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Electrode kinetics, passive state formation

Fig. 4 shows a simple phase diagram for a metal (1) covered with a passivating oxide layer (2) contacting the electrolyte (3) with the reactions at the interfaces and the transfer processes across the film. This model is oversimplified. Most passive layers have a multilayer structure, but usually at least one of these partial layers has barrier character for the transfer of cations and anions. Three main reactions have to be distinguished. The corrosion in the passive state involves the transfer of cations from the metal to the oxide, across the oxide and to the electrolyte (reaction 1). It is a matter of a detailed kinetic investigation as to which part of this sequence of reactions is the rate-determining step. The transfer of O2 or OH- from the electrolyte to the film corresponds to film growth or film dissolution if it occurs in the opposite direction (reaction 2). These anions will combine with cations to new oxide at the metal/oxide and the oxide/electrolyte interface. Finally, one has to discuss electron transfer across the layer which is involved especially when cathodic redox processes have to occur to compensate the anodic metal dissolution and film formation (reaction 3). In addition, one has to discuss the formation of complexes of cations at the surface of the passive layer, which may increase their transfer into the electrolyte and thus the corrosion current density (reaction 4). The scheme of Fig. 4 explains the interaction of the partial electrode processes that are linked to each other by the elec-... [Pg.279]

Corrosion inhibitors are substances whose introduction in small amounts into a corrosion system (aggressive medium, polymer coating, lubricating or packing material, etc.) produces noticeable corrosion abatement in metals. Cl are subdivided into adsorption and passivating Cl by their action mechanism. The former protect metals by affecting the kinetics of the electrode corrosion processes. The latter promote the formation of an oxide or other films on a metal product to transfer the metal into the passive state. [Pg.7]

Factors Involved in Galvanic Corrosion. Emf series and practical nobility of metals and metalloids. The emf. series is a list of half-cell potentials proportional to the free energy changes of the corresponding reversible half-cell reactions for standard state of unit activity with respect to the standard hydrogen electrode (SHE). This is also known as Nernst scale of solution potentials since it allows to classification of the metals in order of nobility according to the value of the equilibrium potential of their reaction of dissolution in the standard state (1 g ion/1). This thermodynamic nobility can differ from practical nobility due to the formation of a passive layer and electrochemical kinetics. [Pg.347]


See other pages where Electrode kinetics, passive state formation is mentioned: [Pg.100]    [Pg.102]    [Pg.308]    [Pg.343]    [Pg.205]    [Pg.75]    [Pg.256]   
See also in sourсe #XX -- [ Pg.247 ]




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Electrode kinetics, passive state

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Passive electrode

State formation

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