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Hydrogen peroxide electrochemical methods

In the second part of the work, the authors used only GIOD due to the simplicity of detecting hydrogen peroxide electrochemically. To determine MSG, the same FIA system is used, and after its optimization, the method is applied to the previous food samples and, in addition, to apple, orange, and tomato juice. [Pg.521]

The perfluoroalkane sulfonic acids were fkst reported ki 1954. Trifluoromethanesulfonic acid was obtained by the oxidation of bis(ttifluoromethyl thio) mercury with aqueous hydrogen peroxide (1). The preparation of a series of perfluoroalkanesulfonic acids derived from electrochemical fluotination (ECF) of alkane sulfonyl haUdes was also disclosed ki the same year (2). The synthetic operations employed when the perfluoroalkanesulfonic acid is derived from electrochemical fluotination, which is the best method of preparation, are shown ki equations 1—3. [Pg.314]

Many electroless coppers also have extended process Hves. Bailout, the process solution that is removed and periodically replaced by Hquid replenishment solution, must still be treated. Better waste treatment processes mean that removal of the copper from electroless copper complexes is easier. Methods have been developed to eliminate formaldehyde in wastewater, using hydrogen peroxide (qv) or other chemicals, or by electrochemical methods. Ion exchange (qv) and electro dialysis methods are available for bath life extension and waste minimi2ation of electroless nickel plating baths (see... [Pg.134]

Satisfactory 40% peracetic acid is obtainable from Buffalo Electrochemical Corporation, Food Machinery and Chemical Corporation, Buffalo, New York. The specifications given by the manufacturer for its composition are peracetic acid, 40% hydrogen peroxide, 5% acetic acid, 39% sulfuric acid, 1% water, 15%. Its density is 1.15 g./ml. The peracetic acid concentration should be determined by titration. A method for the analysis of peracid solutions is based on the use of ceric sulfate as a titrant for the hydrogen peroxide present, followed by an iodometric determination of the peracid present.3 The checkers found that peracetic acid of a lower concentration (27.5%) may also be used without a decrease in yield. The product was found to be sufficiently pure, after only one recrystallization from 60 ml. of petroleum ether (b.p. 40-60°) and cooling overnight to —18°, to be used in the next step. [Pg.88]

A wide variety of enzymes have been used in conjunction with electrochemical techniques. The only requirement is that an electroactive product is formed during the reaction, either from the substrate or as a cofactor (i.e. NADH). In most cases, the electroactive products detected have been oxygen, hydrogen peroxide, NADH, or ferri/ferrocyanide. Some workers have used the dye intermediates used in classical colorimetric methods because these dyes are typically also electroactive. Although an electroactive product must be formed, it does not necessarily have to arise directly from the enzyme reaction of interest. Several cases of coupling enzyme reactions to produce an electroactive product have been described. The ability to use several coupled enzyme reactions extends the possible use of electrochemical techniques to essentially any enzyme system. [Pg.28]

S. Nagase, N. Ohkoshi, A. Ueda, K. Aoyagi, and A. Koyama, Hydrogen peroxide interferes with detection of nitric oxide by an electrochemical method. Clin. Chem. 43, 1246 (1997). [Pg.47]

Recently, acylsilanes have been utilized as useful intermediates in organic synthesis [57], For example, treatment of acylsilanes with the fluoride ion generates the corresponding acyl anions which react with electrophiles. On the other hand, by using the electrochemical method, acylsilanes serve as acyl cation equivalents because nucleophiles are introduced at the carbonyl carbon. Chemical oxidation of acylsilanes with hydrogen peroxide which affords the corresponding carboxylic acids has been reported [58], However, the anodic oxidation provides a versatile method for the introduction of various nucleophiles... [Pg.74]

There is huge potential in the combination of biocatalysis and electrochemistry through reaction engineering as the linker. An example is a continuous electrochemical enzyme membrane reactor that showed a total turnover number of 260 000 for the enantioselective peroxidase catalyzed oxidation of a thioether into its sulfone by in situ cathodic generated hydrogen peroxide - much higher than achieved by conventional methods [52],... [Pg.292]

Oxidation indices, 656-72 peroxide determination, 762-3 peroxide value, 656, 657-64 colorimetry, 658-61 definition, 657 direct titration, 657 electrochemical methods, 663-4 IR spectrophotometry, 661-3 NIR spectrophotometry, 663 UV-visible spectrophotometry, 658-61 secondary oxidation products, 656, 665-72 tests for stability on storage, 664-5, 672 thermal analysis, 672 Oxidative amperometiy, hydroperoxide determination, 686 Oxidative cleavage alkenes, 1094-5 double bonds, 525-7 Oxidative couphng, hydrogen peroxide determination, 630, 635 Oxidative damage... [Pg.1477]

The poisoning of a catalyst may be shown by adding some hydrogen sulfide solution to the hydrogen peroxide before the colloidal platinum is introduced. No decomposition of the peroxide is observed in this case, since the platinum has been poisoned by the presence of the hydrogen sulfide. This method is applicable to most of the metals below hydrogen in the electrochemical series. [Pg.164]

The production of industrially important perfluoroalkane sulfonic acids is generally accomplished by electrochemical fluorination. This method of preparation remains expensive and proceeds in good yields only for short hydrocarbon chains.30 Recently however, Wakselman and Tordeux have described a chemical method for the preparation of trifluoromethane sulfonic acid.31 The procedure involves reaction of a metal selected from zinc, cadmium, manganese, and aluminum with sulfur dioxide in DMF, followed by the introduction of trifluoromethyl bromide under slight pressure. The intermediate sulfinate is subsequently oxidized by hydrogen peroxide, and then hydrolyzed which leads to formation of the trifluoromethane sulfonic acid. Successful extension of the sulfination process to the modification of PCTFE should result in the formation of a sulfinated polymer which can ultimately be oxidized to give a sulfonic-acid modified polymer. [Pg.136]

Mayer determined acetylcholine and choline by enzyme-mediated liquid chromatography with electrochemical detection [195]. The two compounds were separated by passing the eluted fractions through a post-column reactor containing immobilized Acetylcholineesterase and choline oxidase. In the presence of either compound, the dissolved oxygen was converted into hydrogen peroxide, which was detected amperometrically at a platinum electrode. This method was used to determine choline in rat brain homogenates. [Pg.80]

Hydrogen peroxide containing 30 to 35 per cent b.w. HgOg, manufactured by one of the electrochemical methods described, is as a rule not sufficiently pure for further concentration to 80—... [Pg.417]

Hydrogen peroxide is prepared in industrial scale by an electrochemical method. A convenient source is the inexpensive sodium perborate, NaBO3.4H30 this yields hydrogen peroxide when its aqueous solution is heated ... [Pg.380]

Monitoring of hydrogen peroxide concentrations in aqueous systems is possible on- and off-line. Standard methods of H2O2 measurement include titrimetric, gas-ometric, electrochemical and colorimetric methods, and several others. For a short overview of H2O2 analyses, see Gwivy et al. (2000). [Pg.157]


See other pages where Hydrogen peroxide electrochemical methods is mentioned: [Pg.328]    [Pg.99]    [Pg.348]    [Pg.663]    [Pg.664]    [Pg.355]    [Pg.127]    [Pg.534]    [Pg.214]    [Pg.1083]    [Pg.373]    [Pg.183]    [Pg.201]    [Pg.144]    [Pg.425]    [Pg.348]    [Pg.583]    [Pg.312]    [Pg.214]    [Pg.413]    [Pg.227]    [Pg.115]    [Pg.392]    [Pg.515]    [Pg.123]    [Pg.11]    [Pg.479]    [Pg.386]    [Pg.664]    [Pg.665]    [Pg.425]    [Pg.109]    [Pg.545]    [Pg.557]   


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