Abstract
The influence of the oxidized carbon moieties in the nanostructured carbon-supported Pd catalysts was studied for the furfural hydrogenation (2-propanol, 35 °C, 6 bar H2). The mesoporous carbon replicas synthesized using two systems: SBA-15-furfuryl alcohol or nanostructured SiO2-sucrose and oxidized with nitric acid or hydrogen peroxide were used as the supports. The catalysts (1.5–2 wt% Pd) of similar Pd particles size (ca. 4 nm) were synthesized by the “water-in-oil” microemulsion procedure. Although the carbon-supported Pd, Pt catalysts have been tested for the furfural hydrogenation, the effect of oxygenated carbon groups have not been yet investigated. Present results showed that the surface O/Pd atomic ratio influenced the rate and product distribution. Over initial carbon-supported Pd, the rate was high and apart from furfuryl alcohol and tetrahydrofurfuryl alcohol certain amount of “other” products was also observed. The oxidized carbon-supported catalysts were less active but more selective towards furan ring hydrogenation with almost completely inhibited “other” products formation reactions. The growing content of surface oxidized groups, in particular the carboxylic ones, corresponded well to the order of decreased activity. This effect has been related to a gradually reduced access of the regents to the Pd-surface sites because of the growing tendency to the hydrogen bonds formation with the participation of the oxygenated carbon groups – furfuryl alcohol – 2-propanol alcohol solvent.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.