• Journal of Photoscience
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• v.10 no.3
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• pp.231-236
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• 2003

TiO$_2$ has been used as photocatalyst since two and half decades ago. The efficiency in its photocatalytic reactions has been improved by increasing the surface area of the photocatalyst by supporting fine TiO$_2$ particles on some porous materials. In this work, heteropolytungstic acid (HPA) - encapsulated into the titanium exchanged SBA-15 mesoporous materials (TiSBA-15) were prepared and characterized. Also their photocatalytic effects on decomposition of phenol were investigated and the photodecomposition rates of the phenol were observed to be increased by 2.5 8 fold, as compared to those observed in the presence of HPA-encapsulated SBA-15 or TiSBA-15 without HPA.

• Korean Journal of Air-Conditioning and Refrigeration Engineering
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• v.19 no.4
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• pp.285-290
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• 2007

This study has been numerically conducted to investigate the removal efficiency of Volatile Organic Compound (VOC) in photocatalytic micro-reactor. This study has placed emphasis on the improvements of the working condition of photocatalytic micro-reactor. The micro-reactor consists of 19 microchannels with a rectangular cross-section. For the validation of the current numerical study, a computation has been carried out to simulate an existing experimental study on the cylindrical reactor, which has shown a good agreement. The degradation characteristics with different inlet concentrations and velocities have been obtained. The current results can be used for the design of advanced photocatalytic micro-reactor.

• Journal of Powder Materials
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• v.24 no.4
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• pp.279-284
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• 2017

The formation mechanism and photocatalytic properties of a multiwalled carbon nanotube (MWCNT)/$TiO_2$-based nanotube (TNTs) composite are investigated. The CNT/TNT composite is synthesized via a solution chemical route. It is confirmed that this 1-D nanotube composite has a core-shell nanotubular structure, where the TNT surrounds the CNT core. The photocatalytic activity investigated based on the methylene blue degradation test is superior to that of with pure TNT. The CNTs play two important roles in enhancing the photocatalytic activity. One is to act as a template to form the core-shell structure while titanate nanosheets are converted into nanotubes. The other is to act as an electron reservoir that facilitates charge separation and electron transfer from the TNT, thus decreasing the electron-hole recombination efficiency.

• Journal of Industrial and Engineering Chemistry
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• v.68
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• pp.311-324
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• 2018

Herein,the Neodymium ion ($Nd^{3+}$) doped CoAl-LDH have been successfully prepared via co-precipitation method and was used as a precursor of Nd-doped CoAl-mixed metal oxides (MMO). The photocatalytic activity of doped LDH and MMO was investigated in the degradation of an azo dye, C.I. Acid Red 14, under visible light irradiation. DRS and PL analysis demonstrated decreasing in the band gap energy and recombination of photo-induced charge carriers of Nd-doped LDH and MMO compared with the pristine CoAL-LDH. Due to significant difference in photocatalytic performance. A power law empirical kinetic model was obtained for predicting the photocatalytic degradation efficiency.

• Journal of Environmental Health Sciences
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• v.25 no.3
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• pp.64-69
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• 1999

This study was carried out the removal of Cr(VI) which was known to the toxic pollutant in industry using the process of UV and TiO$_2$ photocatalyst in a circular type reactor. In this experiment, the series of photocatalytic process for the removal of Cr(VI) has been selected as a model reaction in a circular type reactor in order to obtain the basic data on the influence of various experimental parameters such as circulation flow rate, pH of solution, initial Cr(VI) light illumination and TiO$_2$ dosage, and salicylic acid concentration. The results of this study were as follows; 1. With both UV light illumination and TiO$_2$ present, Cr(VI) was more effectively eliminated than with either UV or TiO$_2$ alone. 2. As the circulation flow rate of solution increased, the removal efficiency of Cr(VI) was increased. However, over 2.4 l/min of circulation flow rate, the efficiency wa limited. 3. A increase in the photocatalytic removal of Cr(VI) was noticed with decreasing pH. 4. An increase in the photocatalytic removal of Cr(VI) was noticed with decreasing Initial Cr(VI) concentration and first order kinetics was observed from the result at different initial concentration of Cr(VI). 5. Photocatalytic removal efficiency of Cr(VI) increased with increasing TiO$_2$ dosage. However, over 1.0 g/l of TiO$_2$ dosage, the efficiency reached a plateau. 6. As low concentration of saliculic acid were added, there was an increase in the removal efficiency of Cr(VI). However, over 300 mg/l of salicylic acid, the efficiecy was decreased. It eas found that application of photocatalysis to water treatment that contains both Cr(VI) and salicylic acid was possible.

• Korean Chemical Engineering Research
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• v.50 no.6
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• pp.945-951
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• 2012

The effect of photocatalyst-carrying media porosity on the photocatalytic removal efficiency of malodor and VOC of waste air was evaluated when the photocatalytic removal efficiency of porous silica-based media was compared with that of glass bead as control. The amount of photocatalyst coated on the surface of porous silica-based media was observed to be $1,716.3{\mu}g/cm^2$, which was 250% as much as that of nonporous glass bead (control) of $670{\mu}g/cm^2$. The removal efficiencies of hydrogen sulfide and toluene in case of porous silica-based media were observed to be 22% and 82%, respectively, while the removal efficiencies of hydrogen sulfide and toluene in case of nonporous glass bead media were observed to be 19% and 53%, respectively. Therefore, the removal efficiencies of hydrogen sulfide and toluene increased by 16% and 55%, respectively, when the removal efficiencies of porous silica-based media were compared with those of nonporous glass bead media. Thus the increment ratio of the removal efficiency of toluene was observed to be 3.4 times higher than that of hydrogen sulfide.

• Nano
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• v.13 no.11
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• pp.1850130.1-1850130.12
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• 2018

A novel strontium titanate/binary metal sulfide ($SrTiO_3/SnCoS_4$) heterostructure was synthesized by a simple two-step hydrothermal method. The visible-light-driven photocatalytic performance of $SrTiO_3/SnCoS_4$ composites was evaluated in the degradation of methyl orange (MO) under visible light irradiation. The photocatalytic performance of $SrTiO_3/SnCoS_4-5%$ is much higher than that of pure $SrTiO_3$, $SnCoS_4$, $SrTiO_3/SnS_2$ and $SrTiO_3/CoS_2$. The $SrTiO_3/SnCoS_4$ composite material with 5 wt.% of $SnCoS_4$ showed the highest photocatalytic efficiency for MO degradation, and the degradation rate could reach 95% after 140 min irradiation time. The enhanced photocatalytic activity was ascribed to not only the improvement of visible light absorption efficiency, but also the construction of a heterostructure which make it possible to effectively separate photoexcited electrons and holes in the two-phase interface.

• Journal of Environmental Science International
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• v.29 no.12
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• pp.1213-1222
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• 2020

In the current study, a Cu2O/TiO2 photoinduced nanocomposite materials prepared by ultrasonification method was evaluated the photocatalytic oxidation efficiency of volatile organic compounds (BTEX) under visible-light irradiation. The results of XRD confirmed the successful preparation of photoinduced nanocomposite materials. However, diffraction peaks belonging to TiO2 were not confirmed for the Cu2O/TiO2. The possible reason for the absence of Cu2O peak is their low content and small particle size. The result of uv-vis spectra exhibited that the fabricated Cu2O/TiO2 can be activated under visible light irradiation. The FE-SEM/EDS and TEM showed the formation of synthesized nanocomposites and componential analysis in the undoped TiO2 and Cu2O/TiO2. The photocatalytic oxidation efficiencies of benzene, toluene, ethylbenzene, and o-xylene with Cu2O/TiO2 were higher than undoped TiO2. According to light sources, the average oxidation efficiencies for BTEX by Cu2OT-0.5 were exhibited in the orer of 8 W day light > violet LEDs > white LEDs. However, the photocatalytic oxidation efficiencies normalized to supplied electric power were calculated to be in the following order of violet LEDs > white LEDs > 8 W day light, indicating that the LEDs could be a much more energy efficient light source for the photo-oxidation of gaseous BTEX using Cu2O/TiO2.

• Korean Journal of Materials Research
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• v.11 no.7
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• pp.537-544
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• 2001

Anatase $TiO_2$thin films as a photocatalyst were prepared by the reactive magnetron sputtering process. The $TiO_2$thin films were deposited on Si substrates under the various conditions : oxygen partial pressure, working pressure, sputtering time, and D.C. power. The photocatalystic degradation of $TiO_2$thin film have been studied to examine the contribution of surface morphology and crystallinity. The thin films with a good crystallinity or a rough surface showed a high photocatalytic degradation rate on phenol and E.coli 078 experiment. Compared with that of only UV radiation, the photocatalytic efficiency of $TiO_2$thin film under the UV radiation and the $O_2$ flow increased. We found that the crystallity and the morphology were the important factors on the photocatalytic efficiency of TiO$_2$thin film.

• Environmental Engineering Research
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• v.21 no.3
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• pp.291-296
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• 2016

Application of photocatalytic nanoparticles has been recently gaining an increased attention as air purifying material for sustainable urban development. The present work reports the photocatalytic removal of gaseous phase nitrogen oxides ($NO_x$) using $TiO_2$-coated zeolite to be applied as a filter media for the urban green infrastructure such as raingardens. The $TiO_2$-coated zeolite was synthesized by simple wet chemistry method and tested in a continuous-flow photo-reactor for its removal efficiency of $NO_x$ under different conditions of the weight percentage of $TiO_2$ coated on the zeolite, and gas retention time. The removal efficiency of $NO_x$ in general increased as the weight percentage of $TiO_2$ coated on the zeolite increased up to 15-20%. Greater than 90% of $NO_x$ was removed at a retention time of one minute using the $TiO_2$-coated zeolite ($TiO_2$ weight percentage = 20%). Overall, $TiO_2$-coated zeolite showed greater efficiency of $NO_x$ removal compared to $TiO_2$ powder probably by providing additional reaction sites from the porous structure of zeolite. It was presumed that the degradation of $NO_x$ is attributed to both the physical adsorption and photocatalytic oxidation that could simultaneously occur at the catalyst surface.