首页> 外文期刊>Journal of Hazardous Materials >Solid phase extraction of cadmium on 2-mercaptobenzothiazole loaded on sulfur powder in the medium of ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate and cold vapor generation-atomic absorption spectrometric determination
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Solid phase extraction of cadmium on 2-mercaptobenzothiazole loaded on sulfur powder in the medium of ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate and cold vapor generation-atomic absorption spectrometric determination

机译:离子液体1-丁基-3-甲基咪唑鎓六氟磷酸盐介质中硫载于2-巯基苯并噻唑上的固相萃取镉及冷蒸气发生原子吸收光谱法

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摘要

A novel solid phase extractor for preconcentration of cadmium at ng l~(-1) levels has been developed. Cadmium ions were retained on a column packed with sulfur powder modified with 2-mercaptobenzothiazole (2-MBT) in the medium of l-butyl-3-methylimidazolium hexafluorophosphate ([bmim]~+PF_6~-) ionic liquid. The presence of ionic liquid during modification of sulfur enhanced the retention of cadmium ions on the column. The retained cadmium ions were eluted with 2 mol L~(-1) solution of HCl and measured by cold vapor generation-atomic absorption spectrometry (CVG-AAS). By using reaction cell-gas liquid separator (RC-CLS), gaseous cadmium vapors were produced and reached the atomic absorption spectrometer, instantaneously. The influence of different variables on both processes of solid phase extraction and CVG-AAS determination of cadmium ions was investigated. The calibration curve was linear in the range of 10-200 ng L~(-1) of cadmium in the initial solution with r = 0.9992 (n = 8) under optimum conditions. The limit of detection based on three times the standard deviation of the blank (3S_b, n = 10) was 4.6 ng L~(-1). The relative standard deviation (R.S.D.) of 25 and 150 ng L~(-1) of cadmium was 4.1 and 2.2% (n=8), respectively. The procedure was validated by the analysis of a certified reference material (DORM-3), water and fish samples.
机译:已经开发了一种新型的固相萃取器,用于以ng l〜(-1)浓度对镉进行预浓缩。镉离子保留在填充有2-巯基苯并噻唑(2-MBT)修饰的硫粉的柱子上,并在六氟磷酸1-丁基-3-甲基咪唑鎓([bmim]〜+ PF_6-)离子液体中。硫磺改性过程中离子液体的存在增强了镉离子在色谱柱上的保留。残留的镉离子用2 mol L〜(-1)的HCl溶液洗脱,并通过冷蒸气发生原子吸收光谱法(CVG-AAS)测定。通过使用反应池气液分离器(RC-CLS),产生气态镉蒸气并立即到达原子吸收光谱仪。研究了不同变量对固相萃取和CVG-AAS测定镉离子过程的影响。在最佳条件下,初始溶液中镉的校正曲线在10-200 ng L〜(-1)范围内为线性,r = 0.9992(n = 8)。基于空白标准偏差(3S_b,n = 10)的三倍的检出限为4.6 ng L〜(-1)。 25和150 ng L〜(-1)的镉的相对标准偏差(R.S.D.)分别为4.1%和2.2%(n = 8)。通过对认证参考物质(DORM-3),水和鱼样品的分析验证了该程序。

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