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Direct introduction of volatile carbon compounds into the spray chamber of an inductively coupled plasma mass spectrometer: Sensitivity enhancement for selenium
Institution:1. Key Laboratory of Mineral Resources, Institute of Geology and Geophysics, Chinese Academy of Sciences, Beijing, 100029, China;2. China University of Geosciences, Beijing, 100083, China;3. Department of Earth Science, University of Ghana, P.O. Box LG 58, Legon–Accra, Ghana;1. Institute of Geology, Czech Academy of Sciences, Rozvojová 269, 16500 Prague 6, Czech Republic;2. Nuclear Physics Institute, Czech Academy of Sciences, Hlavní 130, 25068 Husinec-?e?, Czech Republic;3. University of Graz, Institute of Chemistry, Universitätsplatz 1, 8010 Graz, Austria;4. Department of Biochemistry and Microbiology, Institute of Chemical Technology, Prague, Technická 3, 166 28 Prague, Czech Republic;5. Institute of Geochemistry, Mineralogy and Mineral Resources, Faculty of Science, Charles University, Prague, Albertov 6, 12843 Prague 2, Czech Republic;6. Laboratories of the Geological Institutes, Faculty of Science, Charles University, Albertov 6, 12843 Prague 2, Czech Republic
Abstract:The effect of signal enhancement of elements with ionization potentials in the range from 9 to 11 eV by carbon-containing compounds is a well-known phenomenon in inductively coupled plasma mass spectrometry (ICPMS). It has traditionally been exploited through the addition of organic solvents to the sample matrix or to the mobile phase to improve sensitivity. In the present work, aqueous solutions of volatile carbon compounds (acetone, methanol and acetic acid) were directly introduced into the thermostatted spray chamber rather than being added to the sample matrix. It is presumed that no aerosol is produced from these solutions and only vapors of organic compounds are swept into the plasma together with the sample aerosol. When a 0.40 mol l? 1 aqueous solution of acetone was introduced directly into the spray chamber, the signals for arsenic and selenium were enhanced by a factor of 4.2. The usefulness of this approach was demonstrated through the achievement of lower instrumental detection limits for selenium at m/z 82 (0.1 ng ml? 1) compared to the system without direct introduction of volatile carbon compounds (0.5 ng ml? 1). The method was successfully applied in the determination of traces of selenium in natural water, urine and bovine liver reference material.
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