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Electrodeposition system

Significant advances in waterborne coatings have been made by PPG Industries utilizing epoxies as co-resins. These coatings are used in cathodic electrodeposited systems, widely accepted for automobile primers. Many patents have been issued for this important technology (50,51). [Pg.370]

In his classic treatise, Brenner reported that over 500 alloy electrodeposition systems had then been studied in depth —that number has now been substantially increased — yet barely 10 to 20 have any real degree of industrial exploitation. The list continues to grow and the present type of work on alloys can be divided into three classes ... [Pg.377]

As noted earlier, the kinetics of electrochemical processes are inflnenced by the microstractnre of the electrolyte in the electrode boundary layer. This zone is populated by a large number of species, including the solvent, reactants, intermediates, ions, inhibitors, promoters, and imparities. The way in which these species interact with each other is poorly understood. Major improvements in the performance of batteries, electrodeposition systems, and electroorganic synthesis cells, as well as other electrochemical processes, conld be achieved through a detailed understanding of boundaiy layer stracture. [Pg.174]

Fig. 1. Schematic diagram of automated flow electrodeposition system, for forming thin films using EC-ALE. Fig. 1. Schematic diagram of automated flow electrodeposition system, for forming thin films using EC-ALE.
Electrolyte mixing is necessary to maintain the particles in suspension, unless the particles are neutrally buoyant, and to transport the particles to the surface of the electrode. The hydrodynamics of the electrodeposition system control the rate, direction, and force with which the suspended particles contact the electrode surface. Bringing the particles in contact with the electrode is a necessary step for the incorporation of particles into the metal matrix, although particle-electrode contact does not guarantee incorporation of the particle. Of course, an increase in flow can increase the plating rate as the thickness of the diffusion layer at the electrode surface decreases. [Pg.200]

Initially, a thin layer flow cell (Fig. 19) was used in this group to study the EC ALE formation of compounds [158] and in studies of electrochemical digital etching [312,313], Wei and Rajeshwar [130] used a flow cell system to deposit compound semiconductors as well, however, the major intent of that study was to form superlattices by modulating the deposition of CdSe and ZnSe. Their study appears to be the first example of the use of a flow electrodeposition system to form a compound semiconductor superlattice. [Pg.121]

EIG. 19. Automated flow electrodeposition system, initial design. Thin layer ceU design. [Pg.121]

Follow the column, disk, and electroplating preparation instructions that are given below the procedure. Follow the instructor s directions if the laboratory has a different electrodeposition system and procedure. [Pg.121]

We specifically note in this latter case the link between the geometric features of the electrodeposition system and the electric field distribution near the electrode that influences the growth rate and the final product quality [5], For example, dendrite growth is considered as a cause for failure of rechargeable batteries [6-9]. Thus, a good knowledge of dendrite growth is necessary, in particular for very small batteries with limited electrode separation [10,11]. [Pg.480]

Diener (46) and Tsuchiya (47) have shown carboxyl-reactive nitrile liquids to have utility in both aqueous and non-aqueous anodic and cathodic electrodeposition systems aimed at primers and coatings. Excellent coating adhesion is demonstrated with advantages noted in moisture resistance and reverse impacts. Diener suggests an electrocoat system as a replacement for standard solvent-based primers used with aircraft adhesives. [Pg.10]

The confirmation of the above theories with accent on the analysis of the effect of exchange current density on the thin metal film formation on inert substrates can be obtained in the following way. In Chap. 1 (see Fig. 1.13 and Table 1.2) are given the polarization curves, the exchange current density values, and ijjio ratios for three different electrodeposition systems (Cd, Cu, and Ni) characterized by the substantially different value exchange current densities [13, 63]. [Pg.63]

Huang B et al (1995) Preliminary studies of the use of an automated flow-cell electrodeposition system for the formation of CdTe thin films by electrochemical atomic layer epitaxy. J Electrochem Soc 142 3007-3016... [Pg.430]

When taking an electrochemical process from the laboratory into manufacturing, the current distribution is a key design consideration. For example, in an electrodeposition system, film thickness (proportional to local current density through Faraday s law) may be uniform on a small electrode but highly nonuniform on a large electrode. In a perhaps less obvious... [Pg.464]

Tenting with dry film becomes difficult when annular rings are very small or in some cases when there are no annular rings at all. In such cases, a positive electrodeposition system may be applied to overcome this difficulty. [Pg.742]

In the electrodeposition experiments, a Cu substrate and a prismatic Nd-Fe-B rod were used as a cathode and an anode, respectively. A platinum QRE was used for this electrodeposition system because the applied overpotential was precisely induced on both electrodes. The electrodeposition of the Dy metal from 0.1 mol dm [Dy(TFSA)5] in [P2225] [TFSA] at 393 K was conducted under an Ar atmosphere (H2O <1.0 ppm) in a glove box at 393 K. The applied overpotential on the cathode for the potentiostatic electrolysis was set at —3.8 V based on the above nucleation study. The potentiostatic electrolysis was carried out while stirring the electrolyte at 500 rpm in order to increase the ciurent density of electrodeposition by continuously supplying the electroactive species [Dy(TFSA>5] to the electrode surface. [Pg.142]


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See also in sourсe #XX -- [ Pg.134 ]




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