尿
废水
双酚S
化学
双酚A
双酚
色谱法
同位素稀释
环境化学
排泄
人口
环境工程
环境科学
质谱法
医学
有机化学
生物化学
环境卫生
环氧树脂
作者
Sisi Tang,Chang He,Phong K. Thai,Amy Heffernan,Soumini Vijayasarathy,Leisa-Maree Toms,Kristie Thompson,Peter Hobson,Benjamin J. Tscharke,Jake O’Brien,Kevin V. Thomas,Jochen F. Mueller
标识
DOI:10.1021/acs.est.0c00921
摘要
Health concerns and related regulation of bisphenol A (BPA) in some countries have led to an increase in the production and use of unregulated and poorly understood BPA analogues, including bisphenol S (BPS), bisphenol F (BPF), bisphenol B (BPB), and bisphenol AF (BPAF). To assess the temporal trends of human exposure to BPA analogues, urine and wastewater samples were collected from South East Queensland, Australia between 2012 and 2017 and analyzed for five bisphenols using validated isotope dilution liquid chromatography tandem mass spectrometry methods. BPA and BPS were the predominant bisphenols detected in both urine and wastewater samples, with median concentrations of 2.5 and 0.64 μg/L in urine and 0.94 and 1.1 μg/L in wastewater, respectively. BPB, BPF, and BPAF had low detection frequencies in both urine and wastewater samples. Concentrations of BPA in both urine and wastewater decreased over the sampling period, whereas concentrations of BPS increased, suggesting that BPS has become a BPA replacement. The contributions of urinary excretion to wastewater were calculated by the ratio of daily per capita urinary excretion to wastewater-based mass loads of bisphenols. Urinary BPA and BPS contributed to less than 1% of the load found in wastewater, indicating that much of the BPA and BPS originates from other sources.
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