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  • Polymer and Materials Science  (5)
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 455-465 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dynamic mechanical properties of branched polyethylenes in the molten state were determined in the frequency range 10-3-10 radians/sec. The materials tested have remarkably similar rheological properties even though they vary greatly in molecular weight and molecular weight distribution. The similarity in properties is attributed to the influence of long chain branching on the relaxation spectra. A mechanistic argument is proposed to relate the observed behavior to molecular entanglement coupling. The concept of entanglement coupling involving long-chain branching leads to the expectation that the quasi-Newtonian and non-Newtonian viscosities of branched polymers may be either greater or less than those of linear polymers of the same species, which have comparable molecular weights. This is borne out by experiment.
    Additional Material: 8 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 18 (1974), S. 83-91 
    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: Viscoelastic properties of the BBL ladder polymer were determined by a dynamic mechanical technique for the temperature range -150°C to 250°C and at frequencies of 3.5, 11, and 110 Hz. A secondary loss dispersion centered at -50°C (at 110 Hz) was discovered which probably arises from an in-chain relaxation mechanism. The loss dispersion resembles β-transitions found in more conventional polymers in intensity (maximum tan δ = 0.035), activation energy( E = 19,000 cal/mole), and in its close relation to the high-temperature mechanical properties of the polymers. Only slight changes in the low-temperature loss peak cause significant increases in brittleness. It is proposed that such changes, produced by a variety of environments, result from random chain scission at imperfection points in the ladder structure. For this reason we conclude that improving the environmental stability of BBL is of prime importance in its further development for specific applications.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 19 (1975), S. 1193-1199 
    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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 10 (1976), S. 939-951 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Exturded filaments of unmodified polypropylene (PP) with and without antioxidant were implanted subcutaneously in hamsters in order to determine their rate of degradation. Specimens were removed periodically during a 5 month test period and analyzed by infrared spectroscopy and dynamic mechanical testing. The analyses show that degradation begins to occur after only a few days. Although the reaction sequence is not known, several factors suggest that the in vivo degradation process is similar to autoxidation which occurs in air or oxygen.The infrared data indicate that the hydroxyl content of the implants increases at a rate of 0.061 mg/g polypropylene per day during the initiation phase of the reaction. An induction time of 108 days was established. Carbonyl bonds appear after an implantation time of 50-90 days and increase thereafter. Mechanical tests indicate a decrease in the dynamic loss tangent, tan δ, during the first month of implantation for unmodified polypropylene. No change in the infrared spectra or tan δ was observed, however, for implants containing an antioxidant.Thus, it is apparent that polypropylene filaments implanted subcutaneously in hamsters degrade by an oxidation process which is retarded effectively by using an antioxidant. While the findings reported are specific to subcutaneous polypropylene implants, they suggest that degradation of other systems may involve similar processes. This notion suggests directions for further research on increasing the in vivo stability of synthetic polymers.Long-term effects of polymer implantation upon tissue were not studied in this work.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 2787-2806 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Semiconduction and electron spin resonance studies on a number of conjugated polymers representative of the polyacetylenes, the polybenzimidazoles, and the polyacene quinone radical polymers were made. Observed resistivities ranged from 270 to 1016 ohm-cm. at room temperature. These and the spin concentrations, the relaxation times, and the energies of activation of conductance and spin concentration were found to be functions of the molecular structure. It was considered impressive evidence that impurity effects on the electronic properties of molecular solids are far less than those commonly observed with the covalently bonded semiconductors such as Ge and Si, for example. A detailed analysis was made of the carrier and free radical formation and life-times in these ekaconjugated molecular solids using a simple model.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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