4.7 Article

Suppression of the phenolic SOA formation in the presence of electrolytic inorganic seed

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 851, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.158082

关键词

Phenol; Cresol; SOA; Photooxidation

资金

  1. National Institute of Environmental Research [NIER2020-01-01-010]
  2. National Science Foundation [AGS1923651]
  3. Fine Particle Research Initiative in East Asia Considering National Differences (FRIEND) Project through the National Research Foundation of Korea (NRF) - Ministry of Science and ICT [2020M3G1A1114556]
  4. National Research Foundation of Korea [2020M3G1A1114556] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study found that the presence of salted aqueous aerosol suppresses the formation of secondary organic aerosol (SOA) from phenol compounds. Phenol and o-cresol produce phenoxy radicals through photochemical oxidation, which then undergo heterogeneous reactions with salted aqueous aerosol under sunlight and humidity, leading to the suppression of SOA formation.
Phenolic compounds are largely attributed to wildfire gases and rapidly react with atmospheric oxidants to form persistent phenoxy free radicals, which influence atmospheric chemistry and secondary organic aerosol (SOA) formation. In this study, phenol or o-cresol was photochemically oxidized under various conditions (NOx levels, humidity, and seed conditions) in an outdoor photochemical reactor. Unexpectedly, SOA growth of both phenols was suppressed in the presence of salted aqueous aerosol compared to non-seed SOA. This discovery is different from the typical SOA formation of aromatic or biogenic hydrocarbons, which show noticeably higher SOA yields via organic aqueous reactions. Phenol, o-cresol, and their phenolic products (e.g., catechols) are absorbed in aqueous aerosol and form phenoxy radicals via heterogeneous reactions under sunlight. The resulting phenoxy radicals are redistributed between the gas and particle phases. Gaseous phenoxy radicals quickly react with ozone to form phenyl peroxide radicals and regenerated through a NOx cycle to retard phenol oxidation and SOA formation. The explicit oxidation mechanisms of phenol or o-cresol in the absence of aqueous phase were derived including the Master Chemical Mechanism (MCM v3.3.1) and the path for peroxy radical adducts originating from the addition of an OH radical to phenols to form low volatility products (e.g., multi-hydroxy aromatics). The resulting gas mechanisms of phenol or o-cresol were, then, applied to the Unified Partitioning Aerosol Phase Reaction (UNIPAR) model to predict SOA formation via multiphase partitioning of organics and aerosol-phase oligomerization. The model well simulated chambergenerated phenolic SOA in absence of wet-inorganic seed, but significantly overestimated SOA mass in presence of wet seed. This study suggests that heterogeneous chemistry to form phenoxy radicals needs to be included to improve SOA prediction from phenols. The suppression of atmospheric oxidation due to phenoxy radicals in wet inorganic aerosol can explain the low SOA formation during wildfire episodes.

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