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Volume 12, issue 15
Atmos. Chem. Phys., 12, 6939-6951, 2012
https://doi.org/10.5194/acp-12-6939-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 12, 6939-6951, 2012
https://doi.org/10.5194/acp-12-6939-2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 02 Aug 2012

Research article | 02 Aug 2012

Modeling nitrous acid and its impact on ozone and hydroxyl radical during the Texas Air Quality Study 2006

B. H. Czader1, B. Rappenglück1, P. Percell1, D. W. Byun1,2,†, F. Ngan1,*, and S. Kim1,** B. H. Czader et al.
  • 1Department of Earth and Atmospheric Sciences, University of Houston, Houston, TX, USA
  • 2Air Resources Laboratory, NOAA, Silver Spring, MD 20910, USA
  • *present address: Air Resources Laboratory, NOAA, Silver Spring, MD 20910, USA
  • **present address: Ajou University, Suwon, S. Korea
  • deceased

Abstract. Nitrous acid (HONO) mixing ratios for the Houston metropolitan area were simulated with the Community Multiscale Air Quality (CMAQ) Model for an episode during the Texas Air Quality Study (TexAQS) II in August/September 2006 and compared to in-situ MC/IC (mist-chamber/ion chromatograph) and long path DOAS (Differential Optical Absorption Spectroscopy) measurements at three different altitude ranges. Several HONO sources were accounted for in simulations, such as gas phase formation, direct emissions, nitrogen dioxide (NO2) hydrolysis, photo-induced formation from excited NO2 and photo-induced conversion of NO2 into HONO on surfaces covered with organic materials. Compared to the gas-phase HONO formation there was about a tenfold increase in HONO mixing ratios when additional HONO sources were taken into account, which improved the correlation between modeled and measured values. Concentrations of HONO simulated with only gas phase chemistry did not change with altitude, while measured HONO concentrations decrease with height. A trend of decreasing HONO concentration with altitude was well captured with CMAQ predicted concentrations when heterogeneous chemistry and photolytic sources of HONO were taken into account. Heterogeneous HONO production mainly accelerated morning ozone formation, albeit slightly. Also HONO formation from excited NO2 only slightly affected HONO and ozone (O3) concentrations. Photo-induced conversion of NO2 into HONO on surfaces covered with organic materials turned out to be a strong source of daytime HONO. Since HONO immediately photo-dissociates during daytime its ambient mixing ratios were only marginally altered (up to 0.5 ppbv), but significant increase in the hydroxyl radical (OH) and ozone concentration was obtained. In contrast to heterogeneous HONO formation that mainly accelerated morning ozone formation, inclusion of photo-induced surface chemistry influenced ozone throughout the day.

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