Response surface modelling of lead pre-concentration from food samples by miniaturised homogenous liquid-liquid solvent extraction: Box-Behnken design

In this study, a new method called miniaturised homogenous liquid-liquid extraction, followed by graphite furnace atomic absorption spectrometry, was developed for the extraction and determination of lead from food samples. The procedure was based on the fast extraction of lead from an acetic acid sample solution into 0.5 mL chloroform, as an extraction solvent. After adding water into the mixture, the extracting solvent phase immediately formed a distinct water-immiscible phase below the vial, which could easily be separated, evaporated and re-dissolved in 1.0 mL nitric acid 0.1 mot L-1 for further analysis. The effects of various experimental parameters in extraction step were studied using two optimisation methods, one variable at a time and Box-Behnken design. The results showed that the amount of salt and extraction time did not have effect on the extraction efficiency. Therefore, a three-level Box-Behnken experimental design with three factors, which combined the response surface modelling, was used to optimise lead extraction. Three independent variables, including pH of solution (ranging from 6.5 to 10.5), concentration of dithizone as chelating agent (ranging from 0.05 to 0.5 mu g L-1) and extracting solvent volume (ranging from 300 to 9004) were respectively coded as pH, D and Vat three different levels (-1, 0 and 1). In this study, the optimum condition was determined at pH 8.4, a volume of chloroform at 0.45 mL, and concentration of dithizone at 0.5 mu g L-1. Under the optimum condition, the limit of detection (LOD) was 0.05 mu g L. Furthermore, the relative standard deviation of the ten replicate was <5.0%. The developed procedure was applied to the extraction and determination of lead in the food samples. (C) 2011 Elsevier Ltd. All rights reserved.