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ISFME extraction of As species from some real water samples using an imidazolium-based task-specific ionic liquid (TSIL): Synthesis and characterization

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...

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Bibliographic Details
Published in:Separation science and technology 2024-03, Vol.59 (4), p.580-591
Main Authors: Hosseini, Mehdi, Khoshfetrat, Seyyed Mehdi, Panahimehr, Mohammad, Rezaei, Aram
Format: Article
Language:English
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Summary: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 using 13 CNMR 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.
ISSN:0149-6395
1520-5754
DOI:10.1080/01496395.2024.2328678