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Aluminium forming

The terms hot corrosion or dry corrosion are normally taken to apply to the reactions taking place between metals and gases at temperatures above 100 C i.e. temperatures at which the presence of liquid water is unusual. The obvious cases of wet corrosion at temperatures above 100 C, i.e. in pressurised boilers or autoclaves, are not considered here. In practice, of course, common metals and alloys used at temperatures above normal do not suffer appreciable attack in the atmosphere until the temperature is considerably above 100 C. Thus iron and low-alloy steels form only the thinnest of interference oxide films at about 200 C, copper shows the first evidence of tarnishing at about 180 C, and while aluminium forms a thin oxide film at room temperature, the rate of growth is extremely slow even near the melting point. [Pg.951]

Both silicon and aluminium are added to zinc to control the adverse effects of iron. The former forms a ferro-silicon dross (which may be removed during casting). Aluminium forms an intermetallic compound which is less active as a cathode than FeZn,] . Similarly in aluminium and magnesium alloys, manganese is added to control the iron . Thus in aluminium alloys for example, the cathodic activity of, FeAl, is avoided by transformation of FeAlj to (Fe, Mn)Al/. This material is believed to have a corrosion potential close to that of the matrix and is, therefore, unable to produce significant cathodic activity . [Pg.140]

Fluorimetry is generally used if there is no colorimetric method sufficiently sensitive or selective for the substance to be determined. In inorganic analysis the most frequent applications are for the determination of metal ions as fluorescent organic complexes. Many of the complexes of oxine fluoresce strongly aluminium, zinc, magnesium, and gallium are sometimes determined at low concentrations by this method. Aluminium forms fluorescent complexes with the dyestuff eriochrome blue black RC (pontachrome blue black R), whilst beryllium forms a fluorescent complex with quinizarin. [Pg.734]

The liquid is an aqueous solution of phosphoric acid, always containing 1 to 3 % of aluminium, which is essential to the cement-forming reaction (Table 6.2). Zinc is often found in amounts that range from 0 to 10% to moderate the reaction. Whereas zinc is present as simple ions, aluminium forms a series of complexes with phosphoric acid (Section 6.1.1). This has important consequences, as we shall see, in the cement-forming reaction. [Pg.207]

Aluminium forms a complex that combusts spontaneously in air with diborane. [Pg.176]

Another brine species of high interest with respect to the cell voltage and membrane life is aluminium. In the electrolysis cells aluminium forms an aluminosilica complex [1] that can damage the electrolyser membrane. This has a negative effect similar to that of iron migration in terms of power consumption. The necessity then of iron and aluminium removal (to mention only the most important elements) from the brine to their lowest possible levels is obvious. [Pg.286]

The exceptional properties of the alloy are due in no small way to the yttrium component which together with the aluminium forms a stable and firmly bound oxide layer that exhibits excellent resistance to exhaust gas emissions at high temperatures over prolonged periods.( ) At the same time, it provides an ideal surface to receive another coating of metal or metal oxide which, in the context of catalyst applications, is most essential. At the present time most catalytic convertors utilise ceramic substrates which are prone to damage by both mechanical and thermal shock. [Pg.168]

Aluminium forms numerous series of complex derivatives, the halogen salts showing a marked tendency to form molecular compounds with other metallic halides, with acid chlorides, with chlorides of organic acids, and with ammonia. [Pg.58]

Under similar conditions the cyanides of potassium, magnesium and aluminium form the corresponding thiocyanates. There are indications 4 that the sulphur nitride reacts with ammonium sulphide in the solution to give sulphur, which then interacts with the cyanide ... [Pg.234]

Have you wondered why iron articles turn brownish, copper vessels turn green and aluminium articles become dull This is because iron, copper and aluminium form oxides when exposed to air. Both oxygen and moisture in the air are responsible for the corrosion of metals. Gold and platinum do not corrode. [Pg.87]

Aluminium forms many mixed oxides of which the aluminosilicates are major constituents of minerals. [Pg.74]

The phosphates of iron and aluminium form gelatinous precipitates which are insoluble in weak acids, or in hydrolysed acid phosphates or sulphates. Ferric phosphate may be decomposed, using up more sulphuric acid, as in the equation... [Pg.223]

After reaction with the monomer to form a new propagating chain the position is formally the same as transfer with monomer. However, the two mechanisms can be distinguished kinetically if realkylation of the catalyst is slow compared with propagation. There is no direct evidence for this reaction although it is well established that the relatively stable alkyls of ms nesium and aluminium form metal hydride bonds on decomposition at elevated temperatures [83]. The existence of spontaneous termination has been deduced from a consideration of the kinetics, and by analogy with the effects of hydrogen on the polymerization. [Pg.150]

One example is the displacement reaction. Aluminium is more reactive than iron to put it another way, aluminium forms positive ions more easily than iron does. Iron(IlI) oxide is an ionic compound it contains positive iron ions and negative oxygen ions. If you mix aluminium metal with iron oxide, and provide some energy by heating the mixture, the aluminium atoms will give up electrons and force them on to the iron ions, thus converting the iron oxide into metallic iron ... [Pg.79]

The p>ore arrangement on the alumina surface is random (Fig. 3b). Selfordering of porous alumina appeared in the bottom parts (Fig. 3c,d). Ordering is enhanced with increasing of porous alumina thickness. The important feature of porous aluminium formed at high current densities is the formation of a nanotubular alumina structure. We have found that such structures were observed at forming current densities more than 100 mA/cm. Such forming... [Pg.218]

Aluminium forms fluoro-, chloro- and bromo-complexes, containing tetrahedral AIX4- ions and, in the case of fluorine, AlFg - octahedra. In the cubic cell of cryolite, NagAlFg, the corners and centre are occupied by distorted AlFg " octahedra, and the Na+ ions are arranged as in Fig. 145. In... [Pg.276]

Aluminium forms alloys of valuable properties, that with copper being known as aluminium bronze with magnesium, as magnalium the former resists the action of many salts in solution, such as alkali chlorides, ammonia compounds, caustic, etc. the latter has great tensile strength and can be soldered. [Pg.118]

Aluminium (Al, at. mass 26.98) occurs in solution exclusively in the III oxidation state. The hydroxide Al(OH)3 begins to precipitate at about pH 4. Above pH 9 it is converted into the soluble tetrahydroaluminate anion. Aluminium forms stable complexes with fluoride, oxalate, tartrate, and EDTA, and weak complexes with acetate. [Pg.83]

Aluminium acetate, known as red liquor, or mordant rouge, is used in dyeing for the production of red colour. One method of preparation is to add a solution of alum to acetate of lime liquor. The lime is precipitated as sulphate, its place being taken by the aluminium forming the acetate. [Pg.202]

The furnace consists of a vat, containing electrodes (anodes), and a conducting hearth (the cathode) sloping towards the tapping hole. Aluminium, formed by electrolysis of the alumina, collects on the floor of the vat oxygen is liberated at the anode, which it attacks, forming carbon monoxide and finally carbon dioxide. [Pg.1]


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