Continuous measurements of dissolved Ne, Ar, Kr, and Xe ratios with a field-deployable gas equilibration mass spectrometer
Continuous measurements of dissolved Ne, Ar, Kr, and Xe ratios with a field-deployable gas equilibration mass spectrometer
Date
2016-01-30
Authors
Manning, Cara C.
Stanley, Rachel H. R.
Lott, Dempsey E.
Stanley, Rachel H. R.
Lott, Dempsey E.
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Abstract
Noble gases dissolved in natural waters are useful tracers for quantifying physical processes. Here, we describe a field-deployable gas equilibration mass spectrometer (GEMS) that
provides continuous, real-time measurements of Ne, Ar, Kr, and Xe mole ratios in natural waters. Gas is equilibrated with a membrane contactor cartridge and measured with a quadrupole
mass spectrometer, after in-line purification with reactive metal alloy getters. We use an electron energy of 35 V for Ne to eliminate isobaric interferences, and a higher electron energy for
the other gases to improve sensitivity. The precision is 0.7 % or better and 1.0 % or better for
all mole ratios when the instrument is installed in a temperature-controlled environment and a
variable-temperature environment, respectively. In the lab, the accuracy is 0.9 % or better for all gas ratios using air as the only calibration standard. In the field (and/or at greater levels of
disequilbrium), the accuracy is 0.7 % or better for Ne/Kr, Ne/Ar, and Ar/Kr, and 2.5 % or better for Ne/Xe, Ar/Xe, and Kr/Xe using air as the only calibration standard. The field accuracy
improves to 0.6 % or better for Ne/Xe, Ar/Xe, and Kr/Xe when the data is calibrated using
discrete water samples run on a laboratory-based mass spectrometer. The e-folding response
time is 90–410 s. This instrument enables the collection of a large number of continuous,
high-precision and accuracy noble gas measurements at substantially reduced cost and labor
compared to laboratory-based methods.
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Author Posting. © American Chemical Society, 2016. This is the author's version of the work. It is posted here by permission of American Chemical Society for personal use, not for redistribution. The definitive version was published in Analytical Chemistry 88 (2016): 3040–3048, doi:10.1021/acs.analchem.5b03102.