RESUMO
Commercial rutile TiO2 particles capped with Al2O3 and ZrO2 layers, which are widely used in white pigments, can serve as a starting material for the fabrication of visible light-responsive photocatalysts toward gas-phase NO oxidation. The as-received TiO2 with iron impurities exhibited reduced photocatalytic activity, and the activity was boosted by the deposition of additional iron comparable in quantity to the intrinsic iron impurity level. Analyses using X-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectroscopy, and low-energy ion scattering spectroscopy revealed that the deposited iron and intrinsic impurity iron are dissimilar in terms of location, oxidation states, and interaction with TiO2. This suggests that tracking the structure and impurity levels of photocatalyst elements can be crucial for understanding structure-activity relationships of real catalysts.
RESUMO
Toluene removal rates using activated carbon (AC) at various relative humidity (RH) levels (0%, 30%, 60%) were compared under dark and visible-light conditions. Light exposure significantly increased toluene-removal efficiency independent of RH. When AC was pre-treated with an optimal concentration of HNO3, its toluene-removal efficiency was enhanced further with light, an effect that can be attributed to increased surface-area and porosity. Fourier-transform infrared analysis confirmed that exposure of HNO3-modified AC to light induced partial oxidation of toluene. Within visible-light range (380-650 nm), shorter wavelengths were more effective for toluene-removal compared with longer wavelengths. This suggests that hydroxyl groups formed on AC-surface under light strongly interact with aromatic rings of toluene, allowing for greater uptake of toluene. Moreover, AC can sustain its photo-activity when mixed with cement and cured, suggesting its potential applications in air-purifying building materials. An efficient and practical method for regeneration of spent AC is also demonstrated.
RESUMO
Fe x O y H z nanostructures were incorporated into commercially available and highly porous alumina using the temperature-regulated chemical vapor deposition method with ferrocene as an Fe precursor and subsequent annealing. All processes were conducted under ambient pressure conditions without using any high-vacuum equipment. The entire internal micro- and mesopores of the Al2O3 substrate with a bead diameter of â¼2 mm were evenly decorated with Fe x O y H z nanoparticles. The Fe x O y H z /Al2O3 structures showed substantially high activity for acetaldehyde oxidation. Most importantly, Fe x O y H z /Al2O3 with a high surface area (â¼200 m2/g) and abundant mesopores was found to uptake a large amount of acetaldehyde at room temperature, and subsequent thermal regeneration of Fe x O y H z /Al2O3 in air resulted in the emission of CO2 with only a negligibly small amount of acetaldehyde because Fe x O y H z nanoparticles can catalyze total oxidation of adsorbed acetaldehyde during the thermal treatment. Increase in the humidity of the atmosphere decreased the amount of acetaldehyde adsorbed on the surface due to the competitive adsorption of acetaldehyde and water molecules, although the adsorptive removal of acetaldehyde and total oxidative regeneration were verified under a broad range of humidity conditions (0-70%). Combinatory use of room-temperature adsorption and catalytic oxidation of adsorbed volatile organic compounds using Fe x O y H z /Al2O3 can be of potential application in indoor and outdoor pollution treatments.
