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  • Electronic Resource  (5)
  • 1995-1999  (3)
  • 1980-1984  (2)
  • Polymer and Materials Science  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 1307-1311 
    ISSN: 0887-6266
    Keywords: polymer surfaces ; polymer films ; polymer blends ; phase separation ; polystyrene-polybutadiene ; neutron reflectometry ; ion beam profiling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 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 B: Polymer Physics 34 (1996), S. 901-908 
    ISSN: 0887-6266
    Keywords: hydrogen atom ejection ; radical-pair formation ; computer modelling of in ; n-hydrocarbons and high density polyethylene (HDPE) ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydrogen atom ejection and subsequent radical pair formation have been modeled in a simple atomistic study employing a BIOSYM amorphous polyethylene macrocell. Mean radical pair distances have been obtained for various maximum hydrogen displacement vibrational cone angles (φ) in the model. φ angles extrapolated from these data, which correspond to experimentally determined mean radical pair distances of Dubinskii et al. (ca. 5.6 Å) and Iwasaki et al. (ca. 5.75 Å), are found to be close to φ angles calculated from hydrogen atom ejection theory. The Dubinskii et al. mean is thought to be the best determination, because the associated model φ angle (ca. φ = 15°) is the closest to φ* angles calculated for excited states of methane. The simple computer model thus supports the mechanism of radical pair formation in solid n-hydrocarbons and polyethylenes. In corroborating the theory for radical pair formation, the theory for polyene crosslinking termination reactions in amorphous polyethylenes irradiated in the presence of acetylene is also supported, because the mechanism requires the prior formation of radical pairs that are separated by distances of the order of those found by Dubinskii et al. The model is transferable to the study of radical-pair reactions in solid n-hydrocarbons irrespective of branching and density variations. A distribution function of radical pair distances from this model, which corresponds to the Dubinskii et al. experimentally determined mean distance, is given for amorphous HDPE. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 39 (1996), S. 271-271 
    ISSN: 0959-8103
    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
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 315-321 
    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: Fibers of poly(1,4-phenylene-1,3,4-oxadiazole) have been prepared by dry jet-wet spinning sulfuric acid solutions of the polymer. Polymer was prepared by polymerizing terephthalic acid and hydrazine dihydrochloride in 30% fuming sulfuric acid and directly spinning the resulting solution. Dry jet-wet spinning allows greater flexibility in conditions than does wet spinning in that spinneret temperature and coagulation bath temperature are independent of one another. Therefore, coagulation may be at temperatures well below those needed at the spinneret to maintain a flowing, extrudable solution. Another common advantage of dry jet-wet spinning is application of draw to the extruded fiber before coagulation, but in this system, drawing the fiber before coagulation was shown to be a disadvantage. Fiber properties were maximized by spinning with a spinneret temperature of 58-73°C into a coagulation bath at 3-4°C and with an air gap of 1/4 in. Water as a coagulation medium allowed operation at speeds up to 40 m/min, while with 50% sulfuric acid less than half that speed was reached. Application of draw ratios of 3/1 on the coagulated but still swollen fiber combined with high-temperature treatments at low draw ratios (1.05/l) gave maximum fiber properties-tenacity 6 g/denier, elongation 20-25%, and modulus 200-240 g/denier.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 15 (1981), S. 889-902 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Numerous studies have been carried out on drug-polymer sustained release systems designed for implantation. The majority of these efforts have been directed toward determining the in-vitro rate of drug release from specific systems or drug polymer combinations and the in-vivo studies have attempted to utilize analysis of the blood serum and excretory products as a measure of the release rate and behavior. To gain a better understanding of the influence of the local tissue environment and implant site on release behavior, we have investigated the release behavior of a gentamicin-silicone rubber system implanted in canines. Particular attention has been directed toward investigating the role that the fibrous capsule which eventually surrounds the implant plays in determining the rate and pattern of drug release. The drug burst effect was decreased by the use of a drug-free silicone rubber membrane on the gentamicin-silicone rod implant. Analysis for gentamicin in the tissue adjacent to the implant for periods up to four weeks indicated that the release rate was retarded by the development of the fibrous capsule. The temporal and spatial variations in gentamicin levels in the tissue surrounding the rod implants were determined. In addition, the influence of implant coating and gentamicin loading level in the implant on local tissue concentrations with time were also investigated. These studies provide evidence that the fibrous capsule surrounding a drug-polymer sustained release implant may influence the release behavior of the drug in an avantageous or disadvantageous manner depending upon the desired function of the sustained release system.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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