利用硼-甘露醇配合物对天然岩石样品进行精确的硼同位素分析

Eizo Nakamura , Tsuyoshi Ishikawa , Jean-Luis Birck , Claude J. Allègre
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引用次数: 104

摘要

介绍了天然硅酸盐岩石和水体中硼化学分离和同位素分析的新进展。在甘露醇存在的情况下,使用氢氟酸和盐酸进行样品溶解和随后的离子交换色谱,通过形成硼-甘露醇络合物抑制硼的挥发和同位素分馏。采用Cs2BO2+-石墨热电离质谱法测定硼同位素组成。在化学分离和质谱分析过程中未观察到硼同位素分馏现象。在整个分析过程中,硼的程序空白率为3 ~ 4 ng,回收率为99±1%。测定玄武岩和海水中11B/10B比值的分析精密度和重现性分别为±0.1 ~ 0.1%和±0.2‰。本方法使我们能够测定<的同位素组成;1 μg B在硅酸盐样品和自然流体中具有上述分析误差。该方法在同位素稀释质谱法测定硼浓度方面也有了显著的改进,因为在样品分解过程中,样品和峰之间实现了完全混合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Precise boron isotopic analysis of natural rock samples using a boron-mannitol complex

Newly developed techniques for boron chemical separation and isotopic analysis in natural silicate rocks and waters are described. Sample dissolution and the subsequent ion-exchange chromatography were conducted using hydrofluoric and hydrochloric acids in the presence of mannitol which suppresses boron volatilization and isotopic fractionation by the formation of a boron-mannitol complex. Thermal ionization mass spectrometry using the Cs2BO2+-graphite method was employed for the determination of boron isotopic composition. No boron isotopic fractionation was observed in the course of chemical separation and mass spectrometry. In the whole analytical procedure, procedural blank and recovery yield of boron were 3–4 ng and 99±1%, respectively. The analytical precision and reproducibility of measured 11B/10B ratios were ±0.1−0.1% and ±0.2‰ for the measurements of basalt and seawater, respectively. The present method enables us to determine the isotopic composition of < 1 μg B in silicate samples and in natural fluids with the above-mentioned analytical errors. This method also provides a remarkable improvement in the measurement of boron concentration by isotope dilution mass spectrometry because of the achievement of complete mixing between sample and spike during sample decomposition.

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