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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of statistical physics 5 (1972), S. 173-183 
    ISSN: 1572-9613
    Keywords: Coherent states ; number conservation ; action-angle variables ; conjugate property
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Utilizing the facts (i) that the number of particles in the many-boson system is conserved and (ii) that the Hamiltonian is Hermitian, a new set of variables comprising “action” and “angle” variables has been introduced. These variables are conjugate in the “mean” and provide a rigorous approach to introducing phase variables for “total-number-conserving many-boson systems.”
    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 8 (1964), S. 2653-2659 
    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: Sol rubber dissolved in three solvents - cyclohexane, petroleum ether (40-60°C. fraction), and toluene - was degraded by ultrasonic waves, the degradation kinetics being followed by measuring spectrophotometrically the consumption of the free radical scavenger α,α′-diphenyl-β-picryl hydrazyl. The kinetic data have been examined by the rate equations developed from two different approaches: one by Jellinek and the other by Ovenall. It has been observed that the number of bonds broken as a function of time can be fitted equally well by both equations in the initial stage, but as the time of degradation increases, especially when the number-average degree of polymerization attains a value less than 3Pe/2, the rate can be described better by Jellinek's equation than that of Ovenall. The rate constants K and the final degree of polymerization for rubber are found to depend on the nature of the solvent.
    Additional Material: 4 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 25 (1980), S. 1263-1271 
    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 influence of hydrofuramide (a reaction product of furfural and ammonia) on the network structure and overall kinetics of thiuram vulcanization of natural rubber is reported. The nature of the network structure of the thiuram vulcanizates in the presence and absence of hydrofuramide was determined using triphenyl phosphine (Ph3P) as a chemical probe. The presence of hydrofuramide produces structural complexity of the vulcanizate. The overall kinetics of thiuram vulcanization follows a first-order-rate law in the presence as well as in the absence of hydrofuramide. The rate constant increases while the energy of activation decreases in the presence of hydrofuramide.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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: A convenient method of preparing zinc ethylenediamine complex (ZED) solution for use as solvent for cellulose pulp is described, and the advantages in using this solvent (0.25M zinc in 41% ethylenediamine in water) over cupriethylenediamine (CED) or cuprammonium solutions for viscometric determination of molecular weight of cellulose are indicated. Intrinsic viscosities of eight rayon-grade pulp solutions have been determined at four temperatures: 15, 20, 25, and 30°C. The constants K = 5.85 × 10-5 and a = 0.936 of the Mark-Houwink equation [η] = KMna, required for evaluating the molecular weight of cellulose pulps in ZED solution, have been determined by using the molecular weight values obtained from CED solutions.
    Additional Material: 3 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 7 (1963), S. 2199-2209 
    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 kinetics of low-temperature (60-100°C.) thermal degradation of deproteinized and deresinified petroleum ether soluble fraction of natural rubber in two chemically inert solvents, cyclohexane and trans-decalin, have been studied. The changes in Mw, A2, and (r2)1/2 at various stages of degradation have been obtained from the lightscattering data. The rate constants and the energy of activation for chain scission have been calculated from the observed variation in Mu. The scission has been found to be random and the average energy of activation is 25.8 kcal./mole. This low-energy requirement suggests the presence of weak links in the rubber molecule which get ruptured at low temperature.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 683-692 
    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: Influence of hydrofuramide and ethanolamines on efficient vulcanization (EV), semi-EV, and conventional sulfur vulcanization accelerated by tetramethyl thiuram disulfide is reported. In the case of thiuram vulcanization, the amines increase the cure rate but reduce the crosslink density. The interaction of tetramethyl thiuram disulfide with amines has been studied. The amines interact with thiuram disulfide (TMTD) giving rise to the formation of gaseous products. Thermogravimetric analysis shows weight loss of about 50% in case of TMTD-ethanolamine system and 25% in case of TMTD-hydrofuramide system. Gas chromatographic studies of the gaseous products indicate that it consists mainly of H2S. The other constituents in the gaseous product are CO2 and a thiol. A possible reaction based on these observations to account for decrease in crosslink density in thiuram vulcanization caused by amines is reported.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    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 kinetics of degradation of butyl rubber in two solvents, cyclohexane and toluene, was studied by two independent techniques: viscosity measurements and free-radical estimation as a function of DPPH consumed. The general shape of the rate curves in the two cases is similar, but not identical. The rate given by estimation of DPPH is faster than that obtained from solution viscosity data. This has been attributed to the inherent limitations of the two methods for the quantitative determination of the number of breaks occurring in the polymer molecules. The rate is also reduced as the viscosity of the solution medium is increased, which may be correlated with the reduction of the cavitation effect responsible for degradation. The degradation rates in two solvent media initially having the same viscosity were unequal. This may be due to different solvent-solute characteristics, which means that the viscosity and cavitation change to different extents in the two cases throughout the course of degradation. The limiting degree of Polymerization (DP)∞ obtained after prolonged irradiation has been found to be dependent on parameters such as intensity of irradiation, solution viscosity, and initial DP of the molecules.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1375-1385 
    ISSN: 0887-6266
    Keywords: liquid crystalline aromatic copolymers, solid state order in ; copolymers, wholly aromatic, nature of order in solid state of ; solid state order in aromatic liquid crystalline random copolymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Two different models of order in the solid state of wholly aromatic liquid crystalline copolymers (ALCPs), namely the nonperiodic layer (NPL) model of Windle et al. and the paracrystalline lattice (PCL) model of Biswas and Blackwell, have been analyzed with respect to experimental and theoretical observations. The NPL model proposes the formation of ordered domains by matching random sequences between adjacent chains while the PCL model relies on the presence of conformational correlations between adjacent monomers, without explicit sequence matching, to form ordered domains. The presence of three-dimensional order in the quenched state of ALCPs has been reported previously. The initial stages of crystallization are very likely to be assisted by the presence of small sequence matched domains. However, the probabilities for the formation of NPL domains having sizes comparable to those observed experimentally in the quenched state are extremely small. The PCL model, on the other hand, is not hampered by probability statistics and also provides a better fit to the experimental wide-angle x-ray scattering data along the fiber (Z) axis. The reported calorimetric data on ALCPs are also inconsistent with the presence of significant motion between chains, which is required for the NPL crystal to grow during the process of annealing. In contrast, the observation of a slow crystallization process, which converts the quenched hexagonal phase to the ordered orthorhombic phase, is adequately described by the PCL model as occurring via local conformational changes and small axial shifts between adjacent monomers. The observations from dielectric relaxation, nuclear magnetic resonance and dynamical mechanical spectroscopy studies also favor the PCL model over the NPL model of order in the solid state of ALCPs. © 1992 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 13 (1954), S. 461-469 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The scattering of light by solutions of a well-fractionated sample of polymethyl methacrylate in acetone, methyl ethyl ketone, and benzene, have been measured using 4358 and 5461 A. wave lengths as incident radiations. The average molecular weights of the polymer from turbidity measurements and lengths determined from angular dissymmetries of scattered light are 571,000 and 760 A. in acetone, 38,400,000 and 715 A. in methyl ethyl ketone, and 408,000 and 375 A. in benzene. The abnormal molecular weight observed in methyl ethyl ketone solution may be ascribed to low μ - μ0 value of the medium. The greater molecular extension in ketone than in benzene solutions is explained in terms of the relative magnitudes of solute-solvent interaction. The depolarization ratios ρu, ρv and ρh have been measured and the decrease of ρv and ρh with increase in concentration of the polymer in ketonic solvents and little change under similar conditions in benzene, are discussed in the light of the “molecular field effect” of Gans.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 27 (1958), S. 575-577 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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