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JOURNAL OF GEOPHYSICAL RESEARCH,
VOL. 105, NO. D9,
PAGES 11,585–11,600,
2000
Impact of acetone on ozone production and OH in the upper troposphere at high NOx
Ian Folkins
Atmospheric Science Program, Departments of Physics and Oceanography, Dalhousie University Halifax, Nova Scotia, Canada
Robert Chatfield
Earth Science Division, NASA Ames Research Center, Moffett Field, California
Abstract
The impact of acetone (or any HOx source) on tropospheric photochemistry is largest in the high NOx regime. The fractional increases in OH and ozone production associated with acetone increase rapidly with NOx when NOx mixing ratios become larger than 300 parts per trillion by volume (pptv). This occurs in part because the HOx yield of acetone is larger at higher NOx mixing ratios, going from about 1HOx at NOx∼10 pptv to 3HOx at NOx∼1000 pptv. We also investigate the effect of acetone on the partitioning of the NOy family. Acetone increases the conversion of NO to NO2, HNO4, HNO3, and peroxyacetylnitrate (PAN). Conversion of NO to PAN dominates at low NOx, while conversion of NO to HNO3 dominates at high NOx. These NO decreases significantly diminish the increases in OH and ozone production one would otherwise anticipate from the
increases in HO2. In particular, acetone can be expected to reduce ozone production for NOx<25 pptv. We also show that most of the changes in species concentrations arising from the introduction of a HOx source can be accurately predicted using simple expressions derived from linear perturbation theory. © 2000 American Geophysical
Union
Index Terms: 0322 Atmospheric Composition and Structure: Constituent sources and sinks; 0365 Atmospheric Composition and Structure: Troposphere--composition and chemistry; 0368 Atmospheric Composition and Structure: Troposphere--constituent transport and chemistry; 3210 Mathematical Geophysics: Modeling.
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Citation: Folkins, I., and R. Chatfield, Impact of acetone on ozone production and OH in the upper troposphere at high NOx,
J. Geophys. Res.,
105(D9),
11,585–11,600,
2000.
Copyright 2000 by the American Geophysical Union.
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