Effect of surface modification with silica on the structure and activity of Pt/ZSM-22@SiO2 catalysts in hydrodeoxygenation of methyl palmitate.

To obtain diesel fuels with high combustion properties from hydrotreatment of vegetable oils, inhibiting the formation of multibranched isomers (MuBI) is highly desirable. A core@shell structural ZSM-22@SiO 2 zeolite was designed to passivate external acid sites and promote the formation of monobranched isomers (MoBI), which have much higher cetane numbers than MuBI (>85 vs. <60). A series of ZSM-22@SiO 2 zeolites with different amounts of shell silica were synthesized through a facile crystal growth method. External acid sites could be successfully inactivated using the proposed method. Synthesized zeolites were used as supports for bifunctional catalysts in hydrodeoxygenation of methyl palmitate. The effects of the shell silica amount and SiO 2 /Al 2 O 3 ratio of the core zeolite were investigated. The MoBI percentage in total isomers increased from 71% to 95% at a reaction temperature of 300 °C. However, deoxygenation activity and isomerization selectivity decreased gradually with increasing amount of shell silica. Fourier transform infrared spectroscopy of CO adsorption combined with transmission electron microscopy demonstrated that Pt particles exposed more Pt(1 0 0) facets than Pt(1 1 1) facets in silica-coated catalysts. This could be the most likely reason for the decreased deoxygenation activity. The decrease in the number of Brønsted acid sites could be responsible for the lowered isomerization selectivity. Catalytic performance could be enhanced by reducing the SiO 2 /Al 2 O 3 ratio of core ZSM-22. Catalysts with lower SiO 2 /Al 2 O 3 ratios favored smaller Pt particles and exposed more active Pt(1 1 1) corner sites. Additionally, acid sites played an important role in the adsorption of oxygenates. [ABSTRACT FROM AUTHOR]