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Kinetics self-discharge process

REACTION THERMODYNAMICS AND KINETICS 1.4.1 Self-Discharge Process in a Lead-Acid Battery... [Pg.12]

The necessary porosity for thicker layers was introduced by appropriate current densities [321-323], by co-deposition of composites with carbon black [28, 324] (cf. Fig. 27), by electrodeposition into carbon felt [28], and by fabrication of pellets from chemically synthesized PPy powders with added carbon black [325]. Practical capacities of 90-100 Ah/kg could be achieved in this way even for thicker layers. Self-discharge of PPy was low, as mentioned. However, in lithium cells with solid polymer electrolytes (PEO), high values were reported also [326]. This was attributed to reduction products at the negative electrode to yield a shuttle transport to the positive electrode. The kinetics of the doping/undoping process based on Eq. (59) is normally fast, but complications due to the combined insertion/release of both ions [327-330] or the presence of a large and a small anion [331] may arise. Techniques such as QMB/CV(Quartz Micro Balance/Cyclic Voltammetry) [331] or resistometry [332] have been employed to elucidate the various mechanisms. [Pg.357]

The actual self-discharge rates are determined by the mechanisms of processes occurring in self-discharge. Conway (1999) formulated three kinetic cases for which he obtained diagnostic criteria for identification of such processes. They can be stated as follows ... [Pg.307]


See other pages where Kinetics self-discharge process is mentioned: [Pg.23]    [Pg.48]    [Pg.149]    [Pg.92]    [Pg.165]    [Pg.149]    [Pg.40]    [Pg.138]    [Pg.325]    [Pg.307]    [Pg.138]    [Pg.109]    [Pg.150]    [Pg.817]    [Pg.671]    [Pg.42]    [Pg.41]    [Pg.278]    [Pg.310]    [Pg.271]    [Pg.17]    [Pg.413]    [Pg.45]    [Pg.271]    [Pg.264]    [Pg.407]    [Pg.195]    [Pg.186]    [Pg.361]    [Pg.664]    [Pg.60]   
See also in sourсe #XX -- [ Pg.12 ]




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