FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS
In this study, a novel method based on floatation assistance of homogeneous liquid-liquid microextraction (FA-HLLME), combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed, for the determination of trace uranium in environmental water samples. As one of the miniaturized se...
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Sociedad Chilena de Química
2017
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oai:scielo:S0717-970720170002000082017-06-30FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MSVEYSEH,SOMAYEHNIAZI,ALI Uranium: Determination Liquid-liquid homogeneous microextraction ICP-MS Water samples In this study, a novel method based on floatation assistance of homogeneous liquid-liquid microextraction (FA-HLLME), combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed, for the determination of trace uranium in environmental water samples. As one of the miniaturized separation and extraction techniques, homogenous liquid-liquid microextraction (HLLME) has been widely applied in the field of environmental monitoring and assessment. 1,2-pyridylazo-2-naphthol (PAN) was used as the complexing agent while toluene and methanol were selected as the extraction and homogeneous solvents, respectively. The factors that influenced the extraction efficiency for uranium determination (including pH, extraction and homogeneous solvents, concentration of PAN and NaCl, extraction time) were studied statistically. Under optimum conditions (pH=7.0, 100 μL toluene, 500 μL methanol, 6.4×10-5 mol L-1 PAN, 1.5 mol L-1 NaCl and 60 sec of extraction time), the linear dynamic range for uranium determination was 1.0-500.0 ng L-1 (R²=0.9995), with a corresponding limit of detection (LOD) of was 0.27 ng L-1. The relative standard deviation (R.S.D.) (C=50.0 ng L-1, n=9) was 1.13%, with a corresponding enrichment factor of 360 for uranium extraction. The proposed method was successfully applied for the determination of uranium in different water samples.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.62 n.2 20172017-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000200008en10.4067/S0717-97072017000200008 |
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Scielo Chile |
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Scielo Chile |
language |
English |
topic |
Uranium: Determination Liquid-liquid homogeneous microextraction ICP-MS Water samples |
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Uranium: Determination Liquid-liquid homogeneous microextraction ICP-MS Water samples VEYSEH,SOMAYEH NIAZI,ALI FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
description |
In this study, a novel method based on floatation assistance of homogeneous liquid-liquid microextraction (FA-HLLME), combined with inductively coupled plasma-mass spectroscopy (ICP-MS) was proposed, for the determination of trace uranium in environmental water samples. As one of the miniaturized separation and extraction techniques, homogenous liquid-liquid microextraction (HLLME) has been widely applied in the field of environmental monitoring and assessment. 1,2-pyridylazo-2-naphthol (PAN) was used as the complexing agent while toluene and methanol were selected as the extraction and homogeneous solvents, respectively. The factors that influenced the extraction efficiency for uranium determination (including pH, extraction and homogeneous solvents, concentration of PAN and NaCl, extraction time) were studied statistically. Under optimum conditions (pH=7.0, 100 μL toluene, 500 μL methanol, 6.4×10-5 mol L-1 PAN, 1.5 mol L-1 NaCl and 60 sec of extraction time), the linear dynamic range for uranium determination was 1.0-500.0 ng L-1 (R²=0.9995), with a corresponding limit of detection (LOD) of was 0.27 ng L-1. The relative standard deviation (R.S.D.) (C=50.0 ng L-1, n=9) was 1.13%, with a corresponding enrichment factor of 360 for uranium extraction. The proposed method was successfully applied for the determination of uranium in different water samples. |
author |
VEYSEH,SOMAYEH NIAZI,ALI |
author_facet |
VEYSEH,SOMAYEH NIAZI,ALI |
author_sort |
VEYSEH,SOMAYEH |
title |
FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
title_short |
FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
title_full |
FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
title_fullStr |
FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
title_full_unstemmed |
FLOTATION-ASSISTED HOMOGENEOUS LIQUID-LIQUID MICROEXTRACTION FOR TRACE DETERMINATION OF URANIUM IN WATER SAMPLES BY ICP-MS |
title_sort |
flotation-assisted homogeneous liquid-liquid microextraction for trace determination of uranium in water samples by icp-ms |
publisher |
Sociedad Chilena de Química |
publishDate |
2017 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000200008 |
work_keys_str_mv |
AT veysehsomayeh flotationassistedhomogeneousliquidliquidmicroextractionfortracedeterminationofuraniuminwatersamplesbyicpms AT niaziali flotationassistedhomogeneousliquidliquidmicroextractionfortracedeterminationofuraniuminwatersamplesbyicpms |
_version_ |
1714200910248280064 |