Abstract
Formic acid (HCOOH) is one of the most abundant organic acids in the atmosphere and affects atmospheric acidity and aqueous chemistry. However, the HCOOH sources are not well understood. In a recent field study, we measured atmospheric HCOOH concentrations at a coastal site in southern China. The average concentrations of HCOOH were 191ĝ€¯±ĝ€¯167ĝ€¯ppt in marine air masses and 996ĝ€¯±ĝ€¯433ĝ€¯ppt in coastal air masses. A strong linear correlation between HCOOH concentrations and the surface area densities of submicron particulate matter was observed in coastal air masses. Post-campaign laboratory experiments confirmed that the photochemical ageing of ambient aerosols promoted by heterogeneous reactions with ozone produced a high concentration of HCOOH at a rate of 0.185g h-1 under typical ambient conditions at noon. HCOOH production was strongly affected by nitrate photolysis, as this efficiently produces OH radicals that oxidise organics to form HCOOH. We incorporated this particle-phase source into a photochemical model, and the net HCOOH production rate increased by about 3 times compared with the default Master Chemical Mechanism (MCM). These findings demonstrate that the photochemical ageing of aerosols is an important source of HCOOH that should be included in atmospheric chemistry-Transport models.
| Original language | English |
|---|---|
| Pages (from-to) | 14813-14828 |
| Number of pages | 16 |
| Journal | Atmospheric Chemistry and Physics |
| Volume | 23 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 1 Dec 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 14 Life Below Water
ASJC Scopus subject areas
- Atmospheric Science
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