Electrolysis chromium

Finally, chromium metal can be obtained by electrowinning from chromium-rich liquors by two electrochemical processes chromium-alum electrolysis and chromic acid electrolysis. In chromium-alum electrolysis, the chromium-rich liquor is obtained by leaching high-carbon ferrochrome with recycled spent catholyte containing chromium alum [(NHJCr(S0J.12H30] and makeup sulfuric acid. It contains ammonium chromium alum. In chromic acid electrolysis, chromium trioxide is dissolved in deionized water acidified with sulfuric acid. The performance of each electrowinning process is presented in Table 4.85. 

The starting materials of the aldehyde method may be sulfonated. For example. Cl Acid Blue 9 [2650-18-2] Cl Food Blue 2 (Cl 42090), is manufactured by condensing a-(A/-ethylanilino)-y -toluenesulfonic acid with o-sulfobenzaldehyde. The leuco base is oxidized with sodium dichromate to the dye, which is usually isolated as the ammonium salt. In this case, the removal of the excess amine is not necessary. However, this color caimot be used in the food sector because separation of the chromium compounds from the dye is difficult. An alternative method which gives food-grade Cl Acid Blue 9 (14) and dispenses with the use of sodium dichromate employs oxidative electrolysis of the leuco base (49). 

The sodium chlorate manufacturing process can be divided into six steps (/) brine treatment 2 electrolysis (J) crystallisation and salt recovery (4) chromium removal (5) hydrogen purification and collection and (6) electrical distribution. These steps are outlined in Figure 3. 

Chromic Acid Electrolysis. Alternatively, as shown in Figure 1, chromium metal may be produced electrolyticaUy or pyrometaUurgicaUy from chromic acid, CrO, obtained from sodium dichromate by any of several processes. Small amounts of an ionic catalyst, specifically sulfate, chloride, or fluoride, are essential to the electrolytic production of chromium. Fluoride and complex fluoride catalyzed baths have become especially important in recent years. The cell conditions for the chromic acid process are given in Table 7. 

The final solution should be checked for absence of free cyanide. The hypochlorite or CI2 + NaOH method is by far the most widely used commercially (45). However, other methods are oxidation to cyanate using hydrogen peroxide, o2one, permanganate, or chlorite electrolysis to CO2, NH, and cyanate hydrolysis at elevated temperatures to NH and salts of formic acid air or steam stripping at low pH biological decomposition to CO2 and N2 chromium... 

In order that a chromate film may be deposited, the passivity which develops in a solution of chromate anions alone must be broken down in solution in a controlled way. This is achieved by adding other anions, e.g. sulphate, nitrate, chloride, fluoride, as activators which attack the metal, or by electrolysis. When attack occurs, some metal is dissolved, the resulting hydrogen reduces some of the chromate ion, and a slightly soluble golden-brown or black chromium chromate (CtjOs CrOs xHjO) is formed. 

Oxidation A half-reaction in which there is an increase in oxidation number, 88 chromium, 548 electrolysis and, 498 fluorine, 557 halogens, 557-558 oxoacids, 568-570 oxoanions, 568-570 species strength, 506-507q transition metals, 546t zinc, 86-87... 

A number of electrolytic processes are used for the industrial production of metals. Some metals such as zinc, copper, manganese, gallium, chromium, etc. are electrowon from aqueous baths. Another common electrolytic process used is molten salt electrolysis. The most important application of molten salt electrolysis till now has been in the electrowinning of metals. Today aluminum, magnesium, lithium, sodium, calcium, boron, cerium, tantalum, and mischmetal are produced in tonnage quantities by molten salt electrolysis. As a representative example, the electrowinning process for aluminum is taken up. 

Fig. 29. Scheme of the membrane cell used for the chromium electrolysis [260]... 

Pinacol formation from ketones and aldehydes by cathodic reduction has been enhanced in the presence of Cr(II) complexes. Electrolysis of a mixture of ben-zophenone (364) and chromium chloride hexahydrate in a DMF-NaCl04 system... 

Chromium may be produced from high-carbon ferrochrome by electrolytic process. Alternatively, the metal may be obtained by electrolysis of chromic... 

Electrolysis is a very important industrial process. It can be used for metal-plating - putting very thin coatings of expensive metals, such as silver or chromium, onto articles made of cheaper materials. This both improves their appearance and protects them from corrosion. 

The process of electroplating metals is another important application of electrolysis. Metals that easily corrode (Fe and Cu) can be plated by metals that are resistant to corrosion. Chromo - plating steel parts used in vehicles is a good example of electroplating. Steel bumpers become more corrosion-resistant when they are electroplated with nickel first, then with chromium. 

Dehalogenation. Barton et at. (1, 148) effected dehalogenation of steroidal /i-hydroxy halides with chromium(II) acetate and butancthiol as the proton donor in DMSO. The method is only useful with tertiary halides. A recent improvement that permits reduction of halides of all types uses the ethylenediamine complex of CrtCIOzh and the tetrahydropyranyl ethers of the /J-hydroxy halide. Catalytic amounts of the reducing agent can be used in "indirect electrolysis." The reaction is convenient for preparation of deoxynucleosides.1... 

In 1800. William Nicholson and Anthony Carlisle decomposed water into hydrogen and oxygen by an electric current supplied by a voltaic pile. Whereas Volta had pruduced electricity from chemical action these experimenters reversed the process and utilized electricity to produce chemical changes. In 1807. Sir Humphry Davy discovered two new elements, potassium and sodium, by the electrolysis of ihe respective solid hydroxides, utilizing a voltaic pile as the source of electric power. These electrolytic processes were the forerunners of the many industrial electrolytic processes used today to obtain aluminum, chlorine, hydrogen, or oxygen, for example, or in die electroplating of metals such as silver or chromium. 

Quinones can be synthesized by anodic nuclear aromatic substitution, if high-valent chromium(VI) acts as an electrochemically generated and regenerated chemical oxidant in acidic solution (indirect electrolysis) [6] ... 

Chromium tetraphenyl iodide in methyl alcohol or moist chloroform is treated with silver oxide, or the iodide is subjected to electrolysis, using an alcohol solution with a platinum or mercury cathode and a rotating silver anode. One molecule of wTater is removed by drying over calcium chloride. The base forms orange-coloured plates, M.pt. 104° to 105° C. when placed in a bath previously heated to 95° C. It dissolves readily in water or alcohols, is sparingly soluble in chloroform, insoluble in benzene or ether. Measurements of its conductivity in aqueous solution show that it is comparable in strength with the alkali hydroxides, whilst comparative tests in methyl alcohol solution show that it is a stronger base than chromium pentaphenyl hydroxide. It may readily be converted into the chloride, bromide and iodide. 

Closely related to electrorefining is electroplating, the coating of one metal on the surface of another using electrolysis. For example, steel automobile bumpers are plated with chromium to protect them from corrosion, and silver-plating is commonly used to make items of fine table service. The object to be plated is carefully cleaned and then set up as the cathode of an electrolytic cell that contains a solution of ions of the metal to be deposited. 

Electroplating is the process involving electrolysis to plate, or coat, one metal with another or a plastic with a metal. Often the purpose of electroplating is to give a protective coating to the metal beneath. For example, bath taps are chromium plated to prevent corrosion, and at the same time are given a shiny, more attractive finish (Figure 5.19). 

Cyclic voltammetry and controlled-potential electrolysis are the techniques that have been used to investigate the electrochemistry of oxo-chromium and oxo-molybdenum corrolates. The data have been related to those obtained for similar porphyrin complexes. Redox potentials are reported in Table 17. 

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