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- 2010 (13) (entfernen)
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Schlagworte
- Active sampling (1)
- Bioaccumulation (1)
- Bioisomerization (1)
- Brominated flame retardant (1)
- Certification (1)
- Chiral separation (1)
- Diastereomers (1)
- Enantiomer fraction (1)
- Enantiomer-specific determination (1)
- Enantiomeric fraction (1)
Eingeladener Vortrag
- nein (2)
Time courses of HBCD levels and enantiomeric signatures in herring gull eggs from the German coast
(2010)
Time courses of HBCD levels and enantiomeric signatures in herring gull eggs from the German coast
(2010)
A number of currently recommended sampling techniques for the determination of hydrogen in contaminated groundwater were compared regarding the practical proficiency in field campaigns. Key characteristics of appropriate sampling procedures are reproducibility of results, robustness against varying field conditions such as hydrostatic pressure, aquifer flow, and biological activity. Laboratory set-ups were used to investigate the most promising techniques. Bubble stripping with gas sampling bulbs yielded reproducible recovery of hydrogen and methane which could be verified for groundwater sampled in two field campaigns. The methane content of the groundwater was confirmed by analysis of directly pumped samples thus supporting the trueness of the stripping results. Laboratory set-ups and field campaigns revealed that bubble stripping of hydrogen may be restricted to the type of used pump. Concentrations of dissolved hydrogen after bubble stripping with an electrically driven submersible pump were about one order of magnitude higher than those obtained from diffusion sampling. The gas chromatographic determination for hydrogen and methane requires manual injection of gas samples and detection by a pulsed discharge detector (PDD) and allows limits of quantification of 3 nM dissolved hydrogen and 1 µg L-1 dissolved methane in groundwater. The combined standard uncertainty of the bubble stripping and GC/PDD quantification of hydrogen in field samples was 7% at 7.8 nM and 18% for 78 nM.
Der Einsatz aktiver (Pumpprobennahme,
Schöpfprobennahme) und passiver (Diffusionsprobennahme)
Probennahmetechniken zur Gehaltsbestimmung von
LHKW sowie Ethen und Methan in Grundwasser wird aus
ordnungsbehördlicher Sicht hinsichtlich der Vergleichbarkeit
von Analysendaten untersucht. Am Beispiel einer Kontamination
mit Trichlorethen sowie 1,2-Dichlorethen und
Vinylchlorid kann deutlich gemacht werden, dass die Einsatzmöglichkeit
der passiven Probennahme durch unzureichende
Strömungsverhältnisse im Aquifer sowie biologische
Aktivität im Pegelrohr begrenzt ist. Der aktiven Probennahme
ist bei ungeklärten oder unzureichenden Strömungsverhältnissen
im Grundwasserleiter daher der Vorzug
zu geben. Das gaschromatographische Verfahren für Vinylchlorid
mittels Dampfraumtechnik wird um die Quantifizierung
von Methan und Ethen erweitert. Dabei werden für
die Bewertung von Altlasten relevante Bestimmungsgrenzen
von 0,1 µg/l (Vinylchlorid, Ethen) sowie 5 µg/l (Methan)
erreicht.
Aus der Validierung der Analysenmethode und den
Ergebnissen verschiedener Probennahmen werden Toleranzbereiche
für die Ergebnisse eines Grundwassermonitorings
abgeschätzt. Diese Streubreiten von Monitoring-
Ergebnissen sollten von Ingenieurbüros und zuständigen
Ordnungsbehörden bei der Bewertung der komplexen Abbauprozesse
eines LHKW-Grundwasserschadens beachtet
werden.
HBCD stereoisomer pattern in mirror carps following dietary exposure to pure Gamma-HBCD enantiomers
(2010)
HBCD ISOMERS: Degradation rates and hydroxylated Products from Microsome Incubation Experiments
(2010)
HBCD isomers: degradation rates and hydroxylated products from microsome incubation experiments
(2010)
An international intercomparison involving eight national metrology institutes (NMIs) was conducted to establish their current measurement capabilities for determining five selected congeners from the brominated flame retardant classes polybrominated diphenyl ethers and polybrominated biphenyls. A candidate reference material consisting of polypropylene fortified with technical mixtures of penta-, octa- and decabromo diphenyl ether and decabromo biphenyl, which was thoroughly assessed for material homogeneity and stability, was used as study material. The analytical procedures applied by the participants differed with regard to sample pre-treatment, extraction, clean-up, employed calibrants and type of calibration procedure as well as regarding analytical methods used for separation, identification and quantification of the flame retardant congeners (gas chromatography coupled to an electron capture detector (GC-ECD), gas chromatography-mass spectrometry in the electron ionisation mode (GC-EI-MS), gas chromatography-mass spectrometry in the electron capture negative ionisation mode (GC-ECNI-MS), and liquid chromatography-inductive coupled plasma-mass spectrometry (LC-ICP-MS)). The laboratory means agreed well with relative standard deviations of the mean of means of 1.9%, 4.8%, 5.5% and 5.4% for brominated diphenyl ether (BDE) 47, 183 and 209 and for the brominated biphenyl (BB) congener 209, respectively. For BDE 206, a relative standard deviation of 28.5% was obtained. For all five congeners, within-laboratory relative standard deviations of six measurements obtained under intermediate precision conditions were between 1% and 10%, and reported expanded measurements uncertainties typically ranged from 4% to 10% (8% to 14% for BDE 206). Furthermore, the results are in good agreement with those obtained in the characterization exercise for determining certified values for the flame retardant congeners in the same material. The results demonstrate the state-of-the-art measurement capabilities of NMIs for quantifying representative BDE congeners and BB 209 in a polymer. The outcome of this intercomparison (pilot study) in conjunction with possible improvements for employing exclusively calibrants with thoroughly assessed purity suggests that a key comparison aiming at underpinning calibration and measurement capability (CMC) claims of NMIs can be conducted.