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Wildfires, which have been occurring increasingly in the era of climate change, emit massive amounts of particulate matter (PM) into the atmosphere, strongly affecting air quality and public health. Biomass burning aerosols may contain environmentally persistent free radicals (EPFRs, such as semiquinone radicals) and redox-active compounds that can generate reactive oxygen species (ROS, including ·OH, superoxide and organic radicals) in the aqueous phase. However, there is a lack of data on EPFRs and ROS associated with size-segregated wildfire PM, which limits our understanding of their climate and health impacts. We collected size-segregated ambient PM in Southern California during two wildfire events to measure EPFRs and ROS using electron paramagnetic resonance spectroscopy. EPFRs are likely associated with soot particles as they are predominantly observed in submicron particles (PM 1 , aerodynamic diameter ≤ 1 μm). Upon extraction in water, wildfire PM mainly generates ·OH (28–49%) and carbon-centered radicals (∼50%) with minor contributions from superoxide and oxygen-centered organic radicals (2–15%). Oxidative potential measured with the dithiothreitol assay (OP-DTT) is found to be high in wildfire PM 1 , exhibiting little correlation with the radical forms of ROS ( r 2 ≤ 0.02). These results are in stark contrast with PM collected at highway and urban sites, which generates predominantly ·OH (84–88%) that correlates well with OP-DTT ( r 2 ∼ 0.6). We also found that PM generated by flaming combustion generates more radicals with higher OP-DTT compared to those by smoldering or pyrolysis.
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Plastic burning particulate matter as a source of environmentally persistent free radicals and reactive oxygen and chlorine species
Abstract Burning plastic waste releases massive amounts of atmospheric particulate matter (PM), but its chemical composition and health-related properties are largely unelucidated. Here we characterize chemical composition of PM generated from burning common types of plastics and quantify reactive oxygen/chlorine species and PM oxidative potential (OP). We find that plastic burning PM contains high levels of environmentally persistent free radicals (EPFRs), transition metals, and polycyclic aromatic hydrocarbons. In the aqueous phase, PM generates hydrogen peroxide, •OH radicals, and carbon-centered organic radicals, exhibiting high levels of OP as characterized by dithiothreitol (DTT) and OH assays. Remarkably, plastic burning PM is associated with high concentrations of hypochlorous acid. Kinetic model simulations demonstrate that the PM respiratory deposition leads to •OH formation via complex redox reactions among its constituents and antioxidants in lung lining fluid. Our study highlights significant atmospheric and health implications for unregulated plastic burning, particularly common in many areas of developing countries.
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- Award ID(s):
- 2203419
- PAR ID:
- 10596700
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- npj Clean Air
- Volume:
- 1
- Issue:
- 1
- ISSN:
- 3059-2240
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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