The airborne mass spectrometer AIMS &ndash; Part 1: AIMS-H<sub>2</sub>O for UTLS water vapor measurements

In the upper troposphere and lower stratosphere (UTLS), the accurate quantification of low water vapor concentrations has presented a significant measurement challenge. The instrumental uncertainties are passed on to estimates of H<sub>2</sub>O transport, cloud formation and the role of...

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Bibliographic Details
Main Authors: S. Kaufmann, C. Voigt, T. Jurkat, T. Thornberry, D. W. Fahey, R.-S. Gao, R. Schlage, D. Schäuble, M. Zöger
Format: Article
Language:English
Published: Copernicus Publications 2016-03-01
Series:Atmospheric Measurement Techniques
Online Access:http://www.atmos-meas-tech.net/9/939/2016/amt-9-939-2016.pdf
Description
Summary:In the upper troposphere and lower stratosphere (UTLS), the accurate quantification of low water vapor concentrations has presented a significant measurement challenge. The instrumental uncertainties are passed on to estimates of H<sub>2</sub>O transport, cloud formation and the role of H<sub>2</sub>O in the UTLS energy budget and resulting effects on surface temperatures. To address the uncertainty in UTLS H<sub>2</sub>O determination, the airborne mass spectrometer AIMS-H<sub>2</sub>O, with in-flight calibration, has been developed for fast and accurate airborne water vapor measurements. <br><br> We present a new setup to measure water vapor by direct ionization of ambient air. Air is sampled via a backward facing inlet that includes a bypass flow to assure short residence times (&lt; 0.2 s) in the inlet line, which allows the instrument to achieve a time resolution of  ∼ 4 Hz, limited by the sampling frequency of the mass spectrometer. From the main inlet flow, a smaller flow is extracted into the novel pressure-controlled gas discharge ion source of the mass spectrometer. The air is directed through the gas discharge region where ion–molecule reactions lead to the production of hydronium ion clusters, H<sub>3</sub>O<sup>+</sup>(H<sub>2</sub>O)<sub><i>n</i></sub> (<i>n</i> = 0, 1, 2), in a complex reaction scheme similar to the reactions in the D-region of the ionosphere. These ions are counted to quantify the ambient water vapor mixing ratio. The instrument is calibrated during flight using a new calibration source based on the catalytic reaction of H<sub>2</sub> and O<sub>2</sub> on a Pt surface to generate a calibration standard with well-defined and stable H<sub>2</sub>O mixing ratios. In order to increase data quality over a range of mixing ratios, two data evaluation methods are presented for lower and higher H<sub>2</sub>O mixing ratios respectively, using either only the H<sub>3</sub>O<sup>+</sup>(H<sub>2</sub>O) ions or the ratio of all water vapor dependent ions to the total ion current. Altogether, a range of water vapor mixing ratios from 1 to 500 parts per million by volume (ppmv) can be covered with an accuracy between 7 and 15 %. AIMS-H<sub>2</sub>O was deployed on two DLR research aircraft, the Falcon during CONCERT (CONtrail and Cirrus ExpeRimenT) in 2011, and HALO during ML-CIRRUS (Mid-Latitude CIRRUS) in 2014. The comparison of AIMS-H<sub>2</sub>O with the SHARC tunable diode laser hygrometer during ML-CIRRUS shows a correlation near to 1 in the range between 10 and 500 ppmv for the entire campaign.
ISSN:1867-1381
1867-8548