Abstract
Zeolitic materials incorporating mono- and bimetallic systems of nickel and cobalt were obtained from natural zeolite modified with Ni(2+) and Co(2+) chloride solutions through traditional ion exchange (IE) and impregnation (Imp) processes. Special attention was given to analyzing the cationic and anionic composition of the resulting materials. The catalytic potential was evaluated in the selective hydrogenation of citral, focused on the formation of unsaturated alcohols. The IE process replaced mainly Ca(2+) and Na(+) with Ni(2+) and Co(2+) cations in the zeolite phases (clinoptilolite and mordenite mix), while Imp resulted in higher metal content (2.0-2.7%) but retained significant amounts of chloride (1.9-3.8%), as confirmed by XRD and temperature-programmed reduction. The materials prepared by IE had negligible chloride content (0.02-0.07%), and their specific surface areas (138-146 m(2)/g) were greater than those of the materials obtained by Imp (54-67 m(2)/g). The bimetallic systems exhibited enhanced reducibility of the Co(2+) and Ni(2+) isolated cations, attributed to synergistic interactions that weakened the cation-framework binding. Catalytic activity tests showed that nickel species were primarily responsible for citronellal formation. Among all materials, the bimetallic CoNi(IE) catalyst, prepared by IE, was the only one to produce unsaturated alcohols, suggesting that synergistic Ni-Co interactions played a role in their formation.