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Determination of Arsenic Species Using Functionalized Ionic Liquid by in Situ Dispersive Liquid-Liquid Microextraction Followed by Atomic Absorption Spectrometry Publisher Pubmed



Ashouri V1, 2 ; Adib K3 ; Fariman GA4 ; Ganjali MR5, 6 ; Rahiminasrabadi M1, 2
Authors
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Authors Affiliations
  1. 1. Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
  2. 2. Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran
  3. 3. Department of Chemistry, Faculty of Basic Sciences, Imam Hossein University, Tehran, Iran
  4. 4. Department of Marine Biology, Faculty of Marine Sciences, Chabahar Maritime University, Daneshgah Ave., Chabahar, Iran
  5. 5. Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran, Iran
  6. 6. Biosensor Research Center, Endocrinology & Metabolism Molecular Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Food Chemistry Published:2021


Abstract

Synthesis and application of a task-specific ionic liquids (TSILs) as extracting solvents or chelating agents in dispersive liquid–liquid micro-extraction (DLLME) was evaluated. The developed method was based on the use of an ammonium pyrrolidine dithiocarbamate (APDC) bonded ionic liquid for chelation with As(III), followed by conversion of the As(III) chelated TSIL to a hydrophobic ionic liquid using KPF6 as an anion-exchange reagent. As(V) was reduced to As(III), using a 2/1 w/w blend of KI and Na2S2O3 and then the total amount of As was measured through ETAAS analysis. Under optimal conditions, linear dynamic ranges of 0.2–15 ng mL−1 and 0.2–20 ng mL−1 were observed in the determination of As(III) and total As respectively. The relative standard deviations (RSD%, n = 5) for the determination of As(III) (10 ng mL−1) was 3.2% and the limits of detection and quantitation were determined to be 0.01 ng mL−1 and 0.0.034 ng mL−1; respectively. © 2021 Elsevier Ltd