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Volume 53 Issue 3
May  2022
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ZHAO Xuan, LUO Chun-ying, ZHANG Jing, et al. Determination of Haloacetic Acids, Disinfection Byproducts, in Tap Water with Reversed-Phase Ultra-Performance Liquid Chromatography-High Resolution Mass Spectrometry[J]. Journal of Sichuan University (Medical Sciences), 2022, 53(3): 504-510. DOI: 10.12182/20220560205
Citation: ZHAO Xuan, LUO Chun-ying, ZHANG Jing, et al. Determination of Haloacetic Acids, Disinfection Byproducts, in Tap Water with Reversed-Phase Ultra-Performance Liquid Chromatography-High Resolution Mass Spectrometry[J]. Journal of Sichuan University (Medical Sciences), 2022, 53(3): 504-510. DOI: 10.12182/20220560205
shu

Determination of Haloacetic Acids, Disinfection Byproducts, in Tap Water with Reversed-Phase Ultra-Performance Liquid Chromatography-High Resolution Mass Spectrometry

  • 1.

    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

  • 2.

    Central Laboratory of Physico-Chemistry, Chengdu Center for Disease Control and Prevention, Chengdu 610047, China

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  • Corresponding author:

    ZOU Xiao-li, E-mail:zouxl_1113@163.com

  • Received Date: May 30, 2021
  • Revised Date: November 30, 2021
  • Available Online: May 24, 2022
  • Published Date: May 19, 2022
    Abstract
  •   Objective  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.
      Methods  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-MS2 acquisition mode. In order to adjust for the matrix effect, matrix matching calibration curves were used to quantitate the nine HAAs.
      Results  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%.
      Conclusion  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.
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    • References (21)
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