Hydrogen peroxide materials

This is a disproportionation reaction, and is strongly catalysed by light and by a wide variety of materials, including many metals (for example copper and iron) especially if these materials have a large surface area. Some of these can induce explosive decomposition. Pure hydrogen peroxide can be kept in glass vessels in the dark, or in stone jars or in vessels made of pure aluminium with a smooth surface. 

Method(B). Add3g. (3ml.)ofbenzonitrileto50ml.of lo-volumes hydrogen peroxide in a beaker, stir mechanically and add i ml. of 10% aqueous sodium hydroxide solution. Warm the stirred mixture at 40° until the oily suspension of the nitrile has been completely replaced by the crystalline benzamide (45-60 minutes). Cool the solution until crystallisation of the benzamide is complete, and then filter at the pump and recrystallise as above. One recrystallisation gives the pure benza-mide, m.p. 129-130° yield of purified material, 2-2-5 S ... 

Because of their use in the rubber industry various sulfenamido thiazoles (131) have been prepared. They are obtained in good yields through the oxidation of A-4-thiazoline-2-thiones (130) in aqueous alkaline solution in the presence of an amine or ammonia (Scheme 66) <123, 166, 255, 286, 308, 309). Other oxidizing agents have been proposed (54, 148. 310-313) such as iodine (152), chlorine, or hydrogen peroxide. Disulfides can also be used as starting materials (3141. 

Chlorosulfonic acid Saturated and unsaturated acids, acid anhydrides, nitriles, acrolein, alcohols, ammonia, esters, HCl, HF, ketones, hydrogen peroxide, metal powders, nitric acid, organic materials, water... 

Hydrogen peroxide Copper, chromium, iron, most metals or their salts, alcohols, acetone, organic materials, flammable liquids, combustible materials... 

In 1973 the Semiconductor Equipment and Materials Institute (SEMI) held its first standards meeting. SEMI standards are voluntary consensus specifications developed by the producers, users, and general interest groups in the semiconductor (qv) industry. Examples of electronic chemicals are glacial acetic acid [64-19-7] acetone [67-64-17, ammonium fluoride [12125-01 -8] and ammonium hydroxide [1336-21 -6] (see Ammonium compounds), dichloromethane [75-09-2] (see Cm.OROCARBONSANDcm.OROHYDROCARBONs), hydrofluoric acid [7664-39-3] (see Eluorine compounds, inorganic), 30% hydrogen peroxide (qv) [7722-84-1] methanol (qv) [67-56-1] nitric acid (qv) [7697-37-2] 2-propanoI [67-63-0] (see Propyl alcohols), sulfuric acid [7664-93-9] tetrachloroethane [127-18-4] toluene (qv) [108-88-3] and xylenes (qv) (see also Electronic materials). 

Detecting the presence of small, even invisible, amounts of blood is routine. Physical characteristics of dried stains give minimal information, however, as dried blood can take on many hues. Many of the chemical tests for the presence of blood rely on the catalytic peroxidase activity of heme (56,57). Minute quantities of blood catalyze oxidation reactions between colorless materials, eg, phenolphthalein, luco malachite green, luminol, etc, to colored or luminescent ones. The oxidant is typically hydrogen peroxide or sodium perborate (see Automated instrumentation,hematology). 

The chemical yield of hydrogen peroxide and the anthraquinone per process cycle is very high, but other secondary reactions necessitate regeneration of the working solution and hydrogenation catalyst, and the removal of organic material from the extracted hydrogen peroxide. 

The 30% reagent-grade hydrogen peroxide is purer than the industrial grades, is covered by ACS reagent specification, and is used as a laboratory reagent and in some specialty uses (see Fine chemicals). Several grades are also marketed for electronics use and thus have exceptionally low impurity levels. Some of these latter contain very Httie or no stabilizers (see Electronic materials). 

Hydrogen peroxide concentrations of 35% and above may, and 50% and above do, cause spontaneous combustion of dry grasses, wood, and leaves. Spills of concentrated hydrogen peroxide should be diluted with excess amounts of water immediately. Practically all soHd combustible materials contain sufficient quantities of catalytic impurities to rapidly decompose hydrogen peroxide, especially at 70% concentration and above. 

In spite of widespread usage of these compounds, the stmctures of only the calcium, barium, and strontium compounds are reasonably weU-estabhshed. The materials are generally made by trituratiag the oxides, or hydroxides, with aqueous hydrogen peroxide and dryiag the soHd products. The commercial products are typically mixtures of the peroxides with varyiag amounts of hydroxides, oxides, carbonates, hydrates, and peroxohydrates. 

Calcium Peroxide. Pure calcium peroxide [1305-79-9] Ca02, has been prepared, but the commercial product is a mixture made by reaction of calcium hydroxide and hydrogen peroxide. Commercial material contains either 60 or 75% Ca02 the remainder is a poorly defined mixture of calcium oxide, hydroxide, and carbonate. A well-defined octahydrate [60762-59-6] 8H20, can be crysta11i2ed from aqueous systems. 

When dissolved ia water, the solution is identical with that obtained by dissolving sodium carbonate ia aqueous hydrogen peroxide. There is some evidence for the presence of the traces of tme peroxocarbonate anion, HCO , ia these solutions (95). If the peroxohydrate is heated for about an hour at 100°C and then allowed to cool to room temperature, some decomposition occurs and the product effervesces when placed ia water. Electron spia resonance experiments (64) iadicate that free radicals are present ia this partially decomposed material, but the nature of these radicals is obscure. 

Disinfection destroys pathogenic organisms. This procedure can render an object safe for use. Disinfectants include solutions of hypochlorites, tinctures of iodine or iodophores, phenoHc derivatives, quaternary ammonium salts, ethyl alcohol, formaldehyde, glutaraldehyde, and hydrogen peroxide (see Disinfectants AND antiseptics). Effective use of disinfected materials must be judged by properly trained personnel. 

Other Cellulosics. Rayon is bleached similarly to cotton but under milder conditions since the fibers are more easily damaged and since there is less colored material to bleach. Cellulose acetate and triacetate are not usually bleached. They can be bleached like rayon, except a slightly lower pH is used to prevent hydrolysis. The above fibers are most commonly bleached with hydrogen peroxide. Linen, dax, and jute requite more bleaching and mil der conditions than cotton, so multiple steps are usually used. Commonly an acidic or neutral hypochlorite solution is followed by alkaline hypochlorite, peroxide, chlorite, or permanganate, or a chlorite step is done between two peroxide steps. A one-step process with sodium chlorite and hydrogen peroxide is also used. 

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