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Catalysts nickel-copper boride

Adiponitrile undergoes the typical nitrile reactions, eg, hydrolysis to adipamide and adipic acid and alcoholysis to substituted amides and esters. The most important industrial reaction is the catalytic hydrogenation to hexamethylenediarnine. A variety of catalysts are used for this reduction including cobalt—nickel (46), cobalt manganese (47), cobalt boride (48), copper cobalt (49), and iron oxide (50), and Raney nickel (51). An extensive review on the hydrogenation of nitriles has been recendy pubUshed (10). [Pg.220]

Nickel, either as a Raney catalyst or in the form of nickel boride, is also effective in the reduction of the C=0 bond. An increase in the catalytic activity can be brought about by metal promoters (chromium and molybdenum). Copper chromite may also be used. [Pg.845]

Hydrogenation Copper chromite (Lazier catalyst). Copper chromium oxide (Adkins catalyst). Lindlar catalyst (see also Lithium ethoxyacetylide, Malealdehyde, Nickel boride). Nickel catalysts. Palladium catalysts. Palladium hydroxide on carbon. Perchloric acid (promoter). Platinum catalysts. Raney catalysts, Rhenium catalysts. Rhodium catalysts. Stannous chloride. Tributylborane. Trifluoroicetic acid, Tris (triphenylphosphine)chlororhodium. [Pg.658]

Although palladium occupies the dominant position in semi-hydrogenation catalysts, it is by no means the only metal suitable for formulation into a viable catalyst. Mention has already been made of the nickel boride alternatives, with or without copper promotion, for example. Other examples include the skeletal catalyst Raney nickel [69], alumina-supported nickel [70], and aluminum phosphate-supported nickel [71] (Eqs 21 and 22) ... [Pg.361]


See other pages where Catalysts nickel-copper boride is mentioned: [Pg.236]    [Pg.111]    [Pg.59]    [Pg.133]    [Pg.65]    [Pg.65]    [Pg.253]    [Pg.440]   
See also in sourсe #XX -- [ Pg.236 ]




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Borides

Copper catalyst

Copper nickel catalyst

Nickel boride

Nickel-copper boride

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