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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Precipitation of aqueous transition metals in particulate matter during the dithiothreitol (DTT) oxidative potential assay
Transition metals in particulate matter (PM) are hypothesized to have enhanced toxicity based on their oxidative potential (OP). The acellular dithiothreitol (DTT) assay is widely used to measure the OP of PM and its chemical components. In our prior study, we showed that the DTT assay (pH 7.4, 0.1 M phosphate buffer, 37 °C) provides favorable thermodynamic conditions for precipitation of multiple metals present in PM. This study utilizes multiple techniques to characterize the precipitation of aqueous metals present at low concentrations in the DTT assay. Metal precipitation was identified using laser particle light scattering analysis, direct chemical measurement of aqueous metal removal, and microscopic imaging. Experiments were run with aqueous metals from individual metal salts and a well-characterized urban PM standard (NIST SRM-1648a, Urban Particulate Matter). Our results demonstrated rapid precipitation of metals in the DTT assay. Metal precipitation was independent of DTT but dependent on metal concentration. Metal removal in the chemically complex urban PM samples exceeded the thermodynamic predictions and removal seen in single metal salt experiments, suggesting co-precipitation and/or adsorption may have occurred. These results have broad implications for other acellular assays that study PM metals using phosphate buffer, and subsequently, the PM toxicity inferred from these assays.
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- Award ID(s):
- 1802474
- PAR ID:
- 10348183
- Date Published:
- Journal Name:
- Environmental Science: Processes & Impacts
- Volume:
- 24
- Issue:
- 5
- ISSN:
- 2050-7887
- Page Range / eLocation ID:
- 762 to 772
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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