A robust method for the determination of lead in water samples using flow injection hydride generation atomic absorption spectrometry

Abstract

Flow injection hydride generation atomic absorption spectrometry (FI-HGAAS) is a sensitive technique for the quantification of trace amounts of lead. However, plumbane generation is not straightforward and usually HG methods for lead are not robust enough for routine analysis. The optimum pH range for Pb HG is very narrow, so strict control of the acidity of the reaction medium is required for reliable results and in some cases even acid concentrations used for sample preservation can interfere. Moreover, some elements, like Cu, can interfere in the HG reaction suppressing the Pb signal. In this paper we report the development and validation of a method for the determination of Pb in water samples that is robust towards acidity and Cu levels usually found in water samples. All hydride generation parameters were optimized, but special emphasis was put on robustness. The use of borate as a buffer significantly improved the robustness of the method towards acidity, compared to the typical non-buffered HG. Furthermore, the interference of Cu, Sb and Sn in the HG reaction was overcome using thiocyanate as a masking agent. Other elements do not interfere at levels typically found in water samples. The limit of quantification achieved (0.9 μg L− 1 ) is below the current guideline value for Pb in drinking water (10 μg L− 1 ). The linearity of the method was verified between the LOQ and up to 15 μg L− 1 . An analytical frequency of 25 samples per hour with 3 measurement replicates each was achieved. The method was applied to the analysis of 50 water samples. The concentrations found ranged from