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Silicon finely divided

Schematic diagram showing how placing a thin layer of highly dispersed carbon onto the surface of a metal filament leads to an induced dipolar field having positive and negative image charges. The positive side is always on the metal, which is much less electronegative than carbon. This positive charge makes it much more difficult to remove electrons from the metal surface. The higher the value of a work function, the more difficult it is to remove an electron. Effectively, the layer of carbon increases the work function of the filament metal. Very finely divided silicon dioxide can be used in place of carbon. Schematic diagram showing how placing a thin layer of highly dispersed carbon onto the surface of a metal filament leads to an induced dipolar field having positive and negative image charges. The positive side is always on the metal, which is much less electronegative than carbon. This positive charge makes it much more difficult to remove electrons from the metal surface. The higher the value of a work function, the more difficult it is to remove an electron. Effectively, the layer of carbon increases the work function of the filament metal. Very finely divided silicon dioxide can be used in place of carbon.
Hydrophobic silica defoamers work on a basis which may not be chemical at all. They are basically finely divided sohd sihca particles dispersed in a hydrocarbon or silicone oil which sei ves as a spreading vehicle. Kulkarni [Ind. Eng. Chem. Fundam., 16, 472 (1977)] theorizes that this mixture defoams by the penetration of the silica particle into the bubble and the rupture of the wall. Table 14-23 hsts major types of defoamers and typical applications. [Pg.1444]

Phosphoric Acid Fuel Cell This type of fuel cell was developed in response to the industiy s desire to expand the natural-gas market. The electrolyte is 93 to 98 percent phosphoric acid contained in a matrix of silicon carbide. The electrodes consist of finely divided platinum or platinum alloys supported on carbon black and bonded with PTFE latex. The latter provides enough hydrophobicity to the electrodes to prevent flooding of the structure by the electrolyte. The carbon support of the air elec trode is specially formulated for oxidation resistance at 473 K (392°F) in air and positive potentials. [Pg.2412]

The hydrocarbon can be in either the liquid or vapour phase and the silicon is finely divided. The inclusion of certain solid catalysts in the reactive mass may in some instances greatly facilitate the reaction. A mixture of powdered silicon and copper in the ratio 90 10 is used in the manufacture of alkyl chlorosilanes. [Pg.819]

Silicon Monoxide. SiO, mw 44.09, hard and abrasive, black to brn-black amorph or cubic crysts, mp > 1702°, bp 1880°, d 2.13-.20. Sol in coned aq alk and dil HF+HN03. Prepn is by subliming finely divided silicon at 1250° under high vacuum for 4 hrs. It is used as a coating for precision optical lenses... [Pg.453]

Ferrosilicon containing 30-75% of silicon is hazardous, particularly when finely divided, and must be kept in a moisture-tight drum. In contact with water, the impurities present (arsenide, carbide, phosphide) evolve extremely poisonous arsine, combustible acetylene and spontaneously flammable phosphine [1 2],... [Pg.1550]

Boron (finely divided forms) reacts violently with cone, acid and may attain incandescence. The vapour of phosphorus, heated in nitric acid in presence of air, may ignite. Boron phosphide ignites with the cone, acid [1], Silicon crystallised from its eutectic with aluminium reacts violently with cone, acid [2], arsenic may react violently with the fuming acid, and finely divided carbon similarly with cone, acid [3], Use of cone, acid to clean a stainless steel hose contaminated with phosphorus led to an explosion [4],... [Pg.1593]

In some cases the modulus and strength are so low that fillers are often added for stiffness. Carbon black, as a filler, is used extensively in car tyres, and it is thought that the surface bonding with the rubber occurs, thus providing stiffness. Finely divided silica, which has been surface treated with organometallic silicon and titanium compounds, is also used. [Pg.75]

Chlorine Ammonia, acetylene, alcohols, alkanes, benzene, butadiene, carbon disulfide, dibutyl phthalate, ethers, fluorine, glycerol, hydrocarbons, hydrogen, sodium carbide, finely divided metals, metal acetylides and carbides, nitrogen compounds, nonmetals, nonmetal hydrides, phosphorus compounds, polychlorobi-phenyl, silicones, steel, sulfides, synthetic rubber, turpentine... [Pg.1476]

The silt fraction is particles 0.20-0.002 mm in diameter. This fraction or separate is produced by the same physical breakdown as described earlier for the formation of sand. Silt is more finely divided silica, but the surfaces are basically the same as those of sand (i.e., silicon and oxygen), and oxygen lone pairs of electrons and hydroxyl groups control its chemistry. Because the particles are smaller, they have more surface area per unit mass. This results in the availability of a greater number of bonds for chemical reactions [1],... [Pg.64]

Source of Silica. Silica can migrate either from free silica present in the cracking catalyst or from the silica alumina matrix but not as readily from the zeolite. Figure 11 shows SEM-EDAX silicon scans of cerium/alumina steamed in the presence of these three sources of silica. Again, the bright dots represent silicon. Qualitatively the sample steamed with pure silica contains more silicon than the sample steamed with silica-alumina. The sample steamed with zeolite shows silicon at the surface of the cross-sectioned particle but little in the interior. The surface silicon comes from dusting of the particle with very finely divided zeolite. [Pg.130]

Reaction with amorphous silicon at 900°C, catalyzed by steam produces cadmium orthosilicate, Cd2Si04. The same product also is obtained by reaction with sdica. Finely divided oxide reacts with dimethyl sulfate forming cadmium sulfate. Cadmium oxide, upon rapid heating with oxides of many other metals, such as iron, molybdenum, tungsten, titanium, tantalum, niobium, antimony, and arsenic, forms mixed oxides. For example, rapid heating with ferric oxide at 750°C produces cadmium ferrite, CdFe204 ... [Pg.154]

In finely divided form, hafnium is pyrophoric, igniting in air spontaneously. However, bulk metal reacts slowly in oxygen or air above 400°C. The rate of oxidation increases with temperature. The product is hafnium dioxide, Hf02. It combines with nitrogen, carbon, boron, sulfur and silicon at very high temperatures to form hafnium nitride HfN, hafnium boride HfB, hafnium sulfide HfSi2, respectively. Nitride formation occurs at 900°C. [Pg.332]

Iron reacts with nonmetals forming their binary compounds. It combines readily with halogens. Reaction is vigorous with chlorine at moderate temperature. With oxygen, it readily forms iron oxides at moderate temperatures. In a finely divided state, the metal is pyrophoric. Iron combines partially with nitrogen only at elevated temperatures. It reacts with carbon, sulfur, phosphorus, arsenic, and silicon at elevated temperatures in the absence of air, forming their binary compounds. [Pg.414]

Because the forces of attraction prevail when molecules are brought into sufficiently dose proximity under normal conditions, release is best effected if both the strength of the interaction and the degree of contact are minimized. Aliphatic hydrocarbons and fluorocarbons achieve the former effect, finely divided solids the latter. Materials such as microcrystalline wax [64742 42-3] and hydrophobic silica [7631-86-9] combine both effects. Some authors refer to this combined effect as the ball bearing mechanism. A perfluoroalkylated fullerene nanosphere would perhaps be the ultimate example of this combined effect (17). These very general mechanistic remarks can be supplemented by publications on the mechanism of specific classes of release agents such as metallic stearates (18), fatty acids and fluorinated compounds (19), and silicone-coated rdease papers (20,21). The mechanism of release of certain problem adherents, eg, polyurethanes, has also been addressed (22,23). [Pg.101]

Zinc oxide (ZnO) is widely used as an active filler in rubber and as a weatherability improver in polyolefins and polyesters. Titanium dioxide (TiOj) is widely used as a white pigment and as a weatherability improver in many polymers. Ground barites (BaS04) yield x-ray-opaque plastics with controlled densities. The addition of finely divided calcined alumina or silicon carbide produces abrasive composites. Zirconia, zirconium silicate, and iron oxide, which have specific gravities greater than 4.5, are used to produce plastics with controlled high densities. [Pg.123]

G. S. Serullas treated potassium chlorate with an excess of hydrofluosilicic acid the clear liquid was decanted from the sparingly soluble potassium fluosilicate, the soln. evaporated below 30°, and filtered through glass powder J. J. Berzelius evaporated the acid liquid mixed with finely divided silica below 30° in air, or over cone, sulphuric acid and potassium hydroxide in vacuo. The excess of hydrofluoric acid was volatilized as silicon fluoride, and the clear liquid was then filtered from the excess of silica. R. Bottger treated sodium chlorate with oxalic acid whereby sparingly soluble sodium oxalate was formed J. L. Wheeler, and T. B. Munroe treated sodium chlorate with hydrofluosilicic acid and M. Brandau treated potassium chlorate with aluminium sulphate and sulphuric acid and precipitated the alum so formed with alcohol. Chloric acid is formed in many reactions with hypochlorous and chlorous acid for example, it is formed when an aq. soln. of chlorine or hypochlorous or chlorous acid decomposes in light. It is also formed when an aq. soln. of chlorine dioxide stands in darkness or in light. A mixture of alkali chlorate and chlorite is formed when an aq. soln. of an alkali hydroxide is treated with chlorine dioxide. [Pg.300]

Long-term exposure to finely divided asbestos from construction work poses a health problem. Some evidence for a negative correlation between silicon content of drinking water and heart disease/... [Pg.484]

When finely divided silica is treated with methanol and then pyrolyzed, it becomes activated toward chemisorption of various gases341-343. Recent careful spectroscopic studies by Radzig and coworkers344-347 and by Razskazovskii et aZ.348,349 establish beyond reasonable doubt that the principal reactive sites are divalent silicons, (=Si—0)2 Si , silylene centers 350, which participate in a rich chemistry. [Pg.2530]

Other linear polysilanes can also be used as ceramic precursors. Solid objects of silicon carbide are manufactured by Nippon Soda Co. from polysilastyrene and finely divided silicon carbide powder.133 These materials are blended, injection molded to the... [Pg.244]


See other pages where Silicon finely divided is mentioned: [Pg.927]    [Pg.7]    [Pg.59]    [Pg.945]    [Pg.285]    [Pg.56]    [Pg.131]    [Pg.1924]    [Pg.112]    [Pg.382]    [Pg.58]    [Pg.363]    [Pg.485]    [Pg.62]    [Pg.209]    [Pg.92]    [Pg.385]    [Pg.206]    [Pg.112]    [Pg.117]    [Pg.133]    [Pg.157]    [Pg.742]    [Pg.965]    [Pg.289]    [Pg.2012]    [Pg.2426]   
See also in sourсe #XX -- [ Pg.320 ]




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