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在一个全规模饮用水处理厂中消毒副产物的形成和去除。

Formation and removal of disinfection by-products in a full scale drinking water treatment plant.

机构信息

Univ. Lille CNRS, UMR 8516 - LASIR, Equipe Physico-Chimie de l'Environnement, Lille F-59000, France.

Univ. Lille CNRS, UMR 8516 - LASIR, Equipe Physico-Chimie de l'Environnement, Lille F-59000, France; Delft University of Technology, Faculty of Civil Engineering and Geosciences, Department of Water Management, PO Box 5048, GA Delft 2600, The Netherlands.

出版信息

Sci Total Environ. 2020 Feb 20;704:135280. doi: 10.1016/j.scitotenv.2019.135280. Epub 2019 Nov 16.

Abstract

In this case study, high sensitivity simple methods for the analysis of trihalomethanes (THM4), iodinated-trihalomethanes (I-THMs), haloacetic acids (HAAs), bromide, iodide and iodate have been developed. A one-step procedure for the analysis of haloacetic acids by head-space GC-MS provides good reproducibility and low limits of quantification (≤50 ng L). These methods were applied to characterize the formation of disinfection by-products (DBPs) in a full scale drinking water treatment plant. In this treatment plant, the incorporation of bromine into THMs increases throughout the water treatment line, due to the formation of bromine reactive species favored by the decrease of competition between dissolved organic carbon (DOC) and bromide towards chlorine. A linear correlation has been observed between the bromine incorporation factor and the Br/DOC mass ratio. The conversion of iodine to iodate by chlorination occurs in this water due to the relatively high bromide concentration. Moreover, a higher formation of iodate compared to iodide levels in the raw water is observed indicating a degradation of organic iodinated compounds. The formation of I-THMs was constant in terms of quantity and speciation between campaigns despite fluctuating concentrations of DOC and total iodine in the raw water. A preferential removal of DBPs formed by the intermediate chlorination in the order I-DBPs > Br-DBPs > Cl-DBPs occurs during the subsequent activated carbon filtration. The removal rates range from 25 to 36% for the regulated THM4, from 82 to 93% for the ∑I-THMs and 95% for haloacetic acids. The assessment of the relative toxicity shows that despite a much lower concentration of HAAs (<10% of the total mass of measured DBPs) compared to THMs, these compounds are responsible for 75% of the relative cytotoxicity of the treated water. Bromoacetic acid on its own accounts for more than 60% of the overall toxicity of the 17 compounds included in this study.

摘要

在这项案例研究中,开发了用于分析三卤甲烷 (THM4)、碘代三卤甲烷 (I-THMs)、卤乙酸 (HAAs)、溴化物、碘化物和碘酸盐的高灵敏度简单方法。通过顶空 GC-MS 分析卤乙酸的一步法提供了良好的重现性和低定量限(≤50 ng L)。这些方法应用于表征全规模饮用水处理厂中消毒副产物 (DBP) 的形成。在该处理厂中,由于溴活性物质的形成受到溶解有机碳 (DOC) 和溴化物之间竞争的降低的促进,THMs 中的溴掺入量随着水处理线的增加而增加。已经观察到溴掺入因子与 Br/DOC 质量比之间存在线性相关性。由于相对较高的溴化物浓度,该水中的氯化会将碘转化为碘酸盐。此外,与原水中的碘化物水平相比,观察到较高的碘酸盐形成水平表明有机碘代化合物的降解。尽管原水中的 DOC 和总碘浓度波动,但 I-THMs 的形成在数量和形态上在两次战役之间保持不变。在随后的活性炭过滤过程中,会优先去除通过中间氯化形成的 DBP,其顺序为 I-DBPs>Br-DBPs>Cl-DBPs。去除率范围为 25%至 36%,用于调节 THM4,93%用于∑I-THMs,95%用于卤乙酸。相对毒性评估表明,尽管与 THMs 相比,HAAs(<测量 DBP 总量的 10%)的浓度低得多,但这些化合物对处理水的相对细胞毒性负责 75%。溴乙酸本身占本研究中包括的 17 种化合物总毒性的 60%以上。

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