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  • Electronic Resource  (4)
  • 1955-1959  (4)
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  • Electronic Resource  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 23 (1957), S. 47-55 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The swelling and solution of elastic polymers, like the mixing of liquids, results in the formation of equilibrium systems. In the interaction of conventional glasses and liquids, however, quite different phenomena appear and cause nonequilibrium systems to form. The density of molecules in conventional glasses is similar t o that of tightly packed liquids, but the diffusion rates are very low. Such glasses sorb practically nothing at low vapor pressures. Sorption begins only when the vapor pressure and the concentration of sorbed liquid in the surface layer are sufficient to cause the glass to melt. It should be noted that in this case sorption shows a sharp rise and an equilibrium solution forms. The degree of tight packing of polymeric glasses varies considerably, decreasing with increasing molecular weight and rigidity of the chain molecules. This packing can be estimated by comparing the densities of the polymers with the volume of the molecular groups of which these polymers consist, the latter being obtained from x-ray data, or by comparing the density of the monomer with that of the polymer. Cellulose, which unlike tightly packed glucose sorbs water over the whole range of vapor pressures, is a typical example of a loosely packed polymer. The effect of the density of packing on the sorbing properties of glasses can be more clearly demonstrated by the sorption of ethylbenzene by polystyrenes of different molecular weights. Low molecular weight polystyrenes dissolve in ethylbenzene without any heat production and sorb ethylbenzene from the vapor at high pressures only. This process results in the formation of a solution. High molecular weight polystyrenes, however, dissolve in ethylbenzene, producing heat, and sorb ethylbenzene a t all vapor pressures. The loose packing of polymers is the result of the long relaxation times existent in glasses. When the deformation time of the polymer is less than the volume relaxation time, the polymer becomes porous. Thus both the sorbing properties and the heats of solution of polystyrene become more pronounced during orientation. The degree of tight packing again increases at heats close to the glass point. Thus polymeric glasses hold an intermediate position between liquids and hard porous sorbents, such as silica gel, in regard to their sorbing properties. Unlike hard sorbents, however, they are apt to change their structure not only under external influence but also in the process of sorption.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 30 (1958), S. 247-258 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In order to determine the structure and phase state of polymers and to define the spacing of molecular groups of atoms of which molecules of the substance under investigation consist, it is necessary to estimate the mutual distribution of macromolecules. The results of a number of investigations carried out by the electron microscope and by direct structural techniques make it possible to obtain such an estimation. In this work the formation of ordered structures in amorphous polymers has been found by investigating solutions of polymers with the electron microscope. The study of thin oriented films of polymers by the above method confirms the possibility of mutual distribution of amorphous polymer chains and of crystallizable polymer chains after destroying the crystals. In investigating thin films of crystallizable polymers by the x-ray and the electron diffraction techniques at temperatures above and below the crystallization temperatures, a high degree of ordering has been found for the amorphous state of these polymers, too. From the data obtained, the conclusion is to be drawn that a fair mutual ordering of chain molecules can arise even in the amorphous state of polymers. Crystallization of polymers is but the last step in the process of mutual ordering of chain molecules.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High polymers with a regular chain structure have been produced by polymerization of ethylene with complexes containing crystalline organolithium compounds and titanium tetrachloride in organic solvents. For this purpose RLi compounds have been prepared, R being methyl, ethyl, butryl, dodeeyl, tolyl, mesityl, naphthyl, benzyl, and other aliphatic and aromatic groups. The investigation of the polymerization has led to the elucidation of the influence of the nature of the organic radical bound with lithium on the properties of polythene formed. Thermomechanical data, infrared and X-ray spectra, as well as viscometric molecular weight determination, have shown all specimens of polyethylene to be highly crystalline and of a regular chain structure. The polymers obtained have mechanical properties characteristic of polyethylenes of this type but with elongations that strongly differ in polymers produced using organolithium complexes with different radicals at the lithium. With some specimen, elongation has been found to reach extremely high values. Some suggestions have been made as to the causes of influence of different organic radicals in RLi on the properties of polymers.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 39 (1959), S. 559-566 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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