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Dimerization potential step chronoamperometry

Calculation stability implies that At/Ay2 <0.5. The fulfillment of this condition may become a problem when fast reactions, or more precisely, large values of the kinetic parameter, are involved since most of the variation of C then occurs within a reaction layer much thinner than the diffusion layer. Making Ay sufficiently small for having enough points inside this layer thus implies diminishing At, and thus increasing the number of calculation lines, to an extent that may rapidly become prohibitive. This is, however, not much of a difficulty in a number of cases since the pure kinetic conditions are reached before the problem arises. This is, for example, the case with the calculation alluded to in Section 2.2.5, where application of double potential step chronoamperometry to various dimerizations mechanisms was depicted. In this case the current ratio becomes nil when the pure kinetic conditions are reached. [Pg.124]

Double-potential-step chronoamperometry is particularly suited for studying systems that follow EC [11] or dimerization [12] mechanisms. [Pg.60]


See other pages where Dimerization potential step chronoamperometry is mentioned: [Pg.174]    [Pg.129]    [Pg.186]    [Pg.1201]    [Pg.764]    [Pg.639]    [Pg.377]   
See also in sourсe #XX -- [ Pg.105 , Pg.382 , Pg.383 ]




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