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  • 1
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 80 (1996), S. 1074-1078 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The oxygen-free x-ray storage phosphor BaFBr, doped with Sr2+ and having Br− vacancies due to fluorine excess, is shown to have a high photostimulability shifted appreciably to lower photon energy compared to nondoped BaFBr because of the predominant generation of FA(Sr2+) centers on the Br− sublattice upon room-temperature x irradiation. The FA(Br−,Sr2+) centers are less stable than unperturbed F(Br−) centers. Therefore, the redshift of the photostimulability disappears upon thermal activation above room temperature. From the failure to observe an F center infrared emission, it is concluded that F and FA centers are spatially correlated to hole centers of yet unknown nature. © 1996 American Institute of 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 79 (1996), S. 4157-4165 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: The x-ray storage phosphor BaFBr:Eu2+ may be made sensitive to stimulation further into the infrared by doping with Ca2+ or Sr2+. This enables the use of light-emitting diodes instead of gas lasers for photostimulation. It is shown by electron paramagnetic resonance (EPR), electron nuclear double resonance (ENDOR), and optically detected EPR and ENDOR that upon x irradiation FA(Br−, Ca2+) centers are formed as photostimulable electron traps in Ca2+-doped BaFBr, in which one of the two nearest Ba2+ neighbors along the c axis is replaced by Ca2+. The FA(Br−, Ca2+) center has tetragonal symmetry as has the F(Br−) center. The optical absorption band of those FA(Br−, Ca2+) centers is red shifted. No FA(Br−, Ca2+) centers have been detected upon additive coloration only. The red shift of the photostimulation spectrum is caused by formation of the FA(Br−, Ca2+, or Sr2+) centers as electron traps. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 22 (1989), S. 3312-3317 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Chemistry of materials 6 (1994), S. 1784-1789 
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 2365-2370 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 26 (1987), S. 135-143 
    ISSN: 1435-1528
    Keywords: Simple shear ; simple extension ; constitutive equation ; strain-energy function ; Valanis-Landel hypothesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract The nonlinear viscoelastic properties of a fairly large class of polymeric fluids can be described with the factorable single integral constitutive equation. For this class of fluids, a connection between the rheological behaviour in different flow geometries can be defined if the strain tensor (or the damping function) is expressed as a function of the invariants of a tensor which describes the macroscopic strain, such as the Finger tensor. A number of these expressions, proposed in the literature, are tested on the basis of the measuring data for a low-density polyethylene melt. In the factorable BKZ constitutive equation the strain-energy function must be expressed as a function of the invariants of the Finger tensor. The paper demonstrates that the strain-energy function can be calculated from the simple shear and simple elongation strain measures, if it is assumed to be of the shape proposed by Valanis and Landel. The measuring data for the LDPE melt indicate that the Valanis-Landel hypothesis concerning the shape of the strainenergy function is probably not valid for polymer melts.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 24 (1985), S. 152-158 
    ISSN: 1435-1528
    Keywords: Mirror relation ; nonlinear viscoelasticity ; polyethylene ; polypropylene ; first normal-stress difference
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract An attempt is made to incorporate into a quasilinear viscoelastic constitutive equation of the Boltzmann superposition type the two mirror relations of Gleissle, as well as his relation between the steady-state first normal-stress difference and the shear viscosity curve. It is shown that the three relations can hold separately within this constitutive model, but not simultaneously, because they require a different nonlinear strain measure, namelyS 12 (γ) =γ − a (γ − 1) (a = 0 forγ ≦ 1,a = 1 forγ ≧ 1) for the mirroring of the viscosities,S 12 (γ) =γ − a (γ−k 2/γ) (a = 0 forγ ≦k, a = 1 forγ ≧k) for the mirroring of the first normal-stress coefficients, and $$S_{12} (\gamma ) = \frac{1}{2}\gamma \{ 1 - erf [ln (\gamma /2 \sqrt k )/\sqrt {2 ln k} ]\}$$ for the third relation. Hereγ denotes the shear strain and erf the error function. Experimental data on melts of a low-density polyethylene, a high-density polyethylene and a polypropylene show that the mirror relations are passable approximations, but that the third relation meets reality surprisingly close if the right value ofk is used.
    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 27 (1989), S. 1009-1016 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress relaxation after a simple elongational step strain, creep under a constant simple elongational stress, and stress build-up under a constant Hencky strain rate have been measured for ultrahigh-molecular-weight polyethylene (UHMW-PE) fibers. The data from the various experiments are consistent with the Boltzman superposition principle in the experimental region of small strains or short times. This leads to a simple constitutive equation in which temperature can be incorporated via time-temperature superposition. The measured power-law relaxation of the UHMW-PE fiber leads to analytical expressions for the dynamic quantities in simple elongation.The constitutive equation is the one-dimensional equivalent of the gel equation derived for cross-linking gels at the gel point. The similarity between the rheological behavior of fibers and cross-linking gels at the transition point might lead to an enhanced understanding of the molecular processes occurring during deformation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1703-1711 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This investigation concerns the important class of fluids whose rheological properties are described by a quasilinear viscoelastic constitutive equation of the Boltzmann superposition type. The first Cox-Merz relation is closely approximated by such a fluid if its nonlinearity in shear can be described by the strain measure $ S_{12} (\gamma) = \int_0^\gamma {J_0} (\upsilon)dv $, irrespective of the distribution of its relaxation times and, hence, its linear viscoelastic properties. Here γ equals the shear strain and J0 the zeroth-order Bessel function. The second Cox-Merz relation is met by materials with a different nonlinearity, namely S12(γ) = Si(γ), where Si is the sine integral. Experimental data on melts of a polystyrene and a low-density polyethylene sample were utilized to demonstrate that both Cox-Merz relations cannot hold simultaneously.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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