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首页> 外文期刊>Human and Experimental Toxicology >Application of response surface methodology for optimization of ionic liquid-based dispersive liquid-liquid microextraction of cadmium from water samples
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Application of response surface methodology for optimization of ionic liquid-based dispersive liquid-liquid microextraction of cadmium from water samples

机译:响应面法在优化离子液体水样中微量镉分离中的应用

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摘要

A new, rapid, and simple method for the determination of cadmium in water samples was developed using ionic liquid-based dispersive liquid-liquid microextraction (IL-DLLME) coupled to flame atomic absorption spectrometry (FAAS). In the proposed approach, 2-(5-boromo-2-pyridylazo)-5-(diethyamino) phenol was used as a chelating agent and 1-hexyl-3-methylimidazolium bis(trifluoro methylsulfonyl)imide and acetone were selected as extraction and dispersive solvents, respectively. Sample pH, concentration of chelating agent, amount of ionic liquid (extraction solvent), disperser solvent volume, extraction time, salt effect, and centrifugation speed were selected as interested variables in IL-DLLME process. The significant variables affecting the extraction efficiency were determined using a Placket-Burman design. Thereafter, the significant variables were optimized using a Box-Behnken design and the quadratic model between the dependent and the independent variables was built. The optimum experimental conditions obtained from this statistical evaluation included: pH: 6.7; concentration of chelating agent: 1.1 × 10-3 mol L-1; and ionic liquid: 50.0 mg. Under the optimum conditions, the preconcentration factor obtained was 100. Calibration graph was linear in the range of 0.2-60 μg L-1 with correlation coefficient of 0.9992. The limit of detection was 0.06 μg L-1, which is lower than other reported approaches applied to the determination of cadmium using FAAS. The relative SD (n = 8) was 2.4%. The proposed method was successfully applied to the determination of trace amounts of cadmium in the real water samples with satisfactory results.
机译:建立了一种基于离子液体的分散液-液微萃取(IL-DLLME)和火焰原子吸收光谱法(FAAS)结合的测定水样品中镉的新方法,该方法简便,快捷。在所提出的方法中,使用2-(5-boromo-2-pyridylazoazo)-5-(diethyamino)苯酚作为螯合剂,并选择1-己基-3-甲基咪唑双(三氟甲基磺酰基)酰亚胺和丙酮作为萃取剂。分散溶剂。选择样品的pH值,螯合剂的浓度,离子液体(萃取溶剂)的量,分散剂的溶剂体积,萃取时间,盐效应和离心速度作为IL-DLLME过程中的重要变量。使用Placket-Burman设计确定影响萃取效率的重要变量。此后,使用Box-Behnken设计对重要变量进行优化,并建立因变量和自变量之间的二次模型。从该统计评估获得的最佳实验条件包括:pH:6.7; pH:6.7。螯合剂浓度:1.1×10-3 mol L-1;和离子液体:50.0 mg。在最佳条件下,获得的预浓系数为100。校正图在0.2-60μgL-1范围内呈线性,相关系数为0.9992。检出限为0.06μgL-1,低于使用FAAS测定镉的其他报道方法。相对SD(n = 8)为2.4%。该方法成功用于实际水样中痕量镉的测定,结果令人满意。

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