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  • Polymer and Materials Science  (6)
  • 74.25.Fy
  • 1980-1984  (6)
Collection
Keywords
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    A new family of crystallizable polyelectrolyte complexes (1981)
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 2 (1981), S. 343-346 
    Details
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/marc.1981.030020505
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  • 2
    Electronic Resource
    Electronic Resource
    A fluorescence quenching study of interpolyelectrolyte reactions (1984)
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 5 (1984), S. 709-714 
    Details
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/marc.1984.030051102
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  • 3
    Electronic Resource
    Electronic Resource
    Mechanism of alternating copolymerization of methyl methacrylate with styrene in the presence of diethylaluminum chloride (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 619-638 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A kinetic study of the propagation mechanism of the alternating copolymerization of styrene (St) with methyl methacrylate (MMA) in the presence of a complexing agent (diethylaluminum chloride, DEAC) in bulk and in tetrachloroethylene solutions at a molar ratio DEAC/MMA = 0.5 has been carried out. It has been shown that the copolymerization is a chain radical process characterized by a short active-center lifetime, bimolecular termination, and high rate of chain transfer to the complexed MMA. A kinetic scheme has been proposed for the propagation mechanism of alternating copolymerization in the presence of a complexing agent not requiring independent measurements of the equilibrium constant of complexation. It has been found that spontaneous and UV-initiated copolymerizations in the system have different mechanisms of initiation and a common mechanism of propagation. The propagation proceeds by addition of single monomers as well as donor-acceptor complexes of the comonomers to the propagation radicals, with the first mechanism being predominant. Inclusion of the monomers in the complex leads to an increase of the St reactivity and to a decrease of the MMA reactivity in propagation to the corresponding macroradicals in comparison with the reactivity of the free monomers. A number of kinetic and statistical parameters of the propagation reaction have been calculated.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170200304
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  • 4
    Electronic Resource
    Electronic Resource
    Effect of sovents on radiation-induced ionic graft polymerization (1980)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 871-878 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The influence of various solvents on radiation-induced cationic (grafting of vinyl-n-butyl ether onto polyethylene) and anionic (grafting of 2-methyl-5-vinylpyridine onto polyethylene) graft polymerization was studied. This ionic grafting was performed in thoroughly dried systems at room temperature. It was established that electron-acceptor solvents promote cationic grafting but that electron-donor solvents promote the anionic. A clear correlation between the donor number of solvents and grafting value by the anionic mechanism was shown. There was no correlation between dielectric constants and grafting values. The reaction orders, according to monomer concentration by 2-methyl-5-vinylpyridine grafting in various solvents, were equal to approximately 1.5 and 2 for the radical and anionic mechanisms, respectively. The effect of solvents on radiation-induced ionic graft polymerization is discussed. The results of this study indicate the correct choice of solvents for radiation-induced ionic grafting.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1980.170180308
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  • 5
    Electronic Resource
    Electronic Resource
    Catalytic behaviour of metalcomplexes immobilized in functional polymeric carriers (1981)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 5 (1981), S. 121-154 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The general principles of construction of gel-immobilized catalyst systems (GICS) are reported as well as some peculiarities of the polymerization of ethylene and of the dimerization of ethylene and propylene in the presence of these systems.GICS consist of a transition metal complex and a specially designed polymeric support. Advantages offered by gel-immobilized catalyst systems are discussed with respect to homogeneous and microheterogeneous metal complex catalysts.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1981.020051981109
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  • 6
    Electronic Resource
    Electronic Resource
    A new class of complex water-soluble polyelectrolytes (1984)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 6 (1984), S. 259-276 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Water-soluble nonstoichiometric polyelectrolyte complexes (N-PEC) constitute a new class of polyelectrolytes. N-PEC are formed as a result of interaction between oppositely charged polyelectrolytes taken in non-equivalent rations and thus they are macromolecular compounds. An N-PEC particle can be represented as a macromolecule of a segmented block copolymer. The behaviour of the N-PEC in aqueous-salt media shows their polyelectrolyte nature, but in contrast to ordinary polyelectrolytes, they undergo considerable conformational changes. These transitions precede phase separations, which are unique and are accompanied by the phenomena of disproportionation. Using N-PEC as enzyme carriers it is possible to produce self-regulating systems with a feedback and also thermostable systems, which are the simplest models of a spore. The N-PEC formed by synthetic polyelectrolytes and some proteins, show a pronounced physiological activity and belong to the class of highly immunogenic antigens.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1984.020061984120
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