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  • Articles  (3)
  • Polymer and Materials Science  (3)
  • 1995-1999  (3)
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  • Chemistry and Pharmacology  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 2013-2025 
    ISSN: 0887-624X
    Keywords: vacuum ultraviolet oxidation ; polyethylene ; polypropylene ; plasma-polymer interaction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The emission from low-pressure microwave plasmas in the vacuum-ultraviolet (VUV) region (λ 〈 200 nm) was investigated in order to use these plasmas as light sources for the study of the VUV photochemistry of polyethylene (PE) and polypropylene (PP) as part of the study of plasma-polymer interaction. These polymers, immersed in low-presure oxygen, were exposed to radiation with wavelengths down to 112 nm, the cut off of magnesium fluoride used as a window to separate the polymer specimen from the plasma light source. Total oxygen incorporation in the surface [O], and the formation of hydroxyl, carbonyl, and carboxyl groups were measured using XPS in combination with chemical derivatizations, particularly their dependence upon the radiation spectrum and the oxygen pressure around the sample. In most experiments the surface oxygen concentration [O] attained a constant value that appears to be related to the initial oxidation rate; this suggests a competition between oxygen incorporation and chain scission reactions, followed by the removal of volatile oxidation products. PE is usually oxidized to a higher level than PP, the latter appearing to be more susceptible to reaction with atomic oxygen than PE. A general initiation mechanism for the VUV experiments is proposed that allows us to explain the observed differences in behavior between PE and PP, and the results obtained under different irradiation conditions. The nature of oxidation products is in both cases very similar to what is observed after direct plasma treatment of the polymers. We conclude that short wavelength radiation contributes very appreciably to the observed surface modification effects during plasma treatment of PE and PP. © 1995 John Wiley & Sons, Inc.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1511-1516 
    ISSN: 0887-624X
    Keywords: poly(ethylene terephthalate) ; surface treatment ; VUV photochemistry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(ethylene terephthalate) was exposed to radiation from different kinds of low-pressure plasmas in an oxygen atmosphere. The lower wavelength limit of the spectrum investigated, λ = 112 nm, is the cut-off of magnesium fluoride used for separating the specimen chamber from the plasma light source. The total surface oxygen concentration, and the formation of hydroxyl, carbonyl, and carboxyl groups were evaluated from XPS measurements in combination with chemical derivatizations, and their dependences on the radiation spectrum and the oxygen pressure in the sample chamber have been investigated. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 59 (1996), S. 119-124 
    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: Thin polyethylene films cast on copper or gold were treated with low-pressure oxygen plasma. Changes in the chemical structure of these films were investigated by infrared spectroscopy using a reflection method in combination with chemical derivatization (CD) reactions. The potential of the CD is demonstrated for hydroxyl groups and carbonyl groups by the reaction with trifluoroacetic anhydride and hydrazine. The reaction conditions were varied to check for side reactions. The results of the derivatization are discussed in terms of secondary structures. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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