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  • Amico acids  (1)
  • Keywords. Pitting corrosion; Silver anode; Perchlorate anion.  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 130 (1999), S. 1207-1216 
    ISSN: 1434-4475
    Keywords: Keywords. Pitting corrosion; Silver anode; Perchlorate anion.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung.  Passivierung und Lochfraßkorrosion einer Silberelektrode in Natriumperchlorat enthaltenden Natriumhydroxidlösungen wurden mit potentiodynamischen und potentiostatischen Methoden untersucht. In perchloratfreier alkalischer Lösung zeigt das Voltammogramm vor Beginn der Sauerstoffentwicklung drei anodische Peaks. Die ersten beiden entsprechen der Oxidation von Ag und der Bildung einer passivierenden Ag2O-Schicht auf der Elektrodenoberfläche, der dritte einer Umwandlung von Ag2O in AgO. In Gegenwart von ClO4 − wurde eine ausgeprägte Abhängigkeit der Voltammogramme von der Perchloratkonzentration festgestellt. Durch die Anwesenheit von ClO4 − wird die Intensität der drei anodischen Peaks erhöht, und ab einem gewissen Potential bricht die Passivierung unter Eintreten von Lochfraßkorrosion zusammen. Das Lochfraßpotential nimmt linear mit der Konzentration von ClO4 − ab und steigt mit der Scangeschwindigkeit. Die potentiostatischen Strom/Zeit-Diagramme zeigen, daß die Lochfraßkorrosion als diffusionskontrolliertes dreidimensionales Wachstum charakterisiert werden kann.
    Notes: Summary.  The passivation and pitting breakdown of a silver electrode in sodium hydroxide solutions containing sodium perchlorate was studied using potentiodynamic and potentiostatic techniques. In perchlorate-free alkali solution, the voltammogram exhibits three anodic peaks prior to oxygen evolution. The first two peaks correspond to the oxidation of Ag and formation of a passive film of Ag2O on the electrode surface, the third to the conversion of Ag2O to AgO. In the presence of ClO4 −, the voltammogram depends considerably on perchlorate concentration. ClO4 − increases the height of the three anodic peaks, and at potentials above a limiting value breakdown of the anodic passivity and initiation of pitting corrosion occurs. The pitting potential decreases linearly with ClO4 − concentration but increases with scan rate. The potentiostatic current/time transients show that pitting corrosion can be described in terms of an instantaneous three dimensional growth under diffusion control.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 61 (1981), S. 227-242 
    ISSN: 1573-5036
    Keywords: Amico acids ; Carbon dioxide evolution ; Casein ; Decomposition ; Glucose ; Humification ; Mineralization ; Respiration rate ; Phenolic compounds
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The course of the CO2 evolution rates of soil samples has been followed continuously in the absence and in the presence of various organic compounds. After an incubation period of 300 hours at 13 and 20°C the CO2 evolution from pasture soil (containing 1.76% soil organic carbon) amounted to 0.13 and 0.44μg CO2−C.g soil−1.h−1, respectively. For arable soil (containing 1.20% soil organic carbon) the rates amounted to 0.04 and 0.09 μg CO2−C.g soil−1.h−1, respectively. At 20°C larger amounts of the organic substrates added to the soil supplied with 20 μg NH4NO3−N.g soil−1 were lost as CO2 than at 13°C, indicating a higher efficiency of the growth of microorganisms at lower temperatures. In the absence of NH4NO3 the respiration rates were initially higher than in its presence, suggesting that a part of the soil microflora is inhibited by low concentrations of NH4NO3. The amounts of carbon lost were low for phenolcarboxylic acids with OH groups in the ortho position. The replacement of one of these groups by a methoxyl group resulted in a larger amount of the C lost as CO2. The replacement of the COOH group by a C=C−COOH group had a decreasing effect on the decomposition of the phenolic acids tested. The decomposition of vanillic acid,p-hydroxybenzoic acid, and of the benzoic acids with OH groups in the meta position was as complete as that of glucose, amino acids or casein. The decomposition of bacterial cells to CO2 was considerably less than that of glucose. No evidence could be obtained that the low percentage of substrate converted to CO2 at the time of maximal respiration rate was due to the decreasing diffusion rate of substrate to the microbial colonies in the soil during the consumption of substrate.
    Type of Medium: Electronic Resource
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