Anode anodic oxidation

Eloxierung anodization, anodic oxidation Eluat eluate eluieren eluate eluotrope Reihe (Ldsungsmittelreihe) eluotropic series Elutionskraft... 

Siher(Il) oxide, AgO, is a black solid, Ag Ag 02, obtained by anodic or persulphate oxidation of an AgNOs solution. Continued anodic oxidation gives impure Ag203. Argentates, e.g. K.AgO, containing silver(I) are known. 

The metal anodic oxidation reaction, Fe Fe + 2e, can be written in tlie standard (reduction) notation as ... 

The above rate law has been observed for many metals and alloys either anodically oxidized or exposed to oxidizing atmospheres at low to moderate temperatures—see e.g. [60]. It should be noted that a variety of different mechanisms of growth have been proposed (see e.g. [61, 62]) but they have in common that they result in either the inverse logaritlnnic or the direct logarithmic growth law. For many systems, the experimental data obtained up to now fit both growth laws equally well, and, hence, it is difficult to distinguish between them. 

Young L 1961 Anodic Oxide Fiims London Aoademio)... 

This is a process of anodic oxidation. The ammonium peroxo-disulphate formed is then hydrolysed and the solution distilled in... 

Films, anodic oxide Films, passivating Films, plastic Film theory Film wrappers Filter Filter aid Filter aids Filter fabrics Filtering centrifuges Filter media Filters... 

At low temperatures, oxidation with chromic acid gives propynal [624-67-9] C2H2O (14), or propynoic acid [471-25-0] C2H2O2 (15), which can also be prepared in high yields by anodic oxidation (16). 

Perfluoroepoxides have also been prepared by anodic oxidation of fluoroalkenes (39), the low temperature oxidation of fluoroalkenes with potassium permanganate (40), by addition of difluorocarbene to perfluoroacetyl fluoride (41) or hexafluoroacetone (42), epoxidation of fluoroalkenes with oxygen difluoride (43) or peracids (44), the photolysis of substituted l,3-dioxolan-4-ones (45), and the thermal rearrangement of perfluorodioxoles (46). 

The scope of oxidation chemistry is enormous and embraces a wide range of reactions and processes. This article provides a brief introduction to the homogeneous free-radical oxidations of paraffinic and alkylaromatic hydrocarbons. Heterogeneous catalysis, biochemical and hiomimetic oxidations, oxidations of unsaturates, anodic oxidations, etc, even if used to illustrate specific points, are arbitrarily outside the purview of this article. There are, even so, many unifying features among these areas. 

C. HIO is prepared by oxidation of iodine with perchloric acid, nitric acid, or hydrogen peroxide or oxidation of iodine in aqueous suspension to iodic acid by silver nitrate. Iodic acid is also formed by anodic oxidation at a platinum electrode of iodine dissolved in hydrochloric acid (113,114). 

The best known oxoanion of iron is the ferrate(VI) prepared by oxidizing a suspension of hydrous iron(III) oxide in concentrated alkah with potassium hypochlorite or by anodic oxidation of iron in concentrated alkah. Crystals of potassium ferrate [13718-66-6], K FeO, are deep purple, orthorhombic, and contain discrete tetrahedral [FeOJ anions. Barium ferrate [13773-23A] can be precipitated from solutions of soluble ferrate salts. 

Electrolytic Manganese Dioxide. The anodic oxidation of an Mn(II) salt to manganese dioxide dates back to 1830, but the usefuhiess of electrolyticaHy prepared manganese dioxide for battery purposes was not recognized until 1918 (69). Initial use of electrolytic manganese dioxide (EAfD) for battery use was ia Japan (70) where usage continues. 

The purple permanganate ion [14333-13-2], MnOu can be obtained from lower valent manganese compounds by a wide variety of reactions, eg, from manganese metal by anodic oxidation from Mn(II) solution by oxidants such as o2one, periodate, bismuthate, and persulfate (using Ag" as catalyst), lead peroxide in acid, or chlorine in base or from MnO by disproportionation, or chemical or electrochemical oxidation. 

The roasting process, or variations of it, are most common. Liquid-phase processes are ia operation, however, both ia the United States and the former USSR. The former USSR is the only place where KMnO was produced by anodic oxidation of ferromanganese. Table 17 summarizes the various KMnO manufactuting faciUties worldwide as of this writing. 

Finishes for aluminum products can be both decorative and useful. Processes in use include anodic oxidation, chemical conversion coating, electrochemical graining, electroplating (qv), thin film deposition, porcelain enameling, and painting. Some alloys respond better than others to such treatments. 

The anodic oxidation of hydroquiaone ethers to quiaone ketals yields synthetically useful iatermediates that can be hydroly2ed to quiaones at the desired stage of a sequence (76). The yields of iatermediate diacetal are 83% for chlorine and 75% for bromine. 

Anodic Oxidation. The abiUty of tantalum to support a stable, insulating anodic oxide film accounts for the majority of tantalum powder usage (see Thin films). The film is produced or formed by making the metal, usually as a sintered porous pellet, the anode in an electrochemical cell. The electrolyte is most often a dilute aqueous solution of phosphoric acid, although high voltage appHcations often require substitution of some of the water with more aprotic solvents like ethylene glycol or Carbowax (49). The electrolyte temperature is between 60 and 90°C. 

Many studies (50—56) have attempted to explain bulk conduction through anodic oxide films on tantalum foils or sputtered tantalum substrates. 

Flaws in the anodic oxide film are usually the primary source of electronic conduction. These flaws are either stmctural or chemical in nature. The stmctural flaws include thermal crystalline oxide, nitrides, carbides, inclusion of foreign phases, and oxide recrystaUi2ed by an appHed electric field. The roughness of the tantalum surface affects the electronic conduction and should be classified as a stmctural flaw (58) the correlation between electronic conduction and roughness, however, was not observed (59). Chemical impurities arise from metals alloyed with the tantalum, inclusions in the oxide of material from the formation electrolyte, and impurities on the surface of the tantalum substrate that are incorporated in the oxide during formation. 

Fig. 7. Anodic oxide films on tantalum before ( ) and after ( ...

Fig. 8. Model of the conductivity profile in an anodic oxide film on tantalum after heat treatment, where Tj < r, < T,.

For steel, the typical anodic oxidation reaction is This reaction is accompanied by the following ... 

In the electrolysis zone, the electrochemical reactions take place. Two basic electrode configurations are used (/) monopolar cells where the same cell voltage is appHed to all anode/cathode combinations and (2) bipolar cells where the same current passes through all electrodes (Eig. 4). To minimize the anodic oxidation of OCL , the solution must be quickly moved out of this zone to a reaction zone. Because the reaction to convert OCk to CIO (eq. 

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