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Evaluating and elucidating the formation of nitrogen-contained disinfection by-products during pre-ozonation and chlorination

机译:评估和阐明预臭氧化和氯化过程中含氮消毒副产物的形成

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The effects of pre-ozonation on the formation of haloacetonitriles (HANs), trichloronitromethane (TCNM), and haloketones (HKs) during chlorination were evaluated. Ozone dose used in this study was 8.0, 10.0 and 25.0 mg O_3/min. Results showed high UV_(254) reduction (>80%) and relatively low dissolved organic carbon removal (40-70%) after ozonation, indicating that ozone might change significantly the chemical properties of natural organic matter presented in the raw water. Undesired ozonation by-products such as aldehydes and ketones were also formed during ozonation. At high ozone dose of 25.0 mg O_3/min, the formation of dichloroacetonitrile and bromochloroacetonitrile were reduced significantly. Chlorination of the ozonated water formed high concentration of TCNM and HKs were 8-10 and 31-48 μg/L, respectively. It was also found that continuous hydrolysis at longer reaction time rapidly decreased the formation of HKs. Ozonation prior to chlorination practice exhibited a negative effect on TCNM and HKs reduction. A model based on the dissolved organic carbon and chlorine decay was developed not only for determining the reaction rate constants, e.g. formation and hydrolysis of HANs, HKs and TCNM, but also for interpreting the mechanisms of formation and hydrolysis for HANs, HKs and TCNM during the chlorination of natural organic matter.
机译:评估了预臭氧化对氯化过程中卤代乙腈(HANs),三氯硝基甲烷(TCNM)和卤代酮(HKs)形成的影响。本研究中使用的臭氧剂量为8.0、10.0和25.0 mg O_3 / min。结果表明,臭氧化后,UV_(254)的还原率较高(> 80%),溶解的有机碳去除率相对较低(40-70%),这表明臭氧可能会显着改变原水中天然有机物的化学性质。在臭氧化过程中还形成了不希望的臭氧化副产物,例如醛和酮。在25.0 mg O_3 / min的高臭氧剂量下,二氯乙腈和溴氯乙腈的形成显着减少。臭氧化水的氯化形成高浓度的TCNM和HKs分别为8-10和31-48μg/ L。还发现在更长的反应时间连续水解迅速减少了HKs的形成。氯化操作之前进行臭氧处理对TCNM和HKs的减少有负面影响。建立了基于溶解的有机碳和氯气衰减的模型,不仅用于确定反应速率常数,例如,HANs,HKs和TCNM的形成和水解,也用于解释天然有机物氯化过程中HANs,HKs和TCNM的形成和水解的机理。

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