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Salts orthophosphate

Orthophosphate salts are generally prepared by the partial or total neutralization of orthophosphoric acid. Phase equiUbrium diagrams are particularly usehil in identifying conditions for the preparation of particular phosphate salts. The solution properties of orthophosphate salts of monovalent cations are distincdy different from those of the polyvalent cations, the latter exhibiting incongment solubiUty in most cases. The commercial phosphates include alkah metal, alkaline-earth, heavy metal, mixed metal, and ammonium salts of phosphoric acid. Sodium phosphates are the most important, followed by calcium, ammonium, and potassium salts. [Pg.331]

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. [Pg.332]

Potassium Phosphates. The K2O—P20 —H2O system parallels the sodium system in many respects. In addition to the three simple phosphate salts obtained by successive replacement of the protons of phosphoric acid by potassium ions, the system contains a number of crystalline hydrates and double salts (Table 7). Monopotassium phosphate (MKP), known only as the anhydrous salt, is the least soluble of the potassium orthophosphates. Monopotassium phosphate has been studied extensively owing to its piezoelectric and ferroelectric properties (see Ferroelectrics). At ordinary temperatures, KH2PO4 is so far above its Curie point as to give piezoelectric effects in which the emf is proportional to the distorting force. There is virtually no hysteresis. [Pg.332]

Evolution of ammonia from a boiling dilute solution of diammonium phosphate gradually reduces the pH. This process is used commercially to control the precipitation of alkaH-soluble—acid-insoluble coUoidal dyes on wool. Other ammonium orthophosphate salts of interest are ammonium hemiphosphate [28537-48-6] NH4H2PO4 H3PO4, and its hydrate [28037-74-3], as well as the trihydrate [78436-07-4] of DAP. [Pg.333]

Many orthophosphate salts, in particular those of polyvalent cations, exhibit incongment solubihty where disporportionation occurs in solution to yield a more basic orthophosphate salt and phosphoric acid. This hydrolytic disproportionation of orthophosphates should not be confused with the... [Pg.333]

TSPP is readily crystallised from water as the decahydrate between —0.4° and 79°C, and as the anhydrous salt above 79°C. The solubiUty of tetrasodium pyrophosphate is illustrated in Figure 8. The pH of a 1% solution is 10.2. TSPP is quite stable in alkaline medium but hydrolyses rapidly to orthophosphate under acid conditions. [Pg.336]

Sodium tripolyphosphate is produced by calcination of an intimate mixture of orthophosphate salts containing the correct overall Na/P mole ratio of 1.67. The proportions of the two anhydrous STP phases are controlled by the calcination conditions. Commercial STP typically contain a few percent of tetrasodium pyrophosphate and some trimetaphosphate. A small amount of unconverted orthophosphates and long-chain polyphosphates also may be present. [Pg.337]

The general manufacturing scheme for phosphate salts is shown in Figure 11. Condensed phosphates are prepared from the appropriate orthophosphate or mixture of orthophosphates, so the preparation of orthophosphates must be considered first for the manufacture of any phosphate salt. Phosphoric acid is neutralized to form a solution or slurry with a carefully adjusted acid/base ratio according to the desired orthophosphate product. The orthophosphate may be recovered either by crystallization from solution, or the entire solution or slurry may be evaporated to dryness. The dewatering (qv) method is determined by the solubihty properties of the product and by its desired physical properties such as crystal size and shape, bulk density, and surface area. Acid orthophosphate salts may be converted to condensed phosphates by thermal dehydration (calcination). [Pg.340]

Alkali Meta.IPhospha.tes, A significant proportion of the phosphoric acid consumed in the manufacture of industrial, food, and pharmaceutical phosphates in the United States is used for the production of sodium salts. Alkali metal orthophosphates generally exhibit congment solubility and are therefore usually manufactured by either crystallisation from solution or drying of the entire reaction mass. Alkaline-earth and other phosphate salts of polyvalent cations typically exhibit incongment solubility and are prepared either by precipitation from solution having a metal oxide/P20 ratio considerably lower than that of the product, or by drying a solution or slurry with the proper metal oxide/P20 ratio. [Pg.341]

Silver Phosphates. Silver phosphate [7784-09-0], or silver orthophosphate, Ag3P04, is a bright yellow material formed by treating silver nitrate with a soluble phosphate salt or phosphoric acid. Silver pyrophosphate [13465-97-9], is a white salt prepared by the addition of a soluble... [Pg.90]

Na[Sb(OH)g], respectively. The latter compound is one of the least soluble sodium salts known and is useful in sodium analysis. Numerous polyantimonate(V) derivatives are prepared by heat treatment of mixtures of antimony trioxide and other metal oxides or carbonates. Of these, K Sb O [12056-59-6] and K Sb O [52015-49-3] have been characterized by x-ray. These consist of three-dimensional networks of SbO in which corners and edges are shared with K" ions located in tunnels through the network (23). Simple species such as SbO and Sb20 2, analogous to orthophosphate and pyrophosphate, apparendy do not exist. [Pg.203]

In the presynthetic surfactant era, soap was budt (and stiU is) with alkaline salts such as soda ash, sdicates, orthophosphates, and borates. These materials buffer the wash solution to a high pH and prevent soap protonation thus the soap remains effective. Another type of budder is the neutral... [Pg.529]

The method may be standardised, if desired, with pure potassium dihydrogen-orthophosphate (see below) sufficient 1 1 hydrochloric acid must be present to prevent precipitation of quinoline molybdate the molybdophosphate complex is readily formed at a concentration of 20 mL of concentrated hydrochloric acid per 100 mL of solution especially when warm, and precipitation of the quinoline salt should take place slowly from boiling solution. A blank determination should always be made it is mostly due to silica. [Pg.304]

The most general method for the simultaneous analysis of oxyanions by gas chromatography is the formation of trimethylsilyl derivatives. Trimethylsilyl derivatives of silicate, carbonate, oxalate, borate, phosphite, phosphate, orthophosphate, arsenite, arsenate, sulfate and vanadate, usually as their ammonium salts, are readily prepared by reaction with BSTFA-TMCS (99 1). Fluoride can be derivatized in aqueous solution with triethylchlorosilane and the triethylfluorosilane formed extracted into an immiscible organic solvent for analysis by gas chromatography [685). [Pg.959]

In 1970, Monroe and Rooker(28) claimed the use of aluminum salts of acid orthophosphate esters as viscosity builders for use in fracturing fluids. The application of these materials began a new era of hydrocarbon gelling agents. Monroe(29) later claimed the use of Fe30it as a metal activator of phosphate esters and in 1971 described several other metals(30) that could be used with amine neutralization agents. Numerous metallic ionic derivatives can be used as effective "activators" or crosslinkers to prepare a gel. [Pg.66]

Poklacki, E.S. "Polyamine Salts of Aluminum Alkyl Orthophosphates," US Patent 4,007,128(1977). [Pg.664]

The most common buffering system containing a weak base together with its salt formed with a strong acid is ammonia with ammonium sulphate. Some useful buffers are obtained from combinations of unrelated acids or bases with salts. The following combinations find occasional use in textile coloration processes, but the acetates and orthophosphates are most frequently used ... [Pg.38]

Orthopedic devices, 3 721-735 joint replacement, 3 727-735 Orthopedic marrow needles, 3 743-744 Orthophosphate (PO4), in soil, 11 112 Orthophosphates, 18 830-841 20 637 magnesium, 18 839 manufacture of, 18 853-855 Orthophosphate salts, 18 836 Orthophosphoric acid, 18 815, 817-826 condensation of, 18 826 properties of, 18 817-819 solubility of boron halides in, 4 140t orf/zo-phthalic resins, 20 101, 113 formulation of, 20 102 Orthorhombic crystal system, 8 114t Orthorhombic phosphorus pentoxide, 19 49 Orthorhombic structure, of ferroelectric crystals, 11 95, 96 Orthorhombic symmetry, 8 114t Orthosilicate monomers, in silicate glasses, 22 453... [Pg.658]

Although all three phosphates tested caused substantial decreases in calcium solubility following the gastric digestion, this trend was reversed upon completion of the second phase of the digestion. Only orthophosphate caused a decrease in calcium solubility from the soy following the complete digestion, while all three phosphates enhanced calcium solubility from the meat. Thus, phosphates are unlikely to interfere with calcium absorption due to the formation of insoluble salts in the gut. [Pg.34]

Adsorption inhibitors act by forming a film on the metal surface. The action of traditional oil-based red lead paint formulations presumably involves the formation of soaps and the precipitation of complex ferric salts that reinforce the oxide film. There has been substantial interest in recent years in development of replacements for lead-based and chromate-based inhibitor systems. Adsorption inhibitors based on pol3rmers have been of particular interest. In this volume, Johnson et al. and Eng and Ishida discuss inhibitors for copper 2-undecylimidazole is shown to be effective in acid media, where it suppresses the oxygen reduction reaction almost completely. Polyvlnyllmidazoles are shown to be effective oxidation inhibitors for copper at elevated temperatures. Also in this volume, Chen discusses the use of N-(hydroxyalkyl)acrylamide copolymers in conjunction with phosphate-orthophosphate inhibitor systems for cooling systems. [Pg.5]

Kinesin and dynein are two microtubule-associated ATP-dependent motors responsible for intracellular motility. Gilbert et al made direct measurements of the dissociation kinetics of kinesin from microtubules (MTs), the release of orthophosphate and ADP, and the rebinding of this motor to MTs. They observed processivity in ATP hydrolysis amounting to 10 molecules ATP per site at low salt concentration and 1 molecule of ATP per site at a higher concentration of salt. After hydrolysis, the dissociation of kinesin from the MT is rate-limiting, and rebinding of kinesin-ADP to MTs is fast. The authors discuss how this behavior differs from that of skeletal myosin. [Pg.572]

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. [Pg.295]

Magnesium orthophosphate Mg3(P04)2 constitutes rhombic crystals melts at 1,184°C insoluble in water soluble in ammonium salt solution. [Pg.533]


See other pages where Salts orthophosphate is mentioned: [Pg.406]    [Pg.323]    [Pg.536]    [Pg.328]    [Pg.150]    [Pg.28]    [Pg.513]    [Pg.523]    [Pg.788]    [Pg.599]    [Pg.265]    [Pg.538]    [Pg.67]    [Pg.664]    [Pg.38]    [Pg.410]    [Pg.305]    [Pg.317]    [Pg.649]    [Pg.271]    [Pg.85]    [Pg.88]    [Pg.586]    [Pg.399]    [Pg.73]   
See also in sourсe #XX -- [ Pg.311 ]




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