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Metals at the Surface

Figure 17.6 Black, graphitically corroded metal at the surface surrounding bright, unaffected metal. Figure 17.6 Black, graphitically corroded metal at the surface surrounding bright, unaffected metal.
Under potential deposition is a much-studied phenomenon in electrochemistry and is the electrochemical reduction of a metal cation to form a monolayer or submonolayer of the corresponding metal at the surface of an electrode. The critical point is that deposition occurs at a potential higher than that dictated by the reversible potential of the metal/metal cation couple, suggesting that such a upd layer is energetically quite different from the bulk metal. However, subsequent deposition on a upd monolayer occurs at the expected potential, and the resulting surface is typical of the bulk metal. [Pg.92]

Bi-layered Cluster (tlie more electronegative metal at the surface)... [Pg.602]

Range 1 x2 < x < 1. Equilibrium is established after all the nickel has been dissolved. A homogeneous alloy, rich in copper, is formed and the concentration of either metal at the surface is equal to the surface enrichment proper to the concentration of the metal in the segment (see Section II, B). [Pg.76]

Conformational factors play a role with large macromolecules. Changes in the conformation of macromolecules may affect the local environment and, thus, the retention energy of specific coordinating groups. Retention of metals at the surface or inside particles may be influenced by similar effects. [Pg.204]

Antropoff and Germann3 found that the presence of very small amounts of alkali metals, at the surface of metallic calcium, very much accelerates its combination with nitrogen these metals apparently act by removing, locally, a layer of oxygen which usually inhibits the combination of calcium with nitrogen. [Pg.244]

When reduced, the liberated metal does not redeposit uniformly over the electrode surface, but instead forms clusters of the metal at the surface ... [Pg.493]

Heteroatonuc contaminants present in the gas and the tar, like Cl and S, react with the metals at the surface of the catalyst. The process is known as catalyst poisoning because the salts formed are not showing catalytic activity towards tar reforming. Some of this poisoning, basically the one associated with the S can be reversible because hi regeneration temperatures can transform the sulfides to sulfates and subsequently decompose the sulfates to SO2/SO3 and the corresponding metal oxides. This is not the case with Cl. [Pg.1678]

Anodic stripping voltammetry. The initial reduction and collection of metals at the surface of an anode, and the subsequent stripping of the metals by oxidation, resulting in a voltammogram that identifies the metals and their respective concentrations. [Pg.644]

The fact that electrons tend to spill out from the metal reflects the mobility of the electron gas within these systems. The distance involved in the formation of the surface dipole is approximately 100 pm. The exact value of x depends on the crystallographic structure of the metal at the surface and reflects the density of metal atoms associated with this structure. For metals with a low melting point, the data for the polycrystalline surface recorded in table 8.2 give the best indication of surface properties. Since the metal atoms are relatively mobile at room temperature, the system tends to maintain the properties described in the jellium model at the surface. [Pg.401]

There is evidence that solid solution formation plays a role in Cd and Mn sorption in suspensions of calcite (CaCOs). Calcite adsorbs these cations initially by a fast reaction that seems to involve exchange of Ca by the trace metal at the surface, that is,... [Pg.161]

Coke deposits from a commercial ESC plant were also examined. Bulk metals concentrations were determined by ashing at 900°C prior to emission spectroscopy analysis. High levels of metals were found at the radiant coil-coke interface due, presumably, to oxide spallation, but concentrations of metals (primarily chromium, iron and titanium,totalling ca200 ppm) were also found into the bulk of the coke and at the coke-process stream interface (Table I). SXAPS examination of coke heated under vacuum for several hours at 900°C also revealed the appearance of up to 1% concentration of metals at the surface of some coke samples, and significantly chromium, iron and titanium were again the metals observed. [Pg.24]

The concentration of catalyst metal at the surface of the graphite target increases during exposure to the laser, which reduces the rate of SWNT formation. Hence a technique simultaneously irradiating a neat and a catalyst-bearing target has been developed that leads to markedly better yields. The amount of SWNT obtained is further influenced by the temperature. The higher it is, the more nanotubes are produced-below 200°C on the other hand, no SWNTs are observed any more. Usually the apparatus is run at a temperature of 1200°C. [Pg.143]

Discussion Metals that either do not displace hydrogen from acids or react with acids very slowly are more or less rapidly attacked by acids in the presence of oxygen. It is probable that the oxygen converts the metal at the surface into an oxide, which then dissolves in the acid. [Pg.213]

Eddy current losses in the copper depend on whether a Cu/Cu cladding or a ss/Cu cladding is used and are affected by the lay angle, of the flexible cable. If one considers only the inner conductor of the coaxial pair (Fig. 1), three surfaces are exposed to magnetic fields, the top surface (field He) and the two surfaces facing the region between layers (field He/2 sec ). Eddy current losses of a thin layer of normal metal at the surface of a superconductor are approximately given by [ ]... [Pg.454]

To detect gases, the presence of a metal at the surface of the sensitive part of the sensor is necessary for electrical contacts. [Pg.277]

For the mixing with sintered pellets, we have only to prepare a mixture of the two powders before the compression operations. This method does not necessarily favor the presence of the metal at the surface of the sample. [Pg.279]


See other pages where Metals at the Surface is mentioned: [Pg.182]    [Pg.56]    [Pg.399]    [Pg.117]    [Pg.446]    [Pg.288]    [Pg.291]    [Pg.432]    [Pg.281]    [Pg.252]    [Pg.141]    [Pg.311]    [Pg.125]    [Pg.314]    [Pg.361]    [Pg.214]    [Pg.133]    [Pg.2973]    [Pg.176]    [Pg.298]    [Pg.29]    [Pg.52]    [Pg.86]    [Pg.247]    [Pg.694]    [Pg.132]    [Pg.296]    [Pg.363]    [Pg.372]    [Pg.438]    [Pg.126]    [Pg.268]   


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The Metallic Surface

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