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  • Physics  (59)
  • SOLAR PHYSICS
  • 1980-1984
  • 1970-1974  (60)
  • 1971  (60)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 829-839 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mobilities of polymer chain segments in mixtures of rubber and carbon black were investigated by nuclear magnetic resonance. Spin-spin relaxation time (T2) measurements on cis-polybutadiene and ethylene-propylene-diene rubber (EPDM) bound rubbers detected at least two relaxing regions: an immobile region and a relatively free region. The molecular motions in the relatively free region are still constrained compared to those of the pure gum.
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 385-406 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization from the melt of three sharp polyethylene fractions has been studied at 5 kbar. It has been shown that the thickness of so-called extended-chain lamellae is a function of time, temperature, and molecular weight. There is by no means just the fully extended molecular configuration present. Crystallization is qualitatively similar to that of chain-folded crystals at 1 bar, giving an optimum lamellar thickness which increases with time and decreasing supercooling. Fractional crystallization is widespread and is a major cause of disparate lamellar thickness. Isothermal thickening of lamellae during crystallization has been established directly. Morphological detail suggests further that layers can increase their thickness tenfold over their initial size.
    Additional Material: 14 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 2079-2083 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
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  • 4
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of aminolysis of 1,2;3,4-meso-erythritol dicarbonate and 1,2;3,4;5,6-mannitol, sorbitol, and dulcitol tricarbonates by n-butylamine in dimethylformamide solution was investigated. The dicarbonate and tricarbonates are considered respectively as models of dyads and triads in the poly(vinylene carbonate) chain. The theoretical kinetic curves for the dimer and the trimers were calculated by solution of kinetic equations and close agreement with experiment was obtained. A version of the Monte-Carlo method was developed to provide a model for the reaction process by a computer calculation including the neighboring group effect in enhancing reactivity. The theoretical curve for a trimer coincides with the experimental one. These results confirm the accelerating influence of the unreacted neighboring groups. For the polymeric chain the experimental and calculated curves deviate for conversions beyond 10%. This indicates an additional polymer effect, which is as yet unexplained.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 779-799 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extensive gel-permeation chromatography (GPC) results are presented which reveal in much more detail than hitherto the effects of fractionation during the crystallization of polyethylene from solution. It is suggested how these results may be used to assess the affects of fractionation on the production of single crystals. In addition the results are compared with the fractionation which would be expected assuming the crystals to be in equilibrium with the solution. It was found that the results can be explained very well on this basis. A discussion of this rather unexpected result is included.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1777-1791 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ozone has been used as a selective oxidizing agent for degrading polyethylene single crystals at room temperature in order to confirm and extend results on surface structure obtained by use of fuming nitric acid at temperatures above 60°C. The surfaces of the crystals were rendered highly accessible to the ozone gas by preparing the crystalline material in a highly expanded form; the solvent in which the crystals were suspended was removed by sublimation from the solid state. The extent and nature of the reaction were studied by measuring the increase in weight and in density, by direct chemical analyses, and by making use of infrared spectroscopy and gel-permeation chromatography. It was found that the surfaces of the crystals are attacked at room temperature by ozone, with resulting chain scission, and the broad features of the chemical reaction were established. Some folded chains are found to be as long as the original thickness of the crystal, and once folds have been cut, continuing reaction shortens the chains. In the early stages of the degradation, during which most of the weight increase takes place, the density of the crystals increases, and the magnitude of the increase is that expected from the increase in weight alone, i.e., assuming no increase in effective volume.
    Additional Material: 12 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 1807-1837 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Previous studies on selective degradation of polyethylene single crystals with fuming nitric acid have been extended, both by using acid of lower concentration which gave better control over the degradation, and by resorting to ozone as an oxidizing agent which among others enabled the degradation temperature to be conveniently lowered. The molecular weight distribution was followed by gel-permeation chromatography in the course of degradation. Complete consistency between these different methods has been established, modifying some of the previous conclusions reached by this method. The principal feature which emerges is that we have a distribution of fold lengths. The largest straight fold stems can stretch across nearly the entire layer defined by the low-angle x-ray period, while there is a continuous distribution of shorter folds terminating deeper down in the crystals. The limiting depth at which the number of terminating folds becomes negligible can be identified and quantitatively assessed. The method of analysis is described, and individual data are discussed in detail. This picture of a fold surface layer containing essentially adjacently reentrant folds of uneven length agrees with quite recent results on other related chain-folded systems (annealed crystals, short chains, bulk structures) obtained in these laboratories and thus appears to be of general validity. The consequences of the model for our picture on polymer crystals in particular on the nature of the “amorphous” component, are discussed.
    Additional Material: 17 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 363-368 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Average values for dispersion γsd and polar γsd contributions of the solid surface tension γs γsd + γsp for poly(methylene oxide) (PMO) and Na-treated polytetrafluoroethylene (PTFE) are determined by a new computational analysis of wettability data. PMO displays γsd equals; 21.8 ± 0.9 and γsp = 11.5 ± 1.5 dyn/cm while Na-treated PTFE displays γsd = 36.1 ± 3.0 and γsp = 14.5 ± 2.9 dyne/cm. These surfaces present the highest fractional surface polarity ps = γsp/γs = 0.29-0.35 yet encountered for organic polymers or oriented monolayers. These unusual surface tension properties are correlated with surface chemistry and adhesion phenomena.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 645-658 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Fourier transform method of Vonk and Kortleve for the analysis of small-angle x-ray diffraction (SAXRD) from semicrystalline polymers has been compared with a modified direct method, originally due to Tsvankin. SAXRD data for three melt-crystallized polyethylene samples have been analyzed in terms of the mean true periodicity, mean crystal length, and mean length of amorphous segments. The two methods of analysis yield substantially equivalent results for all three samples. Calibration curves for the Tsvankin analysis are tabulated, and the relative merits of the two methods of analysis are discussed. With either method, information about the diffracting structure may be deduced that is not available from a simple measurement of the position of the SAXRD maximum. In fact, direct application of the Bragg law to any but the sharpest maximum yields a spacing (the long period) that lacks direct physical significance.
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 747-754 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The electronic states localized at defects in a polyene chain with alternating bond lengths have been investigated in the Hückel approximation by direct computation on large rings. The defects considered include substitutional impurities and bond distortions. None of the cases treated seem likely to be thermally activated donor or acceptor centers, but several examples of deep or shallow traps for electrons in the conduction band are found.
    Additional Material: 4 Tab.
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