RESUMEN
A small external magnetic field (100-1000 Oe) was demonstrated to enhance the photocatalytic degradation of methyl orange (MO) using TiO2 NPs in micro optofluidic chip (MOFC) reactors. The rectangular shape of the fluidic channel and TiO2 deposited only onto the lower glass substrate leads to a selectively enhancing photocatalytic reactions by magnetic field in specific directions. Utilizing ethyl alcohol as a scavenger presented the difference between generated hot-hole (hVB+) and hot-electron (eCB-) pathways of photocatalytic reactions. Effects of dissolved oxygen (DO) and hydroxyl ions (OH-) are all demonstrated in a magnetic field-enhancing photocatalytic reaction. The experimental results demonstrate great potential for practical applications utilizing low-price fixed magnets in the field of green chemistry.
RESUMEN
The light irradiation parameters, including the wavelength spectrum and intensity of light source, can significantly influence a photocatalytic reaction. This study examines the propylene photo-epoxidation over V-Ti/MCM-41 photocatalyst by using artificial sunlight (Xe lamp with/without an Air Mass 1.5 Global Filter at 1.6/18.5 mW·cm(-2)) and ultraviolet light (Mercury Arc lamp with different filters in the range of 0.1-0.8 mW·cm(-2)). This is the first report of using artificial sunlight to drive the photo-epoxidation of propylene. Over V-Ti/MCM-41 photocatalyst, the propylene oxide (PO) formation rate is 193.0 and 112.1 µmol·gcat (-1)·h(-1) with a PO selectivity of 35.0 and 53.7% under UV light and artificial sunlight, respectively. A normalized light utilization (NLU) index is defined and found to correlate well with the rate of both PO formation and C3H6 consumption in log-log scale. The light utilization with a mercury arc lamp is better than with a xenon lamp. The selectivity to PO remains practically unchanged with respect to NLU, suggesting that the photo-epoxidation occurs through the same mechanism under the conditions tested in this study.
RESUMEN
The removal of volatile organic compounds (VOCs) at ppb level is one of the most critical challenges in clean rooms for the semiconductor industry. Photocatalytic oxidation is an innovative and promising technology for ppb-level VOCs degradation. We have designed a fiber-illuminated honeycomb reactor (FIHR) in which the removal efficiency of m-xylene is significantly enhanced to 96.5% as compared to 22.0% for UV irradiation only. The results indicate that photocatalysts not only play the role to substantially oxidize m-xylene, but also alter the chemical properties of xylene under UV illumination. Using the FIHR with Mn-TiO2 photocatalyst not only increased the m-xylene removal efficiency, but also increased the CO2 selectivity. Interestingly, Mn-TiO2 in FIHR also showed a very good reusability, 93% removal efficiency was still achieved in 72-h in reaction. Thus, the FIHR gave very high removal efficiency for xylene at ppb level under room temperature. The FIHR has great potential application in the clean room for the air purification system in the future.