Journal: Analytical and Bioanalytical Chemistry
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Springer
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Publications 1 - 10 of 117
- A new methodology for precise cadmium isotope analyses of seawaterItem type: Journal Article
Analytical and Bioanalytical ChemistryXue, Zichen; Rehkämper, Mark; Schönbächler, Maria; et al. (2012) - Size-related vaporisation and ionisation of laser-induced glass particles in the inductively coupled plasmaItem type: Journal Article
Analytical and Bioanalytical ChemistryKuhn, Hans Rudolf; Guillong, Marcel; Günther, Detlef (2004) - Critical assessment of the elemental composition of Corning archeological reference glasses by LA-ICP-MSItem type: Journal Article
Analytical and Bioanalytical ChemistryWagner, B.; Nowak, A.; Bulska, E.; et al. (2012)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. - Uptake and release kinetics of 22 polar organic chemicals in the Chemcatcher passive samplerItem type: Journal Article
Analytical and Bioanalytical ChemistryVermeirssen, Etiënne L. M.; Dietschweiler, Conrad; Escher, Beate I.; et al. (2013) - Solution to spectroscopy blog challengeItem type: Journal Article
Analytical and Bioanalytical ChemistryPretsch, Ernö; Zenobi, Renato (2009) - Microvolume trace environmental analysis using peak-focusing online solid-phase extraction–nano-liquid chromatography–high-resolution mass spectrometryItem type: Journal Article
Analytical and Bioanalytical ChemistryStravs, Michael A.; Mechelke, Jonas; Ferguson, P. Lee; et al. (2016)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. - Towards chemical analysis of nanostructures in biofilms II: tip-enhanced Raman spectroscopy of alginatesItem type: Journal Article
Analytical and Bioanalytical ChemistrySchmid, Thomas; Messmer, Andreas; Yeo, Boon-Siang; et al. (2008) - LC-MS/MS determination of potential endocrine disruptors of cortico signalling in rivers and wastewatersItem type: Journal Article
Analytical and Bioanalytical ChemistryAmmann, Adrian A.; Macikova, Petra; Groh, Ksenia J.; et al. (2014)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. - 2013 Bunsen–Kirchhoff Award for Analytical SpectroscopyItem type: Journal Article
Analytical and Bioanalytical ChemistryGünther, Detlef (2012) - Combined biological and chemical assessment of estrogenic activities in wastewater treatment plant effluentsItem type: Journal Article
Analytical and Bioanalytical ChemistryAerni, Hans-Rudolf; Kobler, Bernd; Rutishauser, Barbara V.; et al. (2004)
Publications 1 - 10 of 117