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  • Articles: DFG German National Licenses  (18)
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  • Articles: DFG German National Licenses  (18)
Material
  • 11
    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.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 104 (1967), S. 135-141 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Breitlinien-Protonenresonanz-Spektren von gerecktem Polyäthylenoxyd (PÄO) wurden bei Temperaturen zwischen -196°C und 66°C in Abhängigkeit vom Drehwinkel γ zwischen der Reckrichtung und dem Magnetfeld aufgenommen. Linienbreite, zweites Moment und beweglicher Anteil wurden bestimmt und zur Diskussion der molekularen Bewegungsvorgänge herangezogen. In Übereinstimmung mit anderen Autoren wurden zwei Bewegungsprozesse unterschieden: 1. Der bei Temperaturen um -45°C einsetzende β-Prozeß findet wahrscheinlich in nichtkristallinen Bereichen statt und verursacht das Erscheinen einer schmalen Linie zusätzlich zur breiten Komponente. 2. Der zwischen 0°C und dem Schmelzpunkt (66°C) auftretende γ-Prozeß führt zu einer starken Abnahme der Linienbreite der breiten Komponente und auch des zweiten Moments. Diese Abnahme ist anisotrop und am größten bei γ = 45°. Als Folge davon ändert sich die Abhängigkeit der Linienbreite und des zweiten Moments vom Drehwinkel γ: Während beide Größen bei tiefen Temperaturen (〈0°C) ein Maximum bei γ = 45° und ein absolutes Minimum bei γ = 0° besitzen, liegt gerade unterhalb des Schmelzpunkts bei γ = 45° ein Minimum und bei γ = 0° ein absolutes Maximum. Diese Veränderung wurde auf Drehbewegungen der helixförmigen Moleküle um ihre Achse in kristallinen Bereichen zurückgeführt.
    Notes: Wide line NMR spectra of cold drawn poly(ethylene oxide) (PEO) were recorded at temperatures between -196°C. and 66°C. as a function of the alignment angle between the draw direction and the magnetic field. Line width, second moment, and mobile fraction were determined and are discussed in terms of segmental motion. In agreement with other authors two motional processes were found. (1) The β-process, commencing at temperatures around -45°C., probably occurs in non-crystalline regions and causes the emergence of a narrow NMR line in addition to the broad one. (2) The β-process was observed between 0°C. and the melting point (66°C.) and led to a pronounced decrease of the width of the broad line and of the second moment. This decrease was anisotropic and was greatest at the alignment angle γ = 45°. As a consequence of this the dependence of the line width and of the second moment on γ is changed: whereas both these quantities show at low temperatures (〈0°C.) a maximum at γ = 45° and an absolute minimum at γ = 0°, near the melting point, a minimum close to γ = 45° and an absolute maximum at γ = 0° were found. These changes are explained by oscillations of the helical molecules around their axes in crystalline regions.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 4 (1966), S. 399-405 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 409-411 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 769-773 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 Part B: Polymer Letters 9 (1971), S. 583-589 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 17
    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.
    Type of Medium: Electronic Resource
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  • 18
    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.
    Type of Medium: Electronic Resource
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