Zhao Xuan, Luo Chun-Ying, Zhang Jing, Yang Mi, Luo Xin-Yue, Zhao Xin-Yue, Wang Lian, Zou Xiao-Li
Department of Public Health Laboratory Science, West China-PUMC C.C.Chen Institute of Health, West China School of Public Health and West China Fourth Hospital, Sichuan University, Chengdu 610041, China.
Central Laboratory of Physico-Chemistry, Chengdu Center for Disease Control and Prevention, Chengdu 610047, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 May;53(3):504-510. doi: 10.12182/20220560205.
To establish a method for quantitative analysis of haloacetic acids (HAAs), disinfection byproducts, in tap water with reversed-phase ultra-performance liquid chromatography-quadrupole-orbitrap high resolution mass spectrometry.
Tap water samples were collected and 0.70 g/L ascorbic acid was added to eliminate residual chlorine. Then, the water samples were directly injected into the instrument for analysis after filtration. After separation on a pentafluorobenzene (PFP) column with an inner diameter of 1.0 mm at a higher linear velocity and a lower volume flow rate compared with those of a narrow-bore column, nine HAAs, namely, monochloroacetic acid (MCAA), monobromoacetic acid (MBAA), dichloroacetic acid (DCAA), bromochloroacetic acid (BCAA), dibromoacetic acid (DBAA), trichloroacetic acid (TCAA), bromodichloroacetic acid(BDCAA), chlorodibromoacetic acid (CDBAA) and tribromoacetic acid (TBAA), were examined by negative electrospray ionization and full MS/dd-MS acquisition mode. In order to adjust for the matrix effect, matrix matching calibration curves were used to quantitate the nine HAAs.
Good linearity was obtained for each of the nine HAAs within their respective linear ranges. The detection limits and quantification limits of the method were 0.020-1.0 μg/L and 0.060-3.0 μg/L. The recoveries were 69.8%-119%.
The proposed method showed strengths in separation speed and qualitative accuracy. It did not require for complicated pretreatment procedures and can meet the need of tap water sample analysis.
建立一种采用反相超高效液相色谱 - 四极杆 - 轨道阱高分辨率质谱法定量分析自来水中消毒副产物卤乙酸(HAAs)的方法。
采集自来水样品,加入0.70 g/L抗坏血酸以消除余氯。然后,水样经过滤后直接进样分析。在内径为1.0 mm的五氟苯(PFP)柱上以比窄径柱更高的线速度和更低的体积流速进行分离后,采用负电喷雾电离和全扫描/数据依赖二级质谱采集模式检测9种卤乙酸,即一氯乙酸(MCAA)、一溴乙酸(MBAA)、二氯乙酸(DCAA)、溴氯乙酸(BCAA)、二溴乙酸(DBAA)、三氯乙酸(TCAA)、溴二氯乙酸(BDCAA)、氯二溴乙酸(CDBAA)和三溴乙酸(TBAA)。为校正基质效应,采用基质匹配校准曲线对9种卤乙酸进行定量。
9种卤乙酸在各自线性范围内均具有良好的线性关系。该方法的检出限和定量限分别为0.020 - 1.0 μg/L和0.060 - 3.0 μg/L。回收率为69.8% - 119%。
所建立的方法在分离速度和定性准确性方面表现出优势。该方法无需复杂的预处理程序,能够满足自来水样品分析的需求。