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Rapid method for determination of homologue imidazolium ionic liquid cations by ion-pair chromatography using a monolithic column

机译:用整体柱离子对色谱法测定同源物质咪唑鎓离子液体阳离子的快速方法

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A fast and gradient ion-pair chromatographic method was developed for determination of five homologue imidazolium ionic liquid cations using a silica-based monolithic column and ultraviolet detection. Chromatographic separations were performed on a Chromolith Speed ROD RP-18e column with 1-heptanesulfonic acid sodium aqueous solution (pH adjusted by citric acid)-acetonitrile as the mobile phase. The effects of chromatographic column, mobile phase, flow rate, and column temperature on retention and separation of the cations were investigated. The retention rules of homologue imidazolium cations were discussed. The results showed that the analysis time could be significantly reduced owing to the application of monolithic column. Simultaneous and fast separation of five imidazolium cations was achieved under the optimum chromatographic conditions. Detection limits (S/N = 3) for the cations were 0.26-1.61 mg/L. Relative standard deviations (n = 5) for peak areas and retention times were less than 0.8%. The method has been successfully applied to the determination of two ionic liquids synthesized by chemistry lab. Recoveries of the cations after spiking were 96.8-101.9%.
机译:开发了一种快速和梯度离子对色谱法,用于测定使用基于二氧化硅的整体柱和紫外检测的五种同源咪唑鎓离子液体阳离子。用1-庚烷磺酸钠水溶液(通过柠檬酸调节pH调节)的铬铜速度棒RP-18E柱进行色谱分离,即乙腈作为流动相。研究了色谱柱,流动相,流速和柱温对阳离子的保留和分离的影响。讨论了同源咪唑阳离子的保留规则。结果表明,由于单片柱的应用,可以显着降低分析时间。在最佳色谱条件下实现了五种咪唑阳离子的同时和快速分离。阳离子的检测限制(S / N = 3)为0.26-1.61 mg / L.峰面积的相对标准偏差(n = 5)和保留次数小于0.8%。该方法已成功地应用于化学实验室合成的两种离子液体的测定。尖峰后阳离子的回收率为96.8-101.9%。

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