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  • Chemistry  (3)
  • Tafel plot
  • 1980-1984  (3)
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Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 4471-4476 
    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: This paper further illustrates the applicability of multiple internal reflectance infrared spectroscopy to the analysis of near-surface photooxidation. The results are compared with transmission infrared spectra to evaluate compositional gradients resulting from photooxidation and the influence of oxygen diffusion. The sample was a solvent-cast film of atactic, narrow distribution polystyrene, Mw of 100,000, that had been drawn to a ratio of 3.0 at 110°C by solid state coextrusion. Irradiation of these thin films, ∼25μm thickness, was performed on exposure to air at 35°C for periods of up to 6 h using a mercury source emitting at 254 nm. On photooxidation, a board peak appears at 3200-3500 cm-1, attributable to hydroperoxide formation. The most dramatic increase in the infrared spectra is found for a carbonyl band at 1730 cm-1. It appears to result from an aromatic acid group since it is shifted to 1660 cm-1 on immersion of the oxidized polystyrene films in aqueous ammonium hydroxide. It is confirmed that the photooxidation of polystyrene occurs preferentially at the surface and that this reaction rate is greatly reduced in the drawn polystyrene film.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 20 (1982), S. 61-67 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: No Abstract
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 15 (1984), S. 300-307 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Raman and infrared spectra of the 7-cis, 9-cis, 11-cis, 9-cis, 13-cis and 11-cis, 13-cis isomers of retinal have been recorded for the first time. The spectra of the all-trans, 9-cis, 11-cis and 13-cis isomers were also recorded for comparison. The isomers were isolated from a photoisomerization mixture of the all-trans isomer and their configurations were identified by means of 1H NMR or Raman spectroscopy. The Raman spectra of the isomers in CCl4 solution were recorded using a flow method, the 457.9 nm line of an Ar+ laser and a Raman spectrometer equipped with a multichannel detector; their infrared spectra were recorded by using an FT-IR spectrophotometer. Comparison of the Raman spectra of the mono-cis isomers revealed key bands which, discriminate between unmethylated-cis (7-cis and 11-cis) and methylated-cis (9-cis and 13-cis) configurations. The key bands were related to local vibrations around the particular cis double bond. Unmethylated-cis configurations show (1) a unique band around 1280-1270 cm-1 due to a coupled mode of A1 type (with reference to the local symmetry C2ν of the cis-C—CH=CH—C group) consisting of the two C—H in-plane bendings and the C=C stretching, (2) a stronger band at 969 cm-1 ascribable to an A2-type coupled mode consisting of the two C—H out-of-plane waggings and the C=C torsion and (3) a unique band at 563 cm-1, tentatively related to an A-type coupled mode consisting of the C—C=C and C=C—C deformations. Methylated-cis configurations show a stronger Raman band around 880 cm-1 due to C—Me stretchings. Raman bands characteristic of each cis configuration (7-cis, 9-cis, 11-cis or 13-cis) also are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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