Abstract

Thirteen commercially available silicate reference materials (RM) and one in‐house reference material, eleven of which have no previously published values, were analysed for nitrogen mass fraction and isotopic ratios with an Elemental Analyser (EA), and a Sealed Tube Combustion line, coupled to a continuous flow isotope ratio mass spectrometer (IRMS). These materials ranged from < 10 μg g−1 to 1% m/m nitrogen mass fractions and δ15N of −0.5 to +19.8‰. Existing nitrogen RM BHVO‐2, MS#5 and SGR‐1b were used to assess the accuracy of the data from the sealed tube combustion line, which was found to be in good agreement with existing published values. In contrast, the EA‐IRMS failed to fully liberate nitrogen from all silicate rocks and minerals (achieving a mean of 44 ± 10% nitrogen yield) resulting in kinetic fractionation of isotope values by −1.4‰ on average. Therefore, sealed tube combustion is better suited for analyses of silicate‐bound nitrogen. The EA worked reliably for organic samples, but care should be taken when using the EA for silicate nitrogen research. Moving forward, it is recommended that BHVO‐2, Biotite‐Fe, FK‐N and UB‐N be used as quality control materials as they appear to be most reproducible in terms of nitrogen mass fraction (relative error < 10%, 1s), and isotopic composition (< 0.6‰, 1s).

Highlights

  • Moving forward, it is recommended that BHVO-2, Biotite-Fe, FK-N and UB-N be used as quality control materials as they appear to be most reproducible in terms of nitrogen mass fraction, and isotopic composition (< 0.6‰, 1s)

  • The Elemental Analyser (EA) method is unsuitable for the quantification of nitrogen mass fractions and isotopic values for silicate samples where nitrogen is lattice-bound

  • Inaccuracies in the EA method have previously been highlighted for Precambrian sedimentary rocks and for BHVO-2 (Brauer and Hahne 2005, Ader et al 2006, Johnson et al 2017, Feng et al 2018)

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Summary

Introduction

Thirteen commercially available silicate reference materials (RM) and one in-house reference material, eleven of which have no previously published values, were analysed for nitrogen mass fraction and isotopic ratios with an Elemental Analyser (EA), and a Sealed Tube Combustion line, coupled to a continuous flow isotope ratio mass spectrometer (IRMS). These materials ranged from < 10 μg g-1 to 1% m/m nitrogen mass fractions and δ15N of -0.5 to +19.8‰. Moving forward, it is recommended that BHVO-2, Biotite-Fe, FK-N and UB-N be used as quality control materials as they appear to be most reproducible in terms of nitrogen mass fraction (relative error < 10%, 1s), and isotopic composition (< 0.6‰, 1s)

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