Source-dependent photoreactivity of dissolved organic matter and its implications for specific disinfection byproduct formation.

IF 12.8 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
Water Research Pub Date : 2026-11-01 Epub Date: 2026-08-06 DOI:10.1016/j.watres.2026.126635
Ruizhe Wang, Yu Luo, Fang Chen, Zhineng Hao, Dong Ren, Junjian Wang
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引用次数: 0

Abstract

Photochemical processing dictates the molecular evolution of dissolved organic matter (DOM) in sunlit waters and its subsequent reactivity during chlorination. However, how source-specific molecular signatures regulate the photochemical transformations of DOM and its associated disinfection by-product (DBP) formation potentials remains poorly understood. Here, DOM samples derived from algae (ADOM), soil (SDOM), litter (LDOM), and wildfire ash (BDOM) were exposed to 28 days of simulated solar irradiation to elucidate source-dependent molecular transformations and their impacts on specific DBP formation. DOM compositional changes were characterized using optical spectroscopy and Fourier transform-ion cyclotron resonance mass spectrometry, and specific DBP formation potentials were assessed via chlorination assays. Distinct molecular signatures differentiated DOM sources, with ADOM enriched in protein- and lipid-like compounds, whereas SDOM, LDOM, and BDOM contained greater proportions of aromatic, lignin-, and tannin-like molecules. Irradiation drove partial convergence of DOM toward a more oxidized state, lower molecular weight, and more aromatic structures via decarboxylation, dealkylation, and deamination. These transformations reduced specific carbonaceous DBP formation (up to 93 %) across most DOM sources, whereas LDOM showed a ∼9 % increase in specific trihalomethane and chloral hydrate formation, likely due to the persistence and transformation of lignin-like precursors. Notably, specific haloacetonitrile formation potentials substantially increased by 99-125 % across all DOM sources, associated with the generation of reactive nitrogenous precursors through photo-oxidation and depolymerization of macromolecules. These findings demonstrate that solar-driven DOM transformation governs distinct carbonaceous and nitrogenous DBP responses, highlighting the need for source-specific molecular insights to predict and manage DBP risks in watersheds.

溶解有机物的源依赖性光反应性及其对特定消毒副产物形成的影响。
光化学过程决定了阳光照射下水体中溶解有机物(DOM)的分子演化及其在氯化过程中的后续反应性。然而,来源特异性分子特征如何调节DOM的光化学转化及其相关的消毒副产物(DBP)形成电位仍然知之甚少。本研究将来自藻类(ADOM)、土壤(SDOM)、凋落物(LDOM)和野火灰烬(BDOM)的DOM样品暴露在28天的模拟太阳照射下,以阐明源依赖的分子转化及其对特定DBP形成的影响。利用光谱学和傅里叶变换-离子回旋共振质谱法对DOM的组成变化进行了表征,并通过氯化分析评估了DBP的形成势。不同的分子特征区分了DOM来源,ADOM富含蛋白质和类脂化合物,而SDOM、LDOM和BDOM含有更多的芳香、木质素和单宁类分子。辐照通过脱羧、脱烷基和脱胺作用,使DOM向更氧化态、更低分子量和更多芳族结构的方向部分收敛。在大多数DOM源中,这些转化降低了碳质DBP的形成(高达93 %),而LDOM显示出三卤甲烷和水合氯醛的形成增加了~ 9 %,可能是由于木质素样前体的持续存在和转化。值得注意的是,在所有DOM源中,特定的卤乙腈生成电位大幅增加了99-125 %,这与通过光氧化和大分子解聚产生活性氮前体有关。这些发现表明,太阳能驱动的DOM转换控制着不同的碳质和氮质DBP响应,强调了对源特异性分子洞察力的需求,以预测和管理流域DBP风险。
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来源期刊
Water Research
Water Research 环境科学-工程:环境
CiteScore
20.80
自引率
9.40%
发文量
1307
审稿时长
38 days
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.
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