Fast miniaturised sample preparation for the screening and comprehensive two-dimensional gas chromatographic determination of polychlorinated biphenyls in sludge.

Polychlorinated biphenyls (PCBs) in sludge are usually extracted by a technique such as Soxhlet with subsequent fractionation prior to long GC runs using GC-ECD or GC-HRMS. In this study, the extraction of selected chlorinated biphenyls (CBs) from a spiked sludge sample by three rapid techniques, i.e.

Miniaturised pressurised liquid extraction of chloroanilines from soil with subsequent analysis by large-volume injection-gas chromatography-mass spectrometry.

A number of chloroanilines were extracted from soil by means of miniaturised pressurised liquid extraction (PLE). The extraction procedure was optimised for both large-volume on-column (LV-OC) and programmed-temperature vaporisation (PTV) injections combined with GC-MS. Hexane was the only extraction solvent suited for LV-OC and hexane/acetone gave the best results when using a PTV.

Evaluation of modulators and electron-capture detectors for comprehensive two-dimensional GC of halogenated organic compounds.

Different cryogenic and a heated GC x GC modulator(s) were evaluated and compared for the analysis of high-boiling halogenated compounds. The cryogenic modulators investigated were: (i) the longitudinally modulated cryogenic system; (ii) the liquid-nitrogen-cooled jet modulator (KT2001); (iii) a dual-jet CO2 modulator (made in-house); (iv) a semi-rotating cryogenic modulator (made in-house) and (v) a CO2 loop modulator (KT2003); the heated modulator was the slotted heater system (sweeper). Each modulator was optimised with respect to analyte peak widths at half height in the second-dimension.

Role of the retaining precolumn in large-volume on-column injections of volatiles to gas chromatography.

In the present study the retaining precolumn, which is commonly used in a set-up for large-volume on-column injections, or when solid-phase extraction (SPE) or liquid chromatography is coupled to gas chromatography (CC), was removed after varying its length from the standard length of 3 m down to zero. A dramatic increase of the evaporation rate of the injected organic solvent was obtained from a typical value of 100 microl/min up to 300 microl/min. The increased evaporation rate allowed (i) injection of a larger volume in the same retention gap, (ii) faster injection/transfer of the organic solvent and (iii) reduction of the transfer temperature.

Current use of pressurised liquid extraction and subcritical water extraction in environmental analysis.

This review updates our knowledge about pressurised liquid extraction (PLE) and subcritical water extraction (SWE), two sample preparation techniques which are increasingly used for the extraction of moderately and non-volatile organic pollutants from a variety of solid and semi-solid environmental matrices. Parameters influencing the extraction yield and selectivity are discussed. The results deriving from the analysis of several different classes of compounds in a variety of matrices are compared with a reference method, e.