Simultaneous Compound-Specific Analysis of δS and δS in Organic Compounds by GC-MC-ICPMS Using Medium- and Low-Mass-Resolution Modes.

Compound-specific isotope analysis of sulfur (δS-CSIA) in organic compounds was established in the last decade employing gas chromatography connected to multiple-collector inductively coupled plasma mass spectrometry (GC-MC-ICPMS). However, δS-CSIA has not yet been reported so far. In this study, we present a method for the simultaneous determination of δS and δS in organic compounds by GC-MC-ICPMS applying medium- and also low-mass-resolution modes. The method was validated using the international isotope reference materials IAEA-S-1, IAEA-S-2, and IAEA-S-3. Overall analytical uncertainty including normalization and reproducibility for δS and δS was usually better than ±0.2 mUr (σ) for analytes containing at least 100 pmol of S. Further, it is demonstrated that, despite small isobaric interferences, results obtained at low mass resolution are indistinguishable from medium mass resolution offering the benefit of increased sensitivity and versatility of this method. Additionally, the method was applied for the δS and δS isotope analysis of industrially produced organic compounds to investigate potential mass-independent fractionation (MIF). The relation between δS and δS in these compounds followed a mass-dependent fractionation trend (MDF; ΔS ≤ ±0.2 mUr). Degradation of dimethyl disulfide by direct photolysis caused a small but significant MIF (ΔS = 0.55 ± 0.04 mUr, = 3), demonstrating sufficient sensitivity of the method for these types of studies.