Calcium ground

Cements are commonly made by heating a mixture of limestone and clay to about 1700 C. The product is ground with gypsum. Chemically cements consist of a mixture of calcium silicates and aluminates with some sulphate present. World production 1976 730 megatonnes. 

For this preparation, which must be performed in the fume-cupboard, assemble the apparatus shown in Fig. 67(A). C is a 150 ml. distilling-flask, to the neck of which is fitted a reflux single-surface water-condenser D, closed at the top E by a calcium chloride tube. The side-arm of C carries a cork F which fits the end E of the condenser for subsequent distillation. The side-arm of C is meanwhile plugged by a small rubber cork, or by a short length of glass rod. (Alternatively, use the ground-glass flask and condenser (Fig. 22 (a) and (c), p. 43), and... 

Higher alcohols. These may be purified by drying with anhydrous potassium carbonate or with anhydrous calcium sulphate, and fractionated after filtration from the desiccant. Bark corks (or ground glass joints) should be used rubber stoppers are slightly attacked. The boiUng points of the fractions to be collected are as follows —... 

Method 1. a-Naphthonitrile. Place 80 g. (54 ml.) of redistilled a-bromonaphthalene (Section IV.20), 43 g. of dry powdered cuprous cyanide (Section II,50,J) and 36 g. (37 ml.) of dry pure pyridine (1) (Section 11,47.22) in a 250 ml. round-bottomed flask fitted with a ground-in reflux condenser carrying a calcium chloride (or cotton wool) guard tube, and heat the mixture in a metal bath at 215-225° for... 

Analgesic tablets are ground into a fine powder, dissolved in HCl, and analyzed for calcium by atomic absorption. A releasing agent of La + is used to prevent an interference due to the formation of calcium pyrophosphate. 

Cascara sagrada is used as a cathartic. It is most useful when prepared as a fluid extract, and tends to be a mild laxative causing Htfle discomfort. However, on prolonged use it may result in characteristic melanotic pigmentation of the rectal mucosa. The bitter taste can be lessened, owing to neutralization of the acid constituents, if the ground substance is moistened and mixed with magnesium or calcium hydroxide. This treatment may lessen the potency of the preparation. 

In cyanidation, the ground ore is leached with a solution of sodium cyanide (0.02—0.05%) or an equivalent of calcium cyanide together with some lime. The leaching solution is aerated to provide oxygen and gold is dissolved with formation of sodium dicyanoauratae(-l) [15280-09-8] 5 2l(J u(C2>5)[) (see... 

Mineral Feed. Mineral feed supplements for domestic animals and fowl usually contain a pure form of pulverized limestone. In fact, some state laws require the supplement to be at least 35% available calcium. Other sources of calcium are bone meal and dicalcium phosphate. Use as mineral feed has been a steadily growing market for limestone. The material is ground to 90% minus 0.15 mm (100 mesh) or 80% minus 0.9074 mm (200 mesh), is low in silica, and has strict tolerances on arsenic and fluorine (see Feeds and feed additives). 

Plastics. The fastest-growing use of whiting (microcarbonate fillers) is in the plastics industry where dry, pulverized limestone is used intensively for most types of plastics. Other carbonate fillers, precipitated calcium carbonate, oyster sheU, marble, and wet-ground limestone, are also used. 

L. Gorbaty and co-workers, "Fine Ground and Precipitated Calcium Carbonate," CEH Product Review, 1993. 

Calcium carbonate, available both from natural sources and as precipitated forms (see Calcium compounds), is most useful in coating because of purity and high brightness, ie, 90—95%. Ground carbonates from marble deposits have high purity levels as do the carbonates from some chalk deposits. 

Some companies have used the Merseburg process to manufacture ammonium sulfate from gypsum, but the process is only economically attractive where sulfur is unavailable or very expensive (32), and is thus not used in the United States. Ammonium carbonate, formed by the reaction of ammonia and carbon dioxide in an aqueous medium, reacts with suspended, finely ground gypsum. Insoluble calcium carbonate and an ammonium sulfate solution are formed. 

In another process, strontium sulfate can be converted to strontium carbonate direcdy by a metathesis reaction wherein strontium sulfate is added to a solution of sodium carbonate to produce strontium carbonate and leave sodium sulfate in solution (6). Prior to this reaction, the finely ground ore is mixed with hydrochloric acid to convert the calcium carbonates and iron oxides to water-soluble chlorides. 

A number of high temperature processes for the production of titanium carbide from ores have been reported (28,29). The aim is to manufacture a titanium carbide that can subsequently be chlorinated to yield titanium tetrachloride. In one process, a titanium-bearing ore is mixed with an alkah-metal chloride and carbonaceous material and heated to 2000°C to yield, ultimately, a highly pure TiC (28). Production of titanium carbide from ores, eg, ilmenite [12168-52-4], EeTiO, and perovskite [12194-71 -7], CaTiO, has been described (30). A mixture of perovskite and carbon was heated in an arc furnace at ca 2100°C, ground, and then leached with water to decompose the calcium carbide to acetjdene. The TiC was then separated from the aqueous slurry by elutriation. Approximately 72% of the titanium was recovered as the purified product. In the case of ilmenite, it was necessary to reduce the ilmenite carbothermaHy in the presence of lime at ca 1260°C. Molten iron was separated and the remaining CaTiO was then processed as perovskite. 

When boric acid is made from colemanite, the ore is ground to a fine powder and stirred vigorously with diluted mother Hquor and sulfuric acid at about 90°C. The by-product calcium sulfate [7778-18-9] is removed by settling and filtration, and the boric acid is crystallised by cooling the filtrate. 

Calcium carbonate [471-34-17, CaCO, mol wt 100.09, occurs naturally as the principal constituent of limestone, marble, and chalk. Powdered calcium carbonate is produced by two methods on the industrial scale. It is quarried and ground from naturally occurring deposits and in some cases beneficiated. 

It is also made by precipitation from dissolved calcium hydroxide and carbon dioxide. The natural ground calcium carbonate and the precipitated material compete industrially based primarily on particle size and the characteristics imparted to a product. 

Natural ground calcium carbonate has been used for years as the primary constituent of putty. Since 1945, the processing of natural calcium carbonate has seen the introduction of beneficiation by flotation (qv) to remove impurities and the development of grinding processes to manufacture finer products. Precipitated calcium carbonate was first introduced in England in 1850 commercial production started in the United States in about 1913. 

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