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Self exchange manganese

DR. SUTIN I think that this is always a problem with exchange reactions involving aquometal ions. The manganese system bears out what Dr. Taube said we have to be sure of the numbers which we are attempting to interpret. In this regard, I believe that the manganese self-exchange rate constant which you referred to was not measured directly. [Pg.132]

Zn(OH)2 is soluble in the alkaline solution as [Zn(OH)3]- until the solution is saturated with K[Zn(OH)3]. In addition Zn(OH)2 can be dehydrated to ZnO. An enhanced power density (when compared with the - Leclanche cell) is accomplished by using particulate zinc (flakes) soaked with the alkaline electrolyte solution. This anode cannot be used as a cell vessel like in the Leclanche cell. Instead it is mounted in the core of the cell surrounded by the separator the manganese dioxide cathode is pressed on the inside of the nickel-plated steel can used as battery container. In order to limit self-discharge by corrosion of zinc in early cells mercury was added, which coated the zinc effectively and suppressed hydrogen evolution because of the extremely low exchange current density... [Pg.20]


See other pages where Self exchange manganese is mentioned: [Pg.311]    [Pg.268]    [Pg.34]    [Pg.140]    [Pg.1122]    [Pg.99]    [Pg.396]    [Pg.85]    [Pg.458]    [Pg.471]    [Pg.1190]    [Pg.191]    [Pg.392]   
See also in sourсe #XX -- [ Pg.29 ]




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