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Silicon (Latin: silicium) is the chemical element in the periodic table that has the symbol Si and atomic number 14. A tetravalent metalloid, silicon is less reactive than its chemical analog carbon. It is the second most abundant element in the Earth's crust, making up 25.7% of it by weight. It occurs in clay, feldspar, granite, quartz and sand, mainly in the form of silicon dioxide (also known as silica) and as silicates, (various compounds containing silicon, oxygen and one or another metal). Silicon is the principal component of most semiconductor devices and, in the form of siliica and silicates, in glass, cement, ceramics. It is also a component of silicones, a name for various plastic substances often confused with silicon itself. Silicon is widely used in semiconductors because it has a lower reverse leakage current than the semiconductor Germanium, and because its native oxide is easily grown in a furnace and forms a better semiconductor/dielectric interface than almost all other material combinations.
Notable characteristicsIn its crystalline form, silicon has a dark gray color and a metallic luster. Even though it is a relatively inert element, silicon still reacts with halogens and dilute alkalis, but most acids (except for a combination of nitric acid and hydrofluoric acid) do not affect it. Elemental silicon transmits more than 95% of all wavelengths of infrared light. Pure silicon has a negative temperature co-efficient of resistance, since the number of free charge carriers increases with temperature. The electrical resistance of single crystal silicon significantly changes under the application of mechanical stress due to the piezoresistive effect. ApplicationsSilicon is a very useful element that is vital to many human industries. Silicon and alloys
Silicon compounds
See also category:Silicon compounds HistorySilicon (Latin silex, silicis, meaning flint) was first identified by Antoine Lavoisier in 1787, and was later mistaken by Humphry Davy, in 1800, for a compound. In 1811 Gay-Lussac and Thénard probably prepared impure amorphous silicon through the heating of potassium with silicon tetrafluoride. In 1824 Berzelius prepared amorphous silicon using approximately the same method of Lussac. Berzelius also purified the product by repeatedly washing it. Because silicon is an important element in semiconductor and high-tech devices, the high-tech region of Silicon Valley, California, is named after this element. OccurrenceMeasured by weight, silicon makes up 25.7% of the Earth's crust and is the second most abundant element on Earth, after oxygen. Pure silicon crystals are rarely found in nature; natural silicon is usually found in the form of silicon dioxide (also known as silica) and silicate. Sand, amethyst, agate, quartz, rock crystal, flint, jasper, and opal are some of the forms in which silicon dioxide appears (they are known as "lithogenic", as opposed to "biogenic", silicas). Granite, asbestos, feldspar, clay, hornblende, and mica are a few of the many silicate minerals. Pure silicon crystals can be found as inclusions such as gold and volcanic exhalations. Silicon is a principal component of aerolites, which are a class of meteoroids, and also of tektites, which are a natural form of glass. See also category:Silicate minerals ProductionSilicon is commercially prepared by the reaction of high-purity silica with wood, charcoal, and coal, in an electric arc furnace using carbon electrodes. At temperatures over 1900 °C, the carbon reduces the silica to silicon according to the chemical equation
Liquid silicon collects in the bottom of the furnace, and is then drained and cooled. The silicon produced via this process is called metallurgical grade silicon and is at least 99% pure. Using this method, silicon carbide, SiC, can form. However, provided the amount of SiO2 is kept high, silicon carbide may be eliminated, as explained by this equation:
In 2000, metallurgical grade silicon cost about $ 0.56 per pound ($1.23/kg).[1]. PurificationThe use of silicon in semiconductor devices demands a much greater purity than afforded by metallurgical grade silicon. Historically, a number of methods have been used to produce high-purity silicon. Physical methodsSilicon wafer with mirror finish (NASA)Early silicon purification techniques were based on the fact that if silicon is melted and re-solidified, the last parts of the mass to solidify contain most of the impurities. The earliest method of silicon purification, first described in 1919 and used on a limited basis to make radar components during World War II, involved crushing metallurgical grade silicon and then partially dissolving the silicon powder in an acid. When crushed, the silicon cracked so that the weaker impurity-rich regions were on the outside of the resulting grains of silicon. As a result, the impurity-rich silicon was the first to be dissolved when treated with acid, leaving behind a more pure product. In zone melting, also called zone refining, the first silicon purification method to be widely used industrially, rods of metallurgical grade silicon are heated to melt at one end. Then, the heater is slowly moved down the length of the rod, keeping a small length of the rod molten as the silicon cools and resolidifies behind it. Since most impurities tend to remain in the molten region rather than resolidify, when the process is complete, most of the impurities in the rod will have been moved into the end that was the last to be melted. This end is then cut off and discarded, and the process repeated if a still higher purity was desired. Chemical methodsToday, silicon is instead purified by converting it to a silicon compound that can be more easily purified than silicon itself, and then converting that silicon element back into pure silicon. Trichlorosilane is the silicon compound most commonly used as the intermediate, although silicon tetrachloride and silane are also used. When these gases are blown over silicon at high temperature, they decompose to high-purity silicon. Silicon in many purified forms.In the Siemens process, high-purity silicon rods are exposed to trichlorosilane at 1150 °C. The trichlorosilane gas decomposes and deposits additional silicon onto the rods, enlarging them according to chemical reactions like
Silicon produced from this and similar processes is called polycrystalline silicon. Polycrystalline silicon typically has impurity levels of 1 part per billion or less. At one time, DuPont produced ultrapure silicon by reacting silicon tetrachloride with high-purity zinc vapors at 950 °C, producing silicon according to the chemical equation
However, this technique was plagued with practical problems (such as the zinc chloride byproduct solidifying and clogging lines) and was eventually abandoned in favor of the Siemens process. CrystallizationAnother sample of silicon.The majority of silicon crystals grown for device production are produced by the Czochralski process, since it is the cheapest method available. However, silicon single-crystals grown by the Czochralski method contain impurities since the crucible which contains the melt dissolves. For certain electronic devices, particularly those required for high power applications, silicon grown by the Czochralski method is not pure enough. For these applications, float-zone silicon (FZ-Si) can be used instead. Different forms of silicon
One can notice the color change in silicon nanopowder. This is caused by the quantum effects which occur in particles of nanometric dimensions. See Quantum_confinement, Quantum dot, Nanoparticle Isotopes
Silicon has numerous known isotopes, with mass numbers ranging from 22 to 44. 28Si (the most abundant isotope, at 92.23%), 29Si (4.67%), and 30Si (3.1%) are stable; 32Si is a radioactive isotope produced by argon decay. Its half-life, has been determined to be approximately 132 years, and it decays by beta emission to 32P (which has a 14.28 day half-life [2]) and then to 32S. PrecautionsA serious lung disease known as silicosis often occurred in miners, stonecutters, and others who were engaged in work where siliceous dust was inhaled in great quantities. Silicon is not siliconeCasual speakers often make the mistake of interchanging the words silicon and silicone; they are not the same. The first, of course, is the element. The second is a class of chemical compounds (in particular, inorganic polymers) that contain the element silicon, the most notable members of the class being silicone rubbers and silicone gels. Silicon-based lifeSince silicon is analogous to carbon, particularly in its valency, some scientists have proposed the possibility of silicon-based life. This concept is especially popular in science fiction. Although there are no known forms of life that rely entirely on silicon-based chemistry, there are some that rely on silicon minerals for specific functions. Some bacteria and other forms of life, such as the protozoa radiolaria, have silicon dioxide skeletons, and the sea hedgehog has its sharps made of silicon dioxide. These forms of silicon dioxide are known as biogenic silica. Silicate bacteria use silicates in their metabolism. Life as we know it could not have developed based on a silicon biochemistry. The main reason for this fact is that life on Earth depends on the carbon cycle: autotrophic entities use carbon dioxide to synthesize organic compounds with carbon, which is then used as food by heterotrophic entities, which produce energy and carbon dioxide from these compounds. If carbon was to be replaced with silicon, there would be a need for a silicon cycle. However, silicon dioxide precipitate in aquous systems, and cannot be transported among living beings through regular ways. CompoundsFor examples of silicon compounds see silicate, silane (SiH4), silicic acid (H4SiO4), silicon carbide (SiC), silicon dioxide (SiO2), silicon tetrachloride (SiCl4), silicon tetrafluoride (SiF4), and trichlorosilane (HSiCl3). See also category:Silicon compounds References
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