• Journal of the Korean Ceramic Society
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• v.46 no.6
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• pp.621-626
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• 2009

Fe-AC/Ti$O_2$ photocatalysts were prepared by a sol-gel method. The photocatalytic properties of Fe-AC/Ti$O_2$ photocatalysts for the purification of water have been investigated. The samples were characterized by scanning electron microscopy (SEM), specific surface area (BET), X-ray diffraction analysis (XRD), and energy dispersive X-ray spectroscopy (EDX). The photocatalytic activities were evaluated by the photocatalytic oxidation of methylene blue (MB) solution. It was found that the prepared Fe-AC/Ti$O_2$ composites have an excellent photocatalytic under visible light irradiation. A small amount of Fe ions in the AC/Ti$O_2$ composites could obviously enhance their photocatalytic activity. The high activities of the Fe-AC/Ti$O_2$ composites could be attributed to the results of the synergetic effects of the enhancement of the Fe element, the photocatalytic activity of Ti$O_2$, and the adsorption of AC.

• Korean Chemical Engineering Research
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• v.57 no.2
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• pp.185-197
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• 2019

Deactivation of porous photocatalytic materials was studied using three types of microstructured particles: macroporous titania particles, titania microspheres, and porous silica microspheres containing CNTs and $TiO_2$ nanoparticles. All particles were synthesized by emulsion-assisted self-assembly using micron-sized droplets as micro-reactors. During repeated cycles of the photocatalytic decomposition reaction, the non-dimensionalized initial rate constants (a) were estimated as a function of UV irradiation time (t) from experimental kinetics data, and the results were plotted for a regression according to the exponentially decaying equation, $a=a_0\;{\exp}(-k_dt)$. The retardation constant ($k_d$) was then compared for macroporous titania microparticles with different pore diameters to examine the effect of pore size on photocatalytic deactivation. Nonporous or larger macropores resulted in smaller values of the deactivation constant, indicating that the adsorption of organic materials during the photocatalytic decomposition reaction hinders the generation of active radicals from the titania surface. A similar approach was adopted to evaluate the activation constant of porous silica particles containing CNT and $TiO_2$ nanoparticles to compare the deactivation during recycling of the photocatalyst. As the amount of CNTs increased, the deactivation constant decreased, indicating that the conductive CNTs enhanced the generation of active radicals in the aqueous medium during photocatalytic oxidation.

• Bulletin of the Korean Chemical Society
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• v.20 no.8
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• pp.957-960
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• 1999

• Journal of Wellbeing Management and Applied Psychology
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• v.5 no.2
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• pp.21-27
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• 2022

Purpose: This study is about photocatalytic technology and plasma oxidation-reduction technology. To the main cause of exposure to odor pollution, two deodorization techniques were applied to develop a module with higher removal efficiency and ozone reduction effect. Research design, data and methodology: A composite module was constructed by arranging two types of dry deodorization equipment (catalyst, adsorbent) in one module. This method was designed to increase the responsiveness to the components of complex odors and the environment. standard, unity, two types of oxidizing photo-catalyst technology and plasma dry deodorization device installed in one module to increase the potential by reduction to 76% of ozone, 100%, and 82%. Results: The complex odor disposal efficiency was 92%. Ammonia was processed with 50% hydrogen sulfide and 100% hydrogen sulfide, and ozone was 0.01ppm, achieving a target value of 0.07ppm or less. The combined odor showed a disposal efficiency of 93%, ammonia was 82% and hydrogen sulfide was 100% processed, and ozone achieved a target value of 0.07 ppm or less. Conclusions: Ozone removal efficiency was 76% by increasing Oxidation-Reduction Reaction(ORR). The H2S removal efficiency of the deodorizer was higher than that of the biofilter system currently used in sewage disposal plants.

• Membrane Journal
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• v.32 no.3
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• pp.181-190
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• 2022

Membrane separation provides various advantages including cost effectiveness and high efficiency over traditional wastewater treatment methods such as flocculation and adsorption. However, the effectiveness of membrane separation greatly declines due to membrane fouling, where pollutants are accumulated on the membrane surface. Among different groups of membranes, ceramic membranes can provide good antifouling properties due to its hydrophilicity and chemical stability. In addition, composite membranes such as graphene oxide modified membranes can help prevent membrane fouling. Recently, hybrid photocatalytic membranes have been proposed as a solution to prevent membrane fouling and provide synergetic effects. Membrane separation can solve the disadvantages of photocatalytic oxidation such as low reutilization rate, while photocatalytic oxidation can help reduce membrane fouling.

• Economic and Environmental Geology
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• v.50 no.3
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• pp.215-224
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• 2017

Arsenic (As) is known to be the most toxic element and frequently detected in groundwater environment. Inorganic As exists as arsenite [As(III)] and arsenate [As(V)] in reduced and oxidized environments, respectively. It has been reported that the toxicity of arsenite is much higher than that of arsenate and furthermore arsenite shows relatively higher mobility in aqueous environments. For this reason, there have been numerous researches on the process for oxidation of arsenite to arsenate to reduce the toxicity of arsenic. In particular, photooxidation has been considered to be simple, economical, and efficient to attain such goal. This study was conducted to evaluate the applicability of naturally-occurring goethite as a photocatalyst to substitute for $TiO_2$ which has been mostly used in the photooxidation processes so far. In addition, the effects of several factors on the overall performance of arsenite photocatalytic oxidation process were evaluated. The results show that the efficiency of the process was affected by total concentration of dissolved cations rather than by the kind of those cations and also the relatively higher pH conditions seemed to be more favorable to the process. In the case of coexistence of arsenite and arsenate, the removal tendency by adsorption onto goethite appeared to be different between arsenite and arsenate due to their different affinities with goethite, but any effect on the photocatalytic oxidation of arsenite was not observed. In terms of effect of humic acid on the process, it is likely that the higher concentration of humic acid reduced the overall performance of the arsenite photocatalytic oxidation as a result of competing interaction of activated oxygen species, such as hydroxyl and superoxide radicals, with arsenite and humic acid. In addition, it is revealed that the injection of oxygen gas improved the process because oxygen contributes to arsenite oxidation as an electron acceptor. Based on the results of the study, consequently, the photocatalytic oxidation of aqueous arsenite using goethite seems to be greatly feasible with the optimization of process.

• Environmental Engineering Research
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• v.14 no.3
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• pp.170-173
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• 2009

This study examined the special technique of photocatalytic degradation (RPODisk) for removal of taste and odor causing materials, algae, and algal toxin. The RPODisk was effective for removal of these troublesome contaminants. It outperformed the fixed media and the UV irradiation for geosmin removal. The RPODisk performance was comparable to the combination of the UV irradiation with TiO2. The RPODisk performance was affected by the rotating speed. The faster the speed was, the better the performance. The RPODisk was also effective for removal of algae and algal toxin. The algal activity reduced by 80% after 30 mins of the treatment. More toxic microcystin (MC)-LR was more difficult to remove than MC-RR. The times for 50% removal were 23.7 mins for MC-LR and 14.1 mins for MC-RR. Almost 100 mins of the contact time was required to completely remove MC-LR at the rotating speed of 260 rpm.

• Journal of Korean Society on Water Environment
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• v.21 no.1
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• pp.46-51
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• 2005

The photocatalytic oxidation of Rhodamine B (RhB) was studied using immobilized $TiO_2$ and rotating disk photocatalytic reactor. Immobilized $TiO_2$ onto the surface of the aluminum plate was employed as the photocatalyst and two 20 W germicidal lamps and two 20 W UV-BLB lamps were used as the light source and the reactor volume was 1.0 L. The effects of parameters such as the number of rotating disk, rpm of rotating disk, the number of coating, $H_2O_2$ and photo-fenton amounts, and the concentrations of anions and cations ($NO_3{^-}$, $SO_4{^{2-}}$, $Cl^-$, $Ca^{2+}$, $Zn^{2+}$, $Na^+$) were examined.

• Rapid Communication in Photoscience
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• v.4 no.1
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• pp.19-21
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• 2015

Zeolite is an ideal host material for encapsulating nano-size metal catalyst species because of its defined microporous structure, prominent adsorption/condensation properties, high surface area, chemical/thermal stability, and transparency to light. In this study, $TiO_2$ photocatalyst was incorporated in highly hydrophobic Y zeolite and its photocatalytic activity was examined in the photocatalytic oxidation of olefins under UV-light irradiation using molecular oxygen as an oxygen source. $TiO_2$ nanoparticles incorporated in hydrophobic Y zeolite exhibited a markedly enhanced photocatalytic activity compared with bare $TiO_2$ owing to its excellent affinity toward organic moieties, which facilitates the mass transfer of organic substrates and allows them to efficiently access to the neighboring active $TiO_2$ surface.

• Journal of Korean Society on Water Environment
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• v.20 no.6
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• pp.577-582
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• 2004

The photocatalytic degradation of atrazine and PCP, a endocrine disruptors, has been investigated over $TiO_2$ photocatalysts under ultraviolet (UV) light irradiation. The effect of operational parameters, i.e., pH, light intensity and persulphate concentration on the degradation rate of aqueous solution of atrazine and PCP has been examined. The results presented in this work demonstrate that, as pH and the light intensity increased, the photocatalytic reaction rates were enhanced. Individual use of $TiO_2$-persulphate was far more effective than using only $TiO_2$ in atrazine and PCP removal. Based on the overall experimental results, the photocatalytic oxidation of atrazine and PCP with the coated $TiO_2$ photocatalyst is found to be very effective under the operational conditions delineated in this study.