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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1083-1091 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements have been made of the anisotropy of viscoelastic behavior in cold-drawn low-density and high-density polyethylene sheets. In the low-density polymer the β transition was shown to be highly anisotropic, maximum losses corresponding to shear on planes containing the axis of drawing and on planes perpendicular to this axis. In high-density polyethylene the α transition shows anisotropy.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 649-652 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1227-1240 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A stepwise segment-by-segment cluster development of the interaction energy of two polymer coils at given distance leads to a closed expression, describing the second virial coefficient A2 in terms of certain intersegmental contact probabilities. An approximate expression for A2(α,z) in good solvents is then derived by using the uniform segment cloud model; the result being equivalent to that obtained by Flory. This expression is combined with the author's theory for α2(z) to give A2(z), and then with a subsequent adaptation of that theory to polyelectrolytes, to derive the dependence of A2 on ionic strength. The α2(z) and A2(z) equations are both compared with recently reported experimental data for NaPSS.
    Additional Material: 6 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 689-703 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reduced specific viscosity of poly(methacrylic acid) has been studied in ethanol-0.002N HCI solvent mixtures as a function of polymer concentration, alcohol concentration, and temperature. In addition, experiments were performed at different HCI concentrations and with KCI instead of HCI. Both intrinsic viscosity and Huggins coefficient were shown to undergo unusually strong variations. Two minima and two maxima could be demonstrated in intrinsic viscosity. The Huggins coefficient seems to show corresponding variations. The first minimum in intrinsic viscosity indicates that the coil volume has collapsed almost to an Einstein sphere. In this region the Huggins coefficient is extremely large (of order 102) and is controlled by coil association. It was shown that several forms of intramolecular interaction must be assumed to be competing to account for this behavior. The presence of HCI, particularly in the preponderantly aqueous phase, is required to suppress the polyelectrolyte effect. It is found, however, that the behavior of the solutions at relatively high ethanol concentrations is more sensitive to HCI content than is that of highly aqueous solutions. KCI can be used to replace HCI over most of the range. Increase in temperature shifts the turning points of the curves to lower alcohol concentrations. Some evidence has been found that the association constant giving rise to dimers increase with rate of shear. The importance of poly(methacrylic acid) as a chemically simple model substance for various biopolymer effects is stressed.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 705-712 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The intrinsic viscosity of poly(methacrylic acid) has been studied in mixtures of 0.002N HCI and a series of aliphatic alcohols. The behavior found previously with ethanol is shown to apply in the case of admixture with methanol, n-propanol, and 1,2-ethanediol. The intrinsic viscosity first drops to a minimum and then increases sharply to a maximum. With ethanol and n-propanol the maximum is followed by another minimum and maximum. With methanol and 1,2-ethanediol this effect is absent or much smaller. Methanol and 1,2-ethanediol are equivalent, molecule for molecule, in their influence on the intrinsic viscosity. With ethanol and n-propanol there are in addition one and two shoulders, respectively, in the passage from the first minimum to the first maximum. Good correlation of the data is obtained if alcohol concentration is plotted as the mole fraction of carbon atoms per OH group (in the alcohol). The first maximum in particular was shown to correspond to the point where the number of water molecules per alcohol in the solvent mixture equals the number of C atoms per hydroxyl in the alcohol. The shoulders and first minima were found to correspond to other simple ratios. This behavior reflects changes in alcohol-water structure. The maximum in the case of ethanol was found to be the most pronounced and ethanol seems to possess optimal properties from this point of view.
    Additional Material: 5 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1817-1833 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements have been made of the anisotropy of viscoelastic behavior in specially oriented sheets of low-density polyethylene. The results for the cold-drawn sheets show a β relaxation process of very characteristic anisotropy. The annealed sheets show two relaxations in this region of temperature. The lower relaxation (about -10°C) is identified as an interlamellar shear process. The higher relaxation (about 70°C) has a very similar anisotropy to the β relaxation in cold-drawn samples. Isotropic sheets of low-density polyethylene have been also investigated. Two β relaxations are found in these materials.
    Additional Material: 13 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 713-726 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Poly(methacrylic acid) has been studied in 0.002N HCl-ethanol mixtures as a function of molecular weight. A different dependence on molecular weight is noted at different alcohol concentrations. Since the intrinsic viscosity passes through a series of extrema with changes in alcohol concentration, the dependence on molecular weight has been considered in two regions of alcohol concentration in particular. The region of the first minimum and the region of the second minimum (or overall maximum). In the region of the first minimum, intrinsic viscosity is proportional to M½, just as in 0.002N HCl. The Huggins coefficient k′ is large (ca. 60) but drops to about 10 when the molecular weight exceeds 320,000. In the region of the second minimum the dependence on molecular weight is complex. Intrinsic viscosity is proportional to molecular weight both at low and at high molecular weight and thus indicates freely draining structures. There is a conformational contraction, however, at molecular weight about 320,000 leading from one type of structure to the other. The structure at higher molecular weight may involve a specially strong bond between specifically grouped segments in the chain. The positions of the extrema along the alcohol concentration axis are not molecular weight dependent, particularly above 320,000. Results available for molecular weight dependence in methanol agree well with this picture. The present results confirm prediction inherent in the model of Silberberg and Priel and Silberberg.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 507-517 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new typical orientation pattern of polyethylene has been observed in extruded, melt-drawn composites containing 10% polyethylene and 90% polystyrene. In these composites, the polyethylene phase is dispersed in the polystyrene matrix as thin, long ribbons (width 1000 Å, thickness 500 Å). The b axis of the crystallites is found oriented preferentially along the long dimension of the ribbons, i.e., in the extrusion direction. The a and c axes of the crystallites show no preferred orientation. This texture pattern is attributed to the fact that, in view of the small cross section of the polyethylene phase, crystallization can proceed only along the long axis of the ribbons. Since the b axis is the direction of fastest growth in polyethylene (and the radial direction in a spherulite), most polyethylene unit cells are oriented with their b axes in the long dimension of the ribbons.
    Additional Material: 10 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1831-1837 
    ISSN: 0887-6266
    Keywords: block copolymer ; wormlike micelle ; fluctuations ; slow mode ; dynamic light scattering ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic light scattering (DLS) has been used to explore the properties of asymmetric styrene-isoprene (SI) block copolymers in concentrated solutions. Concentrations were always well below those necessary to access the order-disorder transition in neutral good solvents. The samples include SI (10-50), SI (36-9), and SIS (10-100-10), where the numerical suffixes denote the block molecular weights in kilodaltons; experimental emphasis was placed on SI (10-50). The DLS intensity correlation functions in the neutral good solvents, THF and toluene, were dominated by a slow mode that first appeared at a concentration c+ ≈ 4 c*, where c* is the coil overlap concentration. The decay rate of this mode scaled approximately as the third power of the scattering wavevector, and the excess scattered intensity decreased with increased scattering angle. These results were tentatively ascribed to the onset of substantial concentration fluctuations, that exhibited cylindrical, or wormlike structures. Measurements in solvents of known selectivity, dioxane and cyclohexane, and on a copolymer of the opposite composition, SI (36-9), indicated that the intermolecular association was driven by the effectively repulsive interactions between styrene and isoprene segments, rather than by solvent selectivity. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1831-1837, 1998
    Additional Material: 8 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 2659-2670 
    ISSN: 0887-6266
    Keywords: absorption ; chain scission ; degradation ; desorption ; epoxy resin ; hygrothermal aging ; intercrosslink molecular weight ; leaching ; water ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hygrothermal aging at elevated temperatures tends to induce degradation in epoxy resins. To predict the effects of this degradation, a knowledge of absorption and transport behavior of water is needed. In this work, a model material (DGEBA/DDA) has been employed to study the water absorption and absorption/desorption behavior during hygrothermal aging at 90°C, accompanied by degradation. The absorption results show an weight increase during the initial aging period followed by a decrease at later times. Absorption/desorption results show a similar phenomenon but with a net, overall weight loss after a certain period of aging. By assuming that water diffusion is approximately Fickian and that degradation of the resin is mainly caused by hydrolysis reactions, a model has been developed to describe the above-observed phenomena. Results show that the model is in good agreement with experimental data. Moreover, the model proposed can be used to estimate the average molecular weight of the intercrosslink chains after aging. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2659-2670, 1997
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