Abstract
The application of inductively coupled plasma – time-of-flight mass spectrometry for the speciation analysis of organolead compounds in environmental waters is described. Construction of the transfer line was achieved by means of a relatively simple and rapid coupling procedure. Derivatization of the ionic lead species was achieved by in-situ propylation with sodium tetrapropylborate; simultaneous extraction of the derivatized compounds in hexane was followed by separation and detection by capillary gas chromatography hyphenated to inductively coupled plasma–time-of-flight mass spectrometry. Detection limits for the different organolead species ranged from 10 to 15 fg (as Pb), corresponding to procedural detection limits between 50 and 75 ng L–1, on the basis of a 50 mL snow sample, extraction with 200 μL hexane, and subsequent injection of 1 μL of the organic extract on to the column. The accuracy of the system was confirmed by additional analysis of the water samples by capillary gas chromatography coupled with microwave-induced plasma–atomic-emission spectrometry and the analysis of a standard reference material CRM 605 (road dust) with a certified content of trimethyllead.
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Received: 6 December 2000 / Revised: 1 January 2001 / Accepted: 14 January 2001
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Heisterkamp, M., Adams, F. Gas chromatography – inductively coupled plasma – time-of-flight mass spectrometry for the speciation analysis of organolead compounds in environmental water samples. Fresenius J Anal Chem 370, 597–605 (2001). https://doi.org/10.1007/s002160100734
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DOI: https://doi.org/10.1007/s002160100734