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Methods development for separation of fungicides using micellar electrokinetic chromatography

机译:利用胶束电动色谱法分离杀真菌剂的方法开发

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摘要

In this study, micellar electrokinetic chromatography (MEKC) was used for the simultaneous separation of three different classes of fungicides. Separations were done at 210 nm with on-column UV detection. Two different types of separation buffer system (borate and formate) were used. The influence of separation buffer concentration and pH, surfactant concentration, separation voltage and addition of organic solvents and modifiers on migration time, efficiencies and resolutions were investigated. Four fungicides from three different classes viz. carbendazim and thiabendazole (benzimidizole), propiconazole (triazole) and vinclozolin (dicarboximide) were successfully separated in less than 15 min using both separation buffer systems with propiconazole giving two stereoisomer peaks. A buffer system consisting of 4 mM borate buffer at pH 10, with 60 mM sodium cholate (SC) gave the best separation result. On the other hand, good separation was also achieved with a running buffer composed of 20 mM formate buffer at pH 7, containing 60 mM SC and 5 mM ß-cyclodextrin (ß-CD). The limit of detections (LODs) of fungicides in borate buffer system were in the range of 9 – 23 ppm and 29 – 52 ppm for formate buffer system. In an effort to reduce the LODs, two on-line preconcentration techniques with formate buffer system were used because of its higher LODs. The two on-line preconcentration techniques, sweeping and stacking with hydrodynamic (HDI) and electrokinetic (EKI) injection were contrasted. The effect of sample matrix, injection time and injection voltage on fungicides separation was studied using the two online preconcentration techniques. Using on-line preconcentration techniques, height and area sensitivity enhancement factor (SEFheight and SEFarea) were found to be between 10 to 99. LODs in the sub-ppm (0.3 – 4 ppm) level were obtained. At least 10-times improvement in detector response was achieved with normal stacking mode MEKC using hydrodynamic injection, NSM-MEKC-HDI. The proposed method was applied to the analysis of spiked fungicides in lake water samples at 2 – 4 ppm. The recovery was between 46.22 % to 93.30 % with RSDs of 10 % to 27 %.
机译:在这项研究中,胶束电动色谱法(MEKC)用于同时分离三种不同类型的杀菌剂。分离是在210 nm处进行柱上UV检测。使用了两种不同类型的分离缓冲液系统(硼酸盐和甲酸盐)。研究了分离缓冲液浓度和pH,表面活性剂浓度,分离电压以及有机溶剂和改性剂的添加对迁移时间,效率和分离度的影响。来自三个不同类别的四种杀菌剂。多菌灵和噻苯达唑(苯并咪唑),丙环唑(三唑)和长春唑啉(二甲酰亚胺)在两种分离缓冲液体系中均成功分离,丙环唑给出两个立体异构体峰。由pH值为10的4 mM硼酸盐缓冲液和60 mM胆酸钠(SC)组成的缓冲液系统可获得最佳分离效果。另一方面,用运行缓冲液(pH值为20的20 mM甲酸缓冲液),60 mM SC和5 mMß-环糊精(ß-CD)组成,也能实现良好的分离。硼酸盐缓冲液系统中杀真菌剂的检出限(LOD)在甲酸缓冲液系统中介于9 – 23 ppm和29 – 52 ppm之间。为了减少LOD,使用了具有甲酸缓冲液系统的两种在线预浓缩技术,因为它具有更高的LOD。对比了两种在线预浓缩技术,即采用流体动力学(HDI)和电动(EKI)注射进行扫除和堆叠。使用两种在线预浓缩技术研究了样品基质,进样时间和进样电压对杀菌剂分离的影响。使用在线预浓缩技术,发现高度和面积灵敏度增强因子(SEFheight和SEFarea)在10到99之间。LOD低于ppm(0.3 – 4 ppm)水平。使用液力注射NSM-MEKC-HDI的常规堆叠模式MEKC可使检测器响应至少提高10倍。所提出的方法用于分析湖水中2-4 ppm的加标杀真菌剂。回收率为46.22%至93.30%,RSD为10%至27%。

著录项

  • 作者

    Aubid Naemah;

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  • 年度 2006
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  • 原文格式 PDF
  • 正文语种 en
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