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  • Polymer and Materials Science  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 517-523 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electropolymerization of cyanogen in acetonitrile containing an electrolyte yields a poly(cyanogen). Its structure involves an open-structured dimer derived from the heterocyclic anion C7N7- mixed with a sequence of nitrile-substituted, conjugated carbon-nitrogen bonds. Although this polymer is an insulating solid, pyrolysis in vacuo to 700°C leads to highly conducting carbon-nitrogen pyropolymers via crosslinking and nitrogen elimination. The 700° pyropolymer has a carbon-nitrogen ratio of 5:1, a room temperature conductivity of 1 Ω-1 cm-1, and an activation energy for conduction of ∼0.03 eV.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 52 (1994), S. 1203-1210 
    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: The synthesis of a series of graphite fiber-polyacrylamide composites was performed electrochemically in dilute sulfuric acid (0.125M)-acrylamide (2M) solution, 1 : 1 sulfuric acid (0.25M) : acetone-acrylamide (2M) solution, and 1 : 1 sulfuric acid (0.25M) : 2-propanol-acrylamide (2M) solution, respectively, using graphite fiber bundles as the working electrode. The graphite fiber-polyacrylamide composites, synthesized in a 1 : 1 2-propanol : sulfuric acid-acrylamide solution, were more easily characterized than those synthesized from the sulfuric acid-acrylamide solution that contained no alcohol. Composites that were synthesized in a dilute sulfuric acid solution were, however, more readily crosslinked. (Fourier transform infrared spectroscopy, FTIR, confirmed the formation of inter-chain and intrachain imide functional groups after the resin was cured at ≈ 200°C.) Polymer weight gain analysis, coupled with surface morphology studies using scanning electron microscopy, showed that the thickness of the coatings, and hence the volume fraction of the resin in the composites, varied linearly with the time of electropolymerization. Scanning electron microscopy revealed an open and folded chain surface structure, which permitted unrestricted permeation of the monomer onto the electrode surface. Differential scanning calorimetry of the electropolymerized resins confirmed a glass transition temperature of between 180 and 207°C. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 107-117 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of anionic initiators with cyanogen was investigated by ultraviolet, visible, and infrared spectroscopy. It is argued that the reaction proceeds via formation of an analog of the heterocyclic anion C7N7- previously known from the reaction of KCN with (CN)2. The analytical results and spectra of the final black product were indicative of the possible formation of open-structured C7N7- dimers. A molecular model of the dimer suggests why the polymerization might terminate at the dimer stage. The pyrolysis of the cyclic acid HC7N7 was studied with the aim of determining the structure and mechanism of the formation of the resulting black product. It is suggested that this thermally induced polymerization reaction probably proceeds via formation of azomethine-type intermolecular crosslinks and may serve as a model for the investigation of the mechanism of nitrile polymerization in pyrolyzed acrylonitrile polymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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