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Flowing electrolyte

Production of potassium permanganate in the CIS is beheved to be from potassium manganate. Electrolysis of potassium manganate in a continuous-flow electrolytic cell with turbulent electrolyte flow and continuous crystallization has been reported (72). [Pg.78]

Fatigue failure due to underdesign or changes in plant operation of cantilever anodes in flowing electrolytes can occur as a result of vortex shedding. However, with proper design and adequate safety factors these failures can be avoided . [Pg.169]

The electrolyte dropping electrode [63] method, introduced in 1976, and subsequently used in conjunction with the four-electrode potentiostat [64], is a hydrodynamic technique, offering controlled convective transport. In essence, this approach is identical to the dropping mercury electrode [65] however, the drop consists of a flowing electrolyte liquid phase which forms a polarized ITIES with an immiscible continuous (receptor) phase. In... [Pg.346]

To illustrate typical simulation results from such multiphysics SOFC models, consider a co-flow and a cross-flow electrolyte-supported cell. The cross-flow geometry is of particular interest because of the complex transport phenomena offered in this cell configuration, a configuration able to provide detailed understanding of mass-transfer limitations. Structured, orthogonal meshes were used for all compu-... [Pg.522]

Figure 44. Geometry and mesh of a five-channel cross-flow electrolyte-supported SOFC. Figure 44. Geometry and mesh of a five-channel cross-flow electrolyte-supported SOFC.
Figure 45. Current distribution (A/m ) at a cell potential of 0.4 V in the five-channel cross-flow electrolyte-supported SOFC (A/m ) under anode and cathode stoichiometries of 1.5 and 2.0, respectively, and a cell temperature of 1000 °C. Figure 45. Current distribution (A/m ) at a cell potential of 0.4 V in the five-channel cross-flow electrolyte-supported SOFC (A/m ) under anode and cathode stoichiometries of 1.5 and 2.0, respectively, and a cell temperature of 1000 °C.
CEC has recently become an alternative to HPLC. A capillary is filled or its internal wall covered with a porous sorbent. The free volume remaining in the capillary is filled with an electrolyte. High voltage (on the order of ten kV) is applied across the length of the capillary. Sample plugs are introduced at one end. Sample components are carried to the other end due to electro-osmosis and - in the case of ions - also electrophoresis. In CEC the more important effect is electro-osmosis, which is essentially a flow mechanism of the electrolyte solution without the need for applied pressure. The separation of the sample components occurs mainly due to phase distribution between the stationary phase and the flowing electrolyte. Thus CEC is very similar to HPLC in a packed capillary except that the flow is not pressure driven and that ionic analytes undergo electrophoresis additionally to phase separation. [Pg.281]

Figure 8 shows the zeta potentials against pH of the flowing electrolyte solution for the virgin EVAL and grafted with pure dextran after urethanation with 100% HMD I. The -pH of... [Pg.228]

Gabrielli and Perrot [23] carried out in situ mass measurements in well-defined flowing electrolyte with an electrochemical quartz crystal microbaiance (EQCM) adapted to a submerged impinging jet cell (wall tube configuration). The authors employed this new device for the study of nickel electrodeposition and evaluation of the cathodic efficiency. Under the conditions of their experiment (nozzle diameter d = 7 mm disc electrode diameter de = 5 mm and nozzle-to-electrode distance H = 2d), the current that flows at the electrode increases with the square root of flow rate (0-10 cm3 s"1). It should be noted that this approach is much simpler to implement than the rotating EQCM, while keeping control of the convective-diffusion conditions. [Pg.466]

Rote et al. (1993, 1994) used a carotid thrombosis model in dogs. A calibrated electromagnetic flow meter was placed on each common carotid artery proximal to both the point of insertion of an intravascular electrode and a mechanical constrictor. The external constrictor was adjusted with a screw until the pulsatile flow pattern decreased by 25 % without altering the mean blood flow. Electrolytic injury to the intimal surface was accomplished with the use of an intravascular electrode composed of a Teflon-insulated silver-coated copper wire connected to the positive pole of a 9-V nickel-cadmium battery in series with a 250000 ohm variable resistor. The cathode was connected to a subcutaneous site. Injury was initiated in the right carotid artery by application of a 150 xA continuous pulse anodal direct current to the intimal surface of the vessel for a maximum duration of 3 h or for 30 min beyond the time of complete vessel occlusion as determined by the blood flow recording. Upon completion of the study on the right carotid, the procedure for induction of vessel wall injury was repeated on the left carotid artery after administration of the test drug. [Pg.285]

The cell construction ensures a high electrode area per volume unit together with small electrode distances, which, even with poorly conductive electrolytes and/or at low current densities, results in good space-time yields. A high turbulence of the flowing electrolyte is due to the mesh structure and ensures high conversion rates. [Pg.660]

J. Eigeldinger, H. Vogt, The bubble coverage of gas-evolving electrodes in a flowing electrolyte, Electrochimica Acta, Volume 45, Issue 27 (2000) pp4449-4456... [Pg.9]

D. (1995) A flowing electrolytic hydride generator for continuous sample introduction in atomic spectrometry, Anal Chim Acta 316 129-44. [Pg.333]

Saleh, M.M. 2007. Simulation of oxygen evolution reaction at porous anode from flowing electrolytes. Journal of Solid State Electrochemistry 11,811-820. [Pg.298]

Electrochemical corrosion is important to the stability and longevity of implants. Evidence suggests that uniform attack and crevice and pitting corrosion are the most important degradation modes with multipart orthopedic devices (17). Corrosion of devices with blood contact is more complex, due to the oxygenated flowing electrolyte. The cost of this corrosion has not been estimated, but it could be substantially greater than the battery market because the latter is a small fraction of the total cost of the device and associated medical operations. [Pg.45]

FIGURE 17.7 Scheme of a portion of the electrocatalyst in a flow electrolytic cell. [Pg.414]

The steady-flow electrolytic process without recycle, shown in Fig. 13.13, was also used at the plant of Emswerke AG at Ems, Switzerland, to produce 400 iun /h of hydrogen enriched... [Pg.739]

An alternative method of bulk electrolysis involves flowing the solution to be electrolyzed continuously through a porous working electrode (38) of large surface area. Flow electrolytic methods can result in high efficiencies and rapid conversions and are especially convenient where large amounts of solution are to be treated. Flow methods are of use in industrial situations (e.g., removal of metals such as copper from waste streams) and have been broadly applied to electrosynthesis, separations, and analysis. [Pg.441]

Figure 11.6.1 Flow electrolytic cells. Left Cell utilizing glassy carbon granule working electrode (k), silver auxiliary electrode (g), Ag/AgCl reference electrode (o, i) with porous glass separator... Figure 11.6.1 Flow electrolytic cells. Left Cell utilizing glassy carbon granule working electrode (k), silver auxiliary electrode (g), Ag/AgCl reference electrode (o, i) with porous glass separator...
The fluid mechanical and electrical equations governing the distribution of ion concentration and potential in flowing electrolyte solutions were set down in Section 3.4. Recall that for dilute solutions the ion flow is due to migration in the electric field, diffusion, and convection. For simplicity of presentation the following discussion will be restricted to a dilute binary electrolyte, that is, an unionized solvent and a dilute fully ionized salt. [Pg.361]


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