Quantification of chlorinated paraffins by chromatography coupled to high-resolution mass spectrometry – Part B: Influence of liquid chromatography separation.

The analysis of chlorinated paraffins (CPs) is today an analytical challenge. Indeed, it is still impractical to describe their real composition in terms of polychlorinated alkanes (PCAs) homologue groups, which dominate technical mixtures. The co-elution of PCA congeners generates interferences due to the competition phenomena which occur during the ionisation process as well as to the dependence of the ionisation sources on the PCA chemistry. Therefore, the aim of this study was to investigate the influence of chromatographic separation, by LC-ESI-HRMS coupling, on the PCA homologue group pattern and, eventually, on their determination in food samples from interlaboratory studies. For this, three different mobile phases and six LC chromatographic columns were studied in order to optimise the analysis of CP mixtures. The first results showed that the use of a MeOH/H 2 O mobile phase reveals more appropriately the higher chlorinated PCAs. However, using ACN/H 2 O led to less ion species, with almost exclusively [M + Cl]- adducts, formed using post-column dichloromethane addition. Regarding the choice of the stationary phases, Hypercarb column provided a completely different homologue group pattern from the other chromatographic columns, in relation with the stronger retention of PCAs. Among the other columns, the C30 column better highlighted the short-chain PCAs compared to the C18 column conventionally used. Because the regulations now concern short-chain CPs, the quantification of food samples was then carried out on the C30 column. The optimised LC-ESI-HRMS conditions using C30 column and MeOH/H 2 O solvent mixture led to a quantification of PCAs in samples from interlaboratory studies with satisfactory accuracy (|Z-score| ≤ 2) and precision (<15%). [Display omitted] • The mobile phase, in LC conditions, influences the detection of homologue groups. • The selectivity of the stationary phase influences the homologue group pattern. • A C30 column reveals more PCAs–C 10-13 compared to other columns. • Systematic bias in the quantification of ΣPCAs-C 10-13 and ΣPCAs-C 14-17 was observed. • LC- and GC-HRMS methods give complementary results for the detection range of PCAs. [ABSTRACT FROM AUTHOR]