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Plate electrolyser

Consequently, working temperatures of metal-winning and metal-plating electrolyses with anodic 02 evolution must be operated below 40°C if titanium anodes are intended to be used. Fortunately usually these types of electrolyses are operated at relatively low current densities allowing for relatively low process temperatures. [Pg.110]

Figure 5. Monopolar plate electrolyser with five channels. The volume rate of flow through each of them is equal to V/5. Figure 5. Monopolar plate electrolyser with five channels. The volume rate of flow through each of them is equal to V/5.
Electrochemical background for the deposition of heavy metals 49 Plate electrolyser 56... [Pg.738]

Rectangular parallel plate electrolysers. General-purpose flow electrolysers can be readily modified to act as packed bed electro-... [Pg.371]

Brown, C.J., Fletcher, D., Walsh, F.C., Robinson, D. and Hammond, J.K. (1992) Local mass transport effects in the FMOl parallel plate electrolyser. Journal of Applied Electrochemistry,... [Pg.110]

Lu, R. and Alkire, R. C., 1989, Mass transfer in parallel plate electrolysers with two phase liquid-liquid flow, J. Electrochem. Soc., 131 1059-1067. [Pg.89]

If I were constructing another one, I would have put the gas vent hole in the uppermost corner of the plates so that draining the electrolyte out would be easier when the electrolyser is turned upside down. I would also have put two gas vent holes on each plate at both upper corners to help in equalising the electrolyte levels in each cell when it s turned upside down. You would need the other hole to allow the air to flow freely between the cells when it s turned upside down to equalise the electrolyte levels. [Pg.39]

The electrolyte is filled in through either of the holes. There is no continuos water replacement mechanism. To equalise the electrolyte levels in each cell, the electrolyser needs to be turned upside down. It s crucially important that there are no holes in plates that are in contact with the electrolyte. The gasses are mixed inside... [Pg.39]

The general procedure for the electrochemical preparation of (10) is as follows. A solution of (9) (3 mmol) in wet acetonitrile (40 ml, 5 vol.% of H20) containing sodium perchlorate (0.25 m) was placed in an undivided electrolysis cell equipped with a platinum plate anode and a platinum plate cathode. The system was subjected to a constant current electrolysis (300 mA current density, 20mAcnr2) at ambient temperature. After 4 faradays per mole of (9) had been consumed, the electrolysed solution was poured into water (50 ml) and extracted with dichloromethane (3 X 30 ml). The organic layer was dried with magnesium sulfate and concentrated under reduced pressure. The residue was chromatographed on silica gel to afford (10) in an excellent yield. [Pg.122]

B. Lorenz2 has shown that it is possible to produce permanganate by electrolysing a solution of caustic potash, if a manganese or ferro-manganese anode be used and a cathode of copper oxide (the positive plate of a cupron cell for example). [Pg.27]

The results from Figure 4 show that a catalyst like Pt is not required to carry out the copper(I) oxidation reaction. Thus, the anode of a single-cell electrolysis cell can be a Pt-free graphite separator plate. A Pt-free anode will reduce the capital cost of a large-scale commercial electrolyser quite significantly. [Pg.80]

Note that the heat exchangers are partially imbedded in the insulation thickness. The top portion of each heat exchanger is exposed to the hot zone radiant environment, which helps to insure that the inlet gas streams achieve the desired electrolyser operating temperature prior to entering the stacks. The temperature at the bottom of each heat exchanger will be close to the inlet stream temperature, minimising the thermal load on the hot zone base plate in the vicinity of the tubing penetrations. [Pg.113]

Fig. 12.2 Plate-and-frame electrolyser schemes (a) undivided cell (b) membrane-divided cell (c) solid polymer electrolyte (SPE) reactor (d) membrane-divided cell with GDE (e) SPE-GDE reactor. Liquid compartments are denoted in grey... Fig. 12.2 Plate-and-frame electrolyser schemes (a) undivided cell (b) membrane-divided cell (c) solid polymer electrolyte (SPE) reactor (d) membrane-divided cell with GDE (e) SPE-GDE reactor. Liquid compartments are denoted in grey...
Gas diffusion electrode — (also gas fed electrode) Electrode employed in fuel cells, - electrolysers, and - sensors. The electrode is a porous body prepared in various ways from a variety of materials [i]. Hydrophilic electrodes are mostly made from metals (e.g., nickel). The material is finely dispersed (e.g., by the Raney process) and manufactured into a sheet or plate. Depending on the wetting properties and the pore size, large pores will be wetted and subsequently filled by the electrolyte solution (or molten electrolyte salt), fine pores are not filled... [Pg.292]

The NaCl produced in the solution is collected and used again by re-cycling Except for the preparation of the electrolyte in the beginning, the supplement of sodium chloride is almost unnecessary only potassium chloride is required. The solution is electrolysed using graphite anodes and steel plate cathodes as in the case of (a) and adding a small amount of potassium bichromate. The pH value is adjusted to about 6.5 6.8, the bath voltage 3 1 3 5 and the temperature about O O C. When potassium chloride is added to the electrolyte, the potassium chlorate crystallizes out The crystals are recrystallized, dried, crushed to powder and sieved to requirements. This process has one more double decomposition step than (a), but needs less electric power than (a). [Pg.91]

The second electrolyser was a research unit assembled for SRNL by the University of South Carolina (USC). It was constructed with platinised carbon cloth electrodes, a Nafion 115 PEM electrolyte, carbon paper flow fields, solid graphite back plates, copper current collectors and stainless steel end plates. The USC electrolyser had an active cell area of 40 cm and a Pt catalyst loading of 0.5 mg/ cm (only one-eighth that of the commercial cell). The carbon-based configuration proved to be much more corrosive resistant than the commercial-type electrolyzer. A photograph of the two electrolyzer units is shown in Figure 3. [Pg.254]

If a solution of ammonio ohlonde be electrolysed, foe negative electrode being mercury and the positive a platinum plate) the mercury la observed to swell up, owing to foe formation of a epongy metallic maw. [Pg.89]

Consider a flow-through electrolyser with plate-shaped electrodes in a rectangular channel (Fig. 3). In this case, the Sherwood number is given as... [Pg.53]

Figure 3. Scheme of a flow-through channel electrolyser with plate electrodes d distance between electrodes, L electrode height, w electrode width, v linear velocity of electrolyte. [Pg.54]

Electrolyser of this type can be used to remove metals from their dilute solutions. For example, an electrolyser of the firm CHEMELEC (England) permits the concentration of heavy metal ions to be lowered to 100 mg per litre at an acceptable current yield (tens of per cent). The metal deposited on a plate or rod-shaped cathode can be used as an anode in galvanic plating. There were some doubts about the purity of the recovered metal, which was supposed to contain microscopic glass particles, presumably from disintegrated glass beads. If this... [Pg.61]

Maintenance of chromium plating baths causes ecological problems that can be solved by electrochemical methods, especially by using membrane electrolysers (i.e. electrodialysis) [39-41]. In these processes, chromium(III) is oxidized at the anode, usually made of lead, to chromium(VI), whereby chromic acid is regenerated. The chromic acid consumed in the plating process is then replaced by adding CrO in the solid form. [Pg.72]


See other pages where Plate electrolyser is mentioned: [Pg.39]    [Pg.56]    [Pg.56]    [Pg.39]    [Pg.56]    [Pg.56]    [Pg.941]    [Pg.155]    [Pg.524]    [Pg.550]    [Pg.941]    [Pg.659]    [Pg.941]    [Pg.464]    [Pg.484]    [Pg.31]    [Pg.109]    [Pg.484]    [Pg.216]    [Pg.230]    [Pg.353]    [Pg.659]    [Pg.941]    [Pg.22]    [Pg.594]    [Pg.151]    [Pg.941]    [Pg.57]    [Pg.68]   
See also in sourсe #XX -- [ Pg.57 ]




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