To evaluate the migration, transformation, and fate of tetrabromobisphenol A (TBBPA) in the environment, the transformation/degradation (T/D) products of TBBPA and byproducts of industrial production should be distinguished. Herein, 7 reported T/D products (R1-R7) and 7 novel byproducts (N1-N7) of TBBPA were identified in industrial-grade TBBPA chemicals by using high-performance liquid chromatography coupled ion trap mass spectrometry and high-resolution mass spectrometry with a suspect screening strategy. The possible formation pathways of these byproducts were attributed to the bromination, debromination, methylation, demethylation, hydroxylation, substitution, and radical coupling reactions of bisphenol A (BPA), BPA impurities, and TBBPA. The detection frequencies of R1-R7 and N3 (80-100%) were higher than those of N1, N2, and N4-N7 (20-60%) in industrial-grade TBBPA chemicals, with contents extended to 2.29% and 0.0989%, respectively. In the soils and sediments near the TBBPA plants, R1-R4 and N1 were detected with the highest concentration of 1.56 × 10 ng g dry weight, while in the river waters, only R1-R4 were detected with the highest concentration of 4.57 × 10 ng L. An analysis indicated the potential toxicity of these compounds, including their hepatotoxicity and carcinogenicity. To accurately estimate the environmental effects of the T/D products of TBBPA, the contributions of byproducts in industrial-grade TBBPA chemicals should be considered separately.
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http://dx.doi.org/10.1039/d5em00030k | DOI Listing |
Circulation
March 2025
Institute of Experimental and Clinical Research (IREC), Pharmacology and Therapeutics (FATH), Cliniques Universitaires St. Luc and Université catholique de Louvain, Brussels, Belgium (L.Y.M.M., H.E., D.d.M., R.V., N.F., J.-L.B.).
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View Article and Find Full Text PDFAnn Intern Med
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Data Sources: Five electronic databases through September 2024.
Hortic Res
March 2025
Department of Biological Sciences, School of Life Science, Anhui Agricultural University, No. 130, West Changjiang Road, Hefei 230036, Anhui, China.
Galloylated flavan-3-ols are key quality and health-related compounds in tea plants of section . and are two representative species known for their high levels of galloylated flavan-3-ols. Building on our knowledge of galloyl catechin biosynthesis in , we now focus on the biosynthesis of galloylated phenolics in , aiming to elucidate the mechanisms underlying the high accumulation of these compounds in species.
View Article and Find Full Text PDFTo facilitate the design, analysis, and optimization of the hydrogen liquefaction system, this study developed a MATLAB-based independent simulation program encompassing unit equipment models and exergy analysis models. The program incorporated REFPROP software to accurately calculate fluid physical properties and the heat of conversion between ortho- and parahydrogen. The proposed hydrogen liquefaction process utilized LN precooling, the helium Joule-Brayton cryogenic cycle, and a throttle valve to efficiently produce liquid hydrogen.
View Article and Find Full Text PDFEnviron Sci Process Impacts
March 2025
Intelligent Policing Key Laboratory of Sichuan Province, Sichuan Police College, Luzhou 646000, China.
To evaluate the migration, transformation, and fate of tetrabromobisphenol A (TBBPA) in the environment, the transformation/degradation (T/D) products of TBBPA and byproducts of industrial production should be distinguished. Herein, 7 reported T/D products (R1-R7) and 7 novel byproducts (N1-N7) of TBBPA were identified in industrial-grade TBBPA chemicals by using high-performance liquid chromatography coupled ion trap mass spectrometry and high-resolution mass spectrometry with a suspect screening strategy. The possible formation pathways of these byproducts were attributed to the bromination, debromination, methylation, demethylation, hydroxylation, substitution, and radical coupling reactions of bisphenol A (BPA), BPA impurities, and TBBPA.
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