As forest coverage and urban greening increase in China, the impact of biogenic volatile organic compounds (BVOCs) on urban atmospheric environment cannot be neglected. As one of the most abundant and reactive BVOCs globally, isoprene plays a crucial role in atmospheric radical chemistry. However, the reports on quantifying the impact of isoprene on atmospheric photochemistry remain scarce. This study selected Xiamen, a typical coastal city in Fujian Province, as the research area. By employing field observation and Photochemical Box Model (PBM), the study investigated the distribution characteristics, pollution mechanisms, and impact on O of the atmospheric photochemical active species isoprene in coastal urban area. The study found that the average concentration of isoprene in summer was 4.7 times higher than that in autumn. Isoprene degradation primarily occurred through oxidation by OH· radicals, reaching 88 % and 86 % in summer and autumn, respectively. Based on scenario simulations using the PBM model, it was observed that isoprene photochemistry led to increased daytime concentrations of ROx radicals (summer: 24 %, autumn: 23 %), peroxyacetyl nitrate (PAN, 49 %, 44 %), and formaldehyde (HCHO, 37 %, 38 %). Additionally, isoprene photochemistry enhanced reaction rates of HO₂· + NO (summer: 21 %, autumn: 16 %) and RO₂· + NO (50 %, 52 %), ultimately resulting in a 19 % and 15 % increase in net O production rates in summer and autumn, respectively. This study provides scientific evidence for exploring the photochemical mechanisms and pollution control strategies of O in coastal atmospheric environments.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.scitotenv.2024.177392 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!