Abstract With the aim of developing more efficient catalysts based on MOF materials for biomass upgrading through the hydrodeoxygenation, a novel Pt/UiO-66-based catalyst was first designed by introducing amino groups,… Click to show full abstract
Abstract With the aim of developing more efficient catalysts based on MOF materials for biomass upgrading through the hydrodeoxygenation, a novel Pt/UiO-66-based catalyst was first designed by introducing amino groups, together with creating mixing-linker defect using 5-amino-isophthalic acid as a mixed linker, were successfully synthesized with a microwave-solvothermal method. XPS and CO-chemisorption measurements revealed that the presence of amino groups significantly enhance the reducibility of the PtCl62- and PtCl42- phases to the Pt0 phase. As a result, the catalytic performance of these catalysts in the HDO of oleic acid was enhanced, as demonstrated by the 1.8–3.2-fold higher turnover frequency compared to the original Pt/UiO-66 catalyst. Interestingly, the presence of amino-defective linker facilitated the transition from decarbonylation to the hydrodeoxygenation reaction, as confirmed by the significant increase in C18/C17 ratio. Importantly, the modified catalysts were shown to possess a good catalytic stability, thus preventing coke deposition on the UiO-66 structure.
               
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