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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 611-621 
    ISSN: 0887-6266
    Keywords: copper ; corrosion ; poly-N-vinylimidazole ; oxidation ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The degradation of poly-N-vinylimidazole films on copper substrates was studied by Fourier transform infrared spectroscopy and x-ray photoelectron spectroscopy. Infrared measurements on samples heated at 300°C for 15 minutes revealed that the oxidation of the polymer was accelerated by the copper. X-ray photoelectron spectroscopy showed that a layer of copper oxide was formed on top of the oxidized film. Copper ions were also detected within the polymer layer. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 15 (1981), S. 29-32 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 31P NMR spectra of the phenyl ester of dichlorophosphoric acid dissolved in Merck nematic phase IV have been recorded and analysed. The values of the dipole dipole couplings have been discussed in terms of several different geometric models. Non-planarity of C-1, O, P and the phenyl ring must be assumed in order to account for the results; a twist angle of 49° was found.
    Additional Material: 2 Ill.
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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: With the use of persulfate containing radioactive sulfur it is shown that the termination reaction of the polymerization of styrene is a coupling of the free radical chains. In the presence of m-dinitrobenzene as a retarder evidence has been presented that the termination reaction is a disproportionation and not a combination of two free radical chains. Mercaptan in the emulsion polymerization of styrene acts solely as a chain transfer agent. Any chemical reaction between persulfate and mercaptan does not contribute to the initiation. In the presence of detergent the rate of initiation of the polymerization of styrene is equal to the rate of thermal dissociation of persulfate: \documentclass{article}\pagestyle{empty}\begin{document}$ {\rm S}_2 {\rm O}_{\rm 8}^{ - - } \to 2{\rm SO}_4 ^ - . $\end{document} Thus, any reaction between persulfate with monomer and detergent does not contribute to the initiation. The much smaller rate of initiation in the absence of detergent is attributed to the slight solubility of styrene, the concentration of the monomer being so small that it cannot capture all the free radicals. The effect of the detergent is a physical one, by its solubilizing action it increases the solubility of the monomer in the water layer to such an extent that the “activator” now becomes 100% efficient.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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