Metallic phases, diffusion process

Processes in which solids play a rate-determining role have as their principal kinetic factors the existence of chemical potential gradients, and diffusive mass and heat transfer in materials with rigid structures. The atomic structures of the phases involved in any process and their thermodynamic stabilities have important effects on drese properties, since they result from tire distribution of electrons and ions during tire process. In metallic phases it is the diffusive and thermal capacities of the ion cores which are prevalent, the electrons determining the thermal conduction, whereas it is the ionic charge and the valencies of tire species involved in iron-metallic systems which are important in the diffusive and the electronic behaviour of these solids, especially in the case of variable valency ions, while the ions determine the rate of heat conduction. 

The tlrermodynamic activity of nickel in the nickel oxide layer varies from unity in contact with tire metal phase, to 10 in contact with the gaseous atmosphere at 950 K. The sulphur partial pressure as S2(g) is of the order of 10 ° in the gas phase, and about 10 in nickel sulphide in contact with nickel. It therefore appears that the process involves tire uphill pumping of sulphur across this potential gradient. This cannot occur by the counter-migration of oxygen and sulphur since the mobile species in tire oxide is the nickel ion, and the diffusion coefficient aird solubility of sulphur in the oxide are both vety low. 

Corrosion by liquid metals is usually controlled by diffusion processes in the solid and liquid phases and, unlike aqueous corrosion, does not generally involve galvanic effects, and, even where electrochemical phenomena are known to occur, it has not, in general, been demonstrated that they have been responsible for a significant portion of the corrosion observed . In... 

Although not strictly included within the scope of the present review, decompositions have been considered in the context of related rate processes including sulphide oxidations, sulphidation of oxides and/or metals and diffusion in sulphide phases [689],... 

SECM-induced transfer [SECMIT Fig. 2(b)] can be used to characterize reversible phase transfer processes at a wide variety of interfaces. The basic idea is to perturb the process, initially at equilibrium, through local amperometry at the UME. Hitherto, diffusion-limited electrolysis has mainly been used in conjunction with metal tips, but ion transfer voltammetric probes (discussed briefly in Section III, and in detail in Chapter 15) can also be used. The application of a potential to the tip, sufficient to deplete the... 

Characteristics and implementation of the treatments depend on the expected results and on the properties of the material considered a variety of processes are employed. In ferrous alloys, in steels, a eutectoid transformation plays a prominent role, and aspects described by time-temperature-transformation diagrams and martensite formation are of relevant interest. See a short presentation of these points in 5.10.4.5. Titanium alloys are an example of the formation of structures in which two phases may be present in comparable quantities. A few remarks about a and (3 Ti alloys and the relevant heat treatments have been made in 5.6.4.1.1. More generally, for the various metals, the existence of different crystal forms, their transformation temperatures, and the extension of solid-solution ranges with other metals are preliminary points in the definition of convenient heat treatments and of their effects. In the evaluation and planning of the treatments, due consideration must be given to the heating and/or cooling rate and to the diffusion processes (in pure metals and in alloys). 

Despite the vast quantity of data on electropolymerization, relatively little is known about the processes involved in the deposition of oligomers (polymers) on the electrode, that is, the heterogeneous phase transition. Research - voltammetric, potential, and current step experiments - has concentrated largely on the induction stage of film formation of PPy [6, 51], PTh [21, 52], and PANI [53]. In all these studies, it has been overlooked that electropolymerization is not comparable with the electrocrystallization of inorganic metallic phases and oxide films [54]. Thus, two-or three-dimensional growth mechanisms have been postulated on the basis that the initial deposition steps involve one- or two-electron transfers of a soluted species and the subsequent formation of ad-molecules at the electrode surface, which may form clusters and nuclei through surface diffusion. These phenomena are still unresolved. 

At present the iron-based alloys diffusion saturation by nitrogen is widely used in industry for the increase of strength, hardness, corrosion resistance of metal production. Inexhaustible and unrealized potentialities of nitriding are opened when applying it in combination with cold working [1-3], It is connected with one of important factors, which affects diffusion processes and phase formation and determines surface layer structure, mechanical and corrosion properties, like crystal defects and stresses [4, 5], The topical question in this direction is clarification of mechanisms of interstitial atoms diffusion and phase formation in cold worked iron and iron-based alloys under nitriding. 

The deposition of metals or other phases from dilute solutions onto the surface of an electrode is a special case of the adsorptive process. The deposition peak is similar to that for any soluble electroactive species. However, the reverse peak is large, sharp, and narrow (usually off the chart see Figure 3.11). This occurs because all die reacting substance is on the electrode surface the diffusion process is eliminated and Eq. (3.50) applies. 

Abstract. In the paper we consider the problems with moving bound that model the kinetics of hydrogen desorption from hydrides of metals. Change of phase, desorption processes and size reduction effect are taken into consideration. Equations are derived at various assumptions for the experimental method of thermal desorption spectrometry. As the high-temperature TDS-spectra peaks are considered, the diffusion may be assumed to be fast. Therefore ordinary differential equations are sufficient. We present the results of numerical experiments for the models with bulk and surface desorption. 

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