4.8 Article

Are Disinfection Byproducts (DBPs) Formed in My Cup of Tea? Regulated, Priority, and Unknown DBPs

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 55, 期 19, 页码 12994-13004

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c03419

关键词

DBPs; tea; TOX; high-resolution mass spectrometry; nontarget analysis

资金

  1. National Science Foundation [CBET 1705206]
  2. University of South Carolina
  3. Chinese Scholarship Council [201906250099, 201906205007]

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The study found that residual chlorine in tap water used to boil tea can react with tea compounds to produce disinfection byproducts (DBPs), contributing to 12% of total DBPs in brewed tea. The total organic halogen in tea nearly doubled compared to tap water, with 96% of halogenated DBPs unknown, likely high-molecular-weight haloaromatic compounds. Identification and further research on these aromatic DBPs is recommended due to potential significant toxicity.
Globally, tea is the second most consumed nonalcoholic beverage next to drinking water and is an important pathway of disinfection byproduct (DBP) exposure. When boiled tap water is used to brew tea, residual chlorine can produce DBPs by the reaction of chlorine with tea compounds. In this study, 60 regulated and priority DBPs were measured in Twinings green tea, Earl Grey tea, and Lipton tea that was brewed using tap water or simulated tap water (nanopure water with chlorine). In many cases, measured DBP levels in tea were lower than in the tap water itself due to volatilization and sorption onto tea leaves. DBPs formed by the reaction of residual chlorine with tea precursors contributed similar to 12% of total DBPs in real tap water brewed tea, with the remaining 88% introduced by the tap water itself. Of that 12%, dichloroacetic acid, trichloroacetic acid, and chloroform were the only contributing DBPs. Total organic halogen in tea nearly doubled relative to tap water, with 96% of the halogenated DBPs unknown. Much of this unknown total organic halogen (TOX) may be high-molecular-weight haloaromatic compounds, formed by the reaction of chlorine with polyphenols present in tea leaves. The identification of 15 haloaromatic DBPs using gas chromatographyhigh-resolution mass spectrometry indicates that this may be the case. Further studies on the identity and formation of these aromatic DBPs should be conducted since haloaromatic DBPs can have significant toxicity.

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