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  • GEOPHYSICS  (1,182)
  • Physics  (555)
  • Animals
  • 1980-1984
  • 1970-1974  (1,737)
  • 1972  (1,737)
Collection
Publisher
Years
  • 1980-1984
  • 1970-1974  (1,737)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1-9 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: It has been shown in this investigation that the permeation of propane and propylene through polyethylene membranes exhibit a generalized behavior in the vicinity of the condensation point of the penetrant. Correlations to evaluate the permeation flux are presented.
    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 10 (1972), S. 43-50 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Natural rubber crosslinked by dicumyl peroxide in amounts up to 25 parts per hundred of rubber (phr) showed a maximum in tensile strength near 1 phr, followed by a steep decrease to a minimum near 5 phr. The ultimate elongation decreased from 870% at 0.5 phr. to about 10% above 10 phr. The modulus increased linearly with increase of crosslinking. The creep rate decreased from 5.6% per decade at 0.5 phr to zero at 5 phr and higher values. Crystallization, with a resultant abrupt increase in creep, was noted in specimens held in the stretched condition for more than one day. Between 5 and 25 phr this system (when crystallization is avoided) appears to function as an ideal elastic network and can be recommended for studies of rubber elasticity since no variation of modulus with time is observed.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 151-157 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The problem of the segregation of subchains in an isolated molecule of an A-B block copolymer is closely related to that of the mutually excluded volume of two chemically differing macromolecules. Therefore, by resorting to the “segment cloud” model used by Flory and Krigbaum to calculate the excluded volume, it was possible to derive an expression for the number of contacts between the two blocks in the same molecule. From the results of the calculation it follows that only partial block segregation can be expected unless the condensation of one of the subcoils to a dense globule occurs, owing to the effect of a poor solvent quality.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 171-189 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The concentration dependence of the reduced viscosity of a number of polyelectrolytes was found to be adequately described by the equation \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm \eta }_{sp} /c = [{\rm \eta }]_\infty [1 + k/\sqrt c ] $\end{document} as long as the concentration is not too low. The parameter [η]∞ represents the intrinsic viscosity of the well-shielded polyion and corresponds to values of [η] determined in salt solutions and may possibly correspond to the theory of Harris and Rice on polyion expansion. Heuristic arguments based in part on the work of Katchalsky et al. lead to a definite expression for the parameter k in terms of molecular properties. This result shows that the above equation is valid only for strong polyelectrolytes with constant activity coefficients of counterion. The calculated values of k agree well with experiment except when specific intramolecular interactions (e.g., internal hydrogen bonding) occur. For highly charged polyions we find, surprisingly, that k depends only on the properties of the polymer backbone and not on electrical properties.
    Additional Material: 4 Ill.
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  • 5
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ten unfractionated poly(2,6-diphenyl-1,4-phenylene oxide) samples were examined by gel permeation chromatography (GPC) and intrinsic viscosity [η] at 50°C in benzene, by intrinsic viscosity at 25°C in chloroform, and by light scattering at 30°C in chloroform. The GPC column was calibrated with ten narrow-distribution polystyrenes and styrene monomer to yield a “universal” relation of log ([η]M) versus elution volume. GPC-average molecular weights, defined as M̄gpc = \documentclass{article}\pagestyle{empty}\begin{document}$\Sigma w_i [\eta ]_i M_i /\Sigma w_i [\eta ]_i$\end{document}, wi denoting the weight fraction of polymer of molecular weight Mi, were computed from the GPC and [η] data on the polyethers. The M̄GPC were then compared with the weight-average M̄w from light scattering. The intrinsic viscosity (dl/g) versus molecular weight relations for the unfractionated poly(2,6-diphenyl-1,4-phenylene oxides) determined over the molecular weight range 14,000 ≤ M̄w ≤ 1,145,000 are log [η] = -3.494 + 0.609 log M̄w (chloroform, 25°C) and log [η] = -3.705 + 0.638 log M̄w (benzene, 50°C). The M̄w(GPC)/M̄n(GPC) ratios for the polymers in the molecular weight range 14,000 ≤ M̄w ≤ 123,000 approximate 1.5 according to computer integrations of the GPC curves with the use of the “universal” calibration and the measured log [η] versus log M̄w relation. The higher molecular weight polymers (326,000 ≤ M̄w ≤ 1,145,000) show slightly broadened distributions.
    Additional Material: 4 Ill.
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  • 6
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The crystallization and melting temperatures of an unfractionated poly(2,6-dimethyl 1,4-phenylene oxide) (PPO) sample, PM2, were determined at 0.25°C/min cooling and heating rates in five binary toluene - PM2 and fifteen ternary toluene - polystyrene - PM2 solutions. The total polymer weight fraction range studied was 0.12-0.40 and the PM2 weight fraction range was 0.026-0.40. The heat of fusion Hf of the PM2 was computed to be 10.1 cal/g from the melting point depressions. A toluene - PM2 pair interaction parameter χ13 = 0.890 - 223.5/T was found. Although a reliable polystyrene-PM2 interaction parameter could not be computed, the data are consistent with χ23 = 0. Setting χ23 = 0 we calculate the toluene - polystyrene interaction parameter to be χ12 = 0.495 - 15.46/T. This χ12 is in remarkable agreement with values reported in osmotic pressure studies.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 381-384 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 385-432 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anisotropic growth of β-form crystals of isotactic polypropylene in type III and type IV spherulites has made possible microanalysis of the unit cell structure, optical properties, and crystal arrangement within the spherulites. Micro x-ray studies of the type III and type IV spherulites show that interspherulitic β-form crystals have a hexagonal unit cell with dimensions; a = 19.08 Å and c = 6.49 Å. The intrinsic refractive indices of these β-form crystals are 1.506 along the a axis and 1.536 along the c axis. The organization of the crystals within the spherulites and the optical properties of the spherulites are also quantitatively evaluated. Both the type III and type IV spherulites have the a axis of the crystal radial while the crystals rotate randomly around the type III spherulite radii and periodically around the type IV spherulite radii. The radial refractive index for both the type III and type IV spherulites has the same value of 1.496. The tangential refractive index of the type III spherulite has a constant value of 1.509; it varies periodically between a minimum of 1.496 and a maximum of 1.519 in the type IV spherulite. Microtechniques such as micro x-ray diffraction, interference microscopy, birefringence, and optical microscopy were required for acquisition of the data.
    Additional Material: 21 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 541-548 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The tack of cis-polybutadiene was measured by means of a Skewis tackmeter, and the results, which showed considerable variability, could be represented by a double exponential cumulative distribution function of Gumbel. It was concluded that there exists a linear relationship between the applied forces (contact and break) and the time that these forces are applied in the tack test. The mechanism of tack is considered in terms of two distinct processes: (a) the development of a bond and (b) the strength of the bond thus formed. The latter is rationalized by applying Eyring's absolute rate theory. A simple equation is derived which predicts an inverse linear relation between the breaking time and breaking force, which is in agreement with the experiment. The theory also suggests that the area of actual interpenetration of polymer interfaces depends largely on the contact pressure, whereas the depth of penetration appears to depend to a similar degree on both contact pressure and contact time.
    Additional Material: 3 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 571-573 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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