Crystal carbides

WC-TiC-TaC(NbC) mixed crystal carbides (solid solutions). The raw materials are the same as for WC-TiC grades, with addition of Ta20s. Any furnace equipment capable of producing a good quality of WC-TiC is suitable. Total reduction and complete diffusion can only be reached by high temperature, good vacuum, and long exposure time. Carburization temperatures are about the same as for WC-TiC. 

Monolayer graphite can be formed on the flat surfaces by heating the single-crystal carbide disks in an ethylene atmosphere. It has been found that the (111) surface is much more reactive than the (001) surface. The forming conditions on carbide surfaces (40-46) are summarized in Table 2. In the case of the TiC( 111) surface, minimal ethylene exposure is 100-200 L at 1100°C. It is very difficult to form MLG on a TiC(OOl) surface, indicating that exposures over 1 million L using ethylene gas are needed (45). In the case of the NbC(lll) surface, minimal ethylene exposure is 100 L at 1000-1100°C, and more than about 25,000 L exposure at 1100-1250°C is needed to form graphite on an NbC(lOO) substrate. 

Shimada, S. (2001). Oxidation and Meehanism of Single Crystal Carbides with Formation of Carbon. Journal of the Ceramic Society of Japan, 109, S33-S42. doi 10.2109/jeersj. 109.1267 S33. 

Figure C2.17.6. Transmission electron micrograph and its Fourier transfonn for a TiC nanocrystal. High-resolution images of nanocrystals can be used to identify crystal stmctures. In tliis case, tire image of a nanocrystal of titanium carbide (right) was Fourier transfonned to produce tire pattern on tire left. From an analysis of tire spot geometry and spacing, one can detennine that tire nanocrystal is oriented witli its 11001 zone axis parallel to tire viewing direction [217].

Figure C2.17.7. Selected area electron diffraction pattern from TiC nanocrystals. Electron diffraction from fields of nanocrystals is used to detennine tire crystal stmcture of an ensemble of nanocrystals [119]. In tliis case, tliis infonnation was used to evaluate the phase of titanium carbide nanocrystals [217].

The salt-like carbides. Among these are aluminium tricarbide imethanide) AI4C3 (containing essentially C ions) in the crystal lattice and the rather more common dicarbides containing the C ion, for example calcium dicarbide CaCjt these carbides are hydrolysed by water yielding methane and ethyne respectively ... 

Many of the binary compounds of the lanthanides, such as oxides, nitrides, and carbides, can exist as non stoichiometric compounds. These form crystals where some of the anions ate missing from the sites the anions normally occupy. 

Lithium Acetylide. Lithium acetyhde—ethylenediamine complex [50475-76-8], LiCM7H -112X01120112X112, is obtained as colodess-to-light-tan, free-flowing crystals from the reaction of /V-lithoethylenediamine and acetylene in an appropriate solvent (131). The complex decomposes slowly above 40°O to lithium carbide and ethylenediamine. Lithium acetyhde—ethylenediamine is very soluble in primary amines, ethylenediamine, and dimethyl sulfoxide. It is slightly soluble in ether, THF, and secondary and tertiary amines, and is insoluble in hydrocarbons. 

Because the time at high temperature is much less, austenite is produced, which is chemically inhomogeneous especially with undissolved carbides, and has a fine grain crystal size. The formation of the hard martensite requites more rapid cooling than for conventional hardening. Thus case hardening by heat treatment intrinsically requites that the surface region to be hardened be relatively thin and cooled rapidly. 

HTS catalyst consists mainly of magnetite crystals stabilized using chromium oxide. Phosphoms, arsenic, and sulfur are poisons to the catalyst. Low reformer steam to carbon ratios give rise to conditions favoring the formation of iron carbides which catalyze the synthesis of hydrocarbons by the Fisher-Tropsch reaction. Modified iron and iron-free HTS catalysts have been developed to avoid these problems (49,50) and allow operation at steam to carbon ratios as low as 2.7. Kinetic and equiUbrium data for the water gas shift reaction are available in reference 51. 

A wide range of cutting-tool materials is available. Properties, performance capabilities, and cost vary widely (2,7). Various steels (see Steel) cast cobalt alloys (see Cobalt and cobalt alloys) cemented, cast, and coated carbides (qv) ceramics (qv), sintered polycrystalline cubic boron nitride (cBN) (see Boron compounds) and sintered polycrystalline diamond tbin diamond coatings on cemented carbides and ceramics and single-crystal natural diamond (see Carbon) are all used as tool materials. Most tool materials used in the 1990s were developed during the twentieth century. The tool materials of the 1990s... 

The crystal stmcture of beryUium carbide is cubic, density = 2.44 g/mL. The melting point is 2250—2400°C and the compound dissociates under vacuum at 2100°C (1). This compound is not used industhaUy, but Be2C is a potential first-waU material for fusion reactors, one on the very limited Ust of possible candidates (see Fusion energy). 

The crystal stmeture and stoichiometry of these materials is determined from two contributions, geometric and electronic. The geometric factor is an empirical one (8) simple interstitial carbides, nitrides, borides, and hydrides are formed for small ratios of nonmetal to metal radii, eg, < 0.59. 

---