Abstract
Ti-containing MCM-41 supports were prepared by: (a) hydrothermal crystallization; (b) post-synthesis grafting; and (c) two-step Ti incorporation—hydrothermal incorporation followed by post-synthesis grafting. XRD revealed little change in crystallinity and long range order of MCM-41 phase after Ti incorporation by different methods. UV-Vis spectra show the presence of tetrahedral Ti sites at lower Ti contents (upto 4.5 mol%), but aggregated titania formation could be observed at higher Ti loadings (>4.5 mol%). The samples exhibit surface areas and pore volumes in the mesoporous range. Vapor phase epoxidation of propene using H 2 and O 2 was carried out over these supports after Au deposition by deposition-precipitation (DP) method. The Ti-MCM-41 supports prepared by two-step Ti incorporation (with up to 4.5 mol% input Ti), which probably have more number of isolated Ti sites, showed higher catalytic activity than Ti-MCM-41 prepared by one-step Ti incorporation method, at comparable propylene oxide selectivities and hydrogen efficiencies. The former catalyst also deactivates more slowly than the latter ones, probably due to a decrease in the number of silanol sites (those responsible for deactivation) due to grafted Ti.
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