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  • Physics  (131)
  • 1980-1984  (79)
  • 1975-1979  (52)
  • 1935-1939
  • 1983  (79)
  • 1979  (52)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1153-1161 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To elucidate mechanisms in electroinitiated polymerization reactions a comparison was conducted between ultraviolet (UV) photoinitiation and electroinitiation of N-vinyl phthalimide with zinc chloride as a catalyst. Both methods give low yields of a complex polymer product. A detailed analysis, infrared (IR), gel permeation chromatography (GPC), elemental, and molecular weight, conducted on the polymeric products, indicated that phthalimide ring opening was occurring and that complex mixtures of poly(N-vinyl phthalimide) derivatives were formed. Both initiation methods gave comparable results, which further indicated mechanistic similarity between photo-and electroinitiation in these donor-acceptor charge transfer polymerizations.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1411-1418 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electroinitiated polymerizations of styrene, 2-vinylnaphthalene, and 9-vinylanthracene were compared in sulfolane and acetone solvents in the presence of ZnCl2. The relative orders of polymerization rates and polymerization efficiencies, in both solvents, were 9-vinylanthracene 〉 2-vinylnaphthalene 〉 styrene, with faster rates and higher efficiencies occurring in sulfolane. Data obtained from viscosity and gel permeation chromatography (GPC) studies indicate that the molecular weights of the polymers produced in these systems are extremely low, 〈5000. Chemical composition and infrared (IR) spectral data suggest that abnormal transfer reactions (possibly from solvent) may be occurring in the electroinitiated 9-vinylanthracene polymerizations. The polymerization mechanism appears to be cationic in these monomer-solvent systems with ZnCl2.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 569-581 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Resonance Raman spectroscopy has been used to measure the strain dependence of four high-frequency vibrational modes in a single crystal of toluene sulfonate diacetylene polymer. The 0.62-μm thick crystal was stretched elastically to 4% strain before fracture occurred. This was equivalent to an ultimate tensile strength of 2.0 × 109 N m-2. The strain dependence of the vibrational modes has been interpreted using a simple point mass and anharmonic spring constant model. A Fermi resonance was observed for two vibrational modes which are degenerate at 2.1% strain and a 1464 cm-1 frequency.
    Additional Material: 11 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 987-999 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The variety of wide-angle x-ray scattering (WAXS) patterns exhibited by nylon-6 fibers with different fabrication histories is rationalized using a model comprising three limiting structures, viz., an α, a γ, and a pleated α structure. The γ and pleated α structures both have a single broad reflection in the range 2θ = 19° -25°, but differ in their annealing behavior. At 205° (in vacuo), the pleated α structure converts to the normal α structure by removal of the pleats, without breaking any hydrogen bonds. The γ structure, however, remains unchanged under this annealing condition since it is necessary to break all the hydrogen bonding in the structure to convert it to the α form. Different fabrication routes produce fibers which resemble the three ideal structures to varying extents. Fibers extruded at low speeds (and hence low spinline tension) resemble a mixed conventional α/pleated α structure with only a small γ component. Increasing the take-up speed (and hence the spinline tension) of the as-spun fiber, or in-line drawing of the low orientation fiber (without prior storage), increases the γ content. If drawing of the low orientation fiber takes place after several hours storage (off-line drawing), a largely α structure is produced. The intensity of the 020 reflection in the γ structure is shown to be very dependent on the degree of crystalline orientation in the sample.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 537-551 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ion implantation of impurities into thin films of poly(p-phenylene sulfide) (PPS) is found to increase the conductivity of the material by up to 12 orders of magnitude. The increase is stable under exposure to ambient conditions, in contrast to the instability of the conductivity increases in PPS produced by chemical doping with AsF5. PPS films 0.1-0.2 μm thick are spin cast from solution onto interdigitated electrodes patterned on an oxidized silicon substrate. The room-temperature interelectrode resistance is measured as a function of implantation fluence. An estimate of film conductivity is obtained from this resistance with a simple model for the electrode and film geometry. A first experiment yielded similar conductivity increases for implantation of either arsenic or krypton. At a fluence of 1 × 1016cm-;2, which corresponds to an average impurity concentration of 2.5 × 1021cm-3, the conductivity reaches an apparently saturated value of 1.5 × 10-5 (Ω cm)-1. Infrared spectra of the films before and after implantation suggest that crosslinking may be present in the implanted films, and Auger studies show stoichiometric changes throughout the implanted layer. These results suggest that the observed conductivity changes are the result of molecular rearrangements produced by the implantation rather than the result of specific chemical doping. Specific chemical doping may, however, explain the results of a second experiment in which implantation of bromine resulted in substantially larger conductivities found to increase at an approximate linear rate from a value of 1.0 × 10-4 (Ω cm)-1 at a fluence of 1 × 1016 cm-2 to a value of 4.0 × 10-4 (Ω cm)-1 at a fluence of 3.16 × 1016 cm-2.
    Additional Material: 9 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1195-1203 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric methods have been employed to study the high-pressure behavior of a polyurethane elastomer (Solithane 113) in the vicinity of its α transition. The α-loss peak is shifted to higher temperatures and broadened somewhat with the application of hydrostatic pressure up to 6.4 kbars. The slope of Tα vs. P, or dTα/dP, obtained at low frequencies was found to be equal to dTg/dP obtained by a volumetric method. Moreover, it attained a nonzero limiting value at high pressures for each frequency tested (3 - 30,000 Hz) and the limiting value itself increased with increasing frequency from 10.5°C/kbar at 3 Hz to 18°C/kbar at 30,000 Hz. The activation enthalpy ΔH* was found to be nearly constant over the pressure range tested, but the activation volume ΔV* decreased with increasing pressure. The relation dTα/dP = T (ΔV*/ΔH*) was shown to hold for the elastomer.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 917-937 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Light scattering from concentrated solutions of cellulose acetate in acetone is discussed in terms of exponential correlation functions for refractive-index fluctuations. These are related to intermolecular aggregation. Light scattering, tensile creep and recovery, and hyperfiltration studies with films of cellulose acetate cast from acetone are discussed in terms of the state of aggregation in the films. It is concluded that intermolecular aggregates are probably small and imperfectly formed regions of microcrystallinity stable up to about 210°C, with the overall state one of near amorphous disorder.
    Additional Material: 13 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1325-1339 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Twinning in macroscopic single crystals of poly(TSHD) has been investigated using scanning electron microscopy. Two particular chain-axis rotation twins have been identified unambiguously. They have K1 twinning planes of (012) and (212). It is also thought that twins with K1 planes of (212) and (202) may possibly occur. The possible mechanisms of twinning in polymer crystals have been discussed and chain-axis rotation twinning in poly(TSHD) has been compared with a similar type of deformation that has been suggested to take place in polyethylene crystals.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 1355-1366 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The resonance Raman spectra of polymer chains in partially polymerized crystals of 1,6-di-p-toluenesulfonyloxy-2,4-hexadiyne are reported. The polymer chain distortion is deduced using the results obtained previously for fully polymerized samples under tensile strain. Changes in crystal lattice dimensions both parallel and lateral to the polymer chains are found to be important in interpreting the variations in frequency of the Raman-active vibrational modes. Further evidence is found for the resonant interaction of backbone and side-group vibrations reported previously. This interaction is affected by the lateral dimensional changes and is also sensitive to residual strain fields in the monomer crystals. It is not necessary in the interpretation of the Raman spectra to take any account of changes in polymer chain length during polymerization.
    Additional Material: 10 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1079-1090 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cellulose triacetate (CTA) forms cholesteric mesophases in trifluoroacetic acetic acid (TFA) and mixtures of TFA and CH2Cl2, 1,2-dichloroethane (1,2-DCE), and CHCl3. Cholesteric pitches and solution flow times indicate that the order of solvent powers is TFA-CH2Cl2 〉 TFA-1,2-DCE 〉 TFA 〉 TFA-CHCl3, which is the order of decreasing acidity of the solvent systems. With TFA-CH2Cl2 as solvent, the one-fourth power of the pitch varies inversely with the CTA concentration, and increases linearly with temperature. The pitch increases exponentially with time and increases faster the more acidic the solvent. In a magnetic field a cholesteric to nematic transition occurs. A minimum in solution viscosity occurs at 34% w/v of CH2Cl2 for solutions in TFA-CH2Cl2. The miscibility gap as a function of molecular weight depends on the solvent composition and is smaller the higher the acidity of the solvent. Agreement between the experimentally observed A and B points and the theoretical points is better for the Khokhlov and Semenov theory for semiflexible chains than for the original Flory theory or the Flory-Ronca modification.
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