傅里叶变换离子回旋共振
天然有机质
溶解有机碳
质谱法
环境化学
化学
水生生态系统
生化工程
吸附
色谱法
工程类
有机化学
作者
Mingqi Ruan,Fengchang Wu,Fuhong Sun,Fanhao Song,Tingting Li,Chen He,Juan Jiang
标识
DOI:10.1080/10643389.2022.2157167
摘要
AbstractAbstractDissolved organic matter (DOM) contains complex molecular compounds that dominate its heterogeneous dynamics and behaviors in aquatic environments. Fourier transform ion cyclotron resonance mass spectrometry (FTICR-MS) with ultra-high resolution has proven to be effective in characterizing aquatic DOM. However, a systematic summary of molecular-level compositions and behaviors of DOM in natural and engineered water systems remains insufficient. This study provides a critical review of DOM characterization by FTICR-MS, with emphasis on composition diversity, chemical properties, transformation, and dynamics in the natural and engineered water systems. First, FTICR-MS strategies for DOM characterization are introduced on data interpretation and collaborative analysis of complementary datasets (e.g. spectroscopic data). Second, DOM characteristics, including spatiotemporal distribution, photochemical activity, microbial modification, and interface adsorption in natural water environments were comprehensively summarized based on current FTICR-MS findings. Third, DOM molecular changes caused by different engineered treatment methods were reviewed to highlight the molecular variation, reaction, and transformation by focusing on the FTICR-MS results. Finally, we summarized current limitations, biases, and future directions of FTICR-MS, and future extended studies of natural/engineered-derived DOM behavior. This FTICR-MS application review provides favorable strategies for understanding the molecular chemistry and behaviors of aquatic DOM.Graphical AbstractKeywords: Aquatic DOMmolecular heterogeneitymolecular evolutionchemical propertiesmigration and transformationenvironmental reactionsHandling Editors: Dan Tsang and Lena Q. Ma Disclosure statementThe authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.Additional informationFundingThis work was financially supported by the National Key Research and Development Program (nos. 2021YFC3201000, 2021YFC3201001), Budget Surplus of Central Financial Science and Technology Plan (no. 2021-JY-09), and China Postdoctoral Science Foundation (nos. 2021TQ0315, 2022M713010).
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