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  • Articles: DFG German National Licenses  (9)
  • Physics  (9)
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  • Articles: DFG German National Licenses  (9)
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  • 1
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of the NMR second moment of a uniaxially oriented sample of polyethylene single crystals in the range of temperatures from -196°C to 130°C and its dependence on the alignment angle γ between the orientation axis (preferential direction of the molecular chains) and the NMR magnetic field are presented. The experimental results are discussed mainly with respect to the high temperature relaxation, called the α process, in polyethylene. They are compared to theoretical predictions made for a number of mechanisms of molecular motion in Part I of this work. Only one of the mechanisms considered is found to be in quantitative agreement with experiment, the mechanism here referred to as flip-flop motion. This consists of thermally activated rotational jumps of the crystalline chain segment between folds around its axis between two equilibrium sites in the lattice. Each rotational jump through 180° is accompanied by a shift of the molecule along its axis by one CH2 group. The discussion of the low-temperature relaxation of polyethylene, the γ process, is based partly on the above measurements and partly on measurements of second moments for unoriented polyethylene samples varying widely in morphology and noncrystalline content. The decrease of the second moment observed with these samples between -196°C and 20°C is taken as a measure of the intensity of the γ process. A linear correlation is found between the decrease in the second moment, designated ΔS, and the noncrystalline content, 1 - αm; this can be represented by ΔS = 1.4 + 22.1(1 - αm). It is shown that neither the crankshaft mechanism not the kink mechanism is able to account quantitatively for this result. The model of a chain end moving in a vacancy fails to adequately describe the angle dependence of ΔS in oriented polyethylene single crystals. The “sandwich model” of a polyethylene single crystal, in which the crystalline core is covered by noncrystalline surface layers, is in better agreement with observations.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 587-598 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: NMR measurements on undrawn polyethylene (PE) samples in contact with a solvent such as C2Cl4 indicate an increase in the mobility of the mobile chain segments as compared to dry samples. Highly drawn PE shows no such effect. This is because Sa, the sorption per unit mass of noncrystalline material present, decreases from 20.9 wt.-% (dry basis), found for undrawn quenched PE, to 0.63 wt.-% after drawing (Sa determined at 25°C. and 0.80 vapor activity). Drawing also reduces the segment mobility according to the NMR spectrum. It is shown that these effects are caused by considerable structural changes occurring in the noncrystalline regions of PE upon drawing. Annealing of drawn PE samples at successively higher temperatures leads to a gradual relaxation of the noncrystalline regions towards the state characteristic of undrawn PE. With increasing annealing temperature Sa as well as the mobility approach values found with undrawn PE.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 791-797 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The NMR second moment of a uniaxially oriented mat of single crystals of n-C32H66 (in the orthorhombic form) was measured at temperatures from -170°C to 70°C and at various alignment angles γ between the orientation axis (preferential direction of the molecular chains) and the NMR magnetic field. Accurate expressions are given for the NMR second moment of an orthorhombic normal paraffin CnH2n+2 of arbitrary molecular chain length n for n ≥ 10, in the following states of molecular motion: no motion (a rigid lattice), rotation of CH3 groups, and rotation of the chains around their axes with superimposed rotation of CH3 groups. In addition to these well-known motions, n-C32H66 is found to exhibit an α process. The corresponding decrease of the NMR second moment shows the dependence on γ predicted for “flip-flop” motion, i.e., rotational jumps of the chain molecules around their axes through 180° and a simultaneous translation along these axes by one CH2 group. The overall decrease in second moment occuring at the transition to the hexagonal rotator phase in n-C32H66 can be quantitatively accounted for. The dependence of this decrease on the alignment angle γ, however, is in disagreement with calculations based on a simple rotation of the chains around their axes. Considerable torsion of the chains superimposed on the rotation would improve agreement between theory and experiment.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 2033-2042 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Wide-line NMR spectra of nylon 66 fibers have been obtained at different alignment angles between the fiber axis and the magnetic field, at varying water contents (H2O and D2O), and at different temperatures. At 28°C the spectrum of the dry fibers consists of a nearly structureless broad line. At water regains of 1.4% by weight (dry basis) and higher a sharp line appears which originates from highly mobile water molecules. The width of this line decreases with increasing water content, implying an increase of water mobility. Moreover, the width is a function of the alignment angle; this shows that the water is not reorienting isotropically owing to specific water-polymer interaction. The amount of mobile water is always smaller than the amount of water absorbed. At water contents close to saturation, a mobile polymer line appears with a width intermediate between the broad line (immobile polymer) and the sharp water line. This line, most clearly observed at an alignment angle of 0°, is due to a shift of the αa process to lower temperatures in the presence of water. A similar line is observed in the dry fibers at 120°C. It is shown that the αa process decreases the NMR second moment only slightly. The shift of the high temperature drop in second moment to lower temperatures in the presence of water is therefore interpreted as due to a shift of the αc process, and not of the αa process, to lower temperatures.
    Additional Material: 6 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. 753-770 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Several molecular mechanisms, proposed in the literature for the low- and high-temperature relaxation processes in linear polyethylene and commonly referred to as γ and α processes, are examined, and their effect on the second moment of the broad line NMR absorption is predicted quantitatively. The following models for the α process are discussed: rotational oscillation of the long chain molecules around their axes, general two-site models where the chain performs thermally activated rotational jumps through an angle τ between two equilibrium positions, a particular two-site model (τ = 180°) denoted as flip-flop motion, and the kink model. For the γ process, the following molecular mechanism are considered: the kink model, a vacancy with a chain end, the crankshaft mechanism. The decrease of the second moment caused by these motions is considered. Characteristic differences between the motional models are predicted with respect to the anisotropy of the decrease in second moment in a uniaxially oriented sample and/or the magnitude of the overall decrease. These differences allow an experimental distinction between the different models.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 2209-2251 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress crazing is studied in three forms of crystalline, isotactic polypropylene (PP): (1) smectic/nonspherulitic, (2) monoclinic/nonspherulitic, and (3) monoclinic/spherulitic PP. Optical and scanning electron microscopy as well as stress - strain measurements are used to characterize crazing behavior in these three forms as a function of temperature (-210 to 60°C) and of the gaseous environment (vacuum, He, N2, Ar, O2, and CO2). Forms 1 and 2 are found to craze much like an amorphous, glassy polymer in the temperature range between -210 and -20°C, irrespective of environment. The plastic crazing strain is large close to the glass-transition range (ca. -20°C) of amorphous PP and in the neighborhood of the condensation temperature of the environmental gas. Near condensation, the gas acts as a crazing agent inasmuch as the stress necessary to promote crazing is lower in its presence than in vacuum. A gas is the more efficient as a crazing agent, the greater is its thermodynamic activity.Spherulitic PP (form 3) crazes in an entirely different manner from an amorphous, glassy polymer, showing that the presence of spherulites influences crazing behavior much more profoundly than the mere presence of a smectic or monoclinic crystal lattice. Below room temperature, crazes are generally restricted in length to a single spherulite, emanating from the center and going along radii perpendicular, within about 15°, to the direction of stress. They never go along spherulite boundaries. Gases near their condensation temperature act as crazing agents much as in nonspherulitic PP. Above room temperature the crazes are no longer related to the spherulite structure, being extremely long and perfectly perpendicular to the stress direction. Apparently the crystals are softened enough by thermally activated segmental motion to permit easy propagation of the craze. The morphology of the fracture surfaces and its dependence on temperature and environment is described and discussed. Concerning the action of gases as crazing agents it is argued that the gas is strongly absorbed at the craze tip, where stress concentration increases both the equilibrium gas solubility and the diffusion constant. Hence, a plasticized zone is formed having a decreased yield stress for plastic flow. This is considered to be the main mechanism by which the gas acts as a crazing agent. In addition, reduction of the surface energy of the polymer by the adsorbed gas eases the hole formation involved in crazing.
    Additional Material: 25 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 359-384 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A Raman band of low frequency, arising from an accordionlike vibration of all-trans \documentclass{article}\pagestyle{empty}\begin{document}$ \rlap{--} ({\rm CH}_2 \rlap{--})_n $\end{document} segments and previously observed in normal paraffins and in polyethylene single crystals, has now also been found in bulk and in cold-drawn polyethylene, both linear and branched. The accordionlike vibration, or longitudinal acoustic mode (LAM), in polyethylene is compared with the LAM in normal paraffins. Whereas the Raman bands corresponding to the third (LAM-3) and higher modes are quite intense in a long-chain paraffin such as n-C94H190, they are so weak in polyethylene as to be unobservable with the apparatus used. This is attributed to the presence of the chain fold in polyethylene. Of the two extreme structural models of the fold here discussed, namely the models of “tight folds” and of “loose loops,” only the latter seems capable of accounting for the weakness of LAM-3 and higher modes in polyethylene. A quantity called “nominal Raman length” is defined as the length of that all-trans n-paraffin that would have the same LAM-1 frequency as the polyethylene sample under consideration. The nominal Raman length is always greater than the average long spacing, deduced from discrete x-ray scattering at small angles after applying a Lorentz correction, and, after allowing for chain tilt, is found equal to the segment length between folds. This can be accounted for by both of the models mentioned. As a test of the theory of surface melting the frequency of the accordion vibration of annealed polyethylene single crystals was measured as a function of temperature up to the melting point; no frequency change with temperature was observable. On the basis of the naive idea that there is complete decoupling of the vibrations in the all-trans chain segment from the disordered (molten) surface layer, one would predict that upon surface melting and the concomitant shortening of the all-trans segment, the LAM-1 frequency should increase. A more careful analysis, taking into account the existence of coupling of the LAM to the surface layer, shows that the outcome of this experiment does not necessarily invalidate the idea of surface melting. Bulk polyethylene samples exposed to 60Co γ-radiation for doses up to 100 Mrad show a slight shift of the Raman band to lower frequencies, whereas no such shift was observed upon absorption of a swelling agent. A search, without success, was made for a longitudinal acoustic mode in polypropylene, poly(vinylidene fluoride), nylon 66, and polyoxymethylene.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 8 (1970), S. 2049-2059 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In studies of various polymers in the solid state by pulsed and wide-line NMR, a relationship between the spin-lattice relaxation time and the fraction of mobile protons in the polymer sample was observed. This effect has been used to determine the degree of polymerization of a series of fumaronitrile homopolymers. The technique should have wide applicability in the direct determination of the number-average molecular weight M̄n, especially for polymers that may be insoluble and/or infusible though not crosslinked.
    Additional Material: 5 Ill.
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  • 9
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this study, wide-line NMR and x-ray diffraction have been used in conjunction to study the crystal structure of poly(vinylidene fluoride). Drawn poly(vinylidene fluoride) film was found to contain two crystal phases, the relative amounts of each depending on the draw temperature. Drawing at 50°C. yields a single phase, designated as phase I, while drawing at temperatures between 120 and 160°C. yields a mixture of phase I and a second phase (phase II). The fraction of phase II increases with increasing draw temperature, but this phase was never obtained without some phase I. A tentative orthorhombic unit cell is proposed for phase II. The structure of phase I has been determined from x-ray data. The unit cell is orthorhombic, space group Cm2m, having lattice constants a = 8.47, b = 4.90, and c (chain axis) = 2.56 A. There are two polymer chains in this unit cell. The conformation of the polymer chains is planar zigzag. The details of this structure have been confirmed by experimentally determining at -196°C. the change in the NMR second moment with the angle between the magnetic field and the draw direction of phase I (drawn at 50°C.), and by comparing these results with a theoretical calculation of the second moments, based on the atomic positions obtained from the proposed structure.
    Additional Material: 3 Ill.
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