Abstract
The detection of methylmercury species (MeHg) in fish tissue was investigated. Samples were digested with KOH-methanol and acidified prior to extraction with methylene chloride. MeHg was back-extracted from the organic phase into water. An aliquot of this aqueous solution (buffered to pH 5) was subjected to derivatization with sodium tetraphenylborate (NaBPh4) and then extracted with toluene. The organic phase containing MePhHg was injected into a gas chromatograph (GC) which is on-line with a microwave-induced plasma atomic emission spectrometer (MIP-AED). The quantification limit was about 0.6 μg/g and 0.1 μg/g of MeHg (as Hg) for 0.08 g of freeze-dried fish powder and 0.5 g of fresh samples, respectively. Two certified reference materials, CRM 464 (tuna fish) from Community Bureau of Reference-BCR and DORM-2 (dogfish muscle) from National Research Council Canada-NRC were selected for checking the accuracy of the method. This methodology was applied to the determination of MeHg in some kinds of fish from ¶the Carmo river with alluvial gold recovery activities (“garimpos”) in Mariana, Minas Gerais, Brazil.
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Received: 16 September 1999 / Revised: 26 October 1999 / Accepted: 1 November 1999
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Palmieri, H., Leonel, L. Determination of methylmercury in fish tissue by gas chromatography with microwave-induced plasma atomic emission spectrometry after derivatization with sodium tetraphenylborate. Fresenius J Anal Chem 366, 466–469 (2000). https://doi.org/10.1007/s002160050094
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DOI: https://doi.org/10.1007/s002160050094