Peroxides sulfides

In the analysis of inorganic anions using acetonitrile-water (3-1-7) containing citric acid and hexadecyltrimethylammonium hydroxide as eluent. Wheals reported that bromide, cyanide, dithionite, ferrocyanide, iodide, metabisulfite, nitrite, perborate, peroxide, sulfide, thiocyanate and thiosulfate respond at a GCE (-1-0.75 V vs Ag/AgCl). Dou and Krull have further shown that post-column irradiation (low pressure Hg arc discharge lamp) can facilitate the EC detection of chromate, dichromate and perchlorate and give improved sensitivity for thiocyanate. Despite this work, however, the application of EC detection to the analysis of these ions in biological systems has not been reported as yet. 

Procedure. A drop of the test solution, or a few grains (or more) of the solid sulfide, according to the expected arsenic content, is placed in a micro crucible and warmed with a few drops of ammonia and 10 % hydrogen peroxide. Sulfides must be completely dissolved, or made colorless. The mixture is then acidified with dilute acetic acid, and 1 or 2 drops of 1 % silver nitrate solution added. A red-brown precipitate or coloration appears if arsenic is present. 

A second sulfur-based oscillator, the hydrogen peroxide-sulfide reaction recently discovered by ORBAN and EPSTEIN [38] shows, in contrast, an almost classic cross-shaped phase diagram. Fig. 3. The Burger-Field system is the first to oscillate in basic solution, while, as we see in Fig. 4, the H O -S oscillations go from acidic to basic pH, making possible dramatic color effects with acid-base indicators. 

On oxidation with potassium permanganate or hydrogen peroxide, sulfides yield corresponding sulfones, some of which have properties suitable for identification (especially aromatic ones). Sulfones have also been identified by mass spectrometry (10). Another identification method makes use of the reaction of sulfides with alkyl halogenides (the formation of sulfonium salts) ... 

The oxidation of 2- and 5-sulfides is usually performed in acetic acid and 30% hydrogen peroxide (213, 229, 263, 345-350) Or with m-chloroperbenzoic acid (341). Ary] (8, 272. 349, 351-353) and alkyl sulfones (129, 203, 214, 270, 274, 275) are thus obtained in good yields. Other oxidative reagents such as KMn04 (7, 273) or CrO (7) in acetic add have also been used. 

Aldehydes are easily oxidized to carboxylic acids under conditions of ozonide hydroly SIS When one wishes to isolate the aldehyde itself a reducing agent such as zinc is included during the hydrolysis step Zinc reduces the ozonide and reacts with any oxi dants present (excess ozone and hydrogen peroxide) to prevent them from oxidizing any aldehyde formed An alternative more modem technique follows ozone treatment of the alkene m methanol with reduction by dimethyl sulfide (CH3SCH3)... 

One equivalent of a peroxy acid or of hydrogen peroxide converts sulfides to sulf oxides two equivalents gives the corresponding sulfone... 

Section 16 16 Oxidation of sulfides yields sulfoxides then sulfones Sodium metaper lodate IS specific for the oxidation of sulfides to sulfoxides and no fur ther Hydrogen peroxide or peroxy acids can yield sulfoxides (1 mole of oxidant per mole of sulfide) or sulfone (2 moles of oxidant per mole of sulfide)... 

Oldhamite, see Calcium sulfide Opal, see Silicon dioxide Orpiment, see Arsenic trisulfide Oxygen powder, see Sodium peroxide... 

Lead dioxide Aluminum carbide, hydrogen peroxide, hydrogen sulfide, hydroxylamine, ni-troalkanes, nitrogen compounds, nonmetal halides, peroxoformic acid, phosphorus, phosphorus trichloride, potassium, sulfur, sulfur dioxide, sulfides, tungsten, zirconium... 

Manganese dioxide Aluminum, hydrogen sulfide, oxidants, potassium azide, hydrogen peroxide, peroxosulfuric acid, sodium peroxide... 

The rate of dissolution is limited by oxygen availabiUty rather than by cyanide concentration. When oxygen solubiUty is reduced by water salinity or by consumption by ore constituents such as sulfide minerals, enrichment of the air with oxygen or addition of hydrogen or calcium peroxide improves leaching kinetics and decreases cyanide consumption (10). 

Peroxomonosulfuric acid oxidi2es cyanide to cyanate, chloride to chlorine, and sulfide to sulfate (60). It readily oxidi2es carboxyflc acids, alcohols, alkenes, ketones, aromatic aldehydes, phenols, and hydroquiaone (61). Peroxomonosulfuric acid hydroly2es rapidly at pH <2 to hydrogen peroxide and sulfuric acid. It is usually made and used ia the form of Caro s acid. 

Diacyl peroxides have been reduced with a variety of reduciag agents, eg, lithium aluminum hydride, sulfides, phosphites, phosphines, and haUde ions (187). Hahdes yield carboxyUc acid salts (RO) gives acid anhydrides. With iodide ion and certain trivalent phosphoms compounds, the reductions are sufftcientiy quantitative for analytical purposes. 

The hberated iodine, as the complex triiodide ion, may be titrated with standard thiosulfate solution. A general iodometric assay method for organic peroxides has been pubUshed (253). Some peroxyesters may be determined by ferric ion-catalyzed iodometric analysis or by cupric ion catalysis. The latter has become an ASTM Standard procedure (254). Other reducing agents are ferrous, titanous, chromous, staimous, and arsenite ions triphenylphosphine diphenyl sulfide and triphenjiarsine (255,256). 

Strontium Oxide, Hydroxide, and Peroxide. Strontium oxide, SrO, is a white powder that has a specific gravity of 4.7 and a melting point of 2430°C. It is made by heating strontium carbonate with carbon in an electric furnace, or by heating celestite with carbon and treating the sulfide formed with caustic soda and then calcining the product (10). It reacts with water to form strontium hydroxide [18480-07-4] and is used as the source of strontium peroxide [1314-18-7],... 

Chemical Properties. The most significant chemical property of L-ascorbic acid is its reversible oxidation to dehydro-L-ascorbic acid. Dehydro-L-ascorbic acid has been prepared by uv irradiation and by oxidation with air and charcoal, halogens, ferric chloride, hydrogen peroxide, 2,6-dichlorophenolindophenol, neutral potassium permanganate, selenium oxide, and many other compounds. Dehydro-L-ascorbic acid has been reduced to L-ascorbic acid by hydrogen iodide, hydrogen sulfide, 1,4-dithiothreitol (l,4-dimercapto-2,3-butanediol), and the like (33). 

Although these curative systems may also be used with the polyepichlorohydrin elastomers containing AGE, the polymers were developed to be cured with conventional mbber curatives, sulfur, and peroxides. These polymers containing the pendent aHyl group are readily cured with a typical sulfur cure system such as zinc oxide, and sulfur along with the activators, tetramethylthiuram mono sulfide [97-74-5] (TMTM) and... 

There are no known practical peroxide cure systems for the PO—AGE polymers. Apparentiy the peroxide attacks the polymer backbone at a rate that is unfavorably competitive with the cross-linking rate. A typical sulfur cure system consists of zinc oxide [1314-13-2] tetramethylthiuram mono sulfide (TMTM), 2-2-mercaptobenzothiazole [149-30-4] (MBT), and sulfur. A sulfur donor cure system is zinc oxide, di-o-tolylguanidine [97-39-2] (DOTG) and tetramethylthiuram hexasulftde. 

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