HR: 1340h
AN: A33D-1536 [Abstracts]
TI: Modeled Effects of Observed Nitryl Chloride Concentrations in the Houston Area
AU: * Simon, H A
EM: hsimon@mail.utexas.edu
AF: Center for Energy and Environmental Resources, University of Texas at Austin, 10100
Burnet Rd.
Building 133
University Mail Code R7100, Austin, TX 78758, United States
AU: Kimura, Y
EM: yosuke@ccwf.cc.utexas.edu
AF: Center for Energy and Environmental Resources, University of Texas at Austin, 10100
Burnet Rd.
Building 133
University Mail Code R7100, Austin, TX 78758, United States
AU: McGaughey, G
EM: garym@mail.utexas.edu
AF: Center for Energy and Environmental Resources, University of Texas at Austin, 10100
Burnet Rd.
Building 133
University Mail Code R7100, Austin, TX 78758, United States
AU: Allen, D T
EM: allen@che.utexas.edu
AF: Center for Energy and Environmental Resources, University of Texas at Austin, 10100
Burnet Rd.
Building 133
University Mail Code R7100, Austin, TX 78758, United States
AB:
The recent TexAQS II field study involved intensive air pollutant measurements over Texas during the summer
and fall of 2006. During TexAQS II, NOAA researchers measured concentrations of nitryl chloride of up to 1 ppb in
the Houston urban area. Nitryl chloride is potentially important to atmospheric chemistry in urban environments
because its photolysis products include both NO2 and chlorine radicals. Chlorine radicals have previously been
shown to significantly increase ozone formation in urban Houston. If the values of nitryl chloride measured in
Galveston Bay are widespread, this compound has the potential to significantly affect the local reactive chlorine
budget and ultimately ozone mixing ratios.
Photochemical modeling was performed using the comprehensive air quality model with extensions (CAMx) to
investigate the possible effects of measured nitryl chloride concentrations on local chemistry. CAMx was
modified to include nitryl chloride and its photolysis reaction (the dominant loss mechanism of this compound).
The rate constant of nitryl chloride photolysis was calculated within the model using a scaling factor to the
photolysis rate constant of formaldehyde. This scaling was done to simplify the execution of the model. It was
found that under standard conditions (ozone column of 300 Dobson units, albedo of 0.06, and a measurement
height of 640 m) this scaling factor varied very little with shifting zenith angles. Calculations at zenith angles of 0,
10, 20, 30, 40, 50, 60, 70, 78, and 86 degrees, showed that scaling factor values had a standard deviation of less
than five percent of the mean value.
The photochemical modeling runs were performed for a series of days during the TexAQS II study. After an initial
3 day ramp-up period, model runs were stopped at 7am every morning (the approximate time of sunrise). At that
time, measured concentrations of nitryl chloride were inserted into the modeling domain in the three by three grid
cell region around the measurement point (a 12 square km region). The parcel of air which contained the initial
nitryl chloride concentrations was followed throughout the day. Chlorine radical and ozone concentrations in this
model run were compared to those predicted in a basecase model run which did not include any nitryl chloride.
The authors would like to acknowledge the NOAA research team led by James Roberts and thank them for
allowing access to their nitryl chloride measurement data.
DE: 0300 ATMOSPHERIC COMPOSITION AND STRUCTURE
DE: 0345 Pollution: urban and regional (0305, 0478, 4251)
DE: 0368 Troposphere: constituent transport and chemistry
DE: 0478 Pollution: urban, regional and global (0345, 4251)
SC: Atmospheric Sciences [A]
MN: 2007 Fall Meeting