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Aqueous Reaction of Dicarbonyls with Ammonia as a Potential Source of Organic Nitrogen in Airborne Nanoparticles.
Stangl, Christopher M; Johnston, Murray V.
Afiliação
  • Stangl CM; Department of Chemistry and Biochemistry, University of Delaware , Newark, Delaware 19716, United States.
  • Johnston MV; Department of Chemistry and Biochemistry, University of Delaware , Newark, Delaware 19716, United States.
J Phys Chem A ; 121(19): 3720-3727, 2017 May 18.
Article em En | MEDLINE | ID: mdl-28440646
ABSTRACT
Nitrogen-containing organic species such as imines and imidazoles can be formed by aqueous reactions of carbonyl-containing compounds in the presence of ammonia. In the work described here, these reactions are studied in airborne aqueous nanodroplets containing ammonium sulfate and glyoxal, methylglyoxal, or glycolaldehyde using a combination of online and offline mass spectrometry. N/C ratios attributed to the organic fraction of the particles (N/Corg) produced from glyoxal and methylglyoxal were quantified across a wide relative humidity (RH) range. As the RH was lowered, glyoxal was found to increase N/Corg, attributed to "salting-in" with increasing solute concentration, while methylglyoxal led to a decrease in N/Corg, attributed to "salting-out". Glycolaldehyde was found to evaporate from the droplets rather than react in the aqueous phase and did not form particulate-phase organic matter from aerosol drying under any of the conditions studied. The results are discussed in the context of ambient nanoparticle composition measurements and suggest that aqueous chemistry may significantly impact nanoparticle composition and growth during new particle formation in locations where emissions of water-soluble dicarbonyls are high, such as the eastern United States.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem A Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem A Ano de publicação: 2017 Tipo de documento: Article