Carbon silicide

Kohlenstoff-hydrat, n. carbohydrate, -kalium, n. potassium carbide, -kem, m. carbon nucleus. -kette,/. carbon chain, -legiening,/, carbon alloy, -metall, n. carbide, kohlenstoffrelch, a. rich in carbon. Kohlenstoff-silicium, n. carbon silicide. -ske-lett, n. carbon skeleton, -stahl, m. carbon steel, -stein, m. carbon brick, -sticlKtoff-titan, n. titanium carbonitride. -sulfid, n. 

CAS/DOT IDENTIFICATION 409-2l-2/none SYNONYMS carbon silicide, carborundum , silicon monocarbide. 

Synonyms/Trade Names Carbon silicide, Carborundum , Silicon monocarbide ... 

CAS 409-21-2 EINECS/ELINCS 206-991-8 Synonyms Carbon silicide Carborundeum Carborundum Silicon monocarbide Silundum Empirical CSi Famula SiC... 

Carbonothioic acid, 0-(6-chloro-3-phenyl-4-pyridazinyl) S-octyl ester. See Pyridate, Carbonothioic dichloride. See Thiophosgene Carbon oxide. See Carbon monoxide Carbon oxide sulfide. See Carbonyl sulfide Carbon oxychloride. See Phosgene Carbon oxysulfide. See Carbonyl sulfide Carbon silicide. See Silicon carbide Carbon sulfide. See Carbon disulfide Carbon tet. See Carbon tetrachloride Carbon tetraboride. See Boron carbide Carbon tetrabromide CAS 558-13-4 EINECS/ELINCS 209-189-6 UN 2516... 

If an excess of magnesium is used, magnesium silicide, Mg2Si, is also produced.) The silicon obtained is a light brown hygroscopic powder. Crystalline or metallic silicon is obtained industrially by the reduction of silica with carbon in an electric arc furnace ... 

Silicon (3), which resembles metals in its chemical behavior, generally has a valence of +4. In a few compounds it exhibits a +2 valence, and in silicides it exists as a negative ion and largely violates the normal valency rules. Silicon, carbon, germanium, tin, and lead comprise the Group 14 (IVA) elements. Silicon and carbon form the carbide, SiC (see Carbides). Silicon and germanium are isomorphous and thus mutually soluble in all proportions. Neither tin nor lead reacts with silicon. Molten silicon is immiscible in both molten tin and molten lead. 

Similar results are obtained for dre deposition of the carbides of these metals using methane as a source of carbon, atrd silicon tetrahalides for the preparation of silicides. These reactions are more complex than dre preparation of the diborides because of the number of carbides atrd silicides that the tratrsition metals form, some of which have wide ranges of non-stoichiometry. The control of the ratio of the partial pressures of dre ingoing gases is therefore important as a process variable. 

Among metal borides of the formula MjM B or (Mj, M/r)2B, the competing structural units are (a) the antiprism and (b) the trigonal metal prism. In many cases the CUAI2 structure with BMg-antiprismatic B coordination is adopted in close resemblance to transition-metal silicides, but no boron-carbon substitution is ob-served - " . 

Silicon, like carbon, is relatively inactive at ordinary temperatures. But, when heated, it reacts vigorously with the halogens (fluorine, chlorine, bromine, cmd iodine) to form halides and with certain metals to form silicides. It is unaffected by all acids except hydrofluoric. At red heat, silicon is attacked by water vapor or by oxygen, forming a surface layer of silicon dioxide. When silicon and carbon are combined at electric furnace temperatures of 2,000 to 2,600 °C (3,600 to 4700 °F), they form silicon carbide (Carborundum = SiC), which is an Importeint abrasive. When reacted with hydrogen, silicon forms a series of hydrides, the silanes. Silicon also forms a series of organic silicon compounds called silicones, when reacted with various organic compounds. 

Field emission displays are VFDs that use field emission cathodes as the electron source. The cathodes can be molybdenum microtips,33-35 carbon films,36,37 carbon nanotubes,38" 16 diamond tips,47 or other nanoscale-emitting materials.48 Niobium silicide applied as a protective layer on silicon tip field emission arrays has been claimed to improve the emission efficiency and stability.49 ZnO Zn is used in monochrome field emission device (FED) displays but its disadvantage is that it saturates at over 200 V.29... 

Berzelius heated a mixture of silica, iron, and carbon to a very high temperature, and obtained iron silicide. When he decomposed this with hydrochloric acid, silica was precipitated, and the amount of hydrogen evolved was in excess of the iron, indicating that some other metal must have been present (9). Berzelius finally showed in 1824 that this other seemingly metallic substance was derived from the silica, and succeeded in preparing the amorphous form of it by two methods. In the first of... 

Accdg to Molina (Ref 1, p 358), the following Piombite was used during WW1 as a bursting charge in cast-iron shells of medium caliber Pb nitrate 75, Ca silicide 16, Pb carbonate (basic)... 

By far the most common industrial refractories are those composed of single or mixed oxides of Al, Ca, Cr, Mg, Si, and Zr (see Tables 1, 4, and 6). These oxides exhibit relatively high degrees of stability under both reducing and oxidizing conditions. Carbon, graphite, and silicon carbide have been used both alone and in combination with the oxides. Refractories made from these materials are used in ton-lot quantities, whereas silicides are used in relatively small quantities for specialty application in the nuclear, electronic, and aerospace industries. 

LSt has been used extensively abroad as igniting charge for LA and to some extent in the US as an ingredient of priming compositions (Ref 24, p 7-12). On p 7-18 of Ref 18, it is stated that LSt has been used in electric primers and the following compn is used for that purpose LSt 39.5, Ba nitrate 44.4, Ca silicide 14.1, carbon black 1.0 gum arabic 1.0%... 

Silicon carbide is comparatively stable. The only violent reaction occurs when SiC is heated with a mixture of potassium dichromate and lead chromate. Chemical reactions do, however, take place between silicon carbide and a variety of compounds at relatively high temperatures. Sodium silicate attacks SiC above 1300°C, and SiC reacts with calcium and magnesium oxides above 1000°C and with copper oxide at 800°C to form the metal silicide. Silicon carbide decomposes in fused alkalies such as potassium chromate or sodium chromate and in fused borax or cryolite, and reacts with carbon dioxide, hydrogen, air, and steam. Silicon carbide, resistant to chlorine below 700°C, reacts to form carbon and silicon tetrachloride at high temperature. SiC dissociates in molten iron and the silicon reacts with oxides present in the melt, a reaction of use in the metallurgy of iron and steel (qv). The dense, self-bonded type of SiC has good resistance to aluminum up to about 800°C, to bismuth and zinc at 600°C, and to tin up to 400°C a new silicon nitride-bonded type exhibits improved resistance to cryolite. 

Vanadium Subsilicide, V2Si, is obtained by fusing a mixture of vanadium trioxide, V2Os, and silicon, with the addition of either a large excess of vanadium or carbon or copper. The carbide or copper alloy produced is decomposed at the temperature employed.11 The silicide forms metallic prisms, of density 5-48 at 17° C., the m.pt. of which is higher than in the ease of the disilicide. It is attacked by the halogens, hydrogen chloride gas, and fused sodium or copper, but hydrochloric acid, nitric acid and sulphuric acid are without action. 

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