Oxide films composition

AES has found applications in measuring semiconductor composition, oxide film composition, silicides, metallization, particle analysis and the effects of surface cleaning. AES measurements are made inahigh vacuum environment(10 10 °torr)... 

The theoretical open-circuit anode potential for iron can be calculated assuming that the activity of Fe " in equilibrium is determined by the solubility of a covering layer of Fe(OH)2, in accord with previous discussions of oxide-film composition on iron exposed to aqueous media (see Section 7.1). Using the Nernst equation, we obtain... 

The equilibrium contact angles of cp Ti and Ti-6A1-4V, both passivated in nitric acid, were 52 2° and 56 4°, respectively (Keller et al, 1994). Wettability was measured employing water drops. This similarity in contact angles reflets the similarity in oxide film composition found in the same work. However, the film on the alloy surface was significantly thicker (8.3 1.2nm) than that on the cp Ti (3.2 0.8nm). 

The percolation argument is based on the idea that with an increasing Cr content an insoluble interlinked cliromium oxide network can fonn which is also protective by embedding the otherwise soluble iron oxide species. As the tlireshold composition for a high stability of the oxide film is strongly influenced by solution chemistry and is different for different dissolution reactions [73], a comprehensive model, however, cannot be based solely on geometrical considerations but has in addition to consider the dissolution chemistry in a concrete way. 

BM Structure, composition, and properties should be similar and (4) the FM-containing elements should be able to bring about chemical reduction/decomposition or physical removal of BM oxide film. 

Electrical and Electronic Applications. Silver neodecanoate [62804-19-7] has been used in the preparation of a capacitor-end termination composition (110), lead and stannous neodecanoate have been used in circuit-board fabrication (111), and stannous neodecanoate has been used to form patterned semiconductive tin oxide films (112). The silver salt has also been used in the preparation of ceramic superconductors (113). Neodecanoate salts of barium, copper, yttrium, and europium have been used to prepare superconducting films and patterned thin-fHm superconductors. To prepare these materials, the metal salts are deposited on a substrate, then decomposed by heat to give the thin film (114—116) or by a focused beam (electron, ion, or laser) to give the patterned thin film (117,118). The resulting films exhibit superconductivity above Hquid nitrogen temperatures. 

Alloys having varying degrees of corrosion resistance have been developed in response to various environmental needs. At the lower end of the alloying scale are the low alloy steels. These are kon-base alloys containing from 0.5—3.0 wt % Ni, Cr, Mo, or Cu and controlled amounts of P, N, and S. The exact composition varies with the manufacturer. The corrosion resistance of the alloy is based on the protective nature of the surface film, which in turn is based on the physical and chemical properties of the oxide film. As a rule, this alloying reduces the rate of corrosion by 50% over the fkst few years of atmosphere exposure. Low alloy steels have been used outdoors with protection. 

Stainless steels contain 11% or more chromium. Table 5.1 lists common commercial grades and compositions of stainless steels. It is chromium that imparts the stainless character to steel. Oxygen combines with chromium and iron to form a highly adherent and protective oxide film. If the film is ruptured in certain oxidizing environments, it rapidly heals with no substantial corrosion. This film does not readily form until at least 11% chromium is dissolved in the alloy. Below 11% chromium, corrosion resistance to oxygenated water is almost the same as in unalloyed iron. 

Tantalum is severely attacked at ambient temperatures and up to about 100°C in aqueous atmospheric environments in the presence of fluorine and hydrofluoric acids. Flourine, hydrofluoric acid and fluoride salt solutions represent typical aggressive environments in which tantalum corrodes at ambient temperatures. Under exposure to these environments the protective TajOj oxide film is attacked and the metal is transformed from a passive to an active state. The corrosion mechanism of tantalum in these environments is mainly based on dissolution reactions to give fluoro complexes. The composition depends markedly on the conditions. The existence of oxidizing agents such as sulphur trioxide or peroxides in aqueous fluoride environments enhance the corrosion rate of tantalum owing to rapid formation of oxofluoro complexes. 

It is hardly surprising that the preparation of surfaces of plain specimens for stress-corrosion tests can sometimes exert a marked influence upon results. Heat treatments carried out on specimens after their preparation is otherwise completed can produce barely perceptible changes in surface composition, e.g. decarburisation of steels or dezincification of brasses, that promote quite dramatic changes in stress-corrosion resistance. Similarly, oxide films, especially if formed at high temperatures during heat treatment or working, may influence results, especially through their effects upon the corrosion potential. 

It is a valve metal and when made anodic in a chloride-containing solution it forms an anodic oxide film of TiOj (rutile form), that thickens with an increase in voltage up to 8-12 V, when localised film breakdown occurs with subsequent pitting. The TiOj film has a high electrical resistivity, and this coupled with the fact that breakdown can occur at the e.m.f. s produced by the transformer rectifiers used in cathodic protection makes it unsuitable for use as an anode material. Nevertheless, it forms a most valuable substrate for platinum, which may be applied to titanium in the form of a thin coating. The composite anode is characterised by the fact that the titanium exposed at discontinuities is protected by the anodically formed dielectric Ti02 film. Platinised titanium therefore provides an economical method of utilising the inertness and electronic conductivity of platinum on a relatively inexpensive, yet inert substrate. 

Titanium is a very difficult metal to electroplate because of the presence of an oxide film. Sophisticated pretreatments with acids to remove the oxide film are necessary to achieve good adhesion. Improvements in the level of adhesion can, however, be obtained by heat treatment of the resultant Pt/Ti composites... 

It has now gained acceptance as an impressed current anode for cathodic protection and has been in use for this purpose since 1971. The anode consists of a thin film of valve and precious metal oxides baked onto a titanium substrate and when first developed was given the proprietary name dimensionally stable anode , sometimes shortened to DSA. Developments on the composition of the oxide film have taken place since Beer s patent, and this type of anode is now marketed under a number of different trade names. 

The metallic substrate, clean and rinsed, is immersed wet in the plating cell. The base metals which are usually plated present an essentially metallic surface to the electrolyte, and the slight corrosive action of the rinse water in preventing the formation of any substantial oxide film is important. A critical balance of corrosion processes in the initial stages is vital to successful electroplating, and for this reason there is a severe restriction on the composition of the electroplating bath which may be used for a particular substrate. This will be discussed later. The substrate is made the cathode of the cell it may be immersed without applied potential ( dead entry) or may be already part of a circuit which is completed as soon as the substrate touches the electrolyte ( live entry). Live entry reduces the tendency for the plating electrolyte to corrode the substrate in the period before the surface... 

All of these three properties of the oxide films on metals are influenced by the anion composition and pH of the solution. In addition the potential of the metal will depend on the presence of oxidising agents in the solution. Inhibition of corrosion by anions thus requires an appropriate combination of anions, pH and oxidising agent in the solution so that the oxide film on the metal is stable (the potential then lying between the Flade potential and the breakdown potential), and protective (the corrosion current through the oxide being low). 

Tafe plots The linear part of the anodic or cathodic polarisation log-current and potential plot is extrapolated to intersect the corrosion potential line ". Low corrosion rates can be measured relatively quickly. Note that resultant oxide films may be of different composition from those occurring in practice owing to the several decades of current applied which may not relate to actual plant practice. Portable apparatus including computing facilities is commercially available for plant testing. 

Sample surface unrepresentative. Heterogeneity of the sample was given above as the cause of Class II deviations. The case in which heterogeneity causes one part of a surface to differ from another is clear enough it is often encountered with minerals. Here we wish to direct attention to cases where a surface, though uniform, differs in composition from the bulk of the sample. The cause may be an oxide film thick enough that composition differences between it and the bulk of the sample influence the analytical results. 

Deconvolution of the XPS spectra for the Ir4/ levels reveals a chemical shift of 1.2 eV for the oxidized Ir species at 1.3 Vsce, indicating that Ir occurs in the valence state IV. Kim et al. [60] and also Hall et al. [76] assigned the binding energy of 62 eV with a chemical shift of 1.1-1.2 eV to Ir02. Work performed by Augustynski et al. [77] lead to the conclusion that the anodic film on Ir is Ir(OH)4, while Peuckert determined the film composition to be IrO(OH)2 [78]. 

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