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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 25 (1986), S. 148-152 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 1451-1460 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pyrolysis of poly(tert-butyl N-vinylcarbamate) at 185-200°C in bulk yields a rigid foam containing cyclic urea units, primary amine units, and a small amount of urea crosslinks. The yield of primary amine units (ca. 13%) and the yields of carbon dioxide (ca. 57%), isobutylene (ca. 57%), and tert-butanol formed in this reaction indicate that it involves pairwise decomposition of adjacent carbamate units to form cyclic urea units, tert-butanol, carbon dioxide, and isobutylene. The vinyl amine units are formed from carbamate units that become flanked by urea units. The amounts of amine units and residual carbamate units were determined as a function of degree of pyrolysis by an ion-exchange technique and agreed with values expected for a random cyclization process. The pyrolyzed polymers are useful as ion-exchange resins and as rigid foams having good thermal stability.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0959-8103
    Keywords: macromonomers ; Macromers® ; styrene graft polymers ; vinyl chloride graft polymers ; 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: Polystyrene macromonomers terminated with methacrylate, vinyl ether, or maleic half ester functionalities were evaluated in free radical initiated copolymerizations with vinyl chloride in aqueous suspension polymerization. Macromers® (M1) terminated with methacrylate disappeared very rapidly in copolymerization with vinyl chloride (M2). The relative reactivity ratio, r2, was determined to be 0.05 in good agreement with literature values of about 0.04. Vinyl ether-terminated Macromers® had unexpectedly uniform reactivity with vinyl chloride in early conversion samples, but macromonomer conversion was incomplete. Macromers® having maleic half ester functionality were incorporated rapidly in vinyl chloride copolymerization at pH 2.5 (r2 = 0.13). However, at pH 10 these Macromers® had reduced reactivity (r2 = 0.34), which improved graft polymer uniformity. These Macromer® copolymerization relative reactivities are shown to be useful in predicting and controlling graft densities and graft polymer heterogeneity which influence morphology, processing, and mechanical properties.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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