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Zirconium oxide melting point

The silvery, shiny, ductile metal is passivated with an oxide layer. Chemically very similar to and always found with zirconium (like chemical twins, with almost identical ionic radii) the two are difficult to separate. Used in control rods in nuclear reactors (e.g. in nuclear submarines), as it absorbs electrons more effectively than any other element. Also used in special lamps and flash devices. Alloys with niobium and tantalum are used in the construction of chemical plants. Hafnium dioxide is a better insulator than Si02. Hafnium carbide (HfC) has the highest melting point of all solid substances (3890 °C record ). [Pg.149]

One early change was the substitution of cerium oxide by mixed oxides based on the latter. Most interesting for this are solid solutions of cerium and zirconium dioxides (with typically Zr cation fractions between 0.3 and 0.5), which have two main advantages firstly, they are more refractory than pure ceria (have higher melting point) and consequently lose surface... [Pg.289]

Zirconium (Zr, CAS 7440-67-7, atomic number 40, atomic mass 91.22) has a melting point of 1852 °C and a boiling point of 4377 °C. It is a hard, lustrous, silvery metal, in contrast to fine zirconium powder, which is black. Zirconium belongs to Subgroup IV of the Periodic Table of the elements, between the elements titanium and hafnium - two metals with which it is often found in nature. Zirconium has oxidation states ranging from II to IV, of which the tetravalent is relatively stable and abundant (Venugopal and Luckey 1979). Zirconium is very corrosion-resistant and is unaffected by alkalis or acids (except for HF). [Pg.1241]

Reduction processes in which a finely powdered pigment-likc oxide is reduced at a temperature below its own melting point and that of the resultii metal furnish the so-called subsieve powders of which titanium, zirconium, amorphous boron, and hydrogen-reduced iron are the most important representatives. [Pg.258]

Ceramic borides, carbides and nitrides are characterized by high melting points, chemical inertness and relatively good oxidation resistance in extreme environments, such as conditions experienced during reentry. This family of ceramic materials has come to be known as Ultra High Temperature Ceramics (UHTCs). Some of the earliest work on UHTCs was conducted by the Air Force in the 1960 s and 1970 s. Since then, work has continued sporadically and has primarily been funded by NASA, the Navy and the Air Force. This article summarizes some of the early works, with a focus on hafnium diboride and zirconium diboride-based compositions. These works focused on identifying additives, such as SiC, to improve mechanical or thermal properties, and/or to improve oxidation resistance in extreme environments at temperatures greater than 2000°C. [Pg.197]

To form a ceramic object with a complex three-dimensional shape, the finely divided ceramic powder, possibly mixed with other powders, is compacted under pressure and then sintered at high temperature. The temperatures required are about 1650°C for alumina, 1700 C for zirconium oxide, and 2050°C for silicon carbide. During sintering the ceramic particles coalesce without actually melting (compare the sintering temperatures with the melting points listed in Table 12.4). [Pg.469]

Rouanet, A. (1971) Zirconium dioxide-lanthanide oxide systems dose to the melting point. Rev. Int. Hautes Temp. Refract., 8 (2), 161-180. [Pg.250]

The other extreme for oxidizers will be those materials with highly endothermic heats of decomposition and high melting points, such as iron (III) oxide, Fe203. Such materials will require a highly exothermic fuel (such as magnesium, aluminum, or zirconium) in order for a reaction to occur. [Pg.75]


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See also in sourсe #XX -- [ Pg.2 , Pg.137 ]




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