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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 47 (1996), S. 559-567 
    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: Die Rolle der Lösungszusammensetzung bei der Korrosion von Kupfer in Leitungswasser: Der Einfluß von gelöster Kieselsäure auf den gleichmäßigen und den lokalen AngriffLochkorrosion an Kupferrohren wurde im Labor in synthetischem Leitungswasser mit unterschiedlicher Wasserchemie unter Stagnationsbedingungen bei Raumtemperatur simuliert. Das Hauptinteresse galt dabei dem Einfluß gelöster Kieselsäure auf den gleichmäßigen und lokalen Korrosionsangriff. Langzeitexperimente wurden mittels Tauchversuchen über einen Zeitraum von 8 Monaten durchgeführt. Kurzzeittests erfolgten mittels potentiodynamischer Versuche. Die Untersuchungen haben ergeben, daß der Einfluß von gelöster Kieselsäure dem Verhalten eines anodischen Inhibitors ähnlich ist. In Gegenwart von gelöster Kieselsäure scheint der Korrosionsmechanismus von Kupfer in zwei Stufen abzulaufen: einer anfänglichen, aktivierungskontrollierten Korrosionsreaktion für einen Zeitraum von zwei Monaten und einer nachfolgenden, bzgl. der gelösten Kieselsäure diffusionskontrollierten Reaktion. Der Einfluß des Verhältnisses von gelöster Kieselsäurekonzentration zu Calciumionenkonzentration scheint eine vorherrschende Wirkung der gelösten Kieselsäure anzuzeigen. Der Einfluß des Verhältnisses von gelöster Kieselsäurekonzentration zu Carbonationenkonzentration scheint darauf hinzuweisen, daß steigende Konzentrationen der gelösten Kieselsäure und/oder abnehmende Bicarbonationenkonzentration die Korrosionsgeschwindigkeit intensivieren. Der Einfluß des Verhältnisses von gelöster Kieselsäurekonzentration zu Sulfationenkonzentration scheint eine bestimmende Wirkung der gelösten Kieselsäure anzuzeigen.
    Notes: Pitting of copper pipes was stimulated in the laboratory in synthetic tap waters with various water chemistries under stagnant conditions at room temperature. The primary interest was the effect of dissolved silica on uniform and localized attack. Long term experiments were conducted by immersion tests over eight months period. Short term tests were conducted using cyclic potentiodynamic tests. It is found that the effect of dissolved silica is similar to the behavior of an anodic inhibitor. The corrosion mechanism of copper in the presence of dissolved silica seems to proceed by a two step mechanism. An initial activation control corrosion reaction for a period of two months and a final diffusion control reaction with respect to dissolved silica. The effect of the ratio of dissolved silica to calcium ion concentration seems to indicate the predominate effect of dissolved silica. The effect of the ratio of dissolved silica to carbonate ion concentration seems to indicate the fact that increasing dissolved silica and/or decreasing bicarbonate ion concentration intensifies the corrosion rate. The effect of the ratio of dissolved silica to sulfate ion concentration seems to indicate the predominate effect of dissolved silica.
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 30 (1998), S. 903-912 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diffuse Interface Model (DIM) is introduced to describe the mechanism of high-temperature corrosion/internal oxidation. The zone has dissolved oxygen and metal atoms diffuse and react resulting in the inward movement of zone. The high-temperature oxidation data for cobalt, iron, and nickel, which are for metal deficit (p-type), have been analyzed using a nonlinear optimization method to obtain the optimal values for different parameters, diffusivity of metal atoms in metal oxide, diffiusivity of gaseous species in the corrosion product, diffusivity of oxidant in the unreacted solid (metal or alloy), the rate constant for the reaction and the fraction of the zone reacted. The expression for diffusivity in the reaction zone has been modified by relating diffusivities of the product layer and the core as function of fraction of zone reacted. The model was applied to the experimental data for the high-temperature oxidation of cobalt, iron, and nickel by pure oxygen at an atmospheric pressure. The model predicts the values of diffusion coefficients, preexponential factors, and activation energies for diffusion process, which are generally compared favorably with those reported in the literature. Linear relationship are derived relating the diffusion coefficient in the core and product layer to the parabolic rate constant which is valid for iron, cobalt, and nickel for high-temperature oxidation (900-1350°C) by oxygen at an atmospheric pressure according to the following equations:\scriptfont4=\seveni \scriptscriptfont4=\fivei $$D_{\rm P}=1.4\times 10^{-8}\ \it k_{g}$$ $$D_{\rm C}=6.9\times 10^{-9}\ \it k_{g}$$The results of the model have been successfully used to predict the experimentally determined parabolic rate constants for the oxidation of cobalt at high temperatures for two different investigators [6,7] under similar conditions. © 1998 John Wiley & Sons, Inc. Int J Chem Kinet 30: 903-912, 1998
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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