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Silicon, elemental copper metal

Aside from the recently described Cu/Th02 catalysts, copper on chromia and copper on silica have been reported to catalyze methanol synthesis at low temperatures and pressures in various communications that are neither patents nor refereed publications. It is not feasible to critically review statements unsupported by published data or verifiable examples. However, physical and chemical interactions similar to those documented in the copper-zinc oxide catalysts are possible in several copper-metal oxide systems and the active form of copper may be stabilized by oxides of zinc, thorium, chromium, silicon, and many other elements. At the same time it is doubtful that more active and selective binary copper-based catalysts than... [Pg.288]

Metals and Elemental Contaminants. Arsenic, lead, copper, and silicon are examples of the various types of metal or elemental impurities that contaminate feedstocks. Some metals exist in crude oil, whereas others maybe introduced through the addition of corrosion inhibitors or antifoaming agents. Becanse of the irreversible effect of metal poisoning of Platforming catalyst, there shonld be only be subparts per billion levels of metals in Platforming feeds. In practice, most metals that are distilled over with the naphtha in the crude distillation colnnm are adsorbed on the catalyst in the hydrotreating unit. [Pg.1969]

The first metal-ate complex, sodium triethylzincate, " was obtained by John Wanklyn who treated diethylzinc with elemental sodium in an attempt to produce ethylsodium. A systematic and reliable approach to ate complexes is the addition of a more polar organometallic reagent (eg., an organolithium) to a less polar organic derivative of an alkali-earth metal, transition element, or metalloid. In this way, a wealth of ate complexes of berrylium, magnesium, zinc, copper, boron, aluminum, silicon, tin, and mercury as well as of nonmetals like phosphorus, sulfur, selenium, tellurium, and even iodine " have been obtained. [Pg.26]

The properties of aluminum alloys (mechanical, physical, and chemical) depend on alloy composition and microstructure as determined by casting conditions and thermomechanical processing. While certain metals alloy with Al rather readily [9], comparatively few have sufficient solubility to serve as major alloying elements. Of the commonly used alloying elements, magnesium, zinc, copper, and silicon have significant solubility, while a number of additional elements (with less that 1% total solubility) are also used to confer important improvements to alloy properties. Such elements include manganese, chromium, zirconium, titanium, and scandium [2,10]. [Pg.707]

Examples of this procedure for dilute solutions of copper, silicon and aluminium shows the widely different behaviour of these elements. The vapour pressures of the pure metals are 1.14 x 10, 8.63 x 10 and 1.51 x 10 amios at 1873 K, and the activity coefficients in solution in liquid iron are 8.0, 7 X 10 and 3 X 10 respectively. There are therefore two elements of relatively high and similar vapour pressures, Cu and Al, and two elements of approximately equal activity coefficients but widely differing vapour pressures. Si and Al. The right-hand side of the depletion equation has the values 1.89, 1.88 X 10- , and 1.44 X 10 respectively, and we may conclude that there will be depletion of copper only, widr insignificant evaporation of silicon and aluminium. The data for the boundaty layer were taken as 5 x lO cm s for the diffusion coefficient, and 10 cm for the boundary layer thickness in liquid iron. [Pg.362]

The discussion so far has been limited to the structure of pure metals, and to the defects which exist in crysteds comprised of atoms of one element only. In fact, of course, pure metals are comparatively rare and all commercial materials contain impurities and, in many cases also, deliberate alloying additions. In the production of commercially pure metals and of alloys, impurities are inevitably introduced into the metal, e.g. manganese, silicon and phosphorus in mild steel, and iron and silicon in aluminium alloys. However, most commercial materials are not even nominally pure metals but are alloys in which deliberate additions of one or more elements have been made, usually to improve some property of the metal examples are the addition of carbon or nickel and chromium to iron to give, respectively, carbon and stainless steels and the addition of copper to aluminium to give a high-strength age-hardenable alloy. [Pg.1270]

Heating with the following solids, their fusions, or vapours (a) oxides, peroxides, hydroxides, nitrates, nitrites, sulphides, cyanides, hexacyano-ferrate(III), and hexacyanoferrate(II) of the alkali and alkaline-earth metals (except oxides and hydroxides of calcium and strontium) (b) molten lead, silver, copper, zinc, bismuth, tin, or gold, or mixtures which form these metals upon reduction (c) phosphorus, arsenic, antimony, or silicon, or mixtures which form these elements upon reduction, particularly phosphates, arsenates,... [Pg.95]

Germanium has a gray shine with a metallic silvery-white luster. It is a brittle element classed as a semimetal or metalloid, meaning it is neither a metal such as iron or copper nor a nonmetal, such as phosphorus, sulfur, or oxygen. Germanium has some properties like a metal and some like a nonmetal. It is a crystal in its pure state, somewhat like silicon. It will combine with oxygen to form germanium dioxide, which is similar to sihcon dioxide (sand). [Pg.198]

Assay of beryllium metal and beryllium compounds is usually accomplished by titration. The sample is dissolved in sulfuric acid. Solution pH is adjusted to 8.5 using sodium hydroxide. The beryllium hydroxide precipitate is redissolved by addition of excess sodium fluoride. Liberated hydroxide is titrated with sulfuric acid. The beryllium content of the sample is calculated from the titration volume. Standards containing known beryllium concentrations must be analyzed along with the samples, as complexation of beryllium by fluoride is not quantitative. Titration rate and hold times are critical therefore use of an automatic titrator is recommended. Other fluoride-complexing elements such as aluminum, silicon, zirconium, hafnium, uranium, thorium, and rare earth elements must be absent, or must be corrected for if present in small amounts. Copper—beryllium and nickel—beryllium alloys can be analyzed by titration if the beryllium is first separated from copper, nickel, and cobalt by ammonium hydroxide precipitation (15,16). [Pg.68]


See other pages where Silicon, elemental copper metal is mentioned: [Pg.89]    [Pg.872]    [Pg.97]    [Pg.422]    [Pg.72]    [Pg.552]    [Pg.653]    [Pg.645]    [Pg.699]    [Pg.207]    [Pg.546]    [Pg.681]    [Pg.632]    [Pg.727]    [Pg.705]    [Pg.691]    [Pg.725]    [Pg.645]    [Pg.219]    [Pg.909]    [Pg.739]    [Pg.161]    [Pg.46]    [Pg.184]    [Pg.9]    [Pg.227]    [Pg.21]    [Pg.159]    [Pg.327]    [Pg.691]    [Pg.105]    [Pg.353]    [Pg.17]    [Pg.151]    [Pg.92]    [Pg.137]   
See also in sourсe #XX -- [ Pg.2 , Pg.5 , Pg.6 ]

See also in sourсe #XX -- [ Pg.2 , Pg.5 , Pg.6 , Pg.11 ]




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