4.7 Article

Environmental photochemistry of organic UV filter butyl methoxydibenzoylmethane: Implications for photochemical fate in surface waters

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 839, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.156145

Keywords

Organic UV filter; Photolysis; Transformation products; Ecotoxicity; Environmental persistence

Funding

  1. Guangdong Basic and Applied Basic Research Foundation [2020B1515130003, 2021A1515011366]

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With the widespread use of sunscreen and other personal care products, organic ultraviolet filters (OUVFs) have been detected in the aquatic environment. This study investigated the photodegradation of butyl methoxydibenzoylmethane (BMDBM), one of the most commonly used OUVFs, and identified its transformation products (TPs). The evaluation of environmental properties suggests that some TPs may have higher mobility than BMDBM. Furthermore, the ecotoxicity of BMDBM and its TPs were assessed using a quantitative structure-activity relationship (QSAR) approach, revealing that most TPs are less ecotoxic than BMDBM.
With the widespread use of sunscreen and other personal care products, organic ultraviolet filters (OUVFs) have become widely detected in the aquatic environment. Direct and indirect photolysis are important transformation pathways of OUVFs in aquatic environments, so their transformation products (TPs) are also chemicals of concern. Butyl methoxydibenzoylmethane (BMDBM) is one of the most commonly used OUVFs worldwide due to its ability to absorb ultraviolet light across a wide range of wavelengths, and it is ubiquitously detected in aquatic environments. In this study, we investigated the photodegradation of BMDBM through direct photolysis and hydroxyl radical (center dot OH) photo-oxidation. TPs were identified using ultrahigh performance liquid chromatography-high resolution mass spectrometry, and reaction mechanisms were proposed. Our results showed that the photodegradation rates for both enol and keto tautomer forms of BMDBM during direct photolysis and center dot OH photooxidation were similar. The formation of TPs resulted from a-cleavage and decarbonylation reactions involving the keto form of BMDBM. Comparisons of the kinetic data and TPs revealed that the direct photolysis mechanism was a significant sink for BMDBM even during center dot OH photooxidation. Evaluations of environmental properties based on the predicted physicochemical properties of BMDBM and TPs suggests that some of the TPs will have higher mobility than BMDBM. The quantitative structure-activity relationship (QSAR) approach was used to evaluate the ecotoxicity of BMDBM and the identified TPs. Most TPs were found to be less ecotoxic than BMDBM; however, TPs that had a diphenyl ring structure could be more ecotoxic than BMDBM. Overall, this study provides new insights into the photochemical behavior and ecotoxicity of BMDBM and its TPs, which are important for assessing the fate, persistence, accumulation, and adverse impacts of these compounds in aquatic environments.

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