Comprehensive simulations of new particle formation events in Beijing with a cluster dynamics–multicomponent sectional model
| Autor: | C. Li, Y. Li, X. Li, R. Cai, Y. Fan, X. Qiao, R. Yin, C. Yan, Y. Guo, Y. Liu, J. Zheng, V.-M. Kerminen, M. Kulmala, H. Xiao, J. Jiang |
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| Jazyk: | angličtina |
| Rok vydání: | 2023 |
| Předmět: | |
| Zdroj: | Atmospheric Chemistry and Physics, Vol 23, Pp 6879-6896 (2023) |
| Druh dokumentu: | article |
| ISSN: | 1680-7316 1680-7324 |
| DOI: | 10.5194/acp-23-6879-2023 |
| Popis: | New particle formation (NPF) and growth are a major source of atmospheric fine particles. In polluted urban environments, NPF events are frequently observed with characteristics distinct from those in clean environments. Here we simulate NPF events in urban Beijing with a discrete-sectional model that couples cluster dynamics and multicomponent particle growth. In the model, new particles are formed by sulfuric acid–dimethylamine nucleation, while particle growth is driven by particle coagulation and the condensation of sulfuric acid, its clusters, and oxygenated organic molecules (OOMs). A variable simulation domain in the particle size space is applied to isolate newly formed particles from preexisting ones, which allows us to focus on new particle formation and growth rather than the evolution of particles of non-NPF origin. The simulation yields a rich set of information including the time-dependent NPF rates, the cluster concentrations, the particle size distributions, and the time- and size-specific particle chemical compositions. These can be compared with the field observations to comprehensively assess the simulation–observation agreement. Sensitivity analysis with the model further quantifies how metrics of NPF events (e.g., particle survival probability) respond to model input variations and serves as a diagnostic tool to pinpoint the key parameter that leads to simulation–observation discrepancies. Seven typical NPF events in urban Beijing were analyzed. We found that with the observed gaseous precursor concentrations and coagulation sink as model inputs, the simulations roughly captured the evolution of the observed particle size distributions; however, the simulated particle growth rate was insufficient to yield the observed particle number concentrations, survival probability, and mode diameter. With the aid of sensitivity analysis, we identified under-detected OOMs as a likely cause for the discrepancy, and the agreement between the simulation and the observation was improved after we modulated particle growth rates in the simulation by adjusting the abundance of OOMs. |
| Databáze: | Directory of Open Access Journals |
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