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Metal surfaces static condition surface

Wlien an electrical coimection is made between two metal surfaces, a contact potential difference arises from the transfer of electrons from the metal of lower work function to the second metal until their Femii levels line up. The difference in contact potential between the two metals is just equal to the difference in their respective work fiinctions. In the absence of an applied emf, there is electric field between two parallel metal plates arranged as a capacitor. If a potential is applied, the field can be eliminated and at this point tire potential equals the contact potential difference of tlie two metal plates. If one plate of known work fiinction is used as a reference electrode, the work function of the second plate can be detennined by measuring tliis applied potential between the plates [ ]. One can detemiine the zero-electric-field condition between the two parallel plates by measuring directly the tendency for charge to flow through the external circuit. This is called the static capacitor method [59]. [Pg.1894]

Table 5.1. Adsorption of organic compounds on metal surfaces under static conditions and on the nascent steel surfaces... Table 5.1. Adsorption of organic compounds on metal surfaces under static conditions and on the nascent steel surfaces...
Adsorption Using data from Table 5.1 Adsorption of organic compounds on the metal surface under static conditions and on the nascent steel surfaces , discuss the adsorption activity for each of the following (a) saturated hydrocarbons (n-hexane, cyclohexane), (b) the compounds which have rr-electrons (benzene, 1-hexene), (c) compounds with functional polar groups (propylamine, propionic acid). [Pg.214]

Carpio and coworkers [4] supported this hypothesis via a potentiodynamic study of a set of HN03-containing slurries. The corrosion currents and potentials under both the static and the dynamic conditions were practically the same. This is consistent with the fact that there was no native copper oxide film formed because of the presence of these slurries. As a matter of fact, the corrosion currents decreased slightly upon abrasion of the copper surface. The contact between the metal surface and the abrasive pad may have limited the mass transport of chemicals to and from the copper surface. This was verified via an AC impedance measurement that showed the importance of the systems mass transport. It was also concluded that in a dissolution-controlled process, mechanical abrasion would not enhance the chemical corrosion rate or reduce the mass transport of reactants and/or products in the system. [Pg.203]

Ethyl chloride shows the same kind of linear response to static exposure but at a much lower level. Under static conditions vinyl chloride is adsorbed more readily on the metal than is ethyl chloride. The two-stage interaction seen with vinyl chloride under sliding conditions may indicate its polymerization on the surface when the exposure factor is high enough. [Pg.260]

Die negative order, that is NO inhibition, in N0-H2 reactions over noble metal catalysts is essentially concerned with the periodic operation effect. The periodic operation effect is perhaps due to the surface state of the Rh catalyst. That is, the catalyst surface under static conditions is easily oxidized by NO, so that NO chemisorbs to a smaller degree and reaction rates are suppressed. However, under the optimum cycling feeds, catalyst surface is sufficiently reduced and suitable surface compositions of reactants are maintained in order for reaction to proceed. As a result, the reaction rate reaches the maximum value. The periodic operation effect can be interpreted in terms of the strong affinity between Rh and oxygen and this concept can be extended to interpret the behaviour observed in the C0-02 (Ref. 8) and CO-NO (Ref. 9) systems. [Pg.194]

Friction and corrosion mutually affect one another. Friction violates integrity of the passivating layers on the friction surface of metal parts. Movement of the friction surfaces relative to each other accelerates supply of corrosion matter to the freshly formed surface areas of the mechanical counterbody and removal of the products of electrode reactions. These stages of the electrode process are less intensive in static conditions and follow the mechanism of diffusion or convection. As can be seen, corrosion serves as a catalyzer of mechanical wear during metal friction in electrol3Tes. Mechano-chemical... [Pg.12]

Ejfect of flow regime experienced The speed with which a metal s surface comes to equilibrium with a water, and in some cases the characteristics of the corrosion product which is developed, can depend on the flow regime that it has experienced. At present, the standard sit-and-soak test defines static conditions. However, if this mechanism was thought potentially to be significant, different flow regimes could be incorporated into an ageing procedure to cover this. [Pg.152]


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See also in sourсe #XX -- [ Pg.162 , Pg.163 ]




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Metal conditions

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