Carbonic acid , formation

Maintaining condensate temperatures at or near saturation points to minimize carbonic acid formation. This includes heating intermediate condensate receivers to maximum practical temperatures. 

The pCOj electrode was first described in 1957 by Stow and later improved to its presently used form by Severinghaus The basic principle of operation relies on equilibration of COj with an aqueous solution. The change in pH in the aqueous solution associated with the equilibration due to carbonic acid formation (H2CO3) is measured and varies with log pCO2] It should be pointed out here that these measurements (and likewise for the pO electrode described below) give CO2 tension not concentration. To obtain concentration, Henry s Law of gas solubUity must be applied. However, for most medical and biological applications the knowledge of the gas tension is sufficient. 

Drugs of this group inhibit activity of carbonic anhydrase, an enzyme that catalyzes the reversible reaction of water and carbon dioxide, which forms carbonic acid. The mechanism of action of this group of drags is not fuUy understood. However, inhibition of carbonic anhydrase activity leads to a reduction of carbonic acid formation and an increase in bicarbonate, sodium, and potassium excretion with urine, which eventually leads to a significant increase in the process of excreting water from the organism. 

The Solubility of Carbon Dioxide in Brines. Information required to describe the carbonate system in a brine includes the solubility of carbon dioxide, the extent of carbonic acid formation, and the distribution of the anionic carbonic acid dissociation products HCO3 and C0 . ... 

Carbonic acid formation decreases local pore solution pH from 14 to 8. This fall initiates passive hydrated ferric oxide film destruction and hydrated calcium carbonate formation ... 

K. Adamczyk, M. Pr mont-Schwartz, D. Pines, E. Pines, and E.TJ. Nibbering, Real-time observation of carbonic acid formation in aqueous solution. Science 326 (2009), pp. 1690-1694. 

Three-dimensional models of sulfuric acid, bicarbonate, carbonic acid, formate, and formic acid were added. 

Carbonic acid (formation is accelerated by carbonic anhydrase enzyme in red ceils)... 

Although, supercritical carbon dioxide has the advantage of being non-toxic and abundant, it is practically immiscible with water. Also, side reactions such as carbamate formation and carbonic acid formation can occur when carbon dioxide is employed as the supercritical fluid in enzymatic reactions. Therefore, supercritical fluids used as the reaction medium in enzyme catalyzed reactions include fluoroform, sulfur hexafluoride and ethane, while lipases are the enzymes utilized in such reactions." However, ethane and propane have the disadvantages of being expensive and flammable. 

Formamide decomposes thermally either to ammonia and carbon monoxide or to hydrocyanic acid and water. Temperatures around 100°C are critical for formamide, in order to maintain the quaUty requited. The lowest temperature range at which appreciable decomposition occurs is 180—190°C. Boiling formamide decomposes at atmospheric pressure at a rate of about 0.5%/min. In the absence of catalysts the reaction forming NH and CO predominates, whereas hydrocyanic acid formation is favored in the presence of suitable catalysts, eg, aluminum oxides, with yields in excess of 90% at temperatures between 400 and 600°C. 

Barium carbonate prevents formation of scum and efflorescence in brick, tile, masonry cement, terra cotta, and sewer pipe by insolubilizing the soluble sulfates contained in many of the otherwise unsuitable clays. At the same time, it aids other deflocculants by precipitating calcium and magnesium as the carbonates. This reaction is relatively slow and normally requites several days to mature even when very fine powder is used. Consequentiy, often a barium carbonate emulsion in water is prepared with carbonic acid to further increase the solubiUty and speed the reaction. 

Cyanohydrin Synthesis. Another synthetically useful enzyme that catalyzes carbon—carbon bond formation is oxynitnlase (EC 4.1.2.10). This enzyme catalyzes the addition of cyanides to various aldehydes that may come either in the form of hydrogen cyanide or acetone cyanohydrin (152—158) (Fig. 7). The reaction constitutes a convenient route for the preparation of a-hydroxy acids and P-amino alcohols. Acetone cyanohydrin [75-86-5] can also be used as the cyanide carrier, and is considered to be superior since it does not involve hazardous gaseous HCN and also virtually eliminates the spontaneous nonenzymatic reaction. (R)-oxynitrilase accepts aromatic (97a,b), straight- (97c,e), and branched-chain aUphatic aldehydes, converting them to (R)-cyanohydrins in very good yields and high enantiomeric purity (Table 10). 

Ammonium nitrate is manufactured by reacting ammonia with nitric acid. Consider the process shown by Fig. 9.19. First, namral gas is reformed and converted into hydrogen, nitrogen and carbon dioxide. Hydrogen and nitrogen are separated an fed to the ammonia synthesis plant. A fraction of the produced ammonia is employed in nitric acid formation. Ammonia is first oxidized with compressed air then absorbed in water to form nitric acid. Finally nitric acid is reacted with anunonia to oduce ammonium nitrate. 

Rearrangements of vinylogous urethanes to vinylogous carbonic acids and decarboxylation are other interesting enamine rearrangements which may be synthetically useful in the formation of cyclic enamines (623,624). 

The solubility of AS2O3 in water, and the species present in solution, depend markedly on pH. In pure water at 25°C the solubility is 2.16 g per lOOg this diminishes in dilute HCl to a minimum of 1.56g per lOOg at about 3 m HCl and then increases, presumably due to the formation of chloro-complexes. In neutral or acid solutions the main species is probably pyramidal As(OH)3, arsenious acid , though this compound has never been isolated either from solution or otherwise (cf. carbonic acid, p. 310). The solubility is much greater in basic solutions and spectroscopic evidence points to... 

The overall process is the addition of a CH-acidic compound to the carbon-carbon double bond of an o ,/3-unsaturated carbonyl compound. The Michael reaction is of particular importance in organic synthesis for the construction of the carbon skeleton. The above CH-acidic compounds usually do not add to ordinary carbon-carbon double bonds. Another and even more versatile method for carbon-carbon bond formation that employs enolates as reactive species is the aldol reaction. 

Soil reaction (pH) The relationship between the environment and development of acid or alkaline conditions in soil has been discussed with respect to formation of soils from the parent rock materials. Soil acidity comes in part by the formation of carbonic acid from carbon dioxide of biological origin and water. Other acidic development may come from acid residues of weathering, shifts in mineral types, loss of alkaline or basic earth elements by leaching, formation of organic or inorganic acids by microbial activity, plant root secretions, and man-made pollution of the soil, especially by industrial wastes. 

Carbon dioxide, which damages condensate return systems via the formation of carbonic acid. 

The corrosion risks to the steam-condensate system resulting from the decomposition of carbonates and the subsequent formation of carbonic acid. 

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