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评价藻类有机物经紫外线照射后氯化(氨)消毒副产物的形成。

Evaluation of disinfection by-product formation during chlor(am)ination from algal organic matter after UV irradiation.

机构信息

State Key Laboratory of Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Tongji University, 1239 Siping Road, Yangpu District, Shanghai, 200092, China.

College of Civil Engineering and Architecture, Zhejiang University of Technology, Hangzhou, 310014, China.

出版信息

Environ Sci Pollut Res Int. 2018 Feb;25(6):5994-6002. doi: 10.1007/s11356-017-0918-x. Epub 2017 Dec 13.

Abstract

This study evaluated the effect of low-pressure ultraviolet (UV) irradiation on the formation of disinfection by-products (DBPs) from algal organic matter of Microcystis aeruginosa during subsequent chlorination and chloramination. The algal organic matter includes extracellular organic matter (EOM) and intracellular organic matter (IOM). The fluorescence excitation-emission matrix spectra indicated that the humic/fulvic acid-like organics of EOM and the protein-like organics of IOM may be preferentially degraded by UV treatment. UV irradiation with low specific UV absorbance values was effective in reducing the formation of trihalomethanes and dichloroacetic acid from EOM and IOM during the subsequent chlorination. During the UV-chloramine process, higher UV dose (1000 mJ/cm) led to the decrease of the formation of dichloroacetic acid, trichloroacetic acid, and haloketones from IOM by an average of 24%. Furthermore, UV irradiation can slightly increase the bromine substitution factors (BSFs) of haloacetic acids from EOM during chlorination, including dihaloacetic acids and trihaloacetic acids in the presence of bromide (50 μg/L). However, UV irradiation did not shift the formation of DBPs from IOM to more brominated species, since the BSFs of trihalomethanes, dihaloacetic acids, trihaloacetic acids, and dihaloacetonitriles almost kept unchanged during UV-chlorine process. As for UV-chloramine process, UV irradiation decreased the BSFs of trihalomethanes, while increased the BSFs of dihaloacetic acid for both EOM and IOM. Overall, the UV pretreatment process is a potential technology in treating algae-rich water.

摘要

本研究评价了低压紫外(UV)辐照对后续氯化和氯胺消毒过程中铜绿微囊藻藻源有机物生成消毒副产物(DBPs)的影响。藻源有机物包括细胞外有机物(EOM)和细胞内有机物(IOM)。荧光激发-发射矩阵光谱表明,EOM 的腐殖酸/富里酸类有机物和 IOM 的蛋白类有机物可能优先被 UV 处理降解。低特定 UV 吸光度值的 UV 辐照可有效降低 EOM 和 IOM 生成三卤甲烷和二氯乙酸的量。在 UV-氯胺工艺中,较高的 UV 剂量(1000 mJ/cm)导致 IOM 生成二氯乙酸、三氯乙酸和卤代酮的量平均减少 24%。此外,UV 辐照可略微增加 EOM 中卤代乙酸的溴取代因子(BSF),包括溴化物(50 μg/L)存在时的二卤乙酸和三卤乙酸。然而,UV 辐照并未将 IOM 中 DBPs 的生成转化为更多的溴代产物,因为三卤甲烷、二卤乙酸、三卤乙酸和二卤乙腈的 BSF 在 UV-氯气工艺过程中几乎保持不变。对于 UV-氯胺工艺,UV 辐照降低了三卤甲烷的 BSF,同时增加了 EOM 和 IOM 中二卤乙酸的 BSF。总体而言,UV 预处理工艺是一种处理富藻水的潜在技术。

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