• Journal of Korean Society for Atmospheric Environment
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• v.32 no.1
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• pp.9-20
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• 2016

Ozone has been a problem in big cities. That is secondary air pollutant produced by nitrogen oxide and VOCs in the atmosphere. In order to solve this, the first to be the analysis of the $NO_x$ and VOCs. The main source of nitrogen oxide is the road mobile. Industrial sources in Seoul are particularly low, and mobile traffics on roads are large, so 45% of total $NO_x$ are estimated that road mobile emissions in Seoul. Thus, it is necessary to clarify the relation with the activity of road mobile source and $NO_x$ concentration. In this study, we analyzed the 4 locations with roadside automatic monitoring systems in their center. The V.K.T. calculating areas are set in circles with 50 meter spacing, 50 meter to 500 meter from their center. We assumed the total V.K.T. in the set radius affect the $NO_x$ concentration in the center. We used the hourly $NO_x$ concentrations data for the 4 observation points in July for the interference of the other sources are minimized. We used the intersection traffic survey data of all direction for construction of the V.K.T. data, the mobile activities on the roads. ArcGIS application was used for calculating the length of roads in the set radius. The V.K.T. data are multiplied by segment traffic volume and length of roads. As a result, the $NO_x$ concentration can be expressed as linear function formula for V.K.T. with high predictive power. Moreover we separated background concentration and concentrations due to road mobile source. These results can be used for forecasting the effect of traffic demand management plan.

• Asian Journal of Atmospheric Environment
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• v.9 no.2
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• pp.146-157
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• 2015

Emissions of ozone precursors ($NO_x$ and VOCs) and photochemical ozone creation potentials (POCPs) of VOC emission sources were investigated in the largest port city (i.e., Busan), Korea during the year 2011. This analysis was performed using the Clean Air Policy Support System (CAPSS) national emission inventory provided by the National Institute of Environmental Research (NIER), Korea. For $NO_x$, the emissions from off-road mobile sources in Busan were the most dominant (e.g., $31,202ton\;yr^{-1}$), accounting for about 60% of the total $NO_x$ emissions. The emission from shipping of off-road mobile sources (e.g., $24,922ton\;yr^{-1}$) was a major contributor to their total emissions, amounting to 47% of the total $NO_x$ emissions due to the port-related activities in Busan. For VOCs, the emission source category of solvent usage was predominant (e.g., $36,062ton\;yr^{-1}$), accounting for approximately 82% of the total VOC emissions. Out of solvent usages, the emission from painting was the most dominant ($22,733ton\;yr^{-1}$), comprising 52% of the total emissions from solvent usages. The most dominant VOC species emitted from their sources in Busan was toluene, followed by xylene, butane, ethylbenzene, n-butanol, isopropyl alcohol, and propane. The major emission sources of toluene and xylene were found to be painting of coil coating and ship building, respectively. The value of POCP for the off-road mobile source (61) was the highest in ten major activity sectors of VOC emissions. Since the POCP value of ship transport of off-road mobile source (72) was also high enough to affect ozone concentration, the ship emission can play a significant role in ozone production of the port city like Busan.

• Journal of Korean Society for Atmospheric Environment
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• v.15 no.E
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• pp.29-38
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• 1999

This study identified emission sources and emissions of air pollutants such as volatile organic compounds (VOCs), solvents, and acid gases produced from chemical plants. We collected air samples from various processes, reactors and facilities using VOC detectors and workers' experience. We identified chemical structures and emission concentrations of air pollutants. We analyzed total emissions of air pollutants emitted from the chemical plants. Also, we developed some emission reduction technologies based on chemical types and emission situations of the identified air pollutants. For reduction of air emissions of acid gases, we employed a method improving solubility of pollutants by reducing scrubber operation temperature, increasing surface area for effective contact of gas and liquid, and modifying or changing chemicals used in the acid scrubbers. In order to reduce air emissions of both amines and acid gases, which have had different emission sources each other but treated by one scrubber, we first could separate gas components. And then different control techniques based on components of pollutants were applied to the emission sources. That is, we first applied condensation and then acid scrubbing method using H2SO4 solution for amine treatment. However, we only used an acid scrubbing method using H2O and NaOH solution for acid gas treatment. In order to reduce air emissions of solvents such as dimethylformamide and toluene, we applied condensation and activated carbon adsorption. In order to reduce air emissions of mixture gases containing acid gases and slovents, which could not be separated in the processes, we employed a combination of various air pollution control devices. That is, the mixture gases were passed into the first condenser, the acid scrubber, the second condenser, and the activated carbon adsorption tower in sequence. In addition, for improvement of condensation efficiency of VOCs, we changed the type of the condensers attached in the reactors as a control device modification. Finally, we could successfully reduce air emissions of pollutants produced from various chenmical processes or facilities by use of proper control methods according to the types and specific emission situations of pollutants.

• Environmental Analysis Health and Toxicology
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• v.21 no.3 s.54
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• pp.219-228
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• 2006

폴리우레탄, 폴리에스테르, 바이페놀, PVC 외 각종 농약 등을 생산하는 울산의 모 화학공장에서, 다양한 종류의 휘발성유기화합물질들(VOCs)이 배출되고 있다. 평균적인 휘발성유기화합물질의 배출 농도는 7283 ppm으로, 톨루엔, 페놀을 포함하여 Trimethyl-pentene, trimethyl-hexene, dimethyl-cyclohexane 등이 검출되었다. Trimethyl-pentene, trimethyl-hexene, dimethyl-cyclohexane등은 인화성이 강하며 화재를 일으킬 위험성이 매우 큰 것으로 알려져 있고, 특히 톨루엔과 페놀의 경우는 호흡이나 피부접촉 등을 통한 인체로의 유입이 있을 경우 유독성을 나타내게 된다. 이러한 VOCs제거를 위하여 겨울철 기간에 파이로트-규모의 바이오필터 적용 실험이 진행되어 졌다. 본 연구의 목적은 바이오필터 운영이 진행되는 가운데 온도, 함수비, 하중, 압력손실 등의 제한요소들이 미디어 내부에서 변화하는 상황에 대한 관찰 및 평가에 있다. 이러한 제한요소들은 바이오필터의 디자인과 오염물질 제거에 심대한 영향을 미치게 된다. 바이오필터는 옥외에 설치되어 총 44일간 운영되어 졌는데, 외부 영하온도의 영향을 최소화하기 위하여, 7cm두께의 파이버-글래스 소재 단열설비가 반응기 외부에 설치되었고 또한 $150^{\circ}C$의 스팀이 바이오필터 반응기와 단열설비 사이에 제공되어 졌다. 바이오필터 반응기 내부에는 23개의 온도 측정 센서와 함수비 센서, 공기샘플포트, 습도계 등이 각기 다른 장소에 설치되어 온도, 함수비 등의 제한요소 영향연구가 진행되었다. 미디어 내부 같은 높이의 서로 반대되는 위치에서 온도차가 13.7도에서 -8.3도까지 차이가 나는 것으로 관찰되었으며, 미디어 높이 위치의 변화에 따라서도 21도에서 2도가지 차이를 나타냈다. 바이오필터 함수비는 실험기간 동안 지속적으로 변화가 발생하였는데, 스팀이 제공되는 동안에는 미디어 함수비가 훨씬 빠른 속도로 증가됨이 관찰되어 졌다.

• Journal of Adhesion and Interface
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• v.20 no.4
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• pp.140-145
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• 2019

In view of environmental considerations, the control of carbon dioxide (CO₂) and volatile organic compounds (VOCs) is one of important issues in the film and coating industries. Therefore, UV-curable system has been developed due to minimize emissions of VOCs and reduce CO₂ emission due to low energy consumption from fast curing. Also, biodegradable polymers economically are attractive because of environmental and economic concerns associated with huge waste plastics. In this study, UV-curable polyurethane acrylates with different compositions of biodegradable polylactide (PLA) diol and poly(ethylene glycol) as diols were synthesized and curing reaction of their end-capped acrylates was performed by UV exposure. Tensile strength, elongation, and Tg of the UV-cured polyurethane acrylates increased with PLA diol content in the diol while their hydrophilicity and thermal stability increased with the PEG content. These results indicated a property of UV-cured polyurethane acrylates could be controlled by environment-friendly diols.

• Applied Chemistry for Engineering
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• v.34 no.3
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• pp.313-317
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• 2023

In this study, the physicochemical characterization and adsorption performance of air pollutants (VOCs, SO₂, and CO₂) were evaluated for the recycling of zeolite used in the ion exchange process. The surface characteristics of the zeolite used were confirmed through Scanning Electron Microscopy (SEM) and X-Ray Diffraction (XRD) analysis, and the composition and specific surface area were measured through X-Ray Fluorescence (XRF) and Brunauer-Emmett-Teller (BET). There was no change in the surface properties of the used zeolite, but the content of potassium and calcium increased and the specific surface area decreased. The toluene, sulfur oxides, and carbon dioxide adsorption performance of the used zeolite was evaluated, and it was confirmed that the performance was improved compared to the fresh zeolite. In particular, for toluene and sulfur oxides, the adsorption amount increased by 2.6 times and 2.3 times, respectively, which might be due to the enhancement of the polymerization reaction and the increase of the base point, according to the composition of the used zeolite.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2003.11a
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• pp.55-58
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• 2003

The ambient concentrations of benzene, toluene, and $\alpha$-/$\beta$-pinene were measured from July, 2002 to August, 2002 at the Gumsung mountain site in Jeonnam province. The mean concentration of benzene for this study was $62.6{\pm}43.9$ pptv (Min. 20.4 ~ Max. 151.2 pptv) , and that of toluene was 619.8 ${\pm}$ 330.2pptv (264.8~1, 386pptv). It was observed that the concentrations of $\alpha$ -pinene and $\beta$ -pinene were $169.0{\pm}97.7$ pptv (72.9~396.1pptv) and $11.2{\pm}27.9$pptv (7.5 ~95.9 pptv) , respectively. The ambient concentrations of aromatic and natural VOCs were found at the pptv level. In this study, the toluenelbenzene ratios were $13.9{\pm}11.2$ , but they were a little higher than those found in the domestic study and approximately 5 times greater than the values in the foreign study. The $\beta$ -/ $\alpha$ -pinene ratios ranged between 0.05 and 0.55, and this range was found to be similar in the foreign study.

• Membrane Journal
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• v.17 no.2
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• pp.99-111
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• 2007

It is impossible to remove toxic organic substances that are recognized as a cancer caused suspicious element in drinking water using the conventional water purification method. This study introduces groundwater into a reaction chamber as an effective amount of water to process this water using a mixed method of AOP oxidation and M/F membrane and purifies it as a desirable level by artificially mixing such toxic substances in order to effectively process the water. Based on this fact, this study configures an optimal operation condition. The VOCs existed in toxic substances was investigated as a term of phenol and toluene, and agricultural chemicals were also investigated as a term of parathion, diazinon and carbaryl. The experiment applied in this study was performed using a single and composite soolution. In the operation condition applied to fully dissolve and remove such substances, the amount of $H_2O_2$ injected in the process was 150 mL of a fixed quantity, the value of pH was configured as $5.5{\sim}6.0$, the temperature was controlled as a range of $12{\sim}16^{\circ}C$, the dissolved amount of ozone was applied more than 5.0 mg/L, the reaction time was determined as an optimal condition, such as $30{\sim}40$ minutes, and the segregation membrane in the same reactor was determined for acquire water drinking of large quantity using a pore size of $0.45{\mu}m$ M/F membrane.

• Journal of Korean Society of Environmental Engineers
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• v.33 no.11
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• pp.790-796
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• 2011

In this study, we measured the concentrations of volatile organic compounds (VOCs) in Shiwha area by using active and passive sampler. We did a comparative analysis of the characteristics of the active sampler and passive sampler. In the case of the passive sampler, the average TVOC concentration of the industrial area was 1.86 times higher than that of the residential area. In the case of the active sampler, the average TVOC concentration of the industrial area was 1.07 times higher than that of the residential area. When using the passive sampler, the concentration of VOCs in the industrial area was noted to be higher than the concentration found in the residential area. However, when we used the thermal desorption tube, the concentration of residential area was higher rather than that of industrial area in some substances such as trichloroethylene, toluene, ethylbenzene, and xylene. Toluene was a larger percentage of the overall BTEX ratio. In case of the passive sampler, the relative ratio of toluene, ethylbenzene, and xylene was higher in the industrial area than in the residential area. In contrast in case of the thermal desorption tube, the ratio of these substances was higher in the residential area rather than in the industrial area. The passive sampling in this study showed an appropriate method to analyze the temporal and spatial concentrations of air contaminants. This assessment would prove to be useful for its observance of standards or epidemical study.

• Journal of Environmental Impact Assessment
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• v.32 no.5
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• pp.353-362
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• 2023

TOC, which can measure more than 90% of organic substances, can be measured quickly and easily,replacing BOD and COD, which were indicators of organic pollutants. According to water quality pollution control standards, when measuring TOC, if the inorganic carbon ratio in the sample is over 50%, the NPOC (Non-Purgeable Organic Carbon) method should be used. If volatile organic compounds (VOCs) are present at a certain concentration, the TC-IC (subtracting inorganic carbon from total carbon) method should be used. To validate the limitations of these analytical conditions, experiments were conducted by varying the ratio of TOC to IC in purified water and measuring the concentration of TOC in test solutions. The results showed no significant difference between the TC-IC method and the NPOC method. When measuring samples with added VOC standard solutions, it was observed that the carbon loss due to purging was not significant when using the NPOC method. Therefore, it is concluded that the choice of analytical method does not lead to significant differences when VOCs are present in the sample. To account for potential variations in results based on water quality pollution control standards and regulations regarding the approval and testing of environmental measurement devices, a comparison of field sample concentration values was made using two widely used types of TOC analyzers in Korea. The results showed variations of 0.02 to 0.83 mg/L between methods depending on the manufacturer, highlighting the need for caution when selecting an instrument.