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Carbon potassium hydroxide used

In some cases this reaction takes place with water alone but usually some other substance is present e.g., calcium hydroxide or carbonate, potassium hydroxide, metallic iron or iron salts which actsasacatalizer. The mono-chlorine derivative of toluene and other benzene homologues may also be used for preparing the aldehydes. In this case the reaction is in two steps, first, reaction with water yielding the alcohol, and second. [Pg.648]

This type of extraction depends upon the use of a reagent which reacts chemically with the compound to be extracted, and is generally employed either to remove small amounts of impurities in an organic compound or to separate the components of a mixture. Examples of such reagents include dilute (5 per cent.) aqueous sodium or potassium hydroxide solution, 5 or 10 per cent, sodium carbonate solution, saturated sodium bicarbonate solution (ca. 5 per cent.), dilute hydrochloric or sulphuric acid, and concentrated sulphuric acid. [Pg.151]

Saturate the distillate with sodium chloride (ca. 8 g.) and extract four times with 5 ml. portions of ether. Dry the combined ethereal extracts with a little anhydrous potassium carbonate or a few pellets of potassium hydroxide. Remove the ether (Fig. 11,13, 4), using a 20-25 ml. distilling flask. When all... [Pg.1112]

Nitromethane also is used in the synthesis of the antiulcer dmg, ranitidine [66357-35-5]. A two-step process utilizing nitromethane, carbon disulfide, potassium hydroxide, and dimethyl sulfate yields l,l-bis(methylthio)-2-nitroethene [13623-94 ] which reacts further to produce ranitidine. [Pg.104]

A variety of shale-protective muds are available which contain high levels of potassium ions (10). The reaction of potassium ions with clay, well known to soil scientists, results in potassium fixation and formation of a less water-sensitive clay. Potassium chloride, potassium hydroxide, potassium carbonate [584-08-7] (99), tetrapotassium pyrophosphate [7320-34-5] (100), and possibly the potassium salts of organic acids, such as potassium acetate [127-08-2] (101) and formate, have all been used as the potassium source. Potassium chloride is generally preferred because of its low cost and availabihty. [Pg.182]

The cmde phthaUc anhydride is subjected to a thermal pretreatment or heat soak at atmospheric pressure to complete dehydration of traces of phthahc acid and to convert color bodies to higher boiling compounds that can be removed by distillation. The addition of chemicals during the heat soak promotes condensation reactions and shortens the time required for them. Use of potassium hydroxide and sodium nitrate, carbonate, bicarbonate, sulfate, or borate has been patented (30). Purification is by continuous vacuum distillation, as shown by two columns in Figure 1. The most troublesome impurity is phthahde (l(3)-isobenzofuranone), which is stmcturaHy similar to phthahc anhydride. Reactor and recovery conditions must be carefully chosen to minimize phthahde contamination (31). Phthahde [87-41-2] is also reduced by adding potassium hydroxide during the heat soak (30). [Pg.484]

Potassium Carbonate. Except for small amounts produced by obsolete processes, eg, the leaching of wood ashes and the Engel-Precht process, potassium carbonate is produced by the carbonation, ie, via reaction with carbon dioxide, of potassium hydroxide. Potassium carbonate is available commercially as a concentrated solution containing ca 47 wt % K CO or in granular crystalline form containing 99.5 wt % K CO. Impurities are small amounts of sodium and chloride plus trace amounts (<2 ppm) of heavy metals such as lead. Heavy metals are a concern because potassium carbonate is used in the production of chocolate intended for human consumption. [Pg.532]

The aromatic ring of alkylphenols imparts an acidic character to the hydroxyl group the piC of unhindered alkylphenols is 10—11 (2). Alkylphenols unsubstituted in the ortho position dissolve in aqueous caustic. As the carbon number of the alkyl chain increases, the solubihty of the alkah phenolate salt in water decreases, but aqueous caustic extractions of alkylphenols from an organic solution can be accomphshed at elevated temperatures. Bulky ortho substituents reduce the solubihty of the alkah phenolate in water. The term cryptophenol has been used to describe this phenomenon. A 35% solution of potassium hydroxide in methanol (Qaisen s alkah) dissolves such hindered phenols (3). [Pg.58]

Typical values for mf n are 0.5 to 2.5. Gommercially used bases include sodium hydroxide, potassium hydroxide, calcium hydroxide (lime), magnesium hydroxide, sodium carbonate, sodium alurninate, calcium carbonate, or various mixtures. For certain appHcations, PAG can be made from waste grades of aluminum chloride [7446-70-0] such as spent catalyst solutions from Friedel-Grafts synthesis (see Friedel-Grafts reaction). [Pg.179]

Semichemical pulping can be accompHshed by a sulfur-free system of sodium hydroxide and sodium carbonate. The sodium carbonate is recovered by simple incineration, and sodium hydroxide is added as makeup. Advantages in recovery operation are obtained if potassium hydroxide is added occasionally to maintain ca 20 mol % potassium carbonate (66). Lastiy, semichemical pulping can be accompHshed by using kraft white Hquor of low strength. [Pg.275]

Manufacture. Several methods have been described for the preparation of -hydroxyben2oic acid. The commercial technique is similar to that of salicylic acid, ie, Kolbe-Schmitt carboxylation of phenol. The modification includes the use of potassium hydroxide in place of caustic (51). The dried potassium phenate is heated under pressure, 270 kPa (2.7 atm) or more, with dry carbon dioxide at 180—250°C. The potassium salt [16782-08-4] of Nhydroxyben2oic acid forms almost quantitatively and can be converted to free acid by using a mineral acid. [Pg.292]

If tin and sulfur are heated, a vigorous reaction takes place with the formation of tin sulfides. At 100—400°C, hydrogen sulfide reacts with tin, forming stannous sulfide however, at ordinary temperatures no reaction occurs. Stannous sulfide also forms from the reaction of tin with an aqueous solution of sulfur dioxide. Molten tin reacts with phosphoms, forming a phosphide. Aqueous solutions of the hydroxides and carbonates of sodium and potassium, especially when warm, attack tin. Stannates are produced by the action of strong sodium hydroxide and potassium hydroxide solutions on tin. Oxidizing agents, eg, sodium or potassium nitrate or nitrite, are used to prevent the formation of stannites and to promote the reactions. [Pg.64]

For the manufacturiag of potassium ethyl xanthate, 400% excess of alcohol and equimolar quantities of 50 wt % aqueous potassium hydroxide and carbon disulfide were used (77). After 30 min at 40°C, the mixture was vacuum dmm dried. The product was obtained ia near quantitative yield and assayed at 95%. It is claimed that potassium amyl xanthate can be made with almost the same ratio of reactants and 80 wt % caustic potash (78). [Pg.366]

The characteristics for aqueous KOH (97—99) solutions vary somewhat for battery electrolytes when additives are used. Furthermore, potassium hydroxide reacts with many organics and with the carbon dioxide in air to form carbonates. The build-up of carbonates in the electrolyte is to be avoided because carbonates reduce electrolyte conductivity and electrode activity in some cases. [Pg.567]

The quality and yield of carbon black depends on the quaUty of the feedstock, reactor design, and input variables. The stmcture is controlled by the addition of alkaU metals to the reaction or mixing 2ones. Usual practice is to use aqueous solutions of alkaU metal salts such as potassium chloride or potassium hydroxide sprayed into the combustion chamber or added to the make oil in the oil injector. Alkaline-earth compounds such as calcium acetate that increase the specific surface area are introduced in a similar manner. [Pg.546]

Sodium and Potassium Hydroxides. Sodium hydroxide [1310-73-2] and potassium hydroxide [1310-58-3] (Class 1, nonregenerative) are commonly used when moisture and carbon dioxide or hydrogen sulfide must be removed simultaneously (4). Fused sticks or solutions of the alkah hydroxides are frequentiy used. These materials must be handled with care to prevent serious skin bums. [Pg.507]


See other pages where Carbon potassium hydroxide used is mentioned: [Pg.291]    [Pg.12]    [Pg.128]    [Pg.128]    [Pg.14]    [Pg.1100]    [Pg.1258]    [Pg.652]    [Pg.84]    [Pg.117]    [Pg.28]    [Pg.130]    [Pg.482]    [Pg.485]    [Pg.461]    [Pg.487]    [Pg.499]    [Pg.715]    [Pg.858]    [Pg.180]    [Pg.460]    [Pg.384]    [Pg.25]    [Pg.522]    [Pg.134]    [Pg.135]    [Pg.129]    [Pg.359]    [Pg.535]    [Pg.11]    [Pg.378]    [Pg.186]    [Pg.157]    [Pg.250]   
See also in sourсe #XX -- [ Pg.303 , Pg.304 ]




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Carbon hydroxide

Hydroxide carbonates

Hydroxides Potassium hydroxide

Potassium carbonate

Potassium hydroxide

Potassium hydroxide carbonate

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