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Phosphate ions

A rather more specific mechanism of microbial immobilization of metal ions is represented by the accumulation of uranium as an extracellular precipitate of hydrogen uranyl phosphate by a Citrobacter species (83). Staggering amounts of uranium can be precipitated more than 900% of the bacterial dry weight Recent work has shown that even elements that do not readily form insoluble phosphates, such as nickel and neptunium, may be incorporated into the uranyl phosphate crystallites (84). The precipitation is driven by the production of phosphate ions at the cell surface by an external phosphatase. [Pg.36]

Other Salts. Indium nitrate trihydrate [13770-61 -1], In(N02)3 3H20, is a soluble salt prepared by dissolution of the metal or oxide in nitric acid. Indium phosphate [14693-82-4], InPO, is precipitated by adding phosphate ions to a solution of an indium salt. It is soluble in water. [Pg.81]

The bath components for a nitrite—nitrate accelerated bath basic to this conversion coating process are (/) 2inc metal or 2inc oxide dissolved in acid (2) phosphate ions added as phosphoric acid (J) addition of an oxidant such as sodium nitrite and (4) addition of nitric acid. Other oxidants such as peroxide, chlorate, chlorate in combination with nitrate, or an organic nitro compound may also be used. [Pg.223]

Vitamin A (845 RE/L) and vitamin D (913 RE/L) may be added to fortify evaporated milk. Other possible ingredients are sodium citrate, disodium phosphate, and salts of carrageenan. Phosphate ions maintain an appropriate salt balance to prevent coagulation of the protein (casein) during sterilization. The amount of phosphate added depends on the amount of calcium and magnesium present. [Pg.365]

CycHc adenosine monophosphate (cAMP), produced from ATP, is involved in a large number of ceUular reactions including glycogenolysis, Hpolysis, active transport of amino acids, and synthesis of protein (40). Inorganic phosphate ions are involved in controlling the pH of blood (41). The principal anion of interceUular fluid is HP (Pig. 3) (41). [Pg.377]

AletabolicFunctions. The chlorides are essential in the homeostatic processes maintaining fluid volume, osmotic pressure, and acid—base equihbria (11). Most chloride is present in body fluids a Htde is in bone salts. Chloride is the principal anion accompanying Na" in the extracellular fluid. Less than 15 wt % of the CF is associated with K" in the intracellular fluid. Chloride passively and freely diffuses between intra- and extracellular fluids through the cell membrane. If chloride diffuses freely, but most CF remains in the extracellular fluid, it follows that there is some restriction on the diffusion of phosphate. As of this writing (ca 1994), the nature of this restriction has not been conclusively estabUshed. There may be a transport device (60), or cell membranes may not be very permeable to phosphate ions minimising the loss of HPO from intracellular fluid (61). [Pg.380]

PMo220 4q, is analytically usehil, being formed in the molybdenum test for phosphate ion. Poly- and heteropolymolybdate ions are used in the precipitation of dyes. The protonated forms of the ions are strongly acidic and many poly- and heteropolymolybdate compounds have catalytic activity that is attributable to their acid—base or redox properties. [Pg.470]

Oxo Ion Salts. Salts of 0x0 anions, such as nitrate, sulfate, perchlorate, iodate, hydroxide, carbonate, phosphate, oxalate, etc, are important for the separation and reprocessing of uranium, hydroxide, carbonate, and phosphate ions are important for the chemical behavior of uranium ia the environment (150—153). [Pg.325]

Phosphate. Phosphoms occurs in water primarily as a result of natural weathering, municipal sewage, and agricultural mnoff The most common form in water is the phosphate ion. A sample containing phosphate can react with ammonium molybdate to form molybdophosphoric acid (H2P(Mo202q)4). This compound is reduced with stannous chloride in sulfuric acid to form a colored molybdenum-blue complex, which can be measured colorimetrically. SiUca and arsenic are the chief interferences. [Pg.231]

The Ca(Il) coaceatratioa ia blood is closely coatroUed aormal values He betweea 2.1 and 2.6 mmol/L (8.5—10.4 mg/dL) of semm (21). The free calcium ion concentration is near 1.2 mmol/L the rest is chelated with blood proteias or, to a lesser extent, with citrate. It is the free Ca(Il) ia the semm that determines the calcium balance with the tissues. The mineral phase of bone is essentially ia chemical equiUbrium with calcium and phosphate ions present ia blood semm, and bone cells can easily promote either the deposition or dissolution of the mineral phase by localized changes ia pH or chelating... [Pg.408]

Three hormones regulate turnover of calcium in the body (22). 1,25-Dihydroxycholecalciferol is a steroid derivative made by the combined action of the skin, Hver, and kidneys, or furnished by dietary factors with vitamin D activity. The apparent action of this compound is to promote the transcription of genes for proteins that faciUtate transport of calcium and phosphate ions through the plasma membrane. Parathormone (PTH) is a polypeptide hormone secreted by the parathyroid gland, in response to a fall in extracellular Ca(Il). It acts on bones and kidneys in concert with 1,25-dihydroxycholecalciferol to stimulate resorption of bone and reabsorption of calcium from the glomerular filtrate. Calcitonin, the third hormone, is a polypeptide secreted by the thyroid gland in response to a rise in blood Ca(Il) concentration. Its production leads to an increase in bone deposition, increased loss of calcium and phosphate in the urine, and inhibition of the synthesis of 1,25-dihydroxycholecalciferol. [Pg.409]

The butter fat is a coarse dispersion readily removable on standing or by a centrifuging operation. The casein will be present in the skimmed milk as colloidally dispersed micelles of diameter of the order of 10 cm, and is associated with calcium and phosphate ions. [Pg.854]

The condition of the curd on precipitation is important. As the milk starts to gel, agitators in the coagulation tanks are started as the temperature is raised to about 65°C. Under these conditions the protein is thrown out in fine particles. Too slow an agitation will produce large clots difficult to wash whilst too fine a curd also presents washing problems. In order to obtain the requisite consistency of the precipitate it may be necessary to add inorganic material to the skimmed milk. For example, the addition of phosphate ions will prevent undesirable flaky polymer. Similarly, calcium-deficient casein will not coagulate satisfactorily and the addition of calcium ions may be necessary. [Pg.855]

Awad, S. A. and Kamel, K. M. Behaviour of Tin as Metal-metal Phosphate Electrode and Mechanism of Promotion and Inhibition of its Corrosion by Phosphate Ions , Journal of Electroanalytical Chemistry, 24, 217-25 (1969)... [Pg.465]

Salts giving an alkaline reaction may be corrosive to the irons, and while neutral solutions can be handled safely there is usually little point in using high-silicon irons for these relatively innocuous solutions. The irons are useful in handling acidic solutions, subject to the restrictions already referred to regarding the halide, sulphite and phosphate ions. [Pg.631]

By structural complementarity, dicationic l,4-diazabicyclo[2.2.2]octane (VII) provides an appropriate recognition site for phosphate ions and two stearyl side chains attached to the amines add lipophilic properties 59,60). Such a carrier model can selectively extract nucleotides from aqueous solution to chloroform solution via lipophilic salt formation. The order of nucleotide affinity is ATP > ADP > AMP. The selectivity ratios were 45 for ADP/AMP and 7500 for ATP/AMP at pH 3. The relative transport rate was ATP > ADP > AMP. The ratios were 60 for ATP/AMP and 51 for ADP/AMP. The modes of interaction of ADP and ATP are proposed to be as shown in Fig. 6. [Pg.128]

H2po.r Dihydrogen phosphate ion 7.21 HP042 Hydrogen phosphate ion... [Pg.51]

As summarized in Figure 27.7, the mevalonate pathway begins with the conversion of acetate to acetyl CoA, followed by Claisen condensation to yield acetoacety) CoA. A second carbonyl condensation reaction with a third molecule of acetyl CoA, this one an aldol-like process, then yields the six-carbon compound 3-hydroxy-3-methylglutaryl CoA, which is reduced to give mevalonate. Phosphorylation, followed by loss of C02 and phosphate ion, completes the process. [Pg.1072]

Step 4 of Figure 27.7 Phosphorylation and Decarboxylation Three addition reactions are needed to convert mevalonate to isopentenyl diphosphate. Th first two are straightforward phosphorylations that occur by nucleophilic sul stitution reactions on the terminal phosphorus of ATP. Mevalonate is first cor verted to mevalonate 5-phosphate (phosphomevalonate) by reaction wit ATP in a process catalyzed by mevalonate kinase. Mevalonate 5-phosphat then reacts with a second ATP to give mevalonate 5-diphosphate (diphosphc mevalonate). The third reaction results in phosphorylation of the tertiar hydroxyi group, followed by decarboxylation and loss of phosphate ion. [Pg.1075]

Figure 29.1 An overview of catabolic pathways for the degradation of food and the production of biochemical energy. The ultimate products of food catabolism are C02 and H2O, with the energy released in the citric acid cycle used to drive the endergonic synthesis of adenosine triphosphate (ATP) from adenosine diphosphate (ADP) plus phosphate ion, HOPO32-. Figure 29.1 An overview of catabolic pathways for the degradation of food and the production of biochemical energy. The ultimate products of food catabolism are C02 and H2O, with the energy released in the citric acid cycle used to drive the endergonic synthesis of adenosine triphosphate (ATP) from adenosine diphosphate (ADP) plus phosphate ion, HOPO32-.
What is the oxidation number of phosphorus in sodium phosphite, Na3P03 In the dihydrogen phosphate ion ... [Pg.88]

Dihydrogen phosphate ion (ftPOr) Hydrogen phosphate ion (HP042-) 6.2 X 10-8 7.21... [Pg.387]

Figure 10-6 continues this pictorial presentation of solubilities. Figure 10-6A shows the positive ions that form hydroxides of low solubility. Figure 10-6B shows the positive ions that have low solubility when combined with phosphate ion, PO 3, carbonate ion, CO 2, and sulfite ion,... [Pg.171]

Phosphates. Insoluble orthophosphates may be precipitated with phosphate ion derived from trimethyl or triethyl phosphate by stepwise hydrolysis. Thus 1.8M sulphuric acid containing zirconyl ions and trimethyl phosphate on... [Pg.425]

Discussion. Phosphate ion is determined nephelometrically following the formation of strychnine molybdophosphate. This turbidity is white in colour and consists of extremely fine particles (compare ammonium molybdophosphate, which is yellow and is composed of rather large grains). The precipitate must not be agitated, as it tends to agglomerate easily it is somewhat sensitive to temperature changes. [Pg.730]

A popular type of internal chemical conditioning, precipitation water treatment program. Relies on the careful management of permanent reserve of phosphate ions in the BW to prevent waterside scale formation. [Pg.749]

A positive iodinating species was postulated to account for the kinetics and isotope effect observed in the iodination of some amines by iodine in aqueous potassium iodide (in some cases in the presence of acetate, lactate, or phosphate ion). The isotope effects (kH/kD values in parenthesis) for these compounds studied were 2,4,6-trideutero-m-dimethylaminobenzenesulphonate ion, 25 °C (1.0) 2,4,6-trideutero-m-dimethyIbenzoate ion, 30 °C (1.4) 2,4,6-trideutero-dimethylaniline, 30 °C, lactate (3.0) 2,4,6-trideuteromethylaniline, 25 °C, acetate (3.2) 2,4,6-trideuteroaniline, 25 °C (3.5), phosphate (4.0) 2,4,6-trideutero-metanilate ion, 35 °C (2.0) 2,4,6-trideutero-m-aminobenzoate ion, 30 °C (4.8), phosphate (3.0) 2,6-dideutero-l-dimethylaminobenzene-4-sulphonate ion, 25 °C, phosphate (1.0) 4-deutero-l-dimethylaminobenzene-3-sulphonate ion, 25 °C, phosphate (1.0). The kinetics of these reactions was given by... [Pg.96]


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Aqueous complexes with phosphate ions

Blood phosphate ions

Calcium ions phosphate ester hydrolysis

Chiral ions phosphate anions

Dihydrogen phosphate ion

Hydrogen phosphate ion

Ion-Promoted Alcoholysis of Phosphates

Magnesium ions phosphate ester hydrolysis

Phosphat-Ion

Phosphat-Ion

Phosphate Buffer with Ammonium Ions

Phosphate Ions Precipitate and Rupture Secreted Matrix Vesicles

Phosphate ion precipitation

Phosphate ions oxidation

Phosphate ions, monohydrogen

Phosphate ions, reaction with hydrogen

Phosphate ions, sequestration

Phosphate, metal ions binding

Phosphates molecular ions

Phosphates with Ion Vacancies

Plutonium ions from nitric acid by tributyl phosphate

Potassium ions, vanadium phosphates

Sequestration of Phosphate Ions Polymeric Drugs for Chronic Renal Failure

Zirconium phosphate ion exchange resins

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