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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.
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)
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.
High-performance liquid chromatography tandem mass spectrometry (HPLC–MS/MS) was applied to sterospecifically quantify the content of α-, β-, and γ-hexabromocyclododecane (HBCD) in six fish species from the Norwegian Etnefjorden. A combination of a β-PM cyclodextrin and an achiral column enabled the paired chromatographic separation of the stereoisomers in the order (-)-α-, (+)-α-, (-)-β-, (+)-β-, (+)-γ- and, (-)-γ-HBCD. The limits of detection were in the range of 6–21 pg g-1 depending on the stereoisomer and the concentrations of α-, β-, and γ-HBCD in fillets ranged from <5.4 ng g-1 to 11.1 µg g-1 lipid weight. α-HBCD enantiomers were throughout dominating, and in most cases the accumulation of the respective first eluted enantiomers ((-)-α-, (-)-β- and (+)-γ-HBCD) was observed. Deviations from the racemic EF-value were considered to be significant if it was outside of the expanded uncertainty range for each of the racemic HBCD-ratios. The composition of HBCD isomers varied between the investigated fish species and the relative high values for the γ-HBCD concentrations for the bottom-dwellers flounder and thorny skate seems to echo the HBCD pattern of ocean sediments.
The resource-saving utilisation of recovered
waste wood is a matter of growing concern. In several
European countries, this utilisation is governed by regulations
and is dependent on the contents of certain trace
elements and organic compounds. Thus, for decisionmaking
with respect to waste wood management (recycling
or combustion), reliable analytical data are needed and, due
to their great economic and environmental impact, must be
assured by appropriate quality control. To support the
improvement in quality assurance in waste wood analysis,
for the first time, a wood reference material was certified
for its mass fractions of arsenic, cadmium, chromium,
copper, lead, mercury, and pentachlorophenol (PCP).
These analytes were selected because they represent typical
constituents of wood preservatives most widely used in the
past. Material preparation and testing of homogeneity and
stability were carried out by BAM Federal Institute for
Materials Research and Testing. The certification measurements
were performed involving selected laboratories
with documented expertise in the field of waste wood
analysis. The certified values and their corresponding
uncertainties were assigned in full compliance with the
requirements of ISO Guide 35. The certified mass fractions
and their expanded uncertainties (k/i> = 2) are as follows:
(3.1 ± 0.5) mg/kg for As, (3.02 ± 0.24) mg/kg for Cd,
(36.4 ± 2.6) mg/kg for Cr, (22.9 ± 1.7) mg/kg for Cu,
(0.60 ± 0.14) mg/kg for Hg, (39 ± 4) mg/kg for Pb, and
(7.9 ± 0.6) mg/kg for PCP. The certified material is
available as European Reference Material ERM®-CD100.