Abstract
The Cs-salt of heteropolyacid with stoichiometry Cs2.5H 0.5PW12O40 (CsHPW) was deposited selectively at the external surface of the SBA-15 silica microcrystals, inside its mesoporous channels and simultaneously at both location modes. The structure, texture and performance of these CsHPW/SBA-15 composites were compared with that of a reference bulk salt of the same composition. Location of CsHPW salt on the external surface of SBA-15 microcrystals leads to disintegration of its agglomerates increasing acidity of the catalytic phase. A novel preparation strategy consisting of grafting the basic Cs-species at the internal pores surface of SBA-15 stabilized the CsHPW phase inside the channels in form of 5-8 nm nanocrystals at 30-70 wt.% loadings. The catalytic tests demonstrated that insertion of the CsHPW catalytic phase inside the nanotubular channels of SBA-15 in combination with location of an additional amount of this phase at the external surface of SBA-15 microcrystals allows to increase the specific activity of this phase in MTBE synthesis, propionylation of anisole and alkylation of catechol with t-butanol by a factor of 1.5-3. This level of specific activity in combination with high total loading of catalytic phase >60 wt.% permit to get composite catalytic materials with catalytic activity higher by a factor of 1.2-1.5 with respect to the bulk CsHPW catalyst and stabilizing the catalytic phase against colloidization in polar media.
| Original language | English |
|---|---|
| Pages (from-to) | 43-55 |
| Number of pages | 13 |
| Journal | Microporous Materials |
| Volume | 80 |
| Issue number | 1-3 |
| DOIs | |
| State | Published - 30 May 2005 |
Keywords
- Acidic catalysis
- Cesium salt
- Heteropolyacid
- Mesostructured silica
ASJC Scopus subject areas
- General Chemistry
- General Materials Science
- Condensed Matter Physics
- Mechanics of Materials