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Hydrogenation is a chemical reaction between molecular hydrogen (H 2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum. The process is commonly employed to reduce or saturate organic compounds. Hydrogenation typically constitutes the addition of pairs of hydrogen atoms to a molecule ...
Hydrogenation of ethene on a catalytic solid surface (1) Adsorption (2) Reaction (3) Desorption. Heterogeneous catalysis is catalysis where the phase of catalysts differs from that of the reagents or products. [1] The process contrasts with homogeneous catalysis where the reagents, products and catalyst exist in the same phase.
Catalytic hydrogenation using platinum(IV) oxide (PtO 2) [23] or Raney nickel [24] Iron metal in refluxing acetic acid [25] Samarium diiodide [26] Raney nickel, platinum on carbon, or zinc dust and formic acid or ammonium formate [6] α,β-Unsaturated nitro compounds can be reduced to saturated amines by: Catalytic hydrogenation over palladium ...
Sulfur removal requires catalytic hydrogenation to convert sulfur compounds in the feedstocks to gaseous hydrogen sulfide (hydrodesulfurization, hydrotreating): + + Hydrogen sulfide is adsorbed and removed by passing it through beds of zinc oxide where it is converted to solid zinc sulfide:
Adams' catalyst, also known as platinum dioxide, is usually represented as platinum(IV) oxide hydrate, PtO 2 •H 2 O. It is a catalyst for hydrogenation and hydrogenolysis in organic synthesis. [1]
The inhibitor can produce this effect by, e.g., selectively poisoning only certain types of active sites. Another mechanism is the modification of surface geometry. For instance, in hydrogenation operations, large planes of metal surface function as sites of hydrogenolysis catalysis while sites catalyzing hydrogenation of unsaturates are ...
The catalytic hydrogenation of nitriles is often the most economical route available for the production of primary amines. [3] Catalysts for the reaction often include group 10 metals such as Raney nickel, [4] [5] [6] palladium black, or platinum dioxide. [1]
The hydrogenation of alkynes is troublesome to control since alkynes tend to be reduced to alkanes, via intermediacy of the cis-alkene. [14] Ethylene reacts with Wilkinson's catalyst to give RhCl(C 2 H 4 )(PPh 3 ) 2 , but it is not a substrate for hydrogenation.