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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 1789-1800 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: From the temperature dependence of integrated intensities and from line widths in high-resolution 1H-NMR spectra, the relaxation times T1 and T2 of protons in CH2 and CH3 groups of polyisobutylene in CCl4 solution have been determined. Although the relaxation time T1 of methylene protons is determined mainly by intragroup interactions, intergroup interactions of two methyl groups from each two consecutive monomer units were found to contribute considerably to T1 of methyl protons. The Structure and mobility of polyisobutylene (PIB) molecules in solution is discussed on the basis of the relaxation time data.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 1623-1632 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Association of syndiotactic (s) poly(methyl methacrylates) (PMMAs) in toluene, benzene, and acetonitrile has been studied by NMR spectroscopy, osmometry, and viscometry. It was found that in solutions of highly syndiotactic PMMA in toluene, most of the polymer exists in the associated state. Association takes place by means of stereospecific intermolecular and intramolecular interactions of long parallel syndiotactic sequences. The minimum length of syndiotactic sequences necessary for association of s-PMMA in toluene is 7-8 monomer units. Viscosity data indicate that in dilute solutions the associated structures appear as large formations which do not have the character of compact particles. The formation of the aggregates of PMMA is a relatively slow process. A model of the structure of the aggregates of s-PMMA in toluene is proposed. As compared with that in toluene, the tendency to aggregation in benzene and acetonitrile is negligible. Integral parameters currently used for the characterization of polymer-solvent interaction, like “good” or θ solvent, are not suitable for predicting the tendency of s-PMMA to aggregation. The formation of aggregates evidently has some connection with the effect of the solvent upon the conformational structure of syndiotactic sequences.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 617-635 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: From analysis of infrared spectra it was found that in syndiotactic (s) poly(methyl methacrylate) (PMMA) in solution, long s sequences contain an increased population of diads with a skeletal conformation tt (in the staggered approximation). Self-aggregation of s-PMMA in solution leads to a further increase of the fraction of long s sequences in the extended chain conformation, and to an ordering of easter groups. When solid s-PMMA is isolated from a solution in which it exists in the aggregated state, these characteristics are preserved in the solid. The polymer appears partially crystalline by x-ray scattering, and it exhibits fibrillar morphology under the electron microscope. Ordered structures of s-PMMA melt at temperatures about 150°C, while the presence of residual solvent decreases the temperature of melting. Solid s-PMMA obtained from solutions in which aggregation of the polymer does not take place, like s-PMMA which did not come into contact with solvent, contains a higher proportion of syndiotactic diads with a skeletal conformation tg; these samples are amorphous and morphologically structureless. Analogies between the structure of ordered s-PMMA and the structure of the PMMA stereocomplex are also discussed.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 5 (1967), S. 2013-2021 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the temperature dependence of infrared spectra of poly(vinyl chloride) samples prepared by different methods, the intensity of the band at 690 cm.1 (proportional to the number of isotactic diads in the sample), as well as that of the tacticity-independent C—H stretching band, was found to be independent of the crystallinity of the sample. These lines were therefore applied for the tacticity determination in poly(vinyl chloride), measured in the form of KBr pellets. The numerical tacticity value was obtained from the known values of absorbance coefficients of SCH and SHH type C—Cl stretching bands in solution, and from the shape of the spectrum.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 2753-2762 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The distribution of chlorine atoms in the chain of solution-chlorinated PVC (CPVC) composed of —CH2—CHCl— (1), —CHCl—CHCl— (2), and —CCl2—CHCl— (3) monomeric units is described by first-order Markoffian statistics based on the assumption that the chlorination mechanism is independent of tacticity. In this case, all the statistical parameters can be obtained from experimentally determined concentrations of CH2, CHCl and CCl2 units. Populations of the sequences (11) and (111) calculated from the statistical parameters agree with experimental values determined from infrared and 220 MHz NMR spectra. From infrared spectra, suspension-chlorinated CPVC contains blocks of intact PVC.
    Additional Material: 3 Ill.
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