A series of WO 3 -SBA-15 materials with different Si/W ratios have been hydrothermally synthesized using tetraethyl orthosilicate (TEOS) as silica precursor, ammonium paratungstate as tungsten precursor, and EO 20 PO 70 EO 20 (P123) as structure-directing reagent. After temperature-programmed carburization (TPC) in flowing CH 4 /H 2 (20/80 v/v mixture), the materials were converted to the corresponding W x C-SBA-15 materials. The structure of the oxide and carbide materials has been characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), nitrogen adsorption−desorption measurements, 29 Si magic-angle spinning (MAS) NMR spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), and thermogravimetric and differential scanning calorimetric analysis (TG-DSC) measurements. The results show that after hydrothermal synthesis using different amounts of tungsten and subsequent carburization, the materials retain the mesopore structure of SBA-15. When Si/W = 30−15, the majority of the tungsten is dispersed in the channels of SBA-15 with the remainder being incorporated into the framework of SBA-15 with the formation of Si−O−W bonds. The tungsten carbide exists as a single W 2 C phase after carburization. At higher tungsten content (Si/W = 7.5), the amount of tungsten in the framework of SBA-15 increases with the formation of both Si−O−W bonds and W−O−W bonds. The tungsten carbide formed after carburization exists as a mixture of W 2 C and WC phases. A model for the distribution of tungsten in SBA-15 is proposed involving three different tungsten species: α-W inside SBA-15 channels, β-W embedded in the internal surfaces of the SBA-15 channels, and γ-W inside the framework of SBA-15. After temperature-programmed carburization, α-W sites are transformed into W 2 C, whereas β-W sites afford WC; in contrast, γ-W sites show little change after carburization.
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Hu et al. (2007) studied this question.
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