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  • 1980-1984  (4)
  • 1975-1979  (3)
  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 3469-3473 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 40 (1975), S. 0 
    ISSN: 1750-3841
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 40 (1975), S. 0 
    ISSN: 1750-3841
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft , Werkstoffwissenschaften, Fertigungsverfahren, Fertigung
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Applied physics 25 (1981), S. 1-6 
    ISSN: 1432-0630
    Schlagwort(e): 82.50
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Maschinenbau , Physik
    Notizen: Abstract The mechanism of isotope scrambling was studied for infrared multiphoton dissociation of trifluoromethane-h (CHF3) and-d (CDF3) mixtures by a CO2 TEA laser. The CO2 laser was tuned to the R(14) line of the 001–100 transition, where CDF3 absorbs the light selectively. Although the highly selective decomposition of CDF3 occurred at low partial pressures of CDF3, significant decomposition of CHF3 was also observed with increasing pressure of CDF3. The selectivity (s) was found to depend only on the pressure of CDF3, a resonant molecule, but not on that of CHF3, an off-resonant molecule. The mechanism involving the formation of two kinds of vibrationally excited molecules, unimolecular decomposition (rate constantk 2 ),V-V energy transfer (k 3b), and collisional deactivation leads to the simple relationship,s=1+(k 2 /k 3b)/[CDF3], which can explain qualitatively the observed results. The ratiok 2 /k 3b has values of 20–200 Torr, probably depending on experimental conditions.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    ISSN: 1432-0649
    Schlagwort(e): 82.50
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract Time-resolved infrared emission spectra in the wavelength region of 2–5 μm were measured for the CO2-laser-induced photolysis of trifluoromethane-d (CDF3) and its mixtures with trifluoromethane-h (CHF3). The reactant pressures were 0.1–20 Torr at room temperature; some collisions were expected to occur within the laser-pulse duration. The emissions due to vibrationally excited CDF 3 * (C-D stretching mode and probably combination mode) and DF* were observed at the same time for the irradiation of pure CDF3. DF* should be produced in the unimolecular decomposition of CDF 3 * . The dependences of the DF* emission on the experimental condition are explicable on the assumption that the collisional energy transfer followed by the decomposition of CDF3 plays an important role in the present IRMPD, besides its direct multiple-photon decomposition. The mixture of CDF3 and CHF3 showed the emissions due to HF* and CHF 3 * in addition to DF* and CDF 3 * . The ratio between the DF* and HF* emission intensities,I DF/I HF, was examined as a function of pressure. The pressure dependences were similar to those of the selectivity determined previously from the concentration changes of CDF3 and CHF3. The irradiation of mixtures with a long furation pulse (80 ns fwhm with a 2μs) resulted in a marked decrease inI DF/I HF.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Journal of optimization theory and applications 38 (1982), S. 191-205 
    ISSN: 1573-2878
    Schlagwort(e): Proper efficient solutions ; improper efficient solutions ; constraint qualification ; objective qualification ; polar cone
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Mathematik
    Notizen: Abstract The properness of the efficient solution of the optimal problem with multicriteria has been independently defined by Kuhn and Tucker, Geoffrion, and Klinger. A theorem of Geoffrion describes the relation between Geoffrion's and Kuhn and Tucker's properness. In this paper, the dual part of the theorem is given, and some geometric approach is applied to derive the optimal conditions of proper efficient solutions and improper efficient solutions.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 729-741 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Initial processes of radiation-induced cationic polymerization of styrene and α-methylstyrene have been studied by means of microsecond pulse radiolysis. For styrene, absorption bands caused by the monomer cation radical St+• appear at 630 and 350 nm in a mixture of isopentane and n-butyl chloride at about -165°C. In parallel with the decay of St+•, three absorption bands appear in the near-infrared (IR) region, and at 600 and 450 nm. The IR and 600 nm bands are assigned to the associated dimer cation radical St2+•, and the 450 nm band to the bonded dimer cation radical St-St+•. The kinetic behavior of these species shows that reaction of St+• with styrene monomer forms both St2+• and St-St+•. With the decay of St-St+•, another absorption band appears at 340 nm, and the lifetime of this band is relatively long. The 340 nm band may be due to carbonium ions of the growing polystyrene. For α-methylstyrene, the monomer cation radical (at 690 and 350 nm), the associated dimer cation radical (in the near-IR region and at 620 nm) and the bonded dimer cation radical (at 480 nm) behave in a manner similar to that of the corresponding styrene species. The absorption band caused by carbonium ions of growing poly(α-methylstyrene) appears at 340 nm.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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