• Login
    View Item 
    •   MINDS@UW Home
    • MINDS@UW Madison
    • College of Letters and Science, University of Wisconsin–Madison
    • Department of Chemistry
    • Bertram Research Group
    • View Item
    •   MINDS@UW Home
    • MINDS@UW Madison
    • College of Letters and Science, University of Wisconsin–Madison
    • Department of Chemistry
    • Bertram Research Group
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Simultaneous Detection of Ozone and Nitrogen Dioxide by Oxygen Anion Chemical Ionization Mass Spectrometry: A Fast Time Response Sensor Suitable for Eddy Covariance Measurements

    Thumbnail
    File(s)
    SIO Ozone Deposition Data (36.61Kb)
    SIO Ozone Deposition Readme (1.310Kb)
    Date
    2020-04-01
    Author
    Novak, Gordon
    Vermeuel, Michael
    Bertram, Timothy
    Publisher
    Atmos. Meas. Tech., Published by Copernicus Publications on behalf of the European Geosciences Union.
    Metadata
    Show full item record
    Abstract
    We report on the development, characterization, and field deployment of a fast time response sensor for measuring ozone (O3) and nitrogen dioxide (NO2) concentrations utilizing chemical ionization time-of-flight mass spectrometry (CI-ToFMS) with oxygen anion (O2−) reagent ion chemistry. We demonstrate that the oxygen anion chemical ionization mass spectrometer (Ox-CIMS) is highly sensitive to both O3 (180 ions s−1 pptv−1 pptv−1) and NO2 (97 ions s−1 pptv−1), corresponding to detection limits (3σ, 1 s averages) of 13 and 9.9 pptv, respectively. In both cases, the detection threshold is limited by the magnitude and variability in the background determination. The short-term precision (1 s averages) is better than 0.3% at 10 ppbv O3 and 4% at 10 pptv NO2. We demonstrate that the sensitivity of the O3 measurement to fluctuations in ambient water vapor and carbon dioxide is negligible for typical conditions encountered in the troposphere. The application of the Ox-CIMS to the measurement of O3 vertical fluxes over the coastal ocean, via eddy covariance (EC), was tested during summer 2018 at Scripps Pier, La Jolla CA. The observed mean ozone deposition velocity (vd(O3)) was 0.011 cm s−1 pptv−1 with a campaign ensemble limit of detection (LOD) of 0.0042 cm s−1 pptv−1 at the 95% confidence level, from each 27-minute sampling period LOD. The campaign mean and one standard deviation range of O3 mixing ratios were 38.9 ± 12.3 ppbv. Several fast ozone titration events from local NO emissions were sampled where unit conversion of O3 to NO2 was observed, highlighting instrument utility as a total odd oxygen (Ox = O3 + NO2) sensor. The demonstrated precision, sensitivity, and time resolution of this instrument highlight its potential for direct measurements of O3 ocean–atmosphere and biosphere–atmosphere exchange from both stationary and mobile sampling platforms.
    Subject
    Chemical Ionization, Mass Spectrometry, Atmospheric Chemistry, CIMS, Ozone
    Permanent Link
    http://digital.library.wisc.edu/1793/79986
    DOI
    https://doi.org/10.5194/amt-2019-445
    Type
    Report
    Citation
    Novak et al., Atmos. Meas. Tech., 2020
    Part of
    • Bertram Research Group

    Contact Us | Send Feedback
     

     

    Browse

    All of MINDS@UWCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

    My Account

    Login

    Contact Us | Send Feedback