A novel multi-element coprecipitation technique for separation and enrichment of metal ions in environmental samples

被引:186
作者
Aydin, Funda Armagan
Soylak, Mustafa [1 ]
机构
[1] Erciyes Univ, Fac Arts & Sci, Dept Chem, TR-38039 Kayseri, Turkey
[2] Tech Res & Qual Control Dept, Gen Directorate State Hydraul Works, TR-06100 Ankara, Turkey
关键词
preconcentration; separation; heavy metals; coprecipitation; 9-phenyl-3-fluorone; environmental samples;
D O I
10.1016/j.talanta.2007.03.007
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A multi-element preconcentration-separation technique for heavy metal ions in environmental samples has been established. The procedure is based on coprecipitation of gold(III), bismuth(III), cobalt(II), chromium(III), iron(III), manganese(II), nicke](11), lead(II), thorium(TV) and uranium(VI) ions by the aid of Cu(Il)-9-phenyl-3-fluorone precipitate. The Cu(Il)-9-phenyl-3-fluorone precipitate was dissolved by the addition 1.0 mL of concentrated HNO3 and then the solution was completed to 5 mL with distilled water. Iron, lead, cobalt, chromium, manganese and nickel levels in the final solution were determined by flame atomic absorption spectrometer, while gold, bismuth, uranium and thorium were determined by inductively coupled plasma mass spectrometer. The optimal conditions are pH 7, amounts of 9-phenyl-3-fluorone: 5 mg and amounts of Cu(11): I mg. The effects of concomitant ions as matrix were also examined. The preconcentration factor was 30. Gold(III), bismuth(III), chromium(III), iron(III), lead(II) and thorium(IV) were quantitatively recovered from the real samples. The detection limits for the analyte elements based on 3 sigma (n = 15) were in the range of 0.05-12.9 mu g L-1. The validation of the presented procedure was checked by the analysis of two certified reference materials (Montana I Soil (NIST-SRM 2710) and Lake Sediment (IAEA-SL-1)). The procedure was successfully applied to some environmental samples including water and sediments. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:134 / 141
页数:8
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