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Design of Primary Lithium Cells

The actual positive electrode in cells with a liquid oxidant is made of an inert porous carbon material, on the surface of which cathodic processes (11.9)-(11.11) occur. [Pg.81]

The cells of the lithium-iodine system stand somewhat apart. In such cells, the oxidant is not elementary iodine as such, but it is complex with poly-2-vinylpyridine [CH2CH(C5H5N)] (P2VP). Its composition can be expressed as P2VP ml2. The content of iodine in the complex decreases under discharge, and solid lithium iodide is formed  [Pg.81]

Solid lithium iodide is used in the cells of the lithium-iodine system. Its specific conductivity at the room temperature is several pS/cm. Such cells are characterized by very long-term discharge (years) with very low currents (tens of pA). [Pg.81]

The oxidant is apart of liquid electrolyte in the cells of the lithium-thionyl chloride and lithium-sulfuryl chloride systems. In the first case, such oxidant electrolyte is the lithium tetrachloroaluminate (LiAlC ) solution in pure thionyl chloride or in thionyl chloride with a sulfur dioxide additive in the second case, it is the solution of the same salt in sulfuryl chloride. [Pg.81]

Individual cells with a lithium anode are designed with the capacity of about 1/20 to 20 Ah. Such cells are released both in conventional nominal sizes (AAA, AA, C, D) and in original alternates, which prevents their assembly in equipment designed for manganese-zinc cells or nickel-cadmium batteries. Nonstandard tabs in the form of flat blades, axial acicular pins, and so on are usually provided in lithium cells to eliminate the possibility of the application of a 3 V lithium cell instead of a 1.5 V [Pg.81]


See other pages where Design of Primary Lithium Cells is mentioned: [Pg.81]    [Pg.81]   


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