Insight into the generation of toxic by-products during UV/H2O2 degradation of carbamazepine: Mechanisms, N-transformation and toxicity

Xiaohan Huang; Gang Lu; Xuanjin Zhu; Chuan Pu; Junjie Guo; Xiangxing Liang

doi:10.1016/j.chemosphere.2024.142175

Insight into the generation of toxic by-products during UV/H₂O₂ degradation of carbamazepine: Mechanisms, N-transformation and toxicity

Chemosphere. 2024 Apr 26:358:142175. doi: 10.1016/j.chemosphere.2024.142175. Online ahead of print.

Authors

Xiaohan Huang¹, Gang Lu², Xuanjin Zhu¹, Chuan Pu¹, Junjie Guo¹, Xiangxing Liang¹

Affiliations

¹ School of Environment, Guangdong Key Laboratory of Environmental Pollution and Health, Jinan University, Guangzhou, 510632, China.
² School of Environment, Guangdong Key Laboratory of Environmental Pollution and Health, Jinan University, Guangzhou, 510632, China. Electronic address: tlugang@jnu.edu.cn.

PMID: 38679173
DOI: 10.1016/j.chemosphere.2024.142175

Abstract

Carbamazepine (CBZ) is a widely used anticonvulsant drug that has been detected in aquatic environments. This study investigated the toxicity of its by-products (CBZ-BPs), which may surpass CBZ. Unlike the previous studies, this study offered a more systematic approach to identifying toxic BPs and inferring degradation pathways. Furthermore, quadrupole time-of-flight (QTOF) and density functional theory (DFT) calculations were employed to analyze CBZ-BP structures and degradation pathways. Evaluation of total organic carbon (TOC) and total nitrogen (TN) mineralization rates, revealed carbon (C) greater susceptibility to mineralization compared with nitrogen (N). Furthermore, three rules were established for CBZ decarbonization and N removal during degradation, observing the transformation of aromatic compounds into aliphatic hydrocarbons and stable N-containing organic matter over time. Five potentially highly toxic BPs were screened from 14 identified BPs, with toxicity predictions guiding the selection of commercial standards for quantification and true toxicity testing. Additionally, BP207 emerged as the most toxic, supported by the predictive toxicity accumulation model (PTAM). Notably, highly toxic BPs feature an acridine structure, indicating its significant contribution to toxicity. These findings offered valuable insights into the degradation mechanisms of emerging contaminants and the biosafety of aquatic environments during deep oxidation.

Keywords: Carbamazepine; Decarbonization rules; Degradation pathway; N-transformation; Toxicity; UV/H(2)O(2).