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  • ZIB Catalog
  • Articles: DFG German National Licenses  (17)
  • Polymer and Materials Science  (17)
  • 11
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 747-756 
    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 isothermal decomposition of a phenolic resin in a phenolic-carbon cloth composite was measured at approximately 0.1 to 0.2 torr over the temperature range of 105°-718°C. The kinetics are initially first order and, in the later stages, second order. An analytic technique is provided for calculating the maximum quantity of resin which will volatilize during decomposition, thereby obviating the necessity of measurements for extended time periods. The amount of resin available for volatilization during decomposition varies with temperature and is in equilibrium with resin, which does not volatilize. Plots of the equilibrium constant versus the reciprocal absolute temperature show that two equilibria are involved: one which predominates up to 352°C and the other above this temperature. The heats of reaction are 2.2 and 15.3 kcal/mole. The first value is associated with hydrogen bonding and the second with decomposition and oxidation activation energies.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 15 (1971), S. 91-103 
    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 isothermal decomposition of a phenolic resin in a phenolic-carbon cloth composite was measured in air at 0.1 to 0.2 torr over the temperature range 104-718°C. Two decomposition rate relationships are presented that can be used to predict decomposition. One assumes two second-order consecutive rate-controlling reactions, and the other assumes a diffusion-limited second-order reaction. Two rate constants govern each relationship, one being operative during the initial decomposition stages, and the other during the final stages. Evidence is presented to support the applicability of both relationships to predict decomposition over the entire temperature range studied. Arrhenius plots of the rate constants consist of several segments linearly connected. Activation energies and frequency factors computed from these segments cover a broad range of values. The activation energies are used to correlate the temperature ranges with the predominant products formed in these ranges.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 163-173 
    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: ABA-type block polymers of styrene (monomer A) and isoprene or butadiene were prepared using two commercially available dilithium adducts of isoprene as initiators. One (DiLi-1) was predominantly dilithio diisoprene and contained a small amount of dimethyl ether (ether/Li 〉 1.0). The second (DiLi-1 C.E.) was a higher molecular weight version of DiLi-1, containing about seven isoprene units per molecule. It contained only a trace of dimethyl ether (ether/Li 〈 0.1). Polymers were made by charging all of the monomers at the start of the reaction. The diene polymerized first, incorporating some styrene. When the diene was consumed, the difunctional polymer chains then added a block of nearly pure polystyrene at each end. Thus an ABA-type polymer was synthesized in one step. These polymers show the usual behavior of pseudo-vulcanized elastomers. Their stress-strain curves are given. The SBS polymers had the higher tensile strengths. None had tensile strengths as high as SBS or SIS polymers made with n- or sec-butyllithium. It was shown that the diene blocks contain appreciable amounts of styrene. This leads to more compatibility between the A and B blocks; it also shortens the styrene blocks compared to the theoretical lengths of “pure” blocks. Both effects can lead to loss of tensile strength. Microstructures of the diene homopolymers made with these initiators are also given.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 5 (1954), S. 208-212 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: The Surfaces Energy of Stable MaterialsAn explanation of the basic meaning and importance of interfacial surface forces in the building up of materials is followed by an examination of the manysided relations between the surface energy and the other properties of solid materials. The relationships between the tensile strength and other mechanical values, the importance of capillary pressure in active fillers and in separation hardening, the place of synthetic materials in the “Paracher Diagram”, their relation to the specific entropy and others factors are examples of this. Some actual numerical values for surface tension of metals in the solid state, inorganic compounds and synthetic materials are mentioned. However, most of these values depend on empirical methods of calculation.
    Notes: Nach einer Darlegung über die grundsätzliche Bedeutung der Grenzflächenkräfte für den Aufbau der Stoffe wird auf die vielseitigen Bezichungen zwischen Oberflächenenergie und anderen Eigenschaften kompakter Materie eingegangen. Zusammenhänge mit der Zerreißfestigkeit und anderen mechanischen Güteziffern, Bedeutung des Kapillardruckes bei aktiven Füllstoffen und bei der Ausscheidungshärtung, die Lage der Kunststoffe im „Parachor-Diagramm“, ihre Beziehung zur spezifischen Entropie u. a. sind Beispiele hierfür. Ferner werden Zahlenwerte für die Oberflächenspannung im festen Zustand von Metallen, anorganischen Verbindungen und Kunststoffen angeführt, die auf verschiedenen meist empirischen Berechnungsverfahren beruhen.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 1 (1950), S. 51-52 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1083-1087 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cleavage of poly(vinyl alcohol) in dimethyl sulfoxide at 42°C has been measured viscometrically in the presence of tert-butyl hydroperoxide and metal complexes. Phthalocyanine complexes of copper(II), iron(III), cobalt(II), and vanadium as VO(II) as well as hemin, hematin, chlorophyllin, and cytochrome c were used. The rates of decomposition of tert-butyl hydroperoxide in the presence of these metal complexes were measured idometrically. These data are compared to results obtained with other metal complexes in similar reactions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 28 (1958), S. 129-150 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Study of the diffusion in polymers of molecules comparable in size and structure to the segments of the chain molecules is suggested as a means of securing information on structure and molecular friction forces in polymers. A convenient method for measuring the diffusivity in polymers of such compounds tagged with C-14 was devised and used to study the diffusivity of octadecane, octadecanol, stearic acid, and octadecyl stearate for a range of temperatures in polymers including natural rubber, GR-S, polybutadiene, polyisoprene, and polyisobutylene. Diffusivities were independent of concentration for the range used. The diffusivities of straight chain hydrocarbons in natural rubber appear to vary inversely as the molecular weight of the diffusing compound. Evidence was found for association effects in the diffusion of stearic acid in natural rubber. Activation energies for diffusion of the compounds were quite similar in any one polymer and of the same order as reported for low molecular weight hydrocarbons and for viscous flow. Larger differences in activation energies were observed for diffusion in the different polymers. Correlations were observed for the diffusivities of octadecane in a series of polymers with their densities and thermal expansivities, especially the latter. Some study was given to the effect on the diffusivity of octadecane of such parameters as polymer unsaturation, solution viscosity, molecular weight, and crosslink density. The diffusivity of octadecane in natural rubber had a pronounced maximum as a function of crosslink density, coinciding with the maximum in tensile strength. Possible implications of this are discussed. The diffusivities of octadecane in a series of elastomers were studied in relation to the internal frictional losses observed for 60 cps vibrations over a range of temperatures. It was concluded that frictional forces deduced from the diffusivity measurements have some correspondence to high frequency viscoelastic phenomena which involve small units of structure comparable in size to the segments of the polymer molecules.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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