Suppr超能文献

离子色谱法同时测定离子液体中的三氟乙酸根、四氟硼酸根和卤离子

[Simultaneous determination of trifluoroacetate, tetrafluoroborate and halide ions in ionic liquid by ion chromatography].

作者信息

Li Siwen, Zhang Xiaodong, Yu Hong

机构信息

College of Chemistry and Chemical Engineering, Harbin Normal University, Harbin 150025, China.

出版信息

Se Pu. 2010 Jul;28(7):708-11. doi: 10.3724/sp.j.1123.2010.00708.

Abstract

A method was developed for the simultaneous determination of trifluoroacetate, tetrafluoroborate and halide ions (FF-, Cl-, Br-) by ion chromatography with direct conductivity detection. The chromatographic separation was performed on a Shim-pack IC-A3 anion-exchange column with potassium biphthalate, phthalic acid + tris (hydroxymethyl) -aminomethane, and p-hydroxybenzoic acid + tris (hydroxymethyl) -aminomethane + boric acid as eluent, separately. The effects of the nature of eluent, eluent concentration, acetonitrile concentration and column temperature on the separation and the retention factors of the anions were investigated. The optimized chromatographic conditions for the determination of the anions were as follows: 1.2 mmol/L potassium biphthalate as eluent, a column temperature of 45 degrees C and a flow rate of 1.0 mL/min. Under the optimal conditions, the anions were baseline separated. Moreover, the symmetries of peaks were better. The limits of detection (S/N = 3) for the anions were in the range of 0.01 - 0.50 mg/L. The relative standard deviations (RSDs) of the chromatographic retention time and peak area for the anions were not more than 0.2% and 1.2% (n = 5), respectively. The method has been applied to the determination of trifluoroacetate, tetrafluoroborate and halide ions in ionic liquids. The spiked recoveries of the anions were from 98.0% to 103.2%. The method is simple, accurate and reliable, and has better practicability.

摘要

建立了一种采用离子色谱直接电导检测法同时测定三氟乙酸根、四氟硼酸根和卤离子(F⁻、Cl⁻、Br⁻)的方法。分别以邻苯二甲酸钾、邻苯二甲酸+三(羟甲基)氨基甲烷以及对羟基苯甲酸+三(羟甲基)氨基甲烷+硼酸为洗脱液,在Shim-pack IC-A3阴离子交换柱上进行色谱分离。考察了洗脱液性质、洗脱液浓度、乙腈浓度和柱温对阴离子分离及保留因子的影响。测定阴离子的优化色谱条件如下:以1.2 mmol/L邻苯二甲酸钾为洗脱液,柱温45℃,流速1.0 mL/min。在最佳条件下,阴离子实现了基线分离,且峰形对称性较好。阴离子的检测限(S/N = 3)在0.01 - 0.50 mg/L范围内。阴离子色谱保留时间和峰面积的相对标准偏差(RSDs)分别不超过0.2%和1.2%(n = 5)。该方法已应用于离子液体中三氟乙酸根、四氟硼酸根和卤离子的测定。阴离子的加标回收率为98.0%至103.2%。该方法简便、准确、可靠,具有较好的实用性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验