Abstract
A procedure is described for the quantitation of tributyltin in aqueous samples and extracts based on its relatively high volatility in halide media, permitting vapour phase sampling from the headspace above such samples. Tributyltin chloride (TBT-Cl) was purged from various chloride containing aqueous matrices and collected on the surface of an iridium treated graphite tube for subsequent quantitation by graphite furnace atomic absorption. Iodide, bromide and chloride matrices were compared for their generation efficiency. The effect of acidity of the sample was also studied. An absolute detection limit of 1.3 ng TBT (as tin) was estimated, corresponding to a detection limit of 0.33 ng ml−1 for a 4 ml sub-sample. Method validation was achieved using NRCC PACS-2 (sediment) Certified Reference Material, for which reasonable agreement between certified and measured values of tributyltin content was obtained. A procedural concentration limit of detection of 66 ng g−1 TBT in the sediment could be achieved.
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