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首页> 外文期刊>Analytica chimica acta >Combination of flow injection with capillary electrophoresis. Part 6. A bias-free sample introduction system based on electroosmotic-flow traction
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Combination of flow injection with capillary electrophoresis. Part 6. A bias-free sample introduction system based on electroosmotic-flow traction

机译:流动注射与毛细管电泳相结合。第6部分。基于电渗流牵引力的无偏差样品引入系统

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A bias-free sample injection method based on electroosmotic-flow (EOF) traction was developed for the combined flow injection-capillary electrophoresis system. A Nafion joint implemented at a capillary fracture close to the capillary inlet was used for isolating the electric field during the split-flow sample injection, the sample solution being drawn into the capillary by EOF without bias effects. An electronic time relay system was adopted to control the switching of high voltage between the capillary inlet end and the joint. The peak area ratios of two model compounds, dimethyl sulfoxide and benzoic acid obtained using the proposed system were identical to those with gravity injection. Relative standard deviations of 0.5-2.5% (n = 32) were achieved for peak height and peak area evaluation in the consecutive injections of a series of replicate sample solutions at a sampling frequency of 15 h(-1). Similar performance of the system was obtained with a reversed EOF background electrolyte after reversing the electrode polarity for a mixture of the anions, Cl-, SO42-, NO3- and F- using indirect UV detection. The performance of the system for the analysis of real samples was demonstrated by bias-free sample injection in the separation of caffeine, theobromine and theophylline in beverage samples with satisfactory recoveries in the 92-107% range. (C) 1999 Elsevier Science B.V. All rights reserved. [References: 18]
机译:针对组合流动注射-毛细管电泳系统,开发了一种基于电渗流(EOF)牵引力的无偏差样品注射方法。在分流样品注入过程中,使用在靠近毛细管入口的毛细管断裂处实现的Nafion接头隔离电场,通过EOF将样品溶液吸入毛细管中,而不会产生偏见。采用电子时间继电器系统来控制毛细管入口端和接头之间的高压切换。使用该系统获得的两种模型化合物二甲基亚砜和苯甲酸的峰面积比与重力注入时的峰面积比相同。在以15 h(-1)的采样频率连续进样一系列重复样品溶液时,对于峰高和峰面积评估,获得了0.5-2.5%的相对标准偏差(n = 32)。使用间接UV检测,将阴离子Cl,SO42,NO3-和F-的混合物的电极极性反转后,使用反转的EOF背景电解质可获得与系统类似的性能。通过无偏样品进样分离饮料样品中的咖啡因,可可碱和茶碱,证明了该系统用于分析真实样品的性能,回收率在92%至107%之间。 (C)1999 Elsevier Science B.V.保留所有权利。 [参考:18]

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