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  • 1
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 71 (1992), S. 5834-5840 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: Polymeric electrolytes of the poly(ethylene) oxide (PEO) potassium thiocyanate system have been studied by analyzing the temperature dependence of the low-frequency (0.3–30 Hz) mechanical characteristics. It is found that the local and cooperative molecular motions characterizing the host polymer are strongly influenced by the addition of the salt, as a result of strong interactions between the polymeric chains and the alkaline salt molecules, which ensure the formation of homogeneous complexes. In the low-concentration region (molar fraction X≤0.08) a relevant enhancement of the noncrystallinity and a considerable shift of the glass-to-rubber transition toward higher temperatures characterize the blends. Further salt addition stiffens the material, this peculiarity being connected to the gradual formation of a crystalline complex with a fixed stoichiometry. It is believed that the observed inversion in the structural trend arises from an increase of the interchain interactions via the polarizing effects of the salt molecules. At low temperatures the single γ relaxation, observed in pure PEO and in complexes of the same kind with smaller cations, is modified by the presence of the salt; two close peaks appear, whose strength follows behavior closely correlated to that of the primary relaxation. A quantitative interpretation in terms of a parallel relaxation permits the microscopic origin to be discussed and the underlying local motions to be ascribed to the amorphous fraction of the polymer.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 69 (1991), S. 704-709 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: A study of the frequency (0.1–30 Hz) and temperature (120–373 K) behavior of the internal friction and of the dynamic modulus was carried out in polyethylene oxide (PEO)-Ba(SCN)2 polymeric electrolytes. The mechanical spectra reveal the presence of the following anelastic relaxations: (a) the γ process due to localized movements within the main chain, (b) a process due to relaxing particles introduced by salt, and (c) the αa process associated to the glass-rubber like transition. Both the γ- and αa -loss peaks are shifted to higher temperatures by the addition of salt. A careful analysis of the observed peculiarities permits us to gain an insight on the microscopic nature of the relaxation mechanisms and to associate the γ relaxation with localized segmental motion within the amorphous phase. In pure PEO and in the complex with the lowest salt content, the loss due to the melting transition of PEO crystals is also observed. The cited loss is lacking in the complexes with a salt molar fraction X〉0.05, which show an enormous enhancement of the strength of the αa relaxation. It is argued that the addition of a salt with a divalent cation to semicrystalline PEO gives rise to completely amorphous single phase structures.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Phytochemistry 14 (1975), S. 943-947 
    ISSN: 0031-9422
    Schlagwort(e): Euphorbiaceae ; Leguminosae ; Pisum sativum ; Ricinus communis ; castor bean ; homoserine dehydrogenase. ; pea
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Phytochemistry 19 (1980), S. 1619-1623 
    ISSN: 0031-9422
    Schlagwort(e): Euphorbiaceae ; Graminae ; Leguminosae ; Pisum sativum ; Ricinus communis ; Triticum aestivum ; castor bean ; homoserine dehydrogenase ; pea ; threonine. ; wheat
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Biologie , Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Solid State Communications 67 (1988), S. 561-564 
    ISSN: 0038-1098
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    ISSN: 0277-5387
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Solid State Ionics 58 (1992), S. 55-60 
    ISSN: 0167-2738
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 327-328 (Jan. 2000), p. 75-78 
    ISSN: 1662-9752
    Quelle: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Thema: Maschinenbau
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 33 (1995), S. 93-104 
    ISSN: 0887-6266
    Schlagwort(e): anelasticity ; internal friction ; anharmonicity ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A study of the thermal and mechanical characteristics of polyethylene oxide-Fe(SCN)3 complexes shows the existence of structures which can be described by considering a crystalline phase of pure polyethelene oxide (PEO) and an amorphous phase of PEO with dissolved salt. Increasing salt contents decrease the content of crystals, favoring the formation of complexes with a high degree of noncrystallinity as a result of strong polymersalt interactions which tend to enhance the distortion degree of the polymeric skeleton. The microscopic homogeneity of the complexes is also confirmed by the presence in the thermal and mechanical spectra of single glass transitions, which shift to higher temperatures with increasing salt content. Two molecular relaxations are present in the mechanical behavior of these systems, the γ-and the αa-processes at low and high temperatures, respectively, and show a relaxation strength which increases with decreasing degree of crystallinity of the polymer up to a X ∼ 0.10 molar fraction. Both relaxations exhibit a marked nonexponentiality which has been well accounted for in terms of a gaussian distribution of relaxation times for the γ-process and of the Kolrausch-Williams-Watt exponential function for the αa-process. In the glassy region, the elastic modulus E' reveals a linear temperature dependence which has been interpreted as arising from the anharmonicity of vibrational modes. Increasing noncrystallinity of the system gives rise to an increase of the anharmonicity parameter, which has been ascribed to the influence of the “free volume” in determining the thermal expansivity. ©1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 425-433 
    ISSN: 0887-6266
    Schlagwort(e): temperature dependence ; frequency dependence ; poly(ethylene oxide) ; dielectric constant ; hydrostatic pressure ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Electrical impedance measurements have been made in the frequency range 5 Hz to 10 MHz in pure poly(ethylene oxide) having a molecular weight of 600,000 from 12 K nearly up to the melting point of the crystalline phase (about 330 K). A pronounced relaxation peak in the dielectric loss and a corresponding step in the dielectric constant have been observed at about 240 K, which can be readily related to the glass-rubber transition in the amorphous region of the polymer. As the temperature approaches the melting point there are large increases in the real ε′ and imaginary e′ parts of the dielectric constant. The frequency dependence of ε′ is characterized by a primary relaxation process, whose frequency increases with increasing temperature as a consequence of decrease of the average structural relaxation time. There is strong evidence that this low-frequency dispersion arises mainly from the diffusive transport of ionic charge carriers rather than a purely orientation relaxation process. In addition, the effects of hydrostatic pressures (0-0.25 GPa) on the frequency dependencies of the real ε′ and imaginary ε′ parts of the dielectric constant have been measured in the temperature range from 254 to 329 K. An advantage of applying pressure is that it shifts the αa relaxation peak into an experimentally accessible frequency window of the equipment; the lowering of frequency results from a decrease in the relaxation volume and a consequent reduction in the mobility of the molecular units. Results are discussed in terms of theoretical models of the effect of pressure on the glass transition, providing information on the cooperative dynamics. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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