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The oxides of iron

Thus an oxidising agent is identified as an electron acceptor and the oxidation of iron(II) by chlorine can be written as two "half equations, viz. [Pg.92]

Consider also the oxidation of iron(II) ions by dichromate(Vl)... [Pg.96]

The treatment units used for color removal are the same as those used for turbidity removal. However, the pH must be increased prior to filtration so that the metal hydroxides are removed by the filters. At low pH values, metal ions or their soluble complexes readily pass through the filters and form insoluble species in storage tanks and in the distribution system. For iron salts, it is important that the pH be greater than 6 as the oxidation of iron(II) to iron(III) occurs rapidly above this pH in the presence of dissolved oxygen or other strong oxidants (18). [Pg.278]

The result is that the oxidation of iron in aerated water (rusting) goes on at a rate which is millions of times faster than that in dry air. Because of the importance of (c), wet oxidation is a particular problem with metals. [Pg.226]

Formation of rust inside a elosed steel tank (oxygen is removed from the atmosphere by the oxidation of iron). [Pg.124]

Several authors " have suggested that in some systems voids, far from acting as diffusion barriers, may actually assist transport by permitting a dissociation-recombination mechanism. The presence of elements which could give rise to carrier molecules, e.g. carbon or hydrogen , and thus to the behaviour illustrated in Fig. 1.87, would particularly favour this mechanism. The oxidant side of the pore functions as a sink for vacancies diffusing from the oxide/gas interface by a reaction which yields gas of sufficiently high chemical potential to oxidise the metal side of the pore. The vacancies created by this reaction then travel to the metal/oxide interface where they are accommodated by plastic flow, or they may form additional voids by the mechanisms already discussed. The reaction sequence at the various interfaces (Fig. 1.87b) for the oxidation of iron (prior to the formation of Fe Oj) would be... [Pg.277]

It has already been shown that bulk lattice diffusion is not generally considered to be the rate-controlling process for the oxidation of iron in most real situations. Hence the classical Wagner treatment, whereby the valency of the alloying element increases or decreases the number of lattice defects. [Pg.970]

Effects of Specific Alloying Elements on the Oxidation of Iron... [Pg.974]

Over the years, Pourbaix and his co-workers in the CEBELCOR Institute, founded under his direction, extended these diagrams by including lines for metastable compounds. Figure 7.66 illustrates such a presentation for the Fe-O system over the temperature range 830-2200 K. Pourbaix used these diagrams as a basis for a discussion of the stability of metallic iron (solid, liquid and vapour phases), the oxides of iron as a function of oxygen pressure and temperature from which he explained the protection of iron at high temperature by immunity and passivation. He also pointed out the... [Pg.1111]

Hematite an oxide of iron corresponding closely to Fe203 produced during the oxidation of iron it is an n-type semiconductor in which diffusion of O ions occurs via anion vacancies. [Pg.1369]

In quantitative analysis we are chiefly concerned with reactions which take place in solution, i.e. ionic reactions. We shall therefore limit our discussion of oxidation-reduction to such reactions. The oxidation of iron(II) chloride by chlorine in aqueous solution may be written ... [Pg.847]

The transport of pre-boiler corrosion debris to the boiler section includes the oxides of iron, copper, nickel, zinc, and chromium and results from the corrosion of pre-heaters and condensers, and the like. Specifically, equipment components variously fabricated from admiralty brass, aluminum brass, cupronickels, and stainless steels are most affected. [Pg.212]

At the even higher temperatures found in HP industrial process or power generating boilers, the oxidation of iron is accomplished by the reduction of hydrogen ions supplied by the HW. The magnetite film is thus formed directly. [Pg.242]

Anodic inhibitors limit the oxidation of iron by sharing the lone pair electrons on the nitrogen with a metal ion or atom and supressing the anodic reaction. Examples are benzotriazole (at high concentrations), pyridines, thiols, and quinolines. [Pg.647]

A rich supply of manganese lies in nodules of ore that litter the ocean floors (Fig. 16.9). These nodules range in diameter from millimeters to meters and are lumps of the oxides of iron, manganese, and other elements. However, because this source is technically difficult to exploit, manganese is currently obtained by the thermite process from pyrolusite, a mineral form of manganese dioxide ... [Pg.783]

Basically, the oxidation of iron pyrite, FeS2, results in the production of iron(III) sulfate and sulfuric acid, H2SO4. However, two overall reaction stoichiometries are possible and each will yield a different acid generation capacity (e.g., Langmuir, 1997 Baird, 1995) ... [Pg.406]

The major raw materials used at present for the production of alumina are bauxites, which are found in the following mineral forms gibbsite (Al(OH)3), boehmite (AlO OH), and diaspore (AlO OH). The major impurities are the oxides of iron, silicon, and titanium, and organic compounds, all of which must be removed before alumina is suitable for aluminum production. The process objectives are, therefore, separation of impurities and compound production in the present case. Bauxite is first dried to facilitate grinding, destroy organic matter, and oxidize the associated ferrous minerals to the ferric state. The temperature of drying is not allowed to exceed 150 °C, because at higher temperature a part of the combined water is expelled and the solubility is affected adversely. [Pg.484]

The oxidation of iron by oxygen is a spontaneous process in acidic, neutral, or basic environments. Iron serves as the anode and reducing agent as it is oxidized to Fe2+ ... [Pg.44]

In a neutral or alkaline solution, the oxidation of iron is represented by... [Pg.44]

As long as the tin coating remains intact, the iron is protected from oxidation. A scratch of the tin surface to expose the iron metal leads to the oxidation of iron in preference to the tin. [Pg.44]

The vast majority of the studies in this field relate to the oxidation of iron ions by molecular oxygen. The oxidation of Fe2+ is first-order with respect to dioxygen and,... [Pg.402]

If the above half-equation is combined with that for the oxidation of iron (II) to iron (III) ions, Fe2+half-equations, the second is multiplied by 6, giving an overall equation for the redox reaction as ... [Pg.48]

Dissolved iron(III) is (i) an intermediate of the oxidative hydrolysis of Fe(II), and (ii) results from the thermal non-reductive dissolution of iron(III)(hydr)oxides, a reaction that is catalyzed by iron(II) as discussed in Chapter 9. Hence, iron(II) formation in the photic zone may occur as an autocatalytic process (see Chapter 10.4). This is also true for the oxidation of iron(II). As has been discussed in Chapter 9.4, the oxidation of iron(II) by oxygen is greatly enhanced if the ferrous iron is adsorbed at a mineral (or biological) surface. Since mineral surfaces are formed via the oxidative hydrolysis of Fe(II), this reaction proceeds as an autocatalytic process (Sung and Morgan, 1980). Both the rate of photochemical iron(II) formation and the rate of oxidation of iron(II) are strongly pH-dependent the latter increases with... [Pg.364]

Consider also the oxidation of iron(II) ions by dichromate(VI) ions in acidic solution. The Cr202- is reduced to Cr3+(aq)... [Pg.96]

Not all hot packs use dissolution processes. For example, one kind of hot pack exploits the crystallization of sodium thiosulfate or sodium acetate. Another kind uses the oxidation of iron (rusting). On the Internet, investigate different kinds of hot packs. Are they all used for the same purpose What are the pros and cons of their designs To start your search, go to the web site above and click on Web Links. [Pg.229]


See other pages where The oxides of iron is mentioned: [Pg.284]    [Pg.102]    [Pg.264]    [Pg.426]    [Pg.46]    [Pg.339]    [Pg.1079]    [Pg.265]    [Pg.274]    [Pg.967]    [Pg.971]    [Pg.487]    [Pg.811]    [Pg.110]    [Pg.164]    [Pg.536]    [Pg.339]    [Pg.151]    [Pg.102]    [Pg.264]    [Pg.373]   


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An Experimental Lecture for Students on the Formation of Iron Oxides

Coagulation of iron oxide particles in the

Iron oxides and the surface textures of catalysts

Oxidation of iron

Reaction between Nitric Oxide and the Surface of Iron

Structures of the individual iron oxides

The hydrous oxides of iron and manganese

The iron oxides

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