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  • 1
    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 Conventional time-temperature (t-T) superposition appears to be inappropriate to the viscoelastic behaviour of amorphous, peroxide cured EPDM networks. A phenomenological approach is presented that reduces these permanent elastomers to thermorheologically simple materials. Although the origin of the anomalous behaviour observed is not yet completely understood, it is attributed to an unusual variation of the equilibrium modulus with temperature.
    Type of Medium: Electronic Resource
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  • 2
    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 Computer simulations show that oligomers with two different terminal groups with dissimilar reactivities for isocyanates give a delayed viscosity rise in polyurethanes. This is a desired behaviour for RIM processes. Therefore, an α-hydroxy-ω-amino poly(ethylene oxide) (HAPEO) has been prepared. The synthesis was carried out by the ethoxylation of 2-hydroxyethyl phthalimide as a blocked amine. Hydrazinolysis appears to be the best way to obtain the deblocked oligomer. The product properties were compared with an oligomeric diamine ether (Jeffamine D2000). The gel time of HAPEO (Mn=500) and JAD2000 (Mn=2000) was the same (2 sec.). The product with HAPEO had a higher modulus, a comparable impact and tensile strength and a lower elongation at break.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 269-272 
    ISSN: 0025-116X
    Keywords: 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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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2223-2231 
    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: The esterification kinetics of difunctional neopentyl glycol and trifunctional trimethylol propane with monofunctional 1,4-tert-butyl benzoic acid was studied in the melt phase at 200°C in the presence of a metal catalyst. The rate of conversion was monitored via titrations and by determination of the relative concentrations of products and reactants using HPLC with a UV detector. A small but significant positive substitution effect was found for neopentyl glycol (KDA = 1.15) and none was found for trimethylol propane. The reaction rate constant of neopentyl glycol with the acid is about 40% higher than that of trimethylol propane with the acid. A second-order overall reaction order was used to compute the rate constants.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 2007-2015 
    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: The esterification kinetics of isophthalic and terephthalic acid, with benzyl alcohol, were studied in the melt phase, which is a heterogeneous system because of the low solubilities of the phthalic acids. The relative concentrations of components and their conversions, α, were determined with HPLC. The effect of insolubility of the phthalic acids on the reaction kinetics can be described in two ways. For terephthalic acid, at 0 ≤ α ≤ 1, and for isophthalic acid, at α 〈 0.6, the esterification kinetics can be described with equations for a homogeneous system with only a substitution effect. An improved and more complete description for isophthalic acid is obtained with equations for a heterogeneous system, with a surface reaction rate constant and a ratio of reactive (at the surface) over nonreactive monomers (in the core, i.e., the surface to volume ratio). This model fits data for α 〈 0.7. The model parameters depend on the reaction temperature and the solubility of the phthalic acid. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2377-2385 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A nonlinear regression analysis is presented to estimate the equilibrium modulus of relaxing rubber networks from G'(ω) or G(t) data. Various semiempirical curve-fitting equations are tested with two-function minimization algorithms.
    Additional Material: 2 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2635-2635 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 317-344 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An experimental study has been made to specify how the time-temperature superposition and the linear viscoelastic characteristics vary with the degree of crosslinking for a broad class of noncrystalline peroxide-cured EPDM networks. A new, very sensitive method is applied to determine the horizontal and vertical shift functions in an independent way. All uncrosslinked samples are thermoelasticoviscously simple with horizontal shift functions aT of the WLF type and vertical shift functions almost independent of temperature, in agreement with recent theoretical understanding. Upon crosslinking, these materials become thermoviscoelastically complex networks, but superposition can still be accomplished by assuming different temperature dependences for the relaxational strength and the equilibrium modulus. The aT functions can be taken independent of the degree of crosslinking. The vertical shift functions bT for the relaxational strength vary with the degree of crosslinking between theoretical predictions for uncrosslinked and perfectly crosslinked EPDM networks. The equilibrium moduli of the lightly cured networks decreases with increasing temperature, which is ascribed to the presence of interchain associations between ethylene sequences in the trans state. Upon further crosslinking, these effects gradually vanish and eventually the networks can be described as viscoelastically simple with an energy elastic contribution due to the ethylene trans-gauche transitions. The linear viscoelastic characteristics, namely the storage and loss moduli and compliances and phase-angle master curves and the relaxation and retardation spectra are discussed as a function of the degree of crosslinking. A sol/gel analysis and equilibrium swelling measurements complete the experimental characterization of three familes of five EPDM networks each.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 1325-1351 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Three EPDM network families with various degrees of chemical crosslinking and slightly crystalline below about 350 K have been characterized by thermoviscoelastic and equilibrium swelling measurements. Between 300 and 450 K the thermoviscoelasticity of these elastomers, whether cured or not, is complex. Important differences from previous results on noncrystalline EPDM networks are their dependence on waiting time and temperature history below 350 K, and an equilibrium modulus for the uncured elastomers. These effects increase with rising ethylene content of the EPDM and are related to the crystallinity in the networks. A previously proposed modified time-temperature (t-T) superposition scheme is also applicable to these data, and the resulting frequency shift functions aT are of the usual WLF type. The vertical shift functions for the relaxational components bT are different from those for the equilibrium moduli. Experimental data demonstrate that the absolute values of the relaxational components, i.e., G″ (ω) and H(τ), are not changed by small variations in crystallinity. In addition, larger variations in crystallinity do not affect their frequency dependence, only their absolute values. On the contrary, the equilibrium modulus, and therefore all characteristics containing this as a component, is extremely sensitive to small variations in crystallinity, and hence in temperature. The linear viscoelastic characteristics of these slightly crystalline networks and their deviations from thermoviscoelastically simple behavior are discussed as functions of the ethylene content, temperature, and degree of crosslinking of the elastomer. The data provide evidence for three contributing factors, namely chemical crosslinks, crystallinity, and a more disordered type of crystallinity termed microparacrystallinity.
    Additional Material: 17 Ill.
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  • 10
    Publication Date: 1993-05-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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