Abstract
A shape-selective core/shell-structured Al-MWW@B-MWW composite catalyst has been hydrothermally synthesized through isomorphically overgrowing borosilicate on premade MCM-22 aluminosilicate. The secondary growth of borosilicate enlarged obviously the thickness of the platelet crystallites of MCM-22 and increased the surface Si/Al ratio from 16 to 222. The Fourier transform infrared (FTIR) spectra of adsorbed 2,6-di-tert-butylpyridine indicated that the Brønsted acid sites located on the external surface were virtually covered completely by the generated B-MWW layer, whereas those acid sites within channels were still accessible and detectable by using pyridine or ammonia as probing molecules. When applied to the disproportionation of toluene on a fixed-bed reactor, the Al-MWW@B-MWW composite catalysts exhibited significantly enhanced para-xylene selectivity in comparison with normal MCM-22 and its physical mixture with B-MWW. Al-MWW@B-MWW's unique catalytic behaviors were ascribed to an effective suppression of para-xylene isomerization as a result of removal of non-shape-selective acid sites on the external surface.
| Original language | English |
|---|---|
| Pages (from-to) | 168-177 |
| Number of pages | 10 |
| Journal | Journal of Catalysis |
| Volume | 283 |
| Issue number | 2 |
| DOIs | |
| State | Published - 27 Oct 2011 |
Keywords
- Borosilicate
- Core/shell zeolite composite
- Disproportionation of toluene
- MCM-22
- Shape-selective catalysis
- para-Xylene