纳克东河下游饮用水处理过程中卤代乙酰胺的形成与归宿:夏冬季比较

Jungmoon Ryu, Hyunjoo Seol, Heejong Son
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引用次数: 1

摘要

目的:对洛东江下游某饮用水处理厂夏季和冬季各工艺过程中氮消毒副产物卤代乙酰胺(haacams)的形成特征和去向进行评价。为了准备逐步加强的dbtp规则,它打算用作操作dwtp的基本数据。方法:夏季(7 ~ 8月)和冬季(12 ~ 1月)在洛东江下游的大型DWTP(18万m3/天)对7台hacam进行了从原水到洁净水的监测。样品提取采用液液萃取法,HAcAms分析采用气相色谱-质谱联用法。结果与讨论:夏季和冬季DWTP中cl2预处理形成的HAcAms浓度分别为9.4~27.2µg/L和1.4~3.5µg/L,夏季比冬季高7.7倍。夏季HAcAms/TOX浓度比为0.09~0.14,冬季为0.01~0.02,预氯化形成的dbp中HAcAms组成比在夏季迅速增加。预氯化作用在夏季形成DCAcAm、BCAcAm、TCAcAm、DBAcAm和BDCAcAm 5种,在冬季形成DCAcAm、BCAcAm、DBAcAm、DBCAcAm和TBAcAm 5种。夏季和冬季,di-HAcAm物种组成比例分别为91%和66%,且dacam浓度高于其他hacam物种。在间歇式生物降解实验中,评价了HAcAms的生物降解性,在实验室规模的BAC工艺实验中(水温20℃,EBCT 10~30 min),双和三HAcAms的去除率分别为75~99%和85~100%。夏季和冬季DWTP工艺对HAcAms的平均去除率分别为81%和54%。洁净水中HAcAm的检测浓度夏季为1.7 ~ 2.4 μg/L,冬季为0.7 ~ 1.2 μg/L,夏季为冬季的2倍。结论:预氯化处理后,HAcAms的形成浓度高于冬季,但在夏季BAC过程中易于去除。而在冬季,预氯处理的HAcAms形成浓度较低,但BAC的去除率低至54%。在DWTP中,HAcAms的主要去除过程和机制是BAC过程和生物降解。在实验室规模的BAC过程模拟中,当HAcAms在夏季高度形成时,EBCT时间延长至30分钟,去除率可达到95%以上。
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Haloacetamides Formation and Fate in Drinking Water Treatment Process of the Lower Nakdong River: Comparison of Summer and Winter Seasons
Objectives : The formation characteristics and fate of haloacetamides (HAcAms), nitrogenous disinfection by-products (DBPs), were evaluated for each process in a drinking water treatment plant (DWTP) located downstream of the Nakdong River in summer and winter. In preparation for the gradually strengthening rules for DBPs, it was intended to be used as basic data for operating DWTPs.Methods : Seven HAcAms were monitored from the raw water to the clean water in the summer (Jul.∼Aug.) and winter (Dec.∼Jan.) at a large DWTP (180,000 m3/day) located downstream of the Nakdong River. Liquid-liquid extraction (LLE) method was used for sample extraction and GC-MS/MS was used for HAcAms analysis.Results and Discussion : The concentrations of HAcAms formed by the pre-Cl2 treatment in the DWTP in summer and winter were 9.4~27.2 µg/L and 1.4~3.5 µg/L, respectively, and were 7.7 times higher in summer than in winter. The HAcAms/TOX concentration ratio was 0.09~0.14 in summer compared to 0.01~0.02 in winter, and the HAcAms composition ratio among DBPs formed by the pre-chlorination increased rapidly in the summer. Five species of DCAcAm, BCAcAm, TCAcAm, DBAcAm, and BDCAcAm were formed in summer by the pre-chlorination, and five species of DCAcAm, BCAcAm, DBAcAm, DBCAcAm, and TBAcAm were formed in winter. The composition ratio of di-HAcAm species accounted for 91% and 66% in summer and winter, respectively, and the DCAcAm concentration was highest compared to other HAcAms species. In the batch biodegradation experiment, it was evaluated that the biodegradation of the HAcAms species was easy, and in the laboratory scale BAC process experiment (water temp. 20℃, EBCT 10~30 min.), di- and tri-HAcAms removal rate were 75~99% and 85~100%, respectively. In summer and winter, the removal rates of HAcAms in the BAC process of the DWTP were 81% and 54% on average, respectively. The HAcAm detection concentrations in the clean water ranged from 1.7 to 2.4 μg/L in summer and 0.7 to 1.2 µg/L in winter, which was twice as high in summer as was compared to winter.Conclusion : The formation concentration of HAcAms was higher than in winter by pre-chlorination, but it was easily removed in the BAC process in summer. However, in winter, the formation concentration of HAcAms was low by pre-chlorine treatment, but the removal rate in the BAC process was as low as 54%. The main removal process and mechanism of HAcAms in the DWTP were the BAC process and biodegradation. In a lab-scale BAC process simulation, a removal rate of more tthan 95% removal efficiency could be expected with the increase of EBCT to 30 minutes when HAcAms was highly formed in summer.
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