科研之友
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摘要
Dissolved organic matter (DOM) is a major sink of radicals in advanced oxidation processes (AOPs) and the radical-induced DOM transformation influences the subsequent water treatment processes or receiving waters. In this study, we quantified and compared DOM transformation by tracking the changes of dissolved organic carbon (DOC), UVA254, and electron donating capacity (EDC) as functions of four one-electron oxidants (SO4 center dot- , Cl2 center dot- , Br2 center dot-, and CO3 center dot- ) exposures as well as the changes of functional groups and molecule distribution. SO4 center dot- had the highest DOC reduction while Cl2 center dot- had the highest EDC reduction, which could be due to their preferential reaction pathways of decarboxylation and converting phenols to quinones, respectively. Br2 center dot- and CO3 center dot- induced less changes in DOC, UVA254, and EDC than SO4 center dot- and Cl2 center dot- . Additionally, DOM enriched with high aromatic contents tended to have higher DOC, UVA254, and EDC reductions. Decreases in hydroxyl and carboxyl groups and increases in carbonyl groups were observed in these four types of radicals treated DOM using Fourier transform infrared spectroscopy. High resolution mass spectrometry using FTICR-MS showed that one-electron oxidants preferred to attack unsaturated carbon skeletons and transformed into molecules featuring high saturation and low aromaticity. Moreover, SO4 center dot- was inclined to decrease oxidation state of carbon and O/C of DOM due to its strong decarboxylation capacity. This study highlights the distinct DOM transformation by four oneelectron oxidants and provides comprehensive insights into the reactions of one-electron oxidants with DOM.
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单位中国科学院; 中山大学
