Determination of organochlorine compounds in fatty matrices: Application of normal-phase LC clean-up coupled on-line to GC/ECD
✍ Scribed by van der Hoff, G. René ;Baumamn, Robert A. ;van Zoonen, Piet ;Brinkman, Udo A. Th.
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 502 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0935-6304
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✦ Synopsis
Abstract
Off‐line normal‐phase LC has been used for the clean‐up of compounds in our laboratory for several years. On‐line coupling of this LC system, which typically yields 12 ml fractions, is not possible due to its large fraction volume. The maximum transfer volume in on‐line LC‐GC/ECD is approx. 300 μl. Therefore down‐scaling of the LC system was attempted in order to reach these low fraction volumes. Miniaturization resulted in a 240 μ1 LC fraction containing the analytes of interest, which is transferred to GC/ECD via an on‐column interface. Sensitivity requires that a minimum amount equivalent to 1–2 mg of sample should reach the GC detector; the selectivity is determined by the separation between the matrix and the last eluting target analyte.
For the analysis of fatty samples, limitations were observed in the separation of dieldrin from triglycerides. Other organochlorine compounds, e.g. polychlorobiphenyls (PCBs), the DDT group, HCB and the HCHs can be analyzed with RSDs of 2–4 % (n = 10) at concentration levels of sub‐μ/kg in milk fat using a 3 μm Hypersil silica 50 × 1.0 mm i.d. LC column.