Ren Jiafeng, Tang Mengmeng, Wang Leyi, Chu Wenhai, Shi Wei, Zhou Qing, Pan Yang
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, Jiangsu 210023, China.
State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China.
Water Res. 2024 Apr 1;253:121264. doi: 10.1016/j.watres.2024.121264. Epub 2024 Feb 5.
Quenching is an important step to terminate disinfection during preparation of disinfected water samples for the analysis of disinfection byproducts (DBPs). However, an incomplete quenching might result in continued reactions of residual chlorine, whereas an excessive quenching might decompose target DBPs. Therefore, an adequate quenching to achieve simultaneous disinfection termination and DBP preservation is of particular importance. In this study, the two-stage reaction kinetics of chlorine and three commonly used quenching agents (i.e., ascorbic acid, sodium thiosulfate, and sodium sulfite) were determined. Stopping quenching during the first stage prevented interactions of residual chlorine with natural organic matter. Complete quenching was achieved by minimizing the quenching time for ascorbic acid and sodium sulfite, while limiting the quenching time to less than 3 min for sodium thiosulfate. At the optimized quenching times, the molar ratios (MRs) of quenching agent to chlorine were 1.05, 1.10, and 0.75 for ascorbic acid, sodium sulfite, and sodium thiosulfate, respectively. The destructive effects of the three quenching agents on total organic halogen (TOX) followed the rank order of ascorbic acid (33.7-64.8 %) < sodium sulfite (41.6-72.8 %) < sodium thiosulfate (43.3-73.2 %), and the destructive effects on aliphatic DBPs also followed the rank order of ascorbic acid (29.5-44.5 %) < sodium sulfite (34.9-51.9 %) < sodium thiosulfate (46.9-53.2 %). For total organic chlorine (TOCl) and aliphatic DBPs, the quenching behavior itself had more significant destructive effect than the quenching agent type/dose and quenching time, but for total organic bromine (TOBr), the destructive effect caused by quenching agent type/dose and quenching time was more significant. High-dose, long-duration quenching enhanced the reduction of TOX, but had little effect on aliphatic DBPs. Additionally, the three quenching agents reduced the levels of halophenols (except for tribromophenol), while maintained or increased the levels of tribromophenol, halobenzoic/salicylic acids, and halobenzaldehydes/salicylaldehydes. To achieve adequate quenching for overall DBP analysis in chlorinated water samples, it is recommended to use ascorbic acid at a quenching agent-to-chlorine MR of 1.0 for a quenching time of < 0.5 h.
在制备用于分析消毒副产物(DBPs)的消毒水样过程中,淬灭是终止消毒的重要步骤。然而,淬灭不完全可能导致余氯继续反应,而过度淬灭可能分解目标DBPs。因此,进行充分淬灭以同时实现消毒终止和DBP保存尤为重要。本研究测定了氯与三种常用淬灭剂(即抗坏血酸、硫代硫酸钠和亚硫酸钠)的两阶段反应动力学。在第一阶段停止淬灭可防止余氯与天然有机物发生相互作用。通过将抗坏血酸和亚硫酸钠的淬灭时间降至最短,同时将硫代硫酸钠的淬灭时间限制在3分钟以内,实现了完全淬灭。在优化的淬灭时间下,抗坏血酸、亚硫酸钠和硫代硫酸钠与氯的摩尔比(MRs)分别为1.05、1.10和0.75。三种淬灭剂对总有机卤素(TOX)的破坏作用顺序为:抗坏血酸(33.7 - 64.8%)<亚硫酸钠(41.6 - 72.8%)<硫代硫酸钠(43.3 - 73.2%),对脂肪族DBPs的破坏作用顺序也为:抗坏血酸(29.5 - 44.5%)<亚硫酸钠(34.9 - 51.9%)<硫代硫酸钠(46.9 - 53.2%)。对于总有机氯(TOCl)和脂肪族DBPs,淬灭行为本身的破坏作用比淬灭剂类型/剂量和淬灭时间更显著,但对于总有机溴(TOBr),淬灭剂类型/剂量和淬灭时间引起的破坏作用更显著。高剂量、长时间淬灭增强了TOX的降低,但对脂肪族DBPs影响不大。此外,三种淬灭剂降低了卤代酚(三溴酚除外)的含量,同时保持或增加了三溴酚、卤代苯甲酸/水杨酸和卤代苯甲醛/水杨醛的含量。为了对氯化水样中的整体DBP分析进行充分淬灭,建议使用抗坏血酸,淬灭剂与氯的MR为1.0,淬灭时间<0.5小时。