Abstract
Aqueous-phase hydrogenation of D-glucose to D-sorbitol was systematically investigated over silica-supported Pt nanoparticles to elucidate structure−reactivity relations and mechanistic insight. D-Glucose hydrogenation over large Pt particles competes with its isomerization to D-fructose over low-coordination (electron-deficient) Pt sites; D-sorbitol production by the former process was structure insensitive for nanoparticles spanning 3−17 nm, whereas isomerization was favored by smaller particles, with both pathways independent of the choice of fumed silica or mesoporous SBA-15 support. While D-fructose was readily hydrogenated to D-mannitol under the same reaction conditions, the latter underwent minimal isomerization to D-sorbitol, which is, therefore, a direct product of D-glucose ring opening and subsequent hydrogenation of the aldose conformer. D-Sorbitol production was favored by low D-glucose concentrations (<10 wt %), high H2 pressures (>40 bar), and low reaction temperatures (<140 °C), which suppressed undesired polymerization side reactions.
| Original language | English |
|---|---|
| Pages (from-to) | 7409-7417 |
| Number of pages | 9 |
| Journal | ACS Catalysis |
| Volume | 6 |
| Issue number | 11 |
| Early online date | 26 Sept 2016 |
| DOIs | |
| Publication status | Published - 4 Nov 2016 |
Keywords
- Glucose
- Hydrogenation
- Platinum
- SBA-15
- Sorbitol