Journal: Analytical and Bioanalytical Chemistry

Loading...

Abbreviation

Publisher

Springer

Journal Volumes

ISSN

1618-2650
1618-2642

Description

Search Results

Publications 1 - 10 of 117
  • Xue, Zichen; Rehkämper, Mark; Schönbächler, Maria; et al. (2012)
    Analytical and Bioanalytical Chemistry
  • Kuhn, Hans Rudolf; Guillong, Marcel; Günther, Detlef (2004)
    Analytical and Bioanalytical Chemistry
  • Wagner, B.; Nowak, A.; Bulska, E.; et al. (2012)
    Analytical and Bioanalytical Chemistry
    Corning archeological reference glasses A, B, C, and D have been made to simulate different historic technologies of glass production and are used as standards in historic glass investigations. In this work, nanoseconds (193, 266 nm) and femtosecond (800 nm) laser ablation were used to study the elemental composition of Corning glasses using laser ablation inductively coupled plasma mass spectrometry. The determined concentrations of 26 oxides (Li2O, B2O3, Na2O, MgO, Al2O3, SiO2, P2O5, K2O, CaO, TiO2, V2O5, Cr2O3, MnO, Fe2O3, CoO, NiO, CuO, ZnO, Rb2O, SrO, ZrO2, SnO2, Sb2O5, BaO, PbO, Bi2O3) are compared with values reported in the literature. Results show variable discrepancies between the data, with the largest differences found for Cr2O3 in Corning A; Li2O, B2O3, and Cr2O3 in Corning B; and MnO, Sb2O5, Cr2O3, and Bi2O3 in Corning C. The best agreement between the measured and literature values was found for Corning D. However, even for this reference, glass re-evaluation of the data was necessary and new values for PbO, BaO, and Bi2O3 are proposed.
  • Vermeirssen, Etiënne L. M.; Dietschweiler, Conrad; Escher, Beate I.; et al. (2013)
    Analytical and Bioanalytical Chemistry
  • Solution to spectroscopy blog challenge
    Item type: Journal Article
    Pretsch, Ernö; Zenobi, Renato (2009)
    Analytical and Bioanalytical Chemistry
  • Stravs, Michael A.; Mechelke, Jonas; Ferguson, P. Lee; et al. (2016)
    Analytical and Bioanalytical Chemistry
    Online solid-phase extraction was combined with nano-liquid chromatography coupled to high-resolution mass spectrometry (HRMS) for the analysis of micropollutants in environmental samples from small volumes. The method was validated in surface water, Microcystis aeruginosa cell lysate, and spent Microcystis growth medium. For 41 analytes, quantification limits of 0.1–28 ng/L (surface water) and 0.1–32 ng/L (growth medium) were obtained from only 88 μL of sample. In cell lysate, quantification limits ranged from 0.1–143 ng/L or 0.33–476 ng/g dry weight from a sample of 88 μL, or 26 μg dry weight, respectively. The method matches the sensitivity of established online and offline solid-phase extraction–liquid chromatography–mass spectrometry methods but requires only a fraction of the sample used by those techniques, and is among the first applications of nano-LC-MS for environmental analysis. The method was applied to the determination of bioconcentration in Microcystis aeruginosa in a laboratory experiment, and the benefit of coupling to HRMS was demonstrated in a transformation product screening.
  • Schmid, Thomas; Messmer, Andreas; Yeo, Boon-Siang; et al. (2008)
    Analytical and Bioanalytical Chemistry
  • Ammann, Adrian A.; Macikova, Petra; Groh, Ksenia J.; et al. (2014)
    Analytical and Bioanalytical Chemistry
    A targeted analytical method was established to determine a large number of chemicals known to interfere with the gluco- and mineralocorticoid signalling pathway. The analytes comprise 30 glucocorticoids and 9 mineralocorticoids. Ten out of these corticosteroids were primary metabolites. Additionally, 14 nonsteroids were included. These analytes represent a broader range of possible adverse modes of action than previously reported. For the simultaneous determination of these structurally diverse compounds, a single-step multimode solid-phase extraction and pre-concentration was applied. Extracts were separated by a short linear HPLC gradient (20 min) on a core shell RP column (2.7 μm particle size) and compounds identified and quantified by LC-MS/MS. The method provided excellent retention time reproducibility and detection limits in the low nanograms per litre range. Untreated hospital wastewater, wastewater treatment plant influent, treated effluent and river waters were analysed to demonstrate the applicability of the method. The results show that not all compounds were sufficiently eliminated by the wastewater treatment, resulting in the presence of several steroids (∼20 ng/L) and nonsteroids in the final effluent, some of them at high concentrations up to 200 ng/L. Most of the detected mono-hydroxylated steroidal transformation products were found at significantly higher concentrations than their parent compounds. We therefore recommend to include these potentially bioactive metabolites in environmental toxicity assessment.
  • Günther, Detlef (2012)
    Analytical and Bioanalytical Chemistry
  • Aerni, Hans-Rudolf; Kobler, Bernd; Rutishauser, Barbara V.; et al. (2004)
    Analytical and Bioanalytical Chemistry
Publications 1 - 10 of 117