Preprints
https://doi.org/10.5194/egusphere-2026-6574
https://doi.org/10.5194/egusphere-2026-6574
06 Nov 2026
 | 06 Nov 2026
Status: this preprint is open for discussion and under review for Atmospheric Chemistry and Physics (ACP).

Online Measurements Reveal Contrasting Particle-Bound Reactive Oxygen Species and Chemical Composition in Emissions from Six Residential Solid Fuels

Lu Lei, Shan Wang, Jonas Enarsson, Jian Zhao, David Nganga, Ying Li, William Smith, Kirsten N. Fossum, Aneta Wierzbicka, Axel Eriksson, Chunshui Lin, Darius Ceburnis, John Wenger, Stig Hellebust, Colin O’Dowd, and Jurgita Ovadnevaite

Abstract. Residential solid fuel combustion is an important source of atmospheric particulate matter (PM), yet source-dependent characteristics in particle-bound reactive oxygen species (ROS) and their chemical drivers remain poorly constrained. Here, we combined online ROS measurements using a Particle Into Nitroxide Quencher with high-resolution aerosol mass spectrometry to systematically characterize real-time emissions from six residential solid fuels under realistic residential burning conditions. Distinct fuel-dependent chemical signatures were identified: wood-based fuels showed high contributions from oxygen-containing organic ions (O/C = 0.61–0.63), whereas manufactured coals were dominated by hydrocarbon-rich fragments and stronger polycyclic aromatic hydrocarbon (PAH)-related signatures (5–7 % of OA). Importantly, these PAH-related ions were strongly associated with mass-normalized ROS (ROSm) across the six fuels (r2 = 0.98 for burn-averaged data), while weaker positive time-resolved correlations suggested additional influences from particle chemistry and combustion conditions. Consistently, manufactured coals exhibited substantially higher ROSm than wood-based fuels and peat (2.2–2.9 vs. 0.2–0.6 pmol BPEAnit-Me equivalents µg-1), together with greater within-burn variability. However, air-volume-normalized ROS (ROSv) revealed contrasting pathways to elevated ROS burden: coals exhibited the highest ROSv (140.1–305.4 pmol m-3) driven by their high intrinsic ROS activity, whereas peat reached similarly elevated levels (107.5 pmol m-3) primarily because of its high PM loading. Overall, by linking real-time particle-bound ROS with aerosol chemistry across six solid fuels, this study reveals distinct chemical and mass-loading contributions to ROS burdens, providing a basis for interpreting source-dependent oxidative characteristics of atmospheric combustion aerosols.

Competing interests: At least one of the (co-)authors is a member of the editorial board of Atmospheric Chemistry and Physics.

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Lu Lei, Shan Wang, Jonas Enarsson, Jian Zhao, David Nganga, Ying Li, William Smith, Kirsten N. Fossum, Aneta Wierzbicka, Axel Eriksson, Chunshui Lin, Darius Ceburnis, John Wenger, Stig Hellebust, Colin O’Dowd, and Jurgita Ovadnevaite

Status: open (until 18 Dec 2026)

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Lu Lei, Shan Wang, Jonas Enarsson, Jian Zhao, David Nganga, Ying Li, William Smith, Kirsten N. Fossum, Aneta Wierzbicka, Axel Eriksson, Chunshui Lin, Darius Ceburnis, John Wenger, Stig Hellebust, Colin O’Dowd, and Jurgita Ovadnevaite
Lu Lei, Shan Wang, Jonas Enarsson, Jian Zhao, David Nganga, Ying Li, William Smith, Kirsten N. Fossum, Aneta Wierzbicka, Axel Eriksson, Chunshui Lin, Darius Ceburnis, John Wenger, Stig Hellebust, Colin O’Dowd, and Jurgita Ovadnevaite
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Latest update: 06 Nov 2026
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Short summary
By linking online ROS measurements with high-resolution aerosol chemical composition, this study reveals distinct chemical fingerprints and particle-bound ROS across six solid fuels. ROS activity was strongly associated with PAH-related ions, while elevated ROS burdens arose from contrasting contributions of intrinsic ROS activity and PM loading. These findings advance understanding of combustion aerosol chemistry and source-dependent oxidative characteristics of atmospheric aerosols.
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