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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 25 (1992), S. 6952-6960 
    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 Chemical Society
    Analytical chemistry 48 (1976), S. 1505-1508 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Physics and Chemistry of Solids 42 (1981), S. 157-162 
    ISSN: 0022-3697
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Physics and Chemistry of Solids 48 (1987), S. 613-619 
    ISSN: 0022-3697
    Keywords: Hydrogen ; PdSi ; amorphous ; chemical potential ; e.m.f. ; high pressure ; site distribution
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 70 (1991), S. 172-181 
    ISSN: 1089-7550
    Source: AIP Digital Archive
    Topics: Physics
    Notes: Nonstationary and stationary concentration profiles of vacancies in a grain boundary are calculated for the case of electromigration and various conditions of vacancy formation and annihilation. If supersaturation of vacancies is assumed for void formation, current densities necessary for voiding have to be larger than a critical value jcrit, which is related to the length l of the grain boundary by the relation ljcrit=const. An estimation of the value of the constant in the last equation is in agreement with experimental values. An approximate equation for the median time to failure (MTF) is derived from the model for grain boundaries conducting the flux of matter parallel or in series. The results explain many features of experimental studies. First values of MTF for a network of grain boundaries obtained by computer simulations are presented as well, and the effect of resistance heating and nonstationarity on the current exponent is discussed in some detail.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Electrochimica Acta 32 (1987), S. 1619-1629 
    ISSN: 0013-4686
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Surface Science 83 (1979), S. 296-300 
    ISSN: 0039-6028
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Communications 35 (1980), S. vi-vii 
    ISSN: 0038-1098
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 42 (1991), S. 169-178 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Auger-spectroscopic investigations into pitting corrosion of FeCr, FeMo and FeCrMo alloysA single pit was produced on binary iron-chromium (Fe17Cr), iron-molybdenum (Fe1Mo, Fe3Mo, and Fe5Mo) and ternary iron-chromium-molybdenum alloys (Fe17CrxMo, x = 1, 3, 7 wt.%) in 0.5 M H2SO4 with Cl- additions (0.02 to 0.08 molar) at room temperature. Compositional changes at the bottom of the pit and in the surrounding passive film were determined using high resolution Auger-Electron Spectroscopy (AES). The chromium and molybdenum content of the passive layers are not changed in the presence of Cl- and there is no incorporation of chlorine in the passive film as long as the films were formed in a chlorine-free electrolyte and Cl- was added later. At the bottom of the pits salt films could be determined in all cases after removing the electrolyte with filter paper. These salt films are strongly enriched in chromium, molybdenum and chlorine. The salt film was not detectable for Fe-Cr after rinsing the samples with distilled water, whereas in the case of molybedenum additions the salt film could not be washed away with water.
    Notes: Ein einzelnes Loch wurde auf der passiven Oberfläche von Eisen-Chrom-(Fe17Cr), Eisen-Molybdän-(Fe1Mo, Fe3Mo und Fe5Mo) und ternären Eisen-Chrom-Molybdän-Legierungen (Fe17CrxMo, x = 1, 3, 7 Gew.%) durch Lochkorrosion in 0,5 M H2SO4 mit Cl--Zusätzen von 0,02 und 0,08 Mol/l bei Raumtemperatur erzeugt. Die Zusammensetzung des Lochbodens und der umgebenden Passivschicht wurde mit Hilfe der hochauflösenden Augerelektronenspektroskopie (AES) bestimmt. Der Chrom- und Molybdängehalt des Passivfilmes wird durch die Anwesenheit der Cl--Ionen nicht verändert, und es wird kein Chlor in den Passivfilm eingebaut, solange der Film in chloridfreiem Elektrolyt gebildet und Cl- später zugesetzt wurde. Auf dem Lochboden konnten in allen Fällen Salzfilme festgestellt werden, nachdem der Elektrolyt mit Filterpapier aufgesogen wurde. Diese Salzfilme waren stark mit Chrom, Molybdän und Chlor angereichert. Bei der Fe-Cr-Legierung konnte der Salzfilm nach Spülung mit Wasser nicht mehr nachgewiesen werden, während bei den molybdänhaltigen Legierungen der Salzfilm mit Wasser nicht entfernt werden konnte.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 31 (1993), S. 1373-1382 
    ISSN: 0887-6266
    Keywords: partial molar volume ; glassy polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The sorption of atoms or molecules in glassy polymers is assumed to occur within a variety of sites belonging to the intermolecular volume and providing different space for the dissolved molecules. If the size of the small molecule is larger than the size of the site, the glassy polymer is elastically distorted during sorption of the solute molecules. Minimizing the total free energy yields the result that large sites are occupied first, giving rise to small volume changes only. By increasing the solute concentration, smaller sites have to be occupied as well and the corresponding volume changes are larger. Thus the molecules can be considered to act as probes for the intermolecular space. A quantitative analysis and comparison with experimental results provides information on the intermolecular space in a glassy polymer. Compared to the dual-sorption model, the model of this study is able to explain the nonlinear relationship between volume change of the polymer and the partial pressure of the solute. At large solute concentrations, swelling of the glassy polymer or its transformation into the rubbery state occurs, which gives rise to structural changes after desorption. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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