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Aluminium metal

Small particles can be introduced into metals or ceramics in other ways. The most obvious is to mix a dispersoid (such as an oxide) into a powdered metal (aluminium and lead are both treated in this way), and then compact and sinter the mixed powders. [Pg.106]

Below -10°C, heat is conducted away too quickly to allow this melting - and because their thermal conductivity is high, skis with exposed metal (aluminium or steel edges) are slower at low temperatures than those without. At these low temperatures, the mechanism of friction is the same as that of metals ice asperities adhere to the ski and must be sheared when it slides. The value of jl (0.4) is close to that calculated from the shearing model in Chapter 25. This is a large value of the coefficient of friction - enough... [Pg.254]

The second category was concerned with adhesion to porous or microfibrous surfaces on metals. Aluminium may be anodised to form an oxide surface comprising pores of diameter of tens of nanometers. Electroforming and chemical oxidation can be used to produce microfibrous or needle-like coatings on metals, including copper, steel and titanium. The substrate topography was demonstrated to play an vital part in adhesion to these surfaces [45-48]. [Pg.334]

Substrate Steel Steel Zinc Multi-metal Aluminium... [Pg.286]

The solution also contains a high concentration of zinc (as zincate), which is noble relative to aluminium. As metallic aluminium is exposed, it corrodes, reducing zincate ions and forming a coating of zinc ... [Pg.354]

In a related process the work is dipped in a catalytic titanium compound and then transferred to a bath of aluminium hydride solution. The solution dries leaving the hydride on the surface and mild heating then turns the hydride into metallic aluminium. The conversion stage occurs slowly at room temperature or in seconds at 100°C. [Pg.468]

Gauge (BWG) Thickness (mm) Copper Values of xw/kw (m2K/kW) Steel Stainless Admiralty steel metal Aluminium... [Pg.518]

An explanation that may be suggested of these facts is that solid solutions of a quadrivalent metal (zinc) in a tervalent metal (aluminium) tend to be unstable because of the difficulty of saturating the valency of isolated quadrivalent atoms by bonds to its lower-valent ligates. With zinc as the solute an increase in free energy at the lower temperatures would accompany the separation into the zinc-poor a phase, in which the versatile zinc atoms tend to assume the valency 3 (less stable, however, for them than their normal valency) in order to fit into the aluminium structure, and the zinc-rich a phase, in which the concentration of zinc atoms is great enough to permit the extra valency of zinc to be satisfied through the formation of Zn-Zn bonds. [Pg.391]

The dangers are the same as with magnesium and sodium, ie those caused by highly reducing metals. Aluminium is less dangerous with sodium. [Pg.176]

The Fine Structure Before and After Each Edge. ELNES is the term use to describe the energy-loss near edge structure, and this can be quite different for an element in different compounds. For example the shape of the aluminium L edges are quite different in EELS spectra from metallic aluminium and aluminium oxide, so that the chemical form of a given element may be indentified from these small variations in intensity after the edge. [Pg.191]

At 240° C mixtures of finely divided metals (aluminium, iron, tungsten) with the peroxide ignite under high friction, and molybdenum powder reacts explosively. [Pg.1827]

The benzotriazole 109 reacts with alkyl or allyl halides in the presence of bismuth(III) chloride and metallic aluminium to give the homoalkylated amines 110 in high yields119. [Pg.556]

With Aluminium.—If a solution of caustic soda is brought into contact with metallic aluminium, chemical reaction takes place, with the production of sodium aluminate and hydrogen, in accordance with the following equation —... [Pg.44]

In the commercial application of this method it is necessary to amalgamate the metallic aluminium h mercury by hand, as advantage is taken of the t that aluminium will reduce aqueous solutions of s of mercury to the metallic state, in accordance with following equation —... [Pg.69]

B. Bogdanovic, M. Schwickardi, Ti-doped alkali metal aluminium hydrides as potential novel reversible hydrogen storage materials, J. Alloys Compd 1-9 (1997) 253-254. [Pg.78]

A very large number of mixed metal aluminium amides has been reported. The majority are lithium-aluminium amide salts that exhibit a variety of different structures. Only a small number of ese compounds are discussed here.39,52,57,72,118-138 simplest is LiAl-(NH2)4 produced from the reaction of lithium and aluminium in liquid ammonia at 80 to 100 °C. The atomic arrangement of LiAl(NH2)4 has been studied by IR-spectroscopy and single crystal X-ray crystallography and was found to be a new variant of the GaPS4-type structure. [Pg.230]

Preparation of Aluminium Hydroxide. Weigh 0.5 g of metallic aluminium and dissolve it in a calculated amount of a 10% alkali solution. Filter the liquid from undissolved impurities and divide it into two unequal parts. Pass a stream of carbon dioxide through the larger part of the filtrate. Explain what occurs. Heat the smaller... [Pg.202]

Lubricate the ground-glass joints in the apparatus with a concentrated sulphuric acid solution. Clean a piece of metallic aluminium with emery paper, make 10-12 g of shavings from it, and put it into flask 1. Pour 30 ml of dry bromine into dropping funnel 2. This amount of bromine is not sufficient for the aluminium to enter into the reaction completely (why is excess aluminium taken )... [Pg.204]

The composition of similar mixtures, containing metallic aluminium, is given below in Table 56 (p. 271). [Pg.254]

The system ammonium nitrate, aluminium, nitro compound (e.g. TNT) would be expected to undergo gradual decomposition, e.g. that in stored shells and bombs filled with such mixtures changes would occur, leading to the oxidation of the aluminium. Obviously, a mixture containing oxidized aluminium has lower explosive power than the same mixture containing metallic aluminium. It was therefore very important to determine the mechanism of the oxidation of aluminium. It became apparent that this is caused by impurities in the ammonium nitrate, not by the... [Pg.267]

After World War I the use of ammonals was restricted to quarrying in coal mines they were banned since their high flame temperature (due to presence of metallic aluminium) makes them inherently dangerous there. [Pg.270]

During World War II the use of aluminium in military explosives was resumed on a wide scale. Thus sea mines and German torpedoes were loaded with a fusible mixture of hexyl and TNT supplemented by 10—25% of metallic aluminium (Trial). [Pg.271]

Since the mixture is highly hygroscopic it should be protected against atmospheric moisture. During melting it is also necessary to avoid contact between the mixture and brass or other copper alloys since the latter are liable to react with metallic aluminium. Kettles should be washed with water every 24 hr to remove all residues of the mixture. [Pg.274]

Reactivity Reacts with active metals (aluminium, magnesium, zinc) (Lewis, 1993)... [Pg.737]

In comparison with metals, aluminium oxide releases very few ions. This is measured in several ways, one of which is by inserting the implant material in artificial saliva for 6 months. After this period the number of released metal ions is measured by means of special trace analysis techniques. [Pg.267]

In the nineteenth century Napoleon III owned a very precious dinner service. It was said to be made of a metal more precious than gold. That metal was aluminium. The reason it was precious was that it was very rarely found as the pure metal. Aluminium is a reactive metal and as such was very difficult to extract from its ore. Reactive metals hold on tightly to the element(s) they have combined with and many are extracted from their ores by electrolysis. [Pg.85]

Generally, it is the unreactive metals for which we find most uses. For example, the metals iron and copper can be found in everyday objects such as car bodies and coins, respectively However, the metal aluminium is an exception. Aluminium appears in the reactivity series just below magnesium and is quite reactive. [Pg.164]

See Lithium Sulfur Potassium Sulfur Rubidium Non-metals Sodium Non-metals Aluminium, Copper, above See Selenium Metals See also Aluminium, Starch, above See also Fibreglass, Iron, above... [Pg.1989]


See other pages where Aluminium metal is mentioned: [Pg.546]    [Pg.216]    [Pg.431]    [Pg.163]    [Pg.480]    [Pg.619]    [Pg.703]    [Pg.250]    [Pg.338]    [Pg.238]    [Pg.334]    [Pg.492]    [Pg.109]    [Pg.13]    [Pg.92]    [Pg.205]    [Pg.248]    [Pg.138]    [Pg.546]    [Pg.328]   
See also in sourсe #XX -- [ Pg.27 ]

See also in sourсe #XX -- [ Pg.297 ]




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A Possible Benchmark for Solid Metal Fluoride, Lewis Acids Aluminium Chlorofluoride

Aluminium and Other Metal Phosphates

Aluminium appearance of metal

Aluminium as a Passive Metal

Aluminium metal hydride

Aluminium metal polishers

Aluminium metallizing plastic

Aluminium rare earth metals

Aluminium refractory metal alloys

Aluminium structure of metal

Aluminium, Hydrogen, and Transition Metals

Anodized anti-corrosion coatings for aluminium using rare earth metals

Coatings for metals other than aluminium

Growth kinetics of intermetallic layers at the transition metal-liquid aluminium interface

Heavy metals, mercury and aluminium

Metal Fluoride Surfaces that Contain Surface Hydroxyl Groups Aluminium Hydroxy Fluorides with the Hexagonal Tungsten Bronze Structure

Metal dusting Aluminium coating

Metal, metals aluminium

Mixed metal oxides aluminium compounds

Poly aluminium-metallized

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