Selective photocatalytic oxidation of cyclohexanol to cyclohexanone: A spectroscopic and kinetic study

In this work, spectroscopic and kinetic studies were performed on photocatalytic oxidation of cyclohexanol to cyclohexanone. The photocatalytic experiments were performed according to a three-level full factorial design and the rate of cyclohexanone production was determined by HPLC analysis. In situ ATR-FTIR analysis of the photocatalytic reaction revealed that cyclohexanol can be selectively converted to cyclohexanone, without the formation of significant amounts of carbonates and carboxylates. A reaction mechanism based on different steps from charge separation to cyclohexanone molecule formation is proposed. The results were utilized to determine the kinetic parameters (with the help of genetic algorithm) and validate the model. The developed kinetic model illustrates that the rate of cyclohexanone production increases as a power function with respect to the light intensity and decreases as an exponential function with respect to time. An excellent selectivity of cyclohexanone was confirmed by spectroscopic and chromatographic studies. This study demonstrates that photocatalysis can be a promising technology for formation of cyclohexanone from cyclohexanol

Metal-Supported TiO₂/SiO₂ Core-Shell Nanosphere Photocatalyst for Efficient Sunlight-Driven Methanol Degradation

The development of novel and active photocatalysts to industrialize photocatalysis technology is still a challenging task. In this work, a novel method is presented to prepare TiO2/SiO2 NSs by covering SiO2 nanospheres (NSs) with titanate-nanodiscs (TNDs) followed by calcination. In this regard, SiO2 NSs are first synthesized and then TNDs are deposited on the SiO2 NSs using a layer-by-layer deposition technique. The morphology of the prepared samples is analyzed via SEM and TEM analyses before and after the deposition. The analysis of metal (Cu, Pt, and Ni) loading on calcined TNDs/SiO2 NSs reveals the highest specific surface area (109 m2/g), absorption wavelength extension (up to 420 nm), and photocatalytic activity for the Cu-loaded sample. In addition, studying the effect of metal content shows that loading 3% Cu leads to the highest photocatalytic activity. Finally, it is demonstrated that H2S treatment can improve the photocatalytic activity by around 15%. These findings suggest the calcined TNDs/SiO2 NSs are a versatile photocatalyst with potential applications in other processes such as hydrogen production and CO2 valorization