Abstract

ABSTRACT To determine of arsenic species in real water samples using electrothermal atomic absorption spectrometry, a high-performance in-situ solvent formation microextraction technique has been developed using homogenous liquid – liquid microextraction concepts. The developed method was based on the use of a synthesized imidazolium-based ionic liquid (IL) modified with ammonium pyrrolidine dithiocarbamate as a task-specific ionic liquid (TSIL), which was chelated with As(III) and then converted to a hydrophobic IL using ammonium hexafluorophosphate in anion exchange reactions. As(V) was reduced to As(III), using a satisfied reducing agent, and the total amount of As was analyzed using ETAAS. TSIL acts simultaneously as an extracting solvent and a chelating agent. The characterization of the synthesized TSIL was performed using13CNMR and FTIR analyses. When optimal conditions were met, linear dynamic ranges of 0.5–50 µg/L and 0.5–20 µg/L were obtained in the determination of As(III) and total As, respectively. The limits of detection (LOD) and quantitation (LOQ) were determined to be 0.021 µg/Land 0.064 µg/L for the determination of As(III) (for concentration 20 µg/L), respectively, and the standard deviation (RSD%, n = 7) was 2.0%. To evaluate the validity of the method, it was successfully applied for As species determination in different real water samples.

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