Acidic aqueous solutions, anodic oxidation

Among the aliphatic alcohols, oxidation of methanol has been studied most extensively [122-125]. At a platinum anode in acidic aqueous solutions, methanol oxidizes completely to CO2. Higher primary alcohols oxidize to aldehydes and acids under these conditions, though detailed mechanistic studies are lacking [126,127]. Anodic oxidation of secondary alcohols in aqueous acid leads to the corresponding ketones in high yield, but the reaction has received little attention over the years [126,128]. Indirect oxidation methods employing mediators are of considerable interest in this area and are treated elsewhere. 

The UPD and anodic oxidation of Pb monolayers on tellurium was investigated also in acidic aqueous solutions of Pb(II) cations and various concentrations of halides (iodide, bromide, and chloride) [103]. The Te substrate was a 0.5 xm film electrodeposited in a previous step on polycrystalline Au from an acidic Te02 solution. Particular information on the time-frequency-potential variance of the electrochemical process was obtained by potentiodynamic electrochemical impedance spectroscopy (PDEIS), as it was difficult to apply stationary techniques for accurate characterization, due to a tendency to chemical interaction between the Pb adatoms and the substrate on a time scale of minutes. The impedance... 

PANI is usually produced by the anodic oxidation of aniline in acidic aqueous solution [5, 139], but can also be produced by chemical oxidation [138b, 140]. Hence, it is not surprising that the oxidation of PANI is pH-dependent and that, therefore, in addition to electron-transfer processes, proton-transfer reactions occur during charging. Although it is usually assumed that PANI has a chain structure (emeraldine) with head-tail connections... 

The photoelectro-Fenton method [98] complements the photo-Fenton and electro-Fenton reactions. In the latter, a potential is applied between two electrodes immersed in a solution containing Fenton reagent and the target compound. The recent study of the herbicide 2,4,5-T, performed in an undivided cell with a Pt anode and an 02-diffusion cathode, showed that the photo-electrochemical process was more powerful than the electro-Fenton process, which can yield only about 60-65% of decontamination. The electro-Fenton method provides complete destruction of all reaction intermediates, except oxalic acid, which, as already mentioned, forms stable complexes with Fe3+ that remain in the solution. The fast photodecarboxylation of such Fe(III)-oxalate complexes by UV fight explains the highest oxidative ability of the photoelectro-Fenton treatment, which allows a fast and total mineralization of highly concentrated acidic aqueous solutions of 2,4,5-T at low current and temperature. A similar behavior was found for the herbicide 3,6-dichloro-2-methoxybenzoic acid [99]. 

Another observation pointing in the same direction has been described in Glaser (115). Sometimes, during the anodic oxidation of TICIO4 in acidic aqueous solution, the anode solution coagulated to a yellowish-white gel. The electrolysis was then stopped and the stopcock between the anodic and cathodic compartments was closed. After some days, the gel changed back into a clear, colorless solution. In addition. 

Propiomazine hydrochloride exhibits an anodic wave at +0.8v in acidic aqueous solution at a concentration range of 10 - to 10 5k using a stationary platinum electrode vs. a calomel reference electrode, suitable for a quantitative assay O. The wave corresponds to the oxidation of the stilfur in the phenothiazine nucleus to the sulfoxide l. 

In Fig. 3, the images of the surface and cross-section of porous aluminium anodic oxide films obtained in the HA mode in 4 % orthophosphoric acid aqueous solution, are presented. It is evident that the oxide film has the regular structure. These films can be used as a porous matrix for selective deposition of magnetic materials. 

Anodic porous alumina is conventionally grown on aluminum foils, as indicated in Fig. 2. Similar self-assembled growth is achieved on Si by depositing an A1 thin film on the front side of a silicon wafer and forming an ohmic contact on the back side that is used as anode. The electrochemical solutions currently used are oxalic or sulfuric acid aqueous solutions. Details for the fabrication of thin alumina templates on Si with adjustable pore size and density are given elsewhere [8]. Electrochemical oxidation of A1 starts from the A1 surface and continues down to the Al/Si interface, following an anodization current density/time curve as shown in Fig. 3. 

However, the extent of oxidation would have to be controlled to avoid deposition of elemental sulfur on the anode, and diffusion of sulfide species through the membrane to the cathode would poison most cathode materials. Similar reactions are utilized in liquid redox processes [1,2] for absorbed H2S oxidation, but with additimial mediators such as (complexed) Fe /Fe in acidic aqueous solutions and [13] in slightly... 

This is essentially a corrosion reaction involving anodic metal dissolution where the conjugate reaction is the hydrogen (qv) evolution process. Hence, the rate depends on temperature, concentration of acid, inhibiting agents, nature of the surface oxide film, etc. Unless the metal chloride is insoluble in aqueous solution eg, Ag or Hg ", the reaction products are removed from the metal or alloy surface by dissolution. The extent of removal is controUed by the local hydrodynamic conditions. 

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. 

In presence of the enzyme glucose oxidase, an aqueous solution of glucose undergoes oxidation to gluconic acid with formation of hydrogen peroxide which can be determined by anodic oxidation at a fixed potential. 

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