A bimetallic Pt8Co1 supported on alkali-treated ZSM-5 zeolite (ZSM-5-AT) was prepared through the impregnation method. The structure and surface properties of the catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), N2-sorption and X-ray photoelectron spectroscopy (XPS) as well as temperature-programmed desorption of NH3 (NH3-TPD) and temperature-programmed reduction of H2 (H2-TPR). The TEM images present that the bimetallic Pt8Co1 nanoparticles with a mean particle size of 4-6 nm were uniformly dispersed on the alkali-treated ZSM-5 zeolite. The bimetallic Pt8Co1/ZSM-5-AT catalyst exhibited an extraordinary COL selectivity of 65% at a >99% CAL conversion efficiency, which showed a much higher catalytic performance (including the activity and selectivity) than the monometallic Pt/ZSM-5-AT and Co/ZSM-5-AT catalysts in the selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL) using hydrogen as reducing agent. The high catalytic activity of the bimetallic catalyst was attributed to the higher electron density of Pt species and more acidic sites of the alkali-treated ZSM-5 zeolite support. The recovery test showed no obvious loss of its initial activity of the Pt8Co1/ZSM-5-AT catalyst for five times.
Keywords: Pt-Co; ZSM-5; cinnamaldehyde; cinnamyl alcohol; selective hydrogenation.