The conversion of greenhouse gases, H2 and CO selectivity, H2/CO ratio, and carbon formation in the dry reforming reaction over Ni‐supported ZSM‐5, Al2O3, and TiO2 are tested under thermal, plasma, and plasma–thermal conditions. It is observed that the dielectric nature, specific surface area, and acid‐base properties of the support influence the performance during the DRM reaction. Typical results indicate that the best activity and syngas yield are achieved with 15Ni/Al2O3 under plasma conditions, possibly due to the high dielectric constant and surface area of Al2O3 and nanosize of Ni. In the thermal condition, the highest conversion of 73% and 68% for CH4 and CO2, respectively, is achieved over 15Ni/ZSM‐5 at 500 °C. Plasma‐assisted thermal conditions provide the highest conversion due to the activation of reactants and their partial conversion in the plasma zone before entering into the catalytic zone. The plasma‐assisted thermocatalytic conversions of CH4 and CO2 reach the best values of 76% and 71%, respectively, on 15Ni/ZSM‐5. Under the same conditions, 68% and 65% conversion of CH4 and CO2, respectively, is achieved with 15Ni/Al2O3 where the selectivity for H2 and CO is 45% and 58%, respectively.
Sodium titanate nanotubes (NaTNTs) were prepared by alkali treatment of anatase titania. They were then ion-exchanged with alkali and alkaline earth metal ions to get ATNTs (A ¼ Li + , K + , Cs + , Mg 2+ , Ca 2+ , Sr 2+ and Ba 2+ ). Gold (1-5 wt%) was supported on these nanotubes by a deposition-precipitation method and investigated as a catalyst for the selective oxidation of benzyl alcohol with air/molecular oxygen (1 atm) under solvent-and alkali-free conditions. Detailed characterization by X-ray powder diffraction, high resolution transmission electron microscopy, N 2 -physisorption, diffuse reflectance UV-visible spectroscopy, X-ray photoelectron spectroscopy and CO 2 -temperature-programmed desorption techniques revealed that the basicity of the catalyst influences the uptake, mean particle size, electronic properties and oxidation activity of the supported gold. Benzaldehyde formed with a selectivity of about 99%. The catalytic activity (turnover frequency) was found to have a direct relationship with the basicity and an inverse relationship with the Au particle size. Among the catalysts investigated, Au/BaTNTs, having higher basicity, smaller Au particles and higher metal dispersion, showed enhanced catalytic activity than the other Au/ATNT catalysts. Pd addition to Au leading to Au-Pd/BaTNTs increased the activity (TOF) but lowered the selectivity for benzaldehyde (80 wt%). Titanate nanotubes donate electron density to Au particles, yielding electron rich Au ions, which are responsible for activating molecular oxygen and oxidizing benzyl alcohol. Au/BaTNTs, having higher basicity and lower size Au nanoparticles than the other Au/ATNT, activates molecular oxygen more easily and thereby enhances the catalytic activity. † Electronic supplementary information (ESI) available: XRD, CO 2 -TPD proles, DRUV-vis spectra and XPS proles of Au/ATNT, N 2 physisorption of supports, correlation proles of basicity versus uptake and particle size of Au and B.E. values versus TOF and catalytic activity data. See
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