Reduction electron beam

CVD processing can be used to provide selective deposition on certain areas of a surface. Selective tungsten CVD is used to fill vias or holes selectively through siUcon oxide layers in siUcon-device technology. In this case, the siUcon from the substrate catalyzes the reduction of tungsten hexafluoride, whereas the siUcon oxide does not. Selective CVD deposition can also be accompHshed using lasers or focused electron beams for local heating. 

Vanadium metal can be prepared either by the reduction of vanadium chloride with hydrogen or magnesium or by the reduction of vanadium oxide with calcium, aluminum, or carbon. The oldest and most commonly used method for producing vanadium metal on a commercial scale is the reduction of V20 with calcium. Recently, a two-step process involving the alurninotherniic reduction of vanadium oxide combined with electron-beam melting has been developed. This method makes possible the production of a purer grade of vanadium metal, ie, of the quaUty required for nuclear reactors (qv). 

The vanadium alloy is purified and consoHdated by one of two procedures, as shown in the flow diagram of the entire aluminothermic reduction process presented in Figure 1. In one procedure, the brittle alloy is cmshed and heated in a vacuum at 1790°C to sublime most of the aluminum, oxygen, and other impurities. The aluminum faciHtates removal of the oxygen, which is the feature that makes this process superior to the calcium process. Further purification and consoHdation of the metal is accompHshed by electron-beam melting of pressed compacts of the vanadium sponge. 

Rolling and swaging Vacuum-sintered bar can be cold rolled, and reductions up to 90% between anneals are possible. Arc-cast and electron-beam-melted material is generally forged at room temperature prior to rolling and swaging. 

Non-thermal plasmas can be produced in a number of ways, including a variety of electrical corona discharges, radio frequency discharges, microwave discharges and electron beams. The most common NTP technologies for emission reduction in engine exhaust streams are the following. 

Metallic niobium is generally produced by aluminothermic reduction ofNb205. Generally an excess of A1 is used, producing a Nb-Al alloy to give Nb which may be melted in vacuum or by electron beam or arc furnace. 

Borothermic reduction of oxides enhanced by electron-beam bombardment. Light lanthanide borides have been prepared from the oxides according to a reaction such as the following one (Latini et al. 2002) ... 

The hybridizing component can also be formed directly on the surface of a pristine or modified nanocarbon using molecular precursors, such as organic monomers, metal salts or metal organic complexes. Depending on the desired compound, in situ deposition can be carried out either in solution, such as via direct network formation via in situ polymerization, chemical reduction, electro- or electroless deposition, and sol-gel processes, or from the gas phase using chemical deposition (i.e. CVD or ALD) or physical deposition (i.e. laser ablation, electron beam deposition, thermal evaporation, or sputtering). 

Thorium metal also can he prepared hy thermal reduction of its hahdes with calcium, magnesium, sodium, or potassium at elevated temperatures (950°C), first in an inert atmosphere and then in vacuum. Fluoride and chloride thorium salts are commonly employed. Berzehus first prepared thorium by heating tetrachloride, ThCh, with potassium. Magnesium and calcium are the most common reductant. These metals are added to thorium halides in excess to ensure complete reduction. Excess magnesium or calcium is removed by heating at elevated temperatures in vacuum. One such thermal reduction of hahdes produces thorium sponge, which can be converted into the massive metal by melting in an electron beam or arc furnace. 

The possible formation of an alloyed or a core-shell cluster depends on the kinetic competition between, on one hand, the irreversible release of the metal ions displaced by the excess ions of the more noble metal after electron transfer and, on the other hand, the radiation-induced reduction of both metal ions, which depends on the dose rate (Table 5). The pulse radiolysis study of a mixed system [66] (Fig. 7) suggested that a very fast and total reduction by the means of a powerful and sudden irradiation delivered for instance by an electron beam (EB) should prevent the intermetal electron transfer and produce alloyed clusters. Indeed, such a decisive effect of the dose rate has been demonstrated [102]. However, the competition imposed by the metal displacement is more or less serious, because, depending on the couple of metals, the process may not occur [53], or, on the contrary, may last only hours, minutes, or even seconds [102]. 

For example, when the mixed solution of Ag(CN)2 and Au(CN)2 is irradiated by y-radiolysis at increasing dose, the spectrum of pure silver clusters is observed first at 400 nm, because Ag is more noble than Au due to the CN ligand. Then, the spectrum is red-shifted to 500 nm when gold is reduced at the surface of silver clusters in a bilayered structure [102], as when the cluster is formed in a two-step operation [168] (Table 5). However, when the same system is irradiated at a high dose rate with an electron beam, allowing the sudden (out of redox thermodynamics equilibrium) and complete reduction of all the ions prior to the metal displacement, the band maximum of the alloyed clusters is at 420 nm [102]. 

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