Issue 7, 2024

Effects of Faraday cup deterioration on Sr and Cr isotope analyses by thermal ionization mass spectrometry

Abstract

By comparing data from an extensive set of Sr and Cr isotope measurements performed on two different thermal ionization mass spectrometers (TIMS), using three sets of Faraday cups with different usage histories, we assess the effects of Faraday cup deterioration on high-precision isotope measurements by TIMS. We find that dynamic 84Sr/86Sr and 87Sr/86Sr measurements provide stable and reproducible results over the entire 56 months of this study, regardless of which set of Faraday cups is used. By contrast, static 84Sr/86Sr and 87Sr/86Sr measurements lead to deviant results, drifts over time, and in general exhibit larger scatter. For the most part, these differences can be attributed to changing Faraday cup efficiencies. For the instruments of this study we find that the center cup is most affected, consistent with this cup often receiving the highest ion beam intensities during measurements conducted in our laboratory. For Cr isotopes, we find that the correlation between mass fractionation-corrected 53Cr/52Cr and 54Cr/52Cr ratios observed for static measurements in several prior studies also reflects different Faraday cup efficiencies. Again, the changing efficiency of predominantly the center cup can account for the observed drift and correlation in 53Cr/52Cr and 54Cr/52Cr. Multi-static Cr isotope measurements reduce this drift, but still result in a residual correlation between the two ratios, suggesting this correlation in part also reflects unaccounted mass fractionation effects.

Graphical abstract: Effects of Faraday cup deterioration on Sr and Cr isotope analyses by thermal ionization mass spectrometry

Article information

Article type
Paper
Submitted
23 Apr 2024
Accepted
04 Jun 2024
First published
10 Jun 2024
This article is Open Access
Creative Commons BY license

J. Anal. At. Spectrom., 2024,39, 1910-1918

Effects of Faraday cup deterioration on Sr and Cr isotope analyses by thermal ionization mass spectrometry

J. M. Schneider and T. Kleine, J. Anal. At. Spectrom., 2024, 39, 1910 DOI: 10.1039/D4JA00153B

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