{"title":"Far UVC photolysis of PDS and H2O2 in saline water generates disinfection By-products","authors":"Jingmeng Guan , Huang Huang , Wenhai Chu , Xin Yang","doi":"10.1016/j.watres.2025.123866","DOIUrl":null,"url":null,"abstract":"<div><div>Far-UVC-driven (222 nm) advanced oxidation processes (UV<sub>222</sub>/AOPs) have gained increasing attentions for water decontamination owing to their high yields of reactive species and rapid degradation rate constants of emerging contaminants. However, the formation of toxic disinfection by-products (DBPs) during UV<sub>222</sub>/AOP treatments of saline water remains unexplored. In this study, we demonstrated that DBPs generated in UV<sub>222</sub>/PDS and UV<sub>222</sub>/H<sub>2</sub>O<sub>2</sub> treatment of saline water with the presence of 0.5 M Cl<sup>⁻</sup> was 3.55–4.50 and 1.47–1.61 times higher, respectively, compared to those generated in UV<sub>254</sub>/PDS and UV<sub>254</sub>/H<sub>2</sub>O<sub>2</sub>. Adsorbable organic halogen (AOX) generated in UV<sub>222</sub>/AOPs was also higher than UV<sub>254</sub>/AOPs. Notably, DBPs and AOX generated from Suwannee River fulvic acid (SRFA) in UV<sub>222</sub>/PDS treatment were 32.33 times and 6.14 times higher than in UV<sub>222</sub>/H<sub>2</sub>O<sub>2</sub>, primarily due to the elevated concentration of reactive halogen species and the accumulation of hypochlorous acid/ hypohalite. Moreover, the presence of Br⁻ in saline water led to the conversion of chlorinated DBPs into brominated DBPs in both UV<sub>222</sub>/PDS and UV<sub>222</sub>/H<sub>2</sub>O<sub>2</sub>, significantly increasing the overall toxicity associated with DBPs. Increasing the pH from 5.0 to 9.0 was found to reduce DBP-associated toxicity. This study highlights the formation of toxic DBPs in UV<sub>222</sub>/AOPs and provides theoretical foundation for the selection and regulation of UV<sub>222</sub>/AOPs from the perspective of DBP control.</div></div>","PeriodicalId":443,"journal":{"name":"Water Research","volume":"283 ","pages":"Article 123866"},"PeriodicalIF":11.4000,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Water Research","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0043135425007742","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Far-UVC-driven (222 nm) advanced oxidation processes (UV222/AOPs) have gained increasing attentions for water decontamination owing to their high yields of reactive species and rapid degradation rate constants of emerging contaminants. However, the formation of toxic disinfection by-products (DBPs) during UV222/AOP treatments of saline water remains unexplored. In this study, we demonstrated that DBPs generated in UV222/PDS and UV222/H2O2 treatment of saline water with the presence of 0.5 M Cl⁻ was 3.55–4.50 and 1.47–1.61 times higher, respectively, compared to those generated in UV254/PDS and UV254/H2O2. Adsorbable organic halogen (AOX) generated in UV222/AOPs was also higher than UV254/AOPs. Notably, DBPs and AOX generated from Suwannee River fulvic acid (SRFA) in UV222/PDS treatment were 32.33 times and 6.14 times higher than in UV222/H2O2, primarily due to the elevated concentration of reactive halogen species and the accumulation of hypochlorous acid/ hypohalite. Moreover, the presence of Br⁻ in saline water led to the conversion of chlorinated DBPs into brominated DBPs in both UV222/PDS and UV222/H2O2, significantly increasing the overall toxicity associated with DBPs. Increasing the pH from 5.0 to 9.0 was found to reduce DBP-associated toxicity. This study highlights the formation of toxic DBPs in UV222/AOPs and provides theoretical foundation for the selection and regulation of UV222/AOPs from the perspective of DBP control.
远uvc驱动的(222 nm)深度氧化工艺(UV222/AOPs)因其高活性物质收率和对新出现污染物的快速降解速率常数而越来越受到人们的关注。然而,在UV222/AOP处理盐水过程中毒性消毒副产物(DBPs)的形成仍未被探索。在这项研究中,我们证明了UV222/PDS和UV222/H2O2处理含0.5 M Cl的盐水所产生的DBPs分别是UV254/PDS和UV254/H2O2处理的3.55-4.50和1.47-1.61倍。UV222/AOPs中产生的可吸附有机卤素(AOX)也高于UV254/AOPs。值得注意的是,UV222/PDS处理下Suwannee河黄腐酸(SRFA)产生的DBPs和AOX分别是UV222/H2O2处理下DBPs和AOX的32.33倍和6.14倍,这主要是由于反应性卤素物种浓度升高和次氯酸/次盐的积累。此外,Br在盐水中的存在导致氯化dbp在UV222/PDS和UV222/H2O2中转化为溴化dbp,显著增加了dbp的总体毒性。将pH从5.0提高到9.0可以降低dbp相关的毒性。本研究突出了UV222/AOPs中毒性DBPs的形成,从DBP控制的角度为UV222/AOPs的选择和调控提供了理论基础。
期刊介绍:
Water Research, along with its open access companion journal Water Research X, serves as a platform for publishing original research papers covering various aspects of the science and technology related to the anthropogenic water cycle, water quality, and its management worldwide. The audience targeted by the journal comprises biologists, chemical engineers, chemists, civil engineers, environmental engineers, limnologists, and microbiologists. The scope of the journal include:
•Treatment processes for water and wastewaters (municipal, agricultural, industrial, and on-site treatment), including resource recovery and residuals management;
•Urban hydrology including sewer systems, stormwater management, and green infrastructure;
•Drinking water treatment and distribution;
•Potable and non-potable water reuse;
•Sanitation, public health, and risk assessment;
•Anaerobic digestion, solid and hazardous waste management, including source characterization and the effects and control of leachates and gaseous emissions;
•Contaminants (chemical, microbial, anthropogenic particles such as nanoparticles or microplastics) and related water quality sensing, monitoring, fate, and assessment;
•Anthropogenic impacts on inland, tidal, coastal and urban waters, focusing on surface and ground waters, and point and non-point sources of pollution;
•Environmental restoration, linked to surface water, groundwater and groundwater remediation;
•Analysis of the interfaces between sediments and water, and between water and atmosphere, focusing specifically on anthropogenic impacts;
•Mathematical modelling, systems analysis, machine learning, and beneficial use of big data related to the anthropogenic water cycle;
•Socio-economic, policy, and regulations studies.