Abstract
Fluorine species were implanted into the framework of Ti-MOR by post-treatment with fluorides in order to modify the microenvironment around Ti active sites and then to improve their catalytic activity in liquid-phase oxidation. The effects of NH4F amount, fluorination temperature, and solvent on the catalytic performance of F-Ti-MOR were investigated in detail. Methanol was found to be superior to water in fluorination. Fluorine implantation increased the electropositivity of Ti active sites through forming SiO3/2F units in the neighborhood, which enhanced the catalytic performance in the ammoximation of cyclohexanone remarkably. F-Ti-MOR prepared under optimized fluorination conditions showed a cyclohexanone conversion of 99% in comparison to only 30% conversion given by primitive Ti-MOR. Meanwhile, the implanted fluorine species captured the organic molecules with a relatively large dimension tightly, creating enormous steric hindrances that prevented other molecules, in particular those with bulky molecular dimensions, from diffusing into channels freely. Thus, F-Ti-MOR showed much lower activity than Ti-MOR in the hydroxylation of aromatics.
| Original language | English |
|---|---|
| Pages (from-to) | 160-169 |
| Number of pages | 10 |
| Journal | Journal of Catalysis |
| Volume | 320 |
| Issue number | 1 |
| DOIs | |
| State | Published - Dec 2014 |
Keywords
- Ammoximation
- Fluorination
- Hydroxylation
- Liquid-phase oxidation
- Ti-MOR
- Titanosilicate