4.8 Article

Formation of Larger Molecular Weight Disinfection Byproducts from Acetaminophen in Chlorine Disinfection

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 23, Pages 16929-16939

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c06394

Keywords

disinfection byproducts; DBPs; chlorination; acetaminophen; oxidative coupling reaction; quantum chemical calculation

Funding

  1. Research Grants Council of Hong Kong
  2. [16212518]
  3. [16210221]

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A new reaction pathway in the chlorination of acetaminophen, involving oxidative coupling reactions via acetaminophen radicals, was investigated in this study. Over 20 polymeric products, some similar to polychlorinated biphenyls, were detected in chlorinated acetaminophen samples using advanced analytical techniques. Quantum chemical calculations revealed the bonding processes and kinetics of both C-C and C-O bonding products. This study suggests that chlorination may cause both degradation and upgradation of phenolic compounds or contaminants.
Acetaminophen is widely used to treat mild to moderate pain and to reduce fever. Under the worldwide COVID-19 pandemic, this over-the-counter pain reliever and fever reducer has been drastically consumed, which makes it even more abundant than ever in municipal wastewater and drinking water sources. Chlorine is the most widely used oxidant in drinking water disinfection, and chlorination generally causes the degradation of organic compounds, including acetaminophen. In this study, a new reaction pathway in the chlorination of acetaminophen, i.e., oxidative coupling reactions via acetaminophen radicals, was investigated both experimentally and computationally. Using an ultraperformance liquid chromatograph coupled to an electrospray ionization triple quadrupole mass spectrometer, we detected over 20 polymeric products in chlorinated acetaminophen samples, some of which have structures similar to the legacy pollutants polychlorinated biphenyls. Both C-C and C-O bonding products were found, and the corresponding bonding processes and kinetics were revealed by quantum chemical calculations. Based on the product confirmation and intrinsic reaction coordinate computations, a pathway for the formation of the polymeric products in the chlorination of acetaminophen was proposed. This study suggests that chlorination may cause not only degradation but also upgradation of a phenolic compound or contaminant.

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