Abstract
Mesoporous TS-1 microspheres, denoted as M-TS-1-MS, were directly synthesized by adding triblock copolymer (F127 or P123) into the synthetic system for crystallizing conventional TS-1 (C-TS-1). With the assistance of surfactant, TS-1 nanoparticles of 50-100 nm were self-assembled into microspheres which contained regular intercrystal mesopores in the range of 6-10 nm in addition to original micropores. The crystallite aggregates in microspheres did not collapse after ultrasonication for 2 h or refluxing in 2 M HNO 3 for 20 h. The high mechanical strength implied their potential applications in slurry reactors where an easy separation of solid catalyst from reaction mixture is required. M-TS-1-MS was comparably active to C-TS-1 in pyridine oxidation and 1-hexene epoxidation with H 2O 2 as the oxidant, whereas exhibited a higher activity in the oxidation of bulky substrates such as 3-picoline and cyclohexene due to the presence of mesopores. By tracking the crystallization process at different stages, a tentative mechanism is proposed to explain the role of triblock copolymer in inducing the aggregation of nanocrystals to microspheres.
| Original language | English |
|---|---|
| Pages (from-to) | 106-114 |
| Number of pages | 9 |
| Journal | Microporous and Mesoporous Materials |
| Volume | 156 |
| DOIs | |
| State | Published - 1 Jul 2012 |
Keywords
- Liquid-phase oxidation
- Mesoporous microspheres
- Self-assembly
- TS-1
- Triblock copolymer