Double salts, precipitation

The isolated double salt precipitated by mercury(II) chloride explodes violently if heated during drying. 

In addition to the use of malo-lactic fermentation in red wines, it also has been tried in V. vinifera cultivar Chardonnay. In the experiments known to the author, the use of the malo-lactic fermentation in Chardonnay has not proved successful from a sensory point of view. In general, the rise in pH was too great and the buffering capacity of the wine too great to permit adequate adjustment with tartaric acid. However, this work is continuing in conjunction with a number of variations in the local viticultural practices to produce Chardonnay of a lower total acidity. In addition to the use of malo-lactic fermentation for the reduction of the acidity, considerable work has been done in Washington on the use of acid reduction with calcium. Both calcium carbonate and the double salt precipitation, as described by Steele (23, 24), have been utilized. Some very significant successes have been achieved, particularly with the double salt method. 

Calcium Double-Salt Precipitation, Am.J. Enol. Vitic. 1979, 30, 327-331. 

The mixed precipitate of double salt and ferrous ferricyanide is filtered out, washed to remove sulphates and sulphocyanides and decomposed by boiling with sodium carbonate, forming the sodium ferrocyanide and setting free the ammonia which is distilled off and collected. The sodium ferrocyanide solution is filtered off from the iron-lime precipitate, concentrated and crystallized as already described on page 404. Unfortunately the double salt precipitate is very difficult to wash, with the result that frequently considerable amounts of sulphates pass into the finished liquor as sodium sulphate. The first crop of crystals is normally a pure, high-grade sodium ferrocyanide. The first mother liquor is concentrated to proper density and crystallized in like manner. 

The process of rare earth recovery is based on rare-earth double-salt precipitation. However, yttrium and the heavy rare earths go with thorium. The rare earths are recoverable from the thorium fraction during the solvent extraction step used for the purification of uranium and thorium. Solvent extraction with TBP (tribulyl phosphate ), from an aqueous 8 N nitric acid solution of thorium and mixed rare earths, enables the recovery of thorium, uranium, cerium and cerium free rare earths (Gupta and Krishnamurthy 2005). Other significant processes involve precipitation of thorium pyrophosphate, or precipitation as basic salts from the leach fiquor. After that comes recovery of the rare earths from solution as double sulphates, fluorides, or hydroxides, and also selective solubilisation of thorium itself in the ore treatment stage. The sulphuric acid route does yield impure products, but it is not used anymore (Gupta and Krishnamurthy 2005). 

Anhydrous aluminum triduotide, A1F., is a white crystalline soHd. Physical properties are Hsted ia Table 2. Aluminum duotide is spatingly soluble ia water (0.4%) and iasoluble ia dilute mineral acids as well as organic acids at ambient temperatures, but when heated with concentrated sulfuric acid, HF is hberated, and with strong alkah solutions, aluminates are formed. A1F. is slowly attacked by fused alkahes with the formation of soluble metal duotides and aluminate. A series of double salts with the duotides of many metals and with ammonium ion can be made by precipitation or by soHd-state reactions. 

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. 

Fra.ctiona.1 Precipituition. A preliminary enrichment of certain lanthanides can be carried out by selective precipitation of the hydroxides or double salts. The lighter lanthanides (La, Ce, Pr, Nd, Sm) do not easily form soluble double sulfates, whereas those of the heavier lanthanides (Ho, Er, Tm, Yb, Lu) and yttrium are soluble. Generally, the use of this method has been confined to cmde separation of the rare-earth mixture into three groups light, medium, and heavy. 

Uses. The principal use of monosodium phosphate is as a water-soluble soHd acid and pH buffer, primarily in acid-type cleaners. The double salt, NaH2P04 H PO, referred to as hemisodium orthophosphate or sodium hemiphosphate, is often generated in situ from monosodium phosphate and phosphoric acid in these types of formulations. Mixtures of mono- and disodium phosphates are used in textile processing, food manufacture, and other industries to control pH at 4—9. Monosodium phosphate is also used in boiler-water treatment, as a precipitant for polyvalent metal ions, and as an animal-feed supplement. 

The central carbon atom is derived from an aromatic aldehyde or a substance capable of generating an aldehyde during the course of the condensation. Malachite green is prepared by heating benzaldehyde under reflux with a slight excess of dimethyl aniline in aqueous acid (Fig. 2). The reaction mass is made alkaline and the excess dimethylaniline is removed by steam distillation. The resulting leuco base is oxidized with freshly prepared lead dioxide to the carbinol base, and the lead is removed by precipitation as the sulfate. Subsequent treatment of the carbinol base with acid produces the dye, which can be isolated as the chloride, the oxalate [2437-29-8] or the zinc chloride double salt [79118-82-4]. 

BaS hydrolyzes to Ba(OH)2 and barium hydrosulfide. Cooling of an aqueous BaS solution can precipitate the double salt barium hydroxide sulfide hydrate [42821-46-3J, Ba(OH)2 Ba(SH)2 -xH O. 

Hydrochloric acid digestion takes place at elevated temperatures and produces a solution of the mixed chlorides of cesium, aluminum, and other alkah metals separated from the sUiceous residue by filtration. The impure cesium chloride can be purified as cesium chloride double salts such as cesium antimony chloride [14590-08-0] 4CsCl SbCl, cesium iodine chloride [15605 2-2], CS2CI2I, or cesium hexachlorocerate [19153 4-7] Cs2[CeClg] (26). Such salts are recrystaUized and the purified double salts decomposed to cesium chloride by hydrolysis, or precipitated with hydrogen sulfide. Alternatively, solvent extraction of cesium chloride direct from the hydrochloric acid leach Hquor can be used. 

The amine (Imol) is added to a solution of anhydrous zinc chloride (Imol) in concentrated hydrochloric acid (42mL) in ethanol (200mL, or less depending on the solubility of the double salt). The solution is stirred for Ih and the precipitated salt is filtered off and recrystallised from ethanol. The free base is recovered by adding excess of 5-ION NaOH (to dissolve the zinc hydroxide that separates) and is steam distilled. Mercuric chloride in hot water can be used instead of zinc chloride and the salt is crystallised from 1% hydrochloric acid. Other double salts have been used, e.g. cuprous salts, but are not as convenient as the above salts. 

Triphenylselenonium chloride may be precipitated from aqueous solution as the zinc chloride double salt.1... 

Silver nitrate (or other soluble salt) reacts with acetylene in presence of ammonia to form silver acetylide, a sensitive and powerful detonator when dry. In the absence of ammonia, or when calcium acetylide is added to silver nitrate solution, explosive double salts of silver acetylide and silver nitrate are produced. Mercury(I) acetylide precipitates silver acetylide from the aqueous nitrate. 

To the solution of the dye so obtained (and filtered if necessary) a clear concentration solution of zinc chloride (12 g.) is added, and then the zinc chloride double salt of the dye is precipitated by addition of saturated brine. (Test with a spot on filter paper to see whether the solution is nearly colourless.) To purify the dye, which has been collected at the pump and washed with brine, it is redissolved in hot water and, after cooling, salted out as above. Yield 9-10 ... 

The mother liquor obtained from the crystallized hydrazine sulfate contains a small amount of hydrazine. If 200 g. of copper sulfate are dissolved in water and added to 10 1. of the filtrates from the above processes, a light-blue crystalline precipitate of the double salt of copper sulfate and hydrazine sulfate will be formed after ten hours. This salt, when suspended in ten times its weight of distilled water and treated with hydrogen sulfide,... 

In aqueous solution, the dihydrate, CaS04 2H2O (soluble in water) undergoes double decomposition reactions with other soluble salts, precipitating out insoluble salts ... 

Europeum generally is produced from two common rare earth minerals monazite, a rare earth-thorium orthophosphate, and bastnasite, a rare earth fluocarbonate. The ores are crushed and subjected to flotation. They are opened by sulfuric acid. Reaction with concentrated sulfuric acid at a temperature between 130 to 170°C converts thorium and the rare earths to their hydrous sulfates. The reaction is exothermic which raises the temperature to 250°C. The product sulfates are treated with cold water which dissolves the thorium and rare earth sulfates. The solution is then treated with sodium sulfate which precipitates rare earth elements by forming rare earth-sodium double salts. The precipitate is heated with sodium hydroxide to obtain rare earth hydrated oxides. Upon heating and drying, cerium hydrated oxide oxidizes to tetravalent ceric(lV) hydroxide. When the hydrated oxides are treated with hydrochloric acid or nitric acid, aU but Ce4+ salt dissolves in the acid. The insoluble Ce4+ salt is removed. 

Aqueous solution of lead dichloride also undergoes double decomposition reactions with several metal salts, precipitating insoluble lead salts. 

Magnesium sulfate undergoes three important types of reactions in aqueous solutions double decomposition, double salt formation, and formation of oxysulfate cements. Many insoluble magnesium salts may be precipitated out by double decomposition reactions ... 

The monazite sand is heated with sulfuric acid at about 120 to 170°C. An exothermic reaction ensues raising the temperature to above 200°C. Samarium and other rare earths are converted to their water-soluble sulfates. The residue is extracted with water and the solution is treated with sodium pyrophosphate to precipitate thorium. After removing thorium, the solution is treated with sodium sulfate to precipitate rare earths as their double sulfates, that is, rare earth sulfates-sodium sulfate. The double sulfates are heated with sodium hydroxide to convert them into rare earth hydroxides. The hydroxides are treated with hydrochloric or nitric acid to solubihze all rare earths except cerium. The insoluble cerium(IV) hydroxide is filtered. Lanthanum and other rare earths are then separated by fractional crystallization after converting them to double salts with ammonium or magnesium nitrate. The samarium—europium fraction is converted to acetates and reduced with sodium amalgam to low valence states. The reduced metals are extracted with dilute acid. As mentioned above, this fractional crystallization process is very tedious, time-consuming, and currently rare earths are separated by relatively easier methods based on ion exchange and solvent extraction. 

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