2014•Journal of Environmental Science and Health Part ARequires access

Trace level enrichment of lead from environmental water samples utilizing dispersive liquid-liquid microextraction and quantitative determination by graphite furnace atomic absorption spectrometry

Endale Teju, Bezuayehu Tadesse, Negussie Megersa

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Abstract

Dispersive liquid-liquid microextraction (DLLME) was developed and successfully applied, as a sample preconcentration and extraction method, for the determination of trace quantities of lead (Pb) in environmental water samples utilizing graphite furnace atomic absorption spectrometer (GFAAS). Experimental parameters optimized include; extraction and disperser solvent types and their volumes, pH, extraction period, effect of the co-existing ions and the amount of chelating agent, ammonium pyrrolidine dithiocarbamate (APDC). Under the optimized conditions, enrichment factor of 195 at 5 μg L(-1) level and detection limit of 0.16 μg L(-1) were obtained. Linearity from 25-75 μg L(-1) with R(2) of 0.995 was achieved. The procedure was validated utilizing four environmental water samples at the spiking levels of 10 and 20 μg L(-1) and the corresponding recoveries ranged from 89.6 to 95.1% and 91.6 to 97.1%, respectively, indicating the reliability and applicability of the method for selective extraction of trace level lead.

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What this paper is about

Dispersive liquid-liquid microextraction (DLLME) was developed and successfully applied, as a sample preconcentration and extraction method, for the determination of trace quantities of lead (Pb) in environmental water samples utilizing graphite furnace atomic absorption spectrometer (GFAAS). Experimental parameters optimized include; extraction and disperser solvent types and their volumes, pH, extraction period, effect of the co-existing ions and the amount of chelating agent, ammonium pyrrolidine dithiocarbamate (APDC). Under the optimized conditions, enrichment factor of 195 at 5 μg L(-1) level and detection limit of 0.16 μg L(-1) were obtained. Linearity from 25-75 μg L(-1) with R(2) of 0.995 was achieved. The procedure was validated utilizing four environmental water samples at the spiking levels of 10 and 20 μg L(-1) and the corresponding recoveries ranged from 89.6 to 95.1% and 91.6 to 97.1%, respectively, indicating the reliability and applicability of the method for selective extraction of trace level lead.

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Available abstract

Dispersive liquid-liquid microextraction (DLLME) was developed and successfully applied, as a sample preconcentration and extraction method, for the determination of trace quantities of lead (Pb) in environmental water samples utilizing graphite furnace atomic absorption spectrometer (GFAAS). Experimental parameters optimized include; extraction and disperser solvent types and their volumes, pH, extraction period, effect of the co-existing ions and the amount of chelating agent, ammonium pyrrolidine dithiocarbamate (APDC). Under the optimized conditions, enrichment factor of 195 at 5 μg L(-1) level and detection limit of 0.16 μg L(-1) were obtained. Linearity from 25-75 μg L(-1) with R(2) of 0.995 was achieved. The procedure was validated utilizing four environmental water samples at the spiking levels of 10 and 20 μg L(-1) and the corresponding recoveries ranged from 89.6 to 95.1% and 91.6 to 97.1%, respectively, indicating the reliability and applicability of the method for selective extraction of trace level lead.

Key concepts: Graphite furnace atomic absorption, Detection limit, Extraction (chemistry), Enrichment factor, Chromatography, Chemistry, Atomic absorption spectroscopy, Analytical Chemistry (journal)

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