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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 1067-1076 
    ISSN: 0887-6266
    Keywords: transmission electron microscopy ; block copolymer ; polyimide ; nanofoam ; porous films ; polymer foam ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transmission electron microscopy was performed on a polymeric nanofoam material, derived from a triblock copolymer composed of a fluorinated polyimide center block, 3F/PMDA (derived from pyromelletic dianhydride (PMDA) and 1,1-bis(4-aminophenyl)-1-phenyl-2,2,2-trifluoroethane (3F)) and polypropylene oxide (PO) end blocks. The cast and imidized polymer exhibits a microphase-separated morphology consisting of PO microdomains within a polyimide matrix. The final nanofoam material is obtained by decomposing PO microdomains into low molecular weight products, which diffuse out of the polyimide matrix leaving nanometer length scale voids. Ruthenium tetroxide staining prior to microscopy was used to enhance the contrast between the 3F/PMDA matrix and the PO microdomains or voids, which permitted a more detailed view of the microstructure of both the foamed and unfoamed materials. From the power spectra of the micrographs, spatial correlation between the PO microdomains in the unfoamed material and between the voids in the foam were found. An interdomain separation distance of ca. 37 nm was observed. Analysis of the image yielded an average area of 411 nm2 for the PO domains. The analysis indicated that the PO domains were oblong, having average major and minor dimensions of 35 and 12.5 nm, respectively. An autocorrelation of the image showed that the domain center of masses were positioned 41 nm apart, in close agreement with the domain spacing (ca. 37 nm) found as described above. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 1067-1076, 1997
    Additional Material: 7 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 19 (1956), S. 485-494 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Attempts have been made, particularly by American workers, to exploit differences in crystalline and amorphous polymer spectra to determine crystalline/amorphous ratios. In most published work authors have been forced to rely on calibration by other methods, especially density. They have justified the use of the spectroscopic method principally on the grounds of speed in obtaining results. We propose a spectroscopic method, applicable to a number of polymers, which is entirely independent of other measurements. We are thus able to compare our results with those obtained by other methods and have in some cases been able to draw useful conclusions from apparent anomalies. Our method depends upon measurement of pure amorphous bands. We consider these to arise from the multiplicity of rotational isomers present in the amorphous phase. The pure amorphous spectrum of many polymers can be obtained, and by this means an absolute calibration of amorphous content is possible. Crystalline bands cannot be so calibrated; they are dangerous to use quantitatively, although superficially more attractive because of their sharpness. The application of the method to some common polymers including polythene, polyethylene terephthalate, and polytetrafluorethylene is described; the results are compared with values obtained by x-ray and density methods.
    Additional Material: 7 Ill.
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  • 3
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 60 (1962), S. S14 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 7 (1951), S. 377-392 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The Morey-Tamblyn turbidity method has been used to investigate the molecular weight distribution in a series of polymethyl methacrylates including commercial and experimental injection moulding powders. Evidence has been obtained that the increase in rate of polymerization occuring in the polymerization of methyl methacrylate (Norrish-Smith effect) causes widening of the distribution in high conversion polymers, but the separation into multiple peaks reported by other authors has not been observed. From an examination of specially prepared polymers, e.g., at small degrees of conversion, it is concluded that chain combination is a more likely termination process than disproportionation.
    Additional Material: 12 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 15 (1955), S. 592-594 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of crystallization of a branched polyethylene have been studied dilatometrically, spectroscopically, and microscopically at small degrees of supercooling (ca. 0-10°C.). In order to assess the extent to which results of different methods are in agreement with each other, apparent induction times and maximuin crystallization rates are compared. On the basis of these data, the results of different experimental techniques using different types of sample are in general agreement. However, there do exist small, but significant, differences which appear to be outside experimental error. The results are shown to be in essential agreement with present theories of nucleation and of crystallization. The observations are interpreted in terms of the processes occurring during crystallization. The relationship of dynamic mechanical properties to previous thermal histories is considered and a qualitative interpretation is presented.
    Additional Material: 11 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Acta Polymerica 46 (1995), S. 60-63 
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: X-ray diffraction measurements on thin films of poly(hexyl-pentylsilane) cast on silicon substrates are presented. The polymer chains pack in a hexagonal lattice which is oriented such that the chains lie parallel to the surface. In addition, a remarkable degree of orientational order was found with the planes containing the neighbor molecules lying in the surface plane. Parallel to the film surface, the average crystallite size is 600 Å, while perpendicular to the surface, there is nearly perfect interchain stacking of the polymers throughout the thickness of the film.
    Additional Material: 7 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2723-2729 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mild, efficient method of nitrating olefins was described recently by Corey and Estreicher. Application of their procedure to diene polymers failed because of the insolubility of the hydrophobic polymer in the aqueous nitromercuration regent. Use of water-immiscible organic cosolvents gave slow nitromercuration with substantial formation of nitrite esters. To overcome these problems a nonaqueous phase transfer-assisted method of rapid selective nitromercuration of diene polymers was developed.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 1505-1516 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Iodine azide adds to cyclohexene in acetonitrile or 4:1 methylene chloride/acetonitrile to give trans-1-azido-2-iodocyclohexane. In methylene chloride this reaction gives a mixture of the cis-and trans-iodoazides owing to competing radical addition. Iodine azide adds to 1-hexene in acetonitrile by an ionic mechanism to give a 3:1 mixture of the 2-azido-1-azido- and 1-azido-2-iodohexanes. Dehydroiodination of the model iodoazides proceeds smoothly with potassium t-butoxide in diethyl ether or THF in the presence of 5 mol % 18-crown-6 at room temperature, giving in the previous example a mixture of 2-azido- and trans-1-azidohexenes. Polybutadiene, carboxyterminated poly(acrylonitrile-co-butadiene), and hydroxy-terminated polybutadiene gave iodoazide derivatives with up to 96% of the theoretical maximum nitrogen content and strong azide IR absorption. High azidoiodination gave polymer with N3/I ratios slightly higher than unity while low percent azidoiodination led to polymer with N3/I ratios of as low as 2:3. All of the nitrogen introduced was in the form of azide function. Dehydroiodination gave polymers with vinyl azide functionality and caused loss of some of the azide groups. All the azidoiodinated polymers decomposed between 120 and 160°C. The dehydroiodinated materials were less stable, decomposing between 100 and 150°C. The temperature of initial decomposition decreased as azide content increased. Polymers with 〉55-60% of the theoretical maximum azide content were shock sensitive.
    Additional Material: 4 Tab.
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