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Calcium hydroxide solubility

Explain why calcium hydroxide (solubility 0.165 g per 100 g water at 20°C) is much more soluble than magnesium hydroxide (solubility 0.0009 g per 100 g water at 20°C). [Pg.411]

From an examination of the literature data the revise is noted between calcium hydroxide solubility and mineralization in the solutions when the sodium chloride concentration is 1.75-3.96 g-eq 1. ... [Pg.389]

Lithium Hydroxide. Lithium hydroxide monohydrate [1310-66-3], Li0H-H2 0, is prepared industrially from the reaction of lithium carbonate and calcium hydroxide in aqueous slurries. The calcium carbonate is subsequently separated to yield a lithium hydroxide solution from which lithium hydroxide monohydrate can be crystallized. Lithium hydroxide is the least soluble alkaH hydroxide, and solubiHty varies Htfle with temperature. [Pg.226]

The second most common alkalinity control agent is lime [1305-78-8] normally in the form of calcium hydroxide [1303-62-0], used in both water and oH muds. In the latter, the lime reacts with added emulsifiers and fatty acids to stabHi2e water-in-oH emulsions. Lime is used in brine systems containing substantial quantities of soluble calcium and in high pH lime muds. Concentrations are ca 6—57 kg/m (2—20 lb /bbl) (see Lime AND LIMESTONE). [Pg.181]

Lime-Sulfuric. Recovery of citric acid by calcium salt precipitation is shown in Figure 3. Although the chemistry is straightforward, the engineering principles, separation techniques, and unit operations employed result in a complex commercial process. The fermentation broth, which has been separated from the insoluble biomass, is treated with a calcium hydroxide (lime) slurry to precipitate calcium citrate. After sufficient reaction time, the calcium citrate slurry is filtered and the filter cake washed free of soluble impurities. The clean calcium citrate cake is reslurried and acidified with sulfuric acid, converting the calcium citrate to soluble citric acid and insoluble calcium sulfate. Both the calcium citrate and calcium sulfate reactions are generally performed in agitated reaction vessels made of 316 stainless steel and filtered on commercially available filtration equipment. [Pg.183]

Calcium Chelates (Salicylates). Several successhil dental cements which use the formation of a calcium chelate system (96) were developed based on the reaction of calcium hydroxide [1305-62-0] and various phenohc esters of sahcyhc acid [69-72-7]. The calcium sahcylate [824-35-1] system offers certain advantages over the more widely used zinc oxide—eugenol system. These products are completely bland, antibacterial (97), facihtate the formation of reparative dentin, and do not retard the free-radical polymerization reaction of acryhc monomer systems. The principal deficiencies of this type of cement are its relatively high solubihty, relatively low strength, and low modulus. Less soluble and higher strength calcium-based cements based on dimer and trimer acid have been reported (82). [Pg.475]

Calcium hydroxide (Ca(OH)2 (slaked lime) ) White powder soluble in water yielding lime water. Alkaline... [Pg.28]

Neutralizers. To maintain pH levels in alkaline regions, it is necessary to neutralize the acidic components of the corrosive medium. Water-soluble, alkaline materials, such as sodium hydroxide (NaOH), ammonium hydroxide (NH OH) and calcium hydroxide [Ca(OH)J, can be used to obtain pH levels around 9.6. However, care must be taken to avoid reaching pH levels that are... [Pg.1332]

The product, calcium hydroxide, is commonly known as slaked lime because, as calcium hydroxide, the thirst of lime for water has been quenched (slaked). Slaked lime is the form in which lime is normally sold because quicklime can set fire to moist wood and paper. In fact, the wooden boats that were once used to transport quicklime sometimes caught fire in the heat of reaction when water seeped into their holds. An aqueous solution of calcium hydroxide, which is slightly soluble in water, is called lime water. It is used as a test for carbon dioxide, with which it reacts to form a suspension of the much less soluble calcium carbonate ... [Pg.716]

C16-0106. Write the equilibrium reaction and equilibrium constant expression for each of the following processes (a) Trichloroacetic acid, CI3 CCO2H, is added to water, (b) Aniline, (Cg H5) NH2, a weak base, is dissolved in water, (c) Solid calcium hydroxide, Ca (OH)2, a sparingly soluble salt, is added to water. [Pg.1203]

Sodium hydroxide (NaOH) (caustic soda) Potassium hydroxide (KOH) (caustic potash) Calcium hydroxide (Ca(OH)2) (slaked lime) Ammonium hydroxide (NH4OH) (aqueous ammonia solution) White deliquescent solid. Sticks, flakes, pellets. Dissolution in water is highly exothermic. Strongly basic. Severe hazard to skin tissue White deliquescent solid. Sticks, flakes, pellets. Dissolution In water is highly exothermic. Strongly basic. Severe hazard to skin tissue White powder soluble in water yielding lime water. Alkaline Weakly alkaline. Emits ammonia gas. Severe eye irritant... [Pg.28]

CCP in milk is mentioned in connection with casein above (Section VI.C). Fluorapatite is a major constituent of phosphate rocks, and a constituent, probably important, of human tooth enamel for those whose drinking water contains significant amounts of naturally occurring or added fluoride. Fluorapatite is significantly less soluble than hydroxyapatite - the relationship between the solubilities of fluorapatite and hydroxyapatite parallels (but is much less extreme than) that between calcium fluoride (Ksp — 3.9 x 10 11 mol3 dm-9) and calcium hydroxide (Ksp = 7.9 x 10 6 mol3 dm 9). Calcium diphosphate, Ca2P207, is believed to be the least soluble of the calcium phosphates. [Pg.332]

In this system, the least soluble component is sodium bicarbonate, so this crystallizes out. On calcination it yields sodium carbonate and the carbon dioxide is recycled. The ammonia is recovered by adding calcium hydroxide, producing calcium chloride waste and liberating the... [Pg.21]

In Investigation 9-A, you will collect solubility data and use these data to determine a Ksp for calcium hydroxide, Ca(OH)2. When you calculate Ksp, you assume that the dissolved ionic compound exists as independent hydrated ions that do not affect one another. This assumption simplifies the investigation, but it is not entirely accurate. Ions do interfere with one another. As a result, the value of Ksp that you calculate will be just an approximation. iCp values that are calculated from data obtained from experiments such as Investgation 9-A are generally higher than the actual values. [Pg.433]

CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE Calcium carbonate (CaCOs), BIOMINERALIZATION SOLUBILITY PRODUCT Calcium hydroxide (Ca(OH)2),... [Pg.728]

The present work deals with the reactive crystallization of magnesium hydroxide, a well-known sparing soluble material, from magnesium chloride with calcium hydroxide. Magnesium hydroxide is produced industrially by the precipitation from brine with... [Pg.344]

Calcium hydroxide has wide industrial applications. It is used to make cement, mortar, plaster, and other building materials. It also is used in water soluble paints, and for fireproofing coatings and lubricants. Other applications are in the manufacture of paper pulp as a preservative for egg in vulcanization of rubber as a depilatory for hides and in preparation of many calcium salts. [Pg.167]

Limewater is a saturated aqueous calcium hydroxide, Ca(OH)2, solution. To make limewater, a small amount of calcium hydroxide is needed. Calcium hydroxide is marketed commercially as slaked lime or hydrated lime. It is used for cement, increasing the pH in soils, and water treatment. Lime may be obtained from building material stores in the cement section and in agricultural stores. The smallest quantities sold are generally 5- or 10-pound bags, which cost a few dollars. Because only a teaspoon of lime is needed (the solubility of calcium hydroxide in water is 0. Ig per 100 mL), ask the sales clerk if there are any broken bags from which you can take a tablespoon of lime. Often there will be enough lime dust where it is stored to obtain an ample amount for this activity. [Pg.321]

The process to obtain morphine from opium involves boiling a water-opium solution and adding calcium hydroxide (Ca(OH2). The calcium hydroxide combines with the morphine to form the water-soluble salt calcium morphenate. As the solution cools, other insoluble alkaloids precipitate out of solution, leaving morphine in solution. The solution is filtered and then reheated. Ammonium chloride (NHCI) is added to increase the solutions pH level to... [Pg.185]

Molecular theory of caustification.—An excess of solid calcium hydroxide is supposed to be present at the start, so that as fast as calcium hydroxide is removed from the soln. by reacting with the potassium carbonate, more passes into soln. Thus the cone, of the calcium hydroxide in the soln. is kept constant. The. solubility of calcium carbonate is very small, and, in consequence, any calcium carbonate in excess of the solubility will be precipitated as fast as it is formed. The reaction proceeds steadily from right to left because, all the time, calcium hydroxide steadily passes into soln., and calcium carbonate is steadily precipitated but the solubility of calcium carbonate steadily increases with increasing cone, of potassium hydroxide. There is a steady transformation of the potassium carbonate into potassium hydroxide in progress The cone, of the potassium carbonate is steadily decreasing, while the cone, of the potassium hydroxide is steadily increasing. Consequently, when the potassium hydroxide has attained a certain cone, so much calcium carbonate will be present in the soln. that the reaction will cease. Hence the cone, of the potassium carbonate should be such that it is all exhausted before the state of equilibrium is reached. If the cone, of the potassium hydroxide should exceed this critical value, the reaction will be reversed, and calcium carbonate will be transformed into calcium hydroxide. [Pg.498]

They also found the yield to be independent of the temp, so that the heat of the reaction is virtually zero, and no improvement can be expected by working at higher temp, under press., as was proposed by E. W. Parnell16 in 1877. According to G. Bod lander and R. Lucas, the hydroxides of barium and strontium are mere soluble than calcium hydroxides, while the carbonates are less soluble than calcium carbonate. Hence, better yields are obtained with these hydroxides. With strontium hydroxide, the reaction is exothermal, so that the yield should be increased by working at lower temp. [Pg.498]

In 1818, A. Arfvedson 17 causticized lithium carbonate by means of calcium hydroxide, but the sparing solubility of lithium carbonate causes but a poor yield. L. Troost made the hydroxide by dissolving in water the oxide obtained by the combustion of the metal and C. G. Gmelin decomposed lithium sulphate by an eq. soln. of barium hydroxide. In either case, the soln. should.be evaporated rapidly to dryness in a silver vessel, and then fused. [Pg.499]

C. W. Scheele (1773) noted that a damp mixture of common salt and calcium hydroxide effloresces after some weeks exposure to air, the efflorescent salt is sodium carbonate. It is probable that calcium bicarbonate is formed, which precipitates soluble sodium bicarbonate, and this explains the formation of the efflorescence of soda from salty soils. The observation made by C. W. Scheele... [Pg.715]


See other pages where Calcium hydroxide solubility is mentioned: [Pg.151]    [Pg.151]    [Pg.164]    [Pg.451]    [Pg.185]    [Pg.1311]    [Pg.593]    [Pg.440]    [Pg.348]    [Pg.364]    [Pg.453]    [Pg.329]    [Pg.430]    [Pg.61]    [Pg.62]    [Pg.1697]    [Pg.296]    [Pg.59]    [Pg.56]    [Pg.154]    [Pg.206]    [Pg.261]    [Pg.264]    [Pg.272]    [Pg.472]    [Pg.498]    [Pg.721]    [Pg.735]   
See also in sourсe #XX -- [ Pg.148 ]

See also in sourсe #XX -- [ Pg.254 , Pg.255 ]

See also in sourсe #XX -- [ Pg.488 ]




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