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Reactions carbon oxides with water

Hydroxides MOH are important compounds for all the alkali metals. They can easily formed by reaction of oxides with water (or atmosphere moisture). They are soluble in water and give strong base. Compounds of oxoacids are commonly encountered, such as carbonate, nitrate, sulphate, etc. as these anions are fairly large, lithium compounds tend to be the most soluble in the series. Many of these compounds crystallise in a variety of hydrated forms (e.g. Na2C03. H2 O with n = 1, 7 or 10). [Pg.65]

Introduce a solution of 15 g. of the diazo ketone in 100 ml. of dioxan dropwise and with stirring into a mixture of 2 g. of silver oxide (1), 3 g. of sodium thiosulphate and 5 g. of anhydrous sodium carbonate in 200 ml. of water at 50-60°. When the addition is complete, continue the stirring for 1 hour and raise the temperature of the mixture gradually to 90-100°. Cool the reaction mixture, dilute with water and acidify with dilute nitric acid. Filter off the a-naphthylacetic acid which separates and recrys-talhse it from water. The yield is 12 g., m.p. 130°. [Pg.904]

The reaction of thiirane 1-oxides with water or methanol is usually acid-catalyzed and gives /3-substituted sulfenic acids which dimerize to thiolsulfinates (54 Scheme 70) (72JA5786). If acetic acid is used a mixture of disulfide (55) and thiolsulfonate (56) is obtained. Treatment of thiirane 1,1-dioxides with hydroxide ion may involve attack on carbon as well as on sulfur as exemplified by 2-phenylthiirane 1,1-dioxide (Scheme 71). [Pg.157]

Using a "home made" aneroid calorimeter, we have measured rates of production of heat and thence rates of oxidation of Athabasca bitumen under nearly isothermal conditions in the temperature range 155-320°C. Results of these kinetic measurements, supported by chemical analyses, mass balances, and fuel-energy relationships, indicate that there are two principal classes of oxidation reactions in the specified temperature region. At temperatures much lc er than 285°C, the principal reactions of oxygen with Athabasca bitumen lead to deposition of "fuel" or coke. At temperatures much higher than 285°C, the principal oxidation reactions lead to formation of carbon oxides and water. We have fitted an overall mathematical model (related to the factorial design of the experiments) to the kinetic results, and have also developed a "two reaction chemical model". [Pg.427]

We propose that the complicated dry oxidation of bitumen can be represented as the sum of contributions from two classes of oxidation reaction. One class of reactions is the partial oxidation that leads to deposition of coke and formation of "oxygenated bitumen", with very little production of carbon oxides and water. This class of reactions is concisely summarized by... [Pg.430]

Helling and Tester (1987) reported the oxidation kinetics of carbon monoxide over the temperature range 420 to 570°C at a pressure of 246 bar (24.6 MPa). Holgate and Tester (1994) examined oxidation kinetics of carbon monoxide. In addition to direct oxidation with oxygen, Helling and Tester found that the reaction of carbon monoxide with water was significant, as the following equations show ... [Pg.410]

Acrylic Acid, Acrylates, and Acrylonitrile. Acrylic acid [79-10-7], C3H402, and acrylates were once prepared by reaction of acetylene and carbon monoxide with water or an alcohol, using nickel carbonyl as catalyst. I11 recent years tliis process has been completely superseded in the United States by newer processes involving oxidation of propylene (2). I11 western Europe, however, acetylene is still important in acrylate manufacture (see Acrylic acid and derivatives Acrylic ester polymers). [Pg.102]

SAFETY PROFILE Confirmed human carcinogen. A poison. Flammable when exposed to heat or flame can react with oxidizing materials. Explosive reaction on contact with water. Ignites on contact with moist air or carbon dioxide. Upon decomposition it emits highly toxic fumes of BeO. See also BERYLLIUM COMPOUNDS. [Pg.529]

Cleaning Up The aqueous layer from the first part of the reaction should be neutralized with sodium carbonate, diluted with water, and flushed down the drain. The aqueous layer containing hydrosulfite, saturated sodium chloride, and sodium hydroxide are treated with household bleach (5.25% sodium hypochlorite solution) until no further reaction is evident. After neutralizing the solution with dilute hydrochloric acid, the solution is diluted with water and flushed down the drain. Shake the mixture of silver oxide, silver, and sodium sulfate with water to dissolve the sodium sulfate, and then recover the mixture of silver and silver oxide by vacuum filtration. [Pg.454]

Maximum concentrations of hypochlorous acid are obtained by treating pure liquid chlorine(I) oxide with water at 0°. Lower concentrations result from use of the gaseous oxide under reduced pressure or from use of solutions of the oxide in carbon tetrachloride. The last procedure is convenient for acid concentrations up to 5 M. The reaction is nearly quantitative, the equilibrium concentrations of hypochlorous acid and chlorine (I) oxide in the two phases at 0° being calculated from the data of... [Pg.160]

Methyl alcohol occurs naturally in plants and animals, including humans, as the product of metabolic reactions that occur in all organisms. It also occurs in the atmosphere as the result of the decomposition of dead organisms in the soil. None of these sources is utilized for the commercial production of methyl alcohol. Instead, the primary method for the preparation of methyl alcohol is to react carbon monoxide with water at a temperature of about 25o°C (48o°F) and pressures of 50 to 100 atmospheres over a mixed catalyst of copper, zinc oxide, and aluminum oxide. Efforts are being made to develop other methods of synthesizing methyl alcohol. In one process, for... [Pg.449]

Write balanced equations for the following reactions (a) barium oxide with water, (b) iron(II) oxide with perchloric acid, (c) sulfur trioxide with vrater, (d) carbon dioxide with aqueous sodium hydroxide. [Pg.282]


See other pages where Reactions carbon oxides with water is mentioned: [Pg.911]    [Pg.235]    [Pg.50]    [Pg.407]    [Pg.851]    [Pg.313]    [Pg.287]    [Pg.1239]    [Pg.466]    [Pg.427]    [Pg.229]    [Pg.71]    [Pg.2548]    [Pg.799]    [Pg.67]    [Pg.126]    [Pg.181]    [Pg.197]    [Pg.212]    [Pg.245]    [Pg.262]    [Pg.421]    [Pg.34]    [Pg.706]    [Pg.187]    [Pg.188]    [Pg.220]    [Pg.40]    [Pg.124]   
See also in sourсe #XX -- [ Pg.323 ]




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Carbon oxidation reaction

Carbon oxidative reactions

Carbon oxides water

Carbon with water

Carbonate reactions with

Carbonated waters

Oxidant water

Oxidation reactions water

Reaction with carbon

Reaction with water

Water carbon)

Water oxidation

Water oxidation with

Water with oxidative

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