Issue 11, 2001

Abstract

An analytical procedure was developed for the determination of tributyltin in aqueous samples. The relatively high volatility of the organometal halide species confers suitability for their headspace sampling from the vapour phase above natural waters or leached solid samples. Tributyltin was collected from the sample headspace above various chloride-containing matrices, including HCl, sodium chloride solution and sea-water, by passive sampling using a polydimethylsiloxane/divinylbenzene (PDMS/DVB)-coated solid-phase microextraction (SPME) fiber. Inductively coupled plasma time-of-flight mass spectrometry (ICP-TOFMS) was used for detection following thermal desorption of analytes from the fiber. A detection limit of 5.8 pg ml−1 (as tin) was realized in aqueous samples. Method validation was achieved using NRCC PACS-2 (Sediment) certified reference material, for which reasonable agreement between certified and measured values for tributyltin content was obtained.

Article information

Article type
Paper
Submitted
07 Apr 2001
Accepted
23 Aug 2001
First published
22 Oct 2001

J. Anal. At. Spectrom., 2001,16, 1313-1316

Speciation without chromatography

Z. Mester, R. E. Sturgeon, J. W. Lam, P. S. Maxwell and L. Péter, J. Anal. At. Spectrom., 2001, 16, 1313 DOI: 10.1039/B105952C

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