4.2 Article

Homogeneous and heterogeneous reactions of anthracene with selected atmospheric oxidants

Journal

JOURNAL OF ENVIRONMENTAL SCIENCES
Volume 25, Issue 9, Pages 1817-1823

Publisher

SCIENCE PRESS
DOI: 10.1016/S1001-0742(12)60233-2

Keywords

anthracene; ozonation; secondary organic aerosol; heterogeneous reaction; aerosol mass spectrometer

Funding

  1. Creative Research Groups of China [50921064]
  2. China Postdoctoral Science Foundation [2011M500433]
  3. GUCAS [Y25102GN00]

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The reactions of gas-phase anthracene and suspended anthracene particles with O-3 and O-3-NO were conducted in a 200-L reaction chamber, respectively. The secondary organic aerosol (SOA) formations from gas-phase reactions of anthracene with O-3 and O-3-NO were observed. Meanwhile, the size distributions and mass concentrations of SOA were monitored with a scanning mobility particle sizer (SMPS) during the formation processes. The rapid exponential growths of SOA reveal that the atmospheric lifetimes of gas-phase anthracene towards O-3 and O-3-NO are less than 20.5 and 4.34 hr, respectively. The particulate oxidation products from homogeneous and heterogeneous reactions were analyzed with a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS). Gas chromatograph/mass spectrometer (GC/MS) analyses of oxidation products of anthracene were carried out for assigning the time-of-flight (TOP) mass spectra of products from homogeneous and heterogeneous reactions. Anthrone, anthraquinone, 9,10-dihydroxyanthracene, and 1,9,10-trihydroxyanthracene were the ozonation products of anthracene, while anthrone, anthraquinone, 9-nitroanthracene, and 1,8-dihydroxyanthraquinone were the main products of anthracene with O-3-NO.

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