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  • Articles: DFG German National Licenses  (3)
  • Chemistry  (3)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 23 (1979), S. 2279-2291 
    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: In poly(vinyl alcohol) and polyacrylamide films containing the corresponding polymer-Cu2+ complexes, the reason why the films may gain surface electrical semiconductivity as high as 10-3 Ω-1 when treated with acetone solution of iodine was investigated. Optical and scanning electron microscope observations indicated that the coagulated polymer-Cu2+ complexes favor the appearance of the high conductivity and that the state of coagulation depends on the anions of the copper salts used as well as two parameters, F1 ≡ [Cu2+]/[MU] and F2 ≡ [OH-]/[Cu2+], where [MU] is the molar concentration of monomeric units of the polymer and [OH-] is that of hydroxide ions added. The effectiveness of the anions in causing coagulation decreases in the order of SO42- 〉 Cl- 〉 NO3- ≈ Br-. The whitish substance that appears on the film surface after the iodine treatment gives x-ray Debye-Scherrer rings characteristic of γ-CuI. The γ-CuI surface layer adheres to the film rather firmly, at least in polyacrylamide, and is responsible for the conductivity. By controlling the state of coagulation of the complexes and hence the formation of the γ-CuI surface layer, we have produced films with anisotropic surface electrical semiconductivity, i.e., σ∥ ≈ 10-4 Ω-1 and σ∥/σ⊥ = 1 ˜ 103. Optical and ESR spectra are also obtained to understand the mechanism of γ-CuI formation and to clarify the optical properties of the films.
    Additional Material: 13 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 26 (1981), S. 1659-1674 
    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: We have studied whether photoconductivity is observed in polymer films containing the first transition metal complexes. Polymers investigated were poly(vinyl alcohol) (PVA), polyacrylamide, poly(acrylic acid), poly(vinyl pyrrolidone), and polyethylene glycol. Transition metal salts used were CrCl3, MnCl2, FeCl3, CoCl2, NiCl2, FeBr3, Fe(NO3)3, Fe2(SO4)3, and Fe(ClO4)3. Only in the PVA-FeCl3 film was relatively large photoconductivity due to the photoreduction of Fe3+ observed. ESR spectra indicate that an Fe3+ ion is chelated with two in-plane OH residues of PVA and coordinated with three Cl-ions on the meridian. UV irradiation causes an electron transfer from Cl- to Fe3+. The produced chlorine atom extracts an electron from the oxygen of a neighboring OH residue. The unpaired electron thus formed can move from one oxygen to another through hydrogen bonding. In other words, the photoconductivity is due to holes produced in the network of PVA hydrogen bonding by the reduction of Fe3+. Finally, we have tried to explain why the photoconductivity is observed only in the PVA-FeCl3 film.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 14 (1976), S. 407-408 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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