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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Large volume injection in ion chromatography separation of rubidium and strontium for on-line inductively coupled plasma mass spectrometry determination of strontium isotope ratios
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Large volume injection in ion chromatography separation of rubidium and strontium for on-line inductively coupled plasma mass spectrometry determination of strontium isotope ratios

机译:离子注入色谱法中大体积进样分离for和锶,在线电感耦合等离子体质谱法测定锶同位素比

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Large volume injection, up to 5 mL, was evaluated and optimised for the on-line ion chromatographic separation of Rb and Sr before ICP-MS measurement of Sr isotope ratios. Flat-topped chromatographic peaks, ideally suited for multicollector ICP-MS isotope ratio measurements, could be obtained when the composition of the mobile phase (nitric acid and 18-crown-6 ether) was identical to the matrix of the sample. Under those conditions rubidium eluted at the dead volume of the column while strontium produced a flat-topped transient signal with several minutes of stable plateau. On-line data acquisition during several minutes at the plateau of Sr signal allowed high precision Sr isotope ratio measurement. The developed procedure was evaluated for Sr isotope ratio measurements on different types of samples, including cider, apples, apple leaves, and soil extracts, in the frame of a long-term project aiming at origin authentication using strontium isotope ratio measurements. It was observed that sample matrix caused broadening of the strontium chromatographic peak and loss of flat-topped peak profile. Under those circumstances the addition of the complexing crown-ether 18-crown-6 both to samples and chromatographic eluent provided two distinct advantages. First, a drastic increase in the retention of strontium was observed which could be modulated by increasing the concentration of nitric acid in the eluent up to 900 mM. This increase in the eluent HNO3 concentration allowed the application of the method to acid soil digests and other high acidity samples. Second, the matrix of the sample did not affect any more the chromatographic peak profile and similar chromatographic separations could be obtained for samples and standards maintaining the flat-topped Sr peak profile. Sample preparation consisted of a simple 1:10 dilution of the cider or pre-treated solid samples by adding HNO3 (900 mM) and 18-crown-6 ether (5 mM) to obtain similar composition in the sample solution and the HPLC eluent. (c) 2007 Elsevier B.V. All rights reserved.
机译:在ICP-MS测量Sr同位素比之前,对Rb和Sr的在线离子色谱分离进行了评估和优化,最大进样量为5 mL。当流动相(硝酸和18-冠-6醚)的组成与样品的基质相同时,可以获得非常适合多收集器ICP-MS同位素比测量的平顶色谱峰。在这些条件下,rub在柱子的死体积上洗脱,而锶产生平顶的瞬态信号,并具有几分钟的稳定平台。在几分钟内在Sr信号的平稳状态下进行在线数据采集,可以进行高精度的Sr同位素比测量。在一项旨在利用锶同位素比测量进行原产地鉴定的长期项目框架中,对所开发的程序进行了评估,以测量不同类型样品(包括苹果酒,苹果,苹果叶和土壤提取物中)的Sr同位素比。观察到样品基质引起锶色谱峰的加宽和平顶峰轮廓的损失。在这种情况下,将络合的冠醚18-cro-6加入样品和色谱洗脱液中可提供两个明显的优势。首先,观察到锶的保留量急剧增加,这可以通过将洗脱液中硝酸的浓度增加到900 mM来调节。洗脱液中HNO3浓度的增加使得该方法可用于酸性土壤消化物和其他高酸性样品。其次,样品的基质不再影响色谱峰轮廓,对于保持平顶Sr峰轮廓的样品和标准品,可以获得相似的色谱分离。样品制备由苹果酒或预处理的固体样品的简单1:1稀释液组成,方法是添加HNO3(900 mM)和18-crown-6醚(5 mM),以在样品溶液和HPLC洗脱液中获得相似的组成。 (c)2007 Elsevier B.V.保留所有权利。

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