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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 2129-2140 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of poly(p-phenylenes) with linear and branched oxyethylene side chains was synthesized. Microphase separation in the solid state causes polymers with linear side chains to form supramolecular structures, which consist of main chain layers separated by an amorphous side chain matrix. If mixed with lithium salts such as lithium triflate (LiOTf) or lithium bis(trifluoromethanesulfone)imide (LiNTf), the polymers form solid solutions. The experimental data suggest that the layered structures undergo a one-dimensional swelling in the direction perpendicular to the main chain layers when blended with LiOTf and that this salt is only incorporated into the side chain matrix. The observed melting point depression in polymer-LiNTf mixtures is explained by the assumption that the salt species are incorporated both into the side chain and the main chain microphase.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 735-744 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The phase separation of random copolymers during free radical copolymerization to high conversion was studied. In order to prepare in situ high impact thermoplastics during the copolymerization process, the attention was focussed on systems in which the more reactive comonomers form thermoplastics, whereas the less reactive components form elastomeric homopolymers. The studied systems (A, B) were (AN, EA), (AN, VA), (CHMA, MA) and (S, BA) (AN: acrylonitrile, EA: ethyl acrylate, VA: vinyl acetate, CHMA: cyclohexyl methacrylate, MA: methyl acrylate, S: styrene, BA: butyl acrylate). These copolymers display varying compositional heterogeneity depending on the different radical reactivity ratios and the feed composition used. Curves of instantaneous copolymer composition versus fractional conversion and the distribution functions of chemical composition were calculated for the various systems. In addition, miscibility diagrams of corresponding low conversion copolymers AxB1-x and AyB1-y, derived from the same monomer pair (A, B) but differing in composition, were recorded at high temperatures. Phase separation was detected by light microscopy and differential scanning calorimetry (DSC) using cast films. The onset of phase separation depending on the actual stage of copolymerization was recorded. The composition of the copolymers at the onset of phase separation was compared with the miscibility of low conversion copolymer blends. A satisfactory prediction of the start of phase separation during copolymerization is presented.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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