Activated Carbon, Carbon Nanofibers and Carbon-Covered Alumina as Support for W2C in Stearic Acid Hydrodeoxygenation

Carbon materials play a crucial role in sorbents and heterogeneous catalysis and are widely used as catalyst support for several reactions. This paper reports on an investigation of tungsten carbide (W2C) catalyst on three types of carbon support, namely activated carbon (AC), carbon nanofibers (CNF) and carbon-covered alumina (CCA). We evaluated their activity and selectivity in stearic acid hydrodeoxygenation at 350 °C and 30 bar H2. Although all three W2C catalysts displayed similar intrinsic catalytic activities, the support did influence product distribution. At low conversions (<5%), W2C/AC yielded the highest amount of oxygenates relative to W2C/CNF and W2C/CCA. This suggests that the conversion of oxygenates into hydrocarbons is more difficult over W2C/AC than over W2C/CNF and W2C/CCA, which we relate to the lower acidity and smaller pore size of W2C/AC. The support also had an influence on the C18-unsaturated/C18-saturated ratio. At conversions below 30%, W2C/CNF presented the highest C18-unsaturated/C18-saturated ratio in product distribution, which we attribute to the higher mesopore volume of CNF. However, at higher conversions (>50%), W2C/CCA presented the highest C18-unsaturated/C18-saturated ratio in product distribution, which appears to be linked to W2C/CCA having the highest ratio of acid/metallic sites.

TiO2Nanocatalysts Supported on a Hybrid Carbon-Covered Alumina Support: Comparison between Visible Light and UV Light Degradation of Rhodamine B

Titania nanoparticles were successfully supported on carbon-covered alumina (CCA) supports via the impregnation method to form carbon-covered alumna titania (CCA/TiO2). The CCA supports were synthesised through an equilibrium adsorption of toluene 2,4-diisocyante where the N=C=O irreversibly adsorbs on the alumina and pyrolysis at 700°C affords CCA supports. These CCA/TiO2nanocatalysts were tested for their photocatalytic activity both under UV and visible light using Rhodamine B as a model pollutant. The reaction rate constant of the CCA/TiO2was found to be higher than that of unsupported titania and the reaction kinetics were found to follow an apparent first-order rate law. The CCA/TiO2nanocatalysts had a much larger surface area than the unsupported titania and they exhibited overall higher photodegradation efficiency under both UV and visible light than unsupported TiO2.