• 한국환경과학회:학술대회논문집
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• 한국환경과학회 2001년도 가을 학술발표회 발표논문집
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• pp.97-98
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• 2001

Acid Orange 7과 Methyl Orange의 경우, UV 빛을 조사하고 $TiO_2$ powder를 투여하였을 때 120분 이내에 탈색이 완전히 이루어짐으로써 색도를 80% 이상 제거할 수 있었다. 광촉매량이 증가할수록 촉매표면적이 증가하여 광반응 속도의 증가를 가져오나, 과도한 촉매량의 투입은 오히려 UV 빛의 효과적인 투과를 방해함으로써 광반응 속도를 감소시킨 것으로 사료된다. 초기 pH는 반응 속도에 큰 영향을 미치지 못하는 것으로 나타났으며, Orange II는 Methyl Orange보다 초기 pH에 다소 큰 영향을 받았다. 초기 농도가 낮을수록 초기 반응 속도는 증가하여 염료 분해 속도가 빠름을 알 수 있었다.

• 한국진공학회지
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• 제21권3호
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• pp.158-163
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• 2012

본 연구에서는 폴리머 애자의 자가세정 코팅을 위한 소재로써 $TiO_2$ 박막을 실리콘과 유리, 폴리머애자 기판위에 증착하였다. $TiO_2$ 박막은 $TiO_2$ 세라믹 타겟이 부착된 RF 마그네트론 스퍼터링 장치를 이용하여 증착하였다. $TiO_2$ 박막은 스퍼터링의 다양한 공정조건 중 RF 파워의 크기에 따라 100 nm의 두께로 증착하였다. RF 파워에 따라 증착되어진 $TiO_2$ 박막의 접촉각, 표면거칠기등 표면 특성을 확인하였으며, UV-visible등 광학적 특성을 고찰하여, 구조적 특성과의 관계를 고찰하였다.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2003년도 춘계학술대회
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• pp.1881-1884
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• 2003

In this experiment, the oxidations of p-Xylene (140-180 ppmv), one of the air pollutants as a VOC, using $UV/TiO_2$ photocatalyst is studied. In order to increase the specific surface area, the filter is coated by nano $TiO_2$ particles. The photodegradation system consists of a VOCs generator, a photocatalyst filter and a measuring equipment. Illumination is generally provided by two of 20 W black light lamps with 380 nm of wavelength. The filter coated by nano $TiO_2$ particles has a passing efficiency over 80% but a pressure drop of 9.0 $mmH_2O$ at 0.45 cm/s. The filter endurance is better than activated carbon at the same pressure drop.

• Advances in nano research
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• 제15권4호
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• pp.295-304
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• 2023

In this paper, a powerful photocatalyst based on carbon nanocomposite is developed in order to obtain a new material applicable in water treatment and especially for the discoloration of effluents used in the textile industry. For that, TiO₂-graphene nanocomposites have been successfully synthesized by a mixture of Functionalized Graphene Sheet (FGS) and tetrachlorotitanium complexes to form FGS-TiO₂ nanocomposite. In the presence of an anionic surfactant, we used a new chemical process to functionalize graphene sheets in order to make them an excellent medium for blocking and preventing the aggregation of TiO₂ nanoparticles. The components of these nanocomposites are characterized by means of X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM), which confirms the successful formation of the FGS-TiO₂ nanocomposite. It was found that the TiO₂ nanoparticles were dispersed uniformly on the graphene plane which possesses better charge separation capability than pure TiO₂. The FGS-TiO₂ nanocomposites exhibited higher photocatalytic activity compared to pure TiO₂ for the removal of three dyes: such as Methylene Blue (MB), Bromophenol Blue (BB) and Alizarin Red-S (AR) in water. The removal process was fast and more efficient with FGS-TiO₂ nanocomposite in daylight (in the absence of UV irradiation) compared to pure TiO₂ nanoparticles without and under UV in all pH range.

• KSBB Journal
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• 제23권1호
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• pp.83-89
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• 2008

음식물쓰레기를 처리하기 위한 3단계 메탄발효시스템으로부터 유출되는 음식물 발효 폐액은 고농도 유기성 폐수이다. 유기성 폐수는 고도처리 시스템에 의해 방류기준에 적합하게 처리되어져야만 한다. 본 연구에서는 유기성 폐수를 처리하기 위해 고효율 $UV/TiO_{2}$ 광촉매 산화공정의 최적 운전 조건을 조사하였다. 첫 번째 공정에서 폐수에 응집제인 $FeCl_{3}$를 전처리 하였으며, 응집을 위한 최적 pH와 응집제의 농도는 각각 pH 4와 2000 mg/L이었다. 이 공정을 통하여 최대 52.6%의 COD가 제거되었다. 두 번째는 $UV/TiO_{2}$ 광촉매 산화공정으로, 최적 운전 조건은 중심파장이 254 nm, 폐수 온도 및 pH가 각각 $40^{\circ}C$와 pH 8, 반응기 주입 공기량이 40 L/min인 것으로 조사되었다. 응집제를 이용한 전처리 공정과 광촉매 산화공정을 병합하여 최적조건에서 폐수를 처리할 경우 T-N과 COD의 제거율은 각각 69.7%와 70.9% 이었다.

• Bulletin of the Korean Chemical Society
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• 제34권7호
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• pp.2056-2062
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• 2013

The dihydroxy naphthalene/$TiO_2$ complexes with different substitution patterns were prepared by surface modification. X-ray diffraction, UV-Vis spectroscopy, photoluminescence, and X-ray photoelectron spectroscopy were used to characterize the prepared composite materials. The results indicated that the surface modification did not influence the crystallization of $TiO_2$. The visible-light absorbances of prepared dihydroxy naphthalene/$TiO_2$ complexes could be assigned to the ligand-to-metal charge transfer. The obtained catalyst exhibited outstanding photocatalytic activity and stability under visible light. A linear relationship existed between the percentages of hydroxynaphthalenes coordinated on $TiO_2$ surface and $H_2$ production ability. The substitution pattern of dihydroxy naphthalene and $CH_3OH$ content could also influence the photocatalytic performance remarkably. The photocatalytic $H_2$ production ability was further improved after loading with ultra low concentration of Pt, 0.02 wt %. The possible mechanism was proposed.

• 산업기술연구
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• 제21권B호
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• pp.21-26
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• 2001

In this study, the effects of crystalinity, composition and particle size of $TiO_2$ catalysts on the degradations of humic acid in aqueous solution was assessed using the commercially avaliable $TiO_2$ particles. Photocatalytic oxidations of humic acid (HA, Aldrich Co.) solution were carried out in case of adding different types of $TiO_2$ catalysts and their decomposition efficiencies were analyzed with respect to pH, DOC and UV absorbances values for the HA solutions and compared one another. The experimental results showed that $TiO_2$ particles(Degussa P-25) mixed with anataze and rutile gave the highest degradation efficiencies, respectively and much lower degradation efficiency in $TiO_2$ paticles of rutile only type. In comparing among ST series of anataze types, it was observed that the degradation efficiencies generally were increased with increasing $TiO_2$ contents and surface area of the particles. Higher degradation efficiency of HA was also found in zeolite type(D-TZ) of $TiO_2$ paticles compared with hydroxyapatite type (D-TH) of $TiO_2$ particles.

• Journal of Applied Biological Chemistry
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• 제49권4호
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• pp.157-161
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• 2006

The performance of abiotic degradation of oxadiazon was investigated by applying zerovalent iron(ZVI), potassium permanganate($KMnO_4$) and titanium dioxide($TiO_2$) in the contaminated water. Experimental conditions allowed the disappearance of oxadiazon in the abiotic system. The degradation of this herbicide was monitored in buffer solutions having pH 3, 5 and 7 in the presence of iron powder in which the maximum degradation rate was achieved at acidic condition(pH 3) by 2% of ZVI treatment. The oxidative degradation of oxadiazon was observed in aqueous solution by $KMnO_4$ at pH 3, 7 and 10 in which the highest disappearance rate was found at neutral pH when treated with 2% of $KMnO_4$. The catalytic degradation of oxadiazon in $TiO_2$ suspension was obtained under dark and UV irradiation conditions. UV irradiation enhanced the degradation of oxadiazon in aquatic system in the presence of $TiO_2$. Conclusively, the remediation strategy using these abiotic reagents could be applied to remove oxadiazon from the contaminated water.

• 한국재료학회지
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• 제11권1호
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• pp.61-66
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• 2001

양극산화법을 이용하여 광촉매 특성을 나타내는 $TiO_2$ 피막을 제조하고 염료의 분해반응을 통하여 광분해 효율을 조사하였다 양극산화법에 의해 제조된 산화피막은 모두 광촉매 분해특성이 있었으며 양극산화의 조건에 따라서 $TiO_2$ 피막의 성장거동과 피막 형태에 차이가 나타났다. 황산용액에서 양극산화된 $TiO_2$ 피막은 불규칙적 인 입자모양으로 anatase와 rutile이 혼합된 조직이었으며, 인산이 첨가된 혼합용액에서 형성된 $TiO_2$는 anatase로 셀 모양의 피막형태로 생성되었다. 광촉매 특성에 적합한 양극산화의 인가 전압은 180V인 것으로 나타났다.

• Bulletin of the Korean Chemical Society
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• 제29권4호
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• pp.785-789
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• 2008

The present study is the first report of utilizing $TiO_2$ photocatalyst to analytically calibrate the hydroperoxyl radical ($HO_2\;^{\cdot}$). An in-situ calibration method of $HO_2\;^{\cdot}$ is proposed for air monitoring by using an 2-methyl-6-(pmethoxyphenyl)- 3,7-dihydroimidazo-[1,2-a]pyrazin-3-one (MCLA)-chemiluminescence (CL) technique. In this method, $HO_2\;^{\cdot}$($pK_a$ = 4.80) is produced by the ultraviolet (UV) photolysis of immobilized $TiO_2$ using a constant flow rate of air equilibrated water, in which $HO_2\;^{\cdot}$ is controlled by using various lengths of knotted tubing reactor (KTR). The principle of the proposed calibration is based on the experimentally determined halflife ($t_{1/2}$) of $HO_2\;^{\cdot}$ and its empirically observed pH-dependent rate constant, $k_{obs}$, at a given pH. The concentration of $HO_2\;^{\cdot}$/$O_2\;^{\cdot}$− is increased as pH increases. This pH dependence is due to the different disproportionative reactivities between $HO_2\;^{\cdot}$/$O_2\;^{\cdot}$− and $HO_2\;^{\cdot}$/$O_2\;^{\cdot}$−. Experimental results indicate the practical feasibility of the approach, producing very promising method.