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Electrodeposition controlled

The majority of controlled-potential electrochemistry has been carried out at mercury-pool electrodes. This is because of the vast amount of reference data available from polarography. Furthermore, the uniform and reproducible surface, and the high voltage for solvent reduction make the mercury pool particularly attractive relative to solid electrodes. As with electrodeposition, controlled-potential electrolysis rates are dependent on electrode area, stirring rates, solution volume, solution temperature, and supporting electrolyte. If the diffusion layer is uniform and the applied potential is such that one is on the diffusion plateau, the electrolysis obeys the relation... [Pg.97]

Much information for the electrodeposition control is available in situ from analysis of AC response at controllable potential, especially with multi-frequency low amplitude perturbation overlaid on bidirectional potential scans. The latter technique, potentiodynamic electrochemical impedance spectroscopy. [Pg.419]

The typical surface morphologies of Pb formed in each of types of electrodeposition control are shown in Fig. 1.8. The regular hexagonal crystals of Pb as those... [Pg.16]

Anodic deposition is controlled by either fluid shear (cross-flow filtration) (48), similar to gel-polarization control, or by continual anode replacement (electrodeposited paints) (46). High fluid shear rates can cause deviations from theory when E > (49). The EUF efficiency drops rapidly... [Pg.300]

Electrodeposition of Metals. Citric acid and its salts are used as sequestrants to control deposition rates in both electroplating and electroless plating of metals (153—171). The addition of citric acid to an electroless nickel plating bath results in a smooth, hard, nonporous metal finish. [Pg.186]

It was quite recently reported that La can be electrodeposited from chloroaluminate ionic liquids [25]. Whereas only AlLa alloys can be obtained from the pure liquid, the addition of excess LiCl and small quantities of thionyl chloride (SOCI2) to a LaCl3-sat-urated melt allows the deposition of elemental La, but the electrodissolution seems to be somewhat Idnetically hindered. This result could perhaps be interesting for coating purposes, as elemental La can normally only be deposited in high-temperature molten salts, which require much more difficult experimental or technical conditions. Furthermore, La and Ce electrodeposition would be important, as their oxides have interesting catalytic activity as, for instance, oxidation catalysts. A controlled deposition of thin metal layers followed by selective oxidation could perhaps produce cat-alytically active thin layers interesting for fuel cells or waste gas treatment. [Pg.300]

Most of the cases of fretting met with in practice appear to fall into two distinct classes according to whether or not the surfaces involved in the component are intended to undergo some relative motion. If the surfaces are not intended to move, then the first objective should be to prevent slip, either by eliminating the source of vibration, or by increasing the friction between the surfaces. It is believed that the success of certain soft metal electrodeposits in reducing fretting may be due to the improved fit, and hence possibly increased friction, which is obtained from their use. If the displacements cannot be controlled in this way, it may be possible to interpose a thin sheet of an elastic material which can accept the relative movement without slip. [Pg.1333]

Paints are specially formulated for one of two processes. In the first, anodic electrodeposition, the article to be painted is made the anode in a d.c. circuit. Cathodic electrodeposition is the reverse operation. The process takes place under carefully controlled conditions in a tank. Current passes through the paint causing it to deposit uniformly over the article in a uniform film whose thickness can be accurately controlled. The paint film is insoluble in water and exhibits remarkable adhesion after stoving. Electrodeposition is widely used to apply primers, e.g. by car manufacturers, and one coat finishes. [Pg.328]

The principal use of gold is as a very thin coating about 0-05 /xm thick for electrical and electronic applications. Because of the thinness of gold electrodeposits, porosity must be very carefully controlled since seepage of corrosion products from substrate or undercoat exposed at these pores can have serious adverse effects on both appearance and electrical properties of the composite. The porosity can vary with the thickness of the deposit (Fig. 13.1), and with the type of plating bath and with its method of operation (Fig. 13.2), and the phenomenon has been extensively studied by Clarke and many other workers. [Pg.461]

The anionic composition of the cathodic product is not the only parameter that can be controlled through electrolysis conditions. Grinevitch et al. [559] reported on the investigation of the co-deposition of tantalum and niobium during the electrolysis of fluoride - chloride melts. Appropriate electrodeposition conditions were found that enable to obtain either pure niobium or alloys. [Pg.324]

Pavlovic, M. G. Electrodeposition of Metal Powders with Controlled Particle Grain Size and Morphology 24... [Pg.607]

The influence of added agents and inhibitors is important in processes that involve corrosion, electrodeposition, or etching. Mechanistic details remain essentially nnknown. Improved insight wonld benefit technologies that depend on the formation and stabilization of controlled snrfaces. [Pg.174]

By electrodeposition of CuInSe2 thin films on glassy carbon disk substrates in acidic (pH 2) baths of cupric ions and sodium citrate, under potentiostatic conditions [176], it was established that the formation of tetragonal chalcopyrite CIS is entirely prevalent in the deposition potential interval -0.7 to -0.9 V vs. SCE. Through analysis of potentiostatic current transients, it was concluded that electrocrystallization of the compound proceeds according to a 3D progressive nucleation-growth model with diffusion control. [Pg.117]

Aqueous electrolytes proposed in the literature for cathodic electrodeposition of lead selenide are generally composed of dissolved selenous anhydride and a lead salt, such as nitrate or acetate. Polycrystalline PbSe films have been prepared by conventional electrosynthesis from ordinary acidic solutions of this kind on polycrystalline Pt, Au, Ti, and Sn02/glass electrodes. The main problem with these applications was the PbSe dendritic growth. Better controlled deposition has been achieved by using EDTA in order to prevent PbSeOs precipitation, and also acetic acid to prevent lead salt hydrolysis. [Pg.125]

Aqueous cathodic electrodeposition has been shown to offer a low-cost route for the fabrication of large surface n-CdS/p-CdTe solar cells. In a typical procedure, CdTe films, 1-2 xm thick, are electrodeposited from common acidic tellurite bath over a thin window layer of a CdS-coated substrate under potential-controlled conditions. The as-deposited CdTe films are stoichiometric, exhibit strong preferential (111) orientation, and have n-type conductivity (doping density typically... [Pg.137]

Nishino J, Chatani S, Uotani Y, Nosaka Y (1999) Electrodeposition method for controlled formation of CdS films from aqueous solutions. J Electroanal Chem 473 217-222... [Pg.142]


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See also in sourсe #XX -- [ Pg.48 ]




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