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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 193-208 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The results of an x-ray and polarimetric study of a crystalline modification (form I) of isotactic poly-(S)-4-methyl-1-hexene are reported and discussed. The x-ray fiber spectra of this polymer are practically indistinguishable from those of isotactic poly-(R)-(S)-4-methyl-1-hexene. Although the crystal structure of the latter can be described on the basis of helices of different screw sense packed in a P4 space group, the crystal structure of poly-(S)-4-methyl-1-hexene is better described on the basis of a P1 space group. The conclusion of the x-ray investigation, that in the crystals of the optically active polymer an equal number of right-handed and left-handed helices must be present, is supported by the polarimetric measurements, which have shown that the polymer in the crystalline form I possesses a rather low rotatory power.
    Additional Material: 5 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 2147-2155 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The role of the intrinsic viscosity [η] as separation parameter in gel permeation chromatography (GPC) was studied for dextrans (from Leuconostoc mesenteroids B512) dissolved in water with deactivated silicagel (Porasil) as the column-filling material. For that purpose specific viscosities of dextran fractions eluted by GPC were measured as a function of the elution volume v. Provided that the elution volumes are corrected for zonal spreading, they are related to the intrinsic viscosities in an unambiguous way, probably reflecting a unique relationship between degree of branching and molecular weights. This was further investigated by developing an iteration method to prepare two calibration curves γ(v) and g(v), respectively, relating ln[\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] and InM (M is the molecular weight) to v. It required that the weight-average molecular weight Mw, the number-average molecular weight Mn, and the average intrinsic viscosity [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] for a number of dextran samples (broad distributions) be previously known. The calibration curves found lead to consistent values of the above-mentioned averages. Moreover, they allow-establishment of the [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}]-M relationship over the range 5000 〈 M 〈 500,000.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2021-2031 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods for the determination of the number of the number of polytetrahydrofuran branches in neoprene-g-polytetrahydrofuran were examined. Only two suitable methods were found; namely, termination of oxonium ions by triphenylphosphine followed by 31P-NMR and termination with NH4OH—NH4Cl buffer and reaction with fluorescamine followed by fluorescence spectroscopy. Both methods led to the conclusion that Neoprene W has 9 ± 1 active halogens per mole that can be used to initiate tetrahydrofuran polymerization when silver salts are added. Among the methods examined in this study the fluorescence method was the most reliable, most reproducible, fastest, and simplest.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 3591-3595 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 9 (1971), S. 1647-1657 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of o-isopropylstyrene with free radical (benzoylperoxide, heat) and cationic (AlCl3, AlBr3) initiators has been investigated. It is concluded that, contrary to an earlier prediction and to a claim by Aso et al., both the radical and carbonium ion polymerizations of o-isopropylstyrene proceed by conventional mechanisms which give the same 1,2 repeat unit.
    Additional Material: 7 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 81-87 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The high degree of flexibility of blends containing minor amounts of partly crystalline copolymers of ethylene and vinyl acetate in paraffin wax seems to be a manifestation of some type of interaction. Low-angle x-ray diffraction of such blends showed a new long spacing intermediate in length between the polymer long spacing and the c axis length of the wax unit cell. This new long spacing appears to be a consequence of isomorphism involving cocrystallization of polymeric ethylene sequences and wax molecules. A lesser type of isomorphic interaction, epitaxy, occurs in polyethylene-wax blends: wax overgrows crystals of already crystallized polyethylene in the same orientation without a change in its c axial dimension.
    Additional Material: 2 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. 1411-1412 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1425-1441 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The angular position of the extrema of the vertically polarized scattering intensity has previously been utilized for a method of particle size analysis for systems of monodisperse, spherical, isotropic particles which conform to the Rayleigh-Gans-Debye theory. The consequences of a finite polydispersity, which is always present in real systems, was not assessed and the application of the method has resulted in erroneous characterization of some latex systems. This work is concerned with (1) reporting the effects of finite polydispersity on the method of analysis, (2) pointing out previous misuse of the method, and (3) introducing a method of analysis which is based on the position of the extrema but which also considers polydispersity and the exact Mie calculation. This method enables one to characterize a scattering system in terms of a modal diameter and a distribution-width parameter by utilizing prepared diagrams for a particular relative refractive index.
    Additional Material: 10 Ill.
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  • 9
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: New structural phenomena which can be produced in polymers at low temperatures or by the action of high forces are described and discussed. Experimental evidence supports the argument that the deformation of polymers can develop not only as a result of conformational changes of the macromolecules proper but also by transformation of more complex structural formations. The consequence of this phenomenon is the possibility of large deformations far below the glass-transition temperature in a crystalline polymer with well-developed supermolecular structure. This type of deformation takes place without molecular orientation. Another phenomenon discussed is the sharp change of supermolecular structure in crystalline polymers caused by the action of a shock wave. These effects ought to be connected with an energetic rather than entropic deformation mechanism because the transformations occur at a supermolecular level. Thus, there can be two extreme types of deformation processes: the well-known conformation changes that occur at a molecular level, and the deformation of supermolecular structures. Examples of the pure form of the latter type of mechanism obtained under extreme conditions are given.
    Additional Material: 17 Ill.
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  • 10
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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