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Fate of isoprene peroxy radical constrains the urban photochemical regime
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DOI：10.1126/sciadv.aea6509.png)
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Abstract
En 中文
Declining nitrogen oxide (NOx = NO + NO2) emissions have transformed oxidation pathways in urban atmospheres, with implications for air quality. Organic peroxy radicals (RO2), key intermediates in volatile organic compound oxidation, typically react with NO to form ozone (O3). Under lower-NO conditions, alternative RO2 fates, including isomerization forming highly oxidized organic molecules (HOMs), can enhance secondary organic aerosol (SOA) production. We combine aircraft observations over four major North American cities with geostationary satellite data to characterize isoprene-derived RO2 fate across urban environments. We infer RO2 bimolecular lifetimes (τbi) as a proxy for isomerization potential, finding longer τbi (17 ± 11 seconds) in New York, Chicago, and Toronto compared to Los Angeles (7 ± 6 seconds). Satellite measurements reveal that long τbi is widespread across urban North America, suggesting that declining NOx is likely to lead to greater HOM formation in urban regions. These findings indicate that atmospheric models omitting RO2 isomerization chemistry may incorrectly simulate organic oxidation and the subsequent oxidation state of volatile organic compounds and SOA.
Keywords:
isoprene peroxy radicals
NOx emissions
urban atmospheres
highly oxidized organic molecules
secondary organic aerosol
Journal
IF:
12.5
Papers:
2.0W
Citations:
18.1W
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