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61.
K. Pretzl G. Ambrosini R. Arsenescu C. Baglin H. P. Beck K. Borer A. Bussière K. Elsener Ph. Gorodetzky J. P. Guillaud P. Hess S. Kabana R. Klingenberg G. Lehmann T. Lindén K. D. Lohmann R. Mommsen U. Moser K. Pretzl J. Schacher R. Spiwoks F. Stoffel J. Tuominiemi M. Weber 《Acta Physica Hungarica A》2001,14(1-4):297-308
Besides the dedicated search for strangelets NA52 measures light (anti)particle and (anti)nuclei production over a wide range of rapidity. Compared to previous runs the statistics has been increased in the 1998 run by more than one order of magnitude for negatively charged objects at different spectrometer rigidities. Together with previous data taking at a rigidity of ?20 GeV/c we obtained $10^6 \bar p, 10^3 \bar d$ and two $\overline {^3 He} $ without centrality requirements. We measured nuclei and antinuclei (p, d, $\bar p,\bar d$ ) near midrapidity covering an impact parameter range of b ~ 2–12 fm. Our results strongly indicate that nuclei and antinuclei are mainly produced via the coalescence mechanism. However, the centrality dependence of the antibaryon to baryon ratios shows that antibaryons are diminished due to annihilation and breakup reactions in the hadron dense environment. The volume of the particle source extracted from coalescence models agrees with results from pion interferometry for an expanding source. The chemical and thermal freeze-out of nuclei and antinuclei appear to coincide with each other and with the thermal freeze-out of hadrons. 相似文献
62.
Lehmann R Huber M Beck A Schindera T Rinkler T Houdali B Weigert C Häring HU Voelter W Schleicher ED 《Electrophoresis》2000,21(14):3010-3015
The aim of this study was to develop and evaluate a capillary zone electrophoretic (CE) procedure for the accurate quantification of the UDP-hexosamines as well as for the corresponding UDP-hexoses in samples from various biological origins. Testing different buffer conditions, voltages, capillary dimensions and temperatures, optimal results were achieved with a 90 mM borate buffer, pH 9.0, at 18 degrees C and 15.5 kV in an uncoated fused-silica capillary of 50 cm x 50 microm and a detection wavelength of lambda = 262 nm. The total procedure, i.e., including variations of the sample preparation, showed coefficients of variation for the peak areas between 4. 1% and 10.4% in mesangial cells (n = 7) and between 7.8 and 10.3% (n = 6) in leukocytes for the components of interest. To improve precision, an internal standard was used for calibration. The limit of detection for all compounds is an absolute amount of 180 fmol, sufficient for the precise analysis of UDP-sugars in a limited amount of biological samples, such as human leukocytes (obtained from a 10 mL blood sample), muscle biopsies (< or = 100 mg), and mesangial kidney cells (ca. 2.5 x 10(5) cells). This reproducible, quantitative analysis of all four UDP-sugars from various biomedically relevant origins by CZE is a definite improvement over the generally used high performance liquid chromatography (HPLC) procedures. The CZE method allows the study of the flux through the hexosamine pathway in diabetes mellitus and other diseases in a simple, quantitative and accurate way. 相似文献
63.
K. B. Lehmann 《Fresenius' Journal of Analytical Chemistry》1894,33(1):123-124
Ohne Zusammenfassung 相似文献
64.
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66.
A. Preiss A. Bauer H.-M. Berstermann S. Gerling R. Haas A. Joos A. Lehmann L. Schmalz K. Steinbach 《Journal of chromatography. A》2009,1216(25):4968-4975
An advanced HPLC-photodiode array detection method for the determination of 12 selected highly polar nitroaromatic compounds in ground water samples of ammunition waste sites has been developed and validated. After solid-phase extraction the limits of detection were in the range 0.1–0.5 μg/l. To prove the applicability of the method to other polar nitroaromatic compounds the retention time of another 32 polar compounds under the specified chromatographic conditions were determined and their UV spectra recorded. To review the method, interlaboratory comparisons were performed with a spiked and a real ground water sample. 相似文献
67.
Ohne Zusammenfassung 相似文献
68.
V. Lehmann 《Fresenius' Journal of Analytical Chemistry》1884,23(1):109
Ohne Zusammenfassung 相似文献
69.
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E. Rupp G. Siebler W. Brachmann F. Lehmann B. Lokau M. Berdau W. Schmitz und A. Noll 《Fresenius' Journal of Analytical Chemistry》1925,67(10):409-411
Ohne Zusammenfassung 相似文献