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Hydrogen iodide carbon dioxide

P. Lemoult obtained phosphorus trisiodomercuriate, P(HgI)8, by the action of phosphine, diluted with hydrogen or carbon dioxide, on a dil, soln. of potassium iodomercuriate. The product is washed and dried in vacuo. It is slowly decomposed by warm water and rapidly by alkali-lye. Nitric acid and aqua regia decompose it violently. F. Venturoli prepared "yellow phosphorus iodobisiodo-mercuriate, I.P (Hgl)2, by the action of phosphorus on an alcoholic soln. of potassium iodide. The product is decomposed by heat into phosphorus, and mercurous and mercuric iodides. [Pg.1041]

The yield of constant-boiling acid is about 110 to 120 ml., or 90 per cent, based on the amount of iodine used. The product has a specific gravity of about 1.7 with a content of 57 per cent hydrogen iodide. If pure iodine and hydrogen sulfide are employed, the acid prepared in this way is quite pure except for a small amount of dissolved iodine produced by air oxidation. If a colorless product is desired, the distillation should be carried out in an atmosphere of hydrogen or carbon dioxide. [Pg.158]

There are two possible pathways to homologate methanol with carbon dioxide the CO2 insertion path and CO insertion path (Scheme 2). As for the former, Fukuoka et al. reported that the cobalt-ruthenium or nickel bimetallic complex catalyzed acetic acid formation from methyl iodide, carbon dioxide and hydrogen, in which carbon dioxide inserted into the carbon-metal bond to form acetate complex [7]. However, the contribution of this path is rather small because no acetic acid or its derivatives are detected in this reaction. Besides, the time course... [Pg.497]

Homogeneous hydrogenation of carbon dioxide to methanol is catalyzed by ruthenium cluster anions in the presence of halide anions. The catalyst system was Ru3(CO)i2 and alkyl iodides in A -methylpyrrolidone (NMP) solution at 513 K. Some methane was also formed. FT-IR spectra of the reactions allowed identification of several ruthenium carbonyl anions. [Pg.760]

Heal content, 110. 116 change (luring a reaction, 110 of a substance, 109 Heat of combustion of diamond, 122 graphite, 122 hydrazine, 47 hydrogen, 40 methane, 123 Heat of formation, 113 Heat of reaction, 135 between elements, table, 112 oxidation of HC1, 160 oxidation of sulfur dioxide, 161 predicting, 112 Heat of reaction to form ammonia, 112 Br atoms, 290 carbon dioxide, 112 carbon monoxide, 112 Cl atoms, 290 CO + Hi, 110 ethane, 112 F atoms, 290 H atoms, 274 hydrogen chloride, 160 hydrogen iodide, 112 iron(Ill) oxide, 162 Li atoms, 290 Li + Br, 290 Li + F, 290 Na + Cl, 290 NHs products, 114 Na atoms, 290 NO, 112 NOj, 112... [Pg.460]

Better results are obtained by transferring 25.0 mL of the diluted hydrogen peroxide solution to a conical flask, and adding 100 mL 1M(1 20) sulphuric acid. Pass a slow stream of carbon dioxide or nitrogen through the flask, add 10 mL of 10 per cent potassium iodide solution, followed by three drops of 3 per cent ammonium molybdate solution. Titrate the liberated iodine immediately with standard 0.1M sodium thiosulphate in the usual way. [Pg.395]

Less than perfect CO utilization. The rate determining step of the process is addition of methyl iodide to [Rh(CO)2l2] , HI generated elsewhere during the reaction cycle (Scheme 9.2) competes for this Rh species generating hydrogen and subsequently carbon dioxide in a water gas shift reaction summarized in Scheme 9.3. The H2 and CO2... [Pg.264]

According to the authors cited above, equation (16) holds for the decomposition of hydrogen iodide on platinum and of nitrous oxide on gold, and furthermore, according to Schwab and Drikos (12), for the oxidation of carbon monoxide to carbon dioxide on copper oxide. [Pg.259]

Nitrogen dioxide oxidizes an aqueous solution of iodide to iodine, hydrogen sulfide to sulfur, and carbon monoxide to carbon dioxide. In such reaction, it is reduced to nitric oxide, rather than nitrogen ... [Pg.650]

Polonium tetraiodide (8) is a black solid which sublimes in nitrogen at 200°C with partial decomposition to the metal. It is formed from the elements at 40°C/1 mm, by treating polonium dioxide or hydroxide with 0.1 N hydriodic acid, and is precipitated from solutions of polonium(lV) in dilute hydrochloric acid on the addition of 0.1 N hydriodic acid. It is also obtained as a black sublimate by heating polonium dioxide in hydrogen iodide at 200°C a black addition compound (PoCVxHI) is formed in the cold. Polonium metal does not react with iodine dissolved in carbon tetrachloride, but with iodine dissolved in benzene it does react to some extent. [Pg.217]

Telluric acid may be determined iodometrically by reduction with either hydrogen bromide or hydrogen chloride.6 The substance is heated in a distillation llask with four times the theoretical quantity of potassium iodide in the presence of the acid, air being excluded from the apparatus by passing a stream of carbon dioxide. The liberated iodine is titrated in the receiver and in the residue.7... [Pg.367]

Tantalum Pentiodide, Tal5, has been obtained by distilling tantalum pentabromide in a stream of dry hydrogen iodide and purifying the product by redistilling it in an atmosphere of carbon dioxide. It is an almost black substance which melts to a brown liquid, and is decomposed by water similarly to the pentabromide, but not so vigorously. [Pg.196]


See other pages where Hydrogen iodide carbon dioxide is mentioned: [Pg.247]    [Pg.50]    [Pg.3015]    [Pg.499]    [Pg.500]    [Pg.892]    [Pg.327]    [Pg.64]    [Pg.76]    [Pg.84]    [Pg.13]    [Pg.892]    [Pg.39]    [Pg.327]    [Pg.154]    [Pg.154]    [Pg.120]    [Pg.143]    [Pg.170]    [Pg.172]    [Pg.175]    [Pg.208]    [Pg.254]    [Pg.295]    [Pg.393]    [Pg.597]    [Pg.608]    [Pg.608]    [Pg.640]    [Pg.672]    [Pg.892]    [Pg.643]    [Pg.249]    [Pg.56]    [Pg.323]    [Pg.915]   
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Carbon dioxide hydrogenation

Hydrogen carbon dioxide

Hydrogen dioxid

Hydrogen dioxide

Hydrogen iodid

Hydrogen iodide

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