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  • Physics  (140)
  • LUNAR AND PLANETARY EXPLORATION
  • 1970-1974  (140)
  • 1972  (140)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 191-192 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 10 (1972), S. 2125-2134 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The validity of Silberberg's hypothesis concerning the conformation of branched polypeptides was tested by studies on solutions and on monolayers. The poly(α-amino acids) investigated consisted of poly-L-lysine backbones with side chains of poly(gamma;-benzyl L-gutamate) and poly(β-benzyl L-aspartate). In solution, the conformation was studied in the mixed solvent chloroform-dichloroacetic acid. Optical rotatory dispersion measurements demonstrated the existence of a helix-coil transition which is a function of the length of the side chain. A significant “transition curve” appeared between 9 and 15 residues. From the results, it may be assumed that the poly-L-lysine backbone is extended in a coiled conformation and the side chains are coiled or helical, depending on the number of glutamate residues. At the air-water interface, a discontinuity in the surface-pressure curve appears between 9 and 15 residues per side chain. The similarity with the results obtained in solution appears significant; however, this has to be confirmed with methods more specific for structural modifications.
    Additional Material: 6 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. 1023-1028 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The adsorption behavior on silica of some polystrenes of moderate molecular weight distribution, both singly and in mixtures, has been examined. The adsorption isotherms indicate that, in both a good solvent (trichloroethylene) and under theta conditions, the species of higher molecular weight is preferentially adsorbed at or near full surface coverage, but that the smaller adsorbate has an improved opportunity for adsorption at low surface coverage. The use of tritiated adsorbates substantiate the isotherm data in cyclohexane solution.
    Additional Material: 4 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. 1285-1296 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: As part of a study of chemical and physical changes accompanying the formation of carbons by the pyrolysis of polymers, conventional electron microscopy, electron diffraction, and scanning electron microscopy techniques have been used to examine structural and morphological features of polyacrylonitrile (PAN) crystals, powder, and fibers, and of Saran and poly(vinylidene chloride) (PVDC) powder. Changes accompanying the heating of these polymers in air and in nitrogen have been investigated. PAN crystals grown from propylene carbonate were similar to those obtained by Klement and Geil. When heated in air at 220°C they retained their morphology, and electron diffraction gave the same reflections as PAN. On further heating to 400°C in nitrogen the morphology was retained, but the diffraction was lost. Crystals treated in nitrogen alone at 200°C showed morphology similar to that of the polymer. PAN powders and fibers retained discernable external features of their morphology on heating to 800°C. These results are discussed with reference to changes which take place when poly(vinylidene chloride) and Saran are heated in the range 150-180°C, which results in the loss of one hydrogen chloride per monomer unit, and are subsequently carbonized at 800°C. The development of pore structure and the adsorptive properties of Saran carbons are also discussed.
    Additional Material: 13 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1337-1349 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two types of emulsion-grade polytetrafluoroethylene particles have been studied. We refer to these as ribbons and rods. The ribbons consist of very thin ribbons or lamellae folded upon themselves a number of times. In typical emulsion-grade material prepared at Allied Chemical, the unraveled ribbon measures about 3.25 μ in length, 0.25 μ in width, and 60Å in thickness. The folded ribbons, which form the particles, are about 0.5 μ long and 0.25 μ wide. Electron diffraction shows that the ribbons are single crystals with the chain axis parallel to the long axis of the ribbons thus forming extended chain crystals. This extended-chain packing is consistent with the observed cleavage or fibrillation of the ribbons and with the molecular weight. The rods are formed in low-yield polymerizations. Electron diffraction also shows that the rods are single crystals with the chain axis parallel to the long axis of the rods. Striations parallel to the long axis are believed to result from stacking of parallel segments. Considerable bending of the long axis of rods is observed.
    Additional Material: 11 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1321-1336 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transient photocurrents in poly(vinyl chloride) films are shown to be due to photo-injection of electrons from metallic cathodes. Most of the injected electrons are promptly trapped, but some drift across the sample to the anode under the influence of an external electric field. The mobility of these electrons, determined by transient photoconductivity techniques, is 4.7 ± 0.5 × 10-4 cm2/V-sec at 27°C, and rises to 3.4 ± 0.5 × 10-3 cm2/V-sec at 43°C, the measuring cell having been evacuated to a pressure of 10-6 torr at both temperatures. Diffusion of helium into the samples appears to decrease the electron, mobility. It is suggested that electron transport is correctly described by using an energy-band model for intramolecular motion and an activated hopping model for intermolecular transfer. Oscillations observed in the transient photocurrents in the frequency range 103-105 Hz are attributed to electron avalanche formation at the anode, with photosuccessors.
    Additional Material: 8 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. 1351-1359 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elongational viscosity of dilute polymer solutions must always be measured under nonsteady-state conditions. To predict the time dependence of this viscosity for a polymer solution in which a constant stretching rate is maintained, a simple model is considered in which the polymer molecules are represented by elastic dumbbells. The non-Hookean elastic force in the dumbbell is determined by the conformational entropy of the chain. Use is made of Peterlin's approximation which replaces the elastic force by a function of the root-mean-square end-to-end distance. Application to the transient state is straightforward; it can be extended to include the effect of “internal” chain viscosity by means of approximations that are similar to Peterlin's.
    Additional Material: 3 Ill.
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  • 8
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An investigation was made of the dynamic mechanical behavior in the rubberlike region of poly(n-butyl methacrylate) (PBuMA) and poly(n-butyl acrylate) (PBuA) networks lightly crosslinked with ethylene dimethacrylate to concentrations from 10-6 to 10-4 mole/cm3. The measurements were carried out by use of an apparatus for low-frequency forced vibrations working in the frequency range 2.5 × 10-4 to 1 Hz. With parameters c1 and c2 of the Williams-Landel-Ferry equation, obtained from data in the main transition region, the data did not reduce in the rubberlike region for the poly(butyl methacrylate) networks; the spread of the deviations decreases with increasing concentration of the crosslinking agent. Superposition could be achieved in all cases when a shift factor was used on the vertical axis. At sufficiently low reduced frequencies and at high temperatures the storage compliance decreases in both series of polymers with increasing concentration of the crosslinking agent as expected. At higher reduced frequencies and at higher temperatures of measurement, however, anomalous behavior was observed with uncrosslinked samples having a lower compliance than those crosslinked to a very low degree. This finding was explained as due to very long relaxation times of the untrapped entanglements present in the noncrosslinked polymer, which are absent in the same polymer crosslinked already to very low degrees. The retardation spectra of both PBuMA and PBuA exhibited secondary relaxation mechanisms which were shifted by four logarithmic decades toward higher retardation times in comparison with the primary retardation maximum.
    Additional Material: 8 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. 283-293 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The elastic behavior of composite and interpenetrating network structures composed of non-Gaussian chains is investigated. The chain probability density given by Nagai is employed utilizing only the leading correction terms for finite chain extensibility. The independent-network hypothesis, proven valid in Gaussian statistics, is shown to be erroneous in non-Gaussian systems. Further, it is found that composite networks composed of monodisperse chains are elastically isotropic, whereas a most probable contourlength distribution yields a large anisotropy but in the direction opposite to that observed experimentally for rubber. On the other hand, retention of the independent-network hypothesis coupled with a most probable distribution successfully accounts for much of the observed anisotropy. Interpenetrating networks are shown to be substantially anisotropic when a most probable contour-length distribution is employed.
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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. 369-373 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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