Ultra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometry
نویسنده:
, , , , ,سال
: 2016
چکیده: Ion pair-based dispersive liquid-liquid
microextraction technique was used for preconcentration and
determination of ultra-trace levels of Co (ІІ) followed by electrothermal
atomic absorption spectrometry (ETAAS). Thiocyanate
(SCN−) forms an anionic complex with Co (ІІ) followed
by addition of cetylpyridinium chloride (CPC) as a positive
counterion to produce hydrophobic cobalt-thiocyanate-CPC
complex. The resulting hydrophobic complex was extracted
into the fine droplets of carbon tetrachloride by dispersive
liquid-liquid microextraction (DLLME). In DLLME, a mixture
of 1.5 mL of acetone (as disperser solvent) containing
40 μL of carbon tetrachloride (as extraction solvent) was rapidly
injected into the sample solution to extract the hydrophobic
cobalt-thiocyanate-CPC complex. Under the optimum
conditions, the calibration curve was linear in the range of
0.08–1.5 μg L−1 of Co (ІІ) with a correlation coefficient of
0.9997. The relative standard deviation (RSD, %) based on six
replicate analyses of 0.5 μg L−1 of Co (ІІ) was 3.7 %, and the
limit of detection (LOD) was 0.02 μg L−1. The accuracy of the
proposed method was evaluated by the analysis of a certified
reference material and spike method. The proposed method
was successfully applied for determination of ultra-trace levels
of Co (ІІ) in different water samples and spinach leaves.
microextraction technique was used for preconcentration and
determination of ultra-trace levels of Co (ІІ) followed by electrothermal
atomic absorption spectrometry (ETAAS). Thiocyanate
(SCN−) forms an anionic complex with Co (ІІ) followed
by addition of cetylpyridinium chloride (CPC) as a positive
counterion to produce hydrophobic cobalt-thiocyanate-CPC
complex. The resulting hydrophobic complex was extracted
into the fine droplets of carbon tetrachloride by dispersive
liquid-liquid microextraction (DLLME). In DLLME, a mixture
of 1.5 mL of acetone (as disperser solvent) containing
40 μL of carbon tetrachloride (as extraction solvent) was rapidly
injected into the sample solution to extract the hydrophobic
cobalt-thiocyanate-CPC complex. Under the optimum
conditions, the calibration curve was linear in the range of
0.08–1.5 μg L−1 of Co (ІІ) with a correlation coefficient of
0.9997. The relative standard deviation (RSD, %) based on six
replicate analyses of 0.5 μg L−1 of Co (ІІ) was 3.7 %, and the
limit of detection (LOD) was 0.02 μg L−1. The accuracy of the
proposed method was evaluated by the analysis of a certified
reference material and spike method. The proposed method
was successfully applied for determination of ultra-trace levels
of Co (ІІ) in different water samples and spinach leaves.
کلیدواژه(گان): Cobalt,Preconcentration,Thiocyanate anion,
Ion pair-based dispersive liquid-liquid microextraction
کالکشن
:
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آمار بازدید
Ultra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometry
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contributor author | محمد افتخاری | en |
contributor author | فرزانه جاودانی اصله | en |
contributor author | محمود چمساز | en |
contributor author | Mohammad Eftekhari | fa |
contributor author | farzaneh javedani asleh | fa |
contributor author | Mahmod CHamsaz | fa |
date accessioned | 2020-06-06T13:27:07Z | |
date available | 2020-06-06T13:27:07Z | |
date issued | 2016 | |
identifier uri | https://libsearch.um.ac.ir:443/fum/handle/fum/3355400 | |
description abstract | Ion pair-based dispersive liquid-liquid microextraction technique was used for preconcentration and determination of ultra-trace levels of Co (ІІ) followed by electrothermal atomic absorption spectrometry (ETAAS). Thiocyanate (SCN−) forms an anionic complex with Co (ІІ) followed by addition of cetylpyridinium chloride (CPC) as a positive counterion to produce hydrophobic cobalt-thiocyanate-CPC complex. The resulting hydrophobic complex was extracted into the fine droplets of carbon tetrachloride by dispersive liquid-liquid microextraction (DLLME). In DLLME, a mixture of 1.5 mL of acetone (as disperser solvent) containing 40 μL of carbon tetrachloride (as extraction solvent) was rapidly injected into the sample solution to extract the hydrophobic cobalt-thiocyanate-CPC complex. Under the optimum conditions, the calibration curve was linear in the range of 0.08–1.5 μg L−1 of Co (ІІ) with a correlation coefficient of 0.9997. The relative standard deviation (RSD, %) based on six replicate analyses of 0.5 μg L−1 of Co (ІІ) was 3.7 %, and the limit of detection (LOD) was 0.02 μg L−1. The accuracy of the proposed method was evaluated by the analysis of a certified reference material and spike method. The proposed method was successfully applied for determination of ultra-trace levels of Co (ІІ) in different water samples and spinach leaves. | en |
language | English | |
title | Ultra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometry | en |
type | Journal Paper | |
contenttype | External Fulltext | |
subject keywords | Cobalt | en |
subject keywords | Preconcentration | en |
subject keywords | Thiocyanate anion | en |
subject keywords | Ion pair-based dispersive liquid-liquid microextraction | en |
journal title | Food Analytical Methods | fa |
pages | 8-Jan | |
journal volume | 0 | |
journal issue | 0 | |
identifier link | https://profdoc.um.ac.ir/paper-abstract-1053186.html | |
identifier articleid | 1053186 |