• 공업화학
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• 제20권1호
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• pp.87-93
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• 2009

팔라듐 금속을 활성탄과 알루미나에 담지시켜 Pd/AC (Pd/활성탄), Pd/AO (Pd/알루미나) 촉매를 제조하고, 오존/촉매공정에 적용하여 담지체의 종류에 따른 촉매 특성을 비교하였다. 담지체를 달리한 촉매 일정량을 오존포화수에 투입하고 오존분해능을 비교해 본 결과, 담지체의 종류에 따른 효율의 변화는 없었다. 오존단독공정과 Pd/AC, Pd/AO 촉매를 이용한 오존/촉매공정에서 dichloroacetic acid (DCAA)의 분해율 및 산화특성(TOC, $COD_{Cr}$)을 비교해 본 결과, 오존/촉매공정의 제거효율이 높았으며, 담지체에 따른 특성변화는 거의 없었다. DCAA 농도를 일정하게 하고 오존공급량을 변화시켜 제거율을 확인한 결과, 어느 수준까지는 오존공급량 증가에 따라 제거율이 상승하였지만, 1.0 L/min 이상의 오존공급량에서는 공급량에 비례하여 제거율이 상승하지 않았다. 이러한 원인은 DCAA의 완전산화에 의해 생성된 중탄산염과 분해과정에서 발생된 염소이온이 하이드록실 라디칼(${\cdot}OH$)의 스케빈저(scavenger)로 작용한 것 같았다.

• Environmental Engineering Research
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• 제11권2호
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• pp.84-90
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• 2006

UV-catalytic oxidation technique was applied for the treatment of bio-refractory character of the leachate, which is generally present in the form of adsorbable organic halogens (AOX). Destruction of AOX was likely to be governed by pH adjustment, quantitative measurement of oxidants, and the selection of oxidation model type. Peroxide induced degradation ($UV/H_2O_2$) facilitated the chemical oxidation of organic halides in acidic medium, however, the system showed least AOX removal efficiency than the other two systems. Increased dosage of hydrogen peroxide (from 0.5 time to 1.0 time concentration) even did not contribute to a significant increase in the removal rate of AOX. In ozone induced degradation system ($UV/O_3$), alkaline medium (pH 10) favored the removal of AOX and the removal rate was found 11% higher than the rate at pH 3. Since efficiency of the $UV/O_3$ increases with the increase of pH, therefore, more OH-radicals were available for the destruction of organic halides. UV-light with the combination of both ozone and hydrogen peroxide ($UV/H_2O_2$ 0.5 time/$O_3$ 25 mg/min) showed the highest removal rate of AOX and the removal efficiency was found 26% higher than the removal efficiency of $UV/O_3$. The system $UV/H2O_2/O_3$ got the economic preference over the other two systems since lower dose of hydrogen peroxide and relatively shorter reaction time were found enough to get the highest AOX removal rate.

• 공업화학
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• 제28권2호
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• pp.193-197
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• 2017

본 연구에서는 대형 직화구이 음식점으로부터 배출되는 유증기 및 미세먼지 제거를 위해 습식 플라즈마 전기집진 공정을 적용할 경우, 집진공정 후단에서 나오는 잔여 오존을 활용하여 제거되지 않은 아세트알데히드와 오존을 제거함으로써 복합악취를 저감할 수 있는 오존 산화 촉매 공정을 개발하였다. 망간산화물 기반 촉매는 분말 촉매 제조 후 압출하여 펠렛 형태로 성형하였으며, 성형촉매 상에서 아세트알데히드와 오존 모두 높은 제거율을 나타낼 수 있도록 최적 조건을 도출하고자 하였다. 제조한 $Mn_2O_3$와 $CuMnO_x$ 촉매는 각각의 성능을 평가하였으며, 이 두 가지 촉매를 2단으로 적용하였을 때 공간속도 $10,000h^{-1}$, 반응온도 $100^{\circ}C$인 조건에서 아세트알데히드는 85% 이상, 오존은 100% 저감시킬 수 있었다.

• 한국환경과학회지
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• 제11권5호
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• pp.419-436
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• 2002

The current paper reports on the enhancement of O$_3$, CO, NO$_2$, and aerosols during the Asian dust event that occurred over Korea on 1 May 1999. To confirm the origin and net flux of the O$_3$, CO, NO$_2$, and aerosols, the meteorological parameters of the weather conditions were investigated using Mesoscale Meteorological Model 5(MM5) and the TOMS total ozone and aerosol index, the back trajectory was identified using the Hybrid Single-Particle Lagrangian Integrated Trajectory Model(HYSPLIT), and the ozone and ozone precursor concentrations were determined using the Urban Ashed Model(UAM). In the presence of sufficiently large concentrations of NO$\sub$x/, the oxidation of CO led to O$_3$ formation with OH, HO$_2$, NO, and NO$_2$ acting as catalysts. The sudden enhancement of O$_3$, CO, NO$_2$ and aerosols was also found to be associated with a deepening cut-off low connected with a surface cyclone and surface anticyclone located to the south of Korea during the Asian dust event. The wave pattern of the upper trough/cut-off low and total ozone level remained stationary when they came into contact with a surface cyclone during the Asian dust event. A typical example of a stratosphere-troposphere exchange(STE) of ozone was demonstrated by tropopause folding due to the jet stream. As such, the secondary maxima of ozone above 80 ppbv that occurred at night in Busan, Korea on 1 May 2001 were considered to result from vertical mixing and advection from a free troposphere-boundary layer exchange in connection with an STE in the upper troposphere. Whereas the sudden enhancement of ozone above 100 ppbv during the day was explained by the catalytic reaction of ozone precursors and transport of ozone from a slow-moving anticyclone area that included a high level of ozone and its precursors coming from China to the south of Korea. The aerosols identified in the free troposphere over Busan, Korea on 1 May 1999 originated from the Taklamakan and Gobi deserts across the Yellow River. In particular, the 1000m profile indicated that the source of the air parcels was from an anticyclone located to the south of Korea. The net flux due to the first invasion of ozone between 0000 LST and 0600 LST on 1 May 1999 agreed with the observed ground-based background concentration of ozone. From 0600 LST to 1200 LST, the net flux of the second invasion of ozone was twice as much as the day before. In this case, a change in the horizontal wind direction may have been responsible for the ozone increase.

• Bulletin of the Korean Chemical Society
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• 제33권1호
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• pp.215-220
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• 2012

ZnO nanoparticles were synthesized through a facile route and were used as ozonation catalysts. With the increase of calcination temperature ($150-300^{\circ}C$), surface hydroxyl groups and catalytic efficiency of asobtained ZnO decreased remarkably, and the ZnO obtained at $150^{\circ}C$ showed the best catalytic activity. Compared with ozonation alone, the degradation efficiency of phenol increased above 50% due to the catalysis of ZnO-150. In the reaction temperatures range from $5^{\circ}C$ to $35^{\circ}C$, ZnO nanocatalyst revealed remarkable catalytic properties, and the catalytic effect of ZnO was better at lower temperature. Through the effect of tertbutanol on degradation of phenol and the catalytic properties of ZnO on degradation of nitrobenzene, it was proposed that the degradation of phenol was ascribed to the direct oxidation by ozone molecules based on solidliquid interface reaction.

• 대한환경공학회지
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• 제36권5호
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• pp.311-316
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• 2014

오존-활성탄 복합공정에 의한 페놀제거 특성과 그에 미치는 운전변수의 영향에 관해 회분식 실험을 통하여 동력학적 연구를 수행하였다. 활성탄은 오존의 자가분해를 촉진시켜 $OH{\cdot}$ 발생시키므로 페놀분해 속도를 증가시키는 것으로 나타났다. 활성탄의 투입량이 증가함에 따라 페놀분해 반응의 유사 일차반응 속도상수가 증가하고 페놀제거의 반감기가 감소하는 것으로 나타났다. 수용액의 pH 증가는 수산화이온이 개시하는 오존분해의 연쇄반응에 의해 $OH{\cdot}$를 생성시키므로 페놀분해 속도를 증가시키는 것으로 나타났다. 페놀의 완전산화 지표인 총유기탄소(TOC) 제거효율은 활성탄을 투입할 때 투입하지 않은 조건보다 약 3.2배 높은 결과를 얻을 수 있었다.

• Journal of Korean Society for Atmospheric Environment
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• 제16권E호
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• pp.39-46
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• 2000

Volatile Organic Compounds (VOCs) are considered as the precursors of atmospheric ozone and photochemical smog formation. In particular, chemical plants have produced a lot of VOCs and thus they have been forced to reduce or remove air emissions from the on-site chemical facilities. For the effective removal of VOCs produced in the chemical plants, the authors employed a titanium oxide(TiO$_2$) mediated photo-catalytic oxidation method. The initiation methods employed in this study to produce oxygen radicals for th photo-catalytic oxidation of the VOCs were Ultra-Violet(UV), Non-Thermal Plasma(NTS), and a combination of Uv and NTP. This study focused on a comparison of the removal efficiencies of VOCs as a function of the initiation method such as NTP and/or UV techniques. Removal efficiency change of VOCs as was investigated as a function of the wavelength of the UV lamp(254, 302, and 365 nm) and the degree of TiO$_2$ coating (10 and 30%). In this study, it was identified that removal efficiencies if the VOCs under the normal air environment were much better than those under the nitrogen gas environment containing small amount of oxygen. Removal efficiency by NTP technique was much better than the UV or the combination of UV and NTP techniques. In a comparison if UV wavelengths employed, it was found that shorter wavelength showed better removal efficiency, compared with longer ones. When the removal efficiencies of VOCs were compared in terms of the degree of TiO$_2$ coating, the higher TiO$_2$coating showed better removal efficiency that the lower TiO$_2$ coating

• 웰빙융합연구
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• 제6권1호
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• pp.17-22
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• 2023

Purpose: VOCs (volatile organic compounds) are all the organic compounds that react with solar rays and increase the concentration of ozone in the troposphere and are partially also known as carcinogens. The adsorption using activated carbon is usually applied to remove VOCs. Research design, data and methodology: The 20 places of surface coating facilities were selected to evaluate the emission amount of VOCs in Seoul. In addition, the removal efficiency of VOCs in 25 places of automobile coating facilities was evaluated. Results: The average emission amount of VOCs was 10.903 kg/hr from automobile coating facilities, while 3.520 kg/hr from other surface coating facilities. The removal efficiency in adsorption with the combustion catalytic process has the mean value of 87.9% and the regeneration efficiency of activated carbon has the mean value of 95.0%. Conclusions: The removal efficiency in adsorption with the biofiltration process has the mean value of 89.8% and the regeneration efficiency of activated carbon has the mean value of 94.8%. The removal efficiency in the plasma catalyst process has the mean value of 79.3%.

• 산업기술연구
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• 제31권B호
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• pp.127-132
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• 2011

Humic substances is accounted for for the largest proportion in natural organic matter(NOM) and NOM is widely distributed in varying concentration in all aquatic and soil. They can affect water quality adversely in several ways by contributing undesirable color, complexing with metal and yielding metal concentrations exceeding normal solubility. Ozonation is one of the efficient treatments for degradation of humic substances which cause some problems in water treatment. Especially, the combination of ozone and granular activated carbon was applied to degradation humic acid in aquatic system. The aim of this work to test the available of acid-treated granular activated carbon as catalyst in the ozonation of humic acid.

• 대한환경공학회지
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• 제33권10호
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• pp.731-738
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• 2011

본 논문에서는 실험실적 규모의 순환형 회분식 반응기에서 수용액상 phenol을 처리하기 위해 $O_3/UV$ radiation, $O_3/Mg(OH)_2/UV$ radiation 그리고 $O_3/MgO/UV$ radiation 고급산화공정(AOPs)에 대한 연구를 수행하였다. 오존의 유량은 1.0 L/min, 오존 농도를 $150{\pm}10mg/L$로 일정하게 유지 하였으며, 산화반응에 나타나는 $COD_{Cr}$ 및 TOC를 각각 측정하였다. $20^{\circ}C$에서 $O_3/UV$ radiation, $O_3/Mg(OH)_2/UV$ radiation 그리고 $O_3/MgO/UV$ radiation에 대한 유사 1차 반응속도 상수는 각각 $9.31{\times}10^{-5}sec^{-1}$, $1.19{\times}10^{-4}sec^{-1}$ 그리고 $1.79{\times}10^{-4}sec^{-1}$, 활성화 에너지는 각각 $3.03kcal{\cdot}mol^{-1}$, $1.79kcal{\cdot}mol^{-1}$ 그리고 $4.23kcal{\cdot}mol^{-1}$ 로 나타났다. 수용액상에서 $Mg(OH)_2$와 MgO가 phenol의 분해와 COD의 제거에 현저한 촉진작용을 나타낸다는 것을 확인하였다. 이러한 실험 결과에 기초하여 $O_3/MgO/UV$ 시스템이 수용액상 phenol을 처리하기 위한 효율적이고 용이한 방법임을 제시하였다.