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Phosphatic acid

We achieved, that by contact of polyurethane foam with water solution of molybdophosphate, contain by pH 1-2,5 mixture of saturated (5 NMR P=-3.20 p.p.m. apply to 85 % H PO ) and unsaturated monovacant (x=0-t-4) (5 NMR P = -0,96 p.p.m.) heteropolycomplexes Keggin staicture, equilibrium discharge in the direction produced of saturated heteropolycomplex of Dowson stmcture and on the surface of polyurethan foam formed 18-molybdo-2-phosphate acid ( P = -2,40 p.p.m. in ether extract). The formed surfaces heteropolycomplex is stable for action 1 M solution of strong acids and basics and have ion exchanged properties in static and dynamic conditions to relation to macro and micro amount of M(I) ... [Pg.260]

Diacylglycerol kinase (DGK) from E. coli is a small 121 amino-acid, integral membrane protein which catalyses the conversion of diacylglycerol and MgATP to phosphatic acid and MgADP. DGK is homotrimeric,... [Pg.74]

Sodium aluminium phosphate, acidic Sodium aluminium silicate Sodium benzoate Sodium calcium polyphosphate Sodium carbonate Sodium ethyl p-hydroxybenzoate Sodium ferrocyanide Sodium gluconate... [Pg.263]

Synonyms magnesium biphosphate primary magnesium phosphate acid magnesium phosphate magnesium tetrahydrogen phosphate... [Pg.532]

The alkylating activity is dependent on the size of the alkyl group with the relative activity following the order methyl ethyl > propyl > butyl. Beyond butyl, the activity is greatly minimized. For alkyl esters of dibasic (e.g., sulfate) andtribasic (e.g., phosphate) acids, the alkylating activity is completely eliminated if any of the alkyl groups are hydrolyzed (e.g., monoalkyl sulfate or dialkyl phosphate) (Table 14.10). [Pg.392]

Since the resulting monoalkyl sulfate or dialkyl phosphate lacks alkylating activity, remove one of the alkyl groups from the esters of dibasic (e.g., sulfate) and tribasic (e.g., phosphate) acids. [Pg.401]

Trlammoninm imidotrithio- Diammonium lmidotri- Ammonium imidotrithio- Imidotrithiophosphoric phosphate. thiophosphate. phosphate. acid. [Pg.726]

J. J. Berzelius made phosphorous acid by treating phosphorous oxide with water —a reaction studied by T. E. Thorpe and A. E. H. Tutton, vide supra. B. D. Steele obtained it by the action of iodine on hypophosphorous acid (q.v.) in the presence of mineral acids and A. Besson, by heating the hemioxide with water in a sealed tube at 100° P20+024-3H20=2H3P0k. Phosphorous acid is also produced by the action of hot dil. nitric acid oh phosphorus the objection to this process, said J. Come, is the simultaneous production of phosphoric acid (q.v.), and this the more, the greater the cone, of the nitric acid. T. Salzer, and J. Philipp also reported that some hypophosphoric acid is produced at the same time. The early workers knew that the aq. soln. of phosphatic acid slowly decomposes, giving off phosphine, hence the faint smell like garlic. C. F. Sehonbein mentioned that freshly prepared phosphatic acid contains a trace of nitric acid as well as ozone. A. Tamm also observed that some phosphorous acid is formed when phosphated steel is dissolved in nitric acid. [Pg.900]

Two acids are known belonging to this group of elements they have not been tabulated on p. 132, because their structure may be compared with that of hydrazine or liquid phosphine, H2N-NH2 or H2P—PH2, in which two atoms of nitrogen—or of phosphorus—are in direct union with each other. These are phosphatic acid, or, as it is... [Pg.137]

To avoid dissolution or extraction of the FR, FR oligomer can be used instead of monomer. Using this approach, Ma et al.39 reported the synthesis of phosphate-polyester copolymers from spirocyclic pentaerythritol di(phosphate acid monochloride)s. It was shown that LOI of the copolymer increases with increasing phosphate content to reach a maximum of 30 vol %. [Pg.137]

B) Choudhury. A, Rao, C, N, R, Understanding the Building-Up Process of Three-Dimensional Open-Framework Metal Phosphates Acid Degradation of the 3D Structures to Lower Dimensional Structures, Chem, Commun. 2003, 366-367. [Pg.367]

Table 2. Adenosine 5 -phosphate acidity constants and their Al3+ complex stability constants ... Table 2. Adenosine 5 -phosphate acidity constants and their Al3+ complex stability constants ...
Fatty acyl- Glycerol Step 1 Phosphatidic CoA + 3-phosphate acid... [Pg.378]

Sodium Aluminum Phosphate, Acidic, occurs as a white powder. It is anhydrous or contains two or four molecules of water of hydration. It is insoluble in water, but is soluble in hydrochloric acid. [Pg.403]

The simulations were performed using the PTPase crystal structures as above. The PTPIB structure was a serine mutant with a phosphotyrosine ligand, which was manually replaced by phenyl phosphate. Acidic and basic residues close to the active site were charged whereas those outside the simulation sphere and distant to the active site were replaced by polar neutral groups giving the system a total charge of zero [37]. [Pg.275]


See other pages where Phosphatic acid is mentioned: [Pg.468]    [Pg.266]    [Pg.63]    [Pg.88]    [Pg.115]    [Pg.445]    [Pg.396]    [Pg.13]    [Pg.39]    [Pg.271]    [Pg.279]    [Pg.100]    [Pg.446]    [Pg.111]    [Pg.899]    [Pg.900]    [Pg.924]    [Pg.69]    [Pg.1103]    [Pg.403]    [Pg.33]    [Pg.219]    [Pg.342]    [Pg.165]    [Pg.170]    [Pg.172]   
See also in sourсe #XX -- [ Pg.899 , Pg.924 , Pg.925 ]

See also in sourсe #XX -- [ Pg.60 ]

See also in sourсe #XX -- [ Pg.22 ]

See also in sourсe #XX -- [ Pg.60 ]




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