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Anodic oxides current efficiency

The oxygen contribution from these reactions is dependent on the nature of the anode material and the pH of the medium. The current efficiency for oxygen is generally 1—3% using commercial metal anodes. If graphite anodes are used, another overall reaction leading to inefficiency is the oxidation of... [Pg.482]

Ethylene glycol can be produced by an electrohydrodimerization of formaldehyde (16). The process has a number of variables necessary for optimum current efficiency including pH, electrolyte, temperature, methanol concentration, electrode materials, and cell design. Other methods include production of valuable oxidized materials at the electrochemical cell s anode simultaneous with formation of glycol at the cathode (17). The compound formed at the anode maybe used for commercial value direcdy, or coupled as an oxidant in a separate process. [Pg.359]

Fused-salt electrolysis of K2NbFy is not an economically feasible process because of the low current efficiency (31). However, electrowinning has been used to obtain niobium from molten alkaU haUde electrolytes (32). The oxide is dissolved in molten alkaU haUde and is deposited in a molten metal cathode, either cadmium or zinc. The reaction is carried out in a ceramic or glass container using a carbon anode the niobium alloys with the cathode metal, from which it is freed by vacuum distillation, and the niobium powder is left behind. [Pg.23]

The standard potential for the anodic reaction is 1.19 V, close to that of 1.228 V for water oxidation. In order to minimize the oxygen production from water oxidation, the cell is operated at a high potential that requires either platinum-coated or lead dioxide anodes. Various mechanisms have been proposed for the formation of perchlorates at the anode, including the discharge of chlorate ion to chlorate radical (87—89), the formation of active oxygen and subsequent formation of perchlorate (90), and the mass-transfer-controUed reaction of chlorate with adsorbed oxygen at the anode (91—93). Sodium dichromate is added to the electrolyte ia platinum anode cells to inhibit the reduction of perchlorates at the cathode. Sodium fluoride is used in the lead dioxide anode cells to improve current efficiency. [Pg.67]

According to Faraday s law, one Faraday (26.80 Ah) should deposit one gram equivalent (8.994 g) of aluminum. In practice only 85—95% of this amount is obtained. Loss of Faraday efficiency is caused mainly by reduced species ( Al, Na, or A1F) dissolving or dispersing in the electrolyte (bath) at the cathode and being transported toward the anode where these species are reoxidized by carbon dioxide forming carbon monoxide and metal oxide, which then dissolves in the electrolyte. Certain bath additives, particularly aluminum fluoride, lower the content of reduced species in the electrolyte and thereby improve current efficiency. [Pg.97]

Discussion. Bromine may be electro-generated with 100 per cent current efficiency by the oxidation of bromide ion at a platinum anode. Bromination of oxine proceeds according to the equation ... [Pg.542]

Carboxylic acids can be converted by anodic oxidation into radicals and/or carbo-cations. The procedure is simple, an undivided beaker-type cell to perform the reaction, current control, and usually methanol as solvent is sufficient. A scale up is fairly easy and the yields are generally good. The pathway towards either radicals or carbocations can be efficiently controlled by the reaction conditions (electrode material, solvent, additives) and the structure of the carboxylic acids. A broad variety of starting compounds is easily and inexpensively available from natural and petrochemical sources, or by highly developed procedures for the synthesis of carboxylic acids. [Pg.142]

Furan was dimethoxylated to give 2,5-dihydro-2,5-dimethoxyfuran, using electrogenerated bromine molecules generated from bromide salts in electrolyte solutions [71]. This reaction was characterized in classical electrochemical reactors such as pump cells, packed bipolar cells and solid polymer electrolyte cells. In the last type of reactor, no bromide salt or electrolyte was used rather, the furan was oxidized directly at the anode. H owever, high consumption of the order of 5-9 kWh kg (at 8-20 V cell voltage) was needed to reach a current efficiency of 75%. [Pg.499]

OH/oxide species. At potentials anodic of 1 V, incomplete oxidation of formaldehyde to formic acid is activated, while methanol oxidation is almost completely hindered. This reflects an easier oxidation of the C-H group in the aldehyde than in the alcohol. For the negative-going scan, where the COadouble-peak stmcture in the current efficiency. [Pg.453]

Mixing of the electrode products causes hydrolytic precipitation of the nickel and, after separation of the nickel hydroxide, the filtrate was returned to the cells. The sequence of the electrolytic purification steps is outlined in Figure 6.28. Nickel hydroxide slurry is first added to the anolyte for the purpose of raising the pH to 3.7 (2 H+ + Ni(OH) = Ni2+ + 2 H20), and iron(II) is oxidized by introducing chlorine. This causes hydrolytic precipitation of the iron(III) and corrects the nickel ion deficiency by the low anodic current efficiency. The iron(III) hydroxide is removed by filteration. The clarified solution is then treated with nickel carbonate and further chlorine to oxidize the cobalt(II) and allow its separation as cobalt(I II) hydroxide. [Pg.724]

However, in a similar solvent with autoprotolysis such as m-cresol, 100% current efficiency could not be obtained in anodic oxidation with respect to base titrations. According to a further study158, the following reaction scheme seems most probable ... [Pg.311]

Satisfactory agreement of experiments with kinetic laws, described by Eqs. (44) and (45), are observed only for tantalum and niobium, when the current efficiency approaches 100%. Even for these metals, certain deviations occur which could be attributed to space charge effects,82 electronic leakage currents,83 or other factors. In the case of aluminum, these deviations are relatively large, as, even in barrier-forming electrolytes, some oxide dissolution takes place from the very beginning of voltage supply to an anodized sample.32... [Pg.426]

Active anodic dissolution occurs when all the electrochemically oxidized aluminum passes into the aqueous phase and the oxide layer does not grow, i.e., the current efficiency of oxide formation... [Pg.433]

The product, l,4-diacetoxy-2-allyl-3-methyl-2-cyclopentene, obtained (45% current efficiency) from 2-allyl-3-methyl-l,3-cyclopentadiene through anodic oxidation with carbon rod anode in acetic acid is successfully used as a starting compound in the synthesis of allethrolone as shown in equation 23. [Pg.754]

The work on the electrochemical generation of a solution of ceric sulphate from slurry of cerous sulphate in 1-2 M sulphuric acid was abandoned by BCR due to difficulties encountered in handling slurried reactants. A 6kW pilot reactor operated at 50 °C using a Ti plate anode and a tungsten wire cathode (electrolyte velocity about 2ms 1) produced 0.5 M Ce(S04)2 on the anode with a current efficiency of 60%. The usefulness of Ce(IV) has been limited by the counter anions [131,132], Problems include instability to oxidation, reactivity with organic substrates and low solubility. Grace found that use of cerium salts of methane sulfonate avoids the above problems. Walsh has summarized the process history, Scheme 6 [133],... [Pg.160]

DSA-02 oxide-coated Ti anode (DSA = Dimensionally Stable Anode) is placed, thus creating a large cathode volume. The effluent solution flows perpendicularly through the electrodes with a typical flow rate of 0.5 dm3 s-1. The flowthrough metal electrodes have an active area approximately 15 times their geometric area. The cell allows air sparging to increase the mass-transfer. The current efficiency is about 40% when the inlet concentration of the metal ions is 150 to 1500 ppm and the concentration at the out-let is about 50 ppm. The cell is currently used for the treatment of recirculated wash-waters from acid copper, copper cyanide, zinc cyanide, zinc chloride, cadmium sulphate, cadmium cyanide and precious metal plating and washwaters from electroless copper deposition. Since the foam metal electrodes are relatively expensive the electrodes... [Pg.190]

In the addition to nonactivated alkenes, where the direct anodic oxidation is less, satisfactorily good yields can be achieved when Mn(OAc)2 is used as mediator (Table 8, entries 6, 7). Sorbic acid precursors have been obtained in larger scale and high current efficiency by a Mn(III)-mediated oxidation of acetic acid/acetic anhydride in the presence of butadiene [112]. [Pg.144]

Since paired electrosynthesis of nitrones from Af-hydroxylamines can proceed by both anodic and cathodic oxidation, the current efficiencies are very high . [Pg.503]


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See also in sourсe #XX -- [ Pg.95 , Pg.98 , Pg.100 ]




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Anode current

Anode efficiency

Anode oxidation

Anodes oxides

Anodic current

Anodic oxidation

Anodic oxidation) current

Anodic oxides

Current anodization

Current efficiency

Oxidation current

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