Speciation of As(III) and As(V) in water samples by graphite furnace atomic absorption spectrometry after solid phase extraction combined with dispersive liquid-liquid microextraction based on the solidification of floating organic drop

被引:94
|
作者
Shamsipur, Mojtaba [1 ]
Fattahi, Nazir [1 ,2 ]
Assadi, Yaghoub [3 ]
Sadeghi, Marzieh [1 ]
Sharafi, Kiomars [2 ]
机构
[1] Razi Univ, Dept Chem, Kermanshah, Iran
[2] Kermanshah Univ Med Sci, RCEDH, Kermanshah, Iran
[3] Daana Pharmaceut Co, Qual Control Dept, Tabriz, Iran
关键词
Dispersive liquid-liquid microextraction; Solid-phase extraction; Graphite furnace atomic absorption; spectrometry; Arsenic speciation; Water analysis; PLASMA-MASS SPECTROMETRY; VERY-LOW AMOUNTS; EMISSION-SPECTROMETRY; ORGANOPHOSPHORUS PESTICIDES; SUPERCRITICAL-FLUID; TRACE AMOUNTS; ANTIMONY; PRECONCENTRATION; CARBON; CHEMILUMINESCENCE;
D O I
10.1016/j.talanta.2014.06.049
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A solid phase extraction (SPE) coupled with dispersive liquid-liquid microextraction based on the solidification of floating organic drop (DLLME-SFO) method, using diethyldithiphosphate (DDTP) as a proper chelating agent, has been developed as an ultra preconcentration technique for the determination of inorganic arsenic in water samples prior to graphite furnace atomic absorption spectrometry (GFAAS). Variables affecting the performance of both steps were thoroughly investigated. Under optimized conditions, 100 mL of As(11) solution was first concentrated using a solid phase sorbent. The extract was collected in 2.0 mL of acetone and 60.0 mu L of 1-undecanol was added into the collecting solvent. The mixture was then injected rapidly into 5.0 mL of pure water for further DLLME-SFO. Total inorganic As(III, V) was extracted similarly after reduction of As(V) to As(III) with potassium iodide and sodium thiosulfate and As(V) concentration was calculated by difference. A mixture of Pd(NO3)(2) and Mg (NO3)(2) was used as a chemical modifier in GFAAS. The analytical characteristics of the method were determined. The calibration graph was linear in the rage of 10-100 ng L-1 with detection limit of 2.5 ng L-1. Repeatability (intra-day) and reproducibility (inter-day) of method based on seven replicate measurements of 80 ng L-1 of As(III) were 6.8% and 7.5%, respectively. The method was successfully applied to speciation of As(III), As(V) and determination of the total amount of As in water samples and in a certified reference material (NIST RSM 1643e). (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:26 / 32
页数:7
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