Determination of lead in environmental waters with dispersive liquid–liquid microextraction prior to atomic fluorescence spectrometry

Abstract

This paper established a new, rapid and sensitive method for the determination of lead in water samples preconcentrated by dispersive liquid–liquid microextraction (DLLME) prior to atomic fluorescence spectrometry. Dithizone was used as the chelating agent. In the DLLME procedure, lead formed lead–dithizone complex and migrated into the carbon tetrachloride micro-droplets. Important factors that would affect the extraction efficiency had been investigated including the kind and volume of extraction solvent and dispersive solvent, sample pH, the amount of chelating agent, extraction time and centrifugation time. The results showed that the coexisting ions containing in water samples had no obvious negative effect on the determination of lead. The experimental results indicated that the proposed method had a good linear range of 0.01–100 ng mL −1 ( r 2 = 0.9990). The precision was 2.12% (RSD, n = 7) and the detection limit was 0.95 ng L −1. Proposed method was validated with four real environmental samples and the results indicated that the proposed method was excellent for the future use and satisfied spiked recoveries were in the range of 92.9–97.4%.