Rapid, accurate and precise determination of tributyltin in sediments and biological samples by species specific isotope dilution-microwave extraction-gas chromatography-ICP mass spectrometry

The rapid and precise determination of tributyltin (TBT) in sediments and biological tissues has been performed by species specific isotope dilution mass spectrometric analysis (IDMS) using an inductively coupled plasma mass spectrometer as detector after capillary gas chromatography (CGC-ICP-MS). A...

Full description

Saved in:
Bibliographic Details
Published inJournal of analytical atomic spectrometry Vol. 18; no. 3; pp. 247 - 253
Main Authors Monperrus, Mathilde, Zuloaga, Olatz, Krupp, Eva, Amouroux, David, Wahlen, Raimund, Fairman, Ben, Donard, Olivier F. X.
Format Journal Article
LanguageEnglish
Published Royal Society of Chemistry 01.01.2003
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The rapid and precise determination of tributyltin (TBT) in sediments and biological tissues has been performed by species specific isotope dilution mass spectrometric analysis (IDMS) using an inductively coupled plasma mass spectrometer as detector after capillary gas chromatography (CGC-ICP-MS). A new labelled TBT standard (117TBTCl in methanolic solution) commercial isotope provided by LGC Limited (Teddington, UK) was used for these determinations. Parameters affecting the ICP-MS performances, such as correction for detector dead time and mass bias correction, were carefully studied. The mass bias was corrected using two different methods: the bracketing mode and an on-line mode based on a continuous nebulisation of an antimony solution ( 121Sb and 123Sb). The on-line mode has been successfully applied for mass bias corrections and allows simultaneous GC-ICP-MS analysis of organotins. Three spiking procedures were compared using isotopically enriched TBT (117TBT) to compare the efficiency of the extraction procedures for the different samples studied. A rapid method was developed (2 min) giving yield to good precision (uncertainty range between 0.7 and 13.7%) using a simultaneous microwave extraction and spiking procedure. The accuracy and precision of the different protocols has been validated on certified reference materials, such as PACS 2 (980 ng Sn g-1) and CRM 462 (70 ng Sn g-1) for the sediments, CRM 477 (2200 ng TBT g-1) and CRM 710 (135.1 ng TBT g-1) for the biological tissues. The results obtained were in all cases in good agreement with the certified reference values. © The Royal Society of Chemistry 2003.
ISSN:0267-9477
1364-5544
DOI:10.1039/b203242m