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Probing the OH Oxidation of Pinonic Acid at the Air-Water Interface Using Field-Induced Droplet Ionization Mass Spectrometry (FIDI-MS).
Huang, Yuanlong; Barraza, Kevin M; Kenseth, Christopher M; Zhao, Ran; Wang, Chen; Beauchamp, J L; Seinfeld, John H.
Afiliação
  • Huang Y; Division of Geological and Planetary Sciences , California Institute of Technology , Pasadena , California 91125 , United States.
  • Barraza KM; Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
  • Kenseth CM; Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
  • Zhao R; Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
  • Wang C; Department of Chemistry and Department of Physical and Environmental Sciences , University of Toronto , Toronto , Ontario M1C 1A4 , Canada.
  • Beauchamp JL; Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
  • Seinfeld JH; Division of Chemistry and Chemical Engineering , California Institute of Technology , Pasadena , California 91125 , United States.
J Phys Chem A ; 122(31): 6445-6456, 2018 Aug 09.
Article em En | MEDLINE | ID: mdl-30011201
ABSTRACT
Gas and aqueous phases are essential media for atmospheric chemistry and aerosol formation. Numerous studies have focused on aqueous-phase reactions as well as coupled gas/aqueous-phase mass transport and reaction. Few studies have directly addressed processes occurring at the air-water interface, especially involving surface-active compounds. We report here the application of field-induced droplet ionization mass spectrometry (FIDI-MS) to chemical reactions occurring at the atmospheric air-water interface. We determine the air-water interfacial OH radical reaction rate constants for sodium dodecyl sulfate (SDS), a common surfactant, and pinonic acid (PA), a surface-active species and proxy for biogenic atmospheric oxidation products, as 2.87 × 10-8 and 9.38 × 10-8 cm2 molec-1 s-1, respectively. In support of the experimental data, a comprehensive gas-surface-aqueous multiphase transport and reaction model of general applicability to atmospheric interfacial processes is developed. Through application of the model, PA is shown to be oxidized exclusively at the air-water interface of droplets with a diameter of 5 µm under typical ambient OH levels. In the absence of interfacial reaction, aqueous- rather than gas-phase oxidation is the major PA sink. We demonstrate the critical importance of air-water interfacial chemistry in determining the fate of surface-active species.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem A Assunto da revista: QUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem A Assunto da revista: QUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos