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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Reversed-phase ion-pair chromatography of hydroxyl functionalized imidazolium ionic liquid cations and its application in analysis of environmental water and measurement of hydrophobicity constants
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Reversed-phase ion-pair chromatography of hydroxyl functionalized imidazolium ionic liquid cations and its application in analysis of environmental water and measurement of hydrophobicity constants

机译:羟基官能化咪唑离子液体阳离子反相离子对色谱及其在环境水分分析中的应用及疏水性常数的测量

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A reversed-phase ion-pair chromatography with ultraviolet detection method for the determination of 1-hydroxyethyl-3-methyl imidazolium cation ([HOEtMIm](+)) and 1-hydroxypropyl-3-methyl imidazolium cation ([HOPrMIm](+)) was developed. The method has been applied to the analysis of hydroxyl functionalized imidazolium ionic liquid cations in Songhua River water samples and the determination of hydrophobicity constants. [HOEtMIm](+) and [HOPrMIm](+) were not completely separated in the reversed-phase chromatography, but complete separation was realized in the reversed-phase ion-pair chromatography. The effects of ion-pair reagents, organic solvents, column temperatures and ultraviolet detection wavelengths on the separation and detection of hydroxyl functionalized imidazolium ionic liquid cations in reversed-phase ion-pair chromato graphy were investigated. Ordinary imidazolium ionic liquids do not interfere with the determination of hydroxyl functionalized imidazolium ionic liquids. The suitable ion-pair reagent was sodium octane-sulfonate. Using reversed-phase C-18 chromatographic column, the mobile phase consisted of 0.5 mmol/L sodium octanesulfonate solution/methanol (85/15, v/v) with column temperature of 40 degrees C, ultraviolet detection wavelength of 210 nm and flow rate of 1.0 mL/min, [HOEtMIm](+) and [HOPrMIm](+) can be achieved baseline separation within 20 min. The detection limits were 0.36 and 0.50 mg/L, respectively. The relative standard deviations of peak area and retention time were less than 0.80%. Recoveries of sample addition were between 97.3% and 100.5%. The method was simple, accurate, reliable, satisfying the requirement of quantitative analysis, and has good practicability.
机译:具有紫外检测方法的反相离子对色谱法测定1-羟乙基-3-甲基咪唑鎓阳离子([HOETMIM](+))和1-羟基丙基-3-甲基咪唑鎓阳离子([HORMIM](+) ) 已开发。该方法已应用于松花河水样品中羟基官能化咪唑鎓离子液体阳离子的分析及疏水性常数的测定。 [Hoetmim](+)和[HORMIM](+)在反相色谱中没有完全分离,但在反相离子对色谱中实现完全分离。研究了离子对试剂,有机溶剂,柱温和紫外线检测波长对反相离子对染色液中羟基官能化咪唑鎓离子液体阳离子分离和检测的影响。普通咪唑鎓离子液体不会干扰羟基官能化咪唑鎓离子液体的测定。合适的离子对试剂是辛烷 - 磺酸钠。使用反相C-18色谱柱,流动相由0.5mmol / L辛磺酸钠溶液/甲醇(85/15,v / v)组成,柱温为40℃,紫外线检测波长为210nm和流速1.0ml / min,[Hoetmim](+)和[Hopmim](+)可以在20分钟内实现基线分离。检测限分别为0.36和0.50mg / L.峰面积和保留时间的相对标准偏差小于0.80%。样品添加的回收率为97.3%至100.5%。该方法简单,准确,可靠,满足定量分析的要求,具有良好的实用性。

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