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  • Polymer and Materials Science  (46)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 62-65 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A highly biaxially oriented isotactic polypropylene was obtained by stretching and rolling repeatedly. In such treatment, it was confirmed by x-ray examination that the 010 spacing was oriented parallel to the plane of rolling.
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 2 (1959), S. 66-70 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Crystallization and orientation of isotactic polypropylene film by stretching were investigated. The specimen used was a film of thickness 0.03 mm. and had ca. 30% crystallinity in the initial state. It was observed both by x-ray examination and measurement of density that the crystallization of the stretched film increased proportionally to the stretching ratio. And it was confirmed that a quasi-crystalline structure was already developed in the low stretching ratio coexisting with the ordinary stable crystalline structures. This quasi-crystal structure can be easily transformed into the ordinary stable state at above 100°C., as well as the quasi-crystal structure in melt spinning filament, as described in a previous paper. It was also confirmed that the ordinary stable crystalline part was biaxially oriented by high stretching at room temperature, that is, (110) plane of the crystallite was preferentially oriented perpendicular to the surface plane of the film in the cross section perpendicular to the stretching axis. This phenomenon was elucidated from both the cohesive interactions between lattice planes and the compressive stress in the stretching process.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 20 (1956), S. 567-577 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The ion exchange equilibrium constants were obtained by measurements of infrared spectra of the ion exchange resin phase, using carboxymethylcellulose film (degree of etherification 0.66) as ion exchanger. The apparent constants are calculated by the following equation: \documentclass{article}\pagestyle{empty}\begin{document}$${\rm p} K_a = r_{\rm B} \log {\rm \varepsilon }_{\rm A} \log k\varepsilon _{\rm B} - (r_{\rm B} - r_{\rm A} ){\rm }\log {\rm }(\varepsilon _{\rm A} + k\varepsilon _{\rm B} ) + r_{\rm A} \log B^{ + r_{\rm B} } - r_{\rm B} \log A^{ + r_{\rm A} } + \log {\rm }(\gamma _{\rm B}^{r_{\rm A} } /\gamma _{\rm A}^{r_{\rm B} } )$$\end{document} where A and B are the concentrations of the two exchangeable cations, respectively, rA is the valence of the A ion, γA is the activity coefficient of the A ion in the electrolyte solution, ∊A is absorption intensity of carbonyl band of the carboxy radical having the A ion in an exchanger, and k is a constant. The dependence of the apparent equilibrium constants on pH and the ionic concentration in the electrolyte was investigated in the Na-H, K-H, NH4-H, Ca-H, and Sr-H exchange systems. Further, the activity coefficients of the exchangeable ions in the resin phase were evaluated in both the uniunivalent and unidivalent exchange systems. It is concluded that the abnormal behavior of the coefficients in the resin phase would be explained by the interaction energy between the ion pairs in the resin phase, independent of the concentration of the electrolyte solutions, in the range of comparatively dilute electrolyte solutions.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 45 (1960), S. 469-473 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of methacrylonitrile induced by ionizing radiation was investigated in bulk in the temperature range of 40 to -196°C. It was found from this investigation that two different polymerization mechanisms can exist in the polymerization under the same conditions at different temperature regions. The two different polymerization phenomena at room and at low temperature regions proceed by two different mechanisms: ionic and radical. It was found that the apparent activation energy in bulk polymerization is 6.3 kcal./mole in the 40 to -10°C. range and ca. 0.3 kcal./mole for polymerization initiated by high energy radiation in the -40 to -196°C. range. The effects of additives in the polymerization at both temperature regions were investigated. The viscosity of the polymer was measured in acetone solution at 25°C. and the infrared spectrum of the polymer was also measured. The authors believe from these experiments that the polymerization at room temperature proceeds by a radical mechanism and that the polymerization in the solid state at low temperature proceeds by an ionic mechanism. An important possibility was emphasized that a stereoregular ionic polymerization would be possible even in solid state of monomer by ionizing radiation.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 27 (1958), S. 596-597 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 459-465 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of acrylonitrile induced by ionizing radiation was investigated in bulk in the temperature range 15 to -196°C. It was found from this investigation that two different mechanisms could exist in the polymerization under the same conditions in different temperature regions. The two polymerization phenomena at room and at very low temperatures were studied from the point of view of radical and ionic polymerization mechanisms. It has been well known that the polymerization at room temperature proceeds by radical mechanism. In the solid state polymerization at very low temperatures the following results were obtained: first, the activation energy is very low, i.e., ca. 0.4 kcal./mole; second, an induction period was not observed under various conditions; third, the monomer containing a radical scavenger was easily polymerized. The authors believe that the facts described above indicate that polymerization in the solid state should proceed by an ionic mechanism.
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 2307-2318 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In a radiation-induced emulsion copolymerization of tetrafluoroethylene with propylene, the effects of pressure and temperature were investigated in the range of 0-40 kg/cm2 and 7-53°C at emulsifier concentration of 0.5 and 2.0%. Both the polymerization rate and the molecular weight of copolymer increase with increasing pressure and decreasing temperature. These facts are mainly due to an increase of the monomer concentration in the polymer particles. The rate of polymer chain formation was found to be independent of pressure and temperature. The initiation reaction is due mainly to the entry of radicals generated in the aqueous phase into the polymer particles. The apparent activation energy is -2.0 to -3.8 kcal/mole for the polymerization in the presence of 0.5% emulsifier, but is nearly zero at an emulsifier concentration of 2.0%. This difference in apparent activation energies at emulsifier concentrations of 0.5 and 2.0% is explained in terms of the termination mechanisms.
    Additional Material: 12 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 1789-1793 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Copolymerization of methyl trifluoroacrylate (MTFA) with ethylene in bulk was induced by γ irradiation. The copolymerization was observed to proceed in the liquid monomer mixture of MTFA and ethylene at 25°C with the dose rates ranging from 5.0 × 104 to 1.0 × 106 rad/hr. A wide range of the initial monomer composition gives an almost equimolar and alternating copolymer. The highest polymerization rate was observed at the equimolar monomer composition. The dose rate exponent of the polymerization rate is unity. The reactivity ratios of r1 (MTFA) and r2 (ethylene) were determined to be 0.034 and 0.14, respectively.
    Additional Material: 6 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 1325-1337 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Radiation-induced terpolymerizations of methyl α,β,β-trifluoroacrylate (MTFA) with tetrafluoroethylene (TFE) and α-olefins, such as ethylene, propylene, and isobutylene, were carried out in bulk at 25°C for the purpose of controlling the content of ester group in the MTFA-α-olefin alternating copolymers. These monomers polymerized to form alternating terpolymers which contained 50 mole % α-olefin in a wide range of monomer composition. The content of MTFA, namely, the ester group in polymer, can be varied without destruction of the alternating structures between fluoroolefins (MTFA, TFE) and α-olefin by changing the MTFA/TFE ratio in the monomer mixture. The relative reactivities of MTFA and TFE in the terpolymerization were discussed according to kinetic treatments by free propagating and complex mechanisms. The relation between the MTFA/TFE ratio in the monomer mixture and that in terpolymer was explained favourbly by the complex mechanism. It was also concluded that the relative reactivity of MTFA is larger than that of TFE in the terpolymerizations.
    Additional Material: 12 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 12 (1974), S. 545-548 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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