PARC an automated apparatus for clean-up procedures used in routine-analysis for PCDD/PCDF and related compounds

Dettmer, Katja; Stieglitz, L.

doi:10.1016/0045-6535(94)90344-1

Cited by 5 publications

(1 citation statement)

References 6 publications

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“…Unambiguous determination of 2,3,7,8-TCDD calls for high-resolution GC/MS, which requires extensive cleanup procedures. These often include liquid chromatography with combinations of several adsorbents such as modified silica gel, aluminum oxide, and activated carbon. − The two main cleanup objectives are to remove co-extracted organic matter from the analytical sample and to eliminate the interference of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and polychlorinated dibenzofurans (PDBFs). These sample preparation steps make the determination of 2,3,7,8-TCDD one of the most time-consuming and costly monitoring methods.…”

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Four-Way Data Coupled to Parallel Factor Model Applied to Environmental Analysis: Determination of 2,3,7,8-Tetrachloro-dibenzo-para-dioxin in Highly Contaminated Waters by Solid−Liquid Extraction Laser-Excited Time-Resolved Shpol'skii Spectroscopy

Goicoechea

Olivieri

et al. 2005

Anal. Chem.

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This article reports the first application of parallel factor analysis to high-order instrumental data generated from Shpol'skii matrixes at liquid helium temperature. Third-order data arrays-consisting of excitation modulated wavelength time matrixes-are collected with the aid of a cryogenic fiber-optic probe, a tunable dye laser, and a multichannel system for phosphorescence detection. The multidimensional data formats are applied to the analysis of 2,3,7,8-tetrachloro-dibenzo-para-dioxin in water samples. The experimental procedure is rapid and environmentally friendly. Complete sample analysis is accomplished in less than 15 min with only 100 muL of organic solvent (n-heptane). The feasibility to directly determine parts-per-trillion concentration levels of the target compound is demonstrated with heavily contaminated samples of unknown composition. The limits of detection, estimated from calibrations based on the univariate method and parallel factor analysis, are 0.060 and 0.092 ng.mL(-1), respectively; both referred to a 100 mL water sample.

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confidence: 99%