Carbon dioxide and ammonia

The reaction commences at about 120° the carbamic acid formed decomposes immediately into carbon dioxide and ammonia. The latter may form the ammonium salt with unreacted acid the ammonium salt also reacts with urea at temperatures above 120° to yield the amide ... 

Only about 10% of the total urea production is used for amino resins, which thus appear to have a secure source of low cost raw material. Urea is made by the reaction of carbon dioxide and ammonia at high temperature and pressure to yield a mixture of urea and ammonium carbamate the latter is recycled. 

Heating the ammonium beryUium carbonate solution to 95°C causes nearly quantitative precipitation of beryUium basic carbonate [66104-24-3], Be(OH)2 2BeC02. Evolved carbon dioxide and ammonia are recovered for recycle as the strip solution. Continued heating of the beryUium basic carbonate slurry to 165°C Hberates the remaining carbon dioxide and the resulting beryUium hydroxide [13327-32-7] intermediate is recovered by filtration. The hydroxide is the basic raw material for processing into beryUium metal, copper—beryUium and other aUoys, and beryUia [1304-56-9] for ceramic products. Approximately 90% of the beryUium content of bertrandite is recovered by this process. 

The acid chloiide (chloioformamide [463-72-9] "uiea chloiide"), NH2COCI, and its salts have been prepared. Ammonium carbamate [1111 -78-OJ can be obtained as a white crystalline sobd by reaction of dry carbon dioxide and ammonia. It is an impurity in commercial ammonium carbonate [506-87-6] (see Ammonium compounds). Esters of carbamic acid are quite stable. The best known is the ethyl ester usually called urethane [51 -79-6],... 

The cmde product containing aminotria ines can be purified by digestion with acids (eg, hydrochloric, nitric, or sulfuric) this hydroly2es the acycHc impurities to carbon dioxide and ammonia and the aminotria ines to CA and ammonia. 

Urea is prepared commercially by the reaction of liquid carbon dioxide and ammonia in silver-lined autoclaves, at temperatures in the range 135-195°C and pressure of 70-230 atm. The reaction proceeds by way of ammonium carbamate ... 

Catabolism converges via the citric acid cycle to three principal end products water, carbon dioxide, and ammonia. 

Carbohydrazide itself is of very low volatility, but it decomposes at relatively low temperatures to produce volatile carbon dioxide and ammonia. In theory, the combined corrosive effects of these two materials should be negated in the condensate system, but in practice, this is not always so and both steel and copper corrosion transport problems may develop, primarily as the result of corrosion-enhancement reactions resulting from oxygen in-leakage. It is presumed, therefore, that (similar to hydrazine) some deliberate after-desuperheating line addition of CHZ is necessary if post-boiler section corrosion is to be avoided. 

The naturally occurring compound urea, CO(NH,), was first synthesized by Friedrich Wohler in Germany in 1828 by heating ammonium cyanate. This synthesis was a significant event because it was the first time that an organic compound had been produced from an inorganic substance. Urea may also be made by the reaction of carbon dioxide and ammonia ... 

Urea, NH2CONH2, is the diamide of carbonic acid, (HO)2CO, and is manufactured in large volume for use in fertilizers and plastics by the reaction of carbon dioxide and ammonia. 

Campbell LL (1960) Rednctive degradation of pyrimidines V. Enzymatic conversion of V-carbamoyl- 3-alanine to [5-alanine, carbon dioxide, and ammonia. J Biol Chem 235 2375-2378. 

Nitrogen compounds commonly determined are creatinine, urea, and uric acid. Creatinine is an end product of the energy process occurring within the muscles, and is thus related to muscle mass. Creatinine in urine is commonly used as an indicator and correction factor of dilution in urine. Creatinine in serum is an indicator of the filtration capacity of the kidney. Urea is the end product of the nitrogen luea cycle, starting with carbon dioxide and ammonia, and is the bulk compoimd of urine. The production of uric acid is associated with the disease gout. In some cases, it appears that the excess of uric acid is a consequence of impaired renal excretion of this substance. 

Kostic et al. reported the use of various palladium(II) aqua complexes as catalysts for the hydration and alcoholysis of nitriles,435,456 decomposition of urea to carbon dioxide and ammonia, and alcoholysis of urea to ammonia and various carbamate esters.457 Labile aqua or other solvent ligands can be displaced by a substrate. In many cases, the coordinated substrate thus becomes activated toward nucleophilic addition of water or alcohols. 

Kostic et al. recently reported the use of various palladium(II) aqua complexes as catalysts for the hydration of nitriles.456 crossrefil. 34 Reactivity of coordination These complexes, some of which are shown in Figure 36, also catalyze hydrolytic cleavage of peptides, decomposition of urea to carbon dioxide and ammonia, and alcoholysis of urea to ammonia and various carbamate esters.420-424, 427,429,456,457 Qggj-jy palladium(II) aqua complexes are versatile catalysts for hydrolytic reactions. Their catalytic properties arise from the presence of labile water or other solvent ligands which can be displaced by a substrate. In many cases the coordinated substrate becomes activated toward nucleophilic additions of water/hydroxide or alcohols. New palladium(II) complexes cis-[Pd(dtod)Cl2] and c - Pd(dtod)(sol)2]2+ contain the bidentate ligand 3,6-dithiaoctane-l,8-diol (dtod) and unidentate ligands, chloride anions, or the solvent (sol) molecules. The latter complex is an efficient catalyst for the hydration and methanolysis of nitriles, reactions shown in Equation (3) 435... 

Figure 36 Complexes catalyzing hydrolytic cleavage of peptides, hydrolysis and alcoholysis of nitriles, decomposition of urea to carbon dioxide and ammonia, and alcoholysis of urea to ammonia and various...

The analytical phase generally involves the use of very dilute solutions and a relatively high ratio of oxidant to substrate. Solutions of a concentration of 0.01 M to 0.001 M (in periodate ion) should be employed in an excess of two to three hundred percent (of oxidant) over the expected consumption, in order to elicit a valid value for the selective oxidation. This value can best be determined by timed measurements of the oxidant consumption, followed by the construction of a rate curve as previously described. If extensive overoxidation occurs, measures should be taken to minimize it, in order that the break in the curve may be recognized, and, thence, the true consumption of oxidant. After the reaction has, as far as possible, been brought under control, the analytical determination of certain simple reaction-products (such as total acid, formaldehyde, carbon dioxide, and ammonia) often aids in revealing what the reacting structures actually were. When possible, these values should be determined at timed intervals and be plotted as a rate curve. A very useful tool in this type of investigation, particularly when applied to carbohydrates, has been the polarimeter. With such preliminary information at hand, a structure can often be proposed, or the best conditions for a synthetic operation can be outlined. 

A study of the kinetics and mechanism of the reaction of thionyl chloride with a series of /wra-substituted acetophenone semicarbazones suggests attack of thionyl chloride above the plane of the hydrazone (E)-isomer. Subsequent cyclization and loss of carbon dioxide and ammonia produces the 1,2,3-thiadiazole system < 1982J(P 1) 1233>. 

AUC [Ammonium uranyl carbonate] A process for converting uranium hexafluoride into uranium dioxide for use as a nuclear reactor fuel. The hexafluoride vapor, together with carbon dioxide and ammonia, are passed into aqueous ammonium carbonate at 70°C, precipitating ammonium uranyl carbonate ... 

Nitric oxide formation from hydroxyurea requires a three-electron oxidation (Scheme 7.15) [114]. Treatment of hydroxyurea with a variety of chemical oxidants produces NO or NO-related species , including nitroxyl (HNO), and these reactions have recently been extensively reviewed [114]. Many of these reactions proceed either through the nitroxide radical (25) or a C-nitroso intermediate (26, Scheme 7.15) [114]. The remainder of the hydroxyurea molecule may decompose into formamide or carbon dioxide and ammonia, depending on the conditions and type of oxidant (one-electron vs. two electron) employed. 

Wright, P. A., Randall, D. J. and Perry, S. F. (1989). Fish gill water boundary layer a site of linkage between carbon dioxide and ammonia excretion, J. Comp. Physiol. B., 158, 627-635. 

Phthalic anhydride and urea, together with copper(I)chloride and ammonium molybdate, are heated to 200°C in trichlorobenzene. The ratios between the components are the same as in the baking process. Carbon dioxide and ammonia are released to yield Copper Phthalocyanine Blue. The reaction is complete after 2 to 3 hours, producing a yield between 85% and more than 95%. 

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