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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 82 (1992), S. 383-396 
    ISSN: 1432-2234
    Keywords: Reptation ; Constraint release ; Viscosity ; Entanglement phenomenon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A numerical solution to the parallel processes model for combined reptation and constraint release in polymer melts is presented. The discrete chain solution to the problem exhibits an exponent of 3 in the molecular weight dependence of the viscosity, just as in the strict reptation case; the magnitude of the viscosity is overestimated and no crossover to reptation is observed, as in Graessley's independent processes model. It is shown that linear combinations of reptation and constraint release, as modeled here, cannot describe the viscosity results observed experimentally.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 1178-1186 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Gradient theory of equilibrium fluid microstructures is extended to nonequilibrium isothermal processes. The theory is applied to steady diffusion across liquid-liquid interfaces. It is shown that local equilibrium across a fluid-fluid interface is maintained even in the presence of very high diffusion fluxes and that the concept of an interface acting as an applied potential energy for a diffusing species is of limited utility. The theory is suited for practical, semiempirical calculations of structure, stress, and isothermal transport in systems containing interfaces.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 15 (1975), S. 386-393 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: A versatile model for ε-caprolactam polymerization is presented. A deterministic, mathematical basis for obtaining the most probable distribution of molecular weights in batch polymerization is developed. Continuous polycaproamide production has been modeled and shown to give othe than most probable distribution in many cases. The effect of adding monofunctional agents has been investigated. Results of some preliminary studies toward determining the optimal reactor configuration are presented.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: A series of polyether polyol (polyoxypropylene capped with polyoxyethylene), 4-4′ diphenylmethane diisocyanate, and 1,4 butane diol urethanes were prepared by reaction injection molding with different levels of catalyst (dibutyl tin dilaurate). The degree of phase separation, morphology, and molecular weight were compared by dynamic mechanical spectroscopy, wide-angle x-ray scattering, optical microscopy, and gel permeation chromatography. Slowly reacted (uncatalyzed) samples displayed better phase separation, crystallinity, low molecular weight, and poor mechanical properties. Fast-polymerized (highly catalyzed) samples showed a high degree of phase intermixing, low crystallinity, high molecular weight, and good mechanical performance. Differences between these two behaviors are discussed with the aid of a simplified phase diagram. Slowly reacted samples phase-separate through nucleation and growth of large spherulites, while quickly reacted samples form a much finer, interconnected microstructure. Infrared studies of phase separation for slow systems are presented and used to discuss phase separation in fast polymerizations.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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