Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry

A novel dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO) for simultaneous separation/preconcentration of ultra trace amounts of mercury was used. A method based on amalgamation was used for collection of gaseous mercury on gold coated sand (Gold...

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Main Authors: Abdollahi Atousa, Amirkavehei Mooud, Gheisari Mohammad Mehdi, Tadayon Fariba
Format: Article
Language:English
Published: EDP Sciences 2014-07-01
Series:E3S Web of Conferences
Subjects:
Online Access:http://dx.doi.org/10.1051/e3sconf/20130141006
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spelling doaj-4733767f7a2d401089abc1e71f663f692021-02-02T07:59:01ZengEDP SciencesE3S Web of Conferences2267-12422014-07-0114100610.1051/e3sconf/20130141006e3sconf_ichmet2013_41006Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometryAbdollahi Atousa0Amirkavehei Mooud1Gheisari Mohammad Mehdi2Tadayon Fariba3Department of Environmental Chemistry, Islamic Azad University Khorasgan (Isfahan) BranchDepartment of Environmental Chemistry, Islamic Azad University Khorasgan (Isfahan) BranchDepartment of Environmental Chemistry, Islamic Azad University Khorasgan (Isfahan) BranchDepartment of Chemistry, Islamic Azad University North Tehran Branch A novel dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO) for simultaneous separation/preconcentration of ultra trace amounts of mercury was used. A method based on amalgamation was used for collection of gaseous mercury on gold coated sand (Gold trap). The concentration of mercury was determined by cold vapor atomic absorption spectrometry (CV-AAS). The DLLME-SFO behavior of mercury by using dithizone as complexing agent was systematically investigated. The factors influencing, the complex formation and extraction of DLLME-SFO method such as type and volume of extraction and disperser solvents, pH, concentration of salt, centrifuging time and concentration of the chelating agent were optimized. The method was successfully applied to the determination of mercury in drinking and natural water and satisfactory relative recoveries (95–105%) were achieved. The proposed procedure was based on very low consumption of organic solvents. The other benefits of the system were sensitive, simple, friendly to the environment, rejection of matrix constituent, low cost, the time consuming and high enrichment factor. http://dx.doi.org/10.1051/e3sconf/20130141006mercuryDispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO)DithizoneCold vapor atomic absorption spectrometry (CV-AAS)
collection DOAJ
language English
format Article
sources DOAJ
author Abdollahi Atousa
Amirkavehei Mooud
Gheisari Mohammad Mehdi
Tadayon Fariba
spellingShingle Abdollahi Atousa
Amirkavehei Mooud
Gheisari Mohammad Mehdi
Tadayon Fariba
Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
E3S Web of Conferences
mercury
Dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
Dithizone
Cold vapor atomic absorption spectrometry (CV-AAS)
author_facet Abdollahi Atousa
Amirkavehei Mooud
Gheisari Mohammad Mehdi
Tadayon Fariba
author_sort Abdollahi Atousa
title Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
title_short Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
title_full Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
title_fullStr Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
title_full_unstemmed Trace mercury determination in drinking and natural water after preconcentration and separation by DLLME-SFO method coupled with cold vapor atomic absorption spectrometry
title_sort trace mercury determination in drinking and natural water after preconcentration and separation by dllme-sfo method coupled with cold vapor atomic absorption spectrometry
publisher EDP Sciences
series E3S Web of Conferences
issn 2267-1242
publishDate 2014-07-01
description A novel dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO) for simultaneous separation/preconcentration of ultra trace amounts of mercury was used. A method based on amalgamation was used for collection of gaseous mercury on gold coated sand (Gold trap). The concentration of mercury was determined by cold vapor atomic absorption spectrometry (CV-AAS). The DLLME-SFO behavior of mercury by using dithizone as complexing agent was systematically investigated. The factors influencing, the complex formation and extraction of DLLME-SFO method such as type and volume of extraction and disperser solvents, pH, concentration of salt, centrifuging time and concentration of the chelating agent were optimized. The method was successfully applied to the determination of mercury in drinking and natural water and satisfactory relative recoveries (95–105%) were achieved. The proposed procedure was based on very low consumption of organic solvents. The other benefits of the system were sensitive, simple, friendly to the environment, rejection of matrix constituent, low cost, the time consuming and high enrichment factor.
topic mercury
Dispersive liquid–liquid microextraction based on solidification of floating organic drop (DLLME-SFO)
Dithizone
Cold vapor atomic absorption spectrometry (CV-AAS)
url http://dx.doi.org/10.1051/e3sconf/20130141006
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