| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1201680 | Journal of Chromatography A | 2011 | 5 Pages |
The present paper describes an investigation directed toward the development of a rapid heart-cutting LC–GC method for the analysis of mineral oil saturated hydrocarbons contained in vegetable oils. The automated LC–GC experiments were carried out by using a system equipped with a syringe-type interface, capable of both heart-cutting and comprehensive (LC × GC) two-dimensional analysis. The first dimension separation was achieved on a 100 mm × 3 mm ID × 5 μm dp silica column, operated under isocratic conditions (hexane). A single 30-s cut, corresponding to a 175 μL volume, was transferred to a programmed temperature vaporizer. After the large volume injection, the target analytes were separated in a rapid manner (∼9 min) using a 15 m × 0.1 mm ID × 0.1 μm micro-bore GC capillary. The overall LC–GC run time enables the analysis of ca. 4 samples/hour. Quantification was performed by using external calibration, in the 1–200 mg/kg range. The method was validated in terms of linearity, precision, limits of detection and quantification, and accuracy. A series of commercial samples were subjected to analysis. Various degrees of contamination were found in all samples, in the 7.6–180.6 mg/kg range.
