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Titanium sesquioxide

Titanium sesquioxide [1344-54-3], chemical formula TijO, exists within a rather narrow [Pg.617]


Alternative methods of production include reduction of HO2 with magnesium, which yields TiO only. When titanium monoxide is heated in air at 150—200°C, titanium sesquioxide, Ti202, forms, and at 250—350°C, it changes to Ti O. ... [Pg.119]

Titanium Sesc uioxide. Ti202 has the comndum stmcture. At room temperature it behaves as a semiconductor having a small (0.2 eV) band gap. At higher temperatures, however, it becomes metallic. This is associated with marked change in the mean Ti—Ti distance. As with TiO, titanium sesquioxide, Ti202, may be made by heating a stoichiometric mixture of titanium metal and titanium dioxide powders at 1600°C under vacuum in an aluminum or molybdenum capsule. [Pg.119]

Titanium pyrophosphate, 25 57 Titanium sesquioxide, 25 14 Titanium sesquisulfide, 25 58 Titanium silicates, 25 56, 102 Titanium silicides, 25 55—56 Titanium—silicon alloy, 22 520 Titanium silicon compounds, 25 55—56 Titanium slag, 19 388, 389 Titanium sponge... [Pg.955]

B. C. Dutt and S. N. Sen found that when nitric oxide is passed into a suspension of barium dioxide in water, barium nitrite, not nitrate, is formed. P. Sabatier and J. B. Senderens observed no change when nitric oxide is passed over Cuprous Oxide at 500°. H. A. Auden and G. J. Fowler observed that dry nitric oxide and Silver oxide, at ordinary temp., form silver and silver nitrate P. Sabatier and J. B. Senderens also obtained silver and silver nitrite by passing nitric oxide into water with silver oxide in suspension. C. F. Schonbein found gold oxide is reduced by moist nitric oxide, forming nitrous acid. P. Sabatier and J. B. Senderens found that titanium sesquioxide forms white titanic oxide when heated in an atm. of nitric oxide and that stannous oxide below 500° burns in an atm. of nitric oxide, forming stannic oxide. If nitric oxide be passed into water with lead dioxide in suspension, the water is coloured, and in about 3 hrs., lead nitrite and nitrate are formed, and later, rhombic crystals of a basic nitrite. B. C. Dutt and S. N. Sen said that the nitrate is formed by the action of the dioxide on the nitrite. Lead dioxide is reduced to lead oxide by nitric oxide at 315°, and H. A. Auden and G. J. Fowler found that the reaction begins at 15°, when a basic lead nitrite is... [Pg.437]

The so-called sesquioxide (PuOi 5 i.75) is a typical mixed oxidation state oxide, similar to those formed by uranium, praseodymium, terbium, titanium, and many other metals. Its composition shows continuous variation with changes in temperature and pressure of oxygen above the oxide. [Pg.1320]

A2Pt207, similar to those reported for tin, ruthenium, titanium, and several other tetravalent ions. Trivalent ions which form cubic platinum pyrochlores range from Sc(III) at 0.87 A to Pr(III) at X.14 A. Distorted pyrochlore structures are formed by lanthanum (1.18 A) and by bismuth (1.11 A). Platinum dioxide oxidizes Sb203 to Sb2(>4 at high pressure. The infrared spectra and thermal stability of the rare earth platinates have been reported previously and will not be repeated here, except to point out the rather remarkable thermal stability of these compounds decomposition to the rare earth sesquioxide and platinum requires temperatures in excess of 1200 °C. [Pg.48]

The most common process for producing large quantities of titanium diboride is by reacting titania (TiO ) with carbon and boron carbide (B C) or boron sesquioxide (B Oj) as follows ... [Pg.639]


See other pages where Titanium sesquioxide is mentioned: [Pg.998]    [Pg.118]    [Pg.2021]    [Pg.1967]    [Pg.2187]    [Pg.2003]    [Pg.617]    [Pg.1844]    [Pg.2142]    [Pg.2137]    [Pg.266]    [Pg.2216]    [Pg.1964]    [Pg.998]    [Pg.118]    [Pg.2021]    [Pg.1967]    [Pg.2187]    [Pg.2003]    [Pg.617]    [Pg.1844]    [Pg.2142]    [Pg.2137]    [Pg.266]    [Pg.2216]    [Pg.1964]    [Pg.141]    [Pg.155]    [Pg.198]    [Pg.152]    [Pg.222]    [Pg.297]    [Pg.79]    [Pg.125]    [Pg.2028]    [Pg.165]    [Pg.433]    [Pg.434]    [Pg.601]    [Pg.54]    [Pg.58]    [Pg.628]   


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