Graphite borides

Metal-Matrix Composites. A metal-matrix composite (MMC) is comprised of a metal ahoy, less than 50% by volume that is reinforced by one or more constituents with a significantly higher elastic modulus. Reinforcement materials include carbides, oxides, graphite, borides, intermetahics or even polymeric products. These materials can be used in the form of whiskers, continuous or discontinuous fibers, or particles. Matrices can be made from metal ahoys of Mg, Al, Ti, Cu, Ni or Fe. In addition, intermetahic compounds such as titanium and nickel aluminides, Ti Al and Ni Al, respectively, are also used as a matrix material (58,59). P/M MMC can be formed by a variety of full-density hot consolidation processes, including hot pressing, hot isostatic pressing, extmsion, or forging. 

AIB2-Type Analogous Tiling Compounds. A series of layered graphitic boride compounds (AlB2-fype analogous... 

Boron forms B—N compounds that are isoelectronic with graphite (see Boron compounds, refractoryboron compounds). The small size also has a significant role in the interstitial alloy-type metal borides boron forms. Boron forms borides with metals that are less electronegative than itself including titanium, zirconium, and hafnium. 

In this method " - the melt eontains boric oxide and the metal oxide in a suitable electrolyte, usually an alkali or alkaline-earth halide or fluoroborate. The cell is operated at 700-1000 C depending on electrolyte composition. To limit corrosion, the container serving as cathode is made of mild steel or of the metal whose boride is sought. The anode is graphite or Fe. Numerous borides are prepared in this way, e.g., alkaline-earth and rare-earth hexaborides " and transition-metal borides, e.g, TiBj NijB, NiB and TaB... 

Application of carbo-thermal reduction. This is a synthesis process for the preparation of powders of carbides, nitrides and borides. Carbon may be graphite, coke, pyrolysed organic polymers. A reference process may be the Acheson process for the production of SiC ... 

Hydrogenation using Raney nickel is carried out under mild conditions and gives cis alkenes from internal alkynes in yields ranging from 50 to 100% [356, 357, 358, 359, 360]. Half hydrogenation of alkynes was also achieved over nickel prepared by reduction of nickel acetate with sodium borohydride (P-2 nickel, nickel boride) [349,361,362] or by reduction with sodium hydride [49], or by reduction of nickel bromide with potassium-graphite [363]. Other catalysts are palladium on charcoal [364], on barium sulfate [365, 366], on... 

The process of forming boron-boron bonds is carried on further in aluminum boride, AIB, which has a very simple hexagonal structure, consisting of hexagonal layers of boron a,toms, like the layers of carbon atoms in graphite, with aluminum atoms in the spaces between the layers (Pig. 11-15). The B—B bond length is 1.73 A, corresponding to n = 0.66 that is, two valence electrons per boron atom are used in the B—B bonds, which are two-thirds bonds. 

Hoyt and Chorne [230] have recently reported the preparation of several self-bonded dense borides. EuBe (90%) was made by hot vacuum pressing in graphite dies at 1800—2000° C. Temperature, pressure and time are important variables. Unsuccessful attempts have been made to prepare EUB4. 

REDUCTION, REAGENTS Aluminum amalgam. Borane-Dimethyl sulfide. Borane-Tetrahydrofurane. t-Butylaminoborane. /-Butyl-9-borabicyclo[3.3.1]nonane. Cobalt boride— f-Butylamineborane. Diisobutylaluminum hydride. Diisopropylamine-Borane. Diphenylamine-Borane. Diphenyltin dihydride. NB-Enantrane. NB-Enantride. Erbium chloride. Hydrazine, lodotrimethylsilane. Lithium-Ammonia. Lithium aluminum hydride. Lithium borohydride. Lithium bronze. Lithium n-butylborohydride. Lithium 9,9-di-n-butyl-9-borabicyclo[3.3.11nonate. Lithium diisobutyl-f-butylaluminum hydride. Lithium tris[(3-ethyl-3pentylK>xy)aluminum hydride. Nickel-Graphite. Potassium tri-sec-butylborohydride. Samarium(II) iodide. Sodium-Ammonia. Sodium bis(2-mcthoxyethoxy)aluminum hydride. 

Aluminium carbide, 1027 Aluminium phosphide, 0083 Bismuth nitride, 0230 Caesium graphite, 2877 Calcium disilicide, 3938 Calcium phosphide, 3941 Calcium silicide, 3937 Copper diphosphide, 4278 Copper monophosphide, 4277 Copper(II) phosphide, 4284 Dialuminium octavanadium tridecasilicide, 0088 Dicobalt boride, 0128 Ditungsten carbide, 0561 Ferrosilicon, 4384 Hexalithium disilicide, 4684 Iron carbide, 0364... 

As for hydrides, borides, and carbides, different types of nitrides are possible depending on the type of metallic element. The classifications of nitrides are similarly referred to as ionic (salt-like), covalent, and interstitial. However, it should be noted that there is a transition of bond types. Within the covalent classification, nitrides are known that have a diamond or graphite structure. Principally, these are the boron nitrides that were discussed in Chapter 8. 

Besides Urushibara Ni and Ni boride catalysts, various finely divided nickel particles have been prepared by reaction of nickel salts with other reducing agents, such as sodium phosphinate 20,85 alkali metal/liquid NH3 21 NaH-f-AmOH (designated Nic) 22,86Na, Mg, and Zn in THF or Mg in EtOH 24 or C8K(potassium graphite)/THF-HMPTA (designated Ni-Grl) 23,87 Some of these have been reported to compare with Raney Ni or Ni borides in their activity and/or selectivity. 

---