Phosphoric acid, meta

Phosphoric acid, meta- HP03 79.99 vitreous, delq. 

PHOSPHORIC ACID, META / PHOSPHORIC ACID, ORTHO 697... 

Bteto-phosphoric acid. See phosphoric acid, meta-. 

Phosphoric acid, meta- HPO3 79.99 vitreous, delq. 2.2-2.5 subl. s. Forms i. Iq. CO2... 

Phosphoric acid magnesium salt (2 3). See Magnesium phosphate tribasic Phosphoric acid, meta. See Metaphosphoric acid... 

Two examples of condensed phosphoricfV) acids are heptaoxo-diphosphoric(V) (pyrophosphoric) and polytrioxophosphoric (meta-phosphoric) acids. 

A satisfactory bath suitable for temperatures up to about 250° may be prepared by mixing four parts by weight of 85 per cent, ortho-phosphoric acid and one part by weight of meta-phosphoric acid the mixed components should first be heated slowly to 260° and held at this temperature imtil evolution of steam and vapours has ceased. This bath is liquid at room temperatures. For temperatures up to 340°, a mixture of two parts of 85 per cent, ortho-phosphoric acid and one part of meta-phosphoric acid may be used this is solid (or very viscous) at about 20°. 

Fig. 5. Vapoi—liquid phase diagram of the H2O—P20 system at 101 kPa (1 atm), where 3 is ortho, 2 pyro, and 1 meta phosphoric acid. The soHd line...

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. 

These compounds were formerly called meta-phosphoric acids and metaphosphates but the lURAC cyclo- nomenclature is preferred as being structurally more informative. The only... 

The earliest formulations, as reported by Rollins (1879), Gaylord (1889), Ames (1893), Hinkins Acree (1901) and Fleck (1902), were variously based on syrupy orthophosphoric acid or unstable mixtures of meta-phosphoric acid and sodium metaphosphate in solution. Some used solid pyrophosphoric acid. Many were grossly inferior cements which were hydrolytically unstable. 

The monomeric metaphosphate ion itself commands a fair amount of attention in discussions of metaphosphates. It is postulated as an intermediate of numerous hydrolysis reactions of phosphoric esters 52 S4,S5) and also of phosphorylation reactions S6> kinetic and mechanistic studies demonstrate the plausibility of such an assumption. In addition, the transient formation of ester derivatives of meta-phosphoric acid — in which the double-bonded oxygen can also be replaced by thio and imino — has also been observed they were detected mainly on the basis of the electrophilic nature of the phosphorus. 

Prior to the use of the adhesives, the dentin surface is etched with a conditioning solution which is usually an aqueous acidic solution of citric acid-ferric chloride, phosphoric acid, or even polyacrylic acid [192]. These solutions tend to demineralize the dentin and expose the collagen (organic fibers in the dentin) [193], and thereby result in higher bond strengths. The effects of various pre-conditioning treatments on the bond strength of 4-META to dentin have been discussed [194]. 

Also, phosphoric acid forms an extensive series of anhydrides (with P—O—P bonds), which further diversify the number and kind of phosphate esters. The most important phosphate esters are derivatives of mono-, di-, and triphosphoric acid (sometimes classified as ortho-, pyro-, and meta-phos-... 

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