• 대한환경공학회지
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• 제27권8호
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• pp.829-836
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• 2005

본 연구에서는 광화학적 산화처리에 의한 아트라진의 분해특성을 분해산물의 분석을 통하여 살펴보았다. 본 실험에서 나타난 주요 분해산물로는 OIET, OIAT, OAAT가 있었고, 이를 통하여 광산화 반응에 의한 아트라진의 주분해반응은 dechlorination과 hydroxylation임을 확인할 수 있었다. TOC의 분석 결과 광산화에 의한 아트라진의 무기화는 기대하기 어려운 것으로 판명되었으며, 염소 이온의 물질수지 분석을 통해 본 광산화 반응에 의해 아트라진의 염소기의 완전한 탈염소가 진행되었음을 알 수 있었다.

• 한국결정성장학회지
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• 제17권5호
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• pp.196-203
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• 2007

We have studied a method for the preparation of hybrid $carbon/TiO_2$ complexes involving pitch coating, pitch binding and the penetration of titanium n-butoxide(TNB) solution with porous carbon. The photocatalysts were investigated with surface textural properties and SEM morphology, structural crystallinity and elemental identification between porous carbon and $TiO_2$, and dye decomposition performance. For the all $carbon/TiO_2$ complexes prepared by some kinds of different methods, the excellent photocatalytic effect for dye degradation should be attributed to the both effects between photo-decomposition of the supported $TiO_2$ and adsorptivity of the porous carbons.

• 한국세라믹학회지
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• 제46권6호
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• pp.561-567
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• 2009

The Fe-ACF/$TiO_2$ composites were prepared by a sol-gel method and were characterized by nitrogen adsorption, Scanning Electron Microscopy (SEM), X-ray Diffraction (XRD), and Energy Dispersive X-ray (EDX). The Fe-ACF/$TiO_2$ composites were developed for the decomposition of organic dyes by using a UV lamp. The decomposition effect was investigated under various conditions, such as three selected non-biodegradable organic dyes like Methylene Blue (MB), Methyl Orange (MO), Rhodamine B (Rh.B), and in the presence of Fe and hydrogen peroxide ($H_2O_2$). The photocatalytic activity was derived from possible combination effects, such as (1) adsorption of ACF, (2) generation of electron/hole by $TiO_2$, (3) photo-Fenton reaction of Fe, and (4) oxidation of $Fe^{2+}\;to\;Fe^{3+}\;by\;H_2O_2$.

• 대한설비공학회:학술대회논문집
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• 대한설비공학회 2009년도 하계학술발표대회 논문집
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• pp.98-101
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• 2009

Photo-catalyst technology to the decomposition of formaldehyde, and many are capable of VOC. In this research, effects of screw type photo-catalyst device will announce the experimental results.

• 한국환경보건학회지
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• 제26권4호
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• pp.29-37
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• 2000

Fenton’s oxidation process is one of the most commonly applied processes to the wastewater which cannot be treated by conventional biological treatment processes. However, it is necessary to minimize the cost of Fenton’s oxidation treatment by modifying the treatment processes or other means of chemical treatment. So, as a method for the chemical oxidation of biorefractory or nonbiodegradable organic pollutants, the Photo-Fenton-Reaction which utilizes iron(11)salt. $H_2O$$_2$ and UV-light simultaneously has been proprosed. Therfore, the purpose of this study is to test a removal efficiency of dye-wastewater and treatment cost with Fenton’s and Photo-Fenton’s oxidation process. The Fe(11)/$H_2O$$_2$ reagent is referred to as the fenton’s reagent. which produces hydroxy radicals by the interaction of Fe(11) with $H_2O$$_2$. In this exoeriment, the main results are as followed; 1. The Fenton oxidation was most efficient in the pH range of 3-5. The optimal condition for initial reaction pH was 3.5 for the high CO $D_{Cr}$ & TOC-removal efficiency. 2. The removal efficiency of TOC and CO $D_{Cr}$ increased up to the molar ration between ferrate and hydrogen peroxide 0.2:1, but above that ratio removal efficiency hardly increased. 3. The highest removal efficiency of TOC and CO $D_{Cr}$ were showed when the mole ration of ferrate to hydrogen peroxide was 0.2:3.4. 4. Without pretreatment process, photo-fenton oxidation which was not absorbed UV light was not different to fenton oxidation. 5. And Fenton oxidtion with pretreatment process was similar to Fenton oxidation in the absence of coagulation, the proper dosage of F $e^{2+}$: $H_2O$$_2$ was 0.2:1 for the optimal removal efficiency of TOC or CO $D_{Cr}$ .6. Also, TOC & CO $D_{Cr}$ removal efficiency in the photo-fenton oxidation with pretreatment was increased when UV light intensity enhanced.7. Optimum light intensity in the range from 0 to 1200 W/$m^2$ showed that UV-intensity with 1200W/$m^2$ was the optimum condition, when F $e_{2+}$:$H_2O$$_2$ ratio for the highest decomposition was 0.2:2.5.EX>$_2$ ratio for the highest decomposition was 0.2:2.5.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2019년도 춘계학술논문요약집
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• pp.301-302
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• 2019

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2018년도 추계학술논문요약집
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• pp.404-405
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• 2018

• 상하수도학회지
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• 제12권1호
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• pp.88-95
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• 1998

The Electron/Hole Pair is generated when the Activation Energy produces by Ultraviolet Ray illumination to the Semiconductor. And $OH^-$ ion produces by Water Photo-Cleavage reacts with Positive Hole. As a result, OH Radical acting as strong oxidant is generated and then Photocatalytic Oxidation Reaction occurs. The Photocatalytic Oxidation can oxidize the chlorophenol to Chloride and Carbon Dioxide easier, safer and shorter than conventional Water Treatment Process With the same degree of chlorination, the $Cl^-$ ion at para (C4) position is most easily replaced by the OH radical. And then, the blocking effect of $OH^-$ ion between the $Cl^-$ ions and $Cl^-$ ions at symmetrical location is easily replaced by the OH radical. For mono-, di-, tri-chlorophenols, there is no obvious difference in decomposition rate, decomposition efficiency and completeness of the decomposition reaction except for 2,3-dichloropheno, 2,4,5-, 2,3,4-trichlorophenol. The decomposition efficiency is higher than 75% and completeness of the decomposition reaction is higher than 70%. Therefore, continuous flow photocatalytic reactor is promising process to remove the chlorinated aromatic compounds which is more toxic than non-chlorinated aromatic compound.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 춘계학술대회 논문집 기술교육전문연구회
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• pp.144-148
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• 2003

알루미나볼 위에 Titanium tetraisopropoxide(TTIP)를 원료로, 화학기상증착법으로 제조된 $TiO_{2}/Al_{2}O_{3}$ 볼을 이용하여 벤젠의 기상 광 분해 실험을 실시하였다. 기상분해 과정의 연속적 측정을 위하여 순환식의 반응장치를 자체 제작하였으며, PID(Photo Ionization Detector)방식의 VOCs meter를 이용하여 광조사에 의한 벤젠의 분해율을 실시간으로 측정하였다. 기상의 벤젠과 $TiO_2/Al_{2}O_{3}$ 볼의 원활한 흡착을 위해 30분간 암반응 시킨 후 광분해율을 측정한 결과 광조사에 의한 분말표면에 흡착된 VOCs의 탈착에 의한 초기 농도증가 현상이 공통적으로 측정되었으며, 흡착 면적이 작을수록 농도 증가 또한 낮게 측정되었다. 또한 최적조건을 기준으로 실시한 분해 실험 결과 60ppm이상의 고농도 영역에서는 VOCs의 분해가 비교적 느리게 진행되었지만, 60ppm이하의 저농도 영역에서는 급속한 VOCs의 분해가 측정되었다. 마찬가지로 반응 표면적이 넓을수록, 광원이 많을수록 그리고 광분해에 사용된 자외선 램프의 강도가 클수록 광반응에 의한 벤젠의 분해율이 증가하였다.

• 한국재료학회지
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• 제14권4호
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• pp.293-299
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• 2004

Transition metal ions doped $TiO_2$ nanostructured powders were prepared with simply heating aqueous $TiOCl_2$ solutions, contained various metal ions (Ni, Al, Fe, Zr, and Nb) of 1.47 mol% added as metal-chlorides, at $100^{\circ}C$ for 4 hrs by homogeneous precipitation process under suppressing conditions of water vaporization. The characterizations for prepared $TiO_2$ powders were carried out to observe doping of metal ions, their concentrations and microstructures using XRD, UV-VIS (DRS), XPS, SEM, TEM and ICP. Also, photo-oxidative abilities were evaluated by decomposition of 4-chlorophenol (4CP) under ultraviolet light irradiations. No secondary oxide phases were formed in all the $VTiO_2$ powders, showing doping with various transition metal ions. When adding ions ($Ni^{2+}$ or$ Al^{3+ }$ and $Zr^{4+}$ ) having valance states or ionic radii greatly different from those of $Ti^{4+}$ , the $TiO_2$ powders of mixed anatase and rutile phases were formed, whereas in the case of additions of $^Fe{3+ }$ and $Nb^{ 5+}$ as well as no addition of metal ion the powders with pure rutile phase alone were formed. Among the prepared $TiO_2$ powders, Ni$^{2+}$ doped $TiO_2$ powders, containing a small amount of anatase phase, showed excellent photo-oxidative ability in 4CP decomposition because of relative decreases in electron-hole recombination and poisoning of $TiO_2$ surface during the photoreaction.n.