This method uses a QuEChERS (quick, easy, cheap, effective, rugged, and safe) single-step acetonitrile (ACN) extraction and salting out liquid-liquid partitioning to extract PAHs from seafood tissue. Stir Bar Sorptive Extraction (SBSE) is then used as a combined cleanup and concentration step, eliminating organic acids and other polar and high molecular weight matrix components and providing a substantial concentration factor to easily meet regulatory limits of detection and requirements established for precision and accuracy for determination of PAHs in seafood tissue.

Direct injection for gas chromatographic profiling of alcoholic beverages is usually preferable, but where spirits and liquors contain appreciable amounts of non-volatile material, some mode of pre-treatment may be required to avoid both inlet and column contamination. This consideration applies in particular to products aged for extended periods in wooden barrels and especially products containing added sugar, as volatile artefacts from sugar decomposition in the hot injection port can also complicate the chromatogram.

USP <467> Residual Solvents [1] is a general chapter in the US Pharmacopeia that describes a headspace gas chromatographic method for the determination of residual solvents in pharmaceutical products, active ingredients, and excipients. As originally written, it described parameters used with balanced-pressure or pressure loop based headspace instruments. Recent updates [2] have included parameters for syringe based systems.

Accurate qualitative and quantitative analysis of perfumed or flavored products is essential to the flavor and fragrance industry. Especially when unknown samples need to be analyzed traditional methods of GC analysis often lead to only vague results and often require time consuming and cumbersome sample preparation techniques such as solvent extraction (liquid/liquid, Soxhlet, Likens-Nickerson).

A novel stir bar sorptive extraction (SBSE) procedure termed sequential SBSE was developed. Compared to conventional SBSE, sequential SBSE provides more uniform enrichment over the entire polarity/volatility range for organic pollutants at ultra-trace levels in water. Sequential SBSE consists of a SBSE performed sequentially on a 5-mL sample first without modifier using one stir bar, then on the same sample after addition of 30 % NaCl using a second stir bar.

Static (equilibrium) headspace sampling is commonly used for GC determination of volatiles in solid and liquid samples. Since this technique relies on the analyte partitioning between the sample and headspace and uses a fixed injection volume it may not provide adequate detection limits, particularly for higher molecular weight, higher boiling analytes, and for polar analytes in aqueous samples.

Fatty acids are of key importance to the food industry. Especially long chain polyunsaturated fatty acids (LC PUFA) are receiving more and more attention due to their positive influence on human health. LC PUFA refined from natural oils are frequently added to food products to gain a positive health effect. Since LC PUFA are rather unstable and prone to oxidation, the quality of oils and fats has to be controlled. Certain aldehydes, ketones and other compounds are markers for oil and fat quality. Some of these have unpleasant odors and/or tastes (e.g. fishy) which are not acceptable to consumers.

A method for characterization of airborne particles including the nanoparticles fraction with a diameter of 29-58 nm in roadside atmosphere has been described. The method consists of thermal extraction (TE) and comprehensive two-dimensional gas chromatography (GC x GC) with novel detection capabilities, including high resolution time-of-flight mass spectrometry (HRTOF-MS), and simultaneous selective and mass spectrometric detection with a nitrogen phosphorous detector (NPD) and a quadrupole mass spectrometer (qMS). Increased selectivity with the GC x GC - HRTOF-MS allows a group type separation of a selected chemical class, e.g.

Aflatoxins are metabolites from molds such as Aspergillus flavus and Aspergillus Parasiticus. Aflatoxins are classified as mycotoxins, they are among the most potent human carcinogens, found mainly in foods and feed of plant origin. High concentrations of aflatoxins have been found, for example, in pistachios, figs and cereals and aflatoxins have also been found in dairy products. Due to the high toxicity of aflatoxins, EU legislation specifies very low acceptable daily intakes and maximum residue limits (0.05-15 μg/kg).

Malachite green (MG) is a triphenyl methane dye that is highly efficient in battling fungi, bacteria and various single cell parasites. MG is traditionally used in aquaculture to treat and prevent fungal infections. MG, which is structurally related to known carcinogenic triphenylmethane dyes, is metabolized to leucomalachite green (LMG) and deposited in the fatty tissue of the fish. MG is under suspicion of being a human carcinogen and for causing damage to the human genetic material. Consumption of fish that is contaminated with MG is assumed to pose a significant health risk to humans.