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Cloud point extraction for ultra-trace Cd determination in microwave-digested biological samples by ETAAS

机译:ETAAS浊点萃取法测定微波消化的生物样品中的痕量镉

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Cloud point extraction (CPE) has been used for the preconcentration of cadmium, after the formation of a complex with 2-(5-bromo-2-pyridylazo)-5-(diethylamino)-phenol (5-Br-PADAP), and further determination by graphite furnace atomic absorption spectrometry (ETAAS) using polyethyleneglicolmono-p-nonyphenylether (PONPE 7.5) as surfactant. The chemical variables that affect the cloud point extraction were optimized. The separation of the two phases was easily accomplished by cooling the Mixture in order to make more Viscous the surfactant-rich phase. In order to establish the optimum conditions for the determination of Cd by ETAAS, Pd + Mg, Pt, Ir, Rh and Ru were studied as chemical modifiers. The best thermal stabilization was obtained with pd + Mg, with a maximum Pyrolysis temperature of 1100 degrees C. Under the optimum conditions i.e., pH 9.0, [5-Br-PADAP] =2.0 x 10 (5) mol L-1, [PONPE 7.5] =0.02% (w/v), an enhancement factor of 22-fold was reached. The lower limit of detection (LOD) obtained under the optimal conditions was 0.008 mu g L-1. The precision for 10 replicate determinations at 0.2 mu g L-1 Cd was 3.5% relative standard deviation (R.S.D.), The calibration graph using the preconcentration method was linear with a correlation coefficient of 0.9984 at levels close to the detection limit up to at least 1.0 mu g L-1, The method was successfully applied to the determination of cadmium in urine samples and in a water standard reference material. (C) 2008 Elsevier B.V. All rights reserved.
机译:与2-(5-溴-2-吡啶基偶氮)-5-(二乙基氨基)-苯酚(5-Br-PADAP)形成络合物后,浊点萃取(CPE)已用于镉的预浓缩。进一步的测定采用石墨炉原子吸收光谱法(ETAAS),使用聚乙二醇单对-壬基苯基醚(PONPE 7.5)作为表面活性剂。优化了影响浊点提取的化学变量。通过使混合物冷却以容易地完成两相的分离,以使粘稠的富含表面活性剂的相更具粘性。为了建立ETAAS测定镉的最佳条件,研究了Pd + Mg,Pt,Ir,Rh和Ru作为化学改性剂。用pd + Mg可获得最佳的热稳定性,最高热解温度为1100摄氏度。在最佳条件下,即pH 9.0,[5-Br-PADAP] = 2.0 x 10(5)mol L-1,[ PONPE 7.5] = 0.02%(w / v),增强因子达到22倍。在最佳条件下获得的检测下限(LOD)为0.008μgL-1。在0.2μg L-1 Cd下进行10次重复测定的准确度为3.5%相对标准偏差(RSD)。使用预浓缩方法的校准图呈线性,相关系数为0.9984,接近检测极限,至少至少1.0μg L-1,该方法已成功应用于尿液样品和水标准参考物质中镉的测定。 (C)2008 Elsevier B.V.保留所有权利。

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