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  • 1
    Publication Date: 2011-08-24
    Description: The bulk heat capacities of Li/BCX and Li/SOClN2 cells were determined at 0 and 100 percent depth-of-discharge for 2.0 V cut-off voltage, in the temperature range 0 to 60 C by a method that did not involve the destruction of the cell nor the contact of cell with a liquid. The heat capacities are found to be dependent on state-of-charge, increasing with depth-of-discharge. The Li/BCX DD-cell has a lower heat capacity than a high rate Li/SOCl2 D-cell. The results obtained by this method compare favorably well with results reported in the literature through other methods. The bulk heat capacities of the cells did not change significantly in the temperature range 0 to 60 C.
    Keywords: INORGANIC AND PHYSICAL CHEMISTRY
    Type: Journal of Power Sources (ISSN 0378-7753); 39; 2, Ju
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  • 2
    Publication Date: 2019-07-12
    Description: Results are presented of the calorimetric determination of the effective thermoneutral potential, Eetp, of Li/BCS and Li/SOCl2 cells in the temperature range 0-60 C through a continuous recording of the cell voltage, heat flow, and current. The average effective thermoneutral potential at 25 C was 4.0 and 3.84 V for BCX and Li/SOCl2 cells, respectively. Based on the classical approach, the reversible cell potential, Er, and temperature dependence of reversible cell potential, dEr/dT, for BCX cell were 3.74 V and -0.952 mV/K, respectively, and for Li/SOCl2, Er = 3.67 V and dEr/dT = 0.567 mV/K. The thermal polarization (Eetp-E1), where E1 is the load voltage, for both cells, showed that they are the most thermally efficient near 40 C. An overall reaction proposed for the BCX chemistry is supported by the calculated thermodynamic parameters.
    Keywords: INORGANIC AND PHYSICAL CHEMISTRY
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 139; 10; p. 2755-2759.
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  • 3
    Publication Date: 2019-08-28
    Description: Hydrogen oxidation currents at a NiOOH/Ni(OH)2 electrode were measured directly at constant potentials for various hydrogen pressures and states of charge. It was found that the hydrogen oxidation current is linearly proportional to the hydrogen pressure at all electrode potentials and that the logarithm of the anodic current is a linear function of electrode potential. It was also found that hydrogen oxidation on the nickel substrate material was strongly inhibited by the presence of nickel hydroxide on the substrate surface. By comparing the currents for hydrogen oxidation and oxygen evolution on the NiOOH/Ni(OH)2 electrode and a nickel substrate, it is suggested that the self-discharge of the NiOOH/Ni(OH)2 electrode is mainly due to electrochemical oxidation of hydrogen on the active electrode material.
    Keywords: INORGANIC AND PHYSICAL CHEMISTRY
    Type: Electrochemical Society, Journal (ISSN 0013-4651); 139; 5, Ma; 1282-128
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