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Atmospheric Measurement Techniques An interactive open-access journal of the European Geosciences Union

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Atmos. Meas. Tech., 5, 3029-3039, 2012
© Author(s) 2012. This work is distributed under
the Creative Commons Attribution 3.0 License.
Research article
07 Dec 2012
Airborne observations of formic acid using a chemical ionization mass spectrometer
M. Le Breton1, M. R. McGillen1,*, J. B. A. Muller1, A. Bacak1, D. E. Shallcross2, P. Xiao2, L. G. Huey3, D. Tanner3, H. Coe1, and C. J. Percival1 1Centre for Atmospheric Science, School of Earth, Atmospheric and Environmental Science, University of Manchester, Oxford Road, Manchester, M13 9PL, UK
2Biogeochemistry Research Centre, School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK
3School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA
*currently at: Chemical Sciences Division, Earth System Research Laboratory, National Oceanic and Atmospheric Administration (NOAA), 325 Broadway, Boulder, CO 80305, USA
Abstract. The first airborne measurements of formic acid mixing ratios over the United Kingdom were measured on the FAAM BAe-146 research aircraft on 16 March 2010 with a chemical ionization mass spectrometer using I reagent ions. The I ionization scheme was able to measure formic acid mixing ratios at 1 Hz in the boundary layer.

In-flight standard addition calibrations from a formic acid source were used to determine the instrument sensitivity of 35 ± 6 ion counts pptv−1 s−1 and a limit of detection of 25 pptv. Routine measurements were made through a scrubbed inlet to determine the instrumental background. Three plumes of formic acid were observed over the UK, originating from London, Humberside and Tyneside. The London plume had the highest formic acid mixing ratio throughout the flight, peaking at 358 pptv. No significant correlations of formic acid with NOx and ozone were found, but a positive correlation was observed between CO and HCOOH within the two plumes where coincident data were recorded.

A trajectory model was employed to determine the sources of the plumes and compare modelled mixing ratios with measured values. The model underestimated formic acid concentrations by up to a factor of 2. This is explained by missing sources in the model, which were considered to be both primary emissions of formic acid of mainly anthropogenic origin and a lack of precursor emissions, such as isoprene, from biogenic sources, whose oxidation in situ would lead to formic acid formation.

Citation: Le Breton, M., McGillen, M. R., Muller, J. B. A., Bacak, A., Shallcross, D. E., Xiao, P., Huey, L. G., Tanner, D., Coe, H., and Percival, C. J.: Airborne observations of formic acid using a chemical ionization mass spectrometer, Atmos. Meas. Tech., 5, 3029-3039,, 2012.
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