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Molecularly imprinted matrix solid-phase dispersion coupled to micellar electrokinetic chromatography for simultaneous determination of triazines in soil, fruit, and vegetable samples

机译:分子印迹基质固相分散体与胶束电动色谱联用,可同时测定土壤,水果和蔬菜样品中的三嗪

摘要

A simple and sensitive method for the simultaneous determination of four triazines from soil, strawberry, and tomato samples was developed by selective molecularly imprinted matrix solid-phase dispersion (MI-MSPD) coupled to micellar electrokinetic chromatography (MEKC). Using atrazine as template, the synthesized molecularly imprinted polymers (MIPs) were employed as the dispersion sorbent of MSPD to successfully extract atrazine and its analogs of simazine, ametryn, and propazine from the three different real samples, while matrix interferences were effectively eliminated simultaneously under the optimum extraction conditions. Excellent separation was achieved within 7 min by using an optimized buffer system composed of 30 mmol/L ammonium acetate, 20 mmol/L SDS, and 15% ACN at pH 9.45, obtained by orthogonal design. Good linearity was obtained in a range of 0.525 mu g/g with the correlation coefficients R2 =0.9991 except for strawberry sample within 125 mu g/g, and limits of detection were between 12.931.5 ng/g in all the three samples. The average recoveries of the four triazines at three different spiked levels were ranged from 53.5 to 98.4% with the relative standard deviations of 1.284.89%. This method was proved convenient, costeffective, and environmental benign and could be used as an alternative tool to the existing methods for analyzing the residues of triazines in soil, fruit, and vegetable samples.
机译:通过选择性分子印迹基质固相分散体(MI-MSPD)结合胶束电动色谱(MEKC),开发了一种同时测定土壤,草莓和番茄样品中四种四嗪的简单而灵敏的方法。以阿特拉津为模板,将合成的分子印迹聚合物(MIPs)作为MSPD的分散吸附剂,成功地从三个不同的真实样品中提取了阿特拉津及其类似物辛他津,萘丙啶和丙嗪的类似物,同时有效地消除了基质干扰。最佳提取条件。使用正交设计获得的优化缓冲液系统,该缓冲液由30 mmol / L醋酸铵,20 mmol / L SDS和15%ACN在pH 9.45组成,在7分钟内可实现出色的分离。除草莓样品在125μg/ g之内外,相关系数R2 = 0.9991,在0.525μg/ g的范围内获得了良好的线性,所有三个样品的检出限在12.931.5 ng / g之间。三种不同加标水平下的四种三嗪的平均回收率在53.5%至98.4%之间,相对标准偏差为1.284.89%。该方法被证明方便,经济高效且对环境无害,可以用作分析土壤,水果和蔬菜样品中三嗪残留量的现有方法的替代工具。

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