Suspensions hydroxide

The calcium oxide so produced is slaked to give a suspension of calcium hydroxide and this is heated with the filtrate from the carbonator which contains ammonium chloride ... 

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 ... 

Amino-4 -methylthiazole slowly decomposes on storage to a red viscous mass. It can be stored as the nitrate, which is readily deposited as pink crystals when dilute nitric acid is added to a cold ethanolic solution of the thiazole. The nitrate can be recrystallised from ethanol, although a faint pink colour persists. Alternatively, water can be added dropwise to a boiling suspension of the nitrate in acetone until the solution is just clear charcoal is now added and the solution, when boiled for a short time, filtered and cooled, deposits the colourless crystalline nitrate, m.p. 192-194° (immersed at 185°). The thiazole can be regenerated by decomposing the nitrate with aqueous sodium hydroxide, and extracting the free base with ether as before. 

Arsonic acids, like carboxylic and sulphonic acids (pp. 349, 353), usually give crystalline benzylthiouronium salts. Add just sufficient dilute aqueous sodium hydroxide dropwise with shaking to a suspension of 0 5 g. of phenylarsonic acid in 10 ml. of water to give a clear solution. Then add 0 5 g. of benzylthiouronium chloride dissolved in 10 ml. of water. Filter off the precipitated benzylthiouronium salt, wash with water and dry m.p. 114-117° it tends to dissociate on attempted recrystallisation. 

Benzylatnine. Warm an alcoholic suspension of 118-5 g. of finely-powdered benzyl phthalimide with 25 g. of 100 per cent, hydrazine hydrate (CAUTION corrosive liquid) a white, gelatinous precipitate is produced rapidly. Decompose the latter (when its formation appears complete) by heating with excess of hydrochloric acid on a steam bath. Collect the phthalyl hydrazide which separates by suction filtration, and wash it with a little water. Concentrate the filtrate by distillation to remove alcohol, cool, filter from the small amount of precipitated phthalyl hydrazide, render alkaline with excess of sodium hydroxide solution, and extract the liberated benzylamine with ether. Dry the ethereal solution with potassium hydroxide pellets, remove the solvent (compare Fig. //, 13, 4) on a water bath and finally distil the residue. Collect the benzylamine at 185-187° the 3ueld is 50 g. 

The palladium - barium sulphate catalyst Is prepared by treating a suspension of20g. of barium sulphate (which has been precipitated in hot solution) in 400 ml. of hot water with a solution of I - 7 g. of palladium chloride (equivalent to I - 0 g. of palladium) in 50 ml. of water and with I - 5 ml. of 40 per cent, formaldehyde solution. The mixture is rendered faintly alkaline to litmus by the addition of sodium hydroxide solution and then boiled for a short time. When the supernatant liquid is clear, the grey precipitate is filtered oS, and wa.shed with hot water until the... 

Preparation of palladium - calcium carbonate catalyst. Prepare 60 g. of precipitated calcium carbonate by mixing hot solutions of the appropriate quantities of A.R. calcium chloride and A.R. sodium carbonate. Suspend the calcium carbonate in water and add a solution containing 1 g. of palladium chloride. Warm the suspension until all the palladium is precipitated as the hydroxide upon the calcium carbonate, i.e., until the supernatant liquid is colourless. Wash several times with... 

C. Palladium on carbon catalyst (5 per cent. Pd). Suspend 41-5 g. of nitric acid - washed activated carbon in 600 ml. of water in a 2-litre beaker and heat to 80°. Add a solution of 4 1 g. of anhydrous palladium chloride (1) in 10 ml. of concentrated hydrochloric acid and 25 ml. of water (prepared as in A), followed by 4 ml. of 37 per cent, formaldehyde solution. Stir the suspension mechanically, render it alkaUne to litmus with 30 per cent, sodium hydroxide solution and continue the stirring for a further 5 minutes. Filter off the catalyst on a Buchner funnel, wash it ten times with 125 ml. portions of water, and dry and store as in B. The yield is 46 g. 

Attention is directed to the fact that if only minute amounts of material are available or if the substance is expensive, considerable economy may be effected by treating, e.g., the aqueous solution or suspension with the necessary quantity of concentrated sodium hydroxide solution or concentrated hydrochloric acid. 

Starch is a polysaccharide found in many plant species. Com and potatoes are two common sources of industrial starch. The composition of starch varies somewhat in terms of the amount of branching of the polymer chains (11). Its principal use as a flocculant is in the Bayer process for extracting aluminum from bauxite ore. The digestion of bauxite in sodium hydroxide solution produces a suspension of finely divided iron minerals and siUcates, called red mud, in a highly alkaline Hquor. Starch is used to settle the red mud so that relatively pure alumina can be produced from the clarified Hquor. It has been largely replaced by acryHc acid and acrylamide-based (11,12) polymers, although a number of plants stiH add some starch in addition to synthetic polymers to reduce the level of residual suspended soHds in the Hquor. Starch [9005-25-8] can be modified with various reagents to produce semisynthetic polymers. The principal one of these is cationic starch, which is used as a retention aid in paper production as a component of a dual system (13,14) or a microparticle system (15). 

A fourth mechanism is called sweep flocculation. It is used primarily in very low soflds systems such as raw water clarification. Addition of an inorganic salt produces a metal hydroxide precipitate which entrains fine particles of other suspended soflds as it settles. A variation of this mechanism is sometimes employed for suspensions that do not respond to polymeric flocculants. A soHd material such as clay is deUberately added to the suspension and then flocculated with a high molecular weight polymer. The original suspended matter is entrained in the clay floes formed by the bridging mechanism and is removed with the clay. 

Aluminum Hydroxide Gel. CoUoidal aluminum hydroxide [21645-51 -2] (Amphogel), AlOH, is a suspension. Each 100 g contain the... 

Mag nesia. ndAlumina. Suspension. A mixture of salts, available as Maalox, Mylanta, Gelusil, and Aludrox, contains magnesium hydroxide [1309-42-8] Mg(OH)2, and variable amounts of aluminum oxide in the form of aluminum hydroxide and hydrated aluminum oxide, ie, 2.9—4.2% magnesium hydroxide and 2.0—2.4% aluminum oxide, Al O, for a mixture of 4.9—6.6% combined magnesium hydroxide and aluminum oxide. This mixture may contain a flavoring and antimicrobial agents in a total amount not to exceed 0.5% (see Aluminum compounds, aluminum oxide). 

The magnesia and alumina suspension is prepared by treatment of an aqueous solution, containing aluminum and magnesium salt in the desired proportion, with sodium hydroxide. The coprecipitated aluminum and magnesium hydroxides are collected by filtration, washed free of soluble salts, and stabilized by the addition of a suitable hexatol. 

Magnesium sulfate heptahydrate may be prepared by neutralization of sulfuric acid with magnesium carbonate or oxide, or it can be obtained directly from natural sources. It occurs abundantly as a double salt and can also be obtained from the magnesium salts that occur in brines used for the extraction of bromine (qv). The brine is treated with calcium hydroxide to precipitate magnesium hydroxide. Sulfur dioxide and air are passed through the suspension to yield magnesium sulfate (see Chemicals frombrine). Magnesium sulfate is a saline cathartic. 

Aqueous work-up of the typical Grignard reaction gives a mixed magnesium hydroxide—haUde solution or suspension which must be disposed of. The cost of disposal of the acidic aqueous waste in accordance with local wastewater treatment regulations must also be considered. 

AH gg = —43.03 kJ/mol ( — 10.28 kcal/mol) including heat of solution, at standard state m = V) and may require a heat sink to prevent boiling of the reaction mixture. A 30% by weight suspension of MgO in 20°C water boils in the absence of any heat sink. The time to reach boiling is dependent on the reactivity of the MgO raw material, and this time can be only several hours for the more reactive grades of MgO. Investigations of the kinetics of formation of magnesium hydroxide by hydration of MgO have been reported (79). 

Structure Modification. Several types of stmctural defects or variants can occur which figure in adsorption and catalysis (/) surface defects due to termination of the crystal surface and hydrolysis of surface cations (2) stmctural defects due to imperfect stacking of the secondary units, which may result in blocked channels (J) ionic species, eg, OH , AIO 2, Na", SiO , may be left stranded in the stmcture during synthesis (4) the cation form, acting as the salt of a weak acid, hydrolyzes in aqueous suspension to produce free hydroxide and cations in solution and (5) hydroxyl groups in place of metal cations may be introduced by ammonium ion exchange, followed by thermal deammoniation. 

Iron Reduction. The reduction of nitrophenols with iron filings or turnings takes place in weakly acidic solution or suspension (30). The aminophenol formed is converted to the water soluble sodium aminopheno1 ate by adding sodium hydroxide before the iron-iron oxide sludge is separated from the reaction mixture (31). Adjustment of the solution pH leads to the precipitation of aminophenols, a procedure performed in the absence of air because the salts are very susceptible to oxidation in aqueous solution. 

Catalytic Reduction. Catalytic reduction usually takes place in solution, emulsion, or suspension in autoclaves or pressurized vessels after the catalyst is added, the vessel is pressurized with hydrogen (32,33). Water and methanol are the preferred solvents. In water the addition of alkaU hydroxide (34), alkah carbonate (35), or acid (36) has been recommended. 

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