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碳酸锶沉淀法作为一种样品制备技术,用于通过四极杆电感耦合等离子体质谱法对矿泉水和葡萄酒中的锶进行同位素比分析。

Strontium carbonate precipitation as a sample preparation technique for isotope ratio analysis of Sr in mineral water and wine by quadrupole-based inductively coupled plasma mass spectrometry.

作者信息

Dronov Michail, Koza Tim, Schwiers Alexander, Schmidt Torsten C, Schram Jürgen

机构信息

Instrumental Analyitcal Chemistry and Centre for Environmental and Water Research (ZWU), University of Duisburg-Essen, Universitätsstr. 5, D-45141, Essen, Germany.

Department of Instrumental and Environmental Analytic, Hochschule Niederrhein, University of Applied Science, Faculty of Chemistry, Frankenring 20, D-47798, Krefeld, Germany.

出版信息

Rapid Commun Mass Spectrom. 2018 Jan 30;32(2):149-158. doi: 10.1002/rcm.8018.

Abstract

RATIONALE

The defined origin of food products is nowadays often seen as a marker of quality. Stontium (Sr) isotope ratio determination can be used to verify the origin of such food products and it has thus become an important technique. Wine samples in particular are often investigated using this technique. Sr isotopic ratio measurements are often disturbed by isobaric Rb interference, making a separation procedure necessary. In this investigation a very simple and effective procedure for the separation of Rb and Sr ions for Sr isotope ratio determination in mineral water and wine samples was developed.

METHODS

The classical Sr-carbonate precipitation reaction for the separation of Sr ions from highly soluble Rb ions was used. For liquid samples, such as mineral water or wine, a prior digestion is not required. This sample preparation procedure was successfully applied for Sr isotope measurements on a widely available quadrupole-based inductively coupled plasma mass spectrometry (ICP-MS) device in combination with the Concentration-Gradient-Method (CGM).

RESULTS

The separation achieved Sr/Rb concentration ratios of 50,000 to 150,000 in water and wine samples. The addition of Ca ions to co-precipitate with the traces of Sr improved the Rb separation and the reproducibility of isotope ratio determination to an uncertainty of ±0.4 ‰ (single standard deviation). This sample preparation approach achieved 2 to 6 times better Rb separation than the commonly applied ion-exchange resin materials.

CONCLUSIONS

The quality of the separation is only limited by the number of precipitation repetitions. Moreover, the applicability of quadrupole-based ICP-MS for the characterisation of samples with respect to their origin by means of Sr isotope ratio determination was demonstrated.

摘要

原理

如今,食品明确的产地常被视为质量的标志。锶(Sr)同位素比值测定可用于验证此类食品的产地,因此已成为一项重要技术。特别是葡萄酒样品,常使用该技术进行研究。Sr同位素比值测量常受到同量异位素铷(Rb)干扰,因此需要进行分离程序。在本研究中,开发了一种非常简单有效的分离Rb和Sr离子的程序,用于测定矿泉水和葡萄酒样品中的Sr同位素比值。

方法

采用经典的Sr-碳酸盐沉淀反应从高溶解性的Rb离子中分离Sr离子。对于液体样品,如矿泉水或葡萄酒,无需预先消化。该样品制备程序已成功应用于一台广泛使用的基于四极杆的电感耦合等离子体质谱仪(ICP-MS)上,结合浓度梯度法(CGM)进行Sr同位素测量。

结果

在水和葡萄酒样品中,分离得到的Sr/Rb浓度比为50000至150000。添加Ca离子与痕量Sr共沉淀可改善Rb的分离效果,并将同位素比值测定的重现性提高到±0.4‰(单标准偏差)的不确定度。这种样品制备方法的Rb分离效果比常用的离子交换树脂材料好2至6倍。

结论

分离质量仅受沉淀重复次数的限制。此外,还证明了基于四极杆的ICP-MS通过Sr同位素比值测定来表征样品产地的适用性。

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