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  • 2000-2004  (2)
  • Capillary electrophoresis  (1)
  • PACS. 36.40.Qv Stability and fragmentation of clusters – 34.70.+e Charge transfer  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 12 (2000), S. 27-32 
    ISSN: 1434-6079
    Keywords: PACS. 36.40.Qv Stability and fragmentation of clusters – 34.70.+e Charge transfer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: Electron multiplicity has been measured for collisions of O8+ and Ar8+ with C60 fullerene in coincidence with the number of electrons stabilized on the projectile. Measurements have been performed at the same velocity v=0.24 a.u. for both systems. The number of active electrons r is deduced from the number of stabilized electrons s and the number of ejected electrons n. The kinetic energy spectra of outgoing projectiles are different for collisions “outside” the C60 cage which show a narrow peak and collisions “inside” the C60 cage which show a broad shifted energy loss peak. The cross-sections for stabilization of s electrons have been measured versus r for each s value corresponding to peripheral collisions, i.e. s=1−4 for O8+ and s=1−7 for Ar8+. Their sum over s, the total cross-section , shows a similar behavior for Ar8+ and O8+ up to r=10. It gives a clear indication of identical multicapture processes for these two systems. The very different s number distribution is interpreted by the different relaxation modes of the multiply excited states of O(8− r )+ and Ar(8− r )+.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; UV detection ; organic acids ; background electrolyte optimization ; wine ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A simple technique is described for the routine capillary electrophoretic determination of organic acids in wine samples. Several aromatic and non-aromatic compounds, including phthalic acid, benzoic acid, sorbic acid, boric acid, and phosphate, were evaluated as background electrolytes in order to obtain the highest resolution and detection sensivity. Factors that affect capillary electrophoretic separation such as the concentration and pH of the background electrolyte (BGE), the concentration of the electroosmotic flow modifier (EOF), and methanol addition to the electrolyte were investigated systematically. Tartaric, malic, succinic, acetic, and lactic acids were determined simultaneously in approximately six minutes using an electrolyte containing 3 mM phosphate and 0.5 mM myristyltrimethylammonium bromide (MTAB) as electroosmotic flow modifier at pH 6.5. This method is quantitative, with recoveries in the 90-102% range and linear up to 50 mg L-1. The precision is better than 1% and the procedure shows the appropriate sensibility, with detection limits between 0.015 and 0.054 mg L-1. The proposed method was successfully employed for the determination of organic acids in wine samples by direct sample injection after appropriate dilution and filtration.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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