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  • Analytical Chemistry and Spectroscopy  (5)
  • 25.70.Gh  (3)
  • 1
    ISSN: 1434-601X
    Keywords: 23.20.Lv ; 25.70.Gh ; 27.60.+j
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Neutron deficient nuclei close to 100Snhave been investigated in-beam by γ-ray spectroscopic methods using the NORDBALL detector array. A beam of 270 MeV 58Niwas used to bombard a target of 54Fe.Reaction channel separation was achieved with a 4π charged particle multidetector setup together with a 1π neutron detector wall placed in the forward direction. Excited states of 102Inwere identified for the first time. The level scheme constructed from γ-γ-particle-coincidence and γ-γ-angular correlation analysis is presented. The structure of 102 In is discussed and compared to neighboring nuclei in the framework of the nuclear shell-model.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-601X
    Keywords: 23.20.Lv ; 25.70.Gh ; 27.60.+j
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Excited states of 108 Te were populated in the 54 Fe + 58 Ni (270 MeV) reaction using the NORDBALL detector array equipped with charged-particle and neutron detector systems for reaction channel separation. Gamma rays belonging to the neutron deficient nucleus 108 Te were identified for the first time. On the basis of γγ-coincidence and angular correlation relations a level scheme was constructed with tentative spin and parity assignments. The structure of the nucleus is discussed in the framework of systematics of heavier Te nuclei.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-601X
    Keywords: 23.20.Lv ; 25.70.Gh ; 27.60.+j
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Proton rich nuclei close to 100 Sn have been investigated inbeam using the NORDBALL detector array. A beam of 270 MeV58 Ni was used to bombard a 54 Fe target. Reaction channel separation was achieved with a 4π charged particle multi-detector set-up together with a 1π neutron detector wall placed in the forward direction. Gamma-ray transitions belonging to the 111 I nucleus were identified for the first time. A level scheme constructed from γ-γ-particle-coincidence analysis is proposed. The level structure is discussed within the framework of the shell model and the systematics of the heavier odd iodine nuclei.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The bands at 2485 and 940 cm-1 observed in the Raman spectra of 2,5-dimercapto-1,3,4-thiadiazole represent the hydrogen-bonded ν(SH) stretching and δ(C-SH) in-plane bending modes, respectively. A quantitative study of the hydrogen bonding was carried out using intensity measurements of the bands assigned to the hydrogen-bonded and the free δ(C-SH) in-plane deformations at 940 and 919 cm-1, respectively, as a function of temperature. The Fourier transform (FT) Raman spectra were recorded over the temperature range 303-403 K using an environmental chamber fitted into the FT Raman sample compartment. The equilibrium constants between the free and the hydrogen-bonded molecules were determined over this temperature range and the average enthalpy for hydrogen-bond formation was obtained (ΔH° = -3.35 ± 0.2 kJ mol-1).
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 475-483 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The application of Raman spectroscopy to polymers and polymerization processes is surveyed and the advent of recent advances in instrumental techniques to polymer analysis is highlighted. Some of the problems of the more widely-used infrared spectroscopic methods, for example in microstructural analysis of polydienes and copolymers, are discussed and the advantages of the Raman spectroscopic technique are explained. The use of near-infrared excitation and Fourier-transform Raman instrumentation for process monitoring and polymer composite studies is discussed. Raman microscopic and waveguide spectroscopic studies of small samples and polymer coatings on substrates are considered. Other applications are mentioned in the areas of polymer orientation, surface-enhanced Raman scattering, conducting polymers, biopolymers and time-resolved studies.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dissociation constants for an acetonitrile-zinc complex, (CH3CN)Zn2+, were measured in aqueous solutions containing zinc salts (40-80%, w/w) and acetonitrile by Raman spectroscopy. Quantitative measurements of the intensity of the free and complexed ν(CN) Raman bands at 2264 and 2320 cm-1, respectively, were used to determine the average enthalpy and entropy of the complex dissociation to free acetonitrile in the temperature range 293-343 K for a 70% (w/w) solution of zinc chloride (0.052 mol) in an aqueous solution containing acetonitrile (0.024 mol); δH° and δS° values of 8.4 ± 0.5 kJ mol-1, respectively, were determined.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 495-500 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The preparation and vibrational spectroscopic characterization of the hitherto unreported products of the copolymerization of 2,3-dimethylbutadiene and methyl methacrylate are presented. The polymers were prepared by free radical polymerization using α,α′-azobisisobutyronitrile as the initiator. Raman and Fourier transform infrared spectroscopic information on the 2,3-dimethylbutadiene-methyl methacrylate copolymer is presented for a range of copolymers differing in the 2,3-dimethylbutadiene to methyl methacrylate ratio. Quantitative information of the microstructure of the polymer and copolymer using the C=C stretching vibrations is provided by Raman spectroscopy. Evidence is presented for the splitting of the C=O stretching vibration, ascribed to aggregated syndiotactic and unaggregated syndio- and isotactic poly(methyl methacrylate) at 1734 and 1724 cm-1, respectively.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 435-441 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to use a Fourier transform (FT) Raman spectrometer as a detector with a gel permeation chromatograph which was otherwise configured in the usual way for the measurement of molar mass distribution in polymers. A low-volume flow cell was constructed and the detector response tested both off-line and, in a preliminary way, in-line with the chromatograph. The particular objective was to establish whether it would be possible to measure the microstructural variation in polybutadiene with polymer molecular weight during the chromatographic process. The detector sensitivity was assessed for a range of polybutadienes with different cis-1,4-, trans-1,4- and vinyl-1,2- contents using tetrahydrofuran as solvent and eluent. Data obtained using visible Raman (488.0 nm) excitation and near-infrared (1064 nm) excitation were compared. Although it has been established that the Raman spectrometer is one of the best instruments for the evaluation of the microstructure of polybutadiene when used in a conventional way, it lacks the necessary sensitivity to provide quantitative information on polydienes which elute from a chromatograph. However, there is no reason in principle why an FT-Raman spectrometer should not be used as a concentration detector and for the simultaneous more detailed analysis of polymer composition or micro-structure during the chromatographic process, provided that the scattering intensity of the solute is high relative to the eluent. The potential advantages and the observed problems of what appears to be a novel experiment with an FT-Raman instrument are discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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