首页> 外文会议>International Conference on Agricultural and Natural Resources Engineering >A Conversion of Sample Medium from Water to Acetonitrile by Subzero Temperature Liquid-Liquid Extraction for Acetonitrile- Salt Stacking in Capillary Electrophoresis
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A Conversion of Sample Medium from Water to Acetonitrile by Subzero Temperature Liquid-Liquid Extraction for Acetonitrile- Salt Stacking in Capillary Electrophoresis

机译:通过亚单温液 - 液 - 液 - 溶液在毛细管电泳中转化水对乙腈的样品培养基转化为乙腈溶液

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In capillary electrophoresis (CE) analysis, acetonitrile-salt stacking (ASS) is an efficient way for enhancing the response signal of the analyte which is dissolved in the aqueous medium of acetonitrile and NaCl. The higher volume fraction of acetonitrile (60 to 80 %) in the sample medium is strictly demanded if ASS is conducted. Consequently, it is necessary to develop a convenient method for converting the water-based sample to the acetonitrile-based sample without any dilution of the analyte during the sample preparation procedure. Acetonitrile subzero temperature liquid-liquid extraction (ASTLLE) is the best choice for this purpose. ASTLLE is based on the unique property of acetonitrile that a phase separation can occur if the homogenous mixture solution of acetonitrile and water is kept at a subzero temperature for a short period. The upper layer is the acetonitrile-rich phase, and the lower layer is the water phase. Accompanying the phase separation, the analytes of relatively weak polarity such as mononitrophenol isomers (at acidic condition) can be transferred to acetonitrile-rich phase. The volume fraction of acetonitrile in the formed acetonitrile-rich phase was estimated on the basis of its viscosity which was determined by CE instrument. It was confirmed that the volume fraction of acetonitrile in the formed acetonitrile-rich phase was in the range of 70-80 % (v/v), indicating that the sample processed by ASTLLE met the ASS demand for high volume fraction of acetonitrile. The combination of ASTLLE and ASS was successfully applied to the analysis of mononitrophenol isomers in acidic aqueous solution. The precisions (RSD) of the migration time and peak area for six replicate runs of the three mononitrophenol isomers were in the range of 1.1~1.3 %, and 5.5~8.5 %, respectively. The lowest detection limit of mononitrophenol isomers was 1x10~(-4) μg·mL~(-1) . The recovery ranged from 96.1 to 113.4 %.
机译:在毛细管电泳(Ce)分析中,乙腈 - 盐堆叠(ASS)是增强溶解在乙腈和NaCl水性介质中的分析物的响应信号的有效方法。如果进行ASAs,则严格要求在样品介质中较高体积的乙腈(60至80%)。因此,有必要开发一种方便的方法,用于将水基样品转化为基于乙腈的样品,而不会在样品制备程序期间稀释分析物。乙腈亚单温液 - 液 - 液 - 液 - 液 - 液 - 液 - 液 - 液萃取(ASTLLE)是此目的的最佳选择。 ASTLLE基于乙腈的独特性质,如果乙腈和水的均匀混合物溶液保持在亚零温度短时间,则可以发生相分离。上层是富含乙腈的相位,下层是水相。伴随相分离,相对弱极性的分析物,例如单硝基苯酚异构体(在酸性条件下)可以转移至富含乙腈的相。富含乙腈的相中乙腈的体积分数基于其通过CE仪器测定的粘度估计。确认形成富含乙腈的相中乙腈的体积分数在70-80%(v / v)的范围内,表明由Astle加工的样品满足了对乙腈的高体积分数的ass的需求。 Astlle和Ass的组合成功地应用于酸性水溶液中单硝基苯酚异构体的分析。迁移时间和六种重复运行的迁移时间和峰面积的峰值区域分别为1.1〜1.3%和5.5〜8.5%。单硝基苯酚异构体的最低检测限为1×10〜(-4)μg·mL〜(-1)。恢复范围从96.1到113.4%。

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