•  English
    • Persian
    • English
  •   Login
  • Ferdowsi University of Mashhad
  • |
  • Information Center and Central Library
    • Persian
    • English
  • Home
  • Source Types
    • Journal Paper
    • Ebook
    • Conference Paper
    • Standard
    • Protocol
    • Thesis
  • Use Help
View Item 
  •   FUM Digital Library
  • Fum
  • Articles
  • ProfDoc
  • View Item
  •   FUM Digital Library
  • Fum
  • Articles
  • ProfDoc
  • View Item
  • All Fields
  • Title
  • Author
  • Year
  • Publisher
  • Subject
  • Publication Title
  • ISSN
  • DOI
  • ISBN
Advanced Search
JavaScript is disabled for your browser. Some features of this site may not work without it.

Ultra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometry

Author:
محمد افتخاری
,
فرزانه جاودانی اصله
,
محمود چمساز
,
Mohammad Eftekhari
,
farzaneh javedani asleh
,
Mahmod CHamsaz
Year
: 2016
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.
URI: https://libsearch.um.ac.ir:443/fum/handle/fum/3355400
Keyword(s): Cobalt,Preconcentration,Thiocyanate anion,

Ion pair-based dispersive liquid-liquid microextraction
Collections :
  • ProfDoc
  • Show Full MetaData Hide Full MetaData
  • Statistics

    Ultra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometry

Show full item record

contributor authorمحمد افتخاریen
contributor authorفرزانه جاودانی اصلهen
contributor authorمحمود چمسازen
contributor authorMohammad Eftekharifa
contributor authorfarzaneh javedani aslehfa
contributor authorMahmod CHamsazfa
date accessioned2020-06-06T13:27:07Z
date available2020-06-06T13:27:07Z
date issued2016
identifier urihttps://libsearch.um.ac.ir:443/fum/handle/fum/3355400
description abstractIon 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
languageEnglish
titleUltra-Trace Determination of Co (ІІ) in Real Samples Using Ion Pair-Based Dispersive Liquid-Liquid Microextraction Followed by Electrothermal Atomic Absorption Spectrometryen
typeJournal Paper
contenttypeExternal Fulltext
subject keywordsCobalten
subject keywordsPreconcentrationen
subject keywordsThiocyanate anionen
subject keywords

Ion pair-based dispersive liquid-liquid microextraction
en
journal titleFood Analytical Methodsfa
pages8-Jan
journal volume0
journal issue0
identifier linkhttps://profdoc.um.ac.ir/paper-abstract-1053186.html
identifier articleid1053186
  • About Us
نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
DSpace software copyright © 2019-2022  DuraSpace