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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. 777-788 
    ISSN: 0887-6266
    Keywords: PMDA-ODA polyimide ; intrinsic molecular properties ; sheet mapping ; fabrication processes ; three-dimensional orientation functions ; anisotropic coefficient of thermal expansion (CTE) ; anisotropic mechanical moduli ; anisotropic compliances ; anisotropic dielectric constants ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A practical methodology for the correlation and prediction of the process-property performance of advanced materials is developed. The model polymer studied is PMDA-ODA polyimide. The connecting link between the process and the properties is the structural state of the polymer. An essential ingredient for a quantitative characterization of the system is a knowledge of its phase state and intrinsic molecular properties. The intrinsic molecular properties define the limiting performance properties available to the polymer. Anisotropic films and sheets produced by five different fabrication processes are examined. Maps of the molecular symmetry axis, the orientation function, and the thickness distributions of two 50-in.-wide sheets fabricated differently are measured nondestructively for process comparison. Four other film fabrication processes are examined and their three-dimensional orientation states determined and correlated. A three-dimensional orientation function triangular plot permits simultaneous representation of the different fabrication processes on the same figure and allows the investigator to choose the most economic and efficient fabrication route. The structure-property study includes the structural correlation and intrinsic molecular property determination of the anisotropic coefficient of thermal expansion (CTE), the anisotropic mechanical moduli and compliances, and the anisotropic dielectric constants. 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 777-788, 1997
    Additional Material: 17 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 19 (1956), S. 463-475 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A polyethyl methacrylate polymer, prepared by the emulsion technique, was fractionated three times to obtain ten fractions. The intrinsic viscosity-molecular weight relations were established in an ideal and in a nonideal solvent at 23°C. Light scattering measurements giving polymer dimensions were compared with the viscosity theories advanced by Debye-Bueche, Kirkwood-Riseman, and Flory-Fox. The calculated values of the effective bond length b for polymethyl methacrylate and polyethyl methacrylate show that polymethyl methacrylate chain has greater hindrance to rotation than the polyethyl methacrylate chain. The results are explained by consideration of the free volume occupied by the solvent molecules.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 12 (1974), S. 1417-1439 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Information, not previously measurable, about the internal crystallization processes occurring within spherulitic films can now be obtained by combining refractive index, birefringence, and small-angle light-scattering measurements. The surroundings of a spherulite in a solid film are composed of both the adjacent spherulites and their interstices (boundaries), and it is shown that different crystallization processes can occur in each of these regions. Upon annealing a quenched isotactic polypropylene film, the rate of crystallization within the interstices of the space-filling spherulites is observed to be greater than the rate of crystallization within the spherulites themselves.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 781-810 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The mechanical properties of poly(ethylene terephthalate) are examined to see if the quantitative morphological criteria previously used to define the structural state of isotactic polypropylene will lead to similar quantitative structure-property correlations when applied to PET. Tenacity, thermal shrinkage in oil and air, tensile modulus, dynamic loss modulus, long spacings, and small-angle x-ray intensities are included in the study. All of the data were obtained from the open literature. In all cases the physical properties correlate simply and quantitatively with the internal structure of the PET, and the character of the correlations leads to new insights into the nature of the internal mechanisms controlling the observed properties. The study shows that only by considering the structural state of a polymer, and not its fabrication parameters, can general, simplifying, quantitative, structure-property correlations be achieved.
    Additional Material: 19 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 2021-2041 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A modus operandi is developed for characterizing, in quantitative morphological terms, the structural changes occurring during the preparation (spinning, drawing, and heat setting) and testing (tensile modulus) of isotactic polypropylene fiber. This involves the application of the following eight different physical techniques: wide-angle x-ray diffraction, birefringence, density, sonic modulus, small-angle x-ray diffraction, dark-field microscopy, small-angle light scattering, and tensile modulus. Structural changes on several organizational levels, the spherulitic, the interlamellar, and the molecular, are determined in this manner and related to the processes involved.
    Additional Material: 15 Ill.
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  • 6
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The small-angle light scattering (SALS) theory for optically anisotropic spheres and disks is examined in depth. An error is found in the existing sphere equations. The correct form of the equations is identified and then experimentally verified for dilute starch suspensions. Increased concentrations and solid films of starch granules are used to identify the effect of concentration on the scattering envelope. Spherulitic films of isotactic polypropylene, isotactic polystyrene, nylon 610, PET, and nylon 66 are then used to examine different aspects of the SALS theory. Experimental observations are found to agree with the predictions of the correct SALS equations. Disk theory is interrogated and correlated with predictions for spheres. It is found that the predicted patterns from spheres and disks are very similar under identical optical conditions, in contradiction to earlier predictions. A method is developed for identifying the optical sign of spherulites too small to be seen in the optical microscope. This study constitutes a comprehensive examination of SALS theory and includes many other aspects of the phenomena. A catalogue of theoretical Vv SALS patterns from spheres and disks is also included.
    Additional Material: 49 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1101-1139 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The submicroscopic morphology of uniaxially deformed isotactic polypropylene films has been examined by small-angle light scattering (SALS), electron microscopy, optical microscopy, small-angle x-ray scattering (SAXS), wide-angle x-ray diffraction, birefringence, sonic modulus, and density methods. Several new interpretations and extensions of existing theories are developed and verified experimentally as follows. (1) The Vv SALS pattern is shown to be a new tool for the identification of the sign of the birefringence of spherulites too small to be seen in the optical microscope. The theoretical dependence of the Vv SALS pattern is developed and verified experimentally with patterns from isotactic polypropylene, polyethylene, Penton, nylon 6,6, poly(ethylene terephthalate), and nylon 6,10. (2) Intraspherulitic lamellar behavior during deformation can be identified from the SAXS pattern. This includes quantitative evaluation of the long spacing between lamellae and their average orientation. (3) The two-phase sonic modulus theory is valid over the wide range of deformations, crystallinities, processing temperatures, and molecular weights used in this study. The deformation of isotactic polypropylene films drawn at 110 and 135°C. has been characterized quantitatively in terms of an integrated picture of mass movement on all morphological levels: the molecular, the interlamellar, and the spherulitic. At both temperatures, the spherulites deform affinely with extension, whereas the deformation mechanisms within the spherulite depend on the location of the radii with respect to the applied load. During spherulite deformation, lamellar orientation and separation processes predominate, whereas at high extensions, fibrillation occurs and crystal cleavage processes predominate. The noncrystalline region orients throughout the draw region. At 135°C. non-orienting relaxation processes appear in the noncrystalline region which retard the rate of molecular orientation with extension.
    Additional Material: 26 Ill.
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  • 8
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A modus operandi is developed for determining the molecular structure of hydroxypropylcellulose (HPC), and characterizing, in quantitative terms, the morphological changes occurring when a water-cast film of the polymer is deformed. This involves the application of the following eleven different physical measurements: wide-angle x-ray diffraction, differential scanning calorimetry, density, melt rheometry, infrared spectroscopy, refractive index, birefringence, sonic modulus, small-angle light scattering, optical and electron microscopy. In addition, a computer was utilized as a mathematical diffractometer. Morphologically, water-cast HPC was observed to have structure at all levels, from the molecular to the supermolecular. The HPC molecule has a backbone of anhydroglucose units twisted into an irregular 31 helix. Intramolecular hydrogen bonding of the poly(propylene oxide) side chains leads to a stiff, rodlike molecule. The molecules are packed into microfibrillar crystallites 470 Å long and 34 Å in diameter. The microfibrils in turn, associate into supermolecular rodlike structures. The structural rearrangements that occur at each morphological level during deformation of HPC film are quantitatively examined and described.
    Additional Material: 36 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 385-432 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Anisotropic growth of β-form crystals of isotactic polypropylene in type III and type IV spherulites has made possible microanalysis of the unit cell structure, optical properties, and crystal arrangement within the spherulites. Micro x-ray studies of the type III and type IV spherulites show that interspherulitic β-form crystals have a hexagonal unit cell with dimensions; a = 19.08 Å and c = 6.49 Å. The intrinsic refractive indices of these β-form crystals are 1.506 along the a axis and 1.536 along the c axis. The organization of the crystals within the spherulites and the optical properties of the spherulites are also quantitatively evaluated. Both the type III and type IV spherulites have the a axis of the crystal radial while the crystals rotate randomly around the type III spherulite radii and periodically around the type IV spherulite radii. The radial refractive index for both the type III and type IV spherulites has the same value of 1.496. The tangential refractive index of the type III spherulite has a constant value of 1.509; it varies periodically between a minimum of 1.496 and a maximum of 1.519 in the type IV spherulite. Microtechniques such as micro x-ray diffraction, interference microscopy, birefringence, and optical microscopy were required for acquisition of the data.
    Additional Material: 21 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 28 (1988), S. 852-856 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The thermal and flow gradients present during thick polymer molding processes can produce layered structures through the thickness which vary in crystallinity, orientation, and axiality. Such structural complexity is difficult, expensive, and time consuming to characterize and presently impossible to predict. In order to overcome these problems emphasis in our laboratory has been directed toward the development of rapid, nondestructive techniques for the quantitative characterization of the structure of thick polymer samples. This includes the characterization of the average structure, the surface structure, and the internal layer structure. The present paper discusses some of these techniques and illustrates their application.
    Additional Material: 5 Ill.
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