The influence of solvent polarity on the dehydrogenation of isoborneol over a Cu/ZnO/Al2O3 catalyst

Abstract Several Cu/ZnO/Al 2 O 3 catalysts with high Cu and ZnO contents were used to study the influence of solvent polarity on the dehydrogenation and dehydration of isoborneol. The employment of a polar solvent enhanced the activity for the main dehydrogenation reaction, while the use of a non-polar solvent favored the dehydration side-reaction. Different techniques were employed to characterize the fresh, treated, and spent catalysts. X-ray powder diffraction (XRD) showed that the copper was in metallic form and zinc in oxide form, transmission electron microscope (TEM) showed differences in catalyst morphology that depended on the polarity of the solvent used, N 2 O titration gave the Cu active site density, and temperature-programmed desorption of NH 3 (NH 3 -TPD) provided the acidity of the materials. The characterization results indicated that in non-polar solvents the copper nanoparticles were sintered and this may have been due to the enhanced activity of adventitious water in those solvents or simply because of interactions between the solvents and the copper and zinc oxide components. The sintering resulted in a decrease in the number of active sites and an increase in acidic sites, which enhanced the undesired dehydration reaction. Based on the results of inductively coupled plasma (ICP) and TEM, a model of the catalyst was proposed to illustrate the effect of solvent polarity on the dehydrogenation of isoborneol.