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Anion-exchange chromatographic separation of Hg for isotope ratio measurements by multicollector ICPMS

机译:汞的阴离子交换色谱分离,通过多收集器ICPMS测定同位素比

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A procedure is described for precise Hg isotope ratio measurements by solution nebulization multicollector inductively coupled plasma mass spectrometry (MC- ICPMS). Hg was released from geological samples using aqua regia extraction and then separated from other matrix elements with the aid of anion-exchange chromatography using strongly basic Dowex 1-X8 anion-exchange resin. Performance of the chromatographic procedure was evaluated using various types of replacement anions for elution of mercury, including L-cysteine, thiourea, NO3-, and SO42-. A solution of 0.15% L-cysteine in 0.06 M HCl was found to be the most convenient eluent for subsequent MC-ICPMS measurements. The optimized procedure provides separation of Hg from virtually all concomitant matrix elements while maintaining quantitative (>95%) recovery. In addition, band displacement chromatographic experiments were conducted to assess whether the anion-exchange purification can produce Hg isotope fractionation artifacts. No isotope fractionation between the Hg(II)-L-cysteine complex in aqueous solution and Hg ions in the anion-exchange resin was observed. Hg isotope ratio measurements were performed using the bracketing standards approach and on-line correction for instrumental mass discrimination using Tl spiking and normalization to the Tl-205/Tl-203 ratio. The absence of spectral interference during Hg isotope ratio measurements was verified using a three-isotope plot. Uncertainties of Hg isotope ratio measurements for replication of the entire procedure, expressed as two standard deviations, are better than +/- 0.08 parts per thousand/amu. The described procedure facilitates study of variations in the isotopic composition of Hg in nature.
机译:描述了通过溶液雾化多收集器电感耦合等离子体质谱法(MC-ICPMS)精确测量Hg同位素比的方法。使用王水萃取从地质样品中释放出汞,然后借助使用强碱性Dowex 1-X8阴离子交换树脂的阴离子交换色谱法将其与其他基质元素分离。使用各种类型的置换阴离子(包括L-半胱氨酸,硫脲,NO3-和SO42-)洗脱汞来评估色谱程序的性能。发现0.15%L-半胱氨酸在0.06 M HCl中的溶液是随后进行MC-ICPMS测量的最方便的洗脱液。优化的程序可将汞从几乎所有伴随的基质元素中分离出来,同时保持定量(> 95%)的回收率。此外,进行了带位移色谱实验以评估阴离子交换纯化是否可以产生Hg同位素分馏伪影。在水溶液中的Hg(II)-L-半胱氨酸络合物与阴离子交换树脂中的Hg离子之间未观察到同位素分馏。使用括号内标准方法进行汞同位素比测量,并使用T1尖峰和归一化为T1-205 / T1-203比对仪器质量进行在线校正。使用三同位素图验证了在汞同位素比测量过程中不存在光谱干扰。整个过程重复进行的汞同位素比测量的不确定度,以两个标准差表示,优于+/- 0.08份/千/ amu。所描述的程序有助于研究自然界中汞同位素组成的变化。

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