The levels of ionic per- and polyfluoroalkyl substances (iPFASs) in atmospheric particulate matter (PM), wastewater, and aqueous aerosol collected at a municipal WWTP in Wuxi were investigated. The concentration of ΣiPFASs in PM collected from the WWTP (72.2 pg/m, monthly average) was slightly higher than that from the control point (58.4 pg/m). Furthermore, the HYSPLIT model implied that the iPFASs pathways of control point and WWTP were totally different under identical meteorological conditions and that WWTP could be a source of iPFASs in urban environment. A comparison of the levels and compositions of iPFASs in aeration tank wastewater (203 ± 118 ng/L), effluent (392 ± 145 ng/L), and aqueous aerosols (58.5 ± 11.7 ng/L) samples using the t-stochastic neighborhood embedding algorithm revealed similar pollution fingerprints in aqueous aerosols and aeration tank wastewater, which implied that aqueous aerosols could be originating from the aeration tanks of WWTP and that aqueous aerosols may serve as a carrier for the transport of iPFASs from wastewater to atmosphere. Forward trajectory analysis indicated that the priority contaminated areas were more than 200 km southeast of the WWTP source, suggesting that iPFASs emitted from the WWTP were likely to undergo long-range atmospheric transport after entering the atmosphere via aqueous aerosols.
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http://dx.doi.org/10.1016/j.envpol.2025.126003 | DOI Listing |
Environ Pollut
March 2025
Key Laboratory of Pollution Processes and Environmental Criteria, Ministry of Education, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, College of Environmental Science and Engineering, Nankai University, Tianjin, 300071, PR China. Electronic address:
The levels of ionic per- and polyfluoroalkyl substances (iPFASs) in atmospheric particulate matter (PM), wastewater, and aqueous aerosol collected at a municipal WWTP in Wuxi were investigated. The concentration of ΣiPFASs in PM collected from the WWTP (72.2 pg/m, monthly average) was slightly higher than that from the control point (58.
View Article and Find Full Text PDFEnviron Sci Technol
March 2025
Department of Atmospheric Sciences, School of Earth Sciences, Zhejiang University, Hangzhou, Zhejiang 310027, China.
Aerosol deposition significantly impacts ocean ecosystems by providing bioavailable iron (Fe). Acid uptake during the transport of Fe-containing particles has been shown to cause Fe dissolution. However, carbonate in dust particles affects the Fe acidification process, influencing Fe dissolution.
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March 2025
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Heterogeneous oxidation of SO by NO on aerosols has recently been found to be one of the major formation pathways of sulfate in the polluted troposphere, but the chemical mechanisms and kinetics remain uncertain. By combining lab experiments, theoretical chemistry calculations, and field measurements, here we show that the SO oxidation by NO is critically dependent on anions at the air-aerosol aqueous interface. The reaction rate of NO with (1.
View Article and Find Full Text PDFJ Phys Chem Lett
March 2025
Laboratory CPCV, Department of Chemistry, École Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005 Paris, France.
Excess proton diffusion at aqueous interfaces is crucial for applications including electrocatalysis, aerosol chemistry, and biological energy conversion. While interfaces have been proposed as pathways for channeling protons, proton diffusion at interfaces remains far less understood than in the bulk. Here we focus on the air-water interface and use density functional theory-based deep potential molecular dynamics simulations to reveal the contrasting interface's impacts: excess proton diffusion slows down compared to the bulk, while water diffusion accelerates.
View Article and Find Full Text PDFFaraday Discuss
March 2025
School of Geography, Earth and Environmental Sciences, University of Birmingham, Birmingham, UK.
Aqueous aerosols are often covered in thin films of surface-active species, such as fatty acids which are prominent components of both sea spray and cooking emissions. The focus of our study is one-molecule thin layers of linoleic acid (LOA) and their behaviours when exposed to ozone in multi-component films at the air-water interface. LOA's two double bonds allow for ozone-initiated autoxidation, a radical self-oxidation process, as well as traditional ozonolysis.
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