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A chemical ionization mass spectrometer for continuous underway shipboard analysis of dimethylsulfide in near-surface seawater

E. S. Saltzman; W. J. De Bruyn; M. J. Lawler; C. A. Marandino; C. A. McCormick
Ocean Science · Vol. 5, Issue 4 · pp. 537-546 · 2009

Abstract

A compact, low-cost atmospheric pressure, chemical ionization mass spectrometer ("mini-CIMS") has been developed for continuous underway shipboard measurements of dimethylsulfide (DMS) in seawater. The instrument was used to analyze DMS in air equilibrated with flowing seawater across a porous Teflon membrane equilibrator. The equilibrated gas stream was diluted with air containing an isotopically-labeled internal standard. DMS is ionized at atmospheric pressure via proton transfer from water vapor, then declustered, mass filtered via quadrupole mass spectrometry, and detected with an electron multiplier. The instrument described here is based on a low-cost residual gas analyzer (Stanford Research Systems), which has been modified for use as a chemical ionization mass spectrometer. The mini-CIMS has a gas phase detection limit of 220 ppt DMS for a 1 min averaging time, which is roughly equivalent to a seawater DMS concentration of 0.1 nM DMS at 20°C. The mini-CIMS has the sensitivity, selectivity, and time response required for underway measurements of surface ocean DMS over the full range of oceanographic conditions. The simple, robust design and relatively low cost of the instrument are intended to facilitate use in process studies and surveys, with potential for long-term deployment on research vessels, ships of opportunity, and large buoys.

Bibliographic Information

JournalOcean Science
PublisherCopernicus Publications / European Geosciences Union
Publication Date2009-11-06
Publication Year2009
Volume5
Issue4
Pages537-546
Document TypeJournal Article
Print ISSN1812-0784
eISSN1812-0792
DOI10.5194/os-5-537-2009
SubjectOceanography; physical oceanography; chemical oceanography; biogeochemistry; ocean modelling

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NARA Access CoverageOA / free full text
Journal Homepagehttps://www.ocean-science.net/
Publisher PageOpen Publisher Page
This article is openly available from the publisher.