Abstract. A typical multi-day ozone (O3) pollution event was chosen to explore
the atmospheric oxidation capacity (AOC), OH reactivity, radical chemistry,
and O3 pollution mechanism in a coastal city of southeastern China, with
an observation-based model coupled to the Master Chemical Mechanism
(OBM-MCM). The hydroxyl radical (OH) was the predominant oxidant (90 ± 25 %) for daytime AOC, while the NO3 radical played an important role in
AOC during the nighttime (72 ± 9 %). Oxygenated volatile organic
compounds (OVOCs; 30 ± 8 %), NO2 (29 ± 8 %), and CO
(25 ± 5 %) were the dominant contributors to OH reactivity,
accelerating the production of O3 and recycling of ROx radicals
(ROx = OH + HO2 + RO2). Photolysis of nitrous acid (HONO,
33 ± 14 %), O3 (25 ± 13 %), formaldehyde (HCHO, 20 ± 5 %), and other OVOCs (17 ± 2 %) was a major ROx source, which
played an initiation role in atmospheric oxidation processes. Combined with
regional transport analysis, the reasons for this O3 episode were the
accumulation of local photochemical production and regional transport. The
results of sensitivity analysis showed that volatile organic compounds (VOCs) were the limiting factor of
radical recycling and O3 formation, and the 5 % reduction of O3
would be achieved by decreasing 20 % anthropogenic VOCs. Controlling
emissions of aromatics, alkenes, and alkanes with ≥4 carbons was
beneficial for ozone pollution mitigation. The findings of this study provide
significant guidance for emission reduction and regional collaboration for
future photochemical pollution control in the relatively clean coastal
cities of China and similar countries.