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 1833.    ---------------.  [KOCH, H., AND RICHTER, H.]  [Isomerization of Butene.]  Oel u. Kohle, vol. 40, 1944, pp. 231-241; British Abs., 1948, B, II, p. 285; Chem. Abs., vol. 44, 1950, p. 5307.

        When a n-C4H8 is isomerized at 190° on a Fischer-Tropsch catalyst, a shifting of the ethylenic linking and cis-trans-conversion takes place, yielding an equilibrium mixture that accords with that calculated by Frost from free energies of the isomers.  At higher temperature and pressure, slight cracking occurs and a red polymer is formed as a byproduct.  Active C catalyzes the shift of the ethylenic linking at 325°, the main reaction being a redistribution of H2, with formation of C4H10 and higher unsaturated hydrocarbons.  Al2O3 catalyzes this shift at 190°, but at 400° iso-C4H8 is formed accompanied by cracking, which gives C3H6 and polymerization leading to C5H10 as main product.  In presence of H2 phosphates of Cd as catalyst formation of iso-C4H8 occurs at a lower temperature and is accompanied by polymerization; at a higher temperature polymerization is reduced, but the catalyst soon loses its activity.  If in the Fischer-Tropsch synthesis, C4H8-isomers are added to the reactant gases, besides hydrogenation, shift of the ethylenic linking occurs, by which the composition of the residual C4H8 approaches the equilibrium for n-C4H8; C5 hydrocarbons are not produced from C4H8 in this reaction.