DEVELOPMENT OF A TECHNIQUE FOR THE ANALYSIS OF INORGANIC MERCURY SALTS IN SOILS BY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY

Citation
Cm. Barshick et al., DEVELOPMENT OF A TECHNIQUE FOR THE ANALYSIS OF INORGANIC MERCURY SALTS IN SOILS BY GAS-CHROMATOGRAPHY MASS-SPECTROMETRY, International journal of mass spectrometry and ion processes, 178(1-2), 1998, pp. 31-41
Citations number
28
Categorie Soggetti
Spectroscopy,"Physics, Atomic, Molecular & Chemical
ISSN journal
13873806
Volume
178
Issue
1-2
Year of publication
1998
Pages
31 - 41
Database
ISI
SICI code
1387-3806(1998)178:1-2<31:DOATFT>2.0.ZU;2-9
Abstract
A technique has been developed to analyze environmentally relevant sam ples for organic and inorganic mercury compounds. A solid phase microe xtraction (SPME) fiber was used as a sampling medium in both water and water/soil slurries. Quantification of inorganic mercury was accompli shed through a chemical alkylation reaction designed to convert an ino rganic mercury salt to an organomercury compound prior to GC/MS analys is; this was found to be the rate limiting step in the analysis. Two a lkylating reagents were investigated: methylpentacyanocobaltate (III) (K-3[Co(CN)(5)CH3]) and methylbis(dimethylglyoximato)pyridinecobalt (I II) (CH3Co(dmgH(2)Py). Methylbis(dimethylglyoximato)pyridinecobalt (II I) was found to be superior for this application because it produced a single reaction product, methylmercury iodide, with an efficiency of similar to 95%. Detection limits were similar to 7 ppb in water and si milar to 2 ppm in soil. The poorer results in soil were due to an incr ease in background signal (similar to 10 times compared to water) and a reduction in analyte signal las much as 100 times). This reduction i n signal intensity is believed to be caused by complex soil chemistry. Manipulation of the solution chemistry [e.g. oxidation of mercury (0) --> mercury (II)], before or during the alkylation step, may improve the detection limits and increase the number of elements amenable to a nalysis. (Int J Mass Spectrom 178 (1998) 31-41) (C) 1998 Elsevier Scie nce B.V.