Instituto de Química, Universidade de São Paulo, Brazil.
Anal Chem. 2012 Sep 18;84(18):7599-602. doi: 10.1021/ac3019312. Epub 2012 Sep 4.
A thin-layer electrochemical flow cell coupled to capillary electrophoresis with contactless conductivity detection (EC-CE-C(4)D) was applied for the first time to the derivatization and quantification of neutral species using aliphatic alcohols as model compounds. The simultaneous electrooxidation of four alcohols (ethanol, 1-propanol, 1-butanol, and 1-pentanol) to the corresponding carboxylates was carried out on a platinum working electrode in acid medium. The derivatization step required 1 min at 1.6 V vs. Ag/AgCl under stopped flow conditions, which was preceded by a 10 s activation at 0 V. The solution close to the electrode surface was then hydrodynamically injected into the capillary, and a 2.5 min electrophoretic separation was carried out. The fully automated flow system operated at a frequency of 12 analyses per hour. Simultaneous determination of the four alcohols presented detection limits of about 5 × 10(-5) mol L(-1). As a practical application with a complex matrix, ethanol concentrations were determined in diluted pale lager beer and in nonalcoholic beer. No statistically significant difference was observed between the EC-CE-C(4)D and gas chromatography with flame ionization detection (GC-FID) results for these samples. The derivatization efficiency remained constant over several hours of continuous operation with lager beer samples (n = 40).
一种薄层电化学流动池与非接触电导检测毛细管电泳(EC-CE-C(4)D)相结合,首次用于衍生化和定量分析中性物质,以脂肪醇为模型化合物。在酸性介质中,四种醇(乙醇、1-丙醇、1-丁醇和 1-戊醇)在铂工作电极上同时电氧化为相应的羧酸盐。衍生化步骤需要在停流条件下以 1.6 V 相对于 Ag/AgCl 进行 1 分钟,在此之前先在 0 V 下激活 10 秒。然后将靠近电极表面的溶液在水力作用下注入毛细管中,并进行 2.5 分钟的电泳分离。全自动流动系统每小时可分析 12 个样品。四种醇的同时测定检测限约为 5×10(-5)mol L(-1)。作为一个复杂基质的实际应用,乙醇浓度在稀释淡拉格啤酒和无酒精啤酒中进行了测定。这些样品的 EC-CE-C(4)D 和火焰离子化检测气相色谱(GC-FID)结果之间没有统计学上的显著差异。对于拉格啤酒样品,衍生化效率在数小时的连续运行中保持不变(n = 40)。