(50c) Investigating the Role of Solid Acid Sites in Surface Reactions of a Model Sugar
AIChE Annual Meeting
Monday, November 16, 2020 - 8:15am to 8:30am
13C MAS NMR spectroscopy with a direct polarization (DP) pulse sequence was used to identify surface species when the catalysts were impregnated with erythrose at room temperature. The following catalysts were tested due to varying degrees of BrÃ¸nsted and Lewis acidity: Î³-Al2O3, CeO2, Nb2O5, SiO2, SnO2, TiO2, and ZrO2. CeO2 and Nb2O5 promoted ring opening as evidenced by the appearance of two peaks in the carbonyl region of the spectrum. Nb2O5 also produced a significant amount of surface species containing aliphatic carbon suggesting further reaction to other species. SnO2, TiO2, and ZrO2 showed the most drastic reactions when the temperature was increased from 25 â°C to 50 â°C. Both carbonyl and aliphatic carbon became significantly more abundant at elevated temperature. In addition, species on TiO2 had the sharpest peaks suggesting it is weakly bound to the active sites due to the moderately acidic nature of TiO2.
Contact time experiments were carried out to determine the mobility of specific functional groups within the surface species present at 25 â°C and 50 â°C. This was done by comparing the relaxation times of different moieties. Some groups were greatly affected by the temperature increase, while others were immune. This is a significant consideration because one can discriminate which moieties are preventing the molecules release into the bulk phase.