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  • METALLIC MATERIALS  (3)
  • INORGANIC AND PHYSICAL CHEMISTRY  (1)
  • 2000-2004
  • 1980-1984  (2)
  • 1975-1979  (2)
  • 1960-1964
  • 1950-1954
  • 1
    Publication Date: 2011-08-17
    Description: As a part of a program for the development of a sulfur probe for monitoring the sulfur potential in coal gasification reactors, an investigation was conducted regarding the efficiency of the solid electrolyte cell Ar+H2+H2S/CaS+CaF2+(Pt)//CaF2//Pt)+CaF2+CaS/H2S+H2+Ar. A demonstration is provided of the theory, design, and operation of a solid-state sulfur probe based on CaF2 electrolyte. It was found that the cell responds to changes in sulfur potential in a manner predicted by the Nernst equation. The response time of the cell at 1225 K, after a small change in temperature or gas composition, was 2.5 Hr, while at a lower temperature of 990 K the response time was approximately 9 hr. The cell emf was insensitive to a moderate increase in the flow rate of the test gas and/or the reference gas. The exact factors affecting the slow response time of galvanic cells based on a CaF2 electrolyte have not yet been determined. The rate-limiting steps may be either the kinetics of electrode reactions or the rate of transport through the electrolyte.
    Keywords: INORGANIC AND PHYSICAL CHEMISTRY
    Type: Electrochemical Society; vol. 125
    Format: text
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  • 2
    Publication Date: 2011-08-18
    Description: (Previously announced in STAR as N81-19276)
    Keywords: METALLIC MATERIALS
    Type: Metallurgical Transactions A - Physical Metallurgy and Materials Science; 14A; Feb. 198
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  • 3
    Publication Date: 2019-06-28
    Description: Corrosion of SAE 310 stainless steel in H2-H2O-H2S gas mixtures was studied at a constant temperature of 1150 K. Reactive gas mixtures were chosen to yield a constant oxygen potential of approximately 6 x 10 to the minus 13th power/cu Nm and sulfur potentials ranging from 0.19 x 10 to the minus 2nd power/cu Nm to 33 x 10 to the minus 2nd power/cu Nm. The kinetics of corrosion were determined using a thermobalance, and the scales were analyzed using metallography, scanning electron microscopy, and energy dispersive X-ray analysis. Two corrosion regimes, which were dependent on sulfur potential, were identified. At high sulfur potentials (p sub S sub 2 less than or equal to 2.7 x 10 to the minus 2nd power/cu Nm) the corrosion rates were high, the kinetics obeyed a linear rate equation, and the scales consisted mainly of sulfide phases similar to those observed from pure sulfication. At low sulfur potentials (P sub S sub 2 less than or equal to 0.19 x 10 to the minus 2nd power/cu Nm) the corrosion rates were low, the kinetics obeyed a parabolic rate equation, and scales consisted mainly of oxide phases.
    Keywords: METALLIC MATERIALS
    Type: NASA-TM-81242 , A-8349
    Format: application/pdf
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  • 4
    Publication Date: 2019-06-27
    Keywords: METALLIC MATERIALS
    Type: Oxidation of Metals; 13; Feb. 197
    Format: text
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