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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 20 (1987), S. 3060-3065 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 13 (1980), S. 681-685 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 102 (1980), S. 632-636 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1536
    Keywords: Preferential sorption ; polymer networks ; crosslinked poly(methyl methacrylate) ; swelling equilibrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Measurements of preferential sorption,λ(Ν 3), determined by refractometry, and swelling equilibrium,Ν 3 −1, of PMMA networks have been carried out in the cosolvent mixture MeCN+BuOH at 25
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 26 (1991), S. 357-362 
    ISSN: 1436-2449
    Keywords: Model networks ; bimodal networks ; dynamic mechanical properties ; poly(dimethylsiloxane)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Elastomeric networks of polydimethylsiloxane prepared by end-linking chains having molecular weights in the range 18,500 to 220 g mol-1 were studied from -128 to 50°C using a Rheovibron DDV III Viscoelastometer. In the case of the unimodal networks, the glass transition temperature Tg was generally insensitive to degree of cross-linking. The intensity of the tan δ relaxation, however, increased by over an order of magnitude over the range of cross-link densities investigated. Bimodal networks prepared from mixtures of relatively long and very short PDMS chains also had values of Tg which were insensitive to degree of cross-linking. Finally, as expected, the intensities of the tan δ peak for the bimodal networks could not be explained on the basis of simple additivity of contributions from the relatively long and the very short network chains.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Experimental values of the storage G′ (ω) and loss G″ (ω) moduli were obtained at different temperatures for several fractions of poly(diethylene glycol terephthalate). By assuming that all the relaxation mechanisms have the same temperature dependence, free volume parameters were obtained. The qualitative analysis of the molecular weight dependence of the viscosity at zero shear rate suggests that well developed entanglements are present in the relatively low molecular weight fractions investigated.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Elastomeric networks of polydimethylsiloxane (PDMS)) prepared previously for studying the effects of dangling chains on equilibrium elastomeric properties are now studied with regard to their dynamic mechanical properties. These model irregular networks had been prepared by end-linking divinyl-terminated PDMS chains having a number-average molecular weight of 11.3×103 g mol-1. The tetrafunctional end-linking agent present was used in varying amounts smaller than that corresponding to stoichiometric balance between its active hydrogen atoms and the chain vinyl groups. The resulting networks were studied from-135 to-28 °C using a Rheovibron DDV III Viscoelastometer. The glass transition temperature Tg was found to be generally insensitive to the concentration of dangling chains, over the range 0 to 41.1 wt %. The intensity of the tan δ relaxation, however, decreased significantly with increase in concentration over most of this range, suggesting the dangling chains facilitated crystallization. At the highest concentration, tan δ begins to increase, however, presumably because the inherent energy-dissipating ability of the dangling chains finally predominates.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 259 (1981), S. 1056-1061 
    ISSN: 1435-1536
    Keywords: Polydimethylsiloxane ; model bimodal networks ; junction functionality ; limited chain extensibility ; swelling
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Summary Elastomeric networks of high extensibility were prepared by end-linking mixtures of vinyl-terminated polydimethylsiloxane chains having molecular weights of approximately 600 and 11,000 g mol−1, with silanes chosen to give junction functionalities ϕ ranging from 3 to 8. The resulting bimodal networks were studied in elongation, at 25 °C, to their rupture points, and in swelling equilibrium in benzene at room temperature. The elongation moduli [f *] were found to be in satisfactory agreement with previous results obtained by end-linking hydroxyl-terminated polydimethylsiloxane chains. Values of [f *] at low and moderate deformations gave relatively low values of the ratio of elasticity constants 2C 2/2C 1, which is a measure of the extent to which the elongation changes from approximately affine to nonaffine as the elongation increases. The low values obtained for this ratio are presumably due to diminished interpenetration of configurational domains in the case of very short chains. In spite of its small magnitude, 2C 2/2C 1 does show some decrease with increase in ϕ, as predicted by the recent molecular theory of rubberlike elasticity developed by Flory. The swelling equilibrium results were also found to be in satisfactory agreement with theory. The elongation moduli increased significantly at high elongations, and the values of the elongation at which the upturn was first discernible were very nearly independent of ϕ, This is consistent with the interpretation of this anomalous behaviour in terms of limited chain extensibility. The maximum extensibility generally decreased somewhat with increase in ϕ and this caused a decrease in both the ultimate strength and the toughness of the elastomer, as measured by the energy required for rupture.
    Type of Medium: Electronic Resource
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  • 10
    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: Elastomeric networks were prepared by end-linking vinyl-terminated polydimethylsiloxane (PDMS) chains having number-average molecular weights of 11.3 × 103 g mol-1. The tetra-functional end-linking agent, Si[OSi(CH3)2H]4, was used in varying amounts smaller than that corresponding to a stoichiometric balance between its active hydrogen atoms and the chain vinyl groups. The number of dangling-chain irregularities thus introduced into the networks was directly determined by iodometric titration for unreacted vinyl groups. The (unfilled) PDMS networks thus obtained were studied in elongation to their rupture points at 25°C (a temperature sufficiently high to prevent complications from strain-induced crystallization), and in swelling equilibrium in benzene at room temperature. Small to moderately large proportions of dangling chains were found to have less of an effect on the elongation modulus than might be expected, and similarly a relatively small effect on the degree of equilibrium swelling. Most importantly, comparisons of constant values of the high deformation modulus show that dangling-chain irregularities decrease both the maximum extensibility of a network and its ultimate strength.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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