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atomic See also:weight 48.1 See also:TITANIUM [See also:symbol Ti (0 = 16)]
, a metallic chemical See also:element
.
Its See also:discovery as an element was due to See also:
The isolation of metallic titanium is very difficult since it readily combines with See also:nitrogen (thus resembling See also:boron and See also:magnesium) and See also:carbon
.
In 1822 See also:Wollaston examined a specimen of those beautiful See also:copper-like crystals which are occasionally met with in iron-See also:furnace slags, and declared them to be metallic titanium
.
This view had currency until 1849, when See also:Wohler showed that the crystals are a See also:compound, Ti(CN)2.3Ti3N2, of a See also:cyanide and a nitride of the metal
.
An impure titanium was made by Wohler and Sainte-Claire Deville in 1857 by See also:heating to redness fluotitanate of See also:potassium (see below) in the vapour of See also:sodium in an See also:atmosphere of dry See also:hydrogen, and extracting the alkaline fluoride formed by See also:water
.
The metal thus produced formed a dark See also:
The product has a brilliant See also: Rutile assumes tetragonal forms isomorphous with cassiterite, SnO2 (and also See also:zircon, ZrSiO4) ; anatase is also tetragonal, and brookite or thorhombic . Rutile is the most See also:stable and anatase the least, a See also:character reflected in the decrease in See also:density from rutile (4.2) and brookite (4.0) to anatase (3.9) . The minerals are generally found together—a feature rarely met with in the See also:case of polymorphs . They have been obtained artificially by Hautefeuille by the interaction of titanium fluoride and See also:steam . At a red See also:heat rutile is produced, at the boiling point of See also:zinc brookite, and of See also:cadmium anatase . It is apparent that these minerals all result in nature from pneumatolytic See also:action . Amorphous titanium oxide may be obtained in a pure See also:form by fusing the mineral, very finely powdered, with six times its See also:weight of potassium bisulphate in a See also:platinum crucible, then extracting the melt with cold water and boiling the filtered See also:solution for a See also:long time . Titanic oxide separates out as a white See also:hydrate, which, however, is generally contaminated with ferric hydrate and often with tin oxide . A better method is Wohler's, in which the finely powdered mineral is fused with twice its weight of potassium carbonate in a platinum crucible, the melt powdered and treated in a platinum See also:basin with aqueous hydrofluoric acid . The alkaline titanate first produced is converted into crystalline fluotitanate, K2TiF6, which is with difficulty soluble and is extracted with hot water and filtered off . The filtrate, which may be collected in See also:glass vessels if an excess of hydrofluoric acid has been avoided, deposits the greater See also:part of the See also:salt on cooling . The crystals are collected, washed, pressed and recrystallized, whereby the impurities are easily removed . The pure salt is dissolved in hot water and decomposed with ammonia to produce a slightly ammoniacal hydrated oxide; this, when ignited in platinum, leaves pure TiO2 in the form of brownish lumps, the specific gravity of which varies from 3:9 to 4.25, according to the temperature at which it was kept in igniting . The more intense the heat the denser the product . The oxide is fusible only in the oxy-hydrogen See also:flame . It is insoluble in all acids, except in hot concentrated sulphuric, when finely powdered . If the sulphuric acid solution be evaporated to dryness the See also:residue, after cooling, dissolves in cold water . The solution, if boiled, deposits its titanic oxide as a hydrate called See also:meta-titanic acid, TiO(OH)2, because it differs in its properties from orthotitanic acid, Ti(OH)4, obtained by decomposing a solution of the chloride in cold water with alkalis . The ortho-See also:body dissolves in cold dilute acids; the meta-body does not . If titanic oxide be fused with excess of alkaline carbonate a titanate, R2TiO3, is formed . This salt is decomposed by -water with the formation of a solution of See also:alkali See also:free of titanium, and a residue of an acid titanate, which is insoluble in water but soluble in cold aqueous mineral acids . The titanates are very similar to the silicates in their tendency to assume complex forms, e.g. the potassium salts are K2TiO2.4H2O, K2Ti3Oi.3H2O and K2Ti6O13•2H2O . Titanium monoxide, TiO, is obtained as See also:black prismatic crystals by heating the dioxide in the electric furnace, or with magnesium powder . Titanium sesquioxide, Ti2O3, is formed by heating the dioxide in hydrogen . A hydrated form is prepared when a solution of titanic acid in hydrochloric acid is digested with copper, or when the trichloride is precipitated with alkalis . Titanium trioxide, TiOa, is obtained as a yellow precipitate by dropping the chloride into See also:alcohol, adding hydrogen peroxide, and finally ammonium carbonate or potash . When shaken with potash and air it undergoes autoxidation, hydrogen peroxide being formed first, which converts the trioxide into the dioxide and possibly pertitanic acid; this acid may contain sexavalent titanium (see W . Manchot and See also:Richter, Ber., 1906, 39, pp . 320, 488, and also See also:Faber, Abst . Journ . Chem . |
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