• Asian Journal of Atmospheric Environment
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• 제6권4호
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• pp.246-258
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• 2012

Particulate matter deposited on leaf surfaces may cause erosion/abrasion of epicuticular wax and the malfunction of stomata. However, the deposition processes of particulate matter, such as elemental carbon (EC), has not been studied sufficiently in Asian forest ecosystems. Deposition processes for particulate ${SO_4}^{2-}$ and EC were studied in a Japanese cedar forest in Kajikawa, Niigata Prefecture, Japan, and in a dry evergreen forest and a dry deciduous forest in Sakaerat, Nakhon Ratchasima province, Thailand. The ${SO_4}^{2-}$ fluxes attributed to rainfall outside the forest canopy (RF), throughfall (TF), and stemflow (SF) showed distinct seasonalities at both sites, increasing from November to February at the Kajikawa site and in March/April at the Sakaerat site. Seasonal west/northwest winds in winter may transport sulfur compounds across the Sea of Japan to the Kajikawa site. At the Sakaerat site, pollutants suspended in the air or dry deposits from the dry season might have been washed away by the first precipitations of the wet season. The EC fluxes from RF and TF showed similar variations by season at the Kajikawa site, while the flux from TF was frequently lower than that from RF at the Sakaerat site. Particulate matter strongly adsorbed onto leaf surfaces is not washed away by rainfall and contributes to the EC flux. At the Kajikawa site, Japanese cedar leaf surfaces accumulated the highest levels of particulate matter and could not be neglected when calculating the total flux. When such leaf-surface particles were considered, the contribution of dry deposition to the total EC flux was estimated to be 67%, 77%, and 82% at the Kajikawa site, and at the evergreen and deciduous forests of the Sakaerat site, respectively. Leaf-surface particles must be included when evaluating the dry and total fluxes of particulate matter, in particular for water-insoluble constituents such as EC.

• Bulletin of the Korean Chemical Society
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• 제35권10호
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• pp.2995-3000
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• 2014

A sensitive concentration method utilising modified gas-purge microsyringe extraction (GP-MSE) was developed. Concentration (reduction in volume) to a microlitre volume was achieved. PAHs were utilised as semivolatile analytes to optimise the various parameters that affect the concentration efficiency. The injection rate and temperature were the key factors that affected the concentration efficiency. An efficient concentration (75.0-96.1%) of PAHs was obtained under the optimised conditions. The method exhibited good reproducibility (RSD values that ranged from 1.5 to 9.0%). The GP-MSE concentration method enhances the volume reduction (concentration factor), leading to a low method detection limit ($0.5-15ngL^{-1}$). Furthermore, this method offers the advantage of small-volume sampling, enabling even the detection of diurnal hourly changes in the concentration of PAHs in ambient air. Utilising this method in combination with GC-MS, the diurnal hourly flux of PAHs from the gas phase of ambient air was measured. Indeed, the proposed technique is a simple, fast, low-cost and environmentally friendly.

• 분석과학
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• 제8권4호
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• pp.731-738
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• 1995

Toxic air pollutants are investigated in a petrochemical industrial park in Taiwan by using a movable open path FTIR. The results show the qualitative and quantitative analysis of emission gases from plants, and also provide the emission rate of different compounds. More than twenty compounds under usual operation are found from this industrial park. The concentration variation with time can be correlated exactly with wind direction. It means that by changing the measuring points, the source of emission can be unambiguously identified. An EPA proved PAL model is applied to estimate the emission rate of either a point or an area source. Local atmospheric stability is determined by releasing the $SF_6$ tracer. The origins of errors come mainly from the uncertainty of source's configuration and the variation of meteorological condition. Through the continuous measurement (half an hour base in this study) of OP-FTIR sensor, the maximum value of emission rate and the annual amount of emission can be derived. The emission rate of the measured toxic gases are derived by the model technique and the results show that the emission amount are in the order of ten to hundred tons per year.

• Environmental Sciences Bulletin of The Korean Environmental Sciences Society
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• 제4권1호
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• pp.31-42
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• 2000

The dry deposition velocities and fluxes of air pollutants such as SO2(g), O3(g), HNO3(g), sub-micron particulates, NO3(s), and SO42-(s) were estimated according to local meteorological elements in the atmospheric boundary layer. The model used for these calculations was the multiple layer resistance model developed by Hicks et al.1). The meteorological data were recorded on an hourly basis from July, 1990 to June, 1991 at the Austin Cary forest site, near Gainesville FL. Weekly integrated samples of ambient dry deposition species were collected at the site using triple-fiter packs. For the study period, the annual average dry deposition velocities at this site were estimated as 0.87$\pm$0.07 cm/s for SO2(g), 0.65$\pm$0.11 cm/s for O3(g), 1.20$\pm$0.14cm/s for HNO3(g), 0.0045$\pm$0.0006 cm/s for sub-micron particulates, and 0.089$\pm$0.014 cm/s for NO3-(s) and SO42-(s). The trends observed in the daily mean deposition velocities were largely seasonal, indicated by larger deposition velocities for the summer season and smaller deposition velocities for the winter season. The monthly and weekly averaged values for the deposition velocities did not show large differences over the year yet did show a tendency of increased deposition velocities in the summer and decreased values in the winter. The annual mean concentrations of the air pollutants obtained by the triple filter pack every 7 days were 3.63$\pm$1.92 $\mu\textrm{g}$/m3 for SO42-, 2.00$\pm$1.22 $\mu\textrm{g}$/m-3 for SO2, 1.30$\pm$0.59 $\mu\textrm{g}$/m-3 for HNO3, and 0.704$\pm$0.419 $\mu\textrm{g}$/m3 for NO3-, respectively. The air pollutant with the largest deposition flux was SO2 followed by HNO3, SO42-(S), and NO3-(S) in order of their magnitude. The sulfur dioxide and NO3- deposition fluxes were higher in the winter than in the summer, and the nitric acid and sulfate deposition fluxes were high during the spring and summer.

• 한국대기환경학회지
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• 제12권1호
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• pp.101-112
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• 1996

Dry and wet deposition is an impertant removal mechanism of the amobient aerosol in the atmospheric environment. Since the deposition flut provides adverse impacts on various encironmental media including aquatic and ecological system as well as human health, it is essential to quantitatively estimate the removal fluxes of many air pollutants. Thus, the purposes of this experimental study are to investigate seasonal deposition flux variations of the total dustfall and various inorganic elements in the local ambient air and then to finally estimate their dry deposition velocities. To perform the study, the total of 90 dustfall samples were collected from January, 1994 thru February, 1995 in 5 different cities of Korea including Seoul, Suwon, Daejon, Kwangju, and Kangrung. Each sample was analyzed by an AAS and an ICP to determine the quantities of the 11 inorganic elements, such as Zn, Cd, Cr, K, Na, Pb, Ca, Fe, Mn, Mi, and Cu. As results, deposition fluxes, soluble/insoluble fractions, and deposition velocities for each element were extensively investigated. The resulting dry deposition velocities of some elements in Suwon were estimated by ranges of 0.57 .sim. 0.87 cm/sec for Zn, 0.35 .sim. 0.45 cm/sec for Pb, 1.25 .sim. 3.52 cm/sec for Ca, 0.21 .sim. 0.48 cm/sec for Fe, 0.95 .sim. 9.31 cm/sec for Mn, and 2.08 cm/sec for Cu.

• 상하수도학회지
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• 제31권6호
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• pp.501-510
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• 2017

In this study, it is estimated that ceramic membrane process which can operate stably in harsh conditions replacing existing organic membrane connected with coagulation, sedimentation etc.. Jar-test was conducted by using artificial raw water containing kaolin and humic acid. It was observed that coagulant (A-PAC, 10.6%) 4mg/l is the optimal dose. As a results of evaluation of membrane single filtration process (A), coagulation-membrane filtration process (B) and coagulation-sedimentation-membrane filtration process (C), TMP variation is stable regardless of in Flux $2m^3/m^2{\cdot}day$. But in Flux $5m^3/m^2{\cdot}day$, it show change of 1-89.3 kpa by process. TMP of process (B) and (C) is increased 11.8, 0.6 kpa each. But, the (A) showed the greatest change of TMP. When evaluate (A) and (C) in Flux $10m^3/m^2{\cdot}day$, TMP of (A) stopped operation being exceeded 120 kpa in 20 minutes. On the other hand, TMP of (C) is increased only 3 kpa in 120 minutes. Through this, membrane filtration process can be operated stably by using the linkage between the pretreatment process and the ceramic membrane filtration process. Turbidity of treated water remained under 0.1 NTU regardless of flux condition and DOC and $UV_{254}$ showed a removal rate of 65-85%, 95% more each at process connected with pretreatment. Physical cleaning was carried out using water and air of 500kpa to show the recovery of pollutants formed on membrane surface by filtration. In (A) process, TMP has increased rapidly and decreased the recovery by physical cleaning as the flux rises. This means that contamination on membrane surface is irreversible fouling difficult to recover by using physical cleaning. Process (B) and (C) are observed high recovery rate of 60% more in high flux and especially recovery rate of process (B) is the highest at 95.8%. This can be judged that the coagulation flocs in the raw water formed cake layer with irreversible fouling and are favorable to physical cleaning. As a result of estimation, observe that ceramic membrane filtration connected with pretreatment improves efficiency of filtration and recovery rate of physical cleaning. And ceramic membrane which is possible to operate in the higher flux than organic membrane can be reduce the area of water purification facilities and secure a stable quantity of water by connecting the ceramic membrane with pretreatment process.

• 자원리싸이클링
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• 제11권6호
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• pp.3-11
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• 2002

최근 전자산업의 발달로 인하여 폐 인쇄회로기판(PCB) 발생량이 증대되고 있으며 이는 유해물질 및 유가금속을 함유하고 있어 환경오염의 방지 측면 및 유용자원의 회수 측면에 있어서 재활용이 시급하다. 또한, 자동차의 배출가스 내의 대기오염 물질의 저감을 위하여 장착된 자동차 촉매에 백금족 금속이 함유되어 있어 폐기되는 자동차 촉매에서의 유가금속 회수 또한 필요하다. 이러한 유가금속을 회수하기 위하여 본 연구에서는 건식방법의 일종으로 고온처리에 의하여 발생하는 유해물질이 적으며 공정이 매우 안정적이라고 알려진 아크 전기로를 이용한 회수 방안을 고찰하였다. 생석회, 전로슬래그, 동슬래그를 사용하여 용제의 종류에 따른 유가 금속의 회수율을 관찰하였으며 직류 및 교류에 의한 영향 그리고 전류의 방향에 따른 유가 금속의 회수율을 살펴보았다. 용제의 종류에 따른 회수율에 있어서 전로슬래그나 동슬래그를 용제로 사용하는 것이 생석회에 비해 용융회수에 더 유리함을 파악하였다. 폐 PCB에 존재하는 유가 금속의 회수에 있어서 직류 및 교류의 영향에 대한 결과는 전체적으로 직류 기저 消 경우가 높은 회수율을 나타내었으며 이는 자동차 폐촉매의 경우에도 같은 양상이 관찰되었다. 폐기되는 PCB 및 자동차 촉매에서의 유가 금속 회수에 관한 본 연구에서 아크로처리에 의한 유가금속의 회수율은 평균적으로 95～97%정도로 상당히 높은 것으로 관찰되었다.

• 대한기계학회논문집B
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• 제36권2호
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• pp.225-232
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• 2012

희박 예혼합 가스터빈 연소기에서 배출되는 NOx, CO 와 같은 오염물질을 예측하기 위해서 화학반응기 네트워크 모델을 개발했다. 본 연구에서는 CHEMKIN 코드와 4 가지 NO 생성 메커니즘을 포함한 GRI 3.0 메탄-공기 연소 메커니즘을 이용해서 가스터빈의 부하조건을 변화시키며 NOx 및 CO 배출의 예측을 수행하였다. 모델의 검증을 위해서 계산된 결과를 모사연소기의 실험 데이터와 비교하였다. 여러부하조건에 따른 4 가지 NO 경로의 기여도를 조사하였다. 또한 인젝터의 질량유동 및 당량비의 불균일성이 NOx 배출이 끼치는 영향을 고찰하고 10ppm 이하의 저 NOx 연소기 개발을 위한 저감 방법을 제안했다.

• 방사성폐기물학회지
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• 제18권2_spc호
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• pp.327-336
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• 2020

HANARO (High-flux Advanced Neutron Application Reactor)는 우라늄의 핵분열 연쇄반응에서 생성된 중성자를 이용하여 다양한 연구개발을 수행하는 열출력 30 MW 규모의 연구용 원자로이다. 탈기탱크는 HANARO의 부속시설에 설치되어 있다. 탈기탱크는 내부환경요인으로 인해 기체오염물질을 발생시킨다. 탈기탱크는 기체오염물질을 허용 가능한 수준 이하로 유지하기위해 필요하며 기체시료채취판넬의 분석기에 의해 모니터링 된다. 응축수가 발생하여 기체시료채취판넬의 분석기 내부로 유입된다면, 분석기의 측정 챔버 내부에 부식이 발생하여 고장을 야기한다. 응축수의 생성 원인은 탈기탱크에 존재하는 기체가 분석기로 유입되는 과정에서 탈기탱크와 분석기사이 온도 차이다. 응축수 생성을 억제하고 계통 내부에 생성된 응축수를 효율적으로 제거하기 위해 탈기탱크와 기체시료채취판넬 사이에 히팅시스템이 설치되었다. 이 연구에서 우리는 히팅시스템의 효율성을 알고자 한다. 또한 Wall Condensation Model을 이용하여 유체 입구온도, 외부온도 및 히팅 케이블 설정온도 변화에 따른 파이프 온도와 평균응축량의 변화를 모델링하였다.

• 한국환경과학회지
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• 제11권6호
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• pp.489-496
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• 2002

The purpose of this study was to investigate spatial distributions of total deposition. A total number 79 samples were collected at 17 sampling sites from September 1999 to January 2000. Total (=wet+dry) atmospheric depositions were collected by filtered deposition sampler at sampling site (the Western Part of Kyongsangnam Province). In addition, the deposition of soluble and insoluble fraction was also investigated to find a suitable simplified collection method for a long-term monitoring of total deposition. The total depositions were measured soluble amount(mm/month), insoluble amount(kg/km$^2$/month), pH, conductivity(E.C.) and eight ionic components. The spatial distribution of deposition flux was to estimated by using a kringing analysis. The 17 sites mean fluxes of water soluble ionic components; SO$_4$$\^$2-/, Cl$\^$-/, NO$_3$$\^$-/, Na$\^$+/, NH$_4$$\^$+/, K$\^$+/, Mg$\^$2+/, Ca$\^$2+/ were 100.7∼315.6kg/km$^2$/month, 30.1∼234.3kg/km$^2$/month, 64.4∼ 139.4kg/km$^2$/month, 7.5∼68.3kg/km$^2$/month, 10.7∼48.7kg/km$^2$/month, 5.6∼27.9kg/km$^2$/month, 4.5∼17.5kg/km$^2$/month, 27.6∼81.7kg/km$^2$/month, respectively.