Ordered mesoporous materials with MFI structured microporous walls - Synthesis and proof of wall microporosity

Ordered mesoporous materials (OMMs) of 1-dimensional hexagonal and 3-dimensional cubic symmetry of the pore systems were synthesized via well-established soft templating routes starting from precursor solutions of MFI-type zeolites (Silicalite-1, TS-1). The products were characterized by XRD, nitrogen and argon physisorption, DTG/DTA, IR. UV-vis spectroscopy, XANES, TEM, Xe-119 NMR, and determination of the pair distribution function (PDF) in order to elucidate their structure, in particular to prove the presence of microporosity in arrays smaller than the coherence lengths of XRD, i.e. in the pore walls. The mesoporosity of the OMMs was well supported by physisorption studies and by TEM while the regularity of the structure was documented by XRD, which also served to exclude the presence of microporous crystalline grains. Instead, microporosity was detected by adsorption/desorption of water on tetrahedrally coordinated Ti-sites (XANES), by Xe-119 NMR, by the comparison of the PDF with those of amorphous and of MFI-type solids, and by sequential decomposition of the structure directing agents for mesa and micropore systems. From comparison of XRD and physisorption data and from the TEM micrographs, the thickness of the microporous mesopore walls was concluded to be approximate to 1.5 nm. Therefore, the failure of Ar physisorption to detect pores of sizes typical of MFI structures was attributed to the small micropore volume and the very short pore extension. The structural integrity of OMMs with 1-dimensional hexagonal pore system could be improved by a hydrothermal post-treatment despite the microporous nature of their pore walls, which resulted in more narrow mesopore size distributions peaking at somewhat larger pore sizes. (C) Elsevier Inc. All rights reserved

Pt nanoparticles inside the mesopores of TiO2-MCM-48: synthesis, characterization and catalytic activity for CO oxidation

TiO2 and Pt nanoparticles were deposited in the channels of siliceous MCM-48 via a sequential incipient wetness-impregnation method employing (NH4)2PtCl4 as platinum source. The resulting composite Pt/TiO2-MCM-48 (1 wt% Pt, ca. 3 wt% Ti) was characterized using XRD, TEM, nitrogen physisorption, hydrogen chemisorption, UV-vis spectroscopy, and XPS; its catalytic activity for CO oxidation was also explored. These data were compared with those of Pt/MCM-48 prepared via an analogous route. The results reveal that the platinum was deposited inside the intact pore system in both cases. It remains inside upon mild reduction but tends to segregate out of the pore system at higher reduction temperatures or during CO oxidation. Both composites were found to be highly active in CO oxidation, with 50% conversion at 460-475 K after activation of the unreduced catalysts in the (net oxidizing) feed. Striking differences in this activation process between Pt/MCM-48 and Pt/TiO2-MCM-48 suggest that the precursor reduction is influenced by an interaction with the TiO2 component in the latter. © 2009 Springer Science+Business Media, LLC