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不同离子液体用于液相色谱-氢化物发生原子荧光光谱法分离和测定葡萄酒品种中砷形态的比较评价

A comparative evaluation of different ionic liquids for arsenic species separation and determination in wine varietals by liquid chromatography - hydride generation atomic fluorescence spectrometry.

作者信息

Castro Grijalba Alexander, Fiorentini Emiliano F, Martinez Luis D, Wuilloud Rodolfo G

机构信息

Laboratory of Analytical Chemistry for Research and Development (QUIANID), Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Padre J. Contreras 1300, P.C 5500 Mendoza, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.

Laboratory of Analytical Chemistry for Research and Development (QUIANID), Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo, Padre J. Contreras 1300, P.C 5500 Mendoza, Argentina.

出版信息

J Chromatogr A. 2016 Sep 2;1462:44-54. doi: 10.1016/j.chroma.2016.07.069. Epub 2016 Jul 27.

Abstract

The application of different ionic liquids (ILs) as modifiers for chromatographic separation and determination of arsenite [As(III)], arsenate [As(V)], dimethylarsonic acid (DMA) and monomethylarsonic acid (MMA) species in wine samples, by reversed-phase high performance liquid chromatography coupled to hydride generation atomic fluorescence spectrometry detection (RP-HPLC-HG-AFS) was studied in this work. Several factors influencing the chromatographic separation of the As species, such as pH of the mobile phase, buffer solution concentration, buffer type, IL concentration and length of alkyl groups in ILs were evaluated. The complete separation of As species was achieved using a C18 column in isocratic mode with a mobile phase composed of 0.5% (v/v) 1-octyl-3-methylimidazolium chloride ([C8mim]Cl) and 5% (v/v) methanol at pH 8.5. A multivariate methodology was used to optimize the variables involved in AFS detection of As species after they were separated by HPLC. The ILs showed remarkable performance for the separation of As species, which was obtained within 18min with a resolution higher than 0.83. The limits of detection for As(III), As(V), MMA and DMA were 0.81, 0.89, 0.62 and 1.00μg As L(-1). The proposed method was applied for As speciation analysis in white and red wine samples originated from different grape varieties.

摘要

本研究采用反相高效液相色谱-氢化物发生原子荧光光谱检测法(RP-HPLC-HG-AFS),研究了不同离子液体(ILs)作为改性剂在葡萄酒样品中砷酸盐[As(III)]、砷酸盐[As(V)]、二甲基砷酸(DMA)和一甲基砷酸(MMA)形态的色谱分离和测定中的应用。评估了影响砷形态色谱分离的几个因素,如流动相的pH值、缓冲溶液浓度、缓冲类型、离子液体浓度和离子液体中烷基的长度。使用C18柱在等度模式下,以由0.5%(v/v)1-辛基-3-甲基咪唑氯盐([C8mim]Cl)和5%(v/v)甲醇组成的流动相在pH 8.5条件下实现了砷形态的完全分离。采用多变量方法对高效液相色谱分离后的砷形态进行原子荧光光谱检测中涉及的变量进行优化。离子液体对砷形态的分离表现出显著性能,在18分钟内实现分离,分离度高于0.83。As(III)、As(V)、MMA和DMA的检测限分别为0.81、0.89、0.62和1.00μg As L(-1)。所提出的方法应用于来自不同葡萄品种的白葡萄酒和红葡萄酒样品中的砷形态分析。

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