• 한국대기환경학회지
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• 제32권4호
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• pp.422-434
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• 2016

This study was conducted to understand roles of $NO_x(=NO+NO_2)$ on high $O_3$ episodes at an urban monitoring station in Seoul. Concentrations of NO, $NO_2$, $NO_y$ and $O_3$ were measured intensively at KIST monitoring station which located at urban center in Seoul metropolitan area during May 18~June 13, 2015. Sampling period was planed because high $O_3$ and PM occurred frequently during from late spring to early summer months in Seoul. The experimental site locates in NW from center of Seoul and is surrounded by residential area. Belt highway of the city runs from north to west side nearby experimental site. Vehicle exhaust emissions due to heavy traffic influenced $NO_x$ concentration at the site during northwesterly wind. Specific $NO_2$ concentration was measured by Blue Light photolytic converter, and it was compared to $NO_2$ concentration measured by molybedenum converter. $[NO_2]_{phtolysis}$ was usually lower than $[NO_2]_{molybedenum}$ during the experiment period; however their diurnal variations were very similar. The linear relationship between these $NO_2$ concentrations was found to be $[NO_2]_{phtolysis}$=0.64 $[NO_2]_{molybedenum}$ - 2.6, $r^2$=0.83 during May 16~8, 2015. The difference between $NO_2$ by molybdenum converter and by photolytic converter (${\Delta}NO_2=[NO_2]_{molybedenum}-[NO_2]_{phtolysis}$) accounted for residual $NO_y$ which can represent $NO_z$ (=$NO_y-NO_x$). $O_3$ concentration showed typical daily trend which has maximum at late afternoon and minimum during the night. $O_3$ increased at a rate of 7 ppb/hr since 8 am. and reached the maximum concentration (~80 ppb) at 3 pm.. The diurnal pattern of $O_3$ was inversely related with that of $NO_2$, suggesting that the formation of $O_3$ was the result of photochemical activity of $NO_2$.

• 한국대기환경학회지
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• 제30권5호
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• pp.504-509
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• 2014

Twenty-five stations of the urban monitoring network in Seoul were assessed with a focus on surveillance function of the exceedances of 8-hour ozone and 24-hour $PM_{10}$ standards. The two standards were selected because their attainment rates were particularly low. Two hierarchical cluster analyses were performed to group stations with similar atmospheric environments-one using daily highest 8-hour [$O_3+NO_2$], 8-hour $O_3$ concentrations plus corresponding 8-hour $NO_2$ concentrations considering the interconversion of $O_3$ and $NO_2$, and the other using 24-hour $PM_{10}$ concentrations. An index to measure higher concentration and exceedances of the standards was introduced. Within a cluster, sufficiently high score was assigned to the trends station or the station with higher index. Scores for $O_3+NO_2$ and $PM_{10}$ of a given station were added and ranked in the descending order to determine the relative importance.

• 한국전기전자재료학회논문지
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• 제37권1호
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• pp.68-73
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• 2024

In this study, the praseodymium-doped yttrium phosphate (YPO₄:Pr³⁺) powder, which is well known for its high luminescent efficiency, and long life in the UV range, was synthesized with various content ratios of Pr₆O₁₁ and calcination temperature. Crystal structure and luminescent properties of various phosphor powders based on different concentrations and calcination conditions were characterized by XRD (X-Ray Diffraction) and PL (photoluminescence) spectrometers. From the XRD analysis, the structure of YPO₄:Pr³⁺ which is calcinated at 1,200℃ was stable tetragonal phase and crystal size was calculated about 25 nm by Scherrer equation. PL emission of YPO₄:Pr³⁺ with a different content ratio of Pr₆O₁₁ by excitation λ_exc=250 nm shows that 0.75 mol% phosphor powder has maximum PL intensity and PL decreases with the increase of the ratio of Pr₆O₁₁ up to 1.25 mol% which is caused by changes of crystallinity of phosphor powders. With increasing dopant ratio, photo-luminescence Emission decreases due to Concentration quenching, which is commonly observed in phosphors. Currently, 0.75 mol% is considered the optimal doping concentration. A hybrid ultraviolet-emitting device incorporating YPO₄:Pr³⁺ fluorescent material with plasma discharge was fabricated to enhance UV germicidal effects while minimizing ozone generation. UV emission from the plasma discharge device was shown at about 200 nm and 350 nm which caused additional emission of the regions of 250 nm, 315 nm, and 370 nm from the YPO₄:Pr³⁺ phosphor.

• 대한환경공학회지
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• 제29권5호
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• pp.556-563
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• 2007

고전압 방전극이 기체상에 위치하고 접지 전극이 수중에 설치된 기체-액체 혼합 방전에 의한 화학적 활성종의 발생 특성에 관해 실험실 규모 실험을 수행하였다. 실험된 전극 구조는 기존의 연구에서 사용해왔던 일반적 전극 배열에서보다 높은 전계 강도(electric field strength)를 형성하고 짧은 폭을 지닌 펄스들을 생성시킴으로써 방전에 의해서 일어나는 화학반응의 에너지 효율성을 높일 수 있는 것으로 나타났다. 방전에 의해 기체상에 생성되는 오존 농도는 실험된 전압 범위의 중간 값인 45 kV 조건에서 가장 높은 것으로 관찰되었다. 용액 전도도가 낮을수록 액체상을 통한 전기 저항이 증가하여 기체상에서 높은 전계 강도가 형성되므로 오존 생성을 촉진시키는 것으로 나타났다. 인가전압이 증가할수록 높은 전계 강도가 형성되어 강한 방전이 이루어지므로 과산화수소 생성속도가 증가하는 것으로 나타났다. 낮은 전압에서는 용액 전도도가 증가하면 과산화수소 분해속도가 증가하기 때문에 과산화수소 생성 속도가 감소하며 높은 전압에서는 용액 전도도가 증가하면 자외선 조사 등에 의해 과산화수소 발생의 중간 생성물인 OH 라디칼의 발생이 촉진되므로 과산화수소 생성 속도가 증가하는 것으로 나타났다. 산소와 아르곤의 혼합기체가 공급될 때, 강하고 안정한 방전이 이루어져 과산화수소 생성속도가 증가하는 것으로 나타났다.

• 대한환경공학회지
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• 제27권10호
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• pp.1108-1113
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• 2005

본 연구는 1,4-dioxane을 함유한 폐수를 $O_3/H_2O_2$ 고급산화공정에서 1,4-dioxane의 제거율 및 생물학적분해 가능성을 실험하였다. 산화공정에 사용한 반응기는 bubble column 형태이며, 초기 pH 및 과산화수소의 초기농도를 달리하여 14-dioxane의 제거특성을 실험하였다. $H_2O_2$의 초기농도는 $40{\sim}120\;mg/L$로 조절하였으며, 초기 pH는 6과 9로 조절하여 산화반응에 의한 1,4-dioxane의 제거율 및 $BOD_5$, TOC 등을 분석하였다. 실험 결과 동일한 초기 pH에서 $H_2O_2$의 초기농도가 높을수록 1,4-dioxane의 제거율은 증가하였다. 오존의 소비량과 과산화수소의 초기농도 사이에는 직선적인 제거율을 나타내었으며, 이러한 이유는 높은 초기 $H_2O_2$ 농도에서 hydroxyl radical($OH{\cdot}$) 및 hydroperoxy ions(${HO_2}^-$)의 생성을 가속화 시킨 것에 기인한다고 판단되었다. $O_3/H_2O_2$ 고급산화공정에서 과산화수소의 초기농도는 1,4-dioxane의 제거와 생물학적 분해가능성을 높이는 것으로 관찰되었다.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2017년도 9th Asian Crop Science Association conference
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• pp.45-45
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• 2017

The Indian meal moth, Plodia interpunctella, is one of the most important pests of stored food in the food processing industry worldwide. To control the Indian meal moth, methyl bromide, phosphine, high carbon dioxide, sulfuryl fluoride and plant essential oil fumigation have been considered. However, these treatments have disadvantages. For example, depleting the ozone layer, showing resistance in insect, low control efficacy or need high cost for treatment. Chlorine dioxide ($ClO_2$) is strong disinfectant and insecticide. The gas caused a malfunction in enzymes. The oxidative stress induced by $ClO_2$ gas treatment damaged to a physiological system and all life stages of P. interpunctella. The gaseous $ClO_2$ is a convincing alternative to methyl bromide for controlling P. interpunctella. The gaseous $ClO_2$ was generated by a chlorine dioxide generator (PurgoFarm Co., Ltd., Hwasung, Korea). It generated highly pure $ClO_2$ gas and the gas blown out through a vent into a test chamber. Gas entry to the chamber was automatically controlled and monitored by a PortaSene II gas leak detector (Analytical Technology, Collegeville, PA, USA). The properly prepared eggs, larvae, pupae, and adults of P. interpunctella were used in this experiment. Data were analyzed using SAS 9.4. Percentage data were statistically analyzed after arcsine-root transformation. Analysis of variance was performed using general linear model, and means were separated by the least significant difference test at P < 0.05. Fumigation is an effective management technique for controlling all stages of P. interpunctella. We found that $ClO_2$ gas treatment directly effects on egg, larvae, pupae and adults of P. interpunctella. The gas treatment with proper concentration for over a day achieved 100 % mortality in all stages of P. interpunctella and short time treatment or low concentration gas treatment results showed that the egg hatchability, pupation rate, and adult emergency rate were lowered compare with untreated control. Also, abnormal pupae or adult rate were increased. Gaseous $ClO_2$ treatment induced insecticidal reactive oxygen species (ROS), and it resulted in fatal oxidative stress in P. interpunctella. Taken together, these results showed that exposure proper concentration and time of the gas control all stages of P. interpunctella by inducing fatal oxidative stress. Further studies will be required to apply the gas treatment under real-world condition and to understanding physiological reaction in P. interpunctella caused by oxidative stress.

• 대한환경공학회지
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• 제22권7호
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• pp.1253-1261
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• 2000

천연유기물질은 지표수와 지하수내 탁도를 유발하고 humic (humic acid와 fulvic acid)과 nonhumic 성분으로 구성된다. 일반적으로 NOM은 소독부산물(DBP) 전구물질로써 수처리시 관심의 대상이 된다. 원수의 특성은 정수공정의 선택과 적용에 중요한 정보를 제공한다. 수원에 따른 NOM의 상당한 차이가 다양한 원수들 사이에서 관찰되었고, 문제시되는 NOM을 제거하고 전환시키기 위한 목적으로 정수공정을 적용한다. 본 연구의 결과, 산화처리에 의해 전체 DOC 농도의 변화는 거의 없었지만, 고분자의 소수성 물질이 저분자의 친수성 물질로 전환되었고, 염소보다 오존의 경우 그 산화력의 차이 때문에 SUVA 값의 감소가 더 크게 나타났다. 응집처리에 의해 hydrophilic 성분보다 분자량이 더 큰 hydrophobic 성분이 응집 침전되어 훨씬 잘 제거되었다. THMFP는 50% 정도까지 제거되었는데, 이것은 상대적으로 THMFP를 잘 유발시킨다는 humic acid 성분의 제거가 원활하게 일어났기 때문이다.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제48권3호
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• pp.215-220
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• 1999

$SO_2$and CO gas removal characteristics of a wire-to-cylinder type nonthermal discharge plasma reactor in various applied voltage (-dc, ac, fast rising pulse and high frequency pulse) and a crossed dc magnetic field have been investigated. The experiment has been emphasized on the oxidizing characteristics of $SO_2$ and CO gas by $O_3$ and the applying of a crossed magnetic field, which would induce the cyclotronic and drift motions of electrons making the residual time longer in the removal airgap space. And it also would enhance the energy of electrons and the electrophysicochemical actions to remove the pollutant gases effectively. It is found thatthe corona onset voltage and the breakdown voltage were decreased with increasing the crossed magnetic field and decrease initial fed $SO_2$and CO concentration. As a result, a higher ozone generation and $SO_2$ and CO gas removal rate of 20[%] can be obtained with -dc, ac and fast rising pulse corona discharges in the crossed dc current-induced magnetic field. But high frequency pulse didn't show effect in applying of a crossed magnetic field.

• 상하수도학회지
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• 제21권1호
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• pp.13-25
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• 2007

The water treatment plants in Seoul Metropolitan Area, which are under Korea Water Resources Corporation(KOWACO)'s management, take water from Paldang Reservoir in Han River System for drinking water supply. There are taste and odor (T&O) problems in the finished water because the conventional treatment processes do not effectively remove the T&O compounds. As part of countermeasures for taste and odor control, KOWACO is planning to introduce advanced water treatment process such as ozone and GAC in near future. This study evaluated the removal characteristics of T&O and dissolved organic matter (DOM) to find design and operation parameters of advanced water treatment processes in a pilot-scale treatment plant. The GAC adsorption capacity for DOC in the two GAC system (GAC and $O_3$-GAC) at an EBCT of 14min was mostly exhausted after 9months. The differency of the removal efficiency of DOC between $O_3$-GAC and GAC increased with increasing operation time because the bioactivity in $O_3$-GAC process was enhanced by post-ozone process. Removal by conventional treatment was unable to reach the target TON(threshold odor number) of 3 but GAC systems at an EBCT(empty bed contact time) of 14 min were able to archive the target with few exception. During the high T&O episodes, PAC as a pretreatment together with GAC could be useful option for T&O control. However, substantial TON removal continued for more than two year (> 90,000 bed volumes). At the spiking of less concentration 26 to 61 ng/L in the influent of GAC systems, GAC absorber and $O_3$-GAC processes could meet the treatment target. The better spike control after 12 and 19 months of operation compared to that after 7 months of operation is a strong indication of biological control. The results presented in this study had shown that $O_3$-GAC process was found to be more effective for T&O control than GAC process. And the main removal mechanism in GAC systems were adsorption capacity and biodegradation.

• 한국대기환경학회지
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• 제21권6호
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• pp.689-697
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• 2005

Hydrogen peroxide is a reservoir of OH radical which is the powerful oxidant in the atmosphere. Therefore, the status of the oxidizing atmosphere could be reflected on the concentration of $H_{2}O_{2}$. In this study, the distribution of $H_{2}O_{2}$ was determined during the intensive aircraft measurements over the Yellow sea in March, December 2002, April, November 2003 and March, October 2004. Flights covered from $124^{circ}E\;to\;129^{circ}E\;and\;35^{circ}N\;to\;37^{circ}N$, and extending to 3,000 m. The flight patterns were set properly to assess the altitudinal and longitudinal distribution for $H_{2}O_{2}$. $H_{2}O_{2}$ was extracted onto aqueous solution using a continuously flowing glass coil and analyzed by a high performance liquid chromatography (HPLC) accompanied with a fluorescence detector using postcolumn enzyme derivatization. Mixing ratios of $O_{3},\;NO_{x}\;and\;SO_{2}$ were measured in real time by commercial analysis instruments. Along the heights, the maximum concentration of $H_{2}O_{2}$ appeared around 1,500 m then gradually decreased with increasing altitude. The vertical behavior of ozone showed the similar trend to $H_{2}O_{2}$. The mean mixing ratio of $NO_{x}$ was about 2 ppbv and not showed clear vertical distribution patterns. The mean value of was the same as $NO_{x}$ however $SO_{2}$ appeared extreme concentration in low altitude. $H_{2}O_{2}\;and\;O_{3}$ showed even longitudinal distribution however $NO_{x}$ mixing ratio in land ($127^{circ}E$) was much higher than over the sea. $SO_{2}$ rather decreased with increasing longitude. $H_{2}O_{2}$ was in inverse proportion to $NO_{x}$ in spring and summer and $SO_{2}$ in spring, which indicated its significant role to NO and $SO_{2}$ oxidation pathways.