4.7 Article

Particle size-resolved emission characteristics of complex polycyclic aromatic hydrocarbon (PAH) mixtures from various combustion sources

Journal

ENVIRONMENTAL RESEARCH
Volume 214, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.envres.2022.113840

Keywords

Polycyclic aromatic hydrocarbons (PAHs); Domestic solid fuel; Cigarette smoking; Cooking; Vehicular exhaust; Emission profile

Funding

  1. National Natural Science Foundation of China [42077365, 41771530]
  2. Guangdong Basic and Applied Basic Research Foundation [2021B1515020040]

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Combustion of domestic solid fuels is a major source of polycyclic aromatic hydrocarbons (PAHs). This study investigates the size-dependent emissions of different types of PAHs from various combustion sources. Biomass burning is found to be the most significant source of PAH emissions. The study also highlights the importance of considering size-resolved atmospheric behaviors and fate of PAHs after their emission.
Combustion of domestic solid fuels is a significant source of polycyclic aromatic hydrocarbons (PAHs). Some oxygenated PAHs (o-PAHs) and PAHs with molecular weight of 302 (MW302 PAHs) are more toxic than the traditional 16 priority PAHs, whereas their emissions were much less elucidated. This study characterized the size-dependent emissions of parent PAHs (p-PAHs), o-PAHs, and MW302 PAHs from various combustion sources. The estimated emission factors (eEFs) from biomass burning sources were highest for most of the PAHs (391-8928 mu g/kg), much higher than that of anthracite coal combustion (43.0-145 mu g/kg), both which were operated in an indoor stove. Cigarette smoking had a high eEF of o-PAHs (240 ng/g). MW302 PAHs were not found in the emissions of smoking, cooking, and vehicular exhausts. Particle-size distributions of PAHs were compound- and source-dependent, and the tendency to associate with smaller particles was observed especially in biomass burning and cigarette smoking sources. Furthermore, the inter-source differences in PAH eEFs were associated with their dominance in fine particles. PAH composition profiles also varied with the particle size, showing increasing contributions of large-molecule PAHs with decreasing sizes in most cases. The size distributions of p-PAHs are much more significantly dependent on their n-octanol/air partition coefficients and vapor pressures than those of o-PAHs, suggesting differences in mechanisms governing their distributions. Several molecular diagnostic ratios (MDRs), including two based on MW302 PAHs, specific to these combustion scenarios were identified. However, the MDRs within some sources are also strongly size-dependent, providing a new explanation for the uncertainty in their application for source identification of PAHs. This work also highlights the necessity for understanding the size-resolved atmospheric behaviors and fate of PAHs after their emission.

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