Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9617740 | Microporous and Mesoporous Materials | 2005 | 13 Pages |
Abstract
The Cs-salt of heteropolyacid with stoichiometry Cs2.5H0.5PW12O40 (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 5-8Â nm nanocrystals at 30-70Â 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 >60Â 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.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
P. Madhusudhan Rao, M.V. Landau, A. Wolfson, A.M. Shapira-Tchelet, M. Herskowitz,