Measurements of HNoâ and NâOâ using ion drift-chemical ionization mass spectrometry during the MILAGRO/MCMA-2006 campaign
An ion drift-chemical ionization mass spectrometer (ID-CIMS) was deployed in Mexico City between 7 and 31 March to measure gas-phase nitric acid (HNOâ) and dinitrogen pentoxide (NâOâ during the Mexico City Metropolitan Area (MCMA)-2006 field campaign. The observation site was located at the Instituto Mexicano del Petróleo in the northern part of Mexico City urban area with major emissions of pollutants from residential, vehicular and industrial sources. Diurnally, HNOâ was less than 200 parts per trillion (ppt) during the night and early morning. The concentration of HNOâ increased steadily from around 09:00 a.m. central standard time (CST), reached a peak value of 0.5 to 3 parts per billion (ppb) in the early afternoon, and then declined sharply to less than half of the peak value near 05:00 p.m. CST. An inter-comparison between the ID-CIMS and an ion chromatograph/mass spectrometer (ICMS) showed a good agreement between the two HNOâ measurements (R²=0.75). The HNOâ mixing ratio was found to anti-correlate with submicron-sized aerosol nitrate, suggesting that the gas-particle partitioning process was a major factor in determining the gaseous HNOâ concentration. Losses by irreversible reactions with mineral dust and via dry deposition also could be important at this site. Most of the times during the MCMA 2006 field campaign, NâOâ was found to be below the detection limit (about 30 ppt for a 10 s integration time) of the ID-CIMS, because of high NO mixing ratio at the surface (>100 ppb) during the night. An exception occurred on 26 March 2006, when about 40 ppt N2Oâ was observed during the late afternoon and early evening hours under cloudy conditions before the build-up of NO at the surface site. The results revealed that during the MCMA-2006 field campaign HNOâ was primarily produced from the reaction of OH with NOâ and regulated by gas/particle transfer and dry deposition. The production of HNOâ from N2Oâ hydrolysis during the nighttime was small because of high NO and low Oâ concentrations near the surface.
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https://n2t.org/ark:/85065/d7pv6kjf
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2016-01-01T00:00:00Z
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2008-11-28T00:00:00Z
Copyright Author(s) 2008. This work is distributed under the Creative Commons Attribution 3.0 License.
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