色谱

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吹扫捕集-气相色谱-串联质谱法同时测定饮用水源中88种挥发性有机物及嗅味物质

郑晓婷, 简镇培, 朱靖岚, 周至城, 杨滨*, 应光国   

  1. 华南师范大学环境学院, 广东省饮用水安全保障工程技术研究中心, 广东 广州 510006
  • 收稿日期:2026-01-09
  • 基金资助:
    国家自然科学基金项目(42377368); 广东省基础与应用基础研究基金项目(2024A1515011534).

Simultaneous determination of 88 volatile organic compounds and odor compounds in drinking water by purge and trap-gas chromatography-tandem mass spectrometry

ZHENG Xiaoting, JIAN Zhenpei, ZHU Jinglan, ZHOU Zhicheng, YANG Bin*, YING Guangguo   

  1. Guangdong Provincial Engineering & Technology Research Center for Drinking Water Safety Assurance, School of Environment, South China Normal University, Guangzhou 510006, China
  • Received:2026-01-09
  • Contact: *Tel:020-39310536,E-mail:bin.yang@m.scnu.edu.cn.
  • Supported by:
    National Natural Science Foundation of China (No. 42377368); Guangdong Basic and Applied Basic Research Foundation (No. 2024A1515011534).

摘要: 为应对饮用水源中频发的水体异味事件,本研究建立并优化了吹扫捕集-气相色谱-三重四极杆串联质谱法(P&T-GC-MS/MS)同时测定水体中88种挥发性有机物及嗅味物质,为饮用水源水质监测提供技术支撑。该方法通过对吹扫时间、脱附温度、进样温度、分流比及质谱检测参数的系统优化,实现了目标物的高效分离与精准定量。实验结果表明,所建立检测方法能实现88种目标物的良好分离,在0.2~60.0 µg/L区间线性关系良好(R²>0.99)。方法检出限为0.02~0.22 µg/L,定量限为0.2~0.87 µg/L,相对标准偏差为0.01%~10.6%,平均回收率为70.8%~112%,各项性能指标均满足痕量分析要求。该方法应用于降雨时期广东清远市清城区及佛山市三水区饮用水源北江河段8个点位的监测,共检出7种目标化合物,除异味物质2-乙基-5,5-二甲基-1,3-二氧六环(2-EDD)外,其余化合物浓度均符合相关标准限值,表明沿岸无企业偷排现象。风险评估结果显示,仅监测点位3存在低生态风险,其余点位无生态风险,且所有点位检出的目标化合物均未对人体构成致癌及非致癌健康风险。

关键词: 吹扫捕集, 气相色谱-串联质谱法, 挥发性有机物, 嗅味物质

Abstract: To address the frequent occurrence of odor incidents in drinking water sources and effectively ensure the safety and stability of water supply quality, this study established and systematically optimized an analytical method based on purge and trap coupled with gas chromatography-triple quadrupole tandem mass spectrometry (P&T-GC-MS/MS), aiming at the simultaneous detection of 88 typical volatile organic compounds and common odor compounds in raw water. A series of core instrument operating conditions were systematically screened and optimized through repeated comparative experiments. The optimal experimental conditions were finally determined as a purge time of 11 minutes, a desorption temperature of 250 ℃, an inlet temperature of 220 ℃, and a split ratio of 10:1. Under these optimized experimental conditions, all 88 target compounds were successfully analyzed with good chromatographic separation and accurate quantitative analysis, which laid a solid foundation for the subsequent method validation and practical application. The results of methodological validation showed that all 88 target compounds exhibited excellent linear relationships in the range of 0.2-60.0 μg/L, with correlation coefficients (R²) all greater than 0.99, indicating high linearity and reliability of the method. The method detection limits (MDLs) of the target compounds ranged from 0.02 to 0.22 μg/L, and the method quantification limits (MQLs) ranged from 0.2 to 0.87 μg/L, which fully met the requirements for trace analysis of volatile organic compounds and odor compounds in drinking water. In addition, the relative standard deviations (RSDs) of the method, which reflect the precision and repeatability of the detection results, were between 0.01% and 10.6%. The average spiked recoveries of the 88 target compounds ranged from 70.8% to 112%, further confirming that all performance indicators of the established method were in line with the strict requirements of trace environmental analysis. Eight representative sampling sites were set along the main stream of the Beijiang River, which serves as an important drinking water source for Qingcheng District and Sanshui District in Guangdong Province. Collected surface water samples were determined by the optimized method, and a total of seven target compounds were detected in the actual water body, mainly including trans-1,2-dichloroethylene, dichloromethane and the typical odor substance 2-ethyl-5,5-dimethyl-1,3-dioxane (2-EDD). The concentration of detected pollutants ranged from not detected to 0.77 μg/L. Among them, the 2-EDD concentration at site 3 reached 365 ng/L, which far exceeded the local standard limit of 0.02 μg/L with an over-standard multiple up to 18 times and caused obvious odor in local source water. Other detected pollutants complied with water quality limits, and no obvious illegal industrial discharge was found along the river. Ecological and human health risks were further evaluated. Only site 3 presented low ecological risk to aquatic systems, while other sites showed no potential ecological risk. Carcinogenic risk indexes were all below safety thresholds, and non-carcinogenic hazard quotients stayed within safe ranges, proving detected substances posed no threat to residents’ health. This method provides a technical reference for drinking water safety control.

Key words: purge and trap, gas chromatography-tandem mass spectrometry (GC-MS/MS), volatile organic compounds, odor compounds