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Water iron and

Chloroform slowly decomposes on prolonged exposure to sunlight in the presence or absence of air and in the dark in the presence of air. The products of oxidative breakdown include phosgene, hydrogen chloride, chlorine, carbon dioxide, and water. At 290°C, chloroform vapor is not attacked by oxygen. In contact with iron and water hydrogen peroxide is also produced, probably by the following reaction sequence (2) ... [Pg.524]

The prime reaction in boiler corrosion is the formation of magnetite and hydrogen from iron and water ... [Pg.840]

Ethyl -aminobenzoate has been prepared by the esterification of p-aminobcnzoic acid1 and by the reduction of ethyl /i-nitrobenzoate with ammonium sulfide.2 Although commer-dally the reagent used is usually iron and water in presence of a little acid, in the laboratory the catalytic reduction as described in the procedure is by far the most convenient. [Pg.66]

To consider these reactions and the problems caused, it may be useful to refer back to the basic corrosion mechanisms of iron and water as shown in section 4.5.1. It can be seen from the second anodic half reaction that ferrous hydroxide is formed from ferrous ions and hydroxide ion where water (condensate) is present. [Pg.286]

After the horses had worked for 2.5 h, the water began to boil. Assuming that all the work done by the horses was converted to heat in the iron and water, use the information in Table 6.2 to determine the work done by the horses per minute. [Pg.380]

The next stage in the process, the reduction of the nitro-groups on the stilbene to amines, which had been developed many years previously, used old iron and water reduction technology, which resulted in significant... [Pg.261]

Figure 3.26 Iron oxide lump under reduction by hydrogen yielding porous iron and water vapour. Figure 3.26 Iron oxide lump under reduction by hydrogen yielding porous iron and water vapour.
The treatment costs for 2.5 million pounds of soil contaminated with metolachlor at a site in southwest Nebraska were estimated to be 65,000. The treatment involved using a Microen-fractionator to mix the excavated soil with zero-valent iron and water. The estimate included labor costs (D21578L, p. 2). [Pg.642]

Reduction with iron and water, with the addition of small amounts of acid (hydrochloric, sulfuric, or acetic acid, and occasionally mixtures of these). This neutral reduction method of Bechamp-Brimmeyr can be carried out oiJy with certain kinds of iron, notably gray-iron casting, which must always be tested pre. viously to establish its usabiL ty. In general, other kinds of iron are twt usable (many examples have been given). [Pg.271]

At an intermediate temperature a state of chemical equilibrium would be achieved in a closed container. If a sample of iron oxide were to be heated to 700° C with hydrogen gas in a container for a long time, the reaction would proceed, with the formation of water vapor, until a certain amount of tvater vapor had been formed. Similarly if metallic iron and water vapor were to be heated in the container some hydrogen and iron oxide would be formed. Ultimately in either case a steady state would be achieved, in which the rate of reduction of iron oxide by hydrogen is just equal to the rate of oxidation of iron by water vapor. This steady state (chemical equilibrium) is analogous to the steady state between a crystal or a liquid and its vapor, discussed in Chapter 3 (physical equilibrium). It has been found possible to develop a quantitative theory of chemical equilibrium, tvhich will be discussed in a later chapter (Chap. 19). [Pg.105]

The reaction of iron and water vapor is complicLted by the fact that iron forms three oxides, which have the formulas FeO, FcaO, and FcsOa. By carefully controlling the con ditions it is possible to carry out the oxidation of iron to these three oxides successively. [Pg.105]

At a high temperature iron reduces water vapor, giving the magnetic oxide of iron inversely, by passing a current of hydrogen over the magnetic ferrous oxide, iron and water vapor are obtained H. Sainte-Claire Deville and Debray have tried to determine the conditions in which these two inverse reactions are produced. [Pg.61]

Burning isn t the only exothermic reaction. There are, for example, emergency heating packs used by mountain rescue people that depend on an exothermic reaction. They contain two chemicals that react exothermically when the barrier between two containers of chemicals is broken. Isn t it dangerous carrying chemicals like that about Not really, because the chemicals are iron and water and the reaction is rusting - but in this case a third chemical is added as a catalyst to speed up the reaction so that the heat is given out much more quickly than normal. [Pg.114]

Balance the equation for the reaction of iron(III) oxide with hydrogen to form iron and water. [Pg.287]

Iron(III) oxide and hydrogen are the reactants. Iron and water are the products. The unbalanced formula equation is... [Pg.287]

The reaction of iron and water vapor results in an equilibrium... [Pg.747]

The reduction is done using iron and water vapor in industry. [Pg.222]

If 478.2 g of aniline, C6H5NH2, are formed from the reaction of 810.5 g of nitrobenzene, C6H5NO2, with excess iron and water, what is the percent yield ... [Pg.399]

Electronic Mechanism. According to Luder and Zuffanti, the use of iron and acids to reduce nitrobenzene to aniline can be explained as follows Any acid (using the word in the Lewis sense) will increase the concentration of hydrogen ions (hydrated, of course) in water solution. The salts (FeCh and RNH3CI) and cations that have appeared in the equations above are acids in this general Sense, and in the presence of iron and water a plentiful supply of both electrons and protons is available. [Pg.138]

Effect of Agitation. Since the reduction process under consideration is a multiphase reaction, it is clear that the best results are obtainable only when the nitro compound, iron, and water-soluble catalyst are in intimate contact. A stirrer that merely pushes the iron around the bottom of the vessel and permits the charge to separate out into layers does not function efli-ciently. It is apparent, therefore, that, a sturdy sleeve-and-propelier or double-impeller type of stirrer will in some cases be superior to the slow-moving plow type, speeding up the reaction considerably. [Pg.142]

Chloroform is prepared as indicated above and by agitating carbon tetrachloride with iron and water for several days. The reaction resembles the reduction of chloroform to methylene... [Pg.262]

Syn. Sesquichloride of Iron Permuriate of Iron.—It is formed when chlorine gas is passed over iron heated to a temperature below redness, when it appears as red iridescent scales, volatile at a temperature little beyond 212 , and soluble in water, alchohol, and ether. A solution of the perchloride is easily obtained by dissolving peroxide of iron in hydrochloric acid Fe, 0, + 3HC1 = Fe, Cl, -t- 3 HO. When evaporated to the consistence of syrup, and cooled, it forms red crystals, which contain water of ciystallisation. When heated, they are partly decomposed, peroxide being formed, and hydrochloric acid passing off, in consequence of the action between perchloride of iron and water. As perchloride of iron is a volcanic product, it is probably in this way that the crystals of peroxide, found in volcanic districts, have been formed. Perchloride of iron is much used in medicine. [Pg.174]

Due to the reason that the colour of polyaniline changes very quickly in the presence of iron and water, the recording of spectra was started as soon as the coated film was placed into the solution. The spectra were... [Pg.573]


See other pages where Water iron and is mentioned: [Pg.35]    [Pg.313]    [Pg.1298]    [Pg.507]    [Pg.17]    [Pg.597]    [Pg.171]    [Pg.218]    [Pg.313]    [Pg.733]    [Pg.514]    [Pg.69]    [Pg.597]    [Pg.189]    [Pg.178]    [Pg.399]    [Pg.774]    [Pg.94]    [Pg.594]    [Pg.172]    [Pg.69]    [Pg.21]   
See also in sourсe #XX -- [ Pg.69 ]




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