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Determination of heavy metals in water samples using dual-cloud point extraction coupled with inductively coupled plasma mass spectrometry

机译:浊点萃取-电感耦合等离子体质谱法测定水样中的重金属

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A dual-cloud point extraction (d-CPE) technique combined with inductively coupled plasma mass spectrometry (ICP-MS) was used for preconcentration and determination of Cr, Ga, Ag, Cd, Mn, Fe, In, Cu, Ni, Co, Pb and Zn in real water samples. An orthogonal array design (OAD) with the OA25 (56) matrix was employed to study the effects of different parameters on the extraction efficiency. Under the best experimental conditions (concentration of complexing reagent 8-hydroxyquinoline, 0.25 mmol La?’1; pH, 6.5; equilibrium temperature, 60 ?°C; surfactant Triton X-114, 0.1%; equilibrium time, 30 min and without salt addition), the enhancement factor ranged from 9.85 to 35.98. The linear dynamic range (LDR) was 1a€“800 ??g La?’1 with correlation coefficients of 0.9974a€“0.9999 and the limits of detection (LODs) were between 0.012 and 0.36 ??g La?’1. Relative standard deviations (RSDs, C = 10 ??g La?’1 and n = 6) were 1.29%a€“5.56%. Finally, the developed method was successfully applied to extraction and determination of the mentioned metal ions in real water samples and satisfactory results were obtained.
机译:采用双浊点萃取(d-CPE)技术与电感耦合等离子体质谱(ICP-MS)结合进行Cr,Ga,Ag,Cd,Mn,Fe,In,Cu,Ni,Co的富集和测定实际水样中的铅,铅和锌。采用带有OA25(56)矩阵的正交阵列设计(OAD)来研究不同参数对提取效率的影响。在最佳实验条件下(配位剂8-羟基喹啉的浓度为0.25 mmol La?1; pH为6.5;平衡温度为60°C;表面活性剂Triton X-114为0.1%;平衡时间为30分钟,无盐另外),增强因子的范围从9.85到35.98。线性动态范围(LDR)为1a“ 800 ?? g La?1”,相关系数为0.9974a“ 0.9999”,检出限(LODs)在0.012和0.36 gg La?’1之间。相对标准偏差(RSD,C = 10 g g La?1和n = 6)为1.29%-5.56%。最终,该方法成功用于实际水样中上述金属离子的提取和测定,并获得满意的结果。

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