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Phosphate compound

Phosphorus [7723-14-0] is a nonmetaUic element having widespread occurrence in nature as phosphate compounds (see Phosphoric acid and phosphates). Fluorapatite [1306-03-4], Ca F(P0 2> is the primary mineral in phosphate rock ores from which useful phosphoms compounds (qv) ate produced. The recovery from the ore into commercial chemicals is accompHshed by two routes the electric furnace process, which yields elemental phosphoms and the wet acid process, which generates phosphoric acid. The former is discussed herein (see Furnaces, electric). Less than 10% of the phosphate rock mined in the world is processed in electric furnaces. Over 90% is processed by the wet process, used primarily to make fertilisers (qv). [Pg.347]

Most of the phosphoms produced as the element is later converted to high purity phosphoric acid and phosphate compounds the remainder is used in direct chemical synthesis to produce high purity products. In contrast, phosphoric acid produced by the wet process is used in lower purity apphcations, especially in fertiliser and to a lesser degree in animal feed (see Feeds AND FEED ADDITIVES). More recendy, a small portion of wet acid is purified in a second process and then also used in high purity acid and phosphate compound apphcations. [Pg.347]

About 264,000 metric tons of elemental capacity is available in North America, plus another 79,000 t (P equivalent) of purified wet phosphoric acid (14). About 85% of the elemental P is burned to P2 5 hydrated to phosphoric acid. Part of the acid (ca 21%) is used direcdy, but the biggest part is converted to phosphate compounds. Sodium phosphates account for 47% calcium, potassium, and ammonium phosphates account for 17%. Pinal apphcations include home laundry and automatic dishwasher detergents, industrial and institutional cleaners, food and beverages, metal cleaning and treatment, potable water and wastewater treatment, antifree2e, and electronics. The purified wet acid serves the same markets. [Pg.354]

Aluminum [7429-90-5] Al, atomic number 13, atomic weight 26.981, is, at 8.8 wt %, the third most abundant element in the earth s cmst. It is usually found in siUcate minerals such as feldspar [68476-25-5] clays, and mica [12001 -26-2]. Aluminum also occurs in hydroxide, oxide—hydroxide, fluoride, sulfate, or phosphate compounds in a large variety of minerals and ores. [Pg.131]

So far, as in Equation (3.33), the hydrolyses of ATP and other high-energy phosphates have been portrayed as simple processes. The situation in a real biological system is far more complex, owing to the operation of several ionic equilibria. First, ATP, ADP, and the other species in Table 3.3 can exist in several different ionization states that must be accounted for in any quantitative analysis. Second, phosphate compounds bind a variety of divalent and monovalent cations with substantial affinity, and the various metal complexes must also be considered in such analyses. Consideration of these special cases makes the quantitative analysis far more realistic. The importance of these multiple equilibria in group transfer reactions is illustrated for the hydrolysis of ATP, but the principles and methods presented are general and can be applied to any similar hydrolysis reaction. [Pg.77]

Suggest an explanation for the exergonic nature of the glycogen synthase reaction (AG° = - 13.3 kj/mol). Consult Chapter 3 to review the energetics of high-energy phosphate compounds if necessary. [Pg.772]

C. K. Jones, D. A. Williams, and C. C. Blair. Gelling agents comprising aluminium phosphate compounds. Patent GB 2326882, 1999. [Pg.410]

Scheme 3.3 Overall photodeprotection reaction of two p-hydroxyphenacyl caged phosphate compounds. See text for more details. (Reprinted in part with permission from reference [49]. Copyright (2006) American Chemical Society.)... Scheme 3.3 Overall photodeprotection reaction of two p-hydroxyphenacyl caged phosphate compounds. See text for more details. (Reprinted in part with permission from reference [49]. Copyright (2006) American Chemical Society.)...
Of these, (2) and (3) and (1) and (5) must develop together and we see this in Table 2.1. The mixture of primitive cells from which we start our discussion all used as messengers in the cytoplasm various phosphate compounds, various substrates and the levels of minerals such as Fe2+, Mg2+ and K+. We labelled this above system as the P/Fe system of communication in the earliest life system. It may be better to view the system as diversifying at first through combination rather than as progressing. There is a part of the... [Pg.25]

A limited amount of work has been carried out using zirconium phosphates, compounds with well-defined coagulation and adsorption properties. The efficiency of coprecipitation was about 70% for free amino acids and albumin. [Pg.368]

The Li+-induced inhibition of the production of the HSV virus may be related to its actions upon viral DNA polymerase production and activity. Li+ reduces both the synthesis of DNA polymerase in tissue culture and the activity of DNA polymerase in vitro, each by about 50%. It has been proposed that Li+ reduces the biosynthesis of viral polypeptides and nucleic acids, and hence inhibits viral DNA replication by competition with Mg2+, a cofactor of many enzymes [243]. However, the inhibitory effect of Li+ on HSV replication in tissue culture is not affected by Mg2+ levels. A more likely hypothesis is the alteration of the intracellular K+ levels, possibly modifying levels of the high-energy phosphate compounds by replacement of either Na+ or K+ in Na+/K+-ATPase [244]. In tissue culture, HSV replication has been shown to be affected by the... [Pg.39]

To conclude, it is pleasant to consider the regular evolution from 0 to 4 of the number of bridging atoms in the following series of phosphate compounds, which is nicely completed by the phosphorus oxynitride PON (237). [Pg.226]

Magnesium phosphate compounds, uses for, 75 416-416 Magnesium phosphide, 19 58 Magnesium preparation, for Grignard reactions, 72 824... [Pg.543]


See other pages where Phosphate compound is mentioned: [Pg.752]    [Pg.355]    [Pg.222]    [Pg.323]    [Pg.331]    [Pg.332]    [Pg.200]    [Pg.491]    [Pg.495]    [Pg.236]    [Pg.66]    [Pg.66]    [Pg.69]    [Pg.428]    [Pg.624]    [Pg.48]    [Pg.343]    [Pg.85]    [Pg.1529]    [Pg.94]    [Pg.162]    [Pg.219]    [Pg.104]    [Pg.223]    [Pg.158]    [Pg.23]    [Pg.230]    [Pg.382]    [Pg.384]    [Pg.194]    [Pg.62]    [Pg.703]    [Pg.111]    [Pg.1194]    [Pg.1198]    [Pg.1225]    [Pg.317]    [Pg.53]   


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Alkyl phosphates, reaction with compounds

Allylic compounds phosphates

Calcium carbonate phosphate compounds

Carbon-substituted compounds - carbamoyl phosphate

Erythrocyte inorganic phosphate compounds

Glyceraldehyde-3-phosphate acyl compound

Historical Perspective on Metabolic Energy and the Thermodynamics of Phosphate Compounds

Hydrolysis of phosphate compounds

Manganese compounds, vanadium phosphates

Nickel compounds, vanadium phosphates

Oligomers phosphatic compounds

Pentose phosphate compounds

Phosphate Films Modified by Organic Compounds

Phosphate caged compounds

Phosphate compounds, bidentate

Phosphate compounds, coordinative

Phosphate compounds, glycolysis reactions

Phosphate compounds, sodium

Phosphates to Acid-soluble Compounds

Phosphates, modified compounds

Rare Earth Phosphate Compounds

Triose phosphate compounds

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