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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 5421-5427 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 88 (2000), S. 2108-2117 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Scanning pyroelectric microscopy was applied to study the local thermal diffusivity in polar perhydrotriphenylene (PHTP) inclusion compounds. A thermal wave technique with special heat flow and pyroelectric detection principles was used to measure the longitudinal (K(parallel)) and transversal (K⊥) thermal diffusivity of needle shaped crystals. As expected, we have found a higher thermal conductivity along the channel direction: K(parallel)〉K⊥. K(parallel) also showed a variation along the needle axis, the K(parallel) values near the capping faces being higher than in the center region. Based on these observations we suggest a relation between the longitudinal thermal conductivity and the local density of orientational defects of the dipolar guest molecules which reaches a maximum in the area around the seed. These findings are in agreement with previous pyroelectric studies, revealing a macrodomain structure and a spatially dependent pyroelectric activity for two different PHTP inclusion compounds. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Ionics 7 (1982), S. 225-242 
    ISSN: 0167-2738
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1435-1536
    Keywords: Key words Dielectric spectroscopy ; ɛ′ to ɛ″ conversion ; relaxation loss ; Ohmic conduction ; space charge relaxations ; interfacial polarization ; polymer ; poly(vinyl-chloride) ; numerical KK-transform
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  A numerical Kramers–Kronig transform is described which allows the calculation of dielectric relaxation losses from dielectric constant data measured at a limited set of frequencies differing by a factor of 2. Conversion formulas for both the central frequencies and for frequencies near the edges of the experimental frequency window are derived. The approach used can be extended easily to measurement frequencies with a different logarithmic spacing. Using this conversion, relaxation and dissipative, conduction losses can be separated. In this way Ohmic conduction processes and simultaneously occurring relaxation processes like dipole or space-charge relaxations can be analysed independently. The results of some simulations and of calculations on experimental data for poly(vinyl-chloride) are used to illustrate the potentials of the ɛ′ to ɛ″ conversion.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The amorphous polyester 1a prepared by melt condensation of 1,5-bis-(9-hydroxy-1,4,7-trioxanonyl)naphthalene (2a) and adipoylchloride (3a), which contains bis-1,4,7-trioxanonyl (triethyleneglycol) segments in its main chain, represents a matrix for ion-conducting materials. Despite the fact that only triethyleneglycol segments are present, which are shorter than the minimum required for full solvation of Li+ cations, ion-conductivities of σ = 3.3 times; 10 - 5 S cm - 1 at 368 K are found for Li+/1a 0.25 (cations per polymer repeat unit). Hence, more than one bis-1,4,7-trioxanonyl segment (either intra- or interchain) has to be involved in Li+ complexation. The σ value compares favorably with previous data for more complex polymer matrices.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 34 (1994), S. 697-706 
    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 low frequency dielectric properties of polymeric blends of polycarbonate (PC) and acrylonitrile-butadiene-styrene (ABS) were studied in the temperature interval of 100 to 170°C. Attention was focused on a 60/40 (m/m) PC/ABS blend. The results were compared with dynamic mechanical measurements in torsion and with the results of a morphological investigation using scanning electron microscopy (SEM). Besides the relaxations at the glass transition temperatures of the components an additional strong low frequency dielectric dispersion was observed, which was not found in mechanical measurements. This low frequency polarization process is due to interfacial polarization at the boundaries between conductive ABS and non-conductive or slightly-conductive PC. It is shown how this process can be described by the dielectric models for two-phase heterogeneous materials. The Looyenga model offers the best description of the detected effects, while the Hanai model is less suitable. The shape factor of the ABS phase as used for modeling the dielectric properties agrees well with the observed morphology using SEM. It is shown for the dielectric measurements on the 75/25, 60/40, and 45/55 (m/m) PC/ABS blends how the connectivity of the ABS phase can be sensitively derived from the eletrical conductivity of the blend, whereas mechanical measurements are highly senstive to the connectivity of the PC phase.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 815-825 
    ISSN: 0887-6266
    Keywords: dielectric spectroscopy ; interfacial tension ; liquid crystalline polymer ; blend ; interfacial polarization ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dielectric spectroscopy is an unexplored technique in the elucidation of the morphology of polymer blends. Especially the appearance of interfacial polarization can reveal important information about the microstructure of a polymer blend. A model system of liquid crystalline polymer fibers lined up in a thermoplastic matrix was investigated. After heating above the melting temperature of both phases, the fibers developed distortions which grew with time. Dielectric spectroscopy was used to follow the change in shape of the distorted fibers. The use of only two frequencies made it possible to increase the number of relevant data points in the initial stages of the fiber breakup process. From these measurements it was possible to calculate the growth rate and hence the interfacial tension between the two polymers. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 815-825, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2835-2848 
    ISSN: 0887-6266
    Keywords: dielectric spectroscopy ; interfacial polarization ; Debye length ; particle size ; polymer blends ; laminates ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In this article we will focus on the dielectric properties of laminates and blends of a partially conducting (the liquid crystalline copolyesteramide Vectra B950) and an insulating (polypropylene or mica) phase. Dielectric spectroscopy was used as a tool to obtain information about the influence of the dimensions of the conducting phase in these laminates and blends. With decreasing thickness of the conducting layer in the laminates, the measured permittivities deviate more and more from the values predicted using conventional dielectric mixture models. From this discrepancy it is possible to calculate the thickness of the charge layer (=Debye length) in the conducting phase and the thickness of this phase itself, using a model derived by Trukhan. This model incorporates not only conduction, but also diffusion of the charges. Similar experiments were performed on a system of Vectra B950 particles in a polypropylene matrix. After the derivation of a new model, which combines the Trukhan model for space charges with the Böttcher equation for dielectric mixtures, we could make a distinction between samples containing large and small particles. For samples containing small particles, it is even possible to determine the variation in particle sizes. However, the use of a Debye length of 1.1 µm obtained from the laminates resulted in particle sizes that were two times higher than the actual values. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2835-2848, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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