Co/Ni/Mg/Al layered double hydroxides as precursors of catalysts for the hydrogenation of nitriles: Hydrogenation of acetonitrile

Layered double hydroxides (LDHs) with a hydrotalcite-like structure and con taining Ni2+/Co2+/Mg2+/Al3+ cations in different amounts were prepared and activated in various conditions. Depending on the chemical composition and the calcination temperature, mixed-oxide and spinel-like phases of complex compositions are obtained. They lead to well-dispersed bimetallic phases of high metal loadings upon reduction. Temperature-programmed reduction by Hz showed that the introduction of Mg decreases the reducibility of metals an d that most of the Ni and Co are together in bimetallic aggregates. These c atalysts were tested in the gasphase hydrogenation of acetonitrile between 350 and 450 K and with a H-2/CH3CN molar ratio of ca. 33. The main product is ethylamine (MEA); secondary products are N-ethyl,ethylimine at low conve rsion, diethylamine and triethylamine at high conversion. The Ni-free catal yst is three orders of magnitude less active than the Ni-containing samples . The by-products are formed by condensation between "imine-" and "amine-li ke" adsorbed species on metal and acid sites (bifunctional mechanism) and o n the metal sites alone as well. The tuned addition of Mg (Mg/(Mg + Ni + Co ) approximate to 0.25) lowers the surface acidity and the bifunctionalized formation of by-products consequently. A net increase in MEA selectivity is further reached thanks to the formation of bimetallic NiCo phases. It is p roposed that by-product formation on the metal surface occurs by condensati on at Ni-0 sites between multibonded adsorbed species, which could be of th e acimidoyl and aminomethylcarbene types. The first role of Co is the dilut ion of the Ni surface in small ensembles less prone to accomodate neighbori ng multibonded species. The IR spectroscopy of adsorbed CO provided evidenc es of the dilution of Ni by Co in bimetallic NiCo particles, A catalyst obt ained from the CoMi/Mg/Al (0.27/0.26/0.22/0.25) LDH, calcined at 393 K and then reduced at 893 K, exhibits the highest selectivity to ethylamine, 98.2 % at 10% CH3CN conversion. (C) 2000 Academic Press.