A gas chromatographic instrument for measurement of hydrogen cyanide in the lower atmosphere
- 1Department of Chemistry, University of New Hampshire, Durham, New Hampshire, USA
- 2Climate Change Research Center, Institute for the Study of Earth Oceans and Space, University of New Hampshire, Durham, New Hampshire, USA
- *now at: Science and Technology Program, University of Washington-Bothell, Bothell, Washington, USA
- **now at: Department of Chemistry, Appalachian State University, Boone, North Carolina, USA
- ***now at: United States Geological Survey, Washington D.C., USA
- ****now at: Department of Earth and Atmospheric Sciences, University of Houston, Houston, Texas, USA
Abstract. A gas-chromatographic (GC) instrument was developed for measuring hydrogen cyanide (HCN) in the lower atmosphere. The main features of the instrument are (1) a cryogen-free cooler for sample dehumidification and enrichment, (2) a porous polymer PLOT column for analyte separation, (3) a flame thermionic detector (FTD) for sensitive and selective detection, and (4) a dynamic dilution system for calibration. We deployed the instrument for a ∼4 month period from January–June, 2010 at the AIRMAP atmospheric monitoring station Thompson Farm 2 (THF2) in rural Durham, NH. A subset of measurements made during 3–31 March is presented here with a detailed description of the instrument features and performance characteristics. The temporal resolution of the measurements was ~20 min, with a 75 s sample capture time. The 1σ measurement precision was <10% and the instrument response linearity was excellent on a calibration scale of 0.10–0.75 ppbv (±5%). The estimated method detection limit (MDL) and accuracy were 0.021 ppbv and 15%, respectively. From 3–31 March 2010, ambient HCN mixing ratios ranged from 0.15–1.0 ppbv (±15%), with a mean value of 0.36 ± 0.16 ppbv (1σ). The approximate mean background HCN mixing ratio of 0.20 ± 0.04 ppbv appeared to agree well with tropospheric column measurements reported previously. The GC-FTD HCN measurements were strongly correlated with acetonitrile (CH3CN) measured concurrently with a proton transfer-reaction mass spectrometer (PTR-MS), as anticipated given our understanding that the nitriles share a common primary biomass burning source to the global atmosphere. The nitriles were overall only weakly correlated with carbon monoxide (CO), which is reasonable considering the greater diversity of sources for CO. However, strong correlations with CO were observed on several nights under stable atmospheric conditions and suggest regional combustion-based sources for the nitriles. These results demonstrate that the GC-FTD instrument is capable of making long term, in-situ measurements of HCN in the lower atmosphere. To date, similar measurements have not been performed, yet they are critically needed to (1) better evaluate the regional scale distribution of HCN in the atmosphere and (2) discern the influence of biomass burning on surface air composition in remote regions.