Carbonate magnesium

Group II hydrogencarbonates have insufficient thermal stability for them to be isolated as solids. However, in areas where natural deposits of calcium and magnesium carbonates are found a reaction between the carbonate, water and carbon dioxide occurs ... 

For temporary hardness due to magnesium carbonate, more lime is required, since the magnesium precipitates as the hydroxide (less soluble than the carbonate) ... 

Thioformamide is prepared in situ at 25 to 30°C. as described previously, and in the presence of magnesium carbonate (492. 512. 578). The mixture is then mildly heated on a water bath, and when temperature reaches 70°C, a-haloaldehyde is added in small quantities. At the end of this addition the reaction mixture is stirred for 2 hr at 100°C. Thiazoles were isolated in the usual manner by a double steam distillation. 

When thioamides such as thiobenzamide are used directly, neither dioxane nor magnesium carbonate is necessary. Instead absolute alcohol with fused sodium acetate in the presence of piperidine is used (457). 

Potassium perchlorate Aluminum plus magnesium, carbon, nickel plus titanium, reducing agents, sulfur, sulfuric acid... 

Processes rendered obsolete by the propylene ammoxidation process (51) include the ethylene cyanohydrin process (52—54) practiced commercially by American Cyanamid and Union Carbide in the United States and by I. G. Farben in Germany. The process involved the production of ethylene cyanohydrin by the base-cataly2ed addition of HCN to ethylene oxide in the liquid phase at about 60°C. A typical base catalyst used in this step was diethylamine. This was followed by liquid-phase or vapor-phase dehydration of the cyanohydrin. The Hquid-phase dehydration was performed at about 200°C using alkah metal or alkaline earth metal salts of organic acids, primarily formates and magnesium carbonate. Vapor-phase dehydration was accomphshed over alumina at about 250°C. 

Alagnesium Fluoroborate. Treatment of magnesium metal, magnesium oxide, or magnesium carbonate with HBF gives magnesium fluoroborate [14708-13-5]. The MgF2 is filtered and the product is sold as a 30% solution. 

Formation of a gelatinous precipitate that is difficult to filter can be avoided by addition of magnesium oxide to the acid solution. In order to increase particle size it is often necessary to keep the solution hot for several hours however, this problem is avoided by heating an intimate mixture of ammonium bifluoride with magnesium carbonate to 150—400°C (11). Particles of Mgp2 similar in size to those of the magnesium carbonate are obtained. 

The same results are obtained by adding magnesium carbonate to an aqueous solution of ammonium bifluoride and ammonium hydroxide and warming to 60°C (12). The resulting precipitate is ammonium magnesium fluoride [35278-29-6] which settles rapidly. 

Light or heavy magnesium carbonate is exposed to a red heat, and carbon dioxide and water are expelled leaving light or heavy magnesium oxide. The density is also influenced by the calcining temperature higher temperatures yield more compact forms. 

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. 

Transparent white pigments (extenders) commonly used in inks, in order of decreasing transparency, ate alumina hydrate, magnesium carbonate, calcium carbonate, blanc fixe (precipitated barium sulfate), talc, and clay. Extenders ate sometimes used to reduce the color strength and change the theology of inks. 

The carbonate minerals that comprise limestone ate calcite [13397-26-7] (calcium carbonate), which is easily the most abundant mineral type aragonite [14791-73-2] (calcium carbonate) dolomite [17069-72-6] (double carbonate of calcium and magnesium) andmagnesite [13717-31 -5] (magnesium carbonate). Individual limstone types ate further described by many common names (1). Some of this nomenclature is repetitious and overlapping. The following terms ate in common use in Europe and the United States. 

Molten magnesium chloride can be formed by the direct carbochlofination of magnesium oxide obtained from the calciaation of magnesium carbonate ores or magnesium hydroxide [1309-42-8]. 

Properties. The physical properties of the normal magnesium carbonates are given in Table 3, those of the basic magnesium carbonates in Table 4. Magnesium carbonate is insoluble in C02-free water. The solubiUty products, iC, for magnesium carbonate and some hydrates foUow (38). 

Table 4. Physical Properties of Basic Magnesium Carbonates ...

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