研究探讨了PMS预氧化结合随后的铁基混凝对有机物和DBP的缓解作用。结果表明,PPFeC工艺对溶解有机碳(DOC)的去除效果优于PMS预氧化法和铁基混凝法。与Fe3+基混凝相比,Fe2+基混凝在PPFeC过程中具有更高的DOC去除率(在天然水中提高了63.5%),DBP浓度和水毒性(在天然水中细胞毒性指数提高了31.3%,遗传毒性指数提高了18.5%)。DBP浓度和毒性随预氧化时间的增加而降低,随PMS浓度的增加而升高。随着沉淀时间和混凝剂浓度的增加,水的DBP浓度和毒性呈先升高后降低的趋势。此外,与SO4˙−和PMS相比,HO·在PPFeC过程中DBP的形成和毒性中起着更重要的作用。因此,采用PMS作为预氧化剂,Fe3+基混凝剂可以可靠地保证饮用水的安全。
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麦克林
Sodium chloride
麦克林
Tyrosine
麦克林
FeSO4
麦克林
Fe2(SO4)3
麦克林
PMS
麦克林
Humic acid
来源期刊
Environmental Science: Water Research & Technology
Environmental Science: Water Research & Technology ENGINEERING, ENVIRONMENTALENVIRONMENTAL SC-ENVIRONMENTAL SCIENCES
CiteScore
8.60
自引率
4.00%
发文量
206
期刊介绍: Environmental Science: Water Research & Technology seeks to showcase high quality research about fundamental science, innovative technologies, and management practices that promote sustainable water.
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