Tandem ICP-mass spectrometry for Sr isotopic analysis without prior Rb/Sr separation

被引:57
作者
Bolea-Fernandez, Eduardo [1 ]
Balcaen, Lieve [1 ]
Resano, Martin [2 ]
Vanhaecke, Frank [1 ]
机构
[1] Univ Ghent, Dept Analyt Chem, B-9000 Ghent, Belgium
[2] Univ Zaragoza, Dept Analyt Chem, Aragon Inst Engn Res I3A, E-50009 Zaragoza, Spain
关键词
DYNAMIC REACTION CELL; LONG-LIVED RADIONUCLIDES; RATIO MEASUREMENTS; METHYL-FLUORIDE; ENVIRONMENTAL-SAMPLES; REACTION GAS; MS; INTERFERENCE; RESOLUTION; BIAS;
D O I
10.1039/c5ja00157a
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The use of a mixture of 10% of CH3F and 90% of He as a reaction gas in tandem ICP-mass spectrometry (ICP-MS/MS) enables the accurate determination of the Sr-87/Sr-86 isotope ratio in geological materials, provided that mass discrimination is corrected for by using a combination of internal (Russell law, assuming a constant Sr-88/Sr-86 isotope ratio) and external correction (using the isotopic reference material NIST SRM 987 SrCO3) in a sample-standard bracketing approach. No prior Rb/Sr separation is required as the isobaric overlap at a mass-to-charge ratio of 87 is avoided by monitoring SrF+ reaction product ions instead of Sr+ ions. Rb shows no reactivity towards CH3F. The double mass selection (MS/MS mode) prevents both spectral overlap from atomic ions at the mass-to-charge ratios of SrF+ reaction product ions and a measurable effect from the matrix on the Sr-87/Sr-86 result. This aspect is critical, as it enables accurate results to be obtained without the need for using a matrix-matched standard to correct for mass discrimination, in contrast to previous work with a quadrupole ICP-MS instrument with a CH3F/Ne-pressurized cell, in which the use of a matrix-matched standard was compulsory. The precision attainable -0.05% RSD external precision - suffices for making the newly developed method useful in a variety of applications.
引用
收藏
页码:303 / 310
页数:8
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