HR: 0800h
AN: A51C-0064 [Abstracts]
TI: Peroxyacetic Acid Ubiquitous During ICARTT (Summer 2004)
AU: * Crounse, J D
EM: crounjd@caltech.edu
AF: California Institute of Technology, MC 150-21
1200 E California Blvd, Pasadena, CA 91125
United States
AU: Kwan, A
EM: kwan@caltech.edu
AF: California Institute of Technology, MC 150-21
1200 E California Blvd, Pasadena, CA 91125
United States
AU: Wennberg, P
EM: wennberg@gps.caltech.edu
AF: California Institute of Technology, MC 150-21
1200 E California Blvd, Pasadena, CA 91125
United States
AU: O'Sullivan, D
EM: osulliva@usna.edu
AF: United States Navel Academy, Chemistry Department
572 Holloway Rd, Annapolis, MD 21402
United States
AU: Shen, H
EM: hshen@gso.uri.edu
AF: University of Rhode Island, Center for Atmospheric Chemistry Studies
Graduate School of Oceanography
South Ferry Rd., Narragansett, RI 02882-1197
United States
AU: Heikes, B
EM: bheikes@gso.uri.edu
AF: University of Rhode Island, Center for Atmospheric Chemistry Studies
Graduate School of Oceanography
South Ferry Rd., Narragansett, RI 02882-1197
United States
AU: Pippin, M
EM: m.r.pippin@larc.nasa.gov
AF: NASA Langley Research Center, Atmospheric Sciences, Hampton, VA 23681
United States
AU: Crawford, J
EM: James.H.Crawford@nasa.gov
AF: NASA Langley Research Center, Atmospheric Sciences, Hampton, VA 23681
United States
AB:
Observations of peroxyacetic acid (PAA) aboard the NASA DC-8 reveal significant levels of this molecule throughout the
troposphere. Constrained box-model simulations significantly underestimate the amount of PAA, particularly in the upper
troposphere (UT). This implies either a large unaccounted for source of PAA or an error in the assumed lifetime of PAA.
This lifetime is thought to be governed by reaction with the hydroxyl radical. The rate coefficient for this reaction has,
however, only been estimated, as no laboratory measurements have been reported. Using the box model, we investigate the
sensitivity of calculated PAA to assumptions about the rate of the reaction of OH with PAA. Alternatively, we calculate the
magnitude of the additional source required to account for the observed PAA mixing ratios. Implications to the chemistry of
the UT will be discussed.
DE: 0300 ATMOSPHERIC COMPOSITION AND STRUCTURE
DE: 0317 Chemical kinetic and photochemical properties
DE: 0322 Constituent sources and sinks
DE: 0368 Troposphere: constituent transport and chemistry
SC: Atmospheric Sciences [A]
MN: Fall Meeting 2005