Boron nitrides high temperature

Preparation. Hexagonal boron nitride can be prepared by heating boric oxide with ammonia, or by heating boric oxide, boric acid, or its salts with ammonium chloride, alkaU cyanides, or calcium cyanamide at atmospheric pressure. Elemental nitrogen does not react with boric oxide even in the presence of carbon, though it does react with elemental boron at high temperatures. Boron nitride obtained from the reaction of boron trichloride or boron trifluoride with ammonia is easily purified. 

Yoo C S, Akella J, Nicol M and Cynn H 1997 Direct elementary synthesis of hexagonal and cubic boron nitrides at high pressures and temperatures Phys. Rev. B 56 140... 

Only thallium of the Group III elements is affected by air at room temperature and thalliumflll) oxide is slowly formed. All the elements, however, burn in air when strongly heated and, with the exception of gallium, form the oxide M2O3 gallium forms a mixed oxide of composition GaO. In addition to oxide formation, boron and aluminium react at high temperature with the nitrogen in the air to form nitrides (BN and AIN). 

By subjecting boron nitride (a white powder) to high pressure and temperature small crystals of a substance harder than diamond, known as borazon, are obtained. This pressure-temperature treatment changes the structure from the original graphite-like layer structure (p. 163) to a diamond-like structure this hard form can withstand temperatures up to 2000 K. 

Sihcon nitride has good strength retention at high temperature and is the most oxidation resistant nitride. Boron nitride [10043-11 -5] has excellent thermal shock resistance and is in many ways similar to graphite, except that it is not an electrical conductor. 

Ceramics (qv) such as those in Table 12 find high temperature use to over 800°C (32). Advanced ceramics finding interest include alumina, partially stabilized zitconia, siUcon nitride, boron nitride, siUcon carbide, boron carbide, titanium diboride, titanium carbide, and sialon (Si—Al—O—N) (33) (see... 

The cubic 2inc blende form of boron nitride is usually prepared from the hexagonal or rhombohedral form at high (4—6 GPa (40—60 kbar)) pressures and temperatures (1400—1700°C). The reaction is accelerated by lithium or alkaline-earth nitrides or amides, which are the best catalysts, and form intermediate Hquid compounds with BN, which are molten under synthesis conditions (11,16). Many other substances can aid the transformation. At higher pressures (6—13 GPa) the cubic or wurt2itic forms are obtained without catalysts (17). 

Uses. Hot-pressed hBN is useful for high temperature electric or thermal insulation, vessels, etc, especially in inert or reducing atmospheres, and for special materials such as IITV semiconductors (qv). Its low thermal expansion makes it resistant to thermal shock. The powder can be used as a mold release agent or as thermal insulation. Boron nitride is also available in fiber form (19). BN deposited pyrolyticaHy on refractory substrates at 1200—1800°C has a turbostratic stmcture and low porosity it has greater chemical resistance and is impervious to helium. 

Cubic boron nitride is obtained from hexagonal boron nitride at high pressure and temperature in the presence of lithium nitride as a catalyst. It is almost as hard as diamond and has superior chemical resistance and a much higher oxidation threshold.Efforts to... 

Ca3(BN2)2 is readily formed when (distilled) calcium metal is melted in the presence of (layer-type) boron nitride. This reaction provides some insight on how alkaline-earth metals like calcium may act as a catalyst in the phase transformation of layered a-BN into its cubic modification. Instead of metals, nowadays alkaline-earth (Ca, Sr, Ba) nitridoborates can be used as a flux catalyst in high-pressure and high-temperature transformation reactions to produce cubic boron nitride [15]. 

Under high pressure and temperature, boron nitride can be converted to a cubic form. The cubic form of (BN) is known as borazon, and it has a structure similar to that of diamond. Its hardness is similar to that of diamond, and it is stable to higher temperatures. The extreme hardness results from the fact that the B-N bonds possess not only the covalent strength comparable to C-C bonds, but also some ionic stabilization due to the difference in electronegativity between B and N. 

The c-BN phase was first obtained in 1957 [525] by exposing hexagonal boron nitride phase (h-BN) to high pressures and low temperatures. A pressure of more than 11 GPa is necessary to induce the hexagonal to cubic transformation, and these experimental conditions prevent any practical application for industrial purposes. Subsequently, it has been found that the transition pressure can be reduced to approximately 5 GPa at very high temperature (1300-1800°C) by using catalysts such as alkali metals, alkali metal nitrides, and Fe-Al or Ag-Cd alloys [526-528]. In addition, water, urea, and boric acid have been successfully used for synthesis of cubic boron nitride from hexagonal phase at 5-6 GPa and temperature above 800-1000°C [529]. It has been... 

Lithium Iron Sulfide (High Temperature). High-temperature molten salt Li—Al/LiCl— KCl/FeS - cells are known for their high energy density and superior safety. At one point they were being actively pursued for electric vehicle and pulse-power applications. Historically, boron nitride (BN) cloth or felt has been used as the separator in flooded-electrolyte cells, while MgO pressed-powder plaques have been used in starved-electrolyte cells. 

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. 

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