Lime, Phosphates

Ceramics and minerals present many common problems, but ceramics warrant special treatment because elements of low atomic number predominate in them and they consequently offer x-ray emission spectrog-raphy of the light elements an excellent opportunity to prove its usefulness. Scott,8 in making this clear, emphasized the absorption and enhancement effects to be expected, and pointed out the need for careful sample preparation. By use of a General Electric XRD-5 spectrograph and associated equipment, he set up working curves for alumina, silica, potash, lime, phosphate, titania, and iron oxide in clays, refractories, and other ceramic materials. 

Adequate levels of lime, phosphate and potash in the soil are especially important for organic dairy farmers, because these nutrients are essential for healthy white clover. The supply of these nutrients and general manure strategy is covered fully by Newton (1993). 

Carbide, Spent, Powdered. Carbonate (See Limestone)... Oxide, Powdered (See Lime). Phosphate, See Phosphates... 

Agricultural practices have also been applied to soil remediation. Most commonly, the uptake of metals by plants is diminished by keeping a neutral soil pH and by amendments with materials having a high capacity to bind metals in possibly slightly mobile fractions. Various materials are used for soil amendments and remediation these are mainly lime, phosphate fertilizers, zeolites, montmorillonite clays, humic... 

This element occurs abundantly in the bones of animals, in combination with oxygen and metals, as phosphate of lime, phosphate of magnesia, ( . It is also an ingredient in some unknown form of combination, of vegetable and animal fibrine and albumen, and is constantly present in the urine and excrements. In the mineral kingdom it occurs as phosphate of lime (apatite), phosphate of alumina (wavellite), phosphates of lead, copper, c. 

Fourcroy examined gall stones and calculi. In 1800 Fourcroy and Vauquelin published an important memoir on the composition of urinary calculi, which somewhat extended the publications of Wollaston — which they do not mention — and of Pearson, who changed Scheele s name lithic acid into uric oxide or ouric oxide Fourcroy and Vauquelin called it adde urique. They analysed over 600 calculi and concluded that they are of twelve main species, consisting of the following substances, or mixtures of them uric acid, urate of ammonia, phosphate of lime, phosphate of magnesia and ammonia. 

At the beginning of the enterprise the furnace was charged with calcined alumina phosphate (imported from the West Indies), lime phosphate (obtained locally), coke and sand. After about 1900 local phosj-phate was replaced by ore from Tennessee and then Florida. Alumina phosphate was dispensed with after 1910. 

It was not Liebig, however, but an Irish doctor, James Murray (1788-1871), who became the first commercial vendor of inorganic fertilizers with his 1841 offer of liquid superphosphate made by dissolving bones in H2 04. Two years later Lawes set up a superphosphate factory at Deptford on the Thames. His fertilizer, patented in May 1842 on the same day Murray got his patent, was a virtually identical product, containing Super-Phosphate of Lime, Phosphate of Ammonia, Silicate of Potass, etc. ... 

Qualitative examples abound. Perfect crystals of sodium carbonate, sulfate, or phosphate may be kept for years without efflorescing, although if scratched, they begin to do so immediately. Too strongly heated or burned lime or plaster of Paris takes up the first traces of water only with difficulty. Reactions of this type tend to be autocat-alytic. The initial rate is slow, due to the absence of the necessary linear interface, but the rate accelerates as more and more product is formed. See Refs. 147-153 for other examples. Ruckenstein [154] has discussed a kinetic model based on nucleation theory. There is certainly evidence that patches of product may be present, as in the oxidation of Mo(lOO) surfaces [155], and that surface defects are important [156]. There may be catalysis thus reaction VII-27 is catalyzed by water vapor [157]. A topotactic reaction is one where the product or products retain the external crystalline shape of the reactant crystal [158]. More often, however, there is a complicated morphology with pitting, cracking, and pore formation, as with calcium carbonate [159]. 

To prepare the standard pH buffer solutions recommended by the National Bureau of Standards (U.S.), the indicated weights of the pure materials in Table 8.15 should be dissolved in water of specific conductivity not greater than 5 micromhos. The tartrate, phthalate, and phosphates can be dried for 2 h at 100°C before use. Potassium tetroxalate and calcium hydroxide need not be dried. Fresh-looking crystals of borax should be used. Before use, excess solid potassium hydrogen tartrate and calcium hydroxide must be removed. Buffer solutions pH 6 or above should be stored in plastic containers and should be protected from carbon doxide with soda-lime traps. The solutions should be replaced within 2 to 3 weeks, or sooner if formation of mold is noticed. A crystal of thymol may be added as a preservative. 

Calcium. Calcium is the fifth most abundant element in the earth s cmst. There is no foreseeable lack of this resource as it is virtually unlimited. Primary sources of calcium are lime materials and gypsum, generally classified as soil amendments (see Calcium compounds). Among the more important calcium amendments are blast furnace slag, calcitic limestone, gypsum, hydrated lime, and precipitated lime. Fertilizers that carry calcium are calcium cyanamide, calcium nitrate, phosphate rock, and superphosphates. In addition, there are several organic carriers of calcium. Calcium is widely distributed in nature as calcium carbonate, chalk, marble, gypsum, fluorspar, phosphate rock, and other rocks and minerals. 

The rat LD qS are 13, 3.6 (oral) and 21, 6.8 (dermal) mg/kg. Parathion is resistant to aqueous hydrolysis, but is hydroly2ed by alkah to form the noninsecticidal diethjlphosphorothioic acid and -nitrophenol. The time required for 50% hydrolysis is 120 d ia a saturated aqueous solution, or 8 h ia a solution of lime water. At temperatures above 130°C, parathion slowly isomerizes to 0,%diethyl 0-(4-nitrophenyl) phosphorothioate [597-88-6] which is much less stable and less effective as an insecticide. Parathion is readily reduced, eg, by bacillus subtilis ia polluted water and ia the mammalian mmen to nontoxic 0,0-diethyl 0-(4-aminophenyl) phosphorothioate, and is oxidized with difficulty to the highly toxic paraoxon [511-45-5] diethyl 4-nitrophenyl phosphate d 1.268, soluble ia water to 2.4 mg/L), rat oral LD q 1.2 mg/kg. 

Miscellaneous. Both whiting and hydrated lime are used as diluents and carriers of pesticides, such as lime—sulfur sprays, Bordeaux, calcium arsenate, etc. The most widely used bleach and sterilizer, high test calcium hypochlorite, is made by interacting lime and chlorine (see Bleaching AGENTS). Calcium and magnesium salts, such as dicalcium phosphate, magnesium chloride, lithium salts, etc, are made directly from calcific and dolomitic lime and limestone. 

Lubricant carriers are applied by dippiag the workpiece ia hot solution or slurries such as lime or phosphate coatings. Details of surface treatments are available (5) (see also Metal surface TiiEATiffiNTs). 

Because monocalcium phosphate is incongmently soluble, it is typically contaminated with various amounts (6—10%) of dicalcium phosphate and free phosphoric acid resulting from in-process disproportionation of the monocalcium salt. Free phosphoric acid may render the product hygroscopic, and absorbed water plus acid catalyzes further decomposition to additional free acid and dicalcium phosphate. For this reason, industrial monocalcium phosphate may contain some dicalcium phosphate resulting from excess lime addition and then aged to ensure the removal of residual free phosphoric acid. 

Tricalcium phosphate, Ca2(P0 2> is formed under high temperatures and is unstable toward reaction with moisture below 100°C. The high temperature mineral whidockite [64418-26-4] although often described as P-tricalcium phosphate, is not pure. Whidockite contains small amounts of iron and magnesium. Commercial tricalcium phosphate prepared by the reaction of phosphoric acid and a hydrated lime slurry consists of amorphous or poody crystalline basic calcium phosphates close to the hydroxyapatite composition and has a Ca/P ratio of approximately 3 2. Because this mole ratio can vary widely (1.3—2.0), free lime, calcium hydroxide, and dicalcium phosphate may be present in variable proportion. The highly insoluble basic calcium phosphates precipitate as fine particles, mosdy less than a few micrometers in diameter. The surface area of precipitated hydroxyapatite is approximately... 

Anhydrous monocalcium phosphate, Ca(H2PObe made in a pan mixer from concentrated phosphoric acid and lime. The high heat of reaction furnishes essentially all the necessary thermal input and subsequent drying is minimized. A small amount of aluminum phosphate or a mixture of sodium and potassium phosphates is added in the form of proprietary stabilizers for coating the particles. Heat treatment converts the coating to a protective polyphosphate (19). 

Tricalcium Phosphate. Commercial tricalcium phosphate (TCP) is actually an amorphous basic calcium phosphate close to hydroxyapatite in composition. Because of its extremely low solubiUty in water, TCP is precipitated almost quantitatively from dilute phosphate solutions with a slurry of hydrated lime. TCP is separated by dmm-, spray-, or flash-drying the TCP slurry, with or without intermediate sedimentation or filtration steps. It is used as an industrial-grade flow conditioner and parting agent. 

Recovering ammonia as a by-product from other processes accounted for less than 1% of the total U.S. ammonia production in 1987. The principal source of by-product ammonia is from the coking of coal. In the coking operation, about 15—20% of the nitrogen present in the coal is Hberated as ammonia and is recovered from the coke oven gas as ammonium sulfate, ammonia Hquor, and ammonium phosphates. The recovery product depends on the scmbbing medium employed, sulfuric acid, milk of lime, and phosphoric acid, respectively. Ammonium sulfate recovery by the so-called semidirect process, is most widely employed. 

Bone, or osseous tissue, is composed of osteocytes and osteoclasts embedded in a calcified matrix. Hard tissue consists of about 50% water and 50% solids. The solids are composed of cartilaginous material hardened with inorganic salts, such as calcium carbonate and phosphate of lime. 

Phosphatation. Phosphoric acid to give a concentration up to 400 mg/kg as P2O5 and calcium hydroxide as milk of lime or sugar solution of... 

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