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Aluminium experiments

The surface state has an influence on the corrosion resistance of aluminium. Experience has shown that scratched, scraped or ground surfaces are sites at which corrosion preferentially develops [5]. This can be observed very frequently on ground and machined surfaces of welded structures of tanks, for example after hydraulic testing. [Pg.217]

Given their organic nature and their low concentration in air, and given that most of them are insoluble in water, it is unlikely that these compounds have any effect on the atmospheric corrosion of aluminium. Experience has shown that a localised somce of emission of chlorinated solvents, which used to exist in certain activities (dyeing, degreasing, etc.), could lead to severe corrosion of aluminium equipment exposed to this aggressive environment. [Pg.253]

Likewise, corrosion results obtained in artificial seawater, prepared in the laboratory from distilled water and the aimed concentration of dissolved inorganic salts, are known to be generally different from those obtained in natural seawater, even if its mineralisation (quantity and nature of dissolved salts) is close to that of natural seawater. For aluminium, experience shows that laboratory results obtained with artificial seawater are generally more severe than those obtained with natural seawater. All the biological components that are involved in the corrosion behaviour of metals in contact with seawater are missing in artificial seawater. [Pg.336]

It is advisable in any case before an experiment to place the weighed aluminium isopropoxide overnight in a shallow dish in a vacuum desiccator over sodium hydroxide. The isopropanol should be dried over anhydrous sodium sulphate, and the clear liquid decanted off before use. [Pg.153]

In the following experiment, salicylic acid is reduced to o-hydroxybenzyl alcohol (or saligenin), which being crystalline is readily isolated the excess of hydride is destroyed by the addition of undried ether, and the aluminium hydroxide then brought into solution by the addition of sulphuric acid. [Pg.155]

Correct-overlapping of joint is an important parameter to make a good joint, as well as to allow no excessive heat at the joints. Based on the recommendations of the leading aluminium section manufacturers, the desired overlaps are shown in Table 29.1, and two such joints are illustrated in Figures 29.4 and 29.6. Laboratory tests and site experience have revealed that a larger overlap is of no additional benefit. For larger sections also, only... [Pg.907]

It remains to be determined whether the previous experiments , which have been interpreted as confirming the cathodic protection of aluminium by zinc, can be truly interpreted in this fashion or whether they are due to the accumulation of Zn in the electrolyte. Under laboratory conditions, and under some practical conditions in stagnant solutions or in recirculating systems, the latter explanation is quite likely. [Pg.234]

Work by the US Bureau of Mines" involving galvanic couple experiments showed that the normally low corrosion rates of molybdenum were reduced further by contact with aluminium, SAE 1 430 steel or magnesium in aerated solutions of synthetic sea water or 3% sodium chloride. [Pg.847]

Remarkably little has been published on corrosion fatigue crack propagation in copper and its alloys. In general little or no influence of marine environments has been observed in crack propagation experiments on manganese and nickel-aluminium bronzes although the frequencies employed were quite high (> 2.5 Hz) ... [Pg.1312]

Where the end use of the product is known, there is usually preference to use either zinc or aluminium, both technically and because of the works problems associated with use of an alloy (identification, separation of overspray). However, in some countries (such as the United States) where there has been a recent-surge in anti-corrosion uses of metal spraying, a zinc-15%-aluminium alloy wire has been widely used. The original commercial experience was with 65-35% alloys used in powder form. Both have many of the advantages of the parent metals. At one time, the zinc-5%-aluminium alloy was also of interest. These alloy coatings may prove particularly satisfactory for sprayed coatings on articles where service conditions are not known in advance. [Pg.430]

Experience in the application of metal-coating processes can materially affect economics. Thus, although it is possible to apply aluminium by... [Pg.455]

Serra, M., Considerations Arising from Experiments on a New Process of Metallic Protection , Rev. Cienc, Appl., 12, 222 (1958). (Translation available as TM398, Aluminium Federation, Birmingham)... [Pg.480]

Repeat the experiment using 50.0 mL of the iron(III) solution in the presence of 100 fig of aluminium ion and 100 fig of nickel ion at pH 2.0 (use a pH meter to adjust the acidity) and measure the absorbance. Confirm that an effective separation has been achieved. [Pg.178]

Repeat the experiment in the presence of 500 jug of iron(III) and 500 jug of aluminium ions no interference will be detected, but cobalt may interfere (Note 2). [Pg.182]

For example /-butyl phenyl ether with aluminium chloride forms para-t-butyl phenol155. Often the de-alkylated phenol is also formed in considerable quantity. The reaction formally resembles the Fries and Claisen rearrangements. Like the Fries rearrangement the question of inter- or intramolecularity has not been settled, although may experiments based on cross-over studies156, the use of optically active ethers157 and comparison with product distribution from Friedel-Crafts alkylation of phenols158 have been carried out with this purpose in view. [Pg.476]

Various extraction methods for phenolic compounds in plant material have been published (Ayres and Loike, 1990 Arts and Hollman, 1998 Andreasen et ah, 2000 Fernandez et al., 2000). In this case phenolic compounds were an important part of the plant material and all the published methods were optimised to remove those analytes from the matrix. Our interest was to find the solvents to modily the taste, but not to extract the phenolic compounds of interest. In each test the technical treatment of the sample was similar. Extraction was carried out at room temperature (approximately 23 °C) for 30 minutes in a horizontal shaker with 200 rpm. Samples were weighed into extraction vials and solvent was added. The vials were closed with caps to minimise the evaporation of the extraction solvent. After 30 minutes the samples were filtered to separate the solvent from the solid. Filter papers were placed on aluminium foil and, after the solvent evaporahon, were removed. Extracted samples were dried at 100°C for 30 minutes to evaporate all the solvent traces. The solvents tested were chloroform, ethanol, diethylether, butanol, ethylacetate, heptane, n-hexane and cyclohexane and they were tested with different solvent/solid ratios. Methanol (MeOH) and acetonitrile (ACN) were not considered because of the high solubility of catechins and lignans to MeOH and ACN. The extracted phloem samples were tasted in the same way as the heated ones. Detailed results from each extraction experiment are presented in Table 14.2. [Pg.283]

Still has also carried out mechanistic experiments from which he could deduce that the major reduction pathway is by attack of hydride ion at the sulphur atom. This conclusion was deduced from the fact that reduction with sodium borodeuteride-aluminium oxide gave a sulphoxide that had only incorporated about 25% mole equivalent of deuterium on to a methyl carbon atom bound to the sulphur atom. The mechanistic pathway for direct reduction is outlined in equation (38), whereas the pathway whereby deuterium could be incorporated is portrayed in equation (39). These reactions support the proposed mechanism for the hydride reduction of sulphones as outlined in Section III.A.l, namely that attack at sulphur by hydride ions may occur, but will be competitive with proton abstraction in cases when the attack at sulphur is not facilitated. [Pg.942]

With very electropositive metais this oxide is reduced very violently following thermite type of reactions. Vioient reactions of this type happen with lithium, magnesium, aluminium and the Al-Mg-Zn alloy. The iron formed is melted due to the exothermicity of this reaction. This experiment is not recommended for lectures. [Pg.204]

Iodine reacts dangerously with numerous elements. Thus, with aluminium, magnesium or powdered zinc, the mixture with iodine in contact with a drop of water gives rise to a flash , which is extremely violent and blinding. In the very spectacular experiment involving ammonium nitrate and zinc described on p.208 and carried out with students, it is recommended to Incorporate a small quantity of iodine before throwing a few drops of water on the mixture. [Pg.225]


See other pages where Aluminium experiments is mentioned: [Pg.82]    [Pg.82]    [Pg.386]    [Pg.943]    [Pg.219]    [Pg.256]    [Pg.307]    [Pg.121]    [Pg.11]    [Pg.297]    [Pg.306]    [Pg.226]    [Pg.233]    [Pg.663]    [Pg.667]    [Pg.672]    [Pg.677]    [Pg.704]    [Pg.1274]    [Pg.1280]    [Pg.129]    [Pg.389]    [Pg.424]    [Pg.428]    [Pg.474]    [Pg.789]    [Pg.1118]    [Pg.171]    [Pg.934]    [Pg.563]    [Pg.179]    [Pg.142]    [Pg.934]   
See also in sourсe #XX -- [ Pg.197 ]




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