VO x /SBA-15 catalysts with five different vanadium loadings were prepared by a modified wet impregnation method, characterized using N 2 adsorption, XRD, EDX, SEM, Raman and UV-vis spectroscopies and H 2 -TPR techniques, and tested in the oxidative dehydrogenation of propane in the temperature range 450-600 • C. For all the catalysts the propane conversion increases with both reaction temperature and vanadium loading, while the selectivity for propene decreases mainly to the benefit of carbon oxides. Several types of VO x species coexist on the catalyst surface, with monomeric and low-polymerized ones leading mainly to propene, while V 2 O 5 crystallites at high vanadium loadings producing more carbon oxides. Propene was determined to be the only primary product irrespective of the vanadium content.
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Catalytic converters with non-linear channel structures were prepared using 3D printing and tested in the oxidation of methane in a simulated dual-fuel engine exhaust stream. The design used a simple repeating angular offset between adjacent layers, which was sufficient to introduce complexity with minimal software programming. All 3D printed substrates were mechanically stable and, following washcoating with a composite catalyst, demonstrated higher catalytic activity in methane oxidation than a commercial honeycomb substrate.The methane conversion at e.g. 510 °C was 12.6% on the commercial sample, 72.6% for 90 °, 80.1% for both 30 ° and 45 °, and 89.6 % for the 60 ° oriented structures. This enhancement is attributed to the increased turbulence/mass transfer and surface area than are possible using conventional straight-channelled substrates.Computational fluid dynamics (CFD) analysis confirmed that the higher methane conversion over 3D printed substrates is due (at least partially) to its higher turbulence kinetic energy. Backpressures over the 3D printed structures were also experimentally measured and compared with the conventional honeycomb monolith.
Hydroxyapatite (HAP) was synthesised in the presence of surfactants and tested as a catalyst in CO oxidation. XRD confirmed that the characteristic HAP crystal phase was practically unaffected by the addition of surfactant. The surfactant altered both the Ca/P ratio and particle size of HAP. Catalyst tests showed that the activity of HAP increased for preparations using TWEEN, PEG and PVA. The temperature for 50% conversion, T50, values decreased from 340 °C for unmodified HAP, to 320 °C for TWEEN and to 315 °C for both PEG and PVA. This enhanced activity is rationalised by the higher BET surface areas and acid site densities in the surfactant-modified preparations: these increased from 52 m 2 g-1 for HAP to 69, 76 and 68 m 2 g-1 , and from 101 μmoles g-1 for HAP to 110, 170 and 126 μmoles g-1 for TWEEN, PEG and PVA, respectively. These findings demonstrate that HAP i.e. without the addition of precious metals to either the surface or framework, is an active CO catalyst and that the straightforward inclusion of surfactant during preparation can optimise the catalytic performance.
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