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Development and multivariate optimization of nanostructured supramolecular liquid-liquid microextraction validated method for highly sensitive determination of methyl parathion in water samples

机译:纳米结构超分子液 - 液微萃取验证方法的开发和多元优化,用于高敏感测定水样中甲基硫磷的研究

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A simple, rapid and environmentally friendly supramolecular solvent-(SUPRAS)-based liquid phase microextraction method combined with high performance liquid chromatography (HPLC) for the determination of methyl parathion (MP) in water samples was developed. Several factors that affect the coacervation process, such as pH, volume and 1-decanol/THF ratio of supramolecular solvent, vortex time, and inorganic salt concentration were investigated and optimized. Under the optimized conditions, the enhancement factor and preconcentration factor were obtained as 139 and 12.7, respectively and the consumptive index (CI) was 0.79 mL. The limits of detection and quantification were found to be 0.27 mu g L-1 and 0.91 mu g L-1, respectively, while the linear range of analytical curve was ranged from 0.91 up to 500.0 mu g L-1 with correlation coefficient of 0.999. The precision was evaluated in terms of intra-day (n = 10) and inter-day (n = 2) repeatability and the relative standard deviation percentages (% RSD) for two-level concentration (5.0 and 200.0 mu g L-1) was <5.3%. Imazethapyr, imazapic and imazepyr evaluated as possible interfering molecules did not show interference in the microextraction process, while 200.0 mu g L-1 MP could be extracted in the respective presence of 2-nitrophenol and 4-nitrophenol at the 1:1 and 1:10 (m/m) ratio. The developed method was successfully applied for the determination of MP in artesian well (20.3 +/- 2.4 mu g L-1) and surface water (12.2 +/- 3.5 mu g L-1 and 12.7 +/- 2.6 mu g L-1). The accuracy was attested by addition and recovery tests of MP obtaining recovery percentages in the range of 92.0-109.9%, thereby confirming the reliability of the proposed method. (C) 2020 Elsevier B.V. All rights reserved.
机译:一个简单,快速的和环境友好的超分子溶剂(SUPRAS)系液相微方法用高效液相色谱法(HPLC)结合为水样中甲基对硫磷(MP)的确定被开发。影响凝聚过程几种因素,如pH值,体积和1-癸醇/超分子溶剂的THF比,涡旋时间,和无机盐浓度进行了研究和优化。在优化条件下,增强因子和富集因子分别得到分别139和12.7,以及消费指数(CI)为0.79毫升。检测和定量的界限被发现是0.27亩克L-1和0.91亩克L-1,分别,同时分析曲线的线性范围为从0.91到500.0亩克L-1范围为0.999的相关系数。精度在对于两电平浓度日内(N = 10)和日间(N = 2)的重复性和相对标准偏差的百分比(%RSD)来评价(5.0和200.0亩克L-1)为<5.3%。咪草烟,甲基咪草烟和imazepyr评价为可能干扰分子没有表现出在微萃取过程干扰,同时200.0亩克L-1 MP可以在2-硝基苯酚和4-硝基苯酚在1-各自的存在提取:1和1: 10(M / m)的比率。发达方法成功应用于为MP的在自流井确定井(20.3 +/- 2.4亩克L-1)和地表水(12.2 +/- 3.5亩克L-1和12.7 +/- 2.6亩克L- 1)。精度是由MP获得恢复百分比在92.0-109.9%的范围内,从而确认了该方法的可靠性的增加和恢复测试证实。 (c)2020 Elsevier B.v.保留所有权利。

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