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  • Articles  (1,152)
  • Analytical Chemistry and Spectroscopy  (1,024)
  • Physical Chemistry  (128)
  • Gas chromatography
  • Wiley-Blackwell  (1,152)
  • 1990-1994  (777)
  • 1975-1979  (375)
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  • Articles  (1,152)
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  • 1
    ISSN: 0049-8246
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: It was demonstrated that a total reflection x-ray fluorescence spectrometer, using monoenergetic synchrotron radiation as the primary x-ray source, is suitable to measure the concentration of transmutational elements in Cu and Fe metal matrices. In a typical irradiation of copper with 590 MeV protons or with spallation neutrons, where the damage dose is 0.4 dpa (displacement per atom), the calculated concentration of transmutational elements is Ni 25, Co 8 and Fe 8 μg g-1. The results show that the minimum detectable concentrations were lower than these values. The energy of the sychrotron radiation was set just below the K-edge energy of the matrix element, eliminating the large peak due to the matrix. As an example, in the case of a Cu (Z = 29) matrix, the minimum detectable concentration for Ni (Z = 28) was as low as 3 μg g-1. In order to check systematically the possible geometric arrangements of beam direction-reflector position-detector position, a new vacuum chamber was designed and tested. It provides all technical components for remote control of the adjustment procedure to align the reflector in total reflection geometry. Two ways of positioning the reflector in the beam, vertical to the plane of polarization and parallel to that plane, were investigated, to find the best excitation conditions and lowest limits of detection. A few pg corresponding to a concentration of ng g-1 of samples where the matrix can be easily removed as in aqueous or acidic solutions and 50 ng g-1 concentration of metals in a light matrix as in oil were found as detection limits.
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0935-6304
    Keywords: Capillary electrophoresis ; Run-to-run reproducibility ; Capillary thermostatting ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Run-to-run sample separation reproducibility has been compared on two commercial high performance capillary electrophoresis units which differ in the mode by which the capillary temperature is thermostatted. Three standard analytes, differing dramatically in molecular character and size, were used for the analysis: benzoic acid, a 14 amino acid peptide from human chorionic gonadotropin, and ribonuclease A represent, respectively, small stable organic molecules, small peptides with little or no secondary structure, and proteins with secondary structure. These standards were evaluated with regard to reproducibility of migration time, peak area, and peak height. The analyses, performed in buffers of optimum pH for the separations, demonstrated that the liquid and forced air convection thermostatted systems both performed extremely well. The reproducibility, as judged by the percent coefficient of variance (% CV) of replicate analyses, was generally found to be less than 1 % (migration time); the reproducibility decreased in the order migration time 〉 peak height 〉 peak area. Whereas the absolute % CV values for MTrel (migration relative to a standard) observed with the liquid thermostatted system were 2- to 4-fold lower than those observed with the forced air convection thermostatted system, there was little statistically significant difference between the two. As expected, the data indicated a reduction in reproducibility as the complexity of the analyte increased, perhaps as the result of an increased potential for wall interactions. Comparing separations in which low (≍1 watt/meter [W/m] of capillary) and high (〉5 W/m) Joule heat was generated by altering the sodium chloride content of the buffer revealed few statistically significant differences in the reproducibility obtained from the two systems. With these particular standard analytes and their respective buffer systems, there appears to be little difference between forced air convection and liquid thermostatting of the capillary.
    Additional Material: 3 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 231-239 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectrometric behaviour of four macroacyclic and five macrocyclic Schiff bases using two ionization methods (electron impact and fast atom bombardment) was studied in detail with the aid of mass-analysed ion kinetic energy (MIKE) spectrometry. It was possible to propose a common electron impact-induced decomposition pattern for the acyclic compounds, whereas for the cyclic compounds, analysed by fast atom bombardment, peculiar fragmentation routes occurred, which were strongly dependent on the macrocyclic structure and on the different side-chains.
    Additional Material: 2 Tab.
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  • 4
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The mass spectrometric behaviour of ten variously substituted mono- and bis-salicylaldimine derivatives has been studied by fast-atom bombardment and metastable-ion studies. In general, well detectable protonated molecules are present and fragmentation processes mainly related to aldimine chain cleavages are evidenced. Interesting cyclization reactions leading to particularly stable product ions are discussed.
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  • 5
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The keV Cs+ liquid secondary-ion mass spectrometry (LSIMS) and 252Cf-plasma desorption (PD) mass spectra of recombinant proteins in the 10-25 kDa mass range are compared. Both techniques showed comparable mass accuracy and sensitivity, and in the case of LSIMS, remarkably short analysis time. Analysis by the PD/nitrocellulose method demonstrated slightly higher sensitivity and relativity lower dependence on the salt and buffer content of the protein sample.
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 6 (1992), S. 741-746 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The mass spectrometric behaviour of four macrocyclic, one macrobicyclic and one macroacyclic Schiff bases, obtained by one-step multiple condensation reactions of 2,6-diformyl-4-methylpropane, 1,3-diamino- 2,2-dimethylpropene, 1,5-diamino-3-oxapentane or tris-(2-aminoethyl) amine under fast-atom bombardment conditions, was studied in detail with the aid of mass-analyzed ion kinetic energy spectrometry. The mass spectrometric behaviour of a mononuclear macrobicy La(III) complex is also described.
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  • 7
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectrometric behaviour of seven polydentate Schiff bases derived from the condensation of formyl or diformyl precursors (2,3-dihydroxy- or 2,5-dihydroxy-benzaldehyde, 3-metoxy- or 3-ethoxy-salicylaldehyde, 3-formyl-salicyclic acid, 4-methoxy- or 4-chloro-2,6-diformylphenol) with 2-aminomethylpyridine have been investigated by fast atom bombardment mass spectrometry and metastable ion studies.
    Additional Material: 2 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 8 (1976), S. 23-24 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 11 (1979), S. 175-185 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Relaxation rates for O2(1Σg+) by nonradiative pathways have been determined using the fast-flow technique. O2(1Σg+) is formed from O2(1Δg) by an energy pooling process. O2(1Δg) is generated by passing purified oxygen through a microwave discharge. Oxygen atoms are removed by distilling mercury vapor through the discharge zone. It has been observed that the wall loss rate for O2(1Σg+) decreases with increasing pressure of oxygen and thus appears to be diffusion controlled. Quenching rate constants for O2, N2, and He have been determined and found to be (1.5 ± 0.1) × 104, (1.0 ± 0.05) × 106 and (1.2 ± 0.1) × 105 l./mol·sec, respectively.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 25 (1993), S. 521-537 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A laser flash photolysis-long path absorption technique has been employed to study the kinetics of the reaction products as a function of temperature (248-346 K), pressure (16-800 torr), and buffer gas identity (N2, CF4). The reaction is found to be in the falloff regime between third and second-order over the entire range of conditions investigated. This is the first study where temperature-dependent measurements of k1(P, T) have been reported at pressures greater than 12 torr; hence, our results help constrain choices of k1(P, T) for use in models of lower stratospheric BrOx chemistry. Approximate falloff parameters in a convenient form for atmospheric modeling are derived. © 1993 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
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